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Perioperative Blood Transfusion in Open Liver Resection

C

Chiang Mai University

Status

Completed

Conditions

Blood Loss, Postoperative

Treatments

Procedure: Open liver resection

Study type

Observational

Funder types

Other

Identifiers

NCT06189911
ANE-2564-08020

Details and patient eligibility

About

This observational study is specifically designed to identify the pre-operative risk factors that significantly contribute to perioperative packed red cell transfusions in open liver resection procedures.

The main question it aims to answer are:

  1. What are the risk factors of peri-operative blood transfusion in open liver resection procedures
  2. What are the difference outcomes between patients who receive blood transfusion and the other group.

Researcher will compare perioperative factor and post operative outcomes between transfused and non-transfused group

Full description

After approval of the study protocol from the institutional review board of Chiangmai University (Approval number: ANE-2564-08020), we performed a retrospective review of all patients who underwent an elective open liver resection in our specialized hepato-biliary center from January 2006 through December 2017. This retrospective inquiry comprised 808 patients.

The data was systematically retrieved from electronic medical records. Baseline characteristics including age, gender, body mass index (BMI), co-morbidity, American Society of Anesthesiologists (ASA) classification, diagnosis, hepatitis profile, Child-Pugh classification, cirrhosis, the largest tumor size, previous liver resection, and pre-operative laboratory investigations were collected.

The following intra-operative data were collected: type of liver resection, hilar resection, vascular reconstruction, volume and type of fluid administration, estimated blood loss, packed red cell and blood product transfusion, and operation time. The definitions of liver resection and the type of hepatectomy were aligned with the anatomic classification of the Brisbane 2000 Terminology

Enrollment

1,201 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All genders age above 18 year old who underwent open liver resection from 2006-2017
  • Elective open liver resection

Exclusion criteria

  • Patients who death during the course of a surgical operation

Trial design

1,201 participants in 2 patient groups

transfused
Description:
Group of patients who received perioperative blood transfusions which was defined as the transfusion of packed red cells during the operation and 48 hours after surgery.
Treatment:
Procedure: Open liver resection
non-transfused
Description:
Group of patients who did not received perioperative blood transfusions
Treatment:
Procedure: Open liver resection

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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