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拉莫三嗪血清浓度与唾液浓度的相关性。

Correlation of lamotrigine concentrations between serum and saliva.

作者信息

Ryan Melody, Grim Shellee A, Miles Michael V, Tang Peter H, Fakhoury Toufic A, Strawsburg Richard H, deGrauw Ton J, Baumann Robert J

机构信息

University of Kentucky Chandler Medical Center, Lexington 40536-0293, USA.

出版信息

Pharmacotherapy. 2003 Dec;23(12):1550-7. doi: 10.1592/phco.23.15.1550.31957.

Abstract

STUDY OBJECTIVE

To compare the relationship between serum and salivary concentrations of lamotrigine in pediatric and adult epilepsy populations.

DESIGN

Paired-sample pharmacokinetic study.

SETTING

University neurology clinic.

PATIENTS

Thirty-seven patients with epilepsy, aged 2-60 years, who were taking lamotrigine and whose physicians had ordered a lamotrigine serum concentration.

MEASUREMENTS AND MAIN RESULTS

Patients spit a minimum of 0.25 ml into a cup to provide saliva samples. Blood samples were obtained by phlebotomy. Serum and salivary lamotrigine concentrations were determined by high-performance liquid chromatography. Linear regression analysis was used to evaluate correlations. Six patients' results were omitted due to the lack of a serum or saliva specimen or clearly erroneous results, leaving 31 patients for analysis. There was a strong correlation between the serum results reported by two reference laboratories (coefficient of correlation [r] = 0.988). The correlations between salivary and serum lamotrigine concentrations were similar for reference laboratory A (r = 0.81) and reference laboratory B (r = 0.84). Saliva:serum concentration ratios ranged from 0.41-1.26 (mean +/- SD 0.62 +/- 0.19) for reference laboratory A and from 0.40-1.19 ((mean +/- SD 0.64 +/- 0.18) for reference laboratory B.

CONCLUSION

There is a good correlation between salivary and serum concentrations for lamotrigine. However, there is wide interpatient variability in the saliva:serum ratio. The data suggest that salivary monitoring may play a role in the monitoring of lamotrigine for adult and pediatric patients.

摘要

研究目的

比较儿童和成人癫痫患者群体中拉莫三嗪的血清浓度与唾液浓度之间的关系。

设计

配对样本药代动力学研究。

地点

大学神经科诊所。

患者

37例年龄在2至60岁之间、正在服用拉莫三嗪且其医生已要求检测拉莫三嗪血清浓度的癫痫患者。

测量与主要结果

患者向杯中吐出至少0.25毫升唾液以提供唾液样本。通过静脉穿刺采集血样。采用高效液相色谱法测定血清和唾液中拉莫三嗪的浓度。使用线性回归分析评估相关性。6例患者的结果因缺乏血清或唾液样本或结果明显错误而被排除,剩余31例患者进行分析。两个参考实验室报告的血清结果之间存在很强的相关性(相关系数[r]=0.988)。参考实验室A(r=0.81)和参考实验室B(r=0.84)的唾液和血清拉莫三嗪浓度之间的相关性相似。参考实验室A的唾液:血清浓度比范围为0.41 - 1.26(均值±标准差0.62±0.19),参考实验室B的为0.40 - 1.19(均值±标准差0.64±0.18)。

结论

拉莫三嗪的唾液浓度与血清浓度之间存在良好的相关性。然而,患者之间的唾液:血清比值存在很大差异。数据表明,唾液监测可能在成人和儿童患者的拉莫三嗪监测中发挥作用。

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