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HIV Opportunistic Infections Coinfections

Category: medicine

Updated: 25 Nov 2025


I’ll structure this as: 1. Core concept of HIV + opportunistic infections (OIs) 2. Key OIs by CD4 level 3. General diagnostic & management principles (incl. IRIS) 4. Prophylaxis (primary + secondary) – with CD4 cut-offs 5. Focus drug notes (TMP-SMX, dapsone, atovaquone, azithromycin, isoniazid, fluconazole) 6. **25 case scenarios** with management + prophylaxis angle > **Exam note**: Doses, thresholds and regimens are based on current HIV/OI guidelines (NIH/CDC/WHO/UpToDate) as of late-2025; always adapt to your local protocol. ([ClinicalInfo][1]) --- ## 1. Concept: HIV, coinfections and opportunistic infections **Definition** * **Opportunistic infection (OI)**: infection that occurs with increased frequency/severity when immunity is impaired, especially **CD4 T-cell depletion** in HIV. * **Coinfection**: presence of HIV plus **another pathogen** (e.g. TB, HBV, HCV, malaria, STIs) which may or may not be opportunistic but interacts with HIV (worse progression, higher viral load, drug interactions). ([CDC][2]) **Pathophysiology** * Progressive HIV replication → CD4 decline → failure of **cell-mediated immunity** → reactivation of latent infections (TB, toxoplasma, CMV) and new infections (PCP, cryptococcus, MAC). * OIs themselves increase HIV viral load transiently and accelerate disease. ([CDC][2]) * Starting ART may trigger **IRIS (Immune Reconstitution Inflammatory Syndrome)**: recovering immune system mounts exaggerated response to existing antigen load → paradoxical clinical deterioration (e.g. worse TB lymphadenitis, increased ICP in cryptococcal meningitis). ([NACO][3]) --- ## 2. Important OIs & typical CD4 thresholds Approximate **CD4 levels** at which OIs are common: * **Any CD4**: TB, bacterial pneumonia/sepsis, oral candidiasis, herpes zoster. * **<200 cells/µL**: * **Pneumocystis jirovecii pneumonia (PCP/PJP)** ([ASM Journals][4]) * Recurrent bacterial pneumonia. * **<100 cells/µL**: * **Toxoplasma gondii encephalitis** (if IgG⁺). ([UpToDate][5]) * **Cryptococcal meningitis**, disseminated cryptococcosis. ([ASM Journals][6]) * **<50 cells/µL**: * **Mycobacterium avium complex (MAC)** (disseminated). ([bhiva.org][7]) * CMV retinitis, CMV colitis. ([nhstaysideadtc.scot.nhs.uk][8]) You’ll often see questions coupling: * CD4 180 → PCP * CD4 60 + ring-enhancing lesions → toxoplasma * CD4 30 + meningitis with ↑OP → cryptococcus * CD4 20 + fever, hepatosplenomegaly, ALP↑ → MAC --- ## 3. Diagnostic & management principles ### A. General diagnostic work-up in advanced HIV * Full history: ART adherence, **CD4 trend**, VL, prior OIs, prophylaxis. * Physical: skin lesions (Kaposi, molluscum), mucosal candidiasis, focal neurologic signs, neck stiffness. * Baseline labs: CBC, LFT, RFT, electrolytes, LDH, blood cultures. * HIV-specific: current VL, CD4 count. * Imaging: * CXR/HRCT for pneumonia (PCP: bilateral interstitial infiltrates). * CT/MRI brain for focal lesions (toxoplasma, lymphoma). * OI-specific tests: * **PCP**: induced sputum / BAL with silver stain, PCR. * **Toxoplasma**: MRI ring-enhancing lesions + IgG serology; definitive = brain biopsy. ([Medscape Education][9]) * **Cryptococcal**: serum/CSF cryptococcal antigen (CrAg), India ink, fungal culture. ([ASM Journals][6]) * **MAC**: blood cultures, bone marrow culture. ([National Health Mission][10]) * **TB**: GeneXpert/NAAT, cultures; extrapulmonary sampling. ### B. General treatment principles 1. **Stabilise the patient first** * ABC, oxygen, treat sepsis, manage raised ICP (cryptococcus), control seizures, correct electrolytes. 