MedPath

Reperfusion Syndrome in liver transplant

Not Applicable
Conditions
Health Condition 1: K77- Liver disorders in diseases classified elsewhere
Registration Number
CTRI/2020/08/026979
Lead Sponsor
Center for liver and Biliary Sciences Max Super Speciality Hospital SaketNew DelhiIndia
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All consecutive LT procedures in adult patients in our unit will be enrolled for collection of data

Exclusion Criteria

1. All Deceased - donor related transplantation (DDLTs)

2.Liver transplants done in patients with ALF

3.LT for non-cirrhotic liver disease

4.Combined liver/kidney transplantation

5.Re-transplantation

6.All liver recipients identified to have cirrhotic cardiomyopathy, grade 3 Diastolic dysfunction on routine preoperative evaluation.

7.All LT recipients on Inotropes before surgery

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To document the incidence of PRS during LDLT and classify severity of PRSTimepoint: at the end of surgery
Secondary Outcome Measures
NameTimeMethod
1.To identify the predictors of PRS.Timepoint: On Postoperative Day 30 or at discharge (whichever is first);2)To examine the postoperative consequences of PRS after LTTimepoint: On Postoperative Day 30 or at discharge (whichever is first)
© Copyright 2025. All Rights Reserved by MedPath