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Impact of proton pump inhibitors and dual antiplatelet therapy cessation on outcomes following percutaneous coronary intervention: Results From the PARIS Registry
Background Proton pump inhibitors (PPI) may decrease the availability of clopidogrel by competitive antagonism, leading to a potential increase in ischemic events. Methods We evaluated patients from the all‐comer PARIS registry treated with dual antiplatelet therapy (DAPT) with aspirin and clopidogr...
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Published in: | Catheterization and cardiovascular interventions 2017-06, Vol.89 (7), p.E217-E225 |
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creator | Chandrasekhar, Jaya Bansilal, Sameer Baber, Usman Sartori, Samantha Aquino, Melissa Farhan, Serdar Vogel, Birgit Faggioni, Michela Giustino, Gennaro Ariti, Cono Colombo, Antonio Chieffo, Alaide Kini, Annapoorna Saporito, Richard Michael Gibson, C. Witzenbichler, Bernhard Cohen, David Moliterno, David Stuckey, Thomas Henry, Timothy Pocock, Stuart Dangas, George Gabriel Steg, P. Mehran, Roxana |
description | Background
Proton pump inhibitors (PPI) may decrease the availability of clopidogrel by competitive antagonism, leading to a potential increase in ischemic events.
Methods
We evaluated patients from the all‐comer PARIS registry treated with dual antiplatelet therapy (DAPT) with aspirin and clopidogrel following coronary stenting for outcomes stratified by PPI use. Two‐year major adverse cardiovascular events (MACE), composite of cardiac death, myocardial infarction, definite or probable stent thrombosis or target lesion revascularization (TLR), and net adverse cardiac events (NACE), composite of MACE or Bleeding Academic Research consortium (BARC) type 3 or 5 bleeding were assessed. We also explored associations between PPI use and patterns of 2‐year DAPT cessation.
Results
The cohort comprised 4635 patients (23% PPI users) with mean age 64.4 ±11.4 years. Two year adjusted risk of MACE (HR: 1.27, 95% CI: 1.04–1.55), NACE (HR: 1.21, 95% CI: 1.01–1.44) and TLR (HR: 1.33, 95% CI: 1.04–1.71) were significantly higher in PPI users vs. non‐users, without a difference in bleeding. Although the incidence of 2‐year DAPT discontinuation and interruption was similar, DAPT disruption was significantly lower among PPI users vs. non‐users (10.0% vs. 14.7%, P |
doi_str_mv | 10.1002/ccd.26716 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1859737351</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1859737351</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3536-6d9bd68cc8c92fb5e4f0801f2dce9f95e91e9f7ef6eccc1f1672720a898fc0c83</originalsourceid><addsrcrecordid>eNp1kd9qFDEUh4MotlYvfAEJeKMX2yaZTjLxrqxWFwpKVfBuyJ45aVMykzF_LPs6PqlZZ_VCEALnEL7zcZIfIc85O-WMiTOA4VRIxeUDcsxbIVZKyG8PDz3X5_KIPEnpjjGmpdCPyZFQsmWy6Y7Jz804G8g0WDrHkMNE5zLO1E23butyiImaaaBDMb422c3eZPSYab7FaOYdBUzJZFfn9qdkCCMmaoP34d5NN3TGCCWbCUNJFEIMk4m7qs8Yf-C0H3xDrzEVnxO9jGHci-mni-vN53p941KOu6fkkTU-4bNDPSFfL999WX9YXX18v1lfXK2gaRu5koPeDrID6EALu23x3LKOcSsGQG11i5rXqtBKBABuuVRCCWY63Vlg0DUn5NXirR_xvWDK_egSoPfL9j3vWq0a1bS8oi__Qe9CiVPdrueaac650k2lXi8UxJBSRNvP0Y31_T1n_T64vgbX_w6usi8OxrIdcfhL_kmqAmcLcO887v5v6tfrt4vyF-Cdpok</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1909111793</pqid></control><display><type>article</type><title>Impact of proton pump inhibitors and dual antiplatelet therapy cessation on outcomes following percutaneous coronary intervention: Results From the PARIS Registry</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Chandrasekhar, Jaya ; Bansilal, Sameer ; Baber, Usman ; Sartori, Samantha ; Aquino, Melissa ; Farhan, Serdar ; Vogel, Birgit ; Faggioni, Michela ; Giustino, Gennaro ; Ariti, Cono ; Colombo, Antonio ; Chieffo, Alaide ; Kini, Annapoorna ; Saporito, Richard ; Michael Gibson, C. ; Witzenbichler, Bernhard ; Cohen, David ; Moliterno, David ; Stuckey, Thomas ; Henry, Timothy ; Pocock, Stuart ; Dangas, George ; Gabriel Steg, P. ; Mehran, Roxana</creator><creatorcontrib>Chandrasekhar, Jaya ; Bansilal, Sameer ; Baber, Usman ; Sartori, Samantha ; Aquino, Melissa ; Farhan, Serdar ; Vogel, Birgit ; Faggioni, Michela ; Giustino, Gennaro ; Ariti, Cono ; Colombo, Antonio ; Chieffo, Alaide ; Kini, Annapoorna ; Saporito, Richard ; Michael Gibson, C. ; Witzenbichler, Bernhard ; Cohen, David ; Moliterno, David ; Stuckey, Thomas ; Henry, Timothy ; Pocock, Stuart ; Dangas, George ; Gabriel Steg, P. ; Mehran, Roxana</creatorcontrib><description>Background
Proton pump inhibitors (PPI) may decrease the availability of clopidogrel by competitive antagonism, leading to a potential increase in ischemic events.
Methods
We evaluated patients from the all‐comer PARIS registry treated with dual antiplatelet therapy (DAPT) with aspirin and clopidogrel following coronary stenting for outcomes stratified by PPI use. Two‐year major adverse cardiovascular events (MACE), composite of cardiac death, myocardial infarction, definite or probable stent thrombosis or target lesion revascularization (TLR), and net adverse cardiac events (NACE), composite of MACE or Bleeding Academic Research consortium (BARC) type 3 or 5 bleeding were assessed. We also explored associations between PPI use and patterns of 2‐year DAPT cessation.
Results
The cohort comprised 4635 patients (23% PPI users) with mean age 64.4 ±11.4 years. Two year adjusted risk of MACE (HR: 1.27, 95% CI: 1.04–1.55), NACE (HR: 1.21, 95% CI: 1.01–1.44) and TLR (HR: 1.33, 95% CI: 1.04–1.71) were significantly higher in PPI users vs. non‐users, without a difference in bleeding. Although the incidence of 2‐year DAPT discontinuation and interruption was similar, DAPT disruption was significantly lower among PPI users vs. non‐users (10.0% vs. 14.7%, P <0.0001). Compared to non‐PPI users on continued DAPT, disruption was associated with higher MACE in both PPI users (HR: 2.34, 95% CI: 1.38–3.97) and non‐users (HR: 1.41, 95% CI: 1.02–1.94) but greater BARC 3,5 bleeding only in non‐PPI users (HR: 2.06, 95% CI: 1.21–3.51).
Conclusions
In clopidogrel treated PCI patients, the 2‐year adjusted risk of MACE and NACE was significantly higher in PPI users driven by higher TLR compared to non‐PPI users, without a difference in bleeding. PPI use was associated with lower incidence of DAPT disruption without an increase in disruption related bleeding compared to non‐PPI users on DAPT. © 2016 Wiley Periodicals, Inc.</description><identifier>ISSN: 1522-1946</identifier><identifier>EISSN: 1522-726X</identifier><identifier>DOI: 10.1002/ccd.26716</identifier><identifier>PMID: 27650638</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Aged ; Angioplasty ; Antagonism ; Antiplatelet therapy ; Aspirin ; Aspirin - administration & dosage ; Aspirin - adverse effects ; Bleeding ; Clopidogrel ; Coronary Thrombosis - etiology ; Death ; Drug Administration Schedule ; Drug Antagonism ; Drug Therapy, Combination ; dual antiplatelet therapy cessation ; Europe ; Female ; Heart ; Heart diseases ; Hemorrhage - chemically induced ; Humans ; Implants ; Incidence ; Inhibitors ; Interruption ; Ischemia ; Kaplan-Meier Estimate ; Male ; Middle Aged ; Myocardial infarction ; Myocardial Infarction - etiology ; Myocardial