2. **Specific OI treatment** * PCP: high-dose TMP-SMX ± steroids. ([ClinicalInfo][11]) * Toxoplasma encephalitis: pyrimethamine + sulfadiazine + leucovorin (or TMP-SMX high-dose). ([ClinicalInfo][12]) * Cryptococcal meningitis: amphotericin B + flucytosine induction → fluconazole consolidation + maintenance. ([New England Journal of Medicine][13]) * MAC: macrolide (clarithro/azithro) + ethambutol ± rifabutin. ([National Health Mission][10]) * TB: standard HRZE with attention to **rifampicin–ART interactions**. 3. **When to start ART in acute OI** (adult, typical exam stance) * **PCP, toxoplasma, MAC, most bacterial OIs**: start ART within ~2 weeks once patient stabilizes. * **TB**: within 2 weeks if CD4 <50; by 8 weeks if ≥50 (and no CNS TB). * **Cryptococcal meningitis & TB meningitis**: delay ART ~4–6 weeks due to severe CNS-IRIS risk. ([The Lancet][14]) 4. **Secondary prophylaxis / chronic maintenance** Continue specific suppressive therapy until immune reconstitution (details in prophylaxis section). 5. **Manage drug interactions & toxicities** * Check for **overlap**: marrow suppression (zidovudine + TMP-SMX + ganciclovir), nephrotoxicity (tenofovir + amphotericin), hepatotoxicity (TB drugs + azoles + ART), QT prolongation (macrolides, fluoroquinolones, some ARVs). --- ## 4. Prophylaxis strategy: what, when to start, when to stop ### A. Primary prophylaxis (prevent first episode) **PCP** * **Indication** (Adults): * CD4 **<200 cells/µL** OR * CD4% <14% OR * Oropharyngeal candidiasis or unexplained fever >2 weeks, even if CD4 >200. ([ASM Journals][4]) * **Preferred regimen**: * TMP-SMX 1 DS (160/800 mg) **once daily**. * **Alternatives** (if sulfa intolerance): * Dapsone 100 mg daily ± pyrimethamine + leucovorin, or * Atovaquone 1500 mg PO daily with food. ([NACO][3]) * **Stop** when CD4 ≥200 for ≥3 months on ART (and VL suppressed). Restart if CD4 <100 or 100–200 with viremia. ([bccfe.ca][15]) **Toxoplasma gondii encephalitis (TE)** * **Indications**: * Toxoplasma IgG positive + CD4 **<100 cells/µL**. ([ClinicalInfo][12]) * **Preferred prophylaxis**: * TMP-SMX 1 DS once daily (same as PCP prophylaxis). * **Alternatives**: * Dapsone 50 mg daily + pyrimethamine 50 mg weekly + leucovorin, etc. ([NACO][3]) * **Stop** when CD4 >200 for ≥3 months on ART (or 100–200 with sustained VL suppression). ([bccfe.ca][16]) **MAC (disseminated)** * **Modern guidelines**: If ART is started promptly and VL suppressed, **routine primary prophylaxis is generally NOT recommended**. ([hiv.uw.edu][17]) * If used (e.g. cannot start ART, CD4 <50): * Azithromycin 1200 mg weekly PO (or 600 mg twice weekly). ([bhiva.org][7]) **Cryptococcus** * Many programs: **CrAg screening** for CD4 <100. * If **asymptomatic CrAg-positive**: high-dose fluconazole 800 mg/day for 2 weeks, then 400 mg/day 8–10 weeks, then 200 mg/day until immune recovery (pre-emptive treatment = a form of prophylaxis). ([ASM Journals][6]) **TB (latent)** * All PLHIV should be screened with symptom screen + TST/IGRA where available. * **Isoniazid preventive therapy (IPT)**: INH 300 mg daily + pyridoxine 25–50 mg daily for 6–9 months in latent TB or high-burden settings, irrespective of CD4. ### B. Secondary prophylaxis (after an OI) * **PCP** – lower-dose