Loading…

Chloroquine as weekly chemoprophylaxis or intermittent treatment to prevent malaria in pregnancy in Malawi: a randomised controlled trial

Sulfadoxine-pyrimethamine resistance threatens efficacy of intermittent preventive treatment of malaria during pregnancy, and alternative regimens need to be identified. With the return of chloroquine efficacy in southern Africa, we postulated that chloroquine either as an intermittent therapy or as...

Full description

Saved in:
Bibliographic Details
Published in:The Lancet infectious diseases 2018-10, Vol.18 (10), p.1097-1107
Main Authors: Divala, Titus H, Mungwira, Randy G, Mawindo, Patricia M, Nyirenda, Osward M, Kanjala, Maxwell, Ndaferankhande, Masiye, Tsirizani, Lufina E, Masonga, Rhoda, Muwalo, Francis, Boudová, Sarah, Potter, Gail E, Kennedy, Jessie, Goswami, Jaya, Wylie, Blair J, Muehlenbachs, Atis, Ndovie, Lughano, Mvula, Priscilla, Mbilizi, Yamikani, Tomoka, Tamiwe, Laufer, Miriam K
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c523t-734c078e931e05f7d5f68470ee49e5aa77dcb9b08f5f9f1b5220e58a2f4519b83
cites cdi_FETCH-LOGICAL-c523t-734c078e931e05f7d5f68470ee49e5aa77dcb9b08f5f9f1b5220e58a2f4519b83
container_end_page 1107
container_issue 10
container_start_page 1097
container_title The Lancet infectious diseases
container_volume 18
creator Divala, Titus H
Mungwira, Randy G
Mawindo, Patricia M
Nyirenda, Osward M
Kanjala, Maxwell
Ndaferankhande, Masiye
Tsirizani, Lufina E
Masonga, Rhoda
Muwalo, Francis
Boudová, Sarah
Potter, Gail E
Kennedy, Jessie
Goswami, Jaya
Wylie, Blair J
Muehlenbachs, Atis
Ndovie, Lughano
Mvula, Priscilla
Mbilizi, Yamikani
Tomoka, Tamiwe
Laufer, Miriam K
description Sulfadoxine-pyrimethamine resistance threatens efficacy of intermittent preventive treatment of malaria during pregnancy, and alternative regimens need to be identified. With the return of chloroquine efficacy in southern Africa, we postulated that chloroquine either as an intermittent therapy or as weekly chemoprophylaxis would be more efficacious than intermittent sulfadoxine-pyrimethamine for prevention of malaria in pregnancy and associated maternal and newborn adverse outcomes. We did an open-label, single-centre, randomised controlled trial at Ndirande Health Centre, Blantyre, in southern Malawi. We enrolled pregnant women (first or second pregnancy) at 20–28 weeks' gestation who were HIV negative. Participants were randomly assigned in a 1:1:1 ratio using a computer-generated list to either intermittent sulfadoxine-pyrimethamine (two doses of 1500 mg sulfadoxine and 75 mg pyrimethamine, 4 weeks apart), intermittent chloroquine (two doses of 600 mg on day 1, 600 mg on day 2, and 300 mg on day 3), or chloroquine prophylaxis (600 mg on day 1 then 300 mg every week). The primary endpoint was placental malaria in the modified intent-to-treat population, which consisted of participants who contributed placental histopathology data at birth. Secondary outcomes included clinical malaria, maternal anaemia, low birthweight, and safety. This trial is registered with ClinicalTrials.gov, number NCT01443130. Between February, 2012, and May, 2014, we enrolled and randomly allocated 900 women, of whom 765 contributed histopathological data and were included in the primary analysis. 108 (14%) women had placental malaria, which was lower than the anticipated prevalence of placental malaria infection. Protection from placental malaria was not improved by chloroquine as either prophylaxis (30 [12%] of 259 had positive histopathology; relative risk [RR] 0·75, 95% CI 0·48–1·17) or intermittent therapy (39 [15%] of 253; RR 1·00, 0·67–1·50) compared with intermittent sulfadoxine-pyrimethamine (39 [15%] of 253). In protocol-specified analyses adjusted for maternal age, gestational age at enrolment, bednet use the night before enrolment, anaemia at enrolment, and malaria infection at enrolment, women taking chloroquine as prophylaxis had 34% lower placental infections than did those allocated intermittent sulfadoxine-pyrimethamine (RR 0·66, 95% CI 0·46–0·95). Clinical malaria was reported in nine women assigned intermittent sulfadoxine-pyrimethamine, four allocated intermitt
