Managing antituberculosis drug therapy by therapeutic drug monitoring of rifampicin and isoniazid

被引:66
作者
Ray, J
Gardiner, I
Marriott, D
机构
[1] St Vincents Hosp, Dept Clin Pharmacol & Toxicol, Sydney, NSW 2010, Australia
[2] St Vincents Hosp, Inst Lab Med, Dept Microbiol, Sydney, NSW 2010, Australia
[3] Westmead Hosp, Dept Resp Med, Sydney, NSW, Australia
关键词
drug monitoring; isoniazid; multidrug resistance; rifampicin; therapy; tuberculosis;
D O I
10.1046/j.1445-5994.2003.00390.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Current therapeutic regimens with rifampicin and isoniazid have proven successful in treating tuberculosis, however, toxicity, therapeutic failure, relapse and multiple drug resistance are serious -concerns. Optimizing drug dose using therapeutic drug monitoring (TDM) may be a better approach than administering therapy as a standard dose. Aims: To establish and evaluate a TDM service to -optimize rifampicin and isoniazid therapy. Methods: A TDM service for rifampicin and isoniazid was established in November 1998. Drug concentration data were collected, with relevant information to interpret the results. The reason for the request, information on concomitant drug administration and a questionnaire to assess clinical response to the drug results were also obtained. Results: Ninety patient episodes were accepted for study. The rifampicin plasma concentrations showed significant scatter, with 46% of the rifampicin concentrations below the normal range and 2% above the normal range. Similarly, 48% of isoniazid concen-trations were below the lower target of the normal range and 29% were above the upper normal limit. There was a greater proportion of isoniazid concentrations above the normal range in female patients. Conclusion: Significant pharmacokinetic variability was observed for rifampicin and isoniazid in the patient population studied. Further, a substantial number of plasma concentrations fell outside the suggested normal range for both drugs. Isoniazid plasma concentrations were significantly higher in female patients compared with male patients. Despite these abnormal results, the dose of rifampicin and isoniazid was altered in only 17% of patients, however, many patients received follow-up education because of the drug result. The service was considered valuable by 83% of respondents to the questionnaire. While TDM of rifampicin and isoniazid is a valuable tool to optimize the dose of these drugs in some patients, there is an urgent need for concentration-effect studies and possibly education on the principles and practice of TDM for these drugs.
引用
收藏
页码:229 / 234
页数:6
相关论文
共 50 条
[41]   EFFECT OF ALOE VERA EXTRACT ON THE HEPATOTOXICITY INDUCED BY ISONIAZID AND RIFAMPICIN DRUG IN MALE WISTAR RATS [J].
Zodape, G. V. ;
Bhise, P. P. .
INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES AND RESEARCH, 2016, 7 (03) :1314-1320
[42]   Gelatin Nanoparticles as Carrier for Effective Antituberculosis Drug Delivery in Combination Therapy [J].
Desai, Shivang K. ;
Bera, Smritilekha ;
Mondal, Dhananjoy .
BIONANOSCIENCE, 2024, 14 (05) :5139-5148
[43]   Lessons from Seven Decades of Antituberculosis Drug Discovery [J].
Barry, Clifton E. .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2011, 11 (10) :1216-1225
[44]   Genetic Risk Factors in Drug-Induced Liver Injury Due to Isoniazid-Containing Antituberculosis Drug Regimens [J].
Nicoletti, Paola ;
Devarbhavi, Harshad ;
Goel, Ashish ;
Venkatesan, Radha ;
Eapen, Chundamannil E. ;
Grove, Jane, I ;
Zafer, Samreen ;
Bjornsson, Einar ;
Lucena, M. Isabel ;
Andrade, Raul J. ;
Pirmohamed, Munir ;
Wadelius, Mia ;
Larrey, Dominique ;
Maitland-van der Zee, Anke-Hilse ;
Ibanez, Luisa ;
Watkins, Paul B. ;
Daly, Ann K. ;
Aithal, Guruprasad P. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2021, 109 (04) :1125-1135
[45]   Comparative bioavailability of rifampicin, isoniazid and pyrazinamide from a four drug fixed dose combination with separate formulations at the same dose levels [J].
Agrawal, S ;
Singh, I ;
Kaur, KJ ;
Bhade, SR ;
Kaul, CL ;
Panchagnula, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 276 (1-2) :41-49
[46]   Analysis of Rifampicin in Dried Blood Spot of Tuberculosis Patients for Therapeutic Drug Monitoring using High Performance Liquid Chromatography [J].
Harahap, Yahdiana ;
Alkindy, Fauzan ;
Ashiila, Ghina ;
Rahmayanti .
JOURNAL OF YOUNG PHARMACISTS, 2018, 10 (01) :48-51
[47]   Glucuronidation in therapeutic drug monitoring [J].
Shipkova, M ;
Wieland, E .
CLINICA CHIMICA ACTA, 2005, 358 (1-2) :2-23
[48]   Therapeutic drug monitoring for immunosuppressants [J].
Wong, SHY .
CLINICA CHIMICA ACTA, 2001, 313 (1-2) :241-253
[49]   The use and therapeutic drug monitoring of teicoplanin in the UK [J].
Darley, ESR ;
MacGowan, AP .
CLINICAL MICROBIOLOGY AND INFECTION, 2004, 10 (01) :62-69
[50]   Therapeutic drug monitoring in tuberculosis [J].
Sarkar, M. ;
Sarkar, J. .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2024, 80 (11) :1659-1684