Competency of Jeffrey Modell Foundation warning signs and routine laboratory tests in suspecting primary immunodeficiencies: A cross-sectional multi-centric prospective study from eastern India

IF 2.4 4区 医学 Q2 RHEUMATOLOGY International Journal of Rheumatic Diseases Pub Date : 2024-11-12 DOI:10.1111/1756-185X.15405
Asmita Ghosh, Moumita Samanta, Parasar Ghosh, Mitali Chatterjee, Rakesh Mondal, Tapas Kumar Sabui
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Abstract

Aim

To test the efficaciousness of the 10 warning signs of Jeffrey Modell Foundation (JMF) and routine laboratory tests in predicting Primary Immunodeficiencies (PIDs).

Methods

Hospitalized children <12 years age satisfying at least two of 10 warning signs were subjected to routine and confirmatory tests.

Results

Of 35 204 admitted patients, 66 satisfied the JMF criteria and 34 had PID. Also, 59% were infants, with a female preponderance. The most common immunodeficiency disorder group were antibody deficiencies and phagocyte defects (35.3%). Chronic granulomatous disease (CGD) was the commonest overall (29.4%). The need for intravenous antibiotics was the most sensitive (91%) criterion for predicting PID. When combined with positive family history of PID, sensitivity (94%) increased further. The two most specific indicators were recurrent ear infections (88%), and family history of PID (88%). The best positive predictor was family history of PID (69%), and the best negative predictor was recurrent sinus infections (58%). Significant association was found between persistent oral thrush and PID (p .043), and insufficient weight gain and antibody deficiencies (p .037). Absolute neutrophil count, CRP, and elevated ESR were also significantly associated with PIDs (p-values being .036, .011, and .014 respectively).

Conclusion

Out of all 10 JMF criteria, the three most important ones to predict PID were need for IV antibiotics, family history of PID, and recurrent ear infections.

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杰弗里-莫德尔基金会预警信号和常规实验室检测在怀疑原发性免疫缺陷方面的能力:印度东部多中心前瞻性横断面研究。
目的:测试杰弗里-莫德尔基金会(Jeffrey Modell Foundation,JMF)的 10 个警告标志和常规实验室检测在预测原发性免疫缺陷症(PID)方面的有效性:在 35 204 名住院患者中,66 人符合 JMF 标准,34 人患有 PID。此外,59%的患者为婴儿,其中女性居多。最常见的免疫缺陷疾病是抗体缺乏和吞噬细胞缺陷(35.3%)。慢性肉芽肿病(CGD)是最常见的疾病(29.4%)。需要静脉注射抗生素是预测 PID 的最敏感标准(91%)。如果结合阳性的 PID 家族史,敏感性(94%)会进一步提高。两个最特异的指标是反复耳部感染(88%)和家族 PID 史(88%)。最佳阳性预测指标是 PID 家族史(69%),最佳阴性预测指标是反复鼻窦感染(58%)。持续性口腔鹅口疮与 PID(P.043)、体重增加不足与抗体缺乏(P.037)之间存在显著关联。绝对中性粒细胞计数、CRP 和 ESR 升高与 PID 也有显著相关性(P 值分别为 0.036、0.011 和 0.014):结论:在所有 10 项 JMF 标准中,对预测 PID 最重要的三项标准是需要静脉注射抗生素、PID 家族史和反复耳部感染。
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来源期刊
CiteScore
3.70
自引率
4.00%
发文量
362
审稿时长
1 months
期刊介绍: The International Journal of Rheumatic Diseases (formerly APLAR Journal of Rheumatology) is the official journal of the Asia Pacific League of Associations for Rheumatology. The Journal accepts original articles on clinical or experimental research pertinent to the rheumatic diseases, work on connective tissue diseases and other immune and allergic disorders. The acceptance criteria for all papers are the quality and originality of the research and its significance to our readership. Except where otherwise stated, manuscripts are peer reviewed by two anonymous reviewers and the Editor.
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