Singh Anika T, Mc Causland Finnian R
University College Dublin School of Medicine and Medical Science, Dublin, Ireland.
Renal Division, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Semin Dial. 2017 Nov;30(6):509-517. doi: 10.1111/sdi.12629. Epub 2017 Jul 9.
Homeostatic regulation of plasma osmolality (POsm) is critical for normal cellular function in humans. Arginine vasopressin (AVP) is the major hormone responsible for the maintenance of POsm and acts to promote renal water retention in conditions of increased POsm. However, AVP also exerts pressor effects, and its release can be stimulated by the development of effective arterial blood volume depletion. Patients with end-stage renal disease on hemodialysis, particularly those with minimal or no residual renal function, have impaired ability to regulate water retention in response to AVP. While hemodialysis can assist with this task, patients are subject to relatively rapid shifts in volume and electrolytes during the procedure. This can result in the development of transient osmotic gradients that lead to the movement of water from the extracellular to the intracellular space. Hypotension may result-both as a consequence of water movement out of the intravascular compartment, but also from impaired AVP release and inadequate vascular tone. In this review, we explore the evidence for POsm changes during hemodialysis, associations with adverse outcomes, and methods to minimize the rapidity of changes in POsm in an effort to reduce patient symptoms and minimize intra-dialytic hypotension.
血浆渗透压(POsm)的稳态调节对人类正常细胞功能至关重要。精氨酸加压素(AVP)是维持POsm的主要激素,在POsm升高的情况下,它可促进肾脏对水的潴留。然而,AVP也具有升压作用,有效动脉血容量减少可刺激其释放。接受血液透析的终末期肾病患者,尤其是那些残余肾功能极少或无残余肾功能的患者,对AVP作出反应来调节水潴留的能力受损。虽然血液透析可以帮助完成这项任务,但患者在透析过程中会出现相对快速的容量和电解质变化。这可能会导致短暂渗透梯度的形成,从而导致水从细胞外间隙向细胞内间隙移动。低血压可能由此产生,这既是水从血管内 compartment 移出的结果,也是AVP释放受损和血管张力不足所致。在本综述中,我们探讨了血液透析期间POsm变化的证据、与不良结局的关联,以及尽量减少POsm变化速度的方法,以减轻患者症状并尽量减少透析中低血压的发生。