Spasticity after stroke: physiology, assessment and treatment
Background: Spasticity following a stroke occurs in about 30% of patients. The mechanisms
underlying this disorder, however, are not well understood. Method: This review aims to …
underlying this disorder, however, are not well understood. Method: This review aims to …
[HTML][HTML] Comparative efficacy and safety of skeletal muscle relaxants for spasticity and musculoskeletal conditions: a systematic review
R Chou, K Peterson, M Helfand - Journal of pain and symptom …, 2004 - Elsevier
Skeletal muscle relaxants are a heterogeneous group of medications used to treat two
different types of underlying conditions: spasticity from upper motor neuron syndromes and …
different types of underlying conditions: spasticity from upper motor neuron syndromes and …
[HTML][HTML] Expert consensus on the diagnosis and treatment of myofascial pain syndrome
QW Cao, BG Peng, L Wang, YQ Huang… - World journal of …, 2021 - ncbi.nlm.nih.gov
Myofascial pain syndrome (MPS) is characterized by myofascial trigger points and fascial
constrictions. At present, domestic and foreign scholars have not reached a consensus on …
constrictions. At present, domestic and foreign scholars have not reached a consensus on …
Myofascial pain disorders: theory to therapy
AH Wheeler - Drugs, 2004 - Springer
Voluntary muscle is the largest human organ system. The musculotendinous contractual unit
sustains posture against gravity and actuates movement against inertia. Muscular injury can …
sustains posture against gravity and actuates movement against inertia. Muscular injury can …
A benefit-risk assessment of baclofen in severe spinal spasticity
A Dario, G Tomei - Drug safety, 2004 - Springer
Baclofen is used for treatment of the spasticity of spinal origin that is a common sequela of
spinal cord injury and multiple sclerosis; spasticity occurs in about 50% of patients affected …
spinal cord injury and multiple sclerosis; spasticity occurs in about 50% of patients affected …
Pharmacological management of spasticity in multiple sclerosis: systematic review and consensus paper
S Otero-Romero, J Sastre-Garriga… - Multiple Sclerosis …, 2016 - journals.sagepub.com
Background and objectives: Treatment of spasticity poses a major challenge given the
complex clinical presentation and variable efficacy and safety profiles of available drugs. We …
complex clinical presentation and variable efficacy and safety profiles of available drugs. We …
Breakthroughs in the spasticity management: are non-pharmacological treatments the future?
A Naro, A Leo, M Russo, C Casella, A Buda… - Journal of clinical …, 2017 - Elsevier
The present paper aims at providing an objective narrative review of the existing non-
pharmacological treatments for spasticity. Whereas pharmacologic and conventional …
pharmacological treatments for spasticity. Whereas pharmacologic and conventional …
Synthetic and natural compounds that interact with human cytochrome P450 1A2 and implications in drug development
Human cytochrome P450 1A2 (CYP1A2) is one of the major CYPs in the liver (&sim13%)
and metabolizes about 20% of clinically used drugs. CYP1A2 is a 515-residue protein with a …
and metabolizes about 20% of clinically used drugs. CYP1A2 is a 515-residue protein with a …
Assessing and treating functional impairment in poststroke spasticity
Poststroke spasticity (PSS) is associated with significant consequences for a patient's
functional status and quality of life. Nonetheless, no uniform definition of spasticity exists that …
functional status and quality of life. Nonetheless, no uniform definition of spasticity exists that …
Ciprofloxacin greatly increases concentrations and cypotensive effect of tizanidine by inhibiting its cytochrome P450 1A2–mediated presystemic metabolism
MT Granfors, JT Backman, M Neuvonen… - Clinical …, 2004 - Wiley Online Library
Background and objective Tizanidine, a centrally acting skeletal muscle relaxant, is
metabolized mainly by cytochrome P450 (CYP) 1A2 and has a low oral bioavailability. The …
metabolized mainly by cytochrome P450 (CYP) 1A2 and has a low oral bioavailability. The …