Mutignani M, Tringali A, Shah S G, Perri V, Familiari P, Iacopini F, Spada C, Costamagna G
Digestive Endoscopy Unit, Catholic University, Rome, Italy.
Endoscopy. 2007 May;39(5):440-7. doi: 10.1055/s-2007-966327.
Self-expandable metal stents (SEMS) are an effective palliative treatment for malignant biliary and duodenal strictures. Combined biliary and duodenal stenting remains a technical challenge, however. The aim of this study was to evaluate the technical feasibility of an endoscopic approach to double stenting of malignant biliary and duodenal strictures.
Consecutive patients referred for palliative gastroduodenal and biliary stenting were followed up prospectively. Patients' demographic characteristics, the site and nature of the strictures, success rates, complications, and survival time were recorded.
A total of 64 patients underwent double stenting. In 46 patients, biliary obstruction occurred before the onset of duodenal obstruction (by a median of 107 days) (group 1); in 14 patients, biliary obstruction occurred concurrently with duodenal obstruction (group 2); and in four patients the duodenal obstruction preceded the biliary obstruction (by a median of 121 days) (group 3). The duodenal strictures were proximal to the papilla in 31 patients, adjacent to the papilla in 25 patients and distal to the papilla in eight patients. The majority of biliary strictures were in the middle or distal third of the bile duct (in 52/64 patients). Duodenal SEMS were successfully deployed in all patients. Combined endoscopic stenting was successful in 100% of patients in group 1, 86% of patients in group 2, and in 100% of patients in group 3. Taking the three groups together, early complications occurred in 6% of patients and late complications occurred in 16% of patients. The overall median survival after combined stenting was 81 days (range 2-447 days).
Combined endoscopic biliary and duodenal SEMS insertion is safe and effective for palliation in malignant biliary and duodenal obstruction. Biliary stenting through the mesh of the duodenal SEMS is technically feasible and has a high success rate.
自膨式金属支架(SEMS)是治疗恶性胆管和十二指肠狭窄的一种有效姑息治疗方法。然而,联合胆管和十二指肠支架置入术仍然是一项技术挑战。本研究的目的是评估内镜下对恶性胆管和十二指肠狭窄进行双支架置入术的技术可行性。
对连续接受姑息性胃十二指肠和胆管支架置入术的患者进行前瞻性随访。记录患者的人口统计学特征、狭窄的部位和性质、成功率、并发症及生存时间。
共有64例患者接受了双支架置入术。46例患者胆管梗阻发生在十二指肠梗阻之前(中位时间为107天)(第1组);14例患者胆管梗阻与十二指肠梗阻同时发生(第2组);4例患者十二指肠梗阻先于胆管梗阻(中位时间为121天)(第3组)。31例患者的十二指肠狭窄位于乳头近端,25例患者的十二指肠狭窄与乳头相邻,8例患者的十二指肠狭窄位于乳头远端。大多数胆管狭窄位于胆管的中下段(64例患者中的52例)。所有患者十二指肠SEMS均成功置入。联合内镜支架置入术在第1组100%的患者、第2组86%的患者和第3组100%的患者中成功。三组患者总体而言,早期并发症发生率为6%,晚期并发症发生率为16%。联合支架置入术后的总体中位生存期为81天(范围为2 - 447天)。
内镜下联合胆管和十二指肠SEMS置入术对恶性胆管和十二指肠梗阻的姑息治疗是安全有效的。通过十二指肠SEMS的网孔进行胆管支架置入术在技术上是可行的,且成功率高。