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Common Obstetric Complaints — How to Write the HOPI and Obstetric Part of History


How to Structure an Obstetric History

Before writing each complaint's HOPI, every obstetric history must open with the following identifying obstetric data:
Mrs. [Name], [Age] years old, [Gravida X, Para A+B], [marital status], [occupation], at [gestational age] weeks by [LMP/ultrasound], with an EDD of [date], presenting with…
  • Gravida (G) = total number of pregnancies including this one
  • Para (P) = A (births ≥24 weeks) + B (losses <24 weeks, miscarriages, TOPs)
  • Example: G4P1+2 = 4 pregnancies, 1 live birth, 2 losses before 24 weeks

The Universal Obstetric Section (Written After the HOPI for Every Case)

This must be documented after the presenting complaint's HOPI, regardless of the chief complaint:

1. History of the Current Pregnancy

  • 1st Trimester: LMP, method of confirmation (urine/serum βhCG, USS), EDD (Naegele's rule: LMP + 9 months 7 days), nausea/vomiting, bleeding/pain (? ectopic/threatened miscarriage), vaginal discharge, urinary symptoms, first antenatal bloods (blood group, Rh, FBC, VDRL, rubella immunity, HBsAg, HIV)
  • 2nd Trimester (14–28 wks): Fetal movements onset (quickening ~18–20 wks), anomaly scan result, OGTT/GDM screen, amniocentesis if applicable, PET screening
  • 3rd Trimester (28 wks–delivery): Frequency and pattern of fetal movements, ANC visits, BP readings, glucose tolerance, symphysio-fundal height, presentation/lie, swelling, headaches, visual disturbances

2. Past Obstetric History (For each previous pregnancy)

  • Gestational age at delivery
  • Mode of delivery (SVD / instrumental / LSCS — indication)
  • Birth weight, sex, outcome (alive/stillbirth/neonatal death)
  • Any complications: PPH, shoulder dystocia, GDM, PET, IUGR, preterm labour

3. Gynaecological History

  • Age of menarche, cycle regularity, dysmenorrhoea
  • Contraceptive method prior to conception
  • Cervical smear history
  • History of STIs, infertility, pelvic surgery, fibroids, ovarian cysts

4. Past Medical & Surgical History

  • Hypertension, diabetes, thyroid disease, anaemia, cardiac disease, renal disease, epilepsy
  • Previous surgeries (especially abdominal/pelvic)
  • Blood transfusions

5. Drug History & Allergies

  • Folic acid, iron, aspirin, antihypertensives, insulin, anticonvulsants
  • Teratogenic exposures

6. Family History

  • Diabetes, hypertension, multiple pregnancy, congenital malformations, thrombophilia

7. Social History

  • Smoking, alcohol, recreational drugs
  • Occupation, support at home, partner details
  • Housing, domestic violence (ask sensitively)


COMPLAINT 1 — Antepartum Haemorrhage (APH) / Vaginal Bleeding in Pregnancy

Chief Complaint

Mrs. X, 28 years, G2P1+0, at 32 weeks gestation by sure LMP (EDD [date]), presented to [facility] with painless/painful per vaginal bleeding of [duration].

HOPI of the Complaint

Characterise the bleeding (SOCRATES-based):
  • Onset: When did the bleeding start? Sudden onset (suggestive of placenta previa) vs. progressive
  • Amount: How much blood? (Estimate by pads soaked per hour — >1 pad/hour = significant; passage of clots; "flooding")
  • Color: Bright red (fresh — previa or local lesion) vs. dark (abruption; concealed)
  • Associated pain: Painless bleeding → placenta previa; painful, constant uterine tenderness → placental abruption
  • Precipitating factors: Any trauma, coitus, recent cervical examination?
  • Passage of tissue/clots: Tissue = possible miscarriage/molar pregnancy
  • Associated symptoms: Fetal movements — present, reduced, or absent? (Abruption can cause fetal distress/death)
  • Preceding discharge: Mucoid show (early labour) vs. watery loss (PROM)
  • Systemic symptoms: Dizziness, fainting, palpitations, syncope (hypovolaemia)
Differentiating features to document:
FeaturePlacenta PreviaPlacental Abruption
PainPainlessPainful (constant)
OnsetSpontaneous, recurrentOften follows trauma/hypertension
Uterine toneSoftTender, "woody-hard"
Fetal movementsUsually normalOften reduced/absent
Revealed bleedingYesMay be concealed (20%)

Obstetric Part (Current Pregnancy)

  • Booking ultrasound — was low-lying placenta reported?
  • Any prior bleeding episodes in this pregnancy?
  • Blood group and Rh type (anti-D prophylaxis if Rh-negative)
  • Antenatal visits — BP at each visit (hypertension → abruption risk)
  • History of smoking, cocaine use (abruption risk factors)
  • Fetal movements history — when last felt
  • History of trauma or domestic violence
— Rosen's Emergency Medicine, Chapter on Complications of Late Pregnancy

COMPLAINT 2 — Pre-Eclampsia / Hypertension in Pregnancy

Chief Complaint

Mrs. X, 32 years, G1P0+0, at 36 weeks gestation, presenting with headache, swelling of the face and hands, and blurring of vision of [duration].

HOPI of the Complaint

  • Headache: Site (frontal/occipital), severity (grade it 1–10), character (throbbing, pressure), onset, duration, progression, any relieving factors (analgesics), photophobia, phonophobia
  • Visual disturbances: Blurring, "flashing lights" (photopsia), scotomata, diplopia — all suggest cerebral vasospasm in severe PET
  • Oedema: Distribution — hands, face (facial puffiness), ankles; pitting vs. non-pitting; when it is worst (morning facial oedema = significant; dependent ankle oedema alone = normal pregnancy); sudden rapid onset
  • Epigastric/RUQ pain: Burning or tightness under the right ribs → hepatic capsule distension (HELLP syndrome); distinguish from heartburn/reflux (very common in pregnancy)
  • Convulsions / loss of consciousness: If present → eclampsia; document sequence, duration, post-ictal state, tongue biting, incontinence
  • Nausea and vomiting: Non-specific but can accompany HELLP
  • Decreased urine output / dark urine: Suggests renal involvement (oliguria <500 mL/24h = severe PET criterion)
  • Fetal movements: Ask carefully — uteroplacental insufficiency reduces fetal movements
Severity markers to elicit:
  • Systolic ≥160 or diastolic ≥110 mmHg = severe
  • Symptoms of end-organ damage: vision, neurological, liver, renal
  • HELLP: haemolysis (jaundice, haematuria), elevated liver enzymes, low platelets (easy bruising, petechiae)

Obstetric Part (Current Pregnancy)

  • BP at booking visit and at each antenatal visit — trend is critical (new rise from baseline)
  • Proteinuria on urine dipstick at antenatal visits
  • Gestational age — PET occurs ≥20 weeks; before 20 weeks consider molar pregnancy
  • Primigravida (highest risk), multiple pregnancy, known chronic hypertension/renal disease
  • BMI, pre-pregnancy weight
  • Family history of pre-eclampsia (mother, sisters)
  • Use of low-dose aspirin from 12 weeks (was it given/taken?)
  • Investigations done so far: USS for IUGR / oligohydramnios (uteroplacental insufficiency)
— Rosen's Emergency Medicine; Creasy & Resnik's Maternal-Fetal Medicine

COMPLAINT 3 — Preterm Labour (PTL)

Chief Complaint

Mrs. X, 26 years, G2P1+0, at 30 weeks gestation, presenting with painful uterine contractions occurring every [X] minutes since [time/duration].

HOPI of the Complaint

  • Contractions: Onset (sudden vs. gradual), frequency (e.g., every 5 minutes), duration per contraction (e.g., 45 seconds), regularity, severity (can she speak through them?), progression (are they getting stronger and more frequent?)
  • Associated show: Passage of blood-stained mucoid discharge (cervical show = cervix dilating)
  • Membrane status: Has she felt a "gush" or constant trickling of fluid? (PROM/PPROM) — fluid — colour, odour, whether it continues to leak
  • Bleeding: Any associated PV bleeding?
  • Fetal movements: Present and normal?
  • Precipitating factors: UTI (dysuria, frequency), uterine anomaly, polyhydramnios (distension), trauma, intercourse, cervical incompetence (previous LLETZ/cone biopsy, previous second-trimester loss)
  • Systemic features: Fever, rigors, offensive discharge (chorioamnionitis); urinary symptoms (UTI is a common trigger)
  • Previous similar episode in this pregnancy?

Obstetric Part (Current Pregnancy)

  • Gestational age confirmation (USS or reliable LMP)
  • Number of fetuses (multiple pregnancy = major risk)
  • Cervical length measured on USS (short cervix <25 mm = high risk)
  • History of cervical cerclage (in situ?)
  • Previous preterm births (strongest predictor of recurrence)
  • Antenatal steroids (betamethasone 12 mg × 2 doses): have they been given?
  • Group B Streptococcus (GBS) swab status
  • Urine culture — UTI excluded?

COMPLAINT 4 — Hyperemesis Gravidarum

Chief Complaint

Mrs. X, 22 years, G1P0+0, at 9 weeks gestation, presenting with persistent nausea and vomiting since [duration], unable to tolerate oral intake.

HOPI of the Complaint

  • Onset: When did it start? (Nausea of NVP typically 4–8 weeks; hyperemesis more severe and prolonged)
  • Frequency of vomiting: How many times per day? (>3–5 = significant; "vomiting after everything I eat or drink")
  • Content of vomit: Food, bile, blood (haematemesis — Mallory-Weiss tear)
  • Oral intake: Can she keep any fluids down? How long has she been unable to eat or drink?
  • Weight loss: Document weight at booking vs. now — weight loss >5% of pre-pregnancy weight is a diagnostic criterion
  • Triggers: Smell, food type, movement
  • Relieving factors: Any medications tried? (antiemetics, ginger)
  • Associated symptoms:
    • Dysuria/frequency (exclude UTI as a trigger)
    • Diarrhoea
    • Headache, confusion (Wernicke's encephalopathy from thiamine deficiency — a serious complication)
    • Jaundice (rare liver involvement)
  • Signs of dehydration: Thirst, dark urine, dizziness on standing, decreased urine output
  • Impact on daily functioning: Work, activity, mood (depression/anxiety common)
Distinguish from:
  • Normal NVP (nausea + vomiting, but no weight loss, maintains some oral intake, resolves by 12–14 weeks)
  • Molar pregnancy (marked βhCG elevation drives hyperemesis; ask about uterus size larger than dates, no fetal movements, grape-like tissue passed)
  • Gastroenteritis, UTI, thyrotoxicosis, hepatitis

Obstetric Part (Current Pregnancy)

  • Gestational age (hyperemesis worst at 8–12 weeks, should improve by 20 weeks)
  • USS — confirm intrauterine pregnancy, singleton vs. multiple (twins = higher βhCG), exclude molar pregnancy
  • βhCG level trend
  • TSH (transient gestational hyperthyroidism occurs in ~60% of HEG cases due to βhCG cross-reactivity with TSH receptor)
  • Previous pregnancy with same problem (tends to recur)
  • Urine dipstick and MSU (exclude UTI, check for ketonuria — indicates starvation)

COMPLAINT 5 — Reduced / Absent Fetal Movements (RFM)

Chief Complaint

Mrs. X, 30 years, G3P2+0, at 38 weeks gestation, presenting with reduced fetal movements since [time].

HOPI of the Complaint

  • Baseline fetal movements: How many movements per hour/day has she been used to? When did she first feel movements (quickening)?
  • Change: Since when has she noticed a reduction? Any complete cessation?
  • Nature of the change: Reduced in frequency, reduced in strength, or completely absent
  • Kick counts: Has she been monitoring? What is the count today vs. usual? (A count of <10 movements in 2 hours = concerning)
  • Associated features:
    • Any vaginal bleeding?
    • Any abdominal pain or uterine tightening?
    • Fever (intrauterine infection)?
    • Any fall or trauma?
    • Polyhydramnios (excessive fluid "cushions" movements, making them harder to feel)
    • Anterior placenta (attenuates sensation)
  • Last time she was certain baby moved?
  • Maternal wellbeing: Any dizziness, decreased activity (sedatives/alcohol can reduce FMs)

Obstetric Part (Current Pregnancy)

  • Gestational age and placental location (anterior placenta = reduced sensation — reassure; does not reduce actual movement)
  • Known IUGR or SGA on previous scans
  • History of pre-eclampsia/gestational hypertension (uteroplacental insufficiency)
  • Gestational diabetes (macrosomia, polyhydramnios)
  • Maternal medications (opiates, sedatives reduce perceived FMs)
  • Results of previous growth scans, Doppler studies
  • Prior episodes of RFM in this pregnancy
  • Obstetric history of previous stillbirth (highest-risk group)

COMPLAINT 6 — Prelabour Rupture of Membranes (PROM / PPROM)

Chief Complaint

Mrs. X, 24 years, G1P0+0, at 28 weeks gestation, presenting with a sudden gush of watery fluid per vaginum since [time].

HOPI of the Complaint

  • Onset: Sudden gush (classic PROM) vs. slow continuous trickle (high leak)
  • Amount: Large gush soaking through clothes vs. mild dampness
  • Colour of fluid: Clear/straw-coloured (normal), green/meconium-stained (fetal distress), blood-stained, offensive smell (chorioamnionitis)
  • Odour: Offensive odour → infection
  • Continued leaking: Is fluid still leaking? Does she still feel wet?
  • Distinguish from: Urinary incontinence (common in pregnancy — ask if she can stop the flow voluntarily, whether it smells like urine), increased vaginal discharge, show
  • Contractions: Any associated uterine contractions? (If yes, in labour)
  • Fetal movements: Present and normal?
  • Signs of infection (chorioamnionitis): Fever, rigors, tachycardia, abdominal tenderness, offensive discharge — if present, this is a medical emergency
  • Time since rupture: Latency period → risk of infection increases with time

Obstetric Part (Current Pregnancy)

  • Gestational age — determines management (conservative vs. delivery)
  • Presentation and lie of the fetus (USS) — cord prolapse risk with non-cephalic presentation
  • Group B Streptococcus (GBS) status
  • Antenatal steroid status (given for lung maturity if <34 weeks?)
  • Cervical cerclage in situ? (Must be removed if PROM occurs)
  • History of cervical procedure (LLETZ, cone biopsy)
  • Recent PV examination or intercourse
  • Urine culture (UTI as precipitant)
  • Previous PPROM (recurrence risk ~16%)

COMPLAINT 7 — Gestational Diabetes (GDM) — Antenatal Visit Complaint

Chief Complaint

Mrs. X, 35 years, G2P1+0, at 26 weeks gestation, referred with elevated blood glucose on routine OGTT screening.

