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维持性血液透析患者的膜生物相容性与营养

Membrane biocompatibility and nutrition in maintenance haemodialysis patients.

作者信息

Lindsay R M, Bergström J

机构信息

Artificial Kidney Research Centre, Victoria Hospital, London, Ontario, Canada.

出版信息

Nephrol Dial Transplant. 1994;9 Suppl 2:150-5.

PMID:8065607
Abstract

The interrelationship between Kt/V (urea), protein catabolic rate, dialysis membrane, nutritional status and outcome: These correlations are summarized in Figure 3. A given dialysis membrane will allow a given Kt/V (urea) and hence, influence urea removal. The balance between urea removal and urea generation will determine the urea pool and the urea concentration for a given volume of distribution. It is postulated that this urea concentration in some way causes 'biofeedback' determining the protein intake of a given patient which, of course, will influence the protein catabolic rate and hence, the urea generation. The protein catabolic rate may be adversely influenced by the use of bioincompatible membranes which produce activated complement, IL-1, tissue necrosing factor, etc. In addition, the membrane will determine the Kt/V (other toxins; 'middle molecules') which may also influence protein intake. The protein intake will affect the overall nutritional status which, in turn, has a major impact on morbidity and mortality. We suggest that the most effective way to influence morbidity and mortality is to ensure that a Kt/V (urea) well in excess of 1 (perhaps between 1.4 and 1.6) is delivered to the patient if a cellulosic membrane is used. It may be possible to deliver less than this value using a biocompatible membrane which has increased Kt/V (middle molecules) for a given Kt/V (urea). Whatever the method of dialysis or Kt/V (urea) applied, attention should also be gi en to nutritional assessment of the patient, and amongst the tools available to the clinician is the estimation of the protein catabolic rate by urea kinetic modelling.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

Kt/V(尿素)、蛋白质分解代谢率、透析膜、营养状况与预后之间的相互关系:这些相关性总结于图3中。特定的透析膜会允许达到特定的Kt/V(尿素),从而影响尿素清除。在给定的分布容积下,尿素清除与尿素生成之间的平衡将决定尿素池及尿素浓度。据推测,这种尿素浓度会以某种方式引起“生物反馈”,从而决定特定患者的蛋白质摄入量,这当然会影响蛋白质分解代谢率,进而影响尿素生成。使用产生活化补体、白细胞介素-1、组织坏死因子等的生物不相容膜可能会对蛋白质分解代谢率产生不利影响。此外,透析膜还将决定Kt/V(其他毒素;“中分子物质”),这也可能影响蛋白质摄入量。蛋白质摄入量会影响整体营养状况,而整体营养状况又会对发病率和死亡率产生重大影响。我们建议,如果使用纤维素膜,影响发病率和死亡率的最有效方法是确保向患者提供远超1(可能在1.4至1.6之间)的Kt/V(尿素)。对于给定的Kt/V(尿素),使用具有更高Kt/V(中分子物质)的生物相容性膜时,可能可以提供低于此值的Kt/V(尿素)。无论采用何种透析方法或应用何种Kt/V(尿素),都应关注患者的营养评估,临床医生可用的工具之一是通过尿素动力学模型估算蛋白质分解代谢率。(摘要截选至250词)

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