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
Hauptverfasser: 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
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container_end_page 209
container_issue
container_start_page 202
container_title Thrombosis research
container_volume 144
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
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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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 (&gt; 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. 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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 (&gt; 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. 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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 &amp; 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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 (&gt; 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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