Obstetrics & Gynecology (OBGYN) ​Obstetrics ​Early Pregnancy: ​Signs to diagnose pregnancy ​Preconceptional care — supplementations & vaccinations ​Parity index ​Teratogens & associated defects ​Trimester-wise screenings ​Leopold maneuvers ​High-Yield Conditions: ​Cervical insufficiency — types of cerclage ​APLA (Antiphospholipid Antibody Syndrome) ​Ectopic pregnancy — expectant, medical & surgical management ​Molar pregnancy — partial vs complete ​Placenta & Amniotic Fluid: ​Placental abnormalities ​Amniotic fluid abnormalities ​Placenta previa vs placental abruption ​PAS (Placenta Accreta Spectrum) ​Multiple Pregnancy: ​Multiple pregnancy mechanics ​MCDA vs DCDA (USG evaluation) ​TTTS (Twin-to-Twin Transfusion Syndrome) ​Medical Disorders in Pregnancy: ​Hypertension in pregnancy ​Preeclampsia & eclampsia — management ​HELLP syndrome ​Diabetes in pregnancy ​Labor & Delivery: ​Modified Bishop score ​Active management of third stage of labor ​Breech presentation — management ​Lovset & Burns Marshall maneuvers ​Shoulder dystocia — HELPERR algorithm ​Postpartum hemorrhage — EMOTIVE protocol ​Gynecology ​Menstrual Disorders: ​Mullerian anomalies ​Primary vs Secondary amenorrhea ​Abnormal uterine bleeding — FIGO classification ​Uterine Conditions: ​Adenomyosis ​Fibroids ​Endometriosis — management ​Endometrial hyperplasia ​High-Yield Clinicals: ​Vaginal infections ​Ovarian cysts & tumors ​Cervical cancer — screening & diagnosis ​HPV vaccination ​PCOS ​Contraception

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OBGYN USMLE high yield obstetrics gynecology structured notes 2024 2025

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Obstetrics & Gynecology (OBGYN) ​Obstetrics ​Early Pregnancy: ​Signs to diagnose pregnancy ​Preconceptional care — supplementations & vaccinations ​Parity index ​Teratogens & associated defects ​Trimester-wise screenings ​Leopold maneuvers ​High-Yield Conditions: ​Cervical insufficiency — types of cerclage ​APLA (Antiphospholipid Antibody Syndrome) ​Ectopic pregnancy — expectant, medical & surgical management ​Molar pregnancy — partial vs complete ​Placenta & Amniotic Fluid: ​Placental abnormalities ​Amniotic fluid abnormalities ​Placenta previa vs placental abruption ​PAS (Placenta Accreta Spectrum) ​Multiple Pregnancy: ​Multiple pregnancy mechanics ​MCDA vs DCDA (USG evaluation) ​TTTS (Twin-to-Twin Transfusion Syndrome) ​Medical Disorders in Pregnancy: ​Hypertension in pregnancy ​Preeclampsia & eclampsia — management ​HELLP syndrome ​Diabetes in pregnancy ​Labor & Delivery: ​Modified Bishop score ​Active management of third stage of labor ​Breech presentation — management ​Lovset & Burns Marshall maneuvers ​Shoulder dystocia — HELPERR algorithm ​Postpartum hemorrhage — EMOTIVE protocol ​Gynecology ​Menstrual Disorders: ​Mullerian anomalies ​Primary vs Secondary amenorrhea ​Abnormal uterine bleeding — FIGO classification ​Uterine Conditions: ​Adenomyosis ​Fibroids ​Endometriosis — management ​Endometrial hyperplasia ​High-Yield Clinicals: ​Vaginal infections ​Ovarian cysts & tumors ​Cervical cancer — screening & diagnosis ​HPV vaccination ​PCOS ​Contraception

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📚 OBGYN Complete Revision Notes

Sources: Rosen's Emergency Medicine, Creasy & Resnik's Maternal-Fetal Medicine, Berek & Novak's Gynecology, and clinical guidelines.

PART 1: OBSTETRICS


1. EARLY PREGNANCY

1.1 Signs to Diagnose Pregnancy

CategorySignDetails
Presumptive (subjective)AmenorrheaMost common symptom
Nausea/vomitingPeaks 8-10 weeks
Breast tenderness, enlargement
Urinary frequency
QuickeningFetal movements felt at 18-20 wks (primi), 16-18 wks (multi)
Chadwick's signBluish discoloration of vagina/cervix (6 wks)
Probable (objective, not conclusive)Goodell's signSoftening of cervix (6 wks)
Hegar's signSoftening of lower uterine segment (6-8 wks)
Ballottement16-28 wks, fetus bounces back on palpation
Positive urine/serum hCGhCG detectable by Day 9-11 post-conception
Palmer's signRegular rhythmic uterine contractions
Piskacek's signAsymmetric uterine enlargement at implantation site
Positive (definitive)Fetal heart tonesDoppler: 10-12 wks; Fetoscope: 20 wks
Fetal movements felt by examiner~20 wks
USG visualization of fetusGestational sac: 4-5 wks TVS; fetal pole + cardiac activity: 6 wks
Memory: Presumptive = Patient feels; Probable = Physician finds; Positive = Proof (USG/FHT)

1.2 Preconceptional Care

Supplementations:
SupplementDosePurposeTiming
Folic acid400 mcg/day (normal)Neural tube defect prevention1 month before conception through 1st trimester
5 mg/day (high-risk: prior NTD, epilepsy, DM, obesity, twins)
Iron60 mg elemental iron + folic acidAnaemia preventionFrom 2nd trimester in normal; preconceptionally in anaemic
Calcium1000-1200 mg/dayBone health, preeclampsia preventionThroughout pregnancy
Vitamin D600-2000 IU/day
Iodine150-220 mcg/dayFetal thyroid development
Vaccinations before pregnancy:
VaccineTimingNotes
MMR (live)At least 1 month before conceptionContraindicated in pregnancy
Varicella (live)At least 1 month beforeContraindicated in pregnancy
HPVComplete before pregnancy (9-26 yrs)Not given during pregnancy
RubellaPre-conception if non-immune
Vaccinations SAFE/recommended during pregnancy:
VaccineTrimesterNotes
Tdap27-36 weeks (ideally 27-32 wks)Every pregnancy; protects newborn from pertussis
InfluenzaAny trimesterInactivated only
COVID-19Any trimester
Hepatitis BAny trimester if non-immune

1.3 Parity Index (GTPAL / Obstetric Formula)

G-T-P-A-L:
  • G = Gravida (total pregnancies, including current)
  • T = Term deliveries (≥37 weeks)
  • P = Preterm deliveries (20-36+6 weeks)
  • A = Abortions (spontaneous + induced, <20 wks)
  • L = Living children
TermDefinition
NulligravidaNever been pregnant
PrimigravidaCurrently/previously pregnant for 1st time
Multigravida≥2 pregnancies
NulliparaNever delivered a viable infant
PrimiparaDelivered once (≥20 wks, alive or dead)
Multipara≥2 deliveries
Grand multipara≥5 deliveries

