Hereditary Hemorrhagic Telangiectasia: A Primer for Critical Care Nurses
Hereditary hemorrhagic telangiectasia is a rare, autosomal dominant genetic disease that causes abnormal growth of blood vessels and, subsequently, life-threatening arteriovenous malformations in vital organs. Epistaxis may be one of the initial clues that a patient has more serious, generalized art...
Gespeichert in:
| Veröffentlicht in: | Critical care nurse 2016-06, Vol.36 (3), p.36-48 |
|---|---|
| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 48 |
|---|---|
| container_issue | 3 |
| container_start_page | 36 |
| container_title | Critical care nurse |
| container_volume | 36 |
| creator | Sacco, Kathleen M Barkley, Jr, Thomas W |
| description | Hereditary hemorrhagic telangiectasia is a rare, autosomal dominant genetic disease that causes abnormal growth of blood vessels and, subsequently, life-threatening arteriovenous malformations in vital organs. Epistaxis may be one of the initial clues that a patient has more serious, generalized arteriovenous malformations. Recommended treatment involves careful evaluation to determine the severity and risk of spontaneous rupture of the malformations and the management of various signs and symptoms. The disease remains undiagnosed in many patients, and health care providers may miss the diagnosis until catastrophic events happen in multiple family members. Prompt recognition of hereditary hemorrhagic telangiectasia and early intervention can halt the dangerous course of the disease. Critical care nurses can assist with early diagnosis within families with this genetic disease, thus preventing early death and disability. |
| doi_str_mv | 10.4037/ccn2016270 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1793907094</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1793907094</sourcerecordid><originalsourceid>FETCH-LOGICAL-c287t-3fbfde293aafa26cb34683d658fd3143d84faa98f68d3d23e30e19bfaee6a5283</originalsourceid><addsrcrecordid>eNpFkL1OwzAYRS0EoqWw8ADII0IK-C-xzYYiIEgVMJQ5cuzPxShpip0MvD1BLTDd5ejq3oPQOSXXgnB5Y-2GEVowSQ7QnGpBMsVycojmhEmd5UKwGTpJ6YMQKpSix2jGJMsZJWSOqgoiuDCY-IUr6PoY3806WLyC1mzWAexgUjC3-A6_xtBBxL6PuIxhCNa0uDQR8PMYE6RTdORNm-Bsnwv09nC_Kqts-fL4VN4tM8uUHDLuG--AaW6MN6ywDReF4q7IlXecCu6U8MZo5QvluGMcOAGqG28ACpMzxRfocte7jf3nCGmou5AstNNc6MdUU6m5JpJoMaFXO9TGPqUIvt5OH6anNSX1j7n639wEX-x7x6YD94f-quLf4Dpo8Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1793907094</pqid></control><display><type>article</type><title>Hereditary Hemorrhagic Telangiectasia: A Primer for Critical Care Nurses</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><source>Journals@Ovid Complete</source><creator>Sacco, Kathleen M ; Barkley, Jr, Thomas W</creator><creatorcontrib>Sacco, Kathleen M ; Barkley, Jr, Thomas W</creatorcontrib><description>Hereditary hemorrhagic telangiectasia is a rare, autosomal dominant genetic disease that causes abnormal growth of blood vessels and, subsequently, life-threatening arteriovenous malformations in vital organs. Epistaxis may be one of the initial clues that a patient has more serious, generalized arteriovenous malformations. Recommended treatment involves careful evaluation to determine the severity and risk of spontaneous rupture of the malformations and the management of various signs and symptoms. The disease remains undiagnosed in many patients, and health care providers may miss the diagnosis until catastrophic events happen in multiple family members. Prompt recognition of hereditary hemorrhagic telangiectasia and early intervention can halt the dangerous course of the disease. Critical care nurses can assist with early diagnosis within families with this genetic disease, thus preventing early death and disability.