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  1. Article ; Online: Have You Heard the News? Artemether-lumefantrine is Now Recommended for ALL Uncomplicated Malaria in the United States, Including in Pregnancy.

    Castro, Laura / Ridpath, Alison / Mace, Kimberly / Gutman, Julie R

    Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

    2023  Volume 78, Issue 2, Page(s) 245–247

    MeSH term(s) Pregnancy ; Female ; Humans ; United States/epidemiology ; Antimalarials/therapeutic use ; Artemether/therapeutic use ; Artemether, Lumefantrine Drug Combination/therapeutic use ; Malaria/drug therapy ; Malaria/epidemiology ; Artemisinins/therapeutic use ; Malaria, Falciparum/drug therapy ; Malaria, Falciparum/epidemiology ; Ethanolamines/therapeutic use ; Fluorenes/therapeutic use ; Drug Combinations
    Chemical Substances Antimalarials ; Artemether (C7D6T3H22J) ; Artemether, Lumefantrine Drug Combination ; Artemisinins ; Ethanolamines ; Fluorenes ; Drug Combinations
    Language English
    Publishing date 2023-10-16
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1099781-7
    ISSN 1537-6591 ; 1058-4838
    ISSN (online) 1537-6591
    ISSN 1058-4838
    DOI 10.1093/cid/ciad638
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Systematic Review and Meta-Analysis of Seasonal Malaria Chemoprevention.

    Thwing, Julie / Williamson, John / Cavros, Irene / Gutman, Julie R

    The American journal of tropical medicine and hygiene

    2023  Volume 110, Issue 1, Page(s) 20–31

    Abstract: Seasonal malaria chemoprevention (SMC) for children under 5 years of age for up to four monthly cycles during malaria transmission season was recommended by the WHO in 2012 and has been implemented in 13 countries in the Sahel, reaching more than 30 ... ...

    Abstract Seasonal malaria chemoprevention (SMC) for children under 5 years of age for up to four monthly cycles during malaria transmission season was recommended by the WHO in 2012 and has been implemented in 13 countries in the Sahel, reaching more than 30 million children annually. Malaria control programs implementing SMC have asked the WHO to consider expanding the age range or number of monthly cycles. We conducted a systematic review and meta-analysis of SMC among children up to 15 years of age and up to six monthly cycles. Twelve randomized studies were included, with outcomes stratified by age (< 5/≥ 5 years), by three or four versus five or six cycles, and by drug where possible. Drug regimens included sulfadoxine-pyrimethamine + amodiaquine, amodiaquine-artesunate, and sulfadoxine-pyrimethamine + artesunate. Included studies were all conducted in Sahelian countries in which high-grade resistance to sulfadoxine-pyrimethamine was rare and in zones with parasite prevalence ranging from 1% to 79%. Seasonal malaria chemoprevention resulted in substantial reductions in uncomplicated malaria incidence measured during that transmission season (rate ratio: 0.27, 95% CI: 0.25-0.29 among children < 5 years; rate ratio: 0.27, 95% CI: 0.25-0.30 among children ≥ 5 years) and in the prevalence of malaria parasitemia measured within 4-6 weeks from the final SMC cycle (risk ratio: 0.38, 95% CI: 0.34-0.43 among children < 5 years; risk ratio: 0.23, 95% CI: 0.11-0.48 among children ≥ 5 years). In high-transmission zones, SMC resulted in a moderately reduced risk of any anemia (risk ratio: 0.77, 95% CI: 0.72-0.83 among children < 5 years; risk ratio: 0.70, 95% CI: 0.52-0.95 among children ≥ 5 years [one study]). Children < 10 years of age had a moderate reduction in severe malaria (risk ratio: 0.53, 95% CI: 0.37-0.76) but no evidence of a mortality reduction. The evidence suggests that in areas in which sulfadoxine-pyrimethamine and amodiaquine remained efficacious, SMC effectively reduced malaria disease burden among children both < 5 and ≥ 5 years old and that the number of cycles should be commensurate with the length of the transmission season, up to six cycles.
    MeSH term(s) Child ; Child, Preschool ; Humans ; Amodiaquine/therapeutic use ; Antimalarials/therapeutic use ; Artesunate/therapeutic use ; Chemoprevention/methods ; Drug Combinations ; Malaria/epidemiology ; Malaria/prevention & control ; Malaria/drug therapy ; Pyrimethamine/therapeutic use ; Seasons ; Sulfadoxine/therapeutic use ; Adolescent
    Chemical Substances Amodiaquine (220236ED28) ; Antimalarials ; Artesunate (60W3249T9M) ; Drug Combinations ; Pyrimethamine (Z3614QOX8W) ; Sulfadoxine (88463U4SM5) ; sulfadoxine-pyrimethamine-artesunate
    Language English
    Publishing date 2023-12-11
    Publishing country United States
    Document type Meta-Analysis ; Systematic Review ; Journal Article
    ZDB-ID 2942-7
    ISSN 1476-1645 ; 0002-9637
    ISSN (online) 1476-1645
    ISSN 0002-9637
    DOI 10.4269/ajtmh.23-0481
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Evidence for treating malaria with artemisinin-based combination therapy in the first trimester of pregnancy.

