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Barriers to timely diagnosis of interstitial lung disease in the real world: the INTENSITY survey

机译:现实世界中及时诊断间质性肺疾病的障碍:强度调查

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摘要

The diagnosis of idiopathic pulmonary fibrosis (IPF) and other interstitial lung diseases (ILD) presents significant clinical challenges. To gain insights regarding the diagnostic experience of patients with ILD and to identify potential barriers to a timely and accurate diagnosis, we developed an online questionnaire and conducted a national survey of adults with a self-reported diagnosis of ILD. A pre-specified total of 600 subjects were recruited to participate in a 40-question online survey. E-mail invitations containing a link to the survey were sent to 16?427 registered members of the Pulmonary Fibrosis Foundation. Additionally, an open invitation was posted on an online forum for patients and caregivers ( www.inspire.com ). The recruitment and screening period was closed once the pre-defined target number of respondents was reached. Eligible participants were adult U.S. residents with a diagnosis of IPF or a non-IPF ILD. A total of 600 eligible respondents met the eligibility criteria and completed the survey. Of these, 55% reported ≥?1 misdiagnosis and 38% reported ≥?2 misdiagnoses prior to the current diagnosis. The most common misdiagnoses were asthma (13.5%), pneumonia (13.0%), and bronchitis (12.3%). The median time from symptom onset to current diagnosis was 7?months (range, 0–252?months), with 43% of respondents reporting a delay of ≥?1?year and 19% reporting a delay of ≥?3?years. Sixty-one percent of respondents underwent at least one invasive diagnostic procedure. While a minority of patients with ILD will experience an appropriate and expedient diagnosis, the more typical diagnostic experience for individuals with ILD is characterized by considerable delays, frequent misdiagnosis, exposure to costly and invasive diagnostic procedures, and substantial use of healthcare resources. These findings suggest a need for physician education, development of clinical practice recommendations, and improved diagnostic tools aimed at improving diagnostic accuracy in patients with ILD.
机译:特发性肺纤维化(IPF)和其他间质性肺疾病(ILD)的诊断提出了重大的临床挑战。为了获得有关ILD患者诊断经验的见识并确定及时准确诊断的潜在障碍,我们开发了在线调查表,并对自我报告为ILD的成年人进行了全国性调查。预先招募了总共600名受试者参加40个问题的在线调查。包含调查链接的电子邮件邀请已发送给肺纤维化基金会的16?427名注册成员。此外,在在线论坛上为患者和护理人员(www.inspire.com)发布了公开邀请。一旦达到预定的目标受访者人数,招聘和筛选期即告结束。符合条件的参与者是诊断为IPF或非IPF ILD的成年美国居民。共有600名符合条件的受访者符合资格标准并完成了调查。其中,55%的患者报告≥≥1错误,38%的患者≥≥2错误。最常见的误诊是哮喘(13.5%),肺炎(13.0%)和支气管炎(12.3%)。从症状发作到当前诊断的中位时间为7个月(范围为0-252个月),其中43%的受访者表示延迟≥1年,而19%的受访者表示延迟≥3年。百分之六十一的受访者至少接受了一种侵入性诊断程序。虽然少数ILD患者会经历适当且方便的诊断,但ILD患者更典型的诊断经验是延迟时间长,误诊频繁,接触昂贵且侵入性的诊断程序以及大量使用医疗资源。这些发现表明需要对医师进行教育,提出临床实践建议,以及旨在提高ILD患者诊断准确性的改进诊断工具。

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