Therapeutic Drug Monitoring

Highly active antiretroviral therapy (HAART) can suppress viral replication and substantially prolong patient life. It can also fail for a number of reasons, including poor adherence, insufficient drug potency, emergence of resistance, cellular factors, and pharmacokinetic factors. Although many antiretroviral drugs are now available, a limited number of combinations has been proven effective for individual patients. With sequential treatment failures, the durability of virologic response tends to decrease with subsequent treatment regimens until the patient is left with few or no therapeutic options. There is evidence that many treatment-naïve patients will switch from their initial regimen within one year. It is imperative that we adopt strategies that will optimize the use of available therapies, so as to achieve long-term viral suppression.

[1]  Allan R Tunkel,et al.  Practice guidelines for the management of bacterial meningitis. , 2004, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[2]  Y. Kanda,et al.  Increased incidence of acute graft-versus-host disease with the continuous infusion of cyclosporine A compared to twice-daily infusion , 2004, Bone Marrow Transplantation.

[3]  G. Stallone,et al.  Experience with cyclosporine: approaching the therapeutic window for C2 levels in maintenance kidney transplant recipients. , 2004, Transplantation proceedings.

[4]  F. Citterio Evolution of the therapeutic drug monitoring of cyclosporine. , 2004, Transplantation proceedings.

[5]  N. Goto,et al.  Clinical success of Neoral absorption profile. , 2004, Transplantation proceedings.

[6]  J. Barkun,et al.  History of C2 monitoring in heart and liver transplant patients treated with cyclosporine microemulsion. , 2004, Transplantation proceedings.

[7]  L. Balant,et al.  Time course of clinical response to venlafaxine: relevance of plasma level and chirality , 2004, European Journal of Clinical Pharmacology.

[8]  M. Strolin Benedetti,et al.  Pharmacokinetics and metabolism of 14C-levetiracetam, a new antiepileptic agent, in healthy volunteers , 2003, European Journal of Clinical Pharmacology.

[9]  B. Jilma,et al.  Therapeutic approaches in the management of oral cyclosporine A intoxication. , 2003, Transplantation.

[10]  P. Jacobson,et al.  Posttransplant day significantly influences pharmacokinetics of cyclosporine after hematopoietic stem cell transplantation. , 2003, Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation.

[11]  D. Holt,et al.  Monitoring Cyclosporin in Blood: Between-Assay Differences at Trough and 2 Hours Post-dose (C2) , 2003, Therapeutic drug monitoring.

[12]  P. Patsalos The pharmacokinetic characteristics of levetiracetam. , 2003, Methods and findings in experimental and clinical pharmacology.

[13]  E. Perucca,et al.  Effects of antiepileptic comedication on levetiracetam pharmacokinetics: a pooled analysis of data from randomized adjunctive therapy trials , 2003, Epilepsy Research.

[14]  W. Sandborn,et al.  Cyclosporin for refractory ulcerative colitis , 2003, Gut.

[15]  P. Keown New concepts in cyclosporine monitoring. , 2002, Current opinion in nephrology and hypertension.

[16]  R. Cramb,et al.  Cyclosporin: revisions in monitoring guidelines and review of current analytical methods , 2002, Annals of clinical biochemistry.

[17]  M. Reis,et al.  Therapeutic Drug Monitoring of Racemic Venlafaxine and Its Main Metabolites in an Everyday Clinical Setting , 2002, Therapeutic drug monitoring.

[18]  M. Ansseau,et al.  Venlafaxine: the relationship between dose, plasma concentration and clinical response in depressive patients. , 2002, Journal of psychopharmacology.

[19]  L. Balant,et al.  Steady-state concentration of venlafaxine enantiomers: model-based analysis of between-patient variability , 2002, European Journal of Clinical Pharmacology.

[20]  C. Flexner,et al.  Concentration-targeted therapy and the future of HIV management. , 2002, AIDS.

[21]  V. Armstrong,et al.  Two-Hour Cyclosporine Concentration Determination: An Appropriate Tool to Monitor Neoral Therapy? , 2002, Therapeutic drug monitoring.

[22]  R. Hoffman,et al.  A Case of Levetiracetam (Keppra®) Poisoning with Clinical and Toxicokinetic Data , 2002, Journal of toxicology. Clinical toxicology.

[23]  N. Fountain,et al.  Pharmacokinetic Study of Levetiracetam in Children , 2001, Epilepsia.

[24]  H. Lafeber,et al.  Pharmacokinetics of Meropenem in Preterm Neonates , 2001, Therapeutic drug monitoring.

[25]  T. Szekeres,et al.  Cyclosporine metabolism in patients after kidney, bone marrow, heart-lung, and liver transplantation in the early and late posttransplant periods. , 2000, American journal of clinical pathology.

[26]  F. Dreifuss,et al.  Levetiracetam for partial seizures , 2000, Neurology.

[27]  P. Haffmans,et al.  Venlafaxine serum levels and CYP2D6 genotype. , 2000, Therapeutic drug monitoring.

[28]  R. Beale,et al.  Pharmacokinetics of meropenem in intensive care unit patients receiving continuous veno‐venous hemofiltration or hemodiafiltration , 2000, Critical care medicine.

[29]  T. Szekeres,et al.  Evaluation of four automated methods for determination of whole blood cyclosporine concentrations. , 1999, American Journal of Clinical Pathology.

[30]  C. Ashley,et al.  The Renal Drug Handbook , 1999 .

[31]  K. Lasseter,et al.  Pharmacokinetics of meropenem in patients with liver disease. , 1997, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[32]  M. Kraml,et al.  A High‐Performance Liquid Chromatographic Method for the Simultaneous Determination of Venlafaxine and O‐Desmethylvenlafaxine in Biological Fluids , 1994, Therapeutic drug monitoring.

[33]  R. Venkataramanan,et al.  Clinical Pharmacokinetics of Cyclosporin , 1986, Clinical pharmacokinetics.

[34]  P. Harrigan,et al.  The use of virtual inhibitory quotient (VIQ) in antiretroviral (ART) experienced patients taking amprenavir/lopinavir combinations , 2002 .

[35]  N. Perico,et al.  Pharmacokinetic study of the new cyclosporine-A formulation (Neoral) in adult allogeneic bone marrow transplant recipients. , 2001, Haematologica.

[36]  Iain M McIntyre,et al.  A study involving venlafaxine overdoses: comparison of fatal and therapeutic concentrations in postmortem specimens. , 1999, Journal of forensic sciences.

[37]  L. Goldfrank Medical toxicology. , 1992, JAMA.

[38]  H. Loosli,et al.  Disposition of cyclosporine in several animal species and man. I. Structural elucidation of its metabolites. , 1984, Drug metabolism and disposition: the biological fate of chemicals.

[39]  T. Anagnostopoulos [TREATMENT OF THE IDIOPATHIC NEPHROTIC SYNDROME IN CHILDREN]. , 1964, Rein et foie, maladies de la nutrition; actualites.