Antiretroviral Agents in HIV-1 (trial)

DHHS Adult HIV 2013

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Table 6. Laboratory Monitoring for Patients Prior to and After Initiation of Antiretroviral Therapy Entry Into Care Follow-up Before ART ART Initiation or Modification 1 2–8 Weeks Post-ART Every 3–6 Months Every 6 Months Every 12 Months Treatment Failure Clinically Indicated CD4 T-cell count ✔ q3–6 mo ✔ ✔ 2 In clinically stable patients with suppressed viral load, CD4 count can be monitored every 6–12 mo ✔ ✔ HIV RNA ✔ q3–6 mo ✔ ✔ 2 ✔ 3 ✔ ✔ Resistance testing ✔ ✔ 4 ✔ ✔ HLA-B*5701 testing ✔ If considering ABC Tropism testing ✔ If considering a CCR5 antagonist ✔ If considering a CCR5 antagonist or for failure of CCR5 antagonist- based regimen ✔ Hepatitis B serolog y 5 ✔ ✔ May repeat if HBsAg (−) and HBsAb (−) at baseline ✔ Basic chemistry 6 ✔ q6–12 mo ✔ ✔ ✔ ✔ ALT, AST, T bili, D bili ✔ q6–12 mo ✔ ✔ ✔ ✔ CBC w/ differential ✔ q3–6 mo ✔ ✔ If on ZDV ✔ ✔ Fasting lipid profile ✔ If normal, annually ✔ ✔ Consider 4–8 weeks after starting new ART ✔ If abnormal at last measurement ✔ If normal at last measurement ✔ Fasting glucose ✔ If normal, annually ✔ ✔ If abnormal at last measurement ✔ If normal at last measurement ✔ Urinalysis 7 ✔ ✔ ✔ If on TDF 8 ✔ ✔ Pregnancy test ✔ If starting EFV ✔ 1 ARV modification may be done for treatment failure, adverse effects, or simplification. 2 If HIV RNA is detectable at 2–8 weeks, repeat every 4–8 weeks until suppression to <200 copies/mL, then every 3–6 months. 3 For adherent patients with suppressed viral load and stable clinical and immunologic status for >2–3 years, some experts may extend the interval for HIV RNA monitoring to every 6 months. 4 For ART-naive patients, if resistance testing was performed at entry into care, repeat testing is optional; for patients with viral suppression who are switching therapy for toxicity or convenience, resistance testing will not be possible and therefore is not necessary. 5 If HBsAg is positive at baseline or prior to initiation of ART, TDF + (FTC or 3TC) should be used as part of ARV regimen to treat both HBV and HIV infections. If HBsAg and HBsAb are negative at baseline, hepatitis B vaccine series should be administered. 6 Serum Na, K, HCO 3 , Cl, BUN, creatinine, glucose (preferably fasting ); some experts suggest monitoring phosphorus while on TDF; determination of renal function should include estimation of CrCl using the Cockcroft-Gault equation or estimation of glomerular filtration rate based on the Modification of Diet in Renal Disease equation. 7 For patients with renal disease, consult "Guidelines for the Management of Chronic Kidney Disease in HIV-Infected Patients: Recommendations of the HIV Medicine Association of the Infectious Diseases Society of America." 8 More frequent monitoring may be indicated for patients with increased risk of renal insufficiency, such as patients with diabetes, hypertension, etc. 23

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