Defining benefit threshold for extracorporeal membrane oxygenation in children with sepsis-a binational multicenter cohort study.


Journal

Critical care (London, England)
ISSN: 1466-609X
Titre abrégé: Crit Care
Pays: England
ID NLM: 9801902

Informations de publication

Date de publication:
30 12 2019
Historique:
received: 25 08 2019
accepted: 26 11 2019
entrez: 1 1 2020
pubmed: 1 1 2020
medline: 29 4 2020
Statut: epublish

Résumé

The surviving sepsis campaign recommends consideration for extracorporeal membrane oxygenation (ECMO) in refractory septic shock. We aimed to define the benefit threshold of ECMO in pediatric septic shock. Retrospective binational multicenter cohort study of all ICUs contributing to the Australian and New Zealand Paediatric Intensive Care Registry. We included patients < 16 years admitted to ICU with sepsis and septic shock between 2002 and 2016. Sepsis-specific risk-adjusted models to establish ECMO benefit thresholds with mortality as the primary outcome were performed. Models were based on clinical variables available early after admission to ICU. Multivariate analyses were performed to identify predictors of survival in children treated with ECMO. Five thousand sixty-two children with sepsis and septic shock met eligibility criteria, of which 80 (1.6%) were treated with veno-arterial ECMO. A model based on 12 clinical variables predicted mortality with an AUROC of 0.879 (95% CI 0.864-0.895). The benefit threshold was calculated as 47.1% predicted risk of mortality. The observed mortality for children treated with ECMO below the threshold was 41.8% (23 deaths), compared to a predicted mortality of 30.0% as per the baseline model (16.5 deaths; standardized mortality rate 1.40, 95% CI 0.89-2.09). Among patients above the benefit threshold, the observed mortality was 52.0% (13 deaths) compared to 68.2% as per the baseline model (16.5 deaths; standardized mortality rate 0.61, 95% CI 0.39-0.92). Multivariable analyses identified lower lactate, the absence of cardiac arrest prior to ECMO, and the central cannulation (OR 0.31, 95% CI 0.10-0.98, p = 0.046) as significant predictors of survival for those treated with VA-ECMO. This binational study demonstrates that a rapidly available sepsis mortality prediction model can define thresholds for survival benefit in children with septic shock considered for ECMO. Survival on ECMO was associated with central cannulation. Our findings suggest that a fully powered RCT on ECMO in sepsis is unlikely to be feasible.

Sections du résumé

BACKGROUND
The surviving sepsis campaign recommends consideration for extracorporeal membrane oxygenation (ECMO) in refractory septic shock. We aimed to define the benefit threshold of ECMO in pediatric septic shock.
METHODS
Retrospective binational multicenter cohort study of all ICUs contributing to the Australian and New Zealand Paediatric Intensive Care Registry. We included patients < 16 years admitted to ICU with sepsis and septic shock between 2002 and 2016. Sepsis-specific risk-adjusted models to establish ECMO benefit thresholds with mortality as the primary outcome were performed. Models were based on clinical variables available early after admission to ICU. Multivariate analyses were performed to identify predictors of survival in children treated with ECMO.
RESULTS
Five thousand sixty-two children with sepsis and septic shock met eligibility criteria, of which 80 (1.6%) were treated with veno-arterial ECMO. A model based on 12 clinical variables predicted mortality with an AUROC of 0.879 (95% CI 0.864-0.895). The benefit threshold was calculated as 47.1% predicted risk of mortality. The observed mortality for children treated with ECMO below the threshold was 41.8% (23 deaths), compared to a predicted mortality of 30.0% as per the baseline model (16.5 deaths; standardized mortality rate 1.40, 95% CI 0.89-2.09). Among patients above the benefit threshold, the observed mortality was 52.0% (13 deaths) compared to 68.2% as per the baseline model (16.5 deaths; standardized mortality rate 0.61, 95% CI 0.39-0.92). Multivariable analyses identified lower lactate, the absence of cardiac arrest prior to ECMO, and the central cannulation (OR 0.31, 95% CI 0.10-0.98, p = 0.046) as significant predictors of survival for those treated with VA-ECMO.
CONCLUSIONS
This binational study demonstrates that a rapidly available sepsis mortality prediction model can define thresholds for survival benefit in children with septic shock considered for ECMO. Survival on ECMO was associated with central cannulation. Our findings suggest that a fully powered RCT on ECMO in sepsis is unlikely to be feasible.

Identifiants

pubmed: 31888705
doi: 10.1186/s13054-019-2685-1
pii: 10.1186/s13054-019-2685-1
pmc: PMC6937937
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

429

Subventions

Organisme : National Health and Medical Research Council of Australia and New Zealand
ID : Practitioner Fellowship
Pays : International
Organisme : Children's Hospital Foundation
ID : NA
Pays : International

Investigateurs

Anusha Ganeshalingam (A)
Claire Sherring (C)
Simon Erickson (S)
Samantha Barr (S)
Andreas Schibler (A)
Debbie Long (D)
Luregn Schlapbach (L)
Jan Alexander (J)
Shane George (S)
Gary Williams (G)
Vicky Smith (V)
Warwick Butt (W)
Carmel Delzoppo (C)
Johnny Millar (J)
Ben Gelbart (B)
Felix Oberender (F)
Subodh Ganu (S)
Georgia Letton (G)
Jonathan Egan (J)
Gail Harper (G)
Marino Festa (M)

Commentaires et corrections

Type : CommentIn

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Auteurs

Luregn J Schlapbach (LJ)

Paediatric Critical Care Research Group, Child Health Research Centre, The University of Queensland, Brisbane, Australia. l.schlapbach@uq.edu.au.
Paediatric Intensive Care Unit, Queensland Children's Hospital, South Brisbane, QLD, 4101, Australia. l.schlapbach@uq.edu.au.
Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. l.schlapbach@uq.edu.au.

Roberto Chiletti (R)

University of Melbourne, Melbourne, Australia.
Paediatric Intensive Care Unit, The Royal Children's Hospital, Melbourne, Australia.

Lahn Straney (L)

Paediatric Critical Care Research Group, Child Health Research Centre, The University of Queensland, Brisbane, Australia.
Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia.

Marino Festa (M)

Paediatric Intensive Care Unit, Children's Hospital Westmead, Sydney, Australia.
Kids Critical Care Research Group, Kids Research, Sydney Children's Hospitals Network, Sydney, Australia.

Daniel Alexander (D)

Paediatric Intensive Care Unit, Perth Children's Hospital, Perth, Australia.

Warwick Butt (W)

Paediatric Intensive Care Unit, The Royal Children's Hospital, Melbourne, Australia.

Graeme MacLaren (G)

Paediatric Intensive Care Unit, The Royal Children's Hospital, Melbourne, Australia.
Cardiothoracic Intensive Care Unit, National University Health System, Singapore, Singapore.

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