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Journal of Translational Internal Medicine logoLink to Journal of Translational Internal Medicine
. 2021 Mar 31;9(1):57–58. doi: 10.2478/jtim-2021-0018

Recovery from Acute Kidney Injury Is a Potent Predictor of Survival and Good Neurological Outcome at Discharge After Out-of-hospital Cardiac Arrest: Fact Or Fiction

Patrick M Honore 1,*, Luc Kugener 1, Sebastien Redant 1, Rachid Attou 1, Andrea Gallerani 1, David De Bels 1
PMCID: PMC8016355  PMID: 33850803

To the Editor

We read with great interest the recent paper by Park et al., who conclude that recovery from acute kidney injury (AKI) is a potent predictor of survival and good neurological outcome at discharge after out-of-hospital cardiac arrest (OHCA).[1] We would like to make some comments. According to the authors, we should interpret these results carefully because the characteristics of OHCA patients are significantly different from critical care patients such as those with severe sepsis.[2] Indeed, whole body ischemia and reperfusion lead to post-cardiac arrest syndrome, including brain injury, myocardial dysfunction, systemic ischemia, and reperfusion response.[3] Various factors, including the duration of ischemia, cause of cardiac arrest, OHCA interventions, and the patient’s baseline health status, could affect neurological outcomes in OHCA patients.[1, 2, 3] We noticed when comparing the two cohorts’ non-recovery versus AKI recovery that for AKI non recovery, age >60 years was significantly higher 64% in AKI non-recovery versus 45% in recovery group (P value of 0.012).[1] Also, the incidence of diabetes mellitus was 35% in the non-recovery group versus 19% in the recovery group (P value of 0.022). Further, the adrenaline dose above 4 mg was 74% in non-recovery versus 17% in recovery (P value of 0.002). The cardiopulmonary resuscitation time >6 min was 74% in non-recovery versus 59% in recovery (P value of 0.002). Lastly, shock was present in 91% of the non-recovery group versus 67 % of the recovery group (P value of 0.001). Altogether and knowing the retrospective multicenter cohort study design, these five significant risk factors for poor neurological outcome are already enough to explain a bad neurological prognosis even without AKI recovery or not. In a recent study of 1,826 patients with OHCA, after excluding patients with an in-hospital cardiac arrest, a non-shockable rhythm, and no adrenaline administration,[4] it was concluded that among survivors, those who received less than 2 mg of adrenaline had a more favorable neurological outcome than those administered >3 mg (cerebral performance category [CPC] 1–2 16.6% vs. 12.5%, P = 0.004). Again, this is a similar finding to the study of Park et al.[1] In another recent trial, the authors concluded that in prolonged OHCA, initial shockable rhythm, age <65 years, and witnessed arrest are predictors for neurological intact survival.[5] Again, the presence of comorbidities like age is crucial for good neurological outcome. It stands to reason that the relationship founded by Park between AKI recovery and good neurological outcome might be only a pure association and nothing else. A randomized controlled study is surely warranted to explore further this finding.

Footnotes

Conflict of Interests

The authors declare no competing interests.

References

  • 1.Park YS, Choi YH, Oh JH, Cho IS, Cha KC, Choi BS. Recovery from acute kidney injury as a potent predictor of survival and good neurological outcome at discharge after out-of-hospital cardiac arrest. Crit Care. 2019;23:256. doi: 10.1186/s13054-019-2535-1. et al. [DOI] [PMC free article] [PubMed] [Google Scholar]
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  • 4.Sigal AP, Sandel KM, Buckler DG, Wasser T, Abella BS. Impact of adrenaline dose and timing on out-of-hospital cardiac arrest survival and neurological outcomes. Resuscitation. 2019;139:182–8. doi: 10.1016/j.resuscitation.2019.04.018. [DOI] [PubMed] [Google Scholar]
  • 5.Ahn S, Lee BK, Youn CS, Kim YJ, Sohn CH, Seo DW. Predictors of good neurologic outcome after resuscitation beyond 30 min in out-of-hospital cardiac arrest patients undergoing therapeutic hypothermia. Intern Emerg Med. 2018;13:413–9. doi: 10.1007/s11739-017-1662-4. et al. [DOI] [PubMed] [Google Scholar]

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