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一小时葡萄糖耐量试验样本的血糖仪分析

Glucometer analysis of one-hour glucose challenge samples.

作者信息

Dillon A E, Menard M K, Rust P, Newman R B, VanDorsten J P

机构信息

Department of Obstetrics and Gynecology, Medical University of South Carolina, Charleston, USA.

出版信息

Am J Obstet Gynecol. 1997 Nov;177(5):1120-3. doi: 10.1016/s0002-9378(97)70026-7.

Abstract

OBJECTIVE

Our purpose was to explore a cost-saving measure for diabetes screening by using glucometer testing on venous whole blood obtained after a 1-hour glucose challenge test. Glucometer results falling above an upper threshold would predict abnormal plasma values and mandate a glucose tolerance test; results below the lower threshold would predict normal plasma values and avoid further testing. Results between the thresholds would require traditional plasma analysis.

STUDY DESIGN

We performed a prospective cohort study on 222 consecutive pregnant women. A standard 50 gm glucose screen was performed with venous blood drawn at 1 hour. We immediately removed a drop of whole blood from the venous sample and analyzed it on a portable glucometer, Accu-Chek III. The remaining sample was submitted immediately for routine plasma analysis. All values were obtained on the same glucometer, which was calibrated daily in our clinic laboratory. Regression analysis was performed on 129 samples to select the two thresholds. The selected thresholds were then applied prospectively to the next 93 consecutive samples for validation.

RESULTS

Excellent correlation (r = 0.9045) exists between the glucometer and laboratory values. Glucometer threshold values of 110 mg/dl and 155 mg/dl were selected because they predicted plasma values < 135 mg/dl or > 135 mg/dl with 95% certainty, respectively. Prospectively, the thresholds were completely accurate in classifying the values.

CONCLUSION

Venous whole blood assayed by glucometer can reliably predict an elevated or normal automated plasma glucose value. By applying thresholds, three fourths of all patients can immediately receive reassuring information, whereas the patients with poorest glucose tolerance are immediately identified and diagnostic testing is scheduled. Additionally, our model reduces the number of automated laboratory studies by 80% and reduces the cost of diabetic screening.

摘要

目的

我们的目的是探索一种成本节约措施,通过对1小时葡萄糖耐量试验后采集的静脉全血进行血糖仪检测来进行糖尿病筛查。血糖仪检测结果高于上限阈值将预测血浆值异常,并需要进行葡萄糖耐量试验;结果低于下限阈值将预测血浆值正常,并避免进一步检测。阈值之间的结果需要进行传统的血浆分析。

研究设计

我们对222名连续的孕妇进行了一项前瞻性队列研究。进行标准的50克葡萄糖筛查,在1小时时采集静脉血。我们立即从静脉样本中取出一滴全血,并用便携式血糖仪Accu-Chek III进行分析。其余样本立即送去进行常规血浆分析。所有值均在同一台血糖仪上获得,该血糖仪每天在我们的临床实验室进行校准。对129个样本进行回归分析以选择两个阈值。然后将选定的阈值前瞻性地应用于接下来的93个连续样本进行验证。

结果

血糖仪与实验室值之间存在极好的相关性(r = 0.9045)。选择血糖仪阈值为110毫克/分升和155毫克/分升,因为它们分别以95%的确定性预测血浆值<135毫克/分升或>135毫克/分升。前瞻性地,这些阈值在对值进行分类时完全准确。

结论

通过血糖仪检测的静脉全血能够可靠地预测自动化血浆葡萄糖值升高或正常。通过应用阈值,四分之三的患者可以立即获得安心的信息,而葡萄糖耐量最差的患者可以立即被识别并安排诊断测试。此外,我们的模型将自动化实验室检测的数量减少了80%,并降低了糖尿病筛查的成本。

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