Kokori Emmanuel, Olatunji Gbolahan, Ukoaka Bonaventure Michael, Abraham Israel Charles, Komolafe Rosemary, Ajekiigbe Victor Oluwatomiwa, Udam Ntishor Gabriel, Eneh Stanley, Ezenwoba Chidiogo, Babalola Adetola Emmanuel, Omoworare Oluwatobi, Aderinto Nicholas
Department of Medicine and Surgery, University of Ilorin, Ilorin, Nigeria.
Department of Internal Medicine, Asokoro District Hospital, Abuja, Nigeria.
Malar J. 2025 Jan 22;24(1):24. doi: 10.1186/s12936-025-05257-1.
Congenital malaria remains a significant public health challenge in Nigeria, particularly in regions with high malaria endemicity. The increased vertical transmission of malaria is partly associated with the high susceptibility of women to malaria during pregnancy. This systematic review aimed to assess the prevalence, characteristics, and treatment outcomes of congenital malaria in Nigeria.
Twelve studies were included in this review. Studies were retrieved from multiple electronic databases such as PubMed, EMBASE, Google Scholar, Scopus, Web of Science, African Journals Online (AJOL), and Cochrane Library and subjected to a multistage screening per established eligibility criteria. The study was registered with PROSPERO and was conducted per PRSIMA-established guidelines. Quality assessment of included studies was done using the Critical Appraisal Skills Programme (CASP) framework, while a narrative synthesis synthesized and summarized extracted data.
The prevalence of congenital malaria in Nigeria ranged from as low as 5.1% to as high as 96.3%. Clinical manifestations were often non-specific, with fever being the most common symptom. Treatment regimens included a variety of antimalarial drugs, such as chloroquine, sulfadoxine-pyrimethamine, amodiaquine, quinine, and artemisinin-based combination therapy. While treatment outcomes were generally positive, some studies reported complications and deaths.
The findings highlight the need for improved diagnostic tools, standardized treatment protocols, and targeted interventions in high-burden areas. Further research is required to investigate the long-term health outcomes of neonates with congenital malaria and to evaluate the effectiveness of different treatment strategies. By addressing these gaps, effective prevention and management strategies can be developed to reduce the burden of congenital malaria in Nigeria.
先天性疟疾在尼日利亚仍然是一项重大的公共卫生挑战,特别是在疟疾高流行地区。疟疾垂直传播的增加部分与孕期妇女对疟疾的高易感性有关。本系统评价旨在评估尼日利亚先天性疟疾的患病率、特征和治疗结果。
本评价纳入了12项研究。研究从多个电子数据库检索,如PubMed、EMBASE、谷歌学术、Scopus、科学网、非洲期刊在线(AJOL)和Cochrane图书馆,并根据既定的纳入标准进行多阶段筛选。该研究在国际前瞻性系统评价注册库(PROSPERO)进行了注册,并按照PRISMA制定的指南进行。使用批判性评估技能计划(CASP)框架对纳入研究进行质量评估,同时进行叙述性综合分析以综合和总结提取的数据。
尼日利亚先天性疟疾的患病率低至5.1%,高至96.3%。临床表现通常不具特异性,发热是最常见的症状。治疗方案包括多种抗疟药物,如氯喹、磺胺多辛-乙胺嘧啶、阿莫地喹、奎宁和青蒿素类联合疗法。虽然治疗结果总体呈阳性,但一些研究报告了并发症和死亡情况。
研究结果凸显了在高负担地区改进诊断工具、标准化治疗方案和针对性干预措施的必要性。需要进一步研究以调查先天性疟疾新生儿的长期健康结局,并评估不同治疗策略的有效性。通过填补这些空白,可以制定有效的预防和管理策略,以减轻尼日利亚先天性疟疾的负担。