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Disease staging: CliniCal anD CoDeD Criteria - HCUP

Disease staging: CliniCal anD CoDeD Criteria - HCUP

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Clinical <strong>Criteria</strong> with Description, Diagnostic Findings and ICD-9-CM codes<br />

DXCat Number: MUS32<br />

MultiStage: No<br />

DXCat Label: Muscular Dystrophy Specificity: A<br />

Etiology: Genetic (or hereditary)<br />

Stage Description Diagnostic findings ICD-9-CM Codes<br />

1.01 Distal muscular dystrophy Distal muscular dystrophy [physical examination or genetic analysis report]<br />

DX 3591;<br />

1.02 Becker muscular dystrophy or limb-girdle<br />

dystrophy<br />

Becker muscular dystrophy [physical examination or genetic analysis report or Western Blot<br />

analysis report]<br />

NO;<br />

OR limb-girdle dystrophy [physical examination or Western Blot analysis report or genetic<br />

1.03 Myotonic dystrophy or ocular muscular<br />

dystrophy or fascioscapulohumeral<br />

analysis reports limb-girdle dystrophy subtype]<br />

Myotonic dystrophy [physical examination or genetic analysis report an unstable expansion of a<br />

CTG trinucleotide repeat sequence in a gene at 19q13.3]<br />

DX 3590, 3592-35923, 35929;<br />

dystrophy or congenital muscular OR ocular muscular dystrophy [physical examination]<br />

dystrophy or oculopharyngeal muscular<br />

dystrophy<br />

OR facioscapulohumeral dystrophy [physical examination or genetic analysis report defect at<br />

chromosome 4q35]<br />

OR congenital muscular dystrophy [physical examination or laminin α2 deficiency by muscle<br />

biopsy or defect in chromosome 6q22-23 by genetic analysis report]<br />

OR oculopharyngeal muscular dystrophy [physical examination or genetic defect in<br />

chromosome 14q]<br />

2.01 Duchennic type muscular dystrophy Duchennic type muscular dystrophy [physical examination or dystrophin in muscle tissue by<br />

Western Blot analysis report or dystrophin gene at short arm of the X chromosome at Xp21 by<br />

genetics report]<br />

2.02 with hypertension Stage 1.01 2.01<br />

AND hypertension:<br />

2.03 with mental retardation Stage 1.01-2.02<br />

AND mental retardation:<br />

2.04 with pneumonia Stage 1.01-2.03<br />

AND pneumonia:<br />

2.05 with cardiomyopathy or cardiac conduction<br />

abnormalities<br />

Stage 1.01-2.04<br />

Cardiomyopathy [echocardiogram report]<br />

OR cardiac conduction abnormalities:<br />

3.01 with congestive heart failure Stage 1.01-2.05<br />

AND congestive heart failure:<br />

3.02 with respiratory failure Stage 1.01-3.01<br />

AND respiratory failure:<br />

3.03 with shock Stage 1.01-3.02<br />

AND shock:<br />

NO;<br />

STAGE 1.01-1.03 + DXCAT CVS13;<br />

STAGE 1.01-2.02 + DXCAT NEU15;<br />

STAGE 1.01-2.03 + (DXCAT RES15<br />

OR DXCAT RES16 OR DXCAT<br />

RES17 OR DXCAT RES12 OR<br />

DXCAT RES19 OR DX 5070);<br />

STAGE 1.01-2.04 + (DX 4250-<br />

4254, 4257-4259 OR DXCAT<br />

CVS08);<br />

STAGE 1.01-2.05 + (GROUP<br />

CHF__HTNIVE OR GROUP<br />

CHF__NON_HTN);<br />

STAGE 1.01-3.01 + GROUP<br />

RESP_FAIL;<br />

STAGE 1.01-3.02 + (GROUP<br />

SHOCKC OR GROUP SHOCKN) ;<br />

Thursday, January 07, 2010 9:22:39 AM<br />

©2010 Thomson Reuters. All rights reserved.

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