Evidence map›Paper›PMID 41613249›Full record

ArticleWellcome open research2022

Surveillance of respiratory viruses at health facilities from across Kenya, 2014.

Nickson Murunga, Bryan Nyawanda, Joyce U Nyiro, Grieven P Otieno, Everlyn Kamau, Charles N Agoti, Clement Lewa, Alex Gichuki, Martin Mutunga, Nancy Otieno and 11 more

Abstract read
In one paragraph

Article in Wellcome open research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
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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

21 authors.

Nickson MurungaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-5304-2210
Bryan NyawandaKEMRI-Centre for Global Health Research, Kisumu, Kenya.ORCID https://orcid.org/0000-0003-0069-1473
Joyce U NyiroKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-7215-6539
Grieven P OtienoKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0002-3053-1369
Everlyn KamauKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Charles N AgotiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0002-2160-567X
Clement LewaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Alex GichukiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Martin MutungaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Nancy OtienoKEMRI-Centre for Global Health Research, Kisumu, Kenya.
Lilian MayiekaKEMRI-Centre for Global Health Research, Kisumu, Kenya.
Melvin OchiengKEMRI-Centre for Global Health Research, Kisumu, Kenya.
Gilbert KikwaiKEMRI-Centre for Global Health Research, Kisumu, Kenya.ORCID https://orcid.org/0000-0002-2307-2280
Elizabeth HunspergerU.S. Centers of Disease Control and Prevention (CDC), Center for Global Health, Division of Global Health Protection, Nairobi, Kenya.ORCID https://orcid.org/0000-0002-4450-621X
Clayton OnyangoU.S. Centers of Disease Control and Prevention (CDC), Center for Global Health, Division of Global Health Protection, Nairobi, Kenya.
Gideon EmukuleU.S. Centers of Disease Control and Prevention (CDC), Center for Global Health, Division of Global Health Protection, Nairobi, Kenya.
Godfrey BigogoKEMRI-Centre for Global Health Research, Kisumu, Kenya.
Jennifer R VeraniU.S. Centers of Disease Control and Prevention (CDC), Center for Global Health, Division of Global Health Protection, Nairobi, Kenya.
Sandra S ChavesU.S. Centers of Disease Control and Prevention (CDC), Center for Global Health, Division of Global Health Protection, Nairobi, Kenya.ORCID https://orcid.org/0000-0002-9453-7057
D James NokesKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-5426-1984
Patrick K MunywokiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-9419-7155

Funding

CGH CDC HHS U01 GH002143Wellcome Trust
6 · The paper itself

Abstract

Background: Acute respiratory illnesses (ARI) are a major cause of morbidity and mortality globally. With (re)emergence of novel viruses and increased access to childhood bacterial vaccines, viruses have assumed greater importance in the aetiology of ARI. There are now promising candidate vaccines against some of the most common endemic respiratory viruses. Optimal delivery strategies for these vaccines, and the need for interventions against other respiratory viruses, requires geographically diverse data capturing temporal variations in virus circulation. Methods: We leveraged three health facility-based respiratory illness surveillance platforms operating in 11 sites across Kenya. Nasopharyngeal (NP) and/or oropharyngeal (OP) specimens, patient demographic, and clinical characteristics were collected in 2014 from individuals of various ages presenting with respiratory symptoms at the surveillance facilities. Real time multiplex polymerase chain reaction was used to detect rhinoviruses, respiratory syncytial virus (RSV), influenza virus, human coronaviruses (hCoV), and adenoviruses. Results: From 11 sites, 5451 NP/OP specimens were collected and tested from patients. Of these, 40.2% were positive for at least one of the targeted respiratory viruses. The most frequently detected were rhinoviruses (17.0%) and RSV A/B (10.5%), followed by influenza A (6.2%), adenovirus (6.0%) and hCoV (4.2%). RSV was most prevalent among infants aged <12 months old (18.9%), adenovirus among children aged 12-23 months old (11.0%), influenza A among children aged 24-59 months (9.3%), and rhinovirus across all age groups (range, 12.7-19.0%). RSV had a higher virus positivity in the inpatient setting (12.5%) compared to outpatient setting (4.8%). The overall percent virus positivity varied by surveillance site, health facility type and case definition used in surveillance. Conclusions: We identify rhinoviruses, RSV, and influenza A as the most prevalent respiratory viruses. Higher RSV positivity in inpatients, and in infants, strengthens the case for RSV vaccination. To inform the design and delivery of public health interventions, long-term surveillance is required to establish regional heterogeneities in respiratory virus circulation and seasonality.

Indexed as

adenovirusesendemic human coronaviruseshuman rhinovirusesinfluenza virusesmultiplex RT-PCRnasopharyngeal swaboropharyngeal swabrespiratory syncytial viruses

Identifiers

PMID41613249
PMCPMC12848351

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.