COPD Assessment Test Score and Perioperative Risk in COPD
Recruiting · NCT07087626 · Observational (researchers observe without assigning treatment) · Lead sponsor: Erzurum City Hospital
View the official record on ClinicalTrials.gov →Interventions studied
What this trial is about
The goal of this observational cohort study is to evaluate whether the COPD Assessment Test (CAT) score can predict the risk of perioperative respiratory complications in patients aged 40 to 70 years with diagnosed Chronic Obstructive Pulmonary Disease (COPD), undergoing elective surgical procedures lasting no longer than 150 minutes. The main questions it aims to answer are: * Is there a statistically significant association between preoperative CAT scores and the incidence of intraoperative and early postoperative respiratory complications in COPD patients? * Can the CAT score be effectively used as a preoperative risk stratification tool to guide anesthetic and surgical decision-making? Researchers will compare two patient groups based on CAT scores: those with CAT \<10 and those with CAT ≥10 to determine whether higher CAT scores are associated with an increased incidence of perioperative respiratory complications. Participants will: * Complete the CAT questionnaire during the preoperative evaluation * Undergo elective surgery with an expected duration of ≤150 minutes * Be monitored intraoperatively for bronchospasm, oxygen desaturation, and ventilation difficulty * Be monitored postoperatively (within the first 72 hours) for hypoxemia, reintubation, bronchospasm episodes, postoperative pneumonia, intensive care unit (ICU) admission, and length of hospital stay * Have perioperative clinical data collected and analyzed for comparative outcomes between CAT score subgroups
Who can take part
Inclusion criteria
- Patients aged between 40 and 70 years
- Diagnosed with stable-stage Chronic Obstructive Pulmonary Disease (COPD) according to GOLD criteria
- Scheduled for elective surgical intervention
- Classified as ASA Physical Status II or III according to the American Society of Anesthesiologists (ASA)
- Planned for postoperative follow-up and eligible for at least 72 hours of observation
- Undergoing surgery with an expected duration of at least 150 minutes
- Willing to participate voluntarily in the study
Exclusion criteria
- Patients younger than 40 years or older than 70 years
- History of COPD exacerbation within the past 4 weeks
- Presence of severe cardiac failure (EF \<30%), end-stage renal disease, or active malignancy
- Neurological disorders or cognitive impairments
- Requirement for invasive mechanical ventilation in the preoperative period
- Altered consciousness or any condition preventing completion of forms before anesthesia
- Undergoing surgery with an expected duration longer than 150 minutes
- Unwillingness to participate in the study voluntarily
Where it is running
1 location listed.
- Erzurum City Hospital - Erzurum, Yakutiye, Turkey (Türkiye)