Patients with positive malaria tests not given artemisinin-based combination therapies: a research synthesis describing under-prescription of antimalarial medicines in Africa.


Journal

BMC medicine
ISSN: 1741-7015
Titre abrégé: BMC Med
Pays: England
ID NLM: 101190723

Informations de publication

Date de publication:
30 Jan 2020
Historique:
received: 20 05 2019
accepted: 17 12 2019
entrez: 31 1 2020
pubmed: 31 1 2020
medline: 19 3 2020
Statut: epublish

Résumé

There has been a successful push towards parasitological diagnosis of malaria in Africa, mainly with rapid diagnostic tests (mRDTs), which has reduced over-prescribing of artemisinin-based combination therapies (ACT) to malaria test-negative patients. The effect on prescribing for test-positive patients has received much less attention. Malaria infection in endemic Africa is often most dangerous for young children and those in low-transmission settings. This study examined non-prescription of antimalarials for patients with malaria infection demonstrated by positive mRDT results, and in particular these groups who are most vulnerable to poor outcomes if antimalarials are not given. Analysis of data from 562,762 patients in 8 studies co-designed as part of the ACT Consortium, conducted 2007-2013 in children and adults, in Cameroon, Ghana, Nigeria, Tanzania, and Uganda, in a variety of public and private health care sector settings, and across a range of malaria endemic zones. Of 106,039 patients with positive mRDT results (median age 6 years), 7426 (7.0%) were not prescribed an ACT antimalarial. The proportion of mRDT-positive patients not prescribed ACT ranged across sites from 1.3 to 37.1%. For patients under age 5 years, 3473/44,539 (7.8%) were not prescribed an ACT, compared with 3833/60,043 (6.4%) of those aged ≥ 5 years. The proportion of < 5-year-olds not prescribed ACT ranged up to 41.8% across sites. The odds of not being prescribed an ACT were 2-32 times higher for patients in settings with lower-transmission intensity (using test positivity as a proxy) compared to areas of higher transmission. mRDT-positive children in low-transmission settings were especially likely not to be prescribed ACT, with proportions untreated up to 70%. Of the 7426 mRDT-positive patients not prescribed an ACT, 4121 (55.5%) were prescribed other, non-recommended non-ACT antimalarial medications, and the remainder (44.5%) were prescribed no antimalarial. In eight studies of mRDT implementation in five African countries, substantial proportions of patients testing mRDT-positive were not prescribed an ACT antimalarial, and many were not prescribed an antimalarial at all. Patients most vulnerable to serious outcomes, children < 5 years and those in low-transmission settings, were most likely to not be prescribed antimalarials, and young children in low-transmission settings were least likely to be treated for malaria. This major public health risk must be addressed in training and practice. Reported in individual primary studies.

Sections du résumé

BACKGROUND BACKGROUND
There has been a successful push towards parasitological diagnosis of malaria in Africa, mainly with rapid diagnostic tests (mRDTs), which has reduced over-prescribing of artemisinin-based combination therapies (ACT) to malaria test-negative patients. The effect on prescribing for test-positive patients has received much less attention. Malaria infection in endemic Africa is often most dangerous for young children and those in low-transmission settings. This study examined non-prescription of antimalarials for patients with malaria infection demonstrated by positive mRDT results, and in particular these groups who are most vulnerable to poor outcomes if antimalarials are not given.
METHODS METHODS
Analysis of data from 562,762 patients in 8 studies co-designed as part of the ACT Consortium, conducted 2007-2013 in children and adults, in Cameroon, Ghana, Nigeria, Tanzania, and Uganda, in a variety of public and private health care sector settings, and across a range of malaria endemic zones.
RESULTS RESULTS
Of 106,039 patients with positive mRDT results (median age 6 years), 7426 (7.0%) were not prescribed an ACT antimalarial. The proportion of mRDT-positive patients not prescribed ACT ranged across sites from 1.3 to 37.1%. For patients under age 5 years, 3473/44,539 (7.8%) were not prescribed an ACT, compared with 3833/60,043 (6.4%) of those aged ≥ 5 years. The proportion of < 5-year-olds not prescribed ACT ranged up to 41.8% across sites. The odds of not being prescribed an ACT were 2-32 times higher for patients in settings with lower-transmission intensity (using test positivity as a proxy) compared to areas of higher transmission. mRDT-positive children in low-transmission settings were especially likely not to be prescribed ACT, with proportions untreated up to 70%. Of the 7426 mRDT-positive patients not prescribed an ACT, 4121 (55.5%) were prescribed other, non-recommended non-ACT antimalarial medications, and the remainder (44.5%) were prescribed no antimalarial.
CONCLUSIONS CONCLUSIONS
In eight studies of mRDT implementation in five African countries, substantial proportions of patients testing mRDT-positive were not prescribed an ACT antimalarial, and many were not prescribed an antimalarial at all. Patients most vulnerable to serious outcomes, children < 5 years and those in low-transmission settings, were most likely to not be prescribed antimalarials, and young children in low-transmission settings were least likely to be treated for malaria. This major public health risk must be addressed in training and practice.
TRIAL REGISTRATION BACKGROUND
Reported in individual primary studies.

Identifiants

pubmed: 31996199
doi: 10.1186/s12916-019-1483-6
pii: 10.1186/s12916-019-1483-6
pmc: PMC6990477
doi:

Substances chimiques

Antimalarials 0
Artemisinins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

17

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Auteurs

Shennae O'Boyle (S)

London School of Hygiene and Tropical Medicine, London, UK. shennae.oboyle@lshtm.ac.uk.

Katia J Bruxvoort (KJ)

London School of Hygiene and Tropical Medicine, London, UK.
Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, USA.

Evelyn K Ansah (EK)

Centre for Malaria Research, University of Health and Allied Sciences, Accra, Ghana.

Helen E D Burchett (HED)

London School of Hygiene and Tropical Medicine, London, UK.

Clare I R Chandler (CIR)

London School of Hygiene and Tropical Medicine, London, UK.

Siân E Clarke (SE)

London School of Hygiene and Tropical Medicine, London, UK.

Catherine Goodman (C)

London School of Hygiene and Tropical Medicine, London, UK.

Wilfred Mbacham (W)

Public Health Biotechnology, University of Yaoundé I, Yaoundé, Cameroon.

Anthony K Mbonye (AK)

Makerere University School of Public Health, Kampala, Uganda.

Obinna E Onwujekwe (OE)

Department of Pharmacology and Therapeutics, University of Nigeria, Enugu, Nigeria.

Sarah G Staedke (SG)

London School of Hygiene and Tropical Medicine, London, UK.

Virginia L Wiseman (VL)

London School of Hygiene and Tropical Medicine, London, UK.
School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia.

Christopher J M Whitty (CJM)

London School of Hygiene and Tropical Medicine, London, UK.

Heidi Hopkins (H)

London School of Hygiene and Tropical Medicine, London, UK.

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