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Clinical Trials/NCT05189678
NCT05189678UnknownNot Applicable

Correlation Between Modified Weakness Index and Postoperative Delirium in Elderly Patients Undergoing Non-cardiac Surgery: a Single-center Prospective Observational Cohort Study

Qianfoshan Hospital1 site in 1 country1 target enrollmentStarted: November 22, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
1
Locations
1
Primary Endpoint
Postoperative Delirium

Study Overview

Brief Summary

  1. To study whether there is a correlation between weakness and postoperative delusions in elderly non-cardiac surgery patients
  2. Can the improved debilitating index predict the delusion after non-cardiac surgery
  3. Which of the debilitating index are independent risk factors associated with postoperative delusions

Detailed Description

Early identification of frailty patients is of great clinical significance for preoperative decision making and prognosis assessment. To date, the incidence of postoperative delirium in elderly patients undergoing noncardiac surgery has not been assessed. This study aimed to investigate the relationship between preoperative frailty assessment and the incidence of postoperative delirium after noncardiac surgery.

  1. To study whether there is a correlation between weakness and postoperative delusions in elderly non-cardiac surgery patients
  2. Can the improved debilitating index predict the delusion after non-cardiac surgery
  3. Which of the debilitating index are independent risk factors associated with postoperative delusions

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
70 Years to 90 Years (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Age ≥ 70 years old;
  • ASA: Grade Ⅰ~Ⅳ;
  • Signed informed consent;
  • Scheduled non-cardiac surgery.

Exclusion Criteria

  • Refuse to participate;
  • Expected length of stay <3 days;
  • The same patient can only be included once, regardless of whether the reason for the second operation is related to the first cause;
  • Emergency surgery patients;
  • Inability to communicate due to illiteracy, language impairment, severe hearing or visual impairment;
  • Central nervous system diseases, including various types of dementia and depression
  • Severe renal insufficiency (requiring dialysis treatment);
  • Severe liver dysfunction (Child-Pugh score ≥10);
  • Patients who have participated in other relevant clinical studies within 3 months MMSE examination has confirmed the existence of cognitive dysfunction: illiteracy ≤17 points, primary school degree ≤20 points, middle school degree (including technical secondary school) ≤22 points, university degree (including junior college) ≤23 points

Outcomes

Primary Outcomes

Postoperative Delirium

Time Frame: Twice a day from day 1 to 3 after surgery (8:00-10:00 am and 18:00-20:00 PM).

Incidence of postoperative delirium after noncardiac surgery.Postoperative delirium usually occurs between 24 hours and 72 hours after surgery, and this study will conduct follow-up assessments at six postoperative time points (once in the morning and afternoon on days 1 to 3 after surgery, 8:00 a.m.-10:00 a.m., 18:00-20:00 pm), as long as there was one time point to assess postoperative delirium, the patient was judged to have developed postoperative delirium.

Secondary Outcomes

  • complications(Within 30 days after surgery)
  • Incidence of 30-day readmission to hospital(Within 30 days after surgery)

Investigators

Sponsor
Qianfoshan Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lili Cao

Professor

Qianfoshan Hospital

Study Sites (1)

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