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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Cangrelor is an intravenous adenosine triphosphate analog that reversibly blocks P2Y12 receptor-mediated platelet activation&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> It has a quick onset of action and a short plasma half-life&#44; enabling complete platelet function recovery within 60 minutes of stopping the infusion&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> Cangrelor is approved for co-administration with aspirin to reduce thrombotic events in patients with coronary artery disease&#44; undergoing percutaneous coronary intervention &#40;PCI&#41;&#44; who have not received an oral P2Y12 inhibitor &#40;P2Y12i&#41; prior to the procedure and in whom oral P2Y12is are not feasible&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Stented patients who need urgent surgery are likely to experience an early suspension of dual antiplatelet therapy &#40;DAPT&#41;&#44; increasing the risk of stent thrombosis&#44; or postponement of surgery due to bleeding risk concerns&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> An effective and safe antiplatelet bridging therapy is of particular relevance in this setting&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">A 79-year-old man with rectal cancer under neoadjuvant chemotherapy suffered a non-ST-segment elevation myocardial infarction&#46; Coronary angiography showed severe and complex osteal disease of the circumflex artery that was treated with a drug-eluting stent&#46; The patient was considered to be at high thrombotic risk and DAPT with aspirin and ticagrelor was recommended for at least 12 months&#46; Optimal timing for his rectal surgery was defined as 30 days after PCI&#46; The high thrombotic risk associated with early suspension of P2Y12i was considered prohibitive&#46; To avoid further delay in cancer surgery and worsening of the patient&#39;s prognosis&#44; a special authorization for the off-label use of cangrelor as an antiplatelet bridging therapy was conceded by the Portuguese National Authority of Medicines and Health Products&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The patient was admitted to the cardiology ward 30 days after PCI for antiplatelet bridging therapy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41;&#46; Ticagrelor was stopped five days before surgery and cangrelor infusion was started 48 hours later &#40;day -3&#41;&#44; at a dose of 0&#46;75 mcg&#47;kg&#47;min&#44; without bolus&#46; Cangrelor infusion was performed for three days and stopped two hours before surgery&#46; Aspirin therapy was not suspended&#46; We used the ROTEM&#174;-Platelet platform &#40;TEM International GmbH&#44; Munich&#44; Germany&#41; to measure platelet function at four points&#44; based on impedance aggregometry &#40;IPA&#41;&#58; Test 1&#44; 12 hours after ticagrelor suspension &#40;day -5&#41;&#59; Test 2&#44; immediately before starting cangrelor &#40;day -3&#41;&#59; Test 3&#44; 24 hours after starting cangrelor &#40;day -2&#41;&#59; and Test 4&#44; one hour before surgery &#40;day 0&#41;&#46; IPA results showed effective antiplatelet inhibition until surgery &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; The patient underwent a laparoscopic rectal resection&#44; without acute bleeding complications&#46; Six hours after surgery&#44; cangrelor was restarted and subsequently stopped on the first morning post-surgery&#44; when oral drug administration became possible&#46; Ticagrelor was resumed&#44; as a loading dose&#44; immediately after cangrelor suspension&#46; During the postoperative period&#44; there were no bleeding or thrombotic complications&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">The use of cangrelor in this setting is supported by the BRIDGE trial&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a> which showed a higher rate of platelet inhibition&#44; without increasing major bleeding&#44; in patients previously treated with oral P2Y12i awaiting cardiac surgery&#46; Cangrelor bridging therapy should be started three days before surgery&#44; maintained for two to seven days&#44; and suspended one to six hours before surgery&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Although glycoprotein &#40;GP&#41; IIb&#47;IIIa inhibitors have also been used as a bridging therapy&#44; their safety and efficacy in this setting have not been clearly established&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a> They act in the final pathway of platelet aggregation&#44; blocking the platelet response to all agonists&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a> They present disadvantages compared to cangrelor&#46; Their plasma half-life is longer and they should be stopped four to six hours before surgery&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;6</span></a> The ideal bridging dose has not yet been determined&#44; so the recommendation is to use the same dose as in PCI&#44; without a loading dose&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> Therapy should not exceed 72 hours to reduce bleeding risk&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">We report the first use of cangrelor as antiplatelet bridging therapy in Portugal&#46; The absence of thrombotic or bleeding complications and the documentation of good platelet inhibition throughout bridging therapy suggest this strategy is safe and effective&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Funding</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors have no funding</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflicts of interest</span><p id="par0045" class="elsevierStylePara elsevierViewall">Dr&#46; 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Letter to the Editor
Cangrelor as antiplatelet bridging therapy in non-cardiac surgery after percutaneous coronary intervention – First-time use in Portugal
Cangrelor como terapêutica antiplaquetária de bridging na cirurgia não cardíaca após intervenção coronária percutânea – Primeira utilização em Portugal
Inês Fialhoa,
Autor para correspondência
inesscfialho@gmail.com

Corresponding author.
