The objective of this this single-center prospective longitudinal study is to evaluate the incidence of diaphragmatic dysfunction after non-intubated video-assisted thoracoscopic surgery (NIVATS).
Participant will be evaluated during surgery, 2 hours and 24 hours after surgery.
Patient aged 18 years or older
Patient who has read and signed the informed consent form for participation in the study
Patient undergoing surgery with video-assisted thoracoscopic surgery without intubation
Known or detected diaphragmatic dysfunction before the intervention
Patient not affiliated with the French social security system
Patient under legal protection, guardianship, or curatorship
Patient already enrolled in another therapeutic study protocol (involving medications or non-drug therapies)