Stull J C, Erenberg A, Leff R D
Division of Clinical/Hospital Pharmacy, College of Pharmacy, University of Iowa, Iowa City 52242.
Crit Care Med. 1988 Sep;16(9):888-91. doi: 10.1097/00003246-198809000-00014.
During continuous drug administration to pediatric patients, unfavorable pharmacologic effects have occurred. These effects were attributed to variations in flow from electronic infusion devices (EIDs). The intent of this investigation was to evaluate the influence of microrate (0.1 to 99.9 ml/h) EID on the accuracy, continuity, and pattern of flow of continuously effused fluid. Using a factorial study design, iv fluid was effused through iv delivery systems using combinations of five microrate EIDs, three iv flow rates, and three sample-collection intervals. Serial weights were measured at the appropriate sample-collection time using a computerized gravimetric technique to determine accuracy, continuity, and pattern of flow. All the EIDs produced accurate flow within 5% of the desired rate of 5 and 10 ml/h. At 1 ml/h, the actual iv flow rate ranged from 65.1% to 91% of the desired rate. Each of the respective EIDs produced various levels of flow continuity; each flow pattern characterized the mechanism of pump operation for each device. Thus, alteration in response (e.g., increased toxicity or decreased efficacy) to a continuous drug infusion must not be attributed exclusively to the drug or clinical condition of the patient. Serious consideration should also be given to the method of drug delivery and, in particular, the continuity of flow that results from a particular EID.
在对儿科患者持续给药期间,出现了不良药理作用。这些作用归因于电子输液装置(EID)流速的变化。本研究的目的是评估微流速(0.1至99.9 ml/h)EID对持续流出液体的准确性、连续性和流速模式的影响。采用析因研究设计,通过静脉输液系统,利用五种微流速EID、三种静脉流速和三种样本采集间隔的组合来输注静脉输液。在适当的样本采集时间使用计算机化重量分析技术测量连续重量,以确定流速的准确性、连续性和模式。所有EID在5和10 ml/h的期望流速的5%范围内产生准确的流速。在1 ml/h时,实际静脉流速为期望流速的65.1%至91%。各个EID产生了不同程度的流速连续性;每种流速模式表征了每个装置的泵操作机制。因此,对持续药物输注的反应改变(如毒性增加或疗效降低)不应仅归因于药物或患者的临床状况。还应认真考虑药物输送方法,特别是特定EID所导致的流速连续性。