About this trial
Postoperative delirium is a common and serious complication in elderly patients undergoing major orthopedic surgery and is associated with increased morbidity, prolonged hospital stay, and higher healthcare costs. Preoperative psychological distress has been suggested as a potential risk factor influencing postoperative outcomes; however, its relationship with delirium and other clinical outcomes remains insufficiently explored.
This prospective observational study aims to investigate the association between preoperative distress levels and postoperative delirium, pain intensity, and length of hospital stay in elderly patients undergoing major orthopedic surgery. Preoperative distress will be assessed using validated tools, and postoperative outcomes including delirium incidence, pain scores, and hospital stay duration will be recorded and analyzed.
The findings of this study are expected to contribute to improved perioperative risk stratification and may support the development of targeted interventions to reduce postoperative complications in this vulnerable patient population.
Eligibility criteria
Qualifiers
Age ≥65 years
Hip fracture surgery
Primary or revision hip arthroplasty
Primary knee arthroplasty
Disqualifiers
Known diagnosis of severe dementia or significant cognitive impairment
Presence of preoperative delirium or an active diagnosis of delirium
Severe hearing or visual impairment preventing effective communication
History of intracranial surgery or neurological diseases significantly increasing the risk of delirium (e.g., advanced Parkinson's disease, severe stroke sequelae)
Trial design
Treatments tested in this trial
- Not listed