Effects of licence change on prescribing and poisons enquiries for antipsychotic agents in England and Scotland

被引:11
作者
Bateman, DN [1 ]
Good, AM [1 ]
Afshari, R [1 ]
Kelly, CA [1 ]
机构
[1] Royal Infirm, Scottish Poisons Informat Bur, Edinburgh, Midlothian, Scotland
关键词
antipsychotics; drug licensing; pharmacoepidemiology; poisoning; poisons information; thioridazine;
D O I
10.1046/j.1365-2125.2003.01792.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aims To examine the effect of licence change for thioridazine at the end of 2000 on the prescription of antipsychotic drugs in England and Scotland, and investigate changes in poisons information inquiries and, for Edinburgh, poisons admissions. Methods Prescription data for antipsychotic drugs were obtained for England and Scotland and quarterly trends examined for 2000 and 2001. Accesses to the UK National Poisons Information Service website TOXBASE for antipsychotic products were examined for the same period. For Scotland telephone enquiry data, and admission data to the Edinburgh Poisons Unit were also evaluated. Trends in poisonings were compared with prescribing change. Results In England prescriptions for thioridazine fell rapidly in 2001 from approximately 35% of market share to less than 5%, and were replaced by risperidone, chlorpromazine and olanzapine. TOXBASE accesses fell from 39.3% of antipsychotics to 4.4%. Accesses for chlorpromazine, olanzapine and risperidone increased. In Scotland prescribing of thioridazine was similar to changes in England, but it was principally replaced by chlorpromazine. These changes were mirrored by TOXBASE accesses, telephone enquiries and in-patient admissions. The ratio of TOXBASE accesses for thioridazine to prescription numbers for the drug increased after the licence change. Conclusions Licence change produced rapid change in prescribing behaviour within 3 months. Prescribing behaviour in England and Scotland was different. Changes in prescribing were mirrored by changes in accesses for poisons information in both England and Scotland, and in Edinburgh by hospital admissions. The increase in the ratio of TOXBASE accesses to prescriptions for thioridazine suggests doctors may have become more aware of its potential toxicity.
引用
收藏
页码:596 / 603
页数:8
相关论文
共 16 条
[1]  
[Anonymous], BMJ
[2]   Web based information on clinical toxicology for the United Kingdom: uptake and utilization of TOXBASE in 2000 [J].
Bateman, DN ;
Good, AM ;
Kelly, CA ;
Laing, WJ .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 54 (01) :3-9
[3]  
Buck H, 1996, AGENDA, V34, P127
[4]   Discontinuation of thioridazine in patients with learning disabilities: balancing cardiovascular toxicity with adverse consequences of changing drugs [J].
Davies, SJC ;
Cooke, LB ;
Moore, AG ;
Potokar, J .
BRITISH MEDICAL JOURNAL, 2002, 324 (7352) :1519-1521
[5]   ELECTROCARDIOGRAPHIC CHANGES AND CARDIAC-ARRHYTHMIAS IN PATIENTS RECEIVING PSYCHOTROPIC-DRUGS [J].
FOWLER, NO ;
MCCALL, D ;
CHOU, TC ;
HOLMES, JC ;
HANENSON, IB .
AMERICAN JOURNAL OF CARDIOLOGY, 1976, 37 (02) :223-230
[6]   Antipsychotic drugs: Prolonged QTc interval, torsade de pointes, and sudden death [J].
Glassman, AH ;
Bigger, JT .
AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (11) :1774-1782
[7]   PLASMA CONCENTRATIONS OF THIORIDAZINE METABOLITES AND ECG ABNORMALITIES [J].
GOTTSCHALK, LA ;
DINOVO, E ;
BIENER, R ;
NANDI, BR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1978, 67 (02) :155-157
[8]   CARDIOTOXICITY OF THIORIDAZINE AND 2 STEREOISOMERIC FORMS OF THIORIDAZINE 5-SULFOXIDE IN THE ISOLATED PERFUSED RAT-HEART [J].
HALE, PW ;
POKLIS, A .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1986, 86 (01) :44-55
[9]   THIORIDAZINE-5-SULFOXIDE CARDIOTOXICITY IN THE ISOLATED, PERFUSED RAT-HEART [J].
HALE, PW ;
POKLIS, A .
TOXICOLOGY LETTERS, 1984, 21 (01) :1-8
[10]   Concentration-related pharmacodynamic effects of thioridazine and its metabolites in humans [J].
HartiganGo, K ;
Bateman, DN ;
Nyberg, G ;
Martensson, E ;
Thomas, SHL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1996, 60 (05) :543-553