HOPI of the Complaint

  • Symptoms of hyperglycaemia: Polyuria, polydipsia, polyphagia, unexplained fatigue — though most GDM is asymptomatic and found on screening
  • Timing of diagnosis: Routine screen (24–28 weeks) vs. early screen (first trimester if high risk)
  • Blood glucose values: Fasting and 2-hour post-load values on OGTT
  • Dietary history: Sugar intake, carbohydrate load, junk food, soft drinks
  • Home glucose monitoring: Is she doing it? Values?
  • Medications taken: Metformin, insulin — response and adherence
  • Hypoglycaemic episodes: Shakiness, sweating, dizziness, palpitations after medication
  • Symptoms of complications: Excessive thirst despite treatment, recurrent thrush (Candida — common with high glucose), blurred vision
  • Known pre-gestational diabetes? (Different diagnosis — document duration, type, complications)

Obstetric Part (Current Pregnancy)

  • USS for fetal growth — macrosomia (abdominal circumference > 95th centile), polyhydramnios (AFI)
  • Fundal height — uterus larger than dates (polyhydramnios/macrosomia)
  • BP and urinalysis (GDM increases risk of PET)
  • Family history of DM type 2
  • Previous GDM (50–70% recurrence risk)
  • Previous macrosomic baby (>4 kg), previous stillbirth, previous shoulder dystocia
  • BMI, weight gain in pregnancy
  • Ethnicity (South Asian, African, Middle Eastern = high risk)
  • Antenatal clinic referrals: dietician, diabetic team, ophthalmology
— Creasy & Resnik's Maternal-Fetal Medicine; Textbook of Family Medicine, 9e

Quick Reference Summary Table

ComplaintKey Hallmark in HOPICritical Obstetric Data Needed
APH / Vaginal BleedingPainless (previa) vs. painful (abruption); amount; fetal movementsPlacental site on USS; Rh type; BP trend
Pre-eclampsiaHeadache + visual changes + oedema ≥20 wks; RUQ pain; urine outputBP trend; proteinuria; USS for IUGR
Preterm LabourContraction frequency/duration; show; membrane statusGestational age; cervical length; steroid status
HyperemesisFrequency/content of vomiting; weight loss; oral intake; ketonuriaGestational age; molar pregnancy excluded; βhCG; TSH
Reduced Fetal MovementsBaseline vs. current count; cessation time; anterior placentaGrowth scans; Doppler; previous stillbirth
PROM / PPROMGush vs. trickle; colour/odour; contractions; signs of infectionGestational age; GBS status; steroid given?
Gestational DiabetesOften asymptomatic; polyuria/polydipsia; OGTT valuesMacrosomia/polyhydramnios on USS; weight gain; family Hx

Sources:
  • Rosen's Emergency Medicine: Concepts and Clinical Practice — Complications of Late Pregnancy
  • Creasy & Resnik's Maternal-Fetal Medicine: Principles and Practice
  • Textbook of Family Medicine, 9e
  • University of Queensland / Qatar University — History & Clinical Examination in Obstetrics (academic reference)

Now write each complaints in their description examples using their format

Here are all 7 complaints written out as full, realistic clinical history examples — exactly as you would write them in a case sheet or present them in a clinical setting.

COMPLAINT 1 — Antepartum Haemorrhage (Placenta Previa)


Mrs. Amina Hassan, 28 years old, Muslim, married, housewife. G3P2+0, at 34 weeks gestation by sure LMP (EDD: 20/07/2026). She was booked at [facility] at 10 weeks.

Chief Complaint (C/O)

  • Per vaginal bleeding × 3 hours

History of Presenting Illness (HOPI)

Mrs. Amina Hassan, a 28-year-old G3P2+0 at 34 weeks gestation, presented to the labor ward with a 3-hour history of per vaginal bleeding. She reports that the bleeding started suddenly and without warning at approximately 6:00 AM while she was sleeping. She denies any preceding trauma, coitus, or strenuous activity prior to the onset.
The bleeding is described as bright red in color, moderate in amount — she has soaked through 2 maternity pads within the 3 hours prior to presentation. She denies passage of any clots or tissue. Notably, the bleeding is entirely painless — she reports no abdominal cramps, uterine tightening, or backache accompanying the blood loss.
She denies any associated watery or mucoid vaginal discharge. Fetal movements were last felt approximately 2 hours ago and are reported as normal in frequency and strength by the patient.
She denies any dizziness, pre-syncope, palpitations, or shortness of breath at rest. She has had no fever, chills, or urinary symptoms.
She reports a similar episode of painless PV bleeding at 28 weeks during this pregnancy, for which she was admitted for 2 days, observed, and discharged after USS confirmed low-lying placenta. She was counselled to avoid coitus and heavy lifting.

Obstetric Part (Current Pregnancy)

She was confirmed pregnant by urine pregnancy test at 5 weeks. LMP was 13/10/2025, regular 28-day cycle, certain date. EDD calculated as 20/07/2026. Gestational age = 34 weeks.
1st Trimester: Confirmed intrauterine pregnancy on USS at 8 weeks. No bleeding or pain. Mild nausea managed conservatively. Booking bloods done — blood group O Rh-positive, FBC normal, VDRL non-reactive, rubella immune, HBsAg negative, HIV negative. Folate and iron supplementation started.
2nd Trimester: Quickening felt at 18 weeks. Anomaly scan at 20 weeks — low-lying posterior placenta reported, covering the internal os (Grade III placenta previa). Fetal anatomy normal. Counselled regarding pelvic rest. OGTT at 26 weeks — normal. Episode of painless PV bleeding at 28 weeks, admitted and managed conservatively with bed rest; anti-D not required (Rh-positive).
3rd Trimester: Fetal movements regular and strong. BP at last ANC visit (32 weeks) — 110/70 mmHg, urine dipstick negative. SFH = 32 cm. No oedema documented. Repeat USS at 32 weeks confirmed persistent low-lying placenta, not resolved. No cervical cerclage in situ. Scheduled for repeat USS at 36 weeks and planned elective LSCS.

Past Obstetric History

PregnancyYearGA at DeliveryModeWeightSexOutcomeComplications
1st202139 wksSVD3.2 kgFAlive, wellNone
2nd202338 wksSVD3.5 kgMAlive, wellNone
3rdCurrent34 wksPlacenta previa

Gynaecological History

Regular cycles, 28-day cycle, 5 days flow, moderate — no dysmenorrhoea. No history of STIs, fibroids, or ovarian cysts. Last cervical smear: 2022 — normal. No contraceptive use between pregnancies (natural family planning).

Past Medical / Surgical History

No known hypertension, diabetes, cardiac, renal, or thyroid disease. No previous abdominal or pelvic surgeries.

Drug History & Allergies

Ferrous sulphate 200 mg BD, Folic acid 5 mg OD. No known drug allergies.

Family History

No family history of multiple pregnancy, diabetes, hypertension, or congenital malformations.

Social History

Non-smoker. No alcohol. No recreational drug use. Lives with husband and two children in permanent housing. Good social support.


COMPLAINT 2 — Pre-Eclampsia


Mrs. Fatima Al-Rashid, 32 years old, married, teacher. G1P0+0, at 37 weeks gestation by sure LMP (EDD: 28/05/2026). Booked at 9 weeks.

Chief Complaint (C/O)

  • Headache × 2 days
  • Blurring of vision × 1 day
  • Swelling of face and hands × 3 days

History of Presenting Illness (HOPI)

Mrs. Fatima Al-Rashid, a 32-year-old primigravida at 37 weeks gestation, presented to the antenatal clinic with a 2-day history of progressive headache, a 1-day history of blurring of vision, and a 3-day history of facial and hand swelling.
Headache: The headache is located at the frontal and occipital regions, constant in nature, described as a "heavy pressure" sensation, graded 7/10 in severity. It is persistent, worsening over the 2 days, and poorly relieved by paracetamol 1 g taken yesterday. There is no fever, neck stiffness, vomiting, or photophobia. She has no prior history of migraine or recurrent headaches.
Visual disturbance: Since yesterday, she reports bilateral blurring of vision and "flashing lights" at the periphery of her vision (photopsia). There is no diplopia, total vision loss, or eye pain. She has not had any eye problems previously.
Oedema: She noticed puffiness of the face on waking 3 days ago — involving the periorbital region and cheeks. Her hands have felt tight and swollen, making it difficult to remove her rings. Ankle swelling has been present since 28 weeks but has significantly worsened. The swelling is pitting in nature. It does not improve with leg elevation overnight (facial and hand oedema is non-dependent and therefore more significant).
She also reports mild epigastric discomfort and right upper quadrant heaviness since this morning, which she initially attributed to heartburn. She denies nausea, vomiting, or jaundice.
She denies any convulsions, loss of consciousness, or confusion.
Urine output: She reports her urine has been reduced over the past 24 hours and appears slightly darker than usual. She denies dysuria or haematuria.
Fetal movements are reported as present and normal — last felt 1 hour ago.
Her blood pressure was measured by her community midwife yesterday as 158/104 mmHg — she was sent immediately to hospital. At today's visit, BP is 162/108 mmHg (confirmed on two readings 4 hours apart).

Obstetric Part (Current Pregnancy)

LMP: 21/08/2025, regular 30-day cycle. EDD: 28/05/2026. GA = 37 weeks.
1st Trimester: Confirmed intrauterine singleton pregnancy on USS at 8 weeks. No bleeding or pain. Mild nausea, no vomiting. Booking BP: 118/72 mmHg — normal. Booking bloods: blood group A Rh-negative, FBC normal (Hb 12.8 g/dL), urine dipstick — negative. Anti-D immunoglobulin given. Low-dose aspirin 75 mg OD commenced at 12 weeks (primigravida, BMI 29 — moderate risk for PET).
2nd Trimester: Quickening at 20 weeks. Anomaly scan at 20 weeks — normal fetal anatomy, normal placenta, no uterine artery notching reported. OGTT at 26 weeks — normal (fasting: 4.2 mmol/L; 2-hr: 6.8 mmol/L). BP at 24 weeks: 122/76 mmHg. Urine dipstick at each visit — negative until 32 weeks.
3rd Trimester: At 32 weeks, BP noted to be 130/84 mmHg — monitored closely. Urine dipstick at 34 weeks showed 1+ proteinuria — urine PCR sent, result pending. Growth scan at 34 weeks showed fetal weight on 15th centile, normal Doppler. At 36 weeks, BP 142/90 mmHg — patient advised to attend immediately if headache, visual disturbance, or worsening swelling develop. She presents today with all three symptoms.

Past Obstetric History

No previous pregnancies.

Gynaecological History

Menarche at 13 years. Regular 30-day cycles, 5 days flow. No dysmenorrhoea. No history of infertility. Last cervical smear: 2024 — normal. No STIs. COCP used for 3 years prior to conception, stopped 6 months before.

Past Medical / Surgical History

No known hypertension prior to pregnancy. No diabetes, renal disease, or cardiac disease. No previous surgeries. No blood transfusions.

Drug History & Allergies

Ferrous sulphate 200 mg BD, Folic acid 5 mg OD, Aspirin 75 mg OD (since 12 weeks). No known drug allergies.

Family History

Mother has hypertension — diagnosed at age 40, on antihypertensives. No family history of diabetes, multiple pregnancy, or congenital malformations. No family history of pre-eclampsia (mother's pregnancies uncomplicated).

Social History

Non-smoker. Occasional alcohol before pregnancy — stopped at conception. No recreational drugs. Works as a teacher (currently on leave). Lives with husband in permanent housing. Good social support.


COMPLAINT 3 — Preterm Labour


Mrs. Grace Okonkwo, 26 years old, Christian, married, trader. G2P1+0, at 30 weeks gestation by USS dating (EDD: 19/07/2026). Booked at 12 weeks.

Chief Complaint (C/O)

  • Painful uterine contractions × 4 hours
  • Watery vaginal discharge × 2 hours

History of Presenting Illness (HOPI)

Mrs. Grace Okonkwo, a 26-year-old G2P1+0 at 30 weeks gestation, presented to the labor ward at 11:00 PM with a 4-hour history of painful uterine contractions and a 2-hour history of watery vaginal discharge.
Contractions: She began experiencing lower abdominal cramps at approximately 7:00 PM. The contractions are rhythmic, occurring every 5–6 minutes, each lasting approximately 40–45 seconds. They are moderate in intensity — she rates the pain as 6/10 and states she is unable to speak through the contractions. They have been progressively worsening in frequency and intensity since onset. The pain radiates from the lower abdomen to the lower back. She denies any precipitating activity, fall, or trauma.
Vaginal discharge / membranes: Approximately 2 hours ago, she noticed a sudden gush of clear watery fluid from her vagina, soaking through her underwear. Since then, there has been a continuous slow trickle of clear fluid. She describes the fluid as odourless. She denies any offensive smell or change in colour to yellow/green.
Show: She noticed a small amount of blood-stained mucoid discharge (show) approximately 30 minutes before the contractions began.
Fetal movements: She reports fetal movements are present but feels they may be slightly less frequent than usual today. She is unsure whether to attribute this to her discomfort.
Signs of infection: She denies fever, rigors, or chills. No dysuria or urinary frequency. No offensive vaginal discharge. She was last seen at ANC 2 weeks ago — urine culture was sent and she has not yet received results.
She denies any per vaginal bleeding. No diarrhoea. No trauma.

Obstetric Part (Current Pregnancy)

Pregnancy confirmed by urine pregnancy test at 5 weeks. LMP uncertain (irregular cycles) → USS at 12 weeks dates pregnancy at 12+3 weeks → EDD: 19/07/2026. GA today = 30 weeks.
1st Trimester: USS confirmed singleton intrauterine pregnancy. Mild nausea managed conservatively. No bleeding. Booking bloods: Blood group B Rh-positive, Hb 10.8 g/dL (mild anaemia — iron supplements started), VDRL non-reactive, HIV negative, HBsAg negative. Urine dipstick normal.
2nd Trimester: Quickening at 19 weeks. Anomaly scan at 20 weeks — normal fetal anatomy, normal placenta (fundal), normal AFI. Cervical length on transvaginal USS at 22 weeks: 22 mm (short cervix — patient was counselled on PTL risk; cervical cerclage was not performed as she declined; progesterone pessaries 200 mg ON commenced and continued). OGTT at 26 weeks — normal.
3rd Trimester: At 28 weeks: SFH = 28 cm, fetal movements normal, BP 108/66 mmHg, urine dipstick negative. GBS swab not yet done. Antenatal steroids (betamethasone) have NOT yet been administered prior to this presentation. Urine C&S sent at last visit 2 weeks ago — results pending.
No cervical cerclage in situ. No uterine anomaly documented on USS.

Past Obstetric History

PregnancyYearGAModeWeightSexOutcomeComplications
1st202336 wksSVD2.4 kgMAlive, wellPreterm delivery — admitted in PTL at 35 wks
2ndCurrent30 wksPreterm labour
(Previous preterm birth is the single strongest risk factor for recurrent preterm labour)

Gynaecological History

Irregular cycles (28–35 days). Menarche at 14 years. No history of cervical procedures (LLETZ, cone biopsy). No STIs. No infertility. Last cervical smear: 2022 — normal.

Past Medical / Surgical History

No chronic illnesses. No previous pelvic or abdominal surgery. No blood transfusions.

Drug History & Allergies

Ferrous sulphate 200 mg BD, Folic acid 5 mg OD, Progesterone pessaries 200 mg ON. NKDA.

Family History

No family history of multiple pregnancy or congenital malformations. No diabetes or hypertension.

Social History

Non-smoker. No alcohol. No recreational drugs. Works as a trader (on feet for long hours — counselled to reduce activity). Lives with husband. Good social support.


