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Efficacy of quinine, artemether-lumefantrine and dihydroartemisinin-piperaquine as rescue treatment for uncomplicated malaria in Ugandan children
The treatment of falciparum malaria poses unique challenges in settings where malaria transmission intensity is high because recurrent infections are common. These could be new infections, recrudescences, or a combination of the two. Though several African countries continue to use quinine as the se...
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Published in: | PloS one 2013-01, Vol.8 (1), p.e53772 |
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description | The treatment of falciparum malaria poses unique challenges in settings where malaria transmission intensity is high because recurrent infections are common. These could be new infections, recrudescences, or a combination of the two. Though several African countries continue to use quinine as the second line treatment for patients with recurrent infections, there is little information on its efficacy when used for rescue therapy. Moreover, such practice goes against the World Health Organisation (WHO) recommendation to use combination therapy for uncomplicated malaria.
We conducted a nested, randomized, open label, three-arm clinical trial of rescue therapy in children 6-59 months old with recurrent malaria infection during 28 days post treatment with artemisinin combination treatment (ACT). Patients were randomly assigned to receive either quinine, artemether-lumefantrine (AL) or dihydroartemisinin-piperaquine (DHAPQ), and actively followed up for 28 days.
Among 220 patients enrolled, 217 (98·6%) were assigned an efficacy outcome and 218 (99·1%) were assessed for safety. The risk of recurrent infection was significantly higher in patients treated with quinine (70%, 74/110, HR = 3·9; 95% CI: 2·4-6·7, p |
doi_str_mv | 10.1371/journal.pone.0053772 |
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We conducted a nested, randomized, open label, three-arm clinical trial of rescue therapy in children 6-59 months old with recurrent malaria infection during 28 days post treatment with artemisinin combination treatment (ACT). Patients were randomly assigned to receive either quinine, artemether-lumefantrine (AL) or dihydroartemisinin-piperaquine (DHAPQ), and actively followed up for 28 days.
Among 220 patients enrolled, 217 (98·6%) were assigned an efficacy outcome and 218 (99·1%) were assessed for safety. The risk of recurrent infection was significantly higher in patients treated with quinine (70%, 74/110, HR = 3·9; 95% CI: 2·4-6·7, p<0·0001) and AL (60%, 21/35, HR = 3·3; 95% CI: 1·8-6·3, p<0·0002), compared to DHAPQ (25%, 18/72). Recrudescence tended to be lower in the DHAPQ (1%, 1/72) than in the quinine (7%, 8/110) or AL (6%, 2/35) group, though it was not statistically significant. No serious adverse events were reported.
Recurrent infections observed after the administration of an ACT can be successfully treated with an alternative ACT rather than with quinine.
Current Controlled Trials ISRCTN99046537.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0053772</identifier><identifier>PMID: 23349741</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Antimalarials - adverse effects ; Antimalarials - therapeutic use ; Artemether ; Artemisinin ; Artemisinins - adverse effects ; Artemisinins - therapeutic use ; Biology ; Child, Preschool ; Children ; Clinical trials ; Dihydroartemisinin ; Disease transmission ; Drug therapy ; Effectiveness ; Ethanolamines - adverse effects ; Ethanolamines - therapeutic use ; Fluorenes - adverse effects ; Fluorenes - therapeutic use ; Health risks ; Humans ; Infant ; Infection ; Infections ; Malaria ; Malaria, Falciparum - drug therapy ; Male ; Medical law ; Medicine ; Patients ; Plasmodium falciparum ; Quinine ; Quinine - adverse effects ; Quinine - therapeutic use ; Quinolines - adverse effects ; Quinolines - therapeutic use ; Recurrent infection ; Safety ; Statistical analysis ; Surveillance ; Therapy ; Treatment Outcome ; Uganda ; Vector-borne diseases</subject><ispartof>PloS one, 2013-01, Vol.8 (1), p.e53772</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Yeka et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2013 Yeka et al 2013 Yeka et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-2a52f13861467f33c7f8feac440c3967cfa697ca7018971df27caaa92d464d7b3</citedby><cites>FETCH-LOGICAL-c758t-2a52f13861467f33c7f8feac440c3967cfa697ca7018971df27caaa92d464d7b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1327798801/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1327798801?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23349741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Gosling, Roly D.</contributor><creatorcontrib>Yeka, Adoke</creatorcontrib><creatorcontrib>Tibenderana, James</creatorcontrib><creatorcontrib>Achan, Jane</creatorcontrib><creatorcontrib>D'Alessandro, Umberto</creatorcontrib><creatorcontrib>Talisuna, Ambrose O</creatorcontrib><title>Efficacy of quinine, artemether-lumefantrine and dihydroartemisinin-piperaquine as rescue treatment for uncomplicated malaria in Ugandan children</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The treatment of falciparum malaria poses unique challenges in settings where malaria transmission intensity is high because recurrent infections are common. These could be new infections, recrudescences, or a combination of the two. Though several African countries continue to use quinine as the second line treatment for patients with recurrent infections, there is little information on its efficacy when used for rescue therapy. Moreover, such practice goes against the World Health Organisation (WHO) recommendation to use combination therapy for uncomplicated malaria.
