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首页> 外文期刊>Pharmacoepidemiology and drug safety >Palatability, adherence and prescribing patterns of antiretroviral drugs for children with human immunodeficiency virus infection in Canada.
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Palatability, adherence and prescribing patterns of antiretroviral drugs for children with human immunodeficiency virus infection in Canada.

机译:在加拿大,针对人类免疫缺陷病毒感染儿童的抗逆转录病毒药物的适口性,依从性和处方方式。

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PURPOSE: To assess the impact of perceived palatability of antiretroviral drugs on adherence to therapy of children infected by human immunodeficiency virus and on prescribing patterns by their caring physicians. METHODS: Design: Two arms--retrospective chart review and a cross-sectional survey. Setting: Tertiary-care pediatric human immunodeficiency virus clinic during a 17-year period. Participants: Children with human immunodeficiency virus infection and physicians actively caring for children with human immunodeficiency virus infection in seven provinces in Canada were surveyed regarding their perception of the palatability of 8-liquid and 15 non-liquid antiretroviral medications and its effect on drug selection. Main Outcome Measure: Effect of taste preferences of antiretroviral drugs on adherence to treatment by infected children and on drug selection by their caring physicians. RESULTS: Forty of 119 children (34%) refused at least once to an antiretroviral medication. In 5%, treatment was discontinued because of poor palatability. Ritonavir was the least palatable drug (50% of children; p = 0.01). Ritonavir use (OR 4.80 [95%CI 1.34-17.20]) and male gender (OR 7.25 [95%CI 2.30-22.90]) were independent predictors of drug discontinuation because of poor taste. Physicians also perceived liquid ritonavir as the least palatable (p = 0.01) and the most likely to be discontinued (p = 0.01). However, they commonly prescribed it as first-line therapy (p = 0.06). CONCLUSIONS: A third of children infected with human immunodeficiency virus fail to adhere to their treatment because of poor drug taste. Physicians are aware of that, but this does not prevent them from selecting the least palatable drugs as first-line therapy.
机译:目的:评估抗逆转录病毒药物的适口性对坚持治疗被人类免疫缺陷病毒感染的儿童的依从性及其护理医生的处方方式的影响。方法:设计:两条手臂-回顾性图表审查和横断面调查。地点:17年期间的三级护理小儿人类免疫缺陷病毒诊所。参与者:对加拿大7个省的人类免疫缺陷病毒感染儿童和医生积极照顾人类免疫缺陷病毒感染儿童的医生进行了调查,了解他们对8液和15液非液抗逆转录病毒药物的适口性及其对药物选择的影响。主要观察指标:抗逆转录病毒药物的口味偏好对感染儿童坚持治疗的意愿及其护理医生的药物选择的影响。结果:119名儿童中有40名(34%)至少一次拒绝使用抗逆转录病毒药物。在5%的患者中,由于可口性差而终止治疗。利托那韦是最可口的药物(50%的儿童; p = 0.01)。利托那韦的使用(OR 4.80 [95%CI 1.34-17.20])和男性(OR 7.25 [95%CI 2.30-22.90])是由于味觉较差而停药的独立预测因子。医师还认为液态利托那韦是最可口的(p = 0.01),最可能被停用(p = 0.01)。但是,他们通常将其指定为一线治疗药物(p = 0.06)。结论:三分之一的感染人类免疫缺陷病毒的儿童由于药物味道差而无法坚持治疗。医师已经意识到了这一点,但这并不能阻止他们选择可口性最低的药物作为一线疗法。

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