PMID- 38432342 OWN - NLM STAT- MEDLINE DCOM- 20240419 LR - 20240419 IS - 1879-1913 (Electronic) IS - 0002-9149 (Linking) VI - 218 DP - 2024 May 1 TI - Safety and Efficacy of Enoxaparin During Low-Risk Elective Percutaneous Coronary Intervention. PG - 63-67 LID - S0002-9149(24)00157-7 [pii] LID - 10.1016/j.amjcard.2024.02.033 [doi] AB - Intravenous unfractionated heparin (UFH) is the most frequently used anticoagulant for percutaneous coronary intervention (PCI). Intravenous enoxaparin, a low-molecular-weight heparin, has superior pharmacokinetic and pharmacodynamic properties compared with UFH. Multiple trials have shown enoxaparin to be safe and effective in PCI. However, there has not been a contemporary study evaluating its safety and efficacy. To assess its efficacy and safety, intravenous enoxaparin during PCI through radial artery access was evaluated in PCI patients from January 2015 to December 2019. Outcomes included procedural success, all-cause mortality, ischemic complications, and bleeding complications from the time of the procedure until hospital discharge. A total of 1019 consecutive eligible patients were identified. Median age was 63 years, and 70% were men. The indication for PCI was stable and unstable angina in two-thirds of cases (77%). Few patients had myocardial infarction (MI) (2.2%) as the indication for intervention. The procedure was successful in 98.2% of cases. There were no deaths. Procedural MI occurred in 0.3% of patients. Acute stent thrombosis occurred in 0.4%. Urgent revascularization and stroke occurred in 0.1% each. Small wrist hematomas occurred in 0.3% and all were managed conservatively. There was one radial artery pseudoaneurysm. There were no cases of major bleeding. In conclusion, this single-center study showed that intravenous enoxaparin is a reasonable alternative anticoagulant for use in low-risk and elective non-MI PCI through radial artery access. CI - Copyright (c) 2024 Elsevier Inc. All rights reserved. FAU - Alturkmani, Hani AU - Alturkmani H AD - Department of Cardiovascular Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas. Electronic address: hani.alturkmani@gmail.com. FAU - Uretsky, Barry AU - Uretsky B AD - Department of Cardiovascular Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas; Department of Cardiology, Central Arkansas Veterans Affairs Healthcare System, Little Rock, Arkansas. FAU - Patel, Swetal AU - Patel S AD - Department of Cardiology, University of Nevada Las Vegas, Las Vegas, Nevada. FAU - Albadaineh, Mu'nes AU - Albadaineh M AD - Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas. FAU - Alqaisi, Omar AU - Alqaisi O AD - Department of Internal Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas. FAU - Alaiwah, Malek AU - Alaiwah M AD - Department of Cardiovascular Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas. FAU - Cross, Michael AU - Cross M AD - Department of Cardiovascular Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas. FAU - Abbasi, Danish AU - Abbasi D AD - Department of Cardiovascular Medicine, University of Arkansas for Medical Sciences, Little Rock, Arkansas. FAU - Rollefson, William AU - Rollefson W AD - Department of Cardiology, Arkansas Heart Hospital, Little Rock, Arkansas. LA - eng PT - Journal Article DEP - 20240301 PL - United States TA - Am J Cardiol JT - The American journal of cardiology JID - 0207277 RN - 0 (Enoxaparin) RN - 9005-49-6 (Heparin) RN - 0 (Anticoagulants) SB - IM MH - Male MH - Humans MH - Middle Aged MH - Female MH - Enoxaparin MH - Heparin MH - *Percutaneous Coronary Intervention MH - Treatment Outcome MH - Anticoagulants MH - *Myocardial Infarction OTO - NOTNLM OT - anticoagulation OT - enoxaparin OT - heparin OT - percutaneous coronary intervention COIS- Declaration of competing interest The authors have no competing interests to declare. EDAT- 2024/03/04 00:43 MHDA- 2024/04/19 06:43 CRDT- 2024/03/03 19:14 PHST- 2023/08/21 00:00 [received] PHST- 2024/02/01 00:00 [revised] PHST- 2024/02/23 00:00 [accepted] PHST- 2024/04/19 06:43 [medline] PHST- 2024/03/04 00:43 [pubmed] PHST- 2024/03/03 19:14 [entrez] AID - S0002-9149(24)00157-7 [pii] AID - 10.1016/j.amjcard.2024.02.033 [doi] PST - ppublish SO - Am J Cardiol. 2024 May 1;218:63-67. doi: 10.1016/j.amjcard.2024.02.033. Epub 2024 Mar 1.