Ischemia - diagnosis ; Myocardial Ischemia - mortality ; Myocardial Ischemia - therapy ; P2Y12 receptor inhibitor ; percutaneous coronary intervention ; Percutaneous Coronary Intervention - adverse effects ; Percutaneous Coronary Intervention - instrumentation ; Percutaneous Coronary Intervention - mortality ; Platelet Aggregation Inhibitors - administration & dosage ; Platelet Aggregation Inhibitors - adverse effects ; Proportional Hazards Models ; Prospective Studies ; proton pump inhibitor ; Proton pump inhibitors ; Proton Pump Inhibitors - administration & dosage ; Proton Pump Inhibitors - adverse effects ; Registries ; Risk assessment ; Risk Factors ; Stents ; thienopyridine ; Thromboembolism ; Thrombosis ; Ticlopidine - administration & dosage ; Ticlopidine - adverse effects ; Ticlopidine - analogs & derivatives ; Time Factors ; Treatment Outcome ; United States</subject><ispartof>Catheterization and cardiovascular interventions, 2017-06, Vol.89 (7), p.E217-E225</ispartof><rights>2016 Wiley Periodicals, Inc.</rights><rights>2017 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3536-6d9bd68cc8c92fb5e4f0801f2dce9f95e91e9f7ef6eccc1f1672720a898fc0c83</citedby><cites>FETCH-LOGICAL-c3536-6d9bd68cc8c92fb5e4f0801f2dce9f95e91e9f7ef6eccc1f1672720a898fc0c83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27650638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chandrasekhar, Jaya</creatorcontrib><creatorcontrib>Bansilal, Sameer</creatorcontrib><creatorcontrib>Baber, Usman</creatorcontrib><creatorcontrib>Sartori, Samantha</creatorcontrib><creatorcontrib>Aquino, Melissa</creatorcontrib><creatorcontrib>Farhan, Serdar</creatorcontrib><creatorcontrib>Vogel, Birgit</creatorcontrib><creatorcontrib>Faggioni, Michela</creatorcontrib><creatorcontrib>Giustino, Gennaro</creatorcontrib><creatorcontrib>Ariti, Cono</creatorcontrib><creatorcontrib>Colombo, Antonio</creatorcontrib><creatorcontrib>Chieffo, Alaide</creatorcontrib><creatorcontrib>Kini, Annapoorna</creatorcontrib><creatorcontrib>Saporito, Richard</creatorcontrib><creatorcontrib>Michael Gibson, C.</creatorcontrib><creatorcontrib>Witzenbichler, Bernhard</creatorcontrib><creatorcontrib>Cohen, David</creatorcontrib><creatorcontrib>Moliterno, David</creatorcontrib><creatorcontrib>Stuckey, Thomas</creatorcontrib><creatorcontrib>Henry, Timothy</creatorcontrib><creatorcontrib>Pocock, Stuart</creatorcontrib><creatorcontrib>Dangas, George</creatorcontrib><creatorcontrib>Gabriel Steg, P.</creatorcontrib><creatorcontrib>Mehran, Roxana</creatorcontrib><title>Impact of proton pump inhibitors and dual antiplatelet therapy cessation on outcomes following percutaneous coronary intervention: Results From the PARIS Registry</title><title>Catheterization and cardiovascular interventions</title><addtitle>Catheter Cardiovasc Interv</addtitle><description>Background
Proton pump inhibitors (PPI) may decrease the availability of clopidogrel by competitive antagonism, leading to a potential increase in ischemic events.
Methods
We evaluated patients from the all‐comer PARIS registry treated with dual antiplatelet therapy (DAPT) with aspirin and clopidogrel following coronary stenting for outcomes stratified by PPI use. Two‐year major adverse cardiovascular events (MACE), composite of cardiac death, myocardial infarction, definite or probable stent thrombosis or target lesion revascularization (TLR), and net adverse cardiac events (NACE), composite of MACE or Bleeding Academic Research consortium (BARC) type 3 or 5 bleeding were assessed. We also explored associations between PPI use and patterns of 2‐year DAPT cessation.
