Chapter 20 
Drugs Affecting Muscle Spasm 
and Spasticity 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Physiology 
• The human body contains approximately 600 skeletal 
muscles. 
• Skeletal muscle movement is voluntary. 
• Striated muscle is composed of two contractile proteins. 
• Muscle contraction is triggered by a sudden inflow of 
calcium ions (Ca2+). 
• In the resting state, the protein tropomyosin winds 
around actin and covers the myosin-binding sites. 
• Muscle contraction stops when Ca2+ is removed from the 
immediate environment of the myofilaments. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Muscle Fibers 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Pathophysiology 
• Muscle spasm 
– A muscle spasm is a sudden, violent involuntary 
contraction of a muscle or group of muscles. 
– Spasms are related to a localized skeletal muscle 
injury or an imbalance in electrolytes. 
– Tonic spasm is characterized by an unusually 
prolonged and strong muscular contraction. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Pathophysiology (cont.) 
• Spasticity 
– Spasticity is a condition in which certain muscles are 
continuously contracted. 
– This contraction causes stiffness or tightness of the 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
muscles. 
– Spasticity may be associated with spinal cord injury.
Centrally Acting Muscle Relaxants 
• They act in the central nervous system (CNS). 
• Prototype drug: cyclobenzaprine (Flexeril) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Cyclobenzaprine: Core Drug Knowledge 
• Pharmacotherapeutics 
– Manages muscle spasms associated with acute 
musculoskeletal disorders 
• Pharmacokinetics 
– Administered: oral. Metabolism: liver. Excreted: 
urine and bile. Onset: 1 hour. Duration: 12 to 24 
hours. 
• Pharmacodynamics 
– Relieves muscle spasms through a central action 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Cyclobenzaprine: Core Drug Knowledge 
(cont.) 
• Contraindications and precautions 
– Hyperthyroidism 
– 14 days within use of MAOIs 
• Adverse effects 
– CNS depression and anticholinergic activity 
– Arrhythmias, seizures, and MIs 
• Drug interactions 
– Tramadol, guanethidine, MAOIs, histamine-1 
blocking agents, and various herbal remedies 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Cyclobenzaprine: Core Patient Variables 
• Health status 
– Assess past medical history and drug allergies. 
• Life span and gender 
– Pregnancy Category B drug 
– Use precaution in administration to the elderly. 
• Lifestyle, diet, and habits 
– Avoid alcohol and other CNS depressant use. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
• Environment 
– Assess the environment where the drug will be given.
Cyclobenzaprine: Nursing Diagnoses and 
Outcomes 
• Risk for Injury related to CNS depressant effects and 
potential cardiovascular effects. 
– Desired outcome: The patient will remain free from 
injury throughout therapy. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Cyclobenzaprine: Planning and 
Interventions 
• Maximizing therapeutic effects 
– Take with full glass of water at evenly spaced 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
intervals. 
– Coordinate physical therapies with administration. 
• Minimizing adverse effects 
– Assess for excessive sedation. 
– Caution the patient about the potential for orthostatic 
hypotension.
Cyclobenzaprine: Teaching, Assessment, 
and Evaluation 
• Patient and family education 
– Take medication as prescribed. 
– Explain adverse effects. 
– Do not take with other OTC medications. 
• Ongoing assessment and evaluation 
– Evaluate the patient’s safety. 
– Monitor the level of sedation. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Cyclobenzaprine is chemically similar to which of the 
following drugs? 
– A. Adrenergic agents 
– B. Benzodiazepines 
– C. Tricyclic antidepressants 
– D. MAOIs
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• C. Tricyclic antidepressants 
• Rationale: Cyclobenzaprine is structurally similar to 
the tricyclic antidepressants.
Centrally Acting Spasmolytics 
• The centrally acting spasmolytics work in the CNS to 
reduce excessive reflex activity. 
• Allow muscle relaxation 
• Prototype drug: baclofen (Lioresal) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Baclofen: Core Drug Knowledge 
• Pharmacotherapeutics 
– Relieves some components of spinal spasticity 
• Pharmacokinetics 
– Administered: oral. Distribution: crosses blood–brain 
barrier. Metabolism: liver. Excreted: urine and bile. 
Peaks: 2 to 3 hours 
• Pharmacodynamics 
– Acts specifically at the spinal end of the upper motor 
neurons at GABAB receptors to cause 
hyperpolarization 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Baclofen: Core Drug Knowledge (cont.) 
• Contraindications and precautions 
– Hypersensitivity and spasticity of cerebral origin 
• Adverse effects 
– Drowsiness, weakness, dizziness and light-headedness, 
headache, nausea and vomiting, 
hypotension, constipation, lethargy and fatigue, 
confusion, insomnia, and increased urinary frequency 
• Drug interactions 
– CNS depressants or TCAs 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Baclofen: Core Patient Variables 
• Health status 
– Assess past medical history and allergies. 
