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Comparison of atropine and glycopyrronium in patients with pre‐existing cardiac disease
Summary The effects of atropine and glycopyrronium, when given intravenously with neostigmine during the reversal of neuromuscular blockade in patients with cardiovascular disease, were compared in a double blind trial. Atropine was associated with a significantly greater elevation of heart rate and...
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Published in: | Anaesthesia 1984-12, Vol.39 (12), p.1207-1213 |
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container_title | Anaesthesia |
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creator | MOSTAFA, S. M. VUCEVIC, M. |
description | Summary
The effects of atropine and glycopyrronium, when given intravenously with neostigmine during the reversal of neuromuscular blockade in patients with cardiovascular disease, were compared in a double blind trial. Atropine was associated with a significantly greater elevation of heart rate and rate‐pressure product than glycopyrronium. This elevation was also more sustained with atropine. The entire atropine population also showed a significantly greater incidence of ST‐segment depression on the electrocardiogram than that observed in those who had received glycopyrronium. Furthermore, patients with ischaemic heart disease and previous myocardial infarction who received atropine showed a significantly greater incidence of dysrhythmias than those given glycopyrronium. It is suggested that at the time of reversal of neuromuscular blockade in patients with cardiovascular disease, glycopyrronium is a more suitable agent than atropine. |
doi_str_mv | 10.1111/j.1365-2044.1984.tb06433.x |
format | article |
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The effects of atropine and glycopyrronium, when given intravenously with neostigmine during the reversal of neuromuscular blockade in patients with cardiovascular disease, were compared in a double blind trial. Atropine was associated with a significantly greater elevation of heart rate and rate‐pressure product than glycopyrronium. This elevation was also more sustained with atropine. The entire atropine population also showed a significantly greater incidence of ST‐segment depression on the electrocardiogram than that observed in those who had received glycopyrronium. Furthermore, patients with ischaemic heart disease and previous myocardial infarction who received atropine showed a significantly greater incidence of dysrhythmias than those given glycopyrronium. It is suggested that at the time of reversal of neuromuscular blockade in patients with cardiovascular disease, glycopyrronium is a more suitable agent than atropine.</description><identifier>ISSN: 0003-2409</identifier><identifier>EISSN: 1365-2044</identifier><identifier>DOI: 10.1111/j.1365-2044.1984.tb06433.x</identifier><identifier>PMID: 6517248</identifier><identifier>CODEN: ANASAB</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aged ; Anesthesia ; Anesthesia depending on patient's condition ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Atropine - pharmacology ; atropine, glycopyrronium ; Biological and medical sciences ; Blood Pressure - drug effects ; Coronary Disease - complications ; Double-Blind Method ; Electrocardiography ; Female ; Glycopyrrolate - pharmacology ; Heart ; Heart Diseases - complications ; Heart Rate - drug effects ; Humans ; Intubation, Intratracheal ; Male ; Medical sciences ; Myocardial Infarction - complications ; Parasympathetic nervous system ; pulse rate ; Pyrrolidines - pharmacology ; Random Allocation ; Surgical Procedures, Operative ; Time Factors</subject><ispartof>Anaesthesia, 1984-12, Vol.39 (12), p.1207-1213</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4527-593f923f6fbfc59079a09ac570771fd85c4e0d14b49f5fe270c4af989061e11e3</citedby><cites>FETCH-LOGICAL-c4527-593f923f6fbfc59079a09ac570771fd85c4e0d14b49f5fe270c4af989061e11e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8957657$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6517248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MOSTAFA, S. M.</creatorcontrib><creatorcontrib>VUCEVIC, M.</creatorcontrib><title>Comparison of atropine and glycopyrronium in patients with pre‐existing cardiac disease</title><title>Anaesthesia</title><addtitle>Anaesthesia</addtitle><description>Summary
The effects of atropine and glycopyrronium, when given intravenously with neostigmine during the reversal of neuromuscular blockade in patients with cardiovascular disease, were compared in a double blind trial. Atropine was associated with a significantly greater elevation of heart rate and rate‐pressure product than glycopyrronium. This elevation was also more sustained with atropine. The entire atropine population also showed a significantly greater incidence of ST‐segment depression on the electrocardiogram than that observed in those who had received glycopyrronium. Furthermore, patients with ischaemic heart disease and previous myocardial infarction who received atropine showed a significantly greater incidence of dysrhythmias than those given glycopyrronium. It is suggested that at the time of reversal of neuromuscular blockade in patients with cardiovascular disease, glycopyrronium is a more suitable agent than atropine.