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Drug treatment and prevention of malaria in pregnancy: a critical review of the guidelines
Malaria caused by Plasmodium falciparum in pregnancy can result in adverse maternal and fetal sequelae. This review evaluated the adherence of the national guidelines drawn from World Health Organization (WHO) regions, Africa, Eastern Mediterranean, Southeast Asia, and Western Pacific, to the WHO re...
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Published in: | Malaria journal 2021-01, Vol.20 (1), p.62-62, Article 62 |
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description | Malaria caused by Plasmodium falciparum in pregnancy can result in adverse maternal and fetal sequelae. This review evaluated the adherence of the national guidelines drawn from World Health Organization (WHO) regions, Africa, Eastern Mediterranean, Southeast Asia, and Western Pacific, to the WHO recommendations on drug treatment and prevention of chloroquine-resistant falciparum malaria in pregnant women.
Thirty-five updated national guidelines and the President's Malaria Initiative (PMI), available in English language, were reviewed. The primary outcome measures were the first-line anti-malarial treatment protocols adopted by national guidelines for uncomplicated and complicated falciparum malaria infections in early (first) and late (second and third) trimesters of pregnancy. The strategy of intermittent preventive treatment of malaria in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP) was also addressed.
This review evaluated the treatment and prevention of falciparum malaria in pregnancy in 35 national guidelines/PMI-Malaria Operational Plans (MOP) reports out of 95 malaria-endemic countries. Of the 35 national guidelines, 10 (28.6%) recommend oral quinine plus clindamycin as first-line treatment for uncomplicated malaria in the first trimester. As the first-line option, artemether-lumefantrine, an artemisinin-based combination therapy, is adopted by 26 (74.3%) of the guidelines for treating uncomplicated or complicated malaria in the second and third trimesters. Intravenous artesunate is approved by 18 (51.4%) and 31 (88.6%) guidelines for treating complicated malaria during early and late pregnancy, respectively. Of the 23 national guidelines that recommend IPTp-SP strategy, 8 (34.8%) are not explicit about directly observed therapy requirements, and three-quarters, 17 (73.9%), do not specify contra-indication of SP in human immunodeficiency virus (HIV)-infected pregnant women receiving cotrimoxazole prophylaxis. Most of the guidelines (18/23; 78.3%) state the recommended folic acid dose.
Several national guidelines and PMI reports require update revisions to harmonize with international guidelines and emergent trends in managing falciparum malaria in pregnancy. National guidelines and those of donor agencies should comply with those of WHO guideline recommendations although local conditions and delayed guideline updates may call for deviations from WHO evidence-based guidelines. |
doi_str_mv | 10.1186/s12936-020-03565-2 |
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Thirty-five updated national guidelines and the President's Malaria Initiative (PMI), available in English language, were reviewed. The primary outcome measures were the first-line anti-malarial treatment protocols adopted by national guidelines for uncomplicated and complicated falciparum malaria infections in early (first) and late (second and third) trimesters of pregnancy. The strategy of intermittent preventive treatment of malaria in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP) was also addressed.
This review evaluated the treatment and prevention of falciparum malaria in pregnancy in 35 national guidelines/PMI-Malaria Operational Plans (MOP) reports out of 95 malaria-endemic countries. Of the 35 national guidelines, 10 (28.6%) recommend oral quinine plus clindamycin as first-line treatment for uncomplicated malaria in the first trimester. As the first-line option, artemether-lumefantrine, an artemisinin-based combination therapy, is adopted by 26 (74.3%) of the guidelines for treating uncomplicated or complicated malaria in the second and third trimesters. Intravenous artesunate is approved by 18 (51.4%) and 31 (88.6%) guidelines for treating complicated malaria during early and late pregnancy, respectively. Of the 23 national guidelines that recommend IPTp-SP strategy, 8 (34.8%) are not explicit about directly observed therapy requirements, and three-quarters, 17 (73.9%), do not specify contra-indication of SP in human immunodeficiency virus (HIV)-infected pregnant women receiving cotrimoxazole prophylaxis. Most of the guidelines (18/23; 78.3%) state the recommended folic acid dose.
