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Qualitative Study of Presumptive Treatment of Childhood Malaria in Third Tier Tertiary Hospitals in Southeast Nigeria: a Focus Group and In-depth Study

Overview
Journal Malar J
Publisher Biomed Central
Specialty Tropical Medicine
Date 2013 Dec 3
PMID 24289161
Citations 8
Authors
Affiliations
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Abstract

Background: Presumptive treatment of childhood-malaria (PTCM) is common in Nigeria. Delayed laboratory result is blamed, with little attention on patients' and providers' roles. This study aimed to determine patient, provider and laboratory attributes that sustain PTCM in Nigeria.

Methods: Data collection was from focus-group discussions for parents/guardians, and in-depth interviews involving providers and laboratory scientists in two tertiary hospitals.

Results: All parents/guardians agreed to a malaria test. Majority accepted to come back later for full treatment, provided that some treatment was commenced. Majority affirmed that their interests are on their children's improvement.The providers practice presumptive treatment of childhood malaria, for the following reasons: (1) malaria is endemic and should be suspected and treated; (2) microscopy takes two days to be available and parents want immediate treatment for their children, thus delay may lead to self-medication; (3) relying on results for decision to treat creates an impression of incompetence; (4) rapid diagnostic test kits (RDTs) are not available in the consulting rooms and there is doubt about their reliability; (5) patients have already wasted time before being reviewed, so wasting more time on investigation is not advisable; (6) withhold of malaria treatment may be feasible in suspected uncomplicated malaria, but if severe, then anti-malarial treatment has to start immediately.Interviews of laboratory scientists showed that (1) malaria microscopy test cannot be urgent; it is done in batches and takes 24 hours to be ready; (2) a request of malaria test with other investigations on the same form, contributes to the delay; (3) RDTs are unavailable in the facilities.

Conclusions: Provision of RDTs is the only feasible means to treatment of confirmed malaria at the time healthcare providers review a patient on day zero. In facilities that depend on microscopy; a common practice in resource poor countries, healthcare providers can depend on parental willingness to return later for full medication, to commence adjunctive care with antipyretics and multivitamins for uncomplicated malaria. In complicated malaria, supportive care - intravenous fluids, blood transfusion, oxygen therapy - can be commenced while awaiting the inclusion of anti-malarial drugs when the diagnosis of malaria is confirmed.

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References
1.
Prudhomme OMeara W, Mangeni J, Steketee R, Greenwood B . Changes in the burden of malaria in sub-Saharan Africa. Lancet Infect Dis. 2010; 10(8):545-55. DOI: 10.1016/S1473-3099(10)70096-7. View

2.
Reyburn H, Mbakilwa H, Mwangi R, Mwerinde O, Olomi R, Drakeley C . Rapid diagnostic tests compared with malaria microscopy for guiding outpatient treatment of febrile illness in Tanzania: randomised trial. BMJ. 2007; 334(7590):403. PMC: 1804187. DOI: 10.1136/bmj.39073.496829.AE. View

3.
Guerra C, Gikandi P, Tatem A, Noor A, Smith D, Hay S . The limits and intensity of Plasmodium falciparum transmission: implications for malaria control and elimination worldwide. PLoS Med. 2008; 5(2):e38. PMC: 2253602. DOI: 10.1371/journal.pmed.0050038. View

4.
Rolland E, Checchi F, Pinoges L, Balkan S, Guthmann J, Guerin P . Operational response to malaria epidemics: are rapid diagnostic tests cost-effective?. Trop Med Int Health. 2006; 11(4):398-408. DOI: 10.1111/j.1365-3156.2006.01580.x. View

5.
Fawole O, Onadeko M . Knowledge and home management of malaria fever by mothers and care givers of under five children. West Afr J Med. 2002; 20(2):152-7. View