Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros

Banco de datos
País/Región como asunto
Tipo del documento
País de afiliación
Intervalo de año de publicación
1.
Neth Heart J ; 29(10): 490-499, 2021 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-34132981

RESUMEN

Sodium-glucose cotransporter 2 (SGLT2) inhibitors include a relatively new class of glucose-lowering drugs that reduce plasma glucose concentrations by inhibiting proximal tubular reabsorption of glucose in the kidney, while increasing its excretion in urine. Recent large randomised controlled trials have demonstrated that many of these agents reduce the occurrence of major adverse cardiovascular events, hospitalisation for heart failure, cardiovascular death and/or chronic kidney disease progression in patients with and without type 2 diabetes mellitus (DM2). Given their unique insulin-independent mode of action and favourable efficacy and adverse-event profile, SGLT2 inhibitors are promising and they offer an interesting therapeutic approach for the cardiologist to incorporate into routine practice. However, despite accumulating data supporting this class of therapy, cardiologists infrequently prescribe SGLT2 inhibitors, potentially due to a lack of familiarity with their use and the reticence to change DM medication. Here, we provide an up-to-date practical guide highlighting important elements of treatment initiation based on real-world evidence and expert opinion. We describe how to change DM medication, including insulin dosing when appropriate, and how to anticipate any adverse events based on real-world experience in patients with DM2 in the Meander Medical Centre in Amersfoort, the Netherlands. This includes a simple algorithm showing how to initiate SGLT2 inhibitor treatment safely, while considering the consequence of the glucosuric effects of these inhibitors for the individual patient.

2.
Neth J Med ; 65(4): 150-2, 2007 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-17452765

RESUMEN

A 69-year-old woman developed Cushing's syndrome after long-term use of Sinatren, an Indonesian over the-counter drug, which was pharmacologically analysed three times before the correct content was discovered. After discontinuation she developed adrenal insufficiency, for which she needed substitution of steroids. Physicians should be aware of the presence of corticosteroids in over-the-counter products, that are not mentioned on the instruction leaflet.


Asunto(s)
Corticoesteroides/efectos adversos , Insuficiencia Suprarrenal/inducido químicamente , Síndrome de Cushing/inducido químicamente , Eccema/tratamiento farmacológico , Medicamentos sin Prescripción/química , Fitoterapia/efectos adversos , Extractos Vegetales/química , Insuficiencia Suprarrenal/diagnóstico , Anciano , Síndrome de Cushing/diagnóstico , Femenino , Humanos , Indonesia , Anamnesis , Medicamentos sin Prescripción/efectos adversos , Extractos Vegetales/efectos adversos , Automedicación
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA