Parasitaemia and fever in uncomplicated Plasmodium vivax malaria: A systematic review and individual patient data meta-analysis.

IF 3.4 2区 医学 Q1 PARASITOLOGY
PLoS Neglected Tropical Diseases Pub Date : 2025-03-28 eCollection Date: 2025-03-01 DOI:10.1371/journal.pntd.0012951
Emily S Groves, Julie A Simpson, Peta Edler, André Daher, Ayodhia P Pasaribu, Dhelio B Pereira, Kavitha Saravu, Lorenz von Seidlein, Megha Rajasekhar, Ric N Price, Robert J Commons
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引用次数: 0

Abstract

Background: Parasite density thresholds used for diagnosing symptomatic malaria are defined by the relationship between parasitaemia and fever. This relationship can inform the design and development of novel diagnostic tests but appropriate parasitaemia thresholds for Plasmodium vivax malaria remain poorly defined.

Methodology/principal findings: We undertook an individual patient data meta-analysis of P. vivax clinical trials mapped to the WorldWide Antimalarial Resistance Network (WWARN) repository and used parasitaemia centiles of febrile patients at enrolment to derive proportions of patients who would have been diagnosed at different parasite densities. Febrile and afebrile patients with recurrent infections were selected to estimate pyrogenic densities using receiver operating characteristic curve analysis. In total 13,263 patients from 50 studies were included in the analysis. In 27 studies (8,378 febrile patients) in which a parasitaemia threshold was not applied as an inclusion criterion, the median parasitaemia at enrolment was 3,280/µL (interquartile range, 968 - 8,320); 90% of patients had a parasitaemia above 278/µL (10th centile), and 95% above 120/µL (5th centile). The 10th centile was higher in children <5 years old (368/µL) compared to adults ≥15 years (240/µL). In high relapse periodicity regions (Southeast Asia and Oceania) febrile patients presented with lower parasitaemias (10th centile 185/µL vs. 504/µL) and a wider range of parasitaemias compared to those from low relapse periodicity regions (interquartile range 760/µL - 8,774/µL vs. 1,204/µL - 8,000/µL). In total 2,270 patients from 41 studies had at least one episode of recurrent P. vivax parasitaemia, of whom 43% (849/1,983) were febrile at their first recurrence. The P. vivax pyrogenic density at first recurrence was 1,063/µL, defining fever with 74% sensitivity and 65% specificity. The pyrogenic density was lower in young children compared to adults ≥15 years (935/µL vs. 1,179/µL).

Conclusions/significance: The derived parasitaemia centiles will inform the use of current and the design of novel point-of-care tests to diagnose patients with symptomatic vivax malaria. Variation by age and location should be considered when selecting diagnostic thresholds and interpreting results.

Trial registration: This trial was registered with PROSPERO: CRD42021254905. The date of the first registration was 17th May 2021.

无并发症间日疟原虫疟疾中的寄生虫血症和发热:系统综述和患者个体数据荟萃分析。
背景:用于诊断有症状疟疾的寄生虫密度阈值由寄生虫血症和发热之间的关系确定。这种关系可以为设计和开发新的诊断测试提供信息,但间日疟原虫疟疾的适当寄生虫血症阈值仍然不明确。研究方法/主要发现:我们对间日疟原虫临床试验的个体患者数据进行了荟萃分析,并将其映射到世界抗疟药网络(WWARN)存储库中,并使用入组时发热患者的寄生虫血症百分位数,得出在不同寄生虫密度下诊断出的患者比例。选择反复感染的发热和不发热患者,利用受者工作特征曲线分析估计热原密度。来自50项研究的13263名患者被纳入分析。在27项研究(8,378名发热患者)中,没有将寄生虫血症阈值作为纳入标准,入组时的中位寄生虫血症为3,280/µL(四分位数范围为968 - 8,320);90%的患者寄生虫血症高于278/µL(第10百分位),95%的患者寄生虫血症高于120/µL(第5百分位)。结论/意义:衍生的寄生虫病百分位将为使用当前和设计新的护理点检测来诊断有症状的间日疟患者提供信息。在选择诊断阈值和解释结果时,应考虑年龄和地点的差异。试验注册:该试验在PROSPERO注册:CRD42021254905。首次注册日期为2021年5月17日。
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来源期刊
PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases PARASITOLOGY-TROPICAL MEDICINE
自引率
10.50%
发文量
723
期刊介绍: PLOS Neglected Tropical Diseases publishes research devoted to the pathology, epidemiology, prevention, treatment and control of the neglected tropical diseases (NTDs), as well as relevant public policy. The NTDs are defined as a group of poverty-promoting chronic infectious diseases, which primarily occur in rural areas and poor urban areas of low-income and middle-income countries. Their impact on child health and development, pregnancy, and worker productivity, as well as their stigmatizing features limit economic stability. All aspects of these diseases are considered, including: Pathogenesis Clinical features Pharmacology and treatment Diagnosis Epidemiology Vector biology Vaccinology and prevention Demographic, ecological and social determinants Public health and policy aspects (including cost-effectiveness analyses).
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