Intensive Care Unit, Department of Anesthesiology, The Jikei University School of Medicine, 3-19-18, Nishi-Shinbashi Minato-ku, Tokyo, 105-8471, Japan.
The Australian and New Zealand Intensive Care Research Centre, Monash University, 553 St Kilda Rd, Melbourne, VIC, 3004, Australia.
BMC Nephrol. 2020 Jan 30;21(1):31. doi: 10.1186/s12882-020-1701-7.
Acute kidney injury (AKI) is a major comorbidity in critically ill patients. Low-dose atrial natriuretic peptide (ANP) has been shown to effectively prevent acute kidney injury (AKI), especially in cardiovascular surgery patients. However, its treatment effects for AKI in critically ill patients are unclear.
This single-center, retrospective, observational study included patients with AKI diagnosed within 7 days after intensive care unit (ICU) admission during the period January 2010 to December 2017. We conducted a propensity-matched analysis to estimate the treatment effect of low-dose carperitide (a recombinant human ANP) on the clinical outcomes. The primary outcome was a composite of death, renal replacement therapy dependence, or no recovery from AKI (defined as an increase of the serum creatinine level to ≥200% of baseline) at hospital discharge.
During the study period, 4479 adult patients were admitted to the ICU. We identified 1374 eligible patients with AKI diagnosed within 7 days after ICU admission. Among these patients, 346 (25.2%) were treated with low-dose carperitide, with an average dose of 0.019 μg kg min. The primary outcome occurred more often in the treatment group than in the control group (29.7% versus 23.4%, respectively; p = 0.022). After propensity score matching, characteristics of 314 patients from each group were well- balanced. Significant difference of the primary outcome, as seen with the full cohort, was no longer obtained; no benefit of carperitide was detected in the matched cohort (29.0% versus 25.2%; p = 0.281).
Low-dose ANP showed no treatment effect in general critically ill patients who developed AKI.
急性肾损伤(AKI)是危重症患者的主要合并症。小剂量心房利钠肽(ANP)已被证明能有效预防急性肾损伤(AKI),特别是在心血管手术患者中。然而,其在危重症患者中治疗 AKI 的效果尚不清楚。
这项单中心、回顾性、观察性研究纳入了 2010 年 1 月至 2017 年 12 月期间 ICU 入院后 7 天内诊断为 AKI 的患者。我们进行了倾向评分匹配分析,以估计小剂量培哚普利(重组人 ANP)对临床结局的治疗效果。主要结局是住院时死亡、需要肾脏替代治疗或 AKI 未恢复(定义为血清肌酐水平升高至基线的 200%以上)的复合终点。
在研究期间,共有 4479 名成年患者入住 ICU。我们确定了 1374 名符合条件的 AKI 患者,这些患者在 ICU 入院后 7 天内被诊断为 AKI。在这些患者中,346 名(25.2%)接受了小剂量培哚普利治疗,平均剂量为 0.019μg/kg/min。治疗组的主要结局发生率高于对照组(分别为 29.7%和 23.4%,p=0.022)。在进行倾向评分匹配后,两组各 314 名患者的特征得到了很好的平衡。与全队列相比,主要结局的显著差异不再存在;在匹配队列中,培哚普利没有获益(分别为 29.0%和 25.2%,p=0.281)。
在一般发生 AKI 的危重症患者中,小剂量 ANP 治疗无效果。