Long-term outcomes during treatment of chronic pain with intrathecal clonidine or clonidine/opioid combinations

• Published in: Journal of pain and symptom management Vol. 26; no. 1; pp. 668 - 677
• Main Authors: Ackerman, Laurie L., Follett, Kenneth A., Rosenquist, Richard W.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.07.2003; Elsevier Science
• Subjects: Adult; Aged; Aged, 80 and over; Analgesics; Analgesics - administration & dosage; Analgesics - adverse effects; Analgesics, Opioid - administration & dosage; Analgesics, Opioid - adverse effects; Biological and medical sciences; Chronic Disease; chronic pain; Clonidine; Clonidine - administration & dosage; Clonidine - adverse effects; Drug Therapy, Combination; Female; Humans; Hydromorphone - administration & dosage; Hydromorphone - adverse effects; Infusion Pumps, Implantable; Injections, Spinal; intrathecal; Male; Medical sciences; Middle Aged; Neuropharmacology; opioids; Pain - drug therapy; Pharmacology. Drug treatments; polyanalgesia; Treatment Outcome; intrathecal; chronic pain; Clonidine; polyanalgesia; opioids; Human; Imidazole derivatives; Drug combination; Toxicity; Treatment efficiency; Opiates; Intrathecal administration; Chemotherapy; Chronic; Pain; Treatment
• DOI: 10.1016/S0885-3924(03)00144-1
• ISSN: 0885-3924

To evaluate the effectiveness of intrathecal clonidine or clonidine/opioid admixture for the treatment of chronic pain states, a retrospective chart audit of 15 patients seen by the Pain Medicine and Neurosurgical Services was performed. Subjects included 9 men and 6 women aged 26–86 years. Diagnoses included complex regional pain syndrome, neuropathic pain, and cancer pain. All patients received a trial of single-shot and/or short-term infusion of clonidine. Those reporting a significant reduction in pain, or at least 50% reduction in their visual analog scale (VAS), received long-term therapy. Intrathecal clonidine as a single-shot dose, infusion, or as intrathecal polytherapy did not improve VAS scales from pre-treatment values in 5 patients. Ten patients reported significant pain relief or >50% decrease in VAS scores with the initial trial and received long-term therapy. Two received clonidine alone for 7–11 months before the therapy failed; others failed after just a few days. Seven of eight initially responded to clonidine alone (75–950 μg/day) before failing and requiring a second drug. Three received hydromorphone (200–8000 μg/day) and four morphine (0.15–15 mg/day) with clonidine. Four patients then failed 2-drug therapy (duration 6–21 months). Two continue with intrathecal clonidine/hydromorphone (duration 19–29 months) and 1 with clonidine/morphine (duration 21 months). After initiation of intrathecal clonidine, one patient reported good relief with clonidine/morphine until his death 5 months later. In this population, intrathecal clonidine was of limited utility for most patients. It may be of benefit for subset(s) of patients, but in our experience, duration of relief is typically <18 months.