Evidence map›Paper›PMID 42469805›Full record

ArticleMalaria journal2026

Identifying populations with high prevalence of non-malarial febrile illnesses across different demographic groups in Malawi.

Peter Austin Morton Ntenda, David Matiya, Precious Kondwani Majoni, Rex Barnett Mbewe, Fentanesh Nibret Tiruneh

Abstract read
In one paragraph

Article in Malaria journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Peter Austin Morton NtendaMalaria Alert Centre, Kamuzu University of Health Sciences, Chichiri, Private Bag 360, Blantyre 3, Malawi. peterantenda@yahoo.com.
David MatiyaMalaria Alert Centre, Kamuzu University of Health Sciences, Chichiri, Private Bag 360, Blantyre 3, Malawi.
Precious Kondwani MajoniMalawi University of Science and Technology, Thyolo, P.O. Box 5196, Limbe, Malawi.
Rex Barnett MbeweMalaria Alert Centre, Kamuzu University of Health Sciences, Chichiri, Private Bag 360, Blantyre 3, Malawi.
Fentanesh Nibret TirunehDepartment of Applied Human Nutrition, Faculty of Chemical and Food Engineering, Bahir Dar Institute of Technology, Bahir Dar University, P.O. Box 79, Bahir Dar, Ethiopia.

Funding

Determinants of poor responsiveness to the booster dose of the RTS,S malaria vaccine in African childrenR01AI182232 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI James Beeson, SURYARAM GUMMULURU · 2025 to 2026
$1.3M
NIAID/NIH 1R01AI182232-01A1NIAID NIH HHS R01 AI182232
6 · The paper itself

Abstract

backgroundMalaria remains a major cause of febrile illness in Malawi; however, the epidemiology of non-malarial febrile illnesses (NMFIs) is less well characterized. Understanding the distribution and determinants of NMFIs across demographic groups is essential for improving case management in malaria-endemic settings.

objectivesThis study aimed to characterized the distribution and predictors of NMFIs among preschool-aged children (PSC), school-aged children (SAC), women of reproductive age (WRA), and men in Malawi.

methodsSecondary data from the 2015-2016 Malawi Micronutrient Survey were analyzed. Multivariable logistic regression models were fitted separately for each population subgroup to identify factors independently associated with NMFIs. Adjusted odds ratios (aORs) and 95% confidence intervals (CIs) were reported.

resultsThe prevalence of NMFIs was highest among PSC (27.0%) and lowest among men (9.1%). Asymptomatic malaria was most common in SAC (28.6%), while symptomatic malaria was highest in PSC (15.9%). Among PSC, age 24-35 months (aOR = 2.5; 95% CI 1.4-4.6), recent diarrhea (aOR = 1.6; 95% CI 1.1-2.5), recent cough (aOR = 3.8; 95% CI 2.5-5.7), wasting (aOR = 2.2; 95% CI 1.0-4.8), and urban residence (aOR = 1.9; 95% CI 1.0-3.5) were associated with increased odds of NMFIs. In SAC, WRA, and men, recent cough was a consistent predictor of NMFIs (aOR = 1.9; 95% CI 0.9-4.2; aOR = 3.1; 95% CI 1.7-5.8; and aOR = 44.3; 95% CI 10.2-192.8, respectively). Among WRA and men, elevated alpha-1-acid glycoprotein levels were also associated with higher odds of NMFIs (aOR = 2.2; 95% CI 1.0-4.8 and aOR = 4.5; 95% CI 1.0-86.4, respectively).

conclusionPSC bear the highest burden of NMFIs and symptomatic malaria, while SAC commonly harbor asymptomatic malaria. Febrile illness management should move beyond malaria-focused approaches to include integrated screening for common non-malarial infections, particularly in young children.

Indexed as

FeverAdolescentAdultChildChild, PreschoolFemaleHumansInfantMalawiMaleMiddle AgedPrevalenceYoung AdultFeverInfectious diseasesInflammationMalariaMalawiPublic health

Identifiers

PMID42469805
PMCPMC13662969

What OpenQuestion holds

Textmetadata
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.