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. Author manuscript; available in PMC: 2019 Nov 15.
Published in final edited form as: Birth Defects Res. 2018 Aug 2;110(19):1404–1411. doi: 10.1002/bdr2.1371

TABLE 1.

Potential and eligible records screened in the 2007–2011 MD STARnet pilot, by ICD code or other method

Method of record identification Records screened (n = 5,243) Screened records of eligible cases (n = 2,862) Percent of records deemed eligible
ICD-9-CM
  359.0 601 109 18.1
  359.1 2,629 1,435 54.6
  359.21 1,030 807 78.3
ICD-10
  G71.0 71 17 23.9
  G71.1 44 18 40.9
 Othera 1,096 665 50.5
 Totalb 5,471 3,051 55.8

Note. ICD-9-CM codes listed are: 359.0 congenital hereditary muscular dystrophy, 359.1 hereditary progressive muscular dystrophy, 359.21 myotonic muscular dystrophy. ICD-10 codes listed are: G71.0 muscular dystrophy and G71.1 myotonic disorders. MD STARnet = muscular dystrophy surveillance, tracking and research network; ICD-9-CM = International Classification of Diseases, Ninth Revision, Clinical Modification; ICD-10 = International Classification of Diseases, Tenth Revision.

a

Cases where ICD code was not documented were found through source lists that did not use ICD codes such as Duchenne or Becker muscular dystrophy cases already in the MD STARnet database and lists from sources that did not use ICD codes to identify cases.

b

Some cases were found at more than one source so number of records is greater than number of cases screened.