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Polymyositis 2

Polymyositis is an autoimmune disease characterized by inflammation and weakness of the muscles. It has a prevalence of 5-22 per 100,000 individuals and is more common in females, African Americans, and those aged 31-60 years old. The cause is unknown but may be related to certain medications, autoimmune diseases, or cancers. Muscle tissue is damaged by autoimmune cells and inflammation, leading to muscle fiber breakdown and weakness. Treatment involves corticosteroids, immunosuppressants, physical therapy, and assistive devices. Prognosis depends on severity and treatment response, but physical therapy can help improve strength and function.

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0% found this document useful (0 votes)
61 views15 pages

Polymyositis 2

Polymyositis is an autoimmune disease characterized by inflammation and weakness of the muscles. It has a prevalence of 5-22 per 100,000 individuals and is more common in females, African Americans, and those aged 31-60 years old. The cause is unknown but may be related to certain medications, autoimmune diseases, or cancers. Muscle tissue is damaged by autoimmune cells and inflammation, leading to muscle fiber breakdown and weakness. Treatment involves corticosteroids, immunosuppressants, physical therapy, and assistive devices. Prognosis depends on severity and treatment response, but physical therapy can help improve strength and function.

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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Polymyositis

Emma Vaitkevicius, Kennedy Klein, Amber


Lister, Madison Chapin, Melissa Takacs
Prevalence, Incidence, and Etiology

● 5-22 per 100,000


● Mean age → 31 - 60 y/o
● Higher prevalence in Females and
African - American populations
Prevalence, Incidence, Etiology

● Idiopathic, meaning no known cause, linked to:


○ Medicine
■ Myotoxic agents
■ Example: cholesterol - lowering drugs
○ Autoimmune diseases
■ lupus, RA, scleroderma, etc.
○ Cancers
■ Hodgkin's lymphoma
● Potential hereditary indication
● No known way to prevent or transmit
Pathology
● Autoimmune disease affecting muscle tissue
● The cells involved
○ Cytotoxic T lymphocytes and macrophages
○ Muscular antigens
● Direct damage to Muscle tissue
○ Autoimmune reaction causes muscle fiber breakdown
○ Breakdown damage causes release of inflammatory mediators
○ Abnormal activation of cytotoxic T cells and macrophages
Pathology
● Secondary problems may include dermatomyositis and inclusion body
myositis (IBM)
● Course of disease:
○ Muscle weakness develops over weeks to months
○ Rare cases- acute muscle weakness
○ No incubation period
● Treatment:
○ Corticosteroids
○ Immunosuppressants
Diagnosis and Treatment
● Diagnosis
○ Blood tests - Increased muscle enzymes
○ Electromyography - Changes in pattern
○ MRI - Detect inflammation
○ Muscle Biopsy - Analyze abnormalities
● Treatment
○ No cure
○ Muscle strengthening (PT)
○ Medication - corticosteroid drug, immunosuppressive agents
○ Thermotherapy
○ Orthotics and assistive devices
Sign and Symptoms
● Bilateral muscle weakness most proximal to the trunk
● If muscle weakness is an extreme case
○ Respiratory failure and pneumonia
● Difficulty swallowing
○ Malnutrition
Prognosis
● Problems
○ Difficulty performing ADLs
○ Increased risk of falling
○ Arthritis
○ Shortness of breath
○ Difficulty swallowing/speaking
○ Heart arrhythmias
● Effect of Treatment
○ Physical therapy can help gain back strength and flexibility
○ Medications prevent symptoms and cause disease to go dormant
Prognosis Cont’d
● Long term disabilities
○ Difficulty swallowing- could lead to malnutrition
■ If throat/neck muscles are affected
○ Aspiration pneumonia
○ Breathing problems
■ If chest muscles are affected
● Physical therapy prognosis
○ PT is a treatment option! Strength and stretching exercises would be utilized to prevent
worsening of symptoms and gain back lost function
○ It has been proven that physical therapy paired with medication has had great impact on
preventing progression of disease
Implications and Disease Management for Physical
Therapists
● Presentations for differential diagnosis
○ Bilateral muscle weakness surrounding trunk muscles
○ Abnormal increase in muscle enzymes in blood tests
○ EMG or MRI performed following blood tests
● Disease management with PT
○ PT can be a significant intervention to maintain and improve muscular strength
○ Earlier treatment better prognosis
○ Muscles that are are affected and not exercised are at increased risk for severe atrophy
● PT implications
○ Studies have shown that aerobic and low-intensity resistance exercise have improved function
○ Focusing on rest days during severe flare ups to prevent further injuries to affected muscles.
Contraindications and Precautions for Physical Therapy
● Contraindications
○ Acute pathology flare ups
○ Severe pain, uncontrolled bp or irregular heartbeat
● Treatment/intervention precautions
○ difficulty swallowing
○ breathing problems
○ aspiration pneumonia
○ Polymyositis linked to other autoimmune disorders and cancers
Clinical Pearls
● Low risk in 18 y/o and younger
● While it can not be cured, it can be managed
● Bilateral muscle weakness mostly proximal to the trunk
○ When experiencing flare ups, as a PT, be cautious for when and how you treat them
● Associated with other conditions
Questions:
1. What are the basic word parts for the term, Polymyositis?
a. Many - muscle - infection
b. one - muscle - infection
c. Many - cell - inflammation
d. Many - muscle - inflammation