doi_str_mv 10.1016/S1473-3099(18)30415-8
format article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2154218286</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A556022839</galeid><els_id>S1473309918304158</els_id><sourcerecordid>A556022839</sourcerecordid><originalsourceid>FETCH-LOGICAL-c523t-734c078e931e05f7d5f68470ee49e5aa77dcb9b08f5f9f1b5220e58a2f4519b83</originalsourceid><addsrcrecordid>eNqFkcFu1DAQhi0EoqXwCCBLSAgOATuxY5sLqlYtIBVxAM6W40x2XRI72N62-wi8Nc6mcOXk37--8cz4R-g5JW8poe27b5SJpmqIUq-pfNMQRnklH6DTYrOKMS4eHvWKnKAnKV0TQgUl7DE6aQhVXKn2FP3e7MYQw6-984BNwrcAP8cDtjuYwhzDvDuM5s4lHCJ2PkOcXM7gM84RTJ6OKuA5ws0iJzOa6EwhF2vrjbeH5fKl-LfuPTY4Gt-HySXosQ0-xzCOReZSND5FjwYzJnh2f56hH5cX3zefqquvHz9vzq8qy-smV6JhlggJqqFA-CB6PrSSCQLAFHBjhOhtpzoiBz6ogXa8rglwaeqBcao62Zyhl-u787I2pKyvwz760lLXlLOaylq2hXq1UlszgnZ-mRbu8tbsU9L6nPOW1LVsVAH5CtoYUoow6Dm6ycSDpkQvSeljUnqJQVOpj0npZYwX92Psuwn6f1V_oynAhxWA8hk3DqJO1oG30LsINus-uP-0-AN-FaU0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2154218286</pqid></control><display><type>article</type><title>Chloroquine as weekly chemoprophylaxis or intermittent treatment to prevent malaria in pregnancy in Malawi: a randomised controlled trial</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Divala, Titus H ; Mungwira, Randy G ; Mawindo, Patricia M ; Nyirenda, Osward M ; Kanjala, Maxwell ; Ndaferankhande, Masiye ; Tsirizani, Lufina E ; Masonga, Rhoda ; Muwalo, Francis ; Boudová, Sarah ; Potter, Gail E ; Kennedy, Jessie ; Goswami, Jaya ; Wylie, Blair J ; Muehlenbachs, Atis ; Ndovie, Lughano ; Mvula, Priscilla ; Mbilizi, Yamikani ; Tomoka, Tamiwe ; Laufer, Miriam K</creator><creatorcontrib>Divala, Titus H ; Mungwira, Randy G ; Mawindo, Patricia M ; Nyirenda, Osward M ; Kanjala, Maxwell ; Ndaferankhande, Masiye ; Tsirizani, Lufina E ; Masonga, Rhoda ; Muwalo, Francis ; Boudová, Sarah ; Potter, Gail E ; Kennedy, Jessie ; Goswami, Jaya ; Wylie, Blair J ; Muehlenbachs, Atis ; Ndovie, Lughano ; Mvula, Priscilla ; Mbilizi, Yamikani ; Tomoka, Tamiwe ; Laufer, Miriam K</creatorcontrib><description>Sulfadoxine-pyrimethamine resistance threatens efficacy of intermittent preventive treatment of malaria during pregnancy, and alternative regimens need to be identified. With the return of chloroquine efficacy in southern Africa, we postulated that chloroquine either as an intermittent therapy or as weekly chemoprophylaxis would be more efficacious than intermittent sulfadoxine-pyrimethamine for prevention of malaria in pregnancy and associated maternal and newborn adverse outcomes. We did an open-label, single-centre, randomised controlled trial at Ndirande Health Centre, Blantyre, in southern Malawi. We enrolled pregnant women (first or second pregnancy) at 20–28 weeks' gestation who were HIV negative. Participants were randomly assigned in a 1:1:1 ratio using a computer-generated list to either intermittent sulfadoxine-pyrimethamine (two doses of 1500 mg sulfadoxine and 75 mg pyrimethamine, 4 weeks apart), intermittent chloroquine (two doses of 600 mg on day 1, 600 mg on day 2, and 300 mg on day 3), or chloroquine prophylaxis (600 mg on day 1 then 300 mg every week). The primary endpoint was placental malaria in the modified intent-to-treat population, which consisted of participants who contributed placental histopathology data at birth. Secondary outcomes included clinical malaria, maternal anaemia, low birthweight, and safety. This trial is registered with ClinicalTrials.gov, number NCT01443130. Between February, 2012, and May, 2014, we enrolled and randomly allocated 900 women, of whom 765 contributed histopathological data and were included in the primary analysis. 