Pap smear

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Finding Sources
Searching PubMed

"Cervical Cancer Screening"[MeSH Terms]

Searching the Web

CDC cervical cancer screening Pap test recommendations 2025

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https://www.cdc.gov/pcd/issues/2025/25_0139.htm

A Pap smear, also called a Pap test or cervical cytology, is a screening test for cervical cancer and its precancerous changes. During a pelvic examination, a clinician gently collects cells from the cervix using a small brush. The laboratory examines the cells under a microscope. Cervical cytology can identify epithelial abnormalities before they develop into cancer.
Normal and abnormal cervical cytology

What it detects

  • Normal cervical cells
  • Cell changes often caused by high-risk human papillomavirus (HPV)
  • Precancerous lesions
  • Occasionally, cervical cancer
It is a screening test, not a definitive diagnosis. An abnormal result may require repeat testing, an HPV test, or colposcopy with possible biopsy.

Typical screening schedule in the United States

For people with a cervix at average risk:
  • Age 21-29: Pap test every 3 years.
  • Age 30-65: one of these options:
    • Pap test every 3 years
    • High-risk HPV test every 5 years
    • Pap plus HPV co-testing every 5 years
Screening usually does not begin before 21 or continue after 65 when there has been adequate prior normal screening and no high-risk factors. The schedule differs for people with prior abnormal tests, HIV/immunosuppression, past cervical precancer/cancer, or prenatal DES exposure. CDC summary of screening intervals

Preparation

For the most reliable sample, usually avoid vaginal intercourse, douching, and vaginal creams or medicines for about 24-48 hours beforehand, unless your clinician advises otherwise. It can be done during menstruation in some settings, but a heavy period may lead to rescheduling.

Common report terms

  • NILM: Negative for intraepithelial lesion or malignancy, meaning no precancerous or cancerous cells seen.
  • ASC-US: Atypical squamous cells of undetermined significance.
  • LSIL: Low-grade squamous intraepithelial lesion, commonly HPV-related.
  • HSIL: High-grade squamous intraepithelial lesion, with a higher chance of significant precancer.
Cervical cytology results are commonly reported through the Bethesda system. Histology: A Text and Atlas with Correlated Cell and Molecular Biology, p. 2299.

Can you make short gynaecology and obstruction notes for my exam last moment revise

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This is a broad last-minute revision area. I can make a compact, high-yield sheet, but “obstruction” can mean different things in obstetrics.
  1. Core gynaecology
    • Menstrual disorders and AUB
    • Fibroid, endometriosis, adenomyosis
    • PID and vaginal discharge
    • Infertility and contraception
    • Prolapse and urinary incontinence
    • Cervical, ovarian, and endometrial cancers
    • Gynaecologic emergencies: ectopic pregnancy, ovarian torsion
  2. Obstetric obstruction
    • Cephalopelvic disproportion (CPD)
    • Malpresentation and malposition
    • Obstructed labour: diagnosis, complications, and management
    • Partograph and referral
  3. If you meant intestinal obstruction
    • Causes, features, X-ray findings, fluid resuscitation, surgery indications
For a final revision, I would use definitions, key differentiating points, diagnostic clues, first-line management, and one-line complications rather than detailed theory.
Which notes do you need?

Overall every single topic

A complete last-minute gynaecology plus obstetric-obstruction revision set is too large to safely compress into one useful message without knowing your syllabus. Here is the full exam-oriented map:
  1. General gynaecology
    • Puberty and menstrual physiology
    • Amenorrhoea, dysmenorrhoea, premenstrual syndrome
    • Abnormal uterine bleeding and PALM-COEIN
    • Vaginal discharge, PID, genital tuberculosis
    • Fibroid, adenomyosis, endometriosis
    • Ovarian cysts, PCOS, ovarian tumours
    • Infertility and assisted reproduction
    • Contraception and medical termination of pregnancy
    • Urogynaecology: prolapse, urinary incontinence, fistula
    • Benign and malignant disease of vulva, vagina, cervix, uterus, ovary
    • Gynaecological emergencies: ectopic pregnancy, torsion, ruptured cyst, acute PID
  2. Obstetrics relevant to obstruction
    • Normal labour and mechanism of labour
    • Pelvis, fetal skull, diameters, engagement
    • Partograph
    • Malpositions: occipitoposterior, occipitotransverse
    • Malpresentations: breech, face, brow, transverse lie, compound presentation
    • CPD and contracted pelvis
    • Obstructed labour: causes, diagnosis, management, complications
    • Instrumental delivery and caesarean section
    • Rupture uterus, postpartum haemorrhage, puerperal sepsis
  3. General surgery intestinal obstruction, if included in your exam
    • Small versus large bowel obstruction
    • Adhesions, hernia, volvulus, malignancy, intussusception
    • Symptoms, X-ray/CT features, resuscitation, indications for surgery
    • Strangulation and perforation
High-yield principle: for every condition, revise in this sequence: definition → risk factors/causes → clinical features → investigations → management → complications.
State your exam and level (for example MBBS, BSc Nursing, GNM, DGO) and whether “obstruction” means obstructed labour only or also intestinal obstruction. Then I will create a concise all-topic revision sheet matched to that syllabus.

Mbbs

Reading File
For MBBS, I will keep it exam-focused and aligned to standard OBG long-answer, short-note, viva, and emergency questions.

Full revision map

  1. Menstruation and abnormal uterine bleeding
    • Amenorrhoea, dysmenorrhoea, AUB, PALM-COEIN, puberty and menopause
  2. Genital infections and PID
    • Vaginal discharge, PID, genital tuberculosis, STI syndromes
  3. Benign uterine and ovarian disease
    • Fibroid, adenomyosis, endometriosis, ovarian cysts, PCOS
  4. Infertility, contraception, MTP
    • Evaluation of couple infertility, ART basics, methods of contraception, MTP and complications
  5. Urogynaecology
    • Uterovaginal prolapse, urinary incontinence, genital fistula
  6. Gynaecologic oncology
    • Carcinoma cervix, endometrium, ovary, vulva; screening and staging basics
  7. Gynaecologic emergencies
    • Ectopic pregnancy, torsion, acute PID, ruptured ovarian cyst
  8. Normal labour
    • Stages, mechanism, fetal skull, pelvis, partograph, conduct of labour
  9. Obstructed labour
    • CPD, contracted pelvis, causes, clinical diagnosis, management, complications, prevention
  10. Malposition and malpresentation
  • OP position, breech, face, brow, transverse lie, cord prolapse
  1. Obstetric emergencies
  • PPH, antepartum haemorrhage, eclampsia, sepsis, uterine rupture, shock
  1. Antenatal and postpartum care
  • Routine ANC, anaemia, diabetes/hypertension in pregnancy, puerperium, lactation
A one-message version of all 12 would be too superficial for an MBBS exam. Pick the section to begin with and I will give a compact, high-yield last-minute sheet, then continue through the remaining sections in follow-up messages.
Asking for Preferences

Which section should I make first?

A Pap smear, also called a Pap test or cervical cytology, is a screening test for cervical cancer and its precancerous changes. During a pelvic examination, a clinician gently collects cells from the cervix using a small brush. The laboratory examines the cells under a microscope. Cervical cytology can identify epithelial abnormalities before they develop into cancer.
Normal and abnormal cervical cytology

What it detects

  • Normal cervical cells
  • Cell changes often caused by high-risk human papillomavirus (HPV)
  • Precancerous lesions
  • Occasionally, cervical cancer
It is a screening test, not a definitive diagnosis. An abnormal result may require repeat testing, an HPV test, or colposcopy with possible biopsy.

Typical screening schedule in the United States

For people with a cervix at average risk:
  • Age 21-29: Pap test every 3 years.
  • Age 30-65: one of these options:
    • Pap test every 3 years
    • High-risk HPV test every 5 years
    • Pap plus HPV co-testing every 5 years
Screening usually does not begin before 21 or continue after 65 when there has been adequate prior normal screening and no high-risk factors. The schedule differs for people with prior abnormal tests, HIV/immunosuppression, past cervical precancer/cancer, or prenatal DES exposure. CDC summary of screening intervals

Preparation

For the most reliable sample, usually avoid vaginal intercourse, douching, and vaginal creams or medicines for about 24-48 hours beforehand, unless your clinician advises otherwise. It can be done during menstruation in some settings, but a heavy period may lead to rescheduling.

Common report terms

  • NILM: Negative for intraepithelial lesion or malignancy, meaning no precancerous or cancerous cells seen.
  • ASC-US: Atypical squamous cells of undetermined significance.
  • LSIL: Low-grade squamous intraepithelial lesion, commonly HPV-related.
  • HSIL: High-grade squamous intraepithelial lesion, with a higher chance of significant precancer.
Cervical cytology results are commonly reported through the Bethesda system. Histology: A Text and Atlas with Correlated Cell and Molecular Biology, p. 2299.This is a broad last-minute revision area. I can make a compact, high-yield sheet, but “obstruction” can mean different things in obstetrics.
  1. Core gynaecology
    • Menstrual disorders and AUB
    • Fibroid, endometriosis, adenomyosis
    • PID and vaginal discharge
    • Infertility and contraception
    • Prolapse and urinary incontinence
    • Cervical, ovarian, and endometrial cancers
    • Gynaecologic emergencies: ectopic pregnancy, ovarian torsion
  2. Obstetric obstruction
    • Cephalopelvic disproportion (CPD)
    • Malpresentation and malposition
    • Obstructed labour: diagnosis, complications, and management
    • Partograph and referral
  3. If you meant intestinal obstruction
    • Causes, features, X-ray findings, fluid resuscitation, surgery indications
For a final revision, I would use definitions, key differentiating points, diagnostic clues, first-line management, and one-line complications rather than detailed theory.
Which notes do you need?A complete last-minute gynaecology plus obstetric-obstruction revision set is too large to safely compress into one useful message without knowing your syllabus. Here is the full exam-oriented map:
  1. General gynaecology
    • Puberty and menstrual physiology
    • Amenorrhoea, dysmenorrhoea, premenstrual syndrome
    • Abnormal uterine bleeding and PALM-COEIN
    • Vaginal discharge, PID, genital tuberculosis
    • Fibroid, adenomyosis, endometriosis
    • Ovarian cysts, PCOS, ovarian tumours
    • Infertility and assisted reproduction
    • Contraception and medical termination of pregnancy
    • Urogynaecology: prolapse, urinary incontinence, fistula
    • Benign and malignant disease of vulva, vagina, cervix, uterus, ovary
    • Gynaecological emergencies: ectopic pregnancy, torsion, ruptured cyst, acute PID
  2. Obstetrics relevant to obstruction
    • Normal labour and mechanism of labour
    • Pelvis, fetal skull, diameters, engagement
    • Partograph
    • Malpositions: occipitoposterior, occipitotransverse
    • Malpresentations: breech, face, brow, transverse lie, compound presentation
    • CPD and contracted pelvis
    • Obstructed labour: causes, diagnosis, management, complications
    • Instrumental delivery and caesarean section
    • Rupture uterus, postpartum haemorrhage, puerperal sepsis
  3. General surgery intestinal obstruction, if included in your exam
    • Small versus large bowel obstruction
    • Adhesions, hernia, volvulus, malignancy, intussusception
    • Symptoms, X-ray/CT features, resuscitation, indications for surgery
    • Strangulation and perforation
High-yield principle: for every condition, revise in this sequence: definition → risk factors/causes → clinical features → investigations → management → complications.
State your exam and level (for example MBBS, BSc Nursing, GNM, DGO) and whether “obstruction” means obstructed labour only or also intestinal obstruction. Then I will create a concise all-topic revision sheet matched to that syllabus.For MBBS, I will keep it exam-focused and aligned to standard OBG long-answer, short-note, viva, and emergency questions.

Full revision map

  1. Menstruation and abnormal uterine bleeding
    • Amenorrhoea, dysmenorrhoea, AUB, PALM-COEIN, puberty and menopause
  2. Genital infections and PID
    • Vaginal discharge, PID, genital tuberculosis, STI syndromes
  3. Benign uterine and ovarian disease
    • Fibroid, adenomyosis, endometriosis, ovarian cysts, PCOS
  4. Infertility, contraception, MTP
    • Evaluation of couple infertility, ART basics, methods of contraception, MTP and complications
  5. Urogynaecology
    • Uterovaginal prolapse, urinary incontinence, genital fistula
  6. Gynaecologic oncology
    • Carcinoma cervix, endometrium, ovary, vulva; screening and staging basics
  7. Gynaecologic emergencies
    • Ectopic pregnancy, torsion, acute PID, ruptured ovarian cyst
  8. Normal labour
    • Stages, mechanism, fetal skull, pelvis, partograph, conduct of labour
  9. Obstructed labour
    • CPD, contracted pelvis, causes, clinical diagnosis, management, complications, prevention
  10. Malposition and malpresentation
  • OP position, breech, face, brow, transverse lie, cord prolapse
  1. Obstetric emergencies
  • PPH, antepartum haemorrhage, eclampsia, sepsis, uterine rupture, shock
  1. Antenatal and postpartum care
  • Routine ANC, anaemia, diabetes/hypertension in pregnancy, puerperium, lactation
A one-message version of all 12 would be too superficial for an MBBS exam. Pick the section to begin with and I will give a compact, high-yield last-minute sheet, then continue through the remaining sections in follow-up messages.

Make notes of every topic of gyne and obs

For MBBS OBG, a full set of short notes covers the following:
  1. Basic gynaecology and reproductive physiology
    • Puberty, menstrual cycle, menopause
    • Amenorrhoea, dysmenorrhoea, PMS
  2. Abnormal uterine bleeding
    • AUB evaluation, PALM-COEIN, medical and surgical management
  3. Genital tract infection
    • Vaginal discharge, STI, PID, genital tuberculosis
  4. Benign gynaecological disorders
    • Fibroid uterus, adenomyosis, endometriosis
    • PCOS, ovarian cysts and benign ovarian tumours
  5. Infertility and reproductive medicine
    • Evaluation of the infertile couple, ovulation induction, ART basics
  6. Contraception and abortion care
    • Natural, barrier, hormonal, IUCD, permanent methods
    • MTP and post-abortion care
  7. Urogynaecology
    • Genital prolapse, urinary incontinence, genital fistula
  8. Gynaecological malignancies and screening
    • Cancer cervix, ovary, endometrium, vulva
    • Pap smear, HPV, staging principles
  9. Gynaecological emergencies
    • Ectopic pregnancy, adnexal torsion, ruptured ovarian cyst, acute PID
  10. Antenatal care and medical disorders in pregnancy
  • Routine ANC, anaemia, hypertension, diabetes, heart disease, infections
  1. Normal labour and delivery
  • Pelvis, fetal skull, stages and mechanism of labour, partograph, induction
  1. Abnormal and obstructed labour
  • CPD, contracted pelvis, obstructed labour, uterine rupture
  • Malposition: OP and OT
  • Malpresentations: breech, face, brow, transverse lie, cord prolapse
  1. Obstetric emergencies
  • APH, PPH, eclampsia, sepsis, shock, amniotic-fluid embolism
  1. Puerperium and newborn care
  • Normal puerperium, lactation, puerperal sepsis, postpartum mental health
  • Immediate newborn care and resuscitation basics
For last-minute revision, each topic should be reduced to definition → causes/risk factors → clinical features → diagnosis → management → complications, with special emphasis on algorithms for emergencies.
Asking for Preferences

Which block should I turn into concise exam notes first?

A Pap smear, also called a Pap test or cervical cytology, is a screening test for cervical cancer and its precancerous changes. During a pelvic examination, a clinician gently collects cells from the cervix using a small brush. The laboratory examines the cells under a microscope. Cervical cytology can identify epithelial abnormalities before they develop into cancer.
Normal and abnormal cervical cytology

What it detects

  • Normal cervical cells
  • Cell changes often caused by high-risk human papillomavirus (HPV)
  • Precancerous lesions
  • Occasionally, cervical cancer
It is a screening test, not a definitive diagnosis. An abnormal result may require repeat testing, an HPV test, or colposcopy with possible biopsy.

Typical screening schedule in the United States

For people with a cervix at average risk:
  • Age 21-29: Pap test every 3 years.
  • Age 30-65: one of these options:
    • Pap test every 3 years
    • High-risk HPV test every 5 years
    • Pap plus HPV co-testing every 5 years
Screening usually does not begin before 21 or continue after 65 when there has been adequate prior normal screening and no high-risk factors. The schedule differs for people with prior abnormal tests, HIV/immunosuppression, past cervical precancer/cancer, or prenatal DES exposure. CDC summary of screening intervals

Preparation

For the most reliable sample, usually avoid vaginal intercourse, douching, and vaginal creams or medicines for about 24-48 hours beforehand, unless your clinician advises otherwise. It can be done during menstruation in some settings, but a heavy period may lead to rescheduling.

