The effect of activated clotting time values for patients undergoing percutaneous coronary intervention: A systematic review and meta-analysis
Abstract Our aim was to illustrate the effect of higher activated clotting time (ACT) values versus lower ACT values on thrombotic or hemorrhagic events in coronary atherosclerotic heart disease (CHD) patients undergoing percutaneous coronary intervention (PCI). PubMed, Embase, Web of Science, and C...
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Veröffentlicht in: | Thrombosis research 2016-08, Vol.144, p.202-209 |
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description | Abstract Our aim was to illustrate the effect of higher activated clotting time (ACT) values versus lower ACT values on thrombotic or hemorrhagic events in coronary atherosclerotic heart disease (CHD) patients undergoing percutaneous coronary intervention (PCI). PubMed, Embase, Web of Science, and Cochrane Library were searched. Observational studies assessing ACT related major adverse cardiac event (MACE) and major bleeding were included. Studies were allocated into three groups. Group 1 included studies with low percentage of participants prescribed with glycoprotein IIb/IIIa inhibitors (≤ 30%), Group 2 with high percentage of participants prescribed with GPI (> 30%), and Group 3 with routine direct thrombin inhibitors (DTI) prescription. The cutoff is designed as 300 s (290–310 s) for Group 1, and 250 s (240–260 s) for Group 2. With regard to MACE and major bleeding in Group 1, there was no significant difference between higher ACT values and lower ACT values (risk ratio [RR] for MACE, 1.16, 95% confidence interval [CI], 0.65–2.05, p = 0.62, I2 = 94%, RR for major bleeding, 0.96, 95% CI, 0.66–1.40, p = 0.83, I2 = 0%). Likewise, no significant difference was found in Group 2 between higher ACT values and lower ACT values (RR for MACE, 1.15, 95% CI, 0.97–1.35, p = 0.10, I2 = 0%, RR for major bleeding, 0.85, 95% CI, 0.45–1.60, p = 0.61, I2 = 83%). In conclusion, ACT may not have a substantial effect on thrombotic or hemorrhagic complications. Under current clinical practice, target ACT may be higher than what is necessary to prevent thrombotic events. We may achieve a relative low ACT level to preserve efficacy and enhance safety. |
doi_str_mv | 10.1016/j.thromres.2016.04.025 |
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fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1810554935</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0049384816303279</els_id><sourcerecordid>1810554935</sourcerecordid><originalsourceid>FETCH-LOGICAL-c489t-a8884159d4ac8781656aecb333a75cce88b3da09a3165f1ee05f8573a45c391b3</originalsourceid><addsrcrecordid>eNqFks9u1DAQxiMEotvCK1Q-cklqx3Zic0BUFf-kShwoZ2vWmbReEnuxnUX7EjwzjrblwIWTNfJvZvR931TVJaMNo6y72jX5IYY5YmraUjdUNLSVz6oNU72uW9G3z6sNpULXXAl1Vp2ntKOU9UzLl9VZ23MtBVeb6vfdAxIcR7SZhJGAze4AGQdip5Cz8_ckuxnJAaYFExlDJHvIDn1OZPEDxvuwMnuMdsngMSyJ2BCDh3gkzmeMh8K64N-Sa5KOKeNc2i2JeHD4i4AfyIwZavAwHZNLr6oXI0wJXz--F9X3jx_ubj7Xt18_fbm5vq2tUDrXoJQSTOpBgFW9Yp3sAO2Wcw69tBaV2vIBqAZevkaGSOWoZM9BSMs12_KL6s1p7j6Gn0VZNrNLFqfppMEwxaiUQnNZ0O6E2hhSijiafXRz0WcYNWsWZmeesjBrFoYKU7IojZePO5btjMPftifzC_D-BGBRWvyIJtlircXBxZKHGYL7_453_4ywk_POwvQDj5h2YYnF2aLHpNZQ8229iPUgWMcpb3vN_wDjGrc_</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1810554935</pqid></control><display><type>article</type><title>The effect of activated clotting time values for patients undergoing percutaneous coronary intervention: A systematic review and meta-analysis</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Gui, Yi-Yue ; Huang, Fang-Yang ; Huang, Bao-Tao ; Peng, Yong ; Liu, Wei ; Chen, Zhang ; Chen, Shi-Jian ; Pu, Xiao-Bo ; Wang, Peng-Ju ; Chen, Mao</creator><creatorcontrib>Gui, Yi-Yue ; Huang, Fang-Yang ; Huang, Bao-Tao ; Peng, Yong ; Liu, Wei ; Chen, Zhang ; Chen, Shi-Jian ; Pu, Xiao-Bo ; Wang, Peng-Ju ; Chen, Mao</creatorcontrib><description>Abstract