Sclerotherapy on Demand with Polidocanol to Treat HHT Nosebleeds

被引:8
作者
Marcos, Sol [1 ]
Maria Botella, Luisa [2 ]
Albinana, Virginia [2 ]
Arbia, Agustina [1 ]
Maria de Rosales, Anna [3 ]
机构
[1] Hosp Univ Fdn Alcorcon, Otorrhinolaringol Dept, Madrid 28922, Spain
[2] CSIC, CIBER Rare Dis Unit 707, Ctr Invest Biol Margarita Salas, Madrid 28040, Spain
[3] Hosp Univ Fdn Alcorcon, Pharmaceut Dept, Madrid 28922, Spain
关键词
HHT; epistaxis; sclerotherapy; polidocanol; propranolol; HHT-ESS; quality of life; HEREDITARY HEMORRHAGIC TELANGIECTASIA; EPISTAXIS SEVERITY SCORE; RENDU-OSLER-WEBER;
D O I
10.3390/jcm10173845
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epistaxis is the most prevalent clinical symptom in Hereditary Haemorrhagic Telangiectasia (HHT), causing anaemia and decreasing the quality of life (QOL). Since 2013, in Hospital Universitario Fundacion Alcorcon, more than 150 HHT patients have been treated by nose sclerotherapy on demand. This study shows the results of 105 patients treated with sclerotherapy between 2017 and 2019. HHT-ESS (epistaxis severity score) was used to measure the severity and frequency of epistaxis. QOL was determined before and after treatment by EuroQol-5D (EQ-5D) and the visual analogue scale (VAS) on the health condition. According to HHT-ESS before treatment, 22 patients presented mild, 35 moderate, and 47 severe epistaxes. Sclerotherapy significantly decreased the frequency and severity of epistaxis, with a significant drop of HHT-ESS in 4.6 points, from 6.23 +/- 2.3 to 1.64 +/- 1.6. Furthermore, the QOL significantly improved, the EQ-5D scale raised from 0.7 +/- 0.26 pre- to 0.92 +/- 0.16 post-treatment (p < 0.05). Additionally, VAS mean value showed a significant increase from 4.38 +/- 2.4 to 8.35 +/- 1.2. The QOL improvement was correlated with the ESS decrease. In conclusion, this study shows that on-demand sclerotherapy at the office significantly reduces HHT epistaxis as well as improved the patients' QOL.
引用
收藏
页数:11
相关论文
共 18 条
[1]  
AASSAR OS, 1991, LARYNGOSCOPE, V101, P977
[2]   Review of Pharmacological Strategies with Repurposed Drugs for Hereditary Hemorrhagic Telangiectasia Related Bleeding [J].
Albinana, Virginia ;
Cuesta, Angel M. ;
de Rojas-P, Isabel ;
Gallardo-Vara, Eunate ;
Recio-Poveda, Lucia ;
Bernabeu, Carmelo ;
Botella, Luisa Maria .
JOURNAL OF CLINICAL MEDICINE, 2020, 9 (06) :1-22
[3]   Prospective randomized trial of sclerotherapy vs standard treatment for epistaxis due to hereditary hemorrhagic telangiectasia [J].
Boyer, Holly ;
Fernandes, Patricia ;
Le, Chap ;
Yueh, Bevan .
INTERNATIONAL FORUM OF ALLERGY & RHINOLOGY, 2015, 5 (05) :435-440
[4]   ULTRASTRUCTURE AND 3-DIMENSIONAL ORGANIZATION OF THE TELANGIECTASES OF HEREDITARY HEMORRHAGIC TELANGIECTASIA [J].
BRAVERMAN, IM ;
KEH, A ;
JACOBSON, BS .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 95 (04) :422-427
[5]   Sclerotherapy and Topical Nasal Propranolol: An Effective and Safe Therapy for HHT-Epistaxis [J].
Esteban-Casado, Santos ;
de Rosales Cabrera, Ana M. Martin ;
Usarralde Perez, Angela ;
Martinez Simon, Jose Javier ;
Zhan Zhou, Estefania ;
Marcos Salazar, M. Sol ;
Perez Encinas, Montserrat ;
Botella Cubells, Luisa .
LARYNGOSCOPE, 2019, 129 (10) :2216-2223
[6]   Thalidomide for Epistaxis in Patients with Hereditary Hemorrhagic Telangiectasia: A Preliminary Study [J].
Fang, Jia ;
Chen, Xiaomeng ;
Zhu, Bijun ;
Ye, Haibo ;
Zhang, Weitian ;
Guan, Jian ;
Su, Kaiming .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2017, 157 (02) :217-221
[7]   International guidelines for the diagnosis and management of hereditary haemorrhagic telangiectasia [J].
Faughnan, M. E. ;
Palda, V. A. ;
Garcia-Tsao, G. ;
Geisthoff, U. W. ;
McDonald, J. ;
Proctor, D. D. ;
Spears, J. ;
Brown, D. H. ;
Buscarini, E. ;
Chesnutt, M. S. ;
Cottin, V. ;
Ganguly, A. ;
Gossage, J. R. ;
Guttmacher, A. E. ;
Hyland, R. H. ;
Kennedy, S. J. ;
Korzenik, J. ;
Mager, J. J. ;
Ozanne, A. P. ;
Piccirillo, J. F. ;
Picus, D. ;
Plauchu, H. ;
Porteous, M. E. M. ;
Pyeritz, R. E. ;
Ross, D. A. ;
Sabba, C. ;
Swanson, K. ;
Terry, P. ;
Wallace, M. C. ;
Westermann, C. J. J. ;
White, R. I. ;
Young, L. H. ;
Zarrabeitia, R. .
JOURNAL OF MEDICAL GENETICS, 2011, 48 (02) :73-87
[8]   Optimal management of hereditary hemorrhagic telangiectasia [J].
Garg, Neetika ;
Khunger, Monica ;
Gupta, Arjun ;
Kumar, Nilay .
JOURNAL OF BLOOD MEDICINE, 2014, 5 :191-206
[9]  
Herdman M, 2001, Aten Primaria, V28, P425
[10]   An Epistaxis Severity Score for Hereditary Hemorrhagic Telangiectasia [J].
Hoag, Jeffrey B. ;
Terry, Peter ;
Mitchell, Sally ;
Reh, Douglas ;
Merlo, Christian A. .
LARYNGOSCOPE, 2010, 120 (04) :838-843