Barbara L, Roda E, Roda A, Casanova S, Festi D, Sama C, Mazella G, Aldini R
Minerva Med. 1977 Oct 17;68(49):3355-82.
The results of a tiral using chenodeoxycholic acid in 400 patients with cholesterol gallstones are reported. The "qualifying points" of such treatment are compared with the literature data in clinical and laboratory terms. 54% of 300 in clinical and laboratory terms. 54% of 300 patients who received less than 12 mg/kg/day achieved dissolution in a mean time of 11 months, while 64% of the remainder (12-15 mg/kg/day) did so in an average of 8 months. Microcalculi proved most sensitive to treatment (65% of positive results). Lithiasis over 5 years standing and over-weight (10% over the ideal figure) were factors that imposed more protracted treatment. Careful selection of candidates was proved important by the results of quarterly liver and intestine performance examinations. These were more extensive and more clearly aimed than those proposed by other workers. They showed that the acid is neither hepato nor enterotoxic. Indeed, no serious side-effects were noted.
报告了一项在400例胆固醇结石患者中使用鹅去氧胆酸的试验结果。从临床和实验室角度将这种治疗的“合格点”与文献数据进行了比较。在临床和实验室方面,300例患者中,每日剂量低于12mg/kg的患者有54%在平均11个月的时间内结石溶解,而其余患者(每日剂量为12 - 15mg/kg)中有64%在平均8个月内结石溶解。微结石对治疗最为敏感(阳性结果占65%)。病程超过5年的结石病和超重(超过理想体重10%)是需要进行更长疗程治疗的因素。季度肝肠功能检查结果证明,仔细挑选候选患者很重要。这些检查比其他研究者提出的检查更全面、目标更明确。检查表明该酸既无肝毒性也无肠毒性。实际上,未观察到严重的副作用。