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Related Experiment Videos

Gabapentin Superadded to a Pre-Existent Regime Containing Amytriptyline for Chronic Sciatica.

Kelvin L Robertson1,2, Laurence A G Marshman2,3

  • 1*Department of Pharmacy, Medical Services Group, The Townsville Hospital, Townsville, Douglas, Queensland kelvin.robertson@health.qld.gov.au.

Pain Medicine (Malden, Mass.)
|April 5, 2016
PubMed
Summary

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Adding gabapentin (GBP) to amytriptyline (AMP) improved chronic sciatica (CS) in 56% of patients. However, side effects were common, leading many to discontinue GBP, though some tolerated it despite adverse events.

Area of Science:

  • Neurology
  • Pharmacology
  • Pain Management

Background:

  • Chronic sciatica (CS) lacks robust evidence for medical management.
  • Current guidelines suggest antidepressants (e.g., amytriptyline, AMP) as first-line for neuropathic pain.
  • Gabapentin (GBP) is often a second-line agent, with guidelines recommending overlap with first-line treatments.

Purpose of the Study:

  • To evaluate the efficacy and side effects of adding gabapentin (GBP) to an existing amytriptyline (AMP) regimen for chronic sciatica (CS).
  • To assess the impact of side effects on treatment outcomes and tolerability.

Main Methods:

  • A prospective cohort study involving patients with unilateral CS receiving AMP.
  • Gabapentin (GBP) was added to the existing AMP regimen for 3 months without other medication changes.
Keywords:
AmitriptylineGabapentinNeuropathicPainSciaticaSide-Effects

Related Experiment Videos

  • Pain reduction (Visual Analog Scale - VAS) and disability (Oswestry Disability Index - ODI) were measured, along with side effects (SE).
  • Main Results:

    • 56% of patients showed reduced VAS and ODI scores with the addition of GBP.
    • Side effects (SE) were reported by 53% of patients, with 23 different types noted.
    • 34% discontinued GBP during the titration period due to SE, and SE were associated with reduced efficacy.

    Conclusions:

    • This is the first prospective study on adding GBP to AMP for CS, reflecting clinical practice and guidelines.
    • Super-added GBP demonstrated further efficacy in over half of the patients.
    • Frequent and diverse side effects were observed, impacting tolerability and efficacy, yet 37% tolerated GBP despite SE.