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首页> 外文期刊>BMC Nephrology >Chloride content of solutions used for regional citrate anticoagulation might be responsible for blunting correction of metabolic acidosis during continuous veno-venous hemofiltration
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Chloride content of solutions used for regional citrate anticoagulation might be responsible for blunting correction of metabolic acidosis during continuous veno-venous hemofiltration

机译:用于区域柠檬酸盐抗凝的溶液中的氯化物含量可能是导致连续静脉-静脉血液滤过过程中代谢性酸中毒的钝化校正的原因

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Background Citrate, the currently preferred anticoagulant for continuous veno-venous hemofiltration (CVVH), may influence acid-base equilibrium. Methods The effect of 2 different citrate solutions on acid-base status was assessed according to the Stewart-Figge approach in two consecutive cohorts of critically ill adult patients. The first group received Prismocitrate 10/2 (PC10/2; 10?mmol citrate/L). The next group was treated with Prismocitrate 18/0 (PC18; 18?mmol citrate/L). Both groups received bicarbonate-buffered fluids in post-dilution. Results At similar citrate flow, the metabolic acidosis present at baseline in both groups was significantly attenuated in PC18 patients but persisted in PC10/2 patients after 24?h of treatment (median pH?7,42 vs 7,28; p =?0.0001). Acidosis in the PC10/2 group was associated with a decreased strong ion difference and an increased strong ion gap (respectively 43 vs. 51?mmol/L and 17 vs. 12?mmol/L, PC10/2 vs. PC18; both p =?0.001). Chloride flow was higher in PC10/2 than in PC18 subjects (25.9 vs 14.3?mmol/L blood; p Conclusion Correction of acidosis was blunted in patients who received 10?mmol citrate/L as regional anticoagulation during CVVH. This could be explained by differences in chloride flow between the applied citrate solutions inducing hyperchloremic acidosis.
机译:背景枸rate酸盐,目前首选的连续静脉-静脉血液滤过(CVVH)抗凝剂,可能会影响酸碱平衡。方法根据Stewart-Figge方法,在连续两个危重病成年患者队列中评估了两种不同柠檬酸盐溶液对酸碱状态的影响。第一组接受Prismocitrate 10/2(PC10 / 2; 10?mmol柠檬酸盐/ L)。下一组用普利司莫特18/0(PC18; 18?mmol柠檬酸盐/ L)治疗。两组均在稀释后接受碳酸氢盐缓冲液。结果在相似的柠檬酸流量下,两组在基线时出现的代谢性酸中毒在PC18患者中均显着减弱,但在治疗24小时后仍在PC10 / 2患者中持续(中位pH值分别为7.42和7,28; p = 0.0001)。 )。 PC10 / 2组的酸中毒与强离子差的减少和强离子间隙的增加有关(分别为43 vs. 51?mmol / L和17 vs. 12?mmol / L,PC10 / 2 vs. PC18;两者均p = 0.001)。 PC10 / 2中的氯离子流量高于PC18受试者(25.9 vs 14.3?mmol / L血液; p结论)在CVVH期间接受10?mmol柠檬酸/ L作为区域抗凝治疗的患者酸中毒的矫正作用减弱。柠檬酸盐溶液之间的氯离子流量差异导致高氯酸中毒。

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