Literature DB >> 25862798

Complications and mortality in hereditary hemorrhagic telangiectasia: A population-based study.

James W Donaldson1, Tricia M McKeever2, Ian P Hall2, Richard B Hubbard2, Andrew W Fogarty2.   

Abstract

OBJECTIVES: Studies report that the risks of significant neurologic complications (including stroke, cerebral abscess, and migraine) and hemorrhagic sequelae are high in patients with hereditary hemorrhagic telangiectasia (HHT), and that life expectancy in this cohort is reduced. However, most published cohorts derive from specialist centers, which may be susceptible to bias.
METHODS: We used a population-based approach to estimate the risks of developing neurologic and hemorrhagic complications of HHT, the association of a diagnosis of HHT with common cardiovascular and malignant comorbidities, and also long-term survival of those with the disease.
RESULTS: From a UK primary care database of 3.5 million patients (The Health Improvement Network), we identified 675 cases with a diagnosis of HHT and compared them with 6,696 controls matched by age, sex, and primary care practice. Risks of stroke (odds ratio [OR] 1.8, 95% confidence interval [CI] 1.2-2.6), cerebral abscess (OR 30.0, CI 3.1-288), and migraine (OR 1.7, CI 1.3-2.2) were elevated over controls. Bleeding complications including epistaxis (OR 11.6, CI 9.1-14.7) and gastrointestinal hemorrhage (OR 6.1, CI 2.8-13.4) were more common in cases with HHT. Survival of cases with HHT was poorer than controls with a hazard ratio for death of 2.0 (CI 1.6-2.6) and a median age at death 3 years younger.
CONCLUSIONS: Patients with HHT are at substantially increased risk of serious neurologic and hemorrhagic complications of the disease. Because a diagnosis of HHT is associated with a significantly poorer survival compared with those who have no disease, evaluation of new strategies to improve clinical management is required.
© 2015 American Academy of Neurology.

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Year:  2015        PMID: 25862798      PMCID: PMC4433463          DOI: 10.1212/WNL.0000000000001538

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  35 in total

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Authors:  Margaret O'Malley; Lisa LaGuardia; Matthew F Kalady; Joseph Parambil; Brandie Heald; Charis Eng; James Church; Carol A Burke
Journal:  Dis Colon Rectum       Date:  2012-08       Impact factor: 4.585

2.  Prevalence of pulmonary arteriovenous malformations (PAVMs) and occurrence of neurological symptoms in patients with hereditary haemorrhagic telangiectasia (HHT).

Authors:  A D Kjeldsen; H Oxhøj; P E Andersen; A Green; P Vase
Journal:  J Intern Med       Date:  2000-09       Impact factor: 8.989

3.  Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

Authors:  C L Shovlin; A E Guttmacher; E Buscarini; M E Faughnan; R H Hyland; C J Westermann; A D Kjeldsen; H Plauchu
Journal:  Am J Med Genet       Date:  2000-03-06

4.  Cerebral abscesses in hereditary haemorrhagic telangiectasia: a clinical and microbiological evaluation.

Authors:  Stéphane Mathis; Sophie Dupuis-Girod; Henri Plauchu; Maurice Giroud; Bruno Barroso; Kim Heang Ly; Pierre Ingrand; Brigitte Gilbert; Gaëlle Godenèche; Jean-Philippe Neau
Journal:  Clin Neurol Neurosurg       Date:  2011-11-16       Impact factor: 1.876

5.  Primary determinants of ischaemic stroke/brain abscess risks are independent of severity of pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia.

Authors:  C L Shovlin; J E Jackson; K B Bamford; I H Jenkins; A R Benjamin; H Ramadan; E Kulinskaya
Journal:  Thorax       Date:  2007-11-02       Impact factor: 9.139

6.  Cerebral vascular malformations in hereditary hemorrhagic telangiectasia.

Authors:  M Neil Woodall; Melissa McGettigan; Ramon Figueroa; James R Gossage; Cargill H Alleyne
Journal:  J Neurosurg       Date:  2013-11-15       Impact factor: 5.115

7.  Cerebral abscesses among Danish patients with hereditary haemorrhagic telangiectasia.

Authors:  A D Kjeldsen; P M Tørring; H Nissen; P E Andersen
Journal:  Acta Neurol Scand       Date:  2013-08-20       Impact factor: 3.209

8.  The UK prevalence of hereditary haemorrhagic telangiectasia and its association with sex, socioeconomic status and region of residence: a population-based study.

Authors:  J W Donaldson; T M McKeever; I P Hall; R B Hubbard; A W Fogarty
Journal:  Thorax       Date:  2013-11-04       Impact factor: 9.139

9.  Medical management with or without interventional therapy for unruptured brain arteriovenous malformations (ARUBA): a multicentre, non-blinded, randomised trial.

