Clinical Outcomes, Management, Healthcare Resource Utilization, and Cost According to the CHA2DS2-VASc Scores in Asian Patients with Nonvalvular Atrial Fibrillation

Abstract

Background: The prognosis among non-valvular atrial fibrillation (NVAF) patients with different CHA2DS2-VASc scores in the contemporary Asian population remains unclear. Additionally, there is a lack of research examining the disparities in management patterns, healthcare resource utilization (HCRU), and cost among these patients. Therefore, this study aims to assess the incidence of clinical outcomes in NVAF patients with different CHA2DS2-VASc scores and explore their management patterns, HCRU, and cost. Methods and Results: This retrospective cohort study assessed patients diagnosed with NVAF between January 2018 and July 2022, utilizing a merged dataset from China. Patients were stratified into 3 cohorts by CHA2DS2-VASc scores: low-risk (0 for males, 1 for females), intermediate-risk (1 for males, 2 for females), and high-risk (≥2 for males, ≥3 for females). One-year incidence rates of clinical outcomes (including ischemic stroke, transient ischemic attack, arterial embolism, and major bleeding) were calculated as events per 100 person-years. Cumulative incidence and crude and adjusted hazard ratios (aHRs) with 95% confidence intervals (CIs) were calculated using the Fine and Gray models. Management patterns, HCRU, and cost were analyzed descriptively. Among 419,490 NVAF patients (mean age: 75.2 years, 45.1% female), 16,541 (3.9%) were classified as low-risk, 38,494 (9.2%) as intermediate-risk, and 364,455 (86.9%) as high-risk. The mean (SD) age-adjusted Charlson comorbidity index score was 4.7 (2.0), increasing with CHA2DS2-VASc scores. The one-year cumulative incidence of ischemic stroke was 3.2% (95% CI, 2.9%–3.5%) for low-risk, 4.9% (95% CI, 4.7–5.2%) for intermediate-risk (aHR, 1.3, 95% CI, 1.2–1.4), and 12.2% (95% CI, 12.1%–12.3%) for high-risk (aHR, 2.5, 95% CI, 2.3–2.8). Meanwhile, the incidence of transient ischemic attack, arterial embolism, and major bleeding showed a similar increasing trend from low-risk to high-risk. Within one year after the index date, 16.4% of patients in the low-risk cohort received oral anticoagulants (OACs), while 11.1% of patients in the high-risk cohort received OACs. The mean (SD) number of all-cause hospitalizations was 0.1 (0.1), 0.1 (0.2), and 0.1 (0.3) per-patient-per-month (PPPM) for low-risk, intermediate-risk, and high-risk, respectively. The mean (SD) length of stay increased from 0.9 (1.1) days PPPM for the low-risk to 1.2 (1.8) days PPPM for the high-risk. Conclusion: This study demonstrates that contemporary Asian NVAF patients with higher CHA2DS2-VASc scores experience higher incidence of adverse outcomes and increased hospital resource consumption. There is insufficient utilization of OACs and other AF management measures across all CHA2DS2-VASc scores groups. These findings provide new evidence for improving patient management and guiding resource allocation in healthcare.

Competing Interest Statement

The authors have declared no competing interest.

Funding Statement

This research did not receive any specific grants from funding agencies in the public, commercial, or not-for-profit sectors.

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

The study protocol received ethical approval from the Nanjing First Hospital Institutional Review Board (IRB) in Jiangsu, China (KY20230615-01-KS-01)

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

Yes

I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

Yes

Data Availability

The data are not publicly available due to the nature of administrative database.

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