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PENG and LFCN Block Versus FIC Block for Multimodal Analgesia After Total Hip Replacement Surgery: a Retrospective Analysis Focused on Movement (Retro-PvF)

Completed
Conditions
Regional Anesthesia Block
Regional Anesthesia
Total Hip Arthroplasty \(THA\)
Total Hip Replacement Surgery
Interventions
Procedure: PENG + LFCN block
Procedure: FIC block
Registration Number
NCT06342102
Lead Sponsor
Ospedale Edoardo Bassini
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
PENG + LFCN BlockPENG + LFCN blockgroup in which PENG + LFCN Block was performed
FIC BlockFIC blockgroup in which FIC Block was performed
Primary Outcome Measures
NameTimeMethod
Movement of the lower limb affected by surgery6 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 Outcome Measures
NameTimeMethod
Morphine Milligram Equivalents (MME) of "pro re nata" (PRN) opioid doses12 hours after surgery

we studied the effect of Regional anesthesia on opioid-sparing

pain control24 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"

Trial Locations

Locations (1)

ASST Nord Milano - Ospedale E. Bassini

🇮🇹

Cinisello Balsamo, Italy/Milano, Italy

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