Results
The cohort comprised 4635 patients (23% PPI users) with mean age 64.4 ±11.4 years. Two year adjusted risk of MACE (HR: 1.27, 95% CI: 1.04–1.55), NACE (HR: 1.21, 95% CI: 1.01–1.44) and TLR (HR: 1.33, 95% CI: 1.04–1.71) were significantly higher in PPI users vs. non‐users, without a difference in bleeding. Although the incidence of 2‐year DAPT discontinuation and interruption was similar, DAPT disruption was significantly lower among PPI users vs. non‐users (10.0% vs. 14.7%, P <0.0001). Compared to non‐PPI users on continued DAPT, disruption was associated with higher MACE in both PPI users (HR: 2.34, 95% CI: 1.38–3.97) and non‐users (HR: 1.41, 95% CI: 1.02–1.94) but greater BARC 3,5 bleeding only in non‐PPI users (HR: 2.06, 95% CI: 1.21–3.51).
Conclusions
In clopidogrel treated PCI patients, the 2‐year adjusted risk of MACE and NACE was significantly higher in PPI users driven by higher TLR compared to non‐PPI users, without a difference in bleeding. PPI use was associated with lower incidence of DAPT disruption without an increase in disruption related bleeding compared to non‐PPI users on DAPT. © 2016 Wiley Periodicals, Inc.</description><subject>Aged</subject><subject>Angioplasty</subject><subject>Antagonism</subject><subject>Antiplatelet therapy</subject><subject>Aspirin</subject><subject>Aspirin - administration & dosage</subject><subject>Aspirin - adverse effects</subject><subject>Bleeding</subject><subject>Clopidogrel</subject><subject>Coronary Thrombosis - etiology</subject><subject>Death</subject><subject>Drug Administration Schedule</subject><subject>Drug Antagonism</subject><subject>Drug Therapy, Combination</subject><subject>dual antiplatelet therapy cessation</subject><subject>Europe</subject><subject>Female</subject><subject>Heart</subject><subject>Heart diseases</subject><subject>Hemorrhage - chemically induced</subject><subject>Humans</subject><subject>Implants</subject><subject>Incidence</subject><subject>Inhibitors</subject><subject>Interruption</subject><subject>Ischemia</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Myocardial infarction</subject><subject>Myocardial Infarction - etiology</subject><subject>Myocardial Ischemia - diagnosis</subject><subject>Myocardial Ischemia - mortality</subject><subject>Myocardial Ischemia - therapy</subject><subject>P2Y12 receptor inhibitor</subject><subject>percutaneous coronary intervention</subject><subject>Percutaneous Coronary Intervention - adverse effects</subject><subject>Percutaneous Coronary Intervention - instrumentation</subject><subject>Percutaneous Coronary Intervention - mortality</subject><subject>Platelet Aggregation Inhibitors - administration & dosage</subject><subject>Platelet Aggregation Inhibitors - adverse effects</subject><subject>Proportional Hazards Models</subject><subject>Prospective Studies</subject><subject>proton pump inhibitor</subject><subject>Proton pump inhibitors</subject><subject>Proton Pump Inhibitors - administration & dosage</subject><subject>Proton Pump Inhibitors - adverse effects</subject><subject>Registries</subject><subject>Risk assessment</subject><subject>Risk Factors</subject><subject>Stents</subject><subject>thienopyridine</subject><subject>Thromboembolism</subject><subject>Thrombosis</subject><subject>Ticlopidine - administration & dosage</subject><subject>Ticlopidine - adverse effects</subject><subject>Ticlopidine - analogs & derivatives</subject><subject>Time Factors</subject><subject>Treatment Outcome</subject><subject>United