Lumbar Erector Spinae Plane Block for Total Hip Arthroplasty Comparing 24-Hour Opioid Requirements: A Randomized Controlled Study

Author:

Townsend Dahlia12ORCID,Siddique Nasir13ORCID,Kimura Atsumi1,Chein Yaacov1,Kamara Eli4,Pope John4,Weiser Mitchell4,Nair Singh1,Muse Iyabo15ORCID

Affiliation:

1. Montefiore Medical Center, Department of Anesthesiology, 111 E. 210th Street, Bronx, NY 10467, USA

2. University of Pittsburgh Medical Center Shadyside, Department of Anesthesiology and Perioperative Medicine, 5230 Centre Ave, Pittsburgh, PA 15232, USA

3. Nova Southeastern University, Dr. Kiran C. Patel College of Allopathic Medicine, 3200 S University Drive, Fort Lauderdale, FL 33328, USA

4. Montefiore Medical Center, Department of Orthopedic Surgery, Division of Joint Replacement, 111 E. 210th Street, Bronx, NY 10467, USA

5. Westchester Medical Center-New York Medical College, Department of Anesthesiology, 100 Woods Road, Valhalla, NY 10595, USA

Abstract

Study Objective. Neuraxial and regional anesthesia have become commonly utilized for patients undergoing total hip arthroplasty to aid in postoperative analgesia, facilitating early ambulation and better functional recovery. This study investigated the efficacy of a lumbar erector spinae plane block (ESPB) on reducing postoperative opioid consumption in total hip arthroplasty performed under spinal anesthesia. Design. Prospective, randomized, controlled trial. Patients. Sixty-three adult patients with an American Society of Anesthesiologists Status I–III who are undergoing elective primary total hip arthroplasty. Interventions. Patients were randomized to the control group (no block) or the ESPB group (preoperative ultrasound-guided lumbar ESPB). Intraoperatively, all patients received spinal anesthesia with moderate sedation. Postoperatively, patients received a standardized multimodal analgesia protocol. Measurements. The primary outcome was cumulative opioid consumption at 24 hours postoperatively. Secondary outcomes included cumulative opioid consumption at 8 hours and through 48 hours postoperatively and pain scores at 24 and 48 hours post surgery. Main Results. Thirty-one patients were randomized to the control group (spinal alone) and 32 patients to the ESPB group. The median opioid requirement in the first 8 hours after surgery was higher in the control group (28 mg of oral morphine equivalents (OME) versus 5 mg of OME in the ESPB group) ( p = 0.013 ). There was no statistically significant difference in opioid consumption between the groups at 24 hours ( p = 0.153 ) or 48 hours ( p = 0.357 ) postoperatively. There was no statistically significant difference in pain scores between the two groups through 24 hours ( p = 0.143 ) or 48 hours ( p = 0.617 ) after surgery. Conclusion. Lumbar ESPB reduces opioid utilization during the first 8 hours postoperatively after total hip arthroplasty but not thereafter. Evaluating the use of either adding a local anesthetic adjunct to the ESPB or using longer-acting local anesthetic warrants further investigation.

Publisher

Hindawi Limited

Subject

Anesthesiology and Pain Medicine,Critical Care and Intensive Care Medicine

Reference18 articles.

1. Hospitalization for total hip replacement among inpatients aged 45 and over: United States, 2000–2010;M. L. Wolford;NCHS Data Brief,2015

2. Multi-modal, pre-emptive analgesia decreases the length of hospital stay following total joint arthroplasty;T. J. Duellman;Orthopedics,2009

3. Update on Selective Regional Analgesia for Hip Surgery Patients

4. Ultrasound guided erector spinae plane block reduces postoperative opioid consumption following breast surgery: A randomized controlled study

5. Ultrasound guided Erector Spinae Plane block at L-4 transverse process level provides effective postoperative analgesia for total hip arthroplasty

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