</description><identifier>ISSN: 0279-5442</identifier><identifier>EISSN: 1940-8250</identifier><identifier>DOI: 10.4037/ccn2016270</identifier><identifier>PMID: 27252100</identifier><language>eng</language><publisher>United States</publisher><subject>Cerebral Hemorrhage - etiology ; Cerebral Hemorrhage - nursing ; Cerebral Hemorrhage - physiopathology ; Combined Modality Therapy ; Critical Care - methods ; Critical Care Nursing - methods ; Early Diagnosis ; Epistaxis - diagnosis ; Epistaxis - etiology ; Genetic Predisposition to Disease ; Hospitals, Community ; Humans ; Intensive Care Units ; Male ; Nurse's Role ; Nursing ; Nursing Diagnosis - methods ; Prognosis ; Risk Assessment ; Survival Rate ; Telangiectasia, Hereditary Hemorrhagic - genetics ; Telangiectasia, Hereditary Hemorrhagic - physiopathology ; Telangiectasia, Hereditary Hemorrhagic - therapy ; Young Adult</subject><ispartof>Critical care nurse, 2016-06, Vol.36 (3), p.36-48</ispartof><rights>2016 American Association of Critical-Care Nurses.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c287t-3fbfde293aafa26cb34683d658fd3143d84faa98f68d3d23e30e19bfaee6a5283</citedby><cites>FETCH-LOGICAL-c287t-3fbfde293aafa26cb34683d658fd3143d84faa98f68d3d23e30e19bfaee6a5283</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27252100$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sacco, Kathleen M</creatorcontrib><creatorcontrib>Barkley, Jr, Thomas W</creatorcontrib><title>Hereditary Hemorrhagic Telangiectasia: A Primer for Critical Care Nurses</title><title>Critical care nurse</title><addtitle>Crit Care Nurse</addtitle><description>Hereditary hemorrhagic telangiectasia is a rare, autosomal dominant genetic disease that causes abnormal growth of blood vessels and, subsequently, life-threatening arteriovenous malformations in vital organs. Epistaxis may be one of the initial clues that a patient has more serious, generalized arteriovenous malformations. Recommended treatment involves careful evaluation to determine the severity and risk of spontaneous rupture of the malformations and the management of various signs and symptoms. The disease remains undiagnosed in many patients, and health care providers may miss the diagnosis until catastrophic events happen in multiple family members. Prompt recognition of hereditary hemorrhagic telangiectasia and early intervention can halt the dangerous course of the disease. Critical care nurses can assist with early diagnosis within families with this genetic disease, thus preventing early death and disability.</description><subject>Cerebral Hemorrhage - etiology</subject><subject>Cerebral Hemorrhage - nursing</subject><subject>Cerebral Hemorrhage - physiopathology</subject><subject>Combined Modality Therapy</subject><subject>Critical Care - methods</subject><subject>Critical Care Nursing - methods</subject><subject>Early Diagnosis</subject><subject>Epistaxis - diagnosis</subject><subject>Epistaxis - etiology</subject><subject>Genetic Predisposition to Disease</subject><subject>Hospitals, Community</subject><subject>Humans</subject><subject>Intensive Care Units</subject><subject>Male</subject><subject>Nurse's Role</subject><subject>Nursing</subject><subject>Nursing Diagnosis - methods</subject><subject>Prognosis</subject><subject>Risk Assessment</subject><subject>Survival Rate</subject><subject>Telangiectasia, Hereditary Hemorrhagic - genetics</subject><subject>Telangiectasia, Hereditary Hemorrhagic - physiopathology</subject><subject>Telangiectasia, Hereditary Hemorrhagic - therapy</subject><subject>Young Adult</subject><issn>0279-5442</issn><issn>1940-8250</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkL1OwzAYRS0EoqWw8ADII0IK-C-xzYYiIEgVMJQ5cuzPxShpip0MvD1BLTDd5ejq3oPQOSXXgnB5Y-2GEVowSQ7QnGpBMsVycojmhEmd5UKwGTpJ6YMQKpSix2jGJMsZJWSOqgoiuDCY-IUr6PoY3806WLyC1mzWAexgUjC3-A6_xtBBxL6PuIxhCNa0uDQR8PMYE6RTdORNm-Bsnwv09nC_Kqts-fL4VN4tM8uUHDLuG--AaW6MN6ywDReF4q7IlXecCu6U8MZo5QvluGMcOAGqG28ACpMzxRfocte7jf3nCGmou5AstNNc6MdUU6m5JpJoMaFXO9TGPqUIvt5OH6anNSX1j7n639wEX-x7x6YD94f-quLf4Dpo8Q</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Sacco, Kathleen M</creator><creator>Barkley, Jr, Thomas W</creator><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>201606</creationdate><title>Hereditary Hemorrhagic Telangiectasia: A Primer for Critical Care Nurses</title><author>Sacco, Kathleen M ; Barkley, Jr, Thomas W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c287t-3fbfde293aafa26cb34683d658fd3143d84faa98f68d3d23e30e19bfaee6a5283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cerebral