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World J Gastroenterol. Feb 14, 2007; 13(6): 906-911
Published online Feb 14, 2007. doi: 10.3748/wjg.v13.i6.906
Unsedated ultrathin upper endoscopy is better than conventional endoscopy in routine outpatient gastroenterology practice: A randomized trial
Lucio Trevisani, Viviana Cifalà, Sergio Sartori, Giuseppe Gilli, Giancarlo Matarese, Vincenzo Abbasciano
Lucio Trevisani, Viviana Cifalà, Sergio Sartori, Giancarlo Matarese, Vincenzo Abbasciano, Digestive Endoscopy Centre, Department of Internal Medicine, S. Anna Hospital, Ferrara, Italy
Giuseppe Gilli, Health Physics Department, S. Anna Hospital, Ferrara, Italy
Author contributions: All authors contributed equally to the work.
Correspondence to: Dr. Lucio Trevisani, Centro di Endoscopia Digestiva, Azienda Ospedaliera-Universitaria “Arcispedale S. Anna”, C.so Giovecca 203, Ferrara 44100, Italy. tvl@unife.it
Telephone: +39-532-237558 Fax: +39-532-236932
Received: October 16, 2006
Revised: November 1, 2006
Accepted: November 23, 2006
Published online: February 14, 2007
Abstract

AIM: to compare the feasibility and patients’ tolerance of esophagogastroduodenoscopy (EGD) using a thin endoscope with those of conventional oral EGD and to determine the optimal route of introduction of small-caliber endoscopes.

METHODS: One hundred and sixty outpatients referred for diagnostic EGD were randomly allocated to 3 groups: conventional (C)-EGD (9.8 mm in diameter), transnasal (TN)-EGD and transoral (TO)-EGD (5.9 mm in diameter). Pre-EGD anxiety was measured using a 100-mm visual analogue scale (VAS). After EGD, patients and endoscopists completed a questionnaire on the pain, nausea, choking, overall discomfort, and quality of the examination either using VAS or answering some questions. The duration of EGD was timed. Blood oxygen saturation (SaO2) and heart rate (HR) were monitored during EGD.

RESULTS: Twenty-one patients refused to participate in the study. The 3 groups were well-matched for age, gender, experience with EGD, and anxiety. EGD was completed in 91.1% (41/45), 97.5% (40/41), and 96.2% (51/53) of cases in TN-EGD, TO-EGD, and C-EGD groups, respectively. TN-EGD lasted longer (3.11 ± 1.60 min) than TO-EGD (2.25 ± 1.45 min) and C-EGD (2.49 ± 1.64 min) (P < 0.05). The overall tolerance was higher (P < 0.05) and the overall discomfort was lower (P < 0.05) in TN-EGD group than in C-EGD group. EGD was tolerated “better than expected” in 73.2% of patients in TN-EGD group and 55% and 39.2% of patients in TO-EGD and C-EGD groups, respectively (P < 0.05). Endoscopy was tolerated “worst than expected” in 4.9% of patients in TN-EGD group and 17.5% and 23.5% of patients in TO-EGD and C-EGD groups, respectively (P < 0.05). TN-EGD caused mild epistaxis in one case. The ability to insufflate air, wash the lens, and suction of the thin endoscope were lower than those of conventional instrument (P < 0.001). All biopsies performed were adequate for histological assessment.

CONCLUSION: Diagnostic TN-EGD is better tolerated than C-EGD. Narrow-diameter endoscope has a level of diagnostic accuracy comparable to that of conventional gastroscope, even though some technical characteristics of these instruments should be improved. Transnasal EGD with narrow-diameter endoscope should be proposed to all patients undergoing diagnostic EGD.

Keywords: Diagnotic esophagogastroduodenoscopy; Endoscopy; Gastroscopy