Table 3. Laboratory Testing Schedule for Monitoring People with HIV Before and After Initiation of Antiretroviral Therapy

Laboratory Testing for Initial Assessment and Monitoring of People with HIV Receiving Antiretroviral Therapy
Laboratory Test Timepoint or Frequency of Testing
Entry Into Care ART Initiationb or Modification 4 to 8 Weeks After ART Initiation or Modification Every 3 Months Every 6 Months Every 12 Months Treatment Failure Clinically Indicated If ART Initiation Is Delayedc

HIV Antigen/
Antibody Test

If HIV diagnosis has not been confirmed

CD4 Count



If CD4 count is <300 cells/mm3

During the first 2 years of ART, if CD4 count is ≥ 300 cells/mm3

After 2 Years on ART with Consistently Suppressed Viral Load

CD4 Count 300–500 cells/mm3

  • Every 12 months

CD4 Count >500 cells/mm3

  • CD4 count monitoring is optional.

Every 3‍–‍6 months

HIV Viral Load





Repeat testing is optional.

Genotypic Resistance Testing (PR/RT Genes)g


Genotypic Resistance Testing (Integrase Genes)g

If transmitted INSTI resistance is suspected or if there is a history of CAB-LA use for PrEP


If transmitted INSTI resistance is suspected or if there is a history of INSTI use


If there is a history of INSTI use

If there is a history of INSTI use

Tropism Testing  

If considering a CCR5 antagonist


If considering a CCR5 antagonist, or for patients with virologic failure on a CCR5 antagonist

HLA-B*5701 Testing  

If considering ABC


Hepatitis B Serology

(HBsAb, HBsAg, HBcAb total)h,i,j

In patients not immune to HBV, consider retesting if switching to a regimen that does not contain TDF or TAF.


Including before starting HCV DAA


Hepatitis C Screening

(HCV antibody or, if indicated, HCV RNA)k


Repeat HCV screening for at-risk patientsl




Basic Metabolic Panelm,n



Every 6‍–‍‍12 months

ALT, AST, Total Bilirubin



Every 6–‍12 months

CBC with Differentialo


When monitoring CD4 count (if required by lab)

When monitoring CD4 count (if required by lab)

When no longer monitoring CD4 count


Lipid Profilep


Consider 1–3 months after ARV initiation or modification


If normal at baseline but with CV risk


If normal at baseline, every 5 years or if clinically indicated

Random or Fasting Glucoseq






E.g., in patients with CKD or DM

Pregnancy Tests


a This table pertains to laboratory tests done to select an ARV regimen and monitor for treatment responses or ART toxicities. Please refer to the HIV Medicine Association of the Infectious Diseases Society of America’s (HIVMA/IDSA) Primary Care Guidance for Persons with HIV for other laboratory tests generally recommended for primary health care maintenance of HIV patients.1

b If ART is initiated soon after HIV diagnosis and entry into care, repeat baseline laboratory testing is not necessary.

c ART is indicated for all people with HIV and should be started as soon as possible. However, if ART initiation is delayed, patients should be retained in care, with periodic monitoring as noted above.

d After 2 years of consistently suppressed HIV RNA, less frequent monitoring (e.g., every 6 months) may be considered.

e If HIV RNA is detectable at 4–8 weeks, repeat testing every 4–8 weeks until viral load is suppressed to <50 copies/mL. Thereafter, repeat testing every 3–6 months.

f For patients on ART, viral load typically is measured every 3–6 months. More frequent monitoring may be considered in individuals having difficulties with ART adherence or at risk for nonadherence. However, for adherent patients with consistently suppressed viral load and stable immunologic status for more than 1 year, monitoring can be extended to 6-month intervals.

g Standard genotypic drug-resistance testing in ARV-naive persons should focus on testing for mutations in the PR and RT genes. If transmitted INSTI resistance is a concern, or if a person has a history of INSTI use as PrEP or treatment, or a person presents with viremia while on an INSTI, providers also should test for resistance mutations in the IN gene. In ARV-naive patients who do not immediately begin ART, repeat testing before initiation of ART is optional if drug-resistance testing was performed at entry into care. In patients with virologic suppression who are switching therapy because of toxicity or for convenience, viral amplification will not be possible; see the Drug-Resistance Testing section for a discussion of the potential limitations and benefits of proviral DNA assays in this situation. Results from prior drug-resistance testing should be considered because they can be helpful in constructing a new regimen.

