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Impact of Anesthesia Maintenance Methods on Incidence of Postoperative Delirium

Primary Purpose

Delirium, Postoperative Complications, Postoperative Cognitive Dysfunction

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Sevoflurane
Propofol
Sponsored by
Peking University First Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Delirium focused on measuring Sevoflurane, Propofol, Aged, Neoplasm, Surgical Procedure, Operative, Delirium, Postoperative Complications, Postoperative Cognitive Dysfunction

Eligibility Criteria

65 Years - 90 Years (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria

Participants will be included if they meet all the following criteria:

  1. Age ≥ 65 years and < 90 years;
  2. Primary malignant tumor;
  3. Do not receive radiation therapy or chemotherapy before surgery;
  4. Scheduled to undergo surgery for the treatment of tumors, with an expected duration of 2 hours or more, under general anesthesia;
  5. Agree to participate, and give signed written informed consent.

Exclusion criteria

Patients will be excluded if they meet any of the following criteria:

  1. Preoperative history of schizophrenia, epilepsy, parkinsonism or myasthenia gravis;
  2. Inability to communicate in the preoperative period (coma, profound dementia, language barrier, or end-stage disease);
  3. Critical illness (preoperative American Society of Anesthesiologists physical status classification ≥ IV), severe hepatic dysfunction (Child-Pugh class C), or severe renal dysfunction (undergoing dialysis before surgery);
  4. Neurosurgery;
  5. Other reasons that are considered unsuitable for participation by the responsible surgeons or investigators (reasons must be recorded in the case report form).

Sites / Locations

  • Peking University First Hospital
  • Beijing Shijitan Hospital
  • Peking University Cancer Hospital
  • Peking University School and Hospital of Stomatology
  • Cancer Hospital of Guangxi Medical University
  • Shenzhen Second People's Hospital
  • Guizhou Provincial People's Hospital
  • Hebei Medical University Forth Hospital
  • The First Affiliated Hospital of Zhengzhou University
  • The Third Xiangya Hospital of Central South University
  • Zhongda Hospital
  • Ningxia People's Hospital
  • Affiliated Hospital of Qinghai University
  • Tang-Du Hospital
  • Shaanxi Provincial People's Hospital
  • Shanxi Province Cancer Hospital
  • Tianjin Nankai Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Sevoflurane group

Propofol group

Arm Description

Sevoflurane will be administered by inhalation for anesthesia maintenance. The concentration of inhaled sevoflurane will be adjusted to maintain the bispectral index (BIS) value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, sevoflurane inhalational concentration will be decreased and fentanyl/sufentanil will be administered when necessary. Sevoflurane inhalation will be stopped at the end of surgery.

Propofol will be administered by intravenous infusion for anesthesia maintenance. The infusion rate of propofol will be adjusted to maintain the BIS value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, propofol infusion rate will be decreased and fentanyl/sufentanil will be administered when necessary. Propofol infusion will be stopped at the end of surgery.

Outcomes

Primary Outcome Measures

Incidence of delirium within 7 days after surgery.
Delirium is assessed twice daily (8-10 AM and 6-8 PM) with the Confusion Assessment Method for patients without endotracheal intubation or the Confusion Assessment Method for the Intensive Care Unit for patients with endotracheal intubation.

Secondary Outcome Measures

Percentage of intensive care unit (ICU) admission after surgery.
Percentage of intensive care unit (ICU) admission after surgery.
Percentage of ICU admission with endotracheal intubation after surgery.
Percentage of ICU admission with endotracheal intubation after surgery.
Length of stay in ICU after surgery.
Length of stay in ICU after surgery (in patients admitted to the ICU after surgery).
Length of stay in hospital after surgery.
Length of stay in hospital after surgery.
Incidence of non-delirium complications within 30 days.
Non-delirium complications are defined as newly occurred events other than delirium that are harmful to patients' recovery and required therapeutic intervention, i.e., grade 2 or higher on the Clavien-Dindo classification.
Cognitive function at 30 days after surgery.
Cognitive function assessed with Telephone Interview for Cognitive Status-Modified (TICS-m).