States</subject><issn>1522-1946</issn><issn>1522-726X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kd9qFDEUh4MotlYvfAEJeKMX2yaZTjLxrqxWFwpKVfBuyJ45aVMykzF_LPs6PqlZZ_VCEALnEL7zcZIfIc85O-WMiTOA4VRIxeUDcsxbIVZKyG8PDz3X5_KIPEnpjjGmpdCPyZFQsmWy6Y7Jz804G8g0WDrHkMNE5zLO1E23butyiImaaaBDMb422c3eZPSYab7FaOYdBUzJZFfn9qdkCCMmaoP34d5NN3TGCCWbCUNJFEIMk4m7qs8Yf-C0H3xDrzEVnxO9jGHci-mni-vN53p941KOu6fkkTU-4bNDPSFfL999WX9YXX18v1lfXK2gaRu5koPeDrID6EALu23x3LKOcSsGQG11i5rXqtBKBABuuVRCCWY63Vlg0DUn5NXirR_xvWDK_egSoPfL9j3vWq0a1bS8oi__Qe9CiVPdrueaac650k2lXi8UxJBSRNvP0Y31_T1n_T64vgbX_w6usi8OxrIdcfhL_kmqAmcLcO887v5v6tfrt4vyF-Cdpok</recordid><startdate>20170601</startdate><enddate>20170601</enddate><creator>Chandrasekhar, Jaya</creator><creator>Bansilal, Sameer</creator><creator>Baber, Usman</creator><creator>Sartori, Samantha</creator><creator>Aquino, Melissa</creator><creator>Farhan, Serdar</creator><creator>Vogel, Birgit</creator><creator>Faggioni, Michela</creator><creator>Giustino, Gennaro</creator><creator>Ariti, Cono</creator><creator>Colombo, Antonio</creator><creator>Chieffo, Alaide</creator><creator>Kini, Annapoorna</creator><creator>Saporito, Richard</creator><creator>Michael Gibson, C.</creator><creator>Witzenbichler, Bernhard</creator><creator>Cohen, David</creator><creator>Moliterno, David</creator><creator>Stuckey, Thomas</creator><creator>Henry, Timothy</creator><creator>Pocock, Stuart</creator><creator>Dangas, George</creator><creator>Gabriel Steg, P.</creator><creator>Mehran, Roxana</creator><general>Wiley Subscription Services, Inc</general><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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>20170601</creationdate><title>Impact of proton pump inhibitors and dual antiplatelet therapy cessation on outcomes following percutaneous coronary intervention: Results From the PARIS Registry</title><author>Chandrasekhar, Jaya ; Bansilal, Sameer ; Baber, Usman ; Sartori, Samantha ; Aquino, Melissa ; Farhan, Serdar ; Vogel, Birgit ; Faggioni, Michela ; Giustino, Gennaro ; Ariti, Cono ; Colombo, Antonio ; Chieffo, Alaide ; Kini, Annapoorna ; Saporito, Richard ; Michael Gibson, C. ; Witzenbichler, Bernhard ; Cohen, David ; Moliterno, David ; Stuckey, Thomas ; Henry, Timothy ; Pocock, Stuart ; Dangas, George ; Gabriel Steg, P. ; Mehran, Roxana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3536-6d9bd68cc8c92fb5e4f0801f2dce9f95e91e9f7ef6eccc1f1672720a898fc0c83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aged</topic><topic>Angioplasty</topic><topic>Antagonism</topic><topic>Antiplatelet therapy</topic><topic>Aspirin</topic><topic>Aspirin - administration & dosage</topic><topic>Aspirin - adverse effects</topic><topic>Bleeding</topic><topic>Clopidogrel</topic><topic>Coronary Thrombosis - etiology</topic><topic>Death</topic><topic>Drug Administration Schedule</topic><topic>Drug Antagonism</topic><topic>Drug Therapy, Combination</topic><topic>dual antiplatelet therapy cessation</topic><topic>Europe</topic><topic>Female</topic><topic>Heart</topic><topic>Heart diseases</topic><topic>Hemorrhage - chemically induced</topic><topic>Humans</topic><topic>Implants</topic><topic>Incidence</topic><topic>Inhibitors</topic><topic>Interruption</topic><topic>Ischemia</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Myocardial infarction</topic><topic>Myocardial Infarction - etiology</topic><topic>Myocardial Ischemia - diagnosis</topic><topic>Myocardial Ischemia - mortality</topic><topic>Myocardial Ischemia - therapy</topic><topic>P2Y12 receptor inhibitor</topic><topic>percutaneous coronary intervention</topic><topic>Percutaneous Coronary Intervention - adverse effects</topic><topic>Percutaneous Coronary Intervention - instrumentation</topic><topic>Percutaneous Coronary Intervention - mortality</topic><topic>Platelet Aggregation Inhibitors - administration & dosage</topic><topic>Platelet Aggregation Inhibitors - adverse effects</topic><topic>Proportional Hazards Models</topic><topic>Prospective Studies</topic><topic>proton pump