Pannu Neesh, Tonelli Marcello
Department of Medicine, Division of Nephrology, Alberta, Canada.
Curr Opin Nephrol Hypertens. 2006 May;15(3):285-90. doi: 10.1097/01.mnh.0000222696.92088.28.
Contrast nephropathy is a common complication associated with angiographic procedures that carries significant morbidity and mortality. Recent clinical trials of prophylactic strategies have reported contradictory results. This review presents recent insights into the pathophysiology of contrast nephropathy and reviews trial results in this context.
A prediction rule has been developed to better identify patients at risk of developing contrast nephropathy. Factors other than osmolality play a significant role in the pathogenesis of contrast nephropathy, at least for agents with osmolalities of 800 mOsm/kg or less. New randomized trial data do not support a role for N-acetylcysteine in contrast nephropathy prophylaxis and there is additional evidence that fenoldopam is ineffective. Pooled analyses of theophylline prophylaxis trials are inconclusive. Theoretical and clinical data suggest that ascorbic acid may be renoprotective, but this requires further study.
The overall incidence of contrast nephropathy remains low. Available evidence supports the use of hydration and low volumes of iso-osmolar or low-osmolar contrast in patients at risk of developing contrast nephropathy. Heterogeneity has affected interpretability of interventional trials of N-acetylcysteine or theophylline prophylaxis strategies. Future clinical trials must identify and target moderate-risk to high-risk patients and ensure that proven therapies are included in trial protocols.
对比剂肾病是血管造影术常见的并发症,具有较高的发病率和死亡率。近期预防性策略的临床试验报告了相互矛盾的结果。本综述介绍了对比剂肾病病理生理学的最新见解,并在此背景下回顾了试验结果。
已制定了一个预测规则,以更好地识别有发生对比剂肾病风险的患者。除渗透压外,其他因素在对比剂肾病的发病机制中也起重要作用,至少对于渗透压为800 mOsm/kg或更低的造影剂是如此。新的随机试验数据不支持N-乙酰半胱氨酸在预防对比剂肾病中的作用,并且有更多证据表明非诺多泮无效。茶碱预防试验的汇总分析尚无定论。理论和临床数据表明,维生素C可能具有肾脏保护作用,但这需要进一步研究。
对比剂肾病的总体发病率仍然较低。现有证据支持对有发生对比剂肾病风险的患者进行水化治疗,并使用低剂量的等渗或低渗对比剂。异质性影响了N-乙酰半胱氨酸或茶碱预防策略干预试验的可解释性。未来的临床试验必须识别并针对中高危患者,并确保试验方案中纳入已证实的治疗方法。