Daily Opioid Use Fluctuates as a Function of Pain, Catastrophizing, and Affect in Patients With Sickle Cell Disease: An Electronic Daily Diary Analysis
Abstract:The present study shows that pain and pain-related cognitive and affective variables are associated with daily variation in prescription opioid use in SCD. The findings may have broad implications for tracking and defining risk for prescription opioid misuse in patients with daily pain.
“…Exclusion criteria for the previous studies included cancer, use of narcotic patches or fentanyl, or chronic kidney disease. For the present study, an additional exclusion criterion was sickle cell disease, as this population often has fluctuating, distorted opioid (and potentially gabapentin) dose requirements …”
The likelihood of gabapentin overuse alone is low but significantly increases with concomitant opioid use, especially when coupled with a history of addiction. History of addiction does not appear to increase risk of gabapentin misuse among those with gabapentin alone.
“…Exclusion criteria for the previous studies included cancer, use of narcotic patches or fentanyl, or chronic kidney disease. For the present study, an additional exclusion criterion was sickle cell disease, as this population often has fluctuating, distorted opioid (and potentially gabapentin) dose requirements …”
The likelihood of gabapentin overuse alone is low but significantly increases with concomitant opioid use, especially when coupled with a history of addiction. History of addiction does not appear to increase risk of gabapentin misuse among those with gabapentin alone.
“…These data suggest that even during a well‐designed clinical trial, patients with recurrent episodes of acute vaso‐occlusive pain administered hydroxyurea therapy may continue to have frequent need for healthcare utilization. Additional important nonpharmacological treatments for pain are increasingly recognized and include an intensive multidisciplinary approach that incorporates self‐efficacy, cognitive behavioral therapy, guided imagery, and catastrophizing management . However, the availability of resources to support these multidisciplinary approaches likely limits their widespread adoption.…”
Section: Introductionmentioning
confidence: 99%
“…guided imagery, and catastrophizing management. [7][8][9] However, the availability of resources to support these multidisciplinary approaches likely limits their widespread adoption. Chronic transfusion therapy offers another possible treatment for patients with frequent pain events.…”
“…In patients with SCD, this part of the brain is hyperactive and may contribute to exaggerated pain perception by the patient. Sociopsychological factors leading to cognitive impairment have been described to influence pain and opioid requirement in patients with SCD (31). In addition, cerebral infarction in SCD subjects also results in a significant decline of neuropsychological functions, IQ, and cognitive score (5, 10, 13, 22, 26, 71, 87).…”
Sickle cell disease (SCD) is a genetic disorder associated with hemolytic anemia, end-organ damage, reduced survival, and pain. One of the unique features of SCD is recurrent and unpredictable episodes of acute pain due to vasoocclusive crisis requiring hospitalization. Additionally, patients with SCD often develop chronic persistent pain. Currently, sickle cell pain is treated with opioids, an approach limited by adverse effects. Because pain can start at infancy and continue throughout life, preventing the genesis of pain may be relatively better than treating the pain once it has been evoked. Therefore, we provide insights into the cellular and molecular mechanisms of sickle cell pain that contribute to the activation of the somatosensory system in the peripheral and central nervous systems. These mechanisms include mast cell activation and neurogenic inflammation, peripheral nociceptor sensitization, maladaptation of spinal signals, central sensitization, and modulation of neural circuits in the brain. In this review, we describe potential preventive/therapeutic targets and their targeting with novel pharmacologic and/or integrative approaches to ameliorate sickle cell pain.
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