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首页> 外文期刊>Journal of oncology pharmacy practice: official publication of the International Society of Oncology Pharmacy Practitioners >White blood cell growth factor use in anoutpatient oncology clinic: Lessons andopportunities learned
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White blood cell growth factor use in anoutpatient oncology clinic: Lessons andopportunities learned

机译:门诊肿瘤诊所使用白细胞生长因子的经验教训和机会

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The increased use and high cost associated with white blood cell growth factors at our outpatient oncology clinic hasprompted this evaluation. The objectives of this study were to categorize the indication for use of pegfilgrastim andfilgrastim; evaluate the administration of these white blood cell growth factors; identify opportunities for cost savings; andidentify ways to increase prescriber adherence to evidence-based practice guidelines. This medication use evaluationstudy involved retrospective data collection from patient medical records. Adult oncology patients treated in the out-patient oncology clinic who received filgrastim or pegfilgrastim were identified and included in this study. Computerizedpatient records were used to collect data on patient demographics, risk factors for febrile neutropenia, prescribingpatterns for filgrastim and pegfilgrastim, and chemotherapy regimens. The number of pegfilgrastim and filgrastim doseswere predominately used for primary prophylaxis following chemotherapy treatment. Of the 234 total doses of pegfil-grastim used in the setting of primary prophylaxis, 28 (12%), 134 (57%), and 72 (31%) doses were given to patientsreceiving chemotherapy regimens associated with a high risk (>20%), intermediate risk (10-20%), and low risk (< 10%) offebrile neutropenia, respectively. The total number of pegfilgrastim doses used in secondary prophylaxis was 78; 20 (26%)and 58 (74%) of these doses were given to patients receiving chemotherapy regimens associated with an intermediaterisk and low risk of febrile neutropenia, respectively. This study revealed a significant portion of prescribed growth factoruse that was not in accordance with clinical practice guidelines.
机译:在我们的门诊肿瘤诊所,与白细胞生长因子相关的使用增加和成本高昂促使了这一评估。这项研究的目的是对使用培非非司亭和非格拉司亭的适应症进行分类。评估这些白细胞生长因子的给药;找出节省成本的机会;并确定增加处方者对循证实践指南的依从性的方法。该药物使用评估研究涉及从患者病历中收集回顾性数据。确定在门诊肿瘤诊所接受非格司亭或吡非司亭治疗的成年肿瘤患者,并将其纳入本研究。使用计算机化的患者记录来收集有关患者人口统计资料,发热性中性粒细胞减少症的危险因素,非格司亭和培非非司亭的处方模式以及化疗方案的数据。 pegfilgrastim和filgrastim剂量的数量主要用于化疗后的一级预防。在主要预防措施中使用的234剂pegfil-grastim总剂量中,接受高风险(> 20)化疗方案的患者给予28(12%),134(57%)和72(31%)剂量(%),中性粒细胞减少症的中度风险(10-20%)和低风险(<10%)。二次预防中使用的pegfilgrastim剂量总数为78。这些剂量中的20(26%)和58(74%)分别用于接受化疗方案的患者,这些方案与中性发热和中性粒细胞减少症的低风险相关。这项研究表明,处方中使用生长因子的很大一部分与临床实践指南不符。

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