Literature DB >> 25261418

Impact of body weight and missed doses on lopinavir concentrations with standard and increased lopinavir/ritonavir doses during late pregnancy.

Tim R Cressey1, Saik Urien2, Edmund V Capparelli3, Brookie M Best3, Sudanee Buranabanjasatean4, Aram Limtrakul5, Boonsong Rawangban6, Prapan Sabsanong7, Jean-Marc Treluyer2, Gonzague Jourdain8, Alice Stek9, Marc Lallemant8, Mark Mirochnick10.   

Abstract

OBJECTIVES: To assess the influence of body weight and missed doses on lopinavir pharmacokinetics with standard and increased doses of lopinavir/ritonavir melt extrusion tablets during late pregnancy. PATIENTS AND METHODS: Lopinavir concentration data during the third trimester of pregnancy were pooled from clinical trials in Thailand (NCT00409591) and the USA (NCT00042289). A total of 154 HIV-infected pregnant women receiving either 400/100 mg (standard) or 600/150 mg (increased) twice daily had lopinavir plasma concentration data available. Population parameters were estimated using non-linear mixed-effects regression models. Monte Carlo simulations were performed to estimate the probability of achieving target lopinavir trough concentrations (>1.0 mg/L) with standard and increased doses of lopinavir/ritonavir during pregnancy.
RESULTS: The median (range) age, weight and gestational age were 28 years (18-43), 62 kg (45-123) and 33 weeks (29-38), respectively. Body weight influenced lopinavir oral clearance (CL/F) and volume of distribution (V/F). Population estimates of lopinavir CL/F and V/F were 6.21 L/h/70 kg and 52.6 L/70 kg, respectively. Based on simulations, the highest risk of subtherapeutic trough concentrations was for women weighing >100 kg using the standard dose (∼ 7%), while the risk was <2% with the 600/150 mg dose for women weighing 40-130 kg. After a missed dose, 61% of women have lopinavir concentrations below target prior to the next dose with the standard dose compared with 42% with the increased dose.
CONCLUSIONS: Standard dosing provides adequate lopinavir trough concentrations for the majority of pregnant women but increased doses may be preferable for women weighing >100 kg and with a history of lopinavir/ritonavir use and/or adherence issues.
© The Author 2014. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  HIV; Thailand; USA; pharmacokinetics

Mesh:

Substances:

Year:  2014        PMID: 25261418      PMCID: PMC4267507          DOI: 10.1093/jac/dku367

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  26 in total

1.  Implementation of a transit compartment model for describing drug absorption in pharmacokinetic studies.

Authors:  Radojka M Savic; Daniël M Jonker; Thomas Kerbusch; Mats O Karlsson
Journal:  J Pharmacokinet Pharmacodyn       Date:  2007-07-26       Impact factor: 2.745

2.  Estimation of population pharmacokinetic parameters of saquinavir in HIV patients with the MONOLIX software.

Authors:  Marc Lavielle; France Mentré
Journal:  J Pharmacokinet Pharmacodyn       Date:  2007-01-09       Impact factor: 2.745

3.  Population pharmacokinetics of lopinavir in combination with ritonavir in HIV-1-infected patients.

Authors:  K M L Crommentuyn; B S Kappelhoff; J W Mulder; A T A Mairuhu; E C M van Gorp; P L Meenhorst; A D R Huitema; J H Beijnen
Journal:  Br J Clin Pharmacol       Date:  2005-10       Impact factor: 4.335

4.  Reduced lopinavir exposure during pregnancy.

Authors:  Alice M Stek; Mark Mirochnick; Edmund Capparelli; Brookie M Best; Chengcheng Hu; Sandra K Burchett; Carol Elgie; Diane T Holland; Elizabeth Smith; Ruth Tuomala; Amanda Cotter; Jennifer S Read
Journal:  AIDS       Date:  2006-10-03       Impact factor: 4.177

5.  Pharmacokinetics and 24-week efficacy/safety of dual boosted saquinavir/lopinavir/ritonavir in nucleoside-pretreated children.

