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Value of preoperative frailty assessment in predicting pulmonary complications after off-pump coronary artery bypass grafting

Value of preoperative frailty assessment in predicting pulmonary complications after off-pump coronary artery bypass grafting

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091184
Enrollment
Unknown
Registered
2024-10-22
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-10-28

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

Conditions

pulmonary complications

Interventions

Control group/non-pulmonary complications group:Patients were evaluated for frailty before surgery
Experimental group/pulmonary complication group:Patients were evaluated for frailty before surgery

Sponsors

Department of Anesthesia and Perioperative Medicine,Jiangsu Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Patients aged 18-80 years who planned to undergo off-pump coronary bypass surgery; (2) ASA classification: ? level; (3) Plan to stay in hospital for >24 hours after surgery; (4) New York College of Cardiology (NYHA) heart function grade II or III, left ventricular ejection fraction (EF) > 50%; More than 70% of the patients with coronary artery blockage had less than 3 vessels.

Exclusion criteria

Exclusion criteria: (1) Emergency operation patients; (2) preoperative history of cerebrovascular disease; (3) Persons with severe visual and hearing impairment and inability to communicate with language; (4) Preoperative COPD, pleural effusion, lung infection, or history of lung surgery (such as lobectomy, segmental resection, and complete resection of one lung) (5) history of cardiac surgery or second cardiac surgery; Acute pericardial tamponade and myocardial infarction, severe sinus bradycardia, atrioventricular block, or sick sinus syndrome; (6) Refuse to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
plumonary complications;

Secondary

MeasureTime frame
Duration of mechanical ventilation;

Countries

China

Contacts

Public ContactYu Chen

The First Affiliated Hospital of Nanjing Medical University(JiangSu province Hospital)

chenyu_njmu@126.com+86 139 5103 3928

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026