Improved Outcomes for Patients Treated with LantusÂ® and ApidraÂ® Regimen Compared with Sliding Scale Insulin
PARIS, June 25 /PRNewswire-FirstCall/ — Sanofi-aventis (EURONEXT: SAN and NYSE: SNY) announced today that results from the RAndomized Study of Basal Bolus Insulin Therapy in the Inpatient Management of Patients with Type 2 Diabetes Undergoing General Surgery (RABBIT-2 Surgery) found that treatment with a basal-bolus regimen that included LantusÃ‚® (insulin glargine [rDNA origin] injection) once-daily and ApidraÃ‚® (insulin glulisine [rDNA origin] injection) before meals improved glycemic control and reduced hospital complications, compared to “sliding scale” insulin (SSI) in general surgery patients with type 2 diabetes. The study results were presented at the American Diabetes Association’s 70th Annual Scientific Sessions.
Basal-bolus insulin regimens are designed to address hyperglycemia before it happens by providing adequate insulin to cover fasting and prandial insulin needs, while SSI regimens provide a corrective dose of insulin after the development of hyperglycemia has occurred.
“Hyperglycemia in hospitalized patients is a common and costly health care problem for patients living with type 2 diabetes,” said Guillermo E. Umpierrez, MD, Professor of Medicine, Division of Endocrinology, Metabolism and Lipids, Emory University School of Medicine and lead author of this investigator-sponsored study. “This study indicates that a basal-bolus insulin regimen consisting of LantusÃ‚® and ApidraÃ‚® may be an effective insulin regimen in the hospital management of general surgery patients with type 2 diabetes.”
The primary endpoint of glycemic control was measured by differences in daily blood glucose (BG) levels and the secondary endpoint was a composite of postoperative complications including wound infection, pneumonia, respiratory failure, acute renal failure, and bacteremia. A blood glucose of < 70 mg/dl was reported in 23.1% of patients in the LantusÃ‚® and ApidraÃ‚® group versus 4.7% of patients in the SSI group (p<0.001), but there were no significant differences in the frequency of severe hypoglycemia (blood glucose < 40 mg/dl) between groups (p=0.057). Difference between groups in the frequency of the composite outcome including wound infection, pneumonia, bacteremia, respiratory failure, and acute renal failure were higher in the SSI group (24.3%) than in LantusÃ‚® and ApidraÃ‚® basal-bolus group (8.6%), p=0.003.
RABBIT-2 Surgery Study Results
This randomized multicenter trial compared the efficacy and safety of LantusÃ‚® and ApidraÃ‚® in a basal-bolus regimen to SSI in non-ICU patients undergoing general surgery. A total of 211 patients were randomized to LantusÃ‚® and ApidraÃ‚® (n=104) or SSI (n=107). Baseline characteristics were comparable between the two arms: age 58+/-11 years, admission blood glucose (BG) 190+/-92 mg/dl, A1C: 7.72+/-2.2% with a BG between 140-400 mg/dl and a history of type 2 diabetes for greater than three months. Outcomes showed:
- The percentage of BG readings <140mg/dl were higher in the LantusÃ‚® and ApidraÃ‚® group than the SSI (53+/-30% versus 31+/-28%, p<0.001)
- There was a significant difference between groups in the frequency of the composite outcome (24.3% and 8.6% in the SSI and LantusÃ‚® and ApidraÃ‚® groups, respectively, p=0.003)
- Reductions in wound infection (2.9% versus 10.3%, p=0.05), non-statistically significant reduction in pneumonia (0% versus 2.8%, p=0.247), and in acute renal failure (3.8% versus 10.3%, p=0.106) with LantusÃ‚® and ApidraÃ‚® as compared with SSI
- Reductions in ICU length of stay (3.2+/-2 versus 1.2+/-0.6 days, p=0.003) were demonstrated with LantusÃ‚® and ApidraÃ‚® as compared with SSI; while not statistically significant, there was a reduction in the number of post-surgical ICU admissions (19.6% versus 12.5%, p=NS) with LantusÃ‚® and ApidraÃ‚® as compared with SSI
- No differences in mortality (1% versus 1%)
Diabetes is a chronic, widespread condition in which the body does not produce or properly use insulin, the hormone needed to transport glucose (sugar) from the blood into the cells of the body for energy. More than 230 million people worldwide are living with the disease and this number is expected to rise to a staggering 350 million within 20 years. It is estimated that nearly 24 million Americans have diabetes, including an estimated 5.7 million who remain undiagnosed. At the same time, approximately 40 percent of those diagnosed are not achieving the blood sugar control target of A1C <7 percent recommended by the ADA. The A1C test measures average blood glucose levels over the past two- to three-month period.
About the sanofi-aventis Diabetes Division
Sanofi-aventis strives to be a 360 degree partner delivering innovative and integrated solutions for people living with diabetes. The Company currently has insulin products, including LantusÃ‚®, ApidraÃ‚® and InsumanÃ‚® — LantusÃ‚® and ApidraÃ‚® are also available as injection pens (LantusÃ‚® SoloSTARÃ‚® and ApidraÃ‚® SoloSTARÃ‚®). Also available in some countries (outside the US) is ClikSTARÃ‚®, a reusable insulin injection pen for LantusÃ‚® or ApidraÃ‚® for people with type 1 or type 2 diabetes. Following the formation of its Diabetes Division, sanofi-aventis has agreements with other companies for the development of blood glucose monitoring solutions and the potential first regenerative treatment for diabetes. Investigational compounds also in the pipeline include a once-daily injectable GLP-1 agonist as a monotherapy and in combination with LantusÃ‚® as well as a long-acting insulin analog.
Sanofi-aventis, a leading global pharmaceutical company, discovers, develops and distributes therapeutic solutions to improve the lives of everyone. Sanofi-aventis is listed in Paris (EURONEXT: SAN) and in New York (NYSE: SNY). For more information, please visit: www.sanofi-aventis.com.
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Media Contacts: --------------- Susan Brooks Susan.Brooks@sanofi-aventis.com 908-981-6566 Marisol Peron Marisol.Peron@sanofi-aventis.com +331 1 53 77 45 02