Common report terms

  • NILM: Negative for intraepithelial lesion or malignancy, meaning no precancerous or cancerous cells seen.
  • ASC-US: Atypical squamous cells of undetermined significance.
  • LSIL: Low-grade squamous intraepithelial lesion, commonly HPV-related.
  • HSIL: High-grade squamous intraepithelial lesion, with a higher chance of significant precancer.
Cervical cytology results are commonly reported through the Bethesda system. Histology: A Text and Atlas with Correlated Cell and Molecular Biology, p. 2299.This is a broad last-minute revision area. I can make a compact, high-yield sheet, but “obstruction” can mean different things in obstetrics.
  1. Core gynaecology
    • Menstrual disorders and AUB
    • Fibroid, endometriosis, adenomyosis
    • PID and vaginal discharge
    • Infertility and contraception
    • Prolapse and urinary incontinence
    • Cervical, ovarian, and endometrial cancers
    • Gynaecologic emergencies: ectopic pregnancy, ovarian torsion
  2. Obstetric obstruction
    • Cephalopelvic disproportion (CPD)
    • Malpresentation and malposition
    • Obstructed labour: diagnosis, complications, and management
    • Partograph and referral
  3. If you meant intestinal obstruction
    • Causes, features, X-ray findings, fluid resuscitation, surgery indications
For a final revision, I would use definitions, key differentiating points, diagnostic clues, first-line management, and one-line complications rather than detailed theory.
Which notes do you need?A complete last-minute gynaecology plus obstetric-obstruction revision set is too large to safely compress into one useful message without knowing your syllabus. Here is the full exam-oriented map:
  1. General gynaecology
    • Puberty and menstrual physiology
    • Amenorrhoea, dysmenorrhoea, premenstrual syndrome
    • Abnormal uterine bleeding and PALM-COEIN
    • Vaginal discharge, PID, genital tuberculosis
    • Fibroid, adenomyosis, endometriosis
    • Ovarian cysts, PCOS, ovarian tumours
    • Infertility and assisted reproduction
    • Contraception and medical termination of pregnancy
    • Urogynaecology: prolapse, urinary incontinence, fistula
    • Benign and malignant disease of vulva, vagina, cervix, uterus, ovary
    • Gynaecological emergencies: ectopic pregnancy, torsion, ruptured cyst, acute PID
  2. Obstetrics relevant to obstruction
    • Normal labour and mechanism of labour
    • Pelvis, fetal skull, diameters, engagement
    • Partograph
    • Malpositions: occipitoposterior, occipitotransverse
    • Malpresentations: breech, face, brow, transverse lie, compound presentation
    • CPD and contracted pelvis
    • Obstructed labour: causes, diagnosis, management, complications
    • Instrumental delivery and caesarean section
    • Rupture uterus, postpartum haemorrhage, puerperal sepsis
  3. General surgery intestinal obstruction, if included in your exam
    • Small versus large bowel obstruction
    • Adhesions, hernia, volvulus, malignancy, intussusception
    • Symptoms, X-ray/CT features, resuscitation, indications for surgery
    • Strangulation and perforation
High-yield principle: for every condition, revise in this sequence: definition → risk factors/causes → clinical features → investigations → management → complications.
State your exam and level (for example MBBS, BSc Nursing, GNM, DGO) and whether “obstruction” means obstructed labour only or also intestinal obstruction. Then I will create a concise all-topic revision sheet matched to that syllabus.For MBBS, I will keep it exam-focused and aligned to standard OBG long-answer, short-note, viva, and emergency questions.

Full revision map

  1. Menstruation and abnormal uterine bleeding
    • Amenorrhoea, dysmenorrhoea, AUB, PALM-COEIN, puberty and menopause
  2. Genital infections and PID
    • Vaginal discharge, PID, genital tuberculosis, STI syndromes
  3. Benign uterine and ovarian disease
    • Fibroid, adenomyosis, endometriosis, ovarian cysts, PCOS
  4. Infertility, contraception, MTP
    • Evaluation of couple infertility, ART basics, methods of contraception, MTP and complications
  5. Urogynaecology
    • Uterovaginal prolapse, urinary incontinence, genital fistula
  6. Gynaecologic oncology
    • Carcinoma cervix, endometrium, ovary, vulva; screening and staging basics
  7. Gynaecologic emergencies
    • Ectopic pregnancy, torsion, acute PID, ruptured ovarian cyst
  8. Normal labour
    • Stages, mechanism, fetal skull, pelvis, partograph, conduct of labour
  9. Obstructed labour
    • CPD, contracted pelvis, causes, clinical diagnosis, management, complications, prevention
  10. Malposition and malpresentation
  • OP position, breech, face, brow, transverse lie, cord prolapse
  1. Obstetric emergencies
  • PPH, antepartum haemorrhage, eclampsia, sepsis, uterine rupture, shock
  1. Antenatal and postpartum care
  • Routine ANC, anaemia, diabetes/hypertension in pregnancy, puerperium, lactation
A one-message version of all 12 would be too superficial for an MBBS exam. Pick the section to begin with and I will give a compact, high-yield last-minute sheet, then continue through the remaining sections in follow-up messages.For MBBS OBG, a full set of short notes covers the following:
  1. Basic gynaecology and reproductive physiology
    • Puberty, menstrual cycle, menopause
    • Amenorrhoea, dysmenorrhoea, PMS
  2. Abnormal uterine bleeding
    • AUB evaluation, PALM-COEIN, medical and surgical management
  3. Genital tract infection
    • Vaginal discharge, STI, PID, genital tuberculosis
  4. Benign gynaecological disorders
    • Fibroid uterus, adenomyosis, endometriosis
    • PCOS, ovarian cysts and benign ovarian tumours
  5. Infertility and reproductive medicine
    • Evaluation of the infertile couple, ovulation induction, ART basics
  6. Contraception and abortion care
    • Natural, barrier, hormonal, IUCD, permanent methods
    • MTP and post-abortion care
  7. Urogynaecology
    • Genital prolapse, urinary incontinence, genital fistula
  8. Gynaecological malignancies and screening
    • Cancer cervix, ovary, endometrium, vulva
    • Pap smear, HPV, staging principles
  9. Gynaecological emergencies
    • Ectopic pregnancy, adnexal torsion, ruptured ovarian cyst, acute PID
  10. Antenatal care and medical disorders in pregnancy
  • Routine ANC, anaemia, hypertension, diabetes, heart disease, infections
  1. Normal labour and delivery
  • Pelvis, fetal skull, stages and mechanism of labour, partograph, induction
  1. Abnormal and obstructed labour
  • CPD, contracted pelvis, obstructed labour, uterine rupture
  • Malposition: OP and OT
  • Malpresentations: breech, face, brow, transverse lie, cord prolapse
  1. Obstetric emergencies
  • APH, PPH, eclampsia, sepsis, shock, amniotic-fluid embolism
  1. Puerperium and newborn care
  • Normal puerperium, lactation, puerperal sepsis, postpartum mental health
  • Immediate newborn care and resuscitation basics
For last-minute revision, each topic should be reduced to definition → causes/risk factors → clinical features → diagnosis → management → complications, with special emphasis on algorithms for emergencies.I can prepare it as a serial MBBS OBG last-minute notebook. It will cover:
  1. Menstrual cycle, puberty, menopause
  2. Amenorrhoea, dysmenorrhoea, AUB and PALM-COEIN
  3. Vaginal discharge, STIs, PID, genital TB
  4. Fibroid, adenomyosis, endometriosis, PCOS, ovarian cysts
  5. Infertility and ART
  6. Contraception, MTP, ectopic pregnancy
  7. Prolapse, incontinence, genital fistula
  8. Gynaecologic cancers and screening
  9. Antenatal care and medical disorders in pregnancy
  10. Normal labour, fetal skull, pelvis, partograph
  11. Induction, augmentation, instrumental delivery, caesarean section
  12. Obstructed labour, CPD, rupture uterus
  13. Malpositions and malpresentations
  14. APH, PPH, hypertensive emergencies, sepsis, shock
  15. Puerperium, lactation, newborn care and resuscitation basics
Each topic will use: definition → causes → key clinical features → diagnosis → management → complications → exam pearls.
I will start with Part 1: Core Gynaecology in the next message, then continue section by section so the notes remain readable and useful for revision.

Ok

Reading File
Finding Sources
Finding Sources
Searching PubMed

"Abnormal Uterine Bleeding" AND management

Searching the Web

ACOG abnormal uterine bleeding amenorrhea dysmenorrhea guidance

MBBS OBG Last-Minute Notes: Part 1 - Core Gynaecology

1. Menstrual cycle

Normal menstruation

  • Cycle interval: usually 21-35 days
  • Duration: 2-7 days
  • Average blood loss: about 30-40 mL. Heavy menstrual bleeding is suggested by flooding, clots, changing protection very frequently, or anaemia.
  • Menarche usually occurs 2-3 years after thelarche.

Phases

Ovarian cycleEndometrial cycleMain hormone/event
Follicular phaseProliferative phaseFSH stimulates follicles; estrogen proliferates endometrium
OvulationLate proliferativeLH surge causes ovulation, about 14 days before next period
Luteal phaseSecretory phaseCorpus luteum produces progesterone
LuteolysisMenstruationFall in estrogen and progesterone causes shedding
High-yield: Progesterone causes secretory changes and raises basal body temperature by about 0.3-0.5°C after ovulation.

2. Amenorrhoea

Definitions

  • Primary amenorrhoea: no menstruation by 15 years in a girl with normal secondary sexual characteristics, or by 13 years if secondary sexual characteristics are absent.
  • Secondary amenorrhoea: absence of menses for 3 months in someone with previously regular cycles, or for 6 months if cycles were irregular. ACOG definition

Primary amenorrhoea: approach

Step 1: Is uterus present? Use USG

Uterus absent
  • Müllerian agenesis (MRKH): normal breasts, scant/absent pubic hair? Typically normal pubic hair, 46,XX.
  • Androgen insensitivity syndrome: normal breasts, absent/scant pubic and axillary hair, 46,XY, undescended testes.
Uterus present
  • Outflow obstruction: imperforate hymen, transverse vaginal septum
    • Cyclical pelvic pain + primary amenorrhoea + hematocolpos
  • Gonadal dysgenesis, e.g. Turner syndrome
    • No secondary sexual characters, streak ovaries, raised FSH
  • Hypothalamic-pituitary causes

Primary amenorrhoea mnemonic

“Breasts? Uterus? FSH?”
  1. Breasts present or absent?
  2. Uterus present or absent?
  3. If uterus present, FSH high or low?

Secondary amenorrhoea: causes and evaluation

Most important first step

Exclude pregnancy with urine/serum beta-hCG.

Common causes

  1. Pregnancy
  2. PCOS
  3. Hyperprolactinaemia
  4. Hypothalamic amenorrhoea: stress, weight loss, excessive exercise, eating disorder
  5. Thyroid disease
  6. Premature ovarian insufficiency
  7. Uterine adhesions, Asherman syndrome
  8. Drugs: antipsychotics, opioids, hormonal contraception

Investigation sequence

  • Pregnancy test
  • TSH and serum prolactin
  • FSH, LH, estradiol if ovarian failure suspected
  • Androgen profile if hirsutism/virilisation
  • Pelvic USG
  • MRI pituitary if persistently elevated prolactin or neurological symptoms

Treatment principles

Treat cause:
  • PCOS: weight management, cycle protection with COC or cyclic progestogen if not seeking pregnancy
  • Hyperprolactinaemia: dopamine agonist after excluding drug cause/pituitary lesion
  • Hypothyroidism: thyroxine
  • Hypothalamic cause: nutrition, reduce exercise/stress, address eating disorder
  • Premature ovarian insufficiency: hormone replacement unless contraindicated, bone-health counselling
  • Asherman syndrome: hysteroscopic adhesiolysis

3. Dysmenorrhoea

Definition

Painful menstruation, usually crampy lower abdominal pain occurring just before or with menses.

Primary dysmenorrhoea

  • No pelvic pathology
  • Starts within 6-12 months after menarche, once ovulatory cycles begin
  • Due to excess endometrial prostaglandins causing uterine hypercontractility and ischemia
  • Pain begins just before/on day 1 of menses and lasts 1-3 days
  • Examination is normal

Secondary dysmenorrhoea

  • Due to pelvic pathology
  • Begins later, may progressively worsen; pain may occur before and continue after menses
  • Causes: endometriosis, adenomyosis, fibroid, PID, ovarian cyst, cervical stenosis, IUCD-related pain

Management

Primary dysmenorrhoea
  1. Reassurance, exercise, heat
  2. NSAIDs, started at onset or 1-2 days before expected menses
  3. Combined hormonal contraception if NSAIDs inadequate or contraception desired
  4. Persistent/refractory symptoms: assess for secondary cause, especially endometriosis
Exam pearl: A young patient with severe dysmenorrhoea not responding to NSAIDs/COC should be evaluated for endometriosis.

4. Premenstrual syndrome and PMDD

PMS

Cyclical physical, psychological, and behavioural symptoms in the luteal phase that resolve after menstruation begins.
Symptoms: irritability, mood swings, breast tenderness, bloating, headache, fatigue, food craving.

PMDD

A severe form with marked affective symptoms and functional impairment.

Diagnosis

  • Symptom diary for at least 2 cycles
  • Symptoms occur in luteal phase and remit shortly after menstruation begins.

Management

  • Lifestyle: exercise, sleep, reduce stress
  • CBT
  • COC, especially selected regimens
  • SSRI for severe PMS/PMDD
  • Refer when severe mood symptoms or suicidal thoughts occur

5. Abnormal uterine bleeding (AUB)

Definition

Bleeding from the uterine corpus that is abnormal in regularity, frequency, duration, or volume in a non-pregnant woman.

First rule

Exclude pregnancy-related causes first: miscarriage, ectopic pregnancy, gestational trophoblastic disease.

FIGO PALM-COEIN classification

Structural causes: PALM

  • P - Polyp
  • A - Adenomyosis
  • L - Leiomyoma/fibroid
  • M - Malignancy and hyperplasia

Non-structural causes: COEIN

  • C - Coagulopathy
  • O - Ovulatory dysfunction
  • E - Endometrial
  • I - Iatrogenic
  • N - Not yet classified
The PALM-COEIN classification remains the standard framework for AUB assessment. ACOG AUB guidance

Important clinical terms

  • Heavy menstrual bleeding (HMB): excessive menstrual blood loss that affects physical, emotional, social, or quality-of-life functioning.
  • Intermenstrual bleeding: bleeding between expected periods.
  • Postcoital bleeding: bleeding after intercourse. Think cervical pathology.
  • Postmenopausal bleeding: endometrial cancer must be excluded.

AUB: clinical assessment

History

  • LMP, cycle pattern, duration and amount of bleeding
  • Pregnancy possibility
  • Drugs: anticoagulants, hormones
  • Symptoms of anaemia
  • PCOS/thyroid symptoms
  • Bleeding disorder history: easy bruising, epistaxis, heavy bleeding since menarche
  • Cancer risk: obesity, chronic anovulation, diabetes, tamoxifen, family history

Examination

  • Assess haemodynamic status if acute heavy bleeding
  • Pallor, BMI, hirsutism, thyroid signs
  • Abdominal mass
  • Speculum examination: vaginal/cervical lesions, bleeding source
  • Bimanual examination: uterine size, fibroids, adnexal mass

Investigations

  • Urine pregnancy test
  • CBC, ferritin if heavy/prolonged bleeding
  • TSH only if clinically indicated
  • Coagulation testing if bleeding disorder suspected
  • Pelvic USG: first-line imaging for structural lesion
  • Endometrial biopsy if:
    • Age 45 years or more with AUB
    • Younger patient with persistent AUB plus risk factors for endometrial hyperplasia/cancer
    • Failed medical treatment or persistent bleeding

Acute AUB: management

If haemodynamically unstable

  1. ABC resuscitation
  2. Two wide-bore IV lines, blood grouping/cross-match
  3. CBC/coagulation profile, fluids, blood products as needed
  4. Urgent senior gynaecology review
  5. Medical control of bleeding if appropriate, or uterine evacuation/tamponade/surgical intervention depending on cause and stability

If stable

Medical options depend on cause, contraindications, and fertility wishes:
  • Tranexamic acid
  • NSAID
  • Combined oral contraceptive
  • Oral progestogen
  • LNG-IUS for long-term heavy bleeding where suitable
Definitive surgery: hysteroscopic polypectomy/myomectomy, endometrial ablation in selected women who have completed childbearing, or hysterectomy when appropriate.

6. Postmenopausal bleeding (PMB)

Definition

Any vaginal bleeding occurring after 12 months of amenorrhoea due to menopause.

Rule

Endometrial carcinoma must be excluded until proven otherwise.

Causes

  • Atrophic endometrium/vaginitis, most common
  • Endometrial polyp
  • Endometrial hyperplasia/carcinoma
  • Cervical malignancy
  • Hormone therapy
  • Trauma/infection

Evaluation

  • Speculum examination
  • Transvaginal USG for endometrial thickness
  • Endometrial biopsy/hysteroscopy when indicated
  • Cervical screening status and cervical assessment
Exam line: “Postmenopausal bleeding is carcinoma of endometrium until proved otherwise.”

7. Menopause

Definition

Permanent cessation of menstruation due to ovarian follicular depletion, diagnosed retrospectively after 12 months of amenorrhoea without another cause.