Authors:  J P Mohr; Michael K Parides; Christian Stapf; Ellen Moquete; Claudia S Moy; Jessica R Overbey; Rustam Al-Shahi Salman; Eric Vicaut; William L Young; Emmanuel Houdart; Charlotte Cordonnier; Marco A Stefani; Andreas Hartmann; Rüdiger von Kummer; Alessandra Biondi; Joachim Berkefeld; Catharina J M Klijn; Kirsty Harkness; Richard Libman; Xavier Barreau; Alan J Moskowitz
Journal:  Lancet       Date:  2013-11-20       Impact factor: 79.321

10.  The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia.

Authors:  Scott D Grosse; Sheree L Boulet; Althea M Grant; Mary M Hulihan; Marie E Faughnan
Journal:  Genet Med       Date:  2013-05-23       Impact factor: 8.822

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  19 in total

1.  Management of epistaxis in hereditary haemorrhagic telangiectasia (HHT) patients using pulsed dye laser and the effect of withholding treatment during the COVID pandemic.

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2.  Characterization of pulmonary arteriovenous malformations in ACVRL1 versus ENG mutation carriers in hereditary hemorrhagic telangiectasia.

Authors:  Weiyi Mu; Zachary A Cordner; Kevin Yuqi Wang; Kate Reed; Gina Robinson; Sally Mitchell; Doris Lin
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3.  Life expextancy of parents with Hereditary Haemorrhagic Telangiectasia.

Authors:  E M de Gussem; C P Edwards; A E Hosman; C J J Westermann; R J Snijder; M E Faughnan; J J Mager
Journal:  Orphanet J Rare Dis       Date:  2016-04-22       Impact factor: 4.123

4.  20-year follow-up study of Danish HHT patients-survival and causes of death.

Authors:  Anette Kjeldsen; Katrine Saldern Aagaard; Pernille Mathiesen Tørring; Sören Möller; Anders Green
Journal:  Orphanet J Rare Dis       Date:  2016-11-22       Impact factor: 4.123

5.  Life-threatening hemoptysis: case of Osler-Weber-Rendu Syndrome.

Authors:  Ricardo Alicea-Guevara; Michael Cruz Caliz; Jose Adorno; Ricardo Fernandez; Kelvin Rivera; Gustavo Gonzalez; Ricardo Alan Hernandez-Castillo; Rosangela Fernandez; Christian Castillo Latorre
Journal:  Oxf Med Case Reports       Date:  2018-03-22

6.  European Reference Network For Rare Vascular Diseases (VASCERN) Outcome Measures For Hereditary Haemorrhagic Telangiectasia (HHT).

Authors:  Claire L Shovlin; Elisabetta Buscarini; Anette D Kjeldsen; Hans Jurgen Mager; Carlo Sabba; Freya Droege; Urban Geisthoff; Sara Ugolini; Sophie Dupuis-Girod
Journal:  Orphanet J Rare Dis       Date:  2018-08-15       Impact factor: 4.123

7.  Orthodeoxia without Platypnea in Hereditary Hemorrhagic Telangiectasia in the Presence of a Cerebral Abscess and Multiple Pulmonary Arteriovenous Malformations: Unusual Complications and Transcatheter Endovascular Treatment.

Authors:  Carlos Salazar; Jacky Bruce Blank; Veronica Palmero
Journal:  Case Rep Pulmonol       Date:  2017-10-12

8.  Intra-venous bevacizumab in hereditary hemorrhagic telangiectasia (HHT): A retrospective study of 46 patients.

Authors:  Alexandre Guilhem; Anne-Emmanuelle Fargeton; Anne-Claire Simon; Pierre Duffau; Jean-Robert Harle; Christian Lavigne; Marie-France Carette; Olivier Bletry; Pierre Kaminsky; Vanessa Leguy; Nathalie Lerolle; Dominique Roux; Marc Lambert; Thierry Chinet; Delphine Bonnet; Sophie Dupuis-Girod; Sophie Rivière
Journal:  PLoS One       Date:  2017-11-30       Impact factor: 3.240

9.  Impact of Age on Outcomes in Hospitalized Patients with Hereditary Hemorrhagic Telangiectasia.

Authors:  Vivek N Iyer; Waleed Brinjikji; Dinesh Apala; Bibek S Pannu; Aditya Kotecha; Michael D Leise; Patrick S Kamath; Sanjay Misra; Giuseppe Lanzino; Michael J Krowka; Christopher P Wood; Karen L Swanson
Journal:  Adv Hematol       Date:  2018-02-11

10.  Pazopanib for severe bleeding and transfusion-dependent anemia in hereditary hemorrhagic telangiectasia.

Authors:  Joseph G Parambil; James R Gossage; Keith R McCrae; Troy D Woodard; K V Narayanan Menon; Kasi L Timmerman; Douglas P Pederson; Dennis L Sprecher; Hanny Al-Samkari
Journal:  Angiogenesis       Date:  2021-07-22       Impact factor: 9.596

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