Killip class at presentation and immediate versus staged multivessel PCI in patients with STEMI

P Philipp Jakob F Ferdinando Varbella A Axel Linke (University Hospital, Dresden, Germany) S Stephan B. Felix M Moritz Seiffert R Rahel Kesterke P Peter Nordbeck B Bernhard Witzenbichler I Irene M. Lang (Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna) M Mirjam Kessler C Christian Valina A Alban Dibra M Miklos Rohla M Marco Moccetti M Matteo Vercellino L Luise Gaede L Lorenz Bott-Flügel J Julia Stehli A Alessandro Candreva M Michael Würdinger F Francesco Paneni C Christian Templin M Matthias Schindler M Manfred Wischnewsky G Greca Zanda G Giorgio Quadri N Norman Mangner (University Hospital, Dresden, Germany) A Aurel Toma G Giulia Magnani P Peter Clemmensen (University Medical Center Hamburg–Eppendorf, Hamburg, Germany) T Thomas Münzel P P. Christian Schulze (University Hospital Jena, Friedrich-Schiller-University, Jena, Germany) K Karl-Ludwig Laugwitz W Wolfgang Rottbauer K Kurt Huber F Franz-Josef Neumann S Steffen Schneider T Thomas Riemer F Franz Weidinger S Stephan Achenbach G Gert Richardt A Adnan Kastrati (Klinik für Herz- und Kreislauferkrankungen, TUM Klinikum Deutsches Herzzentrum, Technische Universität München, Munich) I Ian Ford F Frank Ruschitzka B Barbara E. Stähli

Abstract

Abstract Patients with ST-segment elevation myocardial infarction (STEMI) and higher Killip class are at an increased risk of death. We sought to assess outcomes of an immediate or staged multivessel percutaneous coronary intervention (PCI) in patients with higher Killip class presenting with STEMI and multivessel coronary artery disease (MVD). We conducted a subgroup analysis of the MULTISTARS AMI trial with stratification of patients according to Killip classes. Outcomes of patients with Killip class I and Killip class ≥ II were compared. The primary end point was a composite of all-cause death, non-fatal myocardial infarction, stroke, unplanned ischemia-driven revascularization, or hospitalization for heart failure at 1 year. The primary end point occurred in 15 (17.9%) patients with Killip class ≥ II and 78 (11.4%) patients with Killip class I (HR, 1.57 [95%CI, 0.92–2.70], p-value = 0.11). Comparing an immediate with a staged multivessel PCI strategy, the immediate strategy reduced the primary endpoint in patients with Killip class I (6.8% vs. 15.8%; HR, 0.40 [95%CI, 0.25–0.65], p-value < 0.01), whereas the difference was not significant in patients with Killip class ≥ II (20.0% vs. 15.4%; HR, 1.37 [95%CI, 0.50–3.78], p-value = 0.55). There was a significant treatment-by-subgroup interaction for the primary endpoint (P interaction  = 0.029), with immediate multivessel PCI not showing an advantage in Killip class ≥ II patients. Conclusively, in the MULTISTARS AMI trial, the benefit of immediate multivessel revascularization strategy observed in patients with Killip class I appeared attenuated in those presenting with Killip class ≥ II, suggesting a potential difference in treatment effect that warrants further investigation. (Supported by Boston Scientific; MULTISTARS AMI, NCT03135275)

Article Details

Volume / Issue Vol. 1, Issue 1
Published June 26, 2026
ISSN 2045-2322
Publisher Nature Portfolio

Journal Info

Scientific Reports

Nature Portfolio

ISSN: 2045-2322 Open Access Life Sciences

Authors (45)

P

Philipp Jakob

F

Ferdinando Varbella

A

Axel Linke

University Hospital, Dresden, Germany

S

Stephan B. Felix

M

Moritz Seiffert

R

Rahel Kesterke

P

Peter Nordbeck

B

Bernhard Witzenbichler

I

Irene M. Lang

Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna

M

Mirjam Kessler

C

Christian Valina

A

Alban Dibra

M

Miklos Rohla

M

Marco Moccetti

M

Matteo Vercellino

L

Luise Gaede

L

Lorenz Bott-Flügel

J

Julia Stehli

A

Alessandro Candreva

M

Michael Würdinger

F

Francesco Paneni

C

Christian Templin

M

Matthias Schindler

M

Manfred Wischnewsky

G

Greca Zanda

G

Giorgio Quadri

N

Norman Mangner

University Hospital, Dresden, Germany

A

Aurel Toma

G

Giulia Magnani

P

Peter Clemmensen

University Medical Center Hamburg–Eppendorf, Hamburg, Germany

T

Thomas Münzel

P

P. Christian Schulze

University Hospital Jena, Friedrich-Schiller-University, Jena, Germany

K

Karl-Ludwig Laugwitz

W

Wolfgang Rottbauer

K

Kurt Huber

F

Franz-Josef Neumann

S

Steffen Schneider

T

Thomas Riemer

F

Franz Weidinger

S

Stephan Achenbach

G

Gert Richardt

A

Adnan Kastrati

Klinik für Herz- und Kreislauferkrankungen, TUM Klinikum Deutsches Herzzentrum, Technische Universität München, Munich

I

Ian Ford

F

Frank Ruschitzka

B

Barbara E. Stähli