Impact of Intermittent Mass Testing and Treatment on Incidence of Malaria Infection in a High Transmission Area of Western Kenya

Progress with malaria control in western Kenya has stagnated since 2007. Additional interventions to reduce the high burden of malaria in this region are urgently needed. We conducted a two-arm, community-based, cluster-randomized, controlled trial of active case detection and treatment of malaria i...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The American journal of tropical medicine and hygiene 2020-07, Vol.103 (1), p.369-377
Hauptverfasser: Desai, Meghna R, Samuels, Aaron M, Odongo, Wycliffe, Williamson, John, Odero, Nobert Awino, Otieno, Kephas, Shi, Ya Ping, Kachur, Stephen Patrick, Hamel, Mary J, Kariuki, Simon, Lindblade, Kim A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 377
container_issue 1
container_start_page 369
container_title The American journal of tropical medicine and hygiene
container_volume 103
creator Desai, Meghna R
Samuels, Aaron M
Odongo, Wycliffe
Williamson, John
Odero, Nobert Awino
Otieno, Kephas
Shi, Ya Ping
Kachur, Stephen Patrick
Hamel, Mary J
Kariuki, Simon
Lindblade, Kim A
description Progress with malaria control in western Kenya has stagnated since 2007. Additional interventions to reduce the high burden of malaria in this region are urgently needed. We conducted a two-arm, community-based, cluster-randomized, controlled trial of active case detection and treatment of malaria infections in all residents mass testing and treatment (MTaT) of 10 village clusters (intervention clusters) for two consecutive years to measure differences in the incidence of clinical malaria disease and malaria infections compared with 20 control clusters where MTaT was not implemented. All residents of intervention clusters, irrespective of history of fever or other malaria-related symptoms, were tested three times per year before the peak malaria season using malaria rapid diagnostic tests. All positive cases were treated with dihydroartemisinin-piperaquine. The incidence of clinical malaria was measured through passive surveillance, whereas the cumulative incidence of malaria infection was measured using active surveillance in a cohort comprising randomly selected residents. The incidence of clinical malaria was 0.19 cases/person-year (p-y, 95% CI: 0.13-0.28) in the intervention arm and 0.24 cases/p-y (95% CI: 0.15-0.39) in the control arm (incidence rate ratio [IRR] 0.79, 95% CI: 0.61-1.02). The cumulative incidence of malaria infections was similar between the intervention (2.08 infections/p-y, 95% CI: 1.93-2.26) and control arms (2.19 infections/p-y, 95% CI: 2.02-2.37) with a crude IRR of 0.95 (95% CI: 0.87-1.04). Six rounds of MTaT over 2 years did not have a significant impact on the incidence of clinical malaria or the cumulative incidence of malaria infection in this area of high malaria transmission.