Hormonal changes

  • Low estrogen and inhibin
  • High FSH and LH

Symptoms

Vasomotor: hot flushes, night sweats, palpitations
Genitourinary syndrome of menopause: vaginal dryness, dyspareunia, urinary urgency/recurrent UTI
Psychological: poor sleep, mood change
Long term: osteoporosis, fracture risk, cardiovascular risk

Management

  • Lifestyle: exercise, smoking cessation, calcium/vitamin D adequacy
  • Vaginal moisturisers/lubricants for mild urogenital symptoms
  • Local vaginal estrogen for genitourinary symptoms when suitable
  • Menopausal hormone therapy for troublesome vasomotor symptoms after individual risk assessment
    • Uterus present: estrogen plus progestogen
    • No uterus: estrogen alone

Important cautions for systemic hormone therapy

Avoid or seek specialist opinion with breast/endometrial cancer, unexplained vaginal bleeding, active/past thromboembolism, stroke, or active liver disease.

One-minute recall

  • Amenorrhoea: pregnancy first.
  • Primary amenorrhoea: assess breasts, uterus, then FSH.
  • Dysmenorrhoea: primary = prostaglandin-mediated; refractory pain = consider endometriosis.
  • AUB: pregnancy test → stabilize if heavy → PALM-COEIN → USG ± biopsy.
  • AUB biopsy: ≥45 years, or younger with risk factors/persistent bleeding.
  • PMB: exclude endometrial cancer.
  • Menopause: 12 months amenorrhoea; uterus present means estrogen needs endometrial protection with progestogen.
Recent systematic-review evidence continues to support FIGO-based structured classification for AUB, although it does not alter the above exam framework. PMID: 39234899.
Next: Part 2 - Vaginal discharge, STIs, PID, genital tuberculosis, fibroid, adenomyosis, endometriosis, PCOS, and ovarian cysts.

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CDC pelvic inflammatory disease STI treatment guidelines 2026 bacterial vaginosis trichomoniasis candidiasis

MBBS OBG Last-Minute Notes: Part 2 - Gynaecological Infections and Benign Disorders

1. Vaginal discharge and vaginitis

Normal discharge

Physiological discharge is:
  • Clear or white
  • Non-offensive
  • Non-pruritic
  • Varies with ovulation, pregnancy, and sexual arousal

Common causes: quick comparison

ConditionDischargepHKey findingTreatment principle
CandidiasisThick, white, curdyNormal, <4.5Intense pruritus, erythema; pseudohyphae on KOHAzole antifungal
Bacterial vaginosisThin, homogeneous grey-white, fishy odour>4.5Clue cells, positive whiff testMetronidazole
TrichomoniasisFrothy yellow-green, offensive>4.5Strawberry cervix, motile trichomonadsMetronidazole, treat partner
Gonorrhoea/chlamydia cervicitisMucopurulent endocervical dischargeVariableFriable cervix, contact bleedingNAAT and organism-directed treatment

Candidial vulvovaginitis

Risk factors: diabetes, pregnancy, recent antibiotics, immunosuppression.
Features
  • Intense vulval itching and soreness
  • Dyspareunia, dysuria
  • Thick curdy white discharge
  • Vulval erythema and excoriation
Diagnosis: KOH mount showing budding yeast/pseudohyphae.
Treatment: topical azole or oral fluconazole in non-pregnant uncomplicated cases. In pregnancy, topical azoles are preferred.

Bacterial vaginosis: Amsel criteria

Diagnosis when at least 3 of 4 are present:
  1. Homogeneous thin white/grey discharge
  2. Vaginal pH >4.5
  3. Positive amine or whiff test with KOH
  4. Clue cells on microscopy
Complications: increased risk of PID, postoperative infection, and adverse pregnancy outcomes.
Treatment: metronidazole. Partner treatment is generally not routinely required.

Trichomoniasis

  • STI caused by Trichomonas vaginalis
  • Frothy yellow-green discharge, odour, itching, dysuria
  • Strawberry cervix may occur
  • Diagnose using NAAT where available, or wet mount
Management
  • Oral metronidazole
  • Treat sexual partner(s)
  • Avoid intercourse until both have completed treatment
  • Test for other STIs
  • Retesting in women after treatment is recommended because reinfection is common. CDC trichomoniasis guidance

2. Pelvic inflammatory disease (PID)

Definition

Ascending infection of the upper female genital tract, involving endometrium, fallopian tubes, ovaries, and pelvic peritoneum.

Causative organisms

Usually polymicrobial:
  • Neisseria gonorrhoeae
  • Chlamydia trachomatis
  • Anaerobes
  • Vaginal flora including Gardnerella
  • Mycoplasma genitalium in some cases

Risk factors

  • Multiple/new sexual partners
  • Previous STI or PID
  • Unprotected intercourse
  • Recent uterine instrumentation
  • IUCD insertion, particularly soon after insertion

Clinical features

  • Bilateral lower abdominal/pelvic pain
  • Fever
  • Abnormal vaginal discharge
  • Dyspareunia
  • Intermenstrual or postcoital bleeding
  • Dysuria
  • Cervical motion tenderness
  • Uterine/adnexal tenderness

Diagnosis

A clinical diagnosis. Treat empirically in a sexually active patient with pelvic pain and cervical-motion, uterine, or adnexal tenderness if no other cause is clear.
Tests
  • Pregnancy test, to exclude ectopic pregnancy
  • NAAT for gonorrhoea/chlamydia
  • CBC, CRP
  • HIV and syphilis testing
  • USG if tubo-ovarian abscess suspected

Complications: “I-C-C”

  • Infertility due to tubal damage
  • Chronic pelvic pain
  • Conception outside uterus: ectopic pregnancy
Also: tubo-ovarian abscess, perihepatitis (Fitz-Hugh-Curtis syndrome), recurrent PID.

Management

  • Give broad-spectrum antibiotics covering gonorrhoea, chlamydia, and anaerobes.
  • Treat and test sexual partners.
  • Abstain from intercourse until treatment is completed and partners are treated.
  • Review response within 48-72 hours.
Admit if severe illness, pregnancy, tubo-ovarian abscess, surgical emergency cannot be excluded, oral therapy cannot be tolerated, or no response to outpatient treatment. The CDC recommends reassessment/escalation if there is no improvement within 72 hours. CDC PID guidance

3. Female genital tuberculosis

Site involved

Most commonly fallopian tubes, then endometrium, ovaries, cervix, and vagina.

Clinical features

  • Infertility, most common presentation
  • Menstrual disturbance: oligomenorrhoea, amenorrhoea, AUB
  • Chronic pelvic pain
  • Constitutional symptoms may be absent
  • Adnexal mass or tubo-ovarian mass
  • Ascites in some cases

Diagnosis

  • Endometrial biopsy for histopathology, AFB studies, culture, and molecular tests
  • Hysteroscopy/laparoscopy: adhesions, tubercles, beaded tubes, caseation
  • HSG: beaded or rigid “pipe-stem” tubes, cornual block, uterine synechiae
  • Chest evaluation and evaluation for TB elsewhere

Management

  • Standard anti-tubercular therapy as per national programme
  • Surgery only for selected complications, persistent masses, abscess, severe adhesions, or diagnostic uncertainty
  • Fertility prognosis may remain poor because of irreversible tubal/endometrial damage

4. Fibroid uterus (leiomyoma)

Definition

A benign smooth-muscle tumour of the uterus. It is estrogen-dependent and common during reproductive age.

Types by location

  • Intramural: within myometrium, most common
  • Submucosal: projects toward uterine cavity, most associated with heavy bleeding and infertility
  • Subserosal: projects outward, may cause pressure symptoms
  • Pedunculated variants may undergo torsion

Clinical features: “Bleeding, bulk, baby”

  • Bleeding: heavy menstrual bleeding, anaemia
  • Bulk symptoms: pelvic pressure, urinary frequency, constipation
  • Baby: subfertility, recurrent miscarriage, pregnancy complications
May also cause dysmenorrhoea, palpable mass, or be asymptomatic.

Degenerations

  • Hyaline degeneration, most common
  • Cystic degeneration
  • Red degeneration: often in pregnancy, painful
  • Calcification: after menopause
  • Sarcomatous change is rare

Diagnosis

  • Bimanual examination: enlarged, irregular, firm uterus
  • Pelvic ultrasound: first-line
  • MRI for mapping before selected procedures or uncertain diagnosis
  • CBC for anaemia

Management

Depends on symptoms, age, fibroid size/location, and fertility wish.
  • Expectant management if asymptomatic
  • Tranexamic acid/NSAIDs for heavy bleeding
  • LNG-IUS or hormonal treatment if cavity is suitable
  • GnRH analogues as short-term preoperative treatment in selected patients
  • Myomectomy: fertility preservation
  • Hysterectomy: definitive treatment if family complete and symptoms significant
  • Uterine artery embolisation: selected patients, counselling needed regarding fertility
Exam pearl: A submucosal fibroid has the strongest association with menorrhagia and infertility.

5. Adenomyosis

Definition

Presence of endometrial glands and stroma within the myometrium.

Classic triad

  1. Heavy menstrual bleeding
  2. Progressive dysmenorrhoea
  3. Uniformly enlarged, boggy, tender uterus

Diagnosis

  • USG may show heterogeneous myometrium, myometrial cysts, globular uterus
  • MRI is more accurate if diagnosis remains uncertain

Management

  • NSAIDs, tranexamic acid
  • LNG-IUS is a useful medical option
  • Hormonal suppression in selected cases
  • Hysterectomy is definitive once childbearing is complete

Fibroid versus adenomyosis

FeatureFibroidAdenomyosis
UterusIrregular, firmUniformly enlarged, boggy
LesionWell-defined massDiffuse myometrial infiltration
Common featurePressure symptoms, HMBHMB with severe dysmenorrhoea
Definitive surgeryMyomectomy/hysterectomyHysterectomy

6. Endometriosis

Definition

Endometrial-type glands and stroma outside the uterus.

Common sites

  • Ovary: endometrioma, “chocolate cyst”
  • Pouch of Douglas
  • Uterosacral ligaments
  • Pelvic peritoneum
  • Rectovaginal septum
  • Surgical scar, rarely distant sites

Clinical features: “Pain, period, pregnancy problem”

  • Progressive secondary dysmenorrhoea
  • Deep dyspareunia
  • Chronic pelvic pain
  • Infertility
  • Dyschezia or cyclical bowel/bladder symptoms in deep disease

Diagnosis

  • Clinical suspicion is important
  • Transvaginal USG for ovarian endometrioma
  • MRI for deep infiltrating disease
  • Laparoscopy with histology can confirm diagnosis, but treatment may begin based on clinical/imaging findings

Management

Depends on pain severity and fertility desire.
Pain with no immediate pregnancy plan
  • NSAIDs
  • Combined hormonal contraception or progestogen
  • GnRH agonist/antagonist in selected cases
Infertility or severe disease
  • Laparoscopic excision/ablation of endometriosis and adhesiolysis when appropriate
  • ART/IVF where indicated
Key point: Medical therapy controls symptoms but does not permanently eradicate disease; surgery also has recurrence risk.

7. Polycystic ovary syndrome (PCOS)

Definition

A common endocrine-metabolic disorder with ovulatory dysfunction and hyperandrogenism.

Rotterdam criteria

Diagnosis requires any 2 of 3, after excluding other causes:
  1. Oligo/anovulation
  2. Clinical or biochemical hyperandrogenism
  3. Polycystic ovarian morphology on ultrasound

Clinical features

  • Oligomenorrhoea/amenorrhoea
  • Infertility due to anovulation
  • Hirsutism, acne, androgenic alopecia
  • Obesity, insulin resistance, acanthosis nigricans
  • Increased risk of endometrial hyperplasia from prolonged unopposed estrogen

Investigations

  • Pregnancy test
  • TSH, prolactin
  • Total/free testosterone if hyperandrogenism
  • Screen for glucose intolerance/diabetes and dyslipidaemia
  • USG when needed

Management

Foundation: lifestyle and weight management where relevant.
If menstrual irregularity and no pregnancy desired
  • COC for cycle control and hyperandrogenic symptoms
  • Cyclic progestogen or LNG-IUS for endometrial protection when COC unsuitable
If fertility desired
  • Ovulation induction, commonly letrozole first-line in many current protocols
  • Metformin may be useful in selected patients, especially metabolic risk/insulin resistance
Exam pearl: Long-standing anovulation causes unopposed estrogen exposure and raises risk of endometrial hyperplasia.

8. Ovarian cysts and benign ovarian tumours

Functional cysts

  • Follicular cyst: failure of follicle to rupture
  • Corpus luteum cyst: may bleed or rupture
  • Usually resolve spontaneously within a few menstrual cycles

Important benign tumours

  • Serous cystadenoma: common, usually unilocular
  • Mucinous cystadenoma: can become very large, multilocular
  • Mature cystic teratoma (dermoid): contains ectodermal tissue, hair/teeth/fat; common cause of torsion in young women
  • Endometrioma: chocolate cyst

Red flags for malignancy

  • Solid areas/papillary projections
  • Thick septa
  • Bilateral complex mass
  • Ascites
  • Fixed/nodular pelvic mass
  • Postmenopausal adnexal mass
  • Raised CA-125 is not diagnostic in premenopausal women because it can rise in endometriosis, fibroids, PID, and pregnancy

Adnexal torsion

Emergency.
  • Sudden severe unilateral lower abdominal pain
  • Nausea/vomiting
  • Tender adnexal mass
  • Doppler flow may be present and does not reliably exclude torsion
Management: urgent laparoscopy and detorsion with ovarian conservation when feasible.

One-minute recall

  • PID: lower abdominal pain + cervical motion tenderness = treat empirically after excluding ectopic pregnancy.
  • PID complications: infertility, ectopic pregnancy, chronic pelvic pain.
  • Fibroid: irregular firm uterus; submucosal type causes HMB/infertility.
  • Adenomyosis: uniformly enlarged boggy tender uterus + menorrhagia + dysmenorrhoea.
  • Endometriosis: pelvic pain + deep dyspareunia + infertility; endometrioma = chocolate cyst.
  • PCOS: 2 of 3 Rotterdam criteria; protect endometrium in chronic anovulation.
  • Ovarian torsion: sudden unilateral pain with vomiting = emergency surgery.
Recent evidence continues to support multidisciplinary care for endometriosis-associated chronic pelvic pain, particularly when symptoms are complex or persistent. PMID: 37753632.
Next: Part 3 - Infertility, contraception, MTP, ectopic pregnancy, prolapse, urinary incontinence, and genital fistula.

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WHO abortion care guideline contraception family planning ectopic pregnancy management guidance

MBBS OBG Last-Minute Notes: Part 3 - Infertility, Contraception, MTP, Ectopic Pregnancy, Prolapse, Incontinence, Fistula

1. Infertility

Definition

Failure to achieve pregnancy after:
  • 12 months of regular, unprotected intercourse, or
  • 6 months if the woman is aged 35 years or above.

Types

  • Primary: no previous pregnancy.
  • Secondary: inability to conceive after a previous pregnancy.

Causes: male, female, combined, unexplained

FactorCommon causes
MaleSemen abnormality, varicocele, endocrine disease, infection, erectile/ejaculatory dysfunction
OvulatoryPCOS, hyperprolactinaemia, thyroid disease, premature ovarian insufficiency
Tubal/peritonealPID, genital TB, previous pelvic surgery, endometriosis
UterineFibroid, polyp, adhesions, congenital anomaly
CervicalRare as an isolated cause
UnexplainedNormal standard evaluation but no identified cause

Evaluation of the couple

Always investigate both partners simultaneously.
Male
  • Semen analysis: first-line test
  • Repeat if abnormal
  • Hormonal profile and scrotal USG when indicated
Female
  1. Ovulation assessment: menstrual history, mid-luteal progesterone, ovulation kits where relevant
  2. Ovarian reserve: AMH, antral follicle count, day-2/3 FSH where used
  3. Tubal patency: HSG, laparoscopy with chromopertubation if indicated
  4. Uterine cavity: USG, saline sonography, hysteroscopy if needed

Management

  • Counsel regarding fertile window, weight, smoking/alcohol, and folic acid.
  • Treat cause: ovulation induction for anovulation, surgery for selected uterine/tubal disease, treatment of male factor.
  • ART: IUI, IVF, ICSI.
High-yield: In India, genital TB is an important cause of tubal infertility.

2. Contraception

Ideal contraceptive: “SAFE”

  • Safe
  • Acceptable
  • Feasible/effective
  • Easily reversible when desired

Methods

CategoryExamplesMain point
NaturalFertility awareness, lactational amenorrhoea, withdrawalHigher failure rate in typical use
BarrierMale/female condom, diaphragmCondoms reduce STI transmission
HormonalCOC, progestin-only pill, injectables, implantsHighly effective with correct use
IUCDCopper IUCD, LNG-IUSLong-acting reversible contraception
PermanentVasectomy, tubectomyFor completed family

Combined oral contraceptive pill (COC)

Mechanism
  • Suppresses ovulation by inhibiting FSH/LH
  • Thickens cervical mucus
  • Causes endometrial changes
Advantages
  • Effective, reversible
  • Cycle control
  • Reduces dysmenorrhoea, heavy bleeding, acne
  • Reduces risk of endometrial and ovarian cancer
Important contraindications
  • Pregnancy
  • Current breast cancer
  • Smoking age >35 years
  • Migraine with aura
  • Previous/current VTE or thrombophilia
  • Severe hypertension, ischemic heart disease, stroke
  • Severe liver disease

Progestin-only methods

  • Pill, DMPA injection, implant, LNG-IUS
  • Useful when estrogen is contraindicated
  • Irregular bleeding is common.

