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Protamine for Coronary Perforation in Chronic Total Occlusion Percutaneous Coronary Intervention
Sant Kumar1,2, Sudhir Thotakura1,3, Kathleen E Kearney1
1Division of Cardiology, Department of Medicine, University of Washington, Seattle, WA, USA .
Insights
Protamine administration for chronic total occlusion percutaneous coronary intervention (CTO PCI) perforations is safe. This study found no significant difference in in-hospital or 1-year outcomes between patients who received protamine and those who did not.
Area of Science:
- Cardiology
- Interventional Cardiology
- Vascular Medicine
Background:
- Unfractionated heparin reversal with protamine is common in percutaneous coronary intervention (PCI).
- Data on protamine's safety and outcomes in chronic total occlusion PCI (CTO PCI)-related perforations are limited.
- Assessing protamine's impact in this specific high-risk scenario is crucial for clinical practice.
Purpose of the Study:
- To evaluate the safety and clinical outcomes associated with protamine administration in patients experiencing coronary perforation during CTO PCI.
- To compare in-hospital and 1-year all-cause mortality, cardiac tamponade, and myocardial infarction between patients who received protamine and those who did not.
Main Methods:
- Retrospective analysis of 1,503 CTO PCI procedures from January 2019 to December 2023.
- Patients with coronary perforation (n=199) were stratified based on protamine administration.
- Inverse probability of treatment weighting (IPTW) and doubly robust logistic regression were used for adjusted analyses.
Main Results:
- In-hospital outcomes including death, pericardiocentesis, and periprocedural MI were comparable between protamine and no-protamine groups.
- No acute stent thrombosis or protamine reactions were observed.
- Adjusted analyses showed no significant association between protamine use and adverse in-hospital or 1-year all-cause death.
Conclusions:
- Protamine administration for CTO PCI-related perforation appears safe.
- There is no evidence of additional clinical benefit from protamine use in this context.
- Current practice of protamine use in CTO PCI perforations warrants re-evaluation based on these findings.
Abstract:
Protamine is frequently used to reverse unfractionated heparin, yet contemporary data on its safety and long-term outcomes in chronic total occlusion percutaneous coronary intervention (CTO PCI)-related perforation are limited. We retrospectively analyzed all CTO PCI procedures performed at a single center between January 2019 and December 2023. Patients who experienced coronary perforation were stratified by protamine administration. Inverse probability of treatment weighting (IPTW) and doubly robust logistic regression were used to adjust for baseline and procedural differences. Clinical end points included protamine-related reactions, cardiac tamponade requiring pericardiocentesis, periprocedural myocardial infarction (MI), acute stent thrombosis, in-hospital all-cause death, and 1-year all-cause death. Among 1503 CTO PCI cases, perforation occurred in 199 patients (13.2%): 108 (54.3%) received protamine and 91 (45.7%) did not. Protamine use increased over time ( P -for-trend <0.001). In-hospital outcomes were comparable between groups, including death (4.6% vs. 4.4%; P > 0.999), pericardiocentesis (8.3% vs. 9.9%; P = 0.806), and periprocedural MI (0.9% vs. 2.2%; P = 0.594). IPTW-adjusted analyses yielded similar results. No acute stent thrombosis or protamine reactions occurred. Doubly robust analysis showed no association between protamine use and in-hospital death (aOR 0.85, 95% CI 0.05-13.86; P = 0.917), pericardiocentesis (aOR 0.45, 95% CI 0.10-1.98; P = 0.294), or either outcome (aOR 0.53, 95% CI 0.21-2.85; P = 0.390). At 1 year, all-cause death remained similar (7.4% vs. 6.6%; P > 0.999), with no association on adjusted analysis (aOR 0.63, 95% CI 0.12-3.40; P = 0.591). Protamine administration for CTO PCI-related perforation seems safe, without evidence of additional clinical benefit compared with no protamine use.
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