Prediction of mortality benefit based on periodic repolarisation dynamics in patients undergoing prophylactic implantation of a defibrillator: a prospective, controlled, multicentre cohort study.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
12 Oct 2019
Historique:
received: 23 07 2019
revised: 30 07 2019
accepted: 01 08 2019
pubmed: 7 9 2019
medline: 24 10 2019
entrez: 7 9 2019
Statut: ppublish

Résumé

A small proportion of patients undergoing primary prophylactic implantation of implantable cardioverter defibrillators (ICDs) experiences malignant arrhythmias. We postulated that periodic repolarisation dynamics, a novel marker of sympathetic-activity-associated repolarisation instability, could be used to identify electrically vulnerable patients who would benefit from prophylactic implantation of ICDs by way of a reduction in mortality. We did a prespecified substudy of EUropean Comparative Effectiveness Research to Assess the Use of Primary ProphylacTic Implantable Cardioverter Defibrillators (EU-CERT-ICD), a prospective, investigator-initiated, non-randomised, controlled cohort study done at 44 centres in 15 EU countries. Patients aged 18 years or older with ischaemic or non-ischaemic cardiomyopathy and reduced left ventricular ejection fraction (≤35%) were eligible for inclusion if they met guideline-based criteria for primary prophylactic implantation of ICDs. Periodic repolarisation dynamics from 24-h Holter recordings were assessed blindly in patients the day before ICD implantation or on the day of study enrolment in patients who were conservatively managed. The primary endpoint was all-cause mortality. Propensity scoring and multivariable models were used to assess the interaction between periodic repolarisation dynamics and the treatment effect of ICDs on mortality. Between May 12, 2014, and Sept 7, 2018, 1371 patients were enrolled in our study. 968 of these patients underwent ICD implantation, and 403 were treated conservatively. During follow-up (median 2·7 years [IQR 2·0-3·3] in the ICD group and 1·2 years [0·8-2·7] in the control group), 138 (14%) patients died in the ICD group and 64 (16%) patients died in the control group. We noted a 43% reduction in mortality in the ICD group compared with the control group (adjusted hazard ratio [HR] 0·57 [95% CI 0·41-0·79]; p=0·0008). Periodic repolarisation dynamics significantly predicted the treatment effect of ICDs on mortality (adjusted p=0·0307). The mortality benefits associated with ICD implantation were greater in patients with periodic repolarisation dynamics of 7·5 deg or higher (n=199; adjusted HR 0·25 [95% CI 0·13-0·47] for the ICD group vs the control group; p<0·0001) than in those with periodic repolarisation dynamics less than 7·5 deg (n=1166; adjusted HR 0·69 [95% CI 0·47-1·00]; p=0·0492; p Periodic repolarisation dynamics predict mortality reductions associated with prophylactic implantation of ICDs in contemporarily treated patients with ischaemic or non-ischaemic cardiomyopathy. Periodic repolarisation dynamics could help to guide treatment decisions about prophylactic ICD implantation. The European Community's 7th Framework Programme.

