Arzika Ahmed M, Abdou Amza, Maliki Ramatou, Lebas Elodie, Cook Catherine, Vanderschelden Benjamin, O'Brien Kieran S, Cotter Sun Y, Varnado Nicole E, Callahan E Kelly, Bailey Robin L, West Sheila K, Rosenthal Philip J, Porco Travis C, Lietman Thomas M, Keenan Jeremy D
The Carter Center, Niamey, Niger.
Centre de Recherche et Interventions en Santé Publique, Birni N'Gaoure, Niger.
JAMA Netw Open. 2025 Aug 1;8(8):e2527148. doi: 10.1001/jamanetworkopen.2025.27148.
Mass azithromycin distributions may reduce malaria parasitemia in the short term, but longer-term effectiveness is unclear.
To examine whether biannual mass azithromycin distributions are associated with lower rates of malaria parasitemia in preschool children living in Niger.
DESIGN, SETTING, AND PARTICIPANTS: A cluster randomized trial was performed from November 23, 2014, until June 9, 2020, as an ancillary trial to a larger trial studying the effect of mass azithromycin on child mortality. Study communities (ie, government-defined health catchment areas) in Niger were randomized in a 1:1 ratio to biannual (ie, twice-yearly) mass administration of azithromycin or placebo to all children aged 1 to 59 months and followed up for 5 years. Data analyses were performed from June 25, 2023, to April 27, 2025.
Twice-yearly administration of a single dose of oral azithromycin, 20 mg/kg, or placebo.
The prevalence of parasitemia 4 years after the community started treatment, assessed in a random sample of 40 children per community.
Among the 30 communities in Niger included in the study at baseline, the 15 communities randomized to azithromycin consisted of 1695 children (mean [SD] age, 30.8 [2.8] months; 858 [51.8%] male) and the 15 communities randomized to placebo consisted of 3031 children (mean [SD] age, 30.6 [2.6] months; 157 [52.0%] male). The mean prevalence of malaria parasitemia at baseline was 8.9% (95% CI, 5.1%-15.7%) in the azithromycin arm and 6.7% (95% CI, 4.0%-12.6%) in the placebo arm. At annual follow-up visits up until month 48, parasitemia was not statistically significantly lower in the azithromycin arm compared with the placebo arm, assuming a 10% prevalence in the placebo arm (-3.3 percentage points [PP]; 95% CI, -5.8 to -0.2 PP; permutation P = .05). The Niger Ministry of Health instituted seasonal malaria chemoprevention (SMC) after the month 36 study visit. Analysis restricted to the period before SMC found significantly less parasitemia in the azithromycin arm compared with the placebo arm (4.8 PP lower; 95% CI, -7.4 to -1.3 PP; permutation P = .02).
In this placebo-controlled cluster randomized trial, malaria among children aged 1 to 59 months was lower in communities treated with biannual mass azithromycin, but the effect was significant only for the first 3 years of the trial, before SMC.
ClinicalTrials.gov Identifier: NCT02048007.
大规模阿奇霉素分发可能在短期内降低疟疾寄生虫血症,但长期有效性尚不清楚。
研究在尼日尔生活的学龄前儿童中,每半年一次的大规模阿奇霉素分发是否与较低的疟疾寄生虫血症发生率相关。
设计、地点和参与者:作为一项更大规模研究大规模阿奇霉素对儿童死亡率影响的试验的辅助试验,于2014年11月23日至2020年6月9日进行了一项整群随机试验。尼日尔的研究社区(即政府划定的卫生服务区域)按1:1比例随机分为两组,一组对所有1至59个月大的儿童每半年(即每年两次)进行一次阿奇霉素大规模给药,另一组给予安慰剂,并随访5年。数据分析于2023年6月25日至2025年4月27日进行。
每年两次口服单剂量阿奇霉素,20毫克/千克,或安慰剂。
社区开始治疗4年后寄生虫血症的患病率,在每个社区随机抽取40名儿童进行评估。
在基线时纳入研究的尼日尔30个社区中,随机分配到阿奇霉素组的15个社区包括1695名儿童(平均[标准差]年龄,30.8[2.8]个月;858名[51.8%]为男性),随机分配到安慰剂组的15个社区包括3031名儿童(平均[标准差]年龄,30.6[2.6]个月;157名[52.0%]为男性)。阿奇霉素组基线时疟疾寄生虫血症的平均患病率为8.9%(95%置信区间,5.1%-15.7%),安慰剂组为6.7%(95%置信区间,4.0%-12.6%)。在第48个月之前的年度随访中,假设安慰剂组患病率为10%,阿奇霉素组的寄生虫血症与安慰剂组相比在统计学上无显著降低(-3.3个百分点[PP];95%置信区间,-5.8至-0.2 PP;置换P = 0.05)。在第36个月的研究访视后,尼日尔卫生部实施了季节性疟疾化学预防(SMC)。仅限于SMC实施前的时期进行分析发现,阿奇霉素组的寄生虫血症明显低于安慰剂组(低4.8 PP;95%置信区间,-7.4至-1.3 PP;置换P = 0.02)。
在这项安慰剂对照的整群随机试验中,每半年进行一次大规模阿奇霉素治疗的社区中,1至59个月大儿童的疟疾发病率较低,但仅在试验的前3年(SMC实施前)效果显著。
ClinicalTrials.gov标识符:NCT02048007。