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Impact of Clinical, Unit-Specific Guidelines on Dornase Alfa Use in Critically Ill Pediatric Patients Without Cystic Fibrosis

机译:临床,单位特异性指南对Dornase Alfa的影响,在没有囊性纤维化的批评性儿科患者中使用

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Purpose: The purpose of this study was to evaluate the impact of the implementation of pharmacist-guided, unit-specific dornase alfa utilization guidelines for patients without cystic fibrosis in an academic medical institution. The study reviewed the prescribing patterns in the institution's pediatric intensive care unit (PICU) and pediatric cardiac intensive care unit (PCICU) before and after the implementation of these guidelines. The primary objective of this study was to determine the effects of the guidelines on the number of dornase alfa doses prescribed in critically ill pediatric patients without cystic fibrosis. We also evaluated the pharmacoeconomic effect of the guidelines and the impact on clinical outcomes in these critically ill patients. Methods: This study was a single-center, retrospective evaluation of the implementation of pharmacist-guided, unit-specific dornase alfa guidelines. The guidelines were piloted on November 1, 2015. Pre-guideline implementation data were collected from February 1, 2015 to October 31, 2015. Post-guideline implementation data were collected from December 1, 2016 to August 31, 2016. We included patients admitted to the PICU and PCICU who had received at least 1 dose of dornase alfa and did not have a medical history or suspicion of cystic fibrosis. Results: During the pre-guideline data collection period, 1067 doses of dornase alfa were administered, and following guideline implementation, 239 doses were administered. The average total admission length of stay for patients admitted to the PICU or PCICU before guideline implementation and after implementation was 16.22 and 13.14 days, respectively (P = .042). Conclusions: The implementation of pharmacist-guided, unit-specific dornase alfa guidelines within the PICU and PCICU resulted in a 77.6% reduction in the use of dornase alfa among these units. The implementation of these guidelines led to a cost reduction of approximately US $87 707.76 over a 9-month period for the health system. During the study, the length of stay for patients admitted to the PICU and PCICU did not increase, indicating that the reduction in use of dornase alfa did not negatively affect the overall hospital length of stay for patients.
机译:目的:本研究的目的是评估在学术性医疗机构中对无囊性纤维化患者实施药剂师指导的、针对特定单位的多纳斯阿尔法使用指南的影响。该研究回顾了该机构的儿科重症监护病房(PICU)和儿科心脏重症监护病房(PCICU)在实施这些指南前后的处方模式。本研究的主要目的是确定指南对无囊性纤维化的危重儿童患者服用多纳斯阿尔法剂量的影响。我们还评估了指南的药物经济学效果以及对这些危重患者临床结果的影响。方法:本研究是一项单中心回顾性评估,旨在评估药剂师指导的、针对特定单位的多纳斯阿尔法指南的实施情况。该指南于2015年11月1日试行。从2015年2月1日至2015年10月31日收集了指南实施前的数据。指南实施后的数据收集于2016年12月1日至2016年8月31日。我们纳入了入住PICU和PCICU的患者,他们至少服用了1剂dornase alfa,没有病史或怀疑有囊性纤维化。结果:在指南前数据收集期间,服用了1067剂dornase-alfa,在指南实施后服用了239剂。指南实施前和实施后PICU或PCICU患者的平均总住院时间分别为16.22和13.14天(P=0.042)。结论:在PICU和PCICU内实施药剂师指导的、针对具体单元的多纳斯阿尔法指南,导致这些单元中多纳斯阿尔法的使用减少了77.6%。这些准则的实施使卫生系统在9个月内的成本降低了约87 707.76美元。在研究期间,入住PICU和PCICU的患者的住院时间没有增加,这表明减少使用dornase-alfa不会对患者的总体住院时间产生负面影响。

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