A Pilot Study of Local Anesthesia for Inguinal Hernia Surgery in Older Adults
Study Details
Study Description
Brief Summary
Inguinal hernia repair-the most common general surgery operation in the U.S.-provides a unique opportunity to improve outcomes for older patients by changing surgical practice. Nearly 80% of inguinal hernia operations are performed under general anesthesia versus 15-20% using local anesthesia, despite the absence of evidence for superiority. The choice of anesthesia has particular implications for older adults because they face substantial short- and long-term risk of cognitive and physical decline after exposure to general anesthesia. Consequently, the American College of Surgeons and the American Geriatrics Society have identified a critical need in surgery: determining which operations have better outcomes when performed under local rather than general anesthesia.
Currently, the evidence for choosing an anesthesia technique for inguinal hernia repair in older adults is inconclusive. Several small randomized trials and cohort studies have suggested that using local anesthesia for hernia repair reduces morbidity by one-third, unplanned readmissions by 20%, and operative time and costs by 15% while other studies showed no significant differences. However, there are significant flaws in these studies that severely limit their applicability to older adults: (1) They mainly focused on younger patients with limited comorbidity burden, largely ignoring individuals aged 65 years and older, (2) They did not adequately examine the effects of general anesthesia on cognitive function and quality of life for older adults and their caregivers, (3) They did not consult with stakeholders to identify outcomes relevant to those groups. The current study aims to address these limitations to determine the ideal anesthesia modality for inguinal hernia repair.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
The study rationale is that prior to conducting a multisite randomized trial, it is necessary to identify relevant outcomes, understand barriers to greater use of local anesthesia, test study procedures, and confirm our ability to adequately recruit and randomly assign participants. Additionally, the proposed study will provide the applicant with critical training in the design, conduct, and analysis of clinical trials. This will uniquely position the applicant to change surgical care for older adults.
There have been two prior randomized clinical trials that compared local versus general anesthesia for inguinal hernia repair. One study randomized 616 patients in Sweden to local, regional, or general anesthesia. They did not specifically look at older patients but the mean age in each group was 56 years old. They found that the total operative time was five minutes faster for the local anesthesia group (90 versus 95 minutes) the incidence of postoperative pain requiring opioids and catheterization for urinary retention was decreased by 29% for the local compared to general anesthesia group and the rate of unplanned admission was decreased by 19%. A cost-effectiveness analysis conducted by the same group indicated that hospital costs were lower in the local anesthesia group (a difference of €311/$378) and total healthcare costs were also lower (€316/$384). A second trial from Scotland randomized 279 patients to local or general anesthesia, with a mean age of 55 years for both groups. This study did not find a significant difference in operative time, complications, length of stay, pain, or neurocognitive recovery as measured by a battery of tests. However, they did not specifically analyze outcomes in older patients which would tend to dilute the potential benefits of local anesthesia. Equally important, this study focused almost exclusively on healthy patients with smaller hernias, as evidenced by >90% of patients having an American Society of Anesthesiology score of 1 or 2 and a mean total surgical time of 48 minutes for each group.
There are several observational studies that compare outcomes from hernia repair under local or general anesthesia, and these mostly suggest that local anesthesia is associated with shorter operative time (5-10 minutes), fewer complications (1-3% reduction), and enhanced quality of life. However, only two of these studies look specifically at outcomes for older adults and both suffer from a poor approach to risk adjustment. Additionally, all the observational studies have a limited assessment of complications and failed to effectively evaluate rates of urinary retention and catheterization after surgery. Urinary retention is the most common complication of general anesthesia after hernia repair and results in considerable discomfort for patients who are catheterized to relieve it. Additionally, when patients do not resolve retention in a timely fashion, it results in the need for unplanned admission which increases hospital costs.
The intervention chosen for testing in this study is the choice of anesthesia (local or general) for unilateral inguinal hernia repair. These are the primary methods of anesthesia for inguinal hernia surgery by most surgeons (though some perform the operation under spinal or regional anesthesia, this is rare). Both approaches are used in clinical practice with acceptable known risks and complications. General anesthesia is associated with risks of hypotension, venous thromboembolism, heart attack, stroke, pulmonary dysfunction, cognitive dysfunction, allergic reaction, and malignant hyperthermia. The main risks of local anesthesia include allergic reaction and hypotension (when the anesthetic is improperly injected into a blood vessel).