doi_str_mv 10.4269/ajtmh.19-0735
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7356446</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2424117052</sourcerecordid><originalsourceid>FETCH-LOGICAL-c415t-812a88f6b26d647afb8f56daf84db0083e0ad22b9912d82a909d43437db3cd2c3</originalsourceid><addsrcrecordid>eNpdkc9rFDEUx4Modq0evUrAi5ep-TWZ5CKUonaxxcuKx_AmyexmmcmsSbbQW__0Zmwt6inw3uf7Jd_3RegtJWeCSf0R9mXanVHdkI63z9CKik42VIr2OVoRQlijJe9O0Kuc94RQxSh9iU4444IpIVfobj0dwBY8D3gdi09TKMXHgq8hZ7zxuYS4xRAd3iQPZVpWc6yoDc5H6xfdNYyQAtTh4G0JdR0iBnwZtruqgpinkPMyPq8Wi-BntfUp4m8-3sJr9GKAMfs3j-8p-vHl8-bisrn6_nV9cX7VWEHb0ijKQKlB9kw6KToYejW00sGghOsJUdwTcIz1WlPmFANNtBNc8M713Dpm-Sn69OB7OPaTd7YmSTCaQwoTpFszQzD_bmLYme18Y-pZpRCyGnx4NEjzr2ONYGou68cRop-P2TCuW0llJ3VF3_-H7udjijWeYYIJSjvSsko1D5RNc87JD0-focQs3Zrf3RqqzdJt5d_9neCJ_lMmvwdA3KH9</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2424117052</pqid></control><display><type>article</type><title>Impact of Intermittent Mass Testing and Treatment on Incidence of Malaria Infection in a High Transmission Area of Western Kenya</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Desai, Meghna R ; Samuels, Aaron M ; Odongo, Wycliffe ; Williamson, John ; Odero, Nobert Awino ; Otieno, Kephas ; Shi, Ya Ping ; Kachur, Stephen Patrick ; Hamel, Mary J ; Kariuki, Simon ; Lindblade, Kim A</creator><creatorcontrib>Desai, Meghna R ; Samuels, Aaron M ; Odongo, Wycliffe ; Williamson, John ; Odero, Nobert Awino ; Otieno, Kephas ; Shi, Ya Ping ; Kachur, Stephen Patrick ; Hamel, Mary J ; Kariuki, Simon ; Lindblade, Kim A</creatorcontrib><description>Progress with malaria control in western Kenya has stagnated since 2007. Additional interventions to reduce the high burden of malaria in this region are urgently needed. We conducted a two-arm, community-based, cluster-randomized, controlled trial of active case detection and treatment of malaria infections in all residents mass testing and treatment (MTaT) of 10 village clusters (intervention clusters) for two consecutive years to measure differences in the incidence of clinical malaria disease and malaria infections compared with 20 control clusters where MTaT was not implemented. All residents of intervention clusters, irrespective of history of fever or other malaria-related symptoms, were tested three times per year before the peak malaria season using malaria rapid diagnostic tests. All positive cases were treated with dihydroartemisinin-piperaquine. The incidence of clinical malaria was measured through passive surveillance, whereas the cumulative incidence of malaria infection was measured using active surveillance in a cohort comprising randomly selected residents. The incidence of clinical malaria was 0.19 cases/person-year (p-y, 95% CI: 0.13-0.28) in the intervention arm and 0.24 cases/p-y (95% CI: 0.15-0.39) in the control arm (incidence rate ratio [IRR] 0.79, 95% CI: 0.61-1.02). The cumulative incidence of malaria infections was similar between the intervention (2.08 infections/p-y, 95% CI: 1.93-2.26) and control arms (2.19 infections/p-y, 95% CI: 2.02-2.37) with a crude IRR of 0.95 (95% CI: 0.87-1.04). Six rounds of MTaT over 2 years did not have a significant impact on the incidence of clinical malaria or the cumulative incidence of malaria infection in this area of high malaria transmission.