Preoperative Anemia Affected to Postoperative Outcomes in Liver Resection

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-75
SponsorChiang Mai University

About this trial

To assess the impact of preoperative anemia on postoperative outcomes in patients undergoing liver resection

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All genders, age 20 to 75 years old who undergoing elective liver resection

American Society of Anesthesiologists (ASA) physical status classification of I-III

Disqualifiers

Living donor liver resection

Unresectable tumor

Cardiac arrest during operation

Trial population

Patients who underwent elective liver resection in setting hospital during January, 2006 to December, 2024

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

728 Participants
are grouped into 2 trial groups
Group A: Anemia group
Group B: No anemia group

Trial outcomes

Primary outcomes

1

Postoperative 30-day morbidity rate

• To determine whether preoperative anemia is associated with increased risk of postoperative 30-day morbidity in patients undergoing liver resection.

Time frame
From enrollment to the postoperative day 30

Secondary outcomes

1

Allogenic blood transfusion, comprehensive complication index, postoperative outcomes, and mortality rate

* To determine the incidence of preoperative anemia in liver resection patients. * To determine the incidence of postoperative 30-day morbidities rate * To evaluated the postoperative 30-day morbidities rate, classified using: * Clavien Dindo classification * Comprehensive complication index (CCI) * To determine postoperative major complication, defined as Clavien-Dindo classification grade III or higher or CCI \> 40 * To assess the length of hospital stay * To assess the length of ICU stay and ventilator day * To evaluate postoperative 30-day mortality

Time frame
From enrollment to the postoperative day 30

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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