Regional Anesthesia, Regional Anesthesia Block, Total Hip Arthroplasty \(THA\), Total Hip Replacement Surgery
Conditions
Keywords
PENG, LFCN, fascia iliaca, THA, total hip replacement surgery, analgesia, movement, Peripheral nerve blocks
Brief summary
Total hip arthroplasty is a major surgical procedure performed on a growing number of patients. Optimal pain control with limited muscle weakness is paramount for a swift initiation of physical therapy and ambulation, thus expediting hospital discharge. Amongst the many peripheral nerve blocks, FIB (fascia iliaca block) has been recommended as the block of choice by many international guidelines since it offers the best pain control with a relatively low risk of motor block. PENG (pericapsular nerve group) and its association with LFCN (lateral femoral cutaneous nerve) has been proposed as an effective alternative that offers comparable, If not better, pain control with a considerably lower risk for motor block compared to FIB. Given the novelty of this block, there are few published papers on the subject, mostly case series or case reports thus justifying the need for retrospective study.
Detailed description
The primary outcome was the degree of residual quadriceps femoris muscle paresis assessed with the MRC (medical research council) scale at 6 hours between PENG and LCFN. The secondary outcomes were NRS (numeric rating scale) at 6,12, 24 hours, total opioid consumption expressed as milligrams of morphine equivalents (MME), time to first rescue opioid and time to first postoperative ambulation.
Interventions
The PENG block was performed under ultrasound guidance. After skin disinfection, the needle was advanced between the psoas tendon and pubic ramus where 20 mL of 0.5% ropivacaine were injected. The LFCN block was performed following the PENG block.10 ml of 0.5% ropivacaine were injected near the nerve into the fat-filled flat tunnel (FFFT) located at the level of the superior anterior iliac spine and lateral to the sartorius muscle.
FICB was performed under ultrasound guidance. The needle was advanced above the fascia iliaca and 20 mL of 0.5% ropivacaine were injected
Sponsors
Study design
Eligibility
Inclusion criteria
* elective total hip replacement surgery for non-traumatic hip disease, * age over 18 years, * complete clinical chart including type of peripheral nerve block performed, * signed consent form for spinal anesthesia and peripheral nerve block.
Exclusion criteria
* preoperative opioid therapy, * having received a peripheral nerve block other than PENG + LFCN or FICB, * having received general anesthesia, * incomplete chart, * documented muscle weakness * deviation from the established post-operative analgesia protocol.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Movement of the lower limb affected by surgery | 6 hours after surgery | The Medical Research Council (MRC) Muscle Strength Scale (ranging scale from 0 to 5 0= no visible contraction, 5=normal power) was used to assess the degree of residual quadriceps femoris muscle paresis 6 hours postoperatively. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| pain control | 6 hours after surgery | pain assessment with Numeric Rating Scale (NRS): a 0-10 scale, with zero meaning no pain and 10 meaning the worst pain imaginable |
| Morphine Milligram Equivalents (MME) of pro re nata (PRN) opioid doses | 24 hours after surgery | we studied the effect of Regional anesthesia on opioid-sparing |
Other
| Measure | Time frame | Description |
|---|---|---|
| time to first opioid request | From date of surgery until up to 3 days after | we studied the effect of Regional anesthesia on opioid-sparing |
| time to first postoperative ambulation | From date of surgery until up to 3 days after | we studied the effect of Regional anesthesia on opioid-sparing |
Countries
Italy