Quantifying the Diagnostic Odyssey Burden Among Persons with Inborn Errors of Immunity.

IF 7.2 2区 医学 Q1 IMMUNOLOGY
Sarina Nikzad, Rebekah Johnson, Christopher Scalchunes, Nicholas L Rider
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Abstract

Purpose: Patients with inborn errors of immunity (IEI) have lifelong health complications including severe infections and physical impairments. Previous studies show that a patient's perception of their health is an important predictor of health outcomes. The purpose of this study was to understand factors related to patient reported health status.

Methods: We used data from the Immunodeficiency Foundation (IDF) 2017 National Patient Survey and analyzed factors which correlated with the reported health status (RHS). Among a cohort of 1139 self-reported IEI patients, we identified age at the time of diagnosis, time gap between symptom onset and diagnosis, number of physicians seen, and whether the diagnosis was made in the first 5 years of life as significant. We used a two-tailed t-test, single-factor ANOVA, and Tukey-Kramer post-hoc test to assess statistical significance in the observed difference.

Results: Patients who received a diagnosis before the age of 12 had a significantly better mean RHS (n = 207 pre-12a vs. n = 900 post-12a; p < 0.0001). Patients who received a diagnosis within 10 years of symptom onset showed improved mean RHS (n = 413 pre-10 vs. n = 524 post-10; p < 0.0001). Among patients who had symptom onset within the first 5 years of life, those who received a diagnosis had a significantly improved RHS (3.5 ± 0.92, n = 275 undiagnosed vs. 2.8 ± 0.94, n = 108 diagnosed; p < 0.0001). Finally, RHS was significantly impacted by number of physicians(n ≥ 4) seen prior to diagnosis (3.1 ± 0.96 vs. 3.4 ± 0.80, p < 0.0001).

Conclusion: These findings shed light upon critical factors which impact IEI patient RHS. Specifically, we find that efficient, rapid and early-life IEI identification should improve patient reported health and relevant outcomes. These improvements appear to be independent of the clinician specialty ultimately making the IEI diagnosis.

目的:先天性免疫错误(IEI)患者会出现终生健康并发症,包括严重感染和身体损伤。以往的研究表明,患者对自身健康的看法是预测健康结果的重要因素。本研究旨在了解与患者报告的健康状况相关的因素:我们使用了免疫缺陷基金会(IDF)2017 年全国患者调查的数据,并分析了与报告健康状况(RHS)相关的因素。在 1139 名自我报告的 IEI 患者队列中,我们确定了诊断时的年龄、症状出现与诊断之间的时间间隔、就诊医生的数量以及是否在出生后的前 5 年内确诊等重要因素。我们使用双尾t检验、单因素方差分析和Tukey-Kramer事后检验来评估观察到的差异的统计学意义:结果:12 岁前确诊的患者的平均 RHS 明显更高(12 岁前 207 人 vs. 12 岁后 900 人;P 结论:这些研究结果揭示了导致儿童颅内压增高的关键因素:这些发现揭示了影响 IEI 患者 RHS 的关键因素。具体而言,我们发现高效、快速和早期的 IEI 识别应能改善患者报告的健康状况和相关结果。这些改善似乎与最终做出 IEI 诊断的临床医生专业无关。
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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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