Natural History of COVID-19-Related Atrial Fibrillation

NCT04830774 — Not applicable, Unknown, 200 participants, Texas Cardiac Arrhythmia Research Foundation

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Natural History and Recurrence Rate of Atrial Fibrillation After the First, COVID-19-Related Atrial Arrhythmic Episode: A Prospective Evaluation Using Continuous Cardiac Rhythm Monitoring

RegistryNCT04830774, acronym unCOVer-AF
StatusUnknown
PhaseNot applicable
Study typeInterventional; na, single group, masking: none, screening
Enrollment200 (Estimated)
SponsorTexas Cardiac Arrhythmia Research Foundation (Other)
ConditionsCOVID-19, Atrial Fibrillation New Onset
InterventionsILR, PMK, ICD (Device)
Datesstart 2021-04-15, primary completion 2021-12-31 (estimated), completion 2023-12-31 (estimated), first posted 2021-04-05, last updated 2021-11-23
Locations12 sites in United States, Belgium, Italy

Related Papers Related Patents Related Grants Related Experts
All trials for COVID-19 All trials for Atrial Fibrillation New Onset All trials of ILR, PMK, ICD

-Summary

The unCOVer-AF prospective, multicenter registry aims at determining the natural history of atrial fibrillation (AF) via continuous cardiac rhythm monitoring in patients with a first arrhythmic episode during COVID-19 hospitalization.

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+Detailed description

Coronavirus Disease 2019 (COVID-19) is a novel coronavirus strain disease, which has rapidly spread worldwide with more than 100 million confirmed cases to date. COVID-19 is mainly characterized by respiratory symptoms; however, patients can exhibit a wide range of clinical manifestations, including cardiovascular complications. Among them, supraventricular and ventricular arrhythmias have been described in patients at different stages of disease severity. According to a recent study on 9564 COVID-19 patients, 17.6% developed AF during hospitalization, 65.7% of whom without a past arrhythmic history.

Several factors (e.g., hypoxia, systemic inflammatory response, myocardial injury) may interact with a preexisting substrate and act as a trigger for AF initiation. Nonetheless, the pathophysiology of COVID-19-related new-onset AF remains elusive. It is unknown whether the disease merely acts as a transient arrhythmia initiator or promotes long-term atrial electrophysiological and structural changes which may facilitate AF recurrence and progression.

Therefore, the investigators designed a multicenter, prospective registry to assess the natural history of AF via continuous cardiac rhythm monitoring (ILR, PMK, ICD) in patients with a first AF episode during COVID-19 hospitalization.

+Arms and interventions

ArmTypeInterventionsDescription
COVID-19 patients with new-onset AFOtherDevice: ILR, PMK, ICDConsecutive patients with a confirmed diagnosis of COVID-19 with a first clinical episode of AF at admission or during hospitalization.
  • ILR, PMK, ICD (Device): * Patients receive a newly implanted ILR, PMK, or ICD during COVID-19 hospitalization or within 30 days after hospital discharge and are followed by daily automated remote transmissions. * Patients have a previously implanted ILR, PMK, or ICD and are followed by daily automated remote transmissions

+Outcome measures

Primary outcomes

  • AF Burden [3 years]: AF burden is defined as cumulative duration of all AF episodes lasting ≥30 s from the first adjudicated AF episode onward, divided by total duration of monitoring.
  • AF Progression [3 years]
  • Time to adjudicated ischemic stroke/transient ischemic attack (TIA)/systemic arterial embolism [3 years]

Secondary outcomes

  • Composite of all-cause mortality, stroke and bleeding [3 years]
  • Time to adjudicated cardiovascular death [3 years]

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* Age> 18 years;
* Confirmed infection with SARS-CoV-2;
* Patients with a first clinical episode of AF ≥30 s at admission or during hospitalization for COVID-19;
* Patients with:

  1. implantation of an ILR, a PMK, or an ICD during COVID-19 hospitalization or within 30 days after hospital discharge, or
  2. an ILR, a PMK, or an ICD implanted before COVID-19 hospitalization.

Exclusion Criteria:

* History of AF or flutter irrespective of type;
* Moderate/severe mitral stenosis;
* Mechanical prosthetic heart valve(s);
* Kidney failure treated with permanent dialysis;
* Any condition (e.g. psychiatric illness, dementia) or situation, that in the investigators opinion could put the subject at significant risk, confound the study results, or interfere significantly with the subject participation in the study;
* Unwillingness to participate.

+Locations (12)

FacilityCityCountryStatus
Kansas City Heart Rhythm Institute, Overland ParkKansas City, KansasUnited StatesNot yet recruiting
Texas Cardiac Arrhythmia InstituteAustin, TexasUnited StatesNot yet recruiting
Vrije Universiteit BrusselBrusselsBelgiumNot yet recruiting
Department of Cardiovascular/Respiratory Diseases, Nephrology, Anesthesiology, and Geriatric Sciences, Policlinico Umberto I, Sapienza University of RomeRome, LazioItalyRecruiting
Cardiology Unit, ASST-Fatebenefratelli Sacco, Luigi Sacco University Hospital, Milan, ItalyMilan, LombardyItalyRecruiting
Ospedale San DonatoArezzoItalyNot yet recruiting
Maria Cecilia HospitalCotignolaItalyNot yet recruiting
Universita' VanvitelliNaplesItalyNot yet recruiting
ARNAS Ospedale CivicoPalermoItalyNot yet recruiting
Università di PisaPisaItalyRecruiting
Policlinico GemelliRomaItalyNot yet recruiting
Ospedale San BortoloVicenzaItalyNot yet recruiting

+Publications

  • Mountantonakis SE, Saleh M, Fishbein J, Gandomi A, Lesser M, Chelico J, Gabriels J, Qiu M, Epstein LM; Northwell COVID-19 Research Consortium. Atrial fibrillation is an independent predictor for in-hospital mortality in patients admitted with SARS-CoV-2 infection. Heart Rhythm. 2021 Apr;18(4):501-507. doi: 10.1016/j.hrthm.2021.01.018. Epub 2021 Jan 22. PMID 33493650

+Investigators