Loading…

Bivalirudin Presents a Favorable Safety Profile Regarding Adverse Drug Reactions, Thrombocytopenia, and Bleeding in Chinese Patients With High Bleeding Risk Undergoing Percutaneous Coronary Intervention: A Prospective, Multi-Center, Intensive Monitoring Study

This study aimed to comprehensively explore the occurrence and risk factors for adverse events (AEs) and adverse drug reactions (ADRs) (especially for thrombocytopenia and bleeding) in Chinese patients with high bleeding risk (older adults, or complicated with diabetes mellitus or renal function imp...

Full description

Saved in:
Bibliographic Details
Published in:Frontiers in cardiovascular medicine 2022-06, Vol.9, p.821322-821322
Main Authors: Peng, Xiaoping, Li, Zhenyong, Li, Dunheng, Li, Zhongyin, Lu, Zhaohua, Luo, Caidong, Ji, Zheng
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c463t-328982d785dff8e8dc230e00713f0458460a2247a4cee20f77852fbb98a1183d3
cites cdi_FETCH-LOGICAL-c463t-328982d785dff8e8dc230e00713f0458460a2247a4cee20f77852fbb98a1183d3
container_end_page 821322
container_issue
container_start_page 821322
container_title Frontiers in cardiovascular medicine
container_volume 9
creator Peng, Xiaoping
Li, Zhenyong
Li, Dunheng
Li, Zhongyin
Lu, Zhaohua
Luo, Caidong
Ji, Zheng
description This study aimed to comprehensively explore the occurrence and risk factors for adverse events (AEs) and adverse drug reactions (ADRs) (especially for thrombocytopenia and bleeding) in Chinese patients with high bleeding risk (older adults, or complicated with diabetes mellitus or renal function impairment) undergoing percutaneous coronary intervention (PCI) with bivalirudin as an anticoagulant. A total of 1,226 patients with high bleeding risk who received PCI with bivalirudin as an anticoagulant from 27 Chinese medical centers were enrolled in this prospective, multi-center, intensive monitoring study. AEs, ADRs, thrombocytopenia, and bleeding were collected from admission to 72 h post-bivalirudin administration; subsequently, patients were followed up on the 30th day with the safety data collected as well. Adverse events were observed in 198 (16.2) patients, among which severe AEs occurred in 16 (1.3%) patients. Meanwhile, bivalirudin-related ADRs were reported in 66 (5.4%) patients, among which 5 (0.4%) patients experienced bivalirudin-related severe ADRs. Besides, thrombocytopenia and bleeding occurred in 45 (3.7%) and 19 (1.5%) patients, respectively. The subsequent multivariate logistic analysis revealed that age >75 years [ = 0.017, odds ratio ( ) = 1.856] and spontaneous coronary artery dissection (SCAD) ( = 0.030, = 2.022) were independently related to higher ADR risk; SCAD ( = 0.017, = 2.426) was independently correlated with higher thrombocytopenia risk, while radial artery access ( = 0.015, = 0.352) was independently correlated with lower thrombocytopenia risk; and the administration of bivalirudin preoperatively or intraoperatively ( = 0.013, = 5.097) was independently associated with higher bleeding risk. Bivalirudin presents a favorable safety profile regarding ADRs, thrombocytopenia, and bleeding in Chinese patients with high bleeding risk undergoing PCI.
