Epidural Anesthesia and Long-term Outcomes in Elderly Patients After Surgery

April 12, 2020 updated by: Dong-Xin Wang, Peking University First Hospital

Impact of Epidural Anesthesia-analgesia on Long-term Outcomes in Elderly Patients After Surgery: 5-year Follow-up of a Multicenter Randomized Controlled Trial

Surgical resection is one of the most important treatments for solid organ cancer. Whereas cancer recurrence and/or metastasis are the major reasons of treatment failure. The outcomes after surgery are mainly dependent on the balance between the immune function of the body and the invasiveness of residual cancer. Preclinical and retrospective studies suggest that anaesthetic techniques and drugs may affect the long-term outcomes in patients undergoing cancer surgery. The investigators hypothesize that epidural anesthesia-analgesia may improve long-term survival in the elderly who undergo major surgery for cancer.

Study Overview

Detailed Description

Surgical resection is the main treatment for potentially curable solid organ cancer. However, long-term survival after cancer surgery is far from satisfactory. Quite a number of patients develop tumor metastasis and/or recurrence after surgery, which are associated with poor long-term outcomes. The development of tumor recurrence and/or metastasis after surgery is mostly dependent on the balance between the anti-tumor immune function of the body and the ability of implantation, proliferation and neovascularization of the residual cancer cells.

Studies showed that anaesthetic techniques and drugs may influence the cellular immune function and long-term outcomes. For example, it was found that ketamine and thiopental, but not propofol, suppresses natural killer (NK) cell activity; all three drugs caused a significant reduction in NK cell number; isoflurane and halothane inhibit interferon stimulation of NK cell cytotoxicity; nitrous oxide interferes with deoxyribonucleic acid, purine, and thymidylate synthesis and depresses neutrophil chemotaxis; opioids have been shown to suppress cell-mediated and humoral immunity.

Considering the potential harmful effects of general anesthesia/anesthetics, there is increasing interest on the effect of regional anaesthesia. Retrospective studies investigating the relationship between epidural anesthesia and outcomes after cancer surgery provide different results. In a meta-analysis of retrospective studies, regional anesthesia was associated with improved survival, but had no effect on the occurrence of cancer recurrence/metastasis. The investigators hypothesize that epidural anesthesia may produce favorable effects on long-term survival in the elderly who undergo major surgery for cancer under general anesthesia. However, there are no sufficient evidences in this aspect.

Study Type

Interventional

Enrollment (Actual)

1802

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Beijing, China, 100044
        • Peking University People's Hospital
      • Beijing, China, 100730
        • Beijing Hospital
      • Beijing, China, 100191
        • Peking University Third Hospital
      • Beijing, China, 100038
        • Beijing Shijitan Hospital
    • Beijing
      • Beijing, Beijing, China, 100034
        • Beijing University First Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

60 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Elderly patients (age 60-90 years);
  • Scheduled to undergo noncardiac thoracic or abdominal surgery with an expected duration of 2 hours or longer. For those who undergo thoracoscopic or laparoscopic surgery, the expected length of incision must be 5 centimeters or more;
  • Agree to receive patient-controlled postoperative analgesia.

Exclusion Criteria:

  • Refused to participate;
  • Previous history of schizophrenia, epilepsy or Parkinson disease, or unable to complete preoperative assessment due to severe dementia, language barrier or end-stage disease;
  • History of myocardial infarction or stroke within 3 months before surgery;
  • Presence of any contraindication to epidural anesthesia and analgesia, including abnormal vertebral anatomy, previous spinal trauma or surgery, severe chronic back pain, coagulation disorder (prothrombin time or activated partial prothrombin time longer than 1.5 times of the upper normal limit, or platelet count of less than 80 * 10^9/L), local infection near the site of puncture, and severe sepsis;
  • Severe heart dysfunction (New York Heart Association functional classification 3 or above), severe hepatic insufficiency (Child-Pugh grade C), or severe renal insufficiency (serum creatinine of 442 umol/L or above, with or without serum potassium of 6.5 mmol/L or above, or requirement of renal replacement therapy);
  • Any other conditions that were considered unsuitable for study participation.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Combined epidural-general anesthesia
Patients assigned to this group receive combined epidural-general anesthesia and postoperative patient-controlled epidural analgesia.
Combined epidural-general anesthesia and postoperative epidural analgesia.
Active Comparator: General anesthesia
Patients assigned to this group receive general anesthesia and postoperative patient-controlled intravenous analgesia.
General anesthesia and postoperative intravenous analgesia.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall survival after surgery.
Time Frame: Up to median 5 years after surgery.
Time from surgery to the date of all-cause death.
Up to median 5 years after surgery.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cancer-specific survival after surgery.
Time Frame: Up to median 5 years after surgery.
Time from surgery to the date of cancer-specific death. Patients who die from other causes being censored at the time of death.
Up to median 5 years after surgery.
Recurrence-free survival after surgery.
Time Frame: Up to median 5 years after surgery.
Time from surgery to the date of cancer recurrence/metastasis or all-cause death, whichever comes first.
Up to median 5 years after surgery.
Event-free survival after surgery.
Time Frame: Up to median 5 years after surgery.
Time from surgery to the first date of cancer recurrence/metastasis, new onset cancer, new serious non-cancer disease, or death from any cause.
Up to median 5 years after surgery.

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Overall survival after surgery (cancer patients).
Time Frame: Up to median 5 years after surgery.
Time from surgery to the date of all-cause death.
Up to median 5 years after surgery.
Cancer-specific survival after surgery (cancer patients).
Time Frame: Up to median 5 years after surgery.
Time from surgery to the date of cancer-specific death. Patients who die from other causes being censored at the time of death.
Up to median 5 years after surgery.
Recurrence-free survival after surgery (cancer patients).
Time Frame: Up to median 5 years after surgery.
Time from surgery to the date of cancer recurrence/metastasis or all-cause death, whichever comes first.
Up to median 5 years after surgery.
Event-free survival after surgery (cancer patients).
Time Frame: Up to median 5 years after surgery.
Time from surgery to the first date of cancer recurrence/metastasis, new onset cancer, new serious non-cancer disease, or death from any cause.
Up to median 5 years after surgery.
Cognitive function (3-year survivors).
Time Frame: At the end of the 3rd year after surgery.
Cognitive function is assessed with the modified Telephone Interview for Cognitive Status (TICS-m; a 12-item questionnaire that assesses global cognitive function by verbal communication via telephone. The score ranges from 0 to 50, with higher score indicating better function).
At the end of the 3rd year after surgery.
Quality of life (3-year survivors).
Time Frame: At the end of the 3rd year after surgery.
Quality of life is assessed with the World Health Organization Quality of Life brief version (WHOQOL-BREF; a 24-item questionnaire that assesses the quality of life in physical, psychological, social relationship and environmental domains. The score ranges from 0 to 100 for each domain, with higher score indicating better function).
At the end of the 3rd year after surgery.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2017

Primary Completion (Actual)

September 30, 2019

Study Completion (Actual)

September 30, 2019

Study Registration Dates

First Submitted

November 6, 2017

First Submitted That Met QC Criteria

November 6, 2017

First Posted (Actual)

November 8, 2017

Study Record Updates

Last Update Posted (Actual)

April 14, 2020

Last Update Submitted That Met QC Criteria

April 12, 2020

Last Verified

April 1, 2020

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

Data will ba available on request.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Long-term Outcome

Clinical Trials on Combined epidural-general anesthesia

Subscribe