Can a Protocol for Glycaemic Control Improve Type 2 Diabetes Outcomes After Gastric Bypass?
Can a Protocol for Glycaemic Control Improve Type 2 Diabetes Outcomes After Gastric Bypass?
复制标题
血糖控制方案能否改善胃绕道手术后 2 型糖尿病的预后?
DOI:
10.1007/s11695-011-0543-6
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发表时间:
2012
期刊:
影响因子:
2.9
通讯作者:
Carel W. le Roux
中科院分区:
文献类型:
--
作者:
Wiebke K. Fenske;Dimitri J. Pournaras;Erlend T. Aasheim;Alexander D. Miras;Nicola Scopinaro;Samantha Scholtz;Carel W. le Roux
BackgroundRoux-en-Y gastric bypass surgery (RYGB) is an effective treatment for patients with type 2 diabetes (T2DM). Tight glycaemic control immediately after RYGB for T2DM may improve long-term glycaemic outcomes, but is also associated with a higher risk of hypoglycaemia. We designed a treatment algorithm to achieve optimal glycaemic control in patients with insulin-treated T2DM after RYGB and evaluated its feasibility, safety and efficacy.MethodsFifty patients following protocol-driven diabetes management were discharged on a fixed amount of metformin and glargine, with the insulin dose adjusted according to a standardised insulin sliding scale aiming for a fasting capillary glucose (FCG) of 5.5–6.9 mmol/L. Glycaemic outcome and remission of diabetes (defined as HbA1c < 6% and FCG levels < 5.6 mmol/L for at least 1 year without hypoglycaemic medication) were compared between patients who received protocol-driven treatment and a similar cohort of 49 patients following standard glycaemic management.ResultsAt 1 year follow-up, the protocol-driven group showed a greater improvement in glycaemic control than the non-protocol-driven group (HbA1c −3.0 ± 0.2% vs. −1.2 ± 0.1%,P< 0.001; FCG levels −3.4 ± 0.2 vs. −2.0 ± 0.2 mmol/L,P= 0.02) and a higher remission rate from T2DM (50.0% vs. 6.1%,P< 0.001). No symptomatic hypoglycaemia was reported in either group.ConclusionsThe protocol-driven management proved to be feasible, safe and effective in achieving targeted glycaemic control in T2DM after RYGB. The next step will be to scrutinise the efficacy of protocol-driven management in a randomised controlled clinical trial.
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影响因子:
6.1
作者:
Nasr, CE;Hoogwerf, BJ;Reddy, SSK
通讯作者:
Reddy, SSK
影响因子:
16.2
作者:
American Diabetes Association
通讯作者:
American Diabetes Association
影响因子:
11.5
作者:
H. Yki
通讯作者:
H. Yki
影响因子:
158.5
作者:
Duckworth, William;Abraira, Carlos;Huang, Grant D.
通讯作者:
Huang, Grant D.
影响因子:
158.5
作者:
Gerstein, Hertzel C.;Miller, Michael E.;Friedewald, William T.
通讯作者:
Friedewald, William T.