inhibitor</topic><topic>Proton pump inhibitors</topic><topic>Proton Pump Inhibitors - administration & dosage</topic><topic>Proton Pump Inhibitors - adverse effects</topic><topic>Registries</topic><topic>Risk assessment</topic><topic>Risk Factors</topic><topic>Stents</topic><topic>thienopyridine</topic><topic>Thromboembolism</topic><topic>Thrombosis</topic><topic>Ticlopidine - administration & dosage</topic><topic>Ticlopidine - adverse effects</topic><topic>Ticlopidine - analogs & derivatives</topic><topic>Time Factors</topic><topic>Treatment Outcome</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chandrasekhar, Jaya</creatorcontrib><creatorcontrib>Bansilal, Sameer</creatorcontrib><creatorcontrib>Baber, Usman</creatorcontrib><creatorcontrib>Sartori, Samantha</creatorcontrib><creatorcontrib>Aquino, Melissa</creatorcontrib><creatorcontrib>Farhan, Serdar</creatorcontrib><creatorcontrib>Vogel, Birgit</creatorcontrib><creatorcontrib>Faggioni, Michela</creatorcontrib><creatorcontrib>Giustino, Gennaro</creatorcontrib><creatorcontrib>Ariti, Cono</creatorcontrib><creatorcontrib>Colombo, Antonio</creatorcontrib><creatorcontrib>Chieffo, Alaide</creatorcontrib><creatorcontrib>Kini, Annapoorna</creatorcontrib><creatorcontrib>Saporito, Richard</creatorcontrib><creatorcontrib>Michael Gibson, C.</creatorcontrib><creatorcontrib>Witzenbichler, Bernhard</creatorcontrib><creatorcontrib>Cohen, David</creatorcontrib><creatorcontrib>Moliterno, David</creatorcontrib><creatorcontrib>Stuckey, Thomas</creatorcontrib><creatorcontrib>Henry, Timothy</creatorcontrib><creatorcontrib>Pocock, Stuart</creatorcontrib><creatorcontrib>Dangas, George</creatorcontrib><creatorcontrib>Gabriel Steg, P.</creatorcontrib><creatorcontrib>Mehran, Roxana</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Catheterization and cardiovascular interventions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chandrasekhar, Jaya</au><au>Bansilal, Sameer</au><au>Baber, Usman</au><au>Sartori, Samantha</au><au>Aquino, Melissa</au><au>Farhan, Serdar</au><au>Vogel, Birgit</au><au>Faggioni, Michela</au><au>Giustino, Gennaro</au><au>Ariti, Cono</au><au>Colombo, Antonio</au><au>Chieffo, Alaide</au><au>Kini, Annapoorna</au><au>Saporito, Richard</au><au>Michael Gibson, C.</au><au>Witzenbichler, Bernhard</au><au>Cohen, David</au><au>Moliterno, David</au><au>Stuckey, Thomas</au><au>Henry, Timothy</au><au>Pocock, Stuart</au><au>Dangas, George</au><au>Gabriel Steg, P.</au><au>Mehran, Roxana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of proton pump inhibitors and dual antiplatelet therapy cessation on outcomes following percutaneous coronary intervention: Results From the PARIS Registry</atitle><jtitle>Catheterization and cardiovascular interventions</jtitle><addtitle>Catheter Cardiovasc Interv</addtitle><date>2017-06-01</date><risdate>2017</risdate><volume>89</volume><issue>7</issue><spage>E217</spage><epage>E225</epage><pages>E217-E225</pages><issn>1522-1946</issn><eissn>1522-726X</eissn><abstract>Background
Proton pump inhibitors (PPI) may decrease the availability of clopidogrel by competitive antagonism, leading to a potential increase in ischemic events.
Methods
We evaluated patients from the all‐comer PARIS registry treated with dual antiplatelet therapy (DAPT) with aspirin and clopidogrel following coronary stenting for outcomes stratified by PPI use. Two‐year major adverse cardiovascular events (MACE), composite of cardiac death, myocardial infarction, definite or probable stent thrombosis or target lesion revascularization (TLR), and net adverse cardiac events (NACE), composite of MACE or Bleeding Academic Research consortium (BARC) type 3 or 5 bleeding were assessed. We also explored associations between PPI use and patterns of 2‐year DAPT cessation.
