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Effect of intraoperative blood product transfusion on postoperative pulmonary complications in patients undergoing living donor liver transplantatio

Not Applicable
Conditions
Health Condition 1: K740- Hepatic fibrosis
Registration Number
CTRI/2020/12/029641
Lead Sponsor
Dr Radhika Mathiyazhagan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All adult chronic liver disease patients who had undergone LDLT between Jan 2017 and Dec 2019 at the Institute of Liver and Biliary Sciences.

Exclusion Criteria

Paediatric patients, Acute liver failure patients, Acute on chronic liver failure patients, Patients with moderate to severe HPS, preoperative severe restrictive/ obstructive lung diseases, Patients who had postoperative transfusion of blood and blood products within 48 hours of surgery.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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