• 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

肉芽肿伴多血管炎能否在初级保健中更早诊断?一项病例对照研究。

Can granulomatosis with polyangiitis be diagnosed earlier in primary care? A case-control study.

机构信息

Division of Epidemiology and Public Health, University of Nottingham, Nottingham, UK.

Department of Rheumatology, Ipswich Hospital, Ipswich, UK.

出版信息

QJM. 2018 Jan 1;111(1):39-45. doi: 10.1093/qjmed/hcx194.

DOI:10.1093/qjmed/hcx194
PMID:29340693
Abstract

BACKGROUND

People with granulomatosis with polyangiitis (GPA) commonly described long delays before diagnosis.

AIM

To study the natural history of GPA prior to diagnosis using primary care data, and determine whether clinical features could be identified to help earlier diagnosis.

DESIGN

Case-control study using the Clinical Practice Research Datalink.

METHODS

We compared primary care activity and clinical features between cases and 10 matched controls.

RESULTS

We identified 757 cases and matched 7546 controls. Compared to controls, cases had more GP consultations and overall healthcare activity in the 5 years prior to their diagnosis, with a marked increase in the year before diagnosis, and particularly in the last 3 months. However, consultations were mostly for symptoms that were not specifically related to GPA. In the year prior to diagnosis, the most frequent and strongly predictive clinical features of GPA were Ear Nose and Throat (ENT) symptoms [34.5% of cases, odds ratio (OR) 10.5, 95% confidence intervals (CI) 8.6-12.7], and general (constitutional) symptoms (21.5% of cases, OR 9.0, 95% CI 7.1-11.3). In the year before diagnosis a larger number of cases attended secondary care (382, 50.5%) than had records of clinical features of GPA.

CONCLUSIONS

After discussing our findings, we conclude that it would be difficult to identify cases of GPA earlier in primary care. Our results support a need for heightened awareness of this condition among secondary care clinicians, especially those assessing emergency admissions, and in the clinics which were most frequently attended by cases 3-12 months prior to diagnosis.

摘要

背景

肉芽肿性多血管炎(GPA)患者在确诊前常描述存在较长的延误。

目的

使用初级保健数据研究 GPA 在确诊前的自然病史,并确定是否可以识别出临床特征以帮助更早诊断。

设计

使用临床实践研究数据链接进行病例对照研究。

方法

我们比较了病例和 10 名匹配对照者的初级保健活动和临床特征。

结果

我们确定了 757 例病例,并匹配了 7546 名对照者。与对照组相比,病例在确诊前的 5 年内有更多的全科医生就诊和整体医疗保健活动,在确诊前 1 年,尤其是在最后 3 个月,有明显增加。然而,就诊主要是针对与 GPA 无关的症状。在确诊前 1 年,GPA 的最常见且具有强烈预测性的临床特征是耳鼻喉(ENT)症状[34.5%的病例,比值比(OR)为 10.5,95%置信区间(CI)为 8.6-12.7]和全身(一般)症状(21.5%的病例,OR 为 9.0,95% CI 为 7.1-11.3)。在确诊前 1 年,更多的病例就诊于二级保健(382 例,50.5%),而有 GPA 临床特征记录的病例则较少。

结论

在讨论了我们的发现后,我们得出结论,很难在初级保健中更早地识别 GPA 病例。我们的结果支持二级保健临床医生,尤其是评估急诊入院的临床医生以及在确诊前 3-12 个月就诊最多的诊所,需要提高对这种疾病的认识。

