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基于加权TOPSIS法的药学干预对阿帕替尼处方合理率的影响

许健 孔令提

许健, 孔令提. 基于加权TOPSIS法的药学干预对阿帕替尼处方合理率的影响[J]. 中华全科医学, 2022, 20(9): 1598-1602. doi: 10.16766/j.cnki.issn.1674-4152.002658
引用本文: 许健, 孔令提. 基于加权TOPSIS法的药学干预对阿帕替尼处方合理率的影响[J]. 中华全科医学, 2022, 20(9): 1598-1602. doi: 10.16766/j.cnki.issn.1674-4152.002658
XU Jian, KONG Ling-ti. Pharmaceutical intervention based on weighted TOPSIS method on the rationality rate of apatinib prescription[J]. Chinese Journal of General Practice, 2022, 20(9): 1598-1602. doi: 10.16766/j.cnki.issn.1674-4152.002658
Citation: XU Jian, KONG Ling-ti. Pharmaceutical intervention based on weighted TOPSIS method on the rationality rate of apatinib prescription[J]. Chinese Journal of General Practice, 2022, 20(9): 1598-1602. doi: 10.16766/j.cnki.issn.1674-4152.002658

基于加权TOPSIS法的药学干预对阿帕替尼处方合理率的影响

doi: 10.16766/j.cnki.issn.1674-4152.002658
基金项目: 

安徽省高校自然科学研究项目 KJ2021A0801

详细信息
    通讯作者:

    孔令提, E-mail: 2015200@bbmc.edu.cn

  • 中图分类号: R979.1 R969.3

Pharmaceutical intervention based on weighted TOPSIS method on the rationality rate of apatinib prescription

  • 摘要:   目的  建立阿帕替尼药物利用评价标准,通过适当的药学干预措施促进阿帕替尼的临床合理使用。  方法  参考阿帕替尼说明书以及相关临床指南,制定阿帕替尼药物利用评价标准,利用加权优劣解距离法(TOPSIS)对阿帕替尼药物使用情况进行客观评价,根据评价结果分析可能原因,再制定相应的药学干预措施并给予持续干预,最后再利用加权TOPSIS法对干预后的阿帕替尼药物使用情况进行评价。  结果  基线调查发现阿帕替尼处方合理率较低,79份病历的相对接近度为0.9~1.0,57份病历的相对接近度为0.6~0.9,各评价指标中,“给药剂量及剂量调整”“适应证”及“临床指南推荐联合使用方案”指标的得分较低,均值分别为5.00、8.10和8.10分。结合基线调查情况制定针对性干预措施,包括利用医院合理用药软件制定阿帕替尼诊断限制规则、发动临床药师深入临床科室开展阿帕替尼合理使用专项培训以及持续开展阿帕替尼专项处方点评等,经过药学干预后处方合理率得到很大改善,146份病历的相对接近度为0.9~1.0,21份病历的相对接近度为0.6~0.9,“适应证”和“临床指南推荐联合使用方案”指标的得分有所改善,均值均上升至9.32分。  结论  加权TOPSIS法可以客观、全面地对阿帕替尼使用情况进行评价,便于发现问题并及时干预。

     

  • 表  1  阿帕替尼药物利用评价标准

    Table  1.   Evaluation criteria for apatinib utilization

    指标名称 评价依据 评价结果 分值(分)
    既往化疗方案(X1) (1)无既往化疗史
    (2)有既往化疗史
    0:符合(1)
    1:符合(2)
    0
    10
    用药顺序(X2) (1)既往化疗失败后选择阿帕替尼
    (2)未进行一线化疗,直接使用阿帕替尼
    0:符合(1)
    1:符合(2)
    10
    0
    给药剂量及剂量调整(X3) (1)推荐剂量:850 mg,1次/d(2)出现骨髓抑制或其他不良反应时,建议暂停用药,持续评估患者病情,尽快恢复用药 0:符合(1)或(2)
    1:不符合(1)或(2),便于下文Ci计算
    10
    5
    适应证(X4) (1)晚期或转移性胃恶性肿瘤(胃癌)
    (2)晚期或转移性肝恶性肿瘤(肝细胞癌)
    0:符合(1)或(2)
    1:不符合(1)或(2)
    10
    0
    禁忌人群(X5) 出现过敏反应,以及其他患者无法耐受的不良反应 0:符合其中任意一项或多项
    1:全部不符合
    0
    10
    给药途径(X6) 口服,餐后半小时服用(每日服药的时间应尽可能相同) 0:符合
    1:不符合
    10
    0
    给药间隔及周期(X7) 连续服用,直至疾病进展或出现不可耐受的不良反应 0:符合
    1:不符合
    10
    0
    临床指南推荐联合使用方案(X8) 符合中国临床肿瘤学会胃癌或肝癌指南 0:符合
    1:不符合
    10
    0
    下载: 导出CSV

    表  2  阿帕替尼点评各指标判断矩阵及权向量

    Table  2.   Apatinib review index judgment matrix and weight vector

    项目 X1 X2 X3 X4 X5 X6 X7 X8 权向量
    X1 0 1/3 1/3 1/3 1/3 1/3 1/2 1/2 0.095
    X2 2/3 0 1/2 1/2 1/2 1/2 2/3 2/3 0.143
    X3 2/3 1/2 0 2/3 2/3 2/3 3/4 3/4 0.167
    X4 2/3 1/2 1/3 0 1/2 1/2 2/3 2/3 0.137
    X5 2/3 1/2 1/3 1/2 0 1/2 2/3 2/3 0.137
    X6 2/3 1/2 1/3 1/2 1/2 0 2/3 2/3 0.137
    X7 1/2 1/2 1/4 1/3 1/3 1/3 0 1/2 0.092
    X8 1/2 1/2 1/4 1/3 1/3 1/3 1/2 0 0.092
    下载: 导出CSV

    表  3  干预前后相对接近度比较

    Table  3.   Comparison of relative proximity before and after intervention

    相对接近度范围 干预前病例数 干预后病例数
    1.0≥Ci≥0.9 79 146
    0.9>Ci≥0.8 0 0
    0.8>Ci≥0.7 57 21
    0.7>Ci≥0.6 0 0
    0.6>Ci≥0.5 0 0
    0.5>Ci≥0.4 0 0
    0.4>Ci≥0.3 0 0
    0.3>Ci≥0.2 45 27
    0.2>Ci≥0.1 0 0
    0.1>Ci≥0 19 6
    下载: 导出CSV

    表  4  干预前后各评价指标评分比较(x±s,分)

    Table  4.   Comparison of evaluation indexes before and after intervention (x±s, points)

    评价指标 干预前评分 干预后评分 t P
    既往化疗方案(X1) 6.80±4.67 8.35±3.72 3.668 < 0.001
    用药顺序(X2) 6.80±4.67 8.35±3.72 3.668 < 0.001
    给药剂量及剂量调整(X3) 5.00±0.00 5.00±0.00
    适应证(X4) 8.10±2.43 9.32±1.71 5.822 < 0.001
    禁忌人群(X5) 10.00±0.00 10.00±0.00
    给药途径(X6) 10.00±0.00 10.00±0.00
    给药间隔及周期(X7) 10.00±0.00 10.00±0.00
    临床指南推荐联合使用方案(X8) 8.10±2.43 9.32±1.71 5.822 < 0.001
    下载: 导出CSV
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  • 收稿日期:  2022-04-18
  • 网络出版日期:  2022-11-29

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