– Perform physical assessment. 
• Life span and gender 
– Older patients are more susceptible to sedation. 
• Lifestyle, diet, and habits 
– Caution the patient about the concurrent use of 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
alcohol. 
• Environment 
– Assess the environment where the drug will be given. 
It is usually given at the home.
Baclofen: Nursing Diagnoses and 
Outcomes 
• Acute Pain related to headache, muscle pain, GI 
disturbances, or rash 
– Desired outcome: The patient will be provided with 
measures to decrease the discomfort of drug therapy 
and the possibility of nonadherence. 
• Risk for Disturbed Sensory Perception related to visual 
changes, vestibular dysfunction, and somatosensory 
changes 
– Desired outcome: The patient will be protected 
from injury if dizziness, weakness, visual changes, or 
perceptual changes occur. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Baclofen: Planning and Interventions 
• Maximizing therapeutic effects 
– Take with full glass of water at evenly spaced 
intervals. 
– If GI distress occurs, coordinate with meals. 
• Minimizing adverse effects 
– Ensure patient safety. 
– Do not abruptly stop the medication. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Baclofen: Teaching, Assessment, and 
Evaluation 
• Patient and family education 
– Teach the importance of patient safety. 
– Caution the patient about the concurrent use of 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
alcohol. 
• Ongoing assessment and evaluation 
– Monitor for the emergence of hallucinations or 
psychotic episodes. 
– Assess for improved symptoms of spasticity.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Baclofen therapy is effective at treating muscle spasms 
due to a cerebral vascular accident. 
– A. True 
– B. False
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. False 
• Rationale: Baclofen therapy does not affect skeletal 
muscle spasms resulting from CVA or parkinsonism. 
Baclofen does not treat this condition because of the 
mechanism of action of the drug.
Peripherally Acting Spasmolytics 
• Peripherally acting spasmolytics relax muscles through 
direct action on the skeletal muscle fibers. 
• They do not interfere with neuromuscular 
communication. 
• They have no CNS effects. 
• Prototype drug: dantrolene (Dantrium) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Dantrolene: Core Drug Knowledge 
• Pharmacotherapeutics 
– Used to treat malignant hyperthermia 
• Pharmacokinetics 
– Administered: oral or IV. Metabolism: liver. Excreted: 
kidneys. Peak: 5 hours. T½: 7.3 hours 
• Pharmacodynamics 
– Reduces the amount of Ca2+ released from the 
sarcoplasmic reticulum, thereby relaxing the muscle 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Dantrolene: Core Drug Knowledge (cont.) 
• Contraindications and precautions 
– Liver disease 
• Adverse effects 
– Muscle weakness, fatal hepatitis, seizures, and pleural 
effusion with pericarditis 
• Drug interactions 
– CNS depressants, clofibrate, estrogens, verapamil, 
and warfarin 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Dantrolene: Core Patient Variables 
• Health status 
– Assess past medical and physical assessment. 
• Life span and gender 
– Consider the age before administration. 
• Lifestyle, diet, and habits 
– Assess for lactose intolerance. 
• Environment 
– Can cause photosensitivity 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Dantrolene: Nursing Diagnoses and 
Outcomes 
• Risk for Injury related to muscular weakness 
– Desired outcome: The patient will be injury free 
despite muscular weakness. 
• Risk for diarrhea or constipation related to drug effects 
– Desired outcome: The patient will maintain 
baseline bowel habits. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Dantrolene: Nursing Diagnoses and 
Outcomes (cont.) 
• Risk for Disturbed Sensory Perception: Kinesthetic 
related to dizziness, malaise, and fatigue 
– Desired outcome: The patient will remain free of 
injury from adverse effects. 
• Disturbed Body Image related to drug-related 
dermatologic effects 
– Desired outcome: Any adverse effects will be 
resolved by the end of therapy. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Dantrolene: Planning and Interventions 
• Maximizing therapeutic effects 
– Administer with food or milk to avoid gastric distress. 
– Do not crush extended release capsules. 
• Minimizing adverse effects 
– Provide for patient safety. 
– Advise the use of sunscreen. 
– Titrate dose to maximum effectiveness. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Dantrolene: Teaching, Assessment, and 
Evaluation 
• Patient and family education 
– Explain why the drug is prescribed. 
– Discuss adverse effects of the drug. 
• Ongoing assessment and evaluation 
– Monitor for improvement in symptoms of spasticity 
and decrease in resistance to passive movement. 
– Monitor for adverse effects. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Dantrolene is used to treat which of the following 
condition(s)? 
– A. Hypertensive crisis 
– B. Malignant hyperthermia 
– C. Pain associated with lumbar stenosis 
– D. All of the above
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. Malignant hyperthermia 
• Rationale: IV dantrolene is the drug of choice for 
acute treatment of malignant hyperthermia. 
