Department of Clinical Pharmacy, Institute of Pharmacy, University of Bonn, Bonn, Germany.
Institute of Medical Biometrics, Informatics, and Epidemiology, University Hospital Bonn, Bonn, Germany.
J Oncol Pharm Pract. 2021 Sep;27(6):1439-1446. doi: 10.1177/1078155220962178. Epub 2020 Oct 6.
Head and neck cancer (HNC) patients are particularly vulnerable to drug-related problems (DRPs) given the toxicity of concomitant chemoradiotherapy (CCRT).
To investigate the number and type of potential DRPs (pDRPs) in HNC outpatients undergoing five consecutive cycles of CCRT.
A single-centre, non-randomized, non-interventional, observational study was conducted at the Oncological Outpatient Clinic of the Center for Integrated Oncology at the University Hospital Bonn, Germany. Clinical pharmacists took a comprehensive medication history, documented laboratory data, assessed patients' symptom burden, and retrospectively performed medication reviews at study entry and on the first day of each therapy cycle without any clinical intervention.
In 26 patients, the mean number of pDRPs continuously increased during therapy course, from 4.8 (SD 2.7, range 2-12) at cycle 1 to 6.9 (SD 2.6, range 2-12) at cycle 5, with drug-drug interactions, adverse drug reactions, inappropriate durations of use, and inappropriate dosage intervals being the most common. Considering only new and recurrent pDRPs, the mean number was 4.3 (SD 2.3, range 2-9) at cycle 1 and lower in the further therapy course with an average of 1.3 (SD 1.7, range 0-7) at cycle 2 and 1.9 (SD 1.5, range 0-5) at cycle 5. The number of pDRPs was found to be associated with medication regimen complexity and health-related quality of life assessed in the first therapy cycle.
pDRPs frequently occurred in HNC outpatients demonstrating the need for pharmaceutical care. A methodological framework for repeated medication reviews was established, facilitating implementation into routine healthcare practice.
由于头颈部癌症(HNC)患者在接受同期放化疗(CCRT)时会出现毒性反应,因此他们特别容易出现药物相关问题(DRP)。
调查连续进行五个周期 CCRT 的 HNC 门诊患者的潜在药物相关问题(pDRP)的数量和类型。
这是一项在德国波恩大学医院综合肿瘤中心肿瘤门诊进行的单中心、非随机、非干预性、观察性研究。临床药师详细询问患者的药物使用史,记录实验室数据,评估患者的症状负担,并在研究入组时以及每个治疗周期的第一天进行药物回顾,回顾时不进行任何临床干预。
在 26 名患者中,pDRP 的数量在治疗过程中持续增加,从第 1 周期的 4.8(SD 2.7,范围 2-12)增加到第 5 周期的 6.9(SD 2.6,范围 2-12),药物-药物相互作用、药物不良反应、用药时间不当和剂量间隔不当最为常见。仅考虑新出现和复发的 pDRP,第 1 周期的平均数量为 4.3(SD 2.3,范围 2-9),在进一步的治疗过程中逐渐减少,第 2 周期的平均数量为 1.3(SD 1.7,范围 0-7),第 5 周期的平均数量为 1.9(SD 1.5,范围 0-5)。pDRP 的数量与第 1 个治疗周期中评估的药物治疗方案复杂性和健康相关生活质量有关。
HNC 门诊患者经常出现 pDRP,这表明需要进行药学服务。建立了重复药物审查的方法学框架,便于将其纳入常规医疗保健实践。