Skip to main content
Clinical Trials/NCT03382054
NCT03382054
Completed
N/A

Frailty and Post-operative Complications in Older Surgical Patients: The Implication of Frailty and Preoperative Risk Assessment - A Retrospective Analysis

Charite University, Berlin, Germany1 site in 1 country25,000 target enrollmentJune 1, 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Frailty
Sponsor
Charite University, Berlin, Germany
Enrollment
25000
Locations
1
Primary Endpoint
Postoperative complications
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Frailty is prevalent in older adults and may be a better predictor of post-operative morbidity and mortality than chronological age. Preoperative risk factors and physiological reserves were assessed on patients more than 70 years old who are scheduled for surgery under general or regional anesthesia. The aim of this retrospective analysis was to examine the impact of relevant geriatric assessments on adverse outcomes in older surgical patients.

Detailed Description

The goal of this study is to analyze the effect of frailty status on postoperative outcomes. These include postoperative complications (only ICD-10 coded diagnoses), length of hospitalization (ward/ICU), disposition, and survival. The project will also attempt to find synergism between a positive frailty status and common medical conditions (e.g. diabetes, congestive heart failure, coronary artery disease, dementia, and kidney disease), as well as anesthesiological and surgical processes (e.g. duration and type of anesthesia, surgical risk, and surgical discipline). Different assessment tools will be analyzed regarding their predictive power and clinical practicability. This should help improve preoperative risk assessment and allow for the multidimensional (physical, cognitive, social) identification of relevant frailty characteristics in the perioperative setting. All outcome parameters, including admission and discharge periods, will be collected using coded information from our hospital database. There will be no follow-up measurements after hospital discharge.

Registry
clinicaltrials.gov
Start Date
June 1, 2016
End Date
December 31, 2022
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Claudia Spies

Clinical director of the Department of Anesthesiology and Operative Intensive Care Medicine (CCM, CVK)

Charite University, Berlin, Germany

Eligibility Criteria

Inclusion Criteria

  • Male and female patients with age 70 years and above scheduled for surgery in the Department of Anesthesiology and Intensive Care Medicine (CCM, CVK), Charité - Universitätsmedizin Berlin

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Postoperative complications

Time Frame: 06/2016-12/2022

ICD-10 coded diagnoses for the hospitalization

Secondary Outcomes

  • Morbidity(06/2016-12/2022)
  • Intensive care unit scores(06/2016-12/2022)
  • Mortality(06/2016-12/2022)
  • Ventilation(06/2016-12/2022)
  • Procedures(06/2016-12/2022)
  • Nutritional therapy 2(06/2016-12/2022)
  • Duration of Hospital stay(06/2016-12/2022)
  • Duration of Intensive Care Unit Stay(06/2016-12/2022)
  • Requirements for intensive care unit(06/2016-12/2022)
  • Nutritional therapy 1(06/2016-12/2022)
  • Disease severity(06/2016-12/2022)
  • Postoperative Delirium(06/2016-12/2022)
  • Medical costs(06/2016-12/2022)
  • Physiotherapy(06/2016-12/2022)
  • Post - intensive care syndrome(06/2016-12/2022)

Study Sites (1)

Loading locations...

Similar Trials