D17 SIGN "O" THE TIMES: DIAGNOSIS AND RISK STRATIFICATION OF PULMONARY HYPERTENSION: Prevalence Of Pulmonary Hypertension In A Large Cohort Of Hereditary Hemorrhagic Telangiectasia Patients

Methods We reviewed the medical charts of patients who had undergone RHC in the setting of selective pulmonary angiograms for embolization of pAVMs (between January 2004 and August 2016) at the Yale New Haven Hospital HHT Center. Conclusions In contrast to the findings of other investigators of a hi...

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Veröffentlicht in:	American journal of respiratory and critical care medicine 2017-01, Vol.195
Hauptverfasser:	Chizinga, M, Rudkovskaia, A A, Henderson, K, Pollak, J, Garcia-Tsao, G, Young, L H, Fares, W H
Format:	Artikel
Sprache:	eng
Schlagworte:	Intubation Medical diagnosis Mutation Pulmonary arteries Pulmonary hypertension
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container_title	American journal of respiratory and critical care medicine
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creator	Chizinga, M Rudkovskaia, A A Henderson, K Pollak, J Garcia-Tsao, G Young, L H Fares, W H
description	Methods We reviewed the medical charts of patients who had undergone RHC in the setting of selective pulmonary angiograms for embolization of pAVMs (between January 2004 and August 2016) at the Yale New Haven Hospital HHT Center. Conclusions In contrast to the findings of other investigators of a high prevalence of PH in HHT patients, this study (which up to our knowledge is the largest ever reported catheterization-based study of PH in HHT) shows a much lower prevalence of PH in this patient population, of 14%.
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Conclusions In contrast to the findings of other investigators of a high prevalence of PH in HHT patients, this study (which up to our knowledge is the largest ever reported catheterization-based study of PH in HHT) shows a much lower prevalence of PH in this patient population, of 14%.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><language>eng</language><publisher>New York: American Thoracic Society</publisher><subject>Intubation ; Medical diagnosis ; Mutation ; Pulmonary arteries ; Pulmonary hypertension</subject><ispartof>American journal of respiratory and critical care medicine, 2017-01, Vol.195</ispartof><rights>Copyright American Thoracic Society 2017</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>314,776,780</link.rule.ids></links><search><creatorcontrib>Chizinga, M</creatorcontrib><creatorcontrib>Rudkovskaia, A A</creatorcontrib><creatorcontrib>Henderson, K</creatorcontrib><creatorcontrib>Pollak, J</creatorcontrib><creatorcontrib>Garcia-Tsao, G</creatorcontrib><creatorcontrib>Young, L H</creatorcontrib><creatorcontrib>Fares, W H</creatorcontrib><title>D17 SIGN "O" THE TIMES: DIAGNOSIS AND RISK STRATIFICATION OF PULMONARY HYPERTENSION: Prevalence Of Pulmonary Hypertension In A Large Cohort Of Hereditary Hemorrhagic Telangiectasia Patients</title><title>American journal of respiratory and critical care medicine</title><description>Methods We reviewed the medical charts of patients who had undergone RHC in the setting of selective pulmonary angiograms for embolization of pAVMs (between January 2004 and August 2016) at the Yale New Haven Hospital HHT Center. Conclusions In contrast to the findings of other investigators of a high prevalence of PH in HHT patients, this study (which up to our knowledge is the largest ever reported catheterization-based study of PH in HHT) shows a much lower prevalence of PH in this patient population, of 14%.</description><subject>Intubation</subject><subject>Medical diagnosis</subject><subject>Mutation</subject><subject>Pulmonary arteries</subject><subject>Pulmonary hypertension</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNqNittqwkAURUNpofbyDwf7LOQe9S0k0QzVJGSmUJ9kSI8aiTN2ZiL4cf23pqUf0Je9Nqx1Y42cwAsm_iyyb4dvR97E92fv99aD1kfbdtypY4-sr9SJgJJlAeNyDCzPgJF1RueQknhZlJRQiIsUakJfgbI6ZmRBkmHLAsoFVG-rdVnE9QbyTZXVLCvoYOZQKbzwDkWDUO6g6ruTFFxdIb-eURkUupUCiIAYVlztERJ5kMr8tDkq_GjNb4wnqdSB79sGGHZc7FtsDNcth4qbFoXRT9bdjncan__4aL0sMpbkk7OSnz1qsz3KXolBbZ2ZG07DMAxc73_VNxwsYBY</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Chizinga, M</creator><creator>Rudkovskaia, A A</creator><creator>Henderson, K</creator><creator>Pollak, J</creator><creator>Garcia-Tsao, G</creator><creator>Young, L H</creator><creator>Fares, W H</creator><general>American Thoracic Society</general><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20170101</creationdate><title>D17 SIGN "O" THE TIMES: DIAGNOSIS AND RISK STRATIFICATION OF PULMONARY HYPERTENSION: Prevalence Of Pulmonary Hypertension In A Large Cohort Of Hereditary Hemorrhagic Telangiectasia Patients</title><author>Chizinga, M ; Rudkovskaia, A A ; Henderson, K ; Pollak, J ; Garcia-Tsao, G ; Young, L H ; Fares, W H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_19268666523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Intubation</topic><topic>Medical diagnosis</topic><topic>Mutation</topic><topic>Pulmonary arteries</topic><topic>Pulmonary hypertension</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chizinga, M</creatorcontrib><creatorcontrib>Rudkovskaia, A A</creatorcontrib><creatorcontrib>Henderson, K</creatorcontrib><creatorcontrib>Pollak, J</creatorcontrib><creatorcontrib>Garcia-Tsao, G</creatorcontrib><creatorcontrib>Young, L H</creatorcontrib><creatorcontrib>Fares, W H</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chizinga, M</au><au>Rudkovskaia, A A</au><au>Henderson, K</au><au>Pollak, J</au><au>Garcia-Tsao, G</au><au>Young, L H</au><au>Fares, W H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>D17 SIGN "O" THE TIMES: DIAGNOSIS AND RISK STRATIFICATION OF PULMONARY HYPERTENSION: Prevalence Of Pulmonary Hypertension In A Large Cohort Of Hereditary Hemorrhagic Telangiectasia Patients</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><date>2017-01-01</date><risdate>2017</risdate><volume>195</volume><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>Methods We reviewed the medical charts of patients who had undergone RHC in the setting of selective pulmonary angiograms for embolization of pAVMs (between January 2004 and August 2016) at the Yale New Haven Hospital HHT Center. Conclusions In contrast to the findings of other investigators of a high prevalence of PH in HHT patients, this study (which up to our knowledge is the largest ever reported catheterization-based study of PH in HHT) shows a much lower prevalence of PH in this patient population, of 14%.</abstract><cop>New York</cop><pub>American Thoracic Society</pub></addata></record>
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source	American Thoracic Society (ATS) Journals Online; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Journals@Ovid Complete
subjects	Intubation Medical diagnosis Mutation Pulmonary arteries Pulmonary hypertension
title	D17 SIGN "O" THE TIMES: DIAGNOSIS AND RISK STRATIFICATION OF PULMONARY HYPERTENSION: Prevalence Of Pulmonary Hypertension In A Large Cohort Of Hereditary Hemorrhagic Telangiectasia Patients
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