Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography
Pulmonary arteriovenous malformations (PAVMs) are direct connections between the pulmonary artery and the pulmonary vein, mostly associated with hereditary hemorrhagic telangiectasia (HHT). PAVMs can lead to severe neurologic complications such as stroke and brain abscess. The risk of complications...
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Veröffentlicht in: | Chest 2023-03, Vol.163 (3), p.669-677 |
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description | Pulmonary arteriovenous malformations (PAVMs) are direct connections between the pulmonary artery and the pulmonary vein, mostly associated with hereditary hemorrhagic telangiectasia (HHT). PAVMs can lead to severe neurologic complications such as stroke and brain abscess. The risk of complications decreases after embolization. Therefore, screening for PAVMs using transthoracic contrast echocardiography (TTCE) is recommended, including a rescreening interval of 5 years.
Is extension of the interval for rescreening patients without a pulmonary right-to-left shunt (RLS) of up to 10 years appropriate?
Adult patients with HHT with 5- or 10-year follow-up TTCE, or both, were included. Patients who underwent PAVM embolization in the past or at baseline were excluded. The RLS grades and presence of a treatable PAVM were compared with baseline.
In total, 387 patients (median age, 45 years [interquartile range, 33-54 years]; 56% women) involving 5- and 10-year follow-up data in 363 and 166 patients, respectively, were included. None of the patients (n = 148) without a pulmonary RLS at baseline demonstrated a treatable PAVM after 5 and 10 years. Of the patients with a pulmonary RLS at baseline, 20 patients (9%) and three patients (3%) demonstrated a treatable PAVM at the 5- and 10-year follow-up, respectively. In most patients, the RLS grade remained stable over time.
On the basis of the results of this retrospective study, we believe that the rescreening interval for patients with HHT without a pulmonary RLS at initial screening may be extended to 10 years. Those with a pulmonary RLS should be rescreened every 5 years because treatable PAVMs can evolve. |
doi_str_mv | 10.1016/j.chest.2022.11.005 |
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Is extension of the interval for rescreening patients without a pulmonary right-to-left shunt (RLS) of up to 10 years appropriate?
Adult patients with HHT with 5- or 10-year follow-up TTCE, or both, were included. Patients who underwent PAVM embolization in the past or at baseline were excluded. The RLS grades and presence of a treatable PAVM were compared with baseline.
In total, 387 patients (median age, 45 years [interquartile range, 33-54 years]; 56% women) involving 5- and 10-year follow-up data in 363 and 166 patients, respectively, were included. None of the patients (n = 148) without a pulmonary RLS at baseline demonstrated a treatable PAVM after 5 and 10 years. Of the patients with a pulmonary RLS at baseline, 20 patients (9%) and three patients (3%) demonstrated a treatable PAVM at the 5- and 10-year follow-up, respectively. In most patients, the RLS grade remained stable over time.
On the basis of the results of this retrospective study, we believe that the rescreening interval for patients with HHT without a pulmonary RLS at initial screening may be extended to 10 years. Those with a pulmonary RLS should be rescreened every 5 years because treatable PAVMs can evolve.</description><identifier>EISSN: 1931-3543</identifier><identifier>DOI: 10.1016/j.chest.2022.11.005</identifier><identifier>PMID: 36368615</identifier><language>eng</language><publisher>United States</publisher><subject>Adult ; Arteriovenous Malformations - complications ; Arteriovenous Malformations - diagnostic imaging ; Echocardiography - methods ; Embolization, Therapeutic - methods ; Female ; Humans ; Male ; Middle Aged ; Pulmonary Artery - abnormalities ; Pulmonary Artery - diagnostic imaging ; Pulmonary Veins - abnormalities ; Pulmonary Veins - diagnostic imaging ; Retrospective Studies ; Telangiectasia, Hereditary Hemorrhagic - complications ; Telangiectasia, Hereditary Hemorrhagic - diagnostic imaging</subject><ispartof>Chest, 2023-03, Vol.163 (3), p.669-677</ispartof><rights>Copyright © 2022 American College of Chest Physicians. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/36368615$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hessels, J</creatorcontrib><creatorcontrib>Kroon, S</creatorcontrib><creatorcontrib>Vorselaars, V V M</creatorcontrib><creatorcontrib>Boerman, S</creatorcontrib><creatorcontrib>Mager, J J</creatorcontrib><creatorcontrib>Post, M C</creatorcontrib><title>Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography</title><title>Chest</title><addtitle>Chest</addtitle><description>Pulmonary arteriovenous malformations (PAVMs) are direct connections between the pulmonary artery and the pulmonary vein, mostly associated with hereditary hemorrhagic telangiectasia (HHT). PAVMs can lead to severe neurologic complications such as stroke and brain abscess. The risk of complications decreases after embolization. Therefore, screening for PAVMs using transthoracic contrast echocardiography (TTCE) is recommended, including a rescreening interval of 5 years.
