scholarly journals Use of high-dose oxycodone hydrochloride in patients with visceral and neuropathic pain

2015 ◽  
Vol 3 ◽  
pp. 257-259
Author(s):  
Jakub Kucharz ◽  
Iwona Filipczak-Bryniarska ◽  
Anna Michalowska-Kaczmarczyk ◽  
Roman M. Herman ◽  
Krzysztof Krzemieniecki
2000 ◽  
Vol 19 (6) ◽  
pp. 405-407 ◽  
Author(s):  
Yoko Tarumi ◽  
Sharon Watanabe ◽  
Eduardo Bruera ◽  
Kunihiko Ishitani
Keyword(s):  

2016 ◽  
Vol 6;19 (6;7) ◽  
pp. E905-E915
Author(s):  
Hélène Staquet

Intracerebroventricular (ICV) administration of opioids for control of intractable cancer pain has been used since 1982. We present here our experience of intracerebroventricular administration of pain treatments including ziconotide associated with morphine and ropivacaine for patients resistant to a conventional approach, with nociceptive, neuropathic, or mixed pain. These clinical cases were conducted with patients suffering from refractory pain, more than 6/10 on a numerical pain rating scale (NPRS) while on high-dose medical treatment and/ or intolerance with significant side effects from oral medication. The baseline study visit included a physical examination and an assessment of pain intensity on a NPRS. Under general anesthesia, a neuronavigation device was used to place the catheter on the floor of the third ventricle, supported by an endoscope. Then, drugs were injected in the cerebroventricular system, through a pump (external or subcutaneous). The primary objective was to measure pain evaluation with ICV treatment after a complete withdrawal of other medications. Four patients were enrolled: 3 with intractable cancer pain and one with central neuropathic pain. The median NPRS at baseline was 9.5 [8.5; 19]. The mean NPRS after one month was 3.5 [3; 4.5]. Ziconotide was initiated at 0.48 µg/dy and up to a median of 1.2 µg/dy [1.0; 1.56]. The median dose of morphine and ropivacaine used initially was respectively 0.36 mg/dy [0.24; 0.66] up to 0.6 mg/dy [0.45; 4.63] and 1.2 mg/dy [0; 2.4] up to 2.23 mg/dy [1.2; 3.35]. Minor side effects were initially observed but transiently. One psychiatric agitation required discontinuation of ziconotide infusion. For intractable pain, using ziconotide by intracerebroventricular infusion seems safe and efficient, specifically for chronic neoplastic pain of cervicocephalic, thoracic, or diffuse origin and also for pain arising from a central neuropathic mechanism. Key words: Intracerebroventricular infusion, ziconotide, intractable pain, nociceptive and neuropathic pain


2013 ◽  
Vol 110 (2) ◽  
pp. 287-292 ◽  
Author(s):  
N.A. Manering ◽  
T. Reuter ◽  
H. Ihmsen ◽  
D.C. Yeomans ◽  
A. Tzabazis

2017 ◽  
Vol 40 ◽  
pp. 195-197
Author(s):  
Julian Prosenz ◽  
Herwig Kloimstein ◽  
Ulrich Thaler ◽  
Ruth Drdla-Schutting ◽  
Jürgen Sandkühler ◽  
...  

2001 ◽  
Vol 5 (3) ◽  
pp. 325-329 ◽  
Author(s):  
Chris P. Bleeker ◽  
Robbert C. Bremer ◽  
Dave A. Dongelmans ◽  
Robert T.M. Dongen ◽  
Ben J.P. Crul

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Suk-Yun Kang ◽  
Dae-Hyun Roh ◽  
Ji-Ho Park ◽  
Hye-Jung Lee ◽  
Jang-Hern Lee

Cold allodynia is an important distinctive feature of neuropathic pain. The present study examined whether single or repetitive treatment of diluted bee venom (DBV) reduced cold allodynia in sciatic nerve chronic constriction injury (CCI) rats and whether these effects were mediated by spinal adrenergic receptors. Single injection of DBV (0.25 or 2.5 mg/kg) was performed into Zusanli acupoint 2 weeks post CCI, and repetitive DBV (0.25 mg/kg) was injected for 2 weeks beginning on day 15 after CCI surgery. Single treatment of DBV at a low dose (0.25 mg/kg) did not produce any anticold allodynic effect, while a high dose of DBV (2.5 mg/kg) significantly reduced cold allodynia. Moreover, this effect of high-dose DBV was completely blocked by intrathecal pretreatment of idazoxan (α2-adrenoceptor antagonist), but not prazosin (α1-adrenoceptor antagonist) or propranolol (nonselectiveβ-adrenoceptor antagonist). In addition, coadministration of low-dose DBV (0.25 mg/kg) and intrathecal clonidine (α2-adrenoceptor agonist) synergically reduced cold allodynia. On the other hand, repetitive treatments of low-dose DBV showing no motor deficit remarkably suppressed cold allodynia from 7 days after DBV treatment. This effect was also reversed by intrathecal idazoxan injection. These findings demonstrated that single or repetitive stimulation of DBV could alleviate CCI-induced cold allodynia via activation of spinalα2-adrenoceptor.


2015 ◽  
Vol 18 (10) ◽  
pp. 14
Author(s):  
Ashley Higbea ◽  
Stephen A. Wilson ◽  
Tomoko Sairenji
Keyword(s):  

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