TMP-SMX (e.g. 1 SS daily) until CD4 ≥200 for ≥3 months on ART. ([bccfe.ca][15]) * **Toxoplasma encephalitis** – reduced-dose pyrimethamine + sulfadiazine + leucovorin OR TMP-SMX DS daily until CD4 ≥200 for ≥6 months on ART. ([bccfe.ca][16]) * **Cryptococcal meningitis** – fluconazole 200 mg daily for at least 1 year and until CD4 ≥100–200 with suppressed VL. ([bccfe.ca][18]) * **MAC** – clarithro/azithro + ethambutol until ≥12 months of therapy AND CD4 ≥100 for ≥6 months. ([National Health Mission][10]) --- ## 5. High-yield drug mini-monographs (for OI prophylaxis) ### 5.1 Trimethoprim–Sulfamethoxazole (TMP-SMX, co-trimoxazole) * **Indications in HIV** * Primary & secondary **PCP prophylaxis**. * Toxoplasma prophylaxis in IgG⁺ patients. * Treatment of PCP, toxoplasma (high doses). * **Mechanism**: sequential blockade of folate synthesis (sulfamethoxazole: dihydropteroate synthase; trimethoprim: DHF reductase) → inhibits DNA synthesis. * **Usual prophylactic dosing (adults)** * 1 **DS** (160/800 mg) once daily; or 1 SS daily, or 1 DS three times/week if toxicity. ([AAHIVM][19]) * **Paediatric**: 150 mg/m² trimethoprim component once daily (approx 5 mg/kg TMP). * **PK**: good oral absorption, renal elimination; T½ ~10 h. * **Common AEs**: rash, nausea, mild hyperkalaemia, creatinine rise, photosensitivity. * **Serious AEs**: Stevens–Johnson, TEN, severe neutropenia, thrombocytopenia, hepatitis, aseptic meningitis. * **Contraindications**: severe sulfa allergy, major prior SJS/TEN, severe hepatic failure, marked renal failure without dose adjustment, G6PD deficiency (caution). * **Important interactions**: ↑ toxicity with other antifolates (methotrexate), additive marrow suppression with zidovudine, ganciclovir, interferon; ↑ INR with warfarin. * **Monitoring**: CBC, creatinine, K⁺, LFTs; watch for rash. * **Counselling**: take with water, report rash or mucosal lesions immediately; avoid self-stopping – contact provider to discuss desensitization/alternatives. ### 5.2 Dapsone * **Indications**: alternative PCP/toxoplasma prophylaxis in sulfa-intolerant patients. ([NACO][3]) * **Mechanism**: sulfone that inhibits folate synthesis similar to sulfonamides. * **Dose**: 100 mg PO once daily (or 50 mg daily when combined with pyrimethamine weekly). * **PK**: hepatic metabolism, long T½ (~20–30 h). * **AEs**: haemolysis (esp. G6PD deficiency), methaemoglobinaemia, rash, agranulocytosis, peripheral neuropathy. * **Contraindications**: severe G6PD deficiency, previous severe reaction. * **Monitoring**: baseline G6PD, Hb, retic count/met-Hb if symptomatic. * **Counselling**: report dark urine, SOB, cyanosis; don’t use OTC oxidant drugs without advice. ### 5.3 Atovaquone * **Indication**: PCP prophylaxis/alternative treatment when TMP-SMX not tolerated. ([bccfe.ca][15]) * **Mechanism**: inhibits mitochondrial electron transport in protozoa/fungi. * **Dose**: 1500 mg PO once daily **with fatty meal**. * **AEs**: GI upset, rash, headache; generally well tolerated. * **Interactions**: rifampicin & tetracyclines ↓ atovaquone levels; monitor if combined with ART with GI effects. * **Counselling**: must be taken with high-fat food to work; if severe diarrhoea, efficacy reduced. ### 5.4 Azithromycin (for MAC prophylaxis/treatment) * **Indications**: * Primary prophylaxis against disseminated MAC when CD4 <50 and ART cannot be started. * Part of MAC treatment (with ethambutol ± rifabutin). ([bhiva.org][7]) * **Mechanism**: macrolide – 50S ribosomal subunit inhibition. * **Dose (prophylaxis)**: 1200 mg once weekly OR 600 mg twice weekly PO. * **AEs**: GI upset, QT prolongation, mild LFT derangement. * **Interactions**: fewer CYP interactions than clarithromycin but still caution with QT-prolonging ARVs; avoid with strong QT-prolongers. * **Monitoring**: ECG in high-risk; LFTs if prolonged. ### 5.5 Isoniazid (INH) * **Indications**: latent TB treatment / preventive therapy in PLHIV. * **Mechanism**: inhibits mycolic acid synthesis in mycobacteria. * **Dose**: 300 mg PO once daily + pyridoxine 25–50 mg daily for 6–9 months. * **AEs**: hepatotoxicity, peripheral neuropathy, rash, lupus-like syndrome. * **Contraindications**: acute hepatitis, severe chronic liver disease (relative). * **Monitoring**: LFTs baseline & if symptomatic. * **Counselling**: avoid alcohol; report jaundice, neuropathic symptoms early. ### 5.6 Fluconazole * **Indications**: * Pre-emptive therapy in asymptomatic CrAg-positive patients. * Consolidation and maintenance in cryptococcal meningitis. ([ASM Journals][6]) * **Mechanism**: triazole – inhibits fungal 14-α-demethylase → ergosterol synthesis ↓. * **Doses**: * Pre-emptive: 800 mg/day 2 weeks → 400 mg/day 8–10 weeks → 200 mg/day until CD4 recovery. ([NCBI][20]) * Secondary prophylaxis: 200 mg/day long term. * **AEs**: GI upset, rash, alopecia (long-term), hepatotoxicity, QT prolongation. * **Interactions**: CYP2C9/3A4 inhibitor – ↑ levels of warfarin, some ARVs (esp. nevirapine, some protease inhibitors), some antiepileptics. * **Monitoring**: LFTs, ECG if other QT drugs. --- ## 6. 25 case scenarios – coinfections, OIs, management & prophylaxis Each case: **summary → diagnosis → immediate management → prophylaxis plan.** --- ### Case 1 – First presentation with PCP 32-year-old man, newly diagnosed HIV, CD4 120, subacute non-productive cough, progressive dyspnoea, fever, desaturation on exertion; CXR: bilateral perihilar interstitial infiltrates; ABG: A-a gradient high. * **Likely diagnosis**: PCP. * **Management**: hospitalize; high-dose IV/PO TMP-SMX (15–20 mg/kg/day TMP in 3–4 doses) + steroids if PaO₂ <70; start ART after ~2 weeks once stable. * **Prophylaxis**: after treatment, move to TMP-SMX 1 DS daily as secondary prophylaxis until CD4 ≥200 for ≥3 months. --- ### Case 2 – Oral candidiasis as a red flag 28-year-old woman with long-standing HIV, not on ART for 1 year, presents with painful white plaques in mouth, odynophagia. CD4 170. * **Diagnosis**: oropharyngeal/esophageal candidiasis. * **Management**: fluconazole 200 mg loading then 100–200 mg daily 7–14 days (longer if esophageal); start/optimize ART. * **Prophylaxis**: regardless of CD4 (170 <200 and thrush present) → start PCP prophylaxis with TMP-SMX DS daily. --- ### Case 3 – Toxoplasma encephalitis 40-year-old man with HIV, irregular ART, CD4 60, headache, seizures, right hemiparesis. MRI brain: multiple ring-enhancing lesions in basal ganglia; Toxo IgG positive. * **Diagnosis**: Toxoplasma encephalitis. * **Management**: pyrimethamine + sulfadiazine + leucovorin for at least 6 weeks, then secondary prophylaxis; consider high-dose TMP-SMX if first-line unavailable. Delay ART 1–2 weeks. * **Prophylaxis**: after acute Rx → reduced-dose pyrimethamine-sulfadiazine or TMP-SMX DS OD until CD4 >200 for ≥6 months. --- ### Case 4 – Toxoplasma prophylaxis missed Same patient as Case 3 – review history shows toxo IgG⁺ 1 year earlier, CD4 then 80, but no