doi_str_mv 10.3389/fcvm.2022.821322
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_5626749da52f437ebb33f2a2a2103db2</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_5626749da52f437ebb33f2a2a2103db2</doaj_id><sourcerecordid>2813553666</sourcerecordid><originalsourceid>FETCH-LOGICAL-c463t-328982d785dff8e8dc230e00713f0458460a2247a4cee20f77852fbb98a1183d3</originalsourceid><addsrcrecordid>eNpVkklv2zAQhdUNTZDm3lPBYw-2y0UL3UvhuE1jIEGNLGhvBCWOZKYS6ZKUAP_7UnaaJtCBIufN94bES5L3BM8Y4_NPdTV0M4opnXFKGKUvk2NK58UUZ9mv10_-j5JT7-8xxiRLeZbzt8kRK0jOGSXHL16d6UG22vVKG7R24MEEjyQ6l4N1smwB3cgawi7WbK3j9hoa6aK4QQs1gPOAvrq-iceyCtoaP0G3G2e70la7YLdgtJwgaRQ6awH2bdFnudEmOqG1DHrv91OHDbrQzea_7Fr73-jOKHCNHfdrcFUfpAHbe7S0zhrpdmhlArghMqL1Z7QYp_RbiJMMMEFXfRv0dAmjZrKXGh8L6MoaHawbqTehV7t3yZtath5OH9aT5O782-3yYnr54_tqubicVmnOwpRRPudUFTxTdc2Bq4oyDBgXhNU4zXiaY0lpWsi0AqC4LqKS1mU555IQzhQ7SVYHrrLyXmyd7uIVhJVa7A-sa4R0QVctiCyneZHOlYyElBVQlozVVMaPYKZKGllfDqxtX3agqnhJJ9tn0OcVozeisYMgmOQ5wUUkfHwgOPunBx9Ep30FbXt4Y0E5YVnG8jyPUnyQVvF5vYP60YdgMWZRjFkUYxbFIYux5cPT-R4b_iWP_QVx8eBZ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2813553666</pqid></control><display><type>article</type><title>Bivalirudin Presents a Favorable Safety Profile Regarding Adverse Drug Reactions, Thrombocytopenia, and Bleeding in Chinese Patients With High Bleeding Risk Undergoing Percutaneous Coronary Intervention: A Prospective, Multi-Center, Intensive Monitoring Study</title><source>PubMed Central</source><creator>Peng, Xiaoping ; Li, Zhenyong ; Li, Dunheng ; Li, Zhongyin ; Lu, Zhaohua ; Luo, Caidong ; Ji, Zheng</creator><creatorcontrib>Peng, Xiaoping ; Li, Zhenyong ; Li, Dunheng ; Li, Zhongyin ; Lu, Zhaohua ; Luo, Caidong ; Ji, Zheng</creatorcontrib><description>This study aimed to comprehensively explore the occurrence and risk factors for adverse events (AEs) and adverse drug reactions (ADRs) (especially for thrombocytopenia and bleeding) in Chinese patients with high bleeding risk (older adults, or complicated with diabetes mellitus or renal function impairment) undergoing percutaneous coronary intervention (PCI) with bivalirudin as an anticoagulant. A total of 1,226 patients with high bleeding risk who received PCI with bivalirudin as an anticoagulant from 27 Chinese medical centers were enrolled in this prospective, multi-center, intensive monitoring study. AEs, ADRs, thrombocytopenia, and bleeding were collected from admission to 72 h post-bivalirudin administration; subsequently, patients were followed up on the 30th day with the safety data collected as well. Adverse events were observed in 198 (16.2) patients, among which severe AEs occurred in 16 (1.3%) patients. Meanwhile, bivalirudin-related ADRs were reported in 66 (5.4%) patients, among which 5 (0.4%) patients experienced bivalirudin-related severe ADRs. Besides, thrombocytopenia and bleeding occurred in 45 (3.7%) and 19 (1.5%) patients, respectively. The subsequent multivariate logistic analysis revealed that age &gt;75 years [ = 0.017, odds ratio ( ) = 1.856] and spontaneous coronary artery dissection (SCAD) ( = 0.030, = 2.022) were independently related to higher ADR risk; SCAD ( = 0.017, = 2.426) was independently correlated with higher thrombocytopenia risk, while radial artery access ( = 0.015, = 0.352) was independently correlated with lower thrombocytopenia risk; and the administration of bivalirudin preoperatively or intraoperatively ( = 0.013, = 5.097) was independently associated with higher bleeding risk. Bivalirudin presents a favorable safety profile regarding ADRs, thrombocytopenia, and bleeding in Chinese patients with high bleeding risk undergoing PCI.