4.4 Article

Opioid Taper is Associated with Improved Experimental Pain Tolerance in Patients with Chronic Pain: An Observational Study

Journal

PAIN AND THERAPY
Volume 11, Issue 1, Pages 303-313

Publisher

SPRINGER INT PUBL AG
DOI: 10.1007/s40122-021-00348-8

Keywords

Chronic pain; Cold-pressor test; Opioid; Quantitative sensory testing; Taper

Funding

  1. National Institutes on Drug Abuse [R21 DA046364]
  2. National Institute of Nursing Research [R21 NR019047, F31 NR019527]
  3. National Institute of Environmental Health Sciences [T32 ES007062]

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This study aimed to investigate the improvement of experimental pain responses in patients with chronic pain undergoing opioid taper. The findings suggest that, in a highly individualized and variable taper process, patients experienced significant improvement in pain responses without a decline in function and quality of life. This indicates a potential reduction in opioid-induced hyperalgesia.
Introduction The degree to which opioid-induced hyperalgesia contributes to the pain experience of patients with chronic pain remains relatively undescribed. The objective of this pilot study was to determine if experimental pain responses improve in patients with chronic pain as they undergo a planned opioid taper. Methods This was a prospective observational study. Seven patients with chronic neuropathic pain on at least 120 mg morphine equivalents/day were enrolled. The participants were followed over the course of an individualized opioid taper to a lower dose. Measures of experimental pain sensitivity, including indicators of central pain modulation, were collected on a biweekly basis; in addition, measures of function and quality of life were collected monthly. The effect of opioid taper on pain responses and functional outcomes over time were examined using longitudinal mixed-effects regression modeling and general linear regression modeling with regularization as a function of baseline dose, end dose, and taper rate. Results In this small sample of patients undergoing highly individualized and variable opioid taper, the opioid taper was significantly associated with improved pain responses to the cold-pressor test, with the pain threshold on average increasing by 1.14 s every 6 weeks (p = 0.0084, 95% confidence interval [CI] for 6-week change 0.3039-2.0178) and pain tolerance on average increasing by 2.87 s every 6 weeks (p = 0.0026, 95% CI for 6-week change 1.02-4.7277). Taper-related changes in central pain modulation were not observed, although conditioned modulation trended toward improvement by the completion of opioid taper. Similarly, no declines in function and quality of life were observed with the opioid taper, suggesting stability despite decreased opioid dose. Conclusions Opioid taper was associated with improvements in experimental pain responses without a decline in function and quality of life, suggestive of diminished opioid-induced hyperalgesia in this clinical sample.

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