نتایج جستجو برای: intrathecal opioid therapy

تعداد نتایج: 687650  

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Hirokazu Mizoguchi Hiroyuki Watanabe Takafumi Hayashi Wataru Sakurada Toshiki Sawai Tsutomu Fujimura Tsukasa Sakurada Shinobu Sakurada

The antinociception induced by i.t. or i.c.v. administration of endomorphins is mediated via mu-opioid receptors. However, although endomorphins do not have an appreciable affinity for kappa-opioid receptors, pretreatment with the kappa-opioid receptor antagonist norbinaltorphimine markedly reduces the antinociceptive response to i.c.v. or i.t. administered endomorphin-2 but not endomorphin-1. ...

2012
Seok Myeon Rhee Eun Joo Choi Pyung Bok Lee Francis Sahngun Nahm

Intrathecal drug administration system (ITDAS) can reduce the side effects while increasing the effectiveness of opioids compared to systemic opioid administration. Therefore, the use of ITDAS has increased in the management of cancer pain and chronic intractable pain. Catheter obstruction is a serious complication of ITDAS. Here, we present a case of catheter obstruction by a mass formed at th...

Journal: :Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland 2013
G P Joshi F Bonnet H Kehlet

AIM The aim of this systematic review was to evaluate the available literature on the management of pain after laparoscopic colorectal surgery. METHOD Randomized studies, published in English between January 1995 and July 2011, assessing analgesic and anaesthetic interventions in adults undergoing laparoscopic colorectal surgery, and reporting pain scores, were retrieved from the Embase and M...

ژورنال: اعتیاد پژوهی 2020

Objective: Substance use disorder is one of the chronic and debilitating disorders. The aim of this study was to investigate the effectiveness of acceptance and commitment therapy on self-compassion and self-criticism in individuals with opioid use disorder. Method: The present study was quasi-experimental with a pretest-posttest design with a control group. Thirty people with opioid use disord...

Journal: :P & T : a peer-reviewed journal for formulary management 2011
James O'Donnell F Randy Vogenberg

tion was removed in 1976; physicians with appropriate Drug Enforcement Agency registration may now prescribe methadone for analgesia.3 The unique pharmaco kinetic and pharmacodynamic characteristics of methadone make it a valuable option for the management of chronic pain both as a first-line agent and as a replacement opioid.1,4 Even though methadone may be administered by several routes––oral...

Journal: :Anesthesiology 2007
Heeseung Lee Norah N Naughton James H Woods Mei-Chuan Ko

BACKGROUND Butorphanol is an opioid analgesic with partial agonist actions at micro- and kappa-opioid receptors (MOR and KOR). Previous studies have demonstrated that both MOR antagonists and KOR agonists are effective in alleviating intrathecal morphine-induced itch in primates. The aim of the study was to investigate the effectiveness of butorphanol as an antipruritic and to elucidate the rec...

Journal: :AANA journal 2001
J E Pellegrini S L Bailey J Graves J A Paice S Shott M Faut-Callahan

Nalmefene is a long-acting opioid antagonist that provides long-term relief from side effects of intrathecal morphine sulfate. A randomized, double-blind, placebo-controlled study was conducted to determine whether prophylactic nalmefene could decrease side effects of intrathecal morphine given during cesarean section, without affecting analgesia. Sixty parturients were given 0.25 mg of intrath...

2017
Tony L. Yaksh Casey J. Fisher Tyler M. Hockman Ashley J. Wiese

Targeting analgesic drugs for spinal delivery reflects the fact that while the conscious experience of pain is mediated supraspinally, input initiated by high intensity stimuli, tissue injury and/or nerve injury is encoded at the level of the spinal dorsal horn and this output informs the brain as to the peripheral environment. This encoding process is subject to strong upregulation resulting i...

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