1.4 Teratogens & Associated Defects

TeratogenDefect/Association
ACE Inhibitors / ARBsRenal tubular dysgenesis, oligohydramnios, skull hypoplasia, neonatal renal failure (2nd/3rd trimester)
WarfarinWarfarin embryopathy: nasal hypoplasia, stippled epiphyses, chondrodysplasia punctata (1st trimester); CNS defects (any trimester)
ThalidomidePhocomelia (limb reduction defects), ear abnormalities
Isotretinoin (Accutane)Craniofacial, cardiac, CNS defects; microtia
Valproic acidNeural tube defects (spina bifida), cardiac defects, IUGR
CarbamazepineNeural tube defects (spina bifida), fingernail hypoplasia
PhenytoinFetal hydantoin syndrome: growth restriction, hypoplastic phalanges/nails, craniofacial anomalies
LithiumEbstein anomaly (tricuspid valve)
Diethylstilbestrol (DES)Clear cell adenocarcinoma of vagina/cervix; T-shaped uterus; cervical incompetence
AlcoholFetal alcohol syndrome: microcephaly, smooth philtrum, thin vermillion, growth restriction, intellectual disability
CocainePlacental abruption, microcephaly, limb reduction defects
TetracyclinesTeeth discoloration, inhibited bone growth (2nd/3rd trimester)
AminoglycosidesCN VIII toxicity - deafness
Misoprostol (early)Moebius sequence, limb defects
MethimazoleAplasia cutis, choanal atresia
Radiation >10 radMicrocephaly, growth restriction (safe threshold: <5 rad)
Rubella (1st trimester)Classic triad: cataracts, PDA/pulmonary stenosis, sensorineural deafness
CMVPeriventricular calcifications, sensorineural deafness, chorioretinitis
ToxoplasmaHydrocephalus, intracranial calcifications, chorioretinitis
SyphilisHutchinson's triad, saddle nose, interstitial keratitis, bone changes
VaricellaLimb hypoplasia, skin scarring, eye defects (if 1st/2nd trimester)
Memory (SAFE antibiotics in pregnancy): Penicillins, Cephalosporins, Erythromycin, Azithromycin, Clindamycin (PCEAC)

1.5 Trimester-Wise Screenings

First Trimester (11-13+6 weeks)

TestTimingWhat it screens
Combined First Trimester Screen11-13+6 wksNT (nuchal translucency) + free β-hCG + PAPP-A → T21, T18, T13
Cell-Free DNA (cfDNA/NIPT)10 wks+T21, T18, T13, sex chromosome aneuploidies (screening, not diagnostic)
Dating USG8-13 wks (CRL)Gestational age, viability, chorionicity in twins
Blood group, Rh, antibody screen1st visit
CBC, urine culture, rubella/varicella immunity1st visit
HIV, syphilis, Hep B, Hep C1st visit
Chorionic villus sampling (CVS)10-13 wksDiagnostic - karyotype/microarray

Second Trimester (14-28 weeks)

TestTimingWhat it screens
Quadruple screen (AFP, hCG, uE3, Inhibin A)15-20 wksT21, T18, NTDs
Anomaly USG18-20 wksStructural anomalies
Amniocentesis15-20 wksDiagnostic karyotype
AFP (elevated)15-20 wksNTDs, abdominal wall defects, multiple gestation
Cervical length (high-risk)18-24 wksPreterm birth risk
GDM screening (1-hr GCT)24-28 wksGestational diabetes

Quad Screen Patterns:

ConditionAFPhCGuE3Inhibin A
Trisomy 21 (Down)
Trisomy 18 (Edwards)Normal
NTD (Open)NormalNormalNormal
Molar pregnancy-↑↑↑--

Third Trimester (29-40 weeks)

TestTimingPurpose
GBS (Group B Strep) culture35-37 wksIntrapartum prophylaxis if positive
Repeat antibody screen (Rh-)28 wksAnti-D prophylaxis
BPP/NST28+ wks (high-risk)Fetal well-being
Kick counts28+ wksDaily monitoring

1.6 Leopold Maneuvers

Systematic abdominal palpation at ≥28 weeks to determine fetal lie, presentation, position, and engagement.
ManeuverTechniqueDetermines
1st (Fundal grip)Both hands cup the fundusWhat is in the fundus (head = hard, round, ballotable; breech = soft, irregular)
2nd (Lateral grip)Hands moved to sides of uterusFetal back (firm, smooth) vs. limbs (irregular, nodular) - determines position
3rd (Pawlik's grip)Single hand grasps presenting part above pubisPresentation; engagement (if moveable = not engaged)
4th (Pelvic grip)Face toward patient's feet; fingertips feel into pelvisDegree of descent/engagement; attitude (flexion vs. extension)
Memory: 1 = Fundal (What's up there?); 2 = Sides (Back or Limbs?); 3 = Presentation; 4 = Descent

2. HIGH-YIELD CONDITIONS

2.1 Cervical Insufficiency

Definition: Painless cervical dilation in 2nd trimester without uterine contractions, leading to recurrent mid-trimester pregnancy loss.
Features:
  • History of 2nd trimester losses with painless dilation
  • Short cervix on USG (<25 mm at 16-24 wks)
  • Associated with: DES exposure, prior LEEP/cone biopsy, Mullerian anomalies, connective tissue disorders

Types of Cerclage:

TypeTechniqueIndicationTiming
McDonald cerclagePurse-string suture at cervicovaginal junctionStandard; history-indicated or USG-indicated12-14 wks (history) or when cervix shortens
Shirodkar cerclageSuture placed at internal os level (submucosal) after bladder reflectionPreferred when McDonald fails; anatomically superior12-14 wks
Transabdominal cerclage (TAC)Open or laparoscopic suture at uterine isthmusFailed vaginal cerclage; very short cervix; prior trachelectomyPre-pregnancy or 10-13 wks
Rescue/Emergency cerclagePlaced when cervix is already dilated (1-4 cm, bulging membranes)Acute cervical dilation in 2nd trimester16-24 wks
Cerclage removal: 36-37 weeks (allow vaginal delivery); removed earlier if labor, PPROM, chorioamnionitis
Progesterone supplementation: Vaginal progesterone 200 mg/night or 17-OHPC IM weekly for short cervix

2.2 Antiphospholipid Antibody Syndrome (APLA)

Definition: Autoimmune thrombophilia causing arterial/venous thrombosis and pregnancy morbidity.

Diagnostic Criteria (Revised Sapporo/Sydney Criteria - need ≥1 clinical + ≥1 lab):

Clinical criteria:
  1. Vascular thrombosis (arterial, venous, or small vessel)
  2. Pregnancy morbidity:
    • ≥3 unexplained consecutive 1st trimester losses (<10 wks)
    • ≥1 morphologically normal fetal loss ≥10 wks
    • ≥1 preterm birth ≤34 wks due to severe preeclampsia or placental insufficiency
Laboratory criteria (positive on ≥2 occasions, ≥12 weeks apart):
  • Lupus anticoagulant (LA)
  • Anticardiolipin antibodies (IgG or IgM) - medium/high titre (>40 GPL/MPL or >99th percentile)
  • Anti-β2 glycoprotein-I antibodies (IgG or IgM) - >99th percentile

Management in Pregnancy:

SituationTreatment
APLA + obstetric morbidity only (no thrombosis)Low-dose aspirin (75-100 mg/day) + LMWH (prophylactic dose) from conception
APLA + prior thrombosisLow-dose aspirin + LMWH (therapeutic/prophylactic dose)
APLA + SLEAdd hydroxychloroquine
PostpartumContinue anticoagulation for at least 6 weeks (switch to warfarin)
⚠️ Warfarin is contraindicated in 1st trimester; LMWH used throughout pregnancy.

