Hereditary Angioedema : A Review of the Current and Evolving Treatment Landscape
Copyright © 2023 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved..
Hereditary angioedema (HAE) is a rare disease characterized by sudden and often unprovoked episodes of swelling that can be potentially life-threatening when it involves the upper airway. The treatment options for both acute episodes of HAE and LTP, used to minimize the frequency and severity of angioedema attacks, were limited historically to very few options, had considerable side effects, and/or had considerable burden of treatment. Fortunately, through the elucidation of the pathophysiology of HAE, the development of newer targeted therapies has been possible both for acute therapy and long-term prophylaxis and even more are on the horizon. Because of the rapid development of these therapies, it can be challenging for clinicians to keep abreast of newer and developing treatments for HAE. This review article will outline the current and potential future treatments for HAE. It will also highlight important considerations when treating special HAE patient populations including women and pediatric patients.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:11 |
---|---|
Enthalten in: |
The journal of allergy and clinical immunology. In practice - 11(2023), 8 vom: 26. Aug., Seite 2315-2325 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Betschel, Stephen D [VerfasserIn] |
---|
Links: |
---|
Themen: |
Complement C1 Inhibitor Protein |
---|
Anmerkungen: |
Date Completed 11.08.2023 Date Revised 11.08.2023 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.jaip.2023.04.017 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM356203506 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM356203506 | ||
003 | DE-627 | ||
005 | 20231226065951.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.jaip.2023.04.017 |2 doi | |
028 | 5 | 2 | |a pubmed24n1187.xml |
035 | |a (DE-627)NLM356203506 | ||
035 | |a (NLM)37116793 | ||
035 | |a (PII)S2213-2198(23)00457-9 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Betschel, Stephen D |e verfasserin |4 aut | |
245 | 1 | 0 | |a Hereditary Angioedema |b A Review of the Current and Evolving Treatment Landscape |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 11.08.2023 | ||
500 | |a Date Revised 11.08.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2023 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved. | ||
520 | |a Hereditary angioedema (HAE) is a rare disease characterized by sudden and often unprovoked episodes of swelling that can be potentially life-threatening when it involves the upper airway. The treatment options for both acute episodes of HAE and LTP, used to minimize the frequency and severity of angioedema attacks, were limited historically to very few options, had considerable side effects, and/or had considerable burden of treatment. Fortunately, through the elucidation of the pathophysiology of HAE, the development of newer targeted therapies has been possible both for acute therapy and long-term prophylaxis and even more are on the horizon. Because of the rapid development of these therapies, it can be challenging for clinicians to keep abreast of newer and developing treatments for HAE. This review article will outline the current and potential future treatments for HAE. It will also highlight important considerations when treating special HAE patient populations including women and pediatric patients | ||
650 | 4 | |a Review | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Hereditary angioedema | |
650 | 7 | |a Complement C1 Inhibitor Protein |2 NLM | |
700 | 1 | |a Banerji, Aleena |e verfasserin |4 aut | |
700 | 1 | |a Busse, Paula J |e verfasserin |4 aut | |
700 | 1 | |a Cohn, Danny M |e verfasserin |4 aut | |
700 | 1 | |a Magerl, Markus |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t The journal of allergy and clinical immunology. In practice |d 2013 |g 11(2023), 8 vom: 26. Aug., Seite 2315-2325 |w (DE-627)NLM227247523 |x 2213-2201 |7 nnns |
773 | 1 | 8 | |g volume:11 |g year:2023 |g number:8 |g day:26 |g month:08 |g pages:2315-2325 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.jaip.2023.04.017 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 11 |j 2023 |e 8 |b 26 |c 08 |h 2315-2325 |