Low flux or high flux membranes can be applied for hemodialysis. High-flux dialysis is defined as a β2-microglobulin clearance of over 20 mL/min (
1,
2). High flux membranes compared to low flux have larger pores and allow the diffusing of a greater amount of uremic toxins and middle molecules such as β2-microglobuline and may, therefore, decrease the risk of dialysis-related amyloidosis (
3,
4). In addition, these membranes have other advantages such as increasing patients’ survival (
5,
6), reduced admission and morbidity (
7,
8), fewer activations of the coagulation pathway and complement system, lower leukocytosis, fewer activations of inflammatory system and less cytokines secretion, removal of more endotoxines, better lipid profile (
9,
10), reduced infection risk, aluminum toxicity and better preserved renal function (
11,
12).
Furthermore, intradialysis hypoxia was reported in former studies (
13-
15). Although the cause of this hypoxia is not completely clear, sequestration of leukocytes in pulmonary capillary may play an important role (
16). The type of buffer used in dialysis also may be important in hypoxia (
17,
18).