Centre de Recherche en Santé de Nouna, Nouna, Burkina Faso.
Francis I Proctor Foundation, University of California, San Francisco, 490 Illinois St, Floor 2, San Francisco, CA, 94143, USA.
Malar J. 2021 Aug 31;20(1):360. doi: 10.1186/s12936-021-03895-9.
Azithromycin has recently been shown to reduce all-cause childhood mortality in sub-Saharan Africa. One potential mechanism of this effect is via the anti-malarial effect of azithromycin, which may help treat or prevent malaria infection. This study evaluated short- and longer-term effects of azithromycin on malaria outcomes in children.
Children aged 8 days to 59 months were randomized in a 1:1 fashion to a single oral dose of azithromycin (20 mg/kg) or matching placebo. Children were evaluated for malaria via thin and thick smear and rapid diagnostic test (for those with tympanic temperature ≥ 37.5 °C) at baseline and 14 days and 6 months after treatment. Malaria outcomes in children receiving azithromycin versus placebo were compared at each follow-up timepoint separately.
Of 450 children enrolled, 230 were randomized to azithromycin and 220 to placebo. Children were a median of 26 months and 51% were female, and 17% were positive for malaria parasitaemia at baseline. There was no evidence of a difference in malaria parasitaemia at 14 days or 6 months after treatment. In the azithromycin arm, 20% of children were positive for parasitaemia at 14 days compared to 17% in the placebo arm (P = 0.43) and 7.6% vs. 5.6% in the azithromycin compared to placebo arms at 6 months (P = 0.47).
Azithromycin did not affect malaria outcomes in this study, possibly due to the individually randomized nature of the trial. Trial registration This study is registered at clinicaltrials.gov (NCT03676751; registered 19 September 2018).
阿奇霉素最近被证明可以降低撒哈拉以南非洲的全因儿童死亡率。这种效果的一个潜在机制是阿奇霉素的抗疟作用,它可能有助于治疗或预防疟疾感染。本研究评估了阿奇霉素对儿童疟疾结局的短期和长期影响。
8 天至 59 个月大的儿童以 1:1 的比例随机分为单次口服阿奇霉素(20mg/kg)或匹配的安慰剂组。基线时以及治疗后 14 天和 6 个月时,通过薄血涂片和厚血涂片以及快速诊断试验(对体温≥37.5°C 的儿童)评估儿童的疟疾情况。分别比较接受阿奇霉素和安慰剂的儿童在每个随访时间点的疟疾结局。
450 名入组儿童中,230 名随机分配至阿奇霉素组,220 名随机分配至安慰剂组。儿童的中位年龄为 26 个月,51%为女性,基线时 17%的儿童疟原虫阳性。治疗后 14 天或 6 个月时,没有证据表明疟原虫血症有差异。在阿奇霉素组中,20%的儿童在 14 天时疟原虫阳性,安慰剂组为 17%(P=0.43);在 6 个月时,阿奇霉素组为 7.6%,安慰剂组为 5.6%(P=0.47)。
在本研究中,阿奇霉素没有影响疟疾结局,这可能是由于试验采用了个体随机化设计。
本研究在 clinicaltrials.gov 注册(NCT03676751;2018 年 9 月 19 日注册)。