External Oblique Intercostal Plane Block, Laparoscopic Cholecystectomy
Conditions
Keywords
EOIPB, alternative analgesic, laparoscopic cholecystectomy
Brief summary
Pain after laparoscopic cholecystectomy (LC) is a common complaint that prolongs hospital stay and thus increases morbidity. There are three primary sources of pain after LC, incision site, local and systemic effects of pneumoperitoneum, and post cholecystectomy wound to the liver. External oblique intercostal plane block (EOIPB) has recently been described as a novel block for upper abdomen surgery. the probable mechanism of the block with the dyeing of both the anterior and lateral branches of the intercostal nerves T7-T10. This block also provides a dermatomal sensory block at the T6-T10 level in the anterior axillary region and the T6-T9 level in the midline.
Detailed description
EOIPB has the benefit of being performed with the patient supine when compared with QLB and ESPB. It also has an advantage over SIPB in that it produces greater analgesia throughout the midline of the abdomen. The hypothesis of this randomized study is that patients who will undergo EOIPB will have lower opioid consumption in the postoperative period than patients who receive routine multimodal analgesia alone. The study aims to assess pain control in the immediate postoperative period by assessment of Numerical Rating scale (NRS), time for the first analgesic request as well as total morphine intake in the first 24 hours after surgery. Study design: This is a prospective, randomized double blinded control study which will be conducted in department of anesthesia and surgical Intensive care unit at Theodor Bilharz Research Institute after approval by research ethics committee and patient informed consent. 50 patients will be enrolled in the study and divided into two groups either (EOIPB group (E) or Control group (C). Randomization will be done by allocation 1:1 of scheduled cases per day. Sample size: 38 patients
Interventions
DRUGlocal anesthetic injection (bupivacaine)
The in-plane technique with a 22G, 80 mm block needle is used to inject 30 ml of 0.25% bupivacaine into the external oblique intercostal plane on both sides.
OTHERnormal saline injection
the control group will receive 30ml of normal saline bilaterally into the external oblique intercostal plane on both sides
Sponsors
Theodor Bilharz Research Institute
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
the investigator responsible for block administration will not be aware of the content of the medications prepared whether they are the local anesthetics or normal saline. also the patients will not be aware of the group assignment.
Intervention model description
38 patients will be enrolled in the study and divided into two groups either (EOIPB group (E) or Control group (C). Randomization will be done by allocation 1:1 of scheduled cases per day.
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
1. ASA 1-2. 2. Patients undergoing elective laparoscopic cholecystectomy with estimated pneumoperitoneum time of 60 to 90 min.-
Exclusion criteria
1. Coagulation disorders. 2. Liver/ kidney disease 3. Previous abdominal surgery 4. Infection in the block site 5. Chronic opioid use 6. Local anesthetic (LA) allergy, 7. Pregnancy, or BMI ≥35 kg/m2 8. Duration of surgery (≥ 2.5 h due to surgical complications), -
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| total morphine consumption | the first 24 hours postoperatively | the total analgesic (morphine) requirements in the first 24 hours postoperatively will be calculated |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| NRS | 6 hours postoperatively | Numerical rating scale for pain recorded at 15,30, 60 minutes postopetaively. |
Countries
Egypt
Outcome results
None listed