Evidence map›Paper›PMID 39806691›Full record

ArticleBMJ open2024

Cohort profile: the potentially preventable burden of community-acquired pneumonia in South African adults in the era of widespread PCV13 immunisation and antiretroviral therapy roll-out, before and during the COVID-19 pandemic - the multicentre, multimethod PotPrev Study.

Firdaus Nabeemeeah, Nadia Sabet, Kennedy Otwombe, Khuthadzo Hlongwane, Lebohang M Mlambo, Tumelo Moloantoa, Michelle Wong, Phetho Mangena, Pattamukkil Abraham, Floris Swanepoel and 14 more

Abstract readMulticenter Study
In one paragraph

Article in BMJ open, 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

24 authors.

Firdaus NabeemeeahPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Diepkloof, Gauteng, South Africa nabeemeeahf@phru.co.za.
Nadia SabetPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Klerksdorp, North West, South Africa.ORCID 0000-0001-9402-0974
Kennedy OtwombePerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Diepkloof, Gauteng, South Africa.ORCID 0000-0002-7433-4383
Khuthadzo HlongwanePerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Diepkloof, Gauteng, South Africa.
Lebohang M MlamboPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Diepkloof, Gauteng, South Africa.
Tumelo MoloantoaPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Klerksdorp, North West, South Africa.
Michelle WongDivision of Pulmonology, Chris Hani Baragwanath Hospital, Johannesburg, South Africa.
Phetho MangenaDepartment of Internal Medicine, University of Limpopo Faculty of Health Sciences, Sovenga, Limpopo, South Africa.
Pattamukkil AbrahamPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Klerksdorp, North West, South Africa.
Floris SwanepoelPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Diepkloof, Gauteng, South Africa.
Fahima MoosaNational Institute for Communicable Diseases, Johannesburg, South Africa.
Anne von GottbergNational Institute for Communicable Diseases, Johannesburg, South Africa.
Cheryl CohenNational Institute for Communicable Diseases, Johannesburg, South Africa.ORCID 0000-0003-0376-2302
Jo SouthernGlobal Biopharmaceutical Business, Pfizer Inc, Collegeville, Pennsylvania, USA.
Mark FletcherEmerging Markets Region Medical Affairs, Vaccines, Pfizer Inc, Paris, France.
Eileen DunneGlobal Biopharmaceutical Business, Pfizer Inc, Collegeville, Pennsylvania, USA.
Bha Ndungane-TlakulaPfizer Inc, Johannesburg, South Africa.
Elizabeth BegierVaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc, Collegeville, Pennsylvania, USA.ORCID 0000-0002-1287-5416
Sharon GrayGlobal Biopharmaceutical Business, Pfizer Inc, Collegeville, Pennsylvania, USA.
Bradford D GessnerGlobal Biopharmaceutical Business, Pfizer Inc, Collegeville, Pennsylvania, USA.ORCID 0000-0002-6216-7194
Jerusha NaidooVaccines, GSK, Singapore.
Minja MilovanovicPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Diepkloof, Gauteng, South Africa.
Ebrahim VariavaUniversity of the Witwatersrand Johannesburg Faculty of Health Sciences, Johannesburg, Gauteng, South Africa.
Neil MartinsonPerinatal HIV Research Unit (PHRU), University of the Witwatersrand Johannesburg, Johannesburg, Gauteng, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn the setting of an established childhood pneumococcal vaccination programme with immediate initiation and treatment of antiretroviral therapy (ART) for people living with HIV (PLWH), the risk of adult pneumococcal community-acquired pneumonia (CAP) is not recently described. We aimed to investigate CAP incidence, recurrence, mortality, risk factors and microbiology before and during the COVID-19 pandemic.

participantsAdults aged ≥18 years were enrolled in three South African provinces from March 2019 to October 2021, with a brief halt during the initial COVID-19 lockdown. The first group, PdCAP, a surveillance cohort, had their data abstracted to estimate the population incidence of physician-diagnosed CAP by counting incident CAP patients presenting to emergency rooms (ER) and mapping them to catchment areas linked to census data. From those admitted to wards from ERs, a prospective cohort (HospCAP) was enrolled and followed up to 1 year after discharge. Microbiology testing was performed and data were abstracted and collected for economic assessments. A third group (StART) of PLWH without respiratory illness at enrolment, attending primary healthcare clinics to initiate or reinitiate ART, was prospectively enrolled and followed. HospCAP and StART participants (totalling 2950 participants) were followed for at least 1 year and assessed for CAP episodes, hospitalisations and mortality. FINDINGS TO DATE: Surveillance identified 6546 patients attending ERs with physician-diagnosed CAP; 61/6546 (0.9%) died in the ER. We prospectively enrolled 2000 hospitalised patients with CAP of whom 1079/2000 (54.0%) were PLWH. Overall, 271/2000 (13.6%) hospitalised CAP patients died during their first admission and 298/2000 (14.9%) died during follow-up. Among StART cohort, 18/950 (1.9%) died during follow-up. FUTURE PLANS: Planned analyses include incidence estimates of pneumococcal serotype-specific adult CAP and its recurrence, using Urinary Antigen Detection assay results to model the burden of pneumococcal CAP better and health economics analyses.

Indexed as

Community-Acquired InfectionsCOVID-19HIV InfectionsPneumococcal VaccinesPneumonia, PneumococcalAdultAgedAnti-Retroviral AgentsCommunity-Acquired PneumoniaFemaleHumansIncidenceMaleMiddle AgedProspective StudiesRisk Factors13-valent pneumococcal vaccineAnti-Retroviral AgentsPneumococcal VaccinesCOVID-19HIV & AIDSMortalityRespiratory infectionsTuberculosis

Identifiers

PMID39806691
PMCPMC11667277

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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.