Bromide as a marker to measure adherence to drug therapy

被引:5
作者
Braam, RL
van Uum, SHM
Russel, FGM
Swinkels, DW
Thien, T
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Internal Med, NL-6500 HB Nijmegen, Netherlands
[2] Univ Western Ontario, Dept Med, London, ON, Canada
[3] Univ Western Ontario, Lawson Hlth Res Inst, London, ON, Canada
[4] Radboud Univ Nijmegen Med Ctr, Dept Pharmacol & Toxicol, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen Med Ctr, Dept Clin Chem, Nijmegen, Netherlands
关键词
adherence; bromide; drug therapy;
D O I
10.1007/s00228-006-0103-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Objective: Several methods have been described to measure adherence to prescribed drug therapy. However, most of these have been shown to be inaccurate. Bromide is an anion that is readily absorbed in the gut and has an elimination half-life of about 12 days. In the present study, we investigated the pharmacokinetic properties of bromide with the objective to use it as a measure of drug adherence. Methods: Three groups of each 8 healthy volunteers took 15, 24 or 30 mg potassium bromide, respectively, daily for 20 weeks. Serum concentrations of bromide were measured every two weeks. Results: There was a linear relationship between the daily dosage taken and the mean increase of bromide concentration. In every group considerable inter-individual variability was seen. Correction for body weight resulted in an improved correlation between daily bromide dose and increase in concentration (r=0.78, p < 0.01). Conclusions: Unfortunately, the inter-individual variability in clearance of bromide was considerable. This limits the use of bromide to primarily measuring adherence in individual patients during long term follow-up. Bromide appears to be a potentially useful marker to be added to drugs for assessment of individual adherence to long term drug therapy. This needs to be investigated in various patients, particularly for patients with relatively asymptomatic diseases (e.g. hypertension).
引用
收藏
页码:285 / 290
页数:6
相关论文
共 18 条
[1]   Monitoring compliance in resistant hypertension: an important step in patient management [J].
Burnier, M ;
Santschi, V ;
Favrat, B ;
Brunner, HR .
JOURNAL OF HYPERTENSION, 2003, 21 :S37-S42
[2]   COMPLIANCE DECLINES BETWEEN CLINIC VISITS [J].
CRAMER, JA ;
SCHEYER, RD ;
MATTSON, RH .
ARCHIVES OF INTERNAL MEDICINE, 1990, 150 (07) :1509-1510
[3]  
ELLARD GA, 1980, BRIT J CLIN PHARMACO, V10, P369
[4]   LOW-DOSE PHENOBARBITONE AS AN INDICATOR OF COMPLIANCE WITH DRUG-THERAPY [J].
FEELY, M ;
COOKE, J ;
PRICE, D ;
SINGLETON, S ;
MEHTA, A ;
BRADFORD, L ;
CALVERT, R .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1987, 24 (01) :77-83
[5]   MINIMAL DOSES OF DIGOXIN - A NEW MARKER FOR COMPLIANCE TO MEDICATION [J].
MAENPAA, H ;
JAVELA, K ;
PIKKARAINEN, J ;
MALKONEN, M ;
HEINONEN, OP ;
MANNINEN, V .
EUROPEAN HEART JOURNAL, 1987, 8 :31-37
[6]  
MILLER ME, 1984, CLIN CHEM, V30, P781
[7]   Drug therapy - Adherence to medication [J].
Osterberg, L ;
Blaschke, T .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (05) :487-497
[8]   Bromide, the first effective antiepileptic agent [J].
Pearce, JMS .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2002, 72 (03) :412-412
[9]   TIME TO STOP COUNTING THE TABLETS [J].
PULLAR, T ;
KUMAR, S ;
TINDALL, H ;
FEELY, M .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1989, 46 (02) :163-168
[10]  
RITSCHEL WA, 1992, METHOD FIND EXP CLIN, V14, P241