prophylaxis. * **Teaching point**: should have been on **primary prophylaxis** (TMP-SMX DS daily) when IgG⁺ + CD4 <100 to prevent TE. --- ### Case 5 – Cryptococcal meningitis 35-year-old man, CD4 40, presents with subacute headache, fever, blurring of vision; neck stiffness mild; LP: ↑ opening pressure, low glucose, high protein, lymphocytes; CSF India ink +, CrAg strongly positive. * **Diagnosis**: cryptococcal meningitis. * **Management**: * Induction: amphotericin B + flucytosine 2 weeks; manage raised ICP with repeated LPs. * Consolidation: fluconazole 400–800 mg/day 8 weeks. * Maintenance: fluconazole 200 mg/day ≥1 year. ART start delayed ~4–6 weeks. * **Prophylaxis**: maintenance fluconazole (secondary), can stop when CD4 ≥100–200 with sustained viral suppression. --- ### Case 6 – Asymptomatic CrAg-positive screen HIV patient, CD4 45, no symptoms; CrAg screening positive in serum; LP normal. * **Diagnosis**: asymptomatic cryptococcal antigenaemia. * **Management**: oral fluconazole 800 mg/day for 2 weeks → 400 mg/day for 8–10 weeks → 200 mg/day until immune reconstitution; start ART after ~2 weeks if well. * **Prophylaxis**: this regimen is effectively **pre-emptive primary prophylaxis** to prevent meningitis. --- ### Case 7 – Disseminated TB co-infection 29-year-old man, HIV+, newly diagnosed, CD4 110, with fever, weight loss, cough, hepatosplenomegaly, matted cervical nodes; CXR: miliary mottling; Xpert positive for MTB. * **Diagnosis**: disseminated TB in HIV. * **Management**: start HRZE with careful drug–drug interaction planning; start ART within 2 weeks (CD4 <50–100 rule, but many exams accept 2 weeks for severe TB). * **Prophylaxis**: * Household contacts → INH preventive therapy. * After completion of TB therapy, consider INH prophylaxis depending on local guideline & risk. --- ### Case 8 – TB meningitis with HIV 36-year-old HIV+ man CD4 70, chronic headache, fever, cranial nerve palsies; CSF lymphocytic, ADA↑, Xpert positive. * **Diagnosis**: tuberculous meningitis. * **Management**: HRZE with steroids; **delay ART ~4–8 weeks** to reduce CNS IRIS; manage raised ICP. * **Prophylaxis**: as above, no specific secondary prophylaxis, but close follow-up; consider isoniazid preventive therapy after completed regimen in high-risk areas. --- ### Case 9 – MAC in advanced HIV 45-year-old male, CD4 20, not on ART, presents with prolonged fever, weight loss, diarrhoea, abdominal pain, hepatosplenomegaly, high ALP; blood cultures: MAC. * **Diagnosis**: disseminated MAC. * **Management**: azithromycin + ethambutol ± rifabutin for ≥12 months; start ART after 2 weeks. * **Prophylaxis**: secondary prophylaxis continues until CD4 ≥100 for ≥6 months; **primary prophylaxis** with azithro would be considered if he was not starting ART and CD4 <50. --- ### Case 10 – Missed MAC prophylaxis Same patient had CD4 30 six months ago and was not started on ART or MAC prophylaxis. * **Teaching point**: in someone who **cannot** start ART with CD4 <50, MAC prophylaxis with weekly azithromycin (or daily clarithromycin) is indicated. --- ### Case 11 – Recurrent bacterial pneumonias 33-year-old woman, HIV+, CD4 190, two lobar pneumonias in last year, smoker. * **Diagnosis**: recurrent bacterial pneumonia; consider humoral deficiency, smoking, bronchiectasis. * **Management**: treat current episode with appropriate IV antibiotics; smoking cessation; vaccinate with PCV/PPV, influenza. * **Prophylaxis**: ensure PCP prophylaxis (CD4<200), optimize