COMPLAINT 4 — Hyperemesis Gravidarum


Miss Zainab Mohammed, 22 years old, single, student. G1P0+0, at 9 weeks gestation by USS (EDD: 07/12/2026). Booked at 7 weeks.

Chief Complaint (C/O)

  • Persistent nausea and vomiting × 4 weeks
  • Inability to tolerate oral intake × 5 days
  • Weight loss

History of Presenting Illness (HOPI)

Miss Zainab Mohammed, a 22-year-old primigravida at 9 weeks gestation, presented to the antenatal day unit with a 4-week history of severe, persistent nausea and vomiting, worsening over the past 5 days to complete inability to tolerate any oral intake.
Onset and progression: Nausea began at approximately 5 weeks gestation, initially in the mornings, consistent with normal NVP. However, by 6 weeks, vomiting had become continuous — occurring throughout the day and night with no predictable pattern. She denies any specific trigger (smell, food, movement) as "everything triggers it."
Frequency and content: She is currently vomiting 10–15 times per day. The vomit initially contained food, then bile, and for the past 2 days she has been vomiting bile only as she can no longer keep any food down. She denies haematemesis (no blood or coffee-ground material in vomit).
Oral intake: She has been completely unable to tolerate any oral intake — including water and oral medications — for the past 5 days. Any attempt to drink results in immediate vomiting within minutes.
Weight loss: She weighed 62 kg at her booking visit 2 weeks ago. Today she weighs 56.5 kg — a loss of 5.5 kg (8.9% of pre-pregnancy body weight) over 2 weeks.
Symptoms of dehydration: She reports intense thirst, decreased and very dark urine output (she estimates she has urinated only twice in the past 24 hours), dizziness and lightheadedness on standing (postural dizziness), and significant weakness. No syncope.
Neurological symptoms: She denies confusion, diplopia, or ataxia. (Absence of Wernicke's features important to document — but thiamine must be given prophylactically before IV dextrose)
Urinary symptoms: She denies dysuria, frequency, or haematuria (excluding UTI as a precipitant).
Other symptoms: No diarrhoea, no fever, no abdominal pain, no jaundice. No history of thyroid disease symptoms prior to pregnancy (though transient gestational hyperthyroidism will be tested).
Previous treatment: She was prescribed metoclopramide 10 mg TDS by her GP one week ago — she was unable to tolerate the tablets as she vomited immediately after every dose.
Psychosocial impact: She has missed 3 weeks of university classes. She reports feeling extremely distressed, helpless, and low in mood. She lives alone in student accommodation and has no one to assist her with daily activities.

Obstetric Part (Current Pregnancy)

Pregnancy confirmed by urine βhCG at 4 weeks (unplanned pregnancy). LMP: 01/03/2026, regular 28-day cycle. EDD: 07/12/2026. GA = 9 weeks.
USS at 7 weeks: Confirmed single intrauterine gestation, fetal pole seen, fetal cardiac activity confirmed. No features of molar pregnancy — no snowstorm appearance, no grape-like vesicles. No corpus luteum cyst. Crown-rump length appropriate for dates.
Booking bloods (7 weeks): Blood group O Rh-positive. FBC: Hb 12.2 g/dL, WCC 9.8 × 10⁹/L (mildly elevated, likely haemoconcentration). U&E: pending today. LFTs: pending today. Urine dipstick at booking: 2+ ketonuria, no protein, no leucocytes. MSU sent — culture pending.
βhCG trend: 7 weeks — 98,000 IU/L (upper limit of normal for singleton at 9 weeks; NOT markedly elevated to suggest molar pregnancy).
TSH: Sent today — awaiting result (transient gestational hyperthyroidism expected).
No multiple pregnancy. No known uterine/ovarian pathology.

Past Obstetric History

No previous pregnancies.

Gynaecological History

Menarche at 13 years. Regular 28-day cycles, 4 days, moderate. No dysmenorrhoea. COCP used for 2 years — stopped 3 months prior to conception. No STIs. No pelvic surgery.

Past Medical / Surgical History

No known medical conditions. No previous surgeries. NKDA.

Drug History & Allergies

Folic acid 400 mcg OD (prior to admission — unable to take now). Metoclopramide 10 mg TDS (prescribed — unable to tolerate). NKDA.

Family History

Mother had NVP in both pregnancies — no hospitalisation. No family history of diabetes, hypertension, or multiple pregnancy.

Social History

Non-smoker. Occasional alcohol prior to pregnancy — stopped at conception. No recreational drug use. University student, lives alone. Limited social support — parents live in another city. Appears distressed and tearful.


COMPLAINT 5 — Reduced Fetal Movements (RFM)


Mrs. Blessing Eze, 30 years old, married, civil servant. G3P2+0, at 38 weeks gestation by sure LMP (EDD: 14/05/2026). Booked at 10 weeks.

Chief Complaint (C/O)

  • Reduced fetal movements × 12 hours

History of Presenting Illness (HOPI)

Mrs. Blessing Eze, a 30-year-old G3P2+0 at 38 weeks gestation, presented to the labor ward at 8:00 PM with a 12-hour history of reduced fetal movements.
Baseline fetal movements: She has been actively monitoring fetal movements since 28 weeks as advised by her midwife. She reports that her baby typically moves 10–15 times per 2-hour period, predominantly in the afternoons and evenings. She describes the movements as a combination of kicks, rolls, and punches — strong and regular.
Change noticed: Since this morning at approximately 8:00 AM, she noticed the baby has been "unusually quiet." She waited, changed her position, drank cold water, and lay on her left side — manoeuvres that usually stimulate the baby. Despite these measures, she counted only 3 faint movements over a 2-hour period this afternoon. She has not felt any movement at all in the 2 hours prior to presentation.
Quality of movements: The few movements she did feel were much weaker than usual — she describes them as "flutters" rather than the strong kicks she is accustomed to.
Last certain movement: She is certain she felt a strong kick at approximately 7:00 AM this morning. She is uncertain about movements since then.
Associated symptoms:
  • She denies any per vaginal bleeding.
  • She denies abdominal pain, uterine contractions, or tightening.
  • She denies fever, chills, or offensive vaginal discharge.
  • She denies any trauma, fall, or road traffic accident.
  • She denies taking any medications that could sedate her or the baby (no opiates, no sedatives, no alcohol).
  • She reports normal activity levels today — she has not been unusually active or inactive.
Maternal wellbeing: She is anxious but haemodynamically stable. She denies headache, visual disturbance, or oedema (pre-eclampsia screen). No epigastric pain.

Obstetric Part (Current Pregnancy)

LMP: 07/08/2025, regular 28-day cycle. EDD: 14/05/2026. GA = 38 weeks.
1st Trimester: Confirmed intrauterine singleton pregnancy. No complications. Booking bloods normal. Blood group A Rh-positive.
2nd Trimester: Quickening at 18 weeks. Anomaly scan at 20 weeks — normal fetal anatomy, posterior placenta (posterior placenta means fetal movements are felt directly against the uterine wall — not attenuated; this makes the reduced movements more clinically significant). AFI normal. No structural abnormalities.
3rd Trimester: Growth scan at 34 weeks — fetal weight on 10th centile, normal umbilical artery Doppler — classified as SGA (small for gestational age), managed with increased surveillance. Repeat growth scan at 36 weeks — fetal weight now on 7th centile, umbilical artery S/D ratio increased — plan was for delivery at 38 weeks. BP at 36 weeks: 128/80 mmHg. Urine dipstick at 36 weeks: trace protein.
This presentation at 38 weeks is therefore particularly concerning given the background of worsening IUGR and abnormal Doppler trend.
No polyhydramnios or oligohydramnios documented. No GDM. No PET criteria met at last visit, though BP trending up.

Past Obstetric History

PregnancyYearGAModeWeightSexOutcomeComplications
1st201940 wksSVD3.4 kgFAlive, wellNone
2nd202238 wksSVD2.8 kgFAlive, wellSGA — IUGR noted at 34 wks; induced at 38 wks
3rdCurrent38 wksSGA/IUGR, RFM
(Recurrent IUGR — consistent with uteroplacental insufficiency)

Gynaecological History

Regular cycles. No history of uterine or cervical pathology. No STIs.

Past Medical / Surgical History

Mild iron-deficiency anaemia — on iron supplements. No hypertension or diabetes outside of pregnancy. No surgeries.

Drug History & Allergies

Ferrous sulphate 200 mg BD, Folic acid 5 mg OD. NKDA.

Family History

Mother: type 2 diabetes mellitus. No family history of PET or multiple pregnancy.

Social History

Non-smoker. No alcohol. No recreational drugs. Civil servant, currently on maternity leave. Lives with husband and two children. Good support. Visibly anxious.


COMPLAINT 6 — Preterm Prelabour Rupture of Membranes (PPROM)


Mrs. Hauwa Musa, 24 years old, married, tailor. G1P0+0, at 28 weeks gestation by USS (EDD: 11/08/2026). Booked at 10 weeks.

Chief Complaint (C/O)

  • Sudden gush of watery fluid per vaginum × 3 hours

History of Presenting Illness (HOPI)

Mrs. Hauwa Musa, a 24-year-old G1P0+0 at 28 weeks gestation, presented to the labor ward at 2:00 AM with a 3-hour history of per vaginal fluid loss.
Onset: At approximately 11:00 PM, while resting in bed, she experienced a sudden large gush of clear watery fluid from her vagina, which immediately soaked through her underwear and onto the mattress. She describes being "completely wet" without any warning or preceding sensation.
Continued leaking: Since the initial gush, there has been a continuous slow trickling of fluid. She has changed 3 pads over the past 3 hours, each moderately wet. The leaking continues.
Characteristics of fluid: The fluid is described as clear, slightly yellowish, and odourless. She denies any offensive or foul smell. She denies green or brown discolouration (no meconium staining). No blood mixed with the fluid.
Distinguishing from urine: She was asked specifically — she reports the fluid does not smell like urine. She is unable to voluntarily stop the leaking by contracting her pelvic floor (unlike urinary incontinence, which stops with voluntary contraction). She had not been incontinent of urine previously during this pregnancy.
Contractions: She denies any associated uterine contractions, cramps, or backache. She is not in labour at presentation.
Show: She denies any blood-stained mucoid discharge.
Fetal movements: Present and normal — last felt approximately 30 minutes ago.
Signs of infection (chorioamnionitis screen):
  • She denies fever or feeling hot/cold.
  • She denies rigors or chills.
  • She denies offensive vaginal discharge prior to this episode.
  • She denies abdominal tenderness or uterine pain.
  • She denies dysuria or urinary symptoms.
  • She has not been unwell in the days preceding this presentation.
Recent PV examination or intercourse: She denies recent sexual intercourse (last coitus was 2 weeks ago). She denies any recent PV examination. No recent cervical procedure.
Duration since rupture: Approximately 3 hours — she noted the time of the initial gush.

Obstetric Part (Current Pregnancy)

Pregnancy confirmed at 6 weeks by urine βhCG. LMP uncertain — USS at 12 weeks dates pregnancy at 12+2 weeks. EDD: 11/08/2026. GA = 28 weeks.
1st Trimester: Confirmed intrauterine singleton pregnancy on USS at 12 weeks. Normal NT scan. Booking bloods: Blood group B Rh-negative (Anti-D immunoglobulin given at booking and will be required again now). FBC: Hb 11.2 g/dL. VDRL non-reactive. HIV negative. HBsAg negative. Rubella immune. Urine dipstick: normal. MSU: no growth.
2nd Trimester: Quickening at 19 weeks. Anomaly scan at 20 weeks — normal fetal anatomy, fundal placenta, normal AFI, normal cervical length (38 mm). No cervical shortening or funnelling noted at that time. OGTT at 26 weeks — normal. No GBS swab yet performed.
3rd Trimester (28 weeks — today's presentation): Last ANC at 26 weeks — BP 104/68 mmHg, urine dipstick negative, SFH = 26 cm. No concerns documented. No antenatal steroids have yet been administered.
No cervical cerclage in situ. No history of cervical procedures (no LLETZ, no cone biopsy). No known uterine anomaly on any scan. No history of prior preterm birth.
No UTI documented in this pregnancy — though last MSU was at 12 weeks.

Past Obstetric History

No previous pregnancies.

Gynaecological History

Menarche at 13 years. Regular 30-day cycles. No STIs documented. No cervical or uterine procedures. Last cervical smear: never done (first time offered at booking).

Past Medical / Surgical History

No chronic medical conditions. No previous surgeries. No blood transfusions.

Drug History & Allergies

Ferrous sulphate 200 mg BD, Folic acid 5 mg OD. NKDA.

Family History

No family history of multiple pregnancy, diabetes, hypertension, or congenital malformations.

Social History

Non-smoker. No alcohol. No recreational drugs. Works as a tailor (sedentary occupation). Lives with husband. Good social support. Anxious about the baby's wellbeing given early gestation.


COMPLAINT 7 — Gestational Diabetes Mellitus (GDM)


Mrs. Priya Sharma, 35 years old, married, accountant. G2P1+0, at 28 weeks gestation by sure LMP (EDD: 08/08/2026). Booked at 8 weeks.

Chief Complaint (C/O)

  • Referred from ANC clinic with elevated blood glucose on routine OGTT screening
  • Increased thirst and frequency of urination × 3 weeks

History of Presenting Illness (HOPI)

Mrs. Priya Sharma, a 35-year-old G2P1+0 at 28 weeks gestation, was referred to the combined obstetric-diabetic antenatal clinic following an abnormal 75g oral glucose tolerance test (OGTT) performed at her routine 26-week ANC visit. She also reports a 3-week history of increased thirst and urinary frequency.
Abnormal OGTT results: The OGTT performed at 26 weeks showed:
  • Fasting glucose: 5.4 mmol/L (normal <5.1 mmol/L — borderline elevated)
  • 1-hour glucose: 10.8 mmol/L (normal <10.0 mmol/L — elevated)
  • 2-hour glucose: 9.2 mmol/L (normal <8.5 mmol/L — elevated)
  • Diagnosis: GDM confirmed (IADPSG criteria — one or more values at or above threshold)
Symptoms:
  • Polydipsia: She has noticed increased thirst for approximately 3 weeks — drinking significantly more water than usual (approximately 4–5 litres per day versus her usual 1.5 L).
  • Polyuria: Urinary frequency has significantly increased — she is waking 3–4 times per night to urinate (nocturia), and urinating every 45–60 minutes during the day. She denies dysuria, haematuria, or offensive urine (excluding UTI as cause).
  • Fatigue: She reports feeling unusually tired and "heavy" — significantly beyond what she attributes to the pregnancy itself.
  • Recurrent vaginal thrush: She has had two episodes of vulvovaginal candidiasis over the past 6 weeks — treated each time with topical clotrimazole. (Recurrent Candida is a red flag for hyperglycaemia)
  • Blurred vision: She noticed intermittent blurring of vision over the past 2 weeks — she attributes this to "tiredness" but has not seen an optician. (Fluctuating glucose causes osmotic lens changes — urgent ophthalmology referral needed)
She denies polyuria with pain (UTI excluded), no headache or visual field loss (PET excluded at this point), no nausea/vomiting.
Dietary history: She describes a diet high in refined carbohydrates — white rice, white bread, fruit juices, and frequent sweet snacks. She has not received dietetic counselling yet. She has not commenced home glucose monitoring.
No hypoglycaemic symptoms (not on any pharmacological treatment yet).

