Haris Ágnes, Polner Kálmán, Arányi József, Braunitzer Henrik, Kaszás Ilona, Rosivall László, Kökény Gábor, Mucsi István
Nephrology Department, Szent Margit Hospital, 132 Bécsi út, Budapest, 1032, Hungary.
Pathology Department, Szent Margit Hospital, 132 Bécsi út, Budapest, 1032, Hungary.
BMC Nephrol. 2017 Feb 23;18(1):76. doi: 10.1186/s12882-017-0491-z.
The early identification of patients with ANCA-associated vasculitis (AAV) who are at increased risk for inferior clinical outcome at the time of diagnosis might help to optimize the immunosuppressive therapy. In this study we wanted to determine the predictive value of simple clinical characteristics, which may be applicable for early risk-stratification of patients with AAV.
We retrospectively analyzed the outcome of 101 consecutive patients with AAV receiving a protocolized immunosuppressive therapy. Baseline Birmingham Vasculitis Activity Score (BVAS) and non-vasculitic comorbidities were computed, then predictors of early (<90 days) and late (>90 days) mortality, infectious death, relapse and end stage kidney disease (ESKD) were evaluated.
The baseline comorbidity score independently predicted early mortality (HR 1.622, CI 1.006-2.614), and showed association with infectious mortality (HR 2.056, CI 1.247-3.392). Patients with BVAS at or above median (=21) had worse early mortality in univariable analysis (HR 3.57, CI 1.039-12.243) (p = 0.031), and had more frequent relapses (p = 0.01) compared to patients with BVAS below median.
Assessing baseline comorbidities, beside clinical indices characterizing the severity and extension of AAV, might help clinicians in risk-stratification of patients. Future prospective studies are needed to investigate whether therapies based on risk-stratification could improve both short term and long term survival.
在诊断时早期识别抗中性粒细胞胞浆抗体相关性血管炎(AAV)患者中临床结局较差风险增加的患者,可能有助于优化免疫抑制治疗。在本研究中,我们想确定简单临床特征的预测价值,这些特征可能适用于AAV患者的早期风险分层。
我们回顾性分析了101例接受标准化免疫抑制治疗的连续AAV患者的结局。计算基线伯明翰血管炎活动评分(BVAS)和非血管性合并症,然后评估早期(<90天)和晚期(>90天)死亡率、感染性死亡、复发和终末期肾病(ESKD)的预测因素。
基线合并症评分独立预测早期死亡率(HR 1.622,CI 1.006 - 2.614),并与感染性死亡率相关(HR 2.056,CI 1.247 - 3.392)。在单变量分析中,BVAS处于或高于中位数(=2)的患者早期死亡率更差(HR 3.57,CI 1.039 - 12.243)(p = 0.031),与BVAS低于中位数的患者相比,复发更频繁(p = 0.01)。
除了表征AAV严重程度和范围的临床指标外,评估基线合并症可能有助于临床医生对患者进行风险分层。需要未来的前瞻性研究来调查基于风险分层的治疗是否能改善短期和长期生存率。