2.3 Ectopic Pregnancy

Definition: Implantation outside the uterine cavity. Sites: Fallopian tube (95% - ampulla most common 70%), cervix, ovary, abdominal, cornual/interstitial.
Risk factors (from Rosen's EM): Tubal surgery, PID, smoking, IUD, prior ectopic, infertility, assisted reproduction.
Diagnosis:
  • Serum β-hCG + TVS
  • Discriminatory zone: hCG >1500-2000 IU/L → IUP should be visible on TVS
  • TVS findings: No IUP + adnexal mass ± free fluid = ectopic until proven otherwise

Management:

ApproachCriteriaDetails
ExpectanthCG <1000 IU/L AND declining (>15%/48h), no pain, no rupture, small mass <3.5 cmSerial hCG monitoring every 48 hrs until undetectable; 50-70% resolution
Medical - MethotrexatehCG <5000 IU/L (some say <10,000), no cardiac activity, mass <3.5-4 cm, no rupture, renal/hepatic/hematologic normalSingle-dose: MTX 50 mg/m² IM; check hCG day 4 & 7 (expect 15% drop by D4-7); Multi-dose: MTX day 1,3,5,7 + leucovorin rescue
MTX contraindications: hCG >5000, cardiac activity, rupture, IUD in situ, immunocompromised, abnormal LFT/renal, breast-feeding
SurgicalRuptured ectopic, hemodynamic instability, contraindication to MTX, failed medical Rx, heterotopicSalpingostomy (preserve tube, higher recurrence risk) vs. Salpingectomy (preferred, definitive); Laparoscopy preferred over laparotomy
Post-treatment: Anti-D immunoglobulin if Rh-negative; serial hCG until undetectable.

2.4 Molar Pregnancy (Gestational Trophoblastic Disease)

Complete vs. Partial Hydatidiform Mole:

FeatureComplete MolePartial Mole
Karyotype46,XX (90%) or 46,XY - all paternal (androgenetic)69,XXX or 69,XXY - triploid (1 egg + 2 sperm)
OriginEmpty egg + 2 sperm (dispermy) or 1 sperm that duplicatesNormal egg + 2 sperm
Fetal tissueAbsentPresent (abnormal fetus/fetal RBCs)
VilliDiffuse trophoblastic hyperplasia, all villi edematousFocal trophoblastic hyperplasia, some normal villi
USG"Snowstorm" appearance, no fetusFetus present (non-viable), Swiss-cheese placenta
hCGVery high (>100,000)Moderately elevated
SymptomsHyperemesis, early preeclampsia (<20 wks), theca lutein cysts, hyperthyroidism, uterus LGAMilder; often presents as missed abortion
Malignant transformation15-20% → GTN<5% → GTN
p57 immunostainNegative (no maternal chromosomes)Positive

Management:

  1. Suction curettage (method of choice) - even for large moles
  2. Anti-D if Rh-negative
  3. Serial β-hCG monitoring: Weekly until undetectable x3, then monthly x12 months
  4. Contraception for 12 months (OCPs preferred - do NOT delay hCG normalization)
  5. Hysterectomy option in women with completed family (does not eliminate GTN risk monitoring)
GTN criteria: hCG plateau (±10% x4 values over 3 wks), rise (>10% x3 values over 2 wks), persistence at 6 months, or histologic choriocarcinoma → Chemotherapy (single-agent MTX or actinomycin-D for low-risk; EMA-CO for high-risk)

3. PLACENTA & AMNIOTIC FLUID

3.1 Placenta Previa vs. Placental Abruption

FeaturePlacenta PreviaPlacental Abruption
DefinitionPlacenta covers internal cervical os (partially or completely)Premature separation of normally implanted placenta
BleedingPainless, bright red, suddenPainful (may be concealed - 20%); dark blood
UterusSoft, non-tenderRigid/board-like, tender
PresentationOften malpresentation (head not engaged)Normal presentation
Fetal conditionOften stable initiallyFetal distress common
DiagnosisUSG (do NOT do digital PV exam!)Clinical + USG (retroplacental clot) - USG has low sensitivity (50%)
Risk factorsPrior CS/uterine surgery, multiparity, smoking, prior previa, IVFHypertension (most common), trauma, cocaine, smoking, PROM, polyhydramnios
DICRareCommon (Couvelaire uterus → severe)
ManagementStable + <37 wks: expectant; ≥37 wks or bleeding: CSStable + preterm: conservative; fetal distress/severe: emergency delivery

Types of Placenta Previa:

  • Complete (major): Completely covers os
  • Partial: Partially covers os
  • Marginal: Edge reaches but doesn't cover os
  • Low-lying: Within 2 cm of os but not covering it
⚠️ Vasa previa: Fetal vessels cross internal os → at risk of rupture with ROM → sinusoidal FHR + Apt test positive → emergency CS

3.2 Placenta Accreta Spectrum (PAS)

TypeInvasionFrequency
AccretaVilli attach to myometrium (no decidua basalis)75-78%
IncretaVilli invade into myometrium17%
PercretaVilli penetrate through serosa (may invade bladder/bowel)5-7%
Risk factors: Previous CS (strongest - risk rises with each CS: 1CS→0.3%, 2CS→0.6%, 3CS→2.1%), placenta previa, uterine surgery, Asherman's syndrome, advanced maternal age.
Diagnosis: USG (loss of retroplacental clear space, lacunae, bladder wall interruption) + MRI (when USG equivocal)
Management:
  • Planned cesarean hysterectomy at 34-36 weeks (elective, before labor)
  • Multidisciplinary team: MFM, gynecologic oncologist, urology, IR (interventional radiology), blood bank
  • Leave placenta in situ if accreta (do not attempt manual removal)
  • Conservative management (uterus-sparing): possible in carefully selected cases with fertility desire

3.3 Amniotic Fluid Abnormalities

Polyhydramnios (AFI >24 cm or MVP >8 cm)

FeatureDetails
DefinitionAFI >24 cm or maximum vertical pocket >8 cm
CausesIdiopathic (60-70%), fetal: GI obstruction (duodenal/esophageal atresia, tracheoesophageal fistula), CNS abnormalities (anencephaly, NTD), neuromuscular conditions; Maternal: gestational diabetes (most common maternal cause), immune hydrops
AssociationsDuodenal atresia → "double bubble"; Anencephaly
ComplicationsPreterm labor, PPROM, malpresentation, cord prolapse, PPH (uterine atony)
ManagementTreat underlying cause; therapeutic amniocentesis if severe symptoms; indomethacin (reduces fetal urine output - use <32 wks)

Oligohydramnios (AFI <5 cm or MVP <2 cm)

FeatureDetails
DefinitionAFI <5 cm or MVP <2 cm; Severe: AFI <2 cm (anhydramnios)
CausesFetal: IUGR (uteroplacental insufficiency), posterior urethral valves, renal agenesis (Potter sequence), polycystic kidneys; Maternal/iatrogenic: Prolonged pregnancy (post-term), PROM, ACE inhibitors, NSAIDs
AssociationsRenal agenesis → Potter sequence (pulmonary hypoplasia, limb contractures, flattened facies)
ComplicationsCord compression, fetal distress, pulmonary hypoplasia, limb contractures (if early onset)
ManagementSerial monitoring; amnioinfusion intrapartum (for recurrent variable decelerations); delivery if at term or fetal compromise

3.4 Other Placental Abnormalities

AbnormalityDescription
Placenta succenturiataAccessory lobe separate from main placenta; risk of retained lobe → PPH
Bilobed placentaTwo equal lobes; vessels may run between → vasa previa risk
Circumvallate placentaChorionic plate smaller than basal plate with folded-back edges; ↑ APH, preterm labor
Placenta membranaceaPlacenta covers most of uterine surface; ↑ hemorrhage risk
Battledore placentaCord inserts at placental margin (marginal insertion)
Velamentous cord insertionCord inserts into membranes; vessels exposed → vasa previa risk; ↑ IUGR, fetal anomaly
CircumvallateAssociated with 2nd trimester bleeding, IUGR, preterm

4. MULTIPLE PREGNANCY

4.1 Chorionicity & Amnionicity - USG Evaluation

FeatureDCDA (Dichorionic Diamniotic)MCDA (Monochorionic Diamniotic)MCMA (Monochorionic Monoamniotic)
ZygosityDizygotic (mostly) or early division (<3 days) monozygoticMonozygotic (division 4-8 days)Monozygotic (division 8-13 days)
USG marker (1st trimester)Twin peak (Lambda/λ) sign - triangular wedge of placental tissue between membranesT-sign - thin membrane arises perpendicular to uterine wallNo dividing membrane
Membrane thicknessThick (>2 mm), 4 layersThin (<2 mm), 2 layersAbsent
Placenta2 separate or fused11
Best time to determine11-14 weeks (most accurate)
RiskLowestIntermediate (TTTS, sIUGR)Highest (cord entanglement, TTTS)
Memory: Lambda (λ) = DCDA ("Lambda" sounds like "large" - more tissue between); T = MCDA (thin membrane)

