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Anaesthetic Approach for Patient with Hereditary Angioedema
Hereditary Angioedema (HEA), a disease caused by a mutation in the gene that encodes for the production of the fraction C1 in the complement (C1-INH), is a rare pathology (1/50.000) that causes swelling of the skin and submucosa in various organs, either naturally triggered or provoked by physical a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Turkish Anaesthesiology and Intensive Care Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001801/ https://www.ncbi.nlm.nih.gov/pubmed/32076683 http://dx.doi.org/10.5152/TJAR.2019.90522 |
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author | Melo, Maize Cordeiro Boas, Walkiria Wingester Vilas Faria, Marcos Daniel Lima, Alyne Andrade Souza, Rafaela Souto |
author_facet | Melo, Maize Cordeiro Boas, Walkiria Wingester Vilas Faria, Marcos Daniel Lima, Alyne Andrade Souza, Rafaela Souto |
author_sort | Melo, Maize Cordeiro |
collection | PubMed |
description | Hereditary Angioedema (HEA), a disease caused by a mutation in the gene that encodes for the production of the fraction C1 in the complement (C1-INH), is a rare pathology (1/50.000) that causes swelling of the skin and submucosa in various organs, either naturally triggered or provoked by physical and psychological traumas, infections, or by the use of nonsteroidal anti-inflammatory drugs (NSAIDs) and angiotensin-converting enzyme inhibitors (ACEIs). Surgical trauma may spur the HEA crisis, leading to complications such as the swelling of the respiratory tracts and hemodynamic instability. Thus, the pre-surgical approach to HEA patients requires a specific plan that ensures short term prophylaxis, careful intra-operative management, rescue therapy and intensive post-surgery care. We present a report on a video-laparoscopic cholecystectomy approach for a 28-year-old woman diagnosed with asthma and HEA with symptomatic choledocholithiasis. We opted for short-term prophylaxis and immunology with the intravenous application of C1-INH. Ultrasonography imaging showed arterial wall oedema, which could correspond to a manifestation of C1-INH deficiency in the wall of the manipulated arteries during ultrasonography-guided puncture. Once the patient recovered consciousness, she was transferred to the intensive care unit and was discharged on the 6(th) day of hospitalisation. |
format | Online Article Text |
id | pubmed-7001801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Turkish Anaesthesiology and Intensive Care Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70018012020-02-19 Anaesthetic Approach for Patient with Hereditary Angioedema Melo, Maize Cordeiro Boas, Walkiria Wingester Vilas Faria, Marcos Daniel Lima, Alyne Andrade Souza, Rafaela Souto Turk J Anaesthesiol Reanim Case Report Hereditary Angioedema (HEA), a disease caused by a mutation in the gene that encodes for the production of the fraction C1 in the complement (C1-INH), is a rare pathology (1/50.000) that causes swelling of the skin and submucosa in various organs, either naturally triggered or provoked by physical and psychological traumas, infections, or by the use of nonsteroidal anti-inflammatory drugs (NSAIDs) and angiotensin-converting enzyme inhibitors (ACEIs). Surgical trauma may spur the HEA crisis, leading to complications such as the swelling of the respiratory tracts and hemodynamic instability. Thus, the pre-surgical approach to HEA patients requires a specific plan that ensures short term prophylaxis, careful intra-operative management, rescue therapy and intensive post-surgery care. We present a report on a video-laparoscopic cholecystectomy approach for a 28-year-old woman diagnosed with asthma and HEA with symptomatic choledocholithiasis. We opted for short-term prophylaxis and immunology with the intravenous application of C1-INH. Ultrasonography imaging showed arterial wall oedema, which could correspond to a manifestation of C1-INH deficiency in the wall of the manipulated arteries during ultrasonography-guided puncture. Once the patient recovered consciousness, she was transferred to the intensive care unit and was discharged on the 6(th) day of hospitalisation. Turkish Anaesthesiology and Intensive Care Society 2020-02 2019-11-11 /pmc/articles/PMC7001801/ /pubmed/32076683 http://dx.doi.org/10.5152/TJAR.2019.90522 Text en © Copyright 2020 by Turkish Anaesthesiology and Intensive Care Society This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Case Report Melo, Maize Cordeiro Boas, Walkiria Wingester Vilas Faria, Marcos Daniel Lima, Alyne Andrade Souza, Rafaela Souto Anaesthetic Approach for Patient with Hereditary Angioedema |
title | Anaesthetic Approach for Patient with Hereditary Angioedema |
title_full | Anaesthetic Approach for Patient with Hereditary Angioedema |
title_fullStr | Anaesthetic Approach for Patient with Hereditary Angioedema |
title_full_unstemmed | Anaesthetic Approach for Patient with Hereditary Angioedema |
title_short | Anaesthetic Approach for Patient with Hereditary Angioedema |
title_sort | anaesthetic approach for patient with hereditary angioedema |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001801/ https://www.ncbi.nlm.nih.gov/pubmed/32076683 http://dx.doi.org/10.5152/TJAR.2019.90522 |
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