Laparascopic TAP and Hysterectomy Trial #2

The primary goal of our study is to demonstrate that laparoscopically assisted bilateral Transversus Abdominis Plane (TAP) block using liposomal bupivacaine is superior to pre-incisional injection of bupivacaine in terms of peri-operative opiate use, pain scores and overall patient satisfaction up to one week following surgery. Our recent research has already demonstrated the safety of performing Laparoscopic assisted TAP blocks using liposomal bupivacaine.

This trial will evaluate the efficacy of laparoscopic TAP blocks with liposomal bupivacaine by using VAS/numeric pain scores at rest and with cough in recovery at 1 and 2 hours post-op. The trial will also utilize an OBAS patient survey, document peri-operative opioid pain medication used intraoperatively, in PACU and overnight (if admitted), and assess length of time in PACU and same-day discharge versus admission. Opioid pain medication use at home up to one week will also be recorded.

HYPOTHESES/SPECIFIC AIMS The goal of this research project is to prove that a laparoscopically delivered TAP block using a combination of Liposomal bupivacaine (Exparel) and Bupivacaine is an effective and feasible means for decreasing post-operative pain from the immediate post-operative period up to one week.

The research aims to demonstrate that TAP blocks, when delivered laparoscopically and by using Liposomal bupivacaine will show a 20% benefit in post-operative QoR-15 scores on post-operative days 1,2 and 7. Other objectives of our study will be to evaluate peri-operative narcotic medication dosing, VAS/Numeric pain scores with cough at 1 and 2 hours in PACU, overnight narcotic use for patients who are admitted and narcotic pain pill use at home up to 7 days. Finally, the study aims to confirm that this technique is simple to perform, easy to implement and would offer a multi-modal anesthetic alternative to the excessive use of post-operative opioid pain medications.

Patients scheduled for laparoscopic or robotic hysterectomy are screened in the pre-anesthesia care unit and if eligible are invited to enroll in the trial. Primary Attendings for each surgery will advise patients of the option for the trial at pre-operative appointments. Patients who agree to enrollment are appropriately consented and then randomized to either control (pre-incisional anesthetic) or study (TAP) group. The patient remains blinded to the arm of the study, but OR personnel are advised so as to prepare medications and syringes.

Following induction of anesthesia, the patients in the TAP block arm are prepared and draped for surgery allowing for mid-axillary access along the flank bilaterally. Once pneumoperitoneum and a port for the laparoscope were established, TAP block is performed bilaterally by first palpating the external landmark within the Triangle of Petit, 2 cm above the iliac crest. A 21-gauge Stimuplex ® A insulated needle (Braun, Melsungen, Germany) is used to enter the transversus abdominis neurovascular plane. Bilaterally, TAP block patients receive 10cc of liposomal bupivacaine combined with 10cc of 0.25% bupivacaine and 10cc normal saline. Patients in the pre-incisional injection arm of the study receive a total of 20cc of 0.25% bupivacaine total, equally distributed between the incisions. All patients receive routine general anesthesia with opiate use adjusted as determined by the anesthesia provider. The anesthesia team is neither blinded nor given specialized protocol instructions. At the end of each case, narcotic dosage used is documented.

All of the patients will receive phone calls on post-operative days 1,2 and 7. They will be asked their opiate pain medication usage, number of pills used and "Overall Benefit of Anesthesia" (OBAS) scores will be obtained. The OBAS is a simple quality assessment instrument shown to reliably measure benefit from post-operative pain therapy16 (Table 1).

