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Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience

OBJECTIVES: Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease characterised by epistaxis. Surgical procedures for epistaxis vary from diathermocoagulation to nasal closure. The aim of this paper is to report our experience in endoscopic surgical management of epistaxi...

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Autores principales: Pagella, Fabio, Pusateri, Alessandro, Maiorano, Eugenia, Spinozzi, Giuseppe, Ugolini, Sara, Lizzio, Roberta, Mirabella, Rosolino, Tinelli, Carmine, Olivieri, Carla, Matti, Elina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pacini Editore Srl 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982753/
https://www.ncbi.nlm.nih.gov/pubmed/33746224
http://dx.doi.org/10.14639/0392-100X-N0915
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author Pagella, Fabio
Pusateri, Alessandro
Maiorano, Eugenia
Spinozzi, Giuseppe
Ugolini, Sara
Lizzio, Roberta
Mirabella, Rosolino
Tinelli, Carmine
Olivieri, Carla
Matti, Elina
author_facet Pagella, Fabio
Pusateri, Alessandro
Maiorano, Eugenia
Spinozzi, Giuseppe
Ugolini, Sara
Lizzio, Roberta
Mirabella, Rosolino
Tinelli, Carmine
Olivieri, Carla
Matti, Elina
author_sort Pagella, Fabio
collection PubMed
description OBJECTIVES: Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease characterised by epistaxis. Surgical procedures for epistaxis vary from diathermocoagulation to nasal closure. The aim of this paper is to report our experience in endoscopic surgical management of epistaxis in HHT patients. METHODS: This is a descriptive, longitudinal study carried out at the Otorhinolaryngology Department of IRCCS Policlinico San Matteo in Pavia, a reference centre for the treatment and diagnosis of HHT. We retrospectively evaluated HHT patients who underwent surgery for epistaxis from 1996 to 2015, including only those treated with endoscopic surgery. RESULTS: Among the 591 patients hospitalised and screened for HHT, 323 (54.7%) underwent endoscopic surgery for epistaxis, for a total of 679 procedures. General anaesthesia was used in 77.2% of procedures; argon plasma coagulation was the instrument of choice in the majority of patients, followed by lasers and quantum molecular resonance technology. CONCLUSIONS: We report one of the largest cohorts undergoing endoscopic treatment of epistaxis in HHT patients. This mini-invasive surgical treatment allowed us to control epistaxis without major complications and nasal packaging and can be repeated over time. For these reasons, we recommend it as first choice in case of epistaxis in HHT patients.
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spelling pubmed-79827532021-03-25 Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience Pagella, Fabio Pusateri, Alessandro Maiorano, Eugenia Spinozzi, Giuseppe Ugolini, Sara Lizzio, Roberta Mirabella, Rosolino Tinelli, Carmine Olivieri, Carla Matti, Elina Acta Otorhinolaryngol Ital Rhinology OBJECTIVES: Hereditary haemorrhagic telangiectasia (HHT) is a rare autosomal dominant disease characterised by epistaxis. Surgical procedures for epistaxis vary from diathermocoagulation to nasal closure. The aim of this paper is to report our experience in endoscopic surgical management of epistaxis in HHT patients. METHODS: This is a descriptive, longitudinal study carried out at the Otorhinolaryngology Department of IRCCS Policlinico San Matteo in Pavia, a reference centre for the treatment and diagnosis of HHT. We retrospectively evaluated HHT patients who underwent surgery for epistaxis from 1996 to 2015, including only those treated with endoscopic surgery. RESULTS: Among the 591 patients hospitalised and screened for HHT, 323 (54.7%) underwent endoscopic surgery for epistaxis, for a total of 679 procedures. General anaesthesia was used in 77.2% of procedures; argon plasma coagulation was the instrument of choice in the majority of patients, followed by lasers and quantum molecular resonance technology. CONCLUSIONS: We report one of the largest cohorts undergoing endoscopic treatment of epistaxis in HHT patients. This mini-invasive surgical treatment allowed us to control epistaxis without major complications and nasal packaging and can be repeated over time. For these reasons, we recommend it as first choice in case of epistaxis in HHT patients. Pacini Editore Srl 2021-03-19 2021-02 /pmc/articles/PMC7982753/ /pubmed/33746224 http://dx.doi.org/10.14639/0392-100X-N0915 Text en Società Italiana di Otorinolaringoiatria e Chirurgia Cervico-Facciale, Rome, Italy https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en This is an open access article distributed in accordance with the CC-BY-NC-ND (Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International) license. The article can be used by giving appropriate credit and mentioning the license, but only for non-commercial purposes and only in the original version. For further information: https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en
spellingShingle Rhinology
Pagella, Fabio
Pusateri, Alessandro
Maiorano, Eugenia
Spinozzi, Giuseppe
Ugolini, Sara
Lizzio, Roberta
Mirabella, Rosolino
Tinelli, Carmine
Olivieri, Carla
Matti, Elina
Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
title Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
title_full Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
title_fullStr Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
title_full_unstemmed Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
title_short Endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
title_sort endoscopic surgical treatment of epistaxis in hereditary haemorrhagic telangiectasia: our experience
topic Rhinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982753/
https://www.ncbi.nlm.nih.gov/pubmed/33746224
http://dx.doi.org/10.14639/0392-100X-N0915
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