108 (14%) women had placental malaria, which was lower than the anticipated prevalence of placental malaria infection. Protection from placental malaria was not improved by chloroquine as either prophylaxis (30 [12%] of 259 had positive histopathology; relative risk [RR] 0·75, 95% CI 0·48–1·17) or intermittent therapy (39 [15%] of 253; RR 1·00, 0·67–1·50) compared with intermittent sulfadoxine-pyrimethamine (39 [15%] of 253). In protocol-specified analyses adjusted for maternal age, gestational age at enrolment, bednet use the night before enrolment, anaemia at enrolment, and malaria infection at enrolment, women taking chloroquine as prophylaxis had 34% lower placental infections than did those allocated intermittent sulfadoxine-pyrimethamine (RR 0·66, 95% CI 0·46–0·95). Clinical malaria was reported in nine women assigned intermittent sulfadoxine-pyrimethamine, four allocated intermittent chloroquine (p=0·26), and two allocated chloroquine prophylaxis (p=0·063). Maternal anaemia was noted in five women assigned intermittent sulfadoxine-pyrimethamine, 15 allocated intermittent chloroquine (p=0·038), and six assigned chloroquine prophylaxis (p&gt;0·99). Low birthweight was recorded for 31 babies born to women allocated intermittent sulfadoxine-pyrimethamine, 29 assigned intermittent chloroquine (p=0·78), and 41 allocated chloroquine prophylaxis (p=0·28). Four women assigned intermittent sulfadoxine-pyrimethamine had adverse events possibly related to study product compared with 94 women allocated intermittent chloroquine (p&lt;0·0001) and 26 allocated chloroquine prophylaxis (p&lt;0·0001). Three women had severe or life-threatening adverse events related to study product, of whom all were assigned intermittent chloroquine (p=0·25). Chloroquine administered as intermittent therapy did not provide better protection from malaria and related adverse effects compared with intermittent sulfadoxine-pyrimethamine in a setting of high resistance to sulfadoxine-pyrimethamine. Chloroquine chemoprophylaxis might provide benefit in protecting against malaria during pregnancy, but studies with larger sample sizes are needed to confirm these results. US National Institutes of Health.</description><identifier>ISSN: 1473-3099</identifier><identifier>EISSN: 1474-4457</identifier><identifier>DOI: 10.1016/S1473-3099(18)30415-8</identifier><identifier>PMID: 30195996</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Adult ; Age ; Analysis ; Anemia ; Antimalarial agents ; Antimalarials - therapeutic use ; Babies ; Birth weight ; Chloroquine ; Chloroquine - adverse effects ; Chloroquine - therapeutic use ; Clinical trials ; Control ; Drug Combinations ; Drug dosages ; Drug therapy ; Effectiveness ; Female ; Gestation ; Gestational age ; Hemoglobin ; High resistance ; Histochemistry ; Histopathology ; HIV ; Human immunodeficiency virus ; Humans ; Infant, Newborn ; Infections ; Infectious diseases ; Malaria ; Malaria - prevention &amp; control ; Medicine, Preventive ; Obstetrics ; Placenta ; Pregnancy ; Pregnancy Complications, Parasitic - prevention &amp; control ; Pregnant women ; Prevention ; Preventive health services ; Prophylaxis ; Pyrimethamine ; Pyrimethamine - adverse effects ; Pyrimethamine - therapeutic use ; Randomization ; Sulfadoxine ; Sulfadoxine - adverse effects ; Sulfadoxine - therapeutic use ; Therapy ; Vector-borne diseases ; Womens health</subject><ispartof>The Lancet infectious diseases, 2018-10, Vol.18 (10), p.1097-1107</ispartof><rights>2018 Elsevier Ltd</rights><rights>Copyright © 2018 Elsevier Ltd. All rights reserved.