Drugs for Muscles and Joint Disease and Pain

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Presentation transcript:

Drugs for Muscles and Joint Disease and Pain Chapter 13 Drugs for Muscles and Joint Disease and Pain

Muscles and Joints Bones of the skeletal system provide framework of the body Are connected at joints Joint: place of union or junction between 2 or more bones Skeletal muscles: provide movement at joints, contractile tissues

Anatomy of a Joint

Bones, Muscles, and Tendon for Movement at Elbow Joint

Three Types of Muscle

Muscle Relaxants Skeletal muscle contractions voluntarily Neurotransmitter acetylcholine (Ach) binds with receptors on muscle cell membrane calcium is released, causing a contraction Relaxation occurs when ACh is broken down by acetylcholinesterase

Muscle Relaxants Medications Acts on motor neurons or at neuromuscular junction Block normal muscle function by Blocking release of ACh Preventing destruction of Ach Preventing ACh from reaching receptors

Dispensing Issues of Muscle Relaxants To avoid drug interactions, drug history needed before administering Technician often obtains drug history Sedative properties cause patient to relax, reducing reflex impulse conduction

Side Effects of Muscle Relaxants Sedation Reduced mental alertness Reduced motor abilities GI upset Avoid alcohol when taking these drugs

carisoprodol (Soma) Skeletal muscle relaxant subject to abuse Scheduled substance in many states Causes drowsiness and dizziness Toxicity risk increases with alcohol or other CNS depressants

cyclobenzapine (Flexeril) Centrally acting skeletal muscle relaxant related to TCAs Treats muscle spasms associated with acute musculoskeletal conditions Onset of action is within 1 hour Not to be used more than 2 to 3 weeks

Discussion Most muscle relaxants are not controlled substances, so why are they highly abused? They are abused due to the relaxing feeling that patients have from taking them.

Inflammation and Swelling Analgesics used to relieve pain Nonnarcotic analgesic used for mild-to-moderate pain, inflammation, and fever Two types of pain Somatic: dull, throbbing pain from skin, muscle, or bone Visceral: sharp, stabbing pain from organs

Inflammation Pain pathway in tissue injury PGs can cause inflammation, tissue damage, and fever Nonnarcotic analgesics interrupt pathway, inhibiting enzyme to synthesize PGs Relieves inflammation and pain Reduces fever

Pain Pathway in Tissue Injury

NSAIDs Properties of nonsteroidal anti-inflammatory drugs (NSAIDs) Analgesic (pain relieving) Anti-inflammatory Antipyretic (fever reducing) Prototype NSAID is aspirin

Therapeutic Uses of NSAIDs Inflammation and pain of arthritis and rheumatism Headache Menstrual cramps Backache Muscle aches Flu Fever Gouty arthritis

Mechanism of Action of NSAIDs Inhibit PG synthesis in inflamed tissues Prevents sensitization of pain receptors Generally act peripherally, not centrally like other pain killers

The GI System and NSAIDs Primary side effect is GI upset One in five chronic NSAID users develop some type of GI gastropathy Many patients need to take a proton pump inhibitor with NSAIDs

Side Effects of NSAIDs Nausea Abdominal cramps Heartburn Ulcers Indigestion Kidney damage Acute renal failure Fluid retention Hypertension Hyperkalemia Liver abnormalities Bone marrow depression Tinnitus and others

Interactions with NSAIDs Other NSAIDs including aspirin Beta blockers Cyclosporine Digoxin Diuretics Methotrexate Oral hypoglycemics Warfarin

Tips for NSAID Users Take with food Use antacids or proton pump inhibitor Do not use gastric irritants (ETOH) Stop NSAID before any surgical procedure Use the lowest possible dose Be aware of side effects Take sufficient fluids If sensitive to aspirin, avoid NSAIDs

Precautions of NSAIDs Concurrent use with multiple NSAIDs, including aspirin, should be discouraged Could lead to additive or synergistic toxicity Use of NSAIDs and opiates may be synergistic Considerable patient-to-patient variability to different NSAIDs

ibuprofen (Advil, Motrin) Controls fever well Can be alternated with aspirin OTC: 200 mg tablet, caplet, or capsule (solids) Rx: 400 mg, 600 mg, and 800 mg solids (tablets)

naproxen (Naprosyn) Least risky NSAID for cardiovascular events Used in lowest effective dose for least amount of time

COX-2 Inhibitors 2 enzymes critical in inflammation process Cyclooxygenase-1 (COX-1): extensive role in body, including protecting GI lining Cyclooxygenase-2 (COX-2): pain, inflammation Drugs only block the COX-2 enzyme which is induced during inflammation

Therapeutic Uses of COX-2 Inhibitors Rheumatoid arthritis Osteoarthritis Menstrual cramps Acute pain

celecoxib (Celebrex) First COX-2 inhibitor to be approved GI upset is primary side effect Only COX-2 inhibitor on the market All others recalled by FDA

Dispensing Issues of celecoxib (Celebrex) Technician—attach the label “Take with Food” Beware of cross-sensitivity with sulfonamides May increase cardiovascular risk Look-alike and sound-alike Celebrex Cerebyx (anticonvulsant)

allopurinol (Zyloprim) Used to prevent gout attacks Liver function should be monitored Used with caution with diuretics