4.2 Twin-to-Twin Transfusion Syndrome (TTTS)

Mechanism: Unbalanced arteriovenous anastomoses in monochorionic placenta → donor twin becomes oliguric/anhydramniotic; recipient twin becomes polyuric/polyhydramniotic.
Occurs in: 10-15% of MCDA twins

Quintero Staging:

StageFeatures
IDonor: MVP <2 cm; Recipient: MVP >8 cm. Bladder still visible in donor
IIDonor bladder not visible on USG (absent filling)
IIICritically abnormal Dopplers in either twin (absent/reversed EDF in UA, reversed DV flow, pulsatile UV)
IVHydrops in either twin
VDemise of one or both twins
Management:
  • Stage I: Close monitoring (some centers treat)
  • Stages II-IV: Fetoscopic laser photocoagulation (FLP) of placental anastomoses - treatment of choice before 26 weeks
  • Amnioreduction: alternative/adjunct, palliative
  • Selective feticide: if one twin anomalous or after single fetal demise risk assessment

5. MEDICAL DISORDERS IN PREGNANCY

5.1 Hypertension Classification in Pregnancy

TypeDefinitionNotes
Chronic hypertensionBP ≥140/90 before 20 wks or pre-existing
Gestational hypertensionNew BP ≥140/90 after 20 weeks, no proteinuria, resolves by 12 wks postpartum
PreeclampsiaGestational HTN + proteinuria (>300 mg/24h or PCR >0.3 or dipstick 2+) OR end-organ damage (without proteinuria)After 20 wks
Superimposed preeclampsiaChronic HTN + new proteinuria or worsening features
EclampsiaPreeclampsia + seizures (not attributable to other causes)

5.2 Preeclampsia & Eclampsia Management

Preeclampsia Features of Severity (any one = severe):

  • SBP ≥160 or DBP ≥110 (on two readings 4h apart)
  • Thrombocytopenia <100,000
  • Renal insufficiency (creatinine >1.1 mg/dL or doubling)
  • Impaired liver function (transaminases 2x normal) or RUQ/epigastric pain
  • Pulmonary edema
  • New-onset headache not responsive to medication / visual disturbances

Management:

ScenarioManagement
Preeclampsia without severe features at <37 wksOutpatient monitoring; antihypertensives if BP ≥160/110; deliver at 37 weeks
Preeclampsia with severe features at <34 wksHospitalize; MgSO₄ for seizure prophylaxis; antihypertensives; corticosteroids (if <34 wks); deliver at 34 weeks
Preeclampsia with severe features at ≥34 wksStabilize and deliver
Eclampsia (seizures)MgSO₄ + airway protection + antihypertensives + delivery after stabilization

Antihypertensives in Pregnancy:

DrugRouteNotes
LabetalolIV/POFirst-line acute; avoid in asthma
HydralazineIVClassic IV agent; can cause maternal hypotension
NifedipinePOFirst-line oral; do NOT give sublingual
MethyldopaPOChronic hypertension in pregnancy (safe, oldest)
Magnesium sulfateIVSeizure prophylaxis/treatment (NOT antihypertensive)
MgSO₄ Protocol:
  • Loading: 4-6 g IV over 15-20 min
  • Maintenance: 1-2 g/hr infusion
  • Monitor: Urine output (>25 mL/hr), respirations (>12/min), patellar reflexes (present)
  • Toxicity signs: Loss of reflexes (first) → respiratory depression → cardiac arrest
  • Antidote: Calcium gluconate 1 g IV

5.3 HELLP Syndrome

Definition: Severe variant of preeclampsia - Hemolysis, Elevated Liver enzymes, Low Platelets

Diagnostic Criteria:

ParameterCriterion
HemolysisAbnormal peripheral smear (schistocytes), LDH >600 U/L, bilirubin >1.2 mg/dL
Elevated liver enzymesAST/ALT >70 U/L
Low platelets<100,000/µL
Tennessee Classification:
  • Class I: Platelets <50,000
  • Class II: Platelets 50,000-100,000
  • Class III: Platelets 100,000-150,000
Mississippi Classification (Martin):
  • Class 1: Platelets <50,000 + LDH ≥600 + AST/ALT ≥40
  • Class 2: Platelets 50,000-100,000
  • Class 3: Platelets 100,000-150,000
Management:
  • Delivery is definitive treatment (after stabilization)
  • MgSO₄ seizure prophylaxis
  • Corticosteroids (dexamethasone) may improve lab parameters
  • If platelets <20,000 or active bleeding → platelet transfusion
  • If DIC develops → FFP/cryo
  • Watch for subcapsular hepatic hematoma (RUQ pain → CT liver)

5.4 Diabetes in Pregnancy

Classification:

TypeDefinition
Pre-gestational DMDM diagnosed before pregnancy (T1DM or T2DM)
Gestational DM (GDM)Glucose intolerance first diagnosed in pregnancy

GDM Screening (24-28 weeks):

Two-step approach:
  1. 1-hr GCT (50g): Positive if ≥130-140 mg/dL → proceed to 3-hr OGTT
  2. 3-hr OGTT (100g): GDM if ≥2 values meet/exceed:
TimeCarpenter-CoustanNDDG
Fasting≥95 mg/dL≥105 mg/dL
1 hour≥180 mg/dL≥190 mg/dL
2 hours≥155 mg/dL≥165 mg/dL
3 hours≥140 mg/dL≥145 mg/dL
One-step approach (IADPSG): 2-hr 75g OGTT - GDM if any value ≥:
  • Fasting: 92 mg/dL; 1-hr: 180 mg/dL; 2-hr: 153 mg/dL

Fetal Complications:

  • Macrosomia (most common), shoulder dystocia, birth injuries
  • Neonatal hypoglycemia, hypocalcemia, polycythemia, hyperbilirubinemia
  • RDS (delayed lung maturity)
  • Stillbirth (poorly controlled)
  • Congenital anomalies (only in pre-gestational DM - organogenesis in 1st trimester): cardiac (VSD, TGA), NTDs (caudal regression syndrome - pathognomonic for maternal DM)

Management:

  • Diet + exercise first (medical nutrition therapy)
  • Insulin (drug of choice if pharmacologic needed); Metformin/glyburide: acceptable alternatives in GDM
  • Target glucose: Fasting <95, 1-hr postprandial <140, 2-hr postprandial <120 mg/dL
  • Delivery timing: GDM controlled on diet → 40-41 wks; on medication → 39-40 wks; Pre-gestational DM → 39 wks

White Classification (Pre-gestational DM):

ClassCriteria
A1GDM, diet-controlled
A2GDM, medication-required
BOnset ≥20 yrs, duration <10 yrs, no vascular disease
COnset 10-19 yrs or duration 10-19 yrs
DOnset <10 yrs or duration ≥20 yrs or benign retinopathy
FNephropathy
RProliferative retinopathy
TPost-renal transplant
HIschemic heart disease

6. LABOR & DELIVERY

6.1 Modified Bishop Score

Used to assess cervical favorability for induction of labor. Score ≥8 = favorable (predict successful induction like spontaneous labor).
Parameter0123
Dilation (cm)Closed1-23-4≥5
Effacement (%)0-3040-5060-70≥80
Station-3-2-1/0+1/+2
ConsistencyFirmMediumSoft-
PositionPosteriorMidAnterior-
Total max = 13. Score ≥8 → favorable; Score <6 → cervical ripening needed (prostaglandins/mechanical methods)
Memory: DECSP - Dilation, Effacement, Consistency, Station, Position