Full Information

First Posted
January 5, 2016
Last Updated
March 1, 2022
Sponsor
Peking University First Hospital
Collaborators
Hebei Medical University Fourth Hospital, The People's Hospital of Ningxia, Beijing Shijitan Hospital, Capital Medical University, Guizhou Provincial People's Hospital, Affiliated Hospital of Qinghai University, The Third Xiangya Hospital of Central South University, Cancer Hospital of Guangxi Medical University, Shanxi Provincial People's Hospital, Zhongda Hospital, The First Affiliated Hospital of Zhengzhou University, Tang-Du Hospital, Tianjin Nankai Hospital, Shenzhen Second People's Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02662257
Brief Title
Impact of Anesthesia Maintenance Methods on Incidence of Postoperative Delirium
Official Title
Impact of Inhalational Versus Intravenous Anesthesia Maintenance Methods on Incidence of Postoperative Delirium in Elderly Patients After Cancer Surgery: An Open-label, Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
April 1, 2015 (Actual)
Primary Completion Date
September 29, 2017 (Actual)
Study Completion Date
November 26, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University First Hospital
Collaborators
Hebei Medical University Fourth Hospital, The People's Hospital of Ningxia, Beijing Shijitan Hospital, Capital Medical University, Guizhou Provincial People's Hospital, Affiliated Hospital of Qinghai University, The Third Xiangya Hospital of Central South University, Cancer Hospital of Guangxi Medical University, Shanxi Provincial People's Hospital, Zhongda Hospital, The First Affiliated Hospital of Zhengzhou University, Tang-Du Hospital, Tianjin Nankai Hospital, Shenzhen Second People's Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Surgery is one of the major treatment methods for patients with malignant tumor. And, alone with ageing process, more and more elderly patients undergo surgery for malignant tumor. Evidence emerges that choice of anesthetics, i.e., either inhalational or intravenous anesthetics, may influence the outcome of elderly patients undergoing cancer surgery. Delirium is a commonly occurred early postoperative cognitive complication in the elderly, and its occurrence is associated with the worsening outcomes. Choice anesthetics may influence the occurrence of postoperative delirium. However, evidence in this aspect is conflicting.
Detailed Description
It is estimated that 234.2 million major surgical procedures are undertaken every year worldwide. Surgery is one of the major treatment methods for patients with malignant tumor. And, alone with ageing process, more and more elderly patients undergo surgery for malignant tumor. Evidence emerges that choice of anesthetics, i.e., either inhalational or intravenous anesthetics, may influence the outcome of elderly patients undergoing cancer surgery. Delirium is a commonly occurred cognitive complication in elderly patients after surgery. The occurrence of delirium is associated with the worsening outcomes, including increased morbidity and mortality, prolonged hospital stay, elevated medical care cost, and declined cognitive function. High age, major surgery, and critical illness are major risk factors of postoperative delirium (POD). However, the relationship between use of general anesthetics and occurrence of delirium cannot be excluded. There are studies that compared the effects of two kinds of anesthetics on the cognitive outcomes after surgery. In the study of Nishikawa et al., 50 elderly (≥ 65 years) patients undergoing long-duration laparoscope-assisted surgery randomly received sevoflurane or propofol anesthesia. The results showed that, although the incidence of POD was not significantly different between the two groups, the delirium rating scale (DRS) score was significantly lower in the sevoflurane group than in the propofol group at postoperative days 2-3 (P = 0.007 and 0.002, respectively). In the study of Schoen et al., 128 patients undergoing on-pump cardiac surgery were randomized into two groups. The results showed that early postoperative cognitive function was significantly better in sevoflurane group than in the propofol group, especially in those who experienced cerebral desaturation during surgery. On the other hand, some studies reported contrary results. In a large sample size study of 2000 patients undergoing general anesthesia, patients carrying ApoE4 epsilon 4 allele were more likely to develop early postoperative cognitive decline after inhalational anesthesia (odd ratio 3.31, 95% confidence interval 1.25-6.39, P < 0.05), but not after intravenous anesthesia (odd ratio 0.93, 95% confidence interval 0.37-2.39, P > 0.05). In a randomized control trail of 44 patients undergoing carotid endarterectomy, the mini-mental state examination (MMSE) score was significantly higher, whereas blood S100B concentration was significantly lower in the propofol group than in the sevoflurane group at 24 hours after surgery. In the study of Tang et al., 200 elderly (≥ 60 years) patients with mild cognitive impairment who planned to undergo radical rectal resection randomly received either sevoflurane or propofol anesthesia. The results showed that, although there was no difference in the incidence of cognitive dysfunction at 7 days after surgery, the negative cognitive effects was more severe after sevoflurane anesthesia than after propofol anesthesia (P = 0.01). It seems that more evidence suggests the harmful cognitive effects of inhalational anesthetics. However, care must be taken when explaining these results: (1) target patients population were different; (2) sample size were small in the majority of studies; (3) the diagnostic criteria of cognitive complications were different, make it hard to do meta-analysis; (4) the clinical significance the of early postoperative cognitive complication remains to be elucidated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium, Postoperative Complications, Postoperative Cognitive Dysfunction
Keywords
Sevoflurane, Propofol, Aged, Neoplasm, Surgical Procedure, Operative, Delirium, Postoperative Complications, Postoperative Cognitive Dysfunction

