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Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Chapter 20 Drugs Affecting Muscle Spasm and Spasticity

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Page 1: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Chapter 20

Drugs Affecting Muscle Spasm and Spasticity

Chapter 20

Drugs Affecting Muscle Spasm and Spasticity

Page 2: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Physiology 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.

Page 3: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Muscle FibersMuscle Fibers

Page 4: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Pathophysiology 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.

Page 5: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Pathophysiology (cont.)Pathophysiology (cont.)

• Spasticity

– Spasticity is a condition in which certain muscles are continuously contracted.

– This contraction causes stiffness or tightness of the muscles.

– Spasticity may be associated with spinal cord injury.

Page 6: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Centrally Acting Muscle Relaxants Centrally Acting Muscle Relaxants

• They act in the central nervous system (CNS).

• Prototype drug: cyclobenzaprine (Flexeril)

Page 7: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Cyclobenzaprine: Core Drug Knowledge 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

Page 8: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Cyclobenzaprine: Core Drug Knowledge(cont.) 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

Page 9: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Cyclobenzaprine: Core Patient Variables 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.

• Environment

– Assess the environment where the drug will be given.

Page 10: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Cyclobenzaprine: Nursing Diagnoses and Outcomes 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.

Page 11: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Cyclobenzaprine: Planning and InterventionsCyclobenzaprine: Planning and Interventions

• Maximizing therapeutic effects

– Take with full glass of water at evenly spaced intervals.

– Coordinate physical therapies with administration.

• Minimizing adverse effects

– Assess for excessive sedation.

– Caution the patient about the potential for orthostatic hypotension.

Page 12: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Cyclobenzaprine: Teaching, Assessment, and EvaluationCyclobenzaprine: 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.

Page 13: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Cyclobenzaprine is chemically similar to which of the following drugs?

– A. Adrenergic agents

– B. Benzodiazepines

– C. Tricyclic antidepressants

– D. MAOIs

Page 14: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• C. Tricyclic antidepressants

• Rationale: Cyclobenzaprine is structurally similar to the tricyclic antidepressants.

Page 15: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Centrally Acting Spasmolytics Centrally Acting Spasmolytics

• The centrally acting spasmolytics work in the CNS to reduce excessive reflex activity.

• Allow muscle relaxation

• Prototype drug: baclofen (Lioresal)

Page 16: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Baclofen: Core Drug Knowledge 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

Page 17: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Baclofen: Core Drug Knowledge (cont.)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

Page 18: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Baclofen: Core Patient Variables 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 alcohol.

• Environment

– Assess the environment where the drug will be given. It is usually given at the home.

Page 19: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Baclofen: Nursing Diagnoses and Outcomes 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.

Page 20: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Baclofen: Planning and InterventionsBaclofen: 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.

Page 21: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Baclofen: Teaching, Assessment, and EvaluationBaclofen: Teaching, Assessment, and Evaluation

• Patient and family education

– Teach the importance of patient safety.

– Caution the patient about the concurrent use of alcohol.

• Ongoing assessment and evaluation

– Monitor for the emergence of hallucinations or psychotic episodes.

– Assess for improved symptoms of spasticity.

Page 22: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Baclofen therapy is effective at treating muscle spasms due to a cerebral vascular accident.

– A. True

– B. False

Page 23: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• 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.

Page 24: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Peripherally Acting Spasmolytics 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)

Page 25: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dantrolene: Core Drug Knowledge 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

Page 26: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dantrolene: Core Drug Knowledge (cont.)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

Page 27: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dantrolene: Core Patient Variables 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

Page 28: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dantrolene: Nursing Diagnoses and Outcomes 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.

Page 29: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dantrolene: Nursing Diagnoses and Outcomes (cont.)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.

Page 30: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dantrolene: Planning and InterventionsDantrolene: 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.

Page 31: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Dantrolene: Teaching, Assessment, and EvaluationDantrolene: 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.

Page 32: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• 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

Page 33: Ppt chapter 20

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• 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.