6.2 Active Management of Third Stage of Labor

Third stage: from delivery of baby to delivery of placenta (normally <30 min)
AMTSL components (WHO recommended):
  1. Uterotonic within 1 minute of birth - Oxytocin 10 IU IM (drug of choice); alternatives: ergometrine, misoprostol, carbetocin
  2. Controlled cord traction (CCT) - Brandt-Andrews method (uterine stabilization + gentle traction during contraction)
  3. Uterine massage after placenta delivery (controversial - some guidelines omit)
Normal blood loss: <500 mL vaginal delivery; <1000 mL cesarean

6.3 Breech Presentation - Management

Types of breech:
  • Frank breech (65%): Hips flexed, knees extended (pike position)
  • Complete breech (10%): Hips + knees flexed (lotus position)
  • Footling/Incomplete (25%): One or both feet presenting
External Cephalic Version (ECV):
  • Attempt at 36-37 weeks
  • Tocolysis (terbutaline) used
  • Success rate: ~50-60%
  • Contraindications: PPROM, placenta previa, fetal compromise, multiple pregnancy, uterine scar (relative)
Mode of delivery:
  • Planned cesarean preferred for singleton breech at term (Term Breech Trial)
  • Vaginal breech delivery: only at experienced centers - Frank or complete breech, adequate pelvis, flexed fetal head, EFW 2500-4000g, no contraindications

6.4 Lovset Maneuver & Burns Marshall Maneuver

Lovset Maneuver (for delivery of arms in breech):

Used when arms are extended/nuchal.
  1. Hold baby's pelvis (thumbs on sacrum)
  2. Rotate baby 180° (back remains anterior) while applying downward traction
  3. The arm that was posterior (under pubic arch) rotates to anterior and can be swept down
  4. Repeat rotation in opposite direction for second arm

Burns Marshall Maneuver (for aftercoming head in breech):

Used for delivery of the head after trunk is delivered.
  1. After trunk delivery, allow baby to hang by its own weight (1-2 minutes) to increase flexion of head
  2. Grasp baby's ankles with both hands
  3. Swing the trunk upward in a wide arc toward maternal abdomen
  4. The chin, face, brow, vertex deliver over perineum
  5. Suboccipital region is fulcrum on perineum - pivot point is critical
Alternative: Mauriceau-Smellie-Veit maneuver (MSV) for flexion of aftercoming head - finger in mouth + 2 fingers on occiput, traction while assistant applies suprapubic pressure

6.5 Shoulder Dystocia - HELPERR Algorithm

Definition: Failure of fetal shoulders to deliver after delivery of the head; anterior shoulder impacted behind symphysis pubis.
Risk factors: Macrosomia, maternal DM/obesity, prolonged 2nd stage, operative vaginal delivery, prior shoulder dystocia.
Recognition: Turtle sign (head retracts after delivery), failed gentle downward traction.

HELPERR Mnemonic:

LetterActionDetails
HHelpCall for help immediately (senior OB, anesthesia, NICU, extra nurses)
EEvaluate for EpisiotomyGives more room for maneuvers (doesn't directly resolve bony dystocia)
LLegs (McRoberts)Hyperflexion of maternal thighs against abdomen → flattens lumbar lordosis → rotates pubic symphysis superiorly → frees anterior shoulder
PPressure (Suprapubic)Assistant applies suprapubic pressure (NOT fundal) in downward/lateral direction to dislodge anterior shoulder
EEnter (internal rotational maneuvers)Rubin II: Push anterior shoulder toward fetal chest (adduction); Woods screw: Push posterior shoulder toward back; Reverse Woods (Rubin II + Woods simultaneously)
RRemove posterior armSweep posterior arm across chest and deliver → reduces shoulder-to-shoulder diameter
RRoll (Gaskin maneuver)All-fours position → gravity shifts anterior shoulder
Last resort: Zavanelli maneuver (head replacement → CS), deliberate clavicle fracture, symphysiotomy
⚠️ Do NOT apply fundal pressure (worsens impaction)

6.6 Postpartum Hemorrhage - EMOTIVE Protocol

Definition: Blood loss >500 mL (vaginal) or >1000 mL (CS) within 24 hours; or any amount causing hemodynamic instability.
Primary PPH: <24 hours postpartum | Secondary PPH: 24 hrs - 12 weeks
4 T's Causes:
  • Tone (uterine atony) - 80% most common
  • Trauma (lacerations, uterine rupture, hematomas)
  • Tissue (retained placenta/membranes, placenta accreta)
  • Thrombin (coagulopathy, DIC, APLA)

EMOTIVE Protocol (Active Management of PPH):

LetterAction
EExamine (assess cause - 4 T's), Estimate blood loss
MMassage uterus (bimanual compression); give Misoprostol 1000 mcg PR/SL if oxytocin unavailable
OOxytocin IV (10-40 IU in 500 mL NS); IV access x2, send bloods (CBC, coag, X-match)
TTransfuse (blood products: pRBC, FFP 1:1 ratio, platelets, cryoprecipitate); also Tamponade (Bakri balloon)
IInterventional radiology (uterine artery embolization - UAE)
VVasopressors (if hemodynamic compromise); Ventilate if needed
EEvaluate for surgery: B-Lynch suture, uterine artery ligation (O'Leary), internal iliac ligation, hysterectomy (definitive)

Uterotonics Stepwise:

DrugDoseNotes
Oxytocin10 IU IM or IV infusionFirst-line
Ergometrine0.2 mg IM/IVAvoid in hypertension
Oxytocin + ergometrine (Syntometrine)IMCombined
Misoprostol800-1000 mcg PR/SLWhen oxytocin unavailable; low-resource settings
Carboprost (PGF2α)250 mcg IM q15-90 min (max 8 doses)Avoid in asthma
Tranexamic acid1 g IV (within 3 hours)Anti-fibrinolytic; reduces death from bleeding

PART 2: GYNECOLOGY


7. MENSTRUAL DISORDERS

7.1 Mullerian Anomalies (ASRM/AFS Classification)

ClassTypeDescriptionAssociated Conditions
IHypoplasia/AgenesisUterine/vaginal agenesis; includes Mayer-Rokitansky-Kuster-Hauser (MRKH) syndromePrimary amenorrhea, 46,XX, normal ovaries
IIUnicornuateOne horn develops; rudimentary horn may be communicating or non-communicatingRenal anomalies (50%), ectopic pregnancy risk
IIIDidelphysComplete duplication: 2 uteri, 2 cervices, 2 vaginas (or single vagina)Best reproductive outcomes of fusion defects
IVBicornuatePartial fusion failure; 2 horns, 1 cervix; arcuate = minor formRecurrent pregnancy loss, preterm birth
VSeptateMost common Mullerian anomaly; complete septum (to os) or partialHighest recurrent miscarriage rate; resectable (hysteroscopic metroplasty)
VIArcuateMinimal indentation of fundus; often considered normal variantMinimal clinical significance
VIIDES-relatedT-shaped uterusAssociated with DES exposure in utero
Memory: Septate = most common + most abortions (septum has poor blood supply)

7.2 Primary vs. Secondary Amenorrhea

Primary Amenorrhea (no menses by age 15 with secondary sexual characteristics, or age 13 without any):

ConditionFSHKaryotypeKey Features
Gonadal dysgenesis (Turner 45,X)↑↑45,XShort stature, webbed neck, shield chest, coarctation of aorta; streak gonads
MRKH syndromeNormal46,XXAbsent uterus/vagina; normal breasts; normal ovaries
Androgen Insensitivity Syndrome (AIS) - CompleteNormal/↑46,XYFemale phenotype, absent uterus/cervix, blind vagina, testes in labia/inguinal; ↑ LH, testosterone in male range
Constitutional delayNormal46,XXBone age delayed; family history
Imperforate hymen / Transverse vaginal septumNormal46,XXCyclic pelvic pain, hematocolpos → bluish bulging at introitus
Hypothalamic/pituitary causes46,XXKallmann syndrome (+ anosmia), prolactinoma