    Gutman, Julie R / Chico, R Matthew

    The Lancet. Infectious diseases

    2020  Volume 20, Issue 8, Page(s) 880–881

    MeSH term(s) Artemisinins ; Female ; Humans ; Malaria ; Malaria, Falciparum ; Pregnancy ; Quinine
    Chemical Substances Artemisinins ; Quinine (A7V27PHC7A)
    Language English
    Publishing date 2020-04-29
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 2061641-7
    ISSN 1474-4457 ; 1473-3099
    ISSN (online) 1474-4457
    ISSN 1473-3099
    DOI 10.1016/S1473-3099(20)30131-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Response to Behrens and Edwards: Atovaquone-proguanil exposure in pregnancy should not be condemned from current evidence.

    Gutman, Julie R / Tan, Kathrine R

    Travel medicine and infectious disease

    2020  Volume 34, Page(s) 101599

    MeSH term(s) Atovaquone ; Drug Combinations ; Female ; Humans ; Infant ; Pregnancy ; Proguanil/adverse effects ; Retrospective Studies
    Chemical Substances Drug Combinations ; atovaquone, proguanil drug combination ; Proguanil (S61K3P7B2V) ; Atovaquone (Y883P1Z2LT)
    Language English
    Publishing date 2020-02-18
    Publishing country Netherlands
    Document type Letter ; Comment
    ZDB-ID 2170891-5
    ISSN 1873-0442 ; 1477-8939
    ISSN (online) 1873-0442
    ISSN 1477-8939
    DOI 10.1016/j.tmaid.2020.101599
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Mass Drug Administration: Contextual Factor Considerations.

    Schneider, Zachary D / Busbee, Alexandra L / Boily, Marisa C / Shah, Monica P / Hwang, Jimee / Lindblade, Kim A / Gutman, Julie R

    The American journal of tropical medicine and hygiene

    2024  Volume 110, Issue 4_Suppl, Page(s) 30–37

    Abstract: In designing mass drug administration (MDA) campaigns, it is imperative to consider contextual factors that affect uptake of the intervention, including acceptability, cost, feasibility, and health system considerations, to ensure optimal coverage. We ... ...

