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Figure. Bariatric surgical procedures: laparoscopic adjustable gastric banding (A); Roux-en-Y gastric bypass (B); and horizontal (C) or vertical (D) resection of the stomach (sleeve gastrectomy) as part of a biliopancreatic diversion. Reprinted with permission from Nature Publishing Group.

Figure. Bariatric surgical procedures: laparoscopic adjustable gastric banding (A); Roux-en-Y gastric bypass (B); and horizontal (C) or vertical (D) resection of the stomach (sleeve gastrectomy) as part of a biliopancreatic diversion. Reprinted with permission from Nature Publishing Group.53

Table 1. Criteria for Adolescent Bariatric Surgery
Table 1. Criteria for Adolescent Bariatric Surgery
Table 2. Requirements for Adolescent Bariatric Surgery
Table 2. Requirements for Adolescent Bariatric Surgery
Table 3. Data From Adolescent Bariatric Surgery Studiesa
Table 3. Data From Adolescent Bariatric Surgery Studiesa
1.
Barlow SE.Expert Committee.  Expert committee recommendations regarding the prevention, assessment, and treatment of child and adolescent overweight and obesity: summary report.  Pediatrics. 2007;120:(suppl 4)  S164-S19218055651PubMedGoogle ScholarCrossref
2.
Daniels SR, Khoury PR, Morrison JA. The utility of body mass index as a measure of body fatness in children and adolescents: differences by race and gender.  Pediatrics. 1997;99(6):804-8079164773PubMedGoogle ScholarCrossref
3.
Lindsay RS, Hanson RL, Roumain J, Ravussin E, Knowler WC, Tataranni PA. Body mass index as a measure of adiposity in children and adolescents: relationship to adiposity by dual energy x-ray absorptiometry and to cardiovascular risk factors.  J Clin Endocrinol Metab. 2001;86(9):4061-406711549626PubMedGoogle ScholarCrossref
4.
Freedman DS, Mei Z, Srinivasan SR, Berenson GS, Dietz WH. Cardiovascular risk factors and excess adiposity among overweight children and adolescents: the Bogalusa Heart Study.  J Pediatr. 2007;150(1):12.e12-17.e1217188605PubMedGoogle Scholar
5.
Camhi SM, Katzmarzyk PT. Prevalence of cardiometabolic risk factor clustering and body mass index in adolescents.  J Pediatr. 2011;159(2):303-30721429506PubMedGoogle ScholarCrossref
6.
Han TS, Sattar N, Lean M. ABC of obesity. Assessment of obesity and its clinical implications.  BMJ. 2006;333(7570):695-69817008674PubMedGoogle ScholarCrossref
7.
Kuczmarski RJ, Ogden CL, Grummer-Strawn LM,  et al.  CDC growth charts: United States.  Adv Data. 2000;(314):1-2711183293PubMedGoogle Scholar
8.
Ogden CL, Flegal KM. Changes in terminology for childhood overweight and obesity.  Natl Health Stat Report. 2010;(25):1-520939253PubMedGoogle Scholar
9.
Lee H, Lee D, Guo G, Harris KM. Trends in body mass index in adolescence and young adulthood in the United States: 1959-2002.  J Adolesc Health. 2011;49(6):601-60822098770PubMedGoogle ScholarCrossref
10.
Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of obesity and trends in body mass index among US children and adolescents, 1999-2010.  JAMA. 2012;307(5):483-49022253364PubMedGoogle ScholarCrossref
11.
The NS, Suchindran C, North KE, Popkin BM, Gordon-Larsen P. Association of adolescent obesity with risk of severe obesity in adulthood.  JAMA. 2010;304(18):2042-204721063014PubMedGoogle ScholarCrossref
12.
Whitaker RC, Wright JA, Pepe MS, Seidel KD, Dietz WH. Predicting obesity in young adulthood from childhood and parental obesity.  N Engl J Med. 1997;337(13):869-8739302300PubMedGoogle ScholarCrossref
13.
Fontaine KR, Redden DT, Wang C, Westfall AO, Allison DB. Years of life lost due to obesity.  JAMA. 2003;289(2):187-19312517229PubMedGoogle ScholarCrossref
14.
Tsai AG, Williamson DF, Glick HA. Direct medical cost of overweight and obesity in the USA: a quantitative systematic review.  Obes Rev. 2011;12(1):50-6120059703PubMedGoogle ScholarCrossref
15.
McNiece KL, Poffenbarger TS, Turner JL, Franco KD, Sorof JM, Portman RJ. Prevalence of hypertension and pre-hypertension among adolescents.  J Pediatr. 2007;150(6):640.e1-644.e117517252PubMedGoogle Scholar
16.
Din-Dzietham R, Liu Y, Bielo MV, Shamsa F. High blood pressure trends in children and adolescents in national surveys, 1963 to 2002.  Circulation. 2007;116(13):1488-149617846287PubMedGoogle ScholarCrossref
17.
Field AE, Cook NR, Gillman MW. Weight status in childhood as a predictor of becoming overweight or hypertensive in early adulthood.  Obes Res. 2005;13(1):163-16915761176PubMedGoogle ScholarCrossref
18.
Ford CA, Nonnemaker JM, Wirth KE. The influence of adolescent body mass index, physical activity, and tobacco use on blood pressure and cholesterol in young adulthood.  J Adolesc Health. 2008;43(6):576-58319027646PubMedGoogle ScholarCrossref
19.
Li L, Law C, Power C. Body mass index throughout the life-course and blood pressure in mid-adult life: a birth cohort study.  J Hypertens. 2007;25(6):1215-122317563534PubMedGoogle ScholarCrossref
20.
Cook S, Weitzman M, Auinger P, Nguyen M, Dietz WH. Prevalence of a metabolic syndrome phenotype in adolescents: findings from the third National Health and Nutrition Examination Survey, 1988-1994.  Arch Pediatr Adolesc Med. 2003;157(8):821-82712912790PubMedGoogle ScholarCrossref
21.
Pinhas-Hamiel O, Dolan LM, Daniels SR, Standiford D, Khoury PR, Zeitler P. Increased incidence of non-insulin-dependent diabetes mellitus among adolescents.  J Pediatr. 1996;128(5, pt 1):608-6158627431PubMedGoogle ScholarCrossref
22.
Duncan GE. Prevalence of diabetes and impaired fasting glucose levels among US adolescents: National Health and Nutrition Examination Survey, 1999-2002.  Arch Pediatr Adolesc Med. 2006;160(5):523-52816651496PubMedGoogle ScholarCrossref
23.
Pacifico L, Nobili V, Anania C, Verdecchia P, Chiesa C. Pediatric nonalcoholic fatty liver disease, metabolic syndrome and cardiovascular risk.  World J Gastroenterol. 2011;17(26):3082-309121912450PubMedGoogle Scholar
24.
Centers for Disease Control and Prevention (CDC).  Prevalence of abnormal lipid levels among youths—United States, 1999-2006 [published correction appears in MMWR Morb Mortal Wkly Rep. 2010;59(3):78].  MMWR Morb Mortal Wkly Rep. 2010;59(2):29-3320094024PubMedGoogle Scholar
25.
Mark AL. Dietary therapy for obesity: an emperor with no clothes.  Hypertension. 2008;51(6):1426-1434, discussion 143418474832PubMedGoogle ScholarCrossref
26.
Kramer FM, Jeffery RW, Forster JL, Snell MK. Long-term follow-up of behavioral treatment for obesity: patterns of weight regain among men and women.  Int J Obes. 1989;13(2):123-1362663745PubMedGoogle Scholar
27.
Rosenbaum M, Leibel RL, Hirsch J. Obesity.  N Engl J Med. 1997;337(6):396-4079241130PubMedGoogle ScholarCrossref
28.
Dansinger ML, Tatsioni A, Wong JB, Chung M, Balk EM. Meta-analysis: the effect of dietary counseling for weight loss.  Ann Intern Med. 2007;147(1):41-5017606960PubMedGoogle Scholar
29.
Wilfley DE, Stein RI, Saelens BE,  et al.  Efficacy of maintenance treatment approaches for childhood overweight: a randomized controlled trial.  JAMA. 2007;298(14):1661-167317925518PubMedGoogle ScholarCrossref
30.
Tsai AG, Wadden TA. Systematic review: an evaluation of major commercial weight loss programs in the United States.  Ann Intern Med. 2005;142(1):56-6615630109PubMedGoogle Scholar
31.
 Methods for voluntary weight loss and control: NIH Technology Assessment Conference Panel: Consensus Development Conference, 30 March to 1 April 1992.  Ann Intern Med. 1993;119(7, pt 2):764-7708363212PubMedGoogle Scholar
32.
Mark AL. Dietary therapy for obesity is a failure and pharmacotherapy is the future: a point of view.  Clin Exp Pharmacol Physiol. 2006;33(9):857-86216922821PubMedGoogle ScholarCrossref
33.
Maier IB, Stricker L, Ozel Y, Wagnerberger S, Bischoff SC, Bergheim I. A low fructose diet in the treatment of pediatric obesity: a pilot study.  Pediatr Int. 2011;53(3):303-30820831653PubMedGoogle ScholarCrossref
34.
Spieth LE, Harnish JD, Lenders CM,  et al.  A low-glycemic index diet in the treatment of pediatric obesity.  Arch Pediatr Adolesc Med. 2000;154(9):947-95110980801PubMedGoogle Scholar
35.
Willi SM, Oexmann MJ, Wright NM, Collop NA, Key LL Jr. The effects of a high-protein, low-fat, ketogenic diet on adolescents with morbid obesity: body composition, blood chemistries, and sleep abnormalities.  Pediatrics. 1998;101(1, pt 1):61-679417152PubMedGoogle ScholarCrossref
36.
Dietz WH Jr. Childhood obesity: susceptibility, cause, and management.  J Pediatr. 1983;103(5):676-6866631594PubMedGoogle ScholarCrossref
37.
Rogovik AL, Chanoine JP, Goldman RD. Pharmacotherapy and weight-loss supplements for treatment of paediatric obesity.  Drugs. 2010;70(3):335-34620166770PubMedGoogle ScholarCrossref
38.
Butryn ML, Wadden TA, Rukstalis MR,  et al.  Maintenance of weight loss in adolescents: current status and future directions.  J Obes. 2010;2010:78928021274275PubMedGoogle Scholar
39.
Kanekar A, Sharma M. Pharmacological approaches for management of child and adolescent obesity.  J Clin Med Res. 2010;2(3):105-11121629521PubMedGoogle Scholar
40.
Berkowitz RI, Wadden TA, Tershakovec AM, Cronquist JL. Behavior therapy and sibutramine for the treatment of adolescent obesity: a randomized controlled trial.  JAMA. 2003;289(14):1805-181212684359PubMedGoogle ScholarCrossref
41.
Chanoine JP, Hampl S, Jensen C, Boldrin M, Hauptman J. Effect of orlistat on weight and body composition in obese adolescents: a randomized controlled trial.  JAMA. 2005;293(23):2873-288315956632PubMedGoogle ScholarCrossref
42.
Savoye M, Shaw M, Dziura J,  et al.  Effects of a weight management program on body composition and metabolic parameters in overweight children: a randomized controlled trial.  JAMA. 2007;297(24):2697-270417595270PubMedGoogle ScholarCrossref
43.
Picot J, Jones J, Colquitt JL,  et al.  The clinical effectiveness and cost-effectiveness of bariatric (weight loss) surgery for obesity: a systematic review and economic evaluation.  Health Technol Assess. 2009;13(41):1-190, 215-357, iii-iv19726018PubMedGoogle Scholar
44.
O’Brien PE, Dixon JB, Laurie C,  et al.  Treatment of mild to moderate obesity with laparoscopic adjustable gastric banding or an intensive medical program: a randomized trial.  Ann Intern Med. 2006;144(9):625-63316670131PubMedGoogle Scholar
45.
Nguyen NT, Masoomi H, Magno CP, Nguyen XM, Laugenour K, Lane J. Trends in use of bariatric surgery, 2003-2008.  J Am Coll Surg. 2011;213(2):261-26621624841PubMedGoogle ScholarCrossref
46.
Schilling PL, Davis MM, Albanese CT, Dutta S, Morton J. National trends in adolescent bariatric surgical procedures and implications for surgical centers of excellence.  J Am Coll Surg. 2008;206(1):1-1218155562PubMedGoogle ScholarCrossref
47.
Woolford SJ, Clark SJ, Gebremariam A, Davis MM, Freed GL. To cut or not to cut: physicians' perspectives on referring adolescents for bariatric surgery.  Obes Surg. 2010;20(7):937-94220401742PubMedGoogle ScholarCrossref
48.
Iqbal CW, Kumar S, Iqbal AD, Ishitani MB. Perspectives on pediatric bariatric surgery: identifying barriers to referral.  Surg Obes Relat Dis. 2009;5(1):88-9318996760PubMedGoogle ScholarCrossref
49.
 Gastrointestinal surgery for severe obesity: National Institutes of Health Consensus Development Conference Statement.  Am J Clin Nutr. 1992;55:(2 suppl)  615S-619S1733140PubMedGoogle Scholar
50.
Pratt JS, Lenders CM, Dionne EA,  et al.  Best practice updates for pediatric/adolescent weight loss surgery.  Obesity (Silver Spring). 2009;17(5):901-91019396070PubMedGoogle ScholarCrossref
51.
Ibele AR, Mattar SG. Adolescent bariatric surgery.  Surg Clin North Am. 2011;91(6):1339-1351, x22054157PubMedGoogle ScholarCrossref
52.
Brandt ML, Harmon CM, Helmrath MA, Inge TH, McKay SV, Michalsky MP. Morbid obesity in pediatric diabetes mellitus: surgical options and outcomes.  Nat Rev Endocrinol. 2010;6(11):637-64520842181PubMedGoogle ScholarCrossref
53.
Rubino F, R'bibo SL, del Genio F, Mazumdar M, McGraw TE. Metabolic surgery: the role of the gastrointestinal tract in diabetes mellitus.  Nat Rev Endocrinol. 2010;6(2):102-10920098450PubMedGoogle ScholarCrossref
54.
Xanthakos SA, Daniels SR, Inge TH. Bariatric surgery in adolescents: an update.  Adolesc Med Clin. 2006;17(3):589-612, abstract x17030281PubMedGoogle Scholar
55.
Byrne TK. Complications of surgery for obesity.  Surg Clin North Am. 2001;81(5):1181-1193, vii-viii11589251PubMedGoogle ScholarCrossref
56.
Lawson ML, Kirk S, Mitchell T,  et al; Pediatric Bariatric Study Group.  One-year outcomes of Roux-en-Y gastric bypass for morbidly obese adolescents: a multicenter study from the Pediatric Bariatric Study Group.  J Pediatr Surg. 2006;41(1):137-14316410123PubMedGoogle ScholarCrossref
57.
Sugerman HJ, Sugerman EL, DeMaria EJ,  et al.  Bariatric surgery for severely obese adolescents.  J Gastrointest Surg. 2003;7(1):102-107, discussion 107-10812559191PubMedGoogle ScholarCrossref
58.
Cameron JLCA. Current Surgical Therapy. 10th ed. Philadelphia, PA: Elsevier Saunders; 2011
59.
Forfori F, Ferro B, Mancini B,  et al.  Role of thrombolestagrophy in monitoring perioperative coagulation status and effect of thromboprophylaxis in bariatric surgery.  Obes Surg. 2011;22(1):113-11821611876PubMedGoogle ScholarCrossref
60.
Inge TH, Krebs NF, Garcia VF,  et al.  Bariatric surgery for severely overweight adolescents: concerns and recommendations.  Pediatrics. 2004;114(1):217-22315231931PubMedGoogle ScholarCrossref
61.
Angrisani L, Favretti F, Furbetta F,  et al.  Obese teenagers treated by Lap-Band System: the Italian experience.  Surgery. 2005;138(5):877-88116291388PubMedGoogle ScholarCrossref
62.
Treadwell JR, Sun F, Schoelles K. Systematic review and meta-analysis of bariatric surgery for pediatric obesity.  Ann Surg. 2008;248(5):763-77618948803PubMedGoogle ScholarCrossref
63.
Holterman AX, Browne A, Tussing L,  et al.  A prospective trial for laparoscopic adjustable gastric banding in morbidly obese adolescents: an interim report of weight loss, metabolic and quality of life outcomes.  J Pediatr Surg. 2010;45(1):74-78, discussion 78-7920105583PubMedGoogle ScholarCrossref
64.
Nadler EP, Youn HA, Ren CJ, Fielding GA. An update on 73 US obese pediatric patients treated with laparoscopic adjustable gastric banding: comorbidity resolution and compliance data.  J Pediatr Surg. 2008;43(1):141-14618206472PubMedGoogle ScholarCrossref
65.
Widhalm K, Fritsch M, Widhalm H,  et al.  Bariatric surgery in morbidly obese adolescents: long-term follow-up.  Int J Pediatr Obes. 2011;6:(suppl 1)  65-6921905819PubMedGoogle ScholarCrossref
66.
Campos GM, Rabl C, Roll GR,  et al.  Better weight loss, resolution of diabetes, and quality of life for laparoscopic gastric bypass vs banding: results of a 2-cohort pair-matched study.  Arch Surg. 2011;146(2):149-15521339424PubMedGoogle ScholarCrossref
67.