IUCD

Copper IUCD

  • Copper is spermicidal and induces sterile inflammatory reaction.
  • Long acting, hormone-free, can be used for emergency contraception if inserted within the appropriate time window.
  • Adverse effects: heavier/longer menses, dysmenorrhoea, expulsion, rare perforation.

LNG-IUS

  • Causes endometrial suppression and thick cervical mucus.
  • Reduces heavy menstrual bleeding and dysmenorrhoea.
  • Initial irregular spotting is common.
Do not insert IUCD in: current PID, purulent cervicitis, current gonorrhoea/chlamydia infection, pregnancy, unexplained bleeding pending evaluation, distorted uterine cavity.

Emergency contraception

  • Copper IUCD is the most effective method.
  • Oral emergency contraceptive pills are alternatives.
  • It does not interrupt an established pregnancy.

Permanent methods

  • Vasectomy: safer, simpler, more effective than female sterilisation; requires alternative contraception until azoospermia is confirmed.
  • Tubectomy: laparoscopic, mini-laparotomy, interval or postpartum.

3. Medical termination of pregnancy and abortion care

Types

  • Spontaneous abortion: miscarriage.
  • Induced abortion: termination by medical or surgical method.

Clinical types of spontaneous abortion

TypeFeaturesCervixManagement principle
ThreatenedBleeding, mild pain, viable pregnancy possibleClosedObserve, USG, supportive care
InevitableBleeding/pain, products may be feltOpenEvacuation or expectant/medical care as appropriate
IncompleteSome products expelledOpenStabilise, uterine evacuation/medical management
CompleteAll products expelledClosedConfirm completion
MissedNonviable pregnancy retainedClosedExpectant, medical, or surgical evacuation
SepticFever, foul discharge, uterine tendernessVariableResuscitation + broad antibiotics + evacuation after stabilisation

Medical abortion: principles

  • Uses an anti-progestin with a prostaglandin analogue in standard protocols.
  • Confirm intrauterine pregnancy and gestational age as appropriate.
  • Suspect ectopic pregnancy in unilateral pain, collapse, prior ectopic/tubal surgery, or pregnancy occurring with an IUCD in situ.
  • Counsel about bleeding, pain, follow-up, warning signs, and contraception.
Emergency referral: soaking pads rapidly, syncope, severe abdominal pain, fever, foul discharge, persistent heavy bleeding.
Exam point: MTP law and gestational limits vary by country and can change. In an Indian MBBS exam, quote your current national law/guidelines as taught by your department.

4. Ectopic pregnancy

Definition

Implantation of a fertilised ovum outside the endometrial cavity.

Commonest site

Fallopian tube, especially ampulla.

Risk factors

  • Previous ectopic pregnancy
  • PID or tubal surgery
  • Infertility treatment/ART
  • Endometriosis
  • IUCD failure
  • Smoking
  • Previous sterilisation failure

Classical triad

  1. Amenorrhoea
  2. Lower abdominal pain
  3. Vaginal bleeding
But the complete triad is not always present.

Clinical features

  • Unilateral pelvic pain
  • Spotting/bleeding
  • Adnexal tenderness or mass
  • Cervical motion tenderness
  • Shoulder-tip pain, syncope, shock in rupture

Diagnosis

  • Urine/serum beta-hCG
  • Transvaginal USG
  • Serial beta-hCG where pregnancy location is uncertain
  • CBC, blood group and Rh status, cross-match if bleeding suspected

Management

SituationManagement
Unstable/ruptured/suspected major haemoperitoneumImmediate resuscitation and surgery
Stable, selected unruptured ectopicExpectant, medical methotrexate, or surgery depending on clinical criteria
Surgical treatmentLaparoscopic salpingectomy or salpingostomy in selected cases
Methotrexate: only for a stable patient with a confirmed/highly likely unruptured ectopic, reliable follow-up, and no contraindication. Follow serial beta-hCG until resolution.
A ruptured ectopic pregnancy is a life-threatening emergency requiring urgent surgery. ACOG ectopic pregnancy summary

5. Pelvic organ prolapse

Definition

Descent of one or more pelvic organs into or beyond the vagina due to weakness of pelvic floor support.

Types

  • Cystocele: bladder bulges into anterior vaginal wall
  • Urethrocele
  • Uterine prolapse
  • Enterocele: small bowel herniation into posterior vaginal wall
  • Rectocele: rectum bulges into posterior vaginal wall
  • Vault prolapse after hysterectomy

Risk factors

  • Multiparity, traumatic vaginal delivery
  • Prolonged/obstructed labour
  • Menopause and estrogen deficiency
  • Chronic cough, constipation, heavy lifting
  • Obesity
  • Previous pelvic surgery
  • Connective-tissue weakness

Symptoms

  • “Something coming out per vaginum”
  • Dragging pelvic pain/backache
  • Urinary symptoms: frequency, incomplete emptying, stress incontinence
  • Constipation, incomplete rectal emptying
  • Dyspareunia, ulceration or discharge

Assessment

  • Examine standing/straining if necessary
  • Speculum examination to identify compartments
  • Assess urinary symptoms, residual urine, ulceration
  • Screen cervix as appropriate before surgery

Management

  • Weight reduction, avoid constipation/heavy lifting, pelvic-floor exercises
  • Vaginal estrogen for atrophy when appropriate
  • Pessary: suitable for women unfit for surgery, awaiting surgery, or preferring conservative treatment
  • Surgery according to age, sexual activity, fertility wish, and compartment involved:
    • Vaginal hysterectomy with pelvic-floor repair
    • Uterus-preserving prolapse surgery in selected women
    • Colpocleisis in selected women who no longer desire vaginal intercourse

6. Urinary incontinence

Types

TypeTypical featureMechanism
Stress urinary incontinenceLeakage on cough, laugh, exerciseUrethral hypermobility or sphincter weakness
Urgency urinary incontinenceSudden urge followed by leakageDetrusor overactivity
MixedBoth stress and urgency featuresBoth mechanisms
OverflowContinuous dribbling, poor stream, high residual urineRetention/obstruction or weak detrusor
FunctionalCannot reach toilet due to disability/cognitionNon-urological cause

Evaluation

  • History and 3-day bladder diary
  • Urinalysis/culture
  • Pelvic examination for prolapse/atrophy
  • Cough stress test
  • Post-void residual if retention suspected
  • Urodynamics in selected complicated cases before surgery

Management

Stress incontinence
  • Weight loss if relevant
  • Pelvic-floor muscle training: first-line
  • Treat cough/constipation
  • Mid-urethral sling or other surgery in selected cases
Urgency incontinence
  • Bladder training and lifestyle modification
  • Treat UTI, reduce caffeine
  • Antimuscarinic drug or beta-3 agonist if appropriate
  • Refractory cases: specialist options such as botulinum toxin/neuromodulation

7. Genital fistula

Vesicovaginal fistula (VVF)

Abnormal communication between bladder and vagina causing continuous, painless leakage of urine through the vagina.

Causes

  • Prolonged obstructed labour, classically in low-resource settings
  • Pelvic surgery, especially hysterectomy
  • Pelvic malignancy/radiotherapy
  • Trauma

Features

  • Continuous urinary leakage after difficult labour or pelvic surgery
  • Recurrent UTI, excoriation, foul odour, social isolation

Diagnosis

  • Speculum examination
  • Dye test: methylene blue in bladder
  • Cystoscopy, imaging as needed

Management

  • Optimise nutrition, treat infection, protect skin
  • Small early fistula may close with continuous bladder drainage in selected cases
  • Definitive surgical repair after inflammation/edema settle, commonly after about 3 months, unless early repair is clearly appropriate in an expert setting

Rectovaginal fistula

  • Passage of flatus/feces through vagina
  • Common causes: obstructed labour, severe perineal tear, surgery, Crohn disease, malignancy
  • Requires infection control, nutritional optimisation, and planned surgical repair.

One-minute recall

  • Infertility: assess both partners together; semen analysis is the first male test.
  • PCOS: a common cause of anovulatory infertility.
  • Copper IUCD: long-acting, hormone-free, emergency contraception option.
  • Ectopic: amenorrhoea + pain + bleeding until proven otherwise.
  • Ruptured ectopic: resuscitate and operate.
  • Prolapse: cystocele anterior, rectocele posterior, enterocele apical/posterior.
  • Stress incontinence: leaks with cough; pelvic-floor exercise first.
  • VVF: continuous painless leakage of urine per vagina.
Recent review evidence supports the established approach of carefully selecting stable ectopic pregnancies for medical versus surgical care. PMID: 37443463.
Next: Part 4 - Cervical, endometrial, ovarian and vulval cancers; screening and Pap smear.

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MBBS OBG Last-Minute Notes: Part 4 - Gynaecologic Malignancies and Cervical Screening

1. Carcinoma cervix

Etiology and risk factors

Persistent infection with high-risk HPV, especially types 16 and 18, is the essential causative factor in most cases.
Risk factors
  • Early sexual debut
  • Multiple sexual partners/partner with multiple partners
  • High parity
  • Smoking
  • Immunosuppression, especially HIV
  • Lack of screening
  • Persistent high-risk HPV infection

Precancerous lesions

  • CIN 1: low-grade lesion, often transient HPV infection
  • CIN 2 and CIN 3: high-grade precancerous lesions
  • Cytology terms:
    • ASC-US: atypical squamous cells of undetermined significance
    • LSIL: low-grade squamous intraepithelial lesion
    • HSIL: high-grade squamous intraepithelial lesion

Clinical features

Early disease is often asymptomatic.
Later:
  • Postcoital bleeding: classic symptom
  • Intermenstrual or postmenopausal bleeding
  • Foul-smelling watery/blood-stained discharge
  • Pelvic pain, dyspareunia
  • Advanced disease: backache, leg edema, urinary/bowel symptoms, fistula, weight loss

Diagnosis

  • Speculum examination: ulceroproliferative/friable cervical lesion may bleed on touch
  • Biopsy confirms diagnosis
  • Colposcopy-directed biopsy for abnormal screening
  • MRI pelvis is useful for local extent; CT/PET-CT may assess nodal/distant disease depending on local protocol

Spread

  • Direct: vagina, uterus, parametrium, bladder, rectum
  • Lymphatic: pelvic then para-aortic lymph nodes
  • Distant: lung, liver, bone

FIGO staging: very short exam outline

StageKey point
IConfined to cervix
IIBeyond cervix, but not pelvic wall/lower third vagina
IIILower third vagina, pelvic wall, hydronephrosis, or regional nodes
IVBladder/rectal mucosa or distant metastasis

Management principle

  • Early-stage disease: surgery or radiotherapy depending on stage, fertility wishes, and local expertise
  • Locally advanced disease: concurrent chemoradiation with brachytherapy
  • Metastatic/recurrent disease: systemic therapy and palliation where appropriate
Exam pearl: Never diagnose carcinoma cervix from Pap smear alone. It is confirmed by histopathology from biopsy.

2. Pap smear and cervical cancer screening

Pap smear

A Pap smear is cervical cytology. Cells are collected from the transformation zone and examined for precancerous changes.

Important points

  • It is a screening test, not a diagnostic test.
  • Abnormal cytology requires triage, usually HPV testing and/or colposcopy.
  • HPV testing detects high-risk viral infection; it does not by itself diagnose cancer.
  • Screening remains important even after HPV vaccination.

Screening methods

  • HPV DNA testing
  • Cytology/Pap smear
  • Co-testing: HPV plus cytology
  • VIA: visual inspection with acetic acid, used in some resource-limited settings
WHO promotes high-performance HPV testing as the preferred screening approach, generally starting at age 30 in the general population. Women with HIV need earlier and more frequent screening. WHO cervical cancer fact sheet

Prevention

  1. HPV vaccination
  2. Safer sexual practices and smoking cessation
  3. Regular screening
  4. Timely treatment of precancerous lesions

3. Carcinoma endometrium

Types

  • Type I: endometrioid, estrogen-related, often associated with hyperplasia and better prognosis
  • Type II: non-endometrioid, e.g. serous carcinoma, not estrogen-related and generally more aggressive

Risk factors: “Unopposed estrogen”

  • Obesity
  • Chronic anovulation/PCOS
  • Nulliparity
  • Early menarche, late menopause
  • Estrogen-only therapy in a woman with uterus
  • Tamoxifen
  • Diabetes, hypertension
  • Lynch syndrome

Protective factors

  • Combined oral contraceptive pills
  • Pregnancy
  • Progesterone exposure

Clinical features

  • Postmenopausal bleeding: most important presentation
  • AUB in perimenopausal women
  • Watery/blood-stained discharge
  • Advanced disease: pain, mass, weight loss

Diagnosis

  • Transvaginal ultrasound may assess endometrial thickness
  • Endometrial biopsy is diagnostic
  • Hysteroscopy-directed biopsy if focal lesion suspected or biopsy is inadequate

Management

  • Standard definitive treatment: total hysterectomy with bilateral salpingo-oophorectomy, with staging assessment as appropriate
  • Radiotherapy/chemotherapy based on stage, histology, grade, and risk factors
  • Fertility-sparing progestin therapy may be considered only in carefully selected early low-grade cases under specialist supervision
Exam line: “Postmenopausal bleeding is endometrial carcinoma until proved otherwise.”

4. Carcinoma ovary

Important fact

Ovarian cancer is often diagnosed late because symptoms are vague and there is no effective population screening test for average-risk women.

Risk factors

  • Increasing age
  • BRCA1/BRCA2 mutation
  • Lynch syndrome
  • Nulliparity/infertility
  • Endometriosis: associated with some epithelial subtypes
  • Family history of breast/ovarian cancer

Protective factors

  • Combined oral contraceptive use
  • Pregnancy and breastfeeding
  • Risk-reducing salpingo-oophorectomy in selected high-risk mutation carriers

Clinical features: vague but persistent

  • Abdominal distension/bloating
  • Pelvic or abdominal pain
  • Early satiety/loss of appetite
  • Urinary frequency/urgency
  • Weight loss
  • Ascites, pelvic/abdominal mass in advanced disease

Evaluation

  • Pelvic examination
  • Transvaginal/abdominal USG
  • CA-125: useful in evaluation/follow-up but not diagnostic and not a screening test in average-risk women
  • CT for extent and surgical planning
  • Definitive diagnosis is histopathological

Management principle

  • Primary cytoreductive/debulking surgery followed by platinum-based chemotherapy in many cases
  • Neoadjuvant chemotherapy followed by interval debulking surgery in selected advanced disease
  • Targeted/maintenance therapy in selected molecular subgroups
Exam pearl: CA-125 can be elevated in benign conditions including endometriosis, fibroids, PID, pregnancy, and liver disease. Do not use it alone to diagnose ovarian cancer.

5. Carcinoma vulva

Types/pathogenesis

Two main pathways:
  1. HPV-related, often in younger women, associated with vulval HSIL
  2. Non-HPV-related, often older women, associated with chronic dermatoses such as lichen sclerosus

Clinical features

  • Persistent vulval itching: common presenting complaint
  • Vulval lump, ulcer, wart-like lesion, or non-healing sore
  • Bleeding, discharge, pain
  • Inguinal lymphadenopathy

Diagnosis

Biopsy of any suspicious vulval lesion.

Spread

Usually to inguinal and femoral lymph nodes.

Management

  • Wide local excision with assessment/management of groin nodes
  • Radiotherapy/chemoradiation for selected advanced or unresectable disease

6. Carcinoma vagina

Key facts

  • Rare
  • Most are squamous cell carcinomas
  • May be secondary extension/metastasis from cervix, vulva, endometrium, or other organs

Features

  • Postcoital/postmenopausal bleeding
  • Vaginal discharge
  • Mass/ulcer
  • Pain or urinary symptoms in advanced disease

Management

Usually radiotherapy, with surgery in carefully selected cases.

Fast comparison table

CancerMost important risk factorTypical presentationDiagnosisMain treatment principle
CervixPersistent high-risk HPVPostcoital bleedingCervical biopsySurgery early, chemoradiation advanced
EndometriumUnopposed estrogen/obesityPostmenopausal bleedingEndometrial biopsyTH + BSO with staging
OvaryAge, BRCA, family historyBloating, mass, ascitesHistopathologyDebulking surgery + chemotherapy
VulvaHPV or lichen sclerosusPersistent pruritus/ulcerVulval biopsyWide local excision + node assessment

One-minute recall

  • Cervix: HPV related, postcoital bleeding, biopsy confirms.
  • Endometrium: postmenopausal bleeding, endometrial biopsy confirms.
  • Ovary: vague symptoms, CA-125 is not a screening/diagnostic test alone.
  • Vulva: chronic itching or non-healing lesion needs biopsy.
  • Pap smear: screening, not diagnostic.
  • Precancer: CIN 2/3 or HSIL require appropriate evaluation and treatment.
Recent evidence from South Asia continues to show that improving access to HPV-based screening and follow-up is central to cervical cancer prevention. PMID: 38268412.
Next: Part 5 - Antenatal care, normal pregnancy, anaemia, hypertension, diabetes, cardiac disease, and infections in pregnancy.

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preeclampsia AND management

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WHO antenatal care pre-eclampsia gestational diabetes pregnancy guidance

MBBS OBG Last-Minute Notes: Part 5 - Antenatal Care and Medical Disorders in Pregnancy

1. Antenatal care (ANC)

Objectives

  • Ensure maternal and fetal wellbeing
  • Detect high-risk pregnancy early
  • Prevent, diagnose, and treat anaemia, hypertension, diabetes, infection, malpresentation, and fetal growth restriction
  • Counsel regarding diet, supplements, danger signs, birth preparedness, breastfeeding, and contraception

At booking visit

History
  • LMP, calculate EDD using Naegele's rule:
    EDD = LMP + 9 months + 7 days
  • Obstetric history: previous CS, PPH, stillbirth, preeclampsia, preterm birth
  • Medical and surgical illness
  • Drug/allergy history
  • Family history: diabetes, hypertension, twins, congenital anomalies
  • Personal history: diet, tobacco/alcohol, domestic safety
Examination
  • Height, weight, BMI, BP
  • Pallor, edema, thyroid, breast/systemic examination
  • Obstetric examination when appropriate
  • Pelvic examination only when indicated
Basic investigations
  • Hb/CBC, blood group and Rh typing
  • Urine routine: protein and sugar
  • Blood glucose screening as per local protocol
  • HIV, hepatitis B, syphilis screening
  • Urine culture where indicated
  • First-trimester dating scan and anomaly scan according to local protocol

ANC advice

  • Balanced diet and adequate protein
  • Iron-folic acid supplementation, calcium, and relevant local supplements
  • Tetanus/diphtheria-containing vaccination according to national schedule
  • Avoid smoking, alcohol, and non-prescribed drugs
  • Folic acid before conception and during early pregnancy helps prevent neural-tube defects
  • Counsel on institutional delivery and blood donor/birth preparedness

Danger signs: urgent assessment

  • Vaginal bleeding
  • Severe headache, visual symptoms, epigastric/right upper abdominal pain
  • Convulsions
  • Sudden swelling of face/hands
  • Fever
  • Persistent vomiting
  • Leaking per vaginum
  • Decreased fetal movements
  • Severe abdominal pain, breathlessness, or reduced urine output

2. Anaemia in pregnancy

Definition

Commonly, Hb <11 g/dL is used to define anaemia in pregnancy. Iron deficiency is the commonest cause.

Causes

  • Iron deficiency
  • Folate or vitamin B12 deficiency
  • Hemoglobinopathies, e.g. thalassaemia
  • Malaria, helminthic infestation in endemic settings
  • Chronic disease, renal disease
  • Acute blood loss

Effects

MaternalFetal/neonatal
Fatigue, reduced work capacityFetal growth restriction
Heart failure in severe anaemiaPreterm birth
Increased risk from PPH/sepsisLow birth weight
Poor puerperal recoveryPerinatal morbidity/mortality

Diagnosis

  • CBC: microcytic hypochromic picture suggests iron deficiency
  • Serum ferritin is useful for confirming depleted iron stores
  • Peripheral smear
  • Hb electrophoresis if hemoglobinopathy suspected
  • Stool, malaria, B12/folate testing if indicated

Management

  • Identify and treat cause
  • Oral iron for mild/moderate iron deficiency, if tolerated
  • IV iron when oral iron is ineffective/intolerable, malabsorption exists, or late pregnancy/severe deficiency requires faster replacement
  • Blood transfusion only for selected severe/symptomatic cases or acute blood loss, with careful clinical assessment
  • Treat helminthic infestation/malaria according to local guidelines
Exam pearl: Do not label every microcytic anaemia as iron deficiency. Consider thalassaemia, especially with low MCV out of proportion to anaemia or relevant family history.

3. Hypertensive disorders of pregnancy

Classification

  1. Chronic hypertension: present before pregnancy, before 20 weeks, or persists beyond postpartum period.
  2. Gestational hypertension: hypertension after 20 weeks without proteinuria or end-organ dysfunction.
  3. Preeclampsia: new hypertension after 20 weeks with proteinuria or maternal organ dysfunction/uteroplacental dysfunction.
  4. Eclampsia: seizures in a woman with preeclampsia, not explained by another cause.
  5. Chronic hypertension with superimposed preeclampsia.

Preeclampsia

Definition

New BP ≥140/90 mmHg after 20 weeks, with proteinuria or features of organ dysfunction.

Risk factors

  • Previous preeclampsia
  • First pregnancy
  • Multiple gestation
  • Chronic hypertension
  • Diabetes mellitus
  • Chronic kidney disease
  • Obesity
  • Antiphospholipid syndrome/SLE
  • Family history

Severe features

  • BP ≥160 systolic or ≥110 diastolic
  • Persistent severe headache, visual disturbance
  • Epigastric/right upper quadrant pain
  • Pulmonary edema
  • Thrombocytopenia
  • Elevated liver enzymes
  • Renal impairment/oliguria
  • Fetal growth restriction

Investigations

Maternal
  • CBC and platelet count
  • LFT, renal function
  • Urine protein assessment
  • Coagulation profile when severe disease/abruption/DIC suspected
Fetal
  • Growth ultrasound
  • Amniotic fluid assessment
  • Doppler studies and CTG as indicated

Management principle

Definitive treatment is delivery. Timing depends on gestation, maternal condition, and fetal status.
  • Mild/stable disease: close maternal and fetal surveillance, antihypertensive therapy when indicated, planned delivery at appropriate gestation
  • Severe preeclampsia: admit, stabilise, control severe BP, prevent seizures with magnesium sulfate, assess mother and fetus, then deliver when indicated
  • Do not delay delivery in uncontrolled severe hypertension, eclampsia, pulmonary edema, abruption, HELLP syndrome, fetal compromise, or maternal deterioration
WHO describes preeclampsia as a hypertensive disorder after 20 weeks that can progress to life-threatening eclampsia, so early recognition and surveillance are central. WHO preeclampsia guidance

Eclampsia: emergency management

Definition

Generalised tonic-clonic seizure in pregnancy or puerperium due to preeclampsia.

Immediate management: ABC + MgSO₄ + BP control + delivery after stabilisation

  1. Call for help. Place in left lateral position.
  2. Maintain airway, give oxygen, protect from injury.
  3. Secure IV access, send blood tests, catheterise, monitor urine output.
  4. Magnesium sulfate is the anticonvulsant of choice.
  5. Treat severe hypertension with appropriate IV/oral rapid-acting antihypertensive according to protocol.
  6. Assess mother and fetus. Plan delivery after stabilisation. Caesarean is not automatic: route depends on obstetric condition and urgency.

Magnesium sulfate toxicity

Monitor:
  • Respiratory rate
  • Patellar reflex
  • Urine output
Antidote: calcium gluconate.
One-line viva answer: “In eclampsia, the first priority is maternal resuscitation and seizure control with magnesium sulfate, not immediate caesarean delivery.”

4. Gestational diabetes mellitus (GDM)

Definition

Glucose intolerance first recognized during pregnancy, usually diagnosed in the second or third trimester.

Risk factors

  • Previous GDM
  • Obesity
  • Previous macrosomic baby
  • PCOS
  • Family history of type 2 diabetes
  • Previous unexplained stillbirth
  • Glycosuria
  • Advanced maternal age

Maternal complications

  • Preeclampsia
  • Polyhydramnios
  • Operative delivery
  • Future type 2 diabetes

Fetal/neonatal complications

  • Macrosomia
  • Shoulder dystocia and birth trauma
  • Neonatal hypoglycaemia
  • Respiratory distress
  • Polycythaemia, hyperbilirubinaemia
  • Stillbirth in poorly controlled disease

Screening and diagnosis

Screening test and thresholds vary by national/institutional protocol. In Indian MBBS examinations, write the method taught by your department, commonly a 75-g oral glucose test approach.

Management

  1. Diet counselling and exercise as appropriate
  2. Self-monitoring of blood glucose
  3. Fetal growth surveillance
  4. Insulin if glucose targets are not achieved with lifestyle measures
  5. Plan timing/mode of birth based on glycaemic control, fetal growth, and obstetric factors
  6. Reassess glucose postpartum because of future diabetes risk
WHO issued dedicated diabetes-in-pregnancy guidance in 2025, stressing integration of diabetes care into routine antenatal services. WHO diabetes-in-pregnancy recommendations
Exam pearl: GDM causes neonatal hypoglycaemia because the fetus develops hyperinsulinaemia in response to maternal hyperglycaemia; after delivery, maternal glucose supply stops but fetal insulin remains high.

5. Cardiac disease in pregnancy

Important principle

Cardiac disease is a major indirect cause of maternal morbidity. Pregnancy increases blood volume and cardiac output, so decompensation may occur, especially in late pregnancy, labour, and early puerperium.

High-risk lesions

  • Pulmonary hypertension/Eisenmenger syndrome
  • Severe mitral stenosis
  • Mechanical heart valve
  • Severe aortic stenosis
  • Aortic disease with high dissection risk
  • Cardiomyopathy with poor ventricular function

Features of cardiac failure

  • Progressive dyspnoea, orthopnoea, PND
  • Persistent tachycardia
  • Cyanosis
  • Raised JVP, basal crepitations
  • Edema, hepatomegaly

Management principles

  • Multidisciplinary care: obstetrician, cardiologist, anaesthetist, neonatologist
  • Avoid anaemia, infection, excessive exertion, and fluid overload
  • Treat heart failure promptly
  • Vaginal delivery is preferred in many stable cardiac conditions because it avoids surgical stress, but use assisted second stage if needed to reduce maternal pushing
  • Caesarean for obstetric indication or selected severe cardiac disease
  • Careful monitoring in postpartum period because autotransfusion from the uterus can precipitate failure

6. Thyroid disease in pregnancy

Hypothyroidism

Effects

  • Maternal: miscarriage, preeclampsia, anaemia, placental abruption
  • Fetal: neurodevelopmental concern if severe untreated maternal hypothyroidism

Management

  • Levothyroxine is safe in pregnancy
  • Monitor TSH and adjust dose under specialist/local protocol

Hyperthyroidism

Usually due to Graves disease.

Risks

  • Miscarriage, preterm birth, fetal growth restriction
  • Thyroid storm in uncontrolled disease
  • Fetal/neonatal thyrotoxicosis due to maternal antibodies

Management

  • Antithyroid medication under specialist supervision
  • Avoid radioiodine in pregnancy
  • Monitor mother and fetus

7. Infections in pregnancy: fast revision

InfectionImportant fetal/maternal issueCore exam point
RubellaCongenital rubella syndrome: cataract, cardiac defect, deafnessVaccinate before pregnancy, not during pregnancy
ToxoplasmosisChorioretinitis, hydrocephalus, intracranial calcificationAvoid undercooked meat/cat litter exposure
SyphilisStillbirth, congenital syphilisScreen early; penicillin prevents congenital infection
HIVVertical transmissionART, viral-load-based delivery plan, infant prophylaxis
Hepatitis BPerinatal transmissionNeonatal immunoprophylaxis
MalariaMaternal anaemia, miscarriage, stillbirthPrompt diagnosis/treatment in endemic region
UTI/pyelonephritisPreterm labour, maternal sepsisScreen/treat bacteriuria as per protocol

8. Rh-negative pregnancy

Key facts

  • Rh-negative mother carrying an Rh-positive fetus may become sensitised after fetomaternal haemorrhage.
  • Maternal anti-D antibodies can cause hemolytic disease of fetus/newborn in subsequent Rh-positive pregnancy.

Prevention

  • Determine maternal blood group and antibody screen at booking.
  • Give anti-D immunoglobulin to unsensitised Rh-negative women according to local schedule and after sensitising events, e.g. miscarriage, ectopic pregnancy, invasive procedures, APH, abdominal trauma, and delivery of an Rh-positive infant.
  • Do not give anti-D to a woman already sensitised.

One-minute recall

  • ANC: booking history + BP + urine protein/sugar + Hb + blood group/Rh + infection screen + supplements + danger signs.
  • Anaemia: iron deficiency commonest; ferritin supports diagnosis.
  • Preeclampsia: hypertension after 20 weeks plus proteinuria or organ dysfunction.
  • Eclampsia: ABC, magnesium sulfate, control severe BP, deliver after stabilisation.
  • GDM: macrosomia, shoulder dystocia, neonatal hypoglycaemia, future maternal type 2 DM.
  • Cardiac disease: danger period is late pregnancy, labour, and early puerperium.
  • Rh-negative: anti-D for unsensitised mother after sensitising events.
Next: Part 6 - Normal labour, fetal skull, pelvis, mechanism of labour, partograph, induction, augmentation, instrumental delivery, and caesarean section.

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WHO intrapartum care labour induction operative vaginal birth caesarean section recommendations

MBBS OBG Last-Minute Notes: Part 6 - Normal Labour, Induction, Instrumental Delivery, Caesarean Section

1. Labour

Definition

Labour is the process in which regular, painful uterine contractions produce progressive cervical effacement and dilatation, leading to delivery of the fetus and placenta.

True labour versus false labour

FeatureTrue labourFalse labour
ContractionsRegular, increasing frequency/intensityIrregular, do not progressively increase
PainStarts in back, radiates to abdomenUsually lower abdomen
CervixProgressive effacement and dilatationNo progressive change
Sedation/restDoes not stop labourOften settles symptoms

2. Stages of labour

StageDefinitionKey events
First stageOnset of true labour to full cervical dilatation, 10 cmEffacement and dilatation
Second stageFull dilatation to delivery of babyDescent, rotation, expulsion
Third stageDelivery of baby to delivery of placenta and membranesPlacental separation and delivery
Fourth stageFirst 1-2 hours after placentaWatch for PPH and maternal stability

First stage: phases

  • Latent phase: cervical dilatation up to about 5 cm.
  • Active phase: from about 5 cm to full dilatation, with more rapid dilatation.

3. Powers, passage, passenger and psyche

The 4 Ps

  1. Powers - uterine contractions and maternal expulsive effort
  2. Passage - bony pelvis and soft tissues
  3. Passenger - fetus: size, lie, presentation, position, attitude
  4. Psyche - maternal fear, anxiety, support and cooperation
Failure in any one can cause abnormal labour.

4. Fetal skull

Important landmarks

  • Sutures: sagittal, coronal, lambdoid, frontal
  • Fontanelles:
    • Anterior fontanelle: diamond-shaped
    • Posterior fontanelle: triangular
  • Identification of fontanelles during vaginal examination helps determine position and flexion.

Important diameters

DiameterMeasurementClinical importance
Suboccipitobregmatic9.5 cmEngaging diameter in well-flexed vertex
Occipitofrontal11.5 cmDeflexed vertex
Mentovertical13.5 cmBrow presentation, usually cannot deliver vaginally
Submentobregmatic9.5 cmFace presentation with mentum anterior
Biparietal diameter9.5 cmLargest transverse diameter of head
Exam pearl: The best attitude for normal vaginal delivery is complete flexion of the fetal head, presenting the suboccipitobregmatic diameter.

5. Fetal lie, presentation, position, attitude

  • Lie: relation of long axis of fetus to long axis of mother
    • Longitudinal, transverse, oblique
  • Presentation: fetal part occupying lower uterine segment
    • Cephalic, breech, shoulder
  • Position: relation of denominator to maternal pelvis
    • Vertex: occiput
    • Face: mentum
    • Breech: sacrum
    • Shoulder: acromion
  • Attitude: relation of fetal parts to each other
    • Normal: general flexion

6. Pelvis and important diameters

Types of pelvis

  • Gynecoid: most favourable for vaginal birth
  • Android: heart-shaped inlet, more associated with deep transverse arrest/OP position
  • Anthropoid: long AP diameter, may predispose to OP position
  • Platypelloid: flattened, wide transverse diameter

Important pelvic diameters

  • Obstetric conjugate: approximately 10.5 cm
  • Diagonal conjugate: approximately 12.5 cm
  • Interspinous diameter: approximately 10.5 cm, narrowest transverse pelvic diameter
  • Bituberous diameter: approximately 11 cm

Station

Relationship of presenting part to ischial spines:
  • At ischial spines: station 0
  • Above spines: negative stations
  • Below spines: positive stations
Engagement: biparietal diameter has passed the pelvic inlet.

7. Mechanism of normal labour in vertex presentation

In a well-flexed occipitoanterior vertex presentation:
  1. Engagement
  2. Descent
  3. Flexion
  4. Internal rotation
  5. Extension: head is delivered
  6. Restitution
  7. External rotation
  8. Expulsion of shoulders and body

Mnemonic

“Every Daring Fellow In England Reads Easy English”
Engagement, Descent, Flexion, Internal rotation, Extension, Restitution, External rotation, Expulsion.

8. Conduct of normal labour

First stage

  • Admit, assess risk, confirm labour and fetal presentation.
  • Record maternal pulse, BP, temperature, contractions, fetal heart rate, vaginal loss, membrane status.
  • Ensure bladder emptying.
  • Provide emotional support, hydration, pain relief.
  • Perform vaginal examination only when indicated, usually at regular intervals to assess progress.
  • Monitor progression with a partograph or locally approved labour chart.

Second stage

  • Confirm full dilatation.
  • Monitor fetal heart rate and maternal condition.
  • Encourage effective pushing when appropriate.
  • Prepare neonatal resuscitation equipment.
  • Perform episiotomy only when indicated, not routinely.

