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RM involves sending CIED data from a patient’s residence via a transmitter or smartphone app. Routine transmissions are usually sent every 90 days and can also be patient- or alert-initiated. RM is a Class 1, Level of Evidence A, professional society recommendation because of its many clinical outcome benefits [1,2]. These include reduced mortality [3-5], fewer hospitalizations [3,6], fewer inappropriate ICD shocks [7], as well as high patient satisfaction [8].
JMIR Cardio 2025;9:e66215
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Cardiac rehabilitation (CR) is a critical aspect of recovery that is offered to adults who experience cardiac events, such as a myocardial infarction, coronary revascularization, and valve replacement, but is significantly underused.
JMIR Cardio 2024;8:e54823
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The person who discussed RM with the veteran was a physician for 4 (17%), a nurse for 7 (30%), a CIED manufacturer representative for 5 (22%), and unknown for 7 respondents (30%). An additional 2 veterans reported learning about RM by reading a pamphlet. Only 8 (35%) veterans were accompanied by a friend, family member, or caregiver when RM was initially discussed with them; the majority of partially adherent or nonadherent veterans reported being unaccompanied.
JMIR Cardio 2023;7:e50973
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Rows were marked with a red x-mark if the HCQ daily dose was calculated to be ≥5.2 mg/kg/day (vs a green check mark if
The hydroxychloroquine patient safety dashboard (using fictitious data). The dashboard was created using the Microsoft Power BI software. Sta3n: unique medical facility codes for each VA station; Last 4: last 4 digits of a patient’s social security number needed to identify a patient in the computerized patient record system (CPRS).
Initial queries using CDW and Power BI began in June 2020.
JMIR Med Inform 2023;11:e44455
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This is particularly true for the case definition of sarcoidosis, which is considered a diagnosis of exclusion and requires a review of clinical, radiological, and histopathological data for accurate diagnosis [3,7,8]. A few studies have reported the development of sarcoidosis-specific “computationally identifying algorithms” based on structured data elements in the EMR, although they were not validated by manual chart review [9-13].
JMIR Form Res 2022;6(3):e31615
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This paper presents a secondary study focused on acceptability that was conducted as part of the primary Mobile4 Heart study, a pilot randomized controlled trial (RCT) [21].
The parent Mobile4 Heart study was a pilot RCT that evaluated group differences in physical activity and exercise capacity after 2 months of using digital health technologies; the results are presented in a separate publication [21]. The 2-month duration was based on the pilot nature of the RCT.
JMIR Hum Factors 2021;8(3):e25356
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A total of 60 participants were included and randomized (using computer-based randomization) to the intervention group or usual care (control) group (Figure 1). Participants were included in the study if they were at least age 18 years, had a history of CVD, owned a smartphone or tablet, and were within 2 weeks of completing CR.
JMIR Form Res 2021;5(4):e20468
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VA FitHeart, a Mobile App for Cardiac Rehabilitation: Usability Study
Tasks demonstrated by study staff included setting a physical activity goal, making a physical activity entry, viewing a fitness graph, making a weight entry, and viewing an educational module. After the conclusion of the demonstration, participants were asked to complete the demonstrated tasks independently. Study staff recorded task completion success if the participant was able to successfully complete the task.
JMIR Hum Factors 2018;5(1):e3
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Each focus group will have 6-8 participants, which is a size that allows for easy exchanges of ideas and a diversity of perspectives to be represented. We will recruit a convenience sample of 24-32 participants for four focus groups. Aims 1 and 2 will include the same participants who will attend a total of four focus group sessions (Figure 3).
JMIR Res Protoc 2017;6(7):e134
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