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因无症状性中性粒细胞减少而就诊患者的临床结局:以血液学中的种族差异为重点

Clinical outcomes of patients referred for asymptomatic neutropenia: A focus on racial disparities in hematology.

机构信息

Division of Internal Medicine, Oregon Health & Science University, Portland, Oregon, USA.

Department of Biomedical Engineering, Oregon Health & Science University, School of Medicine, Portland, Oregon, USA.

出版信息

Eur J Haematol. 2023 Jul;111(1):41-46. doi: 10.1111/ejh.13963. Epub 2023 Mar 28.

Abstract

BACKGROUND

Asymptomatic neutropenia is a common hematology referral, though standardized reference ranges and published clinical outcomes are lacking.

METHODS

In our retrospective analysis, we evaluated demographics, laboratory, and clinical outcomes of adult patients referred to an academic hematology practice for evaluation of neutropenia from 2010 to 2018. Primary and secondary outcomes included incidence of hematologic disorders and rates of Duffy-null positivity by race, respectively. In a separate analysis, we reviewed absolute neutrophil count (ANC) reference ranges from publicly available Association of American Medical Colleges Medical School Member laboratory directories to assess institutional variations.

RESULTS

In total, 163 patients were included, with disproportionate number of Black patients referred compared to local demographics. Twenty-three percent of patients (n = 38) were found to have a clinically relevant hematologic outcome (mean ANC of 0.59 × 10 /L), and only six were identified with ANC ≥1.0 × 10 /L. Incidence of hematologic outcomes was lowest among Black patients (p = .05), and nearly all Blacks who underwent Duffy-null phenotype testing were positive (93%), compared to 50% of Whites (p = .04). In separate review of laboratory directories, we confirmed wide variation in ANC lower limit of normal (0.91-2.40 × 10 /L).

CONCLUSION

Hematologic disorders were rare in patients with mild neutropenia and among Blacks, highlighting the need to standardize hematological ranges representative of non-White communities.

摘要

背景

无症状性中性粒细胞减少症是一种常见的血液学转诊病症,但缺乏标准化的参考范围和已发表的临床结果。

方法

在我们的回顾性分析中,我们评估了 2010 年至 2018 年期间因中性粒细胞减少症到学术血液科就诊的成年患者的人口统计学、实验室和临床结果。主要和次要结局分别为血液系统疾病的发生率和按种族划分的 Duffy 阴性率。在另一项分析中,我们查阅了美国医师协会医学学校成员实验室目录中公开提供的协会的绝对中性粒细胞计数(ANC)参考范围,以评估机构间的差异。

结果

共有 163 名患者入组,其中黑人患者的转诊比例不成比例,与当地人口统计学数据相比。23%的患者(n=38)发现有临床相关的血液学结果(平均 ANC 为 0.59×10/L),只有 6 名患者 ANC≥1.0×10/L。血液学结果的发生率在黑人中最低(p=0.05),几乎所有接受 Duffy 阴性表型检测的黑人都是阳性(93%),而白人的阳性率为 50%(p=0.04)。在对实验室目录的单独审查中,我们证实 ANC 正常下限存在广泛差异(0.91-2.40×10/L)。

结论

在轻度中性粒细胞减少症患者和黑人中,血液系统疾病很少见,这突出表明需要标准化代表非白人社区的血液学范围。

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本文引用的文献

1
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Blood Adv. 2023 Feb 14;7(3):317-320. doi: 10.1182/bloodadvances.2022007679.
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When non-Whiteness becomes a condition.
Blood. 2021 Jan 7;137(1):13-15. doi: 10.1182/blood.2020008600.
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J Pediatr Hematol Oncol. 2016 Apr;38(3):e140-3. doi: 10.1097/MPH.0000000000000528.

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