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Local anesthesia This arm will receive local anesthesia for their inguinal hernia repair. |
Other: Local anesthesia
This is the treatment group. Patients will receive an injection of a 50:50 mix of 1% lidocaine with epinephrine and 0.25% Marcaine at the surgical site (in the skin and subcutaneous layers + beneath the external oblique aponeurosis). Patients in the local arm will also receive intravenous sedation (propofol or Precedex) and pain medication (morphine or fentanyl) at the discretion of the attending anesthesiologist.
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| Active Comparator: General anesthesia This arm will receive general anesthesia for their inguinal hernia repair. |
Other: General anesthesia
This group is the active comparator. General anesthesia will be administered at the discretion of the anesthesiologist and will involve a combination of inhaled and intravenous anesthesia.
|
Outcome Measures
Primary Outcome Measures
- Rates of enrollment and percentage of eligible patients enrolled [Through study completion, estimated 2 years]
Each week, research assistants will compile running counts of patients screened, found eligible, and enrolled.
- Proportion of participants completing all study visits [Through study completion, estimated 2 years]
Assistants will maintain counts of participants who complete each study visit.
- Proportion of missing data [Through study completion, estimated 2 years]
At each visit, every study visit will be entered into our electronic database and missing items will have a separate code number.
- Time to complete study evaluations and instruments [Time from beginning to end of completing study instrument, up to 2 hours]
Assistants will time participants while completing each study research form and will time the entire encounter.
- Partipant satisfaction [At 6 month follow up]
A 10 point likert scale will measure participant satisfaction. Scores range from 1-10 with higher scores indicating higher satisfaction.
Secondary Outcome Measures
- Carolinas Comfort Scale [Measured at baseline]
The Carolinas Comfort Scale measures quality of life. Possible scores range from 1-6 for each item, with higher scores indicating increased quality of life.
- Carolinas Comfort Scale [Measured at 48 hours after surgery]
The Carolinas Comfort Scale measures quality of life. Possible scores range from 1-6 for each item, with higher scores indicating increased quality of life.
- Carolinas Comfort Scale [Measured at 2 weeks after surgery]
The Carolinas Comfort Scale measures quality of life. Possible scores range from 1-6 for each item, with higher scores indicating increased quality of life.
- Carolinas Comfort Scale [Measured at 6 months after surgery]
The Carolinas Comfort Scale measures quality of life. Possible scores range from 1-6 for each item, with higher scores indicating increased quality of life.
- Physical function [Measured at baseline]
We will measure the patients' ability to perform their activities of daily living with the 6 item katz index. This scale is from 0-6, with higher scores indicating more functional independnce.
- Physical function [Measured at 48 hours after surgery]
We will measure the patients' ability to perform their activities of daily living with the 6 item katz index. This scale is from 0-6, with higher scores indicating more functional independnce.
- Physical function [Measured at 2 weeks after surgery]
We will measure the patients' ability to perform their activities of daily living with the 6 item katz index. This scale is from 0-6, with higher scores indicating more functional independnce.
- Physical function [Measured at 6 months after surgery]
We will measure the patients' ability to perform their activities of daily living with the 6 item katz index. This scale is from 0-6, with higher scores indicating more functional independnce.
- Trail Making Test [Measured at baseline]
Trail Making Test will be used to measure cognitive function. The time to complete the trailmaking test is measured, with those taking greater than expected time being considered deficient.
- Montreal Cognitive Assessment [Measured at baseline]
Montreal Cognitive Assessment 5 minute form to measure cognitive function. For the Montreal Cognitive Assessment, the successfully completed skills are added to achieve a final score from 0-30, with higher numbers indicating closer to normal cognitive function.
- Trail Making Test [Measured at 48 hours after surgery]
The Trail Making Test will be used to measure cognitive function. The time to complete the trailmaking test is measured, with those taking greater than expected time being considered deficient.