Naef M, Mouton WG, Naef U, Kummer O, Muggli B, Wagner HE. Graft survival and complications after laparoscopic gastric banding for morbid obesity—lessons learned from a 12-year experience.  Obes Surg. 2010;20(9):1206-121420524156PubMedGoogle ScholarCrossref
68.
Boza C, Gamboa C, Awruch D, Perez G, Escalona A, Ibañez L. Laparoscopic Roux-en-Y gastric bypass versus laparoscopic adjustable gastric banding: five years of follow-up.  Surg Obes Relat Dis. 2010;6(5):470-47520702146PubMedGoogle ScholarCrossref
69.
Frezza EE, Chiriva-Internati M, Wachtel MS. Analysis of the results of sleeve gastrectomy for morbid obesity and the role of ghrelin.  Surg Today. 2008;38(6):481-48318516524PubMedGoogle ScholarCrossref
70.
Cottam D, Qureshi FG, Mattar SG,  et al.  Laparoscopic sleeve gastrectomy as an initial weight-loss procedure for high-risk patients with morbid obesity.  Surg Endosc. 2006;20(6):859-86316738970PubMedGoogle ScholarCrossref
71.
Till HK, Muensterer O, Keller A,  et al.  Laparoscopic sleeve gastrectomy achieves substantial weight loss in an adolescent girl with morbid obesity.  Eur J Pediatr Surg. 2008;18(1):47-4918302070PubMedGoogle ScholarCrossref
72.
Landau Z, Karplus G, Hanukoglu A, Abiri S, Levy A, Serour F. Laparoscopic sleeve gastrectomy (LSG) in adolescents with morbid obesity [in Hebrew].  Harefuah. 2011;150(10):765-768, 816, 81522111118PubMedGoogle Scholar
73.
Till H, Blüher S, Hirsch W, Kiess W. Efficacy of laparoscopic sleeve gastrectomy (LSG) as a stand-alone technique for children with morbid obesity.  Obes Surg. 2008;18(8):1047-104918459015PubMedGoogle ScholarCrossref
74.
Hutter MM, Schirmer BD, Jones DB,  et al.  First report from the American College of Surgeons Bariatric Surgery Center Network: laparoscopic sleeve gastrectomy has morbidity and effectiveness positioned between the band and the bypass.  Ann Surg. 2011;254(3):410-420; discussion 420-41221865942PubMedGoogle ScholarCrossref
75.
Angrisani L, Cutolo PP, Buchwald JN,  et al.  Laparoscopic reinforced sleeve gastrectomy: early results and complications.  Obes Surg. 2011;21(6):783-79321494813PubMedGoogle ScholarCrossref
76.
Bobowicz M, Lehmann A, Orlowski M, Lech P, Michalik M. Preliminary outcomes 1 year after laparoscopic sleeve gastrectomy based on Bariatric Analysis and Reporting Outcome System (BAROS).  Obes Surg. 2011;21(12):1843-184821491136PubMedGoogle ScholarCrossref
77.
Stroh C, Birk D, Flade-Kuthe R,  et al; Bariatric Surgery Working Group.  Results of sleeve gastrectomy-data from a nationwide survey on bariatric surgery in Germany.  Obes Surg. 2009;19(5):632-64019184256PubMedGoogle ScholarCrossref
78.
Xanthakos SA. Bariatric surgery for extreme adolescent obesity: indications, outcomes, and physiologic effects on the gut-brain axis.  Pathophysiology. 2008;15(2):135-14618585904PubMedGoogle ScholarCrossref
79.
Rand CS, Macgregor AM. Adolescents having obesity surgery: a 6-year follow-up.  South Med J. 1994;87(12):1208-12137973919PubMedGoogle ScholarCrossref
80.
Buchwald H, Williams SE. Bariatric surgery worldwide 2003.  Obes Surg. 2004;14(9):1157-116415527627PubMedGoogle ScholarCrossref
81.
Rao RS, Kini S. Diabetic and bariatric surgery: a review of the recent trends.  Surg Endosc. 2012;26(4):893-90321993947PubMedGoogle ScholarCrossref
82.
Marceau P, Marceau S, Biron S,  et al.  Long-term experience with duodenal switch in adolescents.  Obes Surg. 2010;20(12):1609-161620835899PubMedGoogle ScholarCrossref
83.
Papadia FS, Adami GF, Marinari GM, Camerini G, Scopinaro N. Bariatric surgery in adolescents: a long-term follow-up study.  Surg Obes Relat Dis. 2007;3(4):465-46817400517PubMedGoogle ScholarCrossref
84.
Serrot FJ, Dorman RB, Miller CJ,  et al.  Comparative effectiveness of bariatric surgery and nonsurgical therapy in adults with type 2 diabetes mellitus and body mass index <35 kg/m2.  Surgery. 2011;150(4):684-69122000180PubMedGoogle ScholarCrossref
85.
Adams TD, Gress RE, Smith SC,  et al.  Long-term mortality after gastric bypass surgery.  N Engl J Med. 2007;357(8):753-76117715409PubMedGoogle ScholarCrossref
86.
Barnett SJ. Contemporary surgical management of the obese adolescent.  Curr Opin Pediatr. 2011;23(3):351-35521572387PubMedGoogle ScholarCrossref
87.
Frank P, Crookes PF. Short- and long-term surgical follow-up of the postbariatric surgery patient.  Gastroenterol Clin North Am. 2010;39(1):135-14620202586PubMedGoogle ScholarCrossref
88.
Inge TH, Jenkins TM, Zeller M,  et al.  Baseline BMI is a strong predictor of nadir BMI after adolescent gastric bypass.  J Pediatr. 2010;156(1):103.e1-108.e119775700PubMedGoogle Scholar
89.
Nadler EP, Youn HA, Ginsburg HB, Ren CJ, Fielding GA. Short-term results in 53 US obese pediatric patients treated with laparoscopic adjustable gastric banding.  J Pediatr Surg. 2007;42(1):137-141; discussion 141-13217208554PubMedGoogle ScholarCrossref
90.
Nadler EP, Reddy S, Isenalumhe A,  et al.  Laparoscopic adjustable gastric banding for morbidly obese adolescents affects android fat loss, resolution of comorbidities, and improved metabolic status.  J Am Coll Surg. 2009;209(5):638-64419854406PubMedGoogle ScholarCrossref
91.
Inge TH, Miyano G, Bean J,  et al.  Reversal of type 2 diabetes mellitus and improvements in cardiovascular risk factors after surgical weight loss in adolescents.  Pediatrics. 2009;123(1):214-22219117885PubMedGoogle ScholarCrossref
92.
Teeple EA, Teich S, Schuster DP, Michalsky MP. Early metabolic improvement following bariatric surgery in morbidly obese adolescents.  Pediatr Blood Cancer. 2012;58(1):112-11622021118PubMedGoogle ScholarCrossref
93.
Zitsman JL, Digiorgi MF, Marr JR, Witt MA, Bessler M. Comparative outcomes of laparoscopic adjustable gastric banding in adolescents and adults.  Surg Obes Relat Dis. 2011;7(6):720-72621429814PubMedGoogle ScholarCrossref
94.
Vander Wal JS, Mitchell ER. Psychological complications of pediatric obesity.  Pediatr Clin North Am. 2011;58(6):1393-1401, x22093858PubMedGoogle ScholarCrossref
95.
Järvholm K, Olbers T, Marcus C,  et al.  Short-term psychological outcomes in severely obese adolescents after bariatric surgery.  Obesity (Silver Spring). 2012;20(2):318-32321996668PubMedGoogle ScholarCrossref
96.
Zeller MH, Reiter-Purtill J, Ratcliff MB, Inge TH, Noll JG. Two-year trends in psychosocial functioning after adolescent Roux-en-Y gastric bypass.  Surg Obes Relat Dis. 2011;7(6):727-73221497142PubMedGoogle ScholarCrossref
97.
Xanthakos SA, Inge TH. Nutritional consequences of bariatric surgery.  Curr Opin Clin Nutr Metab Care. 2006;9(4):489-49616778582PubMedGoogle ScholarCrossref
98.
Fullmer MA, Abrams SH, Hrovat K,  et al.  Nutritional strategy for adolescents undergoing bariatric surgery: report of a working group of the Nutrition Committee of NASPGHAN/NACHRI.  J Pediatr Gastroenterol Nutr. 2012;54(1):125-13521857247PubMedGoogle ScholarCrossref
99.
Shankar P, Boylan M, Sriram K. Micronutrient deficiencies after bariatric surgery.  Nutrition. 2010;26(11-12):1031-103720363593PubMedGoogle ScholarCrossref
100.
Towbin A, Inge TH, Garcia VF,  et al.  Beriberi after gastric bypass surgery in adolescence.  J Pediatr. 2004;145(2):263-26715289782PubMedGoogle ScholarCrossref
101.
Kaulfers AM, Bean JA, Inge TH, Dolan LM, Kalkwarf HJ. Bone loss in adolescents after bariatric surgery.  Pediatrics. 2011;127(4):e956-e96121444596PubMedGoogle ScholarCrossref
102.
Michalsky M, Kramer RE, Fullmer MA,  et al.  Developing criteria for pediatric/adolescent bariatric surgery programs.  Pediatrics. 2011;128:(suppl 2)  S65-S7021885647PubMedGoogle ScholarCrossref
Review
Aug 2012

Adolescent Bariatric Surgery

Author Affiliations

Author Affiliations: Division of Diabetes and Endocrinology, Department of Pediatrics (Dr Hsia), Division of Pediatric Surgery, Michael E. DeBakey Department of Surgery (Drs Fallon and Brandt), Baylor College of Medicine, Texas Children's Hospital, Houston.

Arch Pediatr Adolesc Med. 2012;166(8):757-766. doi:10.1001/archpediatrics.2012.1011
Abstract

Pediatric obesity has increased from a relatively uncommon problem to one of the most important public health problems facing children today. Typical “adult” diseases, such as type 2 diabetes mellitus, hypertension, and dyslipidemia, have become increasingly prevalent in the pediatric population. The earlier presentation of these comorbidities will have a significant impact for the future because this population of children will require more medical resources at an earlier age and will have a significantly decreased life expectancy. The significant morbidity of obesity in the pediatric population has led to consideration of more aggressive treatment protocols for obesity in children, including the introduction of surgical management at an earlier age. Surgery for obesity in adolescents has particular risks and benefits that must be accounted for when considering this approach. The unique psychological and emotional needs of adolescent patients make the patient selection process and perioperative management substantially different from those of adult patients. Initial outcomes of bariatric surgery in adolescents are comparable to those seen in adults in the short term. However, the long-term effects of these procedures on the adolescent population are not known. This review discusses the epidemiology of pediatric obesity, the indications for operative therapy in adolescent patients, the common surgical procedures used for weight loss, the reported outcomes of these procedures, and the importance of multidisciplinary management for this unique patient population.

The definition of pediatric obesity is not straightforward. Because directly measuring body fat is difficult and time intensive, the surrogate measurement of body mass index (BMI), which takes into account both weight and height (calculated as weight in kilograms divided by height in meters squared), is most commonly used.1 However, BMI does not always accurately reflect body composition. For example, professional athletes with high muscle mass and an extremely low percentage of body fat may have BMIs in the “obese” range. The use of BMI as a predictor of body fat mass in pediatrics has been found to be variably accurate, with correlation ranging between 0.5 and 0.94, depending on sex and age group.2,3 Despite these limitations, BMI has been shown to be predictive of the presence of cardiovascular risk factors in pediatric patients and is considered the most relevant clinical measure of obesity in children.4,5

In adults, a BMI of 25 or greater is defined as overweight, and a BMI of 30 or greater is defined as obese.6 Adults with a BMI of greater than 40 are considered morbidly obese, and those with a BMI of greater than 50 are considered “super” obese. The use of BMI as a marker of obesity in children is more complicated than it is in adults because age, sex, and growth patterns change the proportion of height to weight.7 The BMI growth curves available from the Centers for Disease Control and Prevention take these variables into account and are considered the standard for assessing obesity in children. The BMI growth curves define a child in the 85th to 94th percentile range as overweight, whereas a child in the greater than 95th percentile is defined as obese.8 More specific guidelines have recently been suggested for adolescents because their BMI measurements may begin to reflect adult physiology, particularly in severely obese patients. An American Academy of Pediatrics expert committee proposed the recognition of a BMI of 30 to 32 for youths 10 to 12 years old and of 34 for youths 14 to 16 years old as the 99th percentile, with any value over the 99th percentile termed “extreme obesity.”1 This correlates with the adult model of reporting a BMI of greater than 40 as “morbidly obese.” Most experts feel that adult measurements and categories should be used for adolescents with a BMI of greater than 40 because their physiology and comorbidities often resemble those of morbidly obese adults.

