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Iron Deficiency in Pediatric Heart Surgery

Iron Deficiency in Pediatric Heart Surgery: Impact on Anemia, Transfusion and Complications, a Retrospective Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06276608
Enrollment
300
Registered
2024-02-26
Start date
2024-02-23
Completion date
2024-06-30
Last updated
2024-02-28

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

Conditions

Cardiac Surgical Procedures, Congenital Heart Disease in Children, Iron Deficiencies, Iron Deficiency Anemia

Brief summary

The prevalence of iron deficiency in pediatric cardiac surgery patients is not very well known. Iron deficiency can lead to anemia, higher transfusion rates and possibly higher complication rates. In this retrospective study, the iron status of all patients undergoing pediatric cardiac surgery at our institution between January 2019 and december 2023 will be analyzed. Together with iron status, transfusion requirements as well as complications will be recorded. Iron status will be reported with descriptive statistics, patients with or without iron deficiency will be compared using non-parametric tests.

Interventions

DIAGNOSTIC_TESTIron status

Iron status will be based on preoperative ferritin levels: a ferritin \< 10 mcg/L will be considered as iron deficiency, ferritin levels \> 10 mcg/L will be considered normal

Sponsors

Queen Fabiola Children's University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 16 Years

Inclusion criteria

* All patients who underwent pediatric cardiac surgery at our institution between January 1, 2019 and December 31, 2023

Exclusion criteria

* Incomplete medical charts * Patients who did not consent to the use of their medical data

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of preoperative iron deficiency (%)24 hoursA preoperative ferritin \< 10 mcg/L will be considered as iron deficiency. Iron deficiency will be reported using descriptive statistics (mean, standard deviation, median, interquartile range, %)
Complications28 daysThe complication rate (%) will be reported. Complications are defined by the occurence of one or more of the following events: * transfusion rate (%) * volume of packed red cells transfused (mL/kg) * perioperative blood loss (mL/kg) * need for surgical re-exploration (%) * intensive care stay (days) * new renal insufficiency (%) * use of inotropes (%) * 28 day mortality (%) The frequency of any single item will also be reported (%)

Countries

Belgium

Contacts

Primary ContactDenis Schmartz, MD
denis.schmartz@hubruxelles.be+3225553919
Backup ContactAriane Willems, MD, PhD
ariane.willems@hubruxelles.be+322477331

Outcome results

None listed

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