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Intravenous citrulline generation test to assess intestinal function in intensive care unit patients

机译:静脉瓜氨酸生成测试以评估重症监护病房患者的肠道功能

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Background: Assessment of a quantifiable small intestinal function test is cumbersome. Fasting citrulline concentrations have been proposed as a measure of enterocyte function and elaborated into a citrulline generation test (CGT), which is applicable only when glutamine is administered orally. CGT is an oral test, limiting its use, for example, in critically ill patients. Objective: Assessment of normative values and feasibility of an intravenously performed CGT in intensive care unit (ICU) patients with presumed gastrointestinal motility disturbances, especially when performed intravenously. Design: CGT reference values were determined in 16 stable ICU patients using two different CGT methods, namely following either enteral or intravenous glutamine administration and both with simultaneous arterial and venous plasma citrulline sampling at six time-points. Plasma amino acid analysis was performed using reverse-phase high-performance liquid chromatography. Results: The median total generation of citrulline in 90 min (CGT iAUCT90) was markedly higher with arterial citrulline sampling compared with venous citrulline sampling, being 724±585 and 556±418 μmol/L/min for enteral glutamine, respectively ( p =0.02) and 977±283 and 769±231 μmol/L/min for intravenous glutamine, respectively ( p =0.0004). The median slope (time-dependent increase) for plasma arterial and venous citrulline during the CGT was 0.20±0.16 and 0.18±0.12 μmol/L/min for enteral glutamine, respectively ( p =0.004) and 0.22±0.16 and 0.19±0.05 μmol/L/min for intravenous glutamine, respectively ( p =0.02). Conclusion: Intravenous glutamine administration combined with arterial plasma citrulline sampling yielded the least variation in CGT characteristics in stable ICU patients. A 2-point measurement test had comparable test characteristics as a 6-point measurement CGT and seems promising.
机译:背景:可量化的小肠功能测试的评估很麻烦。已经提出了空腹瓜氨酸浓度作为肠细胞功能的量度,并且已详细说明为瓜氨酸生成测试(CGT),仅当口服谷氨酰胺时才适用。 CGT是一项口服测试,例如在危重病人中限制了其使用。目的:评估重症监护病房(ICU)可能存在胃肠道动力障碍(尤其是静脉注射)的静脉注射CGT的规范价值和可行性。设计:使用两种不同的CGT方法,即在进行肠内或静脉内谷氨酰胺给药后,同时在六个时间点同时进行动脉和静脉血浆瓜氨酸采样,确定了16位稳定ICU患者的CGT参考值。使用反相高效液相色谱法进行血浆氨基酸分析。结果:90分钟的瓜氨酸总生成量(CGT iAUCT90)与静脉瓜氨酸采样相比,动脉瓜氨酸采样显着更高,肠内谷氨酰胺分别为724±585和556±418μmol/ L / min(p = 0.02 )和静脉内谷氨酰胺分别为977±283和769±231μmol/ L / min(p = 0.00004)。 CGT期间血浆动脉和静脉瓜氨酸的中值斜率(随时间增加)肠内谷氨酰胺分别为0.20±0.16和0.18±0.12μmol/ L / min(p = 0.004)和0.22±0.16和0.19±0.05μmol静脉内谷氨酰胺的/ L / min分别为(p = 0.02)。结论:静脉内谷氨酰胺联合动脉血浆瓜氨酸采样可使稳定ICU患者的CGT特征变化最小。 2点测量测试具有与6点测量CGT相当的测试特性,并且似乎很有希望。

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