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
1228 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sevoflurane group
Arm Type
Active Comparator
Arm Description
Sevoflurane will be administered by inhalation for anesthesia maintenance. The concentration of inhaled sevoflurane will be adjusted to maintain the bispectral index (BIS) value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, sevoflurane inhalational concentration will be decreased and fentanyl/sufentanil will be administered when necessary. Sevoflurane inhalation will be stopped at the end of surgery.
Arm Title
Propofol group
Arm Type
Experimental
Arm Description
Propofol will be administered by intravenous infusion for anesthesia maintenance. The infusion rate of propofol will be adjusted to maintain the BIS value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, propofol infusion rate will be decreased and fentanyl/sufentanil will be administered when necessary. Propofol infusion will be stopped at the end of surgery.
Intervention Type
Drug
Intervention Name(s)
Sevoflurane
Other Intervention Name(s)
Sevoflurane for inhalation
Intervention Description
Sevoflurane will be administered by inhalation for anesthesia maintenance. The concentration of inhaled sevoflurane will be adjusted to maintain the bispectral index (BIS) value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, sevoflurane inhalational concentration will be decreased and fentanyl/sufentanil will be administered when necessary. Sevoflurane inhalation will be stopped at the end of surgery.
Intervention Type
Drug
Intervention Name(s)
Propofol
Other Intervention Name(s)
Propofol for injection
Intervention Description
Propofol will be administered by intravenous infusion for anesthesia maintenance. The infusion rate of propofol will be adjusted to maintain the BIS value between 40 and 60. Analgesia will be supplemented with remifentanil (administered by continuous infusion), sufentanil (administered by intermittent injection/continuous infusion), or fentanyl (administered by intermittent injection). Towards the end of surgery, propofol infusion rate will be decreased and fentanyl/sufentanil will be administered when necessary. Propofol infusion will be stopped at the end of surgery.
Primary Outcome Measure Information:
Title
Incidence of delirium within 7 days after surgery.
Description
Delirium is assessed twice daily (8-10 AM and 6-8 PM) with the Confusion Assessment Method for patients without endotracheal intubation or the Confusion Assessment Method for the Intensive Care Unit for patients with endotracheal intubation.
Time Frame
Up to 7 days after surgery
Secondary Outcome Measure Information:
Title
Percentage of intensive care unit (ICU) admission after surgery.
Description
Percentage of intensive care unit (ICU) admission after surgery.
Time Frame
Within 24 hours after surgery.
Title
Percentage of ICU admission with endotracheal intubation after surgery.
Description
Percentage of ICU admission with endotracheal intubation after surgery.
Time Frame
Within 24 hours after surgery.
Title
Length of stay in ICU after surgery.
Description
Length of stay in ICU after surgery (in patients admitted to the ICU after surgery).
Time Frame
Up to 30 days after surgery.
Title
Length of stay in hospital after surgery.
Description
Length of stay in hospital after surgery.
Time Frame
Up to 30 days after surgery.
Title
Incidence of non-delirium complications within 30 days.
Description
Non-delirium complications are defined as newly occurred events other than delirium that are harmful to patients' recovery and required therapeutic intervention, i.e., grade 2 or higher on the Clavien-Dindo classification.
Time Frame
Up to 30 days after surgery.
Title
Cognitive function at 30 days after surgery.
