Broos Caroline E, Poell Linda H C, Looman Caspar W N, In 't Veen Johannes C C M, Grootenboers Marco J J H, Heller Roxane, van den Toorn Leon M, Wapenaar Monique, Hoogsteden Henk C, Kool Mirjam, Wijsenbeek Marlies S, van den Blink Bernt
Department of Pulmonary Medicine, Erasmus MC, Rotterdam, The Netherlands.
Department of Pulmonary Medicine, Erasmus MC, Rotterdam, The Netherlands.
Respir Med. 2018 May;138S:S31-S37. doi: 10.1016/j.rmed.2017.10.022. Epub 2017 Oct 31.
Prednisone is used as first-line therapy for pulmonary sarcoidosis. What dosing strategy has the best balance between effect and side-effects is largely unknown. We analyzed change in forced vital capacity (FVC) and weight during different prednisone doses used in daily practice for treatment naïve pulmonary sarcoidosis patients.
Multilevel models were used to describe FVC and weight change over time. Correlations were calculated using linear regression models.
Fifty-four patients were included. FVC changed over time (p < 0.001), with an average increase of 9.6% predicted (95% CI: 7.2 to 12.1) at 12 months. Weight changed significantly over time (p < 0.001), with an average increase of 4.3 kg (95% CI: 3.0 to 5.6) at 12 months. Although FVC and weight changed significantly over time, there was little correlation between prednisone dose and FVC change, while weight increase correlated significantly with cumulative prednisone dose at 24 months. In patients treated with a high cumulative prednisone dose, baseline FVC was on average lower (p = 0.001) compared to low dose treated patients, while no significant differences were observed in need for second/third-line therapy or number of exacerbations. A strategy leading to a low cumulative dose at 12 months was defined by rapid dose tapering to 10 mg/day within 3.5 months.
These results suggest that prednisone therapy aimed at improving or preserving FVC in newly- treated pulmonary sarcoidosis can often be reduced in dose, using a treatment regimen that is characterized by early dose tapering.
泼尼松被用作肺结节病的一线治疗药物。在疗效和副作用之间取得最佳平衡的给药策略在很大程度上尚不清楚。我们分析了初治肺结节病患者在日常治疗中使用不同剂量泼尼松时用力肺活量(FVC)和体重的变化。
采用多水平模型描述FVC和体重随时间的变化。使用线性回归模型计算相关性。
纳入54例患者。FVC随时间变化(p < 0.001),12个月时预测平均增加9.6%(95%CI:7.2至12.1)。体重随时间显著变化(p < 0.001),12个月时平均增加4.3 kg(95%CI:3.0至5.6)。尽管FVC和体重随时间显著变化,但泼尼松剂量与FVC变化之间几乎没有相关性,而体重增加与24个月时的累积泼尼松剂量显著相关。与低剂量治疗的患者相比,接受高累积泼尼松剂量治疗的患者基线FVC平均较低(p = 0.001),而在二线/三线治疗需求或加重次数方面未观察到显著差异。在3.5个月内迅速将剂量减至10 mg/天的策略可使12个月时的累积剂量较低。
这些结果表明,对于新治疗的肺结节病,旨在改善或维持FVC的泼尼松治疗通常可以采用早期减药的治疗方案来降低剂量。