Tag: guidelines

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  • Neftaly BHIVA guidelines for the management of tuberculosis in adults living with HIV

    Neftaly BHIVA guidelines for the management of tuberculosis in adults living with HIV

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    Neftaly BHIVA guidelines for the management of tuberculosis in adults living with HIV

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    Certainly! The South African (Neftaly) BHIVA guidelines for the management of tuberculosis (TB) in adults living with HIV** align with international standards but are adapted for local context and resource availability. Below is a summary of the key points from the BHIVA (British HIV Association) guidelines with considerations relevant to South Africa (Neftaly):


    Management of Tuberculosis in Adults Living with HIV (Based on BHIVA & adapted for South Africa):

    1. Screening and Diagnosis

    • All people living with HIV (PLHIV) should be routinely screened for TB symptoms (cough, fever, night sweats, weight loss).
    • Use Xpert MTB/RIF as the first-line diagnostic test for TB (detects TB and rifampicin resistance).
    • Additional tests: Chest X-ray, sputum culture, or urinary LAM (lipoarabinomannan) antigen test in severely immunocompromised patients (CD4 <100).
    • Screen for latent TB infection in asymptomatic patients, especially those with high CD4 counts, using Tuberculin Skin Test (TST) or Interferon-Gamma Release Assays (IGRA), where available.

    2. Treatment of Active TB

    • Use the standard 6-month regimen:
      • Intensive phase (2 months): Isoniazid, Rifampicin, Pyrazinamide, Ethambutol (HRZE)
      • Continuation phase (4 months): Isoniazid and Rifampicin (HR)
    • For rifampicin-resistant TB, follow local guidelines for multidrug-resistant TB (MDR-TB).
    • Adjust antiretroviral therapy (ART) considering drug interactions:
      • Rifampicin is a potent inducer of cytochrome P450 enzymes and reduces the levels of many ART drugs.
      • Preferred ART regimens include Efavirenz-based or Dolutegravir-based regimens, with dosage adjustments as needed.
    • Start ART as soon as possible within 2 weeks of starting TB treatment if CD4 <50 cells/mm³, and within 8 weeks if CD4 >50 cells/mm³.

    3. ART and TB Treatment Drug Interactions

    • Efavirenz: Generally compatible with rifampicin.
    • Dolutegravir: Recommended with a dose adjustment (50 mg twice daily) during rifampicin use.
    • Avoid protease inhibitors with rifampicin or adjust with rifabutin.

    4. Management of TB Immune Reconstitution Inflammatory Syndrome (IRIS)

    • Occurs typically 2-8 weeks after starting ART.
    • Characterized by worsening symptoms/signs of TB.
    • Management includes corticosteroids for moderate-severe cases and continuation of ART and TB treatment.

    5. Preventive Therapy

    • Offer Isoniazid Preventive Therapy (IPT) for 6 months to all PLHIV without active TB, regardless of ART status.
    • Consider IPT after ruling out active TB using symptom screening and diagnostic tests.
    • Continuous monitoring for TB symptoms during IPT.

    6. Monitoring and Follow-up

    • Regular clinical review to monitor adherence, side effects, and treatment response.
    • Laboratory monitoring for liver toxicity and other adverse drug reactions.
    • Monitor viral load and CD4 counts per standard HIV care guidelines.

    Summary Table

    AspectRecommendation
    TB ScreeningRoutine symptom screening; Xpert MTB/RIF first-line test
    Active TB Treatment6-month standard regimen (HRZE → HR)
    ART Initiation TimingWithin 2 weeks if CD4 <50; within 8 weeks if CD4 >50
    Preferred ART RegimensEfavirenz-based or Dolutegravir with dose adjustments
    TB Preventive Therapy6 months Isoniazid for all without active TB
    Manage IRISCorticosteroids if severe, continue ART and TB meds

    If you want, I can provide you with more detailed South African National TB and HIV guidelines or specific BHIVA guideline excerpts. Would you like that?

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  • Neftaly BHIVA guidelines on the management of HIV in pregnancy and postpartum

    Neftaly BHIVA guidelines on the management of HIV in pregnancy and postpartum

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    Neftaly BHIVA guidelines on the management of HIV in pregnancy and postpartum

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    Sure! Here’s a summary of the BHIVA (British HIV Association) guidelines on the management of HIV in pregnancy and postpartum, incorporating key points relevant for clinical practice. These guidelines are well-respected internationally and are updated regularly.


    BHIVA Guidelines on Management of HIV in Pregnancy and Postpartum

    1. Preconception and Antenatal Care

    • Preconception counseling: Women with HIV should receive counseling about family planning, conception options, and importance of viral suppression before pregnancy.
    • Early antenatal booking: Women with HIV should be booked early in pregnancy to optimize care and start interventions promptly.
    • Baseline investigations: Include CD4 count, HIV viral load, genotypic resistance testing (if indicated), and screening for other infections (HBV, HCV, STIs, etc.).
    • ART initiation: Start or continue combination antiretroviral therapy (cART) as soon as pregnancy is confirmed or ideally before conception.
    • Viral suppression goal: Aim for undetectable plasma viral load (<50 copies/mL) by 36 weeks gestation to minimize vertical transmission risk.