ART, vaccinations (PCV13/PPV23, Hib, flu). --- ### Case 12 – CMV retinitis 37-year-old man, CD4 25, blurred vision, floaters; fundoscopy: “pizza pie” haemorrhagic lesions. * **Diagnosis**: CMV retinitis. * **Management**: systemic valganciclovir ± intravitreal ganciclovir; urgent ophthalmology; start ART within 2 weeks. * **Prophylaxis**: secondary prophylaxis with valganciclovir until CD4 >100–150 for ≥3–6 months. --- ### Case 13 – Kaposi sarcoma with pulmonary OIs 30-year-old man, MSM, HIV+, purple papules on skin, CD4 90, cough, dyspnoea; CXR diffuse infiltrates; bronchoscopy: PCP. * **Diagnosis**: Kaposi sarcoma (cutaneous ± pulmonary) + PCP. * **Management**: treat PCP with TMP-SMX + steroids; start ART; chemo for extensive KS. * **Prophylaxis**: TMP-SMX secondary prophylaxis; routine MAC/TE prophylaxis as per CD4. --- ### Case 14 – HBV coinfection 42-year-old man, HIV-HBV coinfected, high HBV DNA, CD4 350, needs ART. * **Management**: start ART containing **tenofovir (TDF/TAF) + lamivudine/emtricitabine** (dual-active for HBV); avoid stopping these abruptly to prevent HBV flare. * **Prophylaxis note**: HBV treatment here acts as **long-term prophylaxis** against HBV reactivation. --- ### Case 15 – HCV coinfection and OI risk 45-year-old woman, HIV-HCV coinfection, on ART with CD4 260, persistent elevated LFTs, planning HCV DAA therapy. * **Management**: choose DAA regimen compatible with ART; counsel about alcohol cessation; monitor drug interactions. * **Prophylaxis**: OI prophylaxis not indicated (CD4>200, no OI); but vaccinate for HAV/HBV if not immune to prevent severe acute hepatitis. --- ### Case 16 – IRIS with TB lymphadenitis Patient with HIV-TB coinfection started ART 1 week after TB therapy (CD4 30). Six weeks later, lymph nodes enlarge, fever worsens, cultures still negative, adherence good. * **Diagnosis**: paradoxical TB-IRIS. * **Management**: continue TB Rx and ART; give NSAIDs or short course steroids in severe cases; exclude true failure or new OI. * **Prophylaxis**: no change in TMP-SMX or other OI prophylaxis; emphasize adherence. --- ### Case 17 – IRIS in cryptococcal disease HIV patient with cryptococcal meningitis started ART 1 week after amphotericin; 2 weeks later, severe headache, raised ICP. * **Diagnosis**: cryptococcal IRIS; ART started too early. * **Management**: manage raised ICP, consider corticosteroids; **do not stop antifungals**, may need to pause ART temporarily in severe CNS IRIS (per specialist decision). * **Prophylaxis**: same secondary fluconazole; future learning: delay ART 4–6 weeks in cryptococcal meningitis. --- ### Case 18 – Pregnancy with advanced HIV & OIs 27-year-old pregnant woman (24 weeks), newly diagnosed HIV, CD4 130, oral candidiasis and chronic cough; CXR: PCP pattern. * **Management**: TMP-SMX is still first-line for PCP in pregnancy (benefit outweighs risk), plus steroids if indicated; start pregnancy-safe ART (e.g. TDF/3TC/DTG as per current guidelines) after PCP stabilises. * **Prophylaxis**: TMP-SMX prophylaxis will continue (also reduces malaria, bacterial infections in pregnancy in endemic areas); monitor folate and haemoglobin. --- ### Case 19 – Paediatric HIV with PCP 5-year-old child, vertically infected HIV, CD4% 11%, severe tachypnoea, hypoxia, bilateral interstitial changes. * **Diagnosis**: PCP pneumonia in child. * **Management**: IV TMP-SMX 15–20 mg/kg/day TMP component in divided doses + steroids; start/optimize paediatric ART. * **Prophylaxis**: after recovery, TMP-SMX 5 mg/kg TMP once daily as secondary prophylaxis until CD4% >15–20% and stable. --- ### Case 20 – Severe sulfa allergy 30-year-old HIV+ man, CD4 70, had life-threatening SJS with TMP-SMX previously; now needs PCP/TE prophylaxis. * **Management**: **avoid all sulfa drugs.