Difference between revisions of "Incidence and prevalence of idiopathic inflammatory myopathies among commercially insured, Medicare supplemental insured, and Medicaid enrolled populations: an administrative claims analysis"

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A review of the article by Smoyer-Tomic et al., ‘Incidence and prevalence of idiopathic inflammatory myopathies among commercially insured, Medicare supplemental insured, and Medicaid enrolled populations: an administrative claims analysis' <ref name=“Smoyer-Tomic 2012”> Smoyer-Tomic 2012. Incidence and prevalence of idiopathic inflammatory myopathies among commercially insured, Medicare supplemental insured, and Medicaid enrolled populations: an administrative claims analysis http://www-ncbi-nlm-nih-gov.ezproxyhost.library.tmc.edu/pubmed/22703603 </ref>
 
  
==Introduction==
 
Autoimmune idiopathic inflammatory myopathies (IIMs) have the following common characteristics: Auto-immune disorder, no known cause, muscle inflammation, and muscle weakness and consist of three types: polymyositis, dermatomyositis, and sporadic inclusion body myositis. Many studies have not examined IIM, however using data gathered from commercial insurance, Medicaid and Medicare, this study examined how common and frequent IIM is.
 
 
==Methods==
 
Data from 2004 - 2008 was gathered from:
 
# 130 unique commercial insurance companies for outpatient pharmacy claims for people under 65 (14 million enrollees annually)
 
# Medicare supplemental insurance paid for by employers for retired and working-age recipients (1.6 million individuals)
 
# Pooled Medicaid healthcare information from 10 states (28 million)
 
The data was filtered for patients over the age of 18 with an IIM treatment and patients who had a muscle biopsy; incidence and prevalence was then calculated.
 
 
==Results==
 
The study identified 2,990 incident cases with 2,477 (83%) were from the commercially insured/Medicare supplemental databases and 513 (17%) were from the Medicaid database with 1,072 had dermatomyositis, 1,784 had polymyositis, and .476 had interstitial myositis. The study also identified 7,155 prevalent patients 39.1% had dermatomyositis, 58.9% had polymyositis, and 9.8% had interstitial myositis.
 
 
==Discussion==
 
 
==Conclusion==
 
 
===Comments===
 
 
== References ==
 
 
<references/>
 
[[Category: Reviews]]
 
[[Category: Databases, Big Data, and Data Quality‏]]
 

Latest revision as of 00:40, 20 November 2015