A 32-year-old with right leg swelling and pain

Last updated: November 12, 2025Bookmark

A 32-year-old P2+0 G33 at 32 weeks of gestation presents to the antenatal clinic with swelling and pain in her right leg for 3 days. On examination, her right leg is swollen, erythematous and has dilated superficial veins. On palpation, it is warm and tender. There is a 4 cm difference in leg circumference.

Measuring Leg Circumference in Deep Venous Thrombosis

Q1. What is the most likely diagnosis?

Reveal answer

32-year-old P2+0 G3 with deep venous thrombosis at 32 weeks of gestation.

Q2. List 2 differentials

Reveal answer

Cellulitis

Superficial thrombophlebitis (has a palpable cord)

Varicose veins

Lymphedema

Compartment syndrome

Ruptured popliteal cyst

Q3. What investigations can be used to confirm the diagnosis?

Reveal answer

Doppler ultrasound of the lower limb: Repeat negative ultrasound on days 3 and 7 in high-risk patients.

Magnetic resonance venography: if inconclusive. Especially for the iliac of pelvic vein thrombus

D-dimer is not useful since pregnancy causes a rise in D-dimer

V/Q SCAN or CTPA can be obtained for suspected PE

Q4. What are the predisposing factors for venous thromboembolism in pregnancy?

Reveal answer

Factors contributing to venous thromboembolism in pregnancy

Component of Virchow’s triadFactors
HypercoagulabilityEstrogen increases the production of fibrinogen, factor VII, IX and X. There is also resistance to protein C in the 2nd and 3rd trimester and reduced activity of protein S and Antithrombin III. The levels of fibrinolysis inhibitors also increases.
StasisEstrogen increases the production of fibrinogen, factor VII, IX and X. There is also resistance to protein C in the 2nd and 3rd trimester and reduced activity of protein S and Antithrombin III. The levels of fibrinolysis inhibitors also increase.
Endothelial injuryEndothelial injury from pre-eclampsia, puerperal sepsis, placental abruption and even delivery itself

Q5. List 5 risk factors for thromboembolism in pregnancy

Reveal answer

Immobility

Parity ≥ 3

Varicose veins (gross)

Age > 35 years

Family history of VTE

Smoker

Obesity

IVF conception

Low-risk thrombophilia

Multiple pregnancies

In Pregnancy Variable Antenatal FactorS Often Indicate Low Molecular Heparin Prophylaxis

Risk factors for thromboembolism in pregnancy

CategoryRisk factors
Pre existing risk factorsMaternal age > 35 years, thrombophilia, obesity (> 80 kg), history of thromboembolism, severe varicose veins, smoking, malignancy
Pregnancy-related risk factorsMultiple gestation, pre-eclampsia, grand multiparity, caesarean delivery (especially emergency), damage to pelvic veins, sepsis, prolonged bed rest
Transient risk factorsDehydration, hyperemesis, sepsis, long-distance travel

Q6. How many risk factors need to be present to classify the patient as either high-risk, medium-risk, or low-risk?

Reveal answer

RiskDescription
High-risk≥ 4 risk factors or previous event
Medium risk3 risk factors or 2+ hospital admissions
Low-risk< 3 risk factors

Q7. What is the definitive treatment for this patient?

Reveal answer

Intravenous unfractionated heparin (UFH) for the acute phase

Check for adequate heparinization with aPTT

Switch to SC LMWH once the acute phase is over

Q8. What options exist for venous thromboembolism prophylaxis (VTE) in pregnancy?

Reveal answer

CategoryMeasures
PharmacologicalLow molecular weight heparin (LMWH – preferred), unfractionated heparin (UFH)
MechanicalThromboembolic detergent stockings, intermittent pneumatic compression (peri-operative period)
General measuresThromboembolic deterrent stockings, intermittent pneumatic compression (peri-operative period)

LMWH and UFH are preferred since they cannot cross the placenta due to their large size and negative charge

Warfarin is contraindicated in pregnancy due to its teratogenic effects: low birth weight, hypoplastic nasal bridge, choanal atresia, cleft lip and palate, laryngomalacia and other skeletal abnormalities. It interferes with the y-carboxylation of osteocalcin and other bone proteins.

