University of Missouri-Kansas City, Kansas City, MO; Saint Luke's Mid America Heart Institute, Kansas City, MO.
Washington University School of Medicine, Barnes Jewish Hospital, St. Louis, MO.
Am Heart J. 2021 Apr;234:51-59. doi: 10.1016/j.ahj.2020.12.013. Epub 2021 Jan 25.
Contrast volume used during percutaneous coronary intervention has a direct relationship with contrast-associated acute kidney injury. While several models estimate the risk of contrast-associated acute kidney injury, only the strategy of limiting contrast volume to 3 × estimated glomerular filtration rate (eGFR) gives actionable estimates of safe contrast volume doses. However, this method does not consider other patient characteristics associated with risk, such as age, diabetes or heart failure.
Using the National Cardiovascular Data Registry acute kidney injury risk model, we developed a novel strategy to define safe contrast limits by entering a contrast term into the model and using it to meet specific (eg, 10%) relative risk reductions. We then estimated acute kidney injury rates when our patient-centered model-derived thresholds were and were not exceeded using data from CathPCI version 5 between April 2018 and June 2019. We repeated the same analysis in a sub-set of patients who received ≤3 × eGFR contrast.
After excluding patients on hemodialysis, below average risk (<7%), missing data and multiple percutaneous coronary interventions, our final analytical cohort included 141,133 patients at high risk for acute kidney injury. The rate of acute kidney injury was 10.0% when the contrast thresholds derived from our patient-centered model were met and 18.2% when they were exceeded (P < .001). In patients who received contrast ≤3 × eGFR (n = 82,318), contrast-associated acute kidney injury rate was 9.8% when the contrast thresholds derived from our patient centered model were met and 14.5% when they were exceeded (P < .001).
A novel strategy for developing personalized contrast volume thresholds, provides actionable information for providers that could decrease rates of contrast-associated acute kidney injury. This strategy needs further prospective testing to assess efficacy in improving patient outcomes.
经皮冠状动脉介入治疗中使用的对比剂体积与对比剂相关的急性肾损伤有直接关系。虽然有几种模型可以评估对比剂相关的急性肾损伤风险,但只有将对比剂体积限制在 3×估计肾小球滤过率(eGFR)的策略才能提供安全的对比剂剂量的可操作估计值。然而,这种方法没有考虑到其他与风险相关的患者特征,如年龄、糖尿病或心力衰竭。
我们使用国家心血管数据注册急性肾损伤风险模型,通过在模型中输入对比剂项并使用该模型来实现特定(例如,10%)相对风险降低,开发了一种新策略来定义安全的对比剂限制。然后,我们使用 2018 年 4 月至 2019 年 6 月期间 CathPCI 版本 5 的数据,分别估计了当我们的以患者为中心的模型得出的阈值被超过和未被超过时急性肾损伤的发生率。我们在接受≤3×eGFR 对比剂的患者亚组中重复了相同的分析。
在排除了血液透析患者、低风险(<7%)患者、缺失数据和多次经皮冠状动脉介入治疗的患者后,我们的最终分析队列包括了 141133 名急性肾损伤高危患者。当我们以患者为中心的模型得出的对比剂阈值得到满足时,急性肾损伤的发生率为 10.0%,而当这些阈值被超过时,发生率为 18.2%(P<0.001)。在接受≤3×eGFR 对比剂的患者中(n=82318),当我们以患者为中心的模型得出的对比剂阈值得到满足时,急性肾损伤的发生率为 9.8%,而当这些阈值被超过时,发生率为 14.5%(P<0.001)。
一种用于开发个性化对比剂体积阈值的新策略为提供者提供了可操作的信息,可能会降低对比剂相关的急性肾损伤的发生率。该策略需要进一步的前瞻性测试,以评估其在改善患者结局方面的效果。