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
[31]   Isoniazid and rifampicin exposure during treatment in drug-susceptible TB [J].
Akkerman, O. W. ;
Dijkwel, R. D. C. ;
Kerstjens, H. A. M. ;
van der Werf, T. S. ;
Srivastava, S. ;
Sturkenboom, M. G. G. ;
Bolhuis, M. S. .
INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2023, 27 (10) :772-777
[32]   Challenges in Antifungal Therapy: Therapeutic Drug Monitoring, Drug-Drug Interactions and Approach to Failure After Primary Therapy [J].
Memisoglu, Funda .
KLIMIK JOURNAL, 2019, 32 :177-186
[33]   CONJUGATES OF SEVERAL LUPANE, OLEANANE, AND URSANE TRITERPENOIDS WITH THE ANTITUBERCULOSIS DRUG ISONIAZID AND PYRIDINECARBOXALDEHYDES [J].
Kazakova, O. B. ;
Medvedeva, N. I. ;
Samoilova, I. A. ;
Baikova, I. P. ;
Tolstikov, G. A. ;
Kataev, V. E. ;
Mironov, V. F. .
CHEMISTRY OF NATURAL COMPOUNDS, 2011, 47 (05) :752-758
[34]   Therapeutic monitoring of isoniazid, rifampicin, ethambutol and pyrazinamide serum levels in the treatment of active pulmonary tuberculosis and determinants of their serum concentrations [J].
Kayhan, Servet ;
Akgunes, Alper .
AFRICAN JOURNAL OF PHARMACY AND PHARMACOLOGY, 2011, 5 (17) :2035-2041
[35]   Conjugates of several lupane, oleanane, and ursane triterpenoids with the antituberculosis drug isoniazid and pyridinecarboxaldehydes [J].
O. B. Kazakova ;
N. I. Medvedeva ;
I. A. Samoilova ;
I. P. Baikova ;
G. A. Tolstikov ;
V. E. Kataev ;
V. F. Mironov .
Chemistry of Natural Compounds, 2011, 47 :752-758
[36]   Dependence of Efavirenz- and Rifampicin-Isoniazid-Based Antituberculosis Treatment Drug-Drug Interaction on CYP2B6 and NAT2 Genetic Polymorphisms: ANRS 12154 Study in Cambodia [J].
Bertrand, Julie ;
Verstuyft, Celine ;
Chou, Monidarin ;
Borand, Laurence ;
Chea, Phalla ;
Nay, Kuy Huong ;
Blanc, Francois-Xavier ;
Mentre, France ;
Taburet, Anne-Marie .
JOURNAL OF INFECTIOUS DISEASES, 2014, 209 (03) :399-408
[37]   Metabolism of the Antituberculosis Drug Ethionamide [J].
Vale, Nuno ;
Gomes, Paula ;
Santos, Helder A. .
CURRENT DRUG METABOLISM, 2013, 14 (01) :151-158
[38]   Therapeutic Drug Monitoring in the Treatment of Tuberculosis [J].
Charles A. Peloquin .
Drugs, 2002, 62 :2169-2183
[39]   Study on the associations between liver damage and antituberculosis drug rifampicin and relative metabolic enzyme gene polymorphisms [J].
Su, Qiang ;
Liu, Qiao ;
Liu, Juan ;
Fu, Lingyun ;
Liu, Tao ;
Liang, Jing ;
Peng, Hong ;
Pan, Xue .
BIOENGINEERED, 2021, 12 (02) :11700-11708
[40]   A DFT approach towards therapeutic potential of Novel borospherene as targeted drug delivery system for isoniazid drug [J].
Hashim, Alaa A. ;
Hussein, Uday Abdul-Reda ;
Bahir, Hala ;
Amir, Ahmed Ali ;
Muhammad, Faris Anad ;
Ahjel, Salam ;
Zabibah, Rahman S. ;
Abbas, Ali Hashim ;
Hason, Ahmad .
MOLECULAR PHYSICS, 2024, 122 (17)