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Assessment of Coverage and Quality of Selected Clinical Chemistry Tests among Medical Laboratories of Health Facilities in Jimma Zone, South West Ethiopia

机译:西南埃塞俄比亚吉姆玛区医学实验室医学实验室覆盖和质量评估

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Background. Medical laboratories play essential roles in measurement of analyte in clinical sample for the diagnosis and monitoring of diseases. Thus, data generated from the laboratory have to be reliable for which strict quality assurance is maintained. Objective. To assess the coverage and quality of selected clinical chemistry tests among medical laboratories of health facilities in, Jimma Zone, South West Ethiopia. Methods. A cross-sectional study was conducted at Jimma Zone on health facilities from August 15 to September 15, 2014. Eighty-six health facility laboratories were included in the study. We classified laboratories into laboratories with clinical chemistry service and those without clinical chemistry service clusters and those with clinical chemistry laboratory were again clustered according to their level. Data were collected by direct observation, interview, and proficiency testing (PT). The collected data were analyzed and compared with CLIA PT goal for TEa by considering total allowable error ± 20%, ±10%, ±15%, and ±20 for each analyte, ALT, glucose, creatinine, and total bilirubin, respectively. Result. From total of 86 health facilities with laboratories, 23.3% (n=20) had clinical chemistry service, of which 77.2% results were reported outside of the allowable error limit. Conclusion. According to this study the availability of clinical chemistry test service was very minimal and facilities giving the service do not fulfill the minimum standard for quality; thus clients were either getting wrong clinical decision or misdiagnosed. Therefore, the external and internal quality assessment programs should be reviewed very well. Those laboratories whose report was outside of the allowable error should have to report results with the appropriate reference range so that physicians consider that. Establishment of local clinical chemistry reference range can also minimize the problem.
机译:背景。医学实验室在临床样本中测量分析物的诊断和监测疾病的诊断和监测中的基本作用。因此,从实验室产生的数据必须可靠地保持严格的质量保证。客观的。评估吉米埃塞俄比亚Jimma区医学实验室医学实验室所选临床化学测试的覆盖和质量。方法。 2014年8月15日至9月15日至9月15日在卫生设施的Jimma区进行了横断面研究。该研究中包含八十六个卫生设施实验室。我们将实验室分类为具有临床化学服务的实验室,没有临床化学服务群的人和临床化学实验室的实验室重新聚集在一起。通过直接观察,面试和能力测试(PT)收集数据。通过考虑分析物,ALT,葡萄糖,肌酐和总胆红素的总允许误差±20%,±10%,±15%和±20,分析了收集的数据并与CLIA PT目标进行了比较。结果。从86个卫生设施与实验室共有86个,23.3%(n = 20)具有临床化学服务,其中77.2%的结果在允许的误差限制之外报告。结论。根据本研究的临床化学测试服务的可用性是非常简单的,并且提供服务的设施不符合最低质量标准;因此,客户要么出现错误的临床决策或误会。因此,外部和内部质量评估计划应非常熟悉。那些报告在允许错误之外的实验室应该必须在适当的参考范围内向结果报告结果,以便医生认为这一点。建立地方临床化学参考范围也可以最大限度地减少问题。

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