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1.
Prim Health Care Res Dev ; 23: e76, 2022 11 25.
Artículo en Inglés | MEDLINE | ID: mdl-36426593

RESUMEN

BACKGROUND: Some symptoms are recognised as red flags for cancer, causing the General Practitioner (GP) to refer the patient for investigation without delay. However, many early symptoms of cancer are vague and unspecific, and in these cases, a delay in referral risks a diagnosis of cancer that is too late. Empowering GPs in their management of patients that may have cancer is likely to lead to more timely cancer diagnoses. AIM: To identify the factors that affect European GPs' empowerment in making an early diagnosis of cancer. METHODS: This was a Delphi study involving GPs in 20 European countries. We presented GPs with 52 statements representing factors that could empower GPs to increase the number of early cancer diagnoses. Over three Delphi rounds, we asked GPs to indicate the clinical relevance of each statement on a Likert scale.The final list of statements indicated those that were considered by consensus to be the most relevant. RESULTS: In total, 53 GPs from 20 European countries completed the Delphi process, out of the 68 GPs who completed round one. Twelve statements satisfied the pre-defined criteria for relevance. Five of the statements related to screening and four to the primary/secondary care interface. The other selected statements concerned information technology (IT) and GPs' working conditions. Statements relating to training, skills and working efficiency were not considered priority areas. CONCLUSION: GPs consider that system factors relating to screening, the primary-secondary care interface, IT and their working conditions are key to enhancing their empowerment in patients that could have cancer. These findings provide the basis for seeking actions and policies that will support GPs in their efforts to achieve timely cancer diagnosis.


Asunto(s)
Médicos Generales , Neoplasias , Humanos , Técnica Delphi , Detección Precoz del Cáncer , Neoplasias/diagnóstico , Atención Secundaria de Salud
2.
EBioMedicine ; 13: 274-283, 2016 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28005535

RESUMEN

OBJECTIVE: A potential mechanism by which obesity could promote hypertension and kidney diseases is through accumulation of adipose tissue in the renal sinus (RS). The aim of the study was to quantify RS and abdominal adipose tissue volumes and to evaluate serum kidney injury molecule (sKIM)-1 and fibroblast growth factor (FGF)-21 association with different adipose tissue compartments. METHODS: The cross-sectional study included 280 and follow-up study-40 asymptomatic participants; aged 38.30±4.10. For all study participants computed tomography examination was performed, sKIM-1 and FGF-21 levels were measured. RESULTS: The results indicated asymmetrical deposition of adipose tissue into the RS even after corresponding kidney volume adjustment. The cross-sectional and the follow-up studies showed that sKIM-1 level was positively associated with RS adipose tissue volume increase for both genders. FGF-21 was positively associated with RS and retroperitoneal adipose tissue amount. CONCLUSIONS: Regardless of gender adipose tissue in RS accumulates asymmetrically-the left RS accumulates a significantly higher amount of adipose tissue. Thus, primarily RS adipose tissue effects should be assessed on the left kidney. Accumulation of adipose tissue in the RS is related with the visceral adipose amount, KIM-1 and FGF-21 concentration increase in the blood serum.


Asunto(s)
Adiposidad , Factores de Crecimiento de Fibroblastos/metabolismo , Receptor Celular 1 del Virus de la Hepatitis A/metabolismo , Grasa Intraabdominal/patología , Riñón/metabolismo , Adulto , Biomarcadores , Estudios Transversales , Femenino , Factores de Crecimiento de Fibroblastos/sangre , Estudios de Seguimiento , Receptor Celular 1 del Virus de la Hepatitis A/sangre , Humanos , Imagenología Tridimensional , Grasa Intraabdominal/diagnóstico por imagen , Riñón/anatomía & histología , Masculino , Tamaño de los Órganos , Tomografía Computarizada por Rayos X
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