Preoperatively, it can be used orally or intravenously 
to prevent malignant hyperthermia in patients 
considered at risk.

Ppt chapter 20

  • 1.
    Chapter 20 DrugsAffecting Muscle Spasm and Spasticity Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 2.
    Physiology • Thehuman body contains approximately 600 skeletal muscles. • Skeletal muscle movement is voluntary. • Striated muscle is composed of two contractile proteins. • Muscle contraction is triggered by a sudden inflow of calcium ions (Ca2+). • In the resting state, the protein tropomyosin winds around actin and covers the myosin-binding sites. • Muscle contraction stops when Ca2+ is removed from the immediate environment of the myofilaments. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 3.
    Muscle Fibers Copyright© 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 4.
    Pathophysiology • Musclespasm – A muscle spasm is a sudden, violent involuntary contraction of a muscle or group of muscles. – Spasms are related to a localized skeletal muscle injury or an imbalance in electrolytes. – Tonic spasm is characterized by an unusually prolonged and strong muscular contraction. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 5.
    Pathophysiology (cont.) •Spasticity – Spasticity is a condition in which certain muscles are continuously contracted. – This contraction causes stiffness or tightness of the Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins muscles. – Spasticity may be associated with spinal cord injury.
  • 6.
    Centrally Acting MuscleRelaxants • They act in the central nervous system (CNS). • Prototype drug: cyclobenzaprine (Flexeril) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 7.
    Cyclobenzaprine: Core DrugKnowledge • Pharmacotherapeutics – Manages muscle spasms associated with acute musculoskeletal disorders • Pharmacokinetics – Administered: oral. Metabolism: liver. Excreted: urine and bile. Onset: 1 hour. Duration: 12 to 24 hours. • Pharmacodynamics – Relieves muscle spasms through a central action Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 8.
    Cyclobenzaprine: Core DrugKnowledge (cont.) • Contraindications and precautions – Hyperthyroidism – 14 days within use of MAOIs • Adverse effects – CNS depression and anticholinergic activity – Arrhythmias, seizures, and MIs • Drug interactions – Tramadol, guanethidine, MAOIs, histamine-1 blocking agents, and various herbal remedies Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 9.
    Cyclobenzaprine: Core PatientVariables • Health status – Assess past medical history and drug allergies. • Life span and gender – Pregnancy Category B drug – Use precaution in administration to the elderly. • Lifestyle, diet, and habits – Avoid alcohol and other CNS depressant use. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins • Environment – Assess the environment where the drug will be given.
  • 10.
    Cyclobenzaprine: Nursing Diagnosesand Outcomes • Risk for Injury related to CNS depressant effects and potential cardiovascular effects. – Desired outcome: The patient will remain free from injury throughout therapy. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 11.
    Cyclobenzaprine: Planning and Interventions • Maximizing therapeutic effects – Take with full glass of water at evenly spaced Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins intervals. – Coordinate physical therapies with administration. • Minimizing adverse effects – Assess for excessive sedation. – Caution the patient about the potential for orthostatic hypotension.
  • 12.
    Cyclobenzaprine: Teaching, Assessment, and Evaluation • Patient and family education – Take medication as prescribed. – Explain adverse effects. – Do not take with other OTC medications. • Ongoing assessment and evaluation – Evaluate the patient’s safety. – Monitor the level of sedation. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 13.
    Copyright © 2012Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Cyclobenzaprine is chemically similar to which of the following drugs? – A. Adrenergic agents – B. Benzodiazepines – C. Tricyclic antidepressants – D. MAOIs
  • 14.
    Copyright © 2012Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • C. Tricyclic antidepressants • Rationale: Cyclobenzaprine is structurally similar to the tricyclic antidepressants.
  • 15.
    Centrally Acting Spasmolytics • The centrally acting spasmolytics work in the CNS to reduce excessive reflex activity. • Allow muscle relaxation • Prototype drug: baclofen (Lioresal) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 16.
    Baclofen: Core DrugKnowledge • Pharmacotherapeutics – Relieves some components of spinal spasticity • Pharmacokinetics – Administered: oral. Distribution: crosses blood–brain barrier. Metabolism: liver. Excreted: urine and bile. Peaks: 2 to 3 hours • Pharmacodynamics – Acts specifically at the spinal end of the upper motor neurons at GABAB receptors to cause hyperpolarization Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 17.
    Baclofen: Core DrugKnowledge (cont.) • Contraindications and precautions – Hypersensitivity and spasticity of cerebral origin • Adverse effects – Drowsiness, weakness, dizziness and light-headedness, headache, nausea and vomiting, hypotension, constipation, lethargy and fatigue, confusion, insomnia, and increased urinary frequency • Drug interactions – CNS depressants or TCAs Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 18.