** Use atovaquone 1500 mg OD with food for PCP; for toxoplasma prophylaxis, dapsone-pyrimethamine-leucovorin is generally contraindicated (sulfa); consider atovaquone ± specialist alternatives. * **Prophylaxis**: atovaquone until CD4 >200 for ≥3 months; robust ART. --- ### Case 21 – Malaria coinfection with HIV HIV-positive man in malaria-endemic region, CD4 220, presents with fever, anaemia, positive P. falciparum smear. * **Management**: weight-based artemisinin-based combination therapy; avoid drug interactions with ART (esp. protease inhibitors). * **Prophylaxis**: OI prophylaxis not indicated by CD4; but TMP-SMX (if used for PCP) also offers some antimalarial effect; use bed nets and vector control. --- ### Case 22 – STI coinfection increasing HIV transmission 25-year-old MSM with HIV (CD4 450, suppressed VL) but presents with painful genital ulcers; T. pallidum positive (syphilis). * **Management**: benzathine penicillin G; partner notification; risk-reduction counselling. * **Prophylaxis angle**: Although not an OI, treating STIs reduces genital inflammation and HIV transmission risk – a form of **secondary prevention** in public health terms. --- ### Case 23 – Recurrent herpes simplex HIV+ patient, CD4 90, recurrent painful genital ulcers, HSV PCR positive. * **Management**: oral acyclovir/valacyclovir treatment; consider chronic suppressive therapy. * **Prophylaxis**: suppressive acyclovir doesn’t prevent classic “AIDS-defining OIs,” but it reduces HSV recurrences; TMP-SMX still required for PCP/TE prophylaxis. --- ### Case 24 – Post-OI CD4 recovery and stopping prophylaxis Patient with prior PCP and TE, now on ART with CD4 260 for 1 year, VL undetectable; still on TMP-SMX DS OD and secondary TE regimen. * **Question**: can prophylaxis be stopped? * **Answer**: Yes – CD4 >200 for >3–6 months with VL suppressed → both PCP and TE prophylaxis can be safely discontinued. ([bccfe.ca][16]) --- ### Case 25 – Poor adherence and recurrent OIs HIV+ man with history of PCP and cryptococcal meningitis, frequently stops ART, CD4 fluctuates 40–250, now off ART and prophylaxis, presents with headache and cough. * **Risk**: relapse of cryptococcal disease or new PCP. * **Management**: full re-evaluation (LP, imaging, sputum/BAL); treat any active OI; intensive adherence counselling; involve psychosocial support. * **Prophylaxis**: restart secondary prophylaxis (fluconazole, TMP-SMX) and ART; emphasize that stopping drugs abruptly is dangerous; consider DOT/adherence aids. --- If you want, next I can: * Turn this into a **single-page high-yield PDF-style note layout**, or * Create **HTML + CSS + JS** sheet with these 25 cases as clickable cards (good for your ErrorOn/NEETPG sites). [1]: https://clinicalinfo.hiv.gov/en/guidelines/hiv-clinical-guidelines-adult-and-adolescent-opportunistic-infections/prophylaxis-prevent-first-episode?utm_source=chatgpt.com "Drug Therapies to Prevent First Episode of Opportunistic ..." [2]: https://www.cdc.gov/mmwr/pdf/rr/rr58e324.pdf?utm_source=chatgpt.com "Guidelines for Prevention and Treatment of Opportunistic ..." [3]: https://naco.gov.in/sites/default/files/7-Guidelines%20for%20Prevention%20and%20Management%20of%20common%20opportunistic%20infections.pdf?utm_source=chatgpt.com "Guidelines for Prevention and Management of Common ..." [4]: https://journals.asm.org/doi/10.1128/cmr.00101-22?utm_source=chatgpt.com "Pneumocystis jirovecii pneumonia in people living with HIV" [5]: https://www.uptodate.com/contents/toxoplasmosis-in-patients-with-hiv?utm_source=chatgpt.com "Toxoplasmosis in patients with HIV - UpToDate" [6]: https://journals.asm.org/doi/10.1128/cmr.00156-22?utm_source=chatgpt.com "Diagnosis and management of cryptococcal meningitis in HIV ..." [7]: https://bhiva.org/wp-content/uploads/2024/11/-file-SwhaEzgXmAGOt-hiv_v12_is2_Iss2Press_Text.pdf?utm_source=chatgpt.com "hiv medicine" [8]: https://www.nhstaysideadtc.scot.nhs.uk/Antibiotic%20site/pdf%20docs/Opportunistic%20infections.pdf?utm_source=chatgpt.com "Opportunistic infections.pdf" [9]: https://emedicine.medscape.com/article/1167298-overview?utm_source=chatgpt.com "CNS Toxoplasmosis in HIV: Overview, Pathophysiology ..." [10]: https://nhm.gov.in/images/pdf/guidelines/nrhm-guidelines/stg/hiv-opportunistic-infections.pdf?utm_source=chatgpt.com "hiv: opportunistic infections" [11]: https://clinicalinfo.hiv.gov/en/guidelines/hiv-clinical-guidelines-adult-and-adolescent-opportunistic-infections/pneumocystis?utm_source=chatgpt.com "Pneumocystis Pneumonia: Adult and Adolescent OIs | NIH" [12]: https://clinicalinfo.hiv.gov/en/guidelines/hiv-clinical-guidelines-adult-and-adolescent-opportunistic-infections/toxoplasmosis?utm_source=chatgpt.com "Toxoplasma gondii Encephalitis: Adult and Adolescent OIs" [13]: https://www.nejm.org/doi/full/10.1056/NEJMoa1110404?utm_source=chatgpt.com "Combination Antifungal Therapy for Cryptococcal Meningitis" [14]: https://www.thelancet.com/journals/laninf/article/PIIS1473-3099%2823%2900731-4/abstract?utm_source=chatgpt.com "Global guideline for the diagnosis and management of ..." [15]: https://bccfe.ca/wp-content/uploads/2024/04/bc-cfe_therapeutic_guidelines_for_opportunistic_infections-pcp-mar-2023_nov8.pdf?utm_source=chatgpt.com "Pneumocystis pneumonia (PCP)" [16]: https://bccfe.ca/wp-content/uploads/2024/04/bc-cfe_therapeutic_guidelines_for_opportunistic_infections-toxoplasmosis.pdf?utm_source=chatgpt.com "toxoplasmosis" [17]: https://www.hiv.uw.edu/pdf/co-occurring-conditions/opportunistic-infections-prevention/core-concept/all?utm_source=chatgpt.com "Opportunistic Infections: Prevention - Core Concepts" [18]: https://bccfe.ca/wp-content/uploads/2024/04/bc-cfe_cryptococcosis_guidelines_oct2023.pdf?utm_source=chatgpt.com "Cryptococcosis" [19]: https://aahivm.org/clinical-research-update-040419/?utm_source=chatgpt.com "Clinical Research Update 4.4.19" [20]: https://www.ncbi.nlm.nih.gov/books/NBK531442/?utm_source=chatgpt.com "Key Recommendations, Rationale and Evidence Summary"

Tags:
HIV HIV coinfection opportunistic infections PCP Pneumocystis jirovecii Toxoplasma encephalitis Cryptococcal meningitis CMV retinitis MAC Mycobacterium avium complex Tuberculosis in HIV TB meningitis IRIS immune reconstitution inflammatory syndrome HIV prophylaxis OI prophylaxis CD4 count based prophylaxis ART initiation timing HIV coinfection management HIV case scenarios HIV MCQs AIDS defining illnesses fungal infections in HIV parasitic infections in HIV viral coinfections HIV bacterial opportunistic infections HIV HIV immunosuppression severe immunodeficiency HIV advanced disease NEET PG HIV INI CET HIV topics