Third stage

Signs of placental separation

  • Gush of blood
  • Lengthening of cord
  • Uterus becomes firm, globular, and rises in abdomen

Active management of third stage of labour

  • Give a uterotonic, usually oxytocin, after birth.
  • Controlled cord traction with uterine support.
  • Assess uterine tone and inspect placenta/membranes for completeness.
This reduces postpartum haemorrhage risk. NICE intrapartum guidance

9. Partograph

Purpose

A graphical record of labour progress and maternal-fetal wellbeing used to identify slow progress and need for timely action.

Components

  1. Fetal condition
    • FHR
    • Liquor
    • Moulding
  2. Progress of labour
    • Cervical dilatation
    • Descent of head
    • Uterine contractions
  3. Maternal condition
    • Pulse, BP, temperature
    • Urine volume, protein, ketones
    • Drugs and IV fluids

Alert and action lines

Traditional partographs use:
  • Alert line: slow progress requiring closer observation/referral.
  • Action line: need for assessment and corrective action.
Do not use the partograph alone to diagnose obstruction. Consider contractions, fetal status, CPD, maternal exhaustion, and full clinical picture.

10. Induction of labour (IOL)

Definition

Artificial initiation of uterine contractions before spontaneous onset of labour, with the aim of vaginal delivery.

Common indications

  • Postdated pregnancy
  • Prelabour rupture of membranes
  • Hypertensive disorders of pregnancy
  • Diabetes with appropriate indication
  • Fetal growth restriction/oligohydramnios
  • Intrauterine fetal death
  • Maternal medical disease where delivery benefits mother/fetus

Contraindications

  • Placenta previa or vasa previa
  • Transverse lie
  • Previous classical uterine incision or major transmural uterine surgery
  • Cord prolapse
  • Cephalopelvic disproportion
  • Active genital herpes
  • Any contraindication to vaginal birth

Bishop score

Assesses cervical favourability:
  • Dilatation
  • Effacement/length
  • Station
  • Consistency
  • Position
A low Bishop score indicates an unfavourable cervix and need for cervical ripening.

Methods

  • Membrane sweeping
  • Prostaglandin cervical ripening
  • Balloon catheter
  • Amniotomy
  • Oxytocin infusion

Essential safety point

Before induction: confirm indication, gestation, presentation, fetal wellbeing, absence of contraindications, and availability of monitoring and emergency caesarean capability. WHO advises that induction should occur where maternal-fetal assessment and caesarean delivery are available if needed. WHO induction guidance

11. Augmentation of labour

Definition

Enhancement of inadequate uterine contractions after spontaneous labour has started.

Methods

  • Amniotomy
  • Oxytocin infusion

Before augmentation

Exclude:
  • CPD
  • Malpresentation/malposition
  • Fetal distress
  • Obstructed labour
  • Full bladder
  • Incorrect diagnosis of active labour
Danger: inappropriate oxytocin in CPD or obstructed labour may cause uterine hyperstimulation, fetal hypoxia, or uterine rupture.

12. Operative vaginal delivery

Types

  • Vacuum extraction/ventouse
  • Forceps delivery

Indications

Maternal
  • Exhaustion
  • Prolonged second stage
  • Need to shorten second stage in selected maternal disease, e.g. significant cardiac disease
Fetal
  • Non-reassuring fetal status in second stage when immediate vaginal delivery is feasible

Prerequisites: “FULL”

  • Fully dilated cervix
  • Unruptured? No, membranes should be ruptured and bladder empty
  • Lie/presentation/position accurately known
  • Low head: engaged, no CPD, adequate pelvis
Also require informed consent, anaesthesia/analgesia, skilled operator, neonatal support, and facility for immediate caesarean if procedure fails.

Forceps versus ventouse

FeatureForcepsVentouse
TractionMore controlled/strongerLess traction force
Maternal traumaHigherLower
Fetal scalp traumaLess scalp injuryMore scalp bruising/cephalohaematoma
Use in face presentationMay be used in selected casesContraindicated
Preterm fetusOften preferred over vacuum in selected situationsGenerally avoided in very preterm baby

Complications

  • Maternal: vaginal/cervical trauma, perineal tears, PPH
  • Fetal: scalp injury, facial injury, cephalohaematoma, rarely intracranial injury

13. Caesarean section (CS)

Definition

Delivery of fetus through abdominal incision and uterine incision.

Common indications

Maternal/obstetric

  • Previous CS in selected situations
  • CPD or obstructed labour
  • Failed induction
  • Placenta previa major
  • Placental abruption with fetal/maternal compromise
  • Cord prolapse with viable fetus
  • Transverse lie
  • Certain malpresentations
  • Previous uterine rupture/classical CS

Fetal

  • Persistent fetal distress
  • Some cases of severe fetal growth restriction or abnormal Doppler
  • Macrosomia in selected high-risk settings

Complications

Intraoperative/earlyLate
Haemorrhage, infection, bladder/bowel injuryAdhesions
Anaesthetic complications, thromboembolismScar ectopic pregnancy
Wound complicationsPlacenta previa/accreta spectrum in later pregnancy
Delayed recoveryUterine rupture risk in future labour

Types of uterine incision

  • Lower-segment transverse incision: commonest; better healing and lower future rupture risk
  • Classical vertical incision: used only in selected situations; higher rupture risk in future pregnancy
Exam pearl: A previous classical CS is generally a contraindication to trial of labour after caesarean.

One-minute recall

  • True labour: regular pains plus progressive cervical change.
  • Normal vertex mechanism: engagement → descent → flexion → internal rotation → extension → restitution → external rotation → expulsion.
  • Station 0: ischial spines.
  • Engagement: biparietal diameter passes pelvic inlet.
  • Induction: check indication, Bishop score, presentation, fetal status, and contraindications.
  • Augmentation: never start oxytocin before excluding CPD/obstruction.
  • Instrumental delivery: full dilatation, ruptured membranes, engaged head, known position, empty bladder, no CPD.
  • CS: lower-segment transverse incision is standard; consider future scar risks.
Next: Part 7 - Obstructed labour, CPD, uterine rupture, malposition, malpresentation, breech, face, brow, transverse lie, and cord prolapse.

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MBBS OBG Last-Minute Notes: Part 7 - Obstructed Labour, Malpositions, Malpresentations and Cord Prolapse

1. Obstructed labour

Definition

Labour in which the presenting part fails to descend despite good uterine contractions because of a mechanical obstruction.

Causes

  1. Cephalopelvic disproportion (CPD)
    • Contracted pelvis
    • Large fetus/macrosomia
    • Deflexed head
  2. Malpresentation
    • Transverse lie
    • Brow presentation
    • Face presentation with mentoposterior position
    • Shoulder presentation
  3. Malposition
    • Persistent occipitoposterior
    • Deep transverse arrest
  4. Soft-tissue obstruction
    • Cervical fibroid
    • Ovarian tumour
    • Full bladder
    • Vaginal septum/scarring

Clinical features

  • Prolonged labour with maternal exhaustion, dehydration, tachycardia
  • Strong, frequent contractions
  • Poor descent despite adequate contractions
  • Bandl's ring or pathological retraction ring: sign of impending rupture
  • Distended bladder, scanty urine
  • Caput succedaneum and marked moulding
  • Cervical edema
  • Foul-smelling liquor and fever if infection has occurred
  • Fetal distress or intrauterine fetal death

Management

  1. Call for senior help and prepare for urgent delivery.
  2. ABC assessment, IV access, fluids, blood grouping/cross-match.
  3. Catheterise bladder and monitor urine output.
  4. Antibiotics if prolonged labour, infection, or operative intervention.
  5. Assess fetal status and cause of obstruction.
  6. Caesarean section is usually required if fetus is alive and obstruction is present.
  7. If fetus is dead and vaginal destructive procedure is appropriate, it should only be performed by an experienced obstetrician in a suitable setting.
Do not augment obstructed labour with oxytocin. It can precipitate uterine rupture.

Complications

MaternalFetal
Uterine ruptureHypoxia/asphyxia
PPH, shock, sepsisBirth trauma
Bladder injuryStillbirth/neonatal death
Vesicovaginal or rectovaginal fistula
Acute kidney injury
Maternal death
Prolonged obstruction can compress the bladder and rectum, producing pressure necrosis and obstetric fistula. MSF obstructed-labour guidance

2. Cephalopelvic disproportion (CPD)

Definition

Mismatch between fetal head size and maternal pelvic capacity such that safe vaginal delivery is not possible.

Causes

  • Contracted pelvis: malnutrition, rickets, trauma, pelvic deformity
  • Large fetus: diabetes, post-term pregnancy
  • Hydrocephalus
  • Malposition/malpresentation causing increased presenting diameter
  • Inadequate flexion of head

Diagnosis

CPD is usually diagnosed during labour by:
  • Poor progress despite adequate contractions
  • Failure of descent
  • Increasing caput and moulding
  • High, unengaged head at term in a primigravida may raise suspicion
Management: caesarean delivery if significant CPD is diagnosed.

3. Uterine rupture

Definition

Complete or incomplete disruption of the uterine wall during pregnancy or labour.

Risk factors

  • Previous caesarean scar, especially classical incision
  • Previous myomectomy entering uterine cavity
  • Obstructed labour
  • Injudicious oxytocin/prostaglandin use
  • Grand multiparity
  • Trauma
  • Malpresentation

Features

  • Sudden severe abdominal pain or pain persisting between contractions
  • Maternal tachycardia, hypotension, shock
  • Vaginal bleeding may be absent or present
  • Loss of uterine contour
  • Cessation of contractions
  • Easily palpable fetal parts
  • Loss of fetal station
  • Fetal bradycardia or absent fetal heart sounds

Management

  • Immediate resuscitation: ABC, two IV lines, fluids, blood products.
  • Urgent laparotomy and delivery.
  • Repair uterus if feasible, or hysterectomy if bleeding/extent of rupture demands it.
  • Broad-spectrum antibiotics and intensive postoperative care.
Viva line: The commonest early sign of scar rupture may be fetal heart-rate abnormality, particularly persistent fetal bradycardia.

4. Occipitoposterior position (OP)

Definition

Vertex presentation in which the occiput is directed posteriorly, usually right occipitoposterior.

Why it matters

An OP fetus may rotate anteriorly and deliver normally, but persistent OP can cause prolonged labour, severe backache, deep transverse arrest, and operative delivery.

Features

  • Severe backache
  • Slow labour/prolonged second stage
  • On vaginal examination: posterior fontanelle felt posteriorly; sagittal suture in oblique diameter
  • Increased caput and moulding if persistent

Management

  • Confirm position clinically and by ultrasound where available.
  • Encourage mobility/position changes and provide analgesia.
  • Monitor labour and fetal status.
  • If full dilatation and head low, skilled manual rotation or operative vaginal birth may be possible.
  • Caesarean if arrest of descent, CPD, high head, or fetal compromise.

5. Deep transverse arrest (DTA)

Definition

Arrest of the head in transverse position at the level of ischial spines or below, due to failure of internal rotation.

Causes

  • Android pelvis
  • Inadequate uterine action
  • CPD
  • Persistent occipitotransverse position

Management

  • Confirm full dilatation, station, position, and absence of CPD.
  • If head is low and conditions are suitable: manual rotation followed by forceps/vacuum by an experienced operator.
  • Caesarean section when rotation/delivery is unsafe or unsuccessful.

6. Breech presentation

Definition

Longitudinal lie with buttocks or lower limbs presenting first.

Types

TypeDescription
Frank breechHips flexed, knees extended
Complete breechHips and knees flexed
Footling breechOne or both hips and knees extended, foot presents first

Causes

  • Prematurity
  • Multiple pregnancy
  • Uterine anomaly/fibroid
  • Placenta previa
  • Polyhydramnios/oligohydramnios
  • Fetal anomaly
  • Previous breech pregnancy

Diagnosis

Abdominal examination
  • Hard, round ballotable head in fundus
  • Soft, irregular breech in lower pole
  • Fetal heart usually heard above umbilicus
Vaginal examination
  • Sacrum, anus, ischial tuberosities, genitalia, feet may be felt.
  • Do not confuse anus with mouth: anus has sphincter tone; mouth has gums.
Confirmation: ultrasound, including fetal anomaly assessment, estimated fetal weight, head attitude, placental location, and liquor.

Management

  • At term, consider external cephalic version (ECV) if no contraindication.
  • Planned caesarean is commonly chosen for many term breech pregnancies.
  • Planned vaginal breech birth is only for carefully selected cases with informed consent, experienced staff, immediate CS facility, and strict criteria.

Principles of vaginal breech delivery

  • “Hands off the breech” until the scapulae are visible.
  • Allow spontaneous descent.
  • Assist delivery of legs/arms only if required.
  • Deliver after-coming head by a recognised manoeuvre such as Mauriceau-Smellie-Veit manoeuvre, by an experienced operator.

Breech complications

  • Cord prolapse, especially footling breech
  • Head entrapment
  • Birth trauma
  • Fetal hypoxia/asphyxia

7. Face presentation

Definition

Cephalic presentation with complete extension of the head. The denominator is the mentum.

Diagnosis

On vaginal examination, feel:
  • Mouth, nose, orbital ridges, malar prominences
  • Avoid repeated traumatic examination.

Mechanism and management

  • Mentum anterior: vaginal delivery may occur because the submentobregmatic diameter presents.
  • Mentum posterior: vaginal delivery is generally not possible in a term fetus because further extension cannot occur. Perform caesarean section.
Key line: Face presentation can deliver vaginally only if the mentum is anterior.

8. Brow presentation

Definition

Partial extension of the fetal head. The presenting diameter is mentovertical, 13.5 cm.

Diagnosis

Frontal sutures, anterior fontanelle, orbital ridges, and root of nose may be felt.

Management

  • Usually transient and may convert to face or vertex.
  • Persistent brow in a term fetus generally cannot deliver vaginally because the mentovertical diameter is too large.
  • Caesarean section is the usual management for persistent brow.

9. Transverse lie and shoulder presentation

Definition

Fetal longitudinal axis lies transverse to the maternal axis. Shoulder/acromion is the denominator.

Causes

  • Multiparity/lax uterus
  • Placenta previa
  • Polyhydramnios
  • Prematurity
  • Uterine anomaly or fibroid
  • Multiple pregnancy
  • Pelvic tumour/contracted pelvis

Diagnosis

  • Abdomen broad transversely
  • Head felt in one iliac fossa and breech in the other
  • Fetal heart often heard near umbilicus
  • Vaginal examination may reveal shoulder, acromion, ribs, axilla, or prolapsed arm

Management

  • Before labour: ECV may be considered if suitable.
  • In labour with live singleton fetus: caesarean section.
  • Neglected transverse lie can become obstructed labour and cause uterine rupture.

10. Compound presentation

Definition

A fetal extremity presents alongside the main presenting part, most commonly a hand beside the head.

Management

  • If hand is beside a well-descending vertex, expectant management may be possible.
  • Avoid forceful manipulation.
  • Caesarean if cord prolapse, persistent obstruction, or failure to progress.

11. Umbilical cord prolapse

Definition

Descent of the cord through the cervix beside or beyond the presenting part after membrane rupture.

Types

  • Overt prolapse: cord felt/seen below presenting part after membrane rupture.
  • Occult prolapse: cord lies alongside presenting part and is not visible/felt.
  • Cord presentation: cord lies between presenting part and cervix while membranes are intact.

Risk factors

  • Malpresentation: transverse lie, footling breech
  • Unengaged/high presenting part
  • Prematurity/low birth weight
  • Polyhydramnios
  • Multiple pregnancy
  • Artificial rupture of membranes with high head
  • Long cord
  • Obstetric manipulations

Diagnosis

  • Sudden fetal bradycardia or recurrent variable decelerations after membrane rupture
  • Cord seen at introitus or felt on vaginal examination

Management: “Call - Lift - Fill - Deliver”

  1. Call for help and start continuous fetal monitoring.
  2. Lift the presenting part manually off the cord during vaginal examination.
  3. Fill the bladder with saline if this will facilitate transfer/delivery and manual elevation cannot be maintained.
  4. Position mother knee-chest or steep head-down lateral position.
  5. Minimise handling of exposed cord. Keep it warm and moist with saline-soaked gauze if outside vagina.
  6. Give oxygen only if maternal hypoxia, not routinely.
  7. Immediate caesarean section unless vaginal birth is truly imminent.
Cord prolapse causes fetal hypoxia through cord compression and vasospasm and requires immediate action. RCOG cord-prolapse guidance

One-minute recall

  • Obstructed labour: failure of descent despite good contractions because of mechanical block.
  • Never use oxytocin in suspected CPD/obstructed labour.
  • Bandl's ring: impending uterine rupture.
  • Uterine rupture: resuscitate, blood, immediate laparotomy.
  • Persistent OP: backache, prolonged labour, deep transverse arrest.
  • Breech: term vaginal birth only in carefully selected cases with expertise.
  • Face: mentum anterior can deliver; mentum posterior requires CS.
  • Brow: persistent brow usually needs CS.
  • Transverse lie in labour: CS.
  • Cord prolapse: elevate presenting part and expedite delivery, usually CS.
Next: Part 8 - Antepartum haemorrhage, postpartum haemorrhage, hypertensive emergencies, sepsis, shock, puerperium, lactation, and newborn resuscitation basics.

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MBBS OBG Last-Minute Notes: Part 8 - APH, PPH, Sepsis, Shock, Puerperium, Lactation and Newborn Care

1. Antepartum haemorrhage (APH)

Definition

Bleeding from or into the genital tract after 24 weeks of gestation and before delivery. Some guidelines use 20 weeks.

