Abstract
Background:
The 2023 SARS-CoV-2 environment differs greatly from the initial outbreak, with new variants and widespread vaccination. Early in the pandemic, blood group A was linked to increased hospitalisation and poor outcomes, but its role now, since the availability of vaccination, is unclear.
Methods:
We analysed data (1 August 2020–31 July 2023) from a prospective cohort of adults hospitalised in Bristol with SARS-CoV-2 and known ABO group (n = 3413). Admission date acted as a proxy for viral strain. Regression models assessed length of stay, survival, cardiovascular complications and ICU admission in non-O groups versus Group O.
Results:
Group A was over-represented and Group O was under-represented, compared to the blood donor population, except during Alpha dominance (p < 0.001; Alpha: p = 0.796). ABO group generally did not affect cardiovascular risk. However, during Wild-Type, Group AB had higher odds of cardiovascular complications (odds ratio [OR] = 3.18, p = 0.060) and intensive care unit [ICU] admission (OR = 4.79, p = 0.013). During Omicron, AB group patients had lower 30-day survival (HR = 2.09, p = 0.018). Group A was less likely to be discharged during Alpha (HR = 0.85, p = 0.013), while Group B was more likely to be discharged during Omicron (HR = 1.30, p = 0.002).
Conclusions:
ABO groups may still influence hospitalisation risk but appear less relevant to outcomes once admitted, likely reflecting advances in care and vaccination.
| Original language | English |
|---|---|
| Article number | e70264 |
| Number of pages | 12 |
| Journal | eJHaem |
| Volume | 7 |
| Issue number | 2 |
| Early online date | 16 Mar 2026 |
| DOIs | |
| Publication status | Published - 1 Apr 2026 |
Bibliographical note
Publisher Copyright:© 2026 The Author(s).
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- respiratory infection
- blood group
- ABO
- COVID‐19
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