Abstract

BackgroundEarly and accurate diagnosis of malaria followed by prompt treatment reduces the risk of severe disease in malaria endemic regions. Presumptive treatment of malaria is widely practised where microscopy or rapid diagnostic tests (RDTs) are not readily available. With the introduction of artemisinin-based combination therapy (ACT) for treatment of malaria in many low-resource settings, there is need to target treatment to patients with parasitologically confirmed malaria in order to improve quality of care, reduce over consumption of anti-malarials, reduce drug pressure and in turn delay development and spread of drug resistance. This study evaluated the effect of malaria RDTs on health workers' anti-malarial drug (AMD) prescriptions among outpatients at low level health care facilities (LLHCF) within different malaria epidemiological settings in Uganda.MethodsAll health workers (HWs) in 21 selected intervention (where RDTs were deployed) LLHF were invited for training on the use RDTs. All HWs were trained to use RDTs for parasitological diagnosis of all suspected malaria cases irrespective of age. Five LLHCFs with clinical diagnosis (CD only) were included for comparison. Subsequently AMD prescriptions were compared using both a 'pre - post' and 'intervention - control' analysis designs. In-depth interviews of the HWs were conducted to explore any factors that influence AMD prescription practices.ResultsA total of 166,131 out-patient attendances (OPD) were evaluated at 21 intervention LLHCFs. Overall use of RDTs resulted in a 38% point reduction in AMD prescriptions. There was a two-fold reduction (RR 0.62, 95% CI 0.55-0.70) in AMD prescription with the greatest reduction in the hypo-endemic setting (RR 0.46 95% CI 0.51-0.53) but no significant change in the urban setting (RR1.01, p-value = 0.820). Over 90% of all eligible OPD patients were offered a test. An average of 30% (range 25%-35%) of the RDT-negative fever patients received AMD prescriptions. When the test result was negative, children under five years of age were two to three times more likely (OR 2.6 p-value <0.001) to receive anti-malarial prescriptions relative to older age group. Of the 63 HWs interviewed 92% believed that a positive RDT result confirmed malaria, while only 49% believed that a negative RDT result excluded malaria infection.ConclusionUse of RDTs resulted in a 2-fold reduction in anti-malarial drug prescription at LLHCFs. The study demonstrated that RDT use is feasible at LLHCFs, and can lead to better targetting of malaria treatment. Nationwide deployment of RDTs in a systematic manner should be prioritised in order to improve fever case management. The process should include plans to educate HWs about the utility of RDTs in order to maximize acceptance and uptake of the diagnostic tools and thereby leading to the benefits of parasitological diagnosis of malaria.

Highlights

  • And accurate diagnosis of malaria followed by prompt treatment reduces the risk of severe disease in malaria endemic regions

  • Descriptive characteristics of health facilities Embedded in the phased implementation of rapid diagnostic tests (RDTs) use at level health care facilities (LLHCF) in Uganda, the evaluation was conducted in 26 health facilities between March and December 2007

  • The highest drop was in the hypo-endemic malaria transmission settings with a twofold reduction in the anti-malarial drug (AMD) prescriptions

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Summary

Introduction

And accurate diagnosis of malaria followed by prompt treatment reduces the risk of severe disease in malaria endemic regions. With the introduction of artemisinin-based combination therapy (ACT) for treatment of malaria in many low-resource settings, there is need to target treatment to patients with parasitologically confirmed malaria in order to improve quality of care, reduce over consumption of anti-malarials, reduce drug pressure and in turn delay development and spread of drug resistance. Presumptive treatment of fever with anti-malarials is widely practised to reduce malariaattributable morbidity and mortality especially at lower level health facilities where microscopy is not readily available [1,2,3]. With the current malaria treatment policy of using artemisinin-based combination therapy (ACT) as firstline therapy for malaria in many African countries, there is increasing need to confirm malaria before therapy in order to limit overuse of ACT, reduce programme costs of anti-malarials, reduce drug pressure and delay emergence of resistance against ACT [5]. There is need for a paradigm shift by clinicians in order to overcome reliance on clinical diagnosis and treatment of malaria and actively consider alternative causes of febrile illnesses

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