Epidemiology and Trends of Hereditary Hemorrhagic Telangiectasia in the United States

被引:8
作者
Ferry, Andrew M. [1 ]
Wright, Alex E. [1 ]
Baillargeon, Gwen [2 ]
Kuo, Yong-Fang [2 ]
Chaaban, Mohamad R. [3 ]
机构
[1] Univ Texas Med Branch, Sch Med, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Prevent Med & Community Hlth, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, Dept Otolaryngol, 301 Univ Blvd, Galveston, TX 77555 USA
关键词
hereditary hemorrhagic telangiectasia; epistaxis; thrombosis; hemorrhage; complications; epidemiology; prevalence; incidence; ICD-10; ARTERIOVENOUS-MALFORMATIONS; VASCULAR MALFORMATIONS; YOUNGS PROCEDURE; RISK; COMPLICATIONS; PREGNANCY; EPISTAXIS; WOMEN;
D O I
10.1177/1945892419886756
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background To our knowledge, no national studies have investigated the epidemiology of hereditary hemorrhagic telangiectasia (HHT) in the United States since the incorporation of the International Statistical Classification of Diseases and Related Health Problems, 10th Revision, Clinical Modification (ICD-10 CM). Objective Our objective is to analyze the epidemiology of HHT from 2013 to 2017 and to determine the relationships between epistaxis and other associated complications of this rare disease. Methods We analyzed the epidemiology of HHT between 2013 and 2017 by accessing data of 87 709 738 patients from the Clinformatics Data Mart using ICD-9 CM and ICD-10 CM codes. Variables analyzed included age, gender, region, clinical setting of diagnosis, hospitalizations, and complications. Bivariate analyses using generalized linear models were conducted to determine the likelihood of HHT patients with epistaxis enduring associated life-threatening complications such as cerebral hemorrhage, thrombosis, and pulmonary hemorrhage compared to HHT patients without epistaxis during the study period. Results The prevalence of HHT increased from 6.1 to 12.1 per 100 000 persons, with patients of ages 18 to 29 years and those older than 60 years seeing the greatest percent increase. The prevalence of HHT in the Southern United States saw a 147% increase. Compared to HHT patients without epistaxis, HHT patients with epistaxis were 3.4 times more likely to experience pulmonary hemorrhage, 3.3 times more likely to have pulmonary emboli, 2.8 times more likely to experience cerebral hemorrhage, and 2.0 times more likely to have thrombosis during the study period. Conclusion Our national study has provided the first incidence and prevalence rates of HHT in the United States since the incorporation of the ICD-10 CM. HHT patients with epistaxis require prompt multidisciplinary treatment of their condition due to their increased risk of life-threatening complications.
引用
收藏
页码:230 / 237
页数:8
相关论文
共 40 条
  • [1] AASSAR OS, 1991, LARYNGOSCOPE, V101, P977
  • [2] Young Adult Preventive Healthcare: Changes in Receipt of Care Pre- to Post-Affordable Care Act
    Adams, Sally H.
    Park, Jane
    Twietmeyer, Lauren
    Brindis, Claire D.
    Irwin, Charles E., Jr.
    [J]. JOURNAL OF ADOLESCENT HEALTH, 2019, 64 (06) : 763 - 769
  • [3] Health screening behaviors among adults with hereditary hemorrhagic telangiectasia in North America
    Baxter, Melanie
    Erby, Lori
    Roter, Debra
    Bernhardt, Barbara A.
    Terry, Peter
    Guttmacher, Alan
    [J]. GENETICS IN MEDICINE, 2017, 19 (06) : 659 - 666
  • [4] Epidemiology and trends of anaphylaxis in the United States, 2004-2016
    Chaaban, Mohamad R.
    Warren, Zachary
    Baillargeon, Jacques G.
    Baillargeon, Gwen
    Resto, Vicente
    Kuo, Yong-Fang
    [J]. INTERNATIONAL FORUM OF ALLERGY & RHINOLOGY, 2019, 9 (06) : 607 - 614
  • [5] Outcomes and Complications of Balloon and Conventional Functional Endoscopic Sinus Surgery
    Chaaban, Mohamad R.
    Rana, Nikunj
    Baillargeon, Jacques
    Baillargeon, Gwen
    Resto, Vicente
    Kuo, Yong-Fang
    [J]. AMERICAN JOURNAL OF RHINOLOGY & ALLERGY, 2018, 32 (05) : 388 - 396
  • [6] Use of balloon sinuplasty in patients with chronic rhinosinusitis in the United States
    Chaaban, Mohamad R.
    Baillargeon, Jacques G.
    Baillargeon, Gwen
    Resto, Vicente
    Kuo, Yong-Fang
    [J]. INTERNATIONAL FORUM OF ALLERGY & RHINOLOGY, 2017, 7 (06) : 600 - 608
  • [7] Outcomes of Pregnancy in Women With Hereditary Hemorrhagic Telangiectasia
    de Gussem, Els M.
    Lausman, Andrea Y.
    Beder, Aarin J.
    Edwards, Christine P.
    Blanker, Marco H.
    Terbrugge, Karel G.
    Mager, Johannes J.
    Faughnan, Marie E.
    [J]. OBSTETRICS AND GYNECOLOGY, 2014, 123 (03) : 514 - 520
  • [8] The UK prevalence of hereditary haemorrhagic telangiectasia and its association with sex, socioeconomic status and region of residence: a population-based study
    Donaldson, J. W.
    McKeever, T. M.
    Hall, I. P.
    Hubbard, R. B.
    Fogarty, A. W.
    [J]. THORAX, 2014, 69 (02) : 161 - 167
  • [9] Complications and mortality in hereditary hemorrhagic telangiectasia A population-based study
    Donaldson, James W.
    McKeever, Tricia M.
    Hall, Ian P.
    Hubbard, Richard B.
    Fogarty, Andrew W.
    [J]. NEUROLOGY, 2015, 84 (18) : 1886 - 1893
  • [10] Life expectancy and comorbidities in patients with hereditary hemorrhagic telangiectasia
    Droege, Freya
    Thangavelu, Kruthika
    Stuck, Boris A.
    Stang, Andreas
    Lang, Stephan
    Geisthoff, Urban
    [J]. VASCULAR MEDICINE, 2018, 23 (04) : 377 - 383