Department of Clinical Sciences, Lund University, Jan Waldenströms gata 35, 214 28, Malmö, Sweden.
Infectious Disease Unit, Skåne University Hospital, Malmö, Sweden.
BMC Emerg Med. 2019 Nov 28;19(1):75. doi: 10.1186/s12873-019-0283-9.
Sepsis is a leading cause of death worldwide and a major challenge for physicians to predict and manage. Proenkephalin A 119-159 (penKid) is a reliable surrogate marker for the more unstable endogenous opioid peptide enkephalin, which has previously been shown to predict both acute and chronic kidney disease. The aim of this prospective observational study was to assess penKid as a predictor of acute kidney injury (AKI), multi-organ failure and mortality in sepsis among unselected sepsis patients presenting to the emergency department (ED).
We enrolled 644 patients consecutively during office-hours (6 AM-6 PM) between December 1, 2013 and February 1, 2015. Fifty-six patients were excluded due to incomplete data. We measured penKid in 588 adult patients (patients under 18 years of age were excluded) with sepsis (≥2SIRS criteria + suspected infection) upon admission to the ED at Skåne University Hospital, Malmö, Sweden. Logistic regression analysis was used to relate levels of penKid at presentation to AKI, multi-organ failure, 28-day mortality and progression of renal SOFA subscore. Odds ratios are presented as the number of standard deviations from the mean of log-transformed penKid.
In age and sex adjusted models, penKid predicted AKI within 48 h and 7 days, but these associations were attenuated after additional adjustment for estimated creatinine-based glomerular filtration rate (eGFR). In models adjusted for age, sex and eGFR, penKid significantly predicted progression from rSOFA = 0 and ≤ 1 to higher rSOFA scores as well as multi-organ failure and mortality. In contrast, eGFR did not predict 28-day mortality.
PenKid is an effective predictor of renal injury, severe multi-organ failure and mortality in unselected sepsis patients presenting to the emergency department.
脓毒症是全球范围内主要的死亡原因,也是医生预测和管理的主要挑战。Proenkephalin A 119-159(penKid)是内源性阿片肽脑啡肽更不稳定的可靠替代标志物,先前已显示可预测急性和慢性肾病。本前瞻性观察研究的目的是评估 penKid 在急诊科就诊的未选择脓毒症患者中作为脓毒症急性肾损伤(AKI)、多器官衰竭和死亡率的预测因子。
我们在 2013 年 12 月 1 日至 2015 年 2 月 1 日办公时间(6 AM-6 PM)连续招募了 644 名患者。由于数据不完整,有 56 名患者被排除在外。我们在瑞典马尔默斯科讷大学医院急诊科收治的 588 名成年脓毒症患者(排除年龄在 18 岁以下的患者)中测量了 penKid。使用逻辑回归分析将入院时的 penKid 水平与 AKI、多器官衰竭、28 天死亡率和肾 SOFA 亚评分的进展相关联。比值比以 log 转换后的 penKid 的均数的标准差倍数表示。
在年龄和性别调整模型中,penKid 预测了 48 小时和 7 天内的 AKI,但这些关联在进一步调整基于估计肌酐的肾小球滤过率(eGFR)后减弱。在调整年龄、性别和 eGFR 的模型中,penKid 显著预测了 rSOFA = 0 和 ≤ 1 到更高 rSOFA 评分以及多器官衰竭和死亡率的进展。相比之下,eGFR 不能预测 28 天死亡率。
在急诊科就诊的未选择脓毒症患者中,penKid 是肾损伤、严重多器官衰竭和死亡率的有效预测因子。