Our aim was to illustrate the effect of higher activated clotting time (ACT) values versus lower ACT values on thrombotic or hemorrhagic events in coronary atherosclerotic heart disease (CHD) patients undergoing percutaneous coronary intervention (PCI). PubMed, Embase, Web of Science, and Cochrane Library were searched. Observational studies assessing ACT related major adverse cardiac event (MACE) and major bleeding were included. Studies were allocated into three groups. Group 1 included studies with low percentage of participants prescribed with glycoprotein IIb/IIIa inhibitors (≤ 30%), Group 2 with high percentage of participants prescribed with GPI (> 30%), and Group 3 with routine direct thrombin inhibitors (DTI) prescription. The cutoff is designed as 300 s (290–310 s) for Group 1, and 250 s (240–260 s) for Group 2. With regard to MACE and major bleeding in Group 1, there was no significant difference between higher ACT values and lower ACT values (risk ratio [RR] for MACE, 1.16, 95% confidence interval [CI], 0.65–2.05, p = 0.62, I2 = 94%, RR for major bleeding, 0.96, 95% CI, 0.66–1.40, p = 0.83, I2 = 0%). Likewise, no significant difference was found in Group 2 between higher ACT values and lower ACT values (RR for MACE, 1.15, 95% CI, 0.97–1.35, p = 0.10, I2 = 0%, RR for major bleeding, 0.85, 95% CI, 0.45–1.60, p = 0.61, I2 = 83%). In conclusion, ACT may not have a substantial effect on thrombotic or hemorrhagic complications. Under current clinical practice, target ACT may be higher than what is necessary to prevent thrombotic events. We may achieve a relative low ACT level to preserve efficacy and enhance safety.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/j.thromres.2016.04.025</identifier><identifier>PMID: 27395438</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Activated clotting time ; Anticoagulants - therapeutic use ; Blood Coagulation Tests ; Coronary Disease - complications ; Coronary Disease - drug therapy ; Coronary Disease - surgery ; Hematology, Oncology and Palliative Medicine ; Hemorrhage ; Hemorrhage - chemically induced ; Humans ; Percutaneous coronary intervention ; Percutaneous Coronary Intervention - adverse effects ; Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors ; Thrombosis ; Thrombosis - etiology ; Thrombosis - prevention & control</subject><ispartof>Thrombosis research, 2016-08, Vol.144, p.202-209</ispartof><rights>2016 Elsevier Ltd</rights><rights>Copyright © 2016 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-a8884159d4ac8781656aecb333a75cce88b3da09a3165f1ee05f8573a45c391b3</citedby><cites>FETCH-LOGICAL-c489t-a8884159d4ac8781656aecb333a75cce88b3da09a3165f1ee05f8573a45c391b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.thromres.2016.04.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27395438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gui, Yi-Yue</creatorcontrib><creatorcontrib>Huang, Fang-Yang</creatorcontrib><creatorcontrib>Huang, Bao-Tao</creatorcontrib><creatorcontrib>Peng, Yong</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Chen, Zhang</creatorcontrib><creatorcontrib>Chen, Shi-Jian</creatorcontrib><creatorcontrib>Pu, Xiao-Bo</creatorcontrib><creatorcontrib>Wang, Peng-Ju</creatorcontrib><creatorcontrib>Chen, Mao</creatorcontrib><title>The effect of activated clotting time values for patients undergoing percutaneous coronary intervention: A systematic review and meta-analysis</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>Abstract Our aim was to illustrate the effect of higher activated clotting time (ACT) values versus lower ACT values on thrombotic or hemorrhagic events in coronary atherosclerotic heart disease (CHD) patients undergoing percutaneous coronary intervention (PCI). PubMed, Embase, Web of Science, and Cochrane Library were searched. Observational studies assessing ACT related major adverse cardiac event (MACE) and major bleeding were included. Studies