Observational study of the relative efficacy of insulin-glucose treatment for hyperkalaemia in patients with liver cirrhosis.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
22 10 2021
Historique:
entrez: 23 10 2021
pubmed: 24 10 2021
medline: 4 11 2021
Statut: epublish

Résumé

To determine if liver cirrhosis is associated with reduced efficacy of insulin-glucose treatment in moderate to severe hyperkalaemia. Retrospective, cohort study. Two secondary and one tertiary care hospital at a large metropolitan healthcare network in Melbourne, Australia. This study included 463 adults with a mean age of 68.7±15.8 years, comprising 79 patients with cirrhosis and 384 without cirrhosis as controls, who received standard insulin-glucose treatment for a serum potassium ≥6.0 mmol/L from October 2016 to March 2020. Patients were excluded if they received an insulin infusion, or if there was inadequate follow-up data for at least 6 hours after IDT due to death, lost to follow-up or inadequate biochemistry monitoring. The mean Model for End-stage Liver Disease score in patients with cirrhosis was 22.2±7.5, and the distribution of the Child-Pugh score for cirrhosis was: class A (24%), class B (46%), class C (30%). The primary outcome was the degree of potassium lowering and the secondary outcome was the proportion of patients who achieved normokalaemia, within 6 hours of treatment. The mean pretreatment potassium for the cohort was 6.57±0.52 mmol/L. After insulin-glucose treatment, mean potassium lowering was 0.84±0.58 mmol/L in patients with cirrhosis compared with 1.33±0.75 mmol/L for controls (p<0.001). The proportion of patients achieving normokalaemia was 33% for patients with cirrhosis, compared with 53% for controls (p=0.001). By multivariable regression, on average, liver cirrhosis was associated with a reduced potassium lowering effect of 0.42 mmol/L (95% CI 0.22 to 0.63 mmol/L, p<0.001) from insulin-glucose treatment, after adjusting for age, serum creatinine, cancer, pretreatment potassium level, β-blocker use and cotreatments (sodium polystyrene sulfonate, salbutamol, sodium bicarbonate). Our observational data suggest reduced efficacy of insulin-glucose treatment for hyperkalaemia in patients with cirrhosis.

Identifiants

pubmed: 34686554
pii: bmjopen-2021-051201
doi: 10.1136/bmjopen-2021-051201
pmc: PMC8543643
doi:

Substances chimiques

Insulin 0
Glucose IY9XDZ35W2

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e051201

Informations de copyright

© Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Références

Ann Gastroenterol. 2014;27(3):237-243
pubmed: 24974878
Clin J Am Soc Nephrol. 2012 May;7(5):712-9
pubmed: 22422536
Pharm Pract (Granada). 2019 Jan-Mar;17(1):1361
pubmed: 31015873
Br J Nutr. 2004 Nov;92(5):799-808
pubmed: 15533269
Obes Rev. 2007 May;8(3):231-51
pubmed: 17444965
J Zhejiang Univ Sci B. 2011 Aug;12(8):677-82
pubmed: 21796809
Gastroenterology. 1992 Jun;102(6):2033-41
pubmed: 1587421
Hepatogastroenterology. 2010 Mar-Apr;57(98):309-15
pubmed: 20583433
Br J Surg. 1973 Aug;60(8):646-9
pubmed: 4541913
Arch Intern Med. 1988 Mar;148(3):547-8
pubmed: 3277570
J Clin Endocrinol Metab. 1991 Sep;73(3):564-8
pubmed: 1874934
Diabetes Care. 2005 May;28(5):1245-9
pubmed: 15855602
J Clin Invest. 1985 May;75(5):1659-65
pubmed: 3889056
J Gastroenterol Hepatol. 2016 May;31(5):988-94
pubmed: 26598065
Clin J Am Soc Nephrol. 2011 Jul;6(7):1533-9
pubmed: 21734082
Scand J Gastroenterol. 2013 Mar;48(3):358-65
pubmed: 23298384
Int Urol Nephrol. 2015 Jun;47(6):991-9
pubmed: 25966806
Am J Physiol Gastrointest Liver Physiol. 2012 Jun 15;302(12):G1458-65
pubmed: 22492691
JAMA. 2016 Feb 23;315(8):801-10
pubmed: 26903338
Clin Kidney J. 2021 Feb 03;14(10):2255-2260
pubmed: 34603702
Liver Transpl Surg. 1996 Nov;2(6):443-54
pubmed: 9346691
Biomed Res Int. 2019 Feb 27;2019:6025726
pubmed: 30937312

Auteurs

Andy K H Lim (AKH)

Department of Medicine, Monash University School of Clinical Sciences at Monash Health, Clayton, Victoria, Australia andy.lim@monash.edu.
General Medicine, Monash Health, Clayton, Victoria, Australia.

Ljiljana Crnobrnja (L)

General Medicine, Monash Health, Clayton, Victoria, Australia.

Manogna Metlapalli (M)

General Medicine, Monash Health, Clayton, Victoria, Australia.

Cathy Jiang (C)

General Medicine, Monash Health, Clayton, Victoria, Australia.

Rene S H Wang (RSH)

General Medicine, Monash Health, Clayton, Victoria, Australia.

Jeanette H Pham (JH)

General Medicine, Monash Health, Clayton, Victoria, Australia.

Joshua H Abasszade (JH)

General Medicine, Monash Health, Clayton, Victoria, Australia.

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Classifications MeSH