</description><identifier>ISSN: 0002-9637</identifier><identifier>ISSN: 1476-1645</identifier><identifier>EISSN: 1476-1645</identifier><identifier>DOI: 10.4269/ajtmh.19-0735</identifier><identifier>PMID: 32342846</identifier><language>eng</language><publisher>United States: Institute of Tropical Medicine</publisher><subject>Adolescent ; Antimalarials - therapeutic use ; Artemisinins - therapeutic use ; Child ; Child, Preschool ; Female ; Health surveillance ; Humans ; Incidence ; Infections ; Intervention ; Kenya - epidemiology ; Malaria ; Malaria, Falciparum - diagnosis ; Malaria, Falciparum - drug therapy ; Malaria, Falciparum - epidemiology ; Malaria, Falciparum - transmission ; Male ; Mass Screening - methods ; Quinolines - therapeutic use</subject><ispartof>The American journal of tropical medicine and hygiene, 2020-07, Vol.103 (1), p.369-377</ispartof><rights>Copyright Institute of Tropical Medicine Jul 2020</rights><rights>The American Society of Tropical Medicine and Hygiene 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-812a88f6b26d647afb8f56daf84db0083e0ad22b9912d82a909d43437db3cd2c3</citedby><cites>FETCH-LOGICAL-c415t-812a88f6b26d647afb8f56daf84db0083e0ad22b9912d82a909d43437db3cd2c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356446/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7356446/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32342846$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Desai, Meghna R</creatorcontrib><creatorcontrib>Samuels, Aaron M</creatorcontrib><creatorcontrib>Odongo, Wycliffe</creatorcontrib><creatorcontrib>Williamson, John</creatorcontrib><creatorcontrib>Odero, Nobert Awino</creatorcontrib><creatorcontrib>Otieno, Kephas</creatorcontrib><creatorcontrib>Shi, Ya Ping</creatorcontrib><creatorcontrib>Kachur, Stephen Patrick</creatorcontrib><creatorcontrib>Hamel, Mary J</creatorcontrib><creatorcontrib>Kariuki, Simon</creatorcontrib><creatorcontrib>Lindblade, Kim A</creatorcontrib><title>Impact of Intermittent Mass Testing and Treatment on Incidence of Malaria Infection in a High Transmission Area of Western Kenya</title><title>The American journal of tropical medicine and hygiene</title><addtitle>Am J Trop Med Hyg</addtitle><description>Progress with malaria control in western Kenya has stagnated since 2007. Additional interventions to reduce the high burden of malaria in this region are urgently needed. We conducted a two-arm, community-based, cluster-randomized, controlled trial of active case detection and treatment of malaria infections in all residents mass testing and treatment (MTaT) of 10 village clusters (intervention clusters) for two consecutive years to measure differences in the incidence of clinical malaria disease and malaria infections compared with 20 control clusters where MTaT was not implemented. All residents of intervention clusters, irrespective of history of fever or other malaria-related symptoms, were tested three times per year before the peak malaria season using malaria rapid diagnostic tests. All positive cases were treated with dihydroartemisinin-piperaquine. The incidence of clinical malaria was measured through passive surveillance, whereas the cumulative incidence of malaria infection was measured using active surveillance in a cohort comprising randomly selected residents. The incidence of clinical malaria was 0.19 cases/person-year (p-y, 95% CI: 0.13-0.28) in the intervention arm and 0.24 cases/p-y (95% CI: 0.15-0.39) in the control arm (incidence rate ratio [IRR] 0.79, 95% CI: 0.61-1.02). The cumulative incidence of malaria infections was similar between the intervention (2.08 infections/p-y, 95% CI: 1.93-2.26) and control arms (2.19 infections/p-y, 95% CI: 2.02-2.37) with a crude IRR of 0.95 (95% CI: 0.87-1.04). Six rounds of MTaT over 2 years did not have a significant impact on the incidence of clinical malaria or the cumulative incidence of malaria infection in this area of high malaria transmission.