</rights><rights>COPYRIGHT 2018 Elsevier B.V.</rights><rights>Copyright Elsevier Limited Oct 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-734c078e931e05f7d5f68470ee49e5aa77dcb9b08f5f9f1b5220e58a2f4519b83</citedby><cites>FETCH-LOGICAL-c523t-734c078e931e05f7d5f68470ee49e5aa77dcb9b08f5f9f1b5220e58a2f4519b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30195996$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Divala, Titus H</creatorcontrib><creatorcontrib>Mungwira, Randy G</creatorcontrib><creatorcontrib>Mawindo, Patricia M</creatorcontrib><creatorcontrib>Nyirenda, Osward M</creatorcontrib><creatorcontrib>Kanjala, Maxwell</creatorcontrib><creatorcontrib>Ndaferankhande, Masiye</creatorcontrib><creatorcontrib>Tsirizani, Lufina E</creatorcontrib><creatorcontrib>Masonga, Rhoda</creatorcontrib><creatorcontrib>Muwalo, Francis</creatorcontrib><creatorcontrib>Boudová, Sarah</creatorcontrib><creatorcontrib>Potter, Gail E</creatorcontrib><creatorcontrib>Kennedy, Jessie</creatorcontrib><creatorcontrib>Goswami, Jaya</creatorcontrib><creatorcontrib>Wylie, Blair J</creatorcontrib><creatorcontrib>Muehlenbachs, Atis</creatorcontrib><creatorcontrib>Ndovie, Lughano</creatorcontrib><creatorcontrib>Mvula, Priscilla</creatorcontrib><creatorcontrib>Mbilizi, Yamikani</creatorcontrib><creatorcontrib>Tomoka, Tamiwe</creatorcontrib><creatorcontrib>Laufer, Miriam K</creatorcontrib><title>Chloroquine as weekly chemoprophylaxis or intermittent treatment to prevent malaria in pregnancy in Malawi: a randomised controlled trial</title><title>The Lancet infectious diseases</title><addtitle>Lancet Infect Dis</addtitle><description>Sulfadoxine-pyrimethamine resistance threatens efficacy of intermittent preventive treatment of malaria during pregnancy, and alternative regimens need to be identified. With the return of chloroquine efficacy in southern Africa, we postulated that chloroquine either as an intermittent therapy or as weekly chemoprophylaxis would be more efficacious than intermittent sulfadoxine-pyrimethamine for prevention of malaria in pregnancy and associated maternal and newborn adverse outcomes. We did an open-label, single-centre, randomised controlled trial at Ndirande Health Centre, Blantyre, in southern Malawi. We enrolled pregnant women (first or second pregnancy) at 20–28 weeks' gestation who were HIV negative. Participants were randomly assigned in a 1:1:1 ratio using a computer-generated list to either intermittent sulfadoxine-pyrimethamine (two doses of 1500 mg sulfadoxine and 75 mg pyrimethamine, 4 weeks apart), intermittent chloroquine (two doses of 600 mg on day 1, 600 mg on day 2, and 300 mg on day 3), or chloroquine prophylaxis (600 mg on day 1 then 300 mg every week). The primary endpoint was placental malaria in the modified intent-to-treat population, which consisted of participants who contributed placental histopathology data at birth. Secondary outcomes included clinical malaria, maternal anaemia, low birthweight, and safety. This trial is registered with ClinicalTrials.gov, number NCT01443130. Between February, 2012, and May, 2014, we enrolled and randomly allocated 900 women, of whom 765 contributed histopathological data and were included in the primary analysis. 