Issue: December 2017
October 30, 2017
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CULPRIT-SHOCK: Culprit lesion only may be superior to immediate multivessel PCI

Issue: December 2017
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Holger Thiele

The 30-day risk for composite death or severe renal failure leading to renal-replacement therapy in patients with multivessel CAD and acute MI with cardiogenic shock was lower among those who underwent PCI of the culprit lesion only compared with those who received immediate multivessel PCI, according to the results of the CULPRIT-SHOCK trial, presented at TCT 2017.

The study results, presented by Holger Thiele, MD, from the Heart Center Leipzig and the University Hospital, Leipzig, Germany, were simultaneously published in The New England Journal of Medicine.

According to Thiele and colleagues, the researchers conducted a 706-patient, multicenter, randomized trial to assess whether PCI of the culprit lesion only with the option of staged revascularization of non-culprit lesions would confer better clinical outcomes when compared with immediate multivessel PCI among patients who have multivessel CAD and acute MI with cardiogenic shock.

The study’s primary endpoint was a composite of death or severe renal failure leading to renal-replacement therapy up to 30 days after revascularization and safety endpoints included bleeding rates defined as type 2, 3, or 5 on the Bleeding Academic Research Consortium scale, and stroke.

The researchers found the composite primary endpoint of death or renal-replacement therapy at 30 days had occurred in 45.9% of patients in the culprit-lesion-only group and 55.4% in the multivessel PCI group (RR = 0.83; 95% CI, 0.71-0.96).

Compared with the multivessel PCI group, the RR for death in the culprit-lesion-only cohort was 0.84 (95% CI, 0.72-0.98), and the RR of renal-replacement therapy was 0.71 (95% CI, 0.49-1.03).

According to the presentation, the two groups showed no significant difference in the time to hemodynamic stabilization, the risk of catecholamine therapy and the duration of such therapy, the levels of troponin T and creatine kinase, and the rates of bleeding and stroke.

Although the European guidelines suggest multivessel PCI of class IIa, level of evidence C lesions, there is no specific recommendation in the U.S. for how to treat these patients. However, recently, there has been appropriate use criteria published suggesting immediate PCI in these patients. Regardless of recommendation, the presentation panel said this important study will be practice-changing.

“Keep it simple is the major message from our trial,” Thiele said in his presentation. “Keep it simple, do PCI of the infarct-related artery and then look how the patient does later, and then you can do stent revascularization.”

In an accompanying editorial, Judith S. Hochman, MD, and Stuart Katz, MD, both from NYU Langone Health, wrote: “The consistent risk estimates for the primary endpoint in the intention-to-treat, per-protocol and as-treated analysis support the robustness of the findings. The CUPLRIT-SHOCK trial provides compelling evidence that a strategy of culprit-lesion-only PCI is preferred over initial multivessel PCI for patients with cardiogenic shock.” – by Dave Quaile

References:

Hochman JS, et al. New Engl J Med. 2017;doi:10.1056/NEJMe1713341.

Thiele H, et al. Late Breaking Clinical Trials 1. Presented at: TCT Scientific Symposium; Oct. 29-Nov. 2, 2017; Denver.

Thiele H, et al. New Engl J Med. 2017;doi:10.1056/NEJMoa1710261.

 

Disclosure: Hochman reports she receives grant support from American Regent and Janssen and receives personal fees from Regeneron. Katz reports no relevant financial disclosures. Thiele reports he receives grant and research support from the European Union and German Cardiac Society German Heart Research Foundation.