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. Author manuscript; available in PMC: 2015 Jun 3.
Published in final edited form as: Genet Med. 2013 May 23;16(1):33–39. doi: 10.1038/gim.2013.66

Table 2.

Frequency of presence of ICD-9-CM codes for signs of HHT recorded among individuals with and without ICD-9-CM code 448.0 in MarketScan Commercial and Supplemental Medicare Databases, 2005–2010 (excluding Michigan)

Condition With HHT (N) % Without HHT (n) % Rate ratio
Epistaxis 411 34.2 294,938 0.82 42
Brain AVM 65 5.4 15,079 0.04 135
Lung AVM 173 14.4 10,285 0.03 480
Unspecified AVM of vascular system 152 12.6 17,441 0.05 252
Arteriovenous fistula, acquired 9 0.8 5,005 0.01 80
Any AVM 285 23.7 45,600 0.13 182
Upper GI angiodysplasia 97 8.1 7,613 0.02 405
Angiodysplasia of the intestine 85 7.1 15,606 0.04 178
Hemorrhage of GI tract, unspecified 212 17.6 274,404 0.76 23
Anemia 602 50.0 1,997,615 5.55 9
Aneurysm or intracerebral hemorrhage 35 2.9 54,313 0.15 19
Hemoptysis 46 3.8 72,879 0.20 19
Dyspnea 382 31.8 3,143,068 8.73 4
Telangiectasia 120 10.0 43,849 0.12 83

AVM, arteriovenous malformation; GI, gastrointestinal; HHT, hereditary hemorrhagic telangiectasia; ICD-9-CM, International Classification of Disease, 9th Revision, Clinical Modification.