108 (14%) women had placental malaria, which was lower than the anticipated prevalence of placental malaria infection. Protection from placental malaria was not improved by chloroquine as either prophylaxis (30 [12%] of 259 had positive histopathology; relative risk [RR] 0·75, 95% CI 0·48–1·17) or intermittent therapy (39 [15%] of 253; RR 1·00, 0·67–1·50) compared with intermittent sulfadoxine-pyrimethamine (39 [15%] of 253). In protocol-specified analyses adjusted for maternal age, gestational age at enrolment, bednet use the night before enrolment, anaemia at enrolment, and malaria infection at enrolment, women taking chloroquine as prophylaxis had 34% lower placental infections than did those allocated intermittent sulfadoxine-pyrimethamine (RR 0·66, 95% CI 0·46–0·95). Clinical malaria was reported in nine women assigned intermittent sulfadoxine-pyrimethamine, four allocated intermittent chloroquine (p=0·26), and two allocated chloroquine prophylaxis (p=0·063). Maternal anaemia was noted in five women assigned intermittent sulfadoxine-pyrimethamine, 15 allocated intermittent chloroquine (p=0·038), and six assigned chloroquine prophylaxis (p&gt;0·99). Low birthweight was recorded for 31 babies born to women allocated intermittent sulfadoxine-pyrimethamine, 29 assigned intermittent chloroquine (p=0·78), and 41 allocated chloroquine prophylaxis (p=0·28). Four women assigned intermittent sulfadoxine-pyrimethamine had adverse events possibly related to study product compared with 94 women allocated intermittent chloroquine (p&lt;0·0001) and 26 allocated chloroquine prophylaxis (p&lt;0·0001). Three women had severe or life-threatening adverse events related to study product, of whom all were assigned intermittent chloroquine (p=0·25). Chloroquine administered as intermittent therapy did not provide better protection from malaria and related adverse effects compared with intermittent sulfadoxine-pyrimethamine in a setting of high resistance to sulfadoxine-pyrimethamine. Chloroquine chemoprophylaxis might provide benefit in protecting against malaria during pregnancy, but studies with larger sample sizes are needed to confirm these results. US National Institutes of Health.</description><subject>Adult</subject><subject>Age</subject><subject>Analysis</subject><subject>Anemia</subject><subject>Antimalarial agents</subject><subject>Antimalarials - therapeutic use</subject><subject>Babies</subject><subject>Birth weight</subject><subject>Chloroquine</subject><subject>Chloroquine - adverse effects</subject><subject>Chloroquine - therapeutic use</subject><subject>Clinical trials</subject><subject>Control</subject><subject>Drug Combinations</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>Effectiveness</subject><subject>Female</subject><subject>Gestation</subject><subject>Gestational age</subject><subject>Hemoglobin</subject><subject>High resistance</subject><subject>Histochemistry</subject><subject>Histopathology</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Malaria</subject><subject>Malaria - prevention &amp; control</subject><subject>Medicine, Preventive</subject><subject>Obstetrics</subject><subject>Placenta</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Parasitic - prevention &amp; control</subject><subject>Pregnant women</subject><subject>Prevention</subject><subject>Preventive health services</subject><subject>Prophylaxis</subject><subject>Pyrimethamine</subject><subject>Pyrimethamine - adverse effects</subject><subject>Pyrimethamine - therapeutic use</subject><subject>Randomization</subject><subject>Sulfadoxine</subject><subject>Sulfadoxine - adverse effects</subject><subject>Sulfadoxine - therapeutic use</subject><subject>Therapy</subject><subject>Vector-borne diseases</subject><subject>Womens health</subject><issn>1473-3099</issn><issn>1474-4457</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1DAQhi0EoqXwCCBLSAgOATuxY5sLqlYtIBVxAM6W40x2XRI72N62-wi8Nc6mcOXk37--8cz4R-g5JW8poe27b5SJpmqIUq-pfNMQRnklH6DTYrOKMS4eHvWKnKAnKV0TQgUl7DE6aQhVXKn2FP3e7MYQw6-984BNwrcAP8cDtjuYwhzDvDuM5s4lHCJ2PkOcXM7gM84RTJ6OKuA5ws0iJzOa6EwhF2vrjbeH5fKl-LfuPTY4Gt-HySXosQ0-xzCOReZSND5FjwYzJnh2f56hH5cX3zefqquvHz9vzq8qy-smV6JhlggJqqFA-CB6PrSSCQLAFHBjhOhtpzoiBz6ogXa8rglwaeqBcao62Zyhl-u787I2pKyvwz760lLXlLOaylq2hXq1UlszgnZ-mRbu8tbsU9L6nPOW1LVsVAH5CtoYUoow6Dm6ycSDpkQvSeljUnqJQVOpj0npZYwX92Psuwn6f1V_oynAhxWA8hk3DqJO1oG30LsINus-uP-0-AN-FaU0</recordid><startdate>201810</startdate><enddate>201810</enddate><creator>Divala, Titus