Direct oral anticoagulants (DOACs) are also not recommended in pregnancy

Q9. Why is low molecular weight heparin (LMWH) preferred over unfractionated heparin (UFH) during pregnancy?

Reveal answer

LMWH has less risk of osteoporosis, less requirement for monitoring, and less possibility for heparin induced thrombocytopaenia

Anti-Xa levels may be checked in obese patients or during renal failure after starting therapy with LMWH.

The target is 0.35 – 0.7 IU/mL

Enoxaparin 1mg/kg/d in 2 divided doses

Dalteparin 100 IU/kg/d with a maximum of 18,000 IU

Q10. Why is UFH preferred in the period immediately before delivery?

Reveal answer

It is easily reversed by protamine sulphate and has a shorter half-life than LMWH Anticoagulant activity is also easily monitored with aPTT

Not specifically related to pregnancy, but UFH can also be used in renal failure

Q11. What is given for venous thromboembolism (VTE) prophylaxis in high-risk patients during pregnancy?

Reveal answer

Gestation by dateThromboprophylaxis
0 – 16 weeksUnfractionated heparin (UFH)
16 – 36 weeksAspirin and Low Molecular Weight heparin (LMWH)
36 weeks to deliveryUnfractionated heparin (UFH)
During labourNone
Post-partumWarfarin or LMWH

UFH is stopped 12-24 hours before delivery

Treatment should continue for at least 6 weeks postpartum, using LMWH for high-risk patients

If required, warfarin can also be given from 16 – 36 weeks

Warfarin is safe to use during breastfeeding

The patient is also allowed to mobilise, elevate the legs, wear thromboembolic deterrent stockings and monitor for early warning signs

Other options include an IVC filter, percutaneous catheter thrombus fragmentation, and surgical embolectomy

Q12. When and for what duration is LMWH given for the prevention of VTE after delivery?

Reveal answer

LMWH is given 4-6 hours post-SVD and 6-12 hours post-caesarean delivery

Duration of VTE post-partum

RiskDuration
High-riskLMWH for at least 6 weeks
Medium-riskLMWH for at least 10 days
Low-riskMobilisation and avoid dehydration

