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LETTERS TO EDITOR
Year : 2018  |  Volume : 24  |  Issue : 1  |  Page : 118-119

Ziconotide: Indications, adverse effects, and limitations in managing refractory chronic pain


Department of Anesthesiology and Pain Management, Basavatarakam Indo-American Cancer Hospital and Research Institute, Hyderabad, Telangana, India

Date of Web Publication15-Jan-2018

Correspondence Address:
Dr. Abhijit S Nair
Department of Anesthesiology and Pain Management, Basavatarakam Indo.American Cancer Hospital and Research Institute, Hyderabad - 500 034, Telangana
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/IJPC.IJPC_113_17

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How to cite this article:
Nair AS, Poornachand A, Kodisharapu PK. Ziconotide: Indications, adverse effects, and limitations in managing refractory chronic pain. Indian J Palliat Care 2018;24:118-9

How to cite this URL:
Nair AS, Poornachand A, Kodisharapu PK. Ziconotide: Indications, adverse effects, and limitations in managing refractory chronic pain. Indian J Palliat Care [serial online] 2018 [cited 2019 Oct 22];24:118-9. Available from: http://www.jpalliativecare.com/text.asp?2018/24/1/118/223209


Sir,

Ziconotide is an N-type calcium channel antagonist which is used to treat chronic pain. It is a synthetic ω-conotoxin MVIIA, a hydrophilic conopeptide toxin which was originally isolated from Conus magus, a species of piscivorous cone snail [Figure 1].[1] At present, ziconotide is the only intrathecal (IT), United States Food and Drug Administration-approved, nonopioid analgesic. Preservative-free morphine is the other drug which is approved for IT use in chronic pain due to cancer and noncancer etiology. IT hydromorphone, clonidine, and baclofen are other drugs used off-label by clinicians. IT baclofen relieves pain due to spasticity in chronic pain conditions. When administered systemically, ziconotide has limited penetration across blood–brain barrier at the cost of unbearable side effects. Therefore, it is administered intrathecally to patients for better penetration across blood–brain barrier, better analgesia, and lesser side effects. Ziconotide blocks N-type calcium channels in the central nervous system, thereby effectively inhibiting neurotransmitter release (norepinephrine) that is responsible for pain at multiple synapses in the nervous system. It also antagonizes N-type calcium channels at the cerebral cortex and the neurohypophysis.[2] IT ziconotide is initially started at a rate of 0.1 μg/h, i.e., 2.4 μg/day as a continuous infusion and is carefully monitored and titrated. The maximum recommended dose is 0.8 μg/h, i.e., 19.2 ug/day. Clinical trials in patients with refractory neuropathic and nociceptive pain have established the feasibility and usefulness of single dose or continuous infusion of IT ziconotide.[3] A continuous IT infusion is managed using an intrathecal drug delivery system (IDSS) infusion or as a patient-controlled analgesia system by the patient. The route of administration of this drug is the hurdle in its regular use. The drug needs to be delivered through an infusion pump (IDSS) and the dose needs to be carefully titrated. Second, adverse events are frequently noted with its use which interrupts the ongoing treatment. The commonly encountered adverse effects are cognitive and neuropsychiatric (confusion, memory impairment, and hallucinations), presyncopal and syncopal episodes, gait disturbances, meningitis, depression, and elevated creatine kinase. Hayek et al. presented their data of 15 patients who were enrolled in ziconotide trial and were followed up for 24 months.[4] Only 4 patients could continue IT medication for 24 months. Rest of the patients had to discontinue it due to the adverse effects. Although the number of cases were less, the cases were followed up for a significant duration to address the adverse effect profile. Recently, Brookes et al. performed a systematic review of randomized controlled trials to investigate the efficacy of ziconotide monotherapy in chronic neuropathic pain.[5] They found that although the monotherapy was effective in pain management, there were serious adverse events which interrupted the ongoing treatment. Ziconotide appears to be a reasonable option for patients with unbearable chronic pain refractory to IT morphine, systemic high-dose opioids, antidepressants, and anti convulsants. The 2016 Polyanalgesic Consensus Conference recommendations are to use ziconotide as an IT monotherapy.[6] However, preservative-free IT morphine or clonidine could be used in refractory patients by careful titration.
Figure 1: Chemical structure of Ziconotide. Image source: National Center for Biotechnology Information. PubChem Compound Database; CID = 16135415, https://pubchem.ncbi.nlm.nih.gov/compound/16135415 (accessed June 29, 2017)

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Financial support and sponsorship

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Conflicts of interest

There are no conflicts of interest.

 
  References Top

1.
McGivern JG. Ziconotide: A review of its pharmacology and use in the treatment of pain. Neuropsychiatr Dis Treat 2007;3:69-85.  Back to cited text no. 1
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2.
Pope JE, Deer TR. Ziconotide: A clinical update and pharmacologic review. Expert Opin Pharmacother 2013;14:957-66.  Back to cited text no. 2
[PUBMED]    
3.
McDowell GC 2nd, Pope JE. Intrathecal ziconotide: Dosing and administration strategies in patients with refractory chronic pain. Neuromodulation 2016;19:522-32.  Back to cited text no. 3
    
4.
Hayek SM, Hanes MC, Wang C, Veizi IE. Ziconotide combination intrathecal therapy for noncancer pain is limited secondary to delayed adverse effects: A Case series with a 24-month follow-up. Neuromodulation 2015;18:397-403.  Back to cited text no. 4
    
5.
Brookes ME, Eldabe S, Batterham A. Ziconotide monotherapy: A Systematic review of randomised controlled trials. Curr Neuropharmacol 2017;15:217-31.  Back to cited text no. 5
[PUBMED]    
6.
Deer TR, Pope JE, Hayek SM, Bux A, Buchser E, Eldabe S, et al. The Polyanalgesic Consensus Conference (PACC): Recommendations on intrathecal drug infusion systems best practices and guidelines. Neuromodulation 2017;20:96-132.  Back to cited text no. 6
[PUBMED]    


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