Department of Gastroenterology, National Clinical Research Center for Digestive Diseases, Changhai Hospital, Shanghai, 200433, China.
Department of Gastroenterology, The First Naval Hospital of Southern Theater Command, Zhanjiang, 524005, Guangdong, China.
BMC Gastroenterol. 2023 Mar 16;23(1):76. doi: 10.1186/s12876-023-02696-5.
Complete and consecutive observation of the gastrointestinal (GI) tract continues to present challenges for current endoscopy systems. We developed a novel upper and mid gastrointestinal (UMGI) capsule endoscopy using the modified detachable string magnetically controlled capsule endoscopy (DS-MCE) and inspection method and aimed to assess the clinical application.
Patients were recruited to undergo UMGI capsule endoscopy followed by esophagogastroduodenoscopy. All capsule procedures in the upper gastrointestinal (UGI) tract were conducted under the control of magnet and string. The main outcome was technical success, and the secondary outcomes included visualization of the UMGI tract, examination time, diagnostic yield, compliance, and safety evaluation.
Thirty patients were enrolled and all UMGI capsule procedures realized repeated observation of the esophagus and duodenum with detection rates of 100.0%, 80.0%, and 86.7% of Z-line, duodenal papilla, and reverse side of pylorus, respectively. String detachment was succeeded in 29 patients (96.7%) and the complete examination rate of UMGI tract was 95.45% (21/22). All UMGI capsule procedures were well tolerated with low discomfort score, and had a good diagnostic yield with per-lesion sensitivity of 96.2% in UGI diseases. No adverse events occurred.
This new capsule endoscopy system provides an alternative screening modality for the UMGI tract, and might be indicated in cases of suspected upper and small bowel GI bleeding. Trial registration DS-MCE-UGI and SB, NCT04329468. Registered 27 March 2020, https://clinicaltrials.gov/ct2/results?cond=&term=NCT04329468 .
目前的内镜系统在对胃肠道(GI)进行完整、连续观察时仍面临挑战。我们开发了一种新型上消化道和中消化道(UGI)胶囊内镜,采用改良的可拆卸式磁控胶囊内镜(DS-MCE)和检查方法,并旨在评估其临床应用。
招募患者进行 UMGI 胶囊内镜检查,随后进行食管胃十二指肠镜检查。上消化道(UGI)内的所有胶囊程序均在磁体和线的控制下进行。主要结果是技术成功,次要结果包括 UMGI 道的可视化、检查时间、诊断率、顺应性和安全性评估。
共纳入 30 例患者,所有 UMGI 胶囊程序均能重复观察食管和十二指肠,Z 线、十二指肠乳头和幽门反侧面的检出率分别为 100.0%、80.0%和 86.7%。29 例患者(96.7%)成功实现了线的脱离,UGI 道的完整检查率为 95.45%(21/22)。所有 UMGI 胶囊程序均能耐受,不适感评分较低,且对 UGI 疾病的病变具有较高的诊断率,病变内的敏感度为 96.2%。未发生不良事件。
这种新型胶囊内镜系统为 UMGI 道提供了一种替代筛查方法,可能适用于疑似上消化道和小肠 GI 出血的病例。
DS-MCE-UGI 和 SB,NCT04329468。注册日期:2020 年 3 月 27 日,https://clinicaltrials.gov/ct2/results?cond=&term=NCT04329468。