Knabe Mate, Heilani Myriam, Wetzka Jens, Welsch Lukas, Dultz Georg, Aschmoneit-Messer Insa, Herrmann Eva, Zeuzem Stefan, May Andrea
Center Gastroenterology Bethanien Bethanien Hospital Frankfurt, Frankfurt, Germany.
Department of Internal Medicine I, Hospital of the Goethe University Frankfurt, Frankfurt, Germany.
Clin Endosc. 2025 Jul;58(4):569-576. doi: 10.5946/ce.2024.308. Epub 2025 Jul 7.
Deep enteroscopy is a challenging and time-consuming procedure. Two devices have become the clinical standards for patients: double-balloon enteroscopy (DBE) and motorized spiral enteroscopy (mSPE). Initially, mSPE demonstrated impressive results, with high rates of total enteroscopy, which were superior to those of all other devices. However, for safety reasons, mSPE was withdrawn from the market, and it remains uncertain whether it will return after technical improvements. This prospective randomized trial aimed to compare the DBE and mSPE.
Patients indicated for enteroscopy were randomized to undergo either mSPE or DBE. The time to diagnosis or complete enteroscopy was measured, and all complications were recorded.
A total of 48 enteroscopic procedures were performed, including 23 mSPE and 25 DBE. No significant difference was noted in the procedure time (p=0.212). The mSPE group exhibited a shorter mean procedure time of 54 (range, 15-114; standard deviation [SD], 26) minutes, whereas the DBE group had a mean procedure time of 63 (range, 20-131; SD, 25) minutes. One perforation was seen in the mSPE group.
DBE and mSPE are both effective enteroscopy methods but showed no significant difference in this randomized trial (German trial registry: DRKS 00025890).
深度肠镜检查是一项具有挑战性且耗时的操作。有两种设备已成为针对患者的临床标准:双气囊小肠镜(DBE)和电动螺旋小肠镜(mSPE)。最初,mSPE显示出令人印象深刻的结果,全小肠检查率很高,优于所有其他设备。然而,出于安全原因,mSPE已退出市场,技术改进后是否会重新上市仍不确定。这项前瞻性随机试验旨在比较DBE和mSPE。
被指定进行肠镜检查的患者被随机分配接受mSPE或DBE检查。测量诊断或完成肠镜检查的时间,并记录所有并发症。
共进行了48例肠镜检查操作,包括23例mSPE和25例DBE。操作时间无显著差异(p = 0.212)。mSPE组的平均操作时间较短,为54(范围15 - 114;标准差[SD],26)分钟,而DBE组的平均操作时间为63(范围20 - 131;SD,25)分钟。mSPE组出现1例穿孔。
DBE和mSPE都是有效的肠镜检查方法,但在这项随机试验中未显示出显著差异(德国试验注册:DRKS 00025890)。