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便携式凝血仪在新生儿常规住院中的验证。

Validation of a Portable Coagulometer for Routine In-Hospital Use for Newborns.

机构信息

1Neonatal Unit, Department of Pediatrics, San Cecilio University Hospital, Granada, Spain. 2Department of Haematology, San Cecilio University Hospital, Granada, Spain. 3Department of Pediatrics, San Cecilio University Hospital, Granada, Spain.

出版信息

Pediatr Crit Care Med. 2017 Nov;18(11):e569-e574. doi: 10.1097/PCC.0000000000001333.

Abstract

OBJECTIVES

To verify the reliability and clinical benefits of the coagulation tests made by a point of care device in newborn admitted to a neonatal unit.

DESIGN

We made a statistical comparison between results obtained by the point of care device versus conventional laboratory analysis.

SETTING

Level 3 neonatal unit.

PATIENTS

Thirty-one infants admitted to the neonatal unit at the San Cecilio University Hospital (Granada, Spain) were recruited to this study.

INTERVENTIONS

All underwent a double analytical determination: a small drop of blood was taken for analysis with a portable coagulometer (qLabs Electrometer Plus) and the rest of the blood sample was analyzed with conventional hospital laboratory equipment.

MEASUREMENTS AND MAIN RESULTS

According to the linearity test performed, the measuring methods presented a good linear regression fit. Lin's concordance coefficient showed a "good" agreement for activated partial prothrombin time and international normalized ratio (>0.61) and a moderate one for prothrombin time (0.41-0.6) for the sample of newborns.

CONCLUSIONS

The portable coagulometer qLabs Electrometer Plus device has the potential to be an alternative to standard hospital coagulation autoanalyzers in a subset of patients where the amount of blood drawn can have significant risks. Our study is the first of its kind to analyze the use of this device with severely ill newborns.

摘要

目的

验证即时检测设备在新生儿病房中进行凝血检测的可靠性和临床获益。

设计

我们对即时检测设备和常规实验室分析的结果进行了统计学比较。

地点

三级新生儿病房。

患者

31 名入住西班牙格拉纳达圣塞西莉亚大学医院新生儿病房的婴儿被纳入本研究。

干预措施

所有婴儿均进行了双重分析测定:用便携式凝血仪(qLabs Electrometer Plus)取一小滴血进行分析,其余血样用常规医院实验室设备进行分析。

测量和主要结果

根据进行的线性检验,测量方法呈现出良好的线性回归拟合。Lin 的一致性系数显示,对于激活部分凝血活酶时间和国际标准化比值(>0.61),以及对于新生儿样本的凝血酶时间(0.41-0.6),具有“良好”的一致性。

结论

便携式凝血仪 qLabs Electrometer Plus 设备有可能成为标准医院凝血自动分析仪的替代方法,适用于那些采血可能带来重大风险的特定患者群体。我们的研究是首次分析该设备在重症新生儿中的应用。

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