Preoperative Cardiac Power Output and P-POSSUM Score

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age65+
SponsorNecmettin Erbakan University

About this trial

This study aims to investigate the relationship between preoperative Cardiac Power Output (CPO), which reflects the pumping capacity of the heart, and the P-POSSUM score, a widely used surgical risk assessment tool, in patients aged 65 years and older undergoing abdominal surgery. Simple and non-invasive measurements performed in the preoperative period will be used to obtain CPO values and to evaluate whether these measurements are helpful in predicting postoperative morbidity and mortality. No additional procedures beyond routine clinical care will be performed as part of this observational study. The findings of this study may contribute to a more accurate assessment of surgical risk and help improve patient safety in the perioperative period.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Undergoing abdominal surgery in general surgery practice (including elective and emergency procedures),

ASA (American Society of Anesthesiologists) class I-III,

Adequate recording with transthoracic echocardiography,

Having given informed consent.

Disqualifiers

Severe valvular disease (severe stenosis or insufficiency),

Unstable coronary artery disease or recent myocardial infarction (within the last 3 months),

Pulmonary hypertension,

Severe arrhythmia (uncontrolled atrial fibrillation, ventricular tachycardia, etc.)

Trial population

This study will include patients aged 65 and over who are scheduled for abdominal surgery at Necmettin Erbakan University Faculty of Medicine Hospital.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

120 Participants
are grouped into 1 trial group
Group A: patients aged 65 years and older undergoing abdominal surgery

Trial outcomes

Primary outcomes

1

30-day postoperative mortality

All-cause mortality occurring within 30 days after abdominal surgery in patients aged 65 years and older (yes/no).

Time frame
Up to 30 days after surgery

Secondary outcomes

1

Postoperative morbidity

Postoperative morbidity assessed using the Postoperative Morbidity Survey (POMS).

Time frame
Up to 30 days after surgery
2

Early postoperative morbidity

Early postoperative morbidity assessed using the Postoperative Morbidity Survey (POMS) on postoperative day 3.

Time frame
Postoperative day 3

Other outcomes

Sponsors and contacts

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