Demma Linda J, Carlson Karen T, Duggan Elizabeth W, Morrow John Gordon, Umpierrez Guillermo
Department of Anesthesiology, Emory University School of Medicine and Emory Healthcare, 1364 Clifton Rd, Atlanta, GA 30322, USA; Department of Anesthesiology, Bassett Healthcare, 1 Atwell Rd, Cooperstown, NY 13326, USA.
Department of Anesthesiology, Emory University School of Medicine and Emory Healthcare, 1364 Clifton Rd, Atlanta, GA 30322, USA; Department of Anesthesiology, Bassett Healthcare, 1 Atwell Rd, Cooperstown, NY 13326, USA.
J Clin Anesth. 2017 Feb;36:184-188. doi: 10.1016/j.jclinane.2016.10.003. Epub 2016 Dec 5.
Among patients with type 2 diabetes treated with insulin, perioperative hyperglycemia and hypoglycemia may cause undesirable symptoms, surgery delay or cancellation, or unexpected hospitalization. Our objective was to compare preoperative glargine dosing regimens on perioperative glycemic control in patients undergoing ambulatory surgery.
Observational study.
Pre- and postoperative holding areas.
One hundred fifty patients with type 2 diabetes using a once daily, evening insulin glargine regimen undergoing ambulatory surgery were included.
None.
To conduct the analysis, patients were divided into four groups based on the percentage of normal evening glargine dose taken. Group 1 took no glargine. Group 2 took 33%-57%. Group 3 took 60%-87% and Group 4 took 100% of their normal dose. The primary outcome was the proportion of patients in each group with blood glucose in the target range (100-180 mg/dL), and the incidence of hypoglycemia (defined as BG <70 mg/dL or symptomatic, requiring glucose).
Group 3 had the highest proportion (78%) of patients within target range (P<.001) and Group 4 had the highest proportion of patients with hypoglycemia (P=.01). Patients in Group 3 were significantly more likely to achieve target blood glucose than patients in either Group 1 (P=.001) or Group 4 (P=.002).
Our study shows that the percent of normal insulin dose given the evening before surgery directly impacts perioperative glucose levels in ambulatory surgery patients. Patients taking 60%-87% of their usual dose the evening before surgery were likely to arrive in target blood glucose range with decreased risk for hypoglycemia. The mean and mode dose taken in Group 3 were 73% and 75%, respectively, suggesting that the optimal dose may be 75% of normal dose.
在接受胰岛素治疗的2型糖尿病患者中,围手术期高血糖和低血糖可能会导致不良症状、手术延迟或取消,或意外住院。我们的目的是比较术前甘精胰岛素给药方案对接受门诊手术患者围手术期血糖控制的影响。
观察性研究。
术前和术后等候区。
纳入150例使用每日一次晚间甘精胰岛素方案的2型糖尿病患者接受门诊手术。
无。
为进行分析,根据术前晚间甘精胰岛素正常剂量的服用比例将患者分为四组。第1组未服用甘精胰岛素。第2组服用33%-57%。第3组服用60%-87%,第4组服用100%的正常剂量。主要结局是每组血糖在目标范围内(100-180mg/dL)的患者比例,以及低血糖发生率(定义为血糖<70mg/dL或有症状,需要补充葡萄糖)。
第3组患者血糖在目标范围内的比例最高(78%)(P<0.001),第4组低血糖患者比例最高(P=0.01)。第3组患者达到目标血糖的可能性显著高于第1组(P=0.001)或第4组(P=0.002)患者。
我们的研究表明,术前一晚给予的正常胰岛素剂量百分比直接影响门诊手术患者围手术期的血糖水平。术前一晚服用其常用剂量60%-87%的患者更有可能达到目标血糖范围,且低血糖风险降低。第3组的平均剂量和众数剂量分别为73%和75%,表明最佳剂量可能为正常剂量的75%。