Overview
This is a single-site, non-randomized study on the outcomes of remote real-time "ePRO monitoring" in thoracic surgery patients. ePRO monitoring is a health information technology intervention comprised of delivering longitudinal electronic patient-reported outcome (ePRO) surveys (e.g., on symptoms, and physical functioning) coupled with automated provider alerts for concerning survey responses.
Description
Thoracic surgery patients are at high risk for severe complications post-surgery, such as respiratory failure, empyema, wound problems, and even mortality. Patients with complications may need readmission and invasive management. Usual care may not capture the symptoms of surgery complications. Well-designed remote monitoring of postoperative patients may enable early intervention and lower the risk of severe complications.
This study evaluates the implementation and effectiveness of perioperative electronic patient-reported outcomes (ePROs) monitoring in thoracic surgery patients. Previous studies demonstrated the feasibility of ePROs monitoring by thoracic surgery patients and providers. This study will explore barriers to implementation before real-world effectiveness studies.
Eligibility
Inclusion Criteria:
Patients participating in ePRO monitoring must meet the following inclusion criteria to
participate in this study:
1. 18 years or older
2. English or Spanish speaking
3. Able to complete a web-based, telephonic (IVR), or CRA (or other IRB-approved research
team member)-administrated symptom survey
4. Planned to undergo major thoracic surgery (involving chest wall incisions and
overnight admission) or been discharged from thoracic surgery within the last 30 days
from or by thoracic surgery service.
Exclusion Criteria:
All patients meeting any of the following exclusion criteria at enrollment will be excluded
from study participation:
1. Not completing planned surgery within 3 months of obtaining informed consent
2. Inability to understand English or Spanish
3. Having undergone only minor thoracic surgery (e.g. bronchoscopy, cervical
mediastinoscopy)
4. Dementia, altered mental status, or any psychiatric condition determined by the
thoracic surgery provider team that would prohibit the understanding or rendering of
informed consent.
5. Current incarceration
6. Pregnancy