</description><subject>Adolescent</subject><subject>Antimalarials - therapeutic use</subject><subject>Artemisinins - therapeutic use</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Health surveillance</subject><subject>Humans</subject><subject>Incidence</subject><subject>Infections</subject><subject>Intervention</subject><subject>Kenya - epidemiology</subject><subject>Malaria</subject><subject>Malaria, Falciparum - diagnosis</subject><subject>Malaria, Falciparum - drug therapy</subject><subject>Malaria, Falciparum - epidemiology</subject><subject>Malaria, Falciparum - transmission</subject><subject>Male</subject><subject>Mass Screening - methods</subject><subject>Quinolines - therapeutic use</subject><issn>0002-9637</issn><issn>1476-1645</issn><issn>1476-1645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc9rFDEUx4Modq0evUrAi5ep-TWZ5CKUonaxxcuKx_AmyexmmcmsSbbQW__0Zmwt6inw3uf7Jd_3RegtJWeCSf0R9mXanVHdkI63z9CKik42VIr2OVoRQlijJe9O0Kuc94RQxSh9iU4444IpIVfobj0dwBY8D3gdi09TKMXHgq8hZ7zxuYS4xRAd3iQPZVpWc6yoDc5H6xfdNYyQAtTh4G0JdR0iBnwZtruqgpinkPMyPq8Wi-BntfUp4m8-3sJr9GKAMfs3j-8p-vHl8-bisrn6_nV9cX7VWEHb0ijKQKlB9kw6KToYejW00sGghOsJUdwTcIz1WlPmFANNtBNc8M713Dpm-Sn69OB7OPaTd7YmSTCaQwoTpFszQzD_bmLYme18Y-pZpRCyGnx4NEjzr2ONYGou68cRop-P2TCuW0llJ3VF3_-H7udjijWeYYIJSjvSsko1D5RNc87JD0-focQs3Zrf3RqqzdJt5d_9neCJ_lMmvwdA3KH9</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Desai, Meghna R</creator><creator>Samuels, Aaron M</creator><creator>Odongo, Wycliffe</creator><creator>Williamson, John</creator><creator>Odero, Nobert Awino</creator><creator>Otieno, Kephas</creator><creator>Shi, Ya Ping</creator><creator>Kachur, Stephen Patrick</creator><creator>Hamel, Mary J</creator><creator>Kariuki, Simon</creator><creator>Lindblade, Kim A</creator><general>Institute of Tropical Medicine</general><general>The American Society of Tropical Medicine and Hygiene</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200701</creationdate><title>Impact of Intermittent Mass Testing and Treatment on Incidence of Malaria Infection in a High Transmission Area of Western Kenya</title><author>Desai, Meghna R ; Samuels, Aaron M ; Odongo, Wycliffe ; Williamson, John ; Odero, Nobert Awino ; Otieno, Kephas ; Shi, Ya Ping ; Kachur, Stephen Patrick ; Hamel, Mary J ; Kariuki, Simon ; Lindblade, Kim A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-812a88f6b26d647afb8f56daf84db0083e0ad22b9912d82a909d43437db3cd2c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adolescent</topic><topic>Antimalarials - therapeutic use</topic><topic>Artemisinins - therapeutic use</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Health surveillance</topic><topic>Humans</topic><topic>Incidence</topic><topic>Infections</topic><topic>Intervention</topic><topic>Kenya - epidemiology</topic><topic>Malaria</topic><topic>Malaria, Falciparum - diagnosis</topic><topic>Malaria, Falciparum - drug therapy</topic><topic>Malaria, Falciparum - epidemiology</topic><topic>Malaria, Falciparum - transmission</topic><topic>Male</topic><topic>Mass Screening - methods</topic><topic>Quinolines - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Desai, Meghna R</creatorcontrib><creatorcontrib>Samuels, Aaron M</creatorcontrib><creatorcontrib>Odongo, Wycliffe</creatorcontrib><creatorcontrib>Williamson, John</creatorcontrib><creatorcontrib>Odero, Nobert Awino</creatorcontrib><creatorcontrib>Otieno, Kephas</creatorcontrib><creatorcontrib>Shi, Ya Ping</creatorcontrib><creatorcontrib>Kachur, Stephen Patrick</creatorcontrib><creatorcontrib>Hamel, Mary J</creatorcontrib><creatorcontrib>Kariuki, Simon</creatorcontrib><creatorcontrib>Lindblade, Kim A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The American journal of tropical medicine and hygiene</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Desai, Meghna R</au><au>Samuels, Aaron M</au><au>Odongo, Wycliffe</au><au>Williamson, John</au><au>Odero, Nobert Awino</au><au>Otieno, Kephas</au><au>Shi, Ya Ping</au><au>Kachur, Stephen Patrick</au><au>Hamel, Mary J</au><au>Kariuki, Simon</au><au>Lindblade, Kim A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Intermittent Mass Testing and Treatment on Incidence of