Defining clinical malaria: the specificity and incidence of endpoints from active and passive surveillance of children in rural Kenya
- PMID: 21179571
- PMCID: PMC3002959
- DOI: 10.1371/journal.pone.0015569
Defining clinical malaria: the specificity and incidence of endpoints from active and passive surveillance of children in rural Kenya
Erratum in
- PLoS One. 2011;6(2). doi: 10.1371/annotation/fd5fdb2c-6cdd-429c-ae5c-24334795fe06 doi: 10.1371/annotation/fd5fdb2c-6cdd-429c-ae5c-24334795fe06
Abstract
Background: Febrile malaria is the most common clinical manifestation of P. falciparum infection, and is often the primary endpoint in clinical trials and epidemiological studies. Subjective and objective fevers are both used to define the endpoint, but have not been carefully compared, and the relative incidence of clinical malaria by active and passive case detection is unknown.
Methods: We analyzed data from cohorts under active and passive surveillance, including 19,462 presentations with fever and 5,551 blood tests for asymptomatic parasitaemia. A logistic regression model was used to calculate Malaria Attributable Fractions (MAFs) for various case definitions. Incidences of febrile malaria by active and passive surveillance were compared in a subset of children matched for age and location.
Results: Active surveillance identified three times the incidence of clinical malaria as passive surveillance in a subset of children matched for age and location. Objective fever (temperature≥37.5°C) gave consistently higher MAFs than case definitions based on subjective fever.
Conclusion: The endpoints from active and passive surveillance have high specificity, but the incidence of endpoints is lower on passive surveillance. Subjective fever had low specificity and should not be used in primary endpoint. Passive surveillance will reduce the power of clinical trials but may cost-effectively deliver acceptable sensitivity in studies of large populations.
Conflict of interest statement
Figures
References
-
- Nevill CG, Some ES, Mung'ala VO, Mutemi W, New L, et al. Insecticide-treated bednets reduce mortality and severe morbidity from malaria among children on the Kenyan coast. Trop Med Int Health. 1996;1:139–146. - PubMed
-
- Ballou WR. The development of the RTS,S malaria vaccine candidate: challenges and lessons. Parasite Immunol. 2009;31:492–500. - PubMed
-
- Moorthy VS, Reed Z, Smith PG. MALVAC 2008: Measures of efficacy of malaria vaccines in phase 2b and phase 3 trials—scientific, regulatory and public health perspectives. Vaccine. 2009;27:624–628. - PubMed
-
- Smith T, Schellenberg JA, Hayes R. Attributable fraction estimates and case definitions for malaria in endemic areas. Stat Med. 1994;13:2345–2358. - PubMed
