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Pediatric Enhanced Recovery After Cardiac Surgery

Pediatric Enhanced Recovery After Cardiac Surgery: a Single-centre Retrospective Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05665712
Acronym
PERCS
Enrollment
483
Registered
2022-12-27
Start date
2019-11-01
Completion date
2023-08-15
Last updated
2023-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Heart Disease, ERAS, Pediatric ALL

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.

Interventions

PROCEDUREenhanced recovery

bundle of factors that have been shown to help with recovery in other surgical services such as good pain control, early ambulation, early nutrition

Sponsors

University of Alberta
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
time to extubation24 hourstime to extubation

Secondary

MeasureTime frameDescription
Length of stay48 hoursLOS in ICU

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026