Secondary Amenorrhea (cessation of previously regular menses for >3 months or irregular menses for >6 months):

First test: Pregnancy test (rule out pregnancy)
CauseFSH/LHEstrogenKey Features/Diagnosis
Hypothalamic amenorrhea↓/normalWeight loss, exercise, stress; FHA; GnRH pulsatility disrupted
HyperprolactinemiaGalactorrhea; elevated prolactin; MRI pituitary (prolactinoma)
Hypothyroidism--TSH elevated; TRH stimulates prolactin
PCOSLH:FSH >2:1Normal/↓Oligomenorrhea, hyperandrogenism, polycystic ovaries
POI/POF (Premature Ovarian Insufficiency)↑↑Age <40; FSH >25-40 IU/L on 2 occasions; may be autoimmune
Asherman's syndromeNormalNormalPost-curettage intrauterine adhesions; hysteroscopy diagnostic + therapeutic
Sheehan's syndromePituitary necrosis after PPH; failure to lactate, loss of pubic hair
Workup algorithm: Pregnancy test → Prolactin + TSH → FSH/LH → Progestogen challenge test (withdrawal bleed = estrogen present, intact outflow) → Estrogen + progestogen challenge (no bleed = outflow obstruction/Asherman's)

7.3 Abnormal Uterine Bleeding - FIGO Classification (PALM-COEIN)

CategoryAcronymNotes
PPolypEndometrial or cervical polyp
AAdenomyosisEctopic glands within myometrium
LLeiomyomaSubmucosal (most symptomatic), intramural, subserosal
MMalignancy / hyperplasiaEndometrial carcinoma, atypical hyperplasia
CCoagulopathyVon Willebrand disease (most common), platelet disorders
OOvulatory dysfunctionPCOS, thyroid, hyperprolactinemia, perimenopause
EEndometrialPrimary endometrial disorder (PALM-COEIN E)
IIatrogenicAnticoagulants, hormonal contraception, tamoxifen
NNot yet classifiedArteriovenous malformations, myometrial hypertrophy
PALM = structural causes (detected on imaging/histology); COEIN = non-structural causes
Terminology:
  • Heavy menstrual bleeding (HMB): >80 mL per cycle
  • Intermenstrual bleeding (IMB)
  • Postmenopausal bleeding (PMB): Any bleeding >12 months after LMP → endometrial biopsy mandatory

8. UTERINE CONDITIONS

8.1 Adenomyosis

FeatureDetails
DefinitionEctopic endometrial glands and stroma within myometrium
Pathology"Junctional zone" thickening >12 mm on MRI; heterogeneous myometrium on USG
Typical patientMultiparous woman, 35-50 years (perimenopausal); often with endometriosis
SymptomsDysmenorrhea (progressive), menorrhagia, dyspareunia, tender globular uterus ("boggy")
DiagnosisMRI (gold standard) - junctional zone thickness; USG - heterogeneous myometrium, asymmetric thickening
TreatmentHormonal (LNG-IUS/Mirena, OCP, progestogens, GnRH analogues); Definitive: hysterectomy (only cure)

8.2 Uterine Fibroids (Leiomyomata)

FeatureDetails
DefinitionBenign smooth muscle tumors (monoclonal); most common benign gynecologic tumor
Hormone-dependenceEstrogen and progesterone dependent; shrink postmenopausally
TypesSubmucosal (→ AUB, most symptomatic), Intramural (→ bulk symptoms), Subserosal (→ pressure), Pedunculated, Cervical, Broad ligament
SymptomsMenorrhagia (most common), dysmenorrhea, bulk symptoms (urinary frequency, constipation), infertility (submucosal)
Degeneration typesRed (carneous - in pregnancy, most common), hyaline (most common overall), cystic, calcific, sarcomatous
DiagnosisUSG (hypoechoic, well-defined masses); MRI (best for mapping pre-myomectomy)

FIGO Leiomyoma Classification (Type 0-8):

  • 0: Pedunculated intracavitary
  • 1: <50% intramural
  • 2: ≥50% intramural
  • 3: Contacts endometrium; 100% intramural
  • 4: Intramural
  • 5: Subserosal ≥50% intramural
  • 6: Subserosal <50% intramural
  • 7: Subserosal pedunculated
  • 8: Other (cervical, parasitic)

Management:

OptionDetails
MedicalNSAIDs, tranexamic acid (bleeding); Progestogens, OCP; GnRH agonists (leuprolide) - shrink fibroids 30-50%, pre-op; Ulipristal acetate (SPRMs)
SurgicalMyomectomy (fertility-sparing; hysteroscopic for submucosal, laparoscopic/open for intramural); Hysterectomy (definitive)
RadiologicalUterine artery embolization (UAE) - not for women desiring pregnancy; MRI-guided focused ultrasound (MRgFUS)

8.3 Endometriosis - Management

Definition: Ectopic endometrial glands and stroma outside uterus (ovaries most common → endometrioma/"chocolate cyst", Douglas pouch, uterosacral ligaments, bowel, bladder).
Triad: Dysmenorrhea + Dyspareunia + Dyschezia (painful defecation)
Gold standard diagnosis: Laparoscopy with biopsy (powder burn/blue lesions, "chocolate cysts")

ASRM Staging (I-IV):

  • I (Minimal), II (Mild), III (Moderate), IV (Severe - extensive adhesions, bilateral endometriomas)

Management by Goal:

GoalTreatment
Pain relief (no fertility desire)NSAIDs; Combined OCP (first-line); Progestogens (norethisterone, DMPA, LNG-IUS); GnRH agonists + add-back therapy; Danazol (androgenic SE, less used)
FertilitySurgical (laparoscopic excision/ablation of lesions, cystectomy for endometrioma); IVF (stage III-IV or tubal involvement)
Definitive (completed family)Total hysterectomy + bilateral salpingo-oophorectomy (BSO); HRT may be needed post-op
EndometriomaLaparoscopic cystectomy (preferred over drainage); cyst >4 cm should be operated before IVF

8.4 Endometrial Hyperplasia

TypeEIN ClassificationMalignant RiskTreatment
Without atypiaNon-EIN~1-3%Progestogen therapy (LNG-IUS preferred, or MPA 10-20 mg/day); repeat biopsy at 6 months
With atypia (EIN)Endometrial Intraepithelial Neoplasia~30-40% concurrent carcinoma; ~50% progress to carcinomaTotal hysterectomy + BSO (recommended if family complete); progestogen if fertility-sparing desired
Risk factors: Unopposed estrogen, obesity, PCOS, HRT (estrogen-only), tamoxifen, nulliparity, late menopause.