Several national guidelines and PMI reports require update revisions to harmonize with international guidelines and emergent trends in managing falciparum malaria in pregnancy. National guidelines and those of donor agencies should comply with those of WHO guideline recommendations although local conditions and delayed guideline updates may call for deviations from WHO evidence-based guidelines.</description><identifier>ISSN: 1475-2875</identifier><identifier>EISSN: 1475-2875</identifier><identifier>DOI: 10.1186/s12936-020-03565-2</identifier><identifier>PMID: 33485330</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Anemia ; Antimalarial agents ; Antimalarials ; Artemether ; Artemisinin ; Artesunate ; Binding sites ; Chloroquine ; Clindamycin ; Complications ; Cotrimoxazole ; Disease prophylaxis ; Dosage and administration ; Drug dosages ; Drug therapy ; Drugs ; Erythrocytes ; Evaluation ; Fetuses ; Folic acid ; Government ; Guidelines ; HIV ; Human diseases ; Human immunodeficiency virus ; Infections ; Intravenous administration ; Malaria ; National guidelines ; Parasites ; Plasmodium falciparum ; Practice guidelines (Medicine) ; Pregnancy ; Pregnant women ; Prenatal care ; Prevention ; Prophylaxis ; Pyrimethamine ; Quinine ; Recent trends ; Regions ; Review ; Reviews ; Stillbirth ; Sulfadoxine ; Treatment guidelines ; Vector-borne diseases ; WHO ; Women ; Womens health</subject><ispartof>Malaria journal, 2021-01, Vol.20 (1), p.62-62, Article 62</ispartof><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-8bbf689382f7f465cc4c309e04c82ab40ec9ecbd69c2d3d260d7e0d6ea4c291a3</citedby><cites>FETCH-LOGICAL-c563t-8bbf689382f7f465cc4c309e04c82ab40ec9ecbd69c2d3d260d7e0d6ea4c291a3</cites><orcidid>0000-0001-6591-7686</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825227/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2490911809?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33485330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Al Khaja, Khalid A J</creatorcontrib><creatorcontrib>Sequeira, Reginald P</creatorcontrib><title>Drug treatment and prevention of malaria in pregnancy: a critical review of the guidelines</title><title>Malaria journal</title><addtitle>Malar J</addtitle><description>Malaria caused by Plasmodium falciparum in pregnancy can result in adverse maternal and fetal sequelae. This review evaluated the adherence of the national guidelines drawn from World Health Organization (WHO) regions, Africa, Eastern Mediterranean, Southeast Asia, and Western Pacific, to the WHO recommendations on drug treatment and prevention of chloroquine-resistant falciparum malaria in pregnant women.
Thirty-five updated national guidelines and the President's Malaria Initiative (PMI), available in English language, were reviewed. The primary outcome measures were the first-line anti-malarial treatment protocols adopted by national guidelines for uncomplicated and complicated falciparum malaria infections in early (first) and late (second and third) trimesters of pregnancy. The strategy of intermittent preventive treatment of malaria in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP) was also addressed.
This review evaluated the treatment and prevention of falciparum malaria in pregnancy in 35 national guidelines/PMI-Malaria Operational Plans (MOP) reports out of 95 malaria-endemic countries. Of the 35 national guidelines, 10 (28.6%) recommend oral quinine plus clindamycin as first-line treatment for uncomplicated malaria in the first trimester. As the first-line option, artemether-lumefantrine, an artemisinin-based combination therapy, is adopted by 26 (74.3%) of the guidelines for treating uncomplicated or complicated malaria in the second and third trimesters. Intravenous artesunate is approved by 18 (51.4%) and 31 (88.6%) guidelines for treating complicated malaria during early and late pregnancy, respectively. Of the 23 national guidelines that recommend IPTp-SP strategy, 8 (34.8%) are not explicit about directly observed therapy requirements, and three-quarters, 17 (73.9%), do not specify contra-indication of SP in human immunodeficiency virus (HIV)-infected pregnant women receiving cotrimoxazole prophylaxis. Most of the guidelines (18/23; 78.3%) state the recommended folic acid dose.
