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...
Saved in:
Published in: | Frontiers in cardiovascular medicine 2022-06, Vol.9, p.821322-821322 |
---|---|
Main Authors: | , , , , , , |
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 >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 >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 >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 |