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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 3.

Frequency by age of presence of ICD-9-CM codes for signs of HHT recorded among individuals with HHT (ICD-9-CM 448.0) in MarketScan Commercial and Supplemental Medicare Databases, 2005–2010 (excluding Michigan)

Condition <30 years (n = 160)
30–59 years (n = 621)
≥60 years (n = 422)
n % n % n %
Epistaxis 30 18.8 209 33.7 172 40.8

Brain AVM 18 11.3 35 5.6 12 2.8

Lung AVM 33 20.6 99 15.9 41 9.7

Unspecified AVM of vascular system 18 11.3 82 13.2 52 12.3

Arteriovenous fistula, acquired 0 5 0.8 4 1.0

Any AVM 52 32.5 154 24.8 79 18.7

Upper GI angiodysplasia 1 0.6 49 7.9 47 11.1

Angiodysplasia of the intestine 2 1.3 39 6.3 44 10.4

Hemorrhage of GI tract, unspecified 8 5.0 86 13.9 118 28.0

Anemia 23 14.4 304 49.0 275 65.2

Aneurysm or intracerebral hemorrhage 4 2.5 12 1.9 19 4.5

Hemoptysis 6 3.8 19 3.1 21 5.0

Dyspnea 37 23.1 175 28.2 170 40.3

Telangiectasia 17 10.6 57 9.2 46 10.9

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