Transfusion Prediction in Major Abdominal Surgery
Development and Validation of a Predictive Model for Transfusion in Major Abdominal Surgery
1 other identifier
observational
128,749
1 country
1
Brief Summary
The transfusion nomogram, integrating preoperative variables, may effectively predict intraoperative transfusion in major abdominal surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 30, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 2, 2025
CompletedFirst Submitted
Initial submission to the registry
February 21, 2025
CompletedFirst Posted
Study publicly available on registry
February 26, 2025
CompletedFebruary 26, 2025
February 1, 2025
6 months
February 21, 2025
February 21, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Intraoperative transfusion
The primary outcome measure is the occurrence of intraoperative blood transfusion. This includes any administration of red blood cells, plasma, or platelets during the surgical procedure. The study aims to predict transfusion requirements based on preoperative clinical factors.
From surgical incision to the end of surgery
Interventions
This is an observational study aimed at developing and validating a predictive model for perioperative blood transfusion. The study utilizes retrospective clinical data from surgical patients to identify key risk factors associated with transfusion requirements. No experimental intervention will be applied to participants, as the study solely focuses on data analysis and model development.
Eligibility Criteria
This study includes adult patients (≥18 years old) who underwent major abdominal surgery at a tertiary medical center. The study population consists of patients with available preoperative clinical and laboratory data, allowing for the development of a predictive model for intraoperative blood transfusion. Patients with known hematologic disorders, coagulopathy, or prior transfusion before surgery are excluded to minimize confounding factors.
You may qualify if:
- Patients aged 18 years and older who underwent major abdominal surgery
You may not qualify if:
- Patients with known hematologic disease or coagulopathy
- Patients who received a blood transfusion before surgery
- Patients with incomplete data or missing laboratory values
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Asan Medical Center
Seoul, Songpa, 05505, South Korea
Related Publications (1)
Sim JH, Oh AR, Kim S, Park YS, Ha S, Kim JU. Development and validation of a predictive model for transfusion in major abdominal surgery: a multicentre retrospective study. Br J Anaesth. 2025 Sep;135(3):623-631. doi: 10.1016/j.bja.2025.05.048. Epub 2025 Jul 18.
PMID: 40681389DERIVED
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
February 21, 2025
First Posted
February 26, 2025
Study Start
June 30, 2024
Primary Completion
December 20, 2024
Study Completion
January 2, 2025
Last Updated
February 26, 2025
Record last verified: 2025-02
Data Sharing
- IPD Sharing
- Will not share