Obstetric Part (Current Pregnancy)

LMP: 01/11/2025, regular 28-day cycle. EDD: 08/08/2026. GA = 28 weeks.
1st Trimester: Confirmed intrauterine singleton pregnancy. BMI at booking: 31.2 kg/m² (obese — GDM risk factor). Booking bloods: Blood group O Rh-positive. Fasting glucose at booking: 5.0 mmol/L (borderline — HbA1c was checked: 5.9% — no pre-gestational diabetes, but impaired fasting glucose noted; early OGTT at 16 weeks performed — normal at that time: fasting 4.4 / 2-hr 7.1 mmol/L). FBC: Hb 11.5 g/dL.
2nd Trimester: Quickening at 19 weeks. Anomaly scan at 20 weeks — normal fetal anatomy; note was made of slight increase in abdominal circumference on 60th centile. AFI normal at 20 weeks. OGTT repeated at 26 weeks (routine second screen due to risk factors) — abnormal as above. Weight gain to date: 10 kg (above recommended gain for overweight BMI, target 7–11 kg total).
3rd Trimester (28 weeks — current visit): SFH today = 30 cm at 28 weeks (2 cm larger than dates — suggests macrosomia or polyhydramnios; USS for growth scan ordered today). BP: 118/74 mmHg. Urine dipstick: 2+ glucose, trace protein. No oedema.
Growth USS requested today to assess for macrosomia and polyhydramnios.

Past Obstetric History

PregnancyYearGAModeWeightSexOutcomeComplications
1st202139 wksSVD4.2 kg (macrosomic)MAlive, wellGDM in 1st pregnancy — diet-controlled; shoulder dystocia documented at delivery
2ndCurrent28 wksGDM recurrence
(GDM recurrence risk after first GDM pregnancy: 50–70%. History of macrosomia and shoulder dystocia in first pregnancy increases risk of recurrence)

Gynaecological History

Regular cycles. No history of PCOS (asked specifically — irregular cycles? excess hair? — denied). No STIs. No previous pelvic surgery.

Past Medical / Surgical History

No known pre-gestational diabetes. No hypertension. Family history of DM2 noted (see below). BMI pre-pregnancy estimated at 29.5 kg/m². No thyroid disease. No previous surgeries. No blood transfusions.

Drug History & Allergies

Ferrous sulphate 200 mg BD, Folic acid 5 mg OD. Not yet commenced on metformin or insulin — first diabetic clinic visit today. NKDA.

Family History

  • Father: Type 2 diabetes mellitus, diagnosed at age 45
  • Paternal aunt: Type 2 diabetes mellitus
  • No family history of type 1 DM, multiple pregnancy, hypertension, or congenital malformations.

Social History

Non-smoker. No alcohol during pregnancy. No recreational drugs. Accountant — desk-based sedentary occupation (minimal physical activity). Lives with husband and son. Good financial resources and social support. Motivated to comply with dietary changes and monitoring.


Summary of Writing Principles Used Across All Cases

ElementHow It Was Written
Opening statementName, age, gravida/parity, gestational age, EDD, then the complaint
Complaint characterisationOnset, duration, progression, severity, quality, radiation, associated features, aggravating/relieving factors, effect on function
Obstetric-specific symptomsFetal movements, bleeding, discharge, contractions addressed in every case
Differentials excluded within HOPIEach case actively excludes competing diagnoses with specific denials
Obstetric part structure1st / 2nd / 3rd trimester progression, with USS findings, bloods, BP, and relevant risk factors documented
Past obstetric historyTable format with GA, mode, weight, outcome, complications — each pregnancy numbered
Linking past to presentPast history complications are noted as risk factors for current presentation

Questions in each part from biodata ?? To ask during clerk using simple word states the questions

Here are all the actual questions you ask the patient during clerking, section by section, in simple everyday language — exactly as you would say them at the bedside.

CLERKING QUESTIONS — OBSTETRICS

From Biodata to the End of History


📋 SECTION 1 — BIODATA

These are the first questions you ask to introduce yourself and identify the patient.

"Good morning/afternoon, my name is Dr. ___. I am going to ask you some questions about yourself and your health. Is that okay?"

#Question to AskWhat You Are Finding Out
1"What is your full name?"Patient identity
2"How old are you?"Age — risk stratification (<20 = young primigravida risk; >35 = advanced maternal age)
3"What is your date of birth?"Confirm age
4"What is your religion?"Cultural/religious considerations for management (e.g., blood transfusion refusal)
5"Are you married, single, or in a relationship?"Marital/relationship status — social support
6"What is your husband's/partner's name and age?"Partner details
7"What do you do for work?"Occupation — physical activity, stress, exposure risks
8"What does your husband/partner do for work?"Partner occupation — financial support
9"Where do you live?"Address — for records and follow-up
10"What is your ethnic background?"Ethnicity — risk for GDM, sickle cell, thalassaemia, PET
11"What is your blood group? Do you know if you are Rhesus positive or negative?"Blood group and Rh status — anti-D management


📋 SECTION 2 — CURRENT PREGNANCY DETAILS

(Ask Early — Before the Complaint)


#Question to AskWhat You Are Finding Out
1"Is this your first pregnancy, or have you been pregnant before?"Gravidity
2"How many times have you given birth to a baby?"Parity (deliveries ≥24 weeks)
3"Have you ever had a miscarriage or lost a pregnancy before 6 months?"Pregnancy losses
4"Have you ever had a termination of pregnancy?"TOPs — ask sensitively, privately
5"When did your last period start? Are you sure of that date?"LMP — to calculate gestational age and EDD
6"Are your periods usually regular? How many days between each period?"Cycle regularity — affects accuracy of EDD
7"How many weeks pregnant are you now?"Gestational age
8"Do you know your due date?"EDD
9"Have you done an ultrasound scan? What did it show?"USS dating and findings
10"Where are you attending antenatal care? When did you first register?"Booking details
11"Have you been attending your antenatal visits regularly?"ANC attendance / compliance


📋 SECTION 3 — CHIEF COMPLAINT


"Now, can you tell me in your own words — what brought you to the hospital today?" (Let her speak freely first — do not interrupt)
Then follow with:
#Question to AskWhat You Are Finding Out
1"When exactly did it start?"Onset
2"Did it start suddenly or gradually?"Mode of onset
3"How long has it been going on?"Duration
4"Has it been getting worse, better, or staying the same?"Progression
5"Is there anything that makes it worse?"Aggravating factors
6"Is there anything that makes it better — like lying down, taking a tablet, or resting?"Relieving factors
7"Have you had this same problem before in this pregnancy or a previous one?"Recurrence / past history relevance


📋 SECTION 4 — HOPI QUESTIONS BY COMPLAINT


🔴 COMPLAINT 1 — Vaginal Bleeding (APH)

#Question to AskWhat You Are Finding Out
1"When did the bleeding start?"Onset
2"Did it come on suddenly or build up slowly?"Sudden = placenta previa
3"How much blood did you lose? Can you show me on this pad — is it like this much?"Amount / severity
4"What colour was the blood — bright red or dark?"Bright red = fresh / previa; dark = abruption
5"Did you pass any clots or tissue?"Clots = significant; tissue = possible miscarriage/molar
6"Do you have any pain in your belly right now?"Painless = previa; painful = abruption
7"Is the pain constant, or does it come and go?"Constant pain = abruption; intermittent = contractions
8"Is your belly feeling hard or tender when I touch it?"Wooden/tender uterus = abruption
9"What were you doing when the bleeding started — were you sleeping, walking, having sex?"Precipitating activity
10"Did anything happen before — any fall, injury, or accident?"Trauma as cause
11"Have you had sex recently — in the last 24–48 hours?"Post-coital bleed
12"Is the baby still moving? When did you last feel the baby move?"Fetal wellbeing
13"Have the movements changed — less than usual, or the same?"Reduced FM = fetal distress (abruption)
14"Have you had any watery discharge or fluid leaking from your vagina?"PROM associated
15"Do you feel dizzy, faint, or your heart racing?"Signs of haemorrhagic shock
16"Have you had any bleeding earlier in this pregnancy?"Previous APH = recurrent placenta previa
17"Did your scan ever mention a low-lying placenta?"Placenta previa on USS

🟠 COMPLAINT 2 — Pre-Eclampsia / Headache + Swelling + High BP

#Question to AskWhat You Are Finding Out
1"Where exactly is the headache — front, back, or all over?"Location — frontal/occipital common in PET
2"How bad is the headache — if 0 is no pain and 10 is the worst, what number?"Severity
3"Is the headache constant or does it come and go?"Constant = more sinister in PET
4"Did you take anything for it? Did it help?"Response to analgesia
5"Is your vision blurred, or do you see flashing lights or spots?"Visual disturbance = cerebral vasospasm
6"Are you seeing double?"Diplopia
7"Have you had any fits, blackouts, or shaking of the body?"Eclampsia — most important question
8"When did you first notice your face was swollen?"Facial oedema onset
9"Is your face puffy when you wake up in the morning?"Morning facial oedema = significant
10"Are your hands swollen? Can you still take off your rings?"Hand oedema
11"Has the swelling in your legs suddenly got much worse?"Rapidly worsening oedema
12"Do you have pain under your right ribs or in your upper stomach?"RUQ pain = liver capsule / HELLP
13"Do you have any pain in the middle of your stomach — like heartburn?"Epigastric pain — differentiate from reflux
14"Is your urine less than usual? Is it dark?"Oliguria = renal involvement
15"Has anyone checked your blood pressure recently? What was it?"BP trend from community/ANC
16"Did your antenatal urine tests ever show protein in your urine?"Proteinuria history
17"Are you still feeling the baby move normally?"Fetal wellbeing — IUGR risk

🟡 COMPLAINT 3 — Preterm Labour

#Question to AskWhat You Are Finding Out
1"Are you having pains in your lower belly or back right now?"Contractions present
2"How often do the pains come — how many minutes apart?"Frequency (every 5 min = active labour)
3"How long does each pain last — seconds or minutes?"Duration per contraction
4"Are they getting stronger and more frequent?"Progression = true labour
5"Can you talk or breathe normally during the pain, or does it stop you?"Severity
6"Does the pain go to your back?"Radiation — true labour often has backache
7"Did you notice any blood-stained jelly-like discharge from your vagina before the pains?"Show
8"Did you feel any water or fluid coming out of your vagina?"PPROM — membranes ruptured
9"Was it a big gush or a slow leak?"Gush = complete PROM; trickle = high leak
10"Did you have any bleeding with the pains?"APH associated with labour
11"Is the baby still moving normally?"Fetal wellbeing
12"Do you have any burning when you pass urine, or is it more frequent?"UTI — common trigger of PTL
13"Do you have a fever or feel hot and shivery?"Chorioamnionitis
14"Do you have any bad-smelling discharge from your vagina?"Infection
15"Did anything happen before the pains — a fall, lifting something heavy, or sex?"Precipitating factor
16"Did your scan ever show that your cervix was short?"Short cervix = PTL risk
17"Did you have an early delivery in your last pregnancy?"Previous PTL = strongest risk factor

🟢 COMPLAINT 4 — Hyperemesis Gravidarum

#Question to AskWhat You Are Finding Out
1"When did the nausea and vomiting start?"Onset (NVP starts ~5–6 wks)
2"How many times do you vomit in a day?"Frequency (>5 = significant)
3"What does the vomit look like — food, yellow/green liquid, or blood?"Content — bile = prolonged; blood = Mallory-Weiss
4"Are you able to keep anything down at all — water, juice, food?"Oral intake
5"Is there anything that makes it worse — smells, certain foods, movement?"Triggers
6"How much weight have you lost? Do you know your weight before pregnancy?"Weight loss (>5% = hyperemesis criteria)
7"When did you last pass urine? What colour was it?"Dark urine = dehydration
8"Do you feel dizzy when you stand up?"Postural dizziness = dehydration
9"Do you have any pain when you vomit, or pain in your stomach?"Rule out surgical cause
10"Are you confused or is your memory different lately?"Wernicke's encephalopathy screening
11"Is your vision normal?"Wernicke's — ophthalmoplegia
12"Do you have any burning when you pass urine, or need to go more often?"UTI as precipitant
13"Have you had diarrhoea?"Gastroenteritis vs hyperemesis
14"Do you have a fever?"Infection as a cause
15"Did you have this problem in a previous pregnancy?"Recurrence history
16"Have you tried any medication or home remedy for the vomiting?"Treatment tried
17"How has this been affecting your day — work, school, daily life?"Functional impact
18"How are you feeling in your mood — are you coping, or feeling very low?"Psychological wellbeing

🔵 COMPLAINT 5 — Reduced Fetal Movements

#Question to AskWhat You Are Finding Out
1"When did you first start feeling the baby move during this pregnancy?"Quickening onset
2"How often does your baby normally move in a day?"Baseline movement pattern
3"When did you first notice the movements had reduced?"Onset of RFM
4"When was the last time you are 100% sure the baby moved?"Time of last certain movement
5"How many times has the baby moved since you noticed the change?"Kick count
6"Did you try drinking cold water or lying on your side to get the baby to move?"Response to stimulation
7"Did the baby move after that, or still nothing?"Persisting RFM despite stimulation = urgent
8"Are the movements weaker than usual, or has the baby completely stopped?"Quality of remaining movements
9"Do you have any pain in your belly?"Abruption associated
10"Have you had any bleeding from your vagina?"APH — abruption
11"Have you had any pains coming and going in your belly?"Contractions
12"Have you taken any tablets, painkillers, or sleeping medicine today?"Sedatives reduce perceived FM
13"Did you eat and drink normally today?"Hypoglycaemia reduces FM
14"Did you have a fall or accident recently?"Trauma — abruption risk
15"Do you have a headache or swelling of your face and hands?"PET screening — uteroplacental insufficiency
16"Did your scan ever say the baby was small for its age?"IUGR — highest risk for stillbirth
17"Have you ever had a stillbirth before?"Highest risk group — handle sensitively

🟣 COMPLAINT 6 — PROM / PPROM

#Question to AskWhat You Are Finding Out
1"Can you describe what happened — what exactly did you feel?"Patient's own account of fluid loss
2"Did it come as a big sudden gush, or a slow trickle?"Gush = complete PROM; trickle = high/partial rupture
3"When exactly did it happen?"Time of rupture → latency period
4"Is it still leaking now, or has it stopped?"Ongoing leakage
5"How many pads have you soaked since it started?"Estimate of volume
6"What colour was the fluid — clear, yellow, green, or bloody?"Clear/straw = normal; green = meconium; offensive = infection
7"Did the fluid have a smell — like urine, or a bad smell?"Offensive odour = chorioamnionitis; urine smell = incontinence
8"Are you sure it is not urine — can you squeeze and stop the leaking?"Distinguish PROM from urinary incontinence
9"Is the fluid still coming even when you are sitting or lying still?"Continuous leak = PROM (urine stops when lying)
10"Do you have any pains in your belly or back — coming and going?"Contractions = labour has started
11"Have you noticed any blood-stained jelly coming out?"Show = cervix dilating
12"Is the baby still moving normally?"Fetal wellbeing
13"Do you have a fever, or do you feel hot and shivery?"Chorioamnionitis
14"Does your belly feel tender or painful when I press it?"Uterine tenderness = chorioamnionitis
15"Have you had any bad-smelling discharge from your vagina before today?"Pre-existing infection
16"Did you have sex recently — in the last 48 hours?"Coitus as precipitant
17"Have you had a recent examination in your vagina at the clinic?"Recent PV exam as precipitant
18"Have you ever had an operation on your cervix — like a biopsy or colposcopy?"Cervical procedure = weakened cervix

