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Cardiogenic Shock Intravascular Cooling Trial (CHILL-SHOCK).
Gupta, Nikhil; Kalathiya, Rohan J; Singh, Nikhil; Bandealy, Nadeem; Neyestanak, Maryam; Besser, Stephanie; Arevalo, Cynthia; Friant, Janet; Blair, John E A; Nathan, Sandeep; Shah, Atman P; Paul, Jonathan.
Afiliación
  • Gupta N; Department of Medicine, University of Chicago, Chicago, IL.
  • Kalathiya RJ; Division of Cardiology, Department of Medicine, Johns Hopkins University, Baltimore, MD.
  • Singh N; Division of Cardiology, Ascension, Chicago, IL.
  • Bandealy N; Department of Medicine, University of Chicago, Chicago, IL.
  • Neyestanak M; Section of Cardiology, Department of Medicine, University of Chicago, Chicago, IL.
  • Besser S; School of Computing, DePaul University, Chicago, IL.
  • Arevalo C; Section of Cardiology, Department of Medicine, University of Chicago, Chicago, IL.
  • Friant J; Section of Cardiology, Department of Medicine, University of Chicago, Chicago, IL.
  • Blair JEA; Division of Cardiology, University of Washington, Seattle, WA.
  • Nathan S; Section of Cardiology, Department of Medicine, University of Chicago, Chicago, IL.
  • Shah AP; Section of Cardiology, Department of Medicine, University of Chicago, Chicago, IL.
  • Paul J; Section of Cardiology, Department of Medicine, University of Chicago, Chicago, IL. Electronic address: jpaul@medicine.bsd.uchicago.edu.
J Card Fail ; 30(7): 952-957, 2024 Jul.
Article en En | MEDLINE | ID: mdl-38458486
ABSTRACT

BACKGROUND:

Cardiogenic shock (CS) is complicated by high mortality rates. Targeted temperature control (TTC) has been proposed as an adjunct therapy in CS. This study aims to examine the safety of TTC in patients presenting with CS. METHODS AND

RESULTS:

In this open-label, randomized controlled pilot trial, 20 patients with hemodynamic criteria for CS were assigned to standard of care plus TTC vs standard of care alone. The primary outcome was a composite safety outcome, including well-described complications of TTC. Secondary outcomes included mortality at 90 days, invasive hemodynamic and echocardiographic parameters, electrocardiographic measurements, and inotrope dosing. There were no significant differences in the composite analysis of prespecified safety outcomes (3 events in the TTC group vs 0 events in the control group; P = 0.24). Patients randomized to TTC demonstrated a statistically significant increase in cardiac index and cardiac power index compared to the control group at 48-96 hours after randomization (3.6 [3.1, 3.9] L/min/m2 vs 2.6 [2.5, 3.15] L/min/m2; P = 0.029 and 0.61 [0.55, 0.7] W/m2 vs 0.53 [0.435, 0.565] W/m2; P = 0.029, respectively).

CONCLUSION:

TTC may be a safe adjunct therapy for patients presenting with CS and may yield improvement in specific hemodynamic parameters.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Choque Cardiogénico / Hipotermia Inducida Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Choque Cardiogénico / Hipotermia Inducida Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article