Literature DB >> 27599329

Effect of Topical Intranasal Therapy on Epistaxis Frequency in Patients With Hereditary Hemorrhagic Telangiectasia: A Randomized Clinical Trial.

Kevin J Whitehead1, Nathan B Sautter2, Justin P McWilliams3, Murali M Chakinala4, Christian A Merlo5, Maribeth H Johnson6, Melissa James7, Eric M Everett8, Marianne S Clancy9, Marie E Faughnan10, S Paul Oh11, Scott E Olitsky12, Reed E Pyeritz13, James R Gossage7.   

Abstract

IMPORTANCE: Epistaxis is a major factor negatively affecting quality of life in patients with hereditary hemorrhagic telangiectasia (HHT; also known as Osler-Weber-Rendu disease). Optimal treatment for HHT-related epistaxis is uncertain.
OBJECTIVE: To determine whether topical therapy with any of 3 drugs with differing mechanisms of action is effective in reducing HHT-related epistaxis. DESIGN, SETTING, AND PARTICIPANTS: The North American Study of Epistaxis in HHT was a double-blind, placebo-controlled randomized clinical trial performed at 6 HHT centers of excellence. From August 2011 through March 2014, there were 121 adult patients who met the clinical criteria for HHT and had experienced HHT-related epistaxis with an Epistaxis Severity Score of at least 3.0. Follow-up was completed in September 2014.
INTERVENTIONS: Patients received twice-daily nose sprays for 12 weeks with either bevacizumab 1% (4 mg/d), estriol 0.1% (0.4 mg/d), tranexamic acid 10% (40 mg/d), or placebo (0.9% saline). MAIN OUTCOMES AND MEASURES: The primary outcome was median weekly epistaxis frequency during weeks 5 through 12. Secondary outcomes included median duration of epistaxis during weeks 5 through 12, Epistaxis Severity Score, level of hemoglobin, level of ferritin, need for transfusion, emergency department visits, and treatment failure.
RESULTS: Among the 121 patients who were randomized (mean age, 52.8 years [SD, 12.9 years]; 44% women with a median of 7.0 weekly episodes of epistaxis [interquartile range {IQR}, 3.0-14.0]), 106 patients completed the study duration for the primary outcome measure (43 were women [41%]). Drug therapy did not significantly reduce epistaxis frequency (P = .97). After 12 weeks of treatment, the median weekly number of bleeding episodes was 7.0 (IQR, 4.5-10.5) for patients in the bevacizumab group, 8.0 (IQR, 4.0-12.0) for the estriol group, 7.5 (IQR, 3.0-11.0) for the tranexamic acid group, and 8.0 (IQR, 3.0-14.0) for the placebo group. No drug treatment was significantly different from placebo for epistaxis duration. All groups had a significant improvement in Epistaxis Severity Score at weeks 12 and 24. There were no significant differences between groups for hemoglobin level, ferritin level, treatment failure, need for transfusion, or emergency department visits. CONCLUSIONS AND RELEVANCE: Among patients with HHT, there were no significant between-group differences in the use of topical intranasal treatment with bevacizumab vs estriol vs tranexamic acid vs placebo and epistaxis frequency. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01408030.

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Year:  2016        PMID: 27599329     DOI: 10.1001/jama.2016.11724

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  18 in total

1.  Selective effects of oral antiangiogenic tyrosine kinase inhibitors on an animal model of hereditary hemorrhagic telangiectasia.

Authors:  Y H Kim; M-J Kim; S-W Choe; D Sprecher; Y J Lee; S P Oh
Journal:  J Thromb Haemost       Date:  2017-05-03       Impact factor: 5.824

Review 2.  ALK1 signaling in development and disease: new paradigms.

Authors:  Beth L Roman; Andrew P Hinck
Journal:  Cell Mol Life Sci       Date:  2017-09-04       Impact factor: 9.261

3.  Intranasal bevacizumab treatment on epistaxis in hereditary haemorrhagic telangiectasia: a case report.

Authors:  Estela García-Martín; Sagrario Pernía-López; Pilar A Martínez-Ortega; Beatriz Monje; Cristina Ruiz-Martínez; María Sanjurjo-Saez
Journal:  Eur J Hosp Pharm       Date:  2017-08-16

4.  Tacrolimus rescues the signaling and gene expression signature of endothelial ALK1 loss-of-function and improves HHT vascular pathology.

Authors:  Santiago Ruiz; Pallavi Chandakkar; Haitian Zhao; Julien Papoin; Prodyot K Chatterjee; Erica Christen; Christine N Metz; Lionel Blanc; Fabien Campagne; Philippe Marambaud
Journal:  Hum Mol Genet       Date:  2017-12-15       Impact factor: 6.150

5.  A mouse model of hereditary hemorrhagic telangiectasia generated by transmammary-delivered immunoblocking of BMP9 and BMP10.

Authors:  Santiago Ruiz; Haitian Zhao; Pallavi Chandakkar; Prodyot K Chatterjee; Julien Papoin; Lionel Blanc; Christine N Metz; Fabien Campagne; Philippe Marambaud
Journal:  Sci Rep       Date:  2016-11-22       Impact factor: 4.379

Review 6.  Hereditary hemorrhagic telangiectasia and pregnancy: potential adverse events and pregnancy outcomes.

Authors:  Omar Bari; Philip R Cohen
Journal:  Int J Womens Health       Date:  2017-05-26

Review 7.  Interdisciplinary Management of Head and Neck Vascular Anomalies: Clinical Presentation, Diagnostic Findings and Minimalinvasive Therapies.

Authors:  Maliha Sadick; Walter A Wohlgemuth; Roland Huelse; Bettina Lange; Thomas Henzler; Stefan O Schoenberg; Haneen Sadick
Journal:  Eur J Radiol Open       Date:  2017-05-14

8.  Integration of clinical parameters, genotype and epistaxis severity score to guide treatment for hereditary hemorrhagic telangiectasia associated bleeding.

Authors:  Joan D Beckman; Quefeng Li; Samuel T Hester; Ofri Leitner; Karen L Smith; Raj S Kasthuri
Journal:  Orphanet J Rare Dis       Date:  2020-07-13       Impact factor: 4.123

9.  Weekly epistaxis duration as an indicator of epistaxis severity in hereditary hemorrhagic telangiectasia-Preliminary results from a randomized controlled trial.

Authors:  Vincent Wu; John M Lee; Nicholas T Vozoris; Marie E Faughnan
Journal:  Laryngoscope Investig Otolaryngol       Date:  2021-04-08

10.  Tranexamic acid for patients with nasal haemorrhage (epistaxis).

Authors:  Jonathan Joseph; Pablo Martinez-Devesa; Jenny Bellorini; Martin J Burton
Journal:  Cochrane Database Syst Rev       Date:  2018-12-31
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