A Study to Investigate Outcomes and Management Effectiveness of Cardiogenic Shock II Patients

Overview

Información sobre este estudio

The purpose of this study is to develop a registry of patients with clinical cardiogenic shock (CS) in order to allow better definition of several key issues regarding cardiogenic shock.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Adult patients meeting criteria for cardiogenic shock during the study period of August 1, 2019 to July 31, 2022.
  • Cardiogenic shock criteria defined as:
    • Systolic blood pressure < 90 mm Hg or mean arterial blood pressure 30 mm Hg below baseline for at least 30 minutes despite volume resuscitation and/or vasoactive therapy; and
    • Evidence of end-organ hypoperfusion (altered mental status, oliguria with urine output <30 mL/hour, cool extremities, lactate >2.0 mmol/L); or
    • Pulmonary edema.
  • The etiology of cardiogenic shock can be categorized into one of the following subtypes:
    • Ischemic (acute myocardial infarction, ischemic cardiomyopathy), myocardial (end-stage heart failure, myocarditis), post-cardiotomy, cardiac tamponade, pulmonary thromboembolus.
  • Subjects requiring mechanical circulatory support for one of the CS subtypes listed above.
  • Age ≥ 18 years old.
  • Consent for study participation has been obtained.

Exclusion Criteria: 

  • Lack of consent for study participation.
  • Shock due to causes other than cardiogenic shock (e.g., sepsis, serious ventricular arrhythmias not due to myocardial ischemia or heart failure, neurogenic, anaphylactic, hemorrhagic/hypovolemic).
  • Shock with unwitnessed out of hospital cardiac arrest.
  • Severe non-cardiac morbidity with expected survival of < 6 months (e.g., malignancy, end-stage liver disease, severe chronic lung disease, severe CNS morbidity).
  • Admission occurring outside the study period.
  • Refusal of active treatment.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Brandon Wiley, M.D.

Cerrado para la inscripción

Contact information:

Misty Radosevich M.D.

(507) 255-4267

Radosevich.Misty@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20467890

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