Is extension of the interval for rescreening patients without a pulmonary right-to-left shunt (RLS) of up to 10 years appropriate?
Adult patients with HHT with 5- or 10-year follow-up TTCE, or both, were included. Patients who underwent PAVM embolization in the past or at baseline were excluded. The RLS grades and presence of a treatable PAVM were compared with baseline.
In total, 387 patients (median age, 45 years [interquartile range, 33-54 years]; 56% women) involving 5- and 10-year follow-up data in 363 and 166 patients, respectively, were included. None of the patients (n = 148) without a pulmonary RLS at baseline demonstrated a treatable PAVM after 5 and 10 years. Of the patients with a pulmonary RLS at baseline, 20 patients (9%) and three patients (3%) demonstrated a treatable PAVM at the 5- and 10-year follow-up, respectively. In most patients, the RLS grade remained stable over time.
On the basis of the results of this retrospective study, we believe that the rescreening interval for patients with HHT without a pulmonary RLS at initial screening may be extended to 10 years. Those with a pulmonary RLS should be rescreened every 5 years because treatable PAVMs can evolve.</description><subject>Adult</subject><subject>Arteriovenous Malformations - complications</subject><subject>Arteriovenous Malformations - diagnostic imaging</subject><subject>Echocardiography - methods</subject><subject>Embolization, Therapeutic - methods</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pulmonary Artery - abnormalities</subject><subject>Pulmonary Artery - diagnostic imaging</subject><subject>Pulmonary Veins - abnormalities</subject><subject>Pulmonary Veins - diagnostic imaging</subject><subject>Retrospective Studies</subject><subject>Telangiectasia, Hereditary Hemorrhagic - complications</subject><subject>Telangiectasia, Hereditary Hemorrhagic - diagnostic imaging</subject><issn>1931-3543</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE1Lw0AYhBdBbK3-AkH26CVxP7K7ibdS6gdUFKkHT2GzeWNSNtm4mxT6702xnubyzDAzCN1QElNC5f0uNjWEIWaEsZjSmBBxhuY04zTiIuEzdBnCjhBCaSYv0IxLLlNJxRx9rffOjkPjOuwq_D7a1nXaH_DSD-Abt4fOjQG_als53-ojFx7wtgb84SwcLSvXDV6HAa9N7Yz2ZeO-ve7rwxU6r7QNcH3SBfp8XG9Xz9Hm7elltdxEPaN0iJgBxSvNqwKYIqXWmTbEKJbJQkBqGCEyKUqtCICkkIApCUuUNEIIyIRM-ALd_eX23v2M0wl52wQD1uoOpu45U1ykSgmqJvT2hI5FC2Xe-6adxub_d_BfW4Fi_w</recordid><startdate>202303</startdate><enddate>202303</enddate><creator>Hessels, J</creator><creator>Kroon, S</creator><creator>Vorselaars, V V M</creator><creator>Boerman, S</creator><creator>Mager, J J</creator><creator>Post, M C</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>202303</creationdate><title>Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography</title><author>Hessels, J ; Kroon, S ; Vorselaars, V V M ; Boerman, S ; Mager, J J ; Post, M C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p211t-2ce73fa3fbe270daa9ac0c7296b5e8c20064bda70ee61e4ecd02476c555e95643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adult</topic><topic>Arteriovenous Malformations - complications</topic><topic>Arteriovenous Malformations - diagnostic imaging</topic><topic>Echocardiography - methods</topic><topic>Embolization, Therapeutic - methods</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pulmonary Artery - abnormalities</topic><topic>Pulmonary Artery - diagnostic imaging</topic><topic>Pulmonary Veins - abnormalities</topic><topic>Pulmonary