Reference Intervals
Biochemistry
ACTHP: <80 ng/L
ALTP: 5–35 U/L
AlbuminP: 35–50 g/L
AldosteroneP: 100–500 pmol/L
Alk. phosphataseP: 30–130 U/L
α-AmylaseP: 0–180 IU/dL
α-FetoproteinS: <10 kU/L
Angiotensin IIP: 5–35 pmol/L
ADHP: 0.9–4.6 pmol/L
ASTP: 5–35 U/L
BicarbonateP: 24–30 mmol/L
BilirubinP: 3–17 μmol/L
BNPP: <50 ng/L
CRPP: <10 mg/L
CalcitoninP: <0.1 mcg/L
Calcium (ionized)P: 1.0–1.25 mmol/L
Calcium (total)P: 2.12–2.60 mmol/L
ChlorideP: 95–105 mmol/L
CholesterolP: <5.0 mmol/L
VLDLP: 0.128–0.645 mmol/L
LDLP: <2.0 mmol/L
HDLP: 0.9–1.93 mmol/L
Cortisol AMP: 450–700 nmol/L
Cortisol MidnightP: 80–280 nmol/L
CK ♂P: 25–195 U/L
CK ♀P: 25–170 U/L
CreatinineP: 70–100 μmol/L
FerritinP: 12–200 mcg/L
FolateS: 2.1 mcg/L
FSHP: 2–8 U/L ♂; >25 menopause
GGT ♂P: 11–51 U/L
GGT ♀P: 7–33 U/L
Glucose (fasting)P: 3.5–5.5 mmol/L
Growth hormoneP: <20 mu/L
HbA1C (DCCT)B: 4–6%
HbA1C (IFCC)B: 20–42 mmol/mol
Iron ♂S: 14–31 μmol/L
Iron ♀S: 11–30 μmol/L
Lactate (venous)P: 0.6–2.4 mmol/L
Lactate (arterial)P: 0.6–1.8 mmol/L
LDHP: 70–250 U/L
LHP: 3–16 U/L
MagnesiumP: 0.75–1.05 mmol/L
OsmolalityP: 278–305 mosmol/kg
PTHP: 0.8–8.5 pmol/L
PotassiumP: 3.5–5.3 mmol/L
Prolactin ♂P: <450 U/L
Prolactin ♀P: <600 U/L
PSAP: 0–4 mcg/mL
Protein (total)P: 60–80 g/L
Red cell folateB: 0.36–1.44 μmol/L
Renin (erect)P: 2.8–4.5 pmol/mL/h
Renin (recumbent)P: 1.1–2.7 pmol/mL/h
SodiumP: 135–145 mmol/L
TBGP: 7–17 mg/L
TSHP: 0.5–4.2 mU/L
T4P: 70–140 nmol/L
Free T4P: 9–22 pmol/L
TIBCS: 54–75 μmol/L
TriglyceridesP: 0.50–2.3 mmol/L
T3P: 1.2–3.0 nmol/L
Troponin TP: <0.1 mcg/L
Urate ♂P: 210–480 μmol/L
Urate ♀P: 150–390 μmol/L
UreaP: 2.5–6.7 mmol/L
Vitamin B12S: 0.13–0.68 nmol/L
Vitamin DS: 50 nmol/L
Arterial Blood Gases
pH7.35–7.45
PaCO₂4.7–6.0 kPa
PaO₂>10.6 kPa
Base excess±2 mmol/L
Urine
Cortisol (free)<280 nmol/24h
Hydroxyindole acetic acid16–73 μmol/24h
Hydroxymethylmandelic acid16–48 μmol/24h
Metanephrines0.03–0.69 μmol/mmol cr.
Osmolality350–1000 mosmol/kg
17-Oxogenic steroids ♂28–30 μmol/24h
17-Oxogenic steroids ♀21–66 μmol/24h
17-Oxosteroids ♂17–76 μmol/24h
17-Oxosteroids ♀14–59 μmol/24h
Phosphate (inorganic)15–50 mmol/24h
Potassium14–120 mmol/24h
Protein<150 mg/24h
Protein/creatinine ratio<3 mg/mmol
Sodium100–250 mmol/24h
Haematology
WCC4.0–11.0 ×10⁹/L
RBC ♂4.5–6.5 ×10¹²/L
RBC ♀3.9–5.6 ×10¹²/L
Hb ♂130–180 g/L
Hb ♀115–160 g/L
PCV ♂0.4–0.54 L/L
PCV ♀0.37–0.47 L/L
MCV76–96 fL
MCH27–32 pg
MCHC300–360 g/L
RDW11.6–14.6%
Neutrophils2.0–7.5 ×10⁹/L (40–75%)
Lymphocytes1.0–4.5 ×10⁹/L (20–45%)
Eosinophils0.04–0.44 ×10⁹/L (1–6%)
Basophils0–0.10 ×10⁹/L (0–1%)
Monocytes0.2–0.8 ×10⁹/L (2–10%)
Platelets150–400 ×10⁹/L
Reticulocytes0.8–2.0% / 25–100 ×10⁹/L
Prothrombin time10–14 s
APTT35–45 s
Paediatric
Pulse Rate (bpm)
Neonate140–160
Infant <1yr120–140
1–5 years110–130
5–12 years80–120
>12 years70–100
Respiratory Rate (tachypnoea)
0–2 months≥60/min
2–12 months≥50/min
1–5 years≥40/min
>5 years≥30/min
Blood Pressure (mmHg)
Term65/45
1 year75/50
4 years85/60
8 years95/65
10 years100/70
Weight Formulas
3–12 months(a + 9)/2 kg
1–6 years2a + 8 kg
>6 years(7a − 5)/2 kg
Haemoglobin (g/dL)
Term newborn13–20
1 month11–18
2 months10–15
1–2 years10–13
>2 years11–14
MUAC (6 months–5 years)
Obese>17.5 cm
Normal13.5–17.4 cm
At risk12.5–13.4 cm
Moderate malnutrition11.5–12.4 cm
Severe malnutrition<11.5 cm
Developmental Milestones
Social smile1.5 months
Head control4 months
Sits unsupported7 months
Crawls10 months
Stands unsupported10–12 months
Walks12–13 months
Talks18 months
CSF WBC (/mm³)
Term newborn0–25
>2 weeks0–5
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