Waniewski J, Sobiecka D, Debowska M, Heimbürger O, Weryński A, Lindholm B
Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Warsaw--Poland.
Int J Artif Organs. 2005 Oct;28(10):976-86. doi: 10.1177/039139880502801004.
Two major types of permanent loss of ultrafiltration capacity (UFC) were previously distinguished among patients treated with CAPD: 1) type HDR with high diffusive peritoneal transport rate of small solutes and low osmotic conductance,but with normal fluid absorption rate, and 2) type HAR with high fluid absorption rate, but with normal diffusive peritoneal transport rate of small solutes and normal osmotic conductance. However, the detailed pattern of changes in peritoneal transport parameters in patients developing loss of ultrafiltration capacity is not known.
Analysis of solute and fluid transport parameters in the same patient before and after UFC loss.
Seven CAPD patients who had undergone repeated dwell studies,which were carried out before and/or after the onset of UFC loss.
Dialysis fluids (2 L) with glucose or a mixture of amino acids as osmotic agent at three basic tonicities were applied during 6 hour dwell studies. Fluid and solute transport parameters were previously shown not to be affected by these dialysis solutions (except by hypertonic amino acid-based solution). Intraperitoneal dialysate volume and fluid absorption rate were assessed using radiolabeled human serum albumin (RISA). Osmotic conductance (a(OS))was estimated by a mathematical model as ultrafiltration rate induced by unit osmolality gradient. Diffusive mass transport coefficients, K(BD), for glucose,urea,and creatinine were estimated using the modified Babb-Randerson-Farrell model.
Five patients had increased K(BD) for small solutes after the onset of UFC loss,and three of them had decreased a(OS),whereas two patients had normal a(OS). In one of them, a(OS) decreased with time after the onset of UFC loss with concomitant normalization of glucose absorption. In all studies of these five patients the fluid absorption rate was within the normal range. Two other patients had increased fluid absorption rate (about 5 ml/min),and one of them also had increased K(BD) for small solutes,in two consecutive dwell studies in each patient with the second study being carried out at 1 and 7 months respectively after the first one. In all four studies in these two patients, the a(OS) was within the normal range. The sodium dip during dialysis with 3.86% glucose-based solution was lost, not only among most patients with UFC loss related to reduced osmotic conductance, but also in patients with increased K(BD).
The occurrence of two major types of UFC loss was confirmed. However, a case of a mixed type of UFC loss with high fluid absorption rate and high K(BD) for small solutes, but normal osmotic conductance, and with normalization of initially high K(BD) for small solutes, linked with decreasing initially normal osmotic conductance,was also found. As a reduced sodium dip with hypertonic glucose solution is not only seen in patients with reduced osmotic conductance, it cannot reliably be used as a single measure of decreased aquaporin function. Permanent ultrafiltration capacity loss may be a dynamic phenomenon with a variety of alterations in peritoneal transport characteristics.
既往在接受持续性非卧床腹膜透析(CAPD)治疗的患者中区分出两种主要类型的超滤功能(UFC)永久性丧失:1)HDR型,小分子溶质的高扩散性腹膜转运率、低渗透传导率,但液体吸收率正常;2)HAR型,高液体吸收率,但小分子溶质的扩散性腹膜转运率正常且渗透传导率正常。然而,超滤功能丧失患者腹膜转运参数的详细变化模式尚不清楚。
分析同一患者超滤功能丧失前后的溶质和液体转运参数。
7例接受CAPD治疗的患者,在超滤功能丧失之前和/或之后进行了多次留腹研究。
在6小时留腹研究期间,应用含葡萄糖或氨基酸混合物作为渗透剂的三种基础张力的透析液(2L)。先前已表明这些透析液(高渗氨基酸基溶液除外)不会影响液体和溶质转运参数。使用放射性标记的人血清白蛋白(RISA)评估腹腔内透析液体积和液体吸收率。渗透传导率(a(OS))通过数学模型估算为单位渗透压梯度诱导的超滤率。使用改良的Babb-Randerson-Farrell模型估算葡萄糖、尿素和肌酐的扩散质量转运系数K(BD)。
5例患者在超滤功能丧失后小分子溶质的K(BD)增加,其中3例a(OS)降低,而2例a(OS)正常。其中1例患者,超滤功能丧失后a(OS)随时间降低,同时葡萄糖吸收恢复正常。在这5例患者的所有研究中,液体吸收率均在正常范围内。另外2例患者液体吸收率增加(约5ml/min),其中1例在每位患者的连续两次留腹研究中小分子溶质的K(BD)也增加,第二次研究分别在第一次研究后的1个月和7个月进行。在这2例患者的所有4项研究中,a(OS)均在正常范围内。不仅在大多数与渗透传导率降低相关的超滤功能丧失患者中观察到使用3.86%葡萄糖基溶液透析期间的钠梯度降低,在K(BD)增加的患者中也观察到。
证实了两种主要类型的超滤功能丧失的存在。然而,还发现了1例混合型超滤功能丧失,其液体吸收率高、小分子溶质的K(BD)高,但渗透传导率正常,且最初较高的小分子溶质K(BD)恢复正常,同时最初正常的渗透传导率降低。由于高渗葡萄糖溶液钠梯度降低不仅见于渗透传导率降低的患者,因此不能可靠地将其作为水通道蛋白功能降低的单一指标。永久性超滤功能丧失可能是一种动态现象,腹膜转运特征有多种改变。