Clinical and haemodynamic effects of sildenafil in pulmonary hypertension: acute and mid-term effects

Aim The treatment of patients with pulmonary arterial hypertension remains a challenge. We set out to investigate the use of sildenafil, a selective inhibitor of phosphodiesterase type 5, in patients with this disease. Methods and results Ten patients (8 females, mean age 34.5±3.3 years) with pulmon...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European heart journal 2004-03, Vol.25 (5), p.431-436
Hauptverfasser: Mikhail, Ghada W, Prasad, Sanjay K, Li, Wei, Rogers, Paula, Chester, Adrian H, Bayne, Stephanie, Stephens, David, Khan, Mohammed, Gibbs, J.S.R, Evans, Timothy W, Mitchell, Andrew, Yacoub, Magdi H, Gatzoulis, Michael A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 436
container_issue 5
container_start_page 431
container_title European heart journal
container_volume 25
creator Mikhail, Ghada W
Prasad, Sanjay K
Li, Wei
Rogers, Paula
Chester, Adrian H
Bayne, Stephanie
Stephens, David
Khan, Mohammed
Gibbs, J.S.R
Evans, Timothy W
Mitchell, Andrew
Yacoub, Magdi H
Gatzoulis, Michael A
description Aim The treatment of patients with pulmonary arterial hypertension remains a challenge. We set out to investigate the use of sildenafil, a selective inhibitor of phosphodiesterase type 5, in patients with this disease. Methods and results Ten patients (8 females, mean age 34.5±3.3 years) with pulmonary hypertension underwent right heart catheterisation with vasodilator testing using incremental doses of intravenous sildenafil without adverse events. All patients were subsequently commenced on oral sildenafil 50 mg t.d.s. Nine patients had repeat right heart catheterisation 3 months after the commencement of oral therapy. There was a significant reduction in mean pulmonary artery pressure (from 55.8±5.9 to 50.4±6.1 mmHg, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.038\) \end{document}) and pulmonary vascular resistance (from 10.1±1.7 to 8.6±1.5 Wood units, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.009\) \end{document}), and an increase in cardiac output (from 4.7±0.3 to 5.0±0.4 l/min, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.15\) \end{document}). Furthermore, there was a significant increase in the 6-minute walk test, a mean of 112 m. In response to a quality-of-life questionnaire, patients indicated marked clinical improvement on sildenafil. Sildenafil was discontinued in 1 patient due to a transient visual disturbance. The only patient previously awaiting transplantation was removed from the active transplantation list. Conclusions Sildenafil is well tolerated in its intravenous and oral forms and appears to improve both pulmonary haemodynamics and the clinical status of patients with pulmonary hypertension after 3 months of oral therapy.
doi_str_mv 10.1016/j.ehj.2004.01.013
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71751278</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1418613621</sourcerecordid><originalsourceid>FETCH-LOGICAL-c503t-d283d6f8251e29720b58fda8815eb422a9d05c2ad9268fe8731026fe158185293</originalsourceid><addsrcrecordid>eNpdkU1v1DAQhi0EotvCD-CCLCR6y-Jx1h_hhlYtparEgQ9VXCxvPNY6JM7WTiT23-N2F4qQRprDPPNq5n0JeQVsCQzku26J227JGVstGZSqn5AFCM6rRq7EU7Jg0IhKSn17Qk5z7hhjWoJ8Tk5AsLrmQi4IrvsQQ2t7aqOjW4vD6PbRDqGl6D22U6ajpzn0DqP1oach0t3cD2O0aU-3-x2mCWMOY3xPbTtP-KAzBFdNmIY_Gi_IM2_7jC-P_Yx8u7z4ur6qbj5__LT-cFO15aCpclzXTnrNBSBvFGcbob2zWoPAzYpz2zgmWm5dw6X2qFUNjEuPIDRowZv6jJwfdHdpvJsxT2YIucW-txHHORsFSgBXuoBv_gO7cU6x3GY4iFWjZKMKBAeoTWPOCb3ZpTCUvw0wcx-A6UwJwNwHYBiUqsvO66PwvBnQPW4cHS_A2yNgc7HdJxvbkP_hhGTigasOXMgT_vo7t-mnkapWwlzd_jDX-jsXXxg3qv4NvWidXQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>215497697</pqid></control><display><type>article</type><title>Clinical and haemodynamic effects of sildenafil in pulmonary hypertension: acute and mid-term effects</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Mikhail, Ghada W ; Prasad, Sanjay K ; Li, Wei ; Rogers, Paula ; Chester, Adrian H ; Bayne, Stephanie ; Stephens, David ; Khan, Mohammed ; Gibbs, J.S.R ; Evans, Timothy W ; Mitchell, Andrew ; Yacoub, Magdi H ; Gatzoulis, Michael A</creator><creatorcontrib>Mikhail, Ghada W ; Prasad, Sanjay K ; Li, Wei ; Rogers, Paula ; Chester, Adrian H ; Bayne, Stephanie ; Stephens, David ; Khan, Mohammed ; Gibbs, J.S.R ; Evans, Timothy W ; Mitchell, Andrew ; Yacoub, Magdi H ; Gatzoulis, Michael A</creatorcontrib><description>Aim The treatment of patients with pulmonary arterial