scholarly journals Glucose control after glucocorticoid administration in hospitalized patients – a retrospective analysis

2022 ◽  
Vol 22 (1) ◽  
Author(s):  
Franzisca Merkofer ◽  
Tristan Struja ◽  
Neele Delfs ◽  
Carlos C. Spagnuolo ◽  
Jason F. Hafner ◽  
...  

Abstract Background Glucocorticoid (GC)-induced hyperglycemia is a frequent adverse effect in hospitalized patients. Guidelines recommend insulin treatment to a target range of 6–10 mmol/L (108–180 mg/dl), but efficacies of particular regimes have not been well-studied. Methods In this retrospective cohort study, hospitalized patients receiving GCs at the medical ward were analyzed by treatment (basal-bolus vs. bolus-only vs. pre-mixed insulin) and compared to a non-insulin-therapy reference group. Coefficients of glucose variation (CV), percentage of glucose readings in range (4–10 mmol/L (72–180 mg/dl)) and hypoglycemia (< 4 mmol/L (< 72 mg/dl)) were evaluated. Results Of 2424 hospitalized patients receiving systemic GCs, 875 (36%) developed GC-induced hyperglycemia. 427 patients (17%) had a previous diagnosis of diabetes. Adjusted relative risk ratios (RRR) for the top tertile of CV (> 29%) were 1.47 (95% Cl 1.01–2.15) for bolus-only insulin, 4.77 (95% CI 2.67–8.51) for basal-bolus insulin, and 4.98 (95% CI 2.02–12.31) for premixed insulin, respectively. Adjusted RRR for percentages of glucose readings in range were 0.98 (95% Cl 0.97–0.99) for basal-bolus insulin, 0.99 (95% Cl 0.98–1.00) for premixed insulin, and 1.01 (95% Cl 1.00–1.01) for bolus-only insulin, respectively. Adjusted RRR for hypoglycemia was 13.17 (95% Cl 4.35–39.90) for basal-bolus insulin, 8.92 (95% Cl 2.60–30.63) for premixed insulin, and 2.99 (95% Cl 1.01–8.87) for bolus-only insulin, respectively. Conclusions Current guidelines recommend a basal-bolus regimen for treatment of GC-induced hyperglycemia, but we found similar outcomes with pre-mixed and bolus-only insulin regimens. As GC-induced hyperglycemia is a frequent issue in hospitalized patients, it might be reasonable to prospectively study the ideal regimen.

Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 2194-PUB
Author(s):  
SUN JOON MOON ◽  
HAN NA JANG ◽  
YE SEUL YANG ◽  
SOO HEON KWAK ◽  
HYE SEUNG JUNG ◽  
...  

2013 ◽  
Vol 68 (1) ◽  
pp. 28-33 ◽  
Author(s):  
C Mathieu ◽  
F Storms ◽  
J Tits ◽  
TF Veneman ◽  
IM Colin

Diabetes Care ◽  
2015 ◽  
Vol 38 (12) ◽  
pp. 2211-2216 ◽  
Author(s):  
Virginia Bellido ◽  
Lorena Suarez ◽  
Maria Galiana Rodriguez ◽  
Cecilia Sanchez ◽  
Marta Dieguez ◽  
...  

2014 ◽  
Vol 28 (6) ◽  
pp. 504-510
Author(s):  
Germin Fahim ◽  
Evangelia Davanos ◽  
Karina Muzykovsky ◽  
Rochelle Rubin

The use of basal-bolus insulin (BBI) regimens for the treatment of inpatient hyperglycemia has become standard of care. The purpose of this study was to develop and evaluate a newly piloted dosing guideline and utilize the results to adjust it prior to its implementation hospital-wide. This was an institutional review board approved, prospective, and multiphase study. An interdisciplinary team was developed and created a dosing guideline, which was followed by a 3-month, single-unit pilot of the guideline in noncritically ill adult patients. The resulting data were used to revise the guideline. Forty-three patients were included. There was a significant decrease in median blood glucose (BG) with use of the guideline (219 mg/dL [162-281] vs 190 mg/dL [136-246], P < .05) in patients not utilizing it. There was also a significant increase in the number of values within the target range of 70 to 180 mg/dL (30.2% vs 41.4%, P < .05). Moreover, there was comparable hypoglycemia before and after the intervention (1.6% vs 2.4%, P = .51). Based on these results, the dosing factor used for the total daily dose of insulin was increased in certain populations. Use of a BBI dosing guideline is safe and effective in decreasing BG values in noncritically ill patients at our institution.


2021 ◽  
Vol 32 (4) ◽  
pp. 567-570
Author(s):  
Dinda M. N. Ratri ◽  
Arina D. Puspitasari ◽  
Cahyo W. Nugroho ◽  
Budi Suprapti ◽  
Suharjono ◽  
...  

Abstract Objectives Previous research suggests that there may be intergender differences in the profile of glycemic control achievable during the treatment of type 2 diabetes mellitus. This preliminary study was conducted to determine differences in glycemic outcomes in type 2 diabetes mellitus patients amongst men and women in an Indonesian hospital. Methods The study was conducted at the outpatient internal medicine polyclinic of Universitas Airlangga Teaching Hospital Surabaya. This observational prospective cohort study examining outcomes for 64 patients (32 men and 32 women) treated with insulin therapy. The primary outcome measure was the extent to which subjects achieved concordance with the target blood glucose parameters based on the American Diabetes Association (ADA) guidance. Results After 3 months of combination basal-bolus insulin treatment, the proportion of subjects who had fasting blood glucose values in the target range did not increase for either gender. For women, there was a significantly higher proportion of subjects who achieved a postprandial glucose value within the target range (p=0.04) Conclusions In this study, patients achieved postprandial glycemic outcomes for women but not men. More research is required to elucidate the possible intergender difference in results for subjects treated with basal-bolus insulin for type 2 diabetes mellitus.


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