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1.
J Drugs Dermatol ; 16(7): 707-710, 2017 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-28697226

RESUMEN

INTRODUCTION: A topical proprietary procedural enhancement system (PES) containing a combination of active ingredients including a tripeptide and hexapeptide (TriHex Technology™, Alastin Procedure Enhancement Invasive System, ALASTIN Skincare™, Inc., Carlsbad, CA) has been used successfully to aid in healing and improve symptomatology following resurfacing procedures.

METHODS: PES (Gentle Cleanser, Regenerating Skin Nectar with TriHex Technology™, Ultra Nourishing Moisturizer with TriHex Technology™, Soothe + Protect Recovery Balm, Broad Spectrum 30+ Sunscreen) was compared to a basic regimen (Aquaphor™, Cerave™ cleanser, Vanicream™, Alastin Broad Spectrum 30+ Sunscreen) in a split face/ décolleté trial following fractional non-ablative thulium-doped resurfacing treatment to the face or décolleté. The skin was pre-conditioned and treated during and after the procedure using the two regimens.

RESULTS: A blinded investigator rated the PES statistically superior to the basic regimen on healing post-laser treatment on day 4 based on lentigines, texture, and Global Skin Quality. Subjects also reported 'better looking and feeling' skin on the PES side.

CONCLUSION: PES appears to improve healing post-non ablative thulium-doped resurfacing treatment to the face/décolleté in comparison with standard of care.

J Drugs Dermatol. 2017;16(7):707-710.

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Asunto(s)
Láseres de Gas/uso terapéutico , Envejecimiento de la Piel/efectos de los fármacos , Envejecimiento de la Piel/patología , Crema para la Piel/administración & dosificación , Protectores Solares/administración & dosificación , Procedimientos Quirúrgicos Dermatologicos/métodos , Cara/patología , Femenino , Humanos , Regeneración de la Piel con Plasma/métodos , Método Simple Ciego , Tórax/efectos de los fármacos , Tórax/patología , Resultado del Tratamiento
2.
BMC Cardiovasc Disord ; 16: 152, 2016 07 16.
Artículo en Inglés | MEDLINE | ID: mdl-27422639

RESUMEN

BACKGROUND: Atrial fibrillation is a major public health problem and is the most common cardiac arrhythmia, affecting an estimated 2.7 million Americans. The true prevalence of atrial fibrillation is likely underestimated because episodes are often sporadic; therefore, it is challenging to detect and record an occurrence in a "real world" setting. To date, mobile health tools that promote earlier detection and treatment of atrial fibrillation and improvement in self-management behaviors and knowledge have not been evaluated. This study will be the first to address the epidemic problem of atrial fibrillation with a novel approach utilizing advancements in mobile health electrocardiogram technology to empower patients to actively engage in their healthcare and to evaluate impact on quality of life and quality-adjusted life years. Furthermore, sending a daily electrocardiogram transmission, coupled with receiving educational and motivational text messages aimed at promoting self-management and a healthy lifestyle may improve the management of chronic cardiovascular conditions (e.g., hypertension, diabetes, heart failure, etc.). Therefore, we are currently conducting a randomized controlled trial to assess the efficacy of a mobile health intervention, iPhone® Helping Evaluate Atrial fibrillation Rhythm through Technology (iHEART) versus usual cardiac care. METHODS: The iHEART study is a single center, prospective, randomized controlled trial. A total of 300 participants with a recent history of atrial fibrillation will be enrolled. Participants will be randomized 1:1 to receive the iHEART intervention, receiving an iPhone® equipped with an AliveCor® Mobile ECG and accompanying Kardia application and behavioral altering motivational text messages or usual cardiac care for 6 months. DISCUSSION: This will be the first study to investigate the utility of a mobile health intervention in a "real world" setting. We will evaluate the ability of the iHEART intervention to improve the detection and treatment of recurrent atrial fibrillation and assess the intervention's impact on improving clinical outcomes, quality of life, quality-adjusted life-years and disease-specific knowledge. TRIAL REGISTRATION: NCT02731326 ; Verified April 2016.


Asunto(s)
Fibrilación Atrial/diagnóstico , Electrocardiografía/instrumentación , Sistema de Conducción Cardíaco/fisiopatología , Frecuencia Cardíaca , Aplicaciones Móviles , Teléfono Inteligente , Telemedicina/instrumentación , Potenciales de Acción , Fibrilación Atrial/fisiopatología , Fibrilación Atrial/terapia , Protocolos Clínicos , Electrocardiografía/métodos , Conductas Relacionadas con la Salud , Conocimientos, Actitudes y Práctica en Salud , Estilo de Vida Saludable , Humanos , Motivación , Ciudad de Nueva York , Educación del Paciente como Asunto , Valor Predictivo de las Pruebas , Estudios Prospectivos , Proyectos de Investigación , Conducta de Reducción del Riesgo , Autocuidado , Procesamiento de Señales Asistido por Computador , Telemedicina/métodos , Envío de Mensajes de Texto
3.
Nurse Pract ; 43(8): 49-55, 2018 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-30028773

RESUMEN

There are limited data on racial and ethnic disparities related to quality of life (QoL) and health literacy in adults with multiple cardiac conditions. This article evaluates the relationship between health literacy and QoL among patients with cardiac conditions in a multiethnic community in New York City.


Asunto(s)
Alfabetización en Salud/estadística & datos numéricos , Cardiopatías/enfermería , Adulto , Etnicidad/estadística & datos numéricos , Disparidades en el Estado de Salud , Cardiopatías/etnología , Humanos , Ciudad de Nueva York , Calidad de Vida
4.
J Atr Fibrillation ; 9(5): 1546, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-29250277

RESUMEN

BACKGROUND: Little attention has focused on the integration of mobile health (mHealth) technology with self-management approaches to improve the detection and management of atrial fibrillation (AF) in clinical practice. OBJECTIVE: The objective of this study was to investigate the differences between mHealth and usual care over a 6-month follow-up period among patients with a known history of atrial fibrillation. METHODS: A pilot cohort from within the larger ongoing randomized trial, iPhone® Helping Evaluate Atrial fibrillation Rhythm through Technology (iHEART), was evaluated to determine differences in detection of AF and atrial flutter (AFL) recurrence rates (following treatment to restore normal rhythm) between patients undergoing daily smartphone ECG monitoring and age and gender matched control patients. SF-36v2TM QoL assessments were administered at baseline and 6 months to a subset of the patients undergoing daily ECG monitoring. Differences between groups were assessed by t-test, Fisher's exact test, and Cox proportional hazard models. RESULTS: Among the 23 patients with smartphone ECG monitors (16 males and 7 females, mean age 55 ± 10), 14 (61%) had detection of recurrent AF/AFL versus 30% of controls. During the follow-up period, patients given smartphone ECG monitors were more than twice as likely to have an episode of recurrent AF/AFL detected (hazard ratio: 2.55; 95% CI: 1.06 - 6.11; p = 0.04). Among the 13 patients with baseline and 6 month QoL assessments, significant improvements were observed in the physical functioning (p = 0.009), role physical (p = 0.007), vitality (p = 0.03), and mental health domains (p = 0.02). CONCLUSIONS: Cardiac mHealth self-monitoring is a feasible and effective mechanism for enhancing AF/AFL detection that improves quality of life.

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