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Clinical Trials/NCT02566343
NCT02566343
Completed
Not Applicable

Preoperative Diagnostic Tests for Pulmonary Risk Assessment in Patients With Chronic Obstructive Pulmonary Disease (COPD) Undergoing Major Surgery

Universitätsklinikum Hamburg-Eppendorf1 site in 1 country365 target enrollmentNovember 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Diseases, Obstructive
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Enrollment
365
Locations
1
Primary Endpoint
Composite end point of postoperative pulmonary complications (PPC) or all cause in-hospital mortality
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This prospective study intends to investigate the incidence of postoperative pulmonary complications (PPC) or in-hospital mortality in patients with COPD or at risk for COPD undergoing high-risk noncardiac major surgery and to identify relevant risk factors. This study aims to quantify and compare the diagnostic performance of preoperative functional tests, exercise capacity, clinical assessment tests and predictive scoring systems to predict PPC or in-hospital mortality in these patients.

Detailed Description

COPD is associated with high perioperative morbidity and mortality and PPC frequently occur in these patients. However, concepts for preoperative pulmonary risk assessment and the predictive value of routine preoperative exercise capacity, clinical assessment and pulmonary function tests are still poorly characterized. Objectives: * To determine the incidence of the composite end point of PPC or all cause in-hospital mortality in patients with confirmed COPD (spirometry) and patients with clinical risk factors in whom spirometry disproved COPD. * To determine the predictive value of exercise capacity, clinical assessment tests, pulmonary function tests and predictive scoring systems to predict the composite end point in these patients. * To identify relevant risk factors and predictors associated with the composite end point. Methodology: Prospective single-centre observational study All patients receive a structured preoperative pulmonary risk assessment with: 1. standardized clinical questionnaire 2. COPD Assessment Test (CAT™) 3. exercise capacity (symptom-limited stair climbing) 4. spirometry 5. capillary blood gas Analysis Postoperative follow-up is planned between the 2nd and 5th day after extubation.

Registry
clinicaltrials.gov
Start Date
November 2014
End Date
July 2016
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years and older
  • High-risk noncardiac major surgery with an anticipated operation time ≥ 120 minutes and/or planned postoperative intensive care unit admission
  • Typical clinical signs for COPD (dyspnea, chronic cough, chronic sputum production, exposure to risk factors)
  • Confirmed COPD (medical history) or clinical risk factors for COPD
  • Positive COPD Assessment Test (CAT™)

Exclusion Criteria

  • \< 18 Years
  • Pregnancy
  • Lack of cooperation
  • Inability to provide functional tests like spirometry or stairclimbing

Outcomes

Primary Outcomes

Composite end point of postoperative pulmonary complications (PPC) or all cause in-hospital mortality

Time Frame: until hospital discharge up to 6 months after surgery

Secondary Outcomes

  • Frequency of unplanned intensive care unit admission, prolonged oxygen requirement, reintubation, non-invasive ventilation (NIV) or extracorporeal lung assist(until hospital discharge up to 6 months after surgery)
  • Carbon dioxide (pCO2) and oxygen (pO2) partial pressures from blood gas analysis(within 1 week after extubation)
  • Duration of postoperative respirator support (h)(until hospital discharge up to 6 months after surgery)
  • Length of stay in the intensive care unit (days)(until hospital discharge up to 6 months after surgery)
  • Duration of hospitalization (days)(until hospital discharge up to 6 months after surgery)
  • Forced expiratory volume in one second to forced vital capacity ratio (FEV1/FVC) and FEV1 % predicted(within 1 week after extubation)
  • New pulmonary radiological findings (e.g. pneumonia or pneumothorax)(until hospital discharge up to 6 months after surgery)
  • Postoperative new respiratory symptoms (e.g. dyspnea or wheezing) or treatment for exacerbation (e.g. new systemic glucocorticosteroids or bronchodilators)(until hospital discharge up to 6 months after surgery)

Study Sites (1)

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