    Abstract In designing mass drug administration (MDA) campaigns, it is imperative to consider contextual factors that affect uptake of the intervention, including acceptability, cost, feasibility, and health system considerations, to ensure optimal coverage. We reviewed the literature on contextual factors influencing MDA delivery to provide programs with information to design a successful campaign. From 1,044 articles screened, 37 included contextual factors relevant to participants' values and preferences, drivers of MDA acceptability, health equity concerns, financial and economic aspects, and feasibility barriers; 13 included relevant modeling data. Key findings were abstracted by two reviewers and summarized. No studies directly assessed values or direct health equity concerns with respect to MDA, which represents an evidence gap as unequal distributions of effects and factors that impact participant acceptability and program feasibility must be considered to ensure equitable access. Participant acceptability was the most widely surveyed factor, appearing in 28 of 37 studies; perceived adverse events were a frequently noted cause of nonparticipation, mentioned in 15 studies. Feasibility considerations included when, where, and how drugs will be delivered and how to address pregnant women, as these can all have substantial implications for participation. Mass drug administration costs (∼$1.04 to $19.40 per person per round) are driven primarily by drug prices, but the delivery mechanism can have varying costs as well, and integration with other interventions may provide cost savings. Both programmatic goals and sociopolitical and economic contexts must be carefully considered before embarking on an MDA program to ensure programmatic success.
    MeSH term(s) Humans ; Female ; Pregnancy ; Mass Drug Administration ; Pregnant Women ; Health Equity ; Cost Savings ; Surveys and Questionnaires
    Language English
    Publishing date 2024-01-23
    Publishing country United States
    Document type Review ; Journal Article
    ZDB-ID 2942-7
    ISSN 1476-1645 ; 0002-9637
    ISSN (online) 1476-1645
    ISSN 0002-9637
    DOI 10.4269/ajtmh.22-0767
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Routine Healthcare Facility- and Antenatal Care-Based Malaria Surveillance: Challenges and Opportunities.

    Gutman, Julie R / Thwing, Julie / Mwesigwa, Julia / McElroy, Peter D / Robertson, Molly

    The American journal of tropical medicine and hygiene

    2022  Volume 108, Issue 2_Suppl, Page(s) 4–7

    Abstract: Most monitoring and evaluation tools for measuring malaria burden, intervention coverage, and impact of interventions use periodic nationally representative cross-sectional household surveys. These provide advantages in terms of selecting a large, ... ...

    Abstract Most monitoring and evaluation tools for measuring malaria burden, intervention coverage, and impact of interventions use periodic nationally representative cross-sectional household surveys. These provide advantages in terms of selecting a large, unbiased, population-based sample; however, they are infrequently conducted, are resource-intensive, and do not provide longitudinal data with sufficient granularity. Given the heterogeneity of malaria transmission within most endemic countries, systems with the capacity to provide more granular and frequent data would be more actionable by national malaria control programs and local implementing partners. There is increasing interest in using routine health facility data, usually from outpatient department visits, for monitoring malaria burden. Data from pregnant women attending antenatal care (ANC) could minimize bias related to fever care-seeking among outpatient department visits and provide more granular parasite prevalence data. Most pregnant women attend ANC at least once and are thus highly representative of the overall pregnant population. A growing body of evidence suggests that malaria parasitemia in pregnant women is correlated with parasitemia in children aged < 5 years in moderate to high transmission areas, allowing for monitoring parasitemia in real time. Additional data are needed to assess whether pregnant women are sufficiently representative of the overall population to yield valid malaria prevalence and intervention coverage estimates. Although use of routinely collected ANC data faces many of the same challenges experienced by other routinely collected health facility data, the opportunity to improve parasite prevalence monitoring and the associated health benefits to mothers and infants of early detection of parasitemia make these efforts valuable.
    MeSH term(s) Infant ; Child ; Female ; Pregnancy ; Humans ; Prenatal Care ; Parasitemia/parasitology ; Cross-Sectional Studies ; Malaria/diagnosis ; Malaria/epidemiology ; Malaria/prevention & control ; Health Facilities ; Patient Acceptance of Health Care
    Language English
    Publishing date 2022-06-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2942-7
    ISSN 1476-1645 ; 0002-9637
    ISSN (online) 1476-1645
    ISSN 0002-9637
    DOI 10.4269/ajtmh.22-0182
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Contextual Factors to Improve Implementation of Malaria Chemoprevention in Children: A Systematic Review.

    Gatiba, Peris / Laury, Jessica / Steinhardt, Laura / Hwang, Jimee / Thwing, Julie I / Zulliger, Rose / Emerson, Courtney / Gutman, Julie R

    The American journal of tropical medicine and hygiene

    2023  Volume 110, Issue 1, Page(s) 69–78

    Abstract: Malaria remains a leading cause of childhood morbidity and mortality in sub-Saharan Africa, particularly among children under 5 years of age. To help address this challenge, the WHO recommends chemoprevention for certain populations. For children and ... ...

    Abstract Malaria remains a leading cause of childhood morbidity and mortality in sub-Saharan Africa, particularly among children under 5 years of age. To help address this challenge, the WHO recommends chemoprevention for certain populations. For children and infants, the WHO recommends seasonal malaria chemoprevention (SMC), perennial malaria chemoprevention (PMC; formerly intermittent preventive treatment in infants [IPTi]), and, more recently, intermittent preventive treatment in school children (IPTsc). This review describes the contextual factors, including feasibility, acceptability, health equity, financial considerations, and values and preferences, that impact implementation of these strategies. A systematic search was conducted on July 5, 2022, and repeated April 13, 2023, to identify relevant literature. Two reviewers independently screened titles for eligibility, extracted data from eligible articles, and identified and summarized themes. Of 6,295 unique titles identified, 65 were included. The most frequently evaluated strategy was SMC (n = 40), followed by IPTi (n = 18) and then IPTsc (n = 6). Overall, these strategies were highly acceptable, although with IPTsc, there were community concerns with providing drugs to girls of reproductive age and the use of nonmedical staff for drug distribution. For SMC, door-to-door delivery resulted in higher coverage, improved caregiver acceptance, and reduced cost. Lower adherence was noted when caregivers were charged with giving doses 2 and 3 unsupervised. For SMC and IPTi, travel distances and inclement weather limited accessibility. Sensitization and caregiver education efforts, retention of high-quality drug distributors, and improved transportation were key to improving coverage. Additional research is needed to understand the role of community values and preferences in chemoprevention implementation.
    MeSH term(s) Infant ; Child ; Female ; Humans ; Child, Preschool ; Antimalarials/therapeutic use ; Malaria/epidemiology ; Malaria/prevention & control ; Malaria/drug therapy ; Chemoprevention/methods ; Weather ; Caregivers ; Seasons
    Chemical Substances Antimalarials
    Language English
    Publishing date 2023-12-11
    Publishing country United States
    Document type Systematic Review ; Journal Article
    ZDB-ID 2942-7
    ISSN 1476-1645 ; 0002-9637
    ISSN (online) 1476-1645
    ISSN 0002-9637
    DOI 10.4269/ajtmh.23-0478
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Mass Drug Administration to Reduce Malaria Transmission: A Systematic Review and Meta-Analysis.

    Schneider, Zachary D / Shah, Monica P / Boily, Marisa C / Busbee, Alexandra L / Hwang, Jimee / Lindblade, Kim A / Gutman, Julie R

    The American journal of tropical medicine and hygiene

    2023  Volume 110, Issue 4_Suppl, Page(s) 17–29

    Abstract: Malaria remains a significant cause of morbidity and mortality, even in low-transmission settings. With the advent of longer acting, more effective, and well-tolerated antimalarials, there is renewed interest in the efficacy of mass drug administration ( ... ...

    Abstract Malaria remains a significant cause of morbidity and mortality, even in low-transmission settings. With the advent of longer acting, more effective, and well-tolerated antimalarials, there is renewed interest in the efficacy of mass drug administration (MDA) to accelerate to elimination. We conducted a systematic review and meta-analysis to assess the efficacy of MDA to reduce the incidence and prevalence of Plasmodium falciparum (Pf) and Plasmodium vivax (Pv) infection. From 1,044 articles screened, 14 articles, including 10 randomized controlled trials (RCTs), were identified. Five included data on Pf only; five included Pf and Pv. Two of the Pf studies were conducted in areas of high-moderate transmission, the remainder were in areas of low-very low transmission. In higher transmission areas, MDA reduced incidence of Pf parasitemia (rate ratio = 0.61, 95% CI: 0.40-0.92; moderate certainty) 1 to 3 months after drug administration; no significant effect of MDA on Pf parasitemia prevalence was detected 1 to 3 months post-MDA (risk ratio [RR] = 1.76, 95% CI: 0.58-5.36; low certainty). In lower transmission settings, both incidence and prevalence of Pf parasitemia were reduced 1 to 3 months post-MDA (rate ratio = 0.37, 95% CI: 0.21-0.66; RR = 0.25, 95% CI: 0.15-0.41, respectively). Pv prevalence was reduced 1 to 3 months post-MDA (RR = 0.15, 95% CI: 0.10-0.24); there were no RCTs providing data on incidence of Pv. There was no significant effect of MDA at later time points. MDA may have short-term benefits; however, there was no evidence for longer term impact, although none of the trials assessed prolonged interventions.
    MeSH term(s) Humans ; Mass Drug Administration ; Parasitemia/prevention & control ; Parasitemia/drug therapy ; Antimalarials/therapeutic use ; Antimalarials/pharmacology ; Malaria/drug therapy ; Malaria, Vivax/drug therapy ; Malaria, Vivax/epidemiology ; Malaria, Vivax/prevention & control ; Plasmodium falciparum
    Chemical Substances Antimalarials
    Language English
    Publishing date 2023-12-20
    Publishing country United States
    Document type Meta-Analysis ; Systematic Review ; Journal Article
    ZDB-ID 2942-7
    ISSN 1476-1645 ; 0002-9637
    ISSN (online) 1476-1645
    ISSN 0002-9637
    DOI 10.4269/ajtmh.22-0766
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Perceptions and drivers of healthcare provider and drug dispenser practices for the treatment of malaria in pregnancy in the context of multiple first-line therapies in western Kenya: a qualitative study.

