Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
1.
Vox Sang ; 117(7): 900-912, 2022 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-35437811

RESUMEN

BACKGROUND AND OBJECTIVES: There is convincing evidence to show that low-dose prophylaxis (LDP) results in reduction in annualized bleeding rate (ABR) and better health-related quality of life (HRQoL) compared with on-demand or episodic treatment (ET) in haemophilia patients. The aim is to review various LDP protocols practised for the treatment of haemophilia, specifically in resource-limited countries. METHODS: A literature survey was made of articles published in English language in PubMed and EMBASE without any time limit using keywords 'low dose', 'prophylaxis' and 'haemophilia' in different combinations. RESULTS: A total of 19 reports involving LDP in patients with haemophilia were included in this review. Almost all studies reported reduction in ABR, improvement in joint function, pain and HRQoL compared with ET, but this did not fully translate into significant improvement in structural arthropathy already caused by earlier bleeds, suggesting that LDP may be less or ineffective in either stopping or reversing the damage. Individualized dose escalation protocols based on pharmacokinetic (PK) or clinical parameters were found to be superior to fixed LDP protocols and cost-effective compared with standard dose protocols. CONCLUSION: The developing countries can initiate LDP as the first step of prophylaxis, but certainly this should not be the final goal of the health care system in any country. Due to the complex pathophysiological mechanisms underlying haemophilic arthropathy, long-term data on LDP in haemophilia patients are warranted.


Asunto(s)
Factor VIII , Hemofilia A , Factor VIII/uso terapéutico , Hemofilia A/complicaciones , Hemofilia A/tratamiento farmacológico , Hemorragia/tratamiento farmacológico , Humanos , Calidad de Vida , Factores de Tiempo
2.
Indian Dermatol Online J ; 4(4): 378-9, 2013 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-24350034
3.
Indian J Pathol Microbiol ; 56(4): 355-8, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24441221

RESUMEN

BACKGROUND: Perforating disorders of the skin, is an often overlooked entity characterized by transepidermal elimination of material from the upper dermis and are classified histopathologically according to the type of epidermal disruption and the nature of the eliminated material. They include Kyrle's disease, perforating folliculitis, reactive perforating collagenosis, and elastosis perforans serpiginosa. AIM: The aim of this study was to delineate the clinical and histopathological features of perforating disorders of the skin. MATERIALS AND METHODS: In our study, we reviewed last 2 years skin biopsies received by us. Hematoxylin and eosin sections were re-examined and histochemical stainings (elastic van Gieson and Masson trichrome stains) were also used for histopathological evaluation. RESULTS: We reviewed five cases of perforating disorders of skin which included two cases of Kyrle's disease, two cases of reactive perforating collagenosis and a single case of perforating folliculitis. Two patients had family history of perforating dermatosis in their siblings and three had associated systemic disease. CONCLUSION: Perforating disorders of the skin should be considered when ulcer with keratotic plugs is found.


Asunto(s)
Enfermedades del Colágeno/patología , Opacidad de la Córnea/patología , Enfermedad de Darier/patología , Foliculitis/patología , Enfermedades Cutáneas Genéticas/patología , Úlcera Cutánea/patología , Piel/patología , Adolescente , Biopsia , Enfermedades del Colágeno/complicaciones , Opacidad de la Córnea/complicaciones , Enfermedad de Darier/complicaciones , Femenino , Foliculitis/complicaciones , Histocitoquímica , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Enfermedades Cutáneas Genéticas/complicaciones , Adulto Joven
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA