Laparoscopic ileal interposition associated to a diverted sleeve gastrectomy is an effective operation for the treatment of type 2 diabetes mellitus patients with BMI 21-29

被引:87
作者
DePaula, A. L. [1 ]
Macedo, A. L. V. [1 ,2 ]
Mota, B. R. [1 ]
Schraibman, V. [1 ,2 ]
机构
[1] Hosp Especialidades Ctr Med La Raza, Dept Surg, Goiania, Go, Brazil
[2] Albert Einstein Hosp, Sao Paulo, Brazil
来源
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES | 2009年 / 23卷 / 06期
关键词
Type 2 diabetes mellitus; Ileal interposition; Neuroendocrine brake; Sleeve gastrectomy; Obesity; Metabolic syndrome; ENTEROINSULAR AXIS; INSULIN-RESISTANCE; GLUCOSE-TOLERANCE; SURGERY; TRANSPOSITION; SECRETION; BYPASS;
D O I
10.1007/s00464-008-0156-x
中图分类号
R61 [外科手术学];
学科分类号
摘要
The objective of this study is to evaluate the clinical results of the laparoscopic interposition of a segment of ileum into the proximal duodenum associated to a sleeve gastrectomy (II-DSG) in order to treat patients with type 2 diabetes mellitus (T2DM) and body mass index (BMI) 21-29 kg/m(2). The laparoscopic procedure was performed in 69 patients, 22 female and 47 male. Mean age was 51 years (range 41-63 years). Mean BMI was 25.7 (21.8-29.2) kg/m(2). All patients had the diagnosis of T2DM for at least 3 years and evidence of stable treatment with oral hypoglycemic agents and or insulin for at least 12 months. Insulin therapy was used by 44% of the patients. Mean duration of T2DM was 11 years (range 3-18 years). Dyslipidemia was diagnosed in 72.5% and hypertension in 66.7%. Nephropathy was characterized in 29% of the patients, retinopathy in 26.1%, and neuropathy in 24.6%. Overall, 95.7% of the patients achieved adequate glycemic control (Hb(A1c) < 7%) without antidiabetic medication. Hb(A1c) below 6% was achieved by 65.2%. Mean postoperative follow-up was 21.7 months (range 7-42 months). Mean postoperative BMI was 21.8 kg/m(2). There was no conversion to open surgery. Median hospital stay was 3.4 days (range 2-58 days). Major postoperative complications were diagnosed in 7.3%. There was no mortality. Fasting glycemia decreased from a mean of 218 to 102 mg/dl, postprandial glycemia from 305 to 141 mg/dl, and homeostasis model assessment of insulin resistance (Homa-IR) from 5.2 to 0.77. All associated comorbidities and complications related to T2DM had significant improvement or control. Arterial hypertension was controlled in 91.3%. Macroalbuminuria was no longer observed. Microalbuminuria resolved in 87.5% of patients. Hypercholesterolemia was normalized in 95% and hypertriglyceridemia in 92% of patients. Laparoscopic II-DSG was an effective operation in controlling T2DM in a nonobese (BM < 30 kg/m(2)) population. Associated diseases and related complications were also improved. A longer follow-up period is needed.
引用
收藏
页码:1313 / 1320
页数:8
相关论文
共 20 条
[11]   A new paradigm for type 2 diabetes mellitus - Could it be a disease of the foregut? [J].
Hickey, MS ;
Pories, WJ ;
MacDonald, KG ;
Cory, KA ;
Dohm, GL ;
Swanson, MS ;
Israel, RG ;
Barakat, HA ;
Considine, RV ;
Caro, JF ;
Houmard, JA .
ANNALS OF SURGERY, 1998, 227 (05) :637-644
[12]   Comparison of rates of resolution of diabetes Mellitus after gastric banding, gastric bypass, and billopancreatic diversion [J].
Parikh, Manish ;
Ayoung-Chee, Patricia ;
Romanos, Eleny ;
Lewis, Nichole ;
Pachter, H. Leon ;
Fielding, George ;
Ren, Christine .
JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS, 2007, 205 (05) :631-635
[13]   The enteroinsular axis and the recovery from type 2 diabetes after bariatric surgery [J].
Patriti, A ;
Facchiano, E ;
Sanna, A ;
Gullà, N ;
Donini, A .
OBESITY SURGERY, 2004, 14 (06) :840-848
[14]   Early improvement of glucose tolerance after ileal transposition in a non-obese type 2 diabetes rat model [J].
Patriti, A ;
Facchiano, E ;
Annetti, C ;
Aisa, MC ;
Galli, F ;
Fanelli, C ;
Donini, A .
OBESITY SURGERY, 2005, 15 (09) :1258-1264
[15]   The entero-insular axis: implications for human metabolism [J].
Ranganath, Lakshminarayan R. .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2008, 46 (01) :43-56
[16]   The mechanism of diabetes control after gastrointestinal bypass surgery reveals a role of the proximal small intestine in the pathophysiology of type 2 diabetes [J].
Rubino, Francesco ;
Forgione, Antonello ;
Cummings, David E. ;
Vix, Michel ;
Gnuli, Donatella ;
Mingrone, Geltrude ;
Castagneto, Marco ;
Marescaux, Jacques .
ANNALS OF SURGERY, 2006, 244 (05) :741-749
[17]   Weight loss through ileal transposition is accompanied by increased ileal hormone secretion and synthesis in rats [J].
Strader, AD ;
Vahl, TP ;
Jandacek, RJ ;
Woods, SC ;
D'Alessio, DA ;
Seeley, RJ .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2005, 288 (02) :E447-E453
[18]   Elevated plasma glucose dependent insulinotropic polypeptide associates with hyperinsulinemia in impaired glucose tolerance [J].
Theodorakis, MJ ;
Carlson, O ;
Muller, DC ;
Egan, JM .
DIABETES CARE, 2004, 27 (07) :1692-1698
[19]   Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33) [J].
Turner, RC ;
Holman, RR ;
Cull, CA ;
Stratton, IM ;
Matthews, DR ;
Frighi, V ;
Manley, SE ;
Neil, A ;
McElroy, K ;
Wright, D ;
Kohner, E ;
Fox, C ;
Hadden, D ;
Mehta, Z ;
Smith, A ;
Nugent, Z ;
Peto, R ;
Adlel, AI ;
Mann, JI ;
Bassett, PA ;
Oakes, SF ;
Dornan, TL ;
Aldington, S ;
Lipinski, H ;
Collum, R ;
Harrison, K ;
MacIntyre, C ;
Skinner, S ;
Mortemore, A ;
Nelson, D ;
Cockley, S ;
Levien, S ;
Bodsworth, L ;
Willox, R ;
Biggs, T ;
Dove, S ;
Beattie, E ;
Gradwell, M ;
Staples, S ;
Lam, R ;
Taylor, F ;
Leung, L ;
Carter, RD ;
Brownlee, SM ;
Fisher, KE ;
Islam, K ;
Jelfs, R ;
Williams, PA ;
Williams, FA ;
Sutton, PJ .
LANCET, 1998, 352 (9131) :837-853
[20]   Gastric inhibitory polypeptide modulates adiposity and fat oxidation under diminished insulin action [J].
Zhou, HY ;
Yamada, Y ;
Tsukiyama, K ;
Miyawaki, K ;
Hosokawa, M ;
Nagashima, K ;
Toyoda, K ;
Naitoh, R ;
Mizunoya, W ;
Fushiki, T ;
Kadowaki, T ;
Seino, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 335 (03) :937-942