Guide-lines for near patient testing: haematology.

Clinical and laboratory haematology Pub Date : 1995-12-01
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Abstract

These guide-lines provide a framework for the local arrangement of near patient testing (NPT) services for haematology tests. The guidance may be applied to medical and surgical units within hospitals (e.g. ITU, renal dialysis units, casualty) as well as general practitioners' surgeries, for blood counts and coagulation testing. The professional head of the central laboratory must take responsibility for all aspects of the NPT service, although there should be full discussion with the clinical departments involved and joint ownership of the results. NPT operators must be trained and accredited by the central laboratory. Equipment selected should normally have received a satisfactory evaluation report from the Medical Devices Agency (MDA), and should generate results that are comparable with those of the central laboratory. If a full MDA operation evaluation has not been performed, the purchaser should perform a local assessment according to the protocol in this document. The suitability of the equipment, imprecision, and comparability must be studied. The NPT equipment must be properly maintained and calibrated, and a record of patient identity, date and time of testing, reagent lot numbers, and operator must be kept. The central laboratory must participate in a suitable external quality assessment programme (EQA), and provide systems for EQA and internal quality control (IQC) of the NPT site.

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近病人检测指南:血液学。
这些准则为血液学检测的近病人检测(NPT)服务的当地安排提供了框架。该指南可适用于医院内的内科和外科单位(例如国际电联、肾透析单位、伤病员)以及全科医生的手术,用于血液计数和凝血试验。中心实验室的专业负责人必须负责NPT服务的所有方面,但应与所涉及的临床部门进行充分讨论并共同拥有结果。不扩散操作人员必须经过中央实验室的培训和认证。所选设备通常应已收到医疗器械管理局(MDA)的满意评价报告,并应产生与中心实验室相当的结果。如果尚未进行全面的MDA操作评估,买方应根据本文件中的协议进行本地评估。必须研究设备的适用性、不精确性和可比性。NPT设备必须妥善维护和校准,必须保留患者身份、检测日期和时间、试剂批号和操作人员的记录。中心实验室必须参加合适的外部质量评价方案(EQA),并提供NPT现场的EQA和内部质量控制(IQC)系统。
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