Evidence map›Paper›PMID 41100690›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2026

Measles Without Rash During Acute Febrile Illness Surveillance in Tanzania, 2023-2024.

Saning'o Lukumay, Domitila Augustino, Queen Saidi Naumanga, S Taylor Payne, Godfrey Guga, Joshua Mungi, Mariamu Temu, Kelvin Msoka, Restituta Mosha, Lea Becker and 3 more

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

13 authors.

Saning'o LukumayHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.ORCID 0009-0005-3061-3611
Domitila AugustinoHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.
Queen Saidi NaumangaDivision of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.ORCID 0009-0007-7988-357X
S Taylor PayneDivision of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
Godfrey GugaHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.ORCID 0000-0002-6444-5311
Joshua MungiHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.
Mariamu TemuHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.
Kelvin MsokaHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.
Restituta MoshaHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.
Lea BeckerDivision of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.
Jie LiuDepartment of Microbial Surveillance and Biosafety, Qingdao University School of Public Health, Qingdao, China.ORCID 0000-0003-2658-5249
Esto MdumaHaydom Lutheran Hospital, Haydom Global Health Institute, Haydom, Tanzania.
Eric R HouptDivision of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA.ORCID 0000-0003-1085-1354

Funding

NIH HHS K24 AI102972)
6 · The paper itself

Abstract

backgroundThe leading causes of fever requiring hospital admission in rural sub-Saharan Africa remain understudied, particularly using modern molecular diagnostics.

methodsWe enrolled 258 patients with acute fever (cases) and 48 controls admitted to 1 hospital in Tanzania for 1 year starting in February 2023. Blood was tested by blood culture, polymerase chain reaction (PCR) for 35 pathogens, and serology for 6 pathogens.

resultsThe leading pathogen detected in cases was measles, with 70 of 258 cases detected by PCR, 74 of 238 by immunoglobulin M serology, and 91 allowing either method. Other pathogens were detected in <5% of cases including, in descending order, Plasmodium, Schistosoma, and Bartonella, among others. Measles was the only pathogen clearly associated with cases versus controls. Of 91 measles cases, only 58 (64%) were clinically suspected and only 56 (62%) met the World Health Organization definition of a clinical measles case, largely because 27 (30%) measles cases did not have recorded rash. Outcomes were poorer for measles without rash versus with rash, with a longer hospital stay (mean, 5.5 vs 3.3 days; P = .010), less full recovery (48% vs 75%; P = .016), and high mortality (7% vs 2%; P = .20). Increased laboratory testing would have detected measles 2 months prior to the first clinical suspicion.

conclusionsMeasles was found to be the leading cause of fever during 1 year of acute febrile illness surveillance in rural Tanzania. Measles can present without notable rash in these settings and has poor outcomes. Increasing laboratory test availability and clinician suspicion for measles is a priority.

Indexed as

ExanthemaFeverMeaslesAcute DiseaseAdolescentCase-Control StudiesChildChild, PreschoolFemaleHumansImmunoglobulin MInfantMaleTanzaniaImmunoglobulin Mfevermeaslesrash

Identifiers

PMID41100690
PMCPMC13341257

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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.