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[长期使用奥曲肽(SMS 201-995)治疗的肢端肥大症患者胆汁生成结石的影响]

[Effects of biliary lithogenesis in acromegalic patients with long-term octreotide (SMS 201-995) treatment].

作者信息

Buscail L E, Puel-Bousquet C, Harris A G, Tauber J P, Escourrou J R, Delvaux M M, Vaysse N M, Bayard F, Ribet A

机构信息

Clinique des Maladies de l'Appareil Digestif et INSERM U151, CHU Rangueil, Toulouse.

出版信息

Gastroenterol Clin Biol. 1991;15(11):800-4.

PMID:1769469
Abstract

This study was performed to evaluate the risk of gallstone formation during long-term treatment with the long-acting somatostatin analog octreotide (SMS 201-995). Twelve patients (8 men, 4 women--mean age 43 years) treated with continuous subcutaneous octreotide infusion for acromegaly (mean duration 26.5 months, mean dose 541 micrograms/day) were included. Bile collection by duodenal intubation was performed before, during, and 45 days after octreotide treatment in 3, 12, and 8 patients, respectively. Abdominal ultrasonography and/or oral cholecystrography were also performed before (n = 9 patients), during (n = 12), and after treatment (n = 10). Bile examination was normal in the 3 patients controlled before treatment but showed that 58.3 percent of the treated patients had cholesterol monohydrate crystals. After discontinuation of octreotide only 25 percent of patients had cholesterol crystals. In 3 patients (25 percent) treated longer than 6 months, cholesterol crystals occurred prior to the occurrence of small radiolucent gallstones: one patient underwent cholecystectomy because of biliary colic, while in the two others, complete dissolution of stones was obtained after 10 months of treatment with ursodeoxycholic acid given in association with octreotide. None of the 9 other acromegalic patients (including 7 treated more than 20 months) developed stones. Cholesterol gallstone formation seems to be increased in acromegalic patients during long-term octreotide treatment but the exact incidence remains to be determined in larger series of patients.

摘要

本研究旨在评估长效生长抑素类似物奥曲肽(SMS 201-995)长期治疗期间胆结石形成的风险。纳入了12例接受奥曲肽皮下持续输注治疗肢端肥大症的患者(8例男性,4例女性,平均年龄43岁)(平均治疗时长26.5个月,平均剂量541微克/天)。分别在3例、12例和8例患者中于奥曲肽治疗前、治疗期间及治疗后45天通过十二指肠插管收集胆汁。在治疗前(9例患者)、治疗期间(12例)及治疗后(10例)还进行了腹部超声检查和/或口服胆囊造影。治疗前接受检查的3例患者胆汁检查正常,但显示58.3%的接受治疗患者有一水合胆固醇晶体。停用奥曲肽后,只有25%的患者有胆固醇晶体。在3例(25%)治疗超过6个月的患者中,胆固醇晶体在小的透光性胆结石出现之前就已出现:1例患者因胆绞痛接受了胆囊切除术,而另外2例患者在与奥曲肽联合使用熊去氧胆酸治疗10个月后结石完全溶解。其他9例肢端肥大症患者(包括7例治疗超过20个月的患者)均未形成结石。在肢端肥大症患者长期奥曲肽治疗期间胆固醇胆结石形成似乎增加,但确切发生率仍有待在更多患者系列中确定。

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