What are the guidelines for screening and treatment of Human Immunodeficiency Virus (HIV)?

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Last updated: November 22, 2025View editorial policy

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HIV Screening and Treatment Guidelines

HIV Screening Recommendations

All persons aged 15-65 years should be screened for HIV at least once in their lifetime, with routine opt-out screening recommended in primary care settings, emergency departments, and for all pregnant women. 1, 2

Universal Screening Populations

  • Adolescents and adults aged 15-65 years should undergo routine HIV screening regardless of perceived risk 1, 2
  • All pregnant women must be screened during each pregnancy, including those who present in labor with unknown HIV status 1, 2
  • Younger adolescents (<15 years) and older adults (>65 years) should be screened if they have any risk factors for HIV 1, 2

High-Risk Populations Requiring Frequent Screening

High-risk individuals should be tested every 3 months as long as risk continues 1:

  • Men who have sex with men (MSM) 1
  • Transfeminine persons 1
  • People who inject drugs outside needle sharing programs 1
  • Persons newly diagnosed with sexually transmitted infections (STIs) or hepatitis C 1
  • Sexual partners of HIV-infected persons 1
  • Persons who exchange sex for money or drugs 1

Optimal Testing Methods

Screening should be performed with fourth-generation HIV antigen/antibody combination assays that detect both HIV antibodies and p24 antigen, allowing detection of recent infection 1, 3, 4

  • Combined HIV antibody and antigen tests are preferred over antibody-only tests because they detect infection earlier 1
  • Rapid HIV tests can be used when immediate results are needed, but oral rapid tests have higher false-positive rates and should be confirmed with whole blood testing 1, 5
  • Third-generation antibody-only tests are acceptable for persons without access to better testing, but miss early infections 1

Critical Testing Algorithm

All reactive screening tests must be confirmed before diagnosis 1, 3:

  1. Initial screening with fourth-generation antigen/antibody combination assay 3
  2. If reactive, perform HIV-1/HIV-2 antibody differentiation immunoassay 3
  3. If differentiation assay is positive, HIV infection is confirmed 3
  4. If differentiation assay is negative, perform HIV RNA testing to rule out acute HIV-1 infection 3

Common Pitfall: Never diagnose HIV based on screening test alone—false-positive results can occur with devastating psychological consequences 3

Window Period Considerations

  • HIV antibody is detectable in ≥95% of patients within 6 months of infection 1
  • Antibody tests cannot exclude infection that occurred less than 6 months before testing 1
  • Fourth-generation tests detect infection earlier than antibody-only tests by identifying p24 antigen 3, 4
  • Approximately 14.5% of new HIV diagnoses in emergency departments represent acute infection detectable only with antigen/antibody tests 4

Special Populations

Pregnant women require specific screening protocols 1, 2:

  • Screen during each pregnancy, even if previously tested negative 1
  • Repeat screening in third trimester for women at ongoing risk 1
  • Offer rapid HIV testing during labor for women with unknown or undocumented status 1

Infants born to HIV-positive mothers 1, 3:

  • Standard antibody tests are unreliable due to maternal antibody transfer 1
  • Definitive diagnosis requires two positive HIV RNA PCR or viral culture tests on separate specimens 3
  • Passively acquired maternal antibody becomes undetectable by 15-18 months of age 1

HIV-2 testing considerations 1, 3:

  • Test persons from West Africa (endemic region) or their sexual partners 1
  • Consider when clinical evidence suggests HIV disease but HIV-1 tests are negative 1

Post-Diagnosis Evaluation

Immediate Laboratory Assessment

Before starting antiretroviral therapy (ART), obtain the following tests, but do not delay ART initiation while waiting for results 1:

HIV staging and monitoring 1:

  • HIV RNA level (viral load) 1
  • CD4 cell count and percentage 1
  • HIV genotype resistance testing 1

General health assessment 1:

  • Complete blood count with differential 1
  • Comprehensive metabolic panel (kidney and liver function, electrolytes) 1
  • Fasting lipid profile 1
  • Fasting blood glucose 1
  • Urinalysis 1
  • Pregnancy test (if applicable) 1

Co-infection screening 1:

  • Hepatitis A, B, and C serologies 1
  • Tuberculosis screening 1
  • Sexually transmitted infection screening 1
  • Toxoplasma gondii serology 1
  • Cytomegalovirus (CMV) serology for patients at low risk 1

Additional baseline tests 1:

  • HLA-B*5701 testing (required before prescribing abacavir) 1
  • CCR5 tropism testing (if considering maraviroc) 1
  • Glucose-6-phosphate dehydrogenase (G6PD) in appropriate racial/ethnic groups 1
  • Cervical Pap test; consider anal Pap test if indicated 1

Special consideration for severely immunocompromised patients 1:

  • Serum cryptococcal antigen test for patients with CD4 count <100/μL, even without symptoms 1

Antiretroviral Therapy Initiation

When to Start Treatment

All persons diagnosed with HIV should be offered ART immediately, regardless of CD4 count or viral load 1, 2

  • Early treatment substantially reduces risk of AIDS-related events and death 1, 2
  • ART substantially decreases risk of HIV transmission to uninfected sex partners 2
  • Treatment should not be delayed for laboratory results unless there is preexisting kidney/liver damage or high likelihood of transmitted drug resistance 1

Initial ART Regimens

ART must consist of combination therapy—never add a single active drug to a failing regimen 1, 6, 7, 6

FDA-approved regimens include 6, 7, 6:

  • Integrase strand transfer inhibitors (INSTIs) in combination with other antiretrovirals 7