⚪ COMPLAINT 7 — Gestational Diabetes (GDM)

#Question to AskWhat You Are Finding Out
1"Were you told about your sugar test results at your last visit? What did they say?"Patient's awareness of OGTT result
2"Have you been feeling more thirsty than usual — drinking a lot more water?"Polydipsia
3"Are you passing urine much more often than before, even at night?"Polyuria / nocturia
4"How many times do you wake at night to pass urine?"Nocturia frequency
5"Are you feeling unusually tired or heavy all the time?"Fatigue from hyperglycaemia
6"Is your vision blurred at times?"Osmotic lens changes
7"Have you had any itching in your private parts, or repeated thrush infection?"Recurrent candidiasis = hyperglycaemia
8"Have you had any tingling or numbness in your hands or feet?"Peripheral neuropathy (unlikely in GDM but screen if pre-gestational DM)
9"Are you burning when you pass urine?"UTI — common with GDM; also causes polyuria
10"Are you checking your blood sugar at home? What numbers are you getting?"Home glucose monitoring values
11"What kind of food do you eat usually — do you eat a lot of rice, bread, sugar, or sweet drinks?"Dietary assessment
12"Have you been given any medication for your sugar — tablets or injections?"Treatment compliance
13"Did you have sugar problems in your last pregnancy?"Previous GDM = recurrence risk
14"Were any of your previous babies very big at birth — over 4 kg?"Macrosomia history
15"Did you ever have a big baby that got stuck during delivery?"Previous shoulder dystocia
16"Has your belly been measuring bigger than expected at your visits?"SFH > dates = macrosomia/polyhydramnios
17"Is the baby moving normally?"Fetal wellbeing
18"Do you have headache or your face and hands swelling?"PET screening — GDM increases PET risk


📋 SECTION 5 — OBSTETRIC HISTORY (PAST PREGNANCIES)

Ask for every previous pregnancy — go through them one by one.
#Question to AskWhat You Are Finding Out
1"How many times have you been pregnant before — including this one?"Total gravidity
2"Let's start from your first pregnancy — what year was that?"Timeline
3"How many months pregnant were you when you delivered?"Gestational age at delivery
4"Did you deliver normally through the vagina, or was it a caesarean section?"Mode of delivery
5"If caesarean — why was it done? Was it planned or an emergency?"Indication for LSCS
6"How much did the baby weigh?"Birth weight
7"Was it a boy or a girl?"Sex of infant
8"Is the baby alive and well today?"Neonatal outcome
9"Were there any problems during the pregnancy, labour, or after delivery?"Complications
10"Did you have a lot of bleeding after the baby was born?"Previous PPH
11"Did you have high blood pressure, swelling, or fits during that pregnancy?"Previous PET/eclampsia
12"Were you told you had sugar problems in that pregnancy?"Previous GDM
13"Was the baby premature — born before 9 months?"Previous preterm delivery
14"Were any of the babies small or not growing well inside the womb?"Previous IUGR/SGA
15"Have you ever lost a pregnancy before — a stillbirth or a baby that died after birth?"Stillbirth / neonatal death — ask very sensitively
16"Have you ever had a miscarriage — lost a pregnancy in the early months?"Early pregnancy loss


📋 SECTION 6 — GYNAECOLOGICAL HISTORY

#Question to AskWhat You Are Finding Out
1"How old were you when your periods first started?"Age of menarche
2"Are your periods usually regular?"Cycle regularity
3"How many days is your cycle — from the first day of one period to the next?"Cycle length
4"How many days does the bleeding last?"Duration of flow
5"Is the flow heavy, moderate, or light?"Amount of flow
6"Do you have pain during your periods?"Dysmenorrhoea
7"Have you ever had a smear test? When was the last one, and what was the result?"Cervical smear history
8"Have you ever been told you have fibroids, ovarian cysts, or polyps?"Uterine/ovarian pathology
9"Have you ever had an operation on your cervix or womb?"Previous cervical/uterine surgery
10"Have you ever had any infections 'down there' — sexually transmitted infections?"STI history
11"Have you ever had problems falling pregnant — did it take a long time?"Fertility history
12"What contraceptive method were you using before this pregnancy?"Contraception history


📋 SECTION 7 — PAST MEDICAL & SURGICAL HISTORY

#Question to AskWhat You Are Finding Out
1"Do you have high blood pressure?"Chronic hypertension
2"Do you have diabetes — sugar in your blood?"Pre-gestational diabetes
3"Do you have any problems with your kidneys?"Renal disease — PET risk
4"Do you have any heart problems?"Cardiac disease
5"Do you have any thyroid problems — has your thyroid been checked?"Thyroid disease
6"Do you have anaemia — low blood?"Chronic anaemia
7"Have you ever had fits or epilepsy?"Epilepsy — drug-drug interaction, teratogenicity
8"Have you ever had asthma or breathing problems?"Asthma
9"Have you ever had malaria during this pregnancy?"Malaria — common in endemic areas, causes anaemia/preterm labour
10"Have you ever been in hospital before, not for pregnancy?"Previous admissions
11"Have you ever had an operation? What was it for, and were there any problems?"Surgical history
12"Have you ever had a blood transfusion?"Blood transfusion history — infections, antibodies
13"Have you ever had tuberculosis — TB — or been treated for it?"TB history
14"Have you ever been told you have HIV? Are you on treatment?"HIV status — PMTCT
15"Do you have sickle cell disease or sickle cell trait?"Haemoglobinopathy


📋 SECTION 8 — DRUG HISTORY & ALLERGIES

#Question to AskWhat You Are Finding Out
1"Are you taking any medicines right now — tablets, injections, or supplements?"Current medications
2"Are you taking your folic acid and iron tablets regularly?"Compliance with antenatal supplements
3"Are you taking aspirin — was it prescribed to you?"Aspirin for PET prevention
4"Are you on any blood pressure medicines?"Antihypertensives
5"Are you on insulin or any diabetes tablets?"Diabetic medications
6"Are you taking any herbal medicines, local herbs, or traditional remedies?"Herbal/traditional medicine — teratogen risk
7"Do you have any allergies to any medicine — did any medicine ever give you a rash, swelling, or difficulty breathing?"Drug allergies


📋 SECTION 9 — FAMILY HISTORY

#Question to AskWhat You Are Finding Out
1"Does anyone in your family have diabetes — your parents, brothers, sisters?"Family DM → GDM risk
2"Does anyone in your family have high blood pressure?"Family hypertension → PET risk
3"Did your mother or sister ever have high blood pressure during their own pregnancy?"Family PET history
4"Are there any twins or triplets in your family?"Multiple pregnancy tendency
5"Is there any hereditary illness in the family — sickle cell, thalassaemia, chromosomal problems?"Genetic conditions
6"Has any baby in the family been born with a defect?"Congenital malformations
7"Is there a history of blood clots — DVT or PE — in the family?"Thrombophilia family history


📋 SECTION 10 — SOCIAL HISTORY

#Question to AskWhat You Are Finding Out
1"Do you smoke cigarettes?"Smoking — IUGR, preterm, abruption risk
2"If yes — how many do you smoke per day, and for how many years?"Pack-year history
3"Do you drink alcohol?"Alcohol — fetal alcohol syndrome
4"If yes — how much do you drink and how often?"Quantity and frequency
5"Do you use any other substances — cannabis, cocaine, or anything else?"Recreational drugs — abruption (cocaine), IUGR
6"Is your relationship with your husband or partner good? Do you feel safe at home?"Domestic violence screening — ask alone, sensitively
7"Do you have family or friends around to help you at home?"Social support network
8"Do you have any financial worries or problems caring for yourself?"Socioeconomic status
9"Are you still working? Is the work physically demanding?"Occupational risks
10"Who will be with you during labour and after delivery?"Birth partner / postnatal support
11"Is this pregnancy planned, or was it a surprise?"Planned vs unplanned — affects engagement with care
12"How are you feeling in yourself emotionally — are you coping with the pregnancy?"Mental health / antenatal depression screening


Quick Memory Aid — Order of Sections

B  → Biodata
C  → Current pregnancy (GA, EDD, G/P)
C  → Chief complaint
H  → HOPI (complaint-specific questions above)
O  → Obstetric history (past pregnancies)
G  → Gynaecological history
M  → Medical and surgical history
D  → Drug history and allergies
F  → Family history
S  → Social history
Tip: In obstetrics, always establish gestational age and parity before exploring the complaint — it changes everything about which conditions are possible and how urgently you need to act.

Now common complaints symptoms with their diagnosis smart memory aid

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🌍 TROPICAL MEDICINE 1 — KMTC EXAM MEMORY AID

Kenya Medical Training College | Clinical Medicine Programme


KMTC Tropical Medicine 1 covers: Malaria · Typhoid Fever · Cholera · Amoebiasis · Schistosomiasis · Trypanosomiasis · Leishmaniasis · Filariasis · Hookworm · Ascariasis · Tapeworm


🦟 DISEASE 1 — MALARIA

Memory Aid: "FALCIPARUM KILLS FAST"

LetterStands For
FFever — cyclical, high-grade
AAnaemia (haemolytic)
LLiver — hepatomegaly, jaundice
CCerebral malaria — seizures, coma
IIV Quinine / Artesunate for severe
PPlasmodium species × 4
AAL (Artemether-Lumefantrine) for uncomplicated
RRDT + Blood film = diagnose
UUncomplicated vs Severe — know the difference
MMosquito (female Anopheles) = vector

The 4 Plasmodium Species — Memory Aid: "FVMO"

SpeciesFever PatternSpecial Feature
FalciparumEvery 48 hrs (tertian)MOST DANGEROUS — cerebral, blackwater fever
VivaxEvery 48 hrs (tertian)Relapses — dormant hypnozoites in liver
MalariaeEvery 72 hrs (quartan)Nephrotic syndrome in children
OvaleEvery 48 hrsRelapses like vivax — mild

Clinical Features — "FAHSC"

  • F — Fever (cyclical — cold stage → hot stage → sweating stage)
  • A — Anaemia + pallor
  • H — Hepatosplenomegaly
  • S — Severe features (see below)
  • C — Chills and rigors

The Fever Stages — Memory Aid: "C-H-S"

  1. Cold/shivering stage (1 hour)
  2. Hot stage — very high temp (2–6 hours)
  3. Sweating/defervescence stage (2–4 hours) — patient feels better, then it repeats

Severe Malaria Features — Memory Aid: "CRABS POO"

LetterFeature
CCerebral malaria (altered consciousness, seizures, coma)
RRenal failure (haemoglobinuria = blackwater fever)
AAnaemia severe (Hb < 5 g/dL)
BBleeding / DIC
SShock (algid malaria)
PPulmonary oedema / ARDS
OOliguria / anuria
OObtunded consciousness

Diagnosis

TestWhat It Shows
Thick blood filmMost sensitive — finds parasites (gold standard)
Thin blood filmIdentifies species
RDT (Rapid Diagnostic Test)Detects falciparum antigen — fast, field use
FBCAnaemia, thrombocytopenia, leukopenia
Blood glucoseHypoglycaemia — especially in children
LFTs/RFTsAssess organ damage in severe malaria

Treatment — Memory Aid: "Uncomplicated = AL; Severe = IV AQ"

Uncomplicated Malaria (P. falciparum)

AL = Artemether-Lumefantrine (Coartem)
  • 4 tablets at 0h, 8h, then 4 tablets BD × 2 days
  • Give with food/fatty meal (increases absorption)
  • First-line in Kenya

Severe/Complicated Malaria

IV Artesunate (preferred) OR IV Quinine
  • Artesunate 2.4 mg/kg IV at 0, 12, 24 hours, then daily
  • Quinine: 20 mg/kg loading dose IV then 10 mg/kg q8h
  • Monitor blood glucose — quinine causes hypoglycaemia
  • Treat cerebral malaria: nurse patient, anticonvulsants for seizures

P. vivax / P. ovale (Relapse Prevention)

Chloroquine + Primaquine
  • Primaquine clears liver hypnozoites (prevents relapse)
  • Check G6PD before giving primaquine (causes haemolysis in G6PD deficiency)

Prevention — "BICS"

  • B — Bednets (insecticide-treated — ITNs)
  • I — Indoor Residual Spraying (IRS)
  • C — Chemoprophylaxis (travellers: doxycycline / atovaquone-proguanil)
  • S — Source reduction (eliminate standing water)


🌡️ DISEASE 2 — TYPHOID FEVER (Enteric Fever)

Memory Aid: "TYPHOID = STEPS"

LetterFeature
SSalmonella typhi (causative organism)
TTemperature — stepladder fever
EEnteric symptoms — constipation then diarrhoea
PPea-soup diarrhoea (late)
SSplenomegaly + rose spots

Causative Organism

  • Salmonella typhi (typhoid) and S. paratyphi A, B, C (paratyphoid)
  • Gram-negative bacillus
  • Route: Faeco-oral — contaminated water and food
  • Reservoir: Humans (carrier state in gallbladder)

Clinical Stages — Memory Aid: "4 WEEKS"

WeekFeatures
Week 1Stepladder fever (rises daily), headache, malaise, constipation, bradycardia relative to temperature
Week 2Sustained fever, rose spots (salmon-coloured spots on trunk), splenomegaly, toxic state
Week 3"Pea-soup" diarrhoea, abdominal distension, risk of intestinal perforation + haemorrhage
Week 4Recovery OR complications (perforation, peritonitis, death)

Classic Signs — Memory Aid: "ROBS"

  • R — Relative bradycardia (pulse slower than expected for the fever)
  • O — Obtunded / toxic look (Typhoid toxaemia)
  • B — Bradycardia + bloated abdomen
  • S — Splenomegaly + rose Spots

Complications — Memory Aid: "P-H-E-N"

  • P — Perforation of ileum (3rd week — surgical emergency)
  • H — Haemorrhage (intestinal)
  • E — Encephalopathy / meningitis
  • N — Nephritis / hepatitis / cholecystitis

Diagnosis

TestFinding
Widal testO antigen ≥1:160, H antigen ≥1:160 (suggestive — not definitive)
Blood cultureGold standard — positive in week 1 (80%)
Stool/urine culturePositive in week 3
FBCLeukopenia (low WBC) — classic finding
LFTsMildly elevated

Treatment

AntibioticNotes
Ciprofloxacin 500 mg BD × 14 daysFirst-line (where susceptible)
Azithromycin 500 mg OD × 7 daysAlternative; good for mild cases
Ceftriaxone 2–4 g IV OD × 10–14 daysSevere cases; IV route
ChloramphenicolHistorical first-line; still used where others unavailable
⚠️ Dexamethasone IV for severe toxaemia/encephalopathy (reduces mortality in severe disease)

