• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于 10 项预警信号标准评估疑似原发性免疫缺陷病患者的发病频率和诊断延迟:伊朗的一项横断面研究。

Evaluation of the frequency and diagnostic delay of primary immunodeficiency disorders among suspected patients based on the 10 warning sign criteria: A cross-sectional study in Iran.

机构信息

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.

出版信息

Allergol Immunopathol (Madr). 2020 Nov-Dec;48(6):711-719. doi: 10.1016/j.aller.2020.03.005. Epub 2020 May 11.

DOI:10.1016/j.aller.2020.03.005
PMID:32404246
Abstract

INTRODUCTION

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.

OBJECTIVE

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

简介

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。

目的

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。

方法

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。

结果

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。

结论

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。

相似文献

1
Evaluation of the frequency and diagnostic delay of primary immunodeficiency disorders among suspected patients based on the 10 warning sign criteria: A cross-sectional study in Iran.基于 10 项预警信号标准评估疑似原发性免疫缺陷病患者的发病频率和诊断延迟:伊朗的一项横断面研究。
Allergol Immunopathol (Madr). 2020 Nov-Dec;48(6):711-719. doi: 10.1016/j.aller.2020.03.005. Epub 2020 May 11.
2
Primary Immunodeficiency Disorders Among North Indian Children.原发性免疫缺陷病在印度北部儿童中的发病情况。
Indian J Pediatr. 2019 Oct;86(10):885-891. doi: 10.1007/s12098-019-02971-y. Epub 2019 Jun 8.
3
The Kuwait National Primary Immunodeficiency Registry 2004-2018.科威特国家原发性免疫缺陷登记处 2004-2018 年。
Front Immunol. 2019 Jul 24;10:1754. doi: 10.3389/fimmu.2019.01754. eCollection 2019.
4
Risk Factors of Pneumonia in Primary Antibody Deficiency Patients Receiving Immunoglobulin Therapy: Data from the US Immunodeficiency Network (USIDNET).原发性抗体缺陷患者接受免疫球蛋白治疗后发生肺炎的危险因素:来自美国免疫缺陷网络(USIDNET)的数据。
J Clin Immunol. 2022 Oct;42(7):1545-1552. doi: 10.1007/s10875-022-01317-2. Epub 2022 Jul 2.
5
Systematic Review of Primary Immunodeficiency Diseases in Malaysia: 1979-2020.马来西亚原发性免疫缺陷疾病的系统评价:1979-2020 年。
Front Immunol. 2020 Aug 26;11:1923. doi: 10.3389/fimmu.2020.01923. eCollection 2020.
6
Consanguinity rate and delay in diagnosis in Turkish patients with combined immunodeficiencies: a single-center study.土耳其联合免疫缺陷患者的血缘关系率和诊断延迟:一项单中心研究。
J Clin Immunol. 2011 Feb;31(1):106-11. doi: 10.1007/s10875-010-9472-8. Epub 2010 Oct 6.
7
Long-term follow-up of ninety eight Iranian patients with primary immune deficiency in a single tertiary centre.在一家三级医疗中心对98例伊朗原发性免疫缺陷患者进行的长期随访。
Allergol Immunopathol (Madr). 2016 Jul-Aug;44(4):322-30. doi: 10.1016/j.aller.2015.09.006. Epub 2016 Jan 20.
8
The spectrum of inborn errors of immunity: a single tertiary center retrospective study in Alborz, Iran.免疫缺陷病谱:伊朗阿尔伯兹一个三级中心的回顾性研究
Eur Ann Allergy Clin Immunol. 2023 Jan;55(1):19-28. doi: 10.23822/EurAnnACI.1764-1489.239. Epub 2021 Dec 17.
9
Alterations in humoral immunity in relatives of patients with common variable immunodeficiency.普通可变免疫缺陷患者亲属的体液免疫改变。
J Investig Allergol Clin Immunol. 2008;18(4):266-71.
10
Clinical and Laboratory Characteristics of Primary Immunodeficiency Patients from a Tertiary Care Center in Pakistan.巴基斯坦一家三级医疗中心原发性免疫缺陷患者的临床和实验室特征
J Pak Med Assoc. 2020 Dec;70(12(B)):2403-2407. doi: 10.47391/JPMA.512.

引用本文的文献

1
Primary Immunodeficiency Registry System: The Minimum Data Set Designing Phase-A Systematic Review and Quantitative Delphi Study.原发性免疫缺陷登记系统:最小数据集设计阶段——一项系统评价和定量德尔菲研究
Health Sci Rep. 2025 Jul 9;8(7):e71015. doi: 10.1002/hsr2.71015. eCollection 2025 Jul.
2
Navigating disruption in the PID landscape: embracing opportunities and anticipating threats in the next ten years.应对原发性免疫缺陷病领域的变革:把握未来十年的机遇并预见威胁
Front Immunol. 2025 Jun 17;16:1596971. doi: 10.3389/fimmu.2025.1596971. eCollection 2025.
3
Systematic screening for primary immunodeficiencies in patients hospitalized for severe infection in pediatric intensive care unit.
对入住儿科重症监护病房因严重感染而住院的患者进行原发性免疫缺陷的系统筛查。
Sci Rep. 2025 Jul 1;15(1):22170. doi: 10.1038/s41598-025-02870-7.
4
"I am sick, but that's not all that I am": patient perspectives on psychological adaptation over time to inborn errors of immunity.“我生病了,但我不止如此”:患者对随时间推移适应先天性免疫缺陷的心理历程的看法
J Community Genet. 2025 Apr;16(2):117-130. doi: 10.1007/s12687-024-00758-z. Epub 2025 Jan 6.
5
The Evolutionary Scenario of Pediatric Unclassified Primary Antibody Deficiency to Adulthood.儿童未分类原发性抗体缺陷至成年期的演变情况。
J Clin Med. 2023 Jun 22;12(13):4206. doi: 10.3390/jcm12134206.
6
Evaluation of the 10 Warning Signs in Primary and Secondary Immunodeficient Patients.原发性和继发性免疫缺陷患者 10 大警示征象评估。
Front Immunol. 2022 May 13;13:900055. doi: 10.3389/fimmu.2022.900055. eCollection 2022.
7
The Epidemiology and Clinical Presentations of Atopic Diseases in Selective IgA Deficiency.选择性IgA缺乏症中特应性疾病的流行病学及临床表现
J Clin Med. 2021 Aug 25;10(17):3809. doi: 10.3390/jcm10173809.