We conducted a nested, randomized, open label, three-arm clinical trial of rescue therapy in children 6-59 months old with recurrent malaria infection during 28 days post treatment with artemisinin combination treatment (ACT). Patients were randomly assigned to receive either quinine, artemether-lumefantrine (AL) or dihydroartemisinin-piperaquine (DHAPQ), and actively followed up for 28 days.
Among 220 patients enrolled, 217 (98·6%) were assigned an efficacy outcome and 218 (99·1%) were assessed for safety. The risk of recurrent infection was significantly higher in patients treated with quinine (70%, 74/110, HR = 3·9; 95% CI: 2·4-6·7, p<0·0001) and AL (60%, 21/35, HR = 3·3; 95% CI: 1·8-6·3, p<0·0002), compared to DHAPQ (25%, 18/72). Recrudescence tended to be lower in the DHAPQ (1%, 1/72) than in the quinine (7%, 8/110) or AL (6%, 2/35) group, though it was not statistically significant. No serious adverse events were reported.
Recurrent infections observed after the administration of an ACT can be successfully treated with an alternative ACT rather than with quinine.
Current Controlled Trials ISRCTN99046537.</description><subject>Antimalarials - adverse effects</subject><subject>Antimalarials - therapeutic use</subject><subject>Artemether</subject><subject>Artemisinin</subject><subject>Artemisinins - adverse effects</subject><subject>Artemisinins - therapeutic use</subject><subject>Biology</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Clinical trials</subject><subject>Dihydroartemisinin</subject><subject>Disease transmission</subject><subject>Drug therapy</subject><subject>Effectiveness</subject><subject>Ethanolamines - adverse effects</subject><subject>Ethanolamines - therapeutic use</subject><subject>Fluorenes - adverse effects</subject><subject>Fluorenes - therapeutic use</subject><subject>Health risks</subject><subject>Humans</subject><subject>Infant</subject><subject>Infection</subject><subject>Infections</subject><subject>Malaria</subject><subject>Malaria, Falciparum - drug therapy</subject><subject>Male</subject><subject>Medical law</subject><subject>Medicine</subject><subject>Patients</subject><subject>Plasmodium falciparum</subject><subject>Quinine</subject><subject>Quinine - adverse effects</subject><subject>Quinine - therapeutic use</subject><subject>Quinolines - adverse effects</subject><subject>Quinolines - therapeutic use</subject><subject>Recurrent infection</subject><subject>Safety</subject><subject>Statistical analysis</subject><subject>Surveillance</subject><subject>Therapy</subject><subject>Treatment Outcome</subject><subject>Uganda</subject><subject>Vector-borne diseases</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk9-K1DAUxoso7rr6BqIBQRDs2DRp094Iy7LqwMKCut6G0_yZydAms0kqzmP4xmZ2ussUFKQXbZPf953kS06WvcTFAhOGP2zc6C30i62zalEUFWGsfJSd4paUeV0W5PHR90n2LITNHmrq-ml2UhJCW0bxafb7UmsjQOyQ0-h2NNZY9R6Bj2pQca183o-D0mCjTxMIrETSrHfSuzvEhL0g35qt8rBXJyQgr4IYFYpeQRyUjUg7j0Yr3LDtU62oJBqgB28AGYtuVskVLBJr00uv7PPsiYY-qBfT-yy7-XT5_eJLfnX9eXlxfpULVjUxL6EqNU77wbRmmhDBdKMVCEoLQdqaCQ11ywSwAjctw1KX6QegLSWtqWQdOcteH3y3vQt8SjNwTErG2qYpcCKWB0I62PCtNwP4HXdg-N2A8yueUjCiV1y2VScww0A7RqGSqbKmXStl1zVpoXXy-jhVG7tBSZFi8dDPTOcz1qz5yv3kpKpw2k4yeDMZeHc7qhD_seSJWkFalbHaJTORzknwc8oaXDNM20Qt_kKlR6YjFek-aZPGZ4J3M0FiovoVVzCGwJffvv4_e_1jzr49YtcK-rgOrh-jcTbMQXoAhXcheKUfksMF37fDfRp83w58aocke3Wc-oPo_v6TP46gCcM</recordid><startdate>20130122</startdate><enddate>20130122</enddate><creator>Yeka, Adoke</creator><creator>Tibenderana, James</creator><creator>Achan, Jane</creator><creator>D'Alessandro, Umberto</creator><creator>Talisuna, Ambrose O</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130122</creationdate><title>Efficacy of quinine, artemether-lumefantrine and dihydroartemisinin-piperaquine as rescue treatment for uncomplicated