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粒细胞计数与中性粒细胞计数的比较诊断性能

Comparative Diagnostic Performance of the Granulocyte and Neutrophil Counts.

作者信息

Pether Nicola S, Brothwood Jessica L, van Berkel Cornelis, Dunwoodie Elaine H, Blake Robert L, Price Christopher P, Jones Richard G, Baker Karl S, Hall Geoff

机构信息

Institute of Health Science, the University of Leeds, UK.

Leeds Teaching Hospitals NHS Trust, Leeds, UK.

出版信息

Pract Lab Med. 2017 Oct 4;9:45-52. doi: 10.1016/j.plabm.2017.10.001. eCollection 2017 Dec.

Abstract

OBJECTIVES

Use of point-of-care testing is increasing, however many haematology analysers can only determine granulocyte count without further differentiation into neutrophils, eosinophils and basophils. Since the diagnosis of life-threatening neutropenia in cancer patients requires a distinct neutrophil count, this study aimed to determine the comparative performance between the neutrophil and granulocyte count.

DESIGN AND METHODS

A database of 508 646 venous full blood count results measured on a laboratory reference analyser was mined from a large oncology unit. The relationship between granulocyte and neutrophil counts was assessed. Multinomial logistic regression was used to classify results into neutropenia grades using an equivalent granulocyte count.

RESULTS

Granulocyte to neutrophil count correlation was 0.997. The accuracy for classification into neutropenia grades using the derived equivalent granulocyte count ranges was 96.4%. Identification of results with a neutrophil count <1.5×10 cells/L using an equivalent granulocyte count of <1.69×10 cells/L resulted in sensitivity, specificity, positive and negative predictive values of 98.0%, 99.5%, 97.8% and 99.5%, respectively.

CONCLUSIONS

These results describe the relationship between granulocyte and neutrophil counts, measured on a laboratory analyser, in a large population of patients with malignancies and receiving anti-cancer therapies. However, this relationship must be established using a point of care testing system with a three-part differential count before considering the possibility that a granulocyte count can guide clinical decisions in the absence of a definitive neutrophil count, to reduce the frequency and severity of neutropenic complications in patients receiving cancer treatments.

摘要

目的

即时检验的使用正在增加,然而许多血液学分析仪只能测定粒细胞计数,而无法进一步区分中性粒细胞、嗜酸性粒细胞和嗜碱性粒细胞。由于癌症患者危及生命的中性粒细胞减少症的诊断需要明确的中性粒细胞计数,本研究旨在确定中性粒细胞计数与粒细胞计数之间的比较性能。

设计与方法

从一个大型肿瘤科室挖掘了一个包含508646例静脉全血细胞计数结果的数据库,这些结果是在实验室参考分析仪上测得的。评估粒细胞计数与中性粒细胞计数之间的关系。使用多项逻辑回归,根据等效粒细胞计数将结果分类为中性粒细胞减少症等级。

结果

粒细胞计数与中性粒细胞计数的相关性为0.997。使用推导的等效粒细胞计数范围对中性粒细胞减少症等级进行分类的准确率为96.4%。使用等效粒细胞计数<1.69×10⁹/L来识别中性粒细胞计数<1.5×10⁹/L的结果,其敏感性、特异性、阳性预测值和阴性预测值分别为98.0%、99.5%、97.8%和99.5%。

结论

这些结果描述了在大量恶性肿瘤患者和接受抗癌治疗的患者中,实验室分析仪测得的粒细胞计数与中性粒细胞计数之间的关系。然而,在考虑粒细胞计数在缺乏明确中性粒细胞计数的情况下可指导临床决策的可能性之前,必须使用具有三分群分类计数功能的即时检验系统来建立这种关系,以降低接受癌症治疗患者中性粒细胞减少症并发症的发生率和严重程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4290/5683674/40b42c171c02/gr1.jpg

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