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MIRACLE2 Score Compared With Downtime and Current Selection Criterion for Invasive Cardiovascular Therapies After OHCA.
Aldous, Robert; Roy, Roman; Cannata, Antonio; Abdrazak, Muhamad; Mohanan, Shamika; Beckley-Hoelscher, Nicholas; Stahl, Daniel; Kanyal, Ritesh; Kordis, Peter; Sunderland, Nicholas; Parczewska, Aleksandra; Kirresh, Ali; Nevett, Joanne; Fothergill, Rachael; Webb, Ian; Dworakowski, Rafal; Melikian, Narbeh; Kalra, Sundeep; Johnson, Thomas W; Sinagra, Gianfranco; Rakar, Serena; Noc, Marko; Patel, Sameer; Auzinger, Georg; Gruchala, Marcin; Shah, Ajay M; Byrne, Jonathan; MacCarthy, Philip; Pareek, Nilesh.
Afiliação
  • Aldous R; King's College Hospital NHS Foundation Trust, London, United Kingdom.
  • Roy R; King's College Hospital NHS Foundation Trust, London, United Kingdom.
  • Cannata A; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Abdrazak M; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Mohanan S; Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
  • Beckley-Hoelscher N; Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
  • Stahl D; Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
  • Kanyal R; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Kordis P; Centre for Intensive Internal Medicine, University Medical Center, Ljubljana, Slovenia.
  • Sunderland N; Bristol Heart Institute, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom.
  • Parczewska A; Department of Cardiology, Medical University of Gdansk, Gdansk, Poland.
  • Kirresh A; Royal Free Hospital NHS Foundation Trust, London, United Kingdom.
  • Nevett J; London Ambulance Service NHS Trust, London, United Kingdom.
  • Fothergill R; London Ambulance Service NHS Trust, London, United Kingdom.
  • Webb I; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Dworakowski R; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Melikian N; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Kalra S; Royal Free Hospital NHS Foundation Trust, London, United Kingdom.
  • Johnson TW; Bristol Heart Institute, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol, United Kingdom.
  • Sinagra G; Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.
  • Rakar S; Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.
  • Noc M; Centre for Intensive Internal Medicine, University Medical Center, Ljubljana, Slovenia.
  • Patel S; Faculty of Life Science and Medicine, King's College London, London, United Kingdom.
  • Auzinger G; Faculty of Life Science and Medicine, King's College London, London, United Kingdom.
  • Gruchala M; Department of Cardiology, Medical University of Gdansk, Gdansk, Poland.
  • Shah AM; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Byrne J; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • MacCarthy P; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom.
  • Pareek N; King's College Hospital NHS Foundation Trust, London, United Kingdom; School of Cardiovascular and Metabolic Medicine and Sciences, British Heart Foundation Centre of Excellence, King's College London, London, United Kingdom. Electronic address: nileshpareek@nhs.net.
JACC Cardiovasc Interv ; 16(19): 2439-2450, 2023 Oct 09.
Article em En | MEDLINE | ID: mdl-37609699
ABSTRACT

BACKGROUND:

The MIRACLE2 score is the only risk score that does not incorporate and can be used for selection of therapies after out-of-hospital cardiac arrest (OHCA).

OBJECTIVES:

This study sought to compare the discrimination performance of the MIRACLE2 score, downtime, and current randomized controlled trial (RCT) recruitment criteria in predicting poor neurologic outcome after out-of-hospital cardiac arrest (OHCA).

METHODS:

We used the EUCAR (European Cardiac Arrest Registry), a retrospective cohort from 6 centers (May 2012-September 2022). The primary outcome was poor neurologic outcome on hospital discharge (cerebral performance category 3-5).

RESULTS:

A total of 1,259 patients (total downtime = 25 minutes; IQR 15-36 minutes) were included in the study. Poor outcome occurred in 41.8% with downtime <30 minutes and in 79.3% for those with downtime >30 minutes. In a multivariable logistic regression analysis, MIRACLE2 had a stronger association with outcome (OR 2.23; 95% CI 1.98-2.51; P < 0.0001) than zero flow (OR 1.07; 95% CI 1.01-1.13; P = 0.013), low flow (OR 1.04; 95% CI 0.99-1.09; P = 0.054), and total downtime (OR 0.99; 95% CI 0.95-1.03; P = 0.52). MIRACLE2 had substantially superior discrimination for the primary endpoint (AUC 0.877; 95% CI 0.854-0.897) than zero flow (AUC 0.610; 95% CI 0.577-0.642), low flow (AUC 0.725; 95% CI 0.695-0.754), and total downtime (AUC 0.732; 95% CI 0.701-0.760). For those modeled for exclusion from study recruitment, the positive predictive value of MIRACLE2 ≥5 for poor outcome was significantly higher (0.92) than the CULPRIT-SHOCK (Culprit lesion only PCI Versus Multivessel PCI in Cardiogenic Shock) (0.80), EUROSHOCK (Testing the value of Novel Strategy and Its Cost Efficacy In Order to Improve the Poor Outcomes in Cardiogenic Shock) (0.74) and ECLS-SHOCK (Extra-corporeal life support in Cardiogenic shock) criteria (0.81) (P < 0.001).

CONCLUSIONS:

The MIRACLE2 score has superior prediction of outcome after OHCA than downtime and higher discrimination of poor outcome than the current RCT recruitment criteria. The potential for the MIRACLE2 score to improve the selection of OHCA patients should be evaluated formally in future RCTs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Reanimação Cardiopulmonar / Parada Cardíaca Extra-Hospitalar Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: JACC Cardiovasc Interv Assunto da revista: ANGIOLOGIA / CARDIOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Reanimação Cardiopulmonar / Parada Cardíaca Extra-Hospitalar Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: JACC Cardiovasc Interv Assunto da revista: ANGIOLOGIA / CARDIOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Reino Unido