Literature DB >> 25986996

Bevacizumab: an option for refractory epistaxis in hereditary haemorrhagic telangiectasia.

Arno Amann1, Normann Steiner, Eberhard Gunsilius.   

Abstract

BACKGROUND: Recurrent epistaxis in hereditary haemorrhagic telangiectasia (HHT) patients significantly decreases their quality of life. Treatment in therapy refractory patients is limited although various options have been tested so far. CASE REPORT: Herein, one patient is described that was treated for HHT for over 20 years with only intermediate benefits. As epistaxis duration and frequency increased continuously, bevacizumab 5 mg/kg was administered every 2 weeks. During the time of treatment (six doses) and up to 3 month afterwards clinical symptoms, blood pressure, cardiac output, pulmonary arterial hypertension (PAH), bleeding duration and frequency were assessed as criteria for treatment benefit.
RESULTS: Duration and frequency of epistaxis decreased immediately after the first application resulting in reduced need of blood transfusions. After completion of six cycles, a further decrease in frequency and duration of bleeding was noted. Cardiac output and PAH decreased or remained stable, respectively, during time and after treatment. No increase in blood pressure could be found but a significant increase in heart rate was experienced after completion of all six applications. Unfortunately, the patient died due to a cerebral abscess.
CONCLUSION: Bevacizumab led to an improvement of HHT related epistaxis, refractory to other treatments.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 25986996     DOI: 10.1007/s00508-015-0789-4

Source DB:  PubMed          Journal:  Wien Klin Wochenschr        ISSN: 0043-5325            Impact factor:   1.704


  13 in total

Review 1.  Hereditary hemorrhagic telangiectasia: from molecular biology to patient care.

Authors:  S Dupuis-Girod; S Bailly; H Plauchu
Journal:  J Thromb Haemost       Date:  2010-03-19       Impact factor: 5.824

2.  Bevacizumab in patients with hereditary hemorrhagic telangiectasia and severe hepatic vascular malformations and high cardiac output.

Authors:  Sophie Dupuis-Girod; Isabelle Ginon; Jean-Christophe Saurin; Denis Marion; Elsa Guillot; Evelyne Decullier; Adeline Roux; Marie-France Carette; Brigitte Gilbert-Dussardier; Pierre-Yves Hatron; Pascal Lacombe; Bernard Lorcerie; Sophie Rivière; Romain Corre; Sophie Giraud; Sabine Bailly; Gilles Paintaud; David Ternant; Pierre-Jean Valette; Henri Plauchu; Frédéric Faure
Journal:  JAMA       Date:  2012-03-07       Impact factor: 56.272

3.  Estriol induced squamous metaplasia on the nasal mucosa in patients with hereditary hemorrhagic telangiectasia.

Authors:  Haneen Sadick; Wolfgang F Bergler; Jasmina Oulmi-Kagermann; Ramin Naim; Maliha Sadick; Karl Hörmann; Frank Riedel
Journal:  Arch Med Res       Date:  2005 Sep-Oct       Impact factor: 2.235

4.  Anti-estrogen therapy for hereditary hemorrhagic telangiectasia - a long-term clinical trial.

Authors:  E Yaniv; M Preis; J Shevro; B Nageris; T Hadar
Journal:  Rhinology       Date:  2011-06       Impact factor: 3.681

5.  Tranexamic acid for epistaxis in hereditary hemorrhagic telangiectasia patients: a European cross-over controlled trial in a rare disease.

Authors:  S Gaillard; S Dupuis-Girod; F Boutitie; S Rivière; S Morinière; P-Y Hatron; G Manfredi; P Kaminsky; A-L Capitaine; P Roy; F Gueyffier; H Plauchu
Journal:  J Thromb Haemost       Date:  2014-07-29       Impact factor: 5.824

6.  Laser ablation of upper gastrointestinal vascular ectasias: long term results.

Authors:  I R Sargeant; L A Loizou; D Rampton; M Tulloch; S G Bown
Journal:  Gut       Date:  1993-04       Impact factor: 23.059

7.  Systemic therapy with bevacizumab in patients with hereditary hemorrhagic telangiectasia (HHT).

Authors:  Ajay Chavan; Silke Schumann-Binarsch; Lars Luthe; Britta Nickau; Albrecht Elsässer; Thomas Kühnel; Urban Geisthoff; Henning Köhne
Journal:  Vasa       Date:  2013-03       Impact factor: 1.961

8.  Hepatic vascular malformations in hereditary hemorrhagic telangiectasia: imaging findings.

Authors:  E Buscarini; L Buscarini; G Civardi; S Arruzzoli; G Bossalini; M Piantanida
Journal:  AJR Am J Roentgenol       Date:  1994-11       Impact factor: 3.959

9.  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

10.  Successful lung transplantation in a case with diffuse pulmonary arteriovenous malformations and hereditary hemorrhagic telangiectasia.

Authors:  H Fukushima; T Mitsuhashi; T Oto; Y Sano; K F Kusano; K Goto; M Okazaki; H Date; Y Kojima; H Yamagishi; T Takahashi
Journal:  Am J Transplant       Date:  2013-10-24       Impact factor: 8.086

View more
  2 in total

1.  Bevacizumab and gastrointestinal bleeding in hereditary hemorrhagic telangiectasia.

Authors:  George Ou; Cherry Galorport; Robert Enns
Journal:  World J Gastrointest Surg       Date:  2016-12-27

2.  Intravenous Bevacizumab Therapy in a Patient with Hereditary Hemorrhagic Telangiectasia, ENG E137K, Alcoholic Cirrhosis, and Portal Hypertension.

Authors:  Luigi F Bertoli; Pauline L Lee; Lauren Lallone; James C Barton
Journal:  Case Rep Gastroenterol       Date:  2017-05-17
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.