Hematologic, hepatic, renal, and lipid laboratory monitoring after initiation of combination antiretroviral therapy in the United States, 2000-2010

J Acquir Immune Defic Syndr. 2013 Jun 1;63(2):216-20. doi: 10.1097/QAI.0b013e31828d69f1.

Abstract

We assessed laboratory monitoring after combination antiretroviral therapy initiation among 3678 patients in a large US multisite clinical cohort, censoring participants at last clinic visit, combination antiretroviral therapy change, or 3 years. Median days (interquartile range) to first hematologic, hepatic, renal, and lipid tests were 30 (18-53), 31 (19-56), 33 (20-59), and 350 (96-1106), respectively. At 1 year, approximately 80% received more than 2 hematologic, hepatic, and renal tests consistent with guidelines. However, only 40% received 1 or more lipid tests. Monitoring was more frequent in specific subgroups, likely reflecting better clinic attendance or clinician perception of higher susceptibility to toxicities.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alanine Transaminase / blood
  • Anti-HIV Agents / adverse effects*
  • Anti-HIV Agents / therapeutic use
  • Antiretroviral Therapy, Highly Active*
  • Aspartate Aminotransferases / blood
  • Bilirubin / blood
  • Blood Cell Count
  • Cohort Studies
  • Creatinine / blood
  • Drug Monitoring*
  • Female
  • HIV Infections / drug therapy*
  • HIV Infections / metabolism
  • Hematologic Tests*
  • Humans
  • Kidney / drug effects*
  • Lipids / blood*
  • Liver / drug effects*
  • Male
  • United States

Substances

  • Anti-HIV Agents
  • Lipids
  • Creatinine
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Bilirubin