H</creator><creator>Mungwira, Randy G</creator><creator>Mawindo, Patricia M</creator><creator>Nyirenda, Osward M</creator><creator>Kanjala, Maxwell</creator><creator>Ndaferankhande, Masiye</creator><creator>Tsirizani, Lufina E</creator><creator>Masonga, Rhoda</creator><creator>Muwalo, Francis</creator><creator>Boudová, Sarah</creator><creator>Potter, Gail E</creator><creator>Kennedy, Jessie</creator><creator>Goswami, Jaya</creator><creator>Wylie, Blair J</creator><creator>Muehlenbachs, Atis</creator><creator>Ndovie, Lughano</creator><creator>Mvula, Priscilla</creator><creator>Mbilizi, Yamikani</creator><creator>Tomoka, Tamiwe</creator><creator>Laufer, Miriam K</creator><general>Elsevier Ltd</general><general>Elsevier B.V</general><general>Elsevier Limited</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>0TZ</scope><scope>3V.</scope><scope>7QL</scope><scope>7RV</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>201810</creationdate><title>Chloroquine as weekly chemoprophylaxis or intermittent treatment to prevent malaria in pregnancy in Malawi: a randomised controlled trial</title><author>Divala, Titus H ; Mungwira, Randy G ; Mawindo, Patricia M ; Nyirenda, Osward M ; Kanjala, Maxwell ; Ndaferankhande, Masiye ; Tsirizani, Lufina E ; Masonga, Rhoda ; Muwalo, Francis ; Boudová, Sarah ; Potter, Gail E ; Kennedy, Jessie ; Goswami, Jaya ; Wylie, Blair J ; Muehlenbachs, Atis ; Ndovie, Lughano ; Mvula, Priscilla ; Mbilizi, Yamikani ; Tomoka, Tamiwe ; Laufer, Miriam K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-734c078e931e05f7d5f68470ee49e5aa77dcb9b08f5f9f1b5220e58a2f4519b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adult</topic><topic>Age</topic><topic>Analysis</topic><topic>Anemia</topic><topic>Antimalarial agents</topic><topic>Antimalarials - therapeutic use</topic><topic>Babies</topic><topic>Birth weight</topic><topic>Chloroquine</topic><topic>Chloroquine - adverse effects</topic><topic>Chloroquine - therapeutic use</topic><topic>Clinical trials</topic><topic>Control</topic><topic>Drug Combinations</topic><topic>Drug dosages</topic><topic>Drug therapy</topic><topic>Effectiveness</topic><topic>Female</topic><topic>Gestation</topic><topic>Gestational age</topic><topic>Hemoglobin</topic><topic>High resistance</topic><topic>Histochemistry</topic><topic>Histopathology</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infections</topic><topic>Infectious diseases</topic><topic>Malaria</topic><topic>Malaria - prevention &amp; control</topic><topic>Medicine, Preventive</topic><topic>Obstetrics</topic><topic>Placenta</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Parasitic - prevention &amp; control</topic><topic>Pregnant women</topic><topic>Prevention</topic><topic>Preventive health services</topic><topic>Prophylaxis</topic><topic>Pyrimethamine</topic><topic>Pyrimethamine - adverse effects</topic><topic>Pyrimethamine - therapeutic use</topic><topic>Randomization</topic><topic>Sulfadoxine</topic><topic>Sulfadoxine - adverse effects</topic><topic>Sulfadoxine - therapeutic use</topic><topic>Therapy</topic><topic>Vector-borne diseases</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Divala, Titus H</creatorcontrib><creatorcontrib>Mungwira, Randy G</creatorcontrib><creatorcontrib>Mawindo, Patricia M</creatorcontrib><creatorcontrib>Nyirenda, Osward M</creatorcontrib><creatorcontrib>Kanjala, Maxwell</creatorcontrib><creatorcontrib>Ndaferankhande, Masiye</creatorcontrib><creatorcontrib>Tsirizani, Lufina E</creatorcontrib><creatorcontrib>Masonga, Rhoda</creatorcontrib><creatorcontrib>Muwalo, Francis</creatorcontrib><creatorcontrib>Boudová, Sarah</creatorcontrib><creatorcontrib>Potter, Gail