Epidemiology and Outcome of Critically Ill Pediatric Cancer and Hematopoietic Stem Cell Transplant Patients Requiring Continuous Renal Replacement Therapy: A Retrospective Nationwide Cohort Study.


Journal

Critical care medicine
ISSN: 1530-0293
Titre abrégé: Crit Care Med
Pays: United States
ID NLM: 0355501

Informations de publication

Date de publication:
11 2019
Historique:
pubmed: 30 8 2019
medline: 26 5 2020
entrez: 30 8 2019
Statut: ppublish

Résumé

Acute kidney injury requiring continuous renal replacement therapy is a serious treatment-related complication in pediatric cancer and hematopoietic stem cell transplant patients. The purpose of this study was to assess epidemiology and outcome of these patients requiring continuous renal replacement therapy in the PICU. A nationwide, multicenter, retrospective, observational study. Eight PICUs of a tertiary care hospitals in the Netherlands. Pediatric cancer and hematopoietic stem cell transplant patients (cancer and noncancer) who received continuous renal replacement therapy from January 2006 to July 2017 in the Netherlands. None. Of 1,927 PICU admissions of pediatric cancer and hematopoietic stem cell transplant patients, 68 of 70 evaluable patients who received continuous renal replacement therapy were included. Raw PICU mortality was 11.2% (216/1,972 admissions). PICU mortality of patients requiring continuous renal replacement therapy was 54.4% (37/68 patients). Fluid overload (odds ratio, 1.08; 95% CI, 1.01-1.17) and need for inotropic support (odds ratio, 6.53; 95% CI, 1.86-23.08) at the start of continuous renal replacement therapy were associated with PICU mortality. Serum creatinine levels increased above 150% of baseline 3 days before the start of continuous renal replacement therapy. Urine production did not reach the critical limit of oliguria. In contrast, body weight (fluid overload) increased already 5 days prior to continuous renal replacement therapy initiation. PICU mortality of pediatric cancer and hematopoietic stem cell transplant patients requiring continuous renal replacement therapy is sadly high. Fluid overload at the initiation of continuous renal replacement therapy is the most important and earliest predictor of PICU mortality. Our results suggest that the most commonly used criteria of acute kidney injury, that is, serum creatinine and urine production, are not useful as a trigger to initiate continuous renal replacement therapy. This highlights the urgent need for prospective studies to generate recommendations for effective therapeutic interventions at an early phase in this specific patient population.

Identifiants

pubmed: 31464768
doi: 10.1097/CCM.0000000000003973
pmc: PMC6798750
doi:

Substances chimiques

Cardiotonic Agents 0
Creatinine AYI8EX34EU

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e893-e901

Investigateurs

Job van Woensel (J)
Reinout Bem (R)
Marc van Heerden (M)
Maaike Riedijk (M)
Matthijs de Hoog (M)
Sascha Verbruggen (S)
Roelie Wösten-van Asperen (R)
Martin Kneyber (M)
Joris Lemson (J)
Dick van Waardenburg (D)
P P Roeleveld (PP)

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Auteurs

Paulien A M A Raymakers-Janssen (PAMA)

Department of Pediatric Intensive Care, Wilhelmina Children's Hospital/University Medical Center Utrecht, Utrecht, The Netherlands.

Marc R Lilien (MR)

Department of Pediatric Nephrology, Wilhelmina Children's Hospital/University Medical Center Utrecht, Utrecht, The Netherlands.

Dick Tibboel (D)

Intensive Care and Department of Pediatric Surgery, Sophia Children's Hospital/Erasmus Medical Center, Rotterdam, The Netherlands.

Martin C J Kneyber (MCJ)

Division of Pediatric Critical Care Medicine, Beatrix Children's Hospital/University Medical Center Groningen, Groningen, The Netherlands.

Sandra Dijkstra (S)

Division of Pediatric Critical Care Medicine, Beatrix Children's Hospital/University Medical Center Groningen, Groningen, The Netherlands.

Job B M van Woensel (JBM)

Department of Pediatric Intensive Care, Amsterdam University Medical Centers, Amsterdam, The Netherlands.

Joris Lemson (J)

Department of Intensive Care Medicine, University Medical Center Nijmegen, Nijmegen, The Netherlands.

Karlien Cransberg (K)

Department of Pediatric Nephrology, Erasmus Medical Center/Sophia Children's Hospital, Rotterdam, The Netherlands.

Marry M van den Heuvel-Eibrink (MM)

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Roelie M Wösten-van Asperen (RM)

Department of Pediatric Intensive Care, Wilhelmina Children's Hospital/University Medical Center Utrecht, Utrecht, The Netherlands.

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