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肾病综合征中类固醇的体重或体表面积剂量:是否存在结局差异?

Weight or body surface area dosing of steroids in nephrotic syndrome: is there an outcome difference?

机构信息

Pediatric Nephrology and Hypertension Division, Children's Hospital of Michigan, 3901 Beaubien St, Detroit, MI 48201, USA.

出版信息

Pediatr Nephrol. 2011 Dec;26(12):2167-71. doi: 10.1007/s00467-011-1961-3. Epub 2011 Jul 16.

Abstract

Although prednisone is the treatment of choice for nephrotic syndrome (NS) in childhood, the dosing regimen varies between 60 mg/m(2)/day, as recommended in early studies, to the often prescribed 2 mg/kg/day dose, which is used in common practice. Mathematical models have demonstrated that weight-based dosing can be less than body surface area (BSA)-based dosing in smaller children. To test our hypothesis that weight-based dosing would result in altered treatment outcomes in children with NS, we analyzed a cohort of 56 children (mean age 5.4 ± 3.8 years) treated with a weight-based dosing regimen. Theoretical underdosing of corticosteroids was tested by calculating a relative underdosing percentage (RUP), which was defined as the dose difference between the theoretical BSA-based dose and the actual weight-based doses divided by the BSA-based dose × 100. We found that the mean "actual" prednisone dose in our patients was 43.6 ± 19.3 mg/day; in contrast, the mean theoretical BSA-based dose was calculated to be 48.8 ± 16.7 mg/day. Among the 56 patients, 43 (76.7%) were initial responders, of whom 58% followed a frequently relapsing (FR) course. RUP was significantly higher in FR (16.6 ± 7.9%) than in infrequent relapsers (8.7 ± 9.8%) (P = 0.03). RUP was not significantly different among initial responders and nonresponders. Based on these results, we conclude that prednisone underdosing, when dosing is prescribed according to weight, does not affect the initial response to treatment, but it does increase the likelihood of a FR course in responders.

摘要

尽管泼尼松是儿童肾病综合征(NS)的治疗选择,但剂量方案在早期研究中推荐为 60mg/m²/天,而在常规实践中常用的是 2mg/kg/天剂量。数学模型表明,对于较小的儿童,体重剂量可能小于基于体表面积(BSA)的剂量。为了验证我们的假设,即基于体重的剂量方案会导致 NS 患儿的治疗结果发生改变,我们分析了一组 56 名儿童(平均年龄 5.4 ± 3.8 岁)的队列,他们接受了基于体重的剂量方案治疗。通过计算相对剂量不足百分比(RUP)来测试皮质类固醇的理论剂量不足,定义为理论 BSA 剂量与实际体重剂量之间的剂量差异除以 BSA 剂量×100。我们发现,我们患者的平均“实际”泼尼松剂量为 43.6 ± 19.3mg/天;相比之下,平均理论 BSA 剂量为 48.8 ± 16.7mg/天。在 56 名患者中,43 名(76.7%)为初始缓解者,其中 58%为频繁复发(FR)者。FR(16.6 ± 7.9%)的 RUP 明显高于非频繁复发者(8.7 ± 9.8%)(P=0.03)。初始缓解者和无缓解者之间的 RUP 无显著差异。基于这些结果,我们得出结论,当根据体重开具处方时,泼尼松剂量不足不会影响初始治疗反应,但会增加缓解者 FR 病程的可能性。

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