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2.
Clin Med (Lond) ; 21(4): e371-e374, 2021 07.
Artigo em Inglês | MEDLINE | ID: mdl-35192480

RESUMO

Giant cell arteritis (GCA) is a systemic vasculitis with numerous potential complications and societal costs. After the publication of international guidelines, we found a number of deficiencies in the local care pathway of patients suspected to have GCA. These included poor referral and management pathways, and absence of dedicated monitoring and follow-up. In this paper, we describe a 10-year transformation which led to our service being nominated for a national award.A comprehensive consensus pathway saw referral numbers rise from 19 to 135 from 2012 to 2019. A consensus management pathway has meant that patients are assessed within 2 days of referral and glucocorticoids started at point of referral. All patients with suspected GCA are clerked and managed according to this agreed pathway which is available on the hospital intranet. The introduction of diagnostic ultrasonography has meant that the need for biopsies has dropped by >80% reducing the annual cost of diagnostics by >£140,000. The introduction of a vasculitis specialist nurse has resulted in improving education, contact and speed of access to our service. The improvements in the service resulted in our service becoming a finalist in the Royal College of Physicians Excellence in Patient Care Award in 2020.


Assuntos
Arterite de Células Gigantes , Biópsia , Arterite de Células Gigantes/diagnóstico , Arterite de Células Gigantes/terapia , Humanos , Qualidade da Assistência à Saúde , Artérias Temporais/diagnóstico por imagem , Artérias Temporais/patologia , Ultrassonografia
3.
Pediatr Dev Pathol ; 17(5): 339-43, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25076388

RESUMO

We confirmed the added value provided by sampling D1 in the diagnosis of CD in comparison to the diagnosis yield when only the more distal duodenum (D2, D3, and/or D4) was sampled. The severity of CD, as assessed by the Marsh-Oberhuber classification, did not increase distally; on the contrary, in 39/60 (65%) of the cohort, the features of CD were either more severe or only present in D1.


Assuntos
Doença Celíaca/patologia , Duodeno/patologia , Mucosa Intestinal/patologia , Adolescente , Atrofia , Biópsia , Doença Celíaca/classificação , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Masculino
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