Evidence map›Paper›PMID 31167228›Full record

ArticlePLoS medicine2019

Malaria morbidity and mortality following introduction of a universal policy of artemisinin-based treatment for malaria in Papua, Indonesia: A longitudinal surveillance study.

Enny Kenangalem, Jeanne Rini Poespoprodjo, Nicholas M Douglas, Faustina Helena Burdam, Ketut Gdeumana, Ferry Chalfein, Prayoga, Franciscus Thio, Angela Devine, Jutta Marfurt and 10 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PLoS medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
10.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Mapping Antimalarial Drug Resistance in Mozambique: A Systematic Review ofInternational journal of molecular sciences · 2024
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  10. High versus low dose of 14 days treatment of primaquine inmedRxiv : the preprint server for health sciences · 2025
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  16. Malarial Pigment Hemozoin in Neutrophils: A Manifestation of Severe MalariaTurkish journal of haematology : official journal of Turkish Society of Haematology · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 9 institutions in 5 countries.

Enny KenangalemTimika Malaria Research Program, Papuan Health and Community Development Foundation, Timika, Papua, Indonesia.
Jeanne Rini PoespoprodjoTimika Malaria Research Program, Papuan Health and Community Development Foundation, Timika, Papua, Indonesia.ORCID 0000-0003-1573-734X
Nicholas M DouglasGlobal and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.ORCID 0000-0002-7214-4244
Faustina Helena BurdamTimika Malaria Research Program, Papuan Health and Community Development Foundation, Timika, Papua, Indonesia.
Ketut GdeumanaPublic Health & Malaria Control Department, PT Freeport Indonesia/International SOS, Kuala Kencana, Papua, Indonesia.
Ferry ChalfeinTimika Malaria Research Program, Papuan Health and Community Development Foundation, Timika, Papua, Indonesia.
PrayogaTimika Malaria Research Program, Papuan Health and Community Development Foundation, Timika, Papua, Indonesia.
Franciscus ThioTimika Malaria Research Program, Papuan Health and Community Development Foundation, Timika, Papua, Indonesia.
Angela DevineGlobal and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.ORCID 0000-0002-3321-8706
Jutta MarfurtGlobal and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
Govert WaramoriPublic Health & Malaria Control Department, PT Freeport Indonesia/International SOS, Kuala Kencana, Papua, Indonesia.
Shunmay YeungFaculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, United Kingdom.ORCID 0000-0002-0997-0850
Rintis NoviyantiEijkman Institute for Molecular Biology, Jakarta, Indonesia.ORCID 0000-0003-1383-3274
Pasi PenttinenPublic Health & Malaria Control Department, PT Freeport Indonesia/International SOS, Kuala Kencana, Papua, Indonesia.ORCID 0000-0001-6929-1086
Michael J BangsPublic Health & Malaria Control Department, PT Freeport Indonesia/International SOS, Kuala Kencana, Papua, Indonesia.
Paulus SugiartoRumah Sakit Mitra Masyarakat, Timika, Papua, Indonesia.
Julie A SimpsonCentre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Australia.ORCID 0000-0002-2660-2013
Yati SoenartoPediatric Research Office, Department of Child Health, Faculty of Medicine, Public Health and Nursing, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Nicholas M AnsteyGlobal and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.
Ric N PriceGlobal and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.ORCID 0000-0003-2000-2874
State University of Papua · IDCharles Darwin University · AUThe University of Melbourne · AUUniversitas Gadjah Mada · IDEijkman Institute for Molecular Biology · IDEuropean Centre for Disease Prevention and Control · SEKasetsart University · THLondon School of Hygiene & Tropical Medicine · GBMahidol University · TH

Funding

Wellcome Trust 200909Wellcome Trust 200909/Z/16/Z
6 · The paper itself

Abstract

backgroundMalaria control activities can have a disproportionately greater impact on Plasmodium falciparum than on P. vivax in areas where both species are coendemic. We investigated temporal trends in malaria-related morbidity and mortality in Papua, Indonesia, before and after introduction of a universal, artemisinin-based antimalarial treatment strategy for all Plasmodium species. METHODS AND

findingsA prospective, district-wide malariometric surveillance system was established in April 2004 to record all cases of malaria at community clinics and the regional hospital and maintained until December 2013. In March 2006, antimalarial treatment policy was changed to artemisinin combination therapy for uncomplicated malaria and intravenous artesunate for severe malaria due to any Plasmodium species. Over the study period, a total of 418,238 patients presented to the surveillance facilities with malaria. The proportion of patients with malaria requiring admission to hospital fell from 26.9% (7,745/28,789) in the pre-policy change period (April 2004 to March 2006) to 14.0% (4,786/34,117) in the late transition period (April 2008 to December 2009), a difference of -12.9% (95% confidence interval [CI] -13.5% to -12.2%). There was a significant fall in the mortality of patients presenting to the hospital with P. falciparum malaria (0.53% [100/18,965] versus 0.32% [57/17,691]; difference = -0.21% [95% CI -0.34 to -0.07]) but not in patients with P. vivax malaria (0.28% [21/7,545] versus 0.23% [28/12,397]; difference = -0.05% [95% CI -0.20 to 0.09]). Between the same periods, the overall proportion of malaria due to P. vivax rose from 44.1% (30,444/69,098) to 53.3% (29,934/56,125) in the community clinics and from 32.4% (9,325/28,789) to 44.1% (15,035/34,117) at the hospital. After controlling for population growth and changes in treatment-seeking behaviour, the incidence of P. falciparum malaria fell from 511 to 249 per 1,000 person-years (py) (incidence rate ratio [IRR] = 0.49 [95% CI 0.48-0.49]), whereas the incidence of P. vivax malaria fell from 331 to 239 per 1,000 py (IRR = 0.72 [95% CI 0.71-0.73]). The main limitations of our study were possible confounding from changes in healthcare provision, a growing population, and significant shifts in treatment-seeking behaviour following implementation of a new antimalarial policy.

conclusionsIn this area with high levels of antimalarial drug resistance, adoption of a universal policy of efficacious artemisinin-based therapy for malaria infections due to any Plasmodium species was associated with a significant reduction in total malaria-attributable morbidity and mortality. The burden of P. falciparum malaria was reduced to a greater extent than that of P. vivax malaria. In coendemic regions, the timely elimination of malaria will require that safe and effective radical cure of both the blood and liver stages of the parasite is widely available for all patients at risk of malaria.

Indexed as

AntimalarialsArtemisininsDrug Resistance, MultipleHumansIncidenceIndonesiaLongitudinal StudiesMalariaPopulation SurveillanceProgram EvaluationProspective StudiesRisk FactorsTime FactorsTreatment OutcomeAntimalarialsartemisininArtemisinins

Identifiers

PMID31167228
PMCPMC6541239
OpenAlexW2947863737

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.