Nielsen Finn Erland, Cordtz Johan Joakim, Rasmussen Thomas Bøjer, Christiansen Christian Fynbo
Department of Emergency Medicine, Slagelse Hospital, Slagelse DK-4200, Denmark.
Department of Emergency Medicine, Bispebjerg and Frederiksberg Hospital, Copenhagen DK-2400 NV, Denmark.
Clin Epidemiol. 2020 Sep 24;12:989-995. doi: 10.2147/CLEP.S254516. eCollection 2020.
We examined the association between creatine phosphokinase level in rhabdomyolysis patients and risk of acute kidney injury, renal replacement therapy, and death within 30 days.
The cohort included patients admitted with rhabdomyolysis from November 1, 2011 to March 1, 2014. Rhabdomyolysis was defined as a creatine phosphokinase level higher than 1000 U/L. Information on laboratory variables was obtained from a laboratory database. Medical data were obtained from registries. Acute kidney injury was defined according to the Kidney Disease Improving Global Outcome (KDIGO) guidelines. The 30-day risk of outcomes was estimated using the cumulative incidence method. Spline regression applied to imputed datasets with adjustment for baseline variables was used to assess the appropriateness of the categorization chosen for creatine phosphokinase (1000-5000 U/L, 5001-15,000 U/L, and 15,000+ U/L).
The study included 1027 patients (58.2% male) with a median age of 73.5 years. The median creatine phosphokinase level at rhabdomyolysis diagnosis was 2257 U/L (interquartile range=1404-3961 U/L). The 30-day risks of acute kidney injury according to the three creatinine phosphokinase levels were 42% (95% CI=38-45%), 44% (95% CI=36-52%), and 74% (95% CI=57-85%), respectively, and the risks of renal replacement therapy for the three levels were 3% (95% CI=2-5%), 4% (95% CI=2-7%), and 11% (3-23%), respectively. The 30-day risk of death was 17% (95% CI=14-20%), 16% (95% CI=11-22%), and 11% (95% CI=3-23%), respectively. With increasing creatine phosphokinase levels, the spline plots supported the increasing risk of acute kidney injury and renal replacement therapy, as well as a decreasing risk of death. However, the risk estimates for renal replacement therapy and death were imprecise.
Elevated initial creatine phosphokinase values were associated with an increased risk of acute kidney injury, while estimates of the risk of renal replacement therapy and death were imprecise.
我们研究了横纹肌溶解症患者的肌酸磷酸激酶水平与急性肾损伤风险、肾脏替代治疗及30天内死亡风险之间的关联。
该队列研究纳入了2011年11月1日至2014年3月1日因横纹肌溶解症入院的患者。横纹肌溶解症定义为肌酸磷酸激酶水平高于1000 U/L。实验室变量信息来自实验室数据库,医疗数据来自登记处。急性肾损伤根据改善全球肾脏病预后组织(KDIGO)指南进行定义。采用累积发病率法估计30天的结局风险。对插补数据集应用样条回归并对基线变量进行调整,以评估为肌酸磷酸激酶选择的分类(1000 - 5000 U/L、5001 - 15000 U/L和15000 + U/L)的合理性。
该研究纳入了1027例患者(58.2%为男性),中位年龄为73.5岁。横纹肌溶解症诊断时的肌酸磷酸激酶水平中位数为2257 U/L(四分位间距 = 1404 - 3961 U/L)。根据肌酸磷酸激酶的三个水平,急性肾损伤的30天风险分别为42%(95%置信区间 = 38 - 45%)、44%(95%置信区间 = 36 - 52%)和74%(95%置信区间 = 57 - 85%),三个水平的肾脏替代治疗风险分别为3%(95%置信区间 = 2 - 5%)、4%(95%置信区间 = 2 - 7%)和11%(3 - 23%)。30天死亡风险分别为17%(95%置信区间 = 14 - 20%)、16%(95%置信区间 = 11 - 22%)和11%(95%置信区间 = 3 - 23%)。随着肌酸磷酸激酶水平升高,样条图显示急性肾损伤和肾脏替代治疗风险增加,死亡风险降低。然而,肾脏替代治疗和死亡的风险估计并不精确。
初始肌酸磷酸激酶值升高与急性肾损伤风险增加相关,而肾脏替代治疗和死亡风险的估计并不精确。