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Clinical Trials/NCT05455528
NCT05455528
Completed
Not Applicable

Preoperative Renal Insufficiency Predicts Postoperative Adverse Outcomes: A Matched Cohort Study Using the NSQIP Database

Taipei Medical University Hospital1 site in 1 country2,421,286 target enrollmentJanuary 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Renal Insufficiency
Sponsor
Taipei Medical University Hospital
Enrollment
2421286
Locations
1
Primary Endpoint
Risk of postoperative mortality
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The main purpose of this study is to evaluate the risk of postoperative mortality and complications in surgical populations with preoperative renal insufficiency.

Detailed Description

This retrospective cohort study use the National Surgical Quality Improvement Program (NSQIP) database to evaluate the risk of postoperative morbidity and mortality in the surgical population. Patients with estimated. glomerular filtration rate(GFR) \< 60 ml/min per 1.73 square meter are defined as the renal insufficiency group. Patients with estimated GFR \> 90 ml/min per 1.73 square meter are defined as patients without renal insufficiency. Propensity score-matching methods and multivariate logistic regression are used to calculate the risk of postoperative morbidity and mortality.

Registry
clinicaltrials.gov
Start Date
January 1, 2022
End Date
July 1, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Chao-Shun Lin

principal investigator

Taipei Medical University Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with estimated GFR \< 60 ml/min per 1.73 square meter or currently on dialysis are included in renal insufficiency group.
  • Patients with estimated GFR \> 90 ml/min per 1.73 square meter are included in non-renal insufficiency group

Exclusion Criteria

  • Patients population with estimated GFR between 60-90 is not included in the study

Outcomes

Primary Outcomes

Risk of postoperative mortality

Time Frame: 30 days after surgery date

Calculate risk of postoperative 30-day in-hospital mortality between groups

Secondary Outcomes

  • Risk of postoperative morbidities(30 days after surgery date)

Study Sites (1)

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