2019
DOI: 10.1016/j.carrev.2018.11.018
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Intravenous Antiplatelet Therapy Bridging in Patients Undergoing Cardiac or Non-Cardiac Surgery Following Percutaneous Coronary Intervention

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Cited by 14 publications
(7 citation statements)
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“…8 Retrospective studies of cangrelor bridging for NCS report either no bleeding or minor procedural bleeding (Table 4), suggesting that this is a safe approach to perioperative platelet inhibition. [13][14][15][16][17][18][19][20][21][22][23][24][25][26][27]…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…8 Retrospective studies of cangrelor bridging for NCS report either no bleeding or minor procedural bleeding (Table 4), suggesting that this is a safe approach to perioperative platelet inhibition. [13][14][15][16][17][18][19][20][21][22][23][24][25][26][27]…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, the BRIDGE trial reported a low incidence of preoperative ischemic events, and retrospective studies of cangrelor bridging for NCS report a low incidence of perioperative MACE (Table 4). 8,[13][14][15][16][17][18][19][20][21][22][23][24][25][26][27] Thus, cangrelor bridging appears to be an effective approach for mitigating the risk of perioperative MACE.…”
Section: Table 4 (Continued)mentioning
confidence: 99%
“…In another study it has been reported that thrombotic events start in the preoperative period (8). Bridging with intravenous glycoprotein IIb/IIIa inhibitors (eptifibatide, tirofiban) with a short half-life has been suggested for these patients in recent years (9,10).…”
Section: Discussionmentioning
confidence: 99%
“…In fact, it has a very short half-life with rapid resumption of platelet function (within 60 minutes), it does not require renal dosing adjustments and has a specific dosing regimen for bridging identified from a dose-finding investigation aimed at achieving "thienopyridine-like" levels of platelet inhibition; moreover, cangrelor has been specifically tested in a prospective, randomized, double-blind, placebo-controlled trial of patients undergoing CABG. 9,33 Conversely, the short-acting GPIs (i.e., eptifibatide and tirofiban) have a longer half-life and slower offset of action (i.e., 4-6 hours) compared with cangrelor, require renal dosing adjustments, and are used at the ACS dosing regimen given that there is no dedicated bridging dose. 34 Moreover, GPIs are known to be associated with an increased risk of thrombocytopenia, particularly with prolonged infusion, a phenomenon associated with worse outcomes, including mortality.…”
Section: Discussionmentioning
confidence: 99%