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Neoplasia detection rates after positive fecal occult blood test results are not affected by endoscopy center: a population-based study.
Bretagne, Jean-François; Hamonic, Stéphanie; Piette, Christine; Manfredi, Sylvain; Mallard, Gaud; Durand, Gérard; Riou, Françoise.
Afiliação
  • Bretagne JF; Department of Gastroenterology, Pontchaillou Hospital, Rennes, France.
Gastrointest Endosc ; 74(1): 141-7, 2011 Jul.
Article em En | MEDLINE | ID: mdl-21704812
BACKGROUND: We previously showed a significant variability in adenoma detection among colonoscopists who were participating in a mass screening program. The reasons for such variability remain largely unknown. OBJECTIVE: To study intercenter variations in neoplasia detection. DESIGN AND SETTING: Secondary analyses of colonoscopy findings from the 2 first rounds of a French screening program: logistic regressions and repeated-measures analyses of variance. MATERIAL: A total of 3487 colonoscopies performed by all 19 endoscopists who performed 30 examinations or more per round at 8 centers (6 private, 2 public). MAIN OUTCOME MEASUREMENTS: Probabilities of detecting 1, 2, or 3 or more adenomas, 1 adenoma 10 mm or larger, or colorectal cancer, as well as the corresponding adjusted (for patient age and sex) per-center detection rates. RESULTS: Endoscopy centers were not significant predictors of the probability of detecting any category of neoplasia with the exception of the 2 adenomas or more category (P < .005). The ranges of the adjusted detection rates for each of these categories were 33.1% to 43.1%, 11.1% to 21.6%, 3.6% to 8.1%, 16.3% to 23.6%, and 8.3% to 12.6%, respectively. When the colonoscopies that were performed by the 11 endoscopists who performed 30 examinations or more per center in 2 or more centers were separately analyzed, no intercenter statistically significant variability was observed with the exception of 1 endoscopist and the 1 adenoma category. In a subgroup of 1100 colonoscopies performed by 6 endoscopists who were working at the same 3 centers, intercenter variability was not statistically significant. LIMITATIONS: Type II error because of sample sizes. CONCLUSIONS: In our setting, intercenter variability did not explain interendoscopist variability for neoplasia detection rate.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Adenoma / Instalações de Saúde Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Adenoma / Instalações de Saúde Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Aged / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2011 Tipo de documento: Article