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Neurology. 2013 Feb 5;80(6):583-9. doi: 10.1212/WNL.0b013e318282334e.

Can outcomes in Duchenne muscular dystrophy be improved by public reporting of data?

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  • 1University of Rochester Medical Center, Rochester, NY, USA.

Abstract

OBJECTIVE:

To review current approaches for obtaining patient data in Duchenne muscular dystrophy (DMD) and consider how monitoring and comparing outcome measures across DMD clinics could facilitate standardized and improved patient care.

METHODS:

We reviewed annual standardized data from cystic fibrosis (CF) clinics and DMD care guidelines and consensus statements; compared current approaches to obtain DMD patient data and outcome measures; and considered the best method for implementing public reporting of outcomes, to drive improvements in health care delivery.

RESULTS:

Current methods to monitor DMD patient information (MD STARnet, DuchenneConnect, and TREAT-NMD) do not yet provide patients with comparative outcome data. The CF patient registry allows for reporting of standard outcomes across clinics and is associated with improved CF outcomes. A similar patient registry is under development for the Muscular Dystrophy Association (MDA) clinic network. Suggested metrics for quality care include molecular diagnosis, ambulatory status and age at loss of ambulation, age requiring ventilator support, and survival.

CONCLUSIONS:

CF longevity has increased by almost 33% from 1986 to 2010, in part due to a CF patient registry that has been stratified by individual care centers since 1999, and publically available since 2006. Implementation of outcome reporting for MDA clinics might promote a similar benefit to patients with DMD.

PMID:
23382369
PMCID:
PMC3589293
DOI:
10.1212/WNL.0b013e318282334e
[PubMed - indexed for MEDLINE]
Free PMC Article
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