Lung Cancer
Conditions
Interventions
Given the observational nature of the study, there is no intervention involved. All patients in a participating center will be treated according to the new ERATS standard care protocol after its imple
Sponsors
Albert Schweitzer Ziekenhuis
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Patients aged 18 years or older undergoing anatomical lung resection for suspected or confirmed lung cancer were eligible for inclusion. Written informed consent
Exclusion criteria
Exclusion criteria: Not meeting inclusion criterium
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary objective of this study is to achieve a 15% improvement in ERATS protocol adherence, increasing from an estimated 65% to over 80%, in relation to the completion of the ERATS implementation trajectory. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary objectives include reducing the length of hospital stay by one day (from six to five days), shortening the time to recovery, decreasing complication and readmission rates, lowering mortality rates, and enhancing patient-reported outcomes measured by EORTC QLQ-C30, EORTC QLQ-LC13, and PROMIS-APS. | — |
Countries
Netherlands
Contacts
Public ContactEM Meyenfeldt
Albert Schweitzer Ziekenhuis
Outcome results
None listed