Implementation and development of a center for hereditary hemorrhagic telangiectasia
Thieme. All rights reserved..
OBJECTIVE: Hereditary Hemorrhagic Telangiectasia (HHT) is a rare and systemic disorder which is characterized by recurrent epistaxis, mucocutaneous telangiectases, and visceral arteriovenous malformations (AVM). An interdisciplinary concept is recommended.
MATERIAL AND METHODS: We performed a retrospective review of consecutive patients who were referred to our newly established HHT Center of Excellence (HHT COE) for evaluation and treatment between April 2014 and August 2019.
RESULTS: A network of over 20 departments was established at the University Hospital Essen. In 261 of the 282 patients (93 %), who were referred to the hospital's COE, the HHT diagnosis was at least possible. Most patients suffered from several symptoms (epistaxis and / or telangiectasia: > 80 %, visceral involvement: 65 %) and received a variety of treatments, often in a multidisciplinary setting. Alongside this direct treatment, the COE leader manages the coordination of the center and its public relations, which involves more than 900 e-mails per year. International collaboration and exchanges of expertise within the European Reference Network on Rare Multisystemic Vascular Diseases (VASCERN) can improve the treatment of patients with HHT particularly where these cases are complex.
CONCLUSIONS: An HHT COE provides an interdisciplinary network where highly specialized diagnostic and therapeutic processes can be updated and optimized continuously.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2021 |
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| Erschienen: |
2021 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:100 |
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| Enthalten in: |
Laryngo- rhino- otologie - 100(2021), 5 vom: 16. Mai, Seite 372-381 |
| Sprache: |
Deutsch |
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| Weiterer Titel: |
Aufbau und Entwicklung eines interdisziplinären Zentrums für hereditäre hämorrhagische Teleangiektasie |
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| Beteiligte Personen: |
Droege, Freya [VerfasserIn] |
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| Links: |
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| Themen: |
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| Anmerkungen: |
Date Completed 06.05.2021 Date Revised 06.05.2021 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1055/a-1402-0543 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM322805163 |
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| 245 | 1 | 0 | |a Implementation and development of a center for hereditary hemorrhagic telangiectasia |
| 246 | 3 | 3 | |a Aufbau und Entwicklung eines interdisziplinären Zentrums für hereditäre hämorrhagische Teleangiektasie |
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| 500 | |a Date Completed 06.05.2021 | ||
| 500 | |a Date Revised 06.05.2021 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a Thieme. All rights reserved. | ||
| 520 | |a OBJECTIVE: Hereditary Hemorrhagic Telangiectasia (HHT) is a rare and systemic disorder which is characterized by recurrent epistaxis, mucocutaneous telangiectases, and visceral arteriovenous malformations (AVM). An interdisciplinary concept is recommended | ||
| 520 | |a MATERIAL AND METHODS: We performed a retrospective review of consecutive patients who were referred to our newly established HHT Center of Excellence (HHT COE) for evaluation and treatment between April 2014 and August 2019 | ||
| 520 | |a RESULTS: A network of over 20 departments was established at the University Hospital Essen. In 261 of the 282 patients (93 %), who were referred to the hospital's COE, the HHT diagnosis was at least possible. Most patients suffered from several symptoms (epistaxis and / or telangiectasia: > 80 %, visceral involvement: 65 %) and received a variety of treatments, often in a multidisciplinary setting. Alongside this direct treatment, the COE leader manages the coordination of the center and its public relations, which involves more than 900 e-mails per year. International collaboration and exchanges of expertise within the European Reference Network on Rare Multisystemic Vascular Diseases (VASCERN) can improve the treatment of patients with HHT particularly where these cases are complex | ||
| 520 | |a CONCLUSIONS: An HHT COE provides an interdisciplinary network where highly specialized diagnostic and therapeutic processes can be updated and optimized continuously | ||
| 650 | 4 | |a Journal Article | |
| 700 | 1 | |a Dingemann, Julia |e verfasserin |4 aut | |
| 700 | 1 | |a Thangavelu, Kruthika |e verfasserin |4 aut | |
| 700 | 1 | |a Kuerten, Cornelius H L |e verfasserin |4 aut | |
| 700 | 1 | |a Dahlfrancis, Philipp Marius |e verfasserin |4 aut | |
| 700 | 1 | |a Kaiser, Christina |e verfasserin |4 aut | |
| 700 | 1 | |a Kaster, Friederike |e verfasserin |4 aut | |
| 700 | 1 | |a Zioga, Eleni |e verfasserin |4 aut | |
| 700 | 1 | |a Meyer, Corinna |e verfasserin |4 aut | |
| 700 | 1 | |a Lueb, Carolin |e verfasserin |4 aut | |
| 700 | 1 | |a Sure, Ulrich |e verfasserin |4 aut | |
| 700 | 1 | |a Lang, Stephan |e verfasserin |4 aut | |
| 700 | 1 | |a Geisthoff, Urban |e verfasserin |4 aut | |
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