Hemorrhage - etiology</topic><topic>Cerebral Hemorrhage - nursing</topic><topic>Cerebral Hemorrhage - physiopathology</topic><topic>Combined Modality Therapy</topic><topic>Critical Care - methods</topic><topic>Critical Care Nursing - methods</topic><topic>Early Diagnosis</topic><topic>Epistaxis - diagnosis</topic><topic>Epistaxis - etiology</topic><topic>Genetic Predisposition to Disease</topic><topic>Hospitals, Community</topic><topic>Humans</topic><topic>Intensive Care Units</topic><topic>Male</topic><topic>Nurse's Role</topic><topic>Nursing</topic><topic>Nursing Diagnosis - methods</topic><topic>Prognosis</topic><topic>Risk Assessment</topic><topic>Survival Rate</topic><topic>Telangiectasia, Hereditary Hemorrhagic - genetics</topic><topic>Telangiectasia, Hereditary Hemorrhagic - physiopathology</topic><topic>Telangiectasia, Hereditary Hemorrhagic - therapy</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sacco, Kathleen M</creatorcontrib><creatorcontrib>Barkley, Jr, Thomas W</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>Critical care nurse</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sacco, Kathleen M</au><au>Barkley, Jr, Thomas W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hereditary Hemorrhagic Telangiectasia: A Primer for Critical Care Nurses</atitle><jtitle>Critical care nurse</jtitle><addtitle>Crit Care Nurse</addtitle><date>2016-06</date><risdate>2016</risdate><volume>36</volume><issue>3</issue><spage>36</spage><epage>48</epage><pages>36-48</pages><issn>0279-5442</issn><eissn>1940-8250</eissn><abstract>Hereditary hemorrhagic telangiectasia is a rare, autosomal dominant genetic disease that causes abnormal growth of blood vessels and, subsequently, life-threatening arteriovenous malformations in vital organs. Epistaxis may be one of the initial clues that a patient has more serious, generalized arteriovenous malformations. Recommended treatment involves careful evaluation to determine the severity and risk of spontaneous rupture of the malformations and the management of various signs and symptoms. The disease remains undiagnosed in many patients, and health care providers may miss the diagnosis until catastrophic events happen in multiple family members. Prompt recognition of hereditary hemorrhagic telangiectasia and early intervention can halt the dangerous course of the disease. Critical care nurses can assist with early diagnosis within families with this genetic disease, thus preventing early death and disability.</abstract><cop>United States</cop><pmid>27252100</pmid><doi>10.4037/ccn2016270</doi><tpages>13</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0279-5442 |
| ispartof | Critical care nurse, 2016-06, Vol.36 (3), p.36-48 |
| issn | 0279-5442 1940-8250 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1793907094 |
| source | MEDLINE; Alma/SFX Local Collection; Journals@Ovid Complete |
| subjects | Cerebral Hemorrhage - etiology Cerebral Hemorrhage - nursing Cerebral Hemorrhage - physiopathology Combined Modality Therapy Critical Care - methods Critical Care Nursing - methods Early Diagnosis Epistaxis - diagnosis Epistaxis - etiology Genetic Predisposition to Disease Hospitals, Community Humans Intensive Care Units Male Nurse's Role Nursing Nursing Diagnosis - methods Prognosis Risk Assessment Survival Rate Telangiectasia, Hereditary Hemorrhagic - genetics Telangiectasia, Hereditary Hemorrhagic - physiopathology Telangiectasia, Hereditary Hemorrhagic - therapy Young Adult |
| title | Hereditary Hemorrhagic Telangiectasia: A Primer for Critical Care Nurses |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T19%3A56%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Hereditary%20Hemorrhagic%20Telangiectasia:%20A%20Primer%20for%20Critical%20Care%20Nurses&rft.jtitle=Critical%20care%20nurse&rft.au=Sacco,%20Kathleen%20M&rft.date=2016-06&rft.volume=36&rft.issue=3&rft.spage=36&rft.epage=48&rft.pages=36-48&rft.issn=0279-5442&rft.eissn=1940-8250&rft_id=info:doi/10.4037/ccn2016270&rft_dat=%3Cproquest_cross%3E1793907094%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1793907094&rft_id=info:pmid/27252100&rfr_iscdi=true |