E</creatorcontrib><creatorcontrib>Kennedy, Jessie</creatorcontrib><creatorcontrib>Goswami, Jaya</creatorcontrib><creatorcontrib>Wylie, Blair J</creatorcontrib><creatorcontrib>Muehlenbachs, Atis</creatorcontrib><creatorcontrib>Ndovie, Lughano</creatorcontrib><creatorcontrib>Mvula, Priscilla</creatorcontrib><creatorcontrib>Mbilizi, Yamikani</creatorcontrib><creatorcontrib>Tomoka, Tamiwe</creatorcontrib><creatorcontrib>Laufer, Miriam K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Lancet Titles</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>The Lancet infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Divala, Titus H</au><au>Mungwira, Randy G</au><au>Mawindo, Patricia M</au><au>Nyirenda, Osward M</au><au>Kanjala, Maxwell</au><au>Ndaferankhande, Masiye</au><au>Tsirizani, Lufina E</au><au>Masonga, Rhoda</au><au>Muwalo, Francis</au><au>Boudová, Sarah</au><au>Potter, Gail E</au><au>Kennedy, Jessie</au><au>Goswami, Jaya</au><au>Wylie, Blair J</au><au>Muehlenbachs, Atis</au><au>Ndovie, Lughano</au><au>Mvula, Priscilla</au><au>Mbilizi, Yamikani</au><au>Tomoka, Tamiwe</au><au>Laufer, Miriam K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chloroquine as weekly chemoprophylaxis or intermittent treatment to prevent malaria in pregnancy in Malawi: a randomised controlled trial</atitle><jtitle>The Lancet infectious diseases</jtitle><addtitle>Lancet Infect Dis</addtitle><date>2018-10</date><risdate>2018</risdate><volume>18</volume><issue>10</issue><spage>1097</spage><epage>1107</epage><pages>1097-1107</pages><issn>1473-3099</issn><eissn>1474-4457</eissn><abstract>Sulfadoxine-pyrimethamine resistance threatens efficacy of intermittent preventive treatment of malaria during pregnancy, and alternative regimens need to be identified. With the return of chloroquine efficacy in southern Africa, we postulated that chloroquine either as an intermittent therapy or as weekly chemoprophylaxis would be more efficacious than intermittent sulfadoxine-pyrimethamine for prevention of malaria in pregnancy and associated maternal and newborn adverse outcomes. We did an open-label, single-centre, randomised controlled trial at Ndirande Health Centre, Blantyre, in southern Malawi. We enrolled pregnant women (first or second pregnancy) at 20–28 weeks' gestation who were HIV negative. Participants were randomly assigned in a 1:1:1 ratio using a computer-generated list to either intermittent sulfadoxine-pyrimethamine (two doses of 1500 mg sulfadoxine and 75 mg pyrimethamine, 4 weeks apart), intermittent chloroquine (two doses of 600 mg on day 1, 600 mg on day 2, and 300 mg on day 3), or chloroquine prophylaxis (600 mg on day 1 then 300 mg every week). The primary endpoint was placental malaria in the modified intent-to-treat population, which consisted of participants who contributed placental histopathology data at birth. Secondary outcomes included clinical malaria, maternal anaemia, low birthweight, and safety. This trial is registered with ClinicalTrials.gov, number NCT01443130. Between February, 2012, and May, 2014, we enrolled and randomly allocated 900 women, of whom 765 contributed histopathological data and were included in the primary analysis. 108 (14%) women had placental malaria, which was lower than the anticipated prevalence of placental malaria infection. Protection from placental malaria was not improved by chloroquine as either prophylaxis (30 [12%] of 259 had positive histopathology; relative risk [RR] 0·75, 95% CI 0·48–1·17) or intermittent therapy (39 [15%] of 253; RR 1·00, 0·67–1·50) compared with intermittent sulfadoxine-pyrimethamine (39 [15%] of 253). In protocol-specified analyses adjusted for maternal age, gestational age at enrolment, bednet use the night before enrolment, anaemia at enrolment, and malaria infection at