Veins - diagnostic imaging</topic><topic>Retrospective Studies</topic><topic>Telangiectasia, Hereditary Hemorrhagic - complications</topic><topic>Telangiectasia, Hereditary Hemorrhagic - diagnostic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hessels, J</creatorcontrib><creatorcontrib>Kroon, S</creatorcontrib><creatorcontrib>Vorselaars, V V M</creatorcontrib><creatorcontrib>Boerman, S</creatorcontrib><creatorcontrib>Mager, J J</creatorcontrib><creatorcontrib>Post, M C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Chest</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hessels, J</au><au>Kroon, S</au><au>Vorselaars, V V M</au><au>Boerman, S</au><au>Mager, J J</au><au>Post, M C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography</atitle><jtitle>Chest</jtitle><addtitle>Chest</addtitle><date>2023-03</date><risdate>2023</risdate><volume>163</volume><issue>3</issue><spage>669</spage><epage>677</epage><pages>669-677</pages><eissn>1931-3543</eissn><abstract>Pulmonary arteriovenous malformations (PAVMs) are direct connections between the pulmonary artery and the pulmonary vein, mostly associated with hereditary hemorrhagic telangiectasia (HHT). PAVMs can lead to severe neurologic complications such as stroke and brain abscess. The risk of complications decreases after embolization. Therefore, screening for PAVMs using transthoracic contrast echocardiography (TTCE) is recommended, including a rescreening interval of 5 years.
Is extension of the interval for rescreening patients without a pulmonary right-to-left shunt (RLS) of up to 10 years appropriate?
Adult patients with HHT with 5- or 10-year follow-up TTCE, or both, were included. Patients who underwent PAVM embolization in the past or at baseline were excluded. The RLS grades and presence of a treatable PAVM were compared with baseline.
In total, 387 patients (median age, 45 years [interquartile range, 33-54 years]; 56% women) involving 5- and 10-year follow-up data in 363 and 166 patients, respectively, were included. None of the patients (n = 148) without a pulmonary RLS at baseline demonstrated a treatable PAVM after 5 and 10 years. Of the patients with a pulmonary RLS at baseline, 20 patients (9%) and three patients (3%) demonstrated a treatable PAVM at the 5- and 10-year follow-up, respectively. In most patients, the RLS grade remained stable over time.
On the basis of the results of this retrospective study, we believe that the rescreening interval for patients with HHT without a pulmonary RLS at initial screening may be extended to 10 years. Those with a pulmonary RLS should be rescreened every 5 years because treatable PAVMs can evolve.</abstract><cop>United States</cop><pmid>36368615</pmid><doi>10.1016/j.chest.2022.11.005</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Arteriovenous Malformations - complications Arteriovenous Malformations - diagnostic imaging Echocardiography - methods Embolization, Therapeutic - methods Female Humans Male Middle Aged Pulmonary Artery - abnormalities Pulmonary Artery - diagnostic imaging Pulmonary Veins - abnormalities Pulmonary Veins - diagnostic imaging Retrospective Studies Telangiectasia, Hereditary Hemorrhagic - complications Telangiectasia, Hereditary Hemorrhagic - diagnostic imaging |
title | Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography |
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