The epidemiology of pediatric obesity

From 1959 to 2002, a slow increase in average BMI was seen in all ages from 12 to 26 years. Since 2002, there has been an even more dramatic increase in average BMI in children.9 The most recent National Health and Nutrition Examination Survey data from 2009 to 2010 report that 31.8% of children aged 2 to 19 years were overweight or obese (≥85th percentile of BMI for age), 16.9% were obese (≥95th percentile), and 12.3% had a BMI in the 97th percentile or greater.10

The implications for future public health are significant because obese children usually become obese adults.11,12 In the Bogalusa Heart Study,4 84% of children with a BMI in the 95th to 98th percentile had a BMI of greater than 30 as adults. Data from the National Longitudinal Study of Adolescent Health11 showed that 37.1% of obese male adolescents and 51.3% of obese female adolescents became severely obese by their early 30s. This can lead to life-threatening comorbidities in many if not all of these young adults. Current estimates predict a decrease in life expectancy in obese adolescents of 5 to 20 years depending on race and sex.13 The direct costs of this epidemic are significant; treatment of obesity-related conditions currently accounts for 5% to 10% of health care spending in the United States.14

McNiece et al15 reported the prevalence of prehypertension or hypertension to be 18.9% after screening 6790 adolescents. Population studies of adolescents conducted from 1988 to 2002 found an increase in the prevalence of prehypertension from 7.7% to 10.0% and an increase in the prevalence of hypertension from 2.7% to 3.7% over that time span.16 Multiple studies17-19 have found that overweight or obese adolescents predictably become hypertensive adults. As of 1994, the prevalence of metabolic syndrome was 35.5% in overweight and obese adolescents.20 Between 1982 and 1994, the prevalence of type 2 diabetes mellitus in children quadrupled from 4% to 16%.21 Studying the National Health and Nutrition Examination Survey data from 1999 to 2002, Duncan22 found that 29% of children with diabetes had type 2 diabetes, a dramatic increase from previous decades. Nonalcoholic fatty liver disease, which can lead to liver failure, is estimated to affect 2.6% to 9.8% of obese adolescents.23 The National Health and Nutrition Examination Survey data from 1999 to 2006 showed that 22.3% of overweight adolescents and 42.9% of obese adolescents 12 to 19 years old had at least 1 abnormal lipid level.24 The increased cost of obesity measured financially or in years is directly related to the increase in comorbid disease seen in obese adolescents.

Rationale for surgical treatment of obesity in adolescents

It is clear that aggressive treatment of pediatric obesity is necessary, but finding a method for successful, sustained treatment remains problematic. Dietary restriction is considered the cornerstone of any treatment program for obesity but is only rarely successful for morbidly obese patients.25-32 Although individuals who are on the K diet (ie, a high-protein, low-carbohydrate, low-fat ketogenic diet), a low-fructose diet, or a low-glycemic index diet all show small, transient improvement in weight loss and in BMI, the clinical significance of this weight loss is not clear, and long-term maintenance of the weight loss is rare.26,28-31,33-35 Some studies25,32 have demonstrated no effect of change in diet on the treatment of pediatric obesity, suggesting that dietary restriction alone is ineffective. Although adults experience the same difficulty losing weight with modification of diet and exercise, children have the additional factors of reliance on their parents and the psychosocial impact of family dynamics. For example, children whose parents are leaner and married tend to lose more weight than those whose parents are heavier and divorced.36

Although some evidence supports the use of pharmacotherapy in the treatment of pediatric obesity, none of the available medications have demonstrated efficacy as independent therapy to reduce both BMI and comorbid disease. A few studies have evaluated metformin's effects on reducing BMI in adolescent patients.37 Although a small decrease in BMI was noted with the use of metformin compared with placebo, the effect only lasted for 12 to 24 weeks after a year of treatment, and no changes were noted in other important health parameters, including insulin levels and hypertension.37 Orlistat, an intestinal lipase inhibitor, was approved for the treatment of obesity in adolescents in 2003 for severely obese patients aged 12 to 16 years. Multiple studies have shown a decrease in BMI with minimal adverse effects, especially when prescribed with a lifestyle modification program.37 However, the use of orlistat alone leads to small changes in BMI (range, −0.5 to −4.2), which limits its use among morbidly obese adolescents.37 In addition, to our knowledge, no study has shown this weight loss to be sustained after stopping the medication.38,39 Combined behavior, diet, and pharmacotherapy programs in adolescents have demonstrated minimal longitudinal efficacy as well; in 3 recent trials,40-42 BMI decreased by an average of 1.82, and only 71% of patients completed therapy after 1 year.

Adult studies have also shown that, compared with medical treatment, surgical treatment is cost-effective when evaluating quality-of-life years gained.43 However, studies comparing medical and surgical therapies for obesity in the pediatric population are rare. In one of the first studies of its kind, O’Brien et al44 compared laparoscopic adjustable gastric banding (LAGB) with a combined medical program of lifestyle change, low-calorie diet, and pharmacotherapy in adolescents and showed statistically significant improvement in weight loss, the presence of metabolic syndrome, and quality of life.

Given the dramatic increase in obesity and related diseases in adults, it is not surprising that there has been a dramatic increase in bariatric surgical procedures, paralleling the increase in the prevalence of morbid obesity. In the United States, procedures for adults have increased from 12 775 to 124 838 per year during the 10-year period from 1998 to 2008.45 Because of the lack of data, procedures for adolescents have been much less commonly performed than procedures for adults. From 1997 to 2003, the number of adolescent bariatric surgical procedures performed in the United States was estimated to have increased 5-fold, from 51 to 282.46 Because of the paucity of long-term outcome data, the role of bariatric surgery in the pediatric patient remains controversial, which may account for the hesitancy on the part of pediatricians and pediatric specialists to consider surgery, even for adolescents with life-threatening comorbidities. Woolford et al47 polled more than 500 pediatric doctors; half of the respondents would not refer their patients for bariatric surgery prior to 18 years of age. In another study,48 only half of the respondents indicated that they would be willing to refer an adolescent patient for bariatric surgery.

Preoperative considerations in adolescent bariatric surgery

The criteria for undergoing bariatric surgery in adults are well established and include a BMI of greater than 40 or a BMI of greater than 35 with comorbid disease or functional limitation, acceptable operative risk, a low probability of success with nonoperative measures, and a motivation to continue medical treatment after surgery.49 Given the unknown long-term risks of the surgery in the still-developing adolescent, more stringent criteria have been proposed for adolescent patients.50 In 2009, the International Pediatric Endosurgery Group published updated guidelines that indicated similar BMI cutoffs for surgery in adolescents as in adults but included important stipulations concerning growth, the commitment to lose weight, assent for surgery, and long-term follow-up51 (Table 1). Additional criteria for surgery in adolescents include a Tanner stage of 4 or greater, 95% skeletal maturity, a demonstrated commitment to lifestyle change, and a stable psychosocial environment (Table 2).51 The importance of adhering to these criteria cannot be understated. In adolescents with comorbidities, the unknown long-term risks of surgery are counterbalanced by the potential benefits of improved quality and length of life. Until the long-term outcomes of bariatric surgery in adolescents are known, surgery should ethically be limited to patients with comorbidities.

Contraindications to adolescent bariatric surgery include a medically correctable cause of obesity, a documented substance abuse problem, a disability that would impair adherence to postoperative treatment, current or planned pregnancy or breastfeeding, and an unwillingness to comprehend and acknowledge the consequences of the procedure, particularly the nutritional concerns.52 Elucidating the presence of these issues prior to offering a patient surgical therapy is a multidisciplinary effort and is often the most important predictor of outcome.

