Lindholm B, Werynski A, Bergström J
Department of Renal Medicine, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden.
Int J Artif Organs. 1990 Jun;13(6):352-8.
Standard peritoneal ultrafiltration characteristics in 18 patients undergoing continuous ambulatory peritoneal dialysis (CAPD) were investigated in a total of 21 single dwell studies of 6 h duration with 2 L of 3.86% glucose dialysis fluid. Intraperitoneal dialysate volumes were determined using radioiodinated serum albumin (RISA). Calculations were based on a novel mathematical method in which RISA elimination from the peritoneal cavity was taken into account. The RISA elimination rate, KE, was calculated as 2.1 +/- 0.5 ml/min. The true dialysate volume after 360 min (2957 +/- 196 ml) was on the average 28% lower than the volume (3737 +/- 260 ml) calculated without correction for the elimination of RISA. The mean maximum true volume plus sampling losses was 3255 ml at 240 min corresponding to a mean ultrafiltration of 762 ml between 3 min and 240 min. Our method of peritoneal volume determination proved to be useful for clinical investigations. The present study demonstrates that CAPD patients, without any major ultrafiltration problems, exhibit relatively small interpatient variations in their peritoneal volume over time curve.
在21项持续6小时、使用2L 3.86%葡萄糖透析液的单次驻留研究中,对18例接受持续性非卧床腹膜透析(CAPD)的患者的标准腹膜超滤特性进行了研究。使用放射性碘标记血清白蛋白(RISA)测定腹腔内透析液体积。计算基于一种新的数学方法,该方法考虑了RISA从腹腔的清除情况。RISA清除率KE计算为2.1±0.5ml/分钟。360分钟后的真实透析液体积(2957±196ml)平均比未校正RISA清除情况下计算出的体积(3737±260ml)低28%。240分钟时平均最大真实体积加采样损失为3255ml,对应3分钟至240分钟间平均超滤762ml。我们的腹膜体积测定方法被证明对临床研究有用。本研究表明,没有任何重大超滤问题的CAPD患者,其腹膜体积随时间变化曲线在患者间的差异相对较小。