</description><identifier>ISSN: 2297-055X</identifier><identifier>EISSN: 2297-055X</identifier><identifier>DOI: 10.3389/fcvm.2022.821322</identifier><identifier>PMID: 37168321</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>adverse events and adverse drug reactions ; bivalirudin ; Cardiovascular Medicine ; high bleeding risk patients ; percutaneous coronary intervention ; thrombocytopenia and bleeding</subject><ispartof>Frontiers in cardiovascular medicine, 2022-06, Vol.9, p.821322-821322</ispartof><rights>Copyright © 2022 Peng, Li, Li, Li, Lu, Luo and Ji.</rights><rights>Copyright © 2022 Peng, Li, Li, Li, Lu, Luo and Ji. 2022 Peng, Li, Li, Li, Lu, Luo and Ji</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c463t-328982d785dff8e8dc230e00713f0458460a2247a4cee20f77852fbb98a1183d3</citedby><cites>FETCH-LOGICAL-c463t-328982d785dff8e8dc230e00713f0458460a2247a4cee20f77852fbb98a1183d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166107/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166107/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37168321$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peng, Xiaoping</creatorcontrib><creatorcontrib>Li, Zhenyong</creatorcontrib><creatorcontrib>Li, Dunheng</creatorcontrib><creatorcontrib>Li, Zhongyin</creatorcontrib><creatorcontrib>Lu, Zhaohua</creatorcontrib><creatorcontrib>Luo, Caidong</creatorcontrib><creatorcontrib>Ji, Zheng</creatorcontrib><title>Bivalirudin Presents a Favorable Safety Profile Regarding Adverse Drug Reactions, Thrombocytopenia, and Bleeding in Chinese Patients With High Bleeding Risk Undergoing Percutaneous Coronary Intervention: A Prospective, Multi-Center, Intensive Monitoring Study</title><title>Frontiers in cardiovascular medicine</title><addtitle>Front Cardiovasc Med</addtitle><description>This study aimed to comprehensively explore the occurrence and risk factors for adverse events (AEs) and adverse drug reactions (ADRs) (especially for thrombocytopenia and bleeding) in Chinese patients with high bleeding risk (older adults, or complicated with diabetes mellitus or renal function impairment) undergoing percutaneous coronary intervention (PCI) with bivalirudin as an anticoagulant. A total of 1,226 patients with high bleeding risk who received PCI with bivalirudin as an anticoagulant from 27 Chinese medical centers were enrolled in this prospective, multi-center, intensive monitoring study. AEs, ADRs, thrombocytopenia, and bleeding were collected from admission to 72 h post-bivalirudin administration; subsequently, patients were followed up on the 30th day with the safety data collected as well. Adverse events were observed in 198 (16.2) patients, among which severe AEs occurred in 16 (1.3%) patients. Meanwhile, bivalirudin-related ADRs were reported in 66 (5.4%) patients, among which 5 (0.4%) patients experienced bivalirudin-related severe ADRs. Besides, thrombocytopenia and bleeding occurred in 45 (3.7%) and 19 (1.5%) patients, respectively. The subsequent multivariate logistic analysis revealed that age &gt;75 years [ = 0.017, odds ratio ( ) = 1.856] and spontaneous coronary artery dissection (SCAD) ( = 0.030, = 2.022) were independently related to higher ADR risk; SCAD ( = 0.017, = 2.426) was independently correlated with higher thrombocytopenia risk, while radial artery access ( = 0.015, = 0.352) was independently correlated with lower thrombocytopenia risk; and the administration of bivalirudin preoperatively or intraoperatively ( = 0.013, = 5.097) was independently associated with higher bleeding risk. Bivalirudin presents a favorable safety profile regarding ADRs, thrombocytopenia, and bleeding in Chinese patients with high bleeding risk undergoing PCI.