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Intrathecal ziconotide for complex regional pain syndrome: seven case reports.
Pain Pract. 2009 Jul-Aug; 9(4):296-303.PP

Abstract

Ziconotide is a nonopioid analgesic currently indicated as monotherapy, but frequently used in combination with opioids, for the management of severe chronic pain in patients for whom intrathecal (IT) therapy is warranted and who are intolerant of, or whose pain is, refractory to other treatments. There is a paucity of information regarding ziconotide use in patients with complex regional pain syndrome (CRPS). Seven cases in which IT ziconotide was used in patients with CRPS were analyzed. All patients (4 male, 3 female; age range, 14 to 52 years) had experienced inadequate pain relief with multiple conventional and interventional treatments. Three patients received ziconotide monotherapy exclusively; 4 patients received ziconotide monotherapy initially, then combination IT therapy. The mean ziconotide dose was 5.2 mcg/d (range, 0.5 to 13 mcg/d) at initiation and 24.7 mcg/d (range, 0.06 to 146 mcg/d) at the last available assessment. The mean duration of ziconotide therapy was 3.1 years (range, 26 days to 8 years). At ziconotide initiation, the mean visual analog scale (VAS) score was 89.3 mm (range, 75 to 100 mm); VAS scores decreased by a mean of 47.5% (range, 5% to 100%) at last assessment. Of the 5 patients who experienced substantial improvement in pain, edema, skin abnormalities, and/or mobility with ziconotide therapy, 2 have discontinued ziconotide and are pain free. Another patient experienced marked reversal of both edema and advanced skin trophic changes. Adverse events included urinary retention, depression, anxiety, and hallucinations. Adverse events generally resolved spontaneously, with treatment, or with ziconotide discontinuation/dose reduction. Although further studies are required, ziconotide holds promise as an effective treatment for CRPS.

Authors+Show Affiliations

The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA. KAPURAL@ccf.orgNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

19500276

Citation

Kapural, Leonardo, et al. "Intrathecal Ziconotide for Complex Regional Pain Syndrome: Seven Case Reports." Pain Practice : the Official Journal of World Institute of Pain, vol. 9, no. 4, 2009, pp. 296-303.
Kapural L, Lokey K, Leong MS, et al. Intrathecal ziconotide for complex regional pain syndrome: seven case reports. Pain Pract. 2009;9(4):296-303.
Kapural, L., Lokey, K., Leong, M. S., Fiekowsky, S., Stanton-Hicks, M., Sapienza-Crawford, A. J., & Webster, L. R. (2009). Intrathecal ziconotide for complex regional pain syndrome: seven case reports. Pain Practice : the Official Journal of World Institute of Pain, 9(4), 296-303. https://doi.org/10.1111/j.1533-2500.2009.00289.x
Kapural L, et al. Intrathecal Ziconotide for Complex Regional Pain Syndrome: Seven Case Reports. Pain Pract. 2009 Jul-Aug;9(4):296-303. PubMed PMID: 19500276.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Intrathecal ziconotide for complex regional pain syndrome: seven case reports. AU - Kapural,Leonardo, AU - Lokey,Kristi, AU - Leong,Michael S, AU - Fiekowsky,Sharon, AU - Stanton-Hicks,Michael, AU - Sapienza-Crawford,Anne J, AU - Webster,Lynn R, Y1 - 2009/05/29/ PY - 2009/6/9/entrez PY - 2009/6/9/pubmed PY - 2009/10/10/medline SP - 296 EP - 303 JF - Pain practice : the official journal of World Institute of Pain JO - Pain Pract VL - 9 IS - 4 N2 - Ziconotide is a nonopioid analgesic currently indicated as monotherapy, but frequently used in combination with opioids, for the management of severe chronic pain in patients for whom intrathecal (IT) therapy is warranted and who are intolerant of, or whose pain is, refractory to other treatments. There is a paucity of information regarding ziconotide use in patients with complex regional pain syndrome (CRPS). Seven cases in which IT ziconotide was used in patients with CRPS were analyzed. All patients (4 male, 3 female; age range, 14 to 52 years) had experienced inadequate pain relief with multiple conventional and interventional treatments. Three patients received ziconotide monotherapy exclusively; 4 patients received ziconotide monotherapy initially, then combination IT therapy. The mean ziconotide dose was 5.2 mcg/d (range, 0.5 to 13 mcg/d) at initiation and 24.7 mcg/d (range, 0.06 to 146 mcg/d) at the last available assessment. The mean duration of ziconotide therapy was 3.1 years (range, 26 days to 8 years). At ziconotide initiation, the mean visual analog scale (VAS) score was 89.3 mm (range, 75 to 100 mm); VAS scores decreased by a mean of 47.5% (range, 5% to 100%) at last assessment. Of the 5 patients who experienced substantial improvement in pain, edema, skin abnormalities, and/or mobility with ziconotide therapy, 2 have discontinued ziconotide and are pain free. Another patient experienced marked reversal of both edema and advanced skin trophic changes. Adverse events included urinary retention, depression, anxiety, and hallucinations. Adverse events generally resolved spontaneously, with treatment, or with ziconotide discontinuation/dose reduction. Although further studies are required, ziconotide holds promise as an effective treatment for CRPS. SN - 1533-2500 UR - https://www.unboundmedicine.com/medline/citation/19500276/Intrathecal_ziconotide_for_complex_regional_pain_syndrome:_seven_case_reports_ L2 - https://doi.org/10.1111/j.1533-2500.2009.00289.x DB - PRIME DP - Unbound Medicine ER -