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Feasibility of a using chest strap and dry electrode system for longer term cardiac arrhythmia monitoring: Results from a pilot observational study.
Saggu, Daljeet Kaur; Udigala, Madappa Nagamalesh; Sarkar, Shantanu; Sathiyamoorthy, Arunkumar; Dash, Satyaprakash; P, V R Mohan; Rajan, Vinayakrishnan; Calambur, Narasimahan.
Afiliación
  • Saggu DK; AIG Hospital, Hyderabad, India. Electronic address: drdaljeetsaggu@gmail.com.
  • Udigala MN; MS Ramaiah Hospital, Bengaluru, India.
  • Sarkar S; Medtronic Inc., Minneapolis, Minnesota, USA.
  • Sathiyamoorthy A; Medtronic Inc., Hyderabad, India.
  • Dash S; Medtronic Inc., Mumbai, India.
  • P VRM; Medtronic Inc., Hyderabad, India.
  • Rajan V; Medtronic Inc., Mumbai, India.
  • Calambur N; AIG Hospital, Hyderabad, India.
Article en En | MEDLINE | ID: mdl-39181329
ABSTRACT
BACKGROUND AND

AIM:

Cardiac arrhythmia diagnostic yield improves with increased duration of monitoring. We investigated patient comfort, diagnostic quality of ECG, and arrhythmia diagnostic yield using a single lead longer term external cardiac monitor (ECM).

METHODS:

The observational ECM feasibility study enrolled patients with increased risk of cardiac arrhythmia. The ECM investigational prototype was designed using a chest strap with dry electrodes connected to module capable of triggered loop recording of ECG, and automatic detection of arrhythmia. In group-A of study (24-h inpatient), patients wore ECM and Holter that recorded ECG from the ECM and adhesive electrodes. In group-B of study (12-weeks ambulatory), at monthly follow-ups patients filled out a comfort survey and device stored arrhythmia episodes were reviewed.

RESULTS:

The study enrolled 34 patients (38 % females, average age 57.5 years, 65 % had palpitations, 12 % had syncope). Diagnostic quality ECG was recorded on 76.5 % of the monitoring duration in 12 of 20 patients with reviewable data in group-A, with motion artifacts causing loss in ECG signal for 18.7 % of the time. In 14 patients in group-B, 94.9 % of the survey responses indicated that ECM was comfortable to wear. Cardiac arrhythmia was observed in 4 of 17 patients (24 %) in group-A and 9 of 14 patients (64 %) in group-B in device recorded episodes. All ECM detected pause and tachycardia were inappropriate detections due to motion artifacts and temporary device removal.

CONCLUSION:

The chest strap-based ECM device was mostly comfortable to wear and recorded diagnostic quality ECG in three-fourth of monitoring period. Cardiac arrhythmia was observed in 64 % of patients over 3-month monitoring along with large number of motion artifact induced inappropriate detections.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Indian Pacing Electrophysiol J Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Indian Pacing Electrophysiol J Año: 2024 Tipo del documento: Article