Evidence map›Paper›PMID 37328808›Full record

ArticleBMC infectious diseases2023

Investigating the etiology of acute febrile illness: a prospective clinic-based study in Uganda.

Brian K Kigozi, Grishma A Kharod, Henry Bukenya, Sean V Shadomy, Dana L Haberling, Robyn A Stoddard, Renee L Galloway, Phionah Tushabe, Annet Nankya, Thomas Nsibambi and 7 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
9.6field-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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
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  7. Article
  8. Multi-Pathogen Surveillance of Acute Febrile Illness in Nigeria Using TaqMan Array Cards: Implementation Successes and Lessons Learned From the SAFIAN Study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
  9. Article
  10. Epidemiology and Clinical Characteristics of Human Rickettsial Infections Detected in Nigeria: Discovery of a Significant Contributor to Acute Febrile Illness.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Article
  11. Article
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  14. Molecular detection and typing of pathogenicEpidemiology and infection · 2025
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  20. PathogenicJournal of bacteriology · 2024
    Review
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

17 authors at 4 institutions in 2 countries.

Brian K KigoziUganda Virus Research Institute, Entebbe, Uganda. brkigozi@infocom.co.ug.
Grishma A Kharod *CDC Division of High-Consequence Pathogens and Pathology, Atlanta, USA.
Henry Bukenya *Uganda Virus Research Institute, Entebbe, Uganda.
Sean V ShadomyCDC Division of High-Consequence Pathogens and Pathology, Atlanta, USA.
Dana L HaberlingCDC Division of High-Consequence Pathogens and Pathology, Atlanta, USA.
Robyn A StoddardCDC Division of High-Consequence Pathogens and Pathology, Atlanta, USA.
Renee L GallowayCDC Division of High-Consequence Pathogens and Pathology, Atlanta, USA.
Phionah TushabeUganda Virus Research Institute, Entebbe, Uganda.
Annet NankyaUganda Virus Research Institute, Entebbe, Uganda.
Thomas NsibambiUganda Virus Research Institute, Entebbe, Uganda.
Edward Katongole MbiddeUganda Virus Research Institute, Entebbe, Uganda.
Julius J LutwamaUganda Virus Research Institute, Entebbe, Uganda.
Jamie L PerniciaroCDC Laboratory Systems, Atlanta, USA.
William L NicholsonCDC Rickettsial Zoonoses Branch, Atlanta, USA.
William A BowerCDC Division of High-Consequence Pathogens and Pathology, Atlanta, USA.
Josephine Bwogi *Uganda Virus Research Institute, Entebbe, Uganda.
David D Blaney *CDC Division of High-Consequence Pathogens and Pathology, Atlanta, USA.
Uganda Virus Research Institute · UGCenters for Disease Control and Prevention · UGMakerere University · UGZoo Atlanta · US

Funding

CDC HHS CK08-004Medical Research Council MC_UU_00033/1
6 · The paper itself

Abstract

backgroundHistorically, malaria has been the predominant cause of acute febrile illness (AFI) in sub-Saharan Africa. However, during the last two decades, malaria incidence has declined due to concerted public health control efforts, including the widespread use of rapid diagnostic tests leading to increased recognition of non-malarial AFI etiologies. Our understanding of non-malarial AFI is limited due to lack of laboratory diagnostic capacity. We aimed to determine the etiology of AFI in three distinct regions of Uganda.

methodsA prospective clinic-based study that enrolled participants from April 2011 to January 2013 using standard diagnostic tests. Participant recruitment was from St. Paul's Health Centre (HC) IV, Ndejje HC IV, and Adumi HC IV in the western, central and northern regions, which differ by climate, environment, and population density. A Pearson's chi-square test was used to evaluate categorical variables, while a two-sample t-test and Krukalis-Wallis test were used for continuous variables.

resultsOf the 1281 participants, 450 (35.1%), 382 (29.8%), and 449 (35.1%) were recruited from the western, central, and northern regions, respectively. The median age (range) was 18 (2-93) years; 717 (56%) of the participants were female. At least one AFI pathogen was identified in 1054 (82.3%) participants; one or more non-malarial AFI pathogens were identified in 894 (69.8%) participants. The non-malarial AFI pathogens identified were chikungunya virus, 716 (55.9%); Spotted Fever Group rickettsia (SFGR), 336 (26.2%) and Typhus Group rickettsia (TGR), 97 (7.6%); typhoid fever (TF), 74 (5.8%); West Nile virus, 7 (0.5%); dengue virus, 10 (0.8%) and leptospirosis, 2 (0.2%) cases. No cases of brucellosis were identified. Malaria was diagnosed either concurrently or alone in 404 (31.5%) and 160 (12.5%) participants, respectively. In 227 (17.7%) participants, no cause of infection was identified. There were statistically significant differences in the occurrence and distribution of TF, TGR and SFGR, with TF and TGR observed more frequently in the western region (p = 0.001; p < 0.001) while SFGR in the northern region (p < 0.001).

conclusionMalaria, arboviral infections, and rickettsioses are major causes of AFI in Uganda. Development of a Multiplexed Point-of-Care test would help identify the etiology of non-malarial AFI in regions with high AFI rates.

Indexed as

MalariaRickettsiaRickettsia InfectionsTyphoid FeverAdolescentFemaleFeverHumansMaleProspective StudiesUgandaAcute Febrile illnessArboviral infectionsBrucellosisLeptospirosisMalariaRickettsiosesTyphoid FeverUganda

Identifiers

PMID37328808
PMCPMC10276394
OpenAlexW4380986465

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.