Description
Cognitive function assessed with Telephone Interview for Cognitive Status-Modified (TICS-m).
Time Frame
On the 30th day after surgery.
Other Pre-specified Outcome Measures:
Title
Intensity of pain within 3 days after surgery.
Description
Intensity of pain is assessed twice daily (8-10 AM and 6-8 PM) with the Numeric Rating Scale (an 11-point rating scale where 0 = no pain and 10 = the worst pain).
Time Frame
Up to 3 days after surgery.
Title
Subjective sleep quality within 7 days after surgery.
Description
Subjective sleep quality is assessed once daily (8-10 AM) with the Numeric Rating Scale (an 11-point rating scale where 0 = the worst sleep and 10 = the best sleep).
Time Frame
Up to 7 days after surgery.
Title
Cognitive dysfunction assessment
Description
Cognitive function assessed with a battery of neuropsychological tests before surgery and on the 7th day after surgery. Performed in part of enrolled patients and in control subjects.
Time Frame
The day before surgery and on the 7th day after surgery
Title
Serum vitamine D concentration
Description
Blood samples are taken the day before surgery. Serum 25-hydroxyvitamin D concentration is measured with liquid chromatography-mass spectrometry. Performed in part of enrolled patients.
Time Frame
The day before surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Participants will be included if they meet all the following criteria: Age ≥ 65 years and < 90 years; Primary malignant tumor; Do not receive radiation therapy or chemotherapy before surgery; Scheduled to undergo surgery for the treatment of tumors, with an expected duration of 2 hours or more, under general anesthesia; Agree to participate, and give signed written informed consent. Exclusion criteria Patients will be excluded if they meet any of the following criteria: Preoperative history of schizophrenia, epilepsy, parkinsonism or myasthenia gravis; Inability to communicate in the preoperative period (coma, profound dementia, language barrier, or end-stage disease); Critical illness (preoperative American Society of Anesthesiologists physical status classification ≥ IV), severe hepatic dysfunction (Child-Pugh class C), or severe renal dysfunction (undergoing dialysis before surgery); Neurosurgery; Other reasons that are considered unsuitable for participation by the responsible surgeons or investigators (reasons must be recorded in the case report form).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dong-Xin Wang, MD, PhD
Organizational Affiliation
Peking University First Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University First Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
10034
Country
China
Facility Name
Beijing Shijitan Hospital
City
Beijing
State/Province
Beijing
Country
China
Facility Name
Peking University Cancer Hospital
City
Beijing
State/Province
Beijing
Country
China
Facility Name
Peking University School and Hospital of Stomatology
City
Beijing
State/Province
Beijing
Country
China
Facility Name
Cancer Hospital of Guangxi Medical University
City
Nanning
State/Province
Guangxi
Country
China
Facility Name
Shenzhen Second People's Hospital
City
Shenzhen
State/Province
Guangzhou
Country
China
Facility Name
Guizhou Provincial People's Hospital
City
Guiyang
State/Province
Guizhou
Country
China
Facility Name
Hebei Medical University Forth Hospital
City
Shijiazhuang
State/Province
Hebei
Country
China
Facility Name
The First Affiliated Hospital of Zhengzhou University
City
Zhengzhou
State/Province
Henan
Country
China
Facility Name
The Third Xiangya Hospital of Central South University
City
Changsha
State/Province
Hunan
Country
China
Facility Name
Zhongda Hospital
City
Nanjing
State/Province
Jiangsu
Country
China
Facility Name
Ningxia People's Hospital
City
Yinchuan
State/Province
