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2.
Dermatol Clin ; 37(3): 307-317, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31084725

RESUMEN

Dermatologic surgery in pregnant/postpartum patients requires deliberate consideration. Although surgery can be safely performed during any trimester, the second trimester and immediate postpartum period is optimal. Surgery should not be delayed for melanoma/high-risk skin cancers. Perioperative positioning, analgesic, antiseptic, and antibiotic selection should be deliberate to avoid risk to the patient/fetus/infant. The left lateral tilt position reduces aortocaval compression syndrome. Lidocaine and epinephrine can be used safely. Alcohol and chlorhexidine are considered safe. Antibiotics commonly used in skin surgery are safe in pregnancy and lactation. Acetaminophen is first line for pain management. Nonsteroidal antiinflammatory drugs should be avoided.


Asunto(s)
Lactancia Materna , Melanoma/cirugía , Complicaciones Neoplásicas del Embarazo/cirugía , Neoplasias Cutáneas/cirugía , Analgésicos/efectos adversos , Anestesia Local/métodos , Antibacterianos/efectos adversos , Procedimientos Quirúrgicos Dermatologicos/métodos , Femenino , Humanos , Posicionamiento del Paciente , Cuidados Posoperatorios , Complicaciones Posoperatorias/etiología , Embarazo , Trimestres del Embarazo
3.
Dermatol Clin ; 37(3): 319-328, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-31084726

RESUMEN

Overall, dermatologic surgery performed in the outpatient setting is very low risk to patients and safer than similar procedures performed under general anesthesia, and is also more cost-effective. There are several approaches to mitigating the risk of complications while optimizing patient outcomes. Strict oversight of the dermatology clinic helps to ensure team members all adhere to standards of care. Vial safety, strict hand hygiene, limiting the use of topical antibiotics, generally continuing all blood thinners perioperatively, and prebiopsy photographs are all examples of approaches to help maximize patient safety.


Asunto(s)
Anestésicos Locales/administración & dosificación , Procedimientos Quirúrgicos Dermatologicos/métodos , Errores de Medicación/prevención & control , Seguridad del Paciente , Infección de la Herida Quirúrgica/prevención & control , Anestesia Local , Anestésicos Locales/efectos adversos , Anticoagulantes/uso terapéutico , Procedimientos Quirúrgicos Dermatologicos/efectos adversos , Humanos , Lesiones por Pinchazo de Aguja/prevención & control , Fotograbar
4.
Dermatol Surg ; 42(3): 392-402, 2016 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-26945321

RESUMEN

BACKGROUND: There is a paucity of studies investigating laser resurfacing in Fitzpatrick skin phototypes (SPT) IV to VI. OBJECTIVE: To assess the efficacy and safety of fractional nonablative laser resurfacing in the treatment of acne scarring in patients with SPT IV to VI. METHODS AND MATERIALS: The authors conducted a randomized, investigator-blinded and rater-blinded, split-face comparative study of adults with SPT IV to VI and facial acne scars treated with 2 different density settings and the same fluence. RESULTS: Quantitative global scarring grading system (QGSGS) scores were significantly improved from baseline at 16 and 24 weeks (p = .0277). Improvements in QGSGS scores after higher and lower density treatments were statistically similar (p = .96). The live-blinded dermatologist, the blinded dermatologist photoraters, and the patients rated scars as being significantly more improved by visual analog scale at weeks 16 and 24 compared with baseline (p < .001) for both treatment densities. Five of 7 and 3 of 7 patients in the higher and lower density group, respectively, experienced mild or moderate hyperpigmentation as an investigator observed site reaction. CONCLUSION: The nonablative 1550-nm fractional laser is safe and efficacious in treating acne scaring in Fitzpatrick skin types IV to VI. Self-limited postinflammatory hyperpigmentation was a common occurrence, especially with higher treatment densities.


Asunto(s)
Acné Vulgar/complicaciones , Cicatriz/radioterapia , Técnicas Cosméticas , Dermatosis Facial/radioterapia , Láseres de Estado Sólido/uso terapéutico , Terapia por Luz de Baja Intensidad/métodos , Cicatriz/etiología , Técnicas Cosméticas/efectos adversos , Método Doble Ciego , Femenino , Humanos , Hiperpigmentación/etiología , Láseres de Estado Sólido/efectos adversos , Terapia por Luz de Baja Intensidad/efectos adversos , Masculino , Dolor/etiología , Índice de Severidad de la Enfermedad , Pigmentación de la Piel
5.
J Am Acad Dermatol ; 70(1): 168-77, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24184141