hypertension remains a challenge. We set out to investigate the use of sildenafil, a selective inhibitor of phosphodiesterase type 5, in patients with this disease. Methods and results Ten patients (8 females, mean age 34.5±3.3 years) with pulmonary hypertension underwent right heart catheterisation with vasodilator testing using incremental doses of intravenous sildenafil without adverse events. All patients were subsequently commenced on oral sildenafil 50 mg t.d.s. Nine patients had repeat right heart catheterisation 3 months after the commencement of oral therapy. There was a significant reduction in mean pulmonary artery pressure (from 55.8±5.9 to 50.4±6.1 mmHg, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.038\) \end{document}) and pulmonary vascular resistance (from 10.1±1.7 to 8.6±1.5 Wood units, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.009\) \end{document}), and an increase in cardiac output (from 4.7±0.3 to 5.0±0.4 l/min, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.15\) \end{document}). Furthermore, there was a significant increase in the 6-minute walk test, a mean of 112 m. In response to a quality-of-life questionnaire, patients indicated marked clinical improvement on sildenafil. Sildenafil was discontinued in 1 patient due to a transient visual disturbance. The only patient previously awaiting transplantation was removed from the active transplantation list. Conclusions Sildenafil is well tolerated in its intravenous and oral forms and appears to improve both pulmonary haemodynamics and the clinical status of patients with pulmonary hypertension after 3 months of oral therapy.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1016/j.ehj.2004.01.013</identifier><identifier>PMID: 15033256</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Administration, Oral ; Adult ; Biological and medical sciences ; Blood Pressure - drug effects ; Cardiology. Vascular system ; Female ; Hemodynamics - drug effects ; Humans ; Hypertension, Pulmonary - drug therapy ; Hypertension, Pulmonary - physiopathology ; Infusions, Intravenous ; Male ; Medical sciences ; Middle Aged ; Phosphodiesterase Inhibitors - administration &amp; dosage ; Piperazines - administration &amp; dosage ; Pneumology ; Pulmonary hypertension ; Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases ; Purines ; Sildenafil ; Sildenafil Citrate ; Sulfones ; Vascular Resistance - drug effects</subject><ispartof>European heart journal, 2004-03, Vol.25 (5), p.431-436</ispartof><rights>2004 INIST-CNRS</rights><rights>Copyright Oxford Publishing Limited(England) Mar 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-d283d6f8251e29720b58fda8815eb422a9d05c2ad9268fe8731026fe158185293</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15560556$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15033256$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mikhail, Ghada W</creatorcontrib><creatorcontrib>Prasad, Sanjay K</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Rogers, Paula</creatorcontrib><creatorcontrib>Chester, Adrian H</creatorcontrib><creatorcontrib>Bayne, Stephanie</creatorcontrib><creatorcontrib>Stephens, David</creatorcontrib><creatorcontrib>Khan, Mohammed</creatorcontrib><creatorcontrib>Gibbs, J.S.R</creatorcontrib><creatorcontrib>Evans, Timothy W</creatorcontrib><creatorcontrib>Mitchell, Andrew</creatorcontrib><creatorcontrib>Yacoub, Magdi H</creatorcontrib><creatorcontrib>Gatzoulis, Michael A</creatorcontrib><title>Clinical and haemodynamic effects of sildenafil in pulmonary hypertension: acute and mid-term effects</title><title>European heart journal</title><addtitle>Eur Heart J</addtitle><description>Aim The treatment of patients with pulmonary arterial hypertension remains a challenge. We set out to investigate the use of sildenafil, a selective inhibitor of phosphodiesterase type 5, in patients with this disease. Methods and results Ten patients (8 females, mean age 34.5±3.3 years) with pulmonary hypertension underwent right heart catheterisation with vasodilator testing using incremental doses of intravenous sildenafil without adverse events. All patients were subsequently commenced on oral sildenafil 50 mg t.d.s. Nine patients had repeat right heart catheterisation 3 months after the commencement of oral therapy. There was a significant reduction in mean pulmonary artery pressure (from 55.8±5.9 to 50.4±6.1 mmHg, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.038\) \end{document}) and pulmonary vascular