Department of Allergy and Immunology, Ali Asghar children's Hospital, Iran University of Medical Sciences, Tehran, Iran.
Research Center of Pediatric Infectious Diseases, Institute of Immunology and Infectious Diseases, Iran University of Medical Sciences, Tehran, Iran.
Allergol Immunopathol (Madr). 2020 Nov-Dec;48(6):711-719. doi: 10.1016/j.aller.2020.03.005. Epub 2020 May 11.
The prevalence of undiagnosed primary immunodeficiency diseases is remarkably high and contributes to increasing the rate of morbidity and mortality among this group of patients.
To examine the 10 warning sign scoring system in patients suspected of primary immune deficiency and also estimate the diagnostic delay in patients with proven disease.
This descriptive cross-sectional study was carried out during the years 2015-2016 in Ali Asghar (AS) Clinic and Hospital. Two hundred patients with suspected primary immune deficiency disease were eligible for inclusion in the study. Multivariable logistic regression analysis was used to determine the relation between findings.
In this study, the majority of suspected cases of immunodeficiency were males (57%) with a mean age of 3.33±2.89 years. Twenty-one (10.5%) patients were diagnosed with immunodeficiency disease. The mean diagnostic delay among primary immune deficient patients was 2.05±1.7 years. There was a significant relationship between having parental consanguinity (OR=2.68, 95% CI: 1.07-6.70), allergies (OR=5.03, 95% CI: 1.13-22.31), vaccine adverse effects (OR=9.31, 95% CI: 1.24-69.96) and primary immune deficiency diagnosis. No association was observed between age (OR=0.98, 95% CI: 0.84-1.14), gender (OR=0.99, 95% CI: 0.39-2.47), immune deficiency scoring (OR=0.68, 95% CI: 0.31-1.45) and primary immune deficiency diagnosis.
Ten warning sign scoring system is of less value to consider a patient suspected of having primary immune deficiency. There is a meaningful delay in diagnosis of primary immune deficiencies especially in antibody deficiency defects which seeks further upgrading of knowledge in physicians.
未确诊的原发性免疫缺陷病的患病率非常高,这导致该类患者的发病率和死亡率不断上升。
研究原发性免疫缺陷患者的 10 项预警信号评分系统,并评估确诊患者的诊断延迟情况。
本研究为 2015-2016 年在阿里阿萨格(AS)诊所和医院进行的描述性横断面研究。共有 200 名疑似原发性免疫缺陷病的患者符合纳入研究标准。采用多变量逻辑回归分析来确定发现之间的关系。
在这项研究中,大多数疑似免疫缺陷的患者为男性(57%),平均年龄为 3.33±2.89 岁。21 名(10.5%)患者被诊断为免疫缺陷病。原发性免疫缺陷患者的平均诊断延迟时间为 2.05±1.7 年。父母近亲结婚(OR=2.68,95%CI:1.07-6.70)、过敏(OR=5.03,95%CI:1.13-22.31)、疫苗不良反应(OR=9.31,95%CI:1.24-69.96)与原发性免疫缺陷诊断之间存在显著关系。年龄(OR=0.98,95%CI:0.84-1.14)、性别(OR=0.99,95%CI:0.39-2.47)、免疫缺陷评分(OR=0.68,95%CI:0.31-1.45)与原发性免疫缺陷诊断之间无关联。
10 项预警信号评分系统对于考虑疑似原发性免疫缺陷的患者的价值较低。原发性免疫缺陷的诊断存在明显延迟,特别是抗体缺陷缺陷的诊断延迟更为明显,这需要进一步提高医生的知识水平。