Diagnostic Accuracy of a Novel Mobile Phone Application for the Detection and Monitoring of Atrial Fibrillation

https://doi.org/10.1016/j.amjcard.2018.01.035Get rights and content

Atrial fibrillation (AF) is the most common sustained cardiac arrhythmia in adults, associated with significant morbidity, increased mortality, and rising health-care costs. Simple and available tools for the accurate detection of arrhythmia recurrence in patients after electrical cardioversion (CV) or ablation procedures for AF can help to guide therapeutic decisions. We conducted a prospective, single-center study to evaluate the accuracy of Cardiio Rhythm Mobile Application (CRMA) for AF detection. Patients >18 years of age who were scheduled for elective CV for AF were enrolled in the study. CRMA finger pulse recordings, utilizing an iPhone camera, were obtained before (pre-CV) and after (post-CV) the CV. The findings were validated against surface electrocardiograms. Ninety-eight patients (75.5% men), mean age of 67.7 ± 10.5 years, were enrolled. No electrocardiogram for validation was available in 1 case. Pre-CV CRMA readings were analyzed in 97 of the 98 patients. Post-CV CRMA readings were analyzed for 92 of 93 patients who underwent CV. One patient left before the recording was obtained. The Cardiio Rhythm Mobile Application correctly identified 94 of 101 AF recordings (93.1%) as AF and 80 of 88 non-AF recordings (90.1%) as non-AF. The sensitivity was 93.1% (95% confidence interval [CI] = 86.9% to 97.2%) and the specificity was 90.9% (95% CI = 82.9% to 96.0%). The positive predictive value was 92.2% (95% CI = 85.8% to 95.8%) and the negative predictive value was 92.0% (95% CI = 94.8% to 95.9%). In conclusion, the CRMA demonstrates promising potential in accurate detection and discrimination of AF from normal sinus rhythm in patients with a history of AF.

Section snippets

Methods

This prospective, single-center study was approved by the institutional review board at the Massachusetts General Hospital (MGH) and is compliant with the Health Insurance Portability and Accountability Act. Consecutive patients with a diagnosis of AF who were scheduled for elective direct current cardioversion (DCCV) at MGH were eligible to participate. Patients younger than 18 years of age were excluded. Informed consent was obtained from patients who agreed to participate in the study before

Results

A total of 100 subjects arriving for elective DCCV at MGH were screened for participation in the study. In 1 case, the patient was not scheduled to undergo CV and was mistakenly recruited. In another case, we were unable to obtain the subject's CRMA recordings because of a technical issue. A total of 98 subjects, 73 men and 24 women, with a mean age 67.7 ± 10.5 years (range 40 to 92 years), were enrolled in the study. Table 1 provides a summary of the patient demographics. At least 1 set of

Discussion

AF continues to be challenging to screen, diagnose, and monitor, especially when the arrhythmia is paroxysmal and/or asymptomatic. Camm et al performed 24-hour ambulatory monitoring in 106 asymptomatic elderly subjects and found 10.5% to have AF.9 In the Framingham Heart Study, 228 of the 562 subjects (40%) with AF were reported to be asymptomatic.10

Tools other than the standard 12-lead ECG are also used for the detection of AF. Taggar et al analyzed 21 studies that investigated 39 different

Disclosures

Drs. Yukkee and Ming-Zher Poh are employees of Cardiio, Inc. and have an ownership stake in the company. Dr Ming-Zher Poh has a patent for the AF detection algorithm described here. There are no other potential conflicts of interest relevant to this study.

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1

These authors contributed equally to this study and to the manuscript preparation.

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