Urea treatment in fluid restriction-refractory hyponatraemia.


Journal

Clinical endocrinology
ISSN: 1365-2265
Titre abrégé: Clin Endocrinol (Oxf)
Pays: England
ID NLM: 0346653

Informations de publication

Date de publication:
04 2019
Historique:
received: 01 11 2018
revised: 12 12 2018
accepted: 31 12 2018
pubmed: 8 1 2019
medline: 9 6 2020
entrez: 8 1 2019
Statut: ppublish

Résumé

Hyponatraemia in hospitalized patients is common and associated with increased mortality. International guidelines give conflicting advice regarding the role of urea in the treatment of SIADH. We hypothesized that urea is a safe, effective treatment for fluid restriction-refractory hyponatraemia. Review of urea for the treatment of hyponatraemia in patients admitted to a tertiary hospital during 2016-2017. Primary end-point: proportion of patients achieving a serum sodium ≥130 mmol/L at 72 hours. Urea was used on 78 occasions in 69 patients. The median age was 67 (IQR 52-76), 41% were female. Seventy (89.7%) had hyponatraemia due to SIADH-CNS pathology (64.3%) was the most common cause. The duration was acute in 32 (41%), chronic in 35 (44.9%) and unknown in the rest. The median nadir serum sodium was 122 mmol/L (IQR 118-126). Fluid restriction was first-line treatment in 65.4%. Urea was used first line in 21.8% and second line in 78.2%. Fifty treatment episodes (64.1%) resulted in serum sodium ≥130 mmol/L at 72 hours. In 56 patients who received other prior treatment, the mean sodium change at 72 hours (6.9 ± 4.8 mmol/L) was greater than with the preceding treatments (-1.0 ± 4.7 mmol/L; P < 0.001). Seventeen patients (22.7%) had side effects (principally distaste), none were severe. No patients developed hypernatraemia, overcorrection (>10 mmol/L in 24 hours or >18 mmol/L in 48 hours), or died. Urea is safe and effective in fluid restriction-refractory hyponatraemia. We recommend urea with a starting dose of ≥30 g/d, in patients with SIADH and moderate to profound hyponatraemia who are unable to undergo, or have failed fluid restriction.

Identifiants

pubmed: 30614552
doi: 10.1111/cen.13930
doi:

Substances chimiques

Urea 8W8T17847W
Sodium 9NEZ333N27

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

630-636

Informations de copyright

© 2019 John Wiley & Sons Ltd.

Auteurs

Jack Lockett (J)

Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

Kathryn E Berkman (KE)

Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia.

Goce Dimeski (G)

Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
Department of Chemical Pathology, Pathology Queensland, Brisbane, Queensland, Australia.

Anthony W Russell (AW)

Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

Warrick J Inder (WJ)

Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia.
Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.

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