Current Environment:

Summary

Laparoscopic cholecystectomy is associated with considerable postoperative pain and surgeon-administered local anesthetic infiltration is the standard practice for achieving post-operative analgesia. However, recent studies have shown that pediatric patients continue to experience significant pain during the first 24 hours. The investigators plan to conduct a prospective, double-blinded, randomized study where patients will be designated into either a test group receiving an ultrasound-guided transversus abdominis plane (TAP) and rectus sheath (RS) blocks with ropivacaine and peri-portal sterile saline or the control group that will receive ultrasound-guided TAP block with sterile saline and peri-portal infiltration of ropivacaine. The anesthesia team and surgical team will both be blinded as well as the research personal in the postoperative period. Patients age 5-17 and American Society of Anesthesiology status I and II undergoing laparoscopic cholecystectomy will be included. The study hypothesis is that ultrasound-guided peripheral nerve blocks, specifically single shot transversus abdominis plane and rectus sheath blocks, are superior to local wound infiltration during laparoscopic cholecystectomy for decreasing postoperative pain and pain related behavior and facilitating functional recovery.

Conditions

Pain, Postoperative

Recruitment Status

Not yet recruiting

Detailed Description

Patients will be randomized into either a test group receiving an ultrasound-guided TAP block with ropivacaine and peri-portal sterile saline or the control group that will receive ultrasound-guided TAP block with sterile saline and peri-portal infiltration of ropivicaine. All patients, who are scheduled to undergo laparoscopic cholecystectomy who meet the inclusion/exclusion criteria, and their parent(s)/guardian(s) will be called by the study staff the afternoon before surgery, who will follow a study script introducing the project and providing them with an opportunity to enroll in this study or opt out. If the patient cannot be reached the day before surgery, they will be offered the opportunity to enroll the day of surgery in the pre-operative holding area. If the decision is made to participate in the study, a physician study investigator will obtain appropriate consent and assent when applicable. Recruitment materials will be provided, if desired. A copy of this consent form will be placed in the Boston Children's Hospital medical record and a separate research record. Stratified randomization of patients will be conducted by the pharmacy to maintain the double-blinded nature of the study. The pharmacy staff will deliver a study syringe labeled "regional" and a study syringe labeled "local". Depending on randomization, the "regional" syringe will be filled with either ropivacaine 0.2% or normal saline to the corresponding volume based on the dosing outlined. Similarly, the local syringe will be filled with the opposite solution. Thus, if the "regional" syringe is filled with ropivacaine, the local syringe will be filled with normal saline, and vice versa. Both surgical and anesthesia teams will be blind to the intervention received by the patient. The patients will be divided into two groups: 1. Abdominal Wall Block with Ropivacaine and 2. Surgical infiltration with Ropivacaine. The abdominal wall block group will receive: bilateral transversus abdominis plane and rectus sheath blocks via ultrasound guidance. A total of 1.0ml/kg distributed between the four blocks (0.4+0.4+0.1+0.1) of 0.2% Ropivacaine (max 50ml) will be injected, as a one time single shot injection, into the fours sites. Surgical infiltration of the four port sites will receive 0.4ml/kg of sterile saline. The surgical infiltration group will receive: surgical infiltration of local anesthetic into the 4 laparoscopic port sites. A total of 0.4 ml/kg (0.1+0.1+0.1+0.1) of 0.5% Ropivacaine, divided between the four port sites (max 20 ml), will be used. A total of 1ml/kg, divided between the TAP (0.4ml/kg on each side) and RS (0.1ml/kg on each side), of sterile saline will be used for the nerve blocks. Intra-operative Methods: After induction of anesthesia, but before the first incision, each patient will receive an ultrasound-guided block by the regional anesthesiologist as follows: A. Block Placement: a. Time out performed for procedure b. Site prepared using aseptic technique c. Localization of the bilateral posterior TAP plane and bilateral rectus sheaths using a portable ultrasound machine i. Aseptic preparation of probe with sterile sheath ii. 38mm linear probe (BK Medical, USA) iii. 15 MegaHertz frequency d. Needle: 22g 80mm echogenic e. Drug administration per protocol and group allocation B. Periportal Infiltration: a. Injection of drug and volume per protocol into the planned insertion sites for the 4 ports. All patients will receive acetaminophen IV 15 mg/kg, dexamethasone 0.1 mg/kg, and morphine 0.05 mg/kg after induction of anesthesia but prior to the first incision. At the conclusion of surgery, prior to emergence, each patient will receive ketorolac IV 0.5 mg/kg (max 30 mg). All intraoperative details of care including vitals signs, medication administration, complications, and timing of events are recorded in the electronic anesthesia record. PACU Methods: Pain will be assessed post-operatively in the PACU (Post-Anesthesia Care Unit) using the FLACC, FACES Pain Rating Scale or Numeric Rating Scale (NRS) as per PACU protocol and as appropriate to patient age. Once the patient is awake and able to respond to questions, a pain score will be obtained and documented by a study investigator until discharge from the recovery room. Morphine 0.05 mg/kg IV will be administered for NRS, FLACC, or FACES score greater than 4. This can be repeated every 10 minutes to a total of 4 doses. Doses, times, and types of all medications administered in the PACU, in addition to the duration of time a patient spends in the PACU, are documented in the electronic medical record (per standard PACU protocol). Post-anesthetic complications are documented by the PACU nurse in the electronic medical record. Trained research personnel will evaluate for the presence or absence of periumbilical analgesia prior to discharge from PACU. The patient will be discharged from the PACU to an in-patient bed when standard PACU discharge criteria are met. Inpatient Methods: All patients will receive standard postoperative orders to include acetaminophen 15 mg/kg IV q 6 hours, ketorolac 0.5 mg/kg IV q6 hours, morphine 0.05 mg/kg IV q 2 hours as needed, and oxycodone 0.15 mg/kg PO Q 4 hours as needed. Pain will be assessed by the unit nurses using the appropriate scale for age. Morphine 0.5 mg/kg IV or oxycodone 0.15mg/kg will be administered for NRS, FLACC, or FACES score greater than 4. Pain Scores will be recorded at 3,6,12 and 24 hours postoperatively with the patient at rest and during coughing. On the morning of POD #1, trained research personnel will administer the appropriate survey of functional recovery. Validated questionnaires to assess postoperative recovery are available for use in pediatric patients < 12 yrs age (Parents Postoperative Pain Management (PPPM)) and adult patients (Post Discharge Surgical Recovery (PDSR) scale (10-13)). No validated survey exists for patients between the ages of 12 -17 and it was decided to extend the PPPM for use on patients up to and including patients 15 years of age and to use the PDSR on any patient older than 15. In addition, parents and patients will fill out a bedside diary in the form of a bingo card (addendum 2). Total intravenous and oral opioid (oral oxycodone or other oral opioid given will be converted to IV morphine equivalents). Doses, times, and types of all medications administered while in the OR, PACU and inpatient units will be abstracted from the patient's electronic medical record soon after the patient is discharged from the hospital to ensure that study protocols were followed. Fentanyl administration will be analyzed separate from other opioids due to its comparatively divergent half-life and potency. Other data related to hospital stay such as length of procedure (surgery start time to surgery stop time), length of time in the OR, length of time in the recovery room, and length of hospital stay, will be also be collected. Any complication or opioid-related side effect will also be collected. Data will be kept in an excel spreadsheet. The spreadsheet will have anonymous patient identifiers and will be kept in a folder on a password protected hard-drive. Only persons involved in the research study will have access to the folder.