相似文献

1
Can granulomatosis with polyangiitis be diagnosed earlier in primary care? A case-control study.肉芽肿伴多血管炎能否在初级保健中更早诊断?一项病例对照研究。
QJM. 2018 Jan 1;111(1):39-45. doi: 10.1093/qjmed/hcx194.
2
Novel insights into the aetiology of granulomatosis with polyangiitis-a case-control study using the Clinical Practice Research Datalink.肉芽肿性多血管炎发病机制的新见解——一项使用临床实践研究数据链接的病例对照研究。
Rheumatology (Oxford). 2018 Jun 1;57(6):1002-1010. doi: 10.1093/rheumatology/kex512.
3
Ear, nose and throat involvement in granulomatosis with polyangiitis: how it presents and how it determines disease severity and long-term outcomes.显微镜下多血管炎累及耳鼻咽喉:其临床表现与疾病严重程度及长期预后的关系。
Clin Rheumatol. 2018 Apr;37(4):1075-1083. doi: 10.1007/s10067-018-4019-0. Epub 2018 Feb 20.
4
Clinical characteristics of patients with granulomatosis with polyangiitis and microscopic polyangiitis in ENT practice: a comparative analysis.在耳鼻喉科实践中,肉芽肿伴多血管炎和显微镜下多血管炎患者的临床特征:对比分析。
Acta Otorhinolaryngol Ital. 2018 Dec;38(6):517-527. doi: 10.14639/0392-100X-1776.
5
Current status of the treatment of microscopic polyangiitis and granulomatosis with polyangiitis in Japan.日本显微镜下多血管炎和肉芽肿性多血管炎的治疗现状。
Clin Exp Nephrol. 2013 Feb;17(1):51-8. doi: 10.1007/s10157-012-0651-1. Epub 2012 Jul 5.
6
Childhood-onset granulomatosis with polyangiitis and microscopic polyangiitis: systematic review and meta-analysis.儿童期起病的肉芽肿性多血管炎和显微镜下多血管炎:系统评价和荟萃分析。
Orphanet J Rare Dis. 2016 Oct 22;11(1):141. doi: 10.1186/s13023-016-0523-y.
7
Clinical features of childhood granulomatosis with polyangiitis (wegener's granulomatosis).儿童肉芽肿性多血管炎(韦格纳肉芽肿)的临床特征。
Pediatr Rheumatol Online J. 2014 May 26;12:18. doi: 10.1186/1546-0096-12-18. eCollection 2014.
8
Histopathological features predictive of a clinical diagnosis of ophthalmic granulomatosis with polyangiitis (GPA).预测眼型肉芽肿伴多血管炎(GPA)临床诊断的组织病理学特征。
Int J Clin Exp Pathol. 2012;5(7):684-9. Epub 2012 Sep 5.
9
Value of non-identified ANCA (non-PR3, non-MPO) in the diagnosis of granulomatosis with polyangiitis (Wegener's granulomatosis).未识别的抗中性粒细胞胞浆抗体(非蛋白酶3,非髓过氧化物酶)在肉芽肿性多血管炎(韦格纳肉芽肿)诊断中的价值
Acta Clin Belg. 2017 Oct;72(5):313-317. doi: 10.1080/17843286.2016.1275374. Epub 2017 Jan 9.
10
A cohort study of comorbidity in patients with granulomatosis with polyangiitis.一项关于肉芽肿性多血管炎患者合并症的队列研究。
Rheumatology (Oxford). 2018 Feb 1;57(2):291-299. doi: 10.1093/rheumatology/kex379.

引用本文的文献

1
The 2025 British Society for Rheumatology management recommendations for ANCA-associated vasculitis.2025年英国风湿病学会抗中性粒细胞胞浆抗体相关性血管炎管理建议
Rheumatology (Oxford). 2025 Aug 1;64(8):4470-4494. doi: 10.1093/rheumatology/keaf240.
2
Patients Diagnosed with Granulomatosis with Polyangiitis: The Journey to Receive Rheumatologist Care.诊断为肉芽肿性多血管炎的患者:接受风湿病学家诊治的历程。
J Clin Med. 2025 May 18;14(10):3523. doi: 10.3390/jcm14103523.
3
Prevalence, incidence and healthcare burden of eosinophilic granulomatosis with polyangiitis in the UK.
嗜酸性肉芽肿性多血管炎在英国的患病率、发病率及医疗负担
ERJ Open Res. 2024 May 13;10(3). doi: 10.1183/23120541.00430-2023. eCollection 2024 May.
4
Diagnostic windows in non-neoplastic diseases: a systematic review.非肿瘤性疾病的诊断窗:系统评价。
Br J Gen Pract. 2023 Aug 31;73(734):e702-e709. doi: 10.3399/BJGP.2023.0044. Print 2023 Sep.
5
Granulomatosis With Polyangiitis Presenting as an Infratemporal Fossa Mass.表现为颞下窝肿块的肉芽肿性多血管炎
Clin Med Insights Case Rep. 2023 Mar 23;16:11795476231161982. doi: 10.1177/11795476231161982. eCollection 2023.
6
Global epidemiology of vasculitis.血管炎的全球流行病学。
Nat Rev Rheumatol. 2022 Jan;18(1):22-34. doi: 10.1038/s41584-021-00718-8. Epub 2021 Dec 1.
7
Clinical Decision Support Systems for Diagnosis in Primary Care: A Scoping Review.临床决策支持系统在初级保健中的诊断应用:范围综述。
Int J Environ Res Public Health. 2021 Aug 10;18(16):8435. doi: 10.3390/ijerph18168435.
8
ANCA associated vasculitis.抗中性粒细胞胞浆抗体相关性血管炎
BMJ. 2020 Apr 14;369:m1070. doi: 10.1136/bmj.m1070.
9
Look granulomatosis with polyangiitis (GPA) straight in the face: missed opportunities leading to a delayed diagnosis.直面显微镜下多血管炎(GPA):导致诊断延误的错失良机。
Auto Immun Highlights. 2019 Sep 17;10(1):8. doi: 10.1186/s13317-019-0118-4. eCollection 2019 Dec.