Endoscopy 2023; 55(S 02): S109
DOI: 10.1055/s-0043-1765261
Abstracts | ESGE Days 2023
Oral presentation
Esophageal diseases – new wine in old barrels 22/04/2023, 13:00 – 14:00 Liffey Meeting Room 2

Efficacy and safety of Hybrid Argon Plasma Coagulation technique in patients with Barrett’s esophagus-related dysplasia: a multicenter italian prospective study initial results

R. Maselli
1   Humanitas Research Hospital, Cascina Perseghetto, Italy
,
D. Massimi
1   Humanitas Research Hospital, Cascina Perseghetto, Italy
,
A. Capogreco
1   Humanitas Research Hospital, Cascina Perseghetto, Italy
,
G. Andrisani
2   Bio-Medico Campus University Hospital, Roma, Italy
,
F. M. Di Matteo
2   Bio-Medico Campus University Hospital, Roma, Italy
,
S. Pecere
3   Agostino Gemelli University Policlinic, Rome, Italy
,
C. Spada
3   Agostino Gemelli University Policlinic, Rome, Italy
,
M. A. La Terra
4   San Giovanni Bosco Hospital, Turin, Italy
,
F. Coppola
4   San Giovanni Bosco Hospital, Turin, Italy
,
C. Hassan
1   Humanitas Research Hospital, Cascina Perseghetto, Italy
,
A. Repici
1   Humanitas Research Hospital, Cascina Perseghetto, Italy
› Author Affiliations
 
 

    Aims Preliminary data from a prospective, single-arm, multicenter observational study to evaluate the initial treatment success of the Hybrid-APC (H-APC) technique, which combines argon plasma coagulation (APC) with a previous saline injection for ablation therapy of neoplastic Barrett's esophagus (BE).

    Methods We prospectively collected data from 24 patients with BE (mean C of 0.64 SD 0,91 and M of 2.28 SD 1,15) who underwent H-APC therapy in 4 Italian hospitals. None of them had previous ablative therapy. Max 5 sessions to reach complete eradication of visible metaplasia and max 50% of the circumference treatment for each session were allowed. After 7 days from each session patients received a phone call to assess pain (0-10, 0=no pain, 10=worst pain) and dysphagia (1-5, 1=No dysphagia 5=unable to swallow anything)

    Results 43% of the patients were treated with endoscopic resection for visible lesion (50% PT1a; 50% HGD), while 57% started directly with ablation (81% LGD; 19 % HGD). CE-D and CE-IM were 100% and 100%, respectively after a mean of 1.5 ablation sessions. 67% of patients achieved primary outcome with just one treatment with a mean duration of 26 minutes SD 12.22. One case of temporary dysphagia, which did not require any treatment (4%) was observed without any other major adverse events and good tolerability profile: 93% of patients did not change their daily activities after treatment with a median pain score of 1,35 SD 2,00 and dysphagia score of 1,4 SD 0,74

    Conclusions H-APC appears to have high efficacy, safety, and tolerability profile, with a limited number of treatment sessions required to achieve initial CE-IM.


    #

    Conflicts of interest

    Medtronic consultantLaborie consultant3DMatrix consultantApollo Endosurgery consultantERBE consultantfujiflm consultant

    Publication History

    Article published online:
    14 April 2023

    © 2023. European Society of Gastrointestinal Endoscopy. All rights reserved.

    Georg Thieme Verlag KG
    Rüdigerstraße 14, 70469 Stuttgart, Germany