Identifying relevant determinants of in-hospital time to diagnosis for ANCA-associated vasculitis patients

Author:

Dirikgil Ebru1,Tas Sander W2,Verburgh Cornelis A3,Soonawala Darius4,Hak A Elisabeth2,Remmelts Hilde H F5,IJpelaar Daphne6,Laverman Gozewijn D7,Rutgers Abraham8,van Laar Jaap M9ORCID,Moens Hein J Bernelot10,Verhoeven Peter M J11,Rabelink Ton J1,Bos Willem Jan W112,Teng Y K Onno1

Affiliation:

1. Department of Nephrology, Leiden University Medical Center , Leiden

2. Department of Rheumatology and Clinical Immunology, Amsterdam University Medical Centers , Amsterdam

3. Department of Nephrology, Spaarne Gasthuis , Haarlem

4. Department of Nephrology, Hagaziekenhuis , Den Haag

5. Department of Nephrology, Meander Medical Center , Amersfoort

6. Department of Nephrology, Groene Hart Hospital , Gouda

7. Department of Nephrology, Ziekenhuisgroep Twente , Almelo/Hengelo

8. Department of Rheumatology and Clinical Immunology, University Medical Center Groningen , Groningen

9. Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht , Utrecht

10. Department of Rheumatology and Clinical Immunology, Ziekenhuisgroep Twente , Almelo/Hengelo

11. The Dutch Vasculitis Foundation , Silvolde

12. Department of Internal Medicine, St. Antonius Hospital , Nieuwegein, The Netherlands

Abstract

Abstract Objectives Diagnosing patients with ANCA-associated vasculitis (AAV) can be challenging owing to its rarity and complexity. Diagnostic delay can have severe consequences, such as chronic organ damage or even death. Given that few studies have addressed diagnostic pathways to identify opportunities to improve, we performed a clinical audit to evaluate the diagnostic phase. Methods This retrospective, observational study of electronic medical records data in hospitals focused on diagnostic procedures during the first assessment until diagnosis. Results We included 230 AAV patients from nine hospitals. First assessments were mainly performed by a specialist in internal medicine (52%), pulmonology (14%), ENT (13%) or rheumatology (10%). The overall median time to diagnosis was 13 [interquartile range: 2–49] days, and in patients primarily examined by a specialist in internal medicine it was 6 [1–25] days, rheumatology 14 [4–45] days, pulmonology 15 [5–70] days and ENT 57 [16–176] days (P = 0.004). Twenty-two of 31 (71%) patients primarily assessed by a specialist in ENT had non-generalized disease, of whom 14 (64%) had ENT-limited activity. Two hundred and nineteen biopsies were performed in 187 patients (81%). Histopathological support for AAV was observed in 86% of kidney biopsies, 64% of lung biopsies and 34% of ENT biopsies. Conclusion In The Netherlands, AAV is diagnosed and managed predominantly by internal medicine specialists. Diagnostic delay was associated with non-generalized disease and ENT involvement at presentation. Additionally, ENT biopsies had a low diagnostic yield, in contrast to kidney and lung biopsies. Awareness of this should lead to more frequent consideration of AAV and early referral for a multidisciplinary approach when AAV is suspected.

Funder

Dutch Arthritis Foundation

Publisher

Oxford University Press (OUP)

Subject

Rheumatology

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