Arizona State University, Edson College, Phoenix, AZ, USA.
UCSF Medical Center, University of California San Francisco, San Francisco, CA, USA.
Rev Endocr Metab Disord. 2021 Dec;22(4):1157-1170. doi: 10.1007/s11154-021-09677-7. Epub 2021 Jul 22.
Hyperkalemia is a common and potentially life-threatening complication following kidney transplantation that can be caused by a composite of factors such as medications, delayed graft function, and possibly potassium intake. Managing hyperkalemia after kidney transplantation is associated with increased morbidity and healthcare costs, and can be a cause of multiple hospital admissions and barriers to patient discharge. Medications used routinely after kidney transplantation are considered the most frequent culprit for post-transplant hyperkalemia in recipients with a well-functioning graft. These include calcineurin inhibitors (CNIs), pneumocystis pneumonia (PCP) prophylactic agents, and antihypertensives (angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, beta blockers). CNIs can cause hyperkalemic renal tubular acidosis. When hyperkalemia develops following transplantation, the potential offending medication may be discontinued, switched to another agent, or dose-reduced. Belatacept and mTOR inhibitors offer an alternative to calcineurin inhibitors in the event of hyperkalemia, however should be prescribed in the appropriate patient. While trimethoprim/sulfamethoxazole (TMP/SMX) remains the gold standard for prevention of PCP, alternative agents (e.g. dapsone, atovaquone) have been studied and can be recommend in place of TMP/SMX. Antihypertensives that act on the Renin-Angiotensin-Aldosterone System are generally avoided early after transplant but may be indicated later in the transplant course for patients with comorbidities. In cases of mild to moderate hyperkalemia, medical management can be used to normalize serum potassium levels and allow the transplant team additional time to evaluate the function of the graft. In the immediate post-operative setting following kidney transplantation, a rapidly rising potassium refractory to medical therapy can be an indication for dialysis. Patiromer and sodium zirconium cyclosilicate (ZS-9) may play an important role in the management of chronic hyperkalemia in kidney transplant patients, although additional long-term studies are necessary to confirm these effects.
高钾血症是肾移植后常见且潜在危及生命的并发症,可由多种因素引起,如药物、移植物延迟功能、以及可能的钾摄入。肾移植后高钾血症的管理与发病率和医疗保健成本增加有关,并且可能是导致多次住院和患者出院障碍的原因。肾移植后常规使用的药物被认为是功能良好的移植物受者发生移植后高钾血症的最常见原因。这些药物包括钙调神经磷酸酶抑制剂(CNIs)、肺孢子菌肺炎(PCP)预防性药物和抗高血压药物(血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂、β受体阻滞剂)。CNIs 可引起高钾性肾小管酸中毒。移植后发生高钾血症时,可能会停用潜在的致病药物,改用其他药物或减少剂量。贝那普利和 mTOR 抑制剂为 CNI 引起的高钾血症提供了替代药物,但应在适当的患者中开具处方。虽然复方磺胺甲噁唑(TMP/SMX)仍然是预防 PCP 的金标准,但替代药物(如氨苯砜、阿托伐醌)已被研究并可替代 TMP/SMX。作用于肾素-血管紧张素-醛固酮系统的抗高血压药物通常在移植后早期避免使用,但对于有合并症的患者,在移植过程中晚期可能需要使用。对于轻度至中度高钾血症,可以使用药物治疗来使血清钾水平正常化,并为移植团队提供更多时间来评估移植物的功能。在肾移植后立即的术后环境中,对药物治疗有抗性的快速升高的血钾可能是透析的指征。帕替莫尔和钠锆硅环硅酸酯(ZS-9)可能在肾移植患者慢性高钾血症的管理中发挥重要作用,尽管需要进行更多的长期研究来证实这些作用。