Sections du résumé

BACKGROUND BACKGROUND
A small proportion of patients undergoing primary prophylactic implantation of implantable cardioverter defibrillators (ICDs) experiences malignant arrhythmias. We postulated that periodic repolarisation dynamics, a novel marker of sympathetic-activity-associated repolarisation instability, could be used to identify electrically vulnerable patients who would benefit from prophylactic implantation of ICDs by way of a reduction in mortality.
METHODS METHODS
We did a prespecified substudy of EUropean Comparative Effectiveness Research to Assess the Use of Primary ProphylacTic Implantable Cardioverter Defibrillators (EU-CERT-ICD), a prospective, investigator-initiated, non-randomised, controlled cohort study done at 44 centres in 15 EU countries. Patients aged 18 years or older with ischaemic or non-ischaemic cardiomyopathy and reduced left ventricular ejection fraction (≤35%) were eligible for inclusion if they met guideline-based criteria for primary prophylactic implantation of ICDs. Periodic repolarisation dynamics from 24-h Holter recordings were assessed blindly in patients the day before ICD implantation or on the day of study enrolment in patients who were conservatively managed. The primary endpoint was all-cause mortality. Propensity scoring and multivariable models were used to assess the interaction between periodic repolarisation dynamics and the treatment effect of ICDs on mortality.
FINDINGS RESULTS
Between May 12, 2014, and Sept 7, 2018, 1371 patients were enrolled in our study. 968 of these patients underwent ICD implantation, and 403 were treated conservatively. During follow-up (median 2·7 years [IQR 2·0-3·3] in the ICD group and 1·2 years [0·8-2·7] in the control group), 138 (14%) patients died in the ICD group and 64 (16%) patients died in the control group. We noted a 43% reduction in mortality in the ICD group compared with the control group (adjusted hazard ratio [HR] 0·57 [95% CI 0·41-0·79]; p=0·0008). Periodic repolarisation dynamics significantly predicted the treatment effect of ICDs on mortality (adjusted p=0·0307). The mortality benefits associated with ICD implantation were greater in patients with periodic repolarisation dynamics of 7·5 deg or higher (n=199; adjusted HR 0·25 [95% CI 0·13-0·47] for the ICD group vs the control group; p<0·0001) than in those with periodic repolarisation dynamics less than 7·5 deg (n=1166; adjusted HR 0·69 [95% CI 0·47-1·00]; p=0·0492; p
INTERPRETATION CONCLUSIONS
Periodic repolarisation dynamics predict mortality reductions associated with prophylactic implantation of ICDs in contemporarily treated patients with ischaemic or non-ischaemic cardiomyopathy. Periodic repolarisation dynamics could help to guide treatment decisions about prophylactic ICD implantation.
FUNDING BACKGROUND
The European Community's 7th Framework Programme.

Identifiants

pubmed: 31488371
pii: S0140-6736(19)31996-8
doi: 10.1016/S0140-6736(19)31996-8
pii:
doi:

Types de publication

Controlled Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1344-1351

Investigateurs

Béla Merkely (B)
Peter Perge (P)
Zoltan Sallo (Z)
Gabor Szeplaki (G)
Markus Zabel (M)
Lars Lüthje (L)
Simon Schlögl (S)
Helge Haarmann (H)
Leonard Bergau (L)
Joachim Seegers (J)
Gerd Hasenfuß (G)
Pascal Munoz-Exposito (P)
Tobias Tichelbäcker (T)
Aleksandra Kirova (A)
Tim Friede (T)
Markus Harden (M)
Marek Malik (M)
Katerina Hnatkova (K)
Marc Vos (M)
Stefan N Willich (SN)
Thomas Reinhold (T)
Rik Willems (R)
Bert Vandenberk (B)
Magdalena Klinika (M)
Krapinske Toplice (K)
Panayota Flevari (P)
Andreas Katsimardos (A)
Dimitrios Katsaras (D)
Robert Hatala (R)
Martin Svetlosak (M)
Andrzej Lubinski (A)
Tomasz Kuczejko (T)
Jim Hansen (J)
Christian Sticherling (C)
David Conen (D)
Sestre Milosrdnice (S)
Nikola Pavlović (N)
Šime Manola (Š)
Ozren Vinter (O)
Ivica Benko (I)
Anton Tuinenburg (A)
Axel Bauer (A)
Christine Meyer-Zürn (C)
Christian Eick (C)
Jesper Hastrup (J)
Josep Brugada (J)
Elena Arbelo (E)
Gabriela Kaliska (G)
Jozef Martinek (J)
Michael Dommasch (M)
Alexander Steger (A)
Stefan Kääb (S)
Moritz F Sinner (MF)
Konstantinos D Rizas (KD)
Wolfgang Hamm (W)
Nikolay Vdovin (N)
Mathias Klemm (M)
Lukas von Stülpnagel (L)
Iwona Cygankiewicz (I)
Pawel Ptaszynski (P)
Krzysztof Kaczmarek (K)
Izabela Poddebska (I)
Svetoslav Iovev (S)
Tomáš Novotný (T)
Milan Kozak (M)
Heikki Huikuri (H)
Tuomas Kenttä (T)
Ari Pelli (A)
Jaroslaw D Kasprzak (JD)
Dariusz Qavoq (D)
Sandro Brusich (S)
Ervin Avdovic (E)
Marina Klasan (M)
Jan Galuszka (J)
Milos Taborsky (M)
Vasil Velchev (V)
Rüdiger Dissmann (R)
Przemysław Guzik (P)
Dieter Bimmel (D)
Christiane Lieberz (C)
Stefan Stefanow (S)
Norman Rüb (N)
Christian Wolpert (C)
Lars S Maier (LS)
Steffen Behrens (S)
Zrinka Jurisic (Z)
Frieder Braunschweig (F)
Florian Blaschke (F)
Burkert Pieske (B)
Zoran Bakotic (Z)
Ante Anic (A)
Robert H G Schwinger (RHG)
Pyotr Platonov (P)