, João B. Augustoa,b, Susana Fevereiroc, Miguel B. Santosa, Sérgio Bravo Baptistad, David Roquea
a Cardiology Department, Hospital Professor Doutor Fernando Fonseca, Amadora, Portugal
b Institute of Cardiovascular Science, University College London, UK
c Transfusion Medicine Department, Hospital de Santa Cruz, Centro Hospitalar Lisboa Ocidental, Carnaxide, Portugal
d University Clinic of Cardiology, Faculty of Medicine at University of Lisbon, Lisboa, Portugal
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Cangrelor is an intravenous adenosine triphosphate analog that reversibly blocks P2Y12 receptor-mediated platelet activation&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> It has a quick onset of action and a short plasma half-life&#44; enabling complete platelet function recovery within 60 minutes of stopping the infusion&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> Cangrelor is approved for co-administration with aspirin to reduce thrombotic events in patients with coronary artery disease&#44; undergoing percutaneous coronary intervention &#40;PCI&#41;&#44; who have not received an oral P2Y12 inhibitor &#40;P2Y12i&#41; prior to the procedure and in whom oral P2Y12is are not feasible&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Stented patients who need urgent surgery are likely to experience an early suspension of dual antiplatelet therapy &#40;DAPT&#41;&#44; increasing the risk of stent thrombosis&#44; or postponement of surgery due to bleeding risk concerns&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> An effective and safe antiplatelet bridging therapy is of particular relevance in this setting&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">A 79-year-old man with rectal cancer under neoadjuvant chemotherapy suffered a non-ST-segment elevation myocardial infarction&#46; Coronary angiography showed severe and complex osteal disease of the circumflex artery that was treated with a drug-eluting stent&#46; The patient was considered to be at high thrombotic risk and DAPT with aspirin and ticagrelor was recommended for at least 12 months&#46; Optimal timing for his rectal surgery was defined as 30 days after PCI&#46; The high thrombotic risk associated with early suspension of P2Y12i was considered prohibitive&#46; To avoid further delay in cancer surgery and worsening of the patient&#39;s prognosis&#44; a special authorization for the off-label use of cangrelor as an antiplatelet bridging therapy was conceded by the Portuguese National Authority of Medicines and Health Products&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The patient was admitted to the cardiology ward 30 days after PCI for antiplatelet bridging therapy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41;&#46; Ticagrelor was stopped five days before surgery and cangrelor infusion was started 48 hours later &#40;day -3&#41;&#44; at a dose of 0&#46;75 mcg&#47;kg&#47;min&#44; without bolus&#46; Cangrelor infusion was performed for three days and stopped two hours before surgery&#46; Aspirin therapy was not suspended&#46; We used the ROTEM&#174;-Platelet platform &#40;TEM International GmbH&#44; Munich&#44; Germany&#41; to measure platelet function at four points&#44; based on impedance aggregometry &#40;IPA&#41;&#58; Test 1&#44; 12 hours after ticagrelor suspension &#40;day -5&#41;&#59; Test 2&#44; immediately before starting cangrelor &#40;day -3&#41;&#59; Test 3&#44; 24 hours after starting cangrelor &#40;day -2&#41;&#59; and Test 4&#44; one hour before surgery &#40;day 0&#41;&#46; IPA results showed effective antiplatelet inhibition until surgery &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; The patient underwent a laparoscopic rectal resection&#44; without acute bleeding complications&#46; Six hours after surgery&#44; cangrelor was restarted and subsequently stopped on the first morning post-surgery&#44; when oral drug administration became possible&#46; Ticagrelor was resumed&#44; as a loading dose&#44; immediately after cangrelor suspension&#46; During the postoperative period&#44; there were no bleeding or thrombotic complications&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">The use of cangrelor in this setting is supported by the BRIDGE trial&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a> which showed a higher rate of platelet inhibition&#44; without increasing major bleeding&#44; in patients previously treated with oral P2Y12i awaiting cardiac surgery&#46; Cangrelor bridging therapy should be started three days before surgery&#44; maintained for two to seven days&#44; and suspended one to six hours before surgery&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;2</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Although glycoprotein &#40;GP&#41; IIb&#47;IIIa inhibitors have also been used as a bridging therapy&#44; their safety and efficacy in this setting have not been clearly established&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a> They act in the final pathway of platelet aggregation&#44; blocking the platelet response to all agonists&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a> They present disadvantages compared to cangrelor&#46; Their plasma half-life is longer and they should be stopped four to six hours before surgery&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;6</span></a> The ideal bridging dose has not yet been determined&#44; so the recommendation is to use the same dose as in PCI&#44; without a loading dose&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> Therapy should not exceed 72 hours to reduce bleeding risk&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">We report the first use of cangrelor as antiplatelet bridging therapy in Portugal&#46; The absence of thrombotic or bleeding complications and the documentation of good platelet inhibition throughout bridging therapy suggest this strategy is safe and effective&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Funding</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors have no funding</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflicts of interest</span><p id="par0045" class="elsevierStylePara elsevierViewall">Dr&#46; 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