Literature DB >> 16227917

[Evaluating malaria attributable morbidity in endemic areas].

C Rogier1, T Fusaï, B Pradines, J-F Trape.   

Abstract

There are no specific clinical signs or symptoms of malaria. Fever attacks, anemia, or signs of severity like coma or respiratory distress cannot easily be attributed to malaria in people who are infected most of the time. Ascribing clinical manifestations to malaria is problematic in populations that are regularly exposed to the transmission of human plasmodia. The more transmission is intense and regular, the higher the prevalence of asymptomatic infections. In areas of intense and perennial malaria transmission, more than 90% of the population may be infected and the simple detection of a plasmodial infection is not enough to attribute clinical manifestations to malaria. Naturally acquired anti-malaria immunity permitting asymptomatic infections is incomplete and temporary. It is an obstacle to the estimation of the malaria burden in endemic areas. The positive association between parasite density and fever allows the attribution of clinical attacks to malaria. The relationship between parasitaemia and the risk of fever is not continuous. An age- and endemicity-dependent threshold effect of parasite density has been demonstrated and can be used to distinguish clinical attacks due to malaria from others. Clinical diagnosis and evaluation of malaria are problematic in three situations: in public health to estimate the malaria burden for health services, in clinical research to evaluate treatments or prophylactic measures (drug, vaccine, anti-vectorial devices), and in basic research on pathophysiology, immunology or genetic susceptibility to clinical malaria. No one diagnostic definition nor procedure for detecting cases is adequate for all three purposes. Case detection may be passive (in health structures for example) or active (in population). The choice of methods for diagnosis and recruitment depends on the objectives and whether a "pragmatic" or "explicative" approach is used. The radical differences between these approaches are often unsuspected or ignored.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16227917     DOI: 10.1016/s0398-7620(05)84607-3

Source DB:  PubMed          Journal:  Rev Epidemiol Sante Publique        ISSN: 0398-7620            Impact factor:   1.019


  4 in total

1.  Usefulness of clinical algorithm as screening process to detected malaria in low-to-moderate transmission areas of scarce health related resources.

Authors:  André R S Périssé; G Thomas Strickland
Journal:  Acta Trop       Date:  2008-05-24       Impact factor: 3.112

2.  Co-circulation of Plasmodium and Bacterial DNAs in Blood of Febrile and Afebrile Children from Urban and Rural Areas in Gabon.

Authors:  Gaël Mourembou; Sydney Maghendji Nzondo; Angélique Ndjoyi-Mbiguino; Jean Bernard Lekana-Douki; Lady Charlène Kouna; Pierre Blaise Matsiegui; Rella Zoleko Manego; Irene Pegha Moukandja; Alpha Kabinet Keïta; Hervé Tissot-Dupont; Florence Fenollar; Didier Raoult
Journal:  Am J Trop Med Hyg       Date:  2016-04-25       Impact factor: 2.345

3.  Pattern of the Antimalarials Prescription during Pregnancy in Bangui, Central African Republic.

Authors:  Alexandre Manirakiza; Georges Soula; Remi Laganier; Elise Klement; Djibrine Djallé; Moyen Methode; Nestor Madji; Luc Salva Heredeïbona; Alain Le Faou; Jean Delmont
Journal:  Malar Res Treat       Date:  2011-07-15

4.  Space-time clustering of childhood malaria at the household level: a dynamic cohort in a Mali village.

Authors:  Jean Gaudart; Belco Poudiougou; Alassane Dicko; Stéphane Ranque; Ousmane Toure; Issaka Sagara; Mouctar Diallo; Sory Diawara; Amed Ouattara; Mahamadou Diakite; Ogobara K Doumbo
Journal:  BMC Public Health       Date:  2006-11-21       Impact factor: 3.295

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.