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ABSTRACT: Objectives
The primary objective was to compare the efficacy of enteral potassium replacement (EPR) and intravenous potassium replacement (IVPR) as first-line therapy. Secondary objectives included comparison of adverse effects and number of doses required to resolve the episode of hypokalaemia.Trial design
The EIPS trial is designed as a randomised, equivalence trial between two treatment arms.Study setting
The study was conducted at the paediatric cardiac intensive care unit (PCICU) at Aga Khan University Hospital, Karachi.Participants
41 patients (aged 1 month to 15 years) who were admitted to PCICU post cardiac surgery were recruited (23 IVPR arm and 18 EPR arm).Intervention
Intervention arms were block randomised on alternate weeks for IVPR and
SUBMITTER: Rehman Siddiqu NU
PROVIDER: S-EPMC5736091 | biostudies-literature | 2017 May
REPOSITORIES: biostudies-literature