resistance (from 10.1±1.7 to 8.6±1.5 Wood units, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.009\) \end{document}), and an increase in cardiac output (from 4.7±0.3 to 5.0±0.4 l/min, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.15\) \end{document}). Furthermore, there was a significant increase in the 6-minute walk test, a mean of 112 m. In response to a quality-of-life questionnaire, patients indicated marked clinical improvement on sildenafil. Sildenafil was discontinued in 1 patient due to a transient visual disturbance. The only patient previously awaiting transplantation was removed from the active transplantation list. Conclusions Sildenafil is well tolerated in its intravenous and oral forms and appears to improve both pulmonary haemodynamics and the clinical status of patients with pulmonary hypertension after 3 months of oral therapy.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Cardiology. Vascular system</subject><subject>Female</subject><subject>Hemodynamics - drug effects</subject><subject>Humans</subject><subject>Hypertension, Pulmonary - drug therapy</subject><subject>Hypertension, Pulmonary - physiopathology</subject><subject>Infusions, Intravenous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Phosphodiesterase Inhibitors - administration &amp; dosage</subject><subject>Piperazines - administration &amp; dosage</subject><subject>Pneumology</subject><subject>Pulmonary hypertension</subject><subject>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</subject><subject>Purines</subject><subject>Sildenafil</subject><subject>Sildenafil Citrate</subject><subject>Sulfones</subject><subject>Vascular Resistance - drug effects</subject><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkU1v1DAQhi0EotvCD-CCLCR6y-Jx1h_hhlYtparEgQ9VXCxvPNY6JM7WTiT23-N2F4qQRprDPPNq5n0JeQVsCQzku26J227JGVstGZSqn5AFCM6rRq7EU7Jg0IhKSn17Qk5z7hhjWoJ8Tk5AsLrmQi4IrvsQQ2t7aqOjW4vD6PbRDqGl6D22U6ajpzn0DqP1oach0t3cD2O0aU-3-x2mCWMOY3xPbTtP-KAzBFdNmIY_Gi_IM2_7jC-P_Yx8u7z4ur6qbj5__LT-cFO15aCpclzXTnrNBSBvFGcbob2zWoPAzYpz2zgmWm5dw6X2qFUNjEuPIDRowZv6jJwfdHdpvJsxT2YIucW-txHHORsFSgBXuoBv_gO7cU6x3GY4iFWjZKMKBAeoTWPOCb3ZpTCUvw0wcx-A6UwJwNwHYBiUqsvO66PwvBnQPW4cHS_A2yNgc7HdJxvbkP_hhGTigasOXMgT_vo7t-mnkapWwlzd_jDX-jsXXxg3qv4NvWidXQ</recordid><startdate>20040301</startdate><enddate>20040301</enddate><creator>Mikhail, Ghada W</creator><creator>Prasad, Sanjay K</creator><creator>Li, Wei</creator><creator>Rogers, Paula</creator><creator>Chester, Adrian H</creator><creator>Bayne, Stephanie</creator><creator>Stephens, David</creator><creator>Khan, Mohammed</creator><creator>Gibbs, J.S.R</creator><creator>Evans, Timothy W</creator><creator>Mitchell, Andrew</creator><creator>Yacoub, Magdi H</creator><creator>Gatzoulis, Michael A</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><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>7QP</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20040301</creationdate><title>Clinical and haemodynamic effects of sildenafil in pulmonary hypertension: acute and mid-term effects</title><author>Mikhail, Ghada W ; Prasad, Sanjay K ; Li, Wei ; Rogers, Paula ; Chester, Adrian H ; Bayne, Stephanie ; Stephens, David ; Khan, Mohammed ; Gibbs, J.S.R ; Evans, Timothy W ; Mitchell, Andrew ; Yacoub, Magdi H ; Gatzoulis, Michael A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-d283d6f8251e29720b58fda8815eb422a9d05c2ad9268fe8731026fe158185293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Administration, Oral</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Cardiology. Vascular system</topic><topic>Female</topic><topic>Hemodynamics - drug effects</topic><topic>Humans</topic><topic>Hypertension, Pulmonary - drug therapy</topic><topic>Hypertension, Pulmonary - physiopathology</topic><topic>Infusions, Intravenous</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Phosphodiesterase Inhibitors - administration &amp; dosage</topic><topic>Piperazines - administration &amp; dosage</topic><topic>Pneumology</topic><topic>Pulmonary hypertension</topic><topic>Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases</topic><topic>Purines</topic><topic>Sildenafil</topic><topic>Sildenafil Citrate</topic><topic>Sulfones</topic><topic>Vascular Resistance - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mikhail, Ghada W</creatorcontrib><creatorcontrib>Prasad, Sanjay K</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Rogers, Paula</creatorcontrib><creatorcontrib>Chester, Adrian