Fusi-Schmidhauser Tanja, Caronzolo Dario, Gamondi Claudia
Palliative Care Department, Institute of Oncology of Southern Switzerland, Bellinzona, Switzerland.
Hospital Pharmacy, Ospedale San Giovanni, Bellinzona, Switzerland.
Support Care Cancer. 2016 Dec;24(12):4971-4978. doi: 10.1007/s00520-016-3357-1. Epub 2016 Jul 23.
The objectives of this study were to trace, monitor, and assess for clinical effectiveness, visual compatibility, and stability of commonly used combinations of drugs for patients hospitalized in a Swiss palliative care unit, over a 12-month period.
In this longitudinal analysis, commonly used multidrug combinations were monitored with a duly created data collection sheet for healthcare professionals. Assessment of visual changes of the mixtures and the evaluation of major changes in the overall symptom control over time were recorded. The clinical changes were classified according to reasonable correlation to the modality of drug administration and not to clinical evolution of the underlying disease.
Over a 12-month period, a total of 48 multidrug infusions were recorded and monitored. The infusions were composed of two, three, four, or five active principles. Infusions were given over a 24-h period, mainly intravenously, either through an implantable venous access port or a peripheral venous access. Main diluent was normal saline solution. Commonly used drug combinations included morphine and haloperidol, morphine, haloperidol and octreotide, morphine, haloperidol, octreotide, and chlorpromazine. No precipitations were observed during the study. Patients maintained a clinical stability and no salient changes in symptom control were attributed to inefficacy of the multidrug infusions.
The use of multidrug infusions for parenteral administration appears to confirm an adequate visual compatibility and stability, while maintaining effectiveness in terms of overall symptom control.
本研究的目的是在12个月的时间里,对瑞士一家姑息治疗病房住院患者常用药物组合的临床疗效、视觉相容性和稳定性进行追踪、监测和评估。
在这项纵向分析中,使用专门为医护人员创建的数据收集表对常用的多药组合进行监测。记录混合物的视觉变化评估以及随时间推移总体症状控制的主要变化评估。临床变化根据与药物给药方式的合理相关性进行分类,而非根据基础疾病的临床进展进行分类。
在12个月的时间里,共记录和监测了48次多药输注。输注由两种、三种、四种或五种活性成分组成。输注在24小时内进行,主要通过植入式静脉通路端口或外周静脉通路静脉给药。主要稀释剂为生理盐水溶液。常用的药物组合包括吗啡和氟哌啶醇、吗啡、氟哌啶醇和奥曲肽、吗啡、氟哌啶醇、奥曲肽和氯丙嗪。研究期间未观察到沉淀现象。患者保持了临床稳定性,且多药输注无效未导致症状控制出现明显变化。
胃肠外给药的多药输注使用似乎证实了足够的视觉相容性和稳定性,同时在总体症状控制方面保持了有效性。