Shenje Justin, Gumbo Tawanda, Wiesner Lubbe, Ntsekhe Mpiko, Mayosi Bongani, Ross Ian
Department of Medicine, University of Cape Town, South Africa.
Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Dallas, TX, USA.
Int J Cardiol Heart Vasc. 2019 Jan 11;22:105-110. doi: 10.1016/j.ijcha.2018.12.008. eCollection 2019 Mar.
In patients with tuberculous pericarditis [TBP] adjunctive prednisolone reduces the incidence of constrictive pericarditis. It is unknown whether prednisolone permeates adequately into pericardial fluid. Drug measurements in pericardial fluid require invasive procedures, and thus less invasive methods are needed to perform full pharmacokinetic characterization of prednisolone in large numbers of patients. We sought to evaluate the relationship between prednisolone concentrations in pericardial fluid, plasma, and saliva.
Plasma, pericardial fluid, and saliva samples were collected at 7 time points from TBP patients randomized to 120 mg prednisolone or placebo. Compartmental pharmacokinetic parameters, peak concentration [C], and 0-24 h area under the concentration-time curve [AUC] were identified in plasma, saliva and pericardial fluid.
There were five patients each in the prednisolone and placebo groups. Prednisolone concentrations were best described using a one compartment model. The absorption half-life into plasma was 1 h, while that into pericardial fluid was 9.4 h, which led to a median time-to-maximum concentration in plasma of 2.0 h versus 5.0 h in pericardial fluid [ = 0.048]. The concentration-time profiles in pericardial fluid versus plasma exhibited system hysteresis. The pericardial fluid-to-plasma C peak concentration ratio was 0.28 ( = 0.032), while the AUC ratio was 0.793. The concentration-time profiles in saliva had a similar shape to those in plasma, but the saliva-to-plasma C was 0.59 [ = 0.032].
The prednisolone AUC achieved in pericardial fluid approximates that in plasma, but the C is low due to delayed absorption. Saliva can be used as surrogate sampling site for pericardial fluid prednisolone.
在结核性心包炎(TBP)患者中,辅助使用泼尼松龙可降低缩窄性心包炎的发生率。目前尚不清楚泼尼松龙是否能充分渗透到心包积液中。心包积液中的药物测量需要侵入性操作,因此需要采用侵入性较小的方法来对大量患者的泼尼松龙进行完整的药代动力学特征分析。我们试图评估心包积液、血浆和唾液中泼尼松龙浓度之间的关系。
从随机接受120mg泼尼松龙或安慰剂的TBP患者中,在7个时间点采集血浆、心包积液和唾液样本。确定血浆、唾液和心包积液中的房室药代动力学参数、峰值浓度(C)以及浓度-时间曲线下0-24小时面积(AUC)。
泼尼松龙组和安慰剂组各有5名患者。泼尼松龙浓度用单室模型描述最佳。进入血浆的吸收半衰期为1小时,而进入心包积液的吸收半衰期为9.4小时,这导致血浆中达到最大浓度的中位时间为2.0小时,而心包积液中为5.0小时(P = 0.048)。心包积液与血浆中的浓度-时间曲线呈现系统滞后现象。心包积液与血浆的C峰值浓度比为0.28(P = 0.032),而AUC比为0.793。唾液中的浓度-时间曲线形状与血浆中的相似,但唾液与血浆的C为0.59(P = 0.032)。
心包积液中达到的泼尼松龙AUC与血浆中的相近,但由于吸收延迟,C较低。唾液可作为心包积液中泼尼松龙的替代采样部位。