Neoplasia detection rates after positive fecal occult blood test results are not affected by endoscopy center: a population-based study

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 Second...

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Veröffentlicht in:Gastrointestinal endoscopy 2011-07, Vol.74 (1), p.141-147
Hauptverfasser: Bretagne, Jean-François, PhD, Hamonic, Stéphanie, MSc, Piette, Christine, MD, Manfredi, Sylvain, PhD, Mallard, Gaud, MD, Durand, Gérard, MD, Riou, Françoise, PhD
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Sprache:eng
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Zusammenfassung: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.
ISSN:0016-5107
1097-6779
DOI:10.1016/j.gie.2011.03.1179