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New-Onset Atrial Fibrillation Complicating Acute Myocardial Infarction in China

The Prognostic Impacts and Clinical Utility of the Characteristics of New-onset Atrial Fibrillation Complicating Acute Myocardial Infarction in China

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05511649
Acronym
NOAFCAMI-China
Enrollment
832
Registered
2022-08-23
Start date
2023-03-01
Completion date
2023-09-23
Last updated
2026-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Myocardial Infarction, New Onset Atrial Fibrillation

Keywords

myocardial infarction, new-onset atrial fibrillation, atrial fibrillation burden, mortality

Brief summary

To investigate the prognostic impacts of the atrial fibrillation burden (AFb) in acute myocardial infarction (AMI) patients who developed paroxysmal new-onset atrial fibrillation (NOAF) during the index AMI hospitalization.

Detailed description

In the present study, investigators retrospectively reviewed the medical records of all acute MI patients who were admitted to the coronary artery unit (CCU) of Shanghai Tenth People's Hospital, KaiFeng Central Hospital, and the First Affiliated Hospital of Zhengzhou University between January 2014 and January 2022. All patients will routinely receive continuous electronic monitoring (CEM) throughout their hospital stay to detect cardiac arrhythmias including the AF events. Of these, patients with AMI without a history of AF who developed a first documented AF episode will be considered for inclusion. The AFb is measured as a percentage (%) by dividing the total AF duration by the total CEM duration.

Interventions

All patients with MI hospitalized in the CCU department of Shanghai Tenth People's Hospital, KaiFeng Central Hospital, and the First Affiliated Hospital of Zhengzhou University will receive 24-hour continuous cardiac monitoring until discharge.

Sponsors

Shanghai 10th People's Hospital
Lead SponsorOTHER
Kaifeng Central Hospital
CollaboratorOTHER
The First Affiliated Hospital of Zhengzhou University
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patients hospitalized for AMI including both STEMI and NSTEMI between January 2014 and January 2022 at the CCU department of Shanghai Tenth People's Hospital, KaiFeng Central Hospital, and the First Affiliated Hospital of Zhengzhou University. 2. Patients who developed a first documented AF (NOAF) during the index AMI hospitalization; 3. Adult patients (\>18 years old).

Exclusion criteria

1. Patients with a medical history of pre-existing AF; 2. Patients with a medical history of rheumatic valvular disease; 3. Patients with a medical history of sick sinus syndrome; 4. Patients undergoing emergent coronary artery bypass surgery; 5. Patients' medical records with serious deficiencies and CEM data cannot be retrieved;

Design outcomes

Primary

MeasureTime frameDescription
All-cause deathFrom the time of AMI discharge until occurrence of an outcome of interest, death, or loss to follow up, maximum up to 10 yearsDeath from any cause

Secondary

MeasureTime frameDescription
Major bleedingFrom the time of AMI discharge until occurrence of an outcome of interest, death, or loss to follow up, maximum up to 10 yearsBleeding event with a Bleeding Academic Research Consortium (BARC) classification of types 3 or 5.
Cardiovascular deathFrom the time of AMI discharge until occurrence of an outcome of interest, death, or loss to follow up, maximum up to 10 yearsDeath from cardiovascular causes
Recurrent myocardial infarctionFrom the time of AMI discharge until occurrence of an outcome of interest, death, or loss to follow up, maximum up to 10 yearsRehospitalization for myocardial infarction
Heart failure hospitalizationFrom the time of AMI discharge until occurrence of an outcome of interest, death, or loss to follow up, maximum up to 10 yearsHF hospitalization was based on clinical symptoms such as dyspnea and fatigue, and signs of peripheral or pulmonary edema that required hospitalization for intravenous diuretic treatment
Ischemic strokeFrom the time of AMI discharge until occurrence of an outcome of interest, death, or loss to follow up, maximum up to 10 yearsIschemic stroke was identified as the presence of a new focal neurologic deficit thought to be ischemic in origin, with signs or symptoms lasting\> 24 hours, and was validated according to radiographic imaging test.

Countries

China

Contacts

PRINCIPAL_INVESTIGATORYidong Wei, M.D., Ph.D.

Shanghai 10th People's Hospital

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026