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1.
J Clin Med ; 12(14)2023 Jul 14.
Article in English | MEDLINE | ID: mdl-37510791

ABSTRACT

Use of guideline-directed medical therapy (GDMT) for treatment of heart failure with reduced ejection fraction (HFrEF) remains unacceptably low. The purpose of this study was to determine whether a digital health tool can augment GDMT for patients with HFrEF. Participants ≥ 18 years old with symptomatic HFrEF (left ventricular ejection fraction ≤ 40%) and with access to a mobile phone with internet were included. Participants were given a blood pressure cuff, instructed in its use, and given regular symptom surveys via cell-phone web-link. Data were transmitted to the Story Health web-based platform, and automated alerts were triggered based on pre-specified vital sign and laboratory data. Health coaches assisted patients with medication education, pharmacy access, and lab access through text messages and phone calls. GDMT titration plans were individually created in the digital platform by local clinicians based on entry vitals and labs. Twelve participants enrolled and completed the study. The median age and LVEF were 52.5 years (IQR, 46.5-63.5) and 25% (IQR, 22.5-35.5), respectively. There were 10 GDMT initiations, 52 up-titrations, and 13 down-titrations. Five participants engaged in focus-group interviews following study completion to understand first-hand perspectives regarding the use of digital tools to manage GDMT. Participants expressed comfort knowing that there were clinicians regularly reviewing their data. This alleviated concerns of uncertainty in daily living, led to an increased feeling of security, and empowered patients to understand decision-making regarding GDMT. Frequent medication changes, and the associated financial impact, were common concerns. Remote titration of GDMT for HFrEF is feasible and appears to be a patient-centered approach to care.

2.
J Interv Card Electrophysiol ; 47(1): 19-27, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27565971

ABSTRACT

Development of new medical technology is a crucial part of the advancement of medicine and our ability to better treat patients and their diseases. This process of development is long and arduous and requires a significant investment of human, financial and material capital. However, technology development can be rewarded richly by its impact on patient outcomes and successful sale of the product. One of the major regulatory hurdles to technology development is the Food and Drug Administration (FDA) approval process, which is necessary before a technology can be marketed and sold in the USA. Many businesses, medical providers and consumers believe that the FDA approval process is the only hurdle prior to use of the technology in day-to-day care. In order for the technology to be adopted into clinical use, reimbursement for both the device as well as the associated work performed by physicians and medical staff must be in place. Work and coverage decisions require Current Procedural Terminology (CPT) code development and Relative Value Scale Update Committee (RUC) valuation determination. Understanding these processes is crucial to the timely availability of new technology to patients and providers. Continued and better partnerships between physicians, industry, regulatory bodies and payers will facilitate bringing technology to market sooner and ensure appropriate utilization.


Subject(s)
Device Approval/standards , Electrophysiologic Techniques, Cardiac/instrumentation , Electrophysiologic Techniques, Cardiac/standards , Product Surveillance, Postmarketing/standards , Technology Assessment, Biomedical/standards , United States Food and Drug Administration/standards , Biotechnology/instrumentation , Biotechnology/standards , Device Approval/legislation & jurisprudence , Guidelines as Topic , Marketing of Health Services/standards , Technology Assessment, Biomedical/legislation & jurisprudence , United States
3.
J Interv Card Electrophysiol ; 32(3): 195-203, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21964620

ABSTRACT

Over the past decade, electroanatomic mapping has emerged as a useful tool for complex ablation procedures. A more recent advancement is the development of image integration. Image integration refers to the process of registering a previously acquired MRI or CT scan of the heart with the mapping space during the ablation procedure. The technique of image integration is now relied on by many electrophysiology laboratories to guide complex ablation procedures, particularly atrial fibrillation ablation and ablation of patients with ventricular tachycardia in the setting of structural heart disease. An even more recent development is image fusion. This refers to taking information about the myocardial substrate, especially intramyocardial scar, and registering it with the active mapping space. This technique remains in its infancy but shows great promise in facilitating complex ablation procedures. The purpose of the article is to review the development, state of the art, and future of these image integration and fusion techniques.


Subject(s)
Body Surface Potential Mapping/methods , Cardiovascular Surgical Procedures/methods , Image Enhancement/methods , Magnetic Resonance Imaging/methods , Subtraction Technique , Surgery, Computer-Assisted/methods , Tomography, X-Ray Computed/methods , Humans
4.
Heart Rhythm ; 8(12): 1869-74, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21798230

ABSTRACT

BACKGROUND: The reported complication rate of catheter ablation of atrial fibrillation (AF) varies. OBJECTIVE: Our goal was to assess temporal trends and the effect of both institutional and individual operators' experience on the incidence of complications. METHODS: All patients undergoing AF ablation at Johns Hopkins Hospital between February 2001 and December 2010 were prospectively enrolled in a database. Major complications were defined as those that were life-threatening, resulted in permanent harm, required intervention, or significantly prolonged hospitalization. RESULTS: Fifty-six major complications occurred in 1190 procedures (4.7%). The majority of complications were vascular (18; 1.5%), followed by pericardial tamponade (13; 1.1%) and cerebrovascular accident (12; 1.1%). No cases of death or atrioesophageal fistula occurred. The overall complication rate decreased from 11.1% in 2002 to 1.6% in 2010 (P <.05). On univariate analysis, demographic and clinical factors associated with the increased risk of complications were CHADS(2) score of ≥2 (hazard ratio [HR] = 2.5; 95% confidence interval [CI] = 1.4-4.4; P = .002), female gender (HR = 2.0; 95% CI = 1.2-3.5; P = .014), and age (HR = 1.03; 95% CI = 1.0-1.1; P = .042). Gender and CHADS(2) score of ≥2 remained independent predictors of complication on multivariable analysis. CONCLUSION: The complication rate of catheter ablation of AF decreased with increased institutional experience. Female gender and CHADS(2) score of ≥2 are significant independent risk factors for complications and should be considered when referring patients for AF ablation.


Subject(s)
Atrial Fibrillation/surgery , Catheter Ablation/adverse effects , Postoperative Complications/epidemiology , Postoperative Complications/prevention & control , Baltimore/epidemiology , Cardiac Tamponade/epidemiology , Cardiac Tamponade/etiology , Clinical Competence , Female , Humans , Iatrogenic Disease , Length of Stay , Male , Middle Aged , Postoperative Complications/etiology , Prospective Studies , Retrospective Studies , Risk Factors , Sex Factors , Stroke/epidemiology , Stroke/etiology
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