Several national guidelines and PMI reports require update revisions to harmonize with international guidelines and emergent trends in managing falciparum malaria in pregnancy. National guidelines and those of donor agencies should comply with those of WHO guideline recommendations although local conditions and delayed guideline updates may call for deviations from WHO evidence-based guidelines.</description><subject>Anemia</subject><subject>Antimalarial agents</subject><subject>Antimalarials</subject><subject>Artemether</subject><subject>Artemisinin</subject><subject>Artesunate</subject><subject>Binding sites</subject><subject>Chloroquine</subject><subject>Clindamycin</subject><subject>Complications</subject><subject>Cotrimoxazole</subject><subject>Disease prophylaxis</subject><subject>Dosage and administration</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>Drugs</subject><subject>Erythrocytes</subject><subject>Evaluation</subject><subject>Fetuses</subject><subject>Folic acid</subject><subject>Government</subject><subject>Guidelines</subject><subject>HIV</subject><subject>Human diseases</subject><subject>Human immunodeficiency virus</subject><subject>Infections</subject><subject>Intravenous administration</subject><subject>Malaria</subject><subject>National guidelines</subject><subject>Parasites</subject><subject>Plasmodium falciparum</subject><subject>Practice guidelines (Medicine)</subject><subject>Pregnancy</subject><subject>Pregnant women</subject><subject>Prenatal care</subject><subject>Prevention</subject><subject>Prophylaxis</subject><subject>Pyrimethamine</subject><subject>Quinine</subject><subject>Recent trends</subject><subject>Regions</subject><subject>Review</subject><subject>Reviews</subject><subject>Stillbirth</subject><subject>Sulfadoxine</subject><subject>Treatment guidelines</subject><subject>Vector-borne diseases</subject><subject>WHO</subject><subject>Women</subject><subject>Womens health</subject><issn>1475-2875</issn><issn>1475-2875</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1r3DAQFaWlSbf9Az0UQy-9ONW35B4KIf1IIJBLe-lFyNLY0WJLW9lOyL-vNpuG3RCE0DDz3pNm9BB6T_AJIVp-nghtmKwxxTVmQoqavkDHhKsSaCVe7sVH6M00rTEmSiv6Gh0xxrVgDB-jP9_y0ldzBjuPEOfKRl9tMtyUOKRYpa4a7WBzsFWI20IfbXR3XypbuRzm4OxQFXSA2y10voaqX4KHIUSY3qJXnR0mePdwrtDvH99_nZ3Xl1c_L85OL2snJJtr3bad1A3TtFMdl8I57hhuAHOnqW05BteAa71sHPXMU4m9AuwlWO5oQyxboYudrk92bTY5jDbfmWSDuU-k3Buby1MHMEQDA9KC4srzsrV2xLWaWE9BNMwXra87rc3SjuBdGUO2w4HoYSWGa9OnG6M0FZSqIvDpQSCnvwtMsxnD5GAYbIS0TIZyjZVguPzcCn18Al2nJccyqoJqcFP-GO-helsaCLFL5V63FTWnUmAupBSioE6eQZXlYQwuRehCyR8Q6I7gcpqmDN1jjwSbrbvMzl2muMvcu8vQQvqwP51Hyn87sX_2espB</recordid><startdate>20210123</startdate><enddate>20210123</enddate><creator>Al Khaja, Khalid A J</creator><creator>Sequeira, Reginald P</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SS</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6591-7686</orcidid></search><sort><creationdate>20210123</creationdate><title>Drug treatment and prevention of malaria in pregnancy: a critical review of the guidelines</title><author>Al Khaja, Khalid A J ; Sequeira, Reginald P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-8bbf689382f7f465cc4c309e04c82ab40ec9ecbd69c2d3d260d7e0d6ea4c291a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Anemia</topic><topic>Antimalarial agents</topic><topic>Antimalarials</topic><topic>Artemether</topic><topic>Artemisinin</topic><topic>Artesunate</topic><topic>Binding sites</topic><topic>Chloroquine</topic><topic>Clindamycin</topic><topic>Complications</topic><topic>Cotrimoxazole</topic><topic>Disease prophylaxis</topic><topic>Dosage and administration</topic><topic>Drug dosages</topic><topic>Drug therapy</topic><topic>Drugs</topic><topic>Erythrocytes</topic><topic>Evaluation</topic><topic>Fetuses</topic><topic>Folic acid</topic><topic>Government</topic><topic>Guidelines</topic><topic>HIV</topic><topic>Human diseases</topic><topic>Human immunodeficiency virus</topic><topic>Infections</topic><topic>Intravenous administration</topic><topic>Malaria</topic><topic>National guidelines</topic><topic>Parasites</topic><topic>Plasmodium falciparum</topic><topic>Practice guidelines (Medicine)</topic><topic>Pregnancy</topic><topic>Pregnant women</topic><topic>Prenatal care</topic><topic>Prevention</topic><topic>Prophylaxis</topic><topic>Pyrimethamine</topic><topic>Quinine</topic><topic>Recent trends</topic><topic>Regions</topic><topic>Review</topic><topic>Reviews</topic><topic>Stillbirth</topic><topic>Sulfadoxine</topic><topic>Treatment