Evidence map›Paper›PMID 31462308›Full record

ArticleOrphanet journal of rare diseases2019

Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia.

C L Shovlin, C M Millar, F Droege, A Kjeldsen, G Manfredi, P Suppressa, S Ugolini, N Coote, A D Fialla, U Geisthoff and 10 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00230685 (Hammersmith Hospital Patients With Pulmonary Arteriovenous Malformations), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00230685 recruitingnot on this map

Hammersmith Hospital Patients With Pulmonary Arteriovenous Malformations (PAVMs) and Hereditary Haemorrhagic Telangiectasia

TypeobservationalSponsorImperial College LondonRan2000 to 2028Enrolled2,000ConditionsTelangiectasia, Hereditary Hemorrhagic
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 41 citations in OpenAlex.

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  13. Central nervous system vascular malformations: A clinical review.Annals of clinical and translational neurology · 2021
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 9 institutions in 6 countries.

C L ShovlinVASCERN HHT Reference Centre, Hammersmith Hospital, Imperial College Healthcare National Health Service Trust, London, and Imperial College London, London, UK. c.shovlin@imperial.ac.uk.
C M MillarEuroBloodNet Reference Centre and Centre for Haematology, Imperial College Academic Health Sciences Centre, Imperial College London, London, UK.
F DroegeVASCERN HHT Reference Centre, Essen University Hospital, Departments of Otorhinolaryngology and Neurosurgery, University of Duisburg-Essen, Essen, Germany.
A KjeldsenVASCERN HHT Reference Centre, Odense Universitetshospital, Syddansk Universitet, Odense, Denmark.
G ManfrediVASCERN HHT Reference Centre, ASST Maggiore Hospital, Crema, Italy.
P SuppressaVASCERN HHT Reference Centre, Centro sovraziendale Malattie rare, Frugoni Internal Medicine Unit - University of Bari A Moro, Bari, Italy.
S UgoliniVASCERN HHT Reference Centre, Department of Otorhinolaryngology, University of Pavia, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.
N CooteVASCERN HHT Reference Centre, Hammersmith Hospital, Imperial College Healthcare National Health Service Trust, London, and Imperial College London, London, UK.
A D FiallaVASCERN HHT Reference Centre, Odense Universitetshospital, Syddansk Universitet, Odense, Denmark.
U GeisthoffVASCERN HHT Reference Centre, Essen University Hospital, Departments of Otorhinolaryngology and Neurosurgery, University of Duisburg-Essen, Essen, Germany.
G M LenatoVASCERN HHT Reference Centre, Centro sovraziendale Malattie rare, Frugoni Internal Medicine Unit - University of Bari A Moro, Bari, Italy.
H J MagerVASCERN HHT Reference Centre, St Antonius Ziekenhuis, Nieuwegein, Netherlands.
F PagellaVASCERN HHT Reference Centre, Department of Otorhinolaryngology, University of Pavia, IRCCS Policlinico San Matteo Foundation, Pavia, Italy.
M C PostVASCERN HHT Reference Centre, St Antonius Ziekenhuis, Nieuwegein, Netherlands.
C SabbàVASCERN HHT Reference Centre, Centro sovraziendale Malattie rare, Frugoni Internal Medicine Unit - University of Bari A Moro, Bari, Italy.
U SureVASCERN HHT Reference Centre, Essen University Hospital, Departments of Otorhinolaryngology and Neurosurgery, University of Duisburg-Essen, Essen, Germany.
P M TorringVASCERN HHT Reference Centre, Odense Universitetshospital, Syddansk Universitet, Odense, Denmark.
S Dupuis-GirodVASCERN HHT Reference Centre, Genetic department, Hospices Civils de Lyon, Femme-Mère-Enfants Hospital, F-69677, Bron, France.
E BuscariniVASCERN HHT Reference Centre, ASST Maggiore Hospital, Crema, Italy.
VASCERN-HHT
University of Southern Denmark · DKNational Health Service · GBUniversity of Pavia · ITAzienda Ospedaliera Ospedale Maggiore · ITEssen University Hospital · DESt. Antonius Ziekenhuis · NLHospices Civils de Lyon · FRImperial College Healthcare NHS Trust · GBNIHR Imperial Biomedical Research Centre · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHereditary 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.

methodsTo 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.

resultsAlthough 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.

conclusionsCurrently, 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.

Indexed as

Administration, OralAgedAged, 80 and overAnticoagulantsAtrial FibrillationDabigatranEpistaxisFemaleHumansMaleMiddle AgedPulmonary EmbolismPyrazolesPyridonesRetrospective StudiesRivaroxabanAnticoagulantsapixabanDabigatranPyrazolesPyridonesRivaroxabanWarfarinApixabanAtrial fibrillationDabigatranEpistaxisHeparinPulmonary emboliRivaroxabanVenous thromboemboliWarfarin

Identifiers

PMID31462308
PMCPMC6714298
OpenAlexW2970133637

What OpenQuestion holds

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LicenceCC BY
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.