1996
DOI: 10.1177/0883073896011001s05
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Intrathecal Baclofen in Cerebral Palsy Movement Disorders

Abstract: Intrathecal baclofen reduces spasticity in individuals with cerebral palsy. Intrathecal doses are far lower than oral doses and the effects are considerably greater, and the side effects are fewer. Response to intrathecal baclofen must be confirmed by a screening trial before implantation of a pump for chronic infusion. Intrathecal baclofen reduces spasticity in the upper and lower extremities and is often associated with improved gait and upper extremity function. Quality of life improves for patients and car… Show more

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Cited by 148 publications
(99 citation statements)
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“…O baclofen pode ser usado tanto por via oral como intratecal 29 . A via intratecal é utilizada em PC com espasticidade severa, e tem a vantagem de que as doses podem ser lentamente ajustadas, e alcançar níveis maiores do que a via oral, com menores efeitos secundários.…”
Section: Cerebral Palsy New Therapeutic Possibilitiesunclassified
“…O baclofen pode ser usado tanto por via oral como intratecal 29 . A via intratecal é utilizada em PC com espasticidade severa, e tem a vantagem de que as doses podem ser lentamente ajustadas, e alcançar níveis maiores do que a via oral, com menores efeitos secundários.…”
Section: Cerebral Palsy New Therapeutic Possibilitiesunclassified
“…Intrathecally administrated baclofen acts directly and selectively at the spinal level. 14,15 Indeed, after lumbar administration, baclofen migrates upwards but the concentrations decline along the neuraxis so that the lumbar/cisternal ratio is approximately 4/1. 16 The systemic passage is less than 1%.…”
Section: Introductionmentioning
confidence: 99%
“…14 In most previous studies, Ashworth scores of different muscles had been added to produce a summed Ashworth score. 2,10,11 This is methodologically incorrect because the Ashworth score is an ordinal level measure. 14 The VAS is a valid and reliable measure in rating pain intensity in adults and children over 6 years of age.…”
Section: Outcome Measuresmentioning
confidence: 99%
“…Furthermore, this one-point reduction had to last for two successive measurements on the same day. 2,10,11 On the day that a positive clinical response was observed, the test treatment ended and the study medication code was broken. Only if this positive clinical response was observed on the first test day did the child and caregivers have the opportunity to experience the results of the second test day before the test treatment was ended.…”
Section: Participants and General Study Designmentioning
confidence: 99%
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