2. All of these individuals have a higher risk of developing polymyositis,


except:
a. 50 y/o female
b. 33 y/o african - american male
c. 16 y/o male
d. 59 y/o male with lupus
Sources
Bronner IM, van der Meulen MF, de Visser M, et al. Long-term outcome in polymyositis and dermatomyositis. Annals of the Rheumatic Diseases. 2006;65(11):1456-
1461. doi:10.1136/ard.2005.045690

Cheeti A, Brent LH, Panginikkod S. Autoimmune Myopathies. June 2022. https://www.ncbi.nlm.nih.gov/books/NBK532860/. Accessed September 28, 2022.

Dalakas MC, Hohlfeld R. Polymyositis and Dermatomyositis. The Lancet. 2003;362(9388):971-982.


https://www.sciencedirect.com/science/article/pii/S0140673603143681?via%3Dihub. Accessed September 28, 2022.

Findlay AR, Goyal NA, Mozaffar T. An overview of polymyositis and dermatomyositis. Muscle & Nerve. 2015;51(5):638-656. doi:10.1002/mus.24566

Polymyositis. Johns Hopkins Medicine. https://www.hopkinsmedicine.org/health/conditions-and-diseases/polymyositis. Published May 13, 2019. Accessed September
28, 2022.

Polymyositis. Mayo Clinic. https://www.mayoclinic.org/diseases-conditions/polymyositis/symptoms-causes/syc-20353208. Published August 10, 2022. Accessed


September 28, 2022.

Sarwar A, Dydyk AM, Jatwani S. Polymyositis. May 2022. https://www.ncbi.nlm.nih.gov/books/NBK563129/. Accessed September 28, 2022.

Valiyil R, Christopher-Stine L. Drug-related myopathies of which the clinician should be aware. Current Rheumatology Reports. 2010;12(3):213-220.
doi:10.1007/s11926-010-0104-3

Van der Meulen MFG, Bronner IM, Hoogendijk JE, et al. Polymyositis. Neurology. 2003;61(3):316-321. doi:10.1212/wnl.61.3.316
Photo Sources
Polymyositis. osmosis. https://www.osmosis.org/learn/Polymyositis. Accessed September 30, 2022.

Silver N. How does polymyositis affect your muscles? Healthline. https://www.healthline.com/health/polymyositis.


Published April 19, 2022. Accessed September 30, 2022.

William C. Shiel Jr. MD. Polymyositis & dermatomyositis treatment, symptoms & diagnosis. MedicineNet.
https://www.medicinenet.com/polymyositis/article.htm. Published January 4, 2021. Accessed September 30, 2022.

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