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SYSTEMIC LUPUS ERYTHEMATOSUS—Results of Treatment with Triamcinolone

机译:系统性红斑狼疮—曲安奈德治疗的结果

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摘要

Twenty-nine patients with systemic lupus erythematosus were treated with a new synthetic unsaturated prednisolone derivative, triamcinolone, for as long as 11 months. This hormone is 1.3 times as powerful as prednisone and 4.4 times more potent than hydrocortisone as an anti-inflammatory agent. The average dose for beginning therapy in cases of mild systemic lupus erythematosus was 20.6 mg. a day. The average maintenance dose used to control mild exacerbations of the disease was 26.0 mg. a day. There was no evidence of sodium retention or potassium loss.Sixteen patients had upper gastrointestinal x-ray studies before and during therapy with triamcinolone. There was no evidence of peptic ulceration except in one patient who was receiving 96 mg. a day. Nine patients had gastric analysis with histamine before and during therapy. No significant changes were noted in results of these tests, even in the patient who had an ulcer. No abnormal increase in uropepsin was noted in cases in which this factor was tested.The pattern of clinical improvement closely paralleled that obtained by previous treatment with older steroids. There was a disappearance of all the clinical and laboratory abnormalities produced by the disease, with the exception of long standing renal involvement. A major difference between triamcinolone and other steroids was a tendency to progressive gradual loss of weight, partly owing to fluid loss. Cushingoid appearance produced by other steroid therapy did not disappear.The cutaneous side effects, particularly Cushingoid appearance, hirsutism and striae were more pronounced than with older steroids. The most serious side effect was muscle weakness which appeared in six patients, all women, in from four to thirty-two weeks after starting triamcinolone. The profound muscle weakness, most pronounced in the quadriceps group, gradually cleared after several weeks of therapy with another steroid.Fourteen patients had received prior steroid therapy with all the older anti-inflammatory hormones and seven of them were better controlled and felt better with triamcinolone.
机译:用新的合成不饱和泼尼松龙衍生物曲安西龙治疗29例系统性红斑狼疮患者长达11个月。这种激素的功效是强的松的1.3倍,而抗氢化剂的功效是氢化可的松的4.4倍。轻度系统性红斑狼疮患者开始治疗的平均剂量为20.6 mg。一天。用于控制疾病轻度加重的平均维持剂量为26.0 mg。一天。没有证据表明钠retention留或钾丢失。十六名患者在曲安西龙治疗之前和期间接受了上消化道X线检查。除一名接受96 mg的患者外,没有消化性溃疡的证据。一天。 9名患者在治疗之前和治疗期间接受了组胺的胃部分析。这些测试的结果没有发现明显的变化,即使在患有溃疡的患者中也是如此。在测试该因子的情况下,未观察到尿素蛋白酶异常增加。临床改善的模式与以前使用较老的类固醇治疗所获得的模式非常相似。除了长期受累的肾脏外,该疾病产生的所有临床和实验室异常均已消失。曲安西龙与其他类固醇之间的主要区别是体重逐渐减少的趋势,部分是由于体液减少。其他类固醇疗法产生的库欣类药物外观并未消失,皮肤副作用,尤其是库欣类药物外观,多毛症和纹状体均比老年类固醇药物更为明显。最严重的副作用是在开始曲安西龙后的四到三十二周内,六名患者(所有妇女)出现了肌肉无力。股四头肌组中最明显的肌肉无力现象在用另一种类固醇激素治疗数周后逐渐消失。十四名患者以前接受过所有较老的抗炎激素的类固醇激素治疗,其中七种使用曲安奈德可以更好地控制和感觉好转。 。

著录项

  • 期刊名称 California Medicine
  • 作者

    Edmund L. Dubois;

  • 作者单位
  • 年(卷),期 1958(89),3
  • 年度 1958
  • 页码 195–203
  • 总页数 9
  • 原文格式 PDF
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