Evidence map›Paper›PMID 38009561›Full record

Observational studyBritish journal of haematology2024

Association of ABO and Rhesus blood groups with severe outcomes from non-SARS-CoV-2 respiratory infection: A prospective observational cohort study in Bristol, UK 2020-2022.

Alice Hathaway, George Qian, Jade King, Serena McGuinness, Nick Maskell, Jennifer Oliver, Adam Finn, Leon Danon, Robert Challen, Ashley M Toye and 2 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in British journal of haematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

12 authors at 4 institutions in 1 country.

Alice HathawaySchool of Biochemistry, University of Bristol, Bristol, UK.
George QianEngineering Mathematics, University of Bristol, Bristol, UK.
Jade KingClinical Research and Imaging Centre, UHBW NHS Trust, Bristol, UK.
Serena McGuinnessBristol Vaccine Centre and Population Health Sciences, University of Bristol, Bristol, UK.
Nick MaskellAcademic Respiratory Unit, University of Bristol, Southmead Hospital, Bristol, UK.
Jennifer OliverBristol Vaccine Centre and Population Health Sciences, University of Bristol, Bristol, UK.
Adam FinnBristol Vaccine Centre, Cellular and Molecular Medicine and Population Health Sciences, University of Bristol, Bristol, UK.
Leon DanonEngineering Mathematics, University of Bristol, Bristol, UK.
Robert ChallenEngineering Mathematics, University of Bristol, Bristol, UK.
Ashley M ToyeSchool of Biochemistry, University of Bristol, Bristol, UK.ORCID 0000-0003-4395-9396
Catherine HyamsBristol Vaccine Centre, Cellular and Molecular Medicine and Population Health Sciences, University of Bristol, Bristol, UK.ORCID 0000-0003-3923-1773
Avon CAP Research Group
University of Bristol · GBAt Bristol · GBNorth Bristol NHS Trust · GBSouthmead Hospital · GB

Funding

British Heart Foundation FS/4yPhD/F/21/34162
6 · The paper itself

Abstract

Despite significant global morbidity associated with respiratory infection, there is a paucity of data examining the association between severity of non-SARS-CoV-2 respiratory infection and blood group. We analysed a prospective cohort of adults hospitalised in Bristol, UK, from 1 August 2020 to 31 July 2022, including patients with acute respiratory infection (pneumonia [n = 1934] and non-pneumonic lower respiratory tract infection [NP-LRTI] [n = 1184]), a negative SARS-CoV-2 test and known blood group status. The likelihood of cardiovascular complication, survival and hospital admission length was assessed using regression models with group O and RhD-negative status as reference groups. Group A and RhD-positive were over-represented in both pneumonia and NP-LRTI compared to a first-time donor population (p < 0.05 in all); contrastingly, group O was under-represented. ABO group did not influence cardiovascular complication risk; however, RhD-positive patients with pneumonia had a reduced odds ratio (OR) for cardiovascular complications (OR = 0.77 [95% CI = 0.59-0.98]). Compared to group O, group A individuals with NP-LRTI were more likely to be discharged within 60 days (hazard ratio [HR] = 1.17 [95% CI = 1.03-1.33]), while group B with pneumonia was less likely (HR = 0.8 [95% CI = 0.66-0.96]). This analysis provides some evidence that blood group status may influence clinical outcome following respiratory infection, with group A having increased risk of hospitalisation and RhD-positive patients having reduced cardiovascular complications.

Indexed as

COVID-19PneumoniaRespiratory Tract InfectionsABO Blood-Group SystemAdultHumansProspective StudiesSARS-CoV-2United KingdomABO Blood-Group Systemblood grouppneumoniarespiratory infection

Identifiers

PMID38009561
PMCPMC7616671
OpenAlexW4389037878

What OpenQuestion holds

Textmetadata
LicenceTDM
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.