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No differences between lopinavir/ritonavir and nonnucleoside reverse transcriptase inhibitor–based an- tiretroviral therapy on clearance of plasmodium falciparum subclinical parasitemia in adults living with HIV starting treatment (A5297

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dc.contributor.author Shaffer, Douglas
dc.contributor.author Kumwenda, Johnstone
dc.contributor.author Chen, Huichao
dc.contributor.author Akelo, Victor
dc.contributor.author Angira, Francis
dc.contributor.author Kosgei, Josphat
dc.contributor.author Tonui, Ronald
dc.contributor.author Ssali, Francis
dc.contributor.author McKhann, Ashley
dc.contributor.author Hogg, Evelyn
dc.contributor.author Stewart, V. Ann
dc.contributor.author Murphy, Sean C.
dc.contributor.author Coombs, Robert
dc.contributor.author Schooley, Robert
dc.date.accessioned 2023-10-04T07:54:25Z
dc.date.available 2023-10-04T07:54:25Z
dc.date.issued 2021-03-01
dc.identifier.uri http://ir.mu.ac.ke:8080/jspui/handle/123456789/8098
dc.description.abstract Background: HIV protease inhibitors anti-Plasmodium falcipa- rum activity in adults remains uncertain. Methods: Adults with HIV CD4+ counts .200 cells/mm3 starting antiretroviral therapy (ART) with P. falciparum subclinical para- sitemia (Pf SCP) were randomized 1:1 to (step 1) protease inhibitor lopinavir/ritonavir (LPV/r)-based (arm A) or nonnucleoside reverse transcriptase inhibitor (nNRTI)-based ART (arm B) for 15 days. In step 2, participants received nNRTI-based ART and trimethoprim/ sulfamethoxazole prophylaxis for 15 days. P. falciparum SCP clearance was measured by polymerase chain reaction. The Fisher exact test [95% exact confidence interval (CI)] was used to compare proportions of P. falciparum SCP clearance (,10 parasites/mL on 3 occasions within 24 hours) between LPV/r and nNRTI arms at day 15. The Kaplan–Meier method and log-rank test were used to compare time-to-clearance. Results: Fifty-two adults from Kenya, Malawi, and Uganda with a median age = 31 (Q1, Q3: 24–39) years, 33% women, with baseline median CD4 + counts of 324 (259–404) cells/mm 3 , median HIV-1 RNA viremia of 5.18 log10 copies/mL (4.60–5.71), and median estimated P. falciparum density of 454 parasites/mL (83–2219) enrolled in the study. Forty-nine (94%) participants completed the study. At day 15, there was no statistically significant difference in the proportions of P. falciparum SCP clearance between the LPV/r (23.1% clearance; 6 of the 26) and nNRTI (26.9% clearance; 7 of the 26) arms [between-arm difference 3.9% (95% CI, 221.1% to 28.4%; P = 1.00)]. No significant difference in time-to-clearance was observed between the arms (P = 0.80). Conclusions: In a small randomized study of adults starting ART with P. falciparum SCP, no statistically significant differences were seen between LPV/r- and nNRTI-based ART in P. falciparum SCP clearance after 15 days of treatment. en_US
dc.language.iso en en_US
dc.publisher Wolters Kluwer Health, Inc. en_US
dc.subject Malaria en_US
dc.subject Subclinical parasitemi en_US
dc.subject HIV en_US
dc.subject ART en_US
dc.subject Protease inhibitors en_US
dc.title No differences between lopinavir/ritonavir and nonnucleoside reverse transcriptase inhibitor–based an- tiretroviral therapy on clearance of plasmodium falciparum subclinical parasitemia in adults living with HIV starting treatment (A5297 en_US
dc.type Article en_US


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