Ultrasound Guided Erector Spinae Block Versus Quadratus Lumborum Block For Postoperative Pain ReliefFollowing Laparoscopic Nephrectomy

Menoufia University

Status: Completed

Conditions: Pain, Postoperative

Treatments: Device: US guided block

Study type: Interventional

Funder types: Other

Identifiers

NCT06655298

6/2023ANET44

Details and patient eligibility

About

The aim of this study is to assess the efficacy of Ultrasound guided erector spinae plane block versus quadratus lumborum block for postoperative analgesia in patient undergoing laparoscopic nephrectomy.

Full description

The study will be a prospective randomized single-blind study. Patients will be randomized into two groups using a closed envelope technique in sequentially numbered opaque envelopes that will be opened before carrying out the block

The study will be conducted on 56 patients, 28 patients in each group:

Group Q; (28 patients) Quadratus lumborum block group; patients will receive general anesthesia initially then bilateral QLB type III (anterior subcoastal approach) with a volume of 30 mL of bupivacaine 0.25% for each side taking care that the patient does not receive a local anesthetic dose higher than the maximum allowed (2.5 mg/kg) .

✓ Group E; (28 patients) Erector spinae plane block; patients will receive general anesthesia initially then bilateral ESPB with a volume of 30 mL of bupivacaine 0.25 % for each side taking care that the patient does not receive a local anesthetic dose higher than the maximum allowed (2.5 mg/kg)

Data Collection:

Baseline:

1. Patient demographic data
2. Hemodynamics (pulse- heart rate- mean blood pressure), baseline before induction of anesthesia.

Intraoperative:

1. Hemodynamics (pulse- heart rate- mean blood pressure):

   They will be monitored and recorded 5 minutes after induction of anesthesia then every 30 min till end of the surgery.

2. Total analgesic consumption needed to reach target Entropy measurement 40-60%.

3. The anesthetic time (it is the time that starts when the anesthesia provider begins to administer the IV anesthetics and ends with tracheal extubation) and surgical time (starts with skin incision and ends with last suture and putting dressings on).

4. The time taken to perform the block.

5. Number of patients needed ephedrine and/or atropine and total amount of their administration will be recorded.

6. Recovery time (time since anesthetics discontinuation till reaching score 9 of Alderete's criteria).

Postoperative:

1. Time of first call for rescue analgesia.

2. Number of patients requested analgesia postoperative.

3. Visual analogue scale (VAS) on admission to post-anesthetic care unit (PACU), every 30 minutes for next 2 hours, every 2 hours for next 6 hours and every 4 hours for the rest of the 24 hours postoperatively.

   • Discharge from PACU will be according to Postanesthesia Discharge Scoring System[14](Appendix3).

4. Hemodynamics (pulse- heart rate- mean blood pressure)

   They will be assessed as follow:

   • On admission to post-anesthetic care unit (PACU) then every 30 minutes at 30, 60, 90, 120 minutes then every 2 hours for next 6 hours then every 6 hours for remaining 24 hours.

5. Vomiting, nausea and starting time of intestinal movements.

6. Duration of the block (from the injection time of local anesthetic till complete return of sensation).

Enrollment: 56 patients

Sex: All

Ages: 21 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• ASA I, II, III scheduled for laparoscopic nepheroctomy

Exclusion criteria

• patient refusal bleeding disorders neurological and psychological diseases

Trial design

Primary purpose: Health Services Research

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Single Blind

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56 participants in 2 patient groups

group Q

Experimental group

Description:

Group Q; (28 patients) Quadratus lumborum block group; patients will receive general anesthesia initially then bilateral QLB type III (anterior subcoastal approach) with a volume of 30 mL of bupivacaine 0.25% for each side taking care that the patient does not receive a local anesthetic dose higher than the maximum allowed (2.5 mg/kg)

Treatment:

Device: US guided block

group E

Experimental group

Description:

Group E; (28 patients) Erector spinae plane block; patients will receive general anesthesia initially then bilateral ESPB with a volume of 30 mL of bupivacaine 0.25 % for each side taking care that the patient does not receive a local anesthetic dose higher than the maximum allowed (2.5 mg/kg)

Treatment:

Device: US guided block