Pediatric Enhanced Recovery After Cardiac Surgery

Completed

• Conditions: ERAS; Pediatric ALL; Congenital Heart Disease

• Registration Number: NCT05665712
• Lead Sponsor: University of Alberta

Brief Summary

Identify our institution's current perioperative management strategies for pediatric cardiac surgery patients. Identify predictive factors for receiving perioperative care following P-ERACS strategies.

Compare outcomes between P-ERACS and non-P-ERACS patients

Detailed Description

study aims to 1) assess our institution's current perioperative management strategies for pediatric cardiac surgery patients, 2) identify which patient population would be appropriate for inclusion in a pediatric ERACS (P-ERACS) program, and 3) compare the outcomes of patients whose perioperative care followed general consensus P-ERACS strategies (P-ERACS patients) and those whose perioperative care did not (non-P-ERACS patients). Results from this study will inform current efforts to establish a local P-ERACS protocol, and facilitate the initiation of a clinical trial to assess adherence to a P-ERACS pathway as well as the impact of such a pathway on patient outcomes.

Study Timeline

• Study Start: 2019-11-01
• Study First Submitted: 2022-12-16
• Study First Submitted QC: 2022-12-16
• Study First Posted: 2022-12-27
• Primary Completion: 2023-08-15
• Study Completion: 2023-08-15
• Status Verified: 2023-10
• Last Update Submitted: 2023-10-03
• Last Update Posted: 2023-10-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 483

Inclusion Criteria

• all pediatric patients (<18 years of age) who underwent elective cardiac surgery requiring cardiopulmonary bypass (CPB)

Exclusion Criteria

• Emergency procedures and transplantation (heart, lung, heart and lung)

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
time to extubation	24 hours	time to extubation

Secondary Outcome Measures

Name	Time	Method
Length of stay	48 hours	LOS in ICU

Trial Locations

Locations (1)

University of Alberta; 🇨🇦 Edmonton, Alberta, Canada