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Axel Bauer (A)

Medizinische Klinik und Poliklinik I, Munich University Clinic, Munich, Germany; University Hospital for Internal Medicine III, Medical University Innsbruck, Innsbruck, Austria; German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany. Electronic address: axel.bauer@i-med.ac.at.

Mathias Klemm (M)

Medizinische Klinik und Poliklinik I, Munich University Clinic, Munich, Germany; German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany.

Konstantinos D Rizas (KD)

Medizinische Klinik und Poliklinik I, Munich University Clinic, Munich, Germany; German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany.

Wolfgang Hamm (W)

Medizinische Klinik und Poliklinik I, Munich University Clinic, Munich, Germany; German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany.

Lukas von Stülpnagel (L)

Medizinische Klinik und Poliklinik I, Munich University Clinic, Munich, Germany; German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany; Department of Electrical and Computer Engineering, Technical University of Munich, Munich, Germany.

Michael Dommasch (M)

German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany; Klinikum rechts der Isar, Medizinische Klinik und Poliklinik I, Technical University of Munich, Munich, Germany.

Alexander Steger (A)

German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany; Klinikum rechts der Isar, Medizinische Klinik und Poliklinik I, Technical University of Munich, Munich, Germany.

Andrezej Lubinski (A)

Department of Cardiology, Medical University of Lodz Hospital, Lodz, Poland.

Panagiota Flevari (P)

Second Department of Cardiology, Attikon University Hospital, Athens, Greece.

Markus Harden (M)

Department of Medical Statistics, Heart Center University Medical Center Göttingen, Göttingen, Germany; German Center for Cardiovascular Research partner site Göttingen, Göttingen, Germany.

Tim Friede (T)

Department of Medical Statistics, Heart Center University Medical Center Göttingen, Göttingen, Germany; German Center for Cardiovascular Research partner site Göttingen, Göttingen, Germany.

Stefan Kääb (S)

Medizinische Klinik und Poliklinik I, Munich University Clinic, Munich, Germany; German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany.

Bela Merkely (B)

Department of Cardiology, Semmelweis University Heart Center, Budapest, Hungary.

Christian Sticherling (C)

University Hospital, University of Basel, Basel, Switzerland.

Rik Willems (R)

University Hospitals of Leuven, Leuven, Belgium.

Heikki Huikuri (H)

Medical Research Center, Oulu University Hospital and University of Oulu, Oulu, Finland.

Marek Malik (M)

Heart and Lung Institute, Imperial College London, London, UK.

Georg Schmidt (G)

German Center for Cardiovascular Research partner site, Munich Heart Alliance, Munich, Germany; Klinikum rechts der Isar, Medizinische Klinik und Poliklinik I, Technical University of Munich, Munich, Germany.

Markus Zabel (M)

Department of Cardiology and Pneumology, Heart Center University Medical Center Göttingen, Göttingen, Germany; German Center for Cardiovascular Research partner site Göttingen, Göttingen, Germany.

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