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维加血液分析仪在大学医院环境中的评估。

Evaluation of the Vega haematology analyser in a university hospital setting.

作者信息

Corberand J X, Segonds C, Fontanilles A M, Cambus J P, Fillola G, Laharrague P

机构信息

Laboratoire d'Hématologie, Hôpital Rangueil, CHU Toulouse, France.

出版信息

Clin Lab Haematol. 1999 Feb;21(1):3-10. doi: 10.1046/j.1365-2257.1999.00182.x.

Abstract

The performance of the ABX Vega haematology analyser was compared with that of the Sysmex NE-8000, with specific attention to flagging performance and ergonomics. Eight hundred routine samples underwent precision and interinstrument variability studies and 168 samples corresponding to various blood disorders were studied meanwhile. Results from the two instruments gave excellent correlation (r > 0.900) for most parameters except MCHC (r = 0.114), basophil and monocyte percentages (r = 0.617 and 0.552, respectively). The reproducibility, repeatability, linearity, carry-over and stability of the Vega were satisfactory; 'flagging' occurred in 31% of routine samples with sensitivity 88.8%, specificity 41.3% and positive predictive value 85.7%. Various flags appeared in 91% (42/46) of cases where blast cells were microscopically identified. In the four remaining cases, CBC anomalies would themselves have justified microscopic examination of a smear. On 'CBC only' mode reagent consumption was significantly reduced. In the laboratory the analyser was best appreciated for its user-friendliness.

摘要

将ABX Vega血液分析仪的性能与Sysmex NE - 8000的性能进行了比较,特别关注了标记性能和人体工程学。对800份常规样本进行了精密度和仪器间变异性研究,同时研究了168份对应各种血液疾病的样本。除MCHC(r = 0.114)、嗜碱性粒细胞和单核细胞百分比(分别为r = 0.617和0.552)外,两种仪器的大多数参数结果具有极好的相关性(r > 0.900)。Vega的重现性、重复性、线性、携带污染和稳定性均令人满意;在31%的常规样本中出现“标记”,敏感性为88.8%,特异性为41.3%,阳性预测值为85.7%。在显微镜下识别出原始细胞的病例中,91%(42/46)出现了各种标记。在其余4例中,全血细胞计数异常本身就足以证明需要对涂片进行显微镜检查。在“仅全血细胞计数”模式下,试剂消耗显著减少。在实验室中,该分析仪因其用户友好性而最受赞赏。

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