Chau Destiny F, Vasilopoulos Terrie, Schoepf Miriam, Zhang Christina, Fahy Brenda G
From the *Division of Pediatric Anesthesiology, Department of Pediatrics, The Children's Hospital of the King's Daughters, Eastern Virginia Medical School, Norfolk, Virginia; †Department of Anesthesiology, University of Florida, College of Medicine, Gainesville, Florida; and ‡Department of Engineering, University of Kentucky, Lexington, Kentucky.
Anesth Analg. 2016 Sep;123(3):705-14. doi: 10.1213/ANE.0000000000001273.
Complex surgical and critically ill pediatric patients rely on syringe infusion pumps for precise delivery of IV medications. Low flow rates and in-line IV filter use may affect drug delivery. To determine the effects of an in-line filter to remove air and/or contaminants on syringe pump performance at low flow rates, we compared the measured rates with the programmed flow rates with and without in-line IV filters.
Standardized IV infusion assemblies with and without IV filters (filter and control groups) attached to a 10-mL syringe were primed and then loaded onto a syringe pump and connected to a 16-gauge, 16-cm single-lumen catheter. The catheter was suspended in a normal saline fluid column to simulate the back pressure from central venous circulation. The delivered infusate was measured by gravimetric methods at predetermined time intervals, and flow rate was calculated. Experimental trials for initial programmed rates of 1.0, 0.8, 0.6, and 0.4 mL/h were performed in control and filter groups. For each trial, the flow rate was changed to double the initial flow rate and was then returned to the initial flow rate to analyze pump performance for titration of rates often required during medication administration. These conditions (initial rate, doubling of initial rate, and return to initial rate) were analyzed separately for steady-state flow rate and time to steady state, whereas their average was used for percent deviation analysis. Differences between control and filter groups were assessed using Student t tests with adjustment for multiplicity (using n = 3 replications per group).
Mean time from 0 to initial flow (startup delay) was <1 minute in both groups with no statistical difference between groups (P = 1.0). The average time to reach steady-state flow after infusion startup or rate changes was not statistically different between the groups (range, 0.8-5.5 minutes), for any flow rate or part of the trial (initial rate, doubling of initial rate, and return to initial rate), although the study was underpowered to detect small time differences. Overall, the mean steady-state flow rate for each trial was below the programmed flow rate with negative mean percent deviations for each trial. In the 1.0-mL/h initial rate trial, the steady-state flow rate attained was lower in the filter than the control group for the initial rate (P = 0.04) and doubling of initial rate (P = 0.04) with a trend during the return to initial rate (P = 0.06), although this same effect was not observed when doubling the initial rate trials of 0.8 or 0.6 mL/h or any other rate trials compared with the control group.
With low flow rates used in complex surgical and pediatric critically ill patients, the addition of IV filters did not confer statistically significant changes in startup delay, flow variability, or time to reach steady-state flow of medications administered by syringe infusion pumps. The overall flow rate was lower than programmed flow rate with or without a filter.
复杂手术及危重症儿科患者依靠注射器输液泵精确输注静脉药物。低流速及使用静脉输液管路过滤器可能会影响药物输送。为确定静脉输液管路过滤器去除空气和/或污染物对低流速下注射器泵性能的影响,我们比较了使用和不使用静脉输液管路过滤器时测量流速与设定流速。
将带和不带静脉输液过滤器(过滤器组和对照组)的标准化静脉输液装置连接到一个10毫升注射器上,进行预充,然后安装到注射器泵上,并连接到一根16号、16厘米长的单腔导管。将导管悬挂在生理盐水液柱中,以模拟中心静脉循环的背压。在预定时间间隔通过重量法测量输注的液体量,并计算流速。在对照组和过滤器组中,对初始设定流速为1.0、0.8、0.6和0.4毫升/小时进行实验性试验。对于每次试验,将流速变为初始流速的两倍,然后再回到初始流速,以分析药物给药过程中经常需要的流速滴定的泵性能。分别对稳态流速和达到稳态的时间分析这些条件(初始流速、初始流速加倍、回到初始流速),而其平均值用于百分比偏差分析。使用Student t检验评估对照组和过滤器组之间的差异,并对多重性进行调整(每组使用n = 3次重复)。
两组从0到初始流速的平均时间(启动延迟)均<1分钟,组间无统计学差异(P = 1.0)。对于任何流速或试验部分(初始流速、初始流速加倍、回到初始流速),输注启动或流速变化后达到稳态流速的平均时间在两组之间无统计学差异(范围为0.8 - 5.5分钟),尽管该研究检测小时间差异的效能不足。总体而言,每次试验的平均稳态流速低于设定流速,每次试验的平均百分比偏差为负值。在1.0毫升/小时初始流速试验中,过滤器组在初始流速(P = 0.04)和初始流速加倍(P = 0.04)时达到的稳态流速低于对照组,在回到初始流速时有这种趋势(P = 0.06),尽管在0.8或0.6毫升/小时初始流速加倍试验或与对照组相比的任何其他流速试验中未观察到相同效果。
对于复杂手术及儿科危重症患者使用的低流速,添加静脉输液过滤器在启动延迟、流速变异性或通过注射器输液泵给药达到药物稳态流速的时间方面未产生统计学上的显著变化。无论有无过滤器,总体流速均低于设定流速。