Authors:  Jintanat Ananworanich; Pope Kosalaraksa; Andrew Hill; Umaporn Siangphoe; Alina Bergshoeff; Chitsanu Pancharoen; Chulapan Engchanil; Kiat Ruxrungtham; David Burger
Journal:  Pediatr Infect Dis J       Date:  2005-10       Impact factor: 2.129

6.  Plasma lopinavir trough levels in a group of pregnant women on lopinavir, ritonavir, zidovudine, and lamivudine.

Authors:  Kaveh Manavi; Amy McDonald; Ali Al-Sharqui
Journal:  AIDS       Date:  2007-03-12       Impact factor: 4.177

7.  Lopinavir exposure with an increased dose during pregnancy.

Authors:  Mark Mirochnick; Brookie M Best; Alice M Stek; Edmund Capparelli; Chengcheng Hu; Sandra K Burchett; Diane T Holland; Elizabeth Smith; Sreedhar Gaddipati; Jennifer S Read
Journal:  J Acquir Immune Defic Syndr       Date:  2008-12-15       Impact factor: 3.731

8.  Simultaneous population pharmacokinetic model for lopinavir and ritonavir in HIV-infected adults.

Authors:  José Moltó; Manuel José Barbanoj; Cristina Miranda; Asunción Blanco; José Ramón Santos; Eugenia Negredo; Joan Costa; Pere Domingo; Bonaventura Clotet; Marta Valle
Journal:  Clin Pharmacokinet       Date:  2008       Impact factor: 6.447

9.  Steady-state lopinavir levels in third trimester of pregnancy.

Authors:  Fiona Lyons; Martin Lechelt; Annemiek De Ruiter
Journal:  AIDS       Date:  2007-05-11       Impact factor: 4.177

10.  Population analysis of the pregnancy-related modifications in lopinavir pharmacokinetics and their possible consequences for dose adjustment.

Authors:  Marion Bouillon-Pichault; Vincent Jullien; Elie Azria; Emmanuelle Pannier; Ghislaine Firtion; Anne Krivine; Alexandra Compagnucci; Olivier Taulera; Laurent Finkielsztejn; Stéphanie Chhun; Gérard Pons; Odile Launay; Jean-Marc Treluyer
Journal:  J Antimicrob Chemother       Date:  2009-04-22       Impact factor: 5.790

View more
  6 in total

1.  A Phase II/III Trial of Lopinavir/Ritonavir Dosed According to the WHO Pediatric Weight Band Dosing Guidelines.

Authors:  Jorge A Pinto; Edmund V Capparelli; Meredith Warshaw; Bonnie Zimmer; Tim R Cressey; Stephen A Spector; Min Qin; Betsy Smith; George K Siberry; Mark Mirochnick
Journal:  Pediatr Infect Dis J       Date:  2018-02       Impact factor: 2.129

2.  Efavirenz pharmacokinetics during pregnancy and infant washout.

Authors:  Regis Kreitchmann; Stein Schalkwijk; Brookie Best; Jiajia Wang; Angela Colbers; Alice Stek; David Shapiro; Tim Cressey; Mark Mirochnick; David Burger
Journal:  Antivir Ther       Date:  2019

3.  Impact of obesity on antiretroviral pharmacokinetics and immuno-virological response in HIV-infected patients: a case-control study.

Authors:  Vincent Madelain; Minh P Le; Karen Champenois; Charlotte Charpentier; Roland Landman; Veronique Joly; Patrick Yeni; Diane Descamps; Yazdan Yazdanpanah; Gilles Peytavin
Journal:  J Antimicrob Chemother       Date:  2017-04-01       Impact factor: 5.790

Review 4.  Pharmacokinetic Enhancement of HIV Antiretroviral Therapy During Pregnancy.

Authors:  Engie Salama; Ahizechukwu C Eke; Brookie M Best; Mark Mirochnick; Jeremiah D Momper
Journal:  J Clin Pharmacol       Date:  2020-08-14       Impact factor: 3.126

Review 5.  Strengths, weaknesses, opportunities and challenges for long acting injectable therapies: Insights for applications in HIV therapy.

Authors:  Andrew Owen; Steve Rannard
Journal:  Adv Drug Deliv Rev       Date:  2016-02-23       Impact factor: 15.470

6.  Successful Prediction of Human Fetal Exposure to P-Glycoprotein Substrate Drugs Using the Proteomics-Informed Relative Expression Factor Approach and PBPK Modeling and Simulation.

Authors:  Olena Anoshchenko; Flavia Storelli; Jashvant D Unadkat
Journal:  Drug Metab Dispos       Date:  2021-08-23       Impact factor: 3.922

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.