Table 1. Overall Benefit of Analgesia Score

1. Please rate your current pain at rest on a scale between 0=minimal pain and 10=maximum imaginable pain
2. Please grade any distress and bother from vomiting in the past 24 h (0=not at all to 10=very much)
3. Please grade any distress and bother from itching in the past 24 h (0=not at all to 10=very much)
4. Please grade any distress and bother from sweating in the past 24 h (0=not at all to 10=very much)
5. Please grade any distress and bother from freezing in the past 24 h (0=not at all to 10=very much)
6. Please grade any distress and bother from dizziness in the past 24 h (0=not at all to 10=very much)
7. How satisfied are you with your pain treatment during the past 24 h (0=not at all to 10= very much) OBJECTIVES The primary goal of our study is to demonstrate that laparoscopically assisted bilateral Transversus Abdominis Plane (TAP) block using liposomal bupivacaine is superior to pre-incisional injection of bupivacaine in terms of peri-operative opiate use, pain scores and overall patient satisfaction up to one week following surgery. Our recent research has already demonstrated the safety of performing Laparoscopic assisted TAP blocks using liposomal bupivacaine. This trial will evaluate the efficacy of laparoscopic TAP blocks with liposomal bupivacaine by using VAS/numeric pain scores at rest and with cough in recovery at 1 and 2 hours post-op. The trial will also utilize an OBAS patient survey, document peri-operative opioid pain medication used intraoperatively, in PACU and overnight (if admitted), and assess length of time in PACU and same-day discharge versus admission. Opioid pain medication use at home up to one week will also be recorded. HYPOTHESES/SPECIFIC AIMS The goal of this research project is to prove that a laparoscopically delivered TAP block using a combination of Liposomal bupivacaine (Exparel) and Bupivacaine is an effective and feasible means for decreasing post-operative pain from the immediate post-operative period up to one week. The research aims to demonstrate that TAP blocks, when delivered laparoscopically and by using Liposomal bupivacaine will show a 20% benefit in post-operative QoR-15 scores on post-operative days 1,2 and 7. Other objectives of our study will be to evaluate peri-operative narcotic medication dosing, VAS/Numeric pain scores with cough at 1 and 2 hours in PACU, overnight narcotic use for patients who are admitted and narcotic pain pill use at home up to 7 days. Finally, the study aims to confirm that this technique is simple to perform, easy to implement and would offer a multi-modal anesthetic alternative to the excessive use of post-operative opioid pain medications. PRELIMINARY WORK IRB protocol #14-132 was discontinued 12/14/15 due to a protocol violation. Because the study could not be completed with its original objectives, we are seeking to repeat the study with a very similar protocol. While talking with patients during the audit of their post-operative phone calls, it became clear that the experimental arm of the study might, in fact, have had a beneficial impact on post-operative recovery. As we do not have that portion of the data, we are seeking to repeat the study with a few minor modifications. METHODS
8. Study Design Proposed study design is for a Prospective Single blinded Randomized Clinical Trial. The study aims to evaluate two arms and compare them: All patients would undergo laparoscopic total hysterectomy or Robotic assisted laparoscopic total hysterectomy with or without removal of adnexa. Patients would not be excluded for having other simultaneous procedures such as appendectomy, excision of endometriosis or pelvic lymph node dissection. Patients in one arm of the study would receive a bilateral Laparoscopic Assisted TAP block with 10cc Liposomal bupivacaine, 10cc 0.25% bupivacaine and 10cc normal saline each bilaterally at the beginning of their surgery. The patients in the control arm of the study would receive pre-incisional injections at the trocar incision sites using a total of 20cc 0.25% bupivacaine.
9. Study Subjects <!-- -->
10. Women undergoing laparoscopic hysterectomy or robotic assisted laparoscopic hysterectomy with or without removal of adnexa would be eligible. Patients will be randomized.
11. Inclusion Criteria: Women undergoing TLH at Erlanger Hospital. They must be 18 years or older due to restrictions on Exparel. Women undergoing simultaneous lymph node dissection, appendectomy, adhesiolysis or other incidental procedures would not be excluded.
12. Exclusion Criteria: Patient refusal. Soft tissue infection of the abdominal wall and skin. Abnormality at the needle insertion site. Chronic opiate use within 3 months prior to surgery. Age less than 18 years. Anticipated need for extension of incision greater than 2cm. Hepatic or renal impairment, current pregnancy or BMI >50.
13. Sample Size: 100 patients, 50 in each arm of the study. The sample size calculation is based on an assumption that a 24% difference in VAS pain scores would be clinically meaningful. A sample size of 41 patients in each cohort would be able to detect a 20% difference in post-operative QoR-15 quality of life post-surgery scores with a power of 80%. This calculation was done with the assistance of Jenny Holcomb, PhD (See accompanying paperwork).
14. Data Collection: Each patient will have paperwork designating name, demographics, telephone numbers as well as pertinent PHI. Documentation of VAS scores, time-frame to first request for opiate pain medications, post-operative pill counts and follow-up phone questionnaire (OBAS) will be collected on accompanying forms.
15. Data Handling: A file, with the paper work on each patient, will be handled by the Principal Investigator, Shanti Mohling, MD and primary Co-investigator, Rayan Elkattah, MD. Two personnel will be recruited to handle post-operative phone calls. They will be carefully screened for reliability and phone-calls assessments will be periodically audited to avoid the concerns occurring with #14-132. The charts will be stored in the primary investigator's private office or in the research specialist's office (Patricia Bush) during analysis.
16. Data Analysis: Following collection of data and collation of all data, the results will be statistically analyzed with the help of statistician Jenny Holcomb, PhD.
17. Time Frame:
18. 12 months for data collection. 2. 18 months time for completion of study including analysis. h. Strengths/Innovation: Adding a simple technique for post-operative pain control to the armamentarium of multi-modal anesthesia techniques will greatly enhance the options for caring for patients around the time of laparoscopic surgery. Currently, I believe the laparoscopic TAP block is a valuable, yet underutilized tool in the field of Minimally Invasive Surgery.
19. Limitations:
20. Liposomal bupivacaine is a milky white color and it would have been very difficult to blind the surgeons infiltrating it as opposed to a placebo.
21. There is a learning curve with developing an ability to do the TAP block laparoscopically, however this technique has now been well practiced by our team.
22. BMI, additional procedures, history of other pain issues, such as fibromyalgia, may all be confounders to this study. All of these will be documented and hopefully averaged in the randomization.

VII. RISKS/BENEFITS

1. Risks and side effects related to the TAP Block with liposomal bupivacaine include bruising at the site of the injections, soreness, and a rare potential for intravascular injection causing cardiac arrhythmia. These risks are similar to the risk of routine bupivacaine in the trocar sites routinely used anyway. Of note, there were no complications of laparoscopic TAP blocks during the course of our recent trial #14-132.
2. There are no known direct benefits to study subjects.
3. If the study demonstrates a benefit of the TAP block in controlling post-operative pain better than simply using pre-incisional injections and decreases patient need for opiate analgesia this will undoubtedly benefit patients in future.
4. There are no potential ethical concerns with this study, especially given that it will be randomized.

BUDGET Primary costs incurred will be files and paper products for VAS scores, charting on recovery and post-op questionnaires. The cost of the procedural medications will be rolled into the global surgical charge as pre-incisional anesthetics are already routinely billed for.

RESEARCH ENVIRONMENT All procedures will all take place at the time of surgery in the operating room. Patients will receive information on the study in pre-op consultation or at the time of arrival to the Pre-op arena.