Department of Protozoology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Department of Medical Technology, Institute of Arts and Sciences, Far Eastern University-Manila, Manila, Philippines.
Parasit Vectors. 2021 May 25;14(1):280. doi: 10.1186/s13071-021-04792-5.
Malaria mixed infections are often unrecognized by microscopists in the hospitals, and a delay or failure to treat Plasmodium-mixed infection may lead to aggravated morbidity and increased mortality. The present study aimed to quantify the pooled proportion and risk of malarial recurrences after the treatment of Plasmodium-mixed infection. The results of the study may provide benefits in the management of Plasmodium-mixed infection in co-endemic regions.
This systematic review and meta-analysis searched the international Prospective Register of Systematic Reviews (PROSPERO; ID = CRD42020199709), MEDLINE, Web of Science, and Scopus for potentially relevant studies in any language published between January 1, 1936, and July 20, 2020, assessing drug efficacy in patients with Plasmodium-mixed infection. The primary outcome was the pooled prevalence of Plasmodium parasitemia after initiating antimalarial treatment for Plasmodium-mixed infection. The secondary outcome was the pooled risk ratio (RR) of malarial recurrence in Plasmodium-mixed infection compared with those in Plasmodium falciparum and Plasmodium vivax mono-infection. The pooled analyses were calculated by random-effects meta-analysis. After the initial treatment in different days of recurrences (≤ 28 days or > 28 days), the risk of Plasmodium parasitemia was compared in subgroup analysis.
Out of 5217 screened studies, 11 were included in the meta-analysis, including 4390 patients from six countries. The pooled prevalence of all recurrences of Plasmodium-mixed parasitemia was 30% (95% confidence interval (CI) 16-43; I: 99.2%; 11 studies). The RR of malarial recurrence within 28 days after the initial treatment (clinical treatment failure) of Plasmodium-mixed parasitemia compared with the treatment of P. falciparum was 1.22 (p: 0.029; 95% CI 1.02-1.47; Cochran Q: 0.93; I: 0%; six studies), while there was no significant difference in the risk of recurrence 28 days after initial treatment compared with the treatment of P. falciparum (p: 0.696, RR: 1.14; 95% CI 0.59-2.18; Cochran Q < 0.05; I: 98.2%; four studies). The subgroup analysis of antimalarial drugs showed that significant malarial recurrence within 28 days was observed in patients treated with artemisinin-based combination therapies (ACTs) with no significant heterogeneity (p: 0.028, RR: 1.31; 95% CI 1.03-1.66; Cochran Q: 0.834; I: 0%).
The present findings showed a high prevalence of malarial recurrence after the initial treatment of Plasmodium-mixed infection. Moreover, significant malaria recurrence of mixed infection occurred within 28 days after treatment with ACTs.
疟疾混合感染经常被医院的显微镜检人员忽视,延迟或未能治疗疟原虫混合感染可能导致发病率恶化和死亡率增加。本研究旨在定量评估治疗疟原虫混合感染后疟疾复发的 pooled proportion 和 risk。研究结果可能有助于在疟疾流行地区管理疟原虫混合感染。
本系统评价和荟萃分析在国际前瞻性注册系统评价(PROSPERO;ID=CRD42020199709)、MEDLINE、Web of Science 和 Scopus 中,以任何语言搜索了 1936 年 1 月 1 日至 2020 年 7 月 20 日期间发表的潜在相关研究,评估了混合疟原虫感染患者的药物疗效。主要结局是启动抗疟治疗后疟原虫寄生虫血症的 pooled prevalence。次要结局是与恶性疟原虫和间日疟原虫单感染相比,混合疟原虫感染的 malaria 复发 pooled risk ratio (RR)。pooled 分析通过随机效应荟萃分析计算。在不同复发天数(≤28 天或>28 天)的初始治疗后,在亚组分析中比较了疟原虫寄生虫血症的风险。
在 5217 项筛选研究中,有 11 项研究被纳入荟萃分析,包括来自六个国家的 4390 名患者。所有混合疟原虫寄生虫血症复发的 pooled prevalence 为 30%(95%置信区间 16-43;I:99.2%;11 项研究)。与恶性疟原虫治疗相比,混合疟原虫寄生虫血症初始治疗后 28 天内(临床治疗失败)疟疾复发的 RR 为 1.22(p:0.029;95%CI 1.02-1.47;Cochran Q:0.93;I:0%;6 项研究),而初始治疗后 28 天与恶性疟原虫治疗相比,复发风险无显著差异(p:0.696,RR:1.14;95%CI 0.59-2.18;Cochran Q<0.05;I:98.2%;4 项研究)。抗疟药物的亚组分析显示,接受基于青蒿素的联合疗法(ACTs)治疗的患者在 28 天内出现显著疟疾复发,且无显著异质性(p:0.028,RR:1.31;95%CI 1.03-1.66;Cochran Q:0.834;I:0%)。
本研究结果显示,混合疟原虫感染初始治疗后疟疾复发的 pooled prevalence 较高。此外,ACT 治疗后 28 天内混合感染疟疾复发显著。