LISA: a web-based decision-support system for trial management of childhood acute lymphoblastic leukaemia

被引:31
作者
Bury, J
Hurt, C
Roy, A
Cheesman, L
Bradburn, M
Cross, S
Fox, J
Saha, V
机构
[1] Univ Sheffield, Sch Med, Acad Unit Pathol, Div Genom Med, Sheffield S10 2RX, S Yorkshire, England
[2] Canc Res UK Adv Computat Lab, London, England
[3] Univ London Queen Mary Coll, Canc Res UK Childrens Canc Grp, London E1 4NS, England
[4] Inst Hlth Sci, Canc Res UK Med Stat Grp, Oxford, England
关键词
childhood haematological malignancies; computing; chemotherapy; clinical trials; acute lymphoblastic leukaemia;
D O I
10.1111/j.1365-2141.2005.05541.x
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Continuation chemotherapy is a key component of the treatment of childhood acute lymphoblastic leukaemia. During this treatment phase, weekly dose adjustments are carried out based on current and historical full blood counts (FBCs). The dose decision pathway is complex and suboptimal therapy may result if information on FBC results is not readily available and/or the prescriber is inexperienced. A web-based decision-support system (Leukaemia Intervention Scheduling and Advice, 'LISA') was designed to facilitate access to FBC information across geographical locations and to assist with dosage adjustments. A balanced-block crossover analysis was performed to evaluate the system. Thirty-six clinicians with varying degrees of experience were each asked to decide on appropriate oral chemotherapy dosages for eight simulated cases: four using LISA and four without. LISA significantly reduced the number of erroneous prescriptions (zero of 144 with LISA vs. 54 of 144 without; P < 0.0001) without affecting the number of times subjects deliberately overrode the protocol (seven of 144 times using LISA and six of 144 without). Using LISA reduced the time taken by novices to reach a decision for each case but increased the time taken by experts. Thirty-five of 36 subjects said they would be likely to use the system if it were available. A system like LISA is likely to be acceptable to clinicians, and has the potential to increase protocol compliance and decrease prescribing errors while allowing clinicians to override the protocol in specific cases where sound reasons exist for doing so.
引用
收藏
页码:746 / 754
页数:9
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