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Perioperative Lung Function Monitoring After Anatomic Lung Resections — PLF  

Surgery Clinical Trial

Official title:
Perioperative Lung Function Monitoring After Anatomic Lung Resections

Clinical Trial Summary

Aim of this study was to prospectively investigate the correlation between postoperative spirometry values and pulmonary complications after anatomic lung resections. In addition, the investigators compared postoperative pulmonary function changes between open and minimally invasive approaches.

Clinical Trial Description

All patients undergoing an anatomical lung resection at the investigators' institution were evaluated for this study. Underage patients and those undergoing extended resections (including resection of the chest wall and/or diaphragm) and/or bronchoplastic procedures were excluded.

In every eligible patient undergoing an anatomic lung resection, preoperative spirometry was performed using a handheld spirometer on the day before surgery and on every second day after surgery was performed until patient discharge. The absolute values of FEV1 were recorded by an independent study nurse and noted on a separate sheet not available to the treating doctors.

At the end of the study period FEV1 values were evaluated especially with focus on their correlation with postoperative pulmonary complications (i.e. pneumonia, acute exacerbation of COPD, air leak and atelectasis). Furthermore lung function values of patients undergoing 'open' resections were compared with patients undergoing minimally invasive resections. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03054675
Study type Observational
Source University Hospital Inselspital, Berne
Contact
Status Completed
Phase N/A
Start date June 1, 2013
Completion date June 30, 2016
View Details
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