Bariatric procedures

Bariatric procedures work by either restricting the amount of oral intake and/or creating a malabsorptive environment. Currently, there are 4 procedures that are used, the majority of which are performed laparoscopically. Laparoscopic adjustable gastric banding and laparoscopic sleeve gastrectomy (LSG) are purely restrictive procedures, the biliopancreatic diversion is a mostly malabsorptive procedure, and the Roux-en-Y gastric bypass (RYGB) is a combination restrictive and malabsorptive surgical procedure (Figure). The selection of the correct procedure is based on an evaluation of the patient's medical, psychological, and social issues, as well as a thorough discussion of the risks and benefits of surgery with the patient and his or her family.

Preoperative evaluation for all patients involves understanding the burden of comorbid disease by the use of appropriate screening tests, including a complete blood count, liver function tests, a lipid profile, thyroid function tests, fasting glucose and insulin measurements, hemoglobin A1c level, urinalysis, vitamin D level, parathyroid hormone level, and Helicobacter pylori testing. Polysomnography is indicated if there is any symptom suggestive of sleep apnea. Abdominal ultrasonography is required if biliary colic symptoms are present and may be helpful to screen for asymptomatic gallstones in all patients. A dual-energy x-ray absorptiometric scan for bone mineral density may be necessary for the appropriate patients.54 Deep venous thrombosis and pulmonary embolism are known complications of bariatric surgery. The incidence of deep venous thrombosis and/or pulmonary embolism after bariatric surgery is 2% in adults, and cases of both deep venous thrombosis and pulmonary embolism have been documented in adolescents.55-57 All patients undergoing bariatric procedures, including adolescents, should receive prophylaxis for deep venous thrombosis with both pharmacologic therapy and mechanical compression stockings.56-58 A coagulation profile such as a thromboelastogram may help in more accurately guiding prophylaxis.59

Common operations
Laparoscopic Adjustable Gastric Banding

Laparoscopic adjustable gastric banding is a purely restrictive procedure in which a synthetic band with an adjustable diameter is placed laparoscopically around the proximal stomach, usually 1 to 2 cm below the gastroesophageal junction. The band is positioned diagonally across the stomach and is then secured in place with 2 sutures to prevent migration. Tubing connecting the band to a subcutaneous injection port is brought through one of the trocar sites above the fascia.58 Saline is injected or removed from the port to adjust the diameter of the band as needed; this usually requires multiple postoperative visits in the first year after surgery to find the optimal diameter for the band. Benefits of this procedure include a lack of staple lines, potential reversibility, and fewer nutritional deficits than the malabsorptive procedures. However, patients are required to follow up at regular intervals for band adjustment. In addition, the device has not been approved for therapy for adolescents in the United States, raising both ethical and financial issues.60 In theory, the synthetic device will have to be replaced after a certain period of time, which would require another operation.61

Laparoscopic adjustable gastric banding does result in significant benefits for adolescent patients. In a recent meta-analysis of adolescent bariatric surgery outcomes, Treadwell et al62 found an aggregate decrease in BMI that ranged from 10.6 to 13.7. They62 also found reports of significant resolution of hypertension and type 2 diabetes in multiple series; data concerning other comorbidities are equivocal. A more recent prospective trial63 examining outcomes in LAGB found a mean decrease in BMI of 9.4, sustained resolution of hypertension, 82% resolution of dyslipidemia and metabolic syndrome, and statistically improved quality-of-life scores. Nadler et al64 reported a 70% total reduction in comorbid conditions after LAGB, and the mean compliance rate with treatment was listed at 89.5%.

Complications of LAGB include tube leaks, band migration, and erosion of the band into the stomach. Treadwell et al62 found an aggregate reoperation rate of 8% for any reason in adolescents, with the most common complication being band migration (3%). In a recent trial,63 5 of 26 patients (19.2%) had complications relating to either the tubing/port system or an actual band malfunction, which is a higher reported complication rate than the recent Treadwell et al meta-analysis.62 Another study64 reported an operative complication rate of 15% and found 35 nonoperative complications in 27 patients, including iron and vitamin D deficiency. To date, no studies have indicated long-term data on whether or not these nutritional deficiencies impact growth or development. One small study by Widhalm et al65 of pediatric patients found a 50% reoperation rate (4 of 8 patients) after LAGB due to failure to lose weight.

Despite the success of the LAGB for weight loss, recent adult studies raise serious concerns about the long-term safety and efficacy of the LAGB. A study of adults by Campos et al66 found that RYGB had a higher rate of early complications (11% vs 2%) but that LAGB had a significantly increased rate of late complications with reoperation occurring much more frequently (13% vs 2%). More concerning are 2 prospective studies67,68 from Europe of long-term outcomes after placement of the LAGB. The study by Naef et al67 followed up with 167 adults for a median time of 79 months. They reported a 40% total complication rate, a 20% reoperation rate, and a failure rate (defined as a percentage of excess weight loss of <30% or removal of band due to complication) between 25% and 30%.67 The study by Boza et al68 followed up with 62 adult patients for 5 years and reported that 45% of patients underwent a failed surgical procedure (<50% excess weight loss) and that 20% of patients required a reoperation.

Laparoscopic Sleeve Gastrectomy

Laparoscopic sleeve gastrectomy is primarily a restrictive procedure, but it is also thought to work by decreasing appetite by removing the portion of the stomach that produces ghrelin.69 This surgical procedure was originally performed as the first step in a staged weight loss procedure for severely obese adults.70 Many of these patients lost enough weight that the second stage of the procedure was not necessary, which led to the adoption of the sleeve gastrectomy as an accepted bariatric procedure. The procedure entails dividing the short gastric vessels and then removing the greater curvature of the stomach from approximately 6 cm proximal to the pylorus to the angle of His.58 The benefits of this procedure include the lack of a foreign body, no need for the frequent adjustments necessary with the LAGB, fewer nutritional deficiencies than seen in malabsorptive procedures, and a decreased risk of dumping syndrome because the vagus nerve is preserved. Drawbacks to the procedure include irreversibility and the current lack of longitudinal data on outcomes.71

The majority of studies on outcomes after the sleeve gastrectomy involve adult patients. A small study72 (n = 7) of pediatric patients (mean age, 16.2 years) demonstrated weight loss in 85.7% of patients, improvement in comorbid conditions, and no operative complications. Another small study73 (n = 4) demonstrated similar findings with all patients achieving weight loss, no patients having operative complications, and no patients having postoperative malnutrition or vitamin deficiency. Adult data from a recent large, multicenter trial by Hutter et al74 comparing LSG with LAGB and RYGB showed a decrease in BMI of 11.87 with LSG that was sustained over 12 months compared with a decrease in BMI of 7.05 with LAGB and 15.34 with RYGB. Hutter et al74 also noted that LSG had higher morbidity and reoperation rates than LAGB but better rates than RYGB. Complications occur in 5% to 14% of patients undergoing an LSG. One study75 found a 5% complication rate in 121 adult patients, including wound infection, stricture, and intraoperative leak. Bobowicz et al76 reported a major complication rate of 7.1% (spleen infarction, incisional hernia, or depression) and a minor complication rate of 8.3% (wound infection, anemia, or hair loss) in 84 adult patients. The study by Stroh et al77 of 3122 patients undergoing LSG reported an overall complication rate of 14.1% and a surgical complication rate of 9.4%; the most common single postoperative complication was a leak from the suture line (7%), followed by stenosis. Long-term complications of the LSG, including nutritional deficiencies and failure to sustain weight loss, are not well described because this is a relatively new procedure.