Malaria Infection in a High Transmission Area of Western Kenya</atitle><jtitle>The American journal of tropical medicine and hygiene</jtitle><addtitle>Am J Trop Med Hyg</addtitle><date>2020-07-01</date><risdate>2020</risdate><volume>103</volume><issue>1</issue><spage>369</spage><epage>377</epage><pages>369-377</pages><issn>0002-9637</issn><issn>1476-1645</issn><eissn>1476-1645</eissn><abstract>Progress with malaria control in western Kenya has stagnated since 2007. Additional interventions to reduce the high burden of malaria in this region are urgently needed. We conducted a two-arm, community-based, cluster-randomized, controlled trial of active case detection and treatment of malaria infections in all residents mass testing and treatment (MTaT) of 10 village clusters (intervention clusters) for two consecutive years to measure differences in the incidence of clinical malaria disease and malaria infections compared with 20 control clusters where MTaT was not implemented. All residents of intervention clusters, irrespective of history of fever or other malaria-related symptoms, were tested three times per year before the peak malaria season using malaria rapid diagnostic tests. All positive cases were treated with dihydroartemisinin-piperaquine. The incidence of clinical malaria was measured through passive surveillance, whereas the cumulative incidence of malaria infection was measured using active surveillance in a cohort comprising randomly selected residents. The incidence of clinical malaria was 0.19 cases/person-year (p-y, 95% CI: 0.13-0.28) in the intervention arm and 0.24 cases/p-y (95% CI: 0.15-0.39) in the control arm (incidence rate ratio [IRR] 0.79, 95% CI: 0.61-1.02). The cumulative incidence of malaria infections was similar between the intervention (2.08 infections/p-y, 95% CI: 1.93-2.26) and control arms (2.19 infections/p-y, 95% CI: 2.02-2.37) with a crude IRR of 0.95 (95% CI: 0.87-1.04). Six rounds of MTaT over 2 years did not have a significant impact on the incidence of clinical malaria or the cumulative incidence of malaria infection in this area of high malaria transmission.</abstract><cop>United States</cop><pub>Institute of Tropical Medicine</pub><pmid>32342846</pmid><doi>10.4269/ajtmh.19-0735</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0002-9637
ispartof The American journal of tropical medicine and hygiene, 2020-07, Vol.103 (1), p.369-377
issn 0002-9637
1476-1645
1476-1645
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7356446
source MEDLINE; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection
subjects Adolescent
Antimalarials - therapeutic use
Artemisinins - therapeutic use
Child
Child, Preschool
Female
Health surveillance
Humans
Incidence
Infections
Intervention
Kenya - epidemiology
Malaria
Malaria, Falciparum - diagnosis
Malaria, Falciparum - drug therapy
Malaria, Falciparum - epidemiology
Malaria, Falciparum - transmission
Male
Mass Screening - methods
Quinolines - therapeutic use
title Impact of Intermittent Mass Testing and Treatment on Incidence of Malaria Infection in a High Transmission Area of Western Kenya
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T16%3A20%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Impact%20of%20Intermittent%20Mass%20Testing%20and%20Treatment%20on%20Incidence%20of%20Malaria%20Infection%20in%20a%20High%20Transmission%20Area%20of%20Western%20Kenya&rft.jtitle=The%20American%20journal%20of%20tropical%20medicine%20and%20hygiene&rft.au=Desai,%20Meghna%20R&rft.date=2020-07-01&rft.volume=103&rft.issue=1&rft.spage=369&rft.epage=377&rft.pages=369-377&rft.issn=0002-9637&rft.eissn=1476-1645&rft_id=info:doi/10.4269/ajtmh.19-0735&rft_dat=%3Cproquest_pubme%3E2424117052%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2424117052&rft_id=info:pmid/32342846&rfr_iscdi=true