Forsblom E, Nurmi A-M, Ruotsalainen E, Järvinen A
Division of Infectious Diseases, Inflammation Center, Helsinki University Central Hospital, Helsinki, Finland.
Division of Infectious Diseases, Department of Medicine, Helsinki University Central Hospital, Aurora Hospital, Nordenskiöldinkatu 26, Building 3, P.O. Box 348, 00029, HUS Helsinki, Finland.
Eur J Clin Microbiol Infect Dis. 2016 Mar;35(3):471-9. doi: 10.1007/s10096-015-2563-y. Epub 2016 Jan 14.
The purpose of this study was to examine the prognostic impact of corticosteroids in hemodynamically stabile Staphylococcus aureus bacteremia (SAB). There were 361 hemodynamically stabile methicillin-sensitive SAB patients with prospective follow-up and grouping according to time-point, dose and indication for corticosteroid therapy. To enable analyses without external interfering corticosteroid therapy all patients with corticosteroid therapy equivalent to prednisone >10 mg/day for ≥1 month prior to positive blood culture results were excluded. Twenty-five percent (92) of patients received corticosteroid therapy of which 11 % (40) had therapy initiated within 1 week (early initiation) and 9 % (31) had therapy initiated 2-4 weeks after (delayed initiation) positive blood culture. Twenty-one patients (6 %) had corticosteroid initiated after 4 weeks and were not included in the analyses. A total of 55 % (51/92) received a weekly prednisone dose >100 mg. Patients with early initiated corticosteroid therapy had higher mortality compared to patients treated without corticosteroid therapy at 28 days (20 % vs. 7 %) (OR, 3.11; 95%CI, 1.27-7.65; p < 0.05) and at 90 days (30 % vs. 10 %) (OR, 4.01; 95%CI, 1.82-8.81; p < 0.001). Considering all prognostic markers, early initiated corticosteroid therapy predicted 28-day (HR, 3.75; 95%CI, 1.60-8.79; p = 0.002) and 90-day (HR, 3.10; 95%CI, 1.50-6.39; p = 0.002) mortality in Cox proportional hazards regression analysis. When including only patients receiving early initiated corticosteroid therapy with prednisone ≥100 mg/week the negative prognostic impact on 28-day mortality was accentuated (HR 4.8, p = 0.001). Corticosteroid therapy initiation after 1 week of positive blood cultures had no independent prognostic impact. Early initiation of corticosteroid therapy may be associate to increased mortality in hemodynamically stabile SAB.
本研究的目的是探讨皮质类固醇对血流动力学稳定的金黄色葡萄球菌菌血症(SAB)患者预后的影响。共有361例血流动力学稳定的甲氧西林敏感SAB患者,根据皮质类固醇治疗的时间点、剂量和指征进行前瞻性随访和分组。为了在不考虑外部干扰性皮质类固醇治疗的情况下进行分析,排除了所有在血培养结果呈阳性前1个月内接受相当于泼尼松>10mg/天皮质类固醇治疗≥1个月的患者。25%(92例)患者接受了皮质类固醇治疗,其中11%(40例)在血培养阳性后1周内开始治疗(早期开始),9%(31例)在血培养阳性后2 - 4周开始治疗(延迟开始)。21例(6%)患者在4周后开始使用皮质类固醇,未纳入分析。共有55%(51/92)患者接受的泼尼松每周剂量>100mg。与未接受皮质类固醇治疗的患者相比,早期开始皮质类固醇治疗的患者在28天时的死亡率更高(20%对7%)(OR,3.11;95%CI,1.27 - 7.65;p<0.05),在90天时的死亡率也更高(30%对10%)(OR,4.01;95%CI,1.82 - 8.81;p<0.001)。考虑所有预后标志物,在Cox比例风险回归分析中,早期开始皮质类固醇治疗可预测28天(HR,3.75;95%CI,1.60 - 8.79;p = 0.002)和90天(HR,3.10;95%CI,1.50 - 6.39;p = 0.002)的死亡率。仅纳入每周接受泼尼松≥100mg早期开始皮质类固醇治疗的患者时,对28天死亡率的负面预后影响更为明显(HR 4.8,p = 0.001)。血培养阳性1周后开始皮质类固醇治疗没有独立的预后影响。早期开始皮质类固醇治疗可能与血流动力学稳定的SAB患者死亡率增加有关。