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一项针对原发性免疫性血小板减少症患者骨髓检查的盲法研究。

A blinded study of bone marrow examinations in patients with primary immune thrombocytopenia.

机构信息

Department of Medicine, Michael G. DeGroote School of Medicine, McMaster University, Hamilton, ON, Canada.

出版信息

Eur J Haematol. 2013 Feb;90(2):121-6. doi: 10.1111/ejh.12041. Epub 2012 Dec 13.

Abstract

OBJECTIVE

The role of bone marrow examinations in patients with primary immune thrombocytopenia (ITP) is uncertain. The objectives of this study were to determine the inter-rater reliability of bone marrow examinations and to identify distinguishing morphological features of ITP bone marrows under controlled conditions.

METHODS

Histological slides of bone marrow biopsy specimens and aspirates from 32 adult patients with severe primary ITP who had failed a median of two treatments, and 51 non-thrombocytopenic controls were retrieved from hospital archives. Slides were arranged in random order in a slide box and coded. Blinded to the diagnosis and platelet counts, three independent hematopathologists were asked to identify the ITP bone marrows and to evaluate megakaryocyte number, morphology, and distribution.

RESULTS

Overall chance-corrected agreement on ITP classification among the three raters was poor [kappa (κ) = 0.30; 95% confidence interval 0.22-0.38]. Raters were generally unable to correctly identify the ITP bone marrows from controls. Increased number of megakaryocytes, while an uncommon finding, was more frequent among ITP patients compared with controls (6/32, 18.8%; vs. 2/51, 3.9%; P = 0.05), and abnormal megakaryocyte morphology often led individual raters to reach a diagnosis of ITP. Overall sensitivity and specificity of bone marrow examinations were 24% and 90%, respectively.

CONCLUSIONS

This study confirms methodologically that bone marrow examinations are unreliable and frequently non-diagnostic in ITP. Thus, they are not useful for patients with typical disease. Rare subsets of patients with severe ITP demonstrated unique features such as increased number of megakaryocytes.

摘要

目的

骨髓检查在原发免疫性血小板减少症(ITP)患者中的作用尚不确定。本研究的目的是确定骨髓检查的观察者间可靠性,并在受控条件下确定 ITP 骨髓的鉴别形态特征。

方法

从医院档案中检索了 32 名患有严重原发性 ITP 的成年患者(中位治疗失败 2 次)的骨髓活检和抽吸组织学切片,以及 51 名非血小板减少症对照者。将切片随机排列在切片盒中并编码。三位独立的血液病理学家在不了解诊断和血小板计数的情况下,被要求识别 ITP 骨髓,并评估巨核细胞数量、形态和分布。

结果

三位观察者对 ITP 分类的总体机会校正一致性较差(kappa (κ) = 0.30;95%置信区间 0.22-0.38)。观察者通常无法正确识别 ITP 骨髓与对照者。巨核细胞数量增加虽然不常见,但在 ITP 患者中比对照组更常见(6/32,18.8%;51/51,3.9%;P = 0.05),异常巨核细胞形态通常导致个别观察者做出 ITP 的诊断。骨髓检查的总体敏感性和特异性分别为 24%和 90%。

结论

本研究从方法学上证实,骨髓检查在 ITP 中不可靠且通常无诊断价值。因此,它们对典型疾病患者没有帮助。严重 ITP 的罕见亚组患者表现出独特的特征,例如巨核细胞数量增加。

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