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Obstetrics

HIV in Pregnancy (eMTCT)

Management of HIV infection during pregnancy, labour, delivery, and the postpartum period, focusing on preventing mother-to-child transmission (PMTCT/eMTCT) and maintaining maternal health through lifelong ART (Option B+).

Also known as: PMTCT, HIV and Pregnancy, Option B+

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Referral and warning signs

When to refer

Refer to comprehensive HIV care/ART clinic for initiation/ongoing management. Refer for complex ART issues, side effects, treatment failure, OIs.

Red flags

  • Signs of severe opportunistic infection
  • Severe ART side effects
  • High maternal VL near delivery
  • Infant testing positive for HIV

Signs and symptoms

  • Often asymptomatic.
  • May present with symptoms of HIV/AIDS opportunistic infections or related conditions.
  • Focus is on screening, diagnosis, and management within pregnancy context.

Risk factors

  • Engaging in behaviours that risk HIV acquisition.
  • Lack of access/uptake of HIV prevention/testing services.

Diagnosis

Clinical assessment

Routine HIV counselling and testing (Opt-out approach) offered at first ANC visit (and partner). Repeat testing in 3rd trimester/labour for initially negative.

Investigations

  • HIV rapid antibody testing (Serial algorithm per national guidelines).
  • Viral Load (VL) monitoring (baseline, periodically).
  • CD4 count (baseline useful for OI risk/prophylaxis).

Diagnostic criteria

Positive HIV antibody test confirmed by national algorithm.

Management

Non-pharmacological management

  • Comprehensive counseling (status, lifelong ART, adherence, disclosure, partner testing, safer sex, infant feeding, FP).
  • Psychosocial support (peer groups).
  • Nutritional counseling.
  • Safe obstetric practices.
  • Linkage to ongoing care.

Pharmacological treatment

  • Maternal ART (Lifelong - Option B+): Initiate preferred first-line ART (typically TDF+3TC+DTG FDC) IMMEDIATELY upon diagnosis, regardless of CD4/gestation. Continue existing effective regimen.
  • Infant ARV Prophylaxis: Daily Nevirapine (NVP) syrup from birth for 6 weeks (standard risk). Extended prophylaxis (12w NVP or NVP+AZT) if high risk (e.g., preterm, mother untreated/high VL). Follow current PMTCT guidelines.
  • Infant Cotrimoxazole Prophylaxis: Start at 6 weeks for ALL HIV-exposed infants, continue until HIV excluded post-breastfeeding.

Monitoring

Maternal: Adherence, VL (e.g., 6m post-start, then annually if suppressed), CD4, OI screening. Infant: Prophylaxis adherence, Growth, Development, HIV testing (6wks PCR, post-BF antibody test).

Complications

  • Mother-to-child transmission (MTCT) of HIV.
  • Increased maternal/infant morbidity/mortality if untreated.
  • Opportunistic infections.
  • ART side effects.
  • Stigma.

Prevention

  • Primary HIV prevention.
  • Effective PMTCT interventions (universal testing, immediate ART, infant prophylaxis, safer feeding).

Patient education

  • Understanding HIV/ART.
  • Lifelong ART.
  • Adherence importance.
  • Infant prophylaxis (ARV, Cotrimoxazole).
  • Infant feeding counseling (exclusive choice BF/replacement).
  • Safer sex.
  • Partner testing/disclosure.
  • Infant HIV testing schedule.
  • Follow-up importance.

Uganda-specific notes

Option B+ is national policy. TDF/3TC/DTG preferred 1st line. PMTCT integrated into MCH. Exclusive breastfeeding for 6m, continued to 1yr recommended for mothers on ART. VL monitoring improving.

References

  • Uganda Clinical Guidelines (UCG) 2023

    Chapter 16, Section 16.2.2

  • Uganda Clinical Guidelines (UCG) 2023

    Chapter 3 (HIV Management)

  • Consolidated Guidelines for Prevention and Treatment of HIV in Uganda, MOH

    (Current National PMTCT/ART protocols)

For learning and professional reference. Use current local guidance and clinical judgement.

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