Department of Clinical Pharmacy, Faculty of Pharmacy, Bezmialem Vakif University, Istanbul, Turkey.
Department of Clinical Pharmacy, Institute of Health Sciences, Marmara University, Istanbul, Turkey.
J Oncol Pharm Pract. 2023 Jul;29(5):1178-1186. doi: 10.1177/10781552221104814. Epub 2022 May 31.
One of the most intriguing situations for healthcare providers is cancer therapy. Drug-drug interactions (DDIs) account for 20-30% of all adverse effects. Cancer patients are more likely to have potential-DDIs since they are taking other drugs with anticancer treatments to prevent the side effects of chemotherapeutic agents. The purpose of this research is to compare various decision support software (CDSS) programs in terms of potential DDIs.
A cross-sectional study was carried out. A clinical pharmacist assessed the treatment regimens of 231 cancer patients. pDDIs were evaluated using three sources: Lexicomp®, Medscape®, and Micromedex®. The ethical approval was given in November 2017 with decision number 21/286.
A total of 231 participants who were receiving therapy and had a median age of 61.5 ± 9.18 years were assessed. Almost half of the patients (49%) were female, and 155 had at least one comorbidity in addition to cancer. Medscape had a substantial pDDI ratio of 7.09%, Micromedex had a ratio of 11.15%, and Lexicomp had a ratio of 19.50%. The total number of pDDIs for major/X/contraindicated were 363-2716 (1.56-11.7 pDDI/patient) for Medscape®, 60-1723 (0.26-7.4 pDDI/patient) for Micromedex, and 145-984 (0.62-2.24 pDDI/patient) for Lexicomp®. One of the most common pDDI found was diclofenac and dexamethasone. Interactions between escitalopram and granisetron were also common, and different CDSSs made different recommendations.
In this study, significant disparities in the quantity and severity of CDSS across distinct CDSS were discovered. One of the major finding of our study was suboptimal prescribing. To address this issue, regulatory organizations should establish and verify validation and reporting mechanisms.
对于医疗保健提供者来说,最有趣的情况之一是癌症治疗。药物-药物相互作用(DDI)占所有不良反应的 20-30%。癌症患者更有可能出现潜在的 DDI,因为他们正在服用其他药物与抗癌治疗以预防化疗药物的副作用。本研究的目的是比较各种决策支持软件(CDSS)程序在潜在 DDI 方面的情况。
进行了一项横断面研究。一名临床药剂师评估了 231 名癌症患者的治疗方案。使用三种来源评估潜在的 DDI:Lexicomp®、Medscape®和 Micromedex®。伦理批准于 2017 年 11 月获得,编号为 21/286。
共评估了 231 名接受治疗且中位年龄为 61.5±9.18 岁的参与者。近一半的患者(49%)为女性,除癌症外,155 名患者还有至少一种合并症。Medscape 的潜在 DDI 比例为 7.09%,Micromedex 的比例为 11.15%,Lexicomp 的比例为 19.50%。Medscape 有 363-2716 个主要/ X/禁忌的潜在 DDI(每患者 1.56-11.7 个潜在 DDI),Micromedex 有 60-1723 个潜在 DDI(每患者 0.26-7.4 个潜在 DDI),Lexicomp 有 145-984 个潜在 DDI(每患者 0.62-2.24 个潜在 DDI)。发现最常见的潜在 DDI 之一是双氯芬酸和地塞米松。艾司西酞普兰和格拉司琼之间的相互作用也很常见,不同的 CDSS 提出了不同的建议。
在这项研究中,不同 CDSS 之间在数量和严重程度上存在显著差异。我们研究的一个主要发现是处方不当。为了解决这个问题,监管机构应建立和验证验证和报告机制。