학술논문

Angiotensin II in liver transplantation (AngLT-1): protocol of a randomised, double-blind, placebo-controlled trial
Document Type
article
Source
BMJ Open. 13(11)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Cardiovascular
Organ Transplantation
Transplantation
Clinical Research
Digestive Diseases
Hypertension
Clinical Trials and Supportive Activities
Kidney Disease
Liver Disease
Rare Diseases
Evaluation of treatments and therapeutic interventions
6.1 Pharmaceuticals
Adult
Humans
Angiotensin II
Liver Transplantation
End Stage Liver Disease
Severity of Illness Index
Living Donors
Vasoconstrictor Agents
Hypotension
Norepinephrine
Double-Blind Method
Catecholamines
Randomized Controlled Trials as Topic
Multicenter Studies as Topic
Vasoconstrictor agents
Liver Cirrhosis
Blood Pressure
Public Health and Health Services
Other Medical and Health Sciences
Biomedical and clinical sciences
Health sciences
Psychology
Language
Abstract
IntroductionCatecholamine vasopressors such as norepinephrine are the standard drugs used to maintain mean arterial pressure during liver transplantation. At high doses, catecholamines may impair organ perfusion. Angiotensin II is a peptide vasoconstrictor that may improve renal perfusion pressure and glomerular filtration rate, a haemodynamic profile that could reduce acute kidney injury. Angiotensin II is approved for vasodilatory shock but has not been rigorously evaluated for treatment of hypotension during liver transplantation. The objective is to assess the efficacy of angiotensin II as a second-line vasopressor infusion during liver transplantation. This trial will establish the efficacy of angiotensin II in decreasing the dose of norepinephrine to maintain adequate blood pressure. Completion of this study will allow design of a follow-up, multicentre trial powered to detect a reduction of organ injury in liver transplantation.Methods and analysisThis is a double-blind, randomised clinical trial. Eligible subjects are adults with a Model for End-Stage Liver Disease Sodium Score ≥25 undergoing deceased donor liver transplantation. Subjects are randomised 1:1 to receive angiotensin II or saline placebo as the second-line vasopressor infusion. The study drug infusion is initiated on reaching a norepinephrine dose of 0.05 µg kg-1 min-1 and titrated per protocol. The primary outcome is the dose of norepinephrine required to maintain a mean arterial pressure ≥65 mm Hg. Secondary outcomes include vasopressin or epinephrine requirement and duration of hypotension. Safety outcomes include incidence of thromboembolism within 48 hours of the end of surgery and severe hypertension. An intention-to-treat analysis will be performed for all randomised subjects receiving the study drug. The total dose of norepinephrine will be compared between the two arms by a one-tailed Mann-Whitney U test.Ethics and disseminationThe trial protocol was approved by the local Institutional Review Board (#20-30948). Results will be posted on ClinicalTrials.gov and published in a peer-reviewed journal.Trial registration numberClinicalTrials.govNCT04901169.