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Low-dose Erythropoietin in the Management of HIV-related Anemia in Uganda
F Ssali1, J Kayiwa1, T Otim1, M Ssemmanda1, and Eugene Kinyanda*2
1Joint Clin Res Ctr, Kampala, Uganda and 2Med Res Council, Entebbe, Uganda
Background: Anemia is commonly observed among
patients with HIV infection. In previous studies it has been observed in 12% to
39 % of individuals with HIV and it is an independent predictor of quality of
life and death. The use of erythropoietin has been recommended in patients with
blood erythropoietin levels ≤500IU/L and previous studies have
used erythropoietin doses of 100 to 300 IU/kg given 3 times a week or 40,000 IU
once weekly. In resource-limited countries, there is a higher risk for anemia
for patients in Sub-Saharan Africa because of the added challenges of
nutritional deficiencies, intestinal parasites and malaria but the cost of the
high dose of erythropoietin is prohibitive. We hypothesized that low-dose
erythropoietin is effective in the management of HIV associated grade 1-2
anemia
Methods: A randomized open-label study included 108
out-patient HIV-infected individuals with grade 1-2 anemia during 2006 to 2007
in Kampala, Uganda. Study participants were randomly assigned to 1 of the 4
study arms and treated for 4 weeks as follows: 27 to the no erythropoietin (arm
A); 25 to 2000 IU 3 times a week (arm B); 30 to 4000 IU once a week (arm C),
and 26 to 2000 IU once a week (arm D). All the participants received oral hematinics.
Hemoglobin was measured for all participants at baseline and at week 4. A self-administered
baseline quality-of-life assessment using the SF-36 questionnaire was done for
all and at week 4 for 60 participants. Changes in hemoglobin and quality-of-life
scores were analyzed using SATA/IC 10 software.
Results: The participants had a
median age of 35±2 years, with 92 of 108 female participants. At week 4,
there was a improvement of 1.73 g/dL (SE 4.03) in the hemoglobin in all the
study arms. When compared with the "no erythropoietin" arm, unit hemoglobin
level improvements were observed to be 2.22±2.20 g/dL (p <0.05) in arm
B; 0.43±2.10 g/dL (p = 0.688) in arm C; and 0.27±2.18 g/dL (p = 0.806)
in the arm D. Quality-of-life scores improved with hemoglobin scores in all the
study arms, but physical vitality was significantly higher in study arm B (p
= 0.017).
Conclusions: Erythropoietin at a dose of 2000 IU 3
times a week is effective in improving the hemoglobin level of patients with
grade1 to 2 anemia. This improvement exceeds that achieved with only oral hematinic
supplementation.
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