de la Roche M R, Gauthier L
Canadian Ministry of National Defence, National Defence Medical Centre, Ottawa, Ontario.
Ann Emerg Med. 1993 Oct;22(10):1551-5. doi: 10.1016/s0196-0644(05)81257-0.
To examine flow rates and quantify red blood cell (RBC) destruction using various catheter sizes, pressures, and dilutions in the transfusion of packed RBCs.
Study equipment was identical to that used in clinical practice. Laboratory tests consisting of plasma free hemoglobin, hematocrit, RBC count, and plasma potassium were used to assess RBC destruction. Statistical analysis was performed using the two-tailed Student's t-test. Statistical significance was considered to be .05.
Packed RBCs were transfused in vitro through 16-, 18-, 20-, and 22-gauge catheters using no pressure, 150 mm Hg, and 300 mm Hg pressure as well as dilutions of 0, 100, and 250 mL normal saline.
Flow rates in milliliters per minute were recorded for all combinations. The extent of RBC destruction was estimated using RBC count, hematocrit, plasma free hemoglobin, and serum potassium.
Increases in flow rates of tenfold simply by diluting the units with 250 mL normal saline and sevenfold with the application of a pressure device were seen at all catheter sizes. The combination of both dilution and pressure increased flow rates 33-fold, varying between 70 and 300 mL/min for 22- and 16-gauge catheters, respectively. No significant difference in RBC destruction was seen among the four catheter sizes.
Flow rates of packed RBCs sufficient for volume resuscitation can be achieved using 20- and 22-gauge catheters without evidence of increased RBC destruction. When it is impossible to obtain large-bore venous access or when such access would necessitate a delay of five to ten minutes, smaller catheters used in conjunction with dilution, pressure, or both should be considered.
在输注浓缩红细胞时,使用不同规格的导管、压力和稀释液,检测流速并量化红细胞(RBC)破坏情况。
研究设备与临床实践中使用的设备相同。通过检测血浆游离血红蛋白、血细胞比容、红细胞计数和血浆钾等实验室指标来评估红细胞破坏情况。采用双侧t检验进行统计分析。统计学显著性水平设定为0.05。
在体外通过16号、18号、20号和22号导管输注浓缩红细胞,分别采用无压力、150 mmHg和300 mmHg的压力,以及0、100和250 mL生理盐水的稀释液。
记录所有组合情况下每分钟的流速(毫升/分钟)。使用红细胞计数、血细胞比容、血浆游离血红蛋白和血清钾来估计红细胞破坏程度。
在所有导管规格下,仅用250 mL生理盐水稀释单位血液可使流速提高10倍,使用压力装置可使流速提高7倍。稀释和压力相结合可使流速提高33倍,22号和16号导管的流速分别在70至300 mL/分钟之间变化。四种导管规格在红细胞破坏方面无显著差异。
使用20号和22号导管可实现足以进行容量复苏的浓缩红细胞流速,且无红细胞破坏增加的证据。当无法获得大口径静脉通路或获得该通路会导致延迟5至10分钟时,可考虑使用较小的导管并结合稀释、压力或两者同时使用。