Evidence map›Paper›PMID 26410081›Full record

ArticleMalaria journal2015

Lack of effect of intermittent preventive treatment for malaria in pregnancy and intense drug resistance in western Uganda.

Vera Braun, Eva Rempis, Alexandra Schnack, Sarah Decker, John Rubaihayo, Nazarius Mbona Tumwesigye, Stefanie Theuring, Gundel Harms, Priscilla Busingye, Frank P Mockenhaupt

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 3 pooled it
8.6field-weighted citation impact, top 2% 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

50 citing papers in PubMed, 3 syntheses or guidelines pooled it, 91 citations in OpenAlex.

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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

10 authors at 4 institutions in 2 countries.

Vera BraunInstitute of Tropical Medicine and International Health, Charité-University Medicine Berlin, Berlin, Germany. verabraun@gmail.com.
Eva RempisInstitute of Tropical Medicine and International Health, Charité-University Medicine Berlin, Berlin, Germany. Eva.Rempis@gmx.de.
Alexandra SchnackInstitute of Tropical Medicine and International Health, Charité-University Medicine Berlin, Berlin, Germany. alexandra.schnack@charite.de.
Sarah DeckerInstitute of Tropical Medicine and International Health, Charité-University Medicine Berlin, Berlin, Germany. sarah.decker@gmail.com.
John RubaihayoPublic Health Department, Mountains of the Moon University, Fort Portal, Uganda. rubaihayoj@yahoo.co.uk.
Nazarius Mbona TumwesigyeSchool of Public Health, College of Health Sciences, Makerere University, Kampala, Uganda. naz@musph.ac.ug.
Stefanie TheuringInstitute of Tropical Medicine and International Health, Charité-University Medicine Berlin, Berlin, Germany. stefanie.theuring@charite.de.
Gundel HarmsInstitute of Tropical Medicine and International Health, Charité-University Medicine Berlin, Berlin, Germany. gundel.harms@charite.de.
Priscilla BusingyeHoly Family Virika Hospital, Fort Portal, Uganda. holyface03@gmail.com.
Frank P MockenhauptInstitute of Tropical Medicine and International Health, Charité-University Medicine Berlin, Berlin, Germany. frank.mockenhaupt@charite.de.
Charité - Universitätsmedizin Berlin · DEMakerere University · UGMountains of the Moon University · UGVirika Hospital · UG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIntermittent preventive treatment in pregnancy (IPTp) with sulfadoxine-pyrimethamine (SP) is widely implemented in sub-Saharan Africa for the prevention of malaria in pregnancy and adverse birth outcomes. However, in areas of intense SP resistance, the efficacy of IPTp may be compromised.

methodsA cross-sectional study among 915 delivering women (728 analysable live singleton deliveries) was conducted in Fort Portal, western Uganda, to assess associations of reported IPTp use, Plasmodium falciparum infection, maternal anaemia, low birth weight, and preterm delivery, and to estimate the degree of SP resistance as reflected by pfdhfr/pfdhps mutations.

resultsPlasmodium falciparum infection was detected by PCR in 8.9 % and by microscopy of placental blood samples in 4.0 %. Infection was significantly associated with stillbirth, early neonatal death, anaemia, low birth weight, and pre-term delivery. Eighty percent of the women had taken at least one dose of IPTp, and more than half had taken two doses. As compared to women without chemoprophylaxis against malaria, IPTp had no significant influence on the presence of P. falciparum infection (13.8 vs. 9.6 %, P = 0.31). Nor was it associated with reductions in anaemia, low birth weight or preterm delivery. P. falciparum with intense SP resistance (pfdhfr/pfdhps quintuple or sextuple mutations) were observed in 93 % (pfdhps 581G, 36 %), and the additional high resistance allele pfhdr 164L in 36 %.

conclusionsIn Fort Portal, Uganda, reported use of IPTp with SP does not provide an observable benefit. The molecular markers of P. falciparum indicate high grade SP resistance reaching the threshold set by WHO for the discontinuation of IPTp with SP. Alternative approaches for the prevention of malaria in pregnancy are urgently needed.

Indexed as

AdolescentAdultAnalysis of VarianceAntimalarialsCross-Sectional StudiesDrug ResistanceFemaleHealth Services AccessibilityHumansInfant, Low Birth WeightInfant, NewbornMalaria, FalciparumPlasmodium falciparumPregnancyPregnancy Complications, ParasiticPremature BirthAntimalarials

Identifiers

PMID26410081
PMCPMC4583758
OpenAlexW2122335316

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.