首页|标本保存时间对电化学发光法检测他克莫司药物浓度结果的影响研究

标本保存时间对电化学发光法检测他克莫司药物浓度结果的影响研究

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目的 探讨标本保存时间对电化学发光法检测他克莫司药物浓度结果的影响。方法 选取168例应用他克莫司药物患者的全血标本作为观察对象,按照标本保存时间的不同将患者分为A组(48例)、B组(30例)、C组(30例)、D组(30例)、E组(30例)。所有患者的全血标本采用电化学发光法进行他克莫司浓度检测,A组采血当天标本在前处理后加入EP管立即检测,B组标本在前处理后加入EP管室温放置30 min检测,C组标本在前处理后加入EP管室温放置60 min检测,D组标本在前处理后放置于2~8℃冰箱冷藏3 d后检测,E组标本在前处理后放置于2~8℃冰箱冷藏7 d后检测。以A组标本检测结果为标准,对比A组与B组、C组、D组、E组标本的他克莫司浓度。结果 A组、B组、C组、D组、E组全血标本中他克莫司浓度分别为(7。92±1。26)、(7。96±1。36)、(8。58±1。48)、(8。01±1。19)、(8。66±1。56)ng/ml。B组、D组全血标本中他克莫司浓度与A组相比,差异无统计学意义(P>0。05)。C组、E组全血标本中他克莫司浓度高于A组,差异有统计学意义(P<0。05)。结论 临床上进行电化学发光法检验时,需要重视标本保存时间的管理,尤其是对特定药品(如他克莫司等)浓度评定时,建议在获得检验样本后,短时间(30 min)内完成各项操作,注意时间不宜过长(≤60 min);如当前检验环境、操作无法满足要求,则建议将检验样本进行冷藏处理,并在解决环境、操作问题后立即进行各项操作,以保证最终结果的准确性,提高检验效能。
Study on the effect of sample preservation time on the results of electrochemiluminescence detection of tacrolimus concentration
Objective To explore the effect of sample preservation time on the results of electrochemiluminescence detection of tacrolimus concentration. Methods The whole blood samples from 168 patients treated with tacrolimus were selected as observation subjects,and were divided into Group A (48 cases),Group B (30 cases),Group C (30 cases),Group D (30 cases),and Group E (30 cases) according to the different preservation times of the samples. Tacrolimus concentration was detected by electrochemiluminescence in all patients. Group A was immediately tested by adding to a EP tube after pre-treatment on the day of blood collection,while Group B was tested by adding to a EP tube at room temperature for 30 min after pre-treatment,Group C was tested by adding a EP tube at room temperature for 60 min after pre-treatment,Group D was pre-treated and placed in a 2-8 ℃ refrigerator for 3 d before testing,and Group E was pre-treated and placed in a 2-8 ℃ refrigerator for 7 d before testing. The results of Group A were used as the standard to compare the concentration of tacrolimus detected in Group B,Group C,Group D and Group E. Results The concentrations of tacrolimus detected in Group A,Group B,Group C,Group D and Group E were (7.92±1.26),(7.96±1.36),(8.58±1.48),(8.01±1.19) and (8.66±1.56) ng/ml,respectively. There was no statistically significant difference in the concentration of tacrolimus in whole blood specimens of Group B and Group D compared with Group A (P>0.05). The concentration of tacrolimus in whole blood samples of Group C and Group E were higher than those of Group A,and the difference was statistically significant (P<0.05). Conclusion In the process of clinical electrochemiluminescence testing,it is necessary to pay attention to the management of specimen preservation time,especially for specific drugs (such as tacrolimus). It is recommended to complete all operations within a short period of time (30 min) after obtaining the test sample,and it is important to note that the time should not be too long (≤ 60 min);if the current test environment and operation can not meet the requirements,then it is recommended that the test samples be refrigerated. If the current test environment and operation can not meet the requirements,it is recommended to refrigerate the test samples and carry out the operations immediately after solving the environmental and operational problems,so as to ensure the accuracy of the final results and improve the efficiency of the test.

Whole blood samplesSample preservation timeElectrochemiluminescenceTacrolimusDrug concentration

钱爱丽、张佳琪

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014030 内蒙古科技大学包头医学院第二附属医院

全血标本 标本保存时间 电化学发光法 他克莫司 药物浓度

2024

中国现代药物应用
中国水利电力医学科学技术学会

中国现代药物应用

影响因子:0.862
ISSN:1673-9523
年,卷(期):2024.18(23)