Major causes

  1. Placenta previa
  2. Placental abruption
  3. Vasa previa
  4. Local genital-tract lesions: cervicitis, cervical polyp/cancer, vaginal trauma
  5. Uterine rupture, rarely before delivery

Placenta previa

Definition

Placenta implanted in the lower uterine segment, partly or completely covering the internal cervical os.

Risk factors

  • Previous caesarean section or uterine surgery
  • Previous placenta previa
  • Multiparity
  • Multiple pregnancy
  • Advanced maternal age
  • Smoking

Classical features

  • Painless
  • Bright-red
  • Recurrent
  • Bleeding in late pregnancy
  • Uterus is soft and non-tender
  • Malpresentation or high/unengaged head may be present

Diagnosis

  • Ultrasound, preferably transvaginal ultrasound when appropriate
  • Do not perform digital vaginal examination until placenta previa is excluded.

Management principle

  • Stabilise mother first: ABC, IV access, blood grouping/cross-match.
  • Assess fetal condition and gestation.
  • Expectant management may be possible in stable, preterm cases with minor bleeding.
  • Major placenta previa, persistent bleeding, fetal compromise, or labour usually requires caesarean delivery.

Placental abruption

Definition

Premature separation of a normally implanted placenta after fetal viability and before delivery.

Risk factors

  • Hypertension/preeclampsia
  • Previous abruption
  • Trauma
  • Smoking/cocaine use
  • PROM
  • Multiple pregnancy with sudden uterine decompression

Clinical features

  • Painful vaginal bleeding
  • Abdominal pain and uterine tenderness
  • Tense, “board-like” uterus
  • Frequent contractions
  • Fetal distress or death
  • Bleeding may be concealed, so visible loss can underestimate severity

Complications

  • Maternal shock
  • DIC
  • Acute kidney injury
  • PPH
  • Fetal hypoxia, prematurity, stillbirth

Management

  • Resuscitate, send CBC, coagulation profile, renal function, group/cross-match.
  • Continuous fetal monitoring if viable fetus.
  • Expedite delivery if maternal instability, fetal compromise, or severe abruption.
  • Vaginal delivery may be preferred if fetus has died and maternal condition allows; otherwise CS when indicated.

Placenta previa versus abruption

FeaturePlacenta previaPlacental abruption
BleedingBright red, visibleDark blood, may be concealed
PainPainlessPainful
UterusSoft, non-tenderTender, tense/woody
Fetal statusOften initially reassuringFrequently compromised
PresentationMalpresentation/high head commonUsually cephalic unless another issue
PV examinationDigital PV contraindicated until excludedMay be done only after previa excluded

2. Postpartum haemorrhage (PPH)

Definition

Traditionally:
  • Blood loss ≥500 mL after vaginal birth, or
  • ≥1000 mL after caesarean birth.
Clinically, treat any postpartum bleeding causing haemodynamic instability as PPH regardless of measured volume.

Types

  • Primary PPH: within 24 hours of birth
  • Secondary PPH: 24 hours to 6 weeks postpartum

Causes: the 4 Ts

CauseExamples
ToneUterine atony, most common cause
TraumaCervical/vaginal/perineal tears, uterine rupture, inversion
TissueRetained placenta, retained products, placenta accreta spectrum
ThrombinDIC, thrombocytopenia, coagulation disorders

Uterine atony

Risk factors

  • Overdistended uterus: multiple pregnancy, polyhydramnios, macrosomia
  • Prolonged labour or precipitate labour
  • Oxytocin augmentation
  • Chorioamnionitis
  • Grand multiparity
  • Uterine relaxants/anaesthesia
  • Previous PPH

Features

  • Heavy vaginal bleeding
  • Uterus is enlarged, soft, and boggy

PPH management: “Call, Resuscitate, Find cause, Treat”

Immediate actions

  1. Call for help: obstetrician, anaesthetist, blood bank, theatre team.
  2. ABC assessment, high-flow oxygen if hypoxaemic.
  3. Two large-bore IV cannulas.
  4. Send blood: CBC, group and cross-match, coagulation profile, fibrinogen.
  5. Warm IV fluids and initiate blood-product replacement as needed.
  6. Monitor pulse, BP, urine output, and blood loss.
  7. Uterine massage and empty the bladder.

Specific treatment

Tone
  • Uterine massage
  • Uterotonics according to institutional protocol
  • Tranexamic acid early in clinically diagnosed PPH
  • Bimanual uterine compression
  • Balloon tamponade if medical treatment fails
  • Compression sutures, uterine/iliac artery ligation or embolisation where available
  • Hysterectomy if life-threatening bleeding persists
Trauma
  • Inspect cervix, vagina, perineum; repair tears.
  • Suspect rupture/inversion if uterus is abnormal or bleeding continues despite a well-contracted uterus.
Tissue
  • Manual removal of retained placenta or evacuation of retained products, with adequate anaesthesia/antibiotics as indicated.
Thrombin
  • Correct coagulopathy with appropriate blood components.
Exam line: “The commonest cause of primary PPH is uterine atony.”
WHO’s updated PPH guidance emphasises early diagnosis, rapid treatment, correction of anaemia, and team-based response. WHO PPH update

Secondary PPH

Causes

  • Retained products of conception
  • Endometritis
  • Subinvolution of placental site
  • Bleeding disorder

Management

  • Assess haemodynamic stability.
  • USG if retained products are suspected.
  • Antibiotics if infection is suspected.
  • Uterotonics and evacuation when indicated.

3. Uterine inversion

Definition

Turning inside out of the uterus, usually after delivery of the baby.

Risk factors

  • Excessive cord traction before placental separation
  • Fundal placenta
  • Uterine atony
  • Fundal pressure

Clinical features

  • Sudden PPH and shock, often disproportionate to visible blood loss
  • Severe pain
  • Fundus not palpable abdominally
  • Mass seen/felt through cervix or vagina

Management

  1. Resuscitate.
  2. Immediate manual replacement of uterus.
  3. Give uterotonics after replacement to maintain contraction.
  4. If unsuccessful, use hydrostatic or surgical correction.

4. Obstetric sepsis and puerperal sepsis

Definition

Puerperal sepsis is infection of the genital tract occurring after childbirth, miscarriage, or abortion.

Risk factors

  • Prolonged labour
  • Prolonged rupture of membranes
  • Multiple vaginal examinations
  • Retained products
  • Caesarean delivery
  • PPH, anaemia, poor asepsis

Features

  • Fever, chills, tachycardia
  • Uterine tenderness
  • Foul-smelling lochia
  • Lower abdominal/pelvic pain
  • Wound infection
  • Hypotension, altered sensorium, oliguria in severe sepsis

Management: do not delay

  • ABC resuscitation, oxygen if needed, IV fluids.
  • Take cultures if this does not delay treatment.
  • Start broad-spectrum IV antibiotics promptly.
  • Identify and control source: retained products, infected wound, abscess, septic pelvic thrombophlebitis.
  • Monitor urine output, lactate where available, and organ dysfunction.
  • Escalate to critical care if shock or organ failure.

5. Obstetric shock

Types

  • Hypovolaemic: haemorrhage, commonest
  • Septic: puerperal sepsis, septic abortion
  • Cardiogenic: heart disease, peripartum cardiomyopathy
  • Anaphylactic
  • Obstructive: pulmonary embolism, amniotic-fluid embolism

Features

  • Tachycardia
  • Hypotension, narrow pulse pressure
  • Cold clammy skin in hypovolaemic shock
  • Oliguria
  • Altered mental state
  • Delayed capillary refill

Management

ABC
  • Airway, breathing, circulation
  • Two wide-bore IV lines
  • Blood samples and cross-match
  • Rapid blood-component replacement when haemorrhage is present
  • Urinary catheter, strict fluid balance
  • Treat cause urgently
High-yield: In obstetric haemorrhage, tachycardia may occur before hypotension. Never wait for severe hypotension before acting.

6. Amniotic-fluid embolism (AFE)

Definition

A rare, unpredictable, catastrophic obstetric emergency due to maternal systemic reaction to amniotic fluid/fetal material entering maternal circulation.

Classical presentation

  • Sudden hypoxia/respiratory distress
  • Hypotension or cardiac collapse
  • DIC with severe bleeding

Management

  • Immediate multidisciplinary resuscitation
  • Oxygenation/ventilation, CPR if required
  • Correct DIC with massive transfusion support
  • Deliver fetus if indicated during maternal resuscitation
  • Critical-care management

7. Puerperium

Definition

Period of approximately 6 weeks after delivery, during which maternal reproductive organs return toward the non-pregnant state.

Normal changes

Uterine involution

  • Immediately after delivery: fundus near the umbilicus
  • Descends about 1 cm/day
  • Usually no longer palpable abdominally by about 2 weeks
  • Returns close to pre-pregnant size by 6 weeks

Lochia

TypeDurationAppearance
Lochia rubraFirst 3-4 daysRed, blood-stained
Lochia serosaAbout day 4-10Pink/brown
Lochia albaUp to 4-6 weeksYellowish-white

Postnatal care

  • Monitor uterine involution, lochia, BP, wound, bowel/bladder function.
  • Encourage early ambulation, nutrition, hygiene, breastfeeding, and contraception counselling.
  • Screen for mood symptoms and domestic/social support.

8. Lactation

Physiology

  • Prolactin: milk production
  • Oxytocin: milk ejection or let-down reflex
  • Suckling increases prolactin and oxytocin release.

Colostrum

  • Present in first few days
  • Yellow, thick, protein-rich
  • Rich in immunoglobulins, particularly IgA
  • Acts as the infant’s first immunological protection

Breastfeeding advice

  • Initiate early, ideally within 1 hour after birth if mother and newborn are stable.
  • Exclusive breastfeeding for the first 6 months is generally recommended.
  • Correct attachment: mouth wide open, chin touching breast, more areola visible above than below, no painful nipple compression.
  • Feed on demand.

Common problems

  • Engorgement: frequent effective feeding, correct attachment.
  • Cracked nipple: improve latch and positioning.
  • Mastitis: continue milk drainage/breastfeeding if possible, analgesia and antibiotics when bacterial infection suspected.
  • Breast abscess: drainage plus antibiotics.

9. Postpartum mental-health conditions

ConditionOnset/featuresManagement principle
Postpartum bluesFirst week, tearfulness, mild mood lability; resolves within 2 weeksReassurance, support
Postpartum depressionPersistent low mood, loss of interest, impaired functionMental-health assessment, psychotherapy ± medication
Postpartum psychosisDelusions, hallucinations, severe agitation/confusion; emergencyUrgent psychiatric and obstetric care, protect mother and infant
Red flag: Suicidal thoughts, thoughts of harming the baby, severe confusion, or hallucinations require urgent emergency assessment.

10. Essential newborn care

Immediately after birth

  1. Dry thoroughly and provide warmth.
  2. Assess breathing, tone, and heart rate.
  3. Delayed cord clamping where appropriate and when resuscitation is not urgently required.
  4. Skin-to-skin contact.
  5. Start breastfeeding early.
  6. Identify baby, examine for congenital anomalies, provide routine prophylaxis and immunisation according to local policy.

11. Basic newborn resuscitation

Initial assessment

Ask:
  • Is the baby term?
  • Is there good tone?
  • Is the baby breathing or crying?
If yes: routine care, warmth, skin-to-skin contact, ongoing observation.

If not breathing/gasping

  1. Warm, position airway, dry, stimulate.
  2. Clear secretions only if airway obstruction is suspected.
  3. Start positive-pressure ventilation if apnoeic/gasping or heart rate remains low.
  4. Reassess heart rate and breathing.
  5. If heart rate remains very low despite effective ventilation, begin chest compressions and escalate to advanced resuscitation.
Most important step in neonatal resuscitation: establish effective ventilation.

One-minute emergency recall

  • APH: placenta previa = painless; abruption = painful + tender tense uterus.
  • Never do a digital PV examination in APH until placenta previa is excluded.
  • PPH causes: 4 Ts = Tone, Trauma, Tissue, Thrombin.
  • PPH first steps: call help, resuscitate, uterine massage, uterotonics, find cause, blood products early.
  • Uterine inversion: PPH + shock + absent fundus.
  • Sepsis: early IV antibiotics plus source control.
  • Puerperium: 6 weeks; lochia rubra → serosa → alba.
  • Lactation: prolactin makes milk; oxytocin ejects milk.
  • Newborn resuscitation: warmth, airway positioning, stimulation, then effective ventilation.
This completes the core MBBS gynaecology and obstetrics revision sequence.

Can you please help me out about the OB-D case? Uh, a woman from marriage since two year came to my OB-D. Uh, she wants to conceive, and she has past history of, uh, PCOS, and, uh, she had a treatment for that before the marriage. After the marriage, she say about-- she says, according to her, her periods was normal, uh, at, uh, first two to three months. After that, she had again, uh, issues in her cycles, uh, and now she wants to conceive. Now, kindly can you, uh... Tell me, uh, how to take history? Uh, what, what should I, workups I do, uh, test and all that, and what treatment should I suggest that patient?

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2023 international evidence based guideline PCOS infertility assessment letrozole first line ovulation induction

This is primary infertility of 2 years, probably due to anovulation from PCOS, but do not assume PCOS is the only cause. Evaluate the couple together before giving ovulation induction.

How to present the case

A woman married for 2 years presents with inability to conceive despite regular unprotected intercourse. She has a past history of PCOS and currently has irregular menstrual cycles, suggesting ovulatory dysfunction. I would take a detailed infertility history, examine both partners where possible, exclude pregnancy and other endocrine causes of irregular cycles, and assess the three basic fertility factors: ovulation, semen parameters, and tubal patency.
The basic infertility work-up before treatment is: semen analysis, confirmation of ovulation, and assessment of tubal patency. Berek & Novak's Gynecology, Initial Assessment.

1. History taking

A. Present complaint

Ask:
  • Duration of marriage and duration of trying to conceive
  • Are they having regular unprotected intercourse? Frequency, ideally every 2-3 days through the cycle
  • Any contraception used after marriage and when stopped?
  • Previous infertility treatment, ovulation-induction drugs, injections, response, and any records
  • Has a pregnancy test been done recently?

B. Menstrual history

Ask specifically:
  • Age at menarche
  • LMP
  • Cycle interval: every how many days?
  • Regular or irregular? Amenorrhoea for how long?
  • Duration and amount of flow
  • Dysmenorrhoea, intermenstrual bleeding, postcoital bleeding
  • Past regularity: when did cycles become irregular?
  • Cyclical breast pain, premenstrual symptoms
Interpretation: Cycles longer than 35 days, very irregular menses, or amenorrhoea suggest anovulation, common in PCOS.

C. Symptoms of PCOS and other endocrine disease

Ask:
  • Weight gain, obesity
  • Hirsutism, acne, scalp hair thinning
  • Acanthosis nigricans
  • Galactorrhoea, headache, visual symptoms: hyperprolactinaemia/pituitary lesion
  • Heat/cold intolerance, altered bowel habits, tremor: thyroid disease
  • Rapid virilisation, deep voice, marked temporal balding: consider androgen-secreting tumour, not ordinary PCOS
  • Stress, excessive exercise, eating disorder, major weight loss

D. Obstetric and gynaecological history

  • Any previous pregnancy, miscarriage, ectopic, MTP, or live birth
  • History of PID, STI, genital tuberculosis, chronic pelvic pain, endometriosis
  • Previous pelvic/abdominal surgery, appendicitis, ectopic surgery
  • Past ovarian cyst/torsion
  • Past uterine curettage: consider intrauterine adhesions if amenorrhoea developed afterwards
  • Cervical procedures or genital TB exposure

E. Past, drug, and family history

  • Diabetes, hypertension, thyroid disease, epilepsy, renal/liver disease
  • Current and past medications, especially antipsychotics, steroids, hormonal drugs
  • Prior PCOS treatment: metformin, COC, clomiphene, letrozole, gonadotropins
  • Family history of diabetes, PCOS, premature menopause, infertility, congenital anomalies

F. Lifestyle history

  • Weight, diet, exercise
  • Smoking, alcohol, drugs
  • Sexual history: dyspareunia, vaginismus, sexual dysfunction
  • Psychological stress

G. Husband's history

This is essential.
  • Age, occupation and heat/toxin exposure
  • Children from previous relationship
  • Puberty and sexual function: libido, erection, ejaculation
  • Mumps orchitis, undescended testis, varicocele, STI, TB
  • Diabetes, surgery, trauma, chemotherapy/radiation
  • Smoking, alcohol, anabolic steroids, medications
  • Semen analysis should be done early, not after months of treating the woman.

2. Examination

General examination

  • Height, weight, BMI, waist circumference
  • BP
  • Pallor, thyroid enlargement
  • Hirsutism score, acne, androgenic alopecia
  • Acanthosis nigricans: insulin resistance
  • Galactorrhoea
  • Signs of virilisation

Systemic examination

  • Thyroid
  • Breast examination if galactorrhoea
  • Cardiovascular and abdominal examination

Gynaecological examination

Only after consent and when appropriate:
  • External genitalia and secondary sexual characters
  • Speculum examination: discharge, cervix, infection
  • Bimanual examination:
    • Uterine size/position
    • Adnexal mass
    • Tenderness
    • Endometriosis signs
    • Pelvic mobility/fixed uterus, suggesting adhesions

3. Investigations

First: exclude pregnancy

  • Urine pregnancy test or serum beta-hCG
Never begin ovulation induction until pregnancy is excluded.