9. HIGH-YIELD GYNECOLOGY CLINICALS

9.1 Vaginal Infections

FeatureBacterial VaginosisCandidal VaginitisTrichomoniasis
OrganismGardnerella vaginalis (+ anaerobes)Candida albicans (90%)Trichomonas vaginalis (STI)
pH>4.5 (alkaline)<4.5 (normal/acidic)>4.5 (alkaline)
DischargeThin, gray-white, homogenous, fishy odorThick, white, cottage cheese, no odorFrothy, yellow-green, malodorous
SymptomsOdor (worse after intercourse/menstruation); minimal itchingPruritus vulvae, burning, dysuriaDysuria, pruritus, dyspareunia
Whiff testPositive (10% KOH → fishy amine odor)NegativeMay be positive
MicroscopyClue cells (epithelial cells coated with bacteria)Pseudohyphae/budding yeastMotile flagellated protozoa; strawberry cervix
Amsel criteria (3/4 = BV)pH >4.5, thin discharge, clue cells >20%, positive whiff test
TreatmentMetronidazole 500 mg PO BD x7d or 0.75% gel; ClindamycinClotrimazole (topical) or Fluconazole 150 mg PO single doseMetronidazole 2g PO single dose; treat partners

9.2 Ovarian Cysts & Tumors

Functional Cysts:

  • Follicular cyst: Most common; failure of follicle to rupture; resolves spontaneously in 4-8 weeks; <8 cm
  • Corpus luteum cyst: After ovulation; may hemorrhage (can mimic ectopic)
  • Theca lutein cysts: Bilateral; associated with molar pregnancy/high hCG; multiple large cysts

Ovarian Tumor Classification:

OriginBenignMalignant
Epithelial (70%)Serous cystadenoma (most common benign), Mucinous cystadenomaSerous cystadenocarcinoma (most common malignant), Mucinous, Endometrioid, Clear cell
Germ cell (20-25%)Mature teratoma/Dermoid (most common in young women; contains hair/teeth/fat; ↑ torsion risk)Dysgerminoma (most common malignant germ cell), Yolk sac tumor (AFP↑), Choriocarcinoma (βhCG↑), Immature teratoma
Sex cord-stromal (5%)Fibroma (Meigs' syndrome: fibroma + ascites + pleural effusion), ThecomaGranulosa cell tumor (estrogen-secreting → endometrial hyperplasia/cancer; Call-Exner bodies), Sertoli-Leydig (androgen-secreting → virilization)

Tumor Markers:

MarkerAssociated Tumor
CA-125Epithelial ovarian cancer (serous); also elevated in endometriosis, PID, fibroids
AFPYolk sac tumor, immature teratoma
β-hCGChoriocarcinoma, dysgerminoma (occasionally)
LDHDysgerminoma
InhibinGranulosa cell tumor, mucinous tumors
CEAMucinous tumors
CA-19.9Mucinous tumors

IOTA Criteria / ADNEX model: Used on USG to assess malignancy risk; ROMA score (CA-125 + HE4) for ovarian cancer risk.


9.3 Cervical Cancer - Screening & Diagnosis

Cervical Screening Guidelines:

AgeScreening Recommendation
<21 yearsNo screening regardless of sexual history
21-29 yearsPap smear every 3 years (cytology alone)
30-65 yearsPap + HPV co-test every 5 years (preferred) OR Pap alone every 3 years OR HPV alone every 5 years
>65 yearsDiscontinue if adequate negative prior screening (3 consecutive negative Paps or 2 consecutive negative co-tests in past 10 years)
After hysterectomy (benign)Discontinue

Cervical Cytology (Bethesda System):

ResultManagement
NILM (Negative for intraepithelial lesion)Routine screening
ASC-US (Atypical squamous cells of undetermined significance)Reflex HPV testing; colposcopy if HPV+; repeat in 1 year if HPV-
ASC-H (Cannot exclude HSIL)Colposcopy
LSIL (Low-grade squamous intraepithelial lesion)Colposcopy (women ≥25)
HSIL (High-grade squamous intraepithelial lesion)Colposcopy + biopsy; consider LEEP
AGC (Atypical glandular cells)Colposcopy + endocervical curettage + endometrial biopsy (if >35 yrs)
CarcinomaColposcopy + biopsy → staging

Cervical Intraepithelial Neoplasia (CIN) Management:

CIN GradeDefinitionManagement
CIN 1Mild dysplasia (1/3 epithelium)Observe; repeat in 1 year
CIN 2Moderate dysplasia (2/3 epithelium)Treat (LEEP/CKC) or observe (young women, small lesion)
CIN 3Severe dysplasia / CIS (full thickness)LEEP (Loop Electrosurgical Excision Procedure) or Cold Knife Cone biopsy

Cervical Cancer Staging (FIGO 2018):

StageDescription
IConfined to cervix
IAMicroscopic invasion only
IA1Stromal invasion ≤3 mm
IA2Stromal invasion >3-5 mm
IBVisible lesion or >5 mm invasion, confined to cervix
IIBeyond cervix but not pelvic wall or lower 1/3 vagina
IIAUpper 2/3 vagina involved, no parametria
IIBParametrial invasion
IIIPelvic wall / lower 1/3 vagina / hydronephrosis
IVBladder/rectum (IVA) or distant mets (IVB)

9.4 HPV Vaccination

VaccineTypes CoveredScheduleTarget
Gardasil 9 (9-valent)HPV 6, 11, 16, 18, 31, 33, 45, 52, 589-14 yrs: 2-dose (0, 6-12 months); ≥15 yrs: 3-dose (0, 2, 6 months)Most widely used; prevents ~90% of cervical cancers
Gardasil 4 (4-valent)HPV 6, 11, 16, 182 or 3 dose
Cervarix (2-valent)HPV 16, 183-dose
HPV 16 & 18 → Cervical cancer (70%), oropharyngeal cancer, anal cancer HPV 6 & 11 → Genital warts (condylomata acuminata), recurrent respiratory papillomatosis
WHO recommendation: Primary target: girls 9-14 years (before sexual debut); Catch-up: up to age 26 routinely; 27-45: shared decision-making.
Contraindications: Severe allergy to yeast or vaccine components; pregnancy (defer, not harmful if given inadvertently).

9.5 PCOS (Polycystic Ovary Syndrome)

Diagnosis - Rotterdam Criteria (2 of 3):

  1. Oligo-/anovulation (irregular cycles or anovulatory cycles)
  2. Clinical or biochemical hyperandrogenism (hirsutism by Ferriman-Gallwey >8, acne, alopecia; or elevated testosterone/DHEAS)
  3. Polycystic ovaries on USG (≥20 follicles 2-9 mm per ovary or ovarian volume >10 mL, in absence of dominant follicle/CL)
Must exclude other causes: congenital adrenal hyperplasia (17-OHP), Cushing's, androgen-secreting tumor, thyroid disease, hyperprolactinemia.

Hormonal Profile:

  • LH:FSH ratio >2:1 (or 3:1)
  • Elevated LH, normal/low FSH
  • Elevated androgens (testosterone, DHEAS, androstenedione)
  • Low SHBG (elevated free androgen index)
  • AMH elevated
  • Insulin resistance (elevated fasting insulin)

Associations:

  • Metabolic syndrome, T2DM (6-7x risk)
  • Endometrial hyperplasia/cancer (chronic anovulation → unopposed estrogen)
  • Subfertility
  • Obstructive sleep apnea
  • Cardiovascular disease risk

Management:

GoalTreatment
LifestyleWeight loss (5-10% body weight → restores cycles in up to 80%); exercise
Menstrual regulationCombined OCP (first-line: suppresses LH, increases SHBG, treats hyperandrogenism); Cyclic progestogens (to prevent endometrial hyperplasia)
HyperandrogenismOCP; Anti-androgens: Spironolactone (100-200 mg/day), cyproterone acetate; Metformin
Fertility/ovulation inductionLetrozole (aromatase inhibitor - first-line per ASRM); Clomiphene citrate (anti-estrogen, traditionally used); Metformin (adjunct); Gonadotrophins; Laparoscopic ovarian drilling (LOD)
Insulin resistance/MetabolicMetformin (reduces insulin resistance, improves cycles, reduces GDM/miscarriage risk in pregnancy)

9.6 Contraception

Efficacy Classification (Pearl Index - pregnancies per 100 woman-years):

