Daphnis Eugene, Stylianou Kostas, Alexandrakis Michael, Xylouri Irene, Vardaki Eleftheria, Stratigis Spyros, Kyriazis John
Department of Nephrology, University Hospital of Heraklion, Heraklion, Greece.
Nephron Clin Pract. 2007;106(4):c143-8. doi: 10.1159/000104424. Epub 2007 Jun 26.
BACKGROUND/AIMS: Intravenous immunoglobulin (IVIG) therapy has been associated with renal adverse effects and electrolyte disturbances.
We retrospectively evaluated a cohort of 66 unselected patients with idiopathic thrombocytopenic purpura, who received 140 courses of IVIG therapy. Acute renal failure (ARF), hyponatremia and hyperkalemia, as potential complications of IVIG therapy, were assessed from 100 IVIG courses with sufficient data for analysis.
Thirteen out of 100 (13%) IVIG courses in 10 (15%) patients were complicated with ARF. Risk factors included advanced age, pre-existing renal impairment, use of diuretics and the presence of diabetes mellitus. All patients recovered renal function 1-2 weeks after IVIG infusion. Serum sodium (sNa) fell by 5.7 and 2.7 mmol/l (p < 0.01) in patients with and without ARF, respectively. Correspondingly, serum potassium increased by 0.7 and 0.23 mmol/l (p < 0.01). There was a strong inverse correlation (r = -0.308; p < 0.01) between changes in sNa and creatinine. Changes in serum potassium could be independently predicted by changes in both sNa and creatinine (R(2) = 0.11; p < 0.01). These data suggested that both hyponatremia and hyperkalemia were (a) due to the translocational effect of the osmotic load of sucrose, and (b) largely depended on the extent of IVIG nephropathy.
In our series, ARF attributable to IVIG therapy, although not rare, was usually mild and fully reversible. High-risk patients were more susceptible to IVIG-related renal complications. Translocational hyponatremia and hyperkalemia following IVIG therapy, although unimportant in patients with normal renal function, may be of clinical significance in patients with severely compromised renal function, resulting in impaired sucrose excretion.
背景/目的:静脉注射免疫球蛋白(IVIG)治疗与肾脏不良反应及电解质紊乱有关。
我们回顾性评估了一组66例未经挑选的特发性血小板减少性紫癜患者,他们接受了140个疗程的IVIG治疗。从100个有足够数据进行分析的IVIG疗程中评估急性肾衰竭(ARF)、低钠血症和高钾血症,作为IVIG治疗的潜在并发症。
10例(15%)患者的100个IVIG疗程中有13个(13%)并发ARF。危险因素包括高龄、既往存在的肾功能损害、使用利尿剂和患有糖尿病。所有患者在IVIG输注后1 - 2周肾功能恢复。有ARF和无ARF的患者血清钠(sNa)分别下降5.7和2.7 mmol/L(p < 0.01)。相应地,血清钾分别升高0.7和0.23 mmol/L(p < 0.01)。sNa变化与肌酐变化之间存在强烈的负相关(r = -0.308;p < 0.01)。血清钾的变化可由sNa和肌酐的变化独立预测(R² = 0.11;p < 0.01)。这些数据表明,低钠血症和高钾血症均(a)归因于蔗糖渗透负荷的转运效应,且(b)很大程度上取决于IVIG肾病的程度。
在我们的系列研究中,IVIG治疗所致的ARF虽然并不罕见,但通常较轻且完全可逆。高危患者更容易发生与IVIG相关的肾脏并发症。IVIG治疗后发生的转运性低钠血症和高钾血症,虽然在肾功能正常的患者中并不严重,但在肾功能严重受损的患者中可能具有临床意义,导致蔗糖排泄受损。