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Métodos Terapéuticos y Terapias MTCI
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1.
J Am Acad Dermatol ; 89(2S): S36-S39, 2023 08.
Artículo en Inglés | MEDLINE | ID: mdl-37591565

RESUMEN

Novel medical and procedural options for androgenetic alopecia have arrived. Low-dose oral minoxidil has made its clinical debut, while data on spironolactone, finasteride, and nutritional supplements have advanced. Minimally invasive technological advancements include photobiomodulation and platelet-rich plasma. Within hair transplantation, follicular unit extraction and robotics are now at the clinicians' fingertips.


Asunto(s)
Alopecia , Finasterida , Humanos , Alopecia/tratamiento farmacológico , Finasterida/uso terapéutico , Terapia Conductista , Minoxidil/uso terapéutico , Suplementos Dietéticos
5.
J Cosmet Laser Ther ; 20(7-8): 385-386, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-29388860

RESUMEN

Pulsed dye laser (PDL) is an effective treatment option for erythematotelangiectatic rosacea. The use of a test spot allows patients to experience the procedure on a small area prior to further treatment. The purpose of this study was to elucidate whether the use of a no charge test spot influenced return rates for further PDL treatment. Data were obtained retrospectively using International Classification of Diseases (ICD)-10 codes for rosacea. Sixty charts were identified: 26 patients initially received a PDL test area free of charge, whereas 34 patients initially underwent full PDL treatment. Patients who experienced the test spot laser treatment had a lower return rate compared to those that directly underwent full PDL treatment. However, this difference was not statistically significant (Fisher's exact test p = 0.2883). Future studies evaluating and identifying factors that influence PDL return rates are needed. Abbreviations: ETR: Erythematotelangiectatic rosacea; PDL: pulsed dye laser; ICD: International classification of diseases.


Asunto(s)
Láseres de Colorantes/estadística & datos numéricos , Terapia por Luz de Baja Intensidad/estadística & datos numéricos , Aceptación de la Atención de Salud/estadística & datos numéricos , Rosácea/radioterapia , Humanos , Estudios Retrospectivos
6.
J Cosmet Laser Ther ; 20(3): 159-167, 2018 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-29020478

RESUMEN

The market for home-use photobiomodulation devices to treat androgenetic alopecia has rapidly expanded, and the Food and Drug Administration (FDA) has recently cleared many devices for this purpose. Patients increasingly seek the advice of dermatologists regarding the safety and efficacy of these hair loss treatments. The purpose of this guide was threefold: (1) to identify all home-use photobiomodulation therapy devices with FDA-clearance for treatment of androgenetic alopecia; (2) to review device design, features and existing clinical evidence; and (3) to discuss practical considerations of photobiomodulation therapy, including patient suitability, treatment goals, safety, and device selection. A search of the FDA 510(k) Premarket Notification database was conducted using product code "OAP" to identify all home-use devices that are FDA-cleared to treat androgenetic alopecia. Thirteen commercially available devices were identified and compared. Devices varied in shape, wavelength, light sources, technical features, price, and level of clinical evidence. To date, there are no head-to-head studies comparing the efficacy of these devices. Photobiomodulation therapy devices have an excellent safety profile and mounting evidence supporting their efficacy. However, long-term, high quality studies comparing these devices in diverse populations are lacking. As these devices become increasingly popular, dermatologists should be familiar with this treatment modality to add to their therapeutic armamentarium. ABBREVIATIONS: AGA, androgenetic alopecia; FDA, Food and Drug Administration; IEC, International Electrotechnical Commission; LED, light-emitting diode; PBMT, photobiomodulation therapy.


Asunto(s)
Alopecia/terapia , Terapia por Luz de Baja Intensidad/instrumentación , Terapia por Luz de Baja Intensidad/métodos , Automanejo/métodos , Aprobación de Recursos , Humanos , Terapia por Luz de Baja Intensidad/efectos adversos , Planificación de Atención al Paciente , Selección de Paciente , Estados Unidos , United States Food and Drug Administration
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