Clinical Epidemiology Division, Dept of Medicine Solna, Karolinska Institutet, Stockholm, Sweden
Respiratory Medicine Division, Dept of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Eur Respir J. 2020 Sep 3;56(3). doi: 10.1183/13993003.00767-2020. Print 2020 Sep.
Serious infections impair quality of life and increase costs. Our aim was to determine if sarcoidosis is associated with a higher rate of serious infection and whether this varies by age, sex, time since diagnosis or treatment status around diagnosis.We compared individuals with sarcoidosis (at least two International Classification of Diseases codes in the Swedish National Patient Register 2003-2013; n=8737) and general population comparators matched 10:1 on age, sex and residential location (n=86 376). Patients diagnosed in 2006-2013 who were dispensed at least one immunosuppressant ±3 months from diagnosis (Swedish Prescribed Drug Register) were identified. Cases and comparators were followed in the National Patient Register for hospitalisations for infection. Using Cox and flexible parametric models, we estimated adjusted hazard ratios (aHR) and 95% confidence intervals for first and recurrent serious infections (new serious infection >30 days after previous).We identified 895 first serious infections in sarcoidosis patients and 3881 in comparators. The rate of serious infection was increased 1.8-fold in sarcoidosis compared to the general population (aHR 1.81, 95% CI 1.65-1.98). The aHR was higher in females than males and during the first 2 years of follow-up. Sarcoidosis cases treated with immunosuppressants around diagnosis had a three-fold increased risk, whereas nontreated patients had a 50% increased risk. The rate of serious infection recurrence was 2.8-fold higher in cases than in comparators.Serious infections are more common in sarcoidosis than in the general population, particularly during the first few years after diagnosis. Patients who need immunosuppressant treatment around diagnosis are twice as likely to develop a serious infection than those who do not.
严重感染会降低生活质量并增加医疗成本。我们旨在确定结节病是否与严重感染发生率升高相关,以及这种相关性是否因年龄、性别、诊断后时间或诊断时的治疗状态而异。我们比较了至少有两个 2003-2013 年瑞典国家患者登记处国际疾病分类代码的结节病患者(n=8737)和年龄、性别和居住地点匹配 10:1 的一般人群对照者(n=86376)。确定了 2006-2013 年诊断且至少在诊断后 3 个月内使用过一种免疫抑制剂(瑞典处方药物登记处)的患者。在国家患者登记处中,通过 Cox 和灵活参数模型,我们针对首次和复发性严重感染(上次严重感染后 30 天以上发生新的严重感染),估计了调整后的危险比(aHR)和 95%置信区间。我们在结节病患者中发现了 895 例首次严重感染,在对照者中发现了 3881 例。与一般人群相比,结节病患者严重感染的发生率增加了 1.8 倍(aHR 1.81,95%CI 1.65-1.98)。女性的 aHR 高于男性,且在随访的前 2 年内更高。诊断时接受免疫抑制剂治疗的病例发生严重感染的风险增加了 3 倍,而未接受治疗的患者风险增加了 50%。与对照者相比,病例的严重感染复发率高 2.8 倍。与一般人群相比,结节病患者的严重感染更为常见,尤其是在诊断后的最初几年。诊断时需要免疫抑制剂治疗的患者发生严重感染的可能性是未接受治疗患者的两倍。