Impact of Sarcopenia Index on Postoperative Pulmonary Complication in Elderly Patients Undergoing OPCAB
1 other identifier
observational
605
1 country
1
Brief Summary
Retrospective data collection. The aim of this study is to determine the effect of preoperative sarcopenia index on postoperative pulmonary complications in elderly patients undergoing off-pump coronary artery bypass graft surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2020
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 29, 2020
CompletedFirst Posted
Study publicly available on registry
December 4, 2020
CompletedStudy Start
First participant enrolled
December 7, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
January 15, 2021
CompletedJuly 28, 2021
July 1, 2021
1 month
November 29, 2020
July 27, 2021
Conditions
Outcome Measures
Primary Outcomes (3)
postoperative pulmonary complications : pneumonia
CXR with at least one of the following: infiltrate, consolidation, cavitation;plus at least one of the following: fever \>38 °C with no other cause, white cell count \<4 or\>12\*109 litre-1, \>70 yr of age with altered mental status with no other cause;-plus at least two of the following: new purulent/ changed sputum, increased secretions/suctioning, new/worse cough/dyspnoea/tachypnoea, rales/ bronchial breath sounds, worsening gas exchange.
During the hospitalization for surgery. This includes the entire postoperative period up to discharge, even if over 30 days.
postoperative pulmonary complications : prolonged ventilation
Indicate whether the patient had prolonged post-operative pulmonary ventilation \> 24.0 hours. The hours of postoperative ventilation time include OR exit until extubation, plus any additional hours following reintubation.
During the hospitalization for surgery. This includes the entire postoperative period up to discharge, even if over 30 days.
postoperative pulmonary complications : reintubation
Indicate whether the patient was intubated for the first time after leaving the OR from the initial procedure, or re-intubated during the hospital stay after the initial extubation.
During the hospitalization for surgery. This includes the entire postoperative period up to discharge, even if over 30 days.
Secondary Outcomes (6)
postoperative complications : Renal failure
During the hospitalization for surgery. This includes the entire postoperative period up to discharge, even if over 30 days.
postoperative complications : Delirium
During the hospitalization for surgery. This includes the entire postoperative period up to discharge, even if over 30 days.
postoperative complications : Reoperation due to bleeding/tamponade
During the hospitalization for surgery. This includes the entire postoperative period up to discharge, even if over 30 days.
postoperative complications : Permanent stroke
During the hospitalization for surgery. This includes the entire postoperative period up to discharge, even if over 30 days.
postoperative complications : Mortality
During the hospitalization in which the operation was performed, even if after 30 days.
- +1 more secondary outcomes
Eligibility Criteria
patients who undersent off-pump coronary artery bypass graft surgery.
You may qualify if:
- Patients who were 65 years of age or older at the time of surgery(off-pump coronary artery bypass graft surgery)
- serum cystatin C and creatinine test results were valid within one week before surgery
You may not qualify if:
- Patients with chronic renal failure (estimated glomerular filtration rate less than 60)
- Patients with acute kidney injury
- Patients with respiratory tract infection within 1 month before surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine
Seoul, South Korea
Study Officials
- PRINCIPAL INVESTIGATOR
Young-Lan Kwak, MD, PhD
Severance Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 29, 2020
First Posted
December 4, 2020
Study Start
December 7, 2020
Primary Completion
January 15, 2021
Study Completion
January 15, 2021
Last Updated
July 28, 2021
Record last verified: 2021-07