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奥曲肽长效注射剂治疗后肢端肥大症的改善情况。

Improvement of acromegaly after octreotide LAR treatment.

作者信息

Mangupli Ruth, Lisette Aponte, Ivett Contreras, Paul Camperos, de los Ríos Victoria Cruz, Luis Cevallos Jose

机构信息

Endocrinology and Metabolism Service, Caracas University Hospital, Caracas, Capital District, Venezuela.

出版信息

Pituitary. 2003;6(1):29-34. doi: 10.1023/a:1026277709967.

Abstract

Octreotide is a somatostatin analog that inhibits growth hormone release showing higher potency than natural somatostatin so it has proved to be effective in acromegaly treatment. The objective of present study was to establish the effects of octreotide LAR (long acting release) preparation in patients with active acromegaly. The following parameters were assessed: clinical response, safety of medication, GH and IGF-1 serum concentrations and pituitary tumor size. Eleven patients (6 men and 5 women) range 41.4 years old with diagnosis of active acromegaly were included. Octreotide was administered at 0.1 mg subcutaneusly dose three times daily for four weeks to test the drug tolerability. Afterwards patients received octreotide LAR 20 mg intramuscularly separated by 28 days periods with an option to continue for 8 months. Basal average GH serum concentrations was 27.6 ng/mL. After 6 months treatment reduction to 5.03 +/- 5.38 ng/mL in 9 patients (p < 0.001) was observed. Basal IGF-1 average serum concentration was 889.55 +/- 167.29 ng/mL with a reduction value to 483.00 +/- 239.71 ng/mL in 9 of 11 patients after 6 months treatment (p < 0.005). The drug was well tolerated with few adverse effects Diarrhea, flatulence and steatorrhea were observed during the administration of subcutaneous octreotide in 18.2% of patients. Two patients had symptomatic biliary lithiasis that was successfully removed by surgery. Clinical symptoms improved and some of them dissapeared such as headaches and sweatings. Tumor shrinkage was observed in 66.7% of cases. Monthly injections of 20 mg of octreotide LAR were effective to reduce GH and IGF-1 levels in patients with active acromegaly accompanied by improvement of clinical symptoms and significant tumor size reduction.

摘要

奥曲肽是一种生长抑素类似物,能抑制生长激素释放,其效力高于天然生长抑素,因此已被证明在肢端肥大症治疗中有效。本研究的目的是确定奥曲肽长效释放制剂对活动性肢端肥大症患者的影响。评估了以下参数:临床反应、药物安全性、生长激素(GH)和胰岛素样生长因子-1(IGF-1)血清浓度以及垂体肿瘤大小。纳入了11例诊断为活动性肢端肥大症的患者(6例男性和5例女性),年龄范围为41.4岁。皮下注射奥曲肽0.1毫克,每日3次,持续4周,以测试药物耐受性。之后,患者每28天接受一次20毫克的奥曲肽长效释放制剂肌肉注射,可选择持续8个月。基础GH血清平均浓度为27.6纳克/毫升。治疗6个月后,9例患者的GH浓度降至5.03±5.38纳克/毫升(p<0.001)。基础IGF-1血清平均浓度为889.55±167.29纳克/毫升,11例患者中有9例在治疗6个月后降至483.00±239.71纳克/毫升(p<0.005)。该药物耐受性良好,不良反应较少。在皮下注射奥曲肽期间,18.2%的患者出现腹泻、肠胃胀气和脂肪泻。2例患者出现有症状的胆结石,通过手术成功切除。临床症状有所改善,一些症状如头痛和出汗消失。66.

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