eMedicine Specialties > Emergency Medicine > Allergy & Immunology
Polymyositis: Follow-up
Updated: Aug 25, 2009
Follow-up
Further Outpatient Care
- Physical therapy should begin early in the course of polymyositis to maintain mobility and strength.
- Findings from continuing clinical assessment and muscle enzyme abnormalities guide the duration of treatment.
Complications
- Pneumonia
- Infection
- Myocardial infarction
- Carcinoma (especially in the breast and lung)
- Severe dysphagia
- Interstitial lung disease
- Aspiration pneumonitis
- Steroid myopathy or other complications of steroid therapy
Prognosis
- Overall, the 5-year mortality rate for polymyositis (PM) and dermatomyositis (DM) is 20%.
- Significant morbidity is associated with these diseases, and medications used in treating them may also cause significant side effects.
- Death is closely related to presence of malignancy or respiratory/pulmonary involvement.2
- Residual weakness occurs in approximately 30% of patients.
- Persistent active disease is present in approximately 20% of patients.
- Survival is less likely in women and African American patients.
- Most patients improve with therapy.
- Full recovery is expected in 50% of patients.
Patient Education
- The Myositis Association of America Web site is an excellent resource for patients with inflammatory myopathies, their families, and the medical community.
Miscellaneous
Medicolegal Pitfalls
- Failure to consider an underlying malignancy when diagnosing DM or PM
More on Polymyositis |
| Overview: Polymyositis |
| Differential Diagnoses & Workup: Polymyositis |
| Treatment & Medication: Polymyositis |
Follow-up: Polymyositis |
| Multimedia: Polymyositis |
| References |
| « Previous Page | Next Page » |
References
Hengstman GJ, van den Hoogen FH, van Engelen BG. Treatment of the inflammatory myopathies: update and practical recommendations. Expert Opin Pharmacother. May 2009;10(7):1183-90. [Medline].
Bronner IM, van der Meulen MF, de Visser M, Kalmijn S, van Venrooij WJ, Voskuyl AE. Long-term outcome in polymyositis and dermatomyositis. Ann Rheum Dis. Nov 2006;65(11):1456-61. [Medline].
Amato AA, Barohn RJ. Idiopathic inflammatory myopathies. Neurol Clin. Aug 1997;15(3):615-48. [Medline].
Chahin N, Engel AG. Correlation of muscle biopsy, clinical course, and outcome in PM and sporadic IBM. Neurology. Sep 26 2007;[Medline].
Christopher-Stine L, Plotz PH. Myositis: an update on pathogenesis. Curr Opin Rheumatol. Nov 2004;16(6):700-6. [Medline].
Dalakas MC, Hohlfeld R. Polymyositis and dermatomyositis. Lancet. Sep 20 2003;362(9388):971-82. [Medline].
Dalakas MC, Sivakumar K. The immunopathologic and inflammatory differences between dermatomyositis, polymyositis and sporadic inclusion body myositis. Curr Opin Neurol. Jun 1996;9(3):235-9. [Medline].
Hengstman GJ, van Engelen BG. Polymyositis, invasion of non-necrotic muscle fibres, and the art of repetition. BMJ. Dec 18 2004;329(7480):1464-7. [Medline]. [Full Text].
Koopman WJ. Polymyositis/dermatomyositis classification criteria. In: Arthritis and Allied Conditions. 1997:17-8.
Mastaglia FL, Ojeda VJ. Inflammatory myopathies: Part 1. Ann Neurol. Mar 1985;17(3):215-27. [Medline].
Nirmalananthan N, Holton JL, Hanna MG. Is it really myositis? A consideration of the differential diagnosis. Curr Opin Rheumatol. Nov 2004;16(6):684-91. [Medline].
Olsen NJ, Park JH. Inflammatory myopathies: issues in diagnosis and management. Arthritis Care Res. Jun 1997;10(3):200-7. [Medline].
Further Reading
Keywords
polymyositis, PM, dermatomyositis, DM, inclusion body myositis, idiopathic inflammatory myopathy, inflammatory muscle disease, immune-mediated muscle inflammation, proximal muscle weakness, dysphagia, aspiration, arthralgias, muscle atrophy, heliotrope rash, purple-red edematous periorbital eruption, scaly purple-erythematous papular eruption over knuckles, Gottron sign, conduction defects, arrhythmias, myocarditis, interstitial lung disease, aspiration pneumonia, skeletal muscle disease
Follow-up: Polymyositis