Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia
by
Ugolini, S.
, Post, M. C.
, Buscarini, E.
, Droege, F.
, Sure, U.
, Geisthoff, U.
, Mager, H. J.
, Dupuis-Girod, S.
, Kjeldsen, A.
, Pagella, F.
, Millar, C. M.
, Sabbà, C.
, Manfredi, G.
, Shovlin, C. L.
, Lenato, G. M.
, Torring, P. M.
, Coote, N.
, Fialla, A. D.
, Suppressa, P.
in
Anticoagulants
/ Apixaban
/ Arteriovenous malformations
/ Atrial fibrillation
/ Bleeding
/ Blood transfusion
/ Cardiac arrhythmia
/ Cardiovascular diseases
/ Care and treatment
/ Dabigatran
/ Dietary supplements
/ Dysplasia
/ Epistaxis
/ Fibrillation
/ Health aspects
/ Hemorrhage
/ Heparin
/ Hereditary hemorrhagic telangiectasia
/ Hospital admission and discharge
/ Hospital patients
/ Human Genetics
/ Management
/ Medical research
/ Medicine
/ Medicine & Public Health
/ NMR
/ Nosebleed
/ Nuclear magnetic resonance
/ Patients
/ Pharmacology/Toxicology
/ Population
/ Pulmonary emboli
/ Pulmonary embolism
/ Rare cardiovascular diseases
/ Rare diseases
/ Respiratory system agents
/ Risk factors
/ Rivaroxaban
/ Safety and security measures
/ Stroke
/ Telangiectasis
/ Thromboembolism
/ Vascular diseases
/ Warfarin
2019
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia
by
Ugolini, S.
, Post, M. C.
, Buscarini, E.
, Droege, F.
, Sure, U.
, Geisthoff, U.
, Mager, H. J.
, Dupuis-Girod, S.
, Kjeldsen, A.
, Pagella, F.
, Millar, C. M.
, Sabbà, C.
, Manfredi, G.
, Shovlin, C. L.
, Lenato, G. M.
, Torring, P. M.
, Coote, N.
, Fialla, A. D.
, Suppressa, P.
in
Anticoagulants
/ Apixaban
/ Arteriovenous malformations
/ Atrial fibrillation
/ Bleeding
/ Blood transfusion
/ Cardiac arrhythmia
/ Cardiovascular diseases
/ Care and treatment
/ Dabigatran
/ Dietary supplements
/ Dysplasia
/ Epistaxis
/ Fibrillation
/ Health aspects
/ Hemorrhage
/ Heparin
/ Hereditary hemorrhagic telangiectasia
/ Hospital admission and discharge
/ Hospital patients
/ Human Genetics
/ Management
/ Medical research
/ Medicine
/ Medicine & Public Health
/ NMR
/ Nosebleed
/ Nuclear magnetic resonance
/ Patients
/ Pharmacology/Toxicology
/ Population
/ Pulmonary emboli
/ Pulmonary embolism
/ Rare cardiovascular diseases
/ Rare diseases
/ Respiratory system agents
/ Risk factors
/ Rivaroxaban
/ Safety and security measures
/ Stroke
/ Telangiectasis
/ Thromboembolism
/ Vascular diseases
/ Warfarin
2019
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia
by
Ugolini, S.
, Post, M. C.
, Buscarini, E.
, Droege, F.
, Sure, U.
, Geisthoff, U.
, Mager, H. J.
, Dupuis-Girod, S.
, Kjeldsen, A.
, Pagella, F.
, Millar, C. M.
, Sabbà, C.
, Manfredi, G.
, Shovlin, C. L.
, Lenato, G. M.
, Torring, P. M.
, Coote, N.
, Fialla, A. D.
, Suppressa, P.
in
Anticoagulants
/ Apixaban
/ Arteriovenous malformations
/ Atrial fibrillation
/ Bleeding
/ Blood transfusion
/ Cardiac arrhythmia
/ Cardiovascular diseases
/ Care and treatment
/ Dabigatran
/ Dietary supplements
/ Dysplasia
/ Epistaxis
/ Fibrillation
/ Health aspects
/ Hemorrhage
/ Heparin
/ Hereditary hemorrhagic telangiectasia
/ Hospital admission and discharge
/ Hospital patients
/ Human Genetics
/ Management
/ Medical research
/ Medicine
/ Medicine & Public Health
/ NMR
/ Nosebleed
/ Nuclear magnetic resonance
/ Patients
/ Pharmacology/Toxicology
/ Population
/ Pulmonary emboli
/ Pulmonary embolism
/ Rare cardiovascular diseases
/ Rare diseases
/ Respiratory system agents
/ Risk factors
/ Rivaroxaban
/ Safety and security measures
/ Stroke
/ Telangiectasis
/ Thromboembolism
/ Vascular diseases
/ Warfarin
2019
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia
Journal Article
Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia
2019
Request Book From Autostore
and Choose the Collection Method
Overview
Background
Hereditary hemorrhagic telangiectasia (HHT) is a rare vascular dysplasia resulting in visceral arteriovenous malformations and smaller mucocutaneous telangiectasia. Most patients experience recurrent nosebleeds and become anemic without iron supplementation. However, thousands may require anticoagulation for conditions such as venous thromboembolism and/or atrial fibrillation. Over decades, tolerance data has been published for almost 200 HHT-affected users of warfarin and heparins, but there are no published data for the newer direct oral anticoagulants (DOACs) in HHT.
Methods
To provide such data, a retrospective audit was conducted across the eight HHT centres of the European Reference Network for Rare Multisystemic Vascular Diseases (VASCERN), in Denmark, France, Germany, Italy, the Netherlands and the UK.
Results
Although HHT Centres had not specifically recommended the use of DOACs, 32 treatment episodes had been initiated by other clinicians in 28 patients reviewed at the Centres, at median age 65 years (range 30–84). Indications were for atrial fibrillation (16 treatment episodes) and venous thromboembolism (16 episodes). The 32 treatment episodes used Apixaban (
n
= 15), Rivaroxaban (
n
= 14), and Dabigatran (
n
= 3). HHT nosebleeds increased in severity in 24/32 treatment episodes (75%), leading to treatment discontinuation in 11 (34.4%). Treatment discontinuation was required for 4/15 (26.7%) Apixaban episodes and 7/14 (50%) Rivaroxaban episodes. By a 4 point scale of increasing severity, there was a trend for Rivaroxaban to be associated with a greater bleeding risk both including and excluding patients who had used more than one agent (age-adjusted coefficients 0.61 (95% confidence intervals 0.11, 1.20) and 0.74 (95% confidence intervals 0.12, 1.36) respectively. Associations were maintained after adjustment for gender and treatment indication. Extreme hemorrhagic responses, worse than anything experienced previously, with individual nosebleeds lasting hours requiring hospital admissions, blood transfusions and in all cases treatment discontinuation, occurred in 5/14 (35.7%) Rivaroxaban episodes compared to 3/15 (20%) Apixaban episodes and published rates of ~ 5% for warfarin and heparin.
Conclusions
Currently, conventional heparin and warfarin remain first choice anticoagulants in HHT. If newer anticoagulants are considered, although study numbers are small, at this stage Apixaban appears to be associated with lesser bleeding risk than Rivaroxaban.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
MBRLCatalogueRelatedBooks
Related Items
Related Items
We currently cannot retrieve any items related to this title. Kindly check back at a later time.
This website uses cookies to ensure you get the best experience on our website.