Ontology highlight
ABSTRACT: Objectives
Studies of the use of IV N-acetylcysteine in the management of non-acetaminophen-induced acute liver failure have evaluated various dosing regimens. The only randomized trial studying this application described a 72-hour regimen. However, observational studies have reported extended duration until normalization of international normalized ratio. This study seeks to compare differences in patient outcomes based on IV N-acetylcysteine duration.Design
Retrospective cohort study.Setting
Medical ICU at a large quaternary care academic medical institution and liver transplant center.Patients
Adult patients admitted to the medical ICU who received IV N-acetylcysteine for the treatment of non-acetaminophen-induced acute liver failure.Interventions
SUBMITTER: Bass SN
PROVIDER: S-EPMC8133178 | biostudies-literature | 2021 May
REPOSITORIES: biostudies-literature