Yeo C J, Cameron J L, Lillemoe K D, Sauter P K, Coleman J, Sohn T A, Campbell K A, Choti M A
Department of Surgery, Johns Hopkins Hospital, Baltimore, Maryland 21287-4606, USA.
Ann Surg. 2000 Sep;232(3):419-29. doi: 10.1097/00000658-200009000-00014.
To evaluate the endpoints of complications (specifically pancreatic fistula and total complications) and death in patients undergoing pancreaticoduodenectomy.
Four randomized, placebo-controlled, multicenter trials from Europe have evaluated prophylactic octreotide (the long-acting synthetic analog of native somatostatin) in patients undergoing pancreatic resection. Each trial reported significant decreases in overall complication rates, and two of the four reported significantly lowered rates of pancreatic fistula in patients receiving prophylactic octreotide. However, none of these four trials studied only pancreaticoduodenal resections, and all trials had high pancreatic fistula rates (>19%) in the placebo group. A fifth randomized trial from the United States evaluated the use of prophylactic octreotide in patients undergoing pancreaticoduodenectomy and found no benefit to the use of octreotide. Prophylactic use of octreotide adds more than $75 to the daily hospital charge in the United States. In calendar year 1996, 288 patients received octreotide on the surgical service at the authors' institution, for total billed charges of $74,652.
Between February 1998 and February 2000, 383 patients were recruited into this study on the basis of preoperative anticipation of pancreaticoduodenal resection. Patients who gave consent were randomized to saline control versus octreotide 250 microg subcutaneously every 8 hours for 7 days, to start 1 to 2 hours before surgery. The primary postoperative endpoints were pancreatic fistula, total complications, death, and length of hospital stay.
Two hundred eleven patients underwent pancreaticoduodenectomy with pancreatic-enteric anastomosis, received appropriate saline/octreotide doses, and were available for endpoint analysis. The two groups were comparable with respect to demographics (54% male, median age 66 years), type of pancreaticoduodenal resection (60% pylorus-preserving), type of pancreatic-enteric anastomosis (87% end-to-side pancreaticojejunostomy), and pathologic diagnosis. The pancreatic fistula rates were 9% in the control group and 11% in the octreotide group. The overall complication rates were 34% in the control group and 40% in the octreotide group; the in-hospital death rates were 0% versus 1%, respectively. The median postoperative length of hospital stay was 9 days in both groups.
These data demonstrate that the prophylactic use of perioperative octreotide does not reduce the incidence of pancreatic fistula or total complications after pancreaticoduodenectomy. Prophylactic octreotide use in this setting should be eliminated, at a considerable cost savings.
评估接受胰十二指肠切除术患者的并发症(特别是胰瘘和总体并发症)及死亡终点。
欧洲的四项随机、安慰剂对照、多中心试验评估了预防性使用奥曲肽(天然生长抑素的长效合成类似物)对接受胰腺切除术患者的影响。每项试验均报告总体并发症发生率显著降低,四项试验中的两项报告接受预防性奥曲肽治疗的患者胰瘘发生率显著降低。然而,这四项试验均未仅研究胰十二指肠切除术,且所有试验的安慰剂组胰瘘发生率均较高(>19%)。美国的第五项随机试验评估了预防性使用奥曲肽对接受胰十二指肠切除术患者的影响,未发现使用奥曲肽有任何益处。在美国,预防性使用奥曲肽使每日住院费用增加超过75美元。1996年,作者所在机构的外科有288例患者接受了奥曲肽治疗,总收费为74,652美元。
1998年2月至2000年2月,基于术前预期进行胰十二指肠切除术,招募了383例患者纳入本研究。同意参与的患者被随机分为生理盐水对照组和奥曲肽组,奥曲肽组每8小时皮下注射250μg,共7天,于手术前1至2小时开始给药。术后主要终点为胰瘘、总体并发症、死亡和住院时间。
211例患者接受了胰十二指肠切除术并进行了胰肠吻合,接受了适当剂量的生理盐水/奥曲肽,可进行终点分析。两组在人口统计学特征(54%为男性,中位年龄66岁)、胰十二指肠切除术类型(60%为保留幽门)、胰肠吻合类型(87%为端侧胰管空肠吻合术)和病理诊断方面具有可比性。对照组胰瘘发生率为9%,奥曲肽组为11%。对照组总体并发症发生率为34%,奥曲肽组为40%;住院死亡率分别为0%和1%。两组术后中位住院时间均为9天。
这些数据表明,围手术期预防性使用奥曲肽并不能降低胰十二指肠切除术后胰瘘或总体并发症的发生率。在这种情况下,应停止预防性使用奥曲肽,可节省可观的费用。