MethodTypical Use FailurePerfect Use FailureNotes
No method85%85%
Condom (male)13%2%Also STI protection
Combined OCP7%0.3%
Progestogen-only pill (POP)7-9%0.3%
DMPA (Depo-Provera)4%0.2%Injection every 3 months
Implant (Nexplanon)0.05%0.05%Most effective reversible
LNG-IUD (Mirena)0.1-0.2%0.1%5-7 years; also treats HMB
Copper IUD0.8%0.6%Non-hormonal; also emergency contraception
Female sterilization0.5%0.5%Permanent
Vasectomy0.15%0.1%
Emergency contraception (LNG - Plan B)-75-89% reduction in pregnancy risk if taken <72h

Combined OCP:

  • Contains: Estrogen (ethinyl estradiol) + progestogen
  • Mechanism: Inhibit ovulation (primary), thicken cervical mucus, thin endometrium
  • Benefits: Regular cycles, reduced dysmenorrhea, improved acne/hirsutism, reduced endometrial/ovarian cancer risk, improved endometriosis/fibroids
  • Contraindications (UKMEC 4 - absolute): Known/suspected pregnancy, undiagnosed vaginal bleeding, current DVT/PE, migraine with aura, >35 yrs + smoking >15/day, current breast cancer, active hepatitis/cirrhosis, hypertriglyceridemia, peripartum cardiomyopathy

Progestogen-Only (Mini-Pill):

  • Safe in: Breastfeeding (preferred; start after 6 weeks), smokers >35 yrs, migraine with aura, history of DVT/PE
  • Mechanism: Primarily thickens cervical mucus; inhibits ovulation at higher doses (desogestrel POP - Cerazette)
  • Key point: Must be taken within 3-hour window daily (12-hour window for desogestrel)

Intrauterine Devices:

FeatureCopper IUDLNG-IUD (Mirena)
Duration5-10 years (Cu-380A up to 10 yrs; also emergency contraception up to 5 days post-coitus)5-7 years
MechanismCopper toxic to sperm + prevents fertilizationThickens mucus, thins endometrium, partial ovulation suppression
Effect on periodsHeavier, more painfulLighter or absent (amenorrhea in 20% by 1 yr) - treats HMB
Best forNon-hormonal option; heavy period contraindicationWomen with HMB; fibroids; endometriosis; breastfeeding

Emergency Contraception:

MethodTimingEfficacy
Levonorgestrel (Plan B, 1.5 mg PO)Within 72 hours (up to 120h)75-89% effective
Ulipristal acetate (Ella, 30 mg PO)Within 120 hoursSlightly superior to LNG; affected by progestogens
Copper IUDWithin 5 days>99% effective (most effective EC)

🔑 HIGH-YIELD SUMMARY TABLE

Key Numbers to Remember

TopicKey Value
Folic acid (normal)400 mcg/day, start 1 month before conception
Folic acid (high-risk)5 mg/day
GDM screening24-28 weeks (1-hr GCT)
GBS culture35-37 weeks
Tdap27-36 weeks every pregnancy
Discriminatory zone (hCG)1500-2000 IU/L → IUP visible on TVS
MTX criteria (hCG)<5000 IU/L (single dose)
Preeclampsia seizure prophylaxisMgSO₄ 4-6g loading, 1-2g/hr maintenance
Bishop score (favorable)≥8
PPH definition>500 mL vaginal, >1000 mL CS
PPH most common causeUterine atony (80%)
Most common Mullerian anomalySeptate uterus
Complete mole karyotype46,XX (androgenetic)
Partial mole karyotype69,XXX or 69,XXY
TTTS treatment of choiceFetoscopic laser photocoagulation
Cervical cancer screening start age21 years
CIN 3 treatmentLEEP
PCOS Rotterdam criteria2 of 3
Most common ovarian tumor (young women)Mature cystic teratoma (dermoid)
Most common malignant ovarian tumorSerous cystadenocarcinoma
Most common benign uterine tumorFibroid (leiomyoma)
Dysgerminoma markerLDH
Granulosa cell tumor markerInhibin
BV treatmentMetronidazole 500 mg BD x7 days
Trichomoniasis treatmentMetronidazole 2g single dose (treat partner)
Candida treatmentFluconazole 150 mg single dose

🧠 Quick Mnemonics

TopicMnemonic
Shoulder dystociaHELPERR (Help, Episiotomy, Legs McRoberts, Pressure suprapubic, Enter internal maneuvers, Remove posterior arm, Roll all-fours)
PPH causes4 T's - Tone, Trauma, Tissue, Thrombin
Bishop scoreDECSP - Dilation, Effacement, Consistency, Station, Position
AUB classificationPALM-COEIN (structural vs non-structural)
First trimester combined screen markersNT + PAPP-A + free β-hCG
Quad screen for T21↓AFP, ↑hCG, ↓uE3, ↑Inhibin A
Ectopic risk factorsSHIP - Sterilization/Salpingitis, History of ectopic, IUD/Infertility, Prior PID/procedure
Leopold maneuversFSPE - Fundal, Sides, Presentation, Engagement
TORCH infectionsToxoplasma, Other (syphilis/VZV), Rubella, CMV, HSV/HIV

Sources: Rosen's Emergency Medicine (Ectopic Pregnancy, Hypertension in Pregnancy sections); Creasy & Resnik's Maternal-Fetal Medicine; Berek & Novak's Gynecology; WHO, ACOG, FIGO, RCOG clinical guidelines.Here's your complete OBGYN revision guide - all topics covered with structured tables. Here's a quick orientation:

What's Covered

OBSTETRICS (Sections 1-6)
  • Section 1 - Early Pregnancy: All three categories of pregnancy signs (presumptive/probable/positive), preconception folic acid dosing and vaccination timing, GTPAL parity index, full teratogen table with defects, trimester-wise screening (quad screen patterns, diagnostic vs screening tests), Leopold maneuvers with what each determines
  • Section 2 - High-Yield Conditions: All four cerclage types with indications, APLA Sapporo diagnostic criteria + LMWH/aspirin management, ectopic pregnancy management tiers (expectant/medical/surgical with exact criteria and MTX contraindications), complete vs partial mole comparison table including p57 staining and malignancy rates
  • Section 3 - Placenta & Fluid: Previa vs abruption side-by-side, PAS spectrum with CS risk percentages, polyhydramnios/oligohydramnios causes and management, placental variants (succenturiata, velamentous, battledore, etc.)
  • Section 4 - Multiple Pregnancy: Lambda vs T sign for chorionicity, Quintero staging for TTTS, fetoscopic laser as treatment of choice
  • Section 5 - Medical Disorders: HTN classification, MgSO₄ protocol with toxicity monitoring, HELLP criteria (Tennessee + Mississippi classification), GDM two-step/one-step screening with cut-off values, White classification, fetal complications
  • Section 6 - Labor & Delivery: Full Modified Bishop Score table (DECSP), AMTSL components, breech types + ECV details, Lovset + Burns Marshall step-by-step, HELPERR algorithm with what each step does, EMOTIVE protocol with uterotonic ladder
GYNECOLOGY (Sections 7-9)
  • Section 7 - Menstrual Disorders: ASRM Mullerian classification I-VII with reproductive impact, primary vs secondary amenorrhea FSH-based workup algorithm, PALM-COEIN table
  • Section 8 - Uterine Conditions: Adenomyosis (MRI junctional zone criterion), fibroid FIGO 0-8 classification + degeneration types, endometriosis stepwise management by goal, endometrial hyperplasia risk stratification and treatment
  • Section 9 - GYN Clinicals: BV/Candida/Trichomoniasis comparison (pH/microscopy/treatment), ovarian tumor classification with tumor markers, cervical screening age-based guidelines + Bethesda CIN management, HPV vaccine schedules, PCOS Rotterdam criteria + Rotterdam management ladder, contraceptive Pearl Index + MEC4 contraindications + emergency contraception timing
The Key Numbers table and Mnemonics at the end serve as your last-day revision anchors. Let me know if you want any section expanded, a practice MCQ set, or a condensed one-page summary for any topic.
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