及时识别和干预缺血性单分子神经病变,防止患者严重残疾
Raja GnanaDev1,2, Aldin Malkoc1,2, Jeffrey Hsu1
1Kaiser Fontana Medical Center, Fontana, CA, USA.
对缺血性单基神经病变 (IMN) 的及时诊断和干预,这是动脉静脉和移植的罕见并发症,可以预防患者的重大残疾. 早期识别是避免长期发病的关键.
科学领域:
- 血管外科 血管外科
- 神经学 神经学
- 腎臟病學 (nephrology) 是一種醫學.
背景情况:
- 缺血性单基神经病变 (IMN) 是一种罕见但严重的并发症,在动脉静脉囊 (AVF) 和动脉静脉移植 (AVG) 形成后出现.
- 延迟IMN的诊断可能会导致严重和潜在的不可逆转的患者残疾.
- 这种情况需要在血液透析接入程序后进行仔细的术后监测.
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