van Berge Henegouwen M I, van Gulik T M, Akkermans L M, Jansen J B, Gouma D J
Department of Surgery, University of Amsterdam, The Netherlands.
Gut. 1997 Dec;41(6):758-62. doi: 10.1136/gut.41.6.758.
Octreotide is used in many centres to prevent complications after pancreatic surgery. Delayed gastric emptying is a another complication occurring in around 30% of patients after pancreatoduodenectomy (PD) and causes prolonged hospital stay. The influence of octreotide on this complication is doubtful.
To assess the effect of octreotide, at the clinical dosage used after pancreatic surgery, on gastric emptying in healthy volunteers.
Eight healthy male volunteers (mean age 22.5 years) participated in this double blind, placebo controlled study. On day 1 subjects received 100 micrograms of octreotide or placebo subcutaneously, three times daily and on day 2, one hour after the fourth injection, gastric emptying, postprandial cholecystokinin (CCK) release, and mouth to caecum transit time (MCTT) were measured. This protocol was repeated after one week, in a crossover design. On the test day subjects received a liquid test meal (1.57 MJ/300 ml) and gastric emptying measurements were performed with applied potential tomography, an non-invasive, validated technique which measures gastric emptying through impedance differences. From the gastric emptying curves, lag time, t50, and postlag emptying rate were measured. MCTT was measured using the hydrogen breath test.
Lag time decreased from 29.6 (6.3) (mean (SEM)) to 12.2 (4.6) minutes (p < 0.05) during octretide treatment; t50 decreased from 87.8 (12.0) to 47.5 (8.2) minutes (p < 0.02) and there was a trend towards an increased postlag emptying rate (0.8 to 1.6% per minute; p = 0.07). MCTT increased from 150 (12.7) to 229 (17.9) minutes during octreotide treatment (p < 0.01). Octreotide suppressed postprandial CCK release (p < 0.05).
MCTT was delayed by octreotide, suggesting impairment of small bowl treatment. Octreotide administered at the clinical dosage for pancreatic surgery accelerates gastric emptying, mainly by shortening the lag time. Suppression of postprandial CCK release may be involved in this process. Octreotide administration is therefore not a contributing factor in the pathogenesis of delayed postoperative gastric emptying after PD and might even play a role in preventing this complication.
许多中心使用奥曲肽预防胰腺手术后的并发症。胃排空延迟是胰十二指肠切除术(PD)后约30%的患者出现的另一种并发症,会导致住院时间延长。奥曲肽对这种并发症的影响尚不确定。
评估胰腺手术后临床使用剂量的奥曲肽对健康志愿者胃排空的影响。
8名健康男性志愿者(平均年龄22.5岁)参与了这项双盲、安慰剂对照研究。第1天,受试者皮下注射100微克奥曲肽或安慰剂,每日3次,第2天,在第4次注射后1小时,测量胃排空、餐后胆囊收缩素(CCK)释放及口至盲肠转运时间(MCTT)。一周后采用交叉设计重复该方案。在测试日,受试者摄入一份液体测试餐(1.57兆焦/300毫升),并应用电位断层扫描技术进行胃排空测量,这是一种通过阻抗差异测量胃排空的无创且经过验证的技术。从胃排空曲线中测量滞后时间、t50以及滞后后排空率。使用氢呼气试验测量MCTT。
在奥曲肽治疗期间,滞后时间从29.6(6.3)(平均值(标准误))分钟降至12.2(4.6)分钟(p<0.05);t50从87.8(12.0)分钟降至47.5(8.2)分钟(p<0.02),且滞后后排空率有增加趋势(从每分钟0.8%增至1.6%;p=0.07)。在奥曲肽治疗期间,MCTT从150(12.7)分钟增至229(17.9)分钟(p<0.01)。奥曲肽抑制餐后CCK释放(p<0.05)。
奥曲肽使MCTT延迟,提示小肠处理功能受损。胰腺手术临床剂量的奥曲肽主要通过缩短滞后时间加速胃排空。餐后CCK释放受抑制可能参与了这一过程。因此,奥曲肽给药并非PD术后胃排空延迟发病机制中的一个促成因素,甚至可能在预防这一并发症中发挥作用。