A. Tests for ovulatory dysfunction and PCOS

  • TSH
  • Serum prolactin
  • Total testosterone or free androgen index if hirsutism/biochemical hyperandrogenism
  • Consider 17-hydroxyprogesterone if non-classic congenital adrenal hyperplasia is suspected
  • FSH, LH, estradiol if ovarian insufficiency/hypothalamic cause is suspected
  • Mid-luteal serum progesterone only if cycles are reasonably predictable and you need to confirm ovulation
  • Transvaginal pelvic ultrasound:
    • Ovarian morphology
    • Endometrial thickness
    • Fibroid, polyp, endometrioma, adnexal mass
PCOS is diagnosed using Rotterdam criteria, after excluding other causes: any two of oligo/anovulation, clinical or biochemical hyperandrogenism, and polycystic ovarian morphology.

B. Metabolic evaluation in PCOS

  • Fasting glucose or preferably 75-g OGTT, depending on local protocol
  • HbA1c where appropriate
  • Lipid profile
  • BP and BMI
PCOS increases metabolic and pregnancy risks, so preconception assessment matters.

C. Couple infertility evaluation

FactorTest
Male factorSemen analysis
OvulationMenstrual history, progesterone if needed, follicular monitoring
Uterus/ovariesTransvaginal USG
TubesHSG, or laparoscopy with chromopertubation when indicated

Tubal patency

Do HSG particularly if:
  • History of PID/STI
  • Genital TB risk/history
  • Previous ectopic pregnancy
  • Previous pelvic surgery
  • Endometriosis symptoms
  • Abnormal semen analysis may change the treatment pathway
In anovulatory PCOS with a normal semen analysis and no tubal-risk history, timing of tubal testing can be individualised before starting ovulation induction. The 2023 international PCOS guideline supports this approach.

4. Management plan

Step 1: Preconception counselling

  • Explain that PCOS commonly causes infertility by anovulation, but treatment can be effective.
  • Aim for intercourse every 2-3 days, or around the fertile period if cycles/ovulation are monitored.
  • Start folic acid before conception.
  • Stop smoking/alcohol and review unsafe medications.
  • Optimise diabetes, hypertension, thyroid disease, and weight.

Step 2: Lifestyle management

If overweight or obese:
  • Healthy calorie deficit, dietitian support if available
  • Regular exercise
  • A modest weight reduction can improve cycles, ovulation, and pregnancy outcomes.
Do not delay all fertility treatment indefinitely for weight loss, especially with increasing age. Use an individualised plan.

Step 3: Protect the endometrium if she is not menstruating

If she has prolonged amenorrhoea, she needs assessment and usually periodic endometrial protection with a progestogen withdrawal regimen, as prescribed by her gynaecologist. Chronic anovulation can expose the endometrium to unopposed estrogen.

Step 4: Ovulation induction, only after basic assessment

If she has anovulatory PCOS and semen and tubal factors are satisfactory:

First-line: letrozole

The current international guideline recommends letrozole as first-line pharmacological ovulation induction in infertile anovulatory women with PCOS who have no other infertility factor. International PCOS guideline
Typical specialist protocol:
  • Given early in the cycle, commonly from day 2 or 3 for 5 days
  • Starting dose and escalation depend on local protocol and prior response
  • Monitor ovulation with follicular ultrasound where available, particularly during initial cycles
  • Timed intercourse or IUI depending on the couple's evaluation
Do not prescribe it casually without confirming she is not pregnant and without a monitoring/follow-up plan.

Alternatives/adjuncts

  • Clomiphene citrate: alternative if letrozole is unavailable/contraindicated by local protocol.
  • Metformin: helpful particularly with insulin resistance, impaired glucose tolerance, or metabolic indications. It is not usually the most effective sole ovulation-induction agent.
  • Gonadotropins: second-line, specialist-supervised because of multiple pregnancy and ovarian hyperstimulation risks.
  • Laparoscopic ovarian drilling: selected resistant cases.
  • IVF/ICSI: third-line after failed ovulation-induction treatment, or earlier if severe male factor, bilateral tubal block, or another clear indication exists.

5. Follow-up during treatment

  • Menstrual calendar and pregnancy test if menses delayed
  • Follicular monitoring if on ovulation induction
  • Confirm ovulation when needed
  • Monitor BP, weight, glucose/metabolic health
  • Refer to infertility specialist if:
    • No ovulation or no pregnancy after several appropriately monitored cycles
    • Abnormal semen analysis
    • Tubal block
    • Significant endometriosis
    • Age 35 or older, especially if delay is likely
    • Severe obesity/metabolic disease or suspected alternative endocrine cause

Short viva answer

In this woman, I would diagnose primary infertility with suspected anovulatory infertility due to PCOS. I will first confirm that she is not pregnant, take a complete menstrual, PCOS, sexual, medical, and past-treatment history, and evaluate the husband simultaneously. Examination will include BMI, BP, signs of hyperandrogenism and insulin resistance, thyroid and pelvic examination. Investigations include TSH, prolactin, androgen testing when indicated, glucose assessment, pelvic USG, semen analysis, assessment of ovulation, and tubal patency testing as indicated. After lifestyle and preconception counselling, I would use supervised letrozole ovulation induction if anovulation from PCOS is confirmed and male/tubal factors have been excluded.

If I receive a patient married since two to three year or maybe five to six years, and now she wants to conceive, uh, what should be the history asked and the, the treatment, the follow-ups, and, uh, workup? Well done. Can you please make a list and...

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ASRM fertility evaluation infertile women committee opinion semen analysis tubal patency ovulation 2025

Infertility Case: History, Work-up, Treatment and Follow-up Checklist

Marriage duration alone is not the diagnosis. Ask whether the couple has had regular unprotected intercourse for at least 12 months without conception. Start evaluation earlier, after 6 months, if the woman is 35 years or older, has irregular/absent menses, suspected tubal disease/endometriosis, prior pelvic infection, or a possible male-factor problem.
Evaluate both partners at the same time. The three core assessments are: ovulation, semen analysis, and tubal patency. Berek & Novak's Gynecology, Initial Assessment.

A. First visit: how to take history

1. Basic infertility history

Ask:
  • Woman’s age and husband’s age
  • Duration of marriage
  • Duration of unprotected intercourse
  • Frequency and timing of intercourse
    • Ask sensitively: “How often do you have intercourse in a typical week?”
  • Any contraception used previously and when it was stopped
  • Primary or secondary infertility
    • Primary: never conceived
    • Secondary: conceived previously but cannot conceive now
  • Previous fertility consultations, reports, medicines, injections, surgeries, IUI, IVF, and outcomes

2. Menstrual history

Ask:
  • Age at menarche
  • LMP
  • Cycle interval, duration, amount of bleeding
  • Regular or irregular cycle?
  • Oligomenorrhoea, amenorrhoea, AUB
  • Dysmenorrhoea, deep dyspareunia, chronic pelvic pain
    • These suggest possible endometriosis.
  • Intermenstrual/postcoital bleeding
  • Premenstrual symptoms
Clinical clue: Regular cycles of about 21-35 days usually suggest ovulation. Irregular, infrequent, or absent menses suggest ovulatory dysfunction, especially PCOS.

3. Past obstetric history

Ask about:
  • Previous pregnancies, miscarriages, MTPs, ectopic pregnancy
  • Previous live births, stillbirths, preterm birth
  • PPH, postpartum sepsis
  • Any Rh-related issue
  • Details of previous ectopic pregnancy or tubal surgery

4. Gynaecological history

Ask:
  • PID/STI, genital TB exposure or treatment
  • Previous pelvic/abdominal surgery: appendicitis, ovarian cystectomy, myomectomy, ectopic surgery
  • Endometriosis or chronic pelvic pain
  • Fibroid, ovarian cyst, congenital uterine anomaly
  • Previous D&C/curettage, particularly if amenorrhoea followed it: consider Asherman syndrome
  • Cervical procedures

5. Endocrine and PCOS history

Ask:
  • Weight gain or obesity
  • Hirsutism, acne, scalp hair loss
  • Galactorrhoea
  • Headache or visual disturbance
  • Symptoms of thyroid disease
  • Excessive exercise, stress, eating disorder, major weight loss
  • Diabetes, hypertension, dyslipidaemia
  • Previous diagnosis/treatment of PCOS, thyroid disease, hyperprolactinaemia

6. Medical, surgical and drug history

Ask about:
  • Diabetes, hypertension, thyroid disease
  • Epilepsy, renal/liver disease, autoimmune disease
  • Tuberculosis, malaria in endemic regions
  • Chemotherapy/radiotherapy
  • Current drugs:
    • Antipsychotics can increase prolactin
    • Hormones, steroids, antiepileptics
    • Any medication potentially unsafe in pregnancy

7. Lifestyle and sexual history

Ask sensitively:
  • Smoking, alcohol, recreational drugs
  • Diet, weight, physical activity
  • Occupational heat/toxin exposure
  • Dyspareunia, vaginismus, low libido
  • Erectile dysfunction, ejaculation difficulty
  • Psychological stress, relationship concerns, domestic safety

B. Husband’s history

Do not focus only on the woman. Male factor contributes to a substantial proportion of infertility cases.
Ask:
  • Previous paternity
  • Mumps orchitis, undescended testes, testicular trauma/torsion
  • Varicocele, hernia/testicular surgery
  • STI, TB, diabetes
  • Erectile/ejaculatory dysfunction
  • Smoking, alcohol, anabolic steroids, recreational drugs
  • Heat exposure, pesticides, solvents, radiation
  • Chemotherapy, radiotherapy, medications
First investigation in the male partner: semen analysis.

C. Examination

General examination

  • Height, weight, BMI, waist circumference
  • BP
  • Pallor
  • Thyroid enlargement
  • Hirsutism, acne, alopecia
  • Acanthosis nigricans: insulin resistance
  • Galactorrhoea
  • Signs of virilisation: deep voice, clitoromegaly, marked temporal baldness. If present, evaluate urgently for causes other than routine PCOS.

Abdominal and pelvic examination

With consent and chaperone:
  • Abdominal scar, mass, tenderness
  • External genitalia and secondary sexual characters
  • Speculum: cervicitis, discharge, cervical lesion
  • Bimanual examination:
    • Uterine size, position, mobility
    • Fibroid
    • Adnexal mass/tenderness
    • Endometriosis signs: fixed retroverted uterus, uterosacral nodularity, tenderness

Husband

  • General examination and secondary sexual characters
  • Testicular size/consistency
  • Epididymis/vas deferens
  • Varicocele
  • Refer for detailed male-factor examination if semen analysis is abnormal.

D. Investigations

1. Essential initial tests

Fertility factorInvestigation
PregnancyUrine pregnancy test or serum beta-hCG before fertility treatment
Male factorSemen analysis
OvulationMenstrual history, ovulation tracking, mid-luteal progesterone when indicated
Uterus/ovariesTransvaginal pelvic ultrasound
Tubal patencyHSG or HyCoSy; laparoscopy only when indicated
The ASRM evaluation framework also includes assessment of ovulatory function, ovarian reserve, uterine anatomy, and tubal patency, while avoiding invasive tests unless clinically indicated. ASRM fertility evaluation

2. Female hormonal tests: only when indicated

  • TSH: irregular cycles or symptoms of thyroid disease
  • Serum prolactin: amenorrhoea, oligomenorrhoea, galactorrhoea
  • Total/free testosterone: hirsutism, acne, suspected hyperandrogenism
  • 17-hydroxyprogesterone: if non-classic CAH suspected
  • FSH, estradiol: concern for ovarian insufficiency
  • AMH and antral follicle count: ovarian reserve assessment, especially if older age, prior ovarian surgery, chemotherapy, or suspected diminished reserve
Do not order every hormone panel routinely in a woman with regular ovulatory cycles and no endocrine symptoms.

3. Metabolic assessment for PCOS

  • BMI and BP
  • 75-g OGTT or glycaemic evaluation as per local protocol
  • Lipid profile
  • HbA1c where appropriate

4. Tubal patency tests

  • HSG: first-line in many settings
  • HyCoSy: alternative in some centres
  • Laparoscopy with dye test: if severe dysmenorrhoea/endometriosis, prior PID, suspected adhesions, pelvic mass, or if another pelvic procedure is indicated
Tubal assessment should be prioritised if there is a history of PID, genital TB, ectopic pregnancy, pelvic surgery, or endometriosis.

5. Tests not done routinely

Avoid routine:
  • Diagnostic laparoscopy for every patient
  • Postcoital test
  • Endometrial biopsy
  • Sperm DNA fragmentation tests
  • Immunological or thrombophilia tests
  • Karyotyping
Order them only when a specific clinical indication exists. ASRM test recommendations

E. Treatment plan by cause

1. General treatment for every couple

  • Explain fertility and the fertile window.
  • Advise intercourse every 2-3 days throughout the cycle, or more frequently around ovulation.
  • Start preconception folic acid.
  • Stop smoking, alcohol, and recreational drugs.
  • Optimise weight, diabetes, thyroid disease, hypertension, and anaemia.
  • Check/review immunisation and medicines before pregnancy.
  • Provide supportive counselling. Infertility can cause substantial emotional distress.

2. Anovulation, such as PCOS

  1. Lifestyle intervention and weight management if overweight.
  2. Treat endocrine causes, e.g. hypothyroidism or hyperprolactinaemia.
  3. If PCOS with anovulatory infertility and no male or tubal factor:
    • Letrozole is first-line ovulation induction under supervision.
    • Clomiphene citrate is an alternative in suitable settings.
    • Metformin may be useful where metabolic indications or insulin resistance are present, but it is not usually the most effective sole ovulation-induction drug.
  4. Second-line: gonadotropins or laparoscopic ovarian drilling in selected cases.
  5. Third-line: IVF, or earlier when there is an independent indication.
The 2023 international PCOS guideline recommends letrozole as first-line pharmacological treatment for anovulatory infertility in PCOS without other infertility factors. PCOS infertility guideline

3. Male-factor infertility

  • Repeat semen analysis if abnormal.
  • Refer to andrologist/urologist.
  • Treat reversible cause where possible.
  • Consider IUI for selected mild abnormalities.
  • IVF/ICSI for significant male factor.

4. Tubal factor

  • Treat active infection first.
  • Consider tubal surgery in selected cases.
  • IVF is often appropriate for bilateral severe tubal disease or hydrosalpinx after appropriate management.

5. Endometriosis

  • Analgesia/medical therapy if pain is the main problem and immediate conception is not desired.
  • Fertility-focused management may involve laparoscopic treatment in selected disease or ART/IVF depending on age, duration, severity, and partner factors.

6. Uterine factor

  • Hysteroscopic removal of polyp/submucosal fibroid
  • Hysteroscopic adhesiolysis for intrauterine adhesions
  • Myomectomy for appropriately selected fibroids

7. Unexplained infertility

After normal ovulation, normal semen, patent tubes, and normal uterine assessment:
  • Counsel about age-related prognosis
  • Expectant management may be reasonable in selected younger couples with shorter duration
  • IUI with ovarian stimulation may be offered
  • IVF depending on age, duration of infertility, and prior treatment failure

F. Follow-up plan

At first follow-up

Review:
  • Semen analysis
  • Pelvic ultrasound
  • Ovulatory and endocrine results
  • Metabolic results
  • Need for HSG/HyCoSy
  • Whether both partners understand timing of intercourse and treatment options

During ovulation induction

  • Confirm she is not pregnant before starting a cycle.
  • Record menstrual dates.
  • Monitor follicular development by ultrasound when indicated.
  • Give timed-intercourse or IUI advice.
  • Check for ovulation and adverse effects.
  • Counsel about multiple pregnancy and ovarian hyperstimulation risk, especially with gonadotropins.

At each follow-up

Assess:
  • Menstrual pattern and ovulation
  • Weight, BP, glucose control in PCOS
  • Treatment adherence/adverse effects
  • Pregnancy test if period is delayed
  • Emotional wellbeing
  • Need to advance to IUI/IVF or refer to a fertility specialist

Refer early to infertility specialist if

  • Woman is 35 years or older, especially if duration is prolonged
  • Woman is over 40
  • Severe male-factor abnormality
  • Bilateral tubal block/hydrosalpinx
  • Suspected diminished ovarian reserve or premature ovarian insufficiency
  • Severe endometriosis
  • Repeated treatment failure
  • Complex endocrine disease or major medical illness

One-page viva summary

In a couple with infertility, I will assess both partners simultaneously. I will confirm the duration of regular unprotected intercourse, take a detailed menstrual, obstetric, sexual, medical, gynaecological, lifestyle, and male-partner history, and perform general and pelvic examination. Initial tests are pregnancy testing, semen analysis, assessment of ovulation, pelvic ultrasound, and assessment of tubal patency where indicated. Treatment is cause-specific, with preconception counselling and lifestyle optimisation for all couples. In anovulatory PCOS without male or tubal factor, supervised letrozole is first-line ovulation induction. Follow-up includes monitoring ovulation, pregnancy testing, metabolic risk control, and timely escalation to IUI, IVF, or specialist referral.
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