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...
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Veröffentlicht in: | European heart journal 2004-03, Vol.25 (5), p.431-436 |
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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 |
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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 & 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</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&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 & dosage</subject><subject>Piperazines - administration & 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 & dosage</topic><topic>Piperazines - administration & 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 & Calcified Tissue Abstracts</collection><collection>ProQuest Health & 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> |
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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 |
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