Evidence map›Paper›PMID 29723189›Full record

ArticlePLoS neglected tropical diseases2018

Prevalence and risk factors of Rift Valley fever in humans and animals from Kabale district in Southwestern Uganda, 2016.

Luke Nyakarahuka, Annabelle de St Maurice, Lawrence Purpura, Elizabeth Ervin, Stephen Balinandi, Alex Tumusiime, Jackson Kyondo, Sophia Mulei, Patrick Tusiime, Julius Lutwama and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 5 pooled it
4.8field-weighted citation impact, top 4% 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

62 citing papers in PubMed, 5 syntheses or guidelines pooled it, 91 citations in OpenAlex.

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2 more citing papers are in PubMed but not listed here.

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

16 authors at 4 institutions in 2 countries.

Luke NyakarahukaUganda Virus Research Institute, Department of Arbovirology, Emerging and Re-emerging Infections, Entebbe, Uganda.ORCID 0000-0002-2944-9157
Annabelle de St MauriceCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Lawrence PurpuraCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Elizabeth ErvinCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Stephen BalinandiCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Entebbe, Uganda.
Alex TumusiimeCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Entebbe, Uganda.
Jackson KyondoUganda Virus Research Institute, Department of Arbovirology, Emerging and Re-emerging Infections, Entebbe, Uganda.
Sophia MuleiUganda Virus Research Institute, Department of Arbovirology, Emerging and Re-emerging Infections, Entebbe, Uganda.
Patrick TusiimeKabale district Health Office, Kabale, Uganda.
Julius LutwamaUganda Virus Research Institute, Department of Arbovirology, Emerging and Re-emerging Infections, Entebbe, Uganda.
John D KlenaCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Shelley BrownCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Barbara KnustCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Pierre E RollinCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Stuart T NicholCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.
Trevor R ShoemakerCenters for Disease Control and Prevention, Division of High Consequence Pathogens and Pathology, Viral Special Pathogens Branch, Atlanta, Georgia, United States of America.ORCID 0000-0001-6874-6309
Centers for Disease Control and Prevention · USUganda Virus Research Institute · UGCenters for Disease Control and Prevention · UGKabale University · UG

Funding

ACL HHS U01CK000333
6 · The paper itself

Abstract

backgroundRift Valley fever (RVF) is a zoonotic disease caused by Rift Valley fever virus (RVFV) found in Africa and the Middle East. Outbreaks can cause extensive morbidity and mortality in humans and livestock. Following the diagnosis of two acute human RVF cases in Kabale district, Uganda, we conducted a serosurvey to estimate RVFV seroprevalence in humans and livestock and to identify associated risk factors.

methodsHumans and animals at abattoirs and villages in Kabale district were sampled. Persons were interviewed about RVFV exposure risk factors. Human blood was tested for anti-RVFV IgM and IgG, and animal blood for anti-RVFV IgG. PRINCIPAL

findings655 human and 1051 animal blood samples were collected. Anti-RVFV IgG was detected in 78 (12%) human samples; 3 human samples (0.5%) had detectable IgM only, and 7 (1%) had both IgM and IgG. Of the 10 IgM-positive persons, 2 samples were positive for RVFV by PCR, confirming recent infection. Odds of RVFV seropositivity were greater in participants who were butchers (odds ratio [OR] 5.1; 95% confidence interval [95% CI]: 1.7-15.1) and those who reported handling raw meat (OR 3.4; 95% CI 1.2-9.8). No persons under age 20 were RVFV seropositive. The overall animal seropositivity was 13%, with 27% of cattle, 7% of goats, and 4% of sheep seropositive. In a multivariate logistic regression, cattle species (OR 9.1; 95% CI 4.1-20.5), adult age (OR 3.0; 95% CI 1.6-5.6), and female sex (OR 2.1; 95%CI 1.0-4.3) were significantly associated with animal seropositivity. Individual human seropositivity was significantly associated with animal seropositivity by subcounty after adjusting for sex, age, and occupation (p < 0.05).

conclusionsAlthough no RVF cases had been detected in Uganda from 1968 to March 2016, our study suggests that RVFV has been circulating undetected in both humans and animals living in and around Kabale district. RVFV seropositivity in humans was associated with occupation, suggesting that the primary mode of RVFV transmission to humans in Kabale district could be through contact with animal blood or body fluids.

Indexed as

AbattoirsAdolescentAdultAnimalsAntibodies, ViralCattleCattle DiseasesChildFemaleGoat DiseasesGoatsHumansMaleMiddle AgedPrevalenceRift Valley FeverAntibodies, Viral

Identifiers

PMID29723189
PMCPMC5953497
OpenAlexW2800315720

What OpenQuestion holds

Textmetadata
LicenceCC0
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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.