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量化免疫缺陷病患者的诊断历程负担

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

作者信息

Nikzad Sarina, Johnson Rebekah, Scalchunes Christopher, Rider Nicholas L

机构信息

Liberty University College of Osteopathic Medicine, Lynchburg, Virginia, USA.

Immune Deficiency Foundation, Hanover, Maryland, USA.

出版信息

J Clin Immunol. 2025 Jan 2;45(1):61. doi: 10.1007/s10875-024-01855-x.

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.

摘要

目的

先天性免疫缺陷(IEI)患者会面临包括严重感染和身体损伤在内的终身健康并发症。先前的研究表明,患者对自身健康的认知是健康结果的重要预测指标。本研究的目的是了解与患者报告的健康状况相关的因素。

方法

我们使用了免疫缺陷基金会(IDF)2017年全国患者调查的数据,并分析了与报告的健康状况(RHS)相关的因素。在1139名自我报告的IEI患者队列中,我们确定诊断时的年龄、症状出现与诊断之间的时间间隔、看过的医生数量以及诊断是否在生命的前5年内做出具有重要意义。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中的统计学显著性。

结果

12岁之前确诊的患者平均RHS显著更好(12岁之前确诊的患者n = 207,12岁之后确诊的患者n = 900;p < 0.0001)。症状出现后10年内确诊的患者平均RHS有所改善(症状出现后10年之前确诊的患者n = 413,症状出现后10年之后确诊的患者n = 524;p < 0.0001)。在生命的前5年内出现症状的患者中,确诊的患者RHS显著改善(未确诊的患者为3.5±0.92,n = 275;确诊的患者为2.8±0.94,n = 108;p < 0.0001)。最后,RHS受到诊断前看过的医生数量(n≥4)的显著影响(3.1±0.96 vs. 3.4±0.80,p < 0.0001)。

结论

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识别应该会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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