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:
- Initial screening with fourth-generation antigen/antibody combination assay 3
- If reactive, perform HIV-1/HIV-2 antibody differentiation immunoassay 3
- If differentiation assay is positive, HIV infection is confirmed 3
- 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:
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
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:
- Screen with rapid HIV antibody test 1
- If negative, offer PEP immediately—do not delay for confirmatory testing 1
- 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