- Montreal Cognitive Assessment [Measured at 48 hours after surgery]
Montreal Cognitive Assessment 5 minute form to measure cognitive function. For the Montreal Cognitive Assessment, the successfully completed skills are added to achieve a final score from 0-30, with higher numbers indicating closer to normal cognitive function.
- Trail Making Test [Measured at 2 weeks after surgery]
The Trail Making Test will be used to measure cognitive function. The time to complete the trailmaking test is measured, with those taking greater than expected time being considered deficient.
- Montreal Cognitive Assessment [Measured at 2 weeks after surgery]
Montreal Cognitive Assessment 5 minute form used to measure cognitive function. For the Montreal Cognitive Assessment, the successfully completed skills are added to achieve a final score from 0-30, with higher numbers indicating closer to normal cognitive function.
- Trail Making Test [Measured at 6 months after surgery]
Trail Making Test used to measure cognitive function. The time to complete the trailmaking test is measured, with those taking greater than expected time being considered deficient.
- Montreal Cognitive Assessment [Measured at 6 months after surgery]
Montreal Cognitive Assessment 5 minute form to measure cognitive function. For the Montreal Cognitive Assessment, the successfully completed skills are added to achieve a final score from 0-30, with higher numbers indicating closer to normal cognitive function.
- Delirium [Measured at baseline]
The Confusion Assessment Method short form consists of 5 questions, if inattention + acute onset and/or fluctuating course + Disorganized thinking and/or Altered level of consciousness are present this test is considered positive for delirium.
- Delirium [Measured at 48 hours after surgery]
The Confusion Assessment Method short form consists of 5 questions, if inattention + acute onset and/or fluctuating course + Disorganized thinking and/or Altered level of consciousness are present this test is considered positive for delirium.
- Delirium [Measured at 2 weeks after surgery]
The Confusion Assessment Method short form consists of 5 questions, if inattention + acute onset and/or fluctuating course + Disorganized thinking and/or Altered level of consciousness are present this test is considered positive for delirium.
- Delirium [Measured at 6 months after surgery]
The Confusion Assessment Method short form consists of 5 questions, if inattention + acute onset and/or fluctuating course + Disorganized thinking and/or Altered level of consciousness are present this test is considered positive for delirium.
- Pain level [Measured at baseline]
10 point visual analog scale. Patients indicate on a scale of 0-10 their current level of pain. Higher numbers indicate higher pain.
- Pain level [Measured at 48 hours after surgery]
10 point visual analog scale. Patients indicate on a scale of 0-10 their current level of pain. Higher numbers indicate higher pain.
- Pain level [Measured at 2 weeks after surgery]
10 point visual analog scale. Patients indicate on a scale of 0-10 their current level of pain. Higher numbers indicate higher pain.
- Pain level [Measured at 6 months after surgery]
10 point visual analog scale. Patients indicate on a scale of 0-10 their current level of pain. Higher numbers indicate higher pain.
- Postoperative complications [Up to 2 weeks]
All complications will be recorded based on VA Surgical Quality Improvement Program definitions.
- Operative time [Time between surgery start and surgery end measured. 1 day of surgery]
The amount of time the surgery takes (minutes)
- Anesthesia time [Time spent in operating room. 1 day of surgery]
The amount of time in the operating room (minutes)
- Recovery time [Time spent in post anesthesia care unit. 1 day of surgery]
Time spent in the post anesthesia care unit and stepdown units.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age >=65 years
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Presenting to clinic with a unilateral inguinal hernia that is not incarcerated
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Considered suitable for either general or local anesthesia
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Willing to complete all study requirements, including follow-up continuing until six months after surgery
Exclusion Criteria:
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The hernia that the patient is being evaluated for has undergone prior repair
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Any contraindications to general anesthesia
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Allergies to local anesthesia
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Evidence of hernia incarceration or strangulation
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Active local or systemic infection that would preclude the use of mesh for hernia repair
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Need for concurrent surgical repair at the time of hernia repair
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English is not the patient's primary language
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Enrollment in other research studies
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- University of Texas Southwestern Medical Center
Investigators
- Principal Investigator: Courtney Balentine, MD, MPH, University of Texas
Study Documents (Full-Text)
More Information
Publications
None provided.- STU-2020-0558