Optimal and Safe Pain Management Approach in Ankle and Hindfoot Fractures: Improving Practitioner Decision

Abstract

Background: Over or sub-optimal analgesic treatment leads to undesired consequences and patient dissatisfaction. The study aims to assess the sub-optimal or optimal pain relief and safety of routinely prescribed oral analgesic(s) at discharge and 1-week post-discharge in ankle and foot fracture surgeries. Methods: The ongoing prospective cohort study data on 54 ankle and hindfoot trauma fracture adult patients enrolled between June 2022 to July 2023 was analyzed. Post-surgery oral analgesics prescribed at hospital discharge and 1-week follow-up were stratified for assessing adverse events and pain (Visual Analogue Scale) at 1- and 2 weeks post-discharge. The relationship of age, gender, and comorbidity was analyzed by multiple logistic regression for adverse events and multiple linear regression for pain score.   Results: Median pain scores at 1- and 2-week follow-ups were 3.2 (IQR=3.0) and 2 (IQR=2.0) respectively. Combinations of tramadol, acetaminophen with naproxen or diclofenac or orphenadrine; and naproxen, pregabalin, with acetaminophen seemed toxic with sub-optimal pain control. Similar results were for celecoxib combined with pregabalin and etoricoxib combined with diclofenac or tramadol. Acetaminophen alone was safe but occasionally showed intolerance. Etoricoxib or diclofenac alone or with acetaminophen was safe and showed better pain control in this cohort. A regression model was non-significant for a relationship between covariates and pain scores or adverse events. Conclusion: Current data suggests that certain oral analgesics or their combinations are harmful with sub-optimal pain control while some are safe and effective. Choosing suitable analgesics or their combinations in specific fractures might reduce patient harm with optimal pain management.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

Yes

Author Declarations

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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

National Bioethics Committee and Aga Khan University Ethical Review Committee approvals were obtained prior to study start-up.

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Data Availability

Data cannot be shared publicly because of human subjects identifiers. Data are available from the Aga Khan University Institutional medical record data Access / Ethics Committee (contact via +92 21 3493 0051 Ext: 4988/2445, erc.pakistan@aku.edu) for researchers who meet the criteria for access to confidential data. On acceptance of the manuscript, the de-identified data will be available by the authors.

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