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. 2012 Sep-Oct;18(5):712-9.
doi: 10.4158/EP11371.OR.

A retrospective study comparing neutral protamine hagedorn insulin with glargine as basal therapy in prednisone-associated diabetes mellitus in hospitalized patients

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A retrospective study comparing neutral protamine hagedorn insulin with glargine as basal therapy in prednisone-associated diabetes mellitus in hospitalized patients

Subarna M Dhital et al. Endocr Pract. 2012 Sep-Oct.

Abstract

Objective: To compare glycemic outcomes in hospitalized patients with or without type 2 diabetes mellitus receiving neutral protamine Hagedorn insulin (NPH) vs glargine as basal insulin for management of glucocorticoid-associated hyperglycemia.

Methods: We conducted a retrospective review of electronic medical records in prednisone-treated adult patients with hyperglycemia in a university hospital. Consecutive patients were selected in both the NPH and glargine cohorts using inclusion and exclusion criteria. Baseline characteristics were assessed in each cohort. Glycemic outcomes were analyzed by comparing fasting blood glucose, mean daily blood glucose concentration, median daily blood glucose concentration, and the number of hypoglycemic episodes on a prespecified index day.

Results: One hundred twenty patients were included: 60 patients in the NPH cohort and 60 patients in the glargine cohort. The weight-based insulin requirement was lower in the NPH cohort than in the glargine cohort (0.27 ± 0.2 units/kg vs 0.34 ± 0.2 units/kg [P = .04] for basal insulin and 0.26 ± 0.2 units/kg vs 0.36 ± 0.2 units/kg [P = .03] for bolus insulin). NPH and glargine cohorts were similar regarding age, sex, race, body mass index, hemoglobin A1c, serum creatinine, and prednisone dosage. Glycemic outcomes in the NPH cohort compared with outcomes in the glargine cohort were similar regarding mean fasting blood glucose concentration (134 ± 49 mg/dL vs 139 ± 54 mg/dL [P = .63]), mean daily blood glucose (167 ± 46 mg/dL vs 165 ± 52 mg/dL [P = .79]), median blood glucose (160 ± 49 mg/dL vs 159 ± 57 mg/dL [P = .90]), and number of hypoglycemic episodes per day (0.12 ± 0.3 vs 0.10 ± 0.3 [P = .77]).

Conclusions: NPH and glargine appear to be equally effective as basal insulin in the management of hyperglycemia in hospitalized patients receiving prednisone. However, the total daily insulin doses used were lower in the NPH cohort.

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Figures

Fig. 1
Fig. 1
Definition of index day for data collection.
Fig. 2
Fig. 2
Total daily prednisone dose in patients receiving neutral protamine Hagedorn (NPH) insulin (n = 60) or insulin glargine (n = 60) as basal insulin in a retrospective study of glucocorticoid-associated hyperglycemia.
Fig. 3
Fig. 3
Glycemic outcomes in patients receiving neutral protamine Hagedorn (NPH) insulin (n = 60) or insulin glargine (n = 60) as basal insulin in a retrospective study of glucocorticoid-associated hyperglycemia. Panel A, Mean fasting blood glucose concentration. Panel B, Mean daily blood glucose concentration. Panel C, Median daily blood glucose concentration. Panel D, Mean number of hypoglycemic episodes per day. Error bars represent standard deviation.

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