Methylene Blue Does Not Improve Vasoplegia After Left Ventricular Assist Device Implantation.


Journal

The Annals of thoracic surgery
ISSN: 1552-6259
Titre abrégé: Ann Thorac Surg
Pays: Netherlands
ID NLM: 15030100R

Informations de publication

Date de publication:
03 2021
Historique:
received: 26 06 2019
revised: 10 04 2020
accepted: 27 05 2020
pubmed: 8 8 2020
medline: 10 3 2021
entrez: 8 8 2020
Statut: ppublish

Résumé

Vasoplegia is a frequent complication of left ventricular assist device (LVAD) implantation. We investigated the effectiveness of methylene blue (MB) for vasoplegia in LVAD recipients. Twenty-seven patients received MB for vasoplegia after LVAD implantation and met study criteria between March 2015 and May 2018. Propensity score inverse probability weighting identified 41 controls who did not receive MB for post-LVAD vasoplegia. Clinical outcomes were compared between control and MB groups and between patients who received doses during (n = 15) and after surgery (n = 12). Hemodynamics and vasopressor requirements were analyzed using analysis of covariance. Median total MB dose was 1.9 mg/kg (interquartile range, 1.2-2.2 mg/kg). Methylene blue recipients experienced a transient initial decline in norepinephrine requirement from 141 ng/kg per min (95% confidence interval [CI], 81-201 ng/kg per min) to 117 ng/kg per min (95% CI, 58-176 ng/kg per min; P = .022) and a delayed decline in vasopressin from 4.8 U/h (95% CI, 3.8-5.8 U/h) to 4.0 U/h (95% CI, 2.8-5.1 U/h) (P = .004). In-hospital mortality, postoperative complications, and end-organ dysfunction did not differ from those of controls. There were no observed differences in mean arterial pressure, vasopressor requirements, or outcomes between patients who received doses during or after surgery. Weighted overall mortality in the entire study cohort was 8.8%. Although MB may affect vasopressor requirements, clinical outcomes in vasoplegia after LVAD implantation did not improve and were not affected by the timing of administration.

Sections du résumé

BACKGROUND
Vasoplegia is a frequent complication of left ventricular assist device (LVAD) implantation. We investigated the effectiveness of methylene blue (MB) for vasoplegia in LVAD recipients.
METHODS
Twenty-seven patients received MB for vasoplegia after LVAD implantation and met study criteria between March 2015 and May 2018. Propensity score inverse probability weighting identified 41 controls who did not receive MB for post-LVAD vasoplegia. Clinical outcomes were compared between control and MB groups and between patients who received doses during (n = 15) and after surgery (n = 12). Hemodynamics and vasopressor requirements were analyzed using analysis of covariance.
RESULTS
Median total MB dose was 1.9 mg/kg (interquartile range, 1.2-2.2 mg/kg). Methylene blue recipients experienced a transient initial decline in norepinephrine requirement from 141 ng/kg per min (95% confidence interval [CI], 81-201 ng/kg per min) to 117 ng/kg per min (95% CI, 58-176 ng/kg per min; P = .022) and a delayed decline in vasopressin from 4.8 U/h (95% CI, 3.8-5.8 U/h) to 4.0 U/h (95% CI, 2.8-5.1 U/h) (P = .004). In-hospital mortality, postoperative complications, and end-organ dysfunction did not differ from those of controls. There were no observed differences in mean arterial pressure, vasopressor requirements, or outcomes between patients who received doses during or after surgery. Weighted overall mortality in the entire study cohort was 8.8%.
CONCLUSIONS
Although MB may affect vasopressor requirements, clinical outcomes in vasoplegia after LVAD implantation did not improve and were not affected by the timing of administration.

Identifiants

pubmed: 32758558
pii: S0003-4975(20)31284-4
doi: 10.1016/j.athoracsur.2020.05.172
pii:
doi:

Substances chimiques

Enzyme Inhibitors 0
Methylene Blue T42P99266K

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

800-808

Informations de copyright

Copyright © 2021 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

Auteurs

Amit Saha (A)

Department of Surgery, Division of Cardiac, Thoracic, and Vascular Surgery, Columbia University Irving Medical Center, New York, New York.

Douglas L Jennings (DL)

Department of Pharmacy, Columbia University Irving Medical Center, New York, New York.

Yuming Ning (Y)

Department of Surgery, Columbia University Irving Medical Center, New York, New York.

Paul Kurlansky (P)

Department of Anesthesiology, Division of Adult Cardiothoracic Anesthesiology, Columbia University Irving Medical Center, New York, New York.

Andrea N Miltiades (AN)

Department of Anesthesiology, Division of Adult Cardiothoracic Anesthesiology, University of Texas Southwestern Medical Center, Dallas, Texas.

Jessica L Spellman (JL)

Department of Anesthesiology, Division of Adult Cardiothoracic Anesthesiology, University of Texas Southwestern Medical Center, Dallas, Texas.

Joseph Sanchez (J)

Department of Anesthesiology, Division of Adult Cardiothoracic Anesthesiology, Columbia University Irving Medical Center, New York, New York.

Melana Yuzefpolskaya (M)

Department of Medicine, Division of Cardiology, Columbia University Irving Medical Center, New York, New York.

Paolo C Colombo (PC)

Department of Medicine, Division of Cardiology, Columbia University Irving Medical Center, New York, New York.

Hiroo Takayama (H)

Department of Anesthesiology, Division of Adult Cardiothoracic Anesthesiology, Columbia University Irving Medical Center, New York, New York.

Yoshifumi Naka (Y)

Department of Anesthesiology, Division of Adult Cardiothoracic Anesthesiology, Columbia University Irving Medical Center, New York, New York.

Koji Takeda (K)

Department of Anesthesiology, Division of Adult Cardiothoracic Anesthesiology, Columbia University Irving Medical Center, New York, New York. Electronic address: kt2485@cumc.columbia.edu.

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