Musculoskeletal Diseases (Exam II) Flashcards
What is the pathophysiology of scleroderma?
- Autoimmune-mediated inflammatory vasculitis
-Fibrosis of skin and internal organs from abnormal deposition of extracellular collagen
-Microvascular changes produce tissue fibrosis and organ sclerosis - Also known as Systemic Sclerosis
What mnemonic guides the main symptoms associated with scleroderma?
Expound on the mnemonic.
- **Calcinosis
- **Raynaud’s
- **Esophageal reflux
- **Sclerodactyly
- **Telangiectasia’s
What signs and symptoms might be seen with Scleroderma?
- Skin: Taut skin, Contractures & myopathy
NS: Nerve compression
CV: Systemic and pulmonary HTN, Dysrhythmias, Vasospasms in small arteries of fingers, CHF
Pulmonary: Pulmonary fibrosis
Renal: Decreased RBF
GI: Xerostomia, poor dentition, fibrosis of GI tract and refulx
What does xerostomia mean?
Dry mouth
What treatments are used for scleroderma?
- Symptoms alleviation
- ACE-inhibitors: only treatment that has shown to alter course of disease
- PPIs for reflux
- Digoxin: improve CO
- Steroids
- CCBs for Raynaud’s
Pulm. HTN tx: PDE inhibitors, O2, anticoagulation and diuretics
What airway and pulmonary considerations exists for scleroderma?
- Pulmonary fibrosis (↓ compliance)
- Decreased ROM for airway
- Avoid increasing PVR
Anesthesia management for Airway and motion
- decreased mandibular motion
- small mouth opening
- decreased neck ROM
- oral bleeding
What dose of metoclopramide would be utilized for GI tract fibrosis from scleroderma?
Trick question. Metoclopramide would not work in this scenario.
What other scleroderma anesthesia management considerations are there?
- risk of corneal abrasions
- keep warm (Raynaud’s)
- VTE 3x more common in this population (steriod stress dose)
What is Duchenne’s Muscular Dystrophy (DMD)?
What initial symptoms are present at 2-5 years of age?
- X-linked dystrophin disorder resulting in muscle atrophy.
Dystrophin is a large protein that plays a major role in stabilization of the muscle membrane - (Ages 2-5) = waddling gait, frequent falling, can’t climb stairs, Gower’s sign.
What s/s are seen with DMD?
List:
CNS
Musculoskeletal
CV
Pulm
GI
- **CNS - intellectual disability
- **MS - kyphosis, muscle atrophy, ↑ CK
- **CV - ↑ HR, cardiomyopathy, short PR & tall R-wave
- **Pulm - weakened respiratory muscles and weak cough, OSA **30% of deaths are due to pulmonary reasons
- **GI - hypomotility & gastroparesis
What are the anesthetic concerns and interventions relevant to DMD patients?
- Airway
- Pulmonary
- CV
- GI
- Airway - weak laryngeal reflexes & cough
- Pulm - weakened muscles, increased secretions, possible vent support up to 36 hours
- CV - Get pre-op EKG & echo
- GI - delayed gastric emptying
What drug should be avoided with DMD patients?
- Succinylcholine (Rhabdo & ↑K⁺, MH)
use NDMBs
What type of anesthesia is prefereable for a DMD patient?
Regional (vs GA)
Why might one use less volatile gasses with DMD patients?
- DMD patients have ↑risk of malignant hyperthermia.
Ensure you have Dantrolene
What is the pathophysiology of myasthenia gravis?
- Chronic Autoimmune disorder
- ↓ function of NMJ post-synaptic ACh receptors.
- Muscle weakness and rapid exhaustion of voluntary muscles
αlpha sub-units of ACh receptor are bound by antibodies.
What organ is linked with the production of anti-ACh antibodies?
- Thymus
Which condition is characterized by partial recovery with rest?
Myasthenia Gravis
What test is used to diagnose myasthenia gravis?
Edrophonium/Tensilon Test
- 1-2 mg IVP
- Myasthenia symptoms improve with injection = (+) test
What signs/symptoms might be seen with myasthenia gravis?
- Ptosis & diplopia
- Dysphagia & dysarthria
- Muscle weakness
- Isolated respiratory failure
- Myocarditis
Differentiate Myasthenic Crisis and Cholinergic Crisis.
- Myasthenic Crisis - Insufficient drug therapy and resulting respiratory failure.
- Cholinergic Crisis - too much -stigmine drug = SLUDGE-M symptoms.
- Differentiate by: Edrophonium/Tensilon Test
1-2 mg IVP
Improves myasthenic crisis, makes cholinergic crisis worse
What drugs are the firstline treatment for Myasthenia Gravis?
What would be done if drugs were ineffective?
- Anticholinesterases
-Pyridostigmine > neostigmine - Surgical Thymectomy: induces remission, reduces need for immunosuppresants
What drugs/treatments other than pyridostigmine or surgery could be used for myasthenia gravis?
- Corticosteroids
- Azathioprine
- Cyclosporine
- Mycophenolate
- Plasmapheresis: removes antibodies from circulation
- Immunoglobulin: temporary effect
What anesthetic considerations exist for myasthenia gravis?
- Aspiration risk & weakened respiratory muscles.
- Sensitivity to NMBs (intubate without if possible)
- No succinylcholine (resistant to it)
What is osteoarthritis (OA)?
What makes the pain better?
- Degeneration of articular cartilage with minimal inflammation.
- Pain better at rest.
- Pain is worse with motion.
What are Heberden nodes?
What disease process do they indicate?
- Bony swellings of the distal interphalangeal joints.
- Osteoarthritis
What spinal complications occur from osteoarthritis?
- Vertebral degeneration
- Nucleus pulposus herniation
- Nerve root compression
What are the treatments for osteoarthritis?
- PT & exercise
- Maintenance of muscle function
- Pain relief
- Joint replacement surgery
Are osteoarthritis or rheumatoid arthritis patients prescribed corticosteroids?
- RA patients (no steroids for OA)
What anesthetic considerations exist for OA?
- Airway ROM
What is rheumatoid arthritis?
What hand condition is often seen on inspection?
- Auto-immune systemic inflammatory disease
- Swelling of the Proximal Interphalangeal, metocarpophalangeal, and elbow joints.
- Rheumatoid factor - IG is present in 90% of pts
What joints are usually spared by rheumatoid arthritis?
- Thoracic & Lumbosacral spine