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本文引用的文献

1
British HIV Association and Children's HIV Association guidelines for the management of HIV infection in pregnant women 2008.英国艾滋病协会与儿童艾滋病协会2008年孕妇HIV感染管理指南
HIV Med. 2008 Aug;9(7):452-502. doi: 10.1111/j.1468-1293.2008.00619.x.
2
Antiretroviral therapy and premature delivery in diagnosed HIV-infected women in the United Kingdom and Ireland.英国和爱尔兰确诊感染艾滋病毒女性的抗逆转录病毒疗法与早产
AIDS. 2007 May 11;21(8):1019-26. doi: 10.1097/QAD.0b013e328133884b.
3
Plasma lopinavir trough levels in a group of pregnant women on lopinavir, ritonavir, zidovudine, and lamivudine.一组接受洛匹那韦、利托那韦、齐多夫定和拉米夫定治疗的孕妇的血浆洛匹那韦谷浓度。
AIDS. 2007 Mar 12;21(5):643-5. doi: 10.1097/QAD.0b013e328031f42e.
4
Reduced lopinavir exposure during pregnancy.孕期洛匹那韦暴露减少。
AIDS. 2006 Oct 3;20(15):1931-9. doi: 10.1097/01.aids.0000247114.43714.90.
5
Pharmacologic optimization of protease inhibitors and nonnucleoside reverse transcriptase inhibitors (POPIN)--a randomized controlled trial of therapeutic drug monitoring and adherence support.蛋白酶抑制剂和非核苷类逆转录酶抑制剂的药物优化(POPIN)——一项治疗药物监测与依从性支持的随机对照试验
J Acquir Immune Defic Syndr. 2006 Apr 1;41(4):461-7. doi: 10.1097/01.qai.0000218345.65434.21.
6
Marked intraindividual variability in antiretroviral concentrations may limit the utility of therapeutic drug monitoring.抗逆转录病毒药物浓度存在显著的个体内变异性,这可能会限制治疗药物监测的效用。
Clin Infect Dis. 2006 Apr 15;42(8):1189-96. doi: 10.1086/501458. Epub 2006 Mar 7.
7
Simultaneous determination of HIV protease inhibitors amprenavir, atazanavir, indinavir, lopinavir, nelfinavir, ritonavir and saquinavir in human plasma by high-performance liquid chromatography-tandem mass spectrometry.高效液相色谱-串联质谱法同时测定人血浆中的HIV蛋白酶抑制剂安普那韦、阿扎那韦、茚地那韦、洛匹那韦、奈非那韦、利托那韦和沙奎那韦
J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Dec 27;829(1-2):82-90. doi: 10.1016/j.jchromb.2005.09.032. Epub 2005 Oct 13.
8
Higher plasma lopinavir concentrations are associated with a moderate rise in cholestasis markers in HIV-infected patients.较高的血浆洛匹那韦浓度与HIV感染患者胆汁淤积标志物的适度升高有关。
J Antimicrob Chemother. 2005 Oct;56(4):790-2. doi: 10.1093/jac/dki314. Epub 2005 Sep 5.
9
Safety and pharmacokinetics of antiretroviral therapy during pregnancy.孕期抗逆转录病毒疗法的安全性和药代动力学
Ther Drug Monit. 2004 Apr;26(2):110-5. doi: 10.1097/00007691-200404000-00004.
10
Pharmacokinetics of saquinavir plus low-dose ritonavir in human immunodeficiency virus-infected pregnant women.沙奎那韦联合低剂量利托那韦在人类免疫缺陷病毒感染孕妇中的药代动力学
Antimicrob Agents Chemother. 2004 Feb;48(2):430-6. doi: 10.1128/AAC.48.2.430-436.2004.

治疗药物监测在接受洛匹那韦治疗的HIV感染孕妇管理中的应用

Utility of therapeutic drug monitoring in the management of HIV-infected pregnant women in receipt of lopinavir.

作者信息

Caswell R J, Phillips D, Chaponda M, Khoo S H, Taylor G P, Ghanem M, Poulton M, Welch J, Gibbons S, Jackson V, Lambert J S

机构信息

Department of GU Medicine and Teaching Primary Care Trust, Coventry PCT, Coventry.

出版信息

Int J STD AIDS. 2011 Jan;22(1):11-4. doi: 10.1258/ijsa.2009.009184.

DOI:10.1258/ijsa.2009.009184
PMID:21364060
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3594887/
Abstract

The pharmacokinetics of antiretroviral drugs in pregnancy is poorly understood. We reviewed the use of therapeutic drug monitoring (TDM) in clinical settings to document plasma concentrations of lopinavir during pregnancy and investigated how clinicians acted upon TDM results. A retrospective review was carried out of all HIV-infected pregnant women taking boosted lopinavir-based highly active antiretroviral therapy (HAART) at five National Health Service (NHS) centres in the UK between May 2004 and March 2007. Seventy-three women in receipt of lopinavir were identified, of whom 89% had plasma lopinavir concentrations above the suggested minimum recommended for wild-type HIV. Initial TDM results prompted dosage change in 10% and assessment of adherence and/or pharmacist review in 11%. TDM was repeated in 29%. TDM can play an important role in the clinical management of HIV-positive pregnant women, allowing informed dose modification and an alternative measure of adherence.

摘要

抗逆转录病毒药物在孕期的药代动力学情况目前了解甚少。我们回顾了治疗药物监测(TDM)在临床环境中的应用,以记录孕期洛匹那韦的血浆浓度,并研究临床医生如何根据TDM结果采取行动。对2004年5月至2007年3月期间在英国五个国民健康服务(NHS)中心接受基于洛匹那韦的强化高效抗逆转录病毒治疗(HAART)的所有感染HIV的孕妇进行了回顾性研究。确定了73名接受洛匹那韦治疗的女性,其中89%的血浆洛匹那韦浓度高于野生型HIV建议的最低推荐浓度。初始TDM结果促使10%的患者改变剂量,11%的患者接受依从性评估和/或药剂师审查。29%的患者重复进行了TDM。TDM在HIV阳性孕妇的临床管理中可发挥重要作用,有助于进行明智的剂量调整以及作为一种评估依从性的替代方法。