    Osoro, Caroline B / Dellicour, Stephanie / Ochodo, Eleanor / Young, Taryn / Ter Kuile, Feiko O / Gutman, Julie R / Hill, Jenny

    Malaria journal

    2023  Volume 22, Issue 1, Page(s) 274

    Abstract: Background: Emergence of Plasmodium falciparum resistance to artemether-lumefantrine in Africa prompted the pilot introduction of multiple first-line therapies (MFT) against malaria in Kenya, potentially exposing women-of-childbearing-age (WOCBAs) to ... ...

    Abstract Background: Emergence of Plasmodium falciparum resistance to artemether-lumefantrine in Africa prompted the pilot introduction of multiple first-line therapies (MFT) against malaria in Kenya, potentially exposing women-of-childbearing-age (WOCBAs) to anti-malarials with unknown safety profiles in the first trimester. This qualitative study explored knowledge and perceptions among healthcare providers providing malaria treatment to WOCBAs and pregnant women.
    Methods: In-depth interviews were conducted with purposively selected public and private health facility (HF) and drug outlet (DO) providers within and outside the pilot-MFT area. County health managers were interviewed about their knowledge of the national treatment guidelines. Transcripts were coded by content analysis using the World Health Organization health system building blocks (leadership/governance, financing, health workforce, health information systems, access to medicines, and service delivery).
    Results: Thirty providers (HF:21, DO:9) and three health managers were interviewed. Eighteen providers were from HFs in the pilot-MFT area; the remaining three and all nine DOs were outside the pilot-MFT area. The analysis revealed that providers had not been trained in malaria case management in the previous twelve months. DO providers were unfamiliar with national treatment guidelines in pregnancy and reported having no pregnancy tests. Health managers were unable to supervise DOs due to resource limitations. Providers from HFs and DOs noted poor sensitivity of malaria rapid diagnostic tests (RDTs) and hesitancy among patients who associated malaria-RDTs with HIV testing. Almost all providers reported anti-malarial stock-outs, with quinine most affected. Patient preference was a major factor in prescribing anti-malarials. Providers in HFs and DOs reported preferentially using artemether-lumefantrine in the first trimester due to the side effects and unavailability of quinine.
    Conclusion: Knowledge of malaria case management in drug outlets and health facilities remains poor. Improved regulation of DO providers is warranted. Optimizing treatment of malaria in pregnancy requires training, availability of malaria commodities, and pregnancy tests.
    MeSH term(s) Pregnancy ; Humans ; Female ; Antimalarials/therapeutic use ; Kenya ; Pharmaceutical Preparations ; Quinine ; Artemether ; Artemether, Lumefantrine Drug Combination/therapeutic use ; Malaria/drug therapy ; Health Personnel
    Chemical Substances Antimalarials ; Pharmaceutical Preparations ; Quinine (A7V27PHC7A) ; Artemether (C7D6T3H22J) ; Artemether, Lumefantrine Drug Combination
    Language English
    Publishing date 2023-09-14
    Publishing country England
    Document type Journal Article
    ZDB-ID 2091229-8
    ISSN 1475-2875 ; 1475-2875
    ISSN (online) 1475-2875
    ISSN 1475-2875
    DOI 10.1186/s12936-023-04698-w
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Healthcare provider and drug dispenser knowledge and adherence to guidelines for the case management of malaria in pregnancy in the context of multiple first-line artemisinin-based combination therapy in western Kenya.