</description><subject>adverse events and adverse drug reactions</subject><subject>bivalirudin</subject><subject>Cardiovascular Medicine</subject><subject>high bleeding risk patients</subject><subject>percutaneous coronary intervention</subject><subject>thrombocytopenia and bleeding</subject><issn>2297-055X</issn><issn>2297-055X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkklv2zAQhdUNTZDm3lPBYw-2y0UL3UvhuE1jIEGNLGhvBCWOZKYS6ZKUAP_7UnaaJtCBIufN94bES5L3BM8Y4_NPdTV0M4opnXFKGKUvk2NK58UUZ9mv10_-j5JT7-8xxiRLeZbzt8kRK0jOGSXHL16d6UG22vVKG7R24MEEjyQ6l4N1smwB3cgawi7WbK3j9hoa6aK4QQs1gPOAvrq-iceyCtoaP0G3G2e70la7YLdgtJwgaRQ6awH2bdFnudEmOqG1DHrv91OHDbrQzea_7Fr73-jOKHCNHfdrcFUfpAHbe7S0zhrpdmhlArghMqL1Z7QYp_RbiJMMMEFXfRv0dAmjZrKXGh8L6MoaHawbqTehV7t3yZtath5OH9aT5O782-3yYnr54_tqubicVmnOwpRRPudUFTxTdc2Bq4oyDBgXhNU4zXiaY0lpWsi0AqC4LqKS1mU555IQzhQ7SVYHrrLyXmyd7uIVhJVa7A-sa4R0QVctiCyneZHOlYyElBVQlozVVMaPYKZKGllfDqxtX3agqnhJJ9tn0OcVozeisYMgmOQ5wUUkfHwgOPunBx9Ep30FbXt4Y0E5YVnG8jyPUnyQVvF5vYP60YdgMWZRjFkUYxbFIYux5cPT-R4b_iWP_QVx8eBZ</recordid><startdate>20220616</startdate><enddate>20220616</enddate><creator>Peng, Xiaoping</creator><creator>Li, Zhenyong</creator><creator>Li, Dunheng</creator><creator>Li, Zhongyin</creator><creator>Lu, Zhaohua</creator><creator>Luo, Caidong</creator><creator>Ji, Zheng</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20220616</creationdate><title>Bivalirudin Presents a Favorable Safety Profile Regarding Adverse Drug Reactions, Thrombocytopenia, and Bleeding in Chinese Patients With High Bleeding Risk Undergoing Percutaneous Coronary Intervention: A Prospective, Multi-Center, Intensive Monitoring Study</title><author>Peng, Xiaoping ; Li, Zhenyong ; Li, Dunheng ; Li, Zhongyin ; Lu, Zhaohua ; Luo, Caidong ; Ji, Zheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c463t-328982d785dff8e8dc230e00713f0458460a2247a4cee20f77852fbb98a1183d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>adverse events and adverse drug reactions</topic><topic>bivalirudin</topic><topic>Cardiovascular Medicine</topic><topic>high bleeding risk patients</topic><topic>percutaneous coronary intervention</topic><topic>thrombocytopenia and bleeding</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, Xiaoping</creatorcontrib><creatorcontrib>Li, Zhenyong</creatorcontrib><creatorcontrib>Li, Dunheng</creatorcontrib><creatorcontrib>Li, Zhongyin</creatorcontrib><creatorcontrib>Lu, Zhaohua</creatorcontrib><creatorcontrib>Luo, Caidong</creatorcontrib><creatorcontrib>Ji, Zheng</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Frontiers in cardiovascular medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, Xiaoping</au><au>Li, Zhenyong</au><au>Li, Dunheng</au><au>Li, Zhongyin</au><au>Lu, Zhaohua</au><au>Luo, Caidong</au><au>Ji, Zheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bivalirudin Presents a Favorable Safety Profile Regarding Adverse Drug Reactions, Thrombocytopenia, and Bleeding in Chinese Patients With High Bleeding Risk Undergoing Percutaneous Coronary Intervention: A Prospective, Multi-Center, Intensive Monitoring Study</atitle><jtitle>Frontiers in cardiovascular medicine</jtitle><addtitle>Front Cardiovasc Med</addtitle><date>2022-06-16</date><risdate>2022</risdate><volume>9</volume><spage>821322</spage><epage>821322</epage><pages>821322-821322</pages><issn>2297-055X</issn><eissn>2297-055X</eissn><abstract>This study aimed to comprehensively explore the occurrence and risk factors