Laparoscopic RYGB

An RYGB is a combination restrictive and malabsorptive procedure. Although LSG and LAGB are gaining in the numbers of procedures performed, RYGB is still one of the most commonly used bariatric procedures for adolescents.54 For the restrictive portion of the procedure, the proximal stomach is divided, creating a small 15 to 20 cm3 gastric pouch. The mid-jejunum is transected approximately 40 cm from the ligament of Treitz, and a Roux limb is brought up to the new gastric pouch. The biliopancreatic limb is attached to the distal jejunum 100 to 125 cm from the gastric pouch.58 Xanthankos78 has hypothesized that superior outcomes from an RYGB are due to an alteration of the gut-brain axis induced by bypassing the duodenum, which induces an anorexigenic state. The benefits of an RYGB include a proven ability to induce long-term weight loss and to decrease comorbid disease.50 However, the procedure is irreversible, causes significant change to the normal gut orientation, and carries a risk of malnutrition if proper attention is not paid to diet and supplementation of essential nutrients.

The efficacy of an RYGB for weight loss is well documented in both adults and adolescents. In the meta-analysis of RYGB procedures among adolescents by Treadwell et al,62 BMI decreased anywhere from 17.8 to 22.3. Resolution of hypertension occurred in more than half of patients, and sleep apnea resolved in all patients.62 Lawson et al56 reported a statistically significant decrease in triglycerides and total cholesterol with an RYGB.

Perioperative complications from an RYGB include pneumonia, deep venous thrombosis, pulmonary embolus, gastrointestinal hemorrhage, anastomotic obstruction leading to rupture of the gastric pouch, obstruction of the jejunojejunal anastomosis, leakage from staple lines or anastomoses, incisional hernias, and wound infections. Long-term complications include stomal stenosis, gastric staple line breakdown with gastrogastric fistula formation, symptomatic cholelithiasis, and internal herniation.54 In a meta-analysis62 of 131 adolescents who underwent an RYGB, there were 4 reported postoperative deaths, with only 1 of the deaths potentially related to the procedure (Clostridium difficile colitis 9 months after surgery). The most commonly encountered complication was protein malnutrition. In 6 studies of adolescents undergoing RYGB, complication rates ranged from 0% (n = 34) to 39% (n = 36).56,62,79 Despite the potential for significant complications from an RYGB, data so far have indicated that this procedure is effective and has a good risk-benefit ratio in the adolescent population, making it the current preferred surgical therapy for adolescents.

Laparoscopie duodenal switch with bioliopancreatic diversion

The duodenal switch with biliopancreatic diversion is a primarily malabsorptive operation that involves a subtotal gastrectomy (sleeve gastrectomy) with preservation of the pylorus and transection of the duodenum 3 to 4 cm from the pylorus with anastomosis to a Roux limb. This leads to a bypass of the distal 250 cm of ileum. Malabsorption is achieved by this bypass, which results in only approximately 100 cm of bowel exposed to both digestive enzymes and food.58 Although the procedure has been determined to be highly effective for weight loss, this procedure is the least common (5% of bariatric procedures) and has fallen out of favor owing to increased nutritional deficiencies and greater operative complexity.80,81

In one series of 10 adolescent patients undergoing biliopancreatic diversion,82 all patients lost a significant amount of weight, and all patients had resolution of their comorbidities. Two patients had operative complications, including obstruction and gastric ulcer, and the reported nutritional deficiencies were mild. In another series of adolescents,83 68 patients were studied retrospectively for long-term outcomes (mean of 11 years). Although immediate postoperative complications were rare, this series83 of patients had 19 reoperations in 14 patients (including 4 obstructions and 5 incisional hernias), 3 deaths (protein malnutrition, pulmonary edema, and pancreatitis), and 9 patients with documented protein malnutrition.

Outcome after adolescent bariatric surgery

The lack of effective medical therapy for morbid obesity has led to increased research in the outcomes of surgical therapy for weight loss. Numerous studies43,44,84 in adults have shown that bariatric surgery is the only intervention to reliably decrease weight in a sustainable fashion and reverse many of the comorbidities associated with obesity. In adults, gastric bypass results in an estimated 40% decrease in adjusted long-term mortality from any cause.85,86 Weight loss in adolescents after bariatric surgery is similar to weight loss in adults after bariatric surgery, with an average of 50% to 60% of excess weight lost in the first year and up to 75% of excess weight lost by the end of the second year.87 Weight loss is typically slower after LAGB. The absolute BMI reduction in adolescents after surgery is approximately 35%, regardless of the BMI before surgery. Thus, adolescents with the highest baseline BMI (≥65) remain extremely obese with BMIs of 40 or greater 1 year after an RYGB.88 In a cohort of 61 adolescents with a mean BMI of 60.2, Inge et al88 reported that only 17% of patients reached a normal BMI after 1 year. In another series89 examining 73 patients who underwent LAGB, the initial mean BMI was 47, and mean weight loss at 1 and 2 years was 56.7% and 60.9%, respectively.

Adults undergoing bariatric surgery have shown a decrease in mortality of 56% for coronary artery disease, 92% for diabetes, and 60% for cancer when compared with a control group.85 These results are due to the resolution of the life-limiting comorbidities of hypertension, diabetes, and dyslipidemia. Similar results have been noted in adolescents undergoing bariatric surgery (Table 3). Hypertension in teenagers resolves in 50% to 100% of patients after surgery.62 A prospective trial63 demonstrated a 33% decrease in hypertension at 6 months and a 100% decrease in hypertension at 12 and 18 months after LAGB. Earlier intervention may result in a higher rate of resolution of hypertension because 19% of adolescents had persistent hypertension after bariatric surgery compared with 41.3% of adults.93 Inge et al91 demonstrated resolution of type 2 diabetes in 91% of patients who underwent an RYGB. One study63 found an improvement in insulin resistance with 39% resolution at 6 months and 72% resolution at 18 months after LAGB. The mechanism involved in the resolution of type 2 diabetes after bariatric surgery is still unclear. There are significant decreases in levels of fasting blood glucose and fasting insulin in patients who underwent an RYGB.56 Lawson et al56 reported significant reductions in triglycerides and total cholesterol, as well as a trend toward reduction in high-density lipoprotein and low-density lipoprotein in adolescents who underwent an RYGB. One study63 reported resolution of dyslipidemia in 27% of patients at 6 months and 67% of patients at 18 months after LAGB. In a comparative study,93 adolescents had an 87.5% improvement rate in dyslipidemia compared with an adult improvement rate of 18.4%, which again illustrates that earlier intervention could improve the rate of postoperative resolution of comorbidities. Other direct gains of weight loss include improvement in arthropathies, sleep apnea, and urinary continence.87

There may also be important psychological benefits from bariatric surgery. Multiple studies have examined the relationship between obesity and psychological illness. Adolescent patients with obesity experience depression, low self-esteem, and social marginalization and have decreased physical activity and lower academic scores.94 Adolescent patients undergoing bariatric surgery are in a vulnerable psychological state and are at high risk of having mental health complications postoperatively. However, studies have found that adolescents undergoing bariatric surgery have improved mental health postoperatively.95 Four months after undergoing an RYGB, most patients had a significantly improved image of themselves and fewer symptoms of depression and anxiety.95 Zeller et al96 reported an improvement in health-related quality of life and in self-image, as well as a decrease in depressive symptoms 24 months after undergoing an RYGB; however, these results were not necessarily maintained after 24 months, especially when weight regain occurred. Persistent attention to the psychological state of the adolescent patient after bariatric surgery is necessary for optimal outcomes.

