Krogsgaard M R, Lund B, Johnsson B
Department of Internal Medicine, Deaconess House Saint Luke's Foundation's Hospital, Hellerup, Denmark.
J Rheumatol. 1995 Sep;22(9):1660-2.
The aim of the study was to establish the antiinflammatory equipotency between prednisolone and deflazacort.
Thirty patients with newly diagnosed polymyalgia rheumatica (PMR) were treated double blind with either prednisolone or deflazacort in a 12-month study. The initial daily dose was 20 mg prednisolone or 24 mg deflazacort.
The clinical control of muscle pain was significantly inferior in the deflazacort group from 6 weeks to 3 months. Otherwise there was no difference in the clinical and biochemical variables. The ratio between antiinflammatory equipotent doses of deflazacort and prednisolone (mg:mg) stabilized at about 1.55 for the daily doses and about 1.40 for the cumulative doses.
In PMR the antiinflammatory equipotency (mg to mg) between deflazacort and prednisolone was close to 1.40 (7:5 mg). Twenty mg prednisolone/day was fully sufficient to suppress symptoms in 94% of the patients.
本研究的目的是确定泼尼松龙与地夫可特之间的抗炎等效性。
在一项为期12个月的研究中,30例新诊断的风湿性多肌痛(PMR)患者被随机分为两组,分别接受泼尼松龙或地夫可特的双盲治疗。初始每日剂量为20mg泼尼松龙或24mg地夫可特。
地夫可特组在6周~3个月时肌肉疼痛的临床控制明显较差。除此之外,临床和生化指标没有差异。地夫可特与泼尼松龙的抗炎等效剂量之比(mg:mg),每日剂量稳定在约1.55,累积剂量稳定在约1.40。
在PMR中,地夫可特与泼尼松龙之间的抗炎等效性(mg:mg)接近1.40(7:5mg)。20mg/天的泼尼松龙足以使94%的患者症状得到缓解。