Initial Treatment for HIV/AIDS-Induced Immune Deficiency Syndrome (IDS)
The initial treatment for HIV/AIDS-induced Immune Deficiency Syndrome (IDS) should be antiretroviral therapy (ART) initiated as soon as possible after diagnosis, ideally within 7 days, using an integrase strand transfer inhibitor (InSTI) plus two nucleoside reverse transcriptase inhibitors (NRTIs) as the preferred regimen. 1
Recommended Initial Regimens
The optimal initial antiretroviral regimens for most patients with newly diagnosed HIV infection are:
First-line preferred regimens (in alphabetical order):
Alternative regimens when first-line options are not available:
- Elvitegravir/cobicistat/tenofovir alafenamide/emtricitabine
- Raltegravir plus tenofovir alafenamide/emtricitabine 2
Timing of ART Initiation
Early initiation of ART is critical as it:
- Reduces mortality and morbidity in all viremic patients regardless of CD4 count
- Decreases the size of the latent HIV reservoir
- Reduces immune activation
- May protect against infection of central memory T cells
- Reduces the risk of HIV transmission 1
Special Considerations
CD4 Count and Viral Load
While ART is recommended for all HIV-infected patients regardless of CD4 count, patients with CD4 counts <200 cells/μL or viral load >100,000 copies/mL require particular attention as certain regimens may have suboptimal virologic suppression in this setting 2.
Opportunistic Infections
The presence of opportunistic infections (OIs) requires special consideration for ART timing:
- Tuberculosis without meningitis: Start ART within 2 weeks after beginning TB treatment, especially with CD4+ counts <50 cells/μL 1
- Tubercular meningitis: Start antitubercular treatment and corticosteroids immediately; begin ART when meningitis is under control (within 2-4 weeks) 1
- Cryptococcal meningitis: Start ART 2-4 weeks after beginning antifungal therapy 1
- Asymptomatic cryptococcal antigenemia: Start ART immediately with fluconazole prophylaxis 1
Immune Reconstitution Inflammatory Syndrome (IRIS)
IRIS is a potential complication that occurs when the immune system begins to recover and responds to previously acquired opportunistic infections. This can lead to paradoxical worsening of symptoms despite effective treatment 3, 4. Corticosteroid therapy may be effective in severe cases of IRIS 4.
Baseline Testing Before ART Initiation
Before starting ART, the following tests should be performed:
- HIV viral load and CD4+ T cell count
- HLA-B*5701 testing if considering abacavir-containing regimens
- Baseline resistance testing (though therapy can be initiated before results are available)
- Renal function tests (especially important if using tenofovir-containing regimens) 1, 5
Monitoring After ART Initiation
- Check HIV viral load 1 month after starting treatment
- Continue monitoring every 3-4 months until viral suppression is achieved
- For stable patients with sustained viral suppression, monitoring can be extended to every 6 months 1
- Monitor for drug-specific adverse effects (e.g., renal function with tenofovir, hypersensitivity with abacavir)
Common Pitfalls to Avoid
Delaying ART initiation: Historical guidelines recommended waiting until CD4 counts fell below certain thresholds, but current evidence strongly supports immediate initiation regardless of CD4 count 2, 1.
Inadequate prophylaxis for opportunistic infections: While ART is the primary treatment, patients with low CD4 counts may need prophylaxis for specific opportunistic infections until immune reconstitution occurs 6.
Poor adherence monitoring: Adherence is critical for successful treatment. Patients starting ART with high CD4+ counts may be at higher risk of treatment discontinuation and require close monitoring 1.
Ignoring potential drug interactions: Many antiretroviral medications have significant interactions with other drugs. Always check for interactions when prescribing additional medications 2.
Failure to recognize IRIS: This inflammatory response can occur within weeks to months after ART initiation and may be mistaken for treatment failure or a new infection 4.
By following these evidence-based guidelines for the initial treatment of HIV/AIDS-induced Immune Deficiency Syndrome, clinicians can significantly improve patient outcomes, reduce mortality and morbidity, and decrease the risk of HIV transmission.