Prevention — "3 C's"

  • Clean water and sanitation
  • Cooked food only
  • Chlorination + vaccine (oral Ty21a or Vi capsular polysaccharide)


💧 DISEASE 3 — CHOLERA

Memory Aid: "RICE WATER"

LetterFeature
R — Rice-water stoolsProfuse, watery, odourless, no blood
I — IV fluids (Ringer's lactate)For severe dehydration
C — Cramping (muscle cramps from K+ loss)Hypokalaemia
E — El Tor biotypeMost common current strain
W — Watery vomiting tooProjectile, effortless
A — Acidosis (metabolic)From bicarbonate loss
T — Tetracycline / DoxycyclineAntibiotic treatment
E — Enormous fluid loss (10–20 L/day)Shock within hours
R — Rehydration = ORS is lifesavingCornerstone of management

Causative Organism

  • Vibrio cholerae O1 (El Tor biotype) and O139
  • Gram-negative curved comma-shaped rod
  • Route: Faeco-oral — contaminated water
  • Produces cholera toxin → ↑ cAMP → massive Cl⁻ and water secretion into gut lumen

Clinical Features

FeatureDetail
Incubation2 hours – 5 days
OnsetSudden profuse watery diarrhoea
Stool appearanceRice-water (watery, grey, flecks of mucus) — no blood, no pus
VomitingEffortless, projectile
DehydrationSunken eyes, skin turgor loss, dry mouth, oliguria → anuria → shock
VoiceHoarse (from dehydration)
Muscle crampsPainful — from Na⁺ and K⁺ loss
"Washerwoman hands"Skin wrinkling from dehydration

WHO Dehydration Assessment — "SOME"

SignNo dehydrationSome dehydrationSevere dehydration
Skin pinchReturns quicklyReturns slowlyReturns very slowly
Oral/EyesNormalSunkenVery sunken, dry
MoodAlertRestless/irritableLethargic/unconscious
Eat/drinkDrinks normallyDrinks eagerlyDrinks poorly or unable

Treatment — "R-A-Z"

StepAction
RehydrationORS for mild-moderate; IV Ringer's Lactate for severe (100 mL/kg over 3–4 hrs adult)
AntibioticsDoxycycline 300 mg single dose (adult); Azithromycin in children/pregnant
ZincChildren under 5: Zinc 20 mg OD × 10–14 days (reduces duration and severity)
ORS composition: Glucose 75 mmol/L + NaCl 2.6g + KCl 1.5g + NaHCO3 2.9g per litre ORS works because sodium-glucose co-transport in the gut is intact even in cholera

Prevention — "WASH"

  • Water — safe, treated water
  • Adequate sanitation — latrines
  • Soap — handwashing
  • Hygiene — food hygiene, proper cooking


🦠 DISEASE 4 — AMOEBIASIS

Memory Aid: "AMEBA BITES"

LetterFeature
A — Amoeba = Entamoeba histolyticaCausative organism
M — Mucus + blood in stoolFlask-shaped ulcers in colon
E — Extraintestinal spread → liver abscessRight lobe — most common
B — Bloody diarrhoea (amoebic dysentery)Stool like "anchovy sauce"
A — Abscess (amoebic liver abscess)RUQ pain + fever + no jaundice
B — Biopsy/stool microscopy — trophozoitesDiagnosis
I — Ingestion of cystsFaeco-oral route
T — Tinidazole / MetronidazoleTreatment
E — Examine stool for cysts and trophozoitesLab diagnosis
S — Spread — blood-borne to liver, lung, brainComplications

Two Forms of Disease

FormFeatures
Intestinal (Amoebic dysentery)Bloody mucoid stools, colicky abdominal pain, tenesmus; flask-shaped ulcers in sigmoid/caecum
Extraintestinal (Amoebic liver abscess)RUQ pain, fever, hepatomegaly, no jaundice; "anchovy-paste" pus on aspiration

Diagnosis

  • Stool microscopy — trophozoites with ingested red blood cells (pathognomonic)
  • Ultrasound — liver abscess (single, right lobe)
  • Serology (ELISA) — for liver abscess
  • Stool: no pus cells (unlike bacillary dysentery)

Treatment

DrugUse
Metronidazole 800 mg TDS × 5–10 daysKills trophozoites (tissue infection)
Diloxanide furoate 500 mg TDS × 10 daysKills cysts in gut lumen (luminal agent) — prevents spread
DrainageLiver abscess — aspiration if no response to drugs or imminent rupture
Always give metronidazole + diloxanide together to prevent recurrence

Amoebic Dysentery vs Bacillary Dysentery — Know the Difference!

FeatureAmoebic (E. histolytica)Bacillary (Shigella)
OnsetGradualAcute
StoolBlood + mucus, offensiveBlood + pus + mucus
Stool microscopyTrophozoites with RBCsPus cells + organisms
FeverMild or absentHigh
TenesmusPresentProminent
ComplicationsLiver abscessRectal prolapse, HUS
TreatmentMetronidazoleCiprofloxacin


🐌 DISEASE 5 — SCHISTOSOMIASIS (Bilharzia)

Memory Aid: "SNAIL FEVER"

LetterFeature
S — Snail = intermediate hostFreshwater snail
N — Nigeria/Kenya — endemicSub-Saharan Africa
A — Adult worms in blood vesselsVenous plexuses
I — Itch on entry (Swimmer's itch)Cercarial dermatitis
L — Liver fibrosis (pipe-stem)Mansoni/japonicum
F — Fresh water exposureRisk factor
E — Eggs cause diseaseGranuloma formation
V — Vesical (bladder) = haematobiumTerminal haematuria
E — EosinophiliaBlood picture
R — Praziquantel = RxSingle treatment

Three Main Species

SpeciesLocation in BodyMain Organ AffectedKey Feature
S. haematobiumVesical (bladder) plexusBladderTerminal haematuria → bladder cancer
S. mansoniMesenteric veinsLiver + ColonPipe-stem fibrosis, portal hypertension
S. japonicumMesenteric veinsLiverMost eggs → worst liver disease

Life Cycle — Memory Aid: "EGGS → SNAIL → CERCARIAE → HUMAN"

  1. Eggs passed in urine/faeces → hatch in fresh water → miracidia
  2. Miracidia infect freshwater snail (intermediate host)
  3. Snail releases cercariae into water
  4. Cercariae penetrate human skin during water contact
  5. Travel to liver → mature into adult worms → lay eggs in blood vessels

Clinical Phases

PhaseFeatures
Swimmer's itchDermatitis at site of cercarial penetration
Katayama fever4–8 weeks post-exposure — fever, urticaria, eosinophilia, organomegaly (acute)
ChronicHaematuria (haematobium); portal hypertension, hepatosplenomegaly (mansoni)

Diagnosis

  • Stool/urine microscopy — find eggs (haematobium: terminal-spined egg in urine; mansoni: lateral-spined egg in stool)
  • Urine dipstick — haematuria
  • Serology
  • Biopsy (rectal/bladder)
  • Eosinophilia on FBC

Treatment

  • Praziquantel 40 mg/kg single dose (or two divided doses same day)
  • Safe, effective, inexpensive


😴 DISEASE 6 — TRYPANOSOMIASIS (African Sleeping Sickness)

Memory Aid: "TSETSE FLY SLEEPS"

LetterFeature
T — Trypanosoma bruceiCausative organism
S — Stage 1 (haemolymphatic)Fever, lymphadenopathy
E — Encephalitis Stage 2 (CNS)Sleeping sickness
T — Tsetse fly vectorGlossina species
S — Swollen lymph nodes (Winterbottom's sign)Posterior cervical nodes
E — East Africa = T.b. rhodesiense (acute)Rhodesiense = Rhodesia = Rapid
F — Fever + chancre at bite siteStage 1 feature
L — Lumbar puncture — CSF: trypanosomesConfirms stage 2
Y — Years — West African form is slowT.b. gambiense = Gradual

Two Forms

FeatureT.b. gambiense (West/Central Africa)T.b. rhodesiense (East Africa)
VectorTsetse fly (Glossina palpalis)Tsetse fly (Glossina morsitans)
CourseChronic (months–years)Acute (weeks)
CNSLateEarly
ReservoirHumansAnimals (cattle, game)

Clinical Features — Two Stages

Stage 1 (Haemolymphatic):
  • Fever, headache, malaise
  • Chancre at bite site
  • Winterbottom's sign — painless posterior cervical lymphadenopathy
  • Hepatosplenomegaly, anaemia
Stage 2 (Encephalitic/Meningoencephalitic):
  • Progressive sleep disturbance (sleeping during day, awake at night)
  • Personality change, confusion, coma
  • Involuntary movements, ataxia
  • Death if untreated

Treatment

StageDrugNotes
Stage 1Pentamidine (gambiense) / Suramin (rhodesiense)IV/IM
Stage 2Melarsoprol (arsenic — toxic)CNS penetration needed
Stage 2 gambienseEflornithine ± NifurtimoxSafer alternative


🌑 DISEASE 7 — LEISHMANIASIS (Kala-Azar)

Memory Aid: "KALA AZAR = BLACK FEVER"

FeatureDetail
OrganismLeishmania donovani
VectorFemale sandfly (Phlebotomus)
DistributionEast Africa (Kenya, Ethiopia, Sudan), India
MeaningKala-azar = Black fever (skin darkening)

Three Forms

FormFeaturesLocation Affected
Visceral (Kala-azar)Fever, splenomegaly, anaemia, weight loss, skin darkeningLiver, spleen, bone marrow
Cutaneous (Oriental sore)Painless ulcer at bite siteSkin only
MucocutaneousDestructive ulcers of nose and mouthSkin + mucous membranes

Visceral Leishmaniasis Signs — Memory Aid: "SAFFAW"

  • S — Splenomegaly (massive)
  • A — Anaemia (pancytopenia)
  • F — Fever (irregular, twice-daily spikes)
  • F — Fatigue + weight loss
  • A — Albumin low (reversed A:G ratio)
  • W — Weakness + skin darkening

Diagnosis

  • Splenic aspirate — most sensitive (but risky)
  • Bone marrow aspirate / lymph node aspirate — safer
  • rK39 rapid test — antigen test (field use, common in Kenya)
  • Leishmania skin test (Montenegro test)
  • FBC: pancytopenia (anaemia + thrombocytopenia + leukopenia)

Treatment

  • Sodium stibogluconate (SSG) 20 mg/kg IM/IV × 30 days — first-line in Kenya/Africa
  • Liposomal Amphotericin B — for resistant/immunocompromised
  • Miltefosine (oral) — emerging alternative


🪱 DISEASE 8 — FILARIASIS

Memory Aid: "WORM IN LYMPH BLOCKS FLOW"

FeatureDetail
OrganismsWuchereria bancrofti (most common), Brugia malayi, Brugia timori
VectorCulex mosquito
PathologyLymphatic obstruction → lymphoedema

Clinical Features — "ELEPHANTS HAVE BIG LEGS"

FeatureDescription
LymphangitisInflammation of lymph vessels — recurrent fever, red streaks
LymphadenopathyInguinal nodes most common
LymphoedemaProgressive swelling of legs, arms, genitals
ElephantiasisGross chronic lymphoedema — skin thickened, hardened
HydroceleScrotal swelling — very common in men
ChyluriaMilky white urine (lymph in urine)

Diagnosis

  • Nocturnal blood film — microfilariae (take blood at night — peak microfilariae 10 PM–2 AM with W. bancrofti)
  • Antigen test (ICT card test)
  • Eosinophilia on FBC

Treatment

  • DEC (Diethylcarbamazine) 6 mg/kg/day × 12 days — kills microfilariae and adult worms
  • Ivermectin + Albendazole — mass drug administration programmes
  • Hydrocele: surgical correction
  • Lymphoedema: limb elevation, compression, hygiene


🪱 DISEASE 9 — INTESTINAL WORMS (Helminths)

Quick Comparison Memory Aid: "HOOK-ROUND-TAPE-PIN"

FeatureHookwormRoundworm (Ascaris)TapewormPinworm
OrganismAncylostoma / NecatorAscaris lumbricoidesTaenia solium/saginataEnterobius
Entry routePenetrate skin (feet)Swallow eggsEat undercooked meatSwallow eggs
Key symptomIron-deficiency anaemiaIntestinal obstructionSegments in stoolPerianal itch at night
Larvae migrationLoeffler's syndrome (lungs)Loeffler's syndrome (lungs)
TreatmentAlbendazole/MebendazoleAlbendazole/MebendazolePraziquantel/NiclosamideMebendazole

Hookworm — Key Points

  • Larvae penetrate bare skin (ground itch = entry)
  • Attach to intestinal wall → suck blood → chronic iron deficiency anaemia
  • Eosinophilia — hallmark of all helminth infections
  • Treat: Albendazole 400 mg single dose + iron supplementation

Roundworm (Ascaris lumbricoides)

  • Largest intestinal nematode (up to 35 cm)
  • Loeffler's syndrome — larvae in lungs → cough, wheeze, eosinophilia
  • Complications: intestinal obstruction, biliary obstruction, volvulus
  • Treat: Albendazole 400 mg single dose

Tapeworm (Taenia)

  • T. solium (pork tapeworm) → cysticercosis (larvae invade brain, eye, muscle) → neurocysticercosis → seizures
  • T. saginata (beef tapeworm) — fewer complications
  • Treat: Praziquantel 5–10 mg/kg single dose OR Niclosamide


🧠 MASTER MEMORY TABLES

VECTORS — "Every Vector Has a Disease"

VectorDisease
Female Anopheles mosquitoMalaria
Culex mosquitoFilariasis (Wuchereria bancrofti)
Tsetse fly (Glossina)Trypanosomiasis (sleeping sickness)
Sandfly (Phlebotomus)Leishmaniasis (kala-azar)
Freshwater snailSchistosomiasis (bilharzia)
Blackfly (Simulium)Onchocerciasis (river blindness)
No vector (faeco-oral)Typhoid, Cholera, Amoebiasis, Hookworm, Ascaris, Tapeworm

DIAGNOSIS GOLD STANDARD — "Know Your Best Test"

DiseaseGold Standard Test
MalariaThick + thin blood film
TyphoidBlood culture (week 1)
CholeraStool culture (Vibrio cholerae)
AmoebiasisStool microscopy (trophozoites with RBCs)
SchistosomiasisStool/urine egg microscopy
TrypanosomiasisCSF microscopy (stage 2)
LeishmaniasisSplenic/bone marrow aspirate
FilariasisNocturnal blood film (microfilariae)

TREATMENTS AT A GLANCE — "One Drug Per Disease"