    2. Antiretroviral Therapy (ART)

    • Use regimens with proven safety in pregnancy — typically, two NRTIs plus either an integrase inhibitor (e.g., dolutegravir) or a boosted protease inhibitor.
    • Avoid drugs with known teratogenic risks or limited safety data unless benefits outweigh risks.
    • Monitor adherence and side effects closely throughout pregnancy.

    3. Monitoring During Pregnancy

    • Viral load testing every 4 weeks until suppressed, then every 8-12 weeks.
    • CD4 count every trimester or as clinically indicated.
    • Regular obstetric monitoring per standard pregnancy guidelines.
    • Monitor for drug toxicity (e.g., renal function, liver function).

    4. Delivery

    • Mode of delivery depends on viral load near delivery:
      • If viral load <50 copies/mL near delivery: Vaginal delivery is recommended.
      • If viral load >50 copies/mL near delivery: Consider elective cesarean section to reduce transmission risk.
    • Intravenous zidovudine may be administered during labor if viral load is not fully suppressed.

    5. Infant Management

    • Post-exposure prophylaxis (PEP): Neonates receive antiretroviral prophylaxis, usually zidovudine alone if maternal viral load is suppressed, or combination therapy if higher risk.
    • Infant HIV testing: PCR testing at birth, 6 weeks, and at regular intervals up to 18 months.
    • Avoid breastfeeding in settings where safe formula feeding is available (in UK and similar contexts). WHO guidelines differ for low-resource settings.

    6. Postpartum Care

    • Continue maternal ART postpartum.
    • Monitor maternal viral load and adherence regularly.
    • Provide contraception counseling and support.
    • Infant HIV testing follow-up and pediatric HIV care if needed.
    • Support mental health and address social factors.

    Key Points Summary:

    • Aim for viral suppression <50 copies/mL by 36 weeks.
    • Start or continue effective ART during pregnancy.
    • Mode of delivery based on viral load.
    • Neonatal ART prophylaxis tailored to risk.
    • Avoid breastfeeding where safe alternatives exist.
    • Close maternal and infant follow-up postpartum.
  • Neftaly BHIVA/BASHH guidelines on the use of HIV pre-exposure prophylaxis (PrEP)

    Neftaly BHIVA/BASHH guidelines on the use of HIV pre-exposure prophylaxis (PrEP)

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    Neftaly BHIVA/BASHH guidelines on the use of HIV pre-exposure prophylaxis (PrEP)

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    The British HIV Association (BHIVA) and the British Association for Sexual Health and HIV (BASHH) released their updated guidelines on the use of HIV pre-exposure prophylaxis (PrEP) in 2025. These guidelines aim to enhance accessibility and equity in HIV prevention, particularly among underserved populations.bhiva.org

    Key Updates in the 2025 Guidelines

    1. Equity-Focused Risk Assessment

    The 2025 guidelines move beyond traditional clinical trial-based eligibility criteria, introducing a more inclusive approach to risk assessment. This shift is designed to reduce barriers and expand access to PrEP, especially for young people, ethnic minorities, heterosexual individuals, transgender and non-binary persons, and people who inject drugs. The goal is to address disparities in HIV incidence and prevention efforts.bhiva.org+1bhiva.org+1

    2. Event-Based Dosing Options

    New dosing strategies, such as event-based dosing, are recommended for all PrEP users. These options offer flexibility and may improve adherence by aligning with individuals’ sexual activity patterns.bhiva.org

    3. Quick-Start Double-Dose PrEP

    The guidelines suggest a “quick-start” approach involving a double-dose of PrEP at initiation. This method aims to provide immediate protection and is suitable for all PrEP users.bhiva.org

    4. Long-Acting Injectable Cabotegravir

    The use of long-acting injectable cabotegravir is addressed, reflecting advancements in PrEP formulations. This option may offer an alternative for individuals seeking non-daily dosing regimens.bhiva.org

    5. Post-Exposure Prophylaxis (PEP) Considerations

    The guidelines provide updated recommendations for individuals transitioning from PEP to PrEP, ensuring continuity in HIV prevention strategies.

    For a comprehensive understanding, the full 2025 guidelines are available for download on the BHIVA website. bhiva.orgbhiva.org

    Additionally, BHIVA offers an E-Learning Module (Module 11) that provides in-depth training on the use of HIV pre-exposure prophylaxis. This resource is designed for healthcare professionals seeking to enhance their knowledge and practice in PrEP management. bhiva.orgbhiva.org

    If you require further information or have specific questions about the guidelines, feel free to ask.

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