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1.
Dig Dis Sci ; 52(10): 2892-6, 2007 Oct.
Article de Anglais | MEDLINE | ID: mdl-17394073

RÉSUMÉ

The aim of this prospective study was to assess patient comfort during nonsedated screening sigmoidoscopy with the use of a standard 60-cm sigmoidoscope compared with a thinner 100-cm upper endoscope. Patients undergoing routine colon cancer screening with sigmoidoscopy were randomly assigned to either a 60-cm sigmoidoscope or a 100-cm upper endoscope. The procedure time, depth of insertion, anatomic landmarks, and presence of polyps were documented. Likert 7-point scales and visual analog scales (VAS) were performed to measure comfort and symptoms immediately after the procedure and again in 1 week. These scales, procedure time, insertion depth, percent reaching transverse colon, and percent with polyps were analyzed. Eighty-one patients were enrolled with 38 in the 100-cm group and 43 in the 60-cm group. Patients in the 100-cm group reported greater comfort on the VAS compared with the 60-cm group (P = .035) as well as less cramping on the initial Likert scale (P = .017). One week later, the 100-cm group reported higher comfort (P = .015) and less bloating (P = .040). Procedure time was longer for the 100-cm group (8.8 versus 5.9 minutes; P = .001). Insertion depth was 74 versus 56 cm (P = .001), and percent reaching splenic flexure was 76% versus 35% (P = .001) in the 100 and 60 cm groups, respectively. More adenomas were found with the 100-cm scope (P = .035). The use of a thinner and longer endoscope is more comfortable than a standard sigmoidoscope. Although a 100-cm endoscope procedure takes longer to perform, it allows better evaluation of the colon and misses fewer adenomas.


Sujet(s)
Tumeurs du côlon/diagnostic , Satisfaction des patients , Sigmoïdoscopes/normes , Rectosigmoïdoscopie/méthodes , Conception d'appareillage , Femelle , Études de suivi , Humains , Mâle , Adulte d'âge moyen , Études prospectives , Reproductibilité des résultats
2.
Surg Endosc ; 17(6): 896-8, 2003 Jun.
Article de Anglais | MEDLINE | ID: mdl-12632138

RÉSUMÉ

The purpose of this study was to establish construct validation of a flexible sigmoidoscopy simulator by comparing training-level grouped subjects. These included clerical staff (n = 10), residents (n = 19), and experts (n = 5). Each participant performed 3 scopes. The ANOVA group-based results for trainer-measured variables are shown in Table 1. These results demonstrate that the flexible sigmoidoscopy simulator distinguished the trained from the untrained and the resident from the expert. Although there was no statistically significant differences between the senior residents and the experts, the expert commonly outperformed the residents. Establishing the transferability of simulator training to real life is next. If the transfer of skill can be established, it may give rise to a new skills training approach.


Sujet(s)
Compétence clinique/normes , Simulation numérique/normes , Rectosigmoïdoscopie/normes , Personnel administratif/classification , Personnel administratif/normes , Personnel administratif/statistiques et données numériques , Compétence clinique/statistiques et données numériques , Simulation numérique/statistiques et données numériques , Humains , Internat et résidence/classification , Internat et résidence/normes , Internat et résidence/statistiques et données numériques , Personnel médical hospitalier/classification , Personnel médical hospitalier/statistiques et données numériques , Personnel médical hospitalier/tendances , Médecins de famille/classification , Médecins de famille/normes , Médecins de famille/statistiques et données numériques , Sigmoïdoscopes/normes , Sigmoïdoscopes/statistiques et données numériques , Sigmoïdoscopes/tendances , Rectosigmoïdoscopie/méthodes , Rectosigmoïdoscopie/statistiques et données numériques , Logiciel/normes , Validation de logiciel
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