For the treatment of stage I-II NSCLC, two mini-invasive techniques are mostly utilized: uni-portal and three-portal VATS. In the uniportal approach, the injury on a single intercostal space could determine a lower level of pain than the three-portal approach, allowing a better postoperative course. Few studies in Literature compare these techniques, and most of them are retrospective. The main purpose of this randomized study is to compare uni-portal VATS with three-portal VATS, in terms of postoperative pain. Secondary objectives of the study are valutations of: * respiratory and functional capacity between the two groups * operative time * number of resected lymphnodes * intra and postoperative complications, such as conversions to open surgery, amount of bleeding, prolonged air leaks, surgical site infections, pulmonary complications.
Randomized cohort clinical trial, prospectic, monocentric. Procedure of randomization: the day before the operation, with the "Random Allocation Rule" technique Arm 1: pulmonary lobectomy and lymphoadenectomy with uni-portal VATS approach Arm 2: pulmonary lobectomy and lymphoadenectomy with three-portal VATS approach Misurations Total analgesic consumption, normalized to morphine milligrams, recorded in the 7 days following the operation. The choice of cumulative analgesic consumption as parameter of primary outcome is because pain valuation with VAS is significantly affected by individual variability. Secondary outcomes: measure of postoperative pain with NRS at 2,6,12,24 hours and at 2,3,4,5,30 days from sugery. A pain score will be assigned to each patient after the total amount of NRS. Respiratory function will be valuated with spirometry after 7 and 30 days from surgery, and compared with pre-operative tests. All intraoperative parameters will be compared between the two groups: operative time (skin to skin), proportion of conversions to open surgery, number of resected lymphnodes, amount of bleeding. Postoperative complications will be analyzed: rate of prolonged air leaks, surgical site infections, cardiac rythhm disfunctions, pulmonary complications, post-thoracotomy syndrome, as well as lenght of stay at the hospital.
Study Type
OBSERVATIONAL
Enrollment
120
VATS uni-portal lobectomy and lymphoadenectomy
VATS three-portal lobectomy and lymphoadenectomy, Copenhagen approach
Thoracic Surgery Unit - Fondazione IRCCS Ca' Granda Policlinico
Milan, Mi, Italy
Measurement of postoperative pain after uni-portal and three-portal VATS
Total analgesic consumption, normalized to morphine milligrams, recorded in the 7 days following the operation.
Time frame: 7 days
Measure of postoperative pain with NRS at 2,6,12,24 hours and at 2,3,4,5,30 days from sugery.
A pain score will be assigned to each patient after the total amount of NRS
Time frame: 30 days
Valuation of respiratory function
Spirometry after 7 and 30 days from surgery, compared with pre-operative tests
Time frame: 30 days
Intraoperative parameters
Operative time (skin to skin, minutes)
Time frame: 1 day
Intraoperative bleeding
Amount of bleeding
Time frame: 1 day
Postoperative air leakage
Rate of prolonged air leaks
Time frame: 15 days
Postoperative complications
Cardiac rythhm disfunctions
Time frame: 1 month
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