malaria in Ugandan children</title><author>Yeka, Adoke ; Tibenderana, James ; Achan, Jane ; D'Alessandro, Umberto ; Talisuna, Ambrose O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-2a52f13861467f33c7f8feac440c3967cfa697ca7018971df27caaa92d464d7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antimalarials - 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These could be new infections, recrudescences, or a combination of the two. Though several African countries continue to use quinine as the second line treatment for patients with recurrent infections, there is little information on its efficacy when used for rescue therapy. Moreover, such practice goes against the World Health Organisation (WHO) recommendation to use combination therapy for uncomplicated malaria.
We conducted a nested, randomized, open label, three-arm clinical trial of rescue therapy in children 6-59 months old with recurrent malaria infection during 28 days post treatment with artemisinin combination treatment (ACT). Patients were randomly assigned to receive either quinine, artemether-lumefantrine (AL) or dihydroartemisinin-piperaquine (DHAPQ), and actively followed up for 28 days.
Among 220 patients enrolled, 217 (98·6%) were assigned an efficacy outcome and 218 (99·1%) were assessed for safety. The risk of recurrent infection was significantly higher in patients treated with quinine (70%, 74/110, HR = 3·9; 95% CI: 2·4-6·7, p<0·0001) and AL (60%, 21/35, HR = 3·3; 95% CI: 1·8-6·3, p<0·0002), compared to DHAPQ (25%, 18/72). Recrudescence tended to be lower in the DHAPQ (1%, 1/72) than in the quinine (7%, 8/110) or AL (6%, 2/35) group, though it was not statistically significant. No serious adverse events were reported.
Recurrent infections observed after the administration of an ACT can be successfully treated with an alternative ACT rather than with quinine.
Current Controlled Trials ISRCTN99046537.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23349741</pmid><doi>10.1371/journal.pone.0053772</doi><tpages>e53772</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antimalarials - adverse effects Antimalarials - therapeutic use Artemether Artemisinin Artemisinins - adverse effects Artemisinins - therapeutic use Biology Child, Preschool Children Clinical trials Dihydroartemisinin Disease transmission Drug therapy Effectiveness Ethanolamines - adverse effects Ethanolamines - therapeutic use Fluorenes - adverse effects Fluorenes - therapeutic use Health risks Humans Infant Infection Infections Malaria Malaria, Falciparum - drug therapy Male Medical law Medicine Patients Plasmodium falciparum Quinine Quinine - adverse effects Quinine - therapeutic use Quinolines - adverse effects Quinolines - therapeutic use Recurrent infection Safety Statistical analysis Surveillance Therapy Treatment Outcome Uganda Vector-borne diseases |
title | Efficacy of quinine, artemether-lumefantrine and dihydroartemisinin-piperaquine as rescue treatment for uncomplicated malaria in Ugandan children |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T11%3A57%3A58IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficacy%20of%20quinine,%20artemether-lumefantrine%20and%20dihydroartemisinin-piperaquine%20as%20rescue%20treatment%20for%20uncomplicated%20malaria%20in%20Ugandan%20children&rft.jtitle=PloS%20one&rft.au=Yeka,%20Adoke&rft.date=2013-01-22&rft.volume=8&rft.issue=1&rft.spage=e53772&rft.pages=e53772-&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0053772&rft_dat=%3Cgale_plos_%3EA478167149%3C/gale_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c758t-2a52f13861467f33c7f8feac440c3967cfa697ca7018971df27caaa92d464d7b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1327798801&rft_id=info:pmid/23349741&rft_galeid=A478167149&rfr_iscdi=true |