Impact on hemoglobin of starting combination antiretroviral therapy with or without zidovudine in anemic HIV-infected patients

J Acquir Immune Defic Syndr. 2008 Jun 1;48(2):163-8. doi: 10.1097/QAI.0b013e3181685714.

Abstract

Objective: To evaluate, among anemic patients with HIV, the impact on hemoglobin (Hb) of initiating zidovudine (AZT)-containing and non-AZT-containing combination antiretroviral therapy (cART).

Methods: We used medical records data collected in 11 US cities from 1998 to 2004. Baseline anemia was described as mild (10 < Hb < or = 12 [women] or 14 [men] g/dL), moderate (8 < Hb < or = 10 g/dL), or severe (Hb < or = 8 g/dL). Improvement of anemia was a > or =1-g/dL increase in Hb, with a decrease in categoric severity. We excluded patients previously treated with erythropoietin or transfusion, and used Cox proportional hazards regression to describe factors associated with hazard of improvement of anemia.

Results: For 1620 patients initiating cART, more than half (54%) of patients had improvement of anemia. Time to improvement of anemia was longer for those initiating AZT-containing regimens and blacks and was shorter for those with moderate and severe anemia or CD4 counts <200 cells/microL.

Conclusions: Most anemic patients initiating cART (with or without AZT) had increases in Hb-especially those with more severe anemia or immunosuppression. Initiation of AZT-containing cART may be considered, even for patients with preexisting anemia; however, improvement of anemia may be delayed for black patients and for patients with mild disease.

MeSH terms

  • Adolescent
  • Adult
  • Anemia / blood
  • Anemia / drug therapy*
  • Anti-HIV Agents / administration & dosage*
  • Drug Therapy, Combination
  • Female
  • HIV Infections / blood
  • HIV Infections / drug therapy*
  • Hemoglobins / analysis
  • Humans
  • Male
  • Middle Aged
  • Proportional Hazards Models
  • Zidovudine / administration & dosage*

Substances

  • Anti-HIV Agents
  • Hemoglobins
  • Zidovudine