Literature DB >> 31158891

Summary of Selected Healthcare Encounters among a Selection of Patients with Myotonic Muscular Dystrophy.

Kevin J Bennett1, Joshua R Mann1, Lijing Ouyang1.   

Abstract

OBJECTIVE: Research has not examined the use of health care by patients with myotonic muscular dystrophy (MMD), but it would provide insights into this population, which is prone to comorbidities and high service needs. This study is an analysis of this understudied subgroup, using a unique linked dataset to examine the characteristics and healthcare utilization patterns for people with MMD.
METHODS: This analysis used 3 South Carolina datasets (2009-2014). The subjects included individuals with at least 1 encounter with an International Classification of Diseases, Ninth Revision, Clinical Modification code of 359.21. The variables included sex, race, visit type, payer, and diagnoses. The analyses examined characteristics and number of encounters.
RESULTS: The subjects were predominately female, white, and 45 to 64 years old. A total of 44.6% of the study population had at least 1 inpatient visit, whereas 64.2% had at least 1 emergency department visit. A majority of the subjects had at least 1 office visit (55.0%), and most (85.3%) did not have a home health encounter.
CONCLUSIONS: Investigation of the reasons for these inpatient and emergency department encounters may be helpful in identifying ways to deliver high-quality care.

Entities:  

Mesh:

Year:  2019        PMID: 31158891      PMCID: PMC7667993          DOI: 10.14423/SMJ.0000000000000987

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  25 in total

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2.  Hospitalizations and emergency room visits for adolescents and young adults with muscular dystrophy living in South Carolina.

Authors:  Joshua R Mann; Julie A Royer; Suzanne Mcdermott; James W Hardin; Orgul Ozturk; Natalie Street
Journal:  Muscle Nerve       Date:  2015-08-14       Impact factor: 3.217

3.  Use of state administrative data sources to study adolescents and young adults with rare conditions.

Authors:  J A Royer; J W Hardin; S McDermott; L Ouyang; J R Mann; O D Ozturk; J Bolen
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4.  Pain in patients with myotonic dystrophy type 2: a postal survey in Finland.

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Journal:  Muscle Nerve       Date:  2012-01       Impact factor: 3.217

5.  Utilizing Combined Claims and Clinical Datasets for Research Among Potential Cases of Rare Diseases.

Authors:  Kevin J Bennett; Joshua Mann; Lijing Ouyang
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Review 6.  Myotonic Dystrophy Type 1 Management and Therapeutics.

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7.  Usual source of care and unmet health care needs: interaction of disability with race and ethnicity.

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Journal:  Med Care       Date:  2014-10       Impact factor: 2.983

8.  Difference, disparity, and disability: a comparison of health, insurance coverage, and health service use on the basis of race/ethnicity among US adults with disabilities, 2006-2008.

Authors:  Stephen P Gulley; Elizabeth K Rasch; Leighton Chan
Journal:  Med Care       Date:  2014-10       Impact factor: 2.983

Review 9.  Does integrated care reduce hospital activity for patients with chronic diseases? An umbrella review of systematic reviews.

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Journal:  BMJ Open       Date:  2016-11-21       Impact factor: 2.692

Review 10.  Myotonic disorders: A review article.

Authors:  Chris Hahn; Mohammad Kian Salajegheh
Journal:  Iran J Neurol       Date:  2016-01-05
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  1 in total

1.  Healthcare resource utilization, total costs, and comorbidities among patients with myotonic dystrophy using U.S. insurance claims data from 2012 to 2019.

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Journal:  Orphanet J Rare Dis       Date:  2022-02-23       Impact factor: 4.303

  1 in total

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