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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c3536-6d9bd68cc8c92fb5e4f0801f2dce9f95e91e9f7ef6eccc1f1672720a898fc0c83
cites cdi_FETCH-LOGICAL-c3536-6d9bd68cc8c92fb5e4f0801f2dce9f95e91e9f7ef6eccc1f1672720a898fc0c83
container_end_page E225
container_issue 7
container_start_page E217
container_title Catheterization and cardiovascular interventions
container_volume 89
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
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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 &lt;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 &amp; 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 &amp; dosage ; Platelet Aggregation Inhibitors - adverse effects ; Proportional Hazards Models ; Prospective Studies ; proton pump inhibitor ; Proton pump inhibitors ; Proton Pump Inhibitors - administration &amp; dosage ; Proton Pump Inhibitors - adverse effects ; Registries ; Risk assessment ; Risk Factors ; Stents ; thienopyridine ; Thromboembolism ; Thrombosis ; Ticlopidine - administration &amp; dosage ; Ticlopidine - adverse effects ; Ticlopidine - analogs &amp; 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 &lt;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 &amp; 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 &amp; 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 &amp; 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 &amp; dosage</subject><subject>Ticlopidine - adverse effects</subject><subject>Ticlopidine - analogs &amp; 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 &amp; 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 &amp; 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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 &lt;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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issn 1522-1946
1522-726X
language eng
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
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