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      Trends and predictive factors for treatment failure following artemisinin-based combination therapy among children with uncomplicated malaria in Ghana: 2005–2018

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          Abstract

          Background

          Since the introduction of artemisinin-based combination therapy (ACT) in Ghana in 2005 there has been a surveillance system by the National Malaria Control Programme (NMCP) and the University of Ghana Noguchi Memorial Institute for Medical Research (UG-NMIMR) to monitor the therapeutic efficacy of ACTs for the treatment of uncomplicated malaria in the country. We report trends and determinants of failure following treatment of Ghanaian children with artesunate-amodiaquine (ASAQ) and artemether-lumefantrine (AL) combinations.

          Methods

          Per protocol analyses as well as cumulative incidence of day 28 treatment failure from Kaplan Meier survival analyses were used to describe trends of failure over the surveillance period of 2005–2018. Univariable and multivariable cox regression analyses were used to assess the determinants of treatment failure over the period.

          Results

          Day 28 PCR-corrected failure, following treatment with ASAQ, significantly increased from 0.0% in 2005 to 2.0% (95% CI: 1.1–3.6) in 2015 (p = 0.013) but significantly decreased to 0.4% (95% CI: 0.1–1.6) in 2018 (p = 0.039). Failure, following treatment with AL, decreased from 4.5% (95% CI: 2.0–9.4) in 2010 to 2.7% (95% CI: 1.4–5.1) in 2018, though not statistically significant (p = 0.426). Risk of treatment failure, from multivariable cox regression analyses, was significantly lower among children receiving ASAQ compared with those receiving AL (HR = 0.24; 95% CI: 0.11–0.53; p < 0.001); lower among children with no parasitaemia on day 3 compared with those with parasitaemia on day 3 (HR = 0.02; 95% CI: 0.01–0.13; p < 0.001); and higher among children who received ASAQ and had axillary temperature ≥ 37.5 °C on day 1 compared with those with axillary temperature < 37.5 °C (HR = 3.96; 95% CI: 1.61–9.75; p = 0.003).

          Conclusions

          Treatment failures for both ASAQ and AL have remained less than 5% (below WHO’s threshold of 10%) in Ghana since 2005. Predictors of treatment failure that need to be considered in the management of uncomplicated malaria in the country should include type of ACT, day 3 parasitaemia, and day 1 axillary temperature of patients being treated.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12879-021-06961-4.

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          Most cited references31

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          Discovery, mechanisms of action and combination therapy of artemisinin.

          Despite great international efforts, malaria still inflicts an enormous toll on human lives, especially in Africa. Throughout history, antimalarial medicines have been one of the most powerful tools in malaria control. However, the acquisition and spread of parasite strains that are resistant to multiple antimalarial drugs have become one of the greatest challenges to malaria treatment, and are associated with the increase in morbidity and mortality in many malaria-endemic countries. To deal with this grave situation, artemisinin-based combinatory therapies (ACTs) have been introduced and widely deployed in malarious regions. Artemisinin is a new class of antimalarial compounds discovered by Chinese scientists from the sweet wormwood Artemisia annua. The potential development of resistance to artemisinins by Plasmodium falciparum threatens the usable lifespan of ACTs, and therefore is a subject of close surveillance and extensive research. Studies at the Thai-Cambodian border, a historical epicenter of multidrug resistance, have detected reduced susceptibility to artemisinins as manifested by prolonged parasite-clearance times, raising considerable concerns on resistance development. Despite this significance, there is still controversy on the mode of action of artemisinins. Although a number of potential cellular targets of artemisinins have been proposed, they remain to be verified experimentally. Here, we review the history of artemisinin discovery, discuss the mode of action and potential drug targets, and present strategies to elucidate resistance mechanisms.
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            History of the discovery of the malaria parasites and their vectors

            Malaria is caused by infection with protozoan parasites belonging to the genus Plasmodium transmitted by female Anopheles species mosquitoes. Our understanding of the malaria parasites begins in 1880 with the discovery of the parasites in the blood of malaria patients by Alphonse Laveran. The sexual stages in the blood were discovered by William MacCallum in birds infected with a related haematozoan, Haemoproteus columbae, in 1897 and the whole of the transmission cycle in culicine mosquitoes and birds infected with Plasmodium relictum was elucidated by Ronald Ross in 1897. In 1898 the Italian malariologists, Giovanni Battista Grassi, Amico Bignami, Giuseppe Bastianelli, Angelo Celli, Camillo Golgi and Ettore Marchiafava demonstrated conclusively that human malaria was also transmitted by mosquitoes, in this case anophelines. The discovery that malaria parasites developed in the liver before entering the blood stream was made by Henry Shortt and Cyril Garnham in 1948 and the final stage in the life cycle, the presence of dormant stages in the liver, was conclusively demonstrated in 1982 by Wojciech Krotoski. This article traces the main events and stresses the importance of comparative studies in that, apart from the initial discovery of parasites in the blood, every subsequent discovery has been based on studies on non-human malaria parasites and related organisms.
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              Guidelines for the treatment of malaria

              (2015)
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                Author and article information

                Contributors
                babuaku@noguchi.ug.edu.gh
                nduah@noguchi.ug.edu.gh
                nquashie@noguchi.ug.edu.gh
                akosua.gyasi@yahoo.com
                patriciaopokuafriyie@gmail.com
                owusuantwif@who.int
                aghansah@noguchi.ug.edu.gh
                keziah.malm@ghsmail.org
                conmarfouk@yahoo.co.uk
                kkoram@noguchi.ug.edu.gh
                Journal
                BMC Infect Dis
                BMC Infect Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                15 December 2021
                15 December 2021
                2021
                : 21
                : 1255
                Affiliations
                [1 ]GRID grid.8652.9, ISNI 0000 0004 1937 1485, Department of Epidemiology, Noguchi Memorial Institute for Medical Research, , University of Ghana, ; Legon, Accra, Ghana
                [2 ]GRID grid.8652.9, ISNI 0000 0004 1937 1485, Centre for Tropical Clinical Pharmacology and Therapeutics, , University of Ghana Medical School, ; Accra, Ghana
                [3 ]GRID grid.434994.7, ISNI 0000 0001 0582 2706, National Malaria Control Programme, Public Health Division, Ghana Health Service, ; Accra, Ghana
                [4 ]World Health Organization, Country Office, Accra, Ghana
                [5 ]GRID grid.8652.9, ISNI 0000 0004 1937 1485, Department of Parasitology, Noguchi Memorial Institute for Medical Research, , University of Ghana, ; Legon, Accra, Ghana
                Author information
                http://orcid.org/0000-0002-1840-6979
                http://orcid.org/0000-0001-8819-1793
                http://orcid.org/0000-0002-2538-0324
                http://orcid.org/0000-0002-2250-0511
                http://orcid.org/0000-0003-4639-1249
                http://orcid.org/0000-0003-4274-6516
                Article
                6961
                10.1186/s12879-021-06961-4
                8672499
                34911501
                24748ed9-aa42-4ccf-8a09-e6f35c82bfd4
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 5 August 2021
                : 8 December 2021
                Categories
                Research
                Custom metadata
                © The Author(s) 2021

                Infectious disease & Microbiology
                trends,predictive factors,acts,treatment failure,ghana
                Infectious disease & Microbiology
                trends, predictive factors, acts, treatment failure, ghana

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