Ningxia
Country
China
Facility Name
Affiliated Hospital of Qinghai University
City
Xining
State/Province
Qinghai
Country
China
Facility Name
Tang-Du Hospital
City
Xi'an
State/Province
Shaanxi
Country
China
Facility Name
Shaanxi Provincial People's Hospital
City
Taiyuan
State/Province
Shanxi
Country
China
Facility Name
Shanxi Province Cancer Hospital
City
Taiyuan
State/Province
Shanxi
Country
China
Facility Name
Tianjin Nankai Hospital
City
Tianjin
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18582931
Citation
Weiser TG, Regenbogen SE, Thompson KD, Haynes AB, Lipsitz SR, Berry WR, Gawande AA. An estimation of the global volume of surgery: a modelling strategy based on available data. Lancet. 2008 Jul 12;372(9633):139-144. doi: 10.1016/S0140-6736(08)60878-8. Epub 2008 Jun 24.
Results Reference
background
PubMed Identifier
14995937
Citation
Nishikawa K, Nakayama M, Omote K, Namiki A. Recovery characteristics and post-operative delirium after long-duration laparoscope-assisted surgery in elderly patients: propofol-based vs. sevoflurane-based anesthesia. Acta Anaesthesiol Scand. 2004 Feb;48(2):162-8. doi: 10.1111/j.0001-5172.2004.00264.x.
Results Reference
background
PubMed Identifier
21518736
Citation
Schoen J, Husemann L, Tiemeyer C, Lueloh A, Sedemund-Adib B, Berger KU, Hueppe M, Heringlake M. Cognitive function after sevoflurane- vs propofol-based anaesthesia for on-pump cardiac surgery: a randomized controlled trial. Br J Anaesth. 2011 Jun;106(6):840-50. doi: 10.1093/bja/aer091. Epub 2011 Apr 25.
Results Reference
background
PubMed Identifier
22108393
Citation
Cai Y, Hu H, Liu P, Feng G, Dong W, Yu B, Zhu Y, Song J, Zhao M. Association between the apolipoprotein E4 and postoperative cognitive dysfunction in elderly patients undergoing intravenous anesthesia and inhalation anesthesia. Anesthesiology. 2012 Jan;116(1):84-93. doi: 10.1097/ALN.0b013e31823da7a2.
Results Reference
background
PubMed Identifier
23725684
Citation
Kalimeris K, Kouni S, Kostopanagiotou G, Nomikos T, Fragopoulou E, Kakisis J, Vasdekis S, Matsota P, Pandazi A. Cognitive function and oxidative stress after carotid endarterectomy: comparison of propofol to sevoflurane anesthesia. J Cardiothorac Vasc Anesth. 2013 Dec;27(6):1246-52. doi: 10.1053/j.jvca.2012.12.009. Epub 2013 May 30.
Results Reference
background
PubMed Identifier
25339455
Citation
Tang N, Ou C, Liu Y, Zuo Y, Bai Y. Effect of inhalational anaesthetic on postoperative cognitive dysfunction following radical rectal resection in elderly patients with mild cognitive impairment. J Int Med Res. 2014 Dec;42(6):1252-61. doi: 10.1177/0300060514549781. Epub 2014 Oct 22.
Results Reference
background
PubMed Identifier
29578249
Citation
Zhang Y, Shan GJ, Zhang YX, Cao SJ, Zhu SN, Li HJ, Ma D, Wang DX; First Study of Perioperative Organ Protection (SPOP1) Investigators. Preoperative vitamin D deficiency increases the risk of postoperative cognitive dysfunction: a predefined exploratory sub-analysis. Acta Anaesthesiol Scand. 2018 Aug;62(7):924-935. doi: 10.1111/aas.13116. Epub 2018 Mar 26.
Results Reference
derived
PubMed Identifier
29187413
Citation
Zhang Y, Li HJ, Wang DX, Jia HQ, Sun XD, Pan LH, Ye QS, Ouyang W, Jia Z, Zhang FX, Guo YQ, Ai YQ, Zhao BJ, Yang XD, Zhang QG, Yin N, Tan HY, Liu ZH, Yu JB, Ma D. Impact of inhalational versus intravenous anaesthesia on early delirium and long-term survival in elderly patients after cancer surgery: study protocol of a multicentre, open-label, and randomised controlled trial. BMJ Open. 2017 Nov 28;7(11):e018607. doi: 10.1136/bmjopen-2017-018607.
Results Reference
derived

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Impact of Anesthesia Maintenance Methods on Incidence of Postoperative Delirium

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