Lung tumor
Conditions
Interventions
None listed
Sponsors
Internatinonal University of Health and Welfare
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Adult patients scheduled to undergo thoracic surgery for pulmonary tumors, with written informed consent
Exclusion criteria
Exclusion criteria: Patients already diagnosed with sleep apnea syndrome (SAS) preoperatively, or those judged unable to complete follow-up
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Apnea-hypopnea index (AHI). 2. Oxygen Desaturation Index (ODI). 3. Sleep efficiency These outcomes will be assessed using simplified polysomnography (PSG) at baseline (preoperatively) and 1 year postoperatively. For patients without a preoperative PSG evaluation, exploratory assessments will be conducted at one, two, three and five years postoperatively, provided that informed consent is obtained at these time points. | — |
Secondary
| Measure | Time frame |
|---|---|
| Arterial blood gas findings at baseline and, exploratorily, at 1 year postoperatively (only in patients with available data) Pulmonary function tests (%VC, FEV1, etc.) Epworth Sleepiness Scale for subjective sleepiness assessment Duration of apnea episodes measured by simplified PSG Quality of life assessment (e.g., SF-36, if available) Prognostic information (recurrence, rehospitalization, mortality) | — |
Countries
Japan
Contacts
Public ContactGaku Yamaguchi
International University of Health and Welfare, Ichikawa Hospital Division of Thoracic Surgery
Outcome results
None listed