Results
The cohort comprised 4635 patients (23% PPI users) with mean age 64.4 ±11.4 years. Two year adjusted risk of MACE (HR: 1.27, 95% CI: 1.04–1.55), NACE (HR: 1.21, 95% CI: 1.01–1.44) and TLR (HR: 1.33, 95% CI: 1.04–1.71) were significantly higher in PPI users vs. non‐users, without a difference in bleeding. Although the incidence of 2‐year DAPT discontinuation and interruption was similar, DAPT disruption was significantly lower among PPI users vs. non‐users (10.0% vs. 14.7%, P <0.0001). Compared to non‐PPI users on continued DAPT, disruption was associated with higher MACE in both PPI users (HR: 2.34, 95% CI: 1.38–3.97) and non‐users (HR: 1.41, 95% CI: 1.02–1.94) but greater BARC 3,5 bleeding only in non‐PPI users (HR: 2.06, 95% CI: 1.21–3.51).
Conclusions
In clopidogrel treated PCI patients, the 2‐year adjusted risk of MACE and NACE was significantly higher in PPI users driven by higher TLR compared to non‐PPI users, without a difference in bleeding. PPI use was associated with lower incidence of DAPT disruption without an increase in disruption related bleeding compared to non‐PPI users on DAPT. © 2016 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>27650638</pmid><doi>10.1002/ccd.26716</doi><tpages>9</tpages></addata></record> |
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recordid | cdi_proquest_miscellaneous_1859737351 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Aged Angioplasty Antagonism Antiplatelet therapy Aspirin Aspirin - administration & dosage Aspirin - adverse effects Bleeding Clopidogrel Coronary Thrombosis - etiology Death Drug Administration Schedule Drug Antagonism Drug Therapy, Combination dual antiplatelet therapy cessation Europe Female Heart Heart diseases Hemorrhage - chemically induced Humans Implants Incidence Inhibitors Interruption Ischemia Kaplan-Meier Estimate Male Middle Aged Myocardial infarction Myocardial Infarction - etiology Myocardial Ischemia - diagnosis Myocardial Ischemia - mortality Myocardial Ischemia - therapy P2Y12 receptor inhibitor percutaneous coronary intervention Percutaneous Coronary Intervention - adverse effects Percutaneous Coronary Intervention - instrumentation Percutaneous Coronary Intervention - mortality Platelet Aggregation Inhibitors - administration & dosage Platelet Aggregation Inhibitors - adverse effects Proportional Hazards Models Prospective Studies proton pump inhibitor Proton pump inhibitors Proton Pump Inhibitors - administration & dosage Proton Pump Inhibitors - adverse effects Registries Risk assessment Risk Factors Stents thienopyridine Thromboembolism Thrombosis Ticlopidine - administration & dosage Ticlopidine - adverse effects Ticlopidine - analogs & derivatives Time Factors Treatment Outcome United States |
title | Impact of proton pump inhibitors and dual antiplatelet therapy cessation on outcomes following percutaneous coronary intervention: Results From the PARIS Registry |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-22T08%3A13%3A52IST&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=Impact%20of%20proton%20pump%20inhibitors%20and%20dual%20antiplatelet%20therapy%20cessation%20on%20outcomes%20following%20percutaneous%20coronary%20intervention:%20Results%20From%20the%20PARIS%20Registry&rft.jtitle=Catheterization%20and%20cardiovascular%20interventions&rft.au=Chandrasekhar,%20Jaya&rft.date=2017-06-01&rft.volume=89&rft.issue=7&rft.spage=E217&rft.epage=E225&rft.pages=E217-E225&rft.issn=1522-1946&rft.eissn=1522-726X&rft_id=info:doi/10.1002/ccd.26716&rft_dat=%3Cproquest_cross%3E1859737351%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3536-6d9bd68cc8c92fb5e4f0801f2dce9f95e91e9f7ef6eccc1f1672720a898fc0c83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1909111793&rft_id=info:pmid/27650638&rfr_iscdi=true |