DiseaseFirst-Line DrugMemory Peg
Malaria (uncomplicated)Artemether-Lumefantrine (AL/Coartem)ALways use AL
Malaria (severe)IV Artesunate (or IV Quinine)Artesunate saves lives
TyphoidCiprofloxacin / CeftriaxoneCipro clears Salmonella
CholeraORS + DoxycyclineRehydrate FIRST
AmoebiasisMetronidazole + DiloxanideMetro kills trophozoites
SchistosomiasisPraziquantel 40 mg/kg × 1 dayPrazi for bilharzia
Trypanosomiasis Stage 1Pentamidine / SuraminPent-a-mide = 5 letters = Stage 1
Trypanosomiasis Stage 2Melarsoprol / EflornithineMelarsoprol = arsenic = dangerous
LeishmaniasisSodium StibogluconateSSG — 30 days
FilariasisDEC (Diethylcarbamazine)DEC kills micro-filariae
Hookworm/AscarisAlbendazole 400 mg single doseAlbendazole = all worms
TapewormPraziquantelPrazi for tape too

COMMON EXAM TRAPS — "Don't Fall For These"

TrapCorrect Answer
Malaria fever patternQuotidian (daily) in early infection — becomes tertian/quartan later
Most dangerous malaria speciesP. falciparum — only one that causes cerebral malaria
Which malaria relapses?P. vivax and P. ovale (not falciparum)
Typhoid blood countLeukopenia (NOT leukocytosis)
Typhoid most dangerous complicationIntestinal perforation (week 3)
Cholera stool descriptionRice-water — NOT bloody (bloody = dysentery)
Schistosoma that causes haematuriaS. haematobium
Vector of filariasisCulex mosquito (not Anopheles)
How to prevent relapse in P. vivaxAdd Primaquine (clears liver hypnozoites) — always check G6PD first
Widal test limitationCan be false-positive after prior typhoid vaccination or previous infection
Amoebic liver abscess — stool result?Stool may be NEGATIVE for E. histolytica in 50% of liver abscess cases
Blackwater fever is caused byP. falciparum — massive haemolysis → haemoglobinuria → dark urine

EOSINOPHILIA DISEASES — "WHATS"

Eosinophilia = Helminths (worms) + allergic conditions
Tropical diseases with eosinophilia:
  • Wuchereria (filariasis)
  • Hookworm
  • Ascaris
  • Toxocara
  • Schistosomiasis
Memory: "Worms Always Have Typical Swarms of eosinophils"

FAECO-ORAL ROUTE DISEASES — "CHAT"

  • C — Cholera
  • H — Hepatitis A/E
  • A — Amoebiasis / Ascaris
  • T — Typhoid
Prevention for all: WASH (Water, Adequate sanitation, Soap, Hygiene)

Sources: Harrison's Principles of Internal Medicine 22e; Lippincott Pharmacology; Rosen's Emergency Medicine; Comprehensive Clinical Nephrology — all cross-referenced with KMTC Tropical Medicine 1 curriculum scope

Can u provide sAqs and LAqs and how to answer medicine in correct way to earn marks? Tricks?

TROPICAL MEDICINE 1 — SAQs, LAQs & EXAM ANSWER TRICKS

KMTC Clinical Medicine | Exam-Oriented Guide


PART A — HOW TO ANSWER MEDICAL EXAM QUESTIONS (THE RULES)


The Golden Rules of Medical Exam Answers

Rule 1 — READ THE COMMAND WORD FIRST

The command word tells you exactly what to write and how much.
Command WordWhat It MeansHow Much to Write
DefineGive the exact meaning1–2 sentences
ListWrite items, one per line, numberedNo explanation needed
StateShort factual statement1 sentence each
DescribeGive details — what, how, whenFull sentences, structured
ExplainGive reason/mechanism behind somethingShow you understand WHY
DiscussCover all aspects — definition, features, managementFull structured answer
EnumerateNumber the points clearlyNumbered list
OutlineSummary — not full depth, but cover key pointsSubheadings + brief detail
CompareShow similarities AND differencesTable format preferred
DifferentiateShow differences onlyTable or two columns

Rule 2 — THE MARK ALLOCATION TELLS YOU HOW MANY POINTS

1 mark = 1 correct point
  • If a question is worth 5 marks → write at least 5 clear, separate points
  • If a question is worth 10 marks → write 10–12 points (give 2 extra as buffer)
  • Never write a paragraph when a list is faster and clearer
  • Never write one long sentence that contains 3 points — split them up

Rule 3 — THE FORMAT THAT EARNS MARKS

HEADING (bold or underlined)
  ↓
Short definition (1–2 lines)
  ↓
Numbered / bulleted points
  ↓
Each point = one idea = one mark
  ↓
End with complications or management if the question allows

Rule 4 — STRUCTURE EVERY CLINICAL ANSWER WITH "DOCS-MC"

Use this for any disease question:
LetterMeaning
DDefinition / causative organism
OOccurrence (epidemiology, risk factors, transmission)
CClinical features (symptoms + signs)
SSpecial investigations / diagnosis
MManagement / treatment
CComplications + prevention

Rule 5 — CLINICAL FEATURES: ALWAYS SEPARATE SYMPTOMS FROM SIGNS

Symptoms = what the patient tells you (subjective) Signs = what you find on examination (objective)
Examiners LOVE this separation — always write both.
Symptoms:
1. Fever
2. Headache
3. Chills and rigors

Signs:
1. Pallor
2. Splenomegaly
3. Jaundice

Rule 6 — MANAGEMENT: USE "ABCDE" FORMAT

LetterMeaning
AAssess/Admit — who needs admission
BBasic investigations — what tests to order
CConservative/supportive — fluids, rest, nutrition
DDrug treatment — specific drugs, doses, duration
EEducation / follow-up / prevention / complications to watch

Rule 7 — NEVER LEAVE ANY QUESTION BLANK

Even if you are unsure:
  • Write the definition
  • Write one or two features you know
  • Write one treatment
  • Partial marks are still marks


PART B — SHORT ANSWER QUESTIONS (SAQs) WITH MODEL ANSWERS

SAQs = typically 5–10 marks each. Write structured, concise, numbered answers.

SAQ 1 — MALARIA

Q: Define malaria and list four clinical features of severe malaria. (5 marks)

Model Answer:
Definition: (1 mark) Malaria is a parasitic infection caused by protozoa of the genus Plasmodium, transmitted to humans by the bite of an infected female Anopheles mosquito.
Four clinical features of severe malaria: (4 marks — 1 mark each)
  1. Impaired consciousness / coma (cerebral malaria)
  2. Severe anaemia (Hb <5 g/dL)
  3. Haemoglobinuria (blackwater fever) — dark/cola-coloured urine
  4. Convulsions / repeated seizures
  5. (Bonus) Pulmonary oedema / respiratory distress
  6. (Bonus) Hypoglycaemia

Q: State four differences between uncomplicated and severe malaria. (4 marks)

Model Answer:
FeatureUncomplicated MalariaSevere Malaria
ConsciousnessAlert, orientedImpaired, coma possible
ComplicationsNoneMulti-organ dysfunction
Treatment routeOral (Artemether-Lumefantrine)IV/IM (Artesunate or Quinine)
AnaemiaMildSevere (Hb <5 g/dL)

Q: Outline the treatment of uncomplicated malaria in an adult. (5 marks)

Model Answer:
Drug of choice: Artemether-Lumefantrine (AL/Coartem) — 1 mark
Dosage: 4 tablets at: (2 marks)
  • 0 hours, 8 hours (Day 1)
  • Morning and evening (Day 2)
  • Morning and evening (Day 3)
  • Total = 6 doses over 3 days
Additional measures: (2 marks)
  1. Give with food or milk (fatty meal increases absorption)
  2. Treat fever with paracetamol 1 g TDS
  3. Encourage oral fluids and rest
  4. Follow up in 48–72 hours; repeat blood film if not improving

Q: List five complications of malaria. (5 marks)

Model Answer:
  1. Cerebral malaria (seizures, coma, death)
  2. Severe anaemia (haemolysis)
  3. Acute renal failure (haemoglobinuria — blackwater fever)
  4. Pulmonary oedema / ARDS
  5. Hypoglycaemia (especially with IV quinine treatment)
  6. (Bonus) Disseminated intravascular coagulation (DIC)
  7. (Bonus) Splenic rupture
  8. (Bonus) Nephrotic syndrome (P. malariae in children)

Q: State two methods of malaria prevention. (2 marks)

Model Answer:
  1. Use of insecticide-treated bed nets (ITNs/LLINs)
  2. Indoor residual spraying (IRS) with insecticides
  3. (Bonus) Chemoprophylaxis for travellers (doxycycline / atovaquone-proguanil)
  4. (Bonus) Elimination of mosquito breeding sites (standing water)


SAQ 2 — TYPHOID FEVER

Q: Define typhoid fever and state its causative organism and mode of transmission. (4 marks)

Model Answer:
Definition: (1 mark) Typhoid fever is a systemic infection characterised by prolonged fever, abdominal symptoms, and bacteraemia.
Causative organism: (1 mark) Salmonella typhi (or Salmonella paratyphi A, B, C for paratyphoid)
Mode of transmission: (2 marks)
  1. Faeco-oral route
  2. Through ingestion of contaminated food and water
  3. (Bonus) Carriers (people who carry bacteria in gallbladder without symptoms) are a source

Q: Describe the clinical features of typhoid fever in each week of illness. (8 marks)

Model Answer:
Week 1: (2 marks)
  • Gradually rising "stepladder" fever (temperature rises each day)
  • Headache, malaise, general body aches
  • Constipation (early)
  • Relative bradycardia (pulse slower than expected for fever height)
Week 2: (2 marks)
  • Sustained high fever
  • Rose spots — salmon-coloured, blanching macules on trunk (rare but pathognomonic)
  • Splenomegaly
  • Toxic, ill-looking patient
Week 3: (2 marks)
  • Pea-soup diarrhoea — profuse, offensive green diarrhoea
  • Abdominal distension
  • Risk of intestinal perforation and haemorrhage (most dangerous complication)
Week 4: (2 marks)
  • Gradual defervescence (temperature settling) in uncomplicated cases
  • OR death from perforation/haemorrhage/septicaemia in complicated cases

Q: List three investigations used to diagnose typhoid fever and state the finding expected in each. (6 marks)

Model Answer:
InvestigationExpected FindingMark
1. Blood cultureGrowth of Salmonella typhi — gold standard, positive especially in week 12 marks
2. Widal testO antigen titre ≥1:160 and/or H antigen ≥1:160 — suggestive of infection2 marks
3. Full Blood Count (FBC)Leukopenia (low white cell count) — classic finding in typhoid2 marks

Q: State four complications of typhoid fever. (4 marks)

Model Answer:
  1. Intestinal perforation — commonest dangerous complication (week 3)
  2. Intestinal haemorrhage
  3. Typhoid encephalopathy / meningitis
  4. Hepatitis / jaundice
  5. (Bonus) Cholecystitis (gallbladder — causes chronic carrier state)
  6. (Bonus) Myocarditis


SAQ 3 — CHOLERA

Q: State the causative organism of cholera and describe the characteristic stool in cholera. (3 marks)

Model Answer:
Causative organism: (1 mark) Vibrio cholerae serotype O1 (El Tor biotype) or O139
Characteristic stool: (2 marks)
  • Described as "rice-water stool"
  • Profuse, watery, pale/grey in colour
  • Contains flecks of mucus
  • Has no blood and no faecal odour
  • Passed in very large volumes (up to 10–20 litres/day)

Q: Outline the management of a patient with severe cholera. (10 marks)

Model Answer:
A — Assessment: (1 mark)
  • Assess level of dehydration (skin turgor, sunken eyes, mental state, urine output)
  • Weigh patient to guide fluid replacement
B — Basic investigations: (1 mark)
  • Stool microscopy and culture
  • U&E (electrolytes — hyponatraemia, hypokalaemia, metabolic acidosis)
  • FBC
C — Supportive/IV Fluid Resuscitation: (4 marks)
  • Severe dehydration: IV Ringer's Lactate (NOT normal saline — RL replaces bicarbonate)
  • Adult: 100 mL/kg over 3–4 hours, then reassess
  • Children: 100 mL/kg over 3–6 hours
  • Switch to ORS when patient can drink
  • ORS for mild-moderate dehydration: 75 mL/kg over 4 hours
D — Drug Treatment: (2 marks)
  • Antibiotics reduce stool volume and duration by ~50%
  • Doxycycline 300 mg single dose (adults, non-pregnant)
  • Azithromycin 1 g single dose (children, pregnant women)
  • Ciprofloxacin 1 g single dose — alternative
E — Education and Prevention: (2 marks)
  • Strict hand hygiene after toilet use
  • Safe water — boil or treat
  • Proper disposal of faeces
  • Zinc supplementation in children (20 mg OD × 10 days)
  • Notification to public health authorities (cholera is a notifiable disease)


SAQ 4 — AMOEBIASIS

Q: Define amoebiasis and state its causative organism. (2 marks)

Model Answer:
  • Amoebiasis is an infection of the intestine (and sometimes other organs) caused by the protozoan Entamoeba histolytica, transmitted by the faeco-oral route through ingestion of cysts in contaminated food or water. (1 mark)
  • Causative organism: Entamoeba histolytica (1 mark)

Q: Differentiate between amoebic dysentery and bacillary (shigella) dysentery. (6 marks)

Model Answer:
FeatureAmoebic DysenteryBacillary (Shigella) Dysentery
OnsetGradual/subacuteSudden/acute
FeverMild or absentHigh fever
Stool appearanceBlood + mucus, offensiveBlood + pus + mucus
Stool microscopyTrophozoites with ingested RBCsPus cells + bacteria
TenesmusPresentSevere/prominent
ComplicationsLiver abscess, spread to lung/brainRectal prolapse, HUS
TreatmentMetronidazole + Diloxanide furoateCiprofloxacin
(6 features × 1 mark = 6 marks)

Q: State the treatment of amoebic liver abscess. (4 marks)

Model Answer:
  1. Metronidazole 800 mg TDS orally for 10 days — kills tissue trophozoites (2 marks)
  2. Diloxanide furoate 500 mg TDS × 10 days — clears luminal cysts and prevents recurrence (1 mark)
  3. Aspiration of abscess — if large (>10 cm), risk of rupture, or no response to drugs within 72 hours (1 mark)


SAQ 5 — SCHISTOSOMIASIS

Q: Name two species of Schistosoma that cause disease in East Africa and state the organ affected by each. (4 marks)

Model Answer:
SpeciesOrgan Affected
Schistosoma haematobiumBladder → haematuria, bladder cancer
Schistosoma mansoniLiver and colon → portal hypertension, pipe-stem fibrosis
(2 marks per species × 2 = 4 marks)

Q: State three clinical features of urinary schistosomiasis. (3 marks)

Model Answer:
  1. Terminal haematuria — blood at end of urination (pathognomonic)
  2. Dysuria and frequency (bladder irritation)
  3. Obstructive uropathy → hydronephrosis (chronic)
  4. (Bonus) Bladder cancer (squamous cell carcinoma — long-term complication)
  5. (Bonus) Swimmer's itch at entry (cercarial dermatitis)


PART C — LONG ANSWER QUESTIONS (LAQs) WITH MODEL ANSWERS

LAQs = typically 15–20 marks. Must be structured with headings, well-organised, and comprehensive.

LAQ 1 — MALARIA (20 marks)

Q: Discuss malaria under the following headings: definition, causative organisms, mode of transmission, clinical features, diagnosis, treatment, and prevention.


