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Anesthesia management for emergency laparotomy in a pediatric patient with suspected hereditary angioedema
Hereditary angioedema (HAE) is caused by complement factor 1 inhibitor (C1-INH) deficiency, and its mode of inheritance is autosomal dominant. We present a case of an 8-year-old patient who required emergency laparotomy after a traffic accident. General anesthesia with tracheal intubation was necess...
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Published in: | Journal of anesthesia 2010-02, Vol.24 (1), p.121-123 |
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description | Hereditary angioedema (HAE) is caused by complement factor 1 inhibitor (C1-INH) deficiency, and its mode of inheritance is autosomal dominant. We present a case of an 8-year-old patient who required emergency laparotomy after a traffic accident. General anesthesia with tracheal intubation was necessary. The patient’s mother and maternal grandmother had been diagnosed with HAE. HAE is associated with high mortality when airway edema is caused by tracheal intubation. It was impossible to rule out HAE preoperatively in the patient. Therefore, we presumed that he had HAE and treated him with pasteurized C1-INH concentrate. The patient underwent laparotomy uneventfully. Several days after the operation, the laboratory data revealed that the perioperative plasma complement 1 q subunit (C1q) protein level and C1-INH function were not lowered. The diagnosis of HAE was not confirmed, but it was not possible to rule out the diagnosis either. The prophylactic use of a C1-INH in this case may be justified, because the procedure was an emergency and because of the high mortality associated with tracheal intubation in patients with HAE. |
doi_str_mv | 10.1007/s00540-009-0832-6 |
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We present a case of an 8-year-old patient who required emergency laparotomy after a traffic accident. General anesthesia with tracheal intubation was necessary. The patient’s mother and maternal grandmother had been diagnosed with HAE. HAE is associated with high mortality when airway edema is caused by tracheal intubation. It was impossible to rule out HAE preoperatively in the patient. Therefore, we presumed that he had HAE and treated him with pasteurized C1-INH concentrate. The patient underwent laparotomy uneventfully. Several days after the operation, the laboratory data revealed that the perioperative plasma complement 1 q subunit (C1q) protein level and C1-INH function were not lowered. The diagnosis of HAE was not confirmed, but it was not possible to rule out the diagnosis either. The prophylactic use of a C1-INH in this case may be justified, because the procedure was an emergency and because of the high mortality associated with tracheal intubation in patients with HAE.</description><identifier>ISSN: 0913-8668</identifier><identifier>EISSN: 1438-8359</identifier><identifier>DOI: 10.1007/s00540-009-0832-6</identifier><identifier>PMID: 20052501</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject>Accidents, Traffic ; Anesthesia ; Anesthesia, General ; Anesthesiology ; Angioedemas, Hereditary - complications ; Angioedemas, Hereditary - drug therapy ; Angioedemas, Hereditary - genetics ; Angioedemas, Hereditary - mortality ; Angioneurotic edema ; Bicycling ; Child ; Children ; Clinical Report ; Complement C1 Inhibitor Protein - therapeutic use ; Critical Care Medicine ; Edema - etiology ; Edema - mortality ; Edema - prevention & control ; Emergency Medicine ; Emergency Treatment ; Health aspects ; Humans ; Intensive ; Intestinal Perforation - surgery ; Intestine, Small - injuries ; Intestine, Small - surgery ; Intubation, Intratracheal - mortality ; Japan ; Laparotomy ; Male ; Medicine ; Medicine & Public Health ; Mortality ; Pain Medicine ; Pediatrics ; Tracheal Diseases - etiology ; Tracheal Diseases - mortality ; Tracheal Diseases - prevention & control ; Treatment Outcome</subject><ispartof>Journal of anesthesia, 2010-02, Vol.24 (1), p.121-123</ispartof><rights>Japanese Society of Anesthesiologists 2009</rights><rights>COPYRIGHT 2010 