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Agreement of measured and calculated serum osmolality during the infusion of mannitol or hypertonic saline in patients after craniotomy: a prospective, double-blinded, randomised controlled trial

机译:开颅手术后患者输注甘露醇或高渗盐水期间测得和计算出的血浆渗透压的协议:一项前瞻性,双盲,随机对照试验

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Background Mannitol and hypertonic saline are used to ameliorate brain edema and intracranial hypertension during and after craniotomy. We hypothesized that the agreement of measured and calculated serum osmolality during the infusion of hypertonic saline would be better than mannitol. The objective was to determine the accuracy of serum osmolality estimation by different formulas during the administration of hyperosmolar agent. Methods A prospective, randomized, double-blinded, controlled trial was conducted in a 30-bed neurosurgical intensive care unit at a university hospital. Thirty-five adult patients requiring the use of hyperosmolar agents for prevention or treatment of brain edema after elective craniotomy were enrolled, and randomly assigned 1:1 to receive 125?mL of either 20 % mannitol (mannitol group) or 3.1 % sodium chloride solution (hypertonic saline group) in 15?min. Serum osmolality, serum sodium and potassium concentration, blood urea nitrogen and blood glucose concentration were measured during the study period. The primary outcome was the agreement of measured and estimated serum osmolality during the infusion of the two experimental agents. We used Bland and Altman’s limits of agreement analysis to clarify the accuracy of estimated serum osmolality. Bias and upper and lower limits of agreement of bias were calculated. Results For each formula, the bias was statistically lower in hypertonic saline group than mannitol group (p? Conclusions Compared to mannitol, a better agreement between measured and estimated serum osmolality was found during the infusion of hypertonic saline. This result indicates that, if hypertonic saline is chosen to prevent or treat brain edema, calculated serum osmolality can be used as a reliable surrogate for osmolality measurement. Trial registration ClinicalTrials.gov identifier: NCT02037815
机译:背景技术甘露醇和高渗盐水用于在开颅手术期间和之后减轻脑水肿和颅内高压。我们假设在高渗盐水输注过程中测得的和计算的血清渗透压的一致性比甘露醇好。目的是确定高渗剂给药期间不同配方的血清渗透压估计的准确性。方法在一家大学医院的30张床的神经外科重症监护室进行了一项前瞻性,随机,双盲,对照试验。选择行开颅手术后需要使用高渗药物预防或治疗脑水肿的35名成年患者,随机分配1:1以接受125?mL的20%甘露醇(甘露醇组)或3.1%氯化钠溶液。 (高渗盐水组)在15分钟内。在研究期间测量血清渗透压,血清钠和钾浓度,血尿素氮和血糖浓度。主要结果是在输注两种实验药物期间测得的血清渗透压和估计的摩尔渗透压浓度一致。我们使用Bland和Altman的一致性极限分析来阐明估计的血清渗透压的准确性。计算偏差和偏差一致性的上下限。结果对于每种配方,高渗盐水组的偏倚在统计学上低于甘露醇组(p?结论)与甘露醇相比,在输注高渗盐水过程中,测得的血清渗透压与估计的摩尔渗透压浓度之间存在更好的一致性。该结果表明,如果高渗盐水选择生理盐水以预防或治疗脑水肿,计算出的血清渗透压可以用作渗透压测量的可靠替代物临床注册ClinicalTrials.gov标识符:NCT02037815

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