h If a patient has HBV infection (as determined by a positive HBsAg or HBV DNA test result), TDF or TAF plus either FTC or 3TC should be used as part of the ARV regimen to treat both HBV and HIV infections (see the Hepatitis B Virus/HIV Coinfection section).

i If HBsAg, HBsAb, and HBcAb test results are negative, HBV vaccine series should be administered. Refer to the HIVMA/IDSA’s Primary Care Guidance for Persons with HIV and the Adult and Adolescent Opportunistic Infection Guidelines for detailed recommendations.1,2

j Most patients with isolated HBcAb have resolved HBV infection with loss of HBsAb. Consider performing an HBV viral load test for confirmation. If the HBV viral load test is positive, the patient may be acutely infected (and will usually display other signs of acute hepatitis) or chronically infected. If the test is negative, the patient should be vaccinated. Refer to the HIVMA/IDSA’s Primary Care Guidance for Persons with HIV and the Adult and Adolescent Opportunistic Infection Guidelines for more detailed recommendations.2

k The HCV antibody test may not be adequate for screening in the setting of recent HCV infection (acquisition within the past 6 months) or advanced immunodeficiency (CD4 count <100 cells/mm3). HCV RNA screening is indicated in persons who have been successfully treated for HCV or who spontaneously cleared prior infection. HCV antibody-negative patients with elevated ALT may need HCV RNA testing.

l Injection drug users, people with a history of incarceration, men with HIV who have unprotected sex with men, and people with percutaneous/parenteral exposure to blood in unregulated settings are at risk of HCV infection.

m Serum Na, K, HCO3, Cl, BUN, creatinine, glucose, and Cr-based eGFR. Serum P should be monitored in patients with CKD who are on TDF-containing regimens.3

n Consult the HIVMA/IDSA’s Clinical Practice Guideline for the Management of Chronic Kidney Disease in Patients Infected with HIV for recommendations on managing patients with renal disease.3 More frequent monitoring may be indicated for patients with evidence of kidney disease (e.g., proteinuria, decreased glomerular dysfunction) or increased risk of renal insufficiency (e.g., patients with diabetes, hypertension).

o CBC with differential should be done when a CD4 count is performed. When CD4 count is no longer being monitored, the recommended frequency of CBC with differential is once a year. More frequent monitoring may be indicated for people receiving medications that potentially cause cytopenia (e.g., TMP-SMX).

p If random lipids are abnormal, fasting lipids should be obtained. Consult the American College of Cardiology/American Heart Association’s 2018 Guideline on the Management of Blood Cholesterol for diagnosis and management of patients with dyslipidemia.4

q If random glucose is abnormal, fasting glucose should be obtained. HbA1C is no longer recommended for diagnosis of diabetes in people with HIV on ART (see the American Diabetes Association Guidelines).5

r Urine glucose and protein should be assessed before initiating TAF- or TDF-containing regimens and monitored during treatment with these regimens.

s For persons of childbearing potential.

Key: 3TC = lamivudine; ABC = abacavir; ALT = alanine aminotransferase; ART = antiretroviral therapy; ARV = antiretroviral; AST = aspartate aminotransferase; BUN = blood urea nitrogen; CAB-LA = cabotegravir long-acting; CBC = complete blood count; CD4 = CD4 T lymphocyte; CKD = chronic kidney disease; Cl = chloride; Cr = creatinine; CV = cardiovascular; DAA = direct-acting antiviral; DM = diabetes mellitus; eGFR = estimated glomerular filtration rate; FTC = emtricitabine; HbA1C = hemoglobin A1c; HBcAb = hepatitis B core antibody; HBsAb = hepatitis B surface antibody; HBsAg = hepatitis B surface antigen; HBV = hepatitis B virus; HCO3 = bicarbonate; HCV = hepatitis C virus; IN = integrase; INSTI = integrase strand transfer inhibitor; K = potassium; Na = sodium; P = phosphorus; PR = protease; PrEP = pre-exposure prophylaxis; RT = reverse transcriptase; TAF = tenofovir alafenamide; TDF = tenofovir disoproxil fumarate; TMP-SMX = trimethoprim-sulfamethoxazole