    Osoro, Caroline B / Dellicour, Stephanie / Ochodo, Eleanor / Young, Taryn / Ter Kuile, Feiko / Gutman, Julie R / Hill, Jenny

    Malaria journal

    2023  Volume 22, Issue 1, Page(s) 262

    Abstract: Background: Concerns about emerging resistance to artemether-lumefantrine (AL) in Africa prompted the pilot introduction of multiple first-line therapies (MFT) in Western Kenya, potentially exposing women-of-childbearing-age (WOCBA) to anti-malarials ... ...

    Abstract Background: Concerns about emerging resistance to artemether-lumefantrine (AL) in Africa prompted the pilot introduction of multiple first-line therapies (MFT) in Western Kenya, potentially exposing women-of-childbearing-age (WOCBA) to anti-malarials with unknown safety profiles in the first trimester. The study assessed healthcare provider knowledge and adherence to national guidelines for managing malaria in pregnancy in the context of the MFT pilot.
    Methods: From March to April 2022, a cross-sectional study was conducted in 50 health facilities (HF) and 40 drug outlets (DO) using structured questionnaires to assess pregnancy detection, malaria diagnosis, and treatment choices by trimester. Differences between HF and DO providers and between MFT and non-MFT HFs were assessed using Chi-square tests.
    Results: Of 174 providers (77% HF, 23% DO), 56% were from MFT pilot facilities. Most providers had tertiary education; 5% HF and 20% DO had only primary or secondary education. More HF than DO providers had knowledge of malaria treatment guidelines (62% vs. 40%, p = 0.023), received training in malaria in pregnancy (49% vs. 20%, p = 0.002), and reported assessing for pregnancy in WOCBA (98% vs. 78%, p < 0.001). Most providers insisted on parasitological diagnosis, with 59% HF using microscopy and 85% DO using rapid diagnostic tests. More HF than DO providers could correctly name the drugs for treating uncomplicated malaria in the first trimester (oral quinine, or AL if quinine is unavailable) (90% vs. 58%, p < 0.001), second and third trimesters (artemisinin-based combination therapy) (84% vs. 70%, p = 0.07), and for severe malaria (parenteral artesunate/artemether) (94% vs. 60%, p < 0.001). Among HF providers, those in the MFT pilot had more knowledge of malaria treatment guidelines (67% vs. 49%, p = 0.08) and had received training on treatment of malaria in pregnancy (56% vs. 32%, p = 0.03). Few providers (10% HF and 12% DO) had adequate knowledge of malaria treatment in pregnancy, defined as the correct drug and dose for uncomplicated and severe malaria in all trimesters.
    Conclusions: Knowledge of national malaria in pregnancy treatment guidelines among providers in Western Kenya is suboptimal. Robust training on appropriate anti-malarial and dosage is needed, particularly given the recent change in recommendation for artemether-lumefantrine use in the first trimester. Supervision of DO and HF practices is essential for correct treatment of malaria in pregnancy in the context of MFT programmes.
    MeSH term(s) Pregnancy ; Female ; Humans ; Case Management ; Antimalarials/therapeutic use ; Kenya ; Quinine ; Cross-Sectional Studies ; Artemether ; Artemether, Lumefantrine Drug Combination/therapeutic use ; Artemisinins/therapeutic use ; Malaria/drug therapy
    Chemical Substances Antimalarials ; Quinine (A7V27PHC7A) ; Artemether (C7D6T3H22J) ; Artemether, Lumefantrine Drug Combination ; artemisinin (9RMU91N5K2) ; Artemisinins
    Language English
    Publishing date 2023-09-08
    Publishing country England
    Document type Journal Article
    ZDB-ID 2091229-8
    ISSN 1475-2875 ; 1475-2875
    ISSN (online) 1475-2875
    ISSN 1475-2875
    DOI 10.1186/s12936-023-04692-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

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