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首页> 外文期刊>International journal of clinical pharmacology and therapeutics >A comparison of non-tapering vs. tapering prednisolone in acute exacerbation of asthma involving use of the low-dose ACTH test.
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A comparison of non-tapering vs. tapering prednisolone in acute exacerbation of asthma involving use of the low-dose ACTH test.

机译:非锥形泼尼松龙与逐渐减量泼尼松龙在哮喘急性加重中的比较,涉及使用低剂量ACTH试验。

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OBJECTIVE: To determine if there is a difference in early relapse rates and adrenal suppression between patients receiving an 8-day course of 40 mg/day prednisolone and those receiving an 8-day tapering course of prednisolone. METHODS: This was a prospective, randomized, open clinical trial conducted in a tertiary care center. All asthmatic patients with exacerbation who were judged well enough for discharge home from the emergency department were eligible for participation. Patients with a history of chronic obstructive pulmonary disease, congestive heart failure, pneumonia, pneumothorax, or other pulmonary process and asthmatics already using inhaled or oral steroids within 2 weeks of admission to the emergency department were excluded. Patients on discharge were administered either on 8-day course of 40 mg/day prednisolone or an 8-day tapering course of prednisolone (tapering from 40 mg to 0 mg). Patients were asked to return on Day 12 for cosyntropin stimulated test and pulmonary function testing and on Day 21 for pulmonary function testing only. RESULTS: A group of 13 patients treated with non-tapering course (40 mg/day) of prednisolone for 8 days were compared to a group of 13 patients treated with a tapering course (40 mg taper by 5 mg/day) for 8 days. There were no differences in the FEV1 percent predicted (Days 12 and 21), the incidence of relapse, or the incidence of adrenal suppression between the 2 groups. CONCLUSION: In this small study, we found no significant difference in relapse rate or adrenal suppression between asthmatics receiving an 8-day tapering dose of prednisolone and those receiving 40 mg/day prednisolone upon discharge from the emergency department.
机译:目的:确定接受泼尼松龙40 mg /天的8天疗程和接受泼尼松龙8天减量疗程的患者的早期复发率和肾上腺抑制作用是否存在差异。方法:这是在三级护理中心进行的前瞻性,随机,开放性临床试验。所有被判断为可以从急诊科出院的哮喘加重急性发作患者都有资格参加。排除有慢性阻塞性肺疾病,充血性心力衰竭,肺炎,气胸或其他肺部疾病史并在入急诊科后两周内已使用吸入或口服类固醇的哮喘患者。出院患者以40 mg /天泼尼松龙的8天疗程或泼尼松龙的8天逐渐减量疗程(从40 mg减至0 mg)给药。要求患者在第12天返回以进行促肾上腺皮质激素刺激测试和肺功能测试,在第21天仅返回肺功能测试。结果:一组13例接受非锥形疗程(40 mg /天)泼尼松龙治疗8天的患者与一组13例接受锥形疗程(40 mg锥度按5 mg /天)治疗8天的患者进行比较。两组之间的FEV1预测百分比(第12天和第21天),复发率或肾上腺抑制率没有差异。结论:在这项小型研究中,我们发现接受8天渐减剂量泼尼松龙的哮喘患者和急诊出院时接受40 mg /天泼尼松龙的哮喘患者的复发率或肾上腺抑制没有显着差异。

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