Kasirye Ronnie P, Baisley Kathy, Munderi Paula, Levin Jonathan, Anywaine Zacchaeus, Nunn Andrew, Kamali Anatoli, Grosskurth Heiner
aMRC/UVRI Uganda Research Unit on AIDS, Entebbe, Uganda bLondon School of Hygiene and Tropical Medicine, London, UK cSchool of Public Health, University of Witwatersrand, Johannesburg, South Africa dMRC Clinical Trials Unit at University College London, UK.
AIDS. 2016 Feb 20;30(4):635-44. doi: 10.1097/QAD.0000000000000956.
Previous unblinded trials have shown increased malaria among HIV-infected adults on antiretroviral therapy (ART) who stop cotrimoxazole (CTX) prophylaxis. We investigated the effect of stopping CTX on malaria in HIV-infected adults on ART in a double-blind, placebo-controlled trial.
HIV-infected Ugandan adults stable on ART and CTX with CD4 cell count at least 250 cells/μl were randomized (1 : 1) to continue CTX or stop CTX and receive matching placebo (COSTOP trial; ISRCTN44723643). Clinical malaria was defined as fever and a positive blood slide, and considered severe if a participant had at least one clinical or laboratory feature of severity or was admitted to hospital. Malaria incidence and rate ratios were estimated using random effects Poisson regression, accounting for multiple episodes.
A total of 2180 participants were enrolled and followed for a median of 2.5 years; 453 malaria episodes were recorded. Malaria incidence was 9.1/100 person-years (pyrs) [95% confidence interval (CI) = 8.2-10.1] and was higher on placebo (rate ratio 3.47; CI = 2.74-4.39). Malaria in the placebo arm decreased over time; although incidence remained higher than in the CTX arm, the difference between arms reduced slightly (interaction P value = 0.10). Fifteen participants experienced severe malaria (<1%); overall incidence was 0.30/100 pyrs (CI = 0.18-0.49). There was one malaria-related death (CTX arm).
HIV-infected adults - who are stable on ART and stop prophylactic CTX - experience more malaria than those that continue, but this difference is less than has been reported in previous trials. Few participants had severe malaria. Further research might be useful in identifying groups that can safely stop CTX prophylaxis.
既往非盲法试验表明,接受抗逆转录病毒治疗(ART)的HIV感染成人在停用复方新诺明(CTX)预防用药后,疟疾发病率有所增加。我们在一项双盲、安慰剂对照试验中,研究了停用CTX对接受ART的HIV感染成人疟疾的影响。
CD4细胞计数至少为250个/μl且在ART和CTX治疗下病情稳定的乌干达HIV感染成人被随机分组(1∶1),分别继续使用CTX或停用CTX并接受匹配的安慰剂(COSTOP试验;ISRCTN44723643)。临床疟疾定义为发热且血涂片检查呈阳性,如果参与者至少有一项严重程度的临床或实验室特征或入院治疗,则视为重症疟疾。使用随机效应泊松回归估计疟疾发病率和率比,并考虑多次发作情况。
总共招募了2180名参与者,中位随访时间为2.5年;记录到453例疟疾发作。疟疾发病率为9.1/100人年(pyrs)[95%置信区间(CI)=8.2 - 10.1],安慰剂组更高(率比3.47;CI = 2.74 - 4.39)。安慰剂组的疟疾发病率随时间下降;尽管发病率仍高于CTX组,但两组之间的差异略有缩小(交互作用P值 = 0.10)。15名参与者发生重症疟疾(<1%);总体发病率为0.30/100 pyrs(CI = 0.18 - 0.49)。有1例与疟疾相关的死亡(在CTX组)。
在ART治疗下病情稳定且停用预防性CTX的HIV感染成人,比继续使用CTX的成人患疟疾的情况更多,但这种差异小于既往试验所报道的情况。很少有参与者发生重症疟疾。进一步的研究可能有助于确定能够安全停用CTX预防用药的人群。