Department of Intensive Care, Austin Hospital, Melbourne, Australia.
Department of Intensive Care, Austin Hospital, Melbourne, Australia; Department of Emergency and Critical Care Medicine, The University of Tokyo Hospital, Tokyo, Japan.
Aust Crit Care. 2024 Jul;37(4):632-637. doi: 10.1016/j.aucc.2023.11.005. Epub 2024 Jan 19.
Continuous haemoglobin, venous blood oxygen saturation, and haematocrit (Hct) monitoring is currently not applied during continuous renal replacement therapy (CRRT). Such Hct monitoring enables estimation of changes in blood volume as percentage change (ΔBV%) from therapy start time and is incorporated into intermittent haemodialysis machines but not CRRT machines despite its potential to optimise fluid management in CRRT patients.
To overcome this problem, we used a standalone monitor (CRIT-LINE®IV, Fresenius Medical Care, Concord, USA) with an associated in-line blood chamber (CRIT-LINE®IV Blood Chamber, Fresenius Medical Care, Concord, USA) and designed our own adaptor connection piece (TekMed and Morriset, Melbourne and Brisbane, Australia) to allow these readings at the vascular access outflow and recorded data for estimated Hct and derived ΔBV% during CRRT.
We report on this technique with an illustrative case example and 12 h of CRRT data on the fluid loss rate prescribed, hourly net patient fluid loss (range: 0-308 mL/h), mean arterial pressure, norepinephrine dose (range: 5-14 mcg/min), estimated continuous Hct and ΔBV%, and the otherwise undetected diagnosis of an approximate 15 % decrease in blood volume during the CRRT.
We have described a technical CRRT circuit modification that can facilitate a previously unavailable assessment of fluid shifts during CRRT. Further application in clinical trials is now possible.
目前,在连续肾脏替代治疗(CRRT)期间不进行连续血红蛋白、静脉血氧饱和度和血细胞比容(Hct)监测。这种 Hct 监测可用于估计从治疗开始时间起血液量的变化,作为百分比变化(ΔBV%),并被纳入间歇性血液透析机中,但不包括 CRRT 机,尽管它有可能优化 CRRT 患者的液体管理。
为了克服这个问题,我们使用了一个独立的监测器(CRIT-LINE®IV,费森尤斯医疗保健,康科德,美国)和一个相关的在线血液室(CRIT-LINE®IV 血液室,费森尤斯医疗保健,康科德,美国),并设计了自己的适配器连接件(TekMed 和 Morriset,墨尔本和布里斯班,澳大利亚),以允许在血管通路流出端进行这些读数,并记录 CRRT 期间估计的 Hct 和衍生的ΔBV%的数据。
我们报告了这项技术,并提供了一个说明性的病例示例和 12 小时的 CRRT 数据,包括规定的液体丢失率、每小时净患者液体丢失(范围:0-308 毫升/小时)、平均动脉压、去甲肾上腺素剂量(范围:5-14 微克/分钟)、估计的连续 Hct 和ΔBV%,以及在 CRRT 期间未检测到的约 15%的血液量减少的诊断。
我们描述了一种技术上的 CRRT 回路修改,可方便地评估 CRRT 期间的液体转移。现在可以进一步在临床试验中应用。