RESUMEN

BACKGROUND: Many studies have identified cardiovascular risk factors in patients with psoriasis. Some psoriasis therapies may increase cardiovascular disease (CVD) and others may decrease CVD. OBJECTIVE: We reviewed the literature to define the impact of common psoriasis therapies on cardiovascular measures and outcomes. RESULTS: Phototherapy has no major cardiovascular impact and may reduce levels of proinflammatory cytokines. Acitretin increases serum lipids and triglycerides, but has not been shown to increase cardiovascular risk. Cyclosporine A increases blood pressure, serum triglycerides, and total cholesterol. Methotrexate is associated with a decreased risk of CVD morbidity and mortality. Among the biologics, data for tumor necrosis factor inhibitors suggest an overall reduction in cardiovascular events. Most data on short-term ustekinumab use suggest no effect on major adverse cardiovascular events, however some authorities remain concerned. Nevertheless, ustekinumab use over a 4-year period shows a decrease in major adverse cardiovascular events when compared both with the general US population and with psoriatics in Great Britain. LIMITATIONS: Most studies lack the power and randomization of large clinical trials and long-term follow-up periods. In addition, the increased risk of CVD associated with psoriasis itself is a confounding factor. CONCLUSION: Some therapies for moderate to severe psoriasis, including methotrexate and tumor necrosis factor inhibitors, may reduce cardiovascular events in psoriatic patients. Ustekinumab appears to be neutral but there may be a long-term benefit. Appropriate patient counseling and selection and clinical follow-up are necessary to maximize safety with these agents. Further long-term study is necessary to quantify the benefits and risks associated with biologic therapies.


Asunto(s)
Enfermedades Cardiovasculares/inducido químicamente , Psoriasis/tratamiento farmacológico , Acitretina/efectos adversos , Anticuerpos Monoclonales Humanizados/efectos adversos , Terapia Biológica/efectos adversos , Enfermedades Cardiovasculares/etiología , Ciclosporina/efectos adversos , Humanos , Inmunosupresores/efectos adversos , Queratolíticos/efectos adversos , Metotrexato/efectos adversos , Ácido Micofenólico/efectos adversos , Ácido Micofenólico/análogos & derivados , Terapia PUVA/efectos adversos , Psoriasis/terapia , Factor de Necrosis Tumoral alfa/antagonistas & inhibidores , Ustekinumab
6.
J Drugs Dermatol ; 12(3): 348-9, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23545921

RESUMEN

Increased cases of acquired epidermodysplasia verruciformis (EDV) have been reported in patients with human immunodeficiency virus (HIV). With regard to management, there are no randomized controlled trials in either immunocompetent or immunocompromised patients, and only a limited number of anecdotal treatment options. Systemic retinoids, either independently or in combination with other treatment modalities, have been used with limited success, demonstrating transient clinical response and recurrence of lesions after cessation of therapy. We report a case of an HIV-positive patient with acquired EDV who achieved sustained clinical resolution even after discontinuation of oral acitretin by applying topical imiquimod to prevent recurrence of his lesions.


Asunto(s)
Acitretina/uso terapéutico , Aminoquinolinas/uso terapéutico , Epidermodisplasia Verruciforme/tratamiento farmacológico , Huésped Inmunocomprometido , Acitretina/administración & dosificación , Adyuvantes Inmunológicos/administración & dosificación , Adyuvantes Inmunológicos/uso terapéutico , Administración Cutánea , Administración Oral , Aminoquinolinas/administración & dosificación , Epidermodisplasia Verruciforme/virología , Infecciones por VIH/complicaciones , Humanos , Imiquimod , Queratolíticos/administración & dosificación , Queratolíticos/uso terapéutico , Masculino , Persona de Mediana Edad , Resultado del Tratamiento
7.
Dermatol Clin ; 27(3): 355-64, vii, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19580929

RESUMEN

Systemic contact dermatitis (SCD) describes a cutaneous eruption in response to systemic exposure to an allergen. The exact pathologic mechanism remains uncertain. The broad spectrum of presentations that are often nonspecific can make it difficult for the clinician to suspect this disease, but it is an important diagnosis to consider in cases of recalcitrant, widespread, or recurrent dermatitis, in which patch testing often reveals allergy to nickel or balsam of Peru. Diagnosis and appropriate management can be life-altering for affected patients. This article on SCD provides an overview of the disease with descriptions of common allergens and some insight into the possible mechanism of action seen in SCD.


Asunto(s)
Alérgenos/efectos adversos , Dermatitis Alérgica por Contacto/etiología , Asteraceae/efectos adversos , Bálsamos/efectos adversos , Dermatitis Alérgica por Contacto/diagnóstico , Dermatitis Alérgica por Contacto/terapia , Dermatología/métodos , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/diagnóstico , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/etiología , Fijadores/efectos adversos , Hipersensibilidad a los Alimentos/complicaciones , Hipersensibilidad a los Alimentos/diagnóstico , Formaldehído/efectos adversos , Humanos , Metales/efectos adversos , Níquel/efectos adversos , Vehículos Farmacéuticos/efectos adversos , Fitoterapia/efectos adversos , Propilenglicol/efectos adversos , Oligoelementos/efectos adversos
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