    • Dolutegravir-based regimens for treatment-naïve or treatment-experienced adults and pediatric patients ≥4 weeks and ≥3 kg 7
  • Non-nucleoside reverse transcriptase inhibitors (NNRTIs) in combination with protease inhibitors and/or nucleoside analogue reverse transcriptase inhibitors (NRTIs) 6

    • Efavirenz 600 mg orally once daily for adults 6
    • Efavirenz for pediatric patients ≥3 months and ≥3.5 kg with weight-based dosing 6

Dosing Considerations

Efavirenz should be taken on an empty stomach, preferably at bedtime 6:

  • Food increases efavirenz concentrations and may increase adverse reactions 6
  • Bedtime dosing improves tolerability of nervous system symptoms 6

Dosage adjustments required for drug interactions 6:

  • When coadministered with voriconazole: decrease efavirenz to 300 mg once daily and increase voriconazole maintenance dose to 400 mg every 12 hours 6
  • When coadministered with rifampin in patients ≥50 kg: increase efavirenz to 800 mg once daily 6

Monitoring During Treatment

Viral Load Monitoring

Measure viral load 4-6 weeks after starting or changing ART regimen 1:

  • If viral load has not declined and adherence appears sufficient, obtain genotype resistance testing 1
  • Once HIV RNA <50 copies/mL, monitor every 3 months until suppressed for at least 1 year 1
  • After 1 year of viral suppression with consistent adherence, monitoring can be reduced to every 6 months 1

If viral load >50 copies/mL is detected 1:

  • Repeat measurement within 4 weeks 1
  • Reassess medication adherence and tolerability 1
  • If adherence is sufficient, obtain genotype resistance testing 1

CD4 Cell Count Monitoring

Measure CD4 counts every 6 months until counts are >250/μL for at least 1 year with concomitant viral suppression 1

  • CD4 counts have substantial variation, especially during acute illness 1
  • Some experts recommend obtaining 2 baseline measurements before treatment decisions 1
  • CD8 cell count and CD4:CD8 ratio should not be used in clinical decision making 1

Ongoing Screening and Monitoring

At each visit, screen for 1:

  • High-risk sexual or drug-use behaviors 1
  • Symptoms of sexually transmitted infections 1
  • Depression (routine screening and treatment recommended) 1
  • Age- and risk-appropriate STI screening at various anatomical sites 1
  • Anal or cervical dysplasia 1
  • Tuberculosis 1
  • Medication toxicity 1

Treatment of Multidrug-Resistant HIV

Salvage Therapy Options

For patients with extremely limited treatment options due to multidrug resistance 1:

  • Ibalizumab (anti-CD4 monoclonal antibody, IV every 2 weeks): approximately 50% of adults with virological failure and multidrug-resistant HIV achieved undetectable viral loads at 12 months when combined with at least 1 other active drug 1

  • Fostemsavir (attachment inhibitor): 60% of patients achieved HIV RNA <40 copies/mL at 96 weeks when combined with at least 1 fully active agent; approximately one-third achieved undetectable viral loads without other fully active agents 1

Optimization of the ART regimen to keep viral load as low as possible is essential when resistance is suspected 1


Engagement in Care and Adherence

Linkage to Care After Diagnosis

Brief, strengths-based case management after HIV diagnosis facilitates linkage to care 1

  • Systematic monitoring of time to care linkage, retention, and viral suppression is recommended in all care settings 1
  • Rapid HIV test algorithms allow same-day referral to treatment from nonclinical settings 1
  • Data-driven risk stratification should identify high-acuity patients for combination intervention strategies 1

Retention Strategies

Systematic monitoring of missed clinic visits with rapid intervention is essential 1:

  • Personal telephone and interactive text reminders before scheduled appointments 1
  • Contact within 24-48 hours after missed appointments 1
  • Use public health surveillance with clinic-level data to guide individual-level reengagement 1

Adherence Monitoring and Support

Monitor adherence using validated self-report instruments and pharmacy refill data 1

For specific populations 1:

  • Integrate directly observed ART in methadone maintenance programs 1
  • Consider directly observed therapy for persons with substance use disorders 1
  • Provide opioid substitution therapy for opioid-dependent patients 1

Cash financial incentives for appointment attendance and viral suppression are generally not recommended 1


Psychosocial Support

Behavioral and psychosocial services are integral to HIV care and should be available on-site or through referral 1

Patients require support for 1:

  • Accepting potential life implications 1
  • Coping with stigma and others' reactions 1
  • Developing strategies for maintaining physical and emotional health 1
  • Initiating behavioral changes to prevent HIV transmission 1
  • Making reproductive choices 1
  • Gaining access to health services and insurance 1
  • Confronting employment discrimination 1

Routine screening and treatment for depression is recommended 1


Prevention Counseling

Post-Exposure Prophylaxis (PEP)

For persons with high-risk exposure within the previous 72 hours 1:

  1. Screen with rapid HIV antibody test 1
  2. If negative, offer PEP immediately—do not delay for confirmatory testing 1
  3. At time of prescribing PEP, obtain: creatinine level, hepatitis B surface antigen, STI screening, combined HIV antibody/antigen test or HIV RNA assay 1

Pre-Exposure Prophylaxis (PrEP)

For persons with ongoing high risk for HIV infection 1:

  • Screen with rapid HIV antibody test or combined antibody/antigen test 1
  • If initial test is negative, offer PrEP without waiting for confirmatory or safety testing results 1

Special Considerations for Hepatic Impairment

Monitor hepatic function before and during efavirenz treatment 6

Efavirenz is not recommended in patients with moderate or severe hepatic impairment (Child-Pugh B or C) 6

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.

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