Evidence map›Paper›PMID 36963090›Full record

ArticlePLOS global public health2023

Different clinical features in Malawian outpatients presenting with COVID-19 prior to and during Omicron variant dominance: A prospective observational study.

Marah G Chibwana, Herbert W Thole, Cat Anscombe, Philip M Ashton, Edward Green, Kayla G Barnes, Jen Cornick, Ann Turner, Desiree Witte, Sharon Nthala and 17 more

Open access · goldFull text read
In one paragraph

Article in PLOS global public health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

27 authors at 6 institutions in 4 countries.

Marah G ChibwanaMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.ORCID https://orcid.org/0000-0002-8940-3855
Herbert W TholeMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.ORCID https://orcid.org/0000-0002-1507-1202
Cat AnscombeMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Philip M AshtonMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Edward GreenDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.
Kayla G BarnesMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Jen CornickMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Ann TurnerInstitute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.
Desiree WitteMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.ORCID https://orcid.org/0000-0002-2607-9816
Sharon NthalaMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Chikondi ThomMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Felistas KanyandulaMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Anna AinaniMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Natasha MtikeMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Hope TambalaBlantyre District Health Office, Ministry of Health, Blantyre, Malawi.
Veronica N'gomaMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Dorah MwafulirwaMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Erick AsimaMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Ben MortonDepartment of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.ORCID https://orcid.org/0000-0002-6164-2854
Markus GmeinerMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.ORCID https://orcid.org/0000-0002-1450-2955
Zaziwe GundahBlantyre District Health Office, Ministry of Health, Blantyre, Malawi.
Gift KawalaziraBlantyre District Health Office, Ministry of Health, Blantyre, Malawi.
Neil FrenchInstitute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.ORCID https://orcid.org/0000-0003-4814-8293
Nicholas FeaseyMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.
Robert S HeydermanNIHR Global Health Research Unit on Mucosal Pathogens, University College London, London, United Kingdom.
Todd D SwarthoutNIHR Global Health Research Unit on Mucosal Pathogens, University College London, London, United Kingdom.ORCID https://orcid.org/0000-0001-5285-7039
Kondwani C JamboMalawi-Liverpool-Wellcome Programme (MLW), Blantyre, Malawi.ORCID https://orcid.org/0000-0002-3195-2210
University of Liverpool · GBMinistry of Health · MWLiverpool School of Tropical Medicine · GBBroad Institute · USUniversity College London · GBUtrecht University · NL

Funding

Medical Research Council MC_PC_19026Medical Research Council MR/T008822/1Wellcome Trust
6 · The paper itself

Abstract

The SARS-CoV-2 Omicron variant has resulted in a high number of cases, but a relatively low incidence of severe disease and deaths, compared to the pre-Omicron variants. Therefore, we assessed the differences in symptom prevalence between Omicron and pre-Omicron infections in a sub-Saharan African population. We collected data from outpatients presenting at two primary healthcare facilities in Blantyre, Malawi, from November 2020 to March 2022. Eligible participants were aged >1month old, with signs suggestive of COVID-19, and those not suspected of COVID-19, from whom we collected nasopharyngeal swabs for SARS-CoV-2 PCR testing, and sequenced positive samples to identify infecting-variants. In addition, we calculated the risk of presenting with a given symptom in individuals testing SARS-CoV-2 PCR positive before and during the Omicron variant-dominated period. Among 5176 participants, 6.4% were under 5, and 77% were aged 18 to 50 years. SARS-CoV-2 infection prevalence peaked in January 2021 (Beta), July 2021 (Delta), and December 2021 (Omicron). We found that cough (risk ratio (RR), 1.50; 95% confidence interval (CI), 1.00 to 2.30), fatigue (RR 2.27; 95% CI, 1.29 to 3.86) and headache (RR 1.64; 95% CI, 1.15 to 2.34) were associated with a high risk of SARS-CoV-2 infection during the pre-Omicron period. In comparison, only headache (RR 1.41; 95% CI, 1.07 to 1.86) did associate with a high risk of SARS-CoV-2 infection during the Omicron-dominated period. In conclusion, clinical symptoms associated with Omicron infection differed from prior variants and were harder to identify clinically with current symptom guidelines. Our findings encourage regular review of case definitions and testing policies to ensure case ascertainment.

Identifiers

PMID36963090
PMCPMC10022204
OpenAlexW4323540069

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read155
identifiers read9
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.