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1.
Artigo em Inglês | WPRIM (Pacífico Ocidental) | ID: wpr-111702

RESUMO

BACKGROUND/AIMS: There is significant co-morbidity between irritable bowel syndrome (IBS) and fibromyalgia syndrome (FMS). However, FMS is diagnosed by physical examination, which limits the conduct of co-morbidity studies in a large population-based study. The purpose of this study was to determine the diagnostic validity of a new symptom-based criteria in patients with FMS and/or IBS using the American College of Rheumatology (ACR) criteria as a gold standard. METHODS: The study participants consisted of women with FMS (n = 30), IBS (n = 27) and controls (n = 28). A new symptom-based diagnostic criteria for FMS comprised a regional pain scale and a visual analogue scale for fatigue. All subjects underwent a physical examination for FMS (ACR criteria) and structured questionnaires of regional pain scale and visual analogue scale for fatigue. A fibromyalgia intensity score was calculated and thresholds of tenderness were determined by a dolorimeter. RESULTS: The number of participants diagnosed with FMS in the entire study population (n = 85) was 31 by the new criteria. Compared to the ACR, the sensitivity of the new criteria was 82.9%, specificity 96.0%, positive predictive value 93.5% and negative predictive value 88.9%. In addition, new criteria were useful for the diagnosis of FMS among the subjects with IBS. A fibromyalgia intensity score was significantly correlated with the threshold of tenderness (r = -0.62, P < 0.001). CONCLUSIONS: The new symptom-based diagnostic criteria for the diagnosis of FMS can be used in large-scale clinical and epidemiological co-morbidity studies, in which physical examination is unfeasible. Gastroenterologists investigating the effects of co-morbid FMS in IBS patients can use these new ciriteria with confidence.


Assuntos
Feminino , Humanos , Comorbidade , Fadiga , Fibromialgia , Síndrome do Intestino Irritável , Exame Físico , Inquéritos e Questionários , Reumatologia , Sensibilidade e Especificidade
2.
J Eval Clin Pract ; 14(5): 799-802, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19018913

RESUMO

BACKGROUND: Various international guidelines recommend the use of non-endoscopic tests [such as urea breath test (UBT)] for the evaluation of dyspeptic patients, unless endoscopy is clinically indicated. AIM: To assess adherence with guidelines for UBT referrals among primary care doctors in Israel. METHODS: Patients referred by primary care doctors to an open-access UBT service were included in the study. Prior to the test, all patients were administered with a short questionnaire regarding their symptoms, previous and concomitant medications including previous Helicobacter pylori eradication. RESULTS: The study sample consisted of 209 patients, aged 18-94 years, M/F = 74/135. The UBT was judged to be appropriate in 94 (45%) subjects, inappropriate in 93 (44.5%) subjects and appropriate but avoidable in 22 (10.5%) subjects, most of them asymptomatic patients following anti H. pylori treatment. The inappropriate indications include 38 (18%) patients with suspected gastro-oesophageal reflux disease symptoms and 21 (10%) dyspeptic patients aged 45 years or more. CONCLUSION: Nearly 45% percent of UBT referrals in primary care practice were inappropriate, and a significant number of dyspeptic patients should have been referred to endoscopy. These findings show a substantial non-compliance with guidelines for H. pylori testing among primary care doctors.


Assuntos
Testes Respiratórios , Fidelidade a Diretrizes/organização & administração , Infecções por Helicobacter/diagnóstico , Guias de Prática Clínica como Assunto , Atenção Primária à Saúde/organização & administração , Encaminhamento e Consulta/organização & administração , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Testes Respiratórios/métodos , Distribuição de Qui-Quadrado , Dispepsia/microbiologia , Feminino , Gastroscopia , Mau Uso de Serviços de Saúde/estatística & dados numéricos , Infecções por Helicobacter/complicações , Helicobacter pylori , Humanos , Israel , Masculino , Pessoa de Meia-Idade , Seleção de Pacientes , Padrões de Prática Médica/organização & administração , Estudos Prospectivos , Ureia/análise
3.
World J Gastroenterol ; 12(24): 3841-7, 2006 Jun 28.
Artigo em Inglês | MEDLINE | ID: mdl-16804968

RESUMO

AIM: To investigate whether Thy1 recognizes oval cells in the fetal liver and to characterize the cultured Thy1- selected cells from E14 rat livers. METHODS: Thy1 populations were analyzed by fluorescence activated cell sorter analysis. Thy1 positive cells were isolated using magnetic beads. Hepatic markers were detected by Western blotting, immunocytochemistry and RT-PCR. RESULTS: The percentage of Thy1-positive cells decreased during early development of fetal rat liver (E13-E16). E14 fetal livers contained 7.8% Thy1 positive cells, of which 61% were positive for alpha-fetoprotein (AFP) and 25% expressed albumin. The Thy1+ population expressed oval cell markers c-Kit and CXCR4, liver enriched-transcription factors HNF1alpha and HNF6, hepatocytic markers albumin, AFP and cytokeratin 18, and biliary marker cytokeratin 19. Thy1- selected cells formed only mesenchymal colonies when plated on collagen and in serum-containing media. Thy1 selected cells were able to form hepatic colonies positive for HNF1alpha, HNF6, albumin, AFP, cytokeratin 18, cytokeratin 19 and glycogen, when grown on STO feeder layers in serum free-media. CONCLUSION: Oval cells positive for Thy1 are present in early liver embryonic stages.


Assuntos
Hepatócitos/citologia , Hepatócitos/imunologia , Fígado/embriologia , Fígado/imunologia , Antígenos Thy-1/análise , Albuminas/análise , Animais , Separação Celular/métodos , Células Cultivadas , Feminino , Fator 1-alfa Nuclear de Hepatócito/análise , Fator 6 Nuclear de Hepatócito/análise , Hepatócitos/química , Imuno-Histoquímica , Queratinas/análise , Fígado/química , Fígado/citologia , MAP Quinase Quinase Quinases/análise , Gravidez , Ratos , Ratos Endogâmicos F344 , Receptores de Citocinas/análise , Receptores de Oncostatina M , alfa-Fetoproteínas/análise
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