</description><subject>Aged</subject><subject>Anesthesia</subject><subject>Anesthesia depending on patient's condition</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Atropine - pharmacology</subject><subject>atropine, glycopyrronium</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - drug effects</subject><subject>Coronary Disease - complications</subject><subject>Double-Blind Method</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Glycopyrrolate - pharmacology</subject><subject>Heart</subject><subject>Heart Diseases - complications</subject><subject>Heart Rate - drug effects</subject><subject>Humans</subject><subject>Intubation, Intratracheal</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Myocardial Infarction - complications</subject><subject>Parasympathetic nervous system</subject><subject>pulse rate</subject><subject>Pyrrolidines - pharmacology</subject><subject>Random Allocation</subject><subject>Surgical Procedures, Operative</subject><subject>Time Factors</subject><issn>0003-2409</issn><issn>1365-2044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><recordid>eNqVkM-O0zAQhy0EWroLj4BkIcQtYZzYccyJqloWpBVc4MDJcp3x4iqxg51q2xuPwDPyJKRq1DtzmcPvmz_6CHnNoGRzvduVrG5EUQHnJVMtL6ctNLyuy8MTsrpET8kKAOqi4qCek-ucdwCsall7Ra4awWTF2xX5sYnDaJLPMdDoqJlSHH1AakJHH_qjjeMxpRj8fqA-0NFMHsOU6aOfftIx4d_ff_Dg8-TDA7Umdd5Y2vmMJuML8syZPuPLpd-Q7x9vv20-Ffdf7z5v1veF5aKShVC1U1XtGrd1ViiQyoAyVkiQkrmuFZYjdIxvuXLCYSXBcuNUq6BhyBjWN-Ttee-Y4q895kkPPlvsexMw7rOWouVMKDGD78-gTTHnhE6PyQ8mHTUDffKqd_okT5_k6ZNXvXjVh3n41XJlvx2wu4wuIuf8zZKbbE3vkgnW5wvWKiEbIWfswxl79D0e_-MBvf6yvmUVyPofOgCXPw</recordid><startdate>198412</startdate><enddate>198412</enddate><creator>MOSTAFA, S. M.</creator><creator>VUCEVIC, M.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><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>7X8</scope></search><sort><creationdate>198412</creationdate><title>Comparison of atropine and glycopyrronium in patients with pre‐existing cardiac disease</title><author>MOSTAFA, S. M. ; VUCEVIC, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4527-593f923f6fbfc59079a09ac570771fd85c4e0d14b49f5fe270c4af989061e11e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Aged</topic><topic>Anesthesia</topic><topic>Anesthesia depending on patient's condition</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Atropine - pharmacology</topic><topic>atropine, glycopyrronium</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - drug effects</topic><topic>Coronary Disease - complications</topic><topic>Double-Blind Method</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Glycopyrrolate - pharmacology</topic><topic>Heart</topic><topic>Heart Diseases - complications</topic><topic>Heart Rate - drug effects</topic><topic>Humans</topic><topic>Intubation, Intratracheal</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myocardial Infarction - complications</topic><topic>Parasympathetic nervous system</topic><topic>pulse rate</topic><topic>Pyrrolidines - pharmacology</topic><topic>Random Allocation</topic><topic>Surgical Procedures, Operative</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MOSTAFA, S. M.</creatorcontrib><creatorcontrib>VUCEVIC, M.</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Anaesthesia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MOSTAFA, S. M.</au><au>VUCEVIC, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of atropine and glycopyrronium in patients with pre‐existing cardiac disease</atitle><jtitle>Anaesthesia</jtitle><addtitle>Anaesthesia</addtitle><date>1984-12</date><risdate>1984</risdate><volume>39</volume><issue>12</issue><spage>1207</spage><epage>1213</epage><pages>1207-1213</pages><issn>0003-2409</issn><eissn>1365-2044</eissn><coden>ANASAB</coden><abstract>Summary
The effects of atropine and glycopyrronium, when given intravenously with neostigmine during the reversal of neuromuscular blockade in patients with cardiovascular disease, were compared in a double blind trial. Atropine was associated with a significantly greater elevation of heart rate and rate‐pressure product than glycopyrronium. This elevation was also more sustained with atropine. The entire atropine population also showed a significantly greater incidence of ST‐segment depression on the electrocardiogram than that observed in those who had received glycopyrronium. Furthermore, patients with ischaemic heart disease and previous myocardial infarction who received atropine showed a significantly greater incidence of dysrhythmias than those given glycopyrronium. It is suggested that at the time of reversal of neuromuscular blockade in patients with cardiovascular disease, glycopyrronium is a more suitable agent than atropine.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>6517248</pmid><doi>10.1111/j.1365-2044.1984.tb06433.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Anesthesia Anesthesia depending on patient's condition Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Atropine - pharmacology atropine, glycopyrronium Biological and medical sciences Blood Pressure - drug effects Coronary Disease - complications Double-Blind Method Electrocardiography Female Glycopyrrolate - pharmacology Heart Heart Diseases - complications Heart Rate - drug effects Humans Intubation, Intratracheal Male Medical sciences Myocardial Infarction - complications Parasympathetic nervous system pulse rate Pyrrolidines - pharmacology Random Allocation Surgical Procedures, Operative Time Factors |
title | Comparison of atropine and glycopyrronium in patients with pre‐existing cardiac disease |
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