Department of Gastroenterology and Hepatology, Tokyo Medical University, Tokyo, Japan.
Department of Gastroenterology and Hepatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Gastrointest Endosc. 2015 Jan;81(1):111-8. doi: 10.1016/j.gie.2014.09.046.
There are currently no prospective, controlled trials of endoscopic transpapillary gallbladder drainage in patients with acute cholecystitis.
We evaluated the technical success rate and efficacy of endoscopic transpapillary gallbladder drainage by using either endoscopic nasogallbladder drainage (ENGBD) or endoscopic gallbladder stenting (EGBS) for patients with acute cholecystitis.
Randomized, controlled study.
Tertiary-care referral centers.
Seventy-three consecutive patients with acute cholecystitis were randomized.
ENGBD by using a 5F or 7F tube (n = 37) or EGBS (n = 36) by using a 7F stent.
Technical success, clinical success, adverse events, and procedure-related pain score.
The overall technical success rates in the ENGBD and EGBS groups were 91.9% and 86.1%, respectively (P > .05). The mean procedure times of ENGBD and EGBS were 20.3 ± 12.1 and 22.2 ± 14.5 minutes, respectively (P > .05). The overall clinical success rates by per protocol analysis were 94.1% and 90.3% in the ENGBD and EGBS groups, respectively, whereas the rates by intention-to-treat analysis were 86.5% and 77.8%, respectively (P > .05). Moderate adverse events were observed in the ENGBD (n = 2) and EGBS (n = 1) groups. The mean visual analog score of postprocedure pain in the ENGBD group was significantly higher than that in the EGBS group (1.3 ± 1.1 vs 0.4 ± 0.8, respectively; P < .001).
Small sample size and the participation of multiple endoscopists who may have different levels of experience in endoscopic transpapillary gallbladder drainage.
Both ENGBD and EGBS appear to be suitable for the treatment of acute cholecystitis in patients who are poor candidates for emergency cholecystectomy. (
UMIN000012316.).
目前尚无急性胆囊炎内镜经乳头胆囊引流的前瞻性、对照试验。
我们通过内镜鼻胆管引流(ENGBD)或内镜胆囊支架置入术(EGBS)评估急性胆囊炎患者内镜经乳头胆囊引流的技术成功率和疗效。
随机对照研究。
三级转诊中心。
73 例连续急性胆囊炎患者随机分组。
使用 5F 或 7F 管进行 ENGBD(n = 37)或使用 7F 支架进行 EGBS(n = 36)。
技术成功率、临床成功率、不良事件和与操作相关的疼痛评分。
ENGBD 和 EGBS 组的总体技术成功率分别为 91.9%和 86.1%(P >.05)。ENGBD 和 EGBS 的平均手术时间分别为 20.3 ± 12.1 分钟和 22.2 ± 14.5 分钟(P >.05)。根据意向治疗分析,ENGBD 和 EGBS 组的总体临床成功率分别为 94.1%和 90.3%,而按方案分析的成功率分别为 86.5%和 77.8%(P >.05)。ENGBD(n = 2)和 EGBS(n = 1)组均观察到中度不良事件。ENGBD 组术后疼痛视觉模拟评分明显高于 EGBS 组(1.3 ± 1.1 与 0.4 ± 0.8,P <.001)。
样本量小,参与的内镜医师可能在经乳头胆囊引流方面经验水平不同。
ENGBD 和 EGBS 似乎均适用于不适合急诊胆囊切除术的急性胆囊炎患者的治疗。(临床试验注册号:UMIN000012316)。