Background Timely and effective pain management is essential in the emergency department, particularly for patients with femoral fractures. Despite their potential benefits, femoral nerve blocks remain underutilized compared to intravenous opioid administration.
Methods This retrospective study evaluated patients with femoral fractures who received either femoral nerve blocks (Group 1) or standard Intravenous opioid treatment (Group 2). Pain reduction was assessed using the Numerical Rating Scale, and Intravenous opioid use was recorded.
Results Group 1 experienced a significantly greater reduction in pain scores (mean decrease of 4.96 vs. 3.99; p < 0.001). While the frequency of Intravenous opioid use was slightly lower in Group 1 (1.35 vs. 1.64; p = 0.063), the trend suggests a reduction in opioid reliance. The average time to additional opioid administration post-femoral nerve blocks was 6.49 hours.
Conclusions Femoral nerve blocks offer superior analgesia for femoral fractures and may reduce opioid use in the emergency departments, potentially easing the burden on emergency staff. Further studies are warranted to validate these findings.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The study was conducted in accordance with the Declaration of Helsinki, and approved by the Institutional Review Board of Taichung Veterans General Hospital (No. CE22273B-1, 18 July 2024).
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
AbbreviationsNRSnumerical rating scaleIVOintravenous opioidERemergency departmentERSemergency room stay timeFNBfemoral nerve blocksPCIpain control interventionISSInjury Severity Score
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