MALARIA

1. Definition (2 marks) Malaria is an acute and sometimes chronic parasitic infection caused by protozoa of the genus Plasmodium, transmitted to humans through the bite of an infected female Anopheles mosquito, characterised by cyclical fever, chills, anaemia, and in severe cases, cerebral involvement and death.

2. Causative Organisms (2 marks) Four species of Plasmodium cause human malaria:
SpeciesFever CycleDistinguishing Feature
P. falciparumTertian (48 hrs)Most dangerous; causes cerebral malaria
P. vivaxTertian (48 hrs)Relapses (liver hypnozoites)
P. malariaeQuartan (72 hrs)Nephrotic syndrome in children
P. ovaleTertian (48 hrs)Relapses; mild disease

3. Mode of Transmission (2 marks)
  1. Primary route: Bite of infected female Anopheles mosquito (vector)
  2. Mosquito bites at night (dusk to dawn)
  3. Other routes (rare): Blood transfusion, needle sharing, transplacental (congenital malaria)

4. Clinical Features (4 marks)
Symptoms:
  1. Cyclical fever with three stages: cold (shivering) → hot (high temperature) → sweating (defervescence)
  2. Headache
  3. Chills and rigors
  4. Nausea, vomiting, loss of appetite
  5. General body weakness and myalgia
  6. Joint pains (arthralgia)
Signs:
  1. Pallor (from haemolytic anaemia)
  2. Splenomegaly (in chronic/repeated infection)
  3. Hepatomegaly
  4. Jaundice (haemolysis)
  5. Temperature >38.5°C
Signs of Severe Malaria (P. falciparum):
  1. Altered consciousness / coma
  2. Repeated seizures (>2 in 24 hours)
  3. Severe anaemia (Hb <5 g/dL)
  4. Haemoglobinuria (dark/black urine — blackwater fever)
  5. Pulmonary oedema / respiratory distress
  6. Hypoglycaemia (blood glucose <2.2 mmol/L)
  7. Circulatory shock (algid malaria)

5. Diagnosis (3 marks)
  1. Thick and thin blood film microscopy — gold standard; identifies species and parasite density
  2. Rapid Diagnostic Test (RDT) — detects P. falciparum HRP2 antigen; fast and field-usable
  3. Full Blood Count (FBC): anaemia, thrombocytopenia, leukopenia
  4. Blood glucose: hypoglycaemia in severe malaria
  5. Renal function tests/LFTs: assess organ damage in severe disease

6. Treatment (4 marks)
A. Uncomplicated Malaria:
  • Artemether-Lumefantrine (AL) — 4 tablets at 0h, 8h, then twice daily × 2 days
  • Give with food/milk
  • Treat fever: Paracetamol 1g TDS
B. Severe Malaria:
  • IV Artesunate 2.4 mg/kg at 0h, 12h, 24h then daily
  • OR IV Quinine 20 mg/kg loading dose then 10 mg/kg q8h
  • Monitor blood glucose (IV quinine causes hypoglycaemia)
  • IV fluids, oxygen, treat seizures (diazepam)
C. Relapse Prevention (P. vivax/P. ovale):
  • Chloroquine + Primaquine (check G6PD status first)

7. Prevention (3 marks)
  1. Insecticide-treated bed nets (ITNs/LLINs) — sleep under net every night
  2. Indoor Residual Spraying (IRS) with insecticides
  3. Chemoprophylaxis for travellers and pregnant women (IPTp in pregnancy — SP monthly)
  4. Environmental control — drain stagnant water, clear bushes near homes
  5. Prompt diagnosis and treatment of all cases (reduces transmission)


LAQ 2 — TYPHOID FEVER (20 marks)

Q: A 20-year-old student presents with 2 weeks of gradually rising fever, headache, and constipation. Discuss this case under: definition, causative organism, pathology, clinical features, complications, investigations, and management.


TYPHOID FEVER

1. Definition (1 mark) Typhoid fever (enteric fever) is a systemic infectious disease caused by Salmonella typhi, characterised by prolonged stepladder fever, abdominal symptoms, and bacteraemia, transmitted by the faeco-oral route.

2. Causative Organism (1 mark)
  • Salmonella typhi (typhoid)
  • Salmonella paratyphi A, B, C (paratyphoid — milder disease)
  • Gram-negative rod, motile, bile-soluble
  • Humans are the only reservoir

3. Pathology (2 marks)
  1. Organism ingested in contaminated food/water
  2. Penetrates intestinal mucosa → enters Peyer's patches (lymphoid tissue in ileum)
  3. Carried to mesenteric lymph nodes → bacteraemia (1st week)
  4. Seeds liver, spleen, gallbladder, bone marrow
  5. Rose spots = emboli of bacteria in dermal capillaries
  6. Week 3: Peyer's patches necrose → ulceration and perforation of ileum

4. Clinical Features (4 marks)
Symptoms:
  1. Fever — stepladder pattern (rises 1°C each day over first week)
  2. Frontal headache — prominent, severe
  3. Constipation (first 1–2 weeks)
  4. Diarrhoea — "pea-soup" in week 3
  5. Abdominal pain and distension
  6. Loss of appetite, malaise, myalgia
Signs:
  1. Relative bradycardia — pulse-temperature dissociation
  2. Rose spots — 2–4 mm salmon-coloured macules on trunk (week 2)
  3. Splenomegaly
  4. Coated tongue
  5. Abdominal tenderness (iliac fossa)
  6. Toxic, ill-looking patient

5. Complications (3 marks)
  1. Intestinal perforation — week 3; presents with sudden severe abdominal pain, peritonitis, shock — SURGICAL EMERGENCY
  2. Intestinal haemorrhage — PR bleeding
  3. Hepatitis and jaundice
  4. Typhoid encephalopathy — confusion, psychosis
  5. Myocarditis — bradycardia may worsen
  6. Chronic carrier state — bacteria persist in gallbladder for >1 year; source of outbreaks

6. Investigations (3 marks)
InvestigationTimingResult
Blood cultureWeek 1 (best — 80% positive)S. typhi growth — gold standard
Stool cultureWeek 3Positive
Urine cultureWeek 3Positive
Widal testWeek 2 onwardsO titre ≥1:160; H titre ≥1:160
FBCAny timeLeukopenia (low WBC)
LFTsAny timeMildly elevated transaminases

7. Management (6 marks)
A — Admission: All confirmed/suspected typhoid cases should be admitted
B — Investigations: As above
C — Supportive Care:
  1. Bed rest
  2. Maintain adequate hydration — oral fluids or IV fluids if vomiting
  3. High-calorie, low-fibre soft diet (avoids mechanical stress on Peyer's patches)
  4. Paracetamol for fever (avoid NSAIDs — risk of GI bleeding)
  5. Tepid sponging for very high temperature
D — Drug Treatment:
DrugDoseDuration
Ciprofloxacin (first-line)500 mg BD orally14 days
Ceftriaxone (severe/IV)2–4 g IV OD10–14 days
Azithromycin500 mg OD7 days
Dexamethasone3 mg/kg then 1 mg/kg q6hFor severe encephalopathy
E — Complications Management:
  • Perforation: IV antibiotics + surgical repair (emergency laparotomy)
  • Haemorrhage: blood transfusion, surgical intervention
F — Prevention:
  1. Safe drinking water (boiling/chlorination)
  2. Proper food hygiene and handwashing
  3. Typhoid vaccination — oral Ty21a (3 doses) or Vi polysaccharide (injection)
  4. Treatment of carriers (ciprofloxacin 6 weeks to clear gallbladder carriage)
  5. Notification to public health


LAQ 3 — CHOLERA (15 marks)

Q: Discuss cholera under: definition, causative organism, pathophysiology, clinical features, diagnosis, and management.

(Use DOCS-MC structure — see above for how to write)

CHOLERA
1. Definition (1 mark) Cholera is an acute diarrhoeal illness caused by enterotoxin-producing Vibrio cholerae, characterised by profuse watery ("rice-water") diarrhoea, vomiting, and rapid dehydration, with the potential to cause death within hours if untreated.
2. Causative Organism (1 mark)
  • Vibrio cholerae serogroup O1 (El Tor biotype) — most common worldwide
  • Vibrio cholerae O139 — second most common
  • Gram-negative, curved comma-shaped rod
  • Transmitted by faeco-oral route — contaminated water and food
3. Pathophysiology (2 marks)
  1. V. cholerae colonises the small intestine
  2. Produces cholera toxin (CT) — binds to enterocyte surface
  3. Toxin → activates adenylate cyclase → ↑ intracellular cAMP
  4. ↑ cAMP → massive secretion of Cl⁻, Na⁺, and water into intestinal lumen
  5. Water and electrolyte absorption is blocked
  6. Result: massive watery diarrhoea and dehydration
4. Clinical Features (3 marks)
Symptoms:
  1. Sudden onset profuse watery diarrhoea
  2. Effortless projectile vomiting
  3. Painless abdomen (no colicky pain — unlike dysentery)
  4. Extreme thirst
  5. Muscle cramps (hypokalaemia)
Signs:
  1. Rice-water stools — pale, watery, odourless with flecks of mucus
  2. Sunken eyes, sunken fontanelle (children)
  3. Loss of skin turgor — "skin tent" sign
  4. Dry mucous membranes
  5. Tachycardia → hypotension → shock (in severe cases)
  6. "Washerwoman hands" — wrinkled skin from dehydration
  7. Hoarse voice, decreased urine output → anuria
5. Diagnosis (2 marks)
  1. Clinical diagnosis in endemic area with typical rice-water stool
  2. Stool microscopy and cultureV. cholerae (confirmation)
  3. Dark-field microscopy — darting motility of vibrios
  4. RDT (Rapid cholera antigen test) — field use
  5. U&E — hyponatraemia, hypokalaemia, metabolic acidosis
6. Management (6 marks)
Priority: REHYDRATION FIRST — before anything else
A — Rehydration (most marks here):
SeverityRouteFluidVolume/Rate
Mild (no dehydration)OralORS50 mL/kg over 4 hrs
Moderate (some dehydration)OralORS75 mL/kg over 4 hrs
Severe (shock)IVRinger's Lactate100 mL/kg: give 30 mL/kg in 30 min, then 70 mL/kg in 2.5 hrs
  • Reassess every 30 minutes in severe cases
  • Monitor urine output, pulse, skin turgor
B — Antibiotics:
  • Doxycycline 300 mg single dose (adults, non-pregnant) — reduces stool output by 50%
  • Azithromycin 1g single dose — children and pregnant women
  • Ciprofloxacin 1g single dose — alternative
C — Zinc supplementation (children):
  • 20 mg OD × 10–14 days
D — Diet:
  • Continue breastfeeding in infants
  • Resume normal feeding as soon as tolerated
E — Public Health:
  • Isolate patient (barrier precautions)
  • Notify public health authorities (notifiable disease)
  • Trace contacts, treat water source
  • Safe disposal of stools


PART D — COMMON SAQ QUESTION STEMS + FAST-WRITE CHECKLISTS

These are the most commonly repeated patterns in KMTC exams.

Fast-Write Checklist: "What are the clinical features of ___?"

Always write in two sections:
SYMPTOMS (what patient complains of):
1.
2.
3.
4.
5.

SIGNS (what you find on examination):
1.
2.
3.
4.
5.
Never mix them — that is a basic error that costs marks.

Fast-Write Checklist: "How would you manage a patient with ___?"

Always write in ABCDE order:
A — Admit / Assess
B — Basic investigations (FBC, RFTs, LFTs, cultures, specific tests)
C — Conservative/supportive (fluids, rest, diet, pain relief)
D — Drug treatment (name, dose, route, duration)
E — Education, prevention, follow-up, when to refer

Fast-Write Checklist: "State the complications of ___?"

Always give 5–6 complications and group them:
EARLY complications:
1.
2.

LATE complications:
3.
4.

LIFE-THREATENING complications:
5.
6.

Fast-Write Checklist: "Differentiate between A and B"

Always use a TABLE:
| Feature | Disease A | Disease B |
|---------|-----------|-----------|
| Onset   |           |           |
| Fever   |           |           |
| Stool   |           |           |
| Cause   |           |           |
| Rx      |           |           |
Tables are faster to write and easier to mark — use them whenever comparing two things.


PART E — TRICKS AND EXAMINER SECRETS


🏆 Top 10 Mark-Earning Tricks

#TrickWhy It Works
1Use numbered lists — never long paragraphsExaminer can tick each point easily = more marks
2Underline or write headings in CAPITALSShows structure; examiner can navigate your answer quickly
3Always write the drug + dose + duration (not just the drug name)Each element = separate mark in many mark schemes
4Say "Gold standard" when naming the best testExaminers love this phrase — shows knowledge depth
5Separate symptoms from signs every timeAutomatic extra structure = marks
6Write at least 2 more points than the marks askedBuffer against marking errors; shows thoroughness
7Never leave blank — write what you know, then move onPartial marks are still marks
8In management, ALWAYS mention prevention and educationOften worth 2 marks that most students miss
9Quote normal vs abnormal values where relevantE.g., "Hb <5 g/dL = severe anaemia" — shows clinical thinking
10In differentials/comparison questions — use a TABLEFastest, clearest format — examiners mark tables quickly

🔴 Most Commonly Lost Marks in Tropical Medicine

MistakeFix
Writing "give antibiotics" without naming the drugAlways write the name, dose, duration
Forgetting to mention preventionInclude prevention in every management answer
Writing "blood test" for diagnosisName the specific test — "thick and thin blood film"
Confusing vectors — Culex vs AnophelesCulex = filariasis; Anopheles = malaria
Confusing symptoms and signsSymptoms = subjective; signs = objective
Forgetting relative bradycardia in typhoidClassic examiner test — temperature-pulse dissociation
Not stating "gold standard" for diagnosisBlood culture for typhoid; thick blood film for malaria
Writing "IV fluids" without specifying which fluidCholera = Ringer's Lactate; specify always
Not mentioning G6PD before PrimaquinePrimaquine → haemolysis in G6PD deficiency
Writing all management as one paragraphUse ABCDE structure with numbered points

🟢 Phrases That Earn Bonus Marks in Answers

  • "This is a notifiable disease — public health authorities must be informed" (cholera, typhoid)
  • "Gold standard investigation is..."
  • "First-line treatment as per WHO/Kenya national guidelines is..."
  • "Complications should be actively monitored for..."
  • "Check G6PD status before prescribing primaquine"
  • "Relative bradycardia is a characteristic feature of typhoid"
  • "Rice-water stool is pathognomonic of cholera"
  • "Terminal haematuria is pathognomonic of Schistosoma haematobium"
  • "Severe malaria requires IV treatment and ICU/HDU admission"
  • "Administer anti-D if Rh-negative" (obstetrics — but same principle: show extra clinical thinking)

Answer Length Guide

Question TypeMarksApproximate LengthTime to Spend
Definition1–21–2 lines1–2 minutes
State/List2–52–5 numbered lines2–3 minutes
Short Answer5–10Half a page8–10 minutes
Long Answer15–201.5–2 full pages20–25 minutes

Final Advice: In medical exams, structure beats bulk. A short, well-organised answer with numbered points, clear headings, specific drug names and doses, and mention of prevention will always outscore a long rambling paragraph — even if the paragraph contains more total knowledge.

Hiv ?? Clinical medicine

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