guidelines</topic><topic>Vector-borne diseases</topic><topic>WHO</topic><topic>Women</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Al Khaja, Khalid A J</creatorcontrib><creatorcontrib>Sequeira, Reginald P</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Public Health Database</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 One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Malaria journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Al Khaja, Khalid A J</au><au>Sequeira, Reginald P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Drug treatment and prevention of malaria in pregnancy: a critical review of the guidelines</atitle><jtitle>Malaria journal</jtitle><addtitle>Malar J</addtitle><date>2021-01-23</date><risdate>2021</risdate><volume>20</volume><issue>1</issue><spage>62</spage><epage>62</epage><pages>62-62</pages><artnum>62</artnum><issn>1475-2875</issn><eissn>1475-2875</eissn><abstract>Malaria caused by Plasmodium falciparum in pregnancy can result in adverse maternal and fetal sequelae. This review evaluated the adherence of the national guidelines drawn from World Health Organization (WHO) regions, Africa, Eastern Mediterranean, Southeast Asia, and Western Pacific, to the WHO recommendations on drug treatment and prevention of chloroquine-resistant falciparum malaria in pregnant women.
Thirty-five updated national guidelines and the President's Malaria Initiative (PMI), available in English language, were reviewed. The primary outcome measures were the first-line anti-malarial treatment protocols adopted by national guidelines for uncomplicated and complicated falciparum malaria infections in early (first) and late (second and third) trimesters of pregnancy. The strategy of intermittent preventive treatment of malaria in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP) was also addressed.
This review evaluated the treatment and prevention of falciparum malaria in pregnancy in 35 national guidelines/PMI-Malaria Operational Plans (MOP) reports out of 95 malaria-endemic countries. Of the 35 national guidelines, 10 (28.6%) recommend oral quinine plus clindamycin as first-line treatment for uncomplicated malaria in the first trimester. As the first-line option, artemether-lumefantrine, an artemisinin-based combination therapy, is adopted by 26 (74.3%) of the guidelines for treating uncomplicated or complicated malaria in the second and third trimesters. Intravenous artesunate is approved by 18 (51.4%) and 31 (88.6%) guidelines for treating complicated malaria during early and late pregnancy, respectively. Of the 23 national guidelines that recommend IPTp-SP strategy, 8 (34.8%) are not explicit about directly observed therapy requirements, and three-quarters, 17 (73.9%), do not specify contra-indication of SP in human immunodeficiency virus (HIV)-infected pregnant women receiving cotrimoxazole prophylaxis. Most of the guidelines (18/23; 78.3%) state the recommended folic acid dose.
Several national guidelines and PMI reports require update revisions to harmonize with international guidelines and emergent trends in managing falciparum malaria in pregnancy. National guidelines and those of donor agencies should comply with those of WHO guideline recommendations although local conditions and delayed guideline updates may call for deviations from WHO evidence-based guidelines.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>33485330</pmid><doi>10.1186/s12936-020-03565-2</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6591-7686</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anemia Antimalarial agents Antimalarials Artemether Artemisinin Artesunate Binding sites Chloroquine Clindamycin Complications Cotrimoxazole Disease prophylaxis Dosage and administration Drug dosages Drug therapy Drugs Erythrocytes Evaluation Fetuses Folic acid Government Guidelines HIV Human diseases Human immunodeficiency virus Infections Intravenous administration Malaria National guidelines Parasites Plasmodium falciparum Practice guidelines (Medicine) Pregnancy Pregnant women Prenatal care Prevention Prophylaxis Pyrimethamine Quinine Recent trends Regions Review Reviews Stillbirth Sulfadoxine Treatment guidelines Vector-borne diseases WHO Women Womens health |
title | Drug treatment and prevention of malaria in pregnancy: a critical review of the guidelines |
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