Persistent acidosis after reperfusion-A prognostic indicator of increased 30-day and in-hospital postoperative mortality in liver transplant recipients.


Journal

Clinical transplantation
ISSN: 1399-0012
Titre abrégé: Clin Transplant
Pays: Denmark
ID NLM: 8710240

Informations de publication

Date de publication:
03 2019
Historique:
received: 14 03 2018
revised: 30 11 2018
accepted: 08 12 2018
pubmed: 1 1 2019
medline: 2 5 2020
entrez: 1 1 2019
Statut: ppublish

Résumé

During liver transplantation, the patient is at risk of developing progressive lactic acidosis. Following reperfusion, correction of acidosis may occur. In some patients, acidosis will worsen, a phenomenon referred to as persistent acidosis after reperfusion (PAAR). We compared postoperative outcomes in patients who manifested PAAR vs those that did not. All adult patients undergoing liver transplantation from 2002 to 2015 were included. PAAR is defined by the presence of a significant negative slope coefficient for base excess values measured after hepatic artery anastomosis through 72 hours postoperatively. Primary outcome was a composite of 30-day and in-hospital mortality. Secondary outcomes included: ICU LOS, total hospital LOS, and re-transplantation rate within 7 days. PAAR occurred in 10% of the transplant recipients. Patients with PAAR had higher MELD, BMI, and eGFR and demonstrated a longer median ICU LOS and hospital median LOS with a trend toward mortality difference. But, after propensity matching, the mortality rate difference became significantly higher in patients with PAAR compared with matched controls while the ICU LOS differences disappeared. The re-transplantation rates were similar also between the PAAR and no PAAR groups. The cohort with PAAR had a significant 30-day and in-hospital increase in mortality after propensity score matching.

Identifiants

pubmed: 30597632
doi: 10.1111/ctr.13473
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13473

Informations de copyright

© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Auteurs

Sang Kim (S)

Department of Anesthesiology, Critical Care and Pain Management, Hospital for Special Surgery, New York, New York.

Samuel DeMaria (S)

Department of Anesthesiology, Perioperative and Pain Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Jiawen Li (J)

Department of Biostatistics and Data Management, Abbott Molecular, Des Plaines, Illinois.

Hung-Mo Lin (HM)

Department of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, New York.

Natalie Smith (N)

Department of Anesthesiology, Perioperative and Pain Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

David Wax (D)

Department of Anesthesiology, Perioperative and Pain Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Bryan Hill (B)

Department of Anesthesiology, Ohio State University Wexner Medical Center, Columbus, Ohio.

Ashley So (A)

Department of Anesthesiology, Perioperative and Pain Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Parissa Tabrizian (P)

Recanati/Miller Transplantation Institute, Icahn School of Medicine at Mount Sinai, New York, New York.

Sander Florman (S)

Recanati/Miller Transplantation Institute, Icahn School of Medicine at Mount Sinai, New York, New York.

Dennis Feierman (D)

Department of Anesthesiology, Maimonides Medical Center, Brooklyn, New York.

Jeron Zerillo (J)

Department of Anesthesiology, Perioperative and Pain Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

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Classifications MeSH