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Impact of New Anthropometric Indices on Outcomes After Cardiac Surgery

Impact of New Anthropometric Indices on Outcomes After Cardiac Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05403294
Enrollment
240
Registered
2022-06-03
Start date
2022-07-27
Completion date
2022-11-01
Last updated
2022-07-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anthropometry, Cardiac Anesthesia, Cardiac Surgery, Cardiometabolic Risk Factors, Coronary Artery Disease

Brief summary

Obesity is associated with a number of risk factors for cardiovascular disease. Body mass index (BMI) is the most commonly recommended and used anthropometric measure to classify general obesity in clinical and epidemiological studies. It is widely accepted that obesity increases the risk of heart disease and is thought to be a risk factor for adverse outcomes after cardiac surgery. However, recent studies show paradoxical results, wherein obese patients can experience fewer adverse events and lower mortality than patients with normal-low body mass index(BMI) . The discriminative capacity of BMI has been criticized because it cannot distinguish muscle mass from fat mass, or reflect fat distribution . Alternatively, abdominal obesity indices, such as waist circumference (WC) and waist-to-height ratio (WHtR), have been suggested to be better predictor of cardiometabolic abnormalities because they modulate the limitation of BMI. However, they were insufficient in studies.For this reason, scientists turned to find a new anthropometric formula that could better detect obesity-related mortality and morbidity and they developed 2 new methods. Body Shape İndex (ABSI) is calculated using waist circumference, BMI and height parameters. Body Roundness İndex (BRI) is calculated using waist circumference and height parameters. These new indices may reflect visceral adiposity and strongly predict cardiovascular risk, postsurgical outcomes and resource utilisation.

Interventions

None listed

Sponsors

TC Erciyes University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* open heart surgery * voluntary patients

Exclusion criteria

* emergency surgery * off-pump or robotic surgery * surgery requiring deep hypothermic circulatory arrest * reluctant patients

Design outcomes

Primary

MeasureTime frameDescription
new atrial fibrillation/flutterwithin 30 days of the procedureNumber of Partients with new atrial fibrillation/flutter
permanent rhythm device insertionwithin 30 days of the procedureNumber of Patients requiring insertion of a permanent device
mortalitywithin 30 days of the procedureNumber of death at 30 days after surgery
postoperative strokewithin 30 days of the procedureNumber of patients with postoperative stroke
cardiac arrestwithin 30 days of the procedurenumber of patients with cardiac arrest

Secondary

MeasureTime frameDescription
prolonged ventilationwithin 30 days of the procedurenumber of patients experiencing prolonged postoperative pulmonary ventilation (\>24 hours)
intensive care unit (ICU) readmissionswithin 30 days of the procedurenumber of patients with intensive care unit readmission
sepsis /deep sternal infectionwithin 30 days of the procedurenumber of patients with sepsis, deep sternal wound infection or mediastinitis
pulmonary complicationswithin 30 days of the procedurenumber of patients with pneumonia or pleural effusion
renal failure / renal dialysiswithin 30 days of the procedurenumber of patient with acute renal failure or worsening renal function result
total intensive care unit (ICU) hourswithin 30 days of the proceduretotal intensive care unit (ICU) hours

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026