enrolment, women taking chloroquine as prophylaxis had 34% lower placental infections than did those allocated intermittent sulfadoxine-pyrimethamine (RR 0·66, 95% CI 0·46–0·95). Clinical malaria was reported in nine women assigned intermittent sulfadoxine-pyrimethamine, four allocated intermittent chloroquine (p=0·26), and two allocated chloroquine prophylaxis (p=0·063). Maternal anaemia was noted in five women assigned intermittent sulfadoxine-pyrimethamine, 15 allocated intermittent chloroquine (p=0·038), and six assigned chloroquine prophylaxis (p&gt;0·99). Low birthweight was recorded for 31 babies born to women allocated intermittent sulfadoxine-pyrimethamine, 29 assigned intermittent chloroquine (p=0·78), and 41 allocated chloroquine prophylaxis (p=0·28). Four women assigned intermittent sulfadoxine-pyrimethamine had adverse events possibly related to study product compared with 94 women allocated intermittent chloroquine (p&lt;0·0001) and 26 allocated chloroquine prophylaxis (p&lt;0·0001). Three women had severe or life-threatening adverse events related to study product, of whom all were assigned intermittent chloroquine (p=0·25). Chloroquine administered as intermittent therapy did not provide better protection from malaria and related adverse effects compared with intermittent sulfadoxine-pyrimethamine in a setting of high resistance to sulfadoxine-pyrimethamine. Chloroquine chemoprophylaxis might provide benefit in protecting against malaria during pregnancy, but studies with larger sample sizes are needed to confirm these results. US National Institutes of Health.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>30195996</pmid><doi>10.1016/S1473-3099(18)30415-8</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1473-3099
ispartof The Lancet infectious diseases, 2018-10, Vol.18 (10), p.1097-1107
issn 1473-3099
1474-4457
language eng
recordid cdi_proquest_journals_2154218286
source ScienceDirect Freedom Collection 2022-2024
subjects Adult
Age
Analysis
Anemia
Antimalarial agents
Antimalarials - therapeutic use
Babies
Birth weight
Chloroquine
Chloroquine - adverse effects
Chloroquine - therapeutic use
Clinical trials
Control
Drug Combinations
Drug dosages
Drug therapy
Effectiveness
Female
Gestation
Gestational age
Hemoglobin
High resistance
Histochemistry
Histopathology
HIV
Human immunodeficiency virus
Humans
Infant, Newborn
Infections
Infectious diseases
Malaria
Malaria - prevention & control
Medicine, Preventive
Obstetrics
Placenta
Pregnancy
Pregnancy Complications, Parasitic - prevention & control
Pregnant women
Prevention
Preventive health services
Prophylaxis
Pyrimethamine
Pyrimethamine - adverse effects
Pyrimethamine - therapeutic use
Randomization
Sulfadoxine
Sulfadoxine - adverse effects
Sulfadoxine - therapeutic use
Therapy
Vector-borne diseases
Womens health
title Chloroquine as weekly chemoprophylaxis or intermittent treatment to prevent malaria in pregnancy in Malawi: a randomised controlled trial
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T16%3A09%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chloroquine%20as%20weekly%20chemoprophylaxis%20or%20intermittent%20treatment%20to%20prevent%20malaria%20in%20pregnancy%20in%20Malawi:%20a%20randomised%20controlled%20trial&rft.jtitle=The%20Lancet%20infectious%20diseases&rft.au=Divala,%20Titus%20H&rft.date=2018-10&rft.volume=18&rft.issue=10&rft.spage=1097&rft.epage=1107&rft.pages=1097-1107&rft.issn=1473-3099&rft.eissn=1474-4457&rft_id=info:doi/10.1016/S1473-3099(18)30415-8&rft_dat=%3Cgale_proqu%3EA556022839%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c523t-734c078e931e05f7d5f68470ee49e5aa77dcb9b08f5f9f1b5220e58a2f4519b83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2154218286&rft_id=info:pmid/30195996&rft_galeid=A556022839&rfr_iscdi=true