Eligibility Criteria

Inclusion Criteria:

Patient age 5-17 years old at time of surgery
ASA status 1-2
Parent is able to provide informed consent and patient's > age 7 able to give assent
Patients scheduled for laparoscopic cholecystectomy
Surgery will involve and be limited to laparoscopic cholecystectomy
Admission status: 24-hour admission to hospital

Exclusion Criteria:

Non-English speaking parents/patient.
All emergency laparoscopic cholecystectomies or conversion to an open procedure
Patients who will remain intubated or require ICU care postoperatively
Significant liver or renal disease
Coagulopathy
Underlying neurocognitive disorder or developmental delay affecting ability to convey feelings of pain to medical staff
Diagnosis of chronic pain syndrome
Active infection over nerve block sites
History of allergy to local anesthetic agents or non-steroidal anti-inflammatory drugs (NSAIDS)
Known alcohol or substance abuse within the past 6 months
Daily Opioid use
ASA class 3 or higher

Intervention

Intervention Type

Intervention Name

Procedure

Abdominal Wall Block

Procedure

Surgical infiltration

Drug

Sterile saline

Drug

Ropivacaine 0.2%

Device

Ultrasound

Drug

Ropivacaine 0.5%

Phase

Phase 3

Gender

All

Minimum Age

5 Years

Maximum Age

17 Years

Download Date

July 27, 2021

Principal Investigator

Karen Boretsky

Primary Contact Information

Karen Boretsky, MD

617-355-7737

karen.boretsky@childrens.harvard.edu

Tricia Vecchione, MD

617-355-7040

tricia.vecchione@childrens.harvard.edu

For more information on this trial, visit clinicaltrials.gov.

Contact

For more information and to contact the study team: