PMID- 36100498 OWN - NLM STAT- MEDLINE DCOM- 20221115 LR - 20230223 IS - 1532-8422 (Electronic) IS - 1053-0770 (Linking) VI - 36 IP - 12 DP - 2022 Dec TI - A Pilot Study to Assess the Clinical Onset of IV Heparin in Interventional Cardiology and Cardiac Surgery. PG - 4281-4288 LID - S1053-0770(22)00546-8 [pii] LID - 10.1053/j.jvca.2022.07.030 [doi] AB - OBJECTIVES: To determine the onset of heparin anticoagulation, using 2 different measures of activated clotting times (ACT), thromboelastography (TEG; R-time), and anti-Xa levels, after administering low- (100 U/kg) and high- (300 U/kg) dose intravenous (IV) heparin to patients undergoing transcatheter aortic valve replacement (TAVR) and cardiac surgery, respectively. DESIGN: Prospective study. SETTING: Single academic institution. PARTICIPANTS: Patients with normal baseline coagulation presenting for TAVR or cardiac valve surgery. INTERVENTIONS: Coagulation studies were performed at baseline, 30 seconds, 90 seconds, and 180 seconds after IV heparin administration. The tests included iSTAT (iACT) and Hemochron ACT (hACT), TEG R-Time, and anti-Xa levels. At the authors' institution, anti-Xa is the preferred measure of heparin anticoagulation when time permits. ACT, a rapid point- of-care test, is used to assess intraprocedural anticoagulation. MEASUREMENTS AND MAIN RESULTS: After both low- and high-dose heparin, there are peak increases in ACT and anti-Xa at 30 seconds, followed by a decline at 90 seconds and plateau at 180 seconds. The TEG R-time remained elevated (>80 minutes) throughout. For TAVR cases, all anti-Xa was >1.5 IU/mL, and was associated with an iACT >180 seconds and an hACT >200 seconds. For cardiac valve surgery cases, all anti-Xa was >2.4 and associated with an iACT >420 seconds and and hACT >340 seconds. Compared with hACT, iACTs were significantly lower at all time points after low-dose heparin, but not after high-dose heparin. CONCLUSIONS: In this pilot study, heparin anticoagulation was detected as early as 30 seconds after IV administration, based on ACT, anti-Xa levels, and TEG R-time. CI - Copyright (c) 2022 Elsevier Inc. All rights reserved. FAU - Asher, Shyamal AU - Asher S AD - Department of Anesthesiology, Rhode Island Hospital, Providence, RI. Electronic address: ashershy@gmail.com. FAU - Maslow, Andrew AU - Maslow A AD - Department of Anesthesiology, Rhode Island Hospital, Providence, RI. FAU - Mishra, Vikas AU - Mishra V AD - Department of Anesthesiology, Rhode Island Hospital, Providence, RI. FAU - Flaherty, Devon AU - Flaherty D AD - Department of Anesthesiology, Rhode Island Hospital, Providence, RI. FAU - Hayward, Geoffrey AU - Hayward G AD - Department of Anesthesiology, Rhode Island Hospital, Providence, RI. FAU - Whiteneck, Stephanie AU - Whiteneck S AD - Department of Hematology, Rhode Island Hospital, Providence, RI. FAU - Cheves, Tracey AU - Cheves T AD - Department of Hematology, Rhode Island Hospital, Providence, RI. FAU - Sweeney, Joseph AU - Sweeney J AD - Department of Hematology, Rhode Island Hospital, Providence, RI. LA - eng PT - Journal Article DEP - 20220805 PL - United States TA - J Cardiothorac Vasc Anesth JT - Journal of cardiothoracic and vascular anesthesia JID - 9110208 RN - 0 (Anticoagulants) RN - 9005-49-6 (Heparin) SB - IM MH - Humans MH - Pilot Projects MH - Anticoagulants MH - Prospective Studies MH - Heparin MH - *Cardiac Surgical Procedures MH - *Cardiology MH - Whole Blood Coagulation Time EDAT- 2022/09/14 06:00 MHDA- 2022/11/16 06:00 CRDT- 2022/09/13 22:04 PHST- 2022/04/20 00:00 [received] PHST- 2022/07/27 00:00 [revised] PHST- 2022/07/29 00:00 [accepted] PHST- 2022/09/14 06:00 [pubmed] PHST- 2022/11/16 06:00 [medline] PHST- 2022/09/13 22:04 [entrez] AID - S1053-0770(22)00546-8 [pii] AID - 10.1053/j.jvca.2022.07.030 [doi] PST - ppublish SO - J Cardiothorac Vasc Anesth. 2022 Dec;36(12):4281-4288. doi: 10.1053/j.jvca.2022.07.030. Epub 2022 Aug 5.