    Baclofen: Core PatientVariables • Health status – Assess past medical history and allergies. – Perform physical assessment. • Life span and gender – Older patients are more susceptible to sedation. • Lifestyle, diet, and habits – Caution the patient about the concurrent use of Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins alcohol. • Environment – Assess the environment where the drug will be given. It is usually given at the home.
  • 19.
    Baclofen: Nursing Diagnosesand Outcomes • Acute Pain related to headache, muscle pain, GI disturbances, or rash – Desired outcome: The patient will be provided with measures to decrease the discomfort of drug therapy and the possibility of nonadherence. • Risk for Disturbed Sensory Perception related to visual changes, vestibular dysfunction, and somatosensory changes – Desired outcome: The patient will be protected from injury if dizziness, weakness, visual changes, or perceptual changes occur. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 20.
    Baclofen: Planning andInterventions • Maximizing therapeutic effects – Take with full glass of water at evenly spaced intervals. – If GI distress occurs, coordinate with meals. • Minimizing adverse effects – Ensure patient safety. – Do not abruptly stop the medication. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 21.
    Baclofen: Teaching, Assessment,and Evaluation • Patient and family education – Teach the importance of patient safety. – Caution the patient about the concurrent use of Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins alcohol. • Ongoing assessment and evaluation – Monitor for the emergence of hallucinations or psychotic episodes. – Assess for improved symptoms of spasticity.
  • 22.
    Copyright © 2012Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Baclofen therapy is effective at treating muscle spasms due to a cerebral vascular accident. – A. True – B. False
  • 23.
    Copyright © 2012Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. False • Rationale: Baclofen therapy does not affect skeletal muscle spasms resulting from CVA or parkinsonism. Baclofen does not treat this condition because of the mechanism of action of the drug.
  • 24.
    Peripherally Acting Spasmolytics • Peripherally acting spasmolytics relax muscles through direct action on the skeletal muscle fibers. • They do not interfere with neuromuscular communication. • They have no CNS effects. • Prototype drug: dantrolene (Dantrium) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 25.
    Dantrolene: Core DrugKnowledge • Pharmacotherapeutics – Used to treat malignant hyperthermia • Pharmacokinetics – Administered: oral or IV. Metabolism: liver. Excreted: kidneys. Peak: 5 hours. T½: 7.3 hours • Pharmacodynamics – Reduces the amount of Ca2+ released from the sarcoplasmic reticulum, thereby relaxing the muscle Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 26.
    Dantrolene: Core DrugKnowledge (cont.) • Contraindications and precautions – Liver disease • Adverse effects – Muscle weakness, fatal hepatitis, seizures, and pleural effusion with pericarditis • Drug interactions – CNS depressants, clofibrate, estrogens, verapamil, and warfarin Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 27.
    Dantrolene: Core PatientVariables • Health status – Assess past medical and physical assessment. • Life span and gender – Consider the age before administration. • Lifestyle, diet, and habits – Assess for lactose intolerance. • Environment – Can cause photosensitivity Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 28.
    Dantrolene: Nursing Diagnosesand Outcomes • Risk for Injury related to muscular weakness – Desired outcome: The patient will be injury free despite muscular weakness. • Risk for diarrhea or constipation related to drug effects – Desired outcome: The patient will maintain baseline bowel habits. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 29.
    Dantrolene: Nursing Diagnosesand Outcomes (cont.) • Risk for Disturbed Sensory Perception: Kinesthetic related to dizziness, malaise, and fatigue – Desired outcome: The patient will remain free of injury from adverse effects. • Disturbed Body Image related to drug-related dermatologic effects – Desired outcome: Any adverse effects will be resolved by the end of therapy. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 30.
    Dantrolene: Planning andInterventions • Maximizing therapeutic effects – Administer with food or milk to avoid gastric distress. – Do not crush extended release capsules. • Minimizing adverse effects – Provide for patient safety. – Advise the use of sunscreen. – Titrate dose to maximum effectiveness. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 31.
    Dantrolene: Teaching, Assessment,and Evaluation • Patient and family education – Explain why the drug is prescribed. – Discuss adverse effects of the drug. • Ongoing assessment and evaluation – Monitor for improvement in symptoms of spasticity and decrease in resistance to passive movement. – Monitor for adverse effects. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 32.
    Copyright © 2012Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Dantrolene is used to treat which of the following condition(s)? – A. Hypertensive crisis – B. Malignant hyperthermia – C. Pain associated with lumbar stenosis – D. All of the above
  • 33.
    Copyright © 2012Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. Malignant hyperthermia • Rationale: IV dantrolene is the drug of choice for acute treatment of malignant hyperthermia. Preoperatively, it can be used orally or intravenously to prevent malignant hyperthermia in patients considered at risk.