Plasma electrolyte imbalance in pediatric kidney transplant recipients.


Journal

Pediatric transplantation
ISSN: 1399-3046
Titre abrégé: Pediatr Transplant
Pays: Denmark
ID NLM: 9802574

Informations de publication

Date de publication:
06 2019
Historique:
received: 29 11 2018
revised: 30 01 2019
accepted: 13 02 2019
pubmed: 12 4 2019
medline: 22 4 2020
entrez: 12 4 2019
Statut: ppublish

Résumé

In current practice, pediatric kidney transplant recipients receive large volumes of intravenous fluid intraoperatively to establish allograft perfusion, and further fluid to replace urinary and insensible losses postoperatively. Acute electrolyte imbalance can result, with potential for neurological sequelae. We aimed to determine the incidence and severity of postoperative plasma electrolyte imbalance in pediatric kidney transplant recipients managed with the current standard intravenous crystalloid regimen. A retrospective analysis of plasma electrolytes in the first 72 hours post-kidney transplant in 76 children transplanted between January 1, 2015, and January 31, 2018, managed with a standard intravenous fluid strategy used in most UK pediatric transplant centers. Of 76 pediatric transplant recipients of median age 9.9 (range 2.2-17.9) years predominantly managed with 0.45% sodium chloride 5% glucose, 45 (59%) developed acute hyponatremia, 23 (30%) hyperkalemia, and 43 (57%) non-anion-gap acidosis in the postoperative period. Hyperglycemia occurred in 74 (97%) patients. Hyperkalemia was more prevalent in deceased than live donor recipients (P = 0.003) and was significantly associated with non-anion-gap acidosis (P < 0.001). Recipient weight was not associated with overt electrolyte imbalance. Postoperative plasma electrolyte imbalance is common in pediatric kidney transplant recipients. Current clinical care strategies mitigate the associated risks of neurological sequelae to some degree. Further studies to optimize intravenous fluid therapy and minimize electrolyte disturbance in this group of patients are needed.

Sections du résumé

BACKGROUND
In current practice, pediatric kidney transplant recipients receive large volumes of intravenous fluid intraoperatively to establish allograft perfusion, and further fluid to replace urinary and insensible losses postoperatively. Acute electrolyte imbalance can result, with potential for neurological sequelae. We aimed to determine the incidence and severity of postoperative plasma electrolyte imbalance in pediatric kidney transplant recipients managed with the current standard intravenous crystalloid regimen.
METHODS
A retrospective analysis of plasma electrolytes in the first 72 hours post-kidney transplant in 76 children transplanted between January 1, 2015, and January 31, 2018, managed with a standard intravenous fluid strategy used in most UK pediatric transplant centers.
RESULTS
Of 76 pediatric transplant recipients of median age 9.9 (range 2.2-17.9) years predominantly managed with 0.45% sodium chloride 5% glucose, 45 (59%) developed acute hyponatremia, 23 (30%) hyperkalemia, and 43 (57%) non-anion-gap acidosis in the postoperative period. Hyperglycemia occurred in 74 (97%) patients. Hyperkalemia was more prevalent in deceased than live donor recipients (P = 0.003) and was significantly associated with non-anion-gap acidosis (P < 0.001). Recipient weight was not associated with overt electrolyte imbalance.
CONCLUSION
Postoperative plasma electrolyte imbalance is common in pediatric kidney transplant recipients. Current clinical care strategies mitigate the associated risks of neurological sequelae to some degree. Further studies to optimize intravenous fluid therapy and minimize electrolyte disturbance in this group of patients are needed.

Identifiants

pubmed: 30973673
doi: 10.1111/petr.13411
doi:

Substances chimiques

Electrolytes 0
Sodium Chloride 451W47IQ8X
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13411

Subventions

Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Auteurs

Wesley Hayes (W)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
University College London Great Ormond Street Institute of Child Health, London, UK.

Catherine Longley (C)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.

Nicola Scanlon (N)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.

William Bryant (W)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.

Jelena Stojanovic (J)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
University College London Great Ormond Street Institute of Child Health, London, UK.

Nicos Kessaris (N)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
Evelina Children's Hospital, London, UK.

William Van't Hoff (W)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
University College London Great Ormond Street Institute of Child Health, London, UK.

Detlef Bockenhauer (D)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
University College London Great Ormond Street Institute of Child Health, London, UK.

Stephen D Marks (SD)

Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.
University College London Great Ormond Street Institute of Child Health, London, UK.

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