Evidence map›Paper›PMID 38820301›Full record

ArticlePloS one2024

SARS-CoV-2 active infection and antibodies amongst health personnel during the outbreak in Cameroon: Strengthening the health system for response to future public health emergencies.

Sen Claudine Henriette Ngomtcho, Blaise Mboringong Akenji, Ketina Hirma Tchio-Nighie, Joseph Fokam, Etienne Guenou, Carolle Nsa'Amang Eyebe, Yvan Junior Nzegni Kamkoum, Valdex Derick Ntale Tchoffo, Collins Buh Nkum, Hervé Christian Tchoudjin Paho and 12 more

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Sen Claudine Henriette NgomtchoNational Public Health Laboratory, Ministry of Public Health, Yaoundé, Cameroon.ORCID 0000-0001-5045-3065
Blaise Mboringong AkenjiNational Public Health Laboratory, Ministry of Public Health, Yaoundé, Cameroon.
Ketina Hirma Tchio-NighieM.A. SANTE (Meilleur Accès aux Soins de Santé), Yaoundé, Cameroon.
Joseph FokamChantal Biya International Reference Centre for Research on HIV/AIDS Prevention and Management (CIRCB), Yaoundé, Cameroon.
Etienne GuenouNational Public Health Laboratory, Ministry of Public Health, Yaoundé, Cameroon.
Carolle Nsa'Amang EyebeDepartment of Biological Sciences, Faculty of Medicine and Pharmaceutical Sciences (FMPS), University of Douala, Douala, Cameroon.
Yvan Junior Nzegni KamkoumDepartment of Microbiology, Hematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences (FMPS), University of Dschang, Dschang, Cameroon.
Valdex Derick Ntale TchoffoDepartment of Microbiology, Hematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences (FMPS), University of Dschang, Dschang, Cameroon.
Collins Buh NkumM.A. SANTE (Meilleur Accès aux Soins de Santé), Yaoundé, Cameroon.ORCID 0000-0002-8637-9685
Hervé Christian Tchoudjin PahoNational Public Health Laboratory, Ministry of Public Health, Yaoundé, Cameroon.
Yvette Marie Solange EbogoNational Public Health Laboratory, Ministry of Public Health, Yaoundé, Cameroon.
Aude NanfakM.A. SANTE (Meilleur Accès aux Soins de Santé), Yaoundé, Cameroon.
Martin Maidadi-FoudiCentre de Recherche en Maladies Emergentes et Re-emergentes (CREMER), Yaoundé, Cameroun.
Crescence FoudaNational Public Health Laboratory, Ministry of Public Health, Yaoundé, Cameroon.
Angyiba Serge AndigemaDepartment of Microbiology, Hematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences (FMPS), University of Dschang, Dschang, Cameroon.
Lilian Nsah Bongdze-EmDepartment of Microbiology, Hematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences (FMPS), University of Dschang, Dschang, Cameroon.
Beri Nadin NforDepartment of Microbiology, Hematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences (FMPS), University of Dschang, Dschang, Cameroon.
Judith TorimiroChantal Biya International Reference Centre for Research on HIV/AIDS Prevention and Management (CIRCB), Yaoundé, Cameroon.
Anne Cécile Zoung-Kanyi BissekDivision for Operational Health Research (DROS), Ministry of Public Health, Yaoundé, Cameroon.
Michel NoubomDepartment of Microbiology, Hematology and Immunology, Faculty of Medicine and Pharmaceutical Sciences (FMPS), University of Dschang, Dschang, Cameroon.
Marie Claire Assoumou OkomoNational Public Health Laboratory, Ministry of Public Health, Yaoundé, Cameroon.
Jérôme AteudjieuM.A. SANTE (Meilleur Accès aux Soins de Santé), Yaoundé, Cameroon.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHealth personnel (HP) are on the frontlines during response to public health emergencies like COVID-19. This risk of exposure suggests the need for safety in responding to any pandemic. Therefore, to ascertain the rate of SARS-CoV-2 infection and immunity, and their determinants amongst HP become relevant.

methodsA cross sectional health facility-based study was carried-out amongst HP in the Centre Region of Cameroon from 1st February to 30th June 2021. Characteristics and access to preventive tools were collected using face-to-face administered questionnaire. Nasopharyngeal swabs and whole blood were collected for PCR, IgG and IgM testing respectively. STATA version 17 software was used for data analysis. Determinants of COVID-19 infection were explored by estimating crude and adjusted Odd Ratio.

resultsOut of 510 HP reached, 458 were enrolled with mean age of 35 (±10) years. Thirty-four (7.4%) were PCR-positive to SARS-CoV-2 with 73.5% being clinicians versus 9 (26.4%) non-clinicians (p = 0.05). Sero-positivity to SARS-CoV-2 IgG/IgM was 40.2% (184/458), with 84.2% being clinicians versus 29 (15.8%) non-clinicians (p = 0.733). Amongst the 34 HP with PCR-positivity, 16 (47%) had no antibodies, while, 15 (44%) were IgG only. An estimate of HP (43.7%) had at least an evidence of PCR, IgG or IgM contact to COVID-19. Determinants of PCR-positivity was being clinical staff (AOR = 0.29, P = 0.039); and that of IgG/IgM were being non clinical staff (AOR = 0.41, p = 0.018) and regular use of face masks (AOR = 0.44, p = 0.001). HP trained on IPC (24%) were mainly from peripheral level (74.7%, p = 0.002).

conclusionActive infections were within the range of pandemic control (<10%). However, around two-fifths of participants have had contact with the virus, indicating that HP remains a population at risk of COVID-19 and other similarly-transmitted epidemic prone diseases, and also an important source of transmission. There is need of vaccine to achieve protectiveness, and optimal response also requires capacity building to improve the health system when challenged by a future pandemic.

Indexed as

Antibodies, ViralCOVID-19Health PersonnelPublic HealthSARS-CoV-2AdultCameroonCross-Sectional StudiesDisease OutbreaksFemaleHumansImmunoglobulin GImmunoglobulin MMaleMiddle AgedAntibodies, ViralImmunoglobulin GImmunoglobulin M

Identifiers

PMID38820301
PMCPMC11142533

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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.