Evidence map›Paper›PMID 36068112›Full record

ArticleVaccine2022

Epidemiology and pre-vaccine burden of rotavirus diarrhea in Democratic Republic of Congo (DRC): Results of sentinel surveillance, 2009-2019.

Christophe Luhata Lungayo, Rachel M Burke, Aimé Cikomola, Elisabeth Mukamba, Eleanor Burnett, Jacqueline E Tate, John Samuel Otomba, Mbule K Albert, Marcellin M Nimpa, M A Dommergues and 8 more

Abstract read
In one paragraph

Article in Vaccine, 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.

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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

18 authors.

Christophe Luhata LungayoExpanded Program of Immunization, Kinshasa, Democratic Republic of Congo; INSERM U-1018, Centre de recherche en Epidémiologie et Santé des Populations (CESP) - U1018 INSERM, Université Paris Saclay, Paris, France. Electronic address: christophe.luhata@gmail.com.
Rachel M BurkeViral Gastroenteritis Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.
Aimé CikomolaExpanded Program of Immunization, Kinshasa, Democratic Republic of Congo.
Elisabeth MukambaExpanded Program of Immunization, Kinshasa, Democratic Republic of Congo.
Eleanor BurnettViral Gastroenteritis Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.
Jacqueline E TateViral Gastroenteritis Branch, Centers for Disease Control and Prevention, Atlanta, Georgia.
John Samuel OtombaWorld Health Organization Country Office, Democratic Republic of Congo.
Mbule K AlbertWorld Health Organization Country Office, Democratic Republic of Congo.
Marcellin M NimpaWorld Health Organization Country Office, Democratic Republic of Congo.
M A DommerguesService de pédiatrie générale, centre hospitalier de Versailles, Le Chesnay, France.
Elisabeth PukutaInstitut National de Recherches Biomédicales (I.N.R.B), République Démocratique du Congo.
Jason M MwendaRegional Office for Africa, World Health Organization, Brazzaville, Congo.
Keith ShabaRegional Office for Africa, World Health Organization, Brazzaville, Congo.
Gilson K PalukuWorld Health Organization, Intercountry Support Team, Libreville, Gabon.
Aboubacar N'diayeWorld Health Organization, Intercountry Support Team, Libreville, Gabon.
John DitekemenaKinshasa School of Public Health, Faculty of Medicine, University of Kinshasa, Democratic Republic of Congo.
Odile LaunayUniversité Paris Descartes, Sorbonne Paris cite, and Inserm CIC 1417, F-CRIN I-Reivac, Assistance Publique Hôpitaux de Paris, CIC Cochin-Pasteur, Paris, France.
Romain JouffroyINSERM U-1018, Centre de recherche en Epidémiologie et Santé des Populations (CESP) - U1018 INSERM, Université Paris Saclay, Paris, France; Intensive Care Unit, Ambroise Paré Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France; IRMES - Institute for Research in Medicine and Epidemiology of Sport, INSEP, Paris, France; EA 7329, Université de Paris, Paris, France; EA 7525 Université des Antilles, Pointe-Pitre, France.

Funding

Intramural CDC HHS CC999999World Health Organization 001
6 · The paper itself

Abstract

introductionSince August 2009, the Democratic Republic of Congo (DRC) has implemented sentinel site surveillance for rotavirus gastroenteritis. Limited hospital studies have been carried out, in DRC, describing the epidemiology of rotavirus diarrhea before rotavirus vaccine introduction in October 2019. This analysis describes the epidemiology of rotavirus gastroenteritis and characteristics of circulating viral strains from 2009 to 2019. MATERIALS AND

methodsWe analyzed demographic and clinic data collected from children < 5 years old enrolled at three rotavirus sentinel surveillance sites in DRC during 2009-2019, prior to rotavirus vaccine introduction in 2019. Data have been described and presented as mean ± standard deviation for quantitative variables with normal distribution, or as median with an interquartile range [Q1-Q3] for quantitative variables with non-normal distribution, or as absolute value with percentage for qualitative variables.

resultsBetween August 2009 and December 2019, 4,928 children < 5 years old were admitted to sentinel surveillance sites for gastroenteritis in the DRC; the rotavirus positivity rate was 60 %. There was a slight male gender predominance (56 %), and the majority of children (79 %) were 0-11 months of age. Every year, the incidence was highest between May and September corresponding to the dry and cool season. Genotyping was performed for 50 % of confirmed rotavirus cases. The most common G genotypes were G1 (39 %) and G2 (24 %) and most common P genotypes were P[6] (49 %) and P[8] (37 %). The most common G-P genotype combinations were G1P[8] (22 %), G2P[6] (16 %) and G1P[6] (14 %). Genotype distribution varied by site, age group, and year.

conclusionFrom 2009 to 2019, rotavirus-associated gastroenteritis represented a significant burden among DRC children under 5 who were admitted to sentinel sites. G1P[8] was the most commonly identified genotype. Continued monitoring after the introduction of rotavirus vaccine will be essential to monitor any changes in epidemiology.

Indexed as

GastroenteritisRotavirusRotavirus InfectionsRotavirus VaccinesChildChild, PreschoolDemocratic Republic of the CongoDiarrheaFecesGenotypeHumansInfantMaleSentinel SurveillanceRotavirus VaccinesDemocratic Republic of CongoEpidemiologyRotavirus gastroenteritisSentinel sitesSurveillance

Identifiers

PMID36068112
PMCPMC11494495

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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.