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Characterization of Arrhythmia-induced Cardiomyopathy

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University Hospital Basel

Status

Enrolling

Conditions

Cardiomyopathy
Arrhythmia-induced Cardiomyopathy (AiCM)

Treatments

Other: Data collection: Major adverse cardiovascular event (MACE) assessment questionnaire (prospective part)
Other: Data collection (retrospective study)
Other: Data collection (prospective study database)
Other: Data collection: Quality of Life (QoL) Questionnaire (prospective part)

Study type

Observational

Funder types

Other

Identifiers

NCT05662293
2021-00873 kt22Badertscher2;

Details and patient eligibility

About

The goal of the this observational study is to gather clinically available data on patients presenting with a suspicion for arrhythmia-induced cardiomyopathy (AiCM) at the University Hospital Basel.

Full description

Current studies indicate that AiCM is an under-recognized and an underestimated clinical entity and its prevalence is poorly documented. This project consists of a retrospective longitudinal cohort and case-control study followed by a prospective observational cohort study.

The retrospective pilot study (1200 patients) is to define the incidence of AiCM in patients who presented to the University Hospital of Basel with a reduced left ventricular ejection fraction before or after the diagnosis of an arrhythmia suggestive to lead to an AiCM.

The prospective study part (1500 patients) is to evaluate the predictors of adverse events and re-hospitalizations in patients with a suspicion of AiCM. The diagnosis of AiCM will be established using a "goldstandard diagnosis": 2 independent cardiologists will adjudicate the diagnosis based on all data from the initial hospital stay and follow-up including ECG, laboratory measurements, vital signs, echocardiography, coronary angiography, stress testing and other cardiovascular diagnostic steps. The most likely diagnosis will be chosen among a list of comprehensive, pre-selected choices. In cases of disagreement of the two reviewers, diagnosis will be discussed with a third senior physician and decision made.

In order to optimize the care of patients with AiCM, the researchers intend to determine the prevalence of AICM, evaluate diagnostic criteria that allow an early diagnosis of AICM, and evaluate the current therapeutic management and prognosis of patients with AICM.

Enrollment

2,700 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Prospective part

Inclusion Criteria:

  • Diagnostic or suspicion of AiCM as presence of specified keyword in patient's file or as screened by colleagues of the internal medicine or cardiology clinics
  • Signed study consent

Exclusion Criteria:

  • Patient's active refusal of the general consent of the University Hospital Basel
  • Age <18 years old
  • Temporary exclusion criteria: Acute health condition such as myocardial infarction, patients presenting with a major trauma, a sepsis, patients shortly after cardiac surgery, and patients in shock (>100 bpm, <90 systolic BP, evidence of organ dysfunction).
  • Life expectancy <1 year (palliative, terminal cancer)

Retrospective part

Inclusion Criteria:

  • Patients with a reduced left-ventricular ejection fraction (LVEF ≤50%) or a reduction of 15% in the ejection fraction (EF) between two echocardiographies and a concomitant diagnosis of any arrhythmia likely to lead to AiCM within one year before or after diagnosis of the reduced LVEF from 2010-2021

Exclusion Criteria:

  • Age < 18 years old
  • Patient's active refusal of the general consent of the University Hospital Basel
  • Acute event clearly leading to an acutely reduced LVEF (massive type I myocardial infarction, cardiogenic shock from a coronary or myocardial etiology, septic shock leading to toxic myopathy, hypovolemic shock with reduced EF, cardiac arrest and/or need for resuscitation).
  • Patients with life expectancy <1 year (palliative, terminal cancer)

Trial design

2,700 participants in 1 patient group

Patients with arrhythmia-induced cardiomyopathy (retrospective/prospective)
Description:
retrospective cohort and case-control study followed by a prospective observational cohort study.
Treatment:
Other: Data collection: Quality of Life (QoL) Questionnaire (prospective part)
Other: Data collection (prospective study database)
Other: Data collection (retrospective study)
Other: Data collection: Major adverse cardiovascular event (MACE) assessment questionnaire (prospective part)

Trial contacts and locations

1

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Central trial contact

Patrick Badertscher, MD; Jeanne du Fay de Lavallaz, MD-PhD

Data sourced from clinicaltrials.gov

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