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c501t-293573768a24c0174e6083565ed966eb72c7f23cb36d0f422fe652611cc1dc8e3</citedby><cites>FETCH-LOGICAL-c501t-293573768a24c0174e6083565ed966eb72c7f23cb36d0f422fe652611cc1dc8e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20052501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yazawa, Tomoko</creatorcontrib><creatorcontrib>O’higashi, Toyohiko</creatorcontrib><creatorcontrib>Daijo, Hiroki</creatorcontrib><creatorcontrib>Shinomura, Tetsutaro</creatorcontrib><title>Anesthesia management for emergency laparotomy in a pediatric patient with suspected hereditary angioedema</title><title>Journal of anesthesia</title><addtitle>J Anesth</addtitle><addtitle>J Anesth</addtitle><description>Hereditary angioedema (HAE) is caused by complement factor 1 inhibitor (C1-INH) deficiency, and its mode of inheritance is autosomal dominant. We present a case of an 8-year-old patient who required emergency laparotomy after a traffic accident. General anesthesia with tracheal intubation was necessary. The patient’s mother and maternal grandmother had been diagnosed with HAE. HAE is associated with high mortality when airway edema is caused by tracheal intubation. It was impossible to rule out HAE preoperatively in the patient. Therefore, we presumed that he had HAE and treated him with pasteurized C1-INH concentrate. The patient underwent laparotomy uneventfully. Several days after the operation, the laboratory data revealed that the perioperative plasma complement 1 q subunit (C1q) protein level and C1-INH function were not lowered. The diagnosis of HAE was not confirmed, but it was not possible to rule out the diagnosis either. The prophylactic use of a C1-INH in this case may be justified, because the procedure was an emergency and because of the high mortality associated with tracheal intubation in patients with HAE.</description><subject>Accidents, Traffic</subject><subject>Anesthesia</subject><subject>Anesthesia, General</subject><subject>Anesthesiology</subject><subject>Angioedemas, Hereditary - complications</subject><subject>Angioedemas, Hereditary - drug therapy</subject><subject>Angioedemas, Hereditary - genetics</subject><subject>Angioedemas, Hereditary - mortality</subject><subject>Angioneurotic edema</subject><subject>Bicycling</subject><subject>Child</subject><subject>Children</subject><subject>Clinical Report</subject><subject>Complement C1 Inhibitor Protein - therapeutic use</subject><subject>Critical Care Medicine</subject><subject>Edema - etiology</subject><subject>Edema - mortality</subject><subject>Edema - prevention & control</subject><subject>Emergency Medicine</subject><subject>Emergency Treatment</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Intensive</subject><subject>Intestinal Perforation - surgery</subject><subject>Intestine, Small - injuries</subject><subject>Intestine, Small - surgery</subject><subject>Intubation, Intratracheal - mortality</subject><subject>Japan</subject><subject>Laparotomy</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mortality</subject><subject>Pain Medicine</subject><subject>Pediatrics</subject><subject>Tracheal Diseases - etiology</subject><subject>Tracheal Diseases - mortality</subject><subject>Tracheal Diseases - prevention & control</subject><subject>Treatment Outcome</subject><issn>0913-8668</issn><issn>1438-8359</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kV2L1DAUhoMo7rj6A7yRgBdedc1Hm6aXw7J-wII3eh0y6WknQ5vUJEXm33uGroIwSAIJyfOe5LwvIW85u-OMtR8zY03NKsa6imkpKvWM7HgtdaVl0z0nO9ZxWWml9A15lfOJMaY4ly_JjUChaBjfkdM-QC5HyN7S2QY7wgyh0CEmirs0QnBnOtnFpljifKY-UEsX6L0tyTu62OIv_C9fjjSveQFXoKdHSIgUm87UhtFH6GG2r8mLwU4Z3jytt-THp4fv91-qx2-fv97vHyuHPyqV6GTTylZpK2rHeFuDwuYa1UDfKQWHVrh2ENIdpOrZUAsxgGoENuYc750GeUs-bHWXFH-u2J2ZfXYwTTZAXLNppewa0WqN5PuNHO0ExochlmTdhTZ7fFEonC1S1RUKnYFkpxhg8Hj8D393hceBJnh3VcA3gUsx5wSDWZKf0TzDmbkEbbagDQZtLkEbhZp3T02uhxn6v4o_ySIgNiDjVRghmVNcU0Dj_1P1N-DoslI</recordid><startdate>20100201</startdate><enddate>20100201</enddate><creator>Yazawa, Tomoko</creator><creator>O’higashi, Toyohiko</creator><creator>Daijo, Hiroki</creator><creator>Shinomura, Tetsutaro</creator><general>Springer Japan</general><general>Springer</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20100201</creationdate><title>Anesthesia management for emergency laparotomy in a pediatric patient with suspected hereditary angioedema</title><author>Yazawa, Tomoko ; O’higashi, Toyohiko ; Daijo, Hiroki ; Shinomura, Tetsutaro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c501t-293573768a24c0174e6083565ed966eb72c7f23cb36d0f422fe652611cc1dc8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Accidents, Traffic</topic><topic>Anesthesia</topic><topic>Anesthesia, General</topic><topic>Anesthesiology</topic><topic>Angioedemas, Hereditary - complications</topic><topic>Angioedemas, Hereditary - drug therapy</topic><topic>Angioedemas, Hereditary - genetics</topic><topic>Angioedemas, Hereditary - mortality</topic><topic>Angioneurotic edema</topic><topic>Bicycling</topic><topic>Child</topic><topic>Children</topic><topic>Clinical Report</topic><topic>Complement C1 Inhibitor Protein - therapeutic use</topic><topic>Critical Care Medicine</topic><topic>Edema - etiology</topic><topic>Edema - mortality</topic><topic>Edema - prevention & control</topic><topic>Emergency Medicine</topic><topic>Emergency Treatment</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Intensive</topic><topic>Intestinal Perforation - surgery</topic><topic>Intestine, Small - injuries</topic><topic>Intestine, Small - surgery</topic><topic>Intubation, Intratracheal - mortality</topic><topic>Japan</topic><topic>Laparotomy</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mortality</topic><topic>Pain Medicine</topic><topic>Pediatrics</topic><topic>Tracheal Diseases - etiology</topic><topic>Tracheal Diseases - mortality</topic><topic>Tracheal Diseases - prevention & control</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yazawa, Tomoko</creatorcontrib><creatorcontrib>O’higashi, Toyohiko</creatorcontrib><creatorcontrib>Daijo, Hiroki</creatorcontrib><creatorcontrib>Shinomura, Tetsutaro</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of anesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yazawa, Tomoko</au><au>O’higashi, Toyohiko</au><au>Daijo, Hiroki</au><au>Shinomura, Tetsutaro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anesthesia management for emergency laparotomy in a pediatric patient with suspected hereditary angioedema</atitle><jtitle>Journal of anesthesia</jtitle><stitle>J Anesth</stitle><addtitle>J Anesth</addtitle><date>2010-02-01</date><risdate>2010</risdate><volume>24</volume><issue>1</issue><spage>121</spage><epage>123</epage><pages>121-123</pages><issn>0913-8668</issn><eissn>1438-8359</eissn><abstract>Hereditary angioedema (HAE) is caused by complement factor 1 inhibitor (C1-INH) deficiency, and its mode of inheritance is autosomal dominant. We present a case of an 8-year-old patient who required emergency laparotomy after a traffic accident. General anesthesia with tracheal intubation was necessary. The patient’s mother and maternal grandmother had been diagnosed with HAE. HAE is associated with high mortality when airway edema is caused by tracheal intubation. It was impossible to rule out HAE preoperatively in the patient. Therefore, we presumed that he had HAE and treated him with pasteurized C1-INH concentrate. The patient underwent laparotomy uneventfully. Several days after the operation, the laboratory data revealed that the perioperative plasma complement 1 q subunit (C1q) protein level and C1-INH function were not lowered. The diagnosis of HAE was not confirmed, but it was not possible to rule out the diagnosis either. 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subjects | Accidents, Traffic Anesthesia Anesthesia, General Anesthesiology Angioedemas, Hereditary - complications Angioedemas, Hereditary - drug therapy Angioedemas, Hereditary - genetics Angioedemas, Hereditary - mortality Angioneurotic edema Bicycling Child Children Clinical Report Complement C1 Inhibitor Protein - therapeutic use Critical Care Medicine Edema - etiology Edema - mortality Edema - prevention & control Emergency Medicine Emergency Treatment Health aspects Humans Intensive Intestinal Perforation - surgery Intestine, Small - injuries Intestine, Small - surgery Intubation, Intratracheal - mortality Japan Laparotomy Male Medicine Medicine & Public Health Mortality Pain Medicine Pediatrics Tracheal Diseases - etiology Tracheal Diseases - mortality Tracheal Diseases - prevention & control Treatment Outcome |
title | Anesthesia management for emergency laparotomy in a pediatric patient with suspected hereditary angioedema |
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