Measuring the accuracy of propofol target-controlled infusion (TCI) before and after surgery with major blood loss

被引:14
作者
Mohler, Thomas [1 ]
Welter, JoEllen [1 ]
Steurer, Martina [2 ]
Neumann, Luis [1 ]
Zueger, Max [3 ]
Kraemer, Thomas [4 ]
Dullenkopf, Alexander [1 ]
机构
[1] Inst Anaesthesia, Intens Care Med, Spital Thurgau, Pfaffenholzstrasse 4, CH-8501 Frauenfeld, Switzerland
[2] Univ Calif San Francisco, Dept Pediat, San Francisco, CA USA
[3] Inst Lab Med, Spital Thurgau, Frauenfeld, Switzerland
[4] Univ Zurich, Forens Pharmacol, Toxicology, Zurich, Switzerland
关键词
Propofol administration; Target controlled infusion; Automated drug delivery devices; PHARMACOKINETIC MODELS; PREDICTIVE PERFORMANCE; DIPRIFUSOR; ANESTHESIA;
D O I
10.1007/s10877-019-00261-8
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Target-controlled infusion (TCI) is based on pharmacokinetic models designed to achieve a desired drug level in the blood. TCI's predictive accuracy of plasma propofol levels at the end of surgery with major blood loss has not been well established. This prospective observational study included adult patients (BMI 20-35 kg/m(2)) undergoing surgery with expected blood loss >= 1500 mL. The study was conducted with the Schnider TCI propofol model (Alaris PK Infusion Pump, CareFusion, Switzerland). Propofol levels were assessed in steady-state at the end of anaesthesia induction (T-initial) and before the end of surgery (T-final). Predicted propofol levels (C-TCI) were compared to measured levels (C-blood). Twenty-one patients were included. The median estimated blood loss was 1600 mL (IQR 1000-2300), and the median fluid balance at T-final was + 3200 mL (IQR 2320-4715). Heart rate, mean arterial blood pressure, and blood lactate did not differ significantly between T-initial and T-final. The median bispectral index (0-100) was 50 (IQR 42-54) and 49 (IQR 42-56) at the two respective time points. At T-initial, median C-TCI was 2.2 mu mol/L (IQR 2-2.45) and C-blood was 2.0 mu mol/L (bias 0.3 mu mol/L, limits of agreement - 1.1 to 1.3, p = 0.33). C-TCI and C-blood at T-final were 2.0 mu mol/L (IQR 1.6-2.2) and 1 mu mol/L (IQR 0.8-1.4), respectively (bias 0.6 mu mol/L, limits of agreement - 0.89 to 1.4, p < 0.0001). Propofol TCI allows clinically unproblematic conduct of general anaesthesia. In cases of major blood loss, the probability of propofol TCI overestimating plasma levels increases. Trial registration German Clinical Trials Register (DRKS; DRKS00009312).
引用
收藏
页码:97 / 103
页数:7
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