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5500 words of medical examination biochemical graduation thesis essay

编辑: 毕业论文 Release time: 2019-05-02 Editor: Graduation Thesis

This literature review is about how to automatically convert the catalog of biochemical testing papers, and related undergraduate graduation thesis about the quality elements of biochemical testing, which can be used for writing biochemical testing papers for university graduates and undergraduate graduation thesis report and excellent scientific research. Appraisal paper reference textbook download. Free to teach you how to write biochemical testing and reference literature and medical test papers .


【Abstract】 With the rapid development of medical testing, whether the detection of high or low quality has become a key factor that harms the medical diagnosis. The test report is not only the basis for the medical diagnosis, but also the key material for recording the diagnosis process. This biochemical test report with reference meaning and value can better present reasonable business for patients. This paper analyzes and discusses the relevant elements that jeopardize the results of biochemical quality supervision, and proposes its own countermeasures for improving the quality of biochemical testing.

[Keywords] Biochemical testing; Quality: Hazardous elements Introduction The transformation of modern science has promoted the increasingly close relationship between medicine and testing. Improving the manipulation of the elements that jeopardize the quality of biochemical testing can produce a biochemical testing report with reference meaning and value for medicine, and then stronger presentation of reasonable business for patients. However, because all stages of the inspection and analysis process are related to the appropriateness of the test results, there is still a quality management level in the specific work of the master's thesis essay on the quality elements of hazardous biochemical testing. Many problems should be valued and improved. In order to summarize the relevant factors that jeopardize the quality of biochemical testing, the article summarizes the three factors that jeopardize quality before, during, and after the analysis of biochemical testing, and discusses how such factors can be improved and quality management is carried out. discuss. The report is now given.

1 Quality hazards of biochemical testing before analysis

1.1 Biochemical specimen collection, storage and transportation When carrying out blood collection, please do what you like. After the end, remove the needle tube and slowly introduce it into the test tube along the wall thickness to avoid hemolysis caused by vapor bubbles. For patients seeking medical treatment, the same blood clot collection as in the hanging bottle should be minimized to avoid the illusion of "reduced results" due to blood being mixed with water at night. The collection of biochemical Plasmodium should be performed on an empty stomach. The stable balance of cardiomyocyte organic matter excretion is fully considered, and it is generally adopted after 12 hours of meals. This can truly reflect the TG, GH, and GLU in the sample. Index of exact organic water content. For the samples collected after meals, attention should be paid to the presence of blood lipids, triglycerides, and organic phosphorus reduction and the increase of ammonia, uric acid, and urea nitrogen. Patients who have taken some medicines before sampling and retesting will cause great harm to specific values. For example, it is reported that 10% fructose solution can only harm the measurement results of phosphorus, blood lipids, K, creatinine, etc. The saline solution will cause harm to the measurement results of nitrogen and total cholesterol. The biochemical Plasmodium should be rechecked immediately after collection, and should not be stored as much as possible. Because many factors such as cell excretion, photoelectricity, exothermic reaction, bacterial refinement, and cholesterol enzyme lysis will harm the biochemical test results, this stage will not exceed the biochemical experiment under the current standards of most clinics. Provisions, because the staff involved in this stage are generally unable to standardize management and standards, leading to key elements of pre-analysis deviations.

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