for adverse events (AEs) and adverse drug reactions (ADRs) (especially for thrombocytopenia and bleeding) in Chinese patients with high bleeding risk (older adults, or complicated with diabetes mellitus or renal function impairment) undergoing percutaneous coronary intervention (PCI) with bivalirudin as an anticoagulant. A total of 1,226 patients with high bleeding risk who received PCI with bivalirudin as an anticoagulant from 27 Chinese medical centers were enrolled in this prospective, multi-center, intensive monitoring study. AEs, ADRs, thrombocytopenia, and bleeding were collected from admission to 72 h post-bivalirudin administration; subsequently, patients were followed up on the 30th day with the safety data collected as well. Adverse events were observed in 198 (16.2) patients, among which severe AEs occurred in 16 (1.3%) patients. Meanwhile, bivalirudin-related ADRs were reported in 66 (5.4%) patients, among which 5 (0.4%) patients experienced bivalirudin-related severe ADRs. Besides, thrombocytopenia and bleeding occurred in 45 (3.7%) and 19 (1.5%) patients, respectively. The subsequent multivariate logistic analysis revealed that age &gt;75 years [ = 0.017, odds ratio ( ) = 1.856] and spontaneous coronary artery dissection (SCAD) ( = 0.030, = 2.022) were independently related to higher ADR risk; SCAD ( = 0.017, = 2.426) was independently correlated with higher thrombocytopenia risk, while radial artery access ( = 0.015, = 0.352) was independently correlated with lower thrombocytopenia risk; and the administration of bivalirudin preoperatively or intraoperatively ( = 0.013, = 5.097) was independently associated with higher bleeding risk. Bivalirudin presents a favorable safety profile regarding ADRs, thrombocytopenia, and bleeding in Chinese patients with high bleeding risk undergoing PCI.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>37168321</pmid><doi>10.3389/fcvm.2022.821322</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2297-055X
ispartof Frontiers in cardiovascular medicine, 2022-06, Vol.9, p.821322-821322
issn 2297-055X
2297-055X
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_5626749da52f437ebb33f2a2a2103db2
source PubMed Central
subjects adverse events and adverse drug reactions
bivalirudin
Cardiovascular Medicine
high bleeding risk patients
percutaneous coronary intervention
thrombocytopenia and bleeding
title Bivalirudin Presents a Favorable Safety Profile Regarding Adverse Drug Reactions, Thrombocytopenia, and Bleeding in Chinese Patients With High Bleeding Risk Undergoing Percutaneous Coronary Intervention: A Prospective, Multi-Center, Intensive Monitoring Study
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T15%3A43%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Bivalirudin%20Presents%20a%20Favorable%20Safety%20Profile%20Regarding%20Adverse%20Drug%20Reactions,%20Thrombocytopenia,%20and%20Bleeding%20in%20Chinese%20Patients%20With%20High%20Bleeding%20Risk%20Undergoing%20Percutaneous%20Coronary%20Intervention:%20A%20Prospective,%20Multi-Center,%20Intensive%20Monitoring%20Study&rft.jtitle=Frontiers%20in%20cardiovascular%20medicine&rft.au=Peng,%20Xiaoping&rft.date=2022-06-16&rft.volume=9&rft.spage=821322&rft.epage=821322&rft.pages=821322-821322&rft.issn=2297-055X&rft.eissn=2297-055X&rft_id=info:doi/10.3389/fcvm.2022.821322&rft_dat=%3Cproquest_doaj_%3E2813553666%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c463t-328982d785dff8e8dc230e00713f0458460a2247a4cee20f77852fbb98a1183d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2813553666&rft_id=info:pmid/37168321&rfr_iscdi=true