Evaluating the pericapsular nerve group block in hip fracture patients: A prospective observational cohort study.
DOI:
https://doi.org/10.51168/sjhrafrica.v7i2.2527Keywords:
hip fracture, PENG block, Analgesic efficacy, Arthroplasty, Postoperative analgesiaAbstract
Background
This study aimed to assess the pericapsular nerve group (PENG) block combined with a spinal anaesthetic compared to only a spinal anaesthetic in patients presenting for hip fracture surgery. The objectives were to determine the ability of a patient to sit for a spinal anaesthetic, rest, dynamic hip pain scores, and the incidence of lower limb motor blockade following the block. Furthermore, time to first request for opioid analgesia post-operatively and the total opioid consumption in morphine equivalents were determined.
Methods
A prospective, observational study with 40 participants who were recruited via purposive sampling. Participants receiving the PENG block combined with a spinal anaesthetic were allocated to the PENG block (Group P, n = 20) and those receiving only a spinal anaesthetic (Group C, n = 20). Group P received bupivacaine 0.25% 20ml injected into the target site in the block area, followed by spinal after 30 minutes in theatre. Group C received a spinal only.
Results
There were no significant differences in participants’ characteristics. Group P had 90% of the participants able to sit adequately without IV analgesia for a spinal versus 45% in Group C. Group P had statistically significantly lower rest (p<0.001) and dynamic (p<0.001) pain scores compared to Group C at 30 minutes following PENG block injection (T1). Thirteen (65%) participants in Group P did not have motor blockade as they were able to lift the blocked leg to 15 degrees at T1. A longer duration to first opioid analgesia required was found in Group P (p <0.001). The total IV morphine equivalent analgesic requirement for Group C was almost double that required for Group P (p = 0.009).
Conclusion
PENG block combined with spinal anaesthesia is better compared to spinal anaesthesia only.
Recommendations
A randomised controlled trial with a larger sample size is recommended.
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