Sep 23, 2026 · 9 min · 5 segments
!https://cathmasters.com/wp-content/uploads/2026/09/15.-ACS-Guidelines-Question-6-with-Dr.-Binita-Shah.webp This episode is part of our comprehensive Decipher the Guidelines Series covering the…
Binita ShahGuest
Saahil JumkhawalaGuest
Grace QiuGuestAmit GoyalHost
We have a sixty-four-year-old male with a history of hypertension and dyslipidemia presenting to the emergency department with crescendo angina.

A diagnosis of non-ST elevation ACS is made, and the patient is scheduled for an early invasive strategy with percutaneous coronary intervention.

Which of the following parenteral anticoagulants is not recommended for use as a standalone agent during the PCI procedure itself? Option A, fondaparinux; option B, bivalirudin; option C, unfractionated heparin; or option D, enoxaparin.

The choice of parenteral anticoagulation for a patient with non-ST elevation ACS undergoing percutaneous coronary intervention is governed by both efficacy in preventing ischemic events and the safety profile regarding bleeding.

In patients with NSTACS, intravenous unfractionated heparin is useful to reduce ischemic events with a class one recommendation, level of evidence C. Bivalirudin, this direct thrombin inhibitor is recommended as an alternative to unfractionated heparin.

In patients with NSTACS undergoing PCI, bivalirudin may be reasonable as an alternative to unfractionated heparin to reduce bleeding and mortality with a class two B recommendation, level of evidence B. Enoxaparin.

In patients with ACS, IV enoxaparin may be considered as an alternative to unfractionated heparin at the time of PCI to reduce ischemic events.

In patients with ACS, fondaparinux should not be used to support PCI, class three recommendation harm with the level of evidence B.

Large-scale trials, notably the OASIS-Five trial, demonstrated that using fondaparinux alone during PCI led to a significantly higher rate of thrombus formation on the diagnostic and therapeutic catheters.

In the OASIS-Five trial, an increase was observed in the rate of catheter-related thrombus with fondaparinux compared with the enoxaparin arm.

Similar results were observed in the OASIS-Six trial, in which a higher rate of guiding catheter thrombosis and more coronary complications with fondaparinux were observed when used during PCI.

The main takeaway here is that parenteral anticoagulation for a patient with non-ST elevation acute coronary syndrome undergoing percutaneous coronary intervention is governed by both efficacy in preventing ischemic events and the safety profile regarding bleeding.

Dr. Shah, would you mind providing some additional perspective on this question and the related guideline recommendations?

We have a sixty-four-year-old male with a history of hypertension and dyslipidemia presenting to the emergency department with crescendo angina.

A diagnosis of non-ST elevation ACS is made, and the patient is scheduled for an early invasive strategy with percutaneous coronary intervention.

Which of the following parenteral anticoagulants is not recommended for use as a standalone agent during the PCI procedure itself? Option A, fondaparinux; option B, bivalirudin; option C, unfractionated heparin; or option D, enoxaparin.

The choice of parenteral anticoagulation for a patient with non-ST elevation ACS undergoing percutaneous coronary intervention is governed by both efficacy in preventing ischemic events and the safety profile regarding bleeding.

In patients with NSTACS, intravenous unfractionated heparin is useful to reduce ischemic events with a class one recommendation, level of evidence C. Bivalirudin, this direct thrombin inhibitor is recommended as an alternative to unfractionated heparin.

In patients with NSTACS undergoing PCI, bivalirudin may be reasonable as an alternative to unfractionated heparin to reduce bleeding and mortality with a class two B recommendation, level of evidence B. Enoxaparin.

In patients with ACS, IV enoxaparin may be considered as an alternative to unfractionated heparin at the time of PCI to reduce ischemic events.

In patients with ACS, fondaparinux should not be used to support PCI, class three recommendation harm with the level of evidence B.

Large-scale trials, notably the OASIS-Five trial, demonstrated that using fondaparinux alone during PCI led to a significantly higher rate of thrombus formation on the diagnostic and therapeutic catheters.

In the OASIS-Five trial, an increase was observed in the rate of catheter-related thrombus with fondaparinux compared with the enoxaparin arm.

Similar results were observed in the OASIS-Six trial, in which a higher rate of guiding catheter thrombosis and more coronary complications with fondaparinux were observed when used during PCI.

The main takeaway here is that parenteral anticoagulation for a patient with non-ST elevation acute coronary syndrome undergoing percutaneous coronary intervention is governed by both efficacy in preventing ischemic events and the safety profile regarding bleeding.

Dr. Shah, would you mind providing some additional perspective on this question and the related guideline recommendations?
The rest of this transcript — segmented and speaker-labeled, so you land on the exact moment something was said
Search every transcript — by keyword, by phrase, or by meaning, across every show Radar indexes
Trends — what is surging across podcasts, measured against its own baseline
Alerts — when a name you follow appears in a newly indexed episode
No account is needed to search Radar.