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Efficacy and safety of biodegradable stents for refractory benign esophageal strictures: The BEST (Biodegradable Esophageal Stent) study

Articolo
Data di Pubblicazione:
2010
Citazione:
Efficacy and safety of biodegradable stents for refractory benign esophageal strictures: The BEST (Biodegradable Esophageal Stent) study / Repici, A.; Vleggaar, F. P.; Hassan, C.; Van Boeckel, P. G.; Romeo, F.; Pagano, N.; Malesci, A.; Siersema, P. D.. - In: GASTROINTESTINAL ENDOSCOPY. - ISSN 0016-5107. - 72:5(2010), pp. 927-934. [10.1016/j.gie.2010.07.031]
Abstract:
Background Benign esophageal strictures refractory to standard dilation therapy present a challenging problem. Temporary plastic and metal stents have been proposed with inconclusive results. Objective To evaluate the efficacy and safety of a new biodegradable stent for the treatment of refractory benign esophageal strictures (RBESs). Design and Setting Prospective study from 2 European endoscopy centers. Patients and Intervention Twenty-one patients (11 men/10 women, mean age 60.2 ± 17.6 years) with RBESs defined according to the Kochman criteria treated by placement of a biodegradable stent (Ella stent). Main Outcome Measurements Clinical and endoscopic follow-up was scheduled at 1, 2, 3, and 6 months and later only in case of dysphagia recurrence. Pre- and poststenting dysphagia status was graded according to a 5-point scale. Minor and major complication rates were prospectively assessed. Results Stent insertion was technically successful in all of the patients. At 4 and 7 weeks, stent migration occurred in 2 patients (9.5%). At 3-month endoscopy, the stent appeared to be almost completely fragmented in all remaining patients. The median pre- and poststenting dysphagia scores were 3 (range 3-4) and 1 (range 0-2), respectively (P < .01), with a median follow-up of 53 weeks (range 25-88 weeks). In detail, 9 of 20 patients (45%) were dysphagia free at the end of the follow-up. No major complications occurred. Severe poststenting pain requiring analgesics developed in 3 patients, and minor bleeding was observed in 1 patient. Limitations Limited follow-up; nonrandomized study. Conclusions In this preliminary study, the biodegradable stent showed a favorable risk/benefit ratio, achieving complete relief of dysphagia in nearly 50% of RBES patients without the occurrence of major complications. The use of this stent may be a valuable alternative to repeat endoscopic dilation. Larger studies with longer follow-up are needed.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Repici, A.; Vleggaar, F. P.; Hassan, C.; Van Boeckel, P. G.; Romeo, F.; Pagano, N.; Malesci, A.; Siersema, P. D.
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/181096
Pubblicato in:
GASTROINTESTINAL ENDOSCOPY
Journal
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URL

https://www.giejournal.org/article/S0016-5107(10)01901-2/abstract
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