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Impact of hyperkalaemia on renin-angiotensin-aldosterone (RAAS) inhibitor reduction or withdrawal following hospitalisation.

Authors :
Ellis HL
Al-Agil M
Kelly PA
Teo J
Sharpe C
Whyte MB
Source :
Clinical and experimental medicine [Clin Exp Med] 2024 Dec 21; Vol. 25 (1), pp. 16. Date of Electronic Publication: 2024 Dec 21.
Publication Year :
2024

Abstract

Background: Inhibitors of the renin-angiotensin-aldosterone system (RAAS), such as ACE inhibitors (ACEi), angiotensin-II receptor blockers and mineralocorticoid receptor antagonists, reduce morbidity and mortality in hypertension, congestive heart failure and chronic kidney disease. However, their use can lead to hyperkalaemia. We examined the proportions of RAAS inhibitor (RAASi) reduction or withdrawal, across GFR strata, following hospitalisation and the effect on patient mortality.<br />Methods: This was a retrospective cohort study of adult patients hospitalised from 1 January2017 to 31 December2020. Biochemistry data, clinical notes and medicines use were extracted using the CogStack platform, from electronic health records. Patients were identified by creatinine measurement during hospitalisation. Hyperkalaemia was defined as potassium > 5.0 mmol/L, with severity categorisation. RAASi discontinuation defined as ≥ 48 h without administration. Mortality risk associated with RAASi cessation was assessed using Cox proportional hazards models.<br />Results: Among 129,172 patients with potassium measurements, 49,011 were hospitalised. Hyperkalaemia prevalence was 8.57% in the emergency department and 16.79% among hospitalised patients. Higher hyperkalaemia levels correlated with increased CKD and heart failure. RAASi use was more common in hyperkalaemic patients, with higher discontinuation rates during hospitalisation (36% with potassium 5-5.5 mmol/L; 61% with potassium > 6.5 mmol/L). By discharge, 32% of patients had RAASi stopped, and 2% doses reduced. Discontinuation of RAASi was associated with 37% worse survival probability.<br />Conclusion: RAASi cessation was greater with hyperkalaemia and associated with increased mortality in hospitalised patients. Reinstitution of RAASi after hospital discharge, or alternative management of hyperkalaemia if maintained on RAASi therapy, may improve clinical outcomes.<br />Competing Interests: Declarations. Competing interests: The authors declare no competing interests. Ethics approval and consent to participate: The King’s College Hospital Research and Innovation Department, after review of the project, considered this as a service evaluation, rather than research. We confirmed this opinion using the HRA ‘Is this research?’ decision tool ( http://www.hra-decisiontools.org.uk/research/ ). We used anonymous data, at scale, at source (within the hospital IT system), and therefore, patient-level consent was not required. Approval for this approach to use of CogStack is within London—South East Research Ethics Committee approval (18/LO/2048) 2nd January 2019. King's Electronic Patient Record Interface (KERRI) committee (project ID 20210405A) approved the project (within the boundaries of CogStack ethical approval 18/LO/2048) on 7th May 2021. Consent to publish: Not applicable.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1591-9528
Volume :
25
Issue :
1
Database :
MEDLINE
Journal :
Clinical and experimental medicine
Publication Type :
Academic Journal
Accession number :
39708241
Full Text :
https://doi.org/10.1007/s10238-024-01531-9