H</creatorcontrib><creatorcontrib>Bayne, Stephanie</creatorcontrib><creatorcontrib>Stephens, David</creatorcontrib><creatorcontrib>Khan, Mohammed</creatorcontrib><creatorcontrib>Gibbs, J.S.R</creatorcontrib><creatorcontrib>Evans, Timothy W</creatorcontrib><creatorcontrib>Mitchell, Andrew</creatorcontrib><creatorcontrib>Yacoub, Magdi H</creatorcontrib><creatorcontrib>Gatzoulis, Michael A</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mikhail, Ghada W</au><au>Prasad, Sanjay K</au><au>Li, Wei</au><au>Rogers, Paula</au><au>Chester, Adrian H</au><au>Bayne, Stephanie</au><au>Stephens, David</au><au>Khan, Mohammed</au><au>Gibbs, J.S.R</au><au>Evans, Timothy W</au><au>Mitchell, Andrew</au><au>Yacoub, Magdi H</au><au>Gatzoulis, Michael A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and haemodynamic effects of sildenafil in pulmonary hypertension: acute and mid-term effects</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>2004-03-01</date><risdate>2004</risdate><volume>25</volume><issue>5</issue><spage>431</spage><epage>436</epage><pages>431-436</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>Aim The treatment of patients with pulmonary arterial hypertension remains a challenge. We set out to investigate the use of sildenafil, a selective inhibitor of phosphodiesterase type 5, in patients with this disease. Methods and results Ten patients (8 females, mean age 34.5±3.3 years) with pulmonary hypertension underwent right heart catheterisation with vasodilator testing using incremental doses of intravenous sildenafil without adverse events. All patients were subsequently commenced on oral sildenafil 50 mg t.d.s. Nine patients had repeat right heart catheterisation 3 months after the commencement of oral therapy. There was a significant reduction in mean pulmonary artery pressure (from 55.8±5.9 to 50.4±6.1 mmHg, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.038\) \end{document}) and pulmonary vascular resistance (from 10.1±1.7 to 8.6±1.5 Wood units, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.009\) \end{document}), and an increase in cardiac output (from 4.7±0.3 to 5.0±0.4 l/min, \batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \(p=0.15\) \end{document}). Furthermore, there was a significant increase in the 6-minute walk test, a mean of 112 m. In response to a quality-of-life questionnaire, patients indicated marked clinical improvement on sildenafil. Sildenafil was discontinued in 1 patient due to a transient visual disturbance. The only patient previously awaiting transplantation was removed from the active transplantation list. Conclusions Sildenafil is well tolerated in its intravenous and oral forms and appears to improve both pulmonary haemodynamics and the clinical status of patients with pulmonary hypertension after 3 months of oral therapy.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>15033256</pmid><doi>10.1016/j.ehj.2004.01.013</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0195-668X
ispartof European heart journal, 2004-03, Vol.25 (5), p.431-436
issn 0195-668X
1522-9645
language eng
recordid cdi_proquest_miscellaneous_71751278
source MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals
subjects Administration, Oral
Adult
Biological and medical sciences
Blood Pressure - drug effects
Cardiology. Vascular system
Female
Hemodynamics - drug effects
Humans
Hypertension, Pulmonary - drug therapy
Hypertension, Pulmonary - physiopathology
Infusions, Intravenous
Male
Medical sciences
Middle Aged
Phosphodiesterase Inhibitors - administration & dosage
Piperazines - administration & dosage
Pneumology
Pulmonary hypertension
Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases
Purines
Sildenafil
Sildenafil Citrate
Sulfones
Vascular Resistance - drug effects
title Clinical and haemodynamic effects of sildenafil in pulmonary hypertension: acute and mid-term effects
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T09%3A08%3A46IST&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=Clinical%20and%20haemodynamic%20effects%20of%20sildenafil%20in%20pulmonary%20hypertension:%20acute%20and%20mid-term%20effects&rft.jtitle=European%20heart%20journal&rft.au=Mikhail,%20Ghada%20W&rft.date=2004-03-01&rft.volume=25&rft.issue=5&rft.spage=431&rft.epage=436&rft.pages=431-436&rft.issn=0195-668X&rft.eissn=1522-9645&rft_id=info:doi/10.1016/j.ehj.2004.01.013&rft_dat=%3Cproquest_cross%3E1418613621%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=215497697&rft_id=info:pmid/15033256&rfr_iscdi=true