were allocated into three groups. Group 1 included studies with low percentage of participants prescribed with glycoprotein IIb/IIIa inhibitors (≤ 30%), Group 2 with high percentage of participants prescribed with GPI (> 30%), and Group 3 with routine direct thrombin inhibitors (DTI) prescription. The cutoff is designed as 300 s (290–310 s) for Group 1, and 250 s (240–260 s) for Group 2. With regard to MACE and major bleeding in Group 1, there was no significant difference between higher ACT values and lower ACT values (risk ratio [RR] for MACE, 1.16, 95% confidence interval [CI], 0.65–2.05, p = 0.62, I2 = 94%, RR for major bleeding, 0.96, 95% CI, 0.66–1.40, p = 0.83, I2 = 0%). Likewise, no significant difference was found in Group 2 between higher ACT values and lower ACT values (RR for MACE, 1.15, 95% CI, 0.97–1.35, p = 0.10, I2 = 0%, RR for major bleeding, 0.85, 95% CI, 0.45–1.60, p = 0.61, I2 = 83%). In conclusion, ACT may not have a substantial effect on thrombotic or hemorrhagic complications. Under current clinical practice, target ACT may be higher than what is necessary to prevent thrombotic events. We may achieve a relative low ACT level to preserve efficacy and enhance safety.</description><subject>Activated clotting time</subject><subject>Anticoagulants - therapeutic use</subject><subject>Blood Coagulation Tests</subject><subject>Coronary Disease - complications</subject><subject>Coronary Disease - drug therapy</subject><subject>Coronary Disease - surgery</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hemorrhage</subject><subject>Hemorrhage - chemically induced</subject><subject>Humans</subject><subject>Percutaneous coronary intervention</subject><subject>Percutaneous Coronary Intervention - adverse effects</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors</subject><subject>Thrombosis</subject><subject>Thrombosis - etiology</subject><subject>Thrombosis - prevention & control</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks9u1DAQxiMEotvCK1Q-cklqx3Zic0BUFf-kShwoZ2vWmbReEnuxnUX7EjwzjrblwIWTNfJvZvR931TVJaMNo6y72jX5IYY5YmraUjdUNLSVz6oNU72uW9G3z6sNpULXXAl1Vp2ntKOU9UzLl9VZ23MtBVeb6vfdAxIcR7SZhJGAze4AGQdip5Cz8_ckuxnJAaYFExlDJHvIDn1OZPEDxvuwMnuMdsngMSyJ2BCDh3gkzmeMh8K64N-Sa5KOKeNc2i2JeHD4i4AfyIwZavAwHZNLr6oXI0wJXz--F9X3jx_ubj7Xt18_fbm5vq2tUDrXoJQSTOpBgFW9Yp3sAO2Wcw69tBaV2vIBqAZevkaGSOWoZM9BSMs12_KL6s1p7j6Gn0VZNrNLFqfppMEwxaiUQnNZ0O6E2hhSijiafXRz0WcYNWsWZmeesjBrFoYKU7IojZePO5btjMPftifzC_D-BGBRWvyIJtlircXBxZKHGYL7_453_4ywk_POwvQDj5h2YYnF2aLHpNZQ8229iPUgWMcpb3vN_wDjGrc_</recordid><startdate>20160801</startdate><enddate>20160801</enddate><creator>Gui, Yi-Yue</creator><creator>Huang, Fang-Yang</creator><creator>Huang, Bao-Tao</creator><creator>Peng, Yong</creator><creator>Liu, Wei</creator><creator>Chen, Zhang</creator><creator>Chen, Shi-Jian</creator><creator>Pu, Xiao-Bo</creator><creator>Wang, Peng-Ju</creator><creator>Chen, Mao</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20160801</creationdate><title>The effect of activated clotting time values for patients undergoing percutaneous coronary intervention: A systematic review and meta-analysis</title><author>Gui, Yi-Yue ; Huang, Fang-Yang ; Huang, Bao-Tao ; Peng, Yong ; Liu, Wei ; Chen, Zhang ; Chen, Shi-Jian ; Pu, Xiao-Bo ; Wang, Peng-Ju ; Chen, Mao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-a8884159d4ac8781656aecb333a75cce88b3da09a3165f1ee05f8573a45c391b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Activated clotting time</topic><topic>Anticoagulants - therapeutic use</topic><topic>Blood Coagulation Tests</topic><topic>Coronary Disease - complications</topic><topic>Coronary Disease - drug therapy</topic><topic>Coronary Disease - surgery</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hemorrhage</topic><topic>Hemorrhage - chemically induced</topic><topic>Humans</topic><topic>Percutaneous coronary intervention</topic><topic>Percutaneous Coronary Intervention - adverse effects</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors</topic><topic>Thrombosis</topic><topic>Thrombosis - etiology</topic><topic>Thrombosis - prevention & control</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gui, Yi-Yue</creatorcontrib><creatorcontrib>Huang, Fang-Yang</creatorcontrib><creatorcontrib>Huang, Bao-Tao</creatorcontrib><creatorcontrib>Peng, Yong</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Chen, Zhang</creatorcontrib><creatorcontrib>Chen, Shi-Jian</creatorcontrib><creatorcontrib>Pu, Xiao-Bo</creatorcontrib><creatorcontrib>Wang, Peng-Ju</creatorcontrib><creatorcontrib>Chen, Mao</creatorcontrib><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>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gui, Yi-Yue</au><au>Huang, Fang-Yang</au><au>Huang, Bao-Tao</au><au>Peng, Yong</au><au>Liu, Wei</au><au>Chen, Zhang</au><au>Chen, Shi-Jian</au><au>Pu, Xiao-Bo</au><au>Wang, Peng-Ju</au><au>Chen, Mao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of activated clotting time values for patients undergoing percutaneous coronary intervention: A systematic review and meta-analysis</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>2016-08-01</date><risdate>2016</risdate><volume>144</volume><spage>202</spage><epage>209</epage><pages>202-209</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><abstract>Abstract Our aim was to illustrate the effect of higher activated clotting time (ACT) values versus lower ACT values on thrombotic or hemorrhagic events in coronary atherosclerotic heart disease (CHD) patients undergoing percutaneous coronary intervention (PCI). PubMed, Embase, Web of Science, and Cochrane Library were searched. Observational studies assessing ACT related major adverse cardiac event (MACE) and major bleeding were included. Studies were allocated into three groups. Group 1 included studies with low percentage of participants prescribed with glycoprotein IIb/IIIa inhibitors (≤ 30%), Group 2 with high percentage of participants prescribed with GPI (> 30%), and Group 3 with routine direct thrombin inhibitors (DTI) prescription. The cutoff is designed as 300 s (290–310 s) for Group 1, and 250 s (240–260 s) for Group 2. With regard to MACE and major bleeding in Group 1, there was no significant difference between higher ACT values and lower ACT values (risk ratio [RR] for MACE, 1.16, 95% confidence interval [CI], 0.65–2.05, p = 0.62, I2 = 94%, RR for major bleeding, 0.96, 95% CI, 0.66–1.40, p = 0.83, I2 = 0%). Likewise, no significant difference was found in Group 2 between higher ACT values and lower ACT values (RR for MACE, 1.15, 95% CI, 0.97–1.35, p = 0.10, I2 = 0%, RR for major bleeding, 0.85, 95% CI, 0.45–1.60, p = 0.61, I2 = 83%). In conclusion, ACT may not have a substantial effect on thrombotic or hemorrhagic complications. Under current clinical practice, target ACT may be higher than what is necessary to prevent thrombotic events. We may achieve a relative low ACT level to preserve efficacy and enhance safety.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>27395438</pmid><doi>10.1016/j.thromres.2016.04.025</doi><tpages>8</tpages></addata></record> |
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subjects | Activated clotting time Anticoagulants - therapeutic use Blood Coagulation Tests Coronary Disease - complications Coronary Disease - drug therapy Coronary Disease - surgery Hematology, Oncology and Palliative Medicine Hemorrhage Hemorrhage - chemically induced Humans Percutaneous coronary intervention Percutaneous Coronary Intervention - adverse effects Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors Thrombosis Thrombosis - etiology Thrombosis - prevention & control |
title | The effect of activated clotting time values for patients undergoing percutaneous coronary intervention: A systematic review and meta-analysis |
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