What are the current guidelines for managing HIV?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 17, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Current Guidelines for HIV Management

Antiretroviral therapy (ART) is recommended for all HIV-infected individuals regardless of CD4 count, not only for individual health benefits but also because of the reduced infectiousness of individuals achieving virologic suppression. 1

Initial Evaluation and Testing

  • A comprehensive medical history, physical examination, and review of systems should be obtained for all patients upon HIV diagnosis 1
  • HIV serologic testing should be performed for patients without documentation of their HIV status 1
  • CD4 cell count with percentage should be obtained at initial evaluation 1
  • HIV RNA (viral load) level should be measured at baseline 1
  • Genotypic resistance testing should be performed before initiating ART to guide regimen selection 1
  • HLA-B*5701 testing is required before using abacavir to prevent hypersensitivity reactions 1
  • Tropism testing is recommended when considering CCR5 inhibitors 1

When to Start ART

  • ART should be initiated immediately upon diagnosis, regardless of CD4 count 1
  • Early initiation of ART reduces mortality by 74% compared to delayed initiation 2
  • Rapid intervention following HIV diagnosis improves linkage to care and viral suppression 1
  • Brief, strengths-based case management is recommended after HIV diagnosis to facilitate linkage to care 1

Recommended Initial ART Regimens

  • Preferred regimens include an integrase strand transfer inhibitor (InSTI) plus two nucleoside reverse transcriptase inhibitors (NRTIs) 1
  • Specifically recommended combinations include:
    • Dolutegravir (DTG) plus tenofovir disoproxil fumarate (TDF)/emtricitabine (FTC) or tenofovir alafenamide (TAF)/FTC 3
    • Bictegravir plus TAF/FTC 4
    • Dolutegravir plus abacavir/lamivudine (for HLA-B*5701 negative patients) 1
    • Dolutegravir plus lamivudine (as a two-drug regimen) 4
  • Once-daily regimens are recommended for treatment-naive patients when possible 1
  • Fixed-dose combinations are recommended to decrease pill burden 1

Monitoring of Treatment Response

  • Viral load should be measured 4-6 weeks after starting ART 1
  • After initial suppression, viral load monitoring is recommended every 3 months until suppressed for at least a year, then every 6 months if adherence is consistent 1
  • CD4 cell counts should be monitored every 6 months until counts are above 250/μL for at least 1 year with viral suppression 1
  • If viral load is above 50 copies/mL after previous suppression, measurement should be repeated within 4 weeks, and adherence should be reassessed 1
  • Age- and risk-appropriate screening for sexually transmitted infections, tuberculosis, and medication toxicity is recommended 1

Adherence Support

  • Systematic monitoring of ART adherence is essential for successful treatment 1
  • Self-reported adherence should be obtained routinely from all patients 1
  • Pharmacy refill data are recommended for adherence monitoring 1
  • Personal telephone and interactive text reminders before scheduled appointments and shortly after missed appointments (24-48 hours) improve adherence 1
  • Individual one-on-one ART education and adherence counseling are recommended 1
  • Opioid substitution therapy is recommended for opioid-dependent patients 1
  • Routine screening and treatment for depression is recommended 1

Management of Treatment Failure

  • If viral load has not declined after starting ART, adherence and medication tolerability should be discussed 1
  • If adherence appears sufficient but viral suppression is not achieved, genotypic resistance testing is recommended 1
  • For patients with persistent quantifiable HIV RNA between 50 and 200 copies/mL, reassessment for causes of virologic failure and close monitoring are recommended 1
  • Tropism testing is recommended at the time of virologic failure of a CCR5 inhibitor 1

HIV Prevention Strategies

  • ART is a key component of HIV prevention as virally suppressed individuals have virtually no risk of transmitting HIV sexually 4
  • Pre-exposure prophylaxis (PrEP) should be considered for HIV-negative individuals at high risk 1
  • Daily TDF/FTC is the recommended PrEP regimen 1
  • TDF-based PrEP is not recommended for individuals with osteopenia, osteoporosis, or creatinine clearance less than 60 mL/min 1

Special Considerations

  • For patients with tuberculosis co-infection, timing of ART initiation should be carefully considered, as early ART has been shown to increase mortality in cryptococcal meningitis 1
  • For patients with substance use disorders, integration of directly observed ART in treatment programs and opioid substitution therapy are recommended 1
  • Screening for and addressing housing instability, food insecurity, psychiatric disorders, and medication adverse effects improves outcomes 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

HIV/AIDS Treatment Regimen in India

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

HIV 101: fundamentals of antiretroviral therapy.

Topics in antiviral medicine, 2019

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.