Abstract

BackgroundThe average time to a diagnosis for people with axial spondyloarthritis (axSpA) is 7-10 years. Delayed diagnosis may result in increased structural damage, worse physical function, and worse quality of life relative to patients with a timely axSpA diagnosis. Understanding patient experiences may provide insights for how to reduce diagnostic delays.ObjectiveTo provide foundational knowledge about patient experiences with healthcare providers leading to an axSpA diagnosis.MethodsWe conducted an exploratory qualitative research study with six focus groups interviews with participants recruited from three rheumatology clinics within the United States (MA (n = 3); CO (n = 2); PA (n = 1)) that included a total of 26 adults (10 females, 16 males) with rheumatologist confirmed diagnosis of axSpA in 2019. Focus groups were ~ 2 h, audio recorded, transcribed, and subject to dual coding. The codes reviewed were in relation to the patients’ diagnostic experiences.ResultsPatients described frustrating and lengthy diagnostic journeys. They recognized that the causes of diagnostic delays in axSpA are multifactorial (e.g., no definitive diagnostic test, disease characteristics, lack of primary care provider’s awareness about axSpA, trust). Patients described how doctors minimized or dismissed complaints about symptoms or told them that their issues were psychosomatic. Patients believed the healthcare system contributed to diagnostic delays (e.g., lack of time in clinical visits, difficulty accessing rheumatologists, health insurance challenges). Advice to physicians to reduce the diagnostic delay included allowing time for patients to give a complete picture of their illness experience, listening to, and believing patients, earlier referral to rheumatology, provision of HLA-B27 gene testing, and that physicians need to partner with their patients.ConclusionsPatients desire a definitive test that could be administered earlier in the course of axSpA. Until such a test is available, patients want clinicians who listen to, believe, and partner with them, and who will follow them until a diagnosis is reached. Educating primary care clinicians about guidelines and referral for diagnosis of axSpA could reduce diagnostic delay.

Highlights

  • The average time to a diagnosis for people with axial spondyloarthritis is 7-10 years

  • We conducted an exploratory qualitative research study with six focus groups interviews with participants recruited from three rheumatology clinics within the United States (MA (n = 3); CO (n = 2); PA (n = 1)) that included a total of 26 adults (10 females, 16 males) with rheumatologist confirmed diagnosis of axial spondyloarthritis (axSpA) in 2019

  • Advice to physicians to reduce the diagnostic delay included allowing time for patients to give a complete picture of their illness experience, listening to, and believing patients, earlier referral to rheumatology, provision of HLA-B27 gene testing, and that physicians need to partner with their patients

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Summary

Introduction

The average time to a diagnosis for people with axial spondyloarthritis (axSpA) is 7-10 years. Axial spondyloarthritis (axSpA), including ankylosing spondylitis and non-radiographic axSpA, is characterized by waxing and waning symptoms of chronic inflammatory back pain with sacroiliac joint involvement [1]. Patients with axSpA often experience low back pain as their initial symptom [2]. In the United States, population-based estimates of the prevalence of axSpA are ~ 1% [4, 5]. This can cause further challenges in a primary care setting where back pain is a common presenting symptom [6], but patients with axSpA appear infrequently. Differentiating common mechanical low back pain from inflammatory back pain can be complicatedfor primary care clinicians [7]

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