Nutritional concerns after bariatric surgery

Close attention to nutritional parameters are necessary after bariatric surgery in adolescents due to the potential for significant metabolic and growth derangements. Both macronutrient intake and micronutrient intake are affected by a decreased total volume intake and in malabsorptive procedures, a decrease in small intestine absorption.97 In the immediate postoperative period, diet advancement protocols are used both to address the smaller stomach volume and to ensure adequate micronutrient intake and macronutrient intake.98

The most common macronutrient concerns for the adolescent bariatric patient are dehydration and protein deficiency.98 Although clinically significant dehydration resulting in end-organ damage, such as renal failure, is rare, dehydration from inadequate intake, vomiting, and dumping syndrome is common.98 Protein malnutrition is usually seen after malabsorptive procedures, particularly the biliopancreatic diversion, and occurs more often in patients who do not follow dietary recommendations.

Water-soluble vitamin deficiencies are usually seen after restrictive procedures owing to decreased liquid intake.52 Vitamin B12 deficiency results from a decrease in intrinsic factor, decreased protein intake, and decreased uptake in an often defunctionalized ileum and can lead to anemia, glossitis, and peripheral neuropathy if unrecognized.99 Folate deficiency, which has been reported in up to 38% of adult patients, is of particular importance in women of child-bearing age owing to the risk of neural tube defects.52 Thiamine deficiency, a precursor to Wernicke encephalopathy, has been seen in up to 49% of patients who underwent an RYGB and has been reported in pediatric patients.52,100 Fat-soluble vitamin deficiencies are more commonly seen in malabsorptive procedures, with up to 60% prevalence.97 Calcium deficiency is of particular concern in adolescent patients given the potential for additional bone mineralization. Kaulfers et al101 found significant bone density loss in patients after bariatric surgery. The multitude and complexity of nutritional deficiencies after these procedures underscore the need for consultation with an experienced dietician both before and after surgery.

The adolescent bariatric surgery team

Morbidly obese adolescents have unique physiologic and psychological issues that mandate special care. The evaluation process for bariatric surgery is more complicated for adolescents than for adults. Adolescents often have trouble accurately reporting dietary attempts at weight loss and food habits. Adolescents are still actively growing, with additional risk for potential nutritional deficiencies postoperatively. In addition, because of the unique psychology of adolescence, many adolescents who meet physical criteria for bariatric surgery do not meet psychological criteria. Owing to these additional challenges, a multidisciplinary team is essential to adequately care for the adolescent bariatric patient. The team should include a surgical director with adequate experience and expertise, a medical director or expert consultant, a psychologist/psychiatrist, a social worker, a dietician, an exercise physiologist or physical therapist with expertise in exercise, and an array of available of consulting services.102 Several models have been proposed and are effective in caring for adolescent bariatric patients. These models include a pediatric surgeon or pediatrician with expertise in obesity, working with an adult bariatric team, or an adult bariatric surgeon, working with a pediatric team. Given the unique social structure and needs of adolescence, support groups that meet on a regular basis provide additional peer interaction and are an important part of the care of these patients.

Pediatric obesity is an important public health problem. There are currently no medical treatments that provide durable and sustainable weight loss for adolescent patients with morbid obesity or that improve the life-threatening comorbidities associated with morbid obesity. Bariatric surgery in adults has been shown to improve or, in many cases, eliminate obesity-related comorbidities. Initial data are supportive that these beneficial effects are also seen in adolescent patients, leading to the consideration of bariatric surgery as an accepted treatment option for morbidly obese adolescents. Adolescents with morbid obesity are a unique and relatively high-risk patient population that requires care by a multidisciplinary team. There are currently no clear guidelines to choose a specific bariatric procedure for a specific adolescent patient. Although the RYGB remains the gold standard bariatric procedure for both adolescents and adults, LAGB and LSG deserve further study, primarily to document the long-term efficacy and risk-benefit ratio. Strict criteria for surgery and the adolescent's understanding of the process are critical for the short-term surgical success and the long-term improvement in comorbidities. Performing bariatric surgery in centers prepared to meet all the special needs of adolescents is essential to minimizing risk and maximizing successful outcomes. Research examining the long-term effects of bariatric surgery in adolescents is ethically essential to help in future patient selection and to determine late clinical outcomes.

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Article Information

Correspondence: Mary L. Brandt, MD, Division of Pediatric Surgery, Texas Children's Hospital, 6701 Fannin St, CCC 1210.00, Houston, TX 77030 (brandt@bcm.edu).

Accepted for Publication: April 11, 2012.

Author Contributions:Study concept and design: Hsia and Brandt. Acquisition of data: Hsia and Fallon. Analysis and interpretation of data: Hsia. Drafting of the manuscript: Hsia, Fallon, and Brandt. Critical revision of the manuscript for important intellectual content: Hsia and Brandt. Administrative, technical, and material support: Hsia. Study supervision: Brandt.

Financial Disclosure: None reported.

Additional Contributions: We thank Emily Larimer, BS, and the members of the Adolescent Bariatric Team for their contributions: David Allen, BS; Margaret Lee, BA, MPH; Karin Price, PhD; Patricia Walters-Salas, BSN, RN-BC, CCM, CBN; and Gia Washington, PhD.

References
1.
Barlow SE.Expert Committee.  Expert committee recommendations regarding the prevention, assessment, and treatment of child and adolescent overweight and obesity: summary report.  Pediatrics. 2007;120:(suppl 4)  S164-S19218055651PubMedGoogle ScholarCrossref
2.
Daniels SR, Khoury PR, Morrison JA. The utility of body mass index as a measure of body fatness in children and adolescents: differences by race and gender.  Pediatrics. 1997;99(6):804-8079164773PubMedGoogle ScholarCrossref
3.
Lindsay RS, Hanson RL, Roumain J, Ravussin E, Knowler WC, Tataranni PA. Body mass index as a measure of adiposity in children and adolescents: relationship to adiposity by dual energy x-ray absorptiometry and to cardiovascular risk factors.  J Clin Endocrinol Metab. 2001;86(9):4061-406711549626PubMedGoogle ScholarCrossref
4.
Freedman DS, Mei Z, Srinivasan SR, Berenson GS, Dietz WH. Cardiovascular risk factors and excess adiposity among overweight children and adolescents: the Bogalusa Heart Study.  J Pediatr. 2007;150(1):12.e12-17.e1217188605PubMedGoogle Scholar
5.
Camhi SM, Katzmarzyk PT. Prevalence of cardiometabolic risk factor clustering and body mass index in adolescents.  J Pediatr. 2011;159(2):303-30721429506PubMedGoogle ScholarCrossref
6.
Han TS, Sattar N, Lean M. ABC of obesity. Assessment of obesity and its clinical implications.  BMJ. 2006;333(7570):695-69817008674PubMedGoogle ScholarCrossref
7.
Kuczmarski RJ, Ogden CL, Grummer-Strawn LM,  et al.  CDC growth charts: United States.  Adv Data. 2000;(314):1-2711183293PubMedGoogle Scholar
8.
Ogden CL, Flegal KM. Changes in terminology for childhood overweight and obesity.  Natl Health Stat Report. 2010;(25):1-520939253PubMedGoogle Scholar
9.
Lee H, Lee D, Guo G, Harris KM. Trends in body mass index in adolescence and young adulthood in the United States: 1959-2002.  J Adolesc Health. 2011;49(6):601-60822098770PubMedGoogle ScholarCrossref
10.
Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of obesity and trends in body mass index among US children and adolescents, 1999-2010.  JAMA. 2012;307(5):483-49022253364PubMedGoogle ScholarCrossref
11.
The NS, Suchindran C, North KE, Popkin BM, Gordon-Larsen P. Association of adolescent obesity with risk of severe obesity in adulthood.  JAMA. 2010;304(18):2042-204721063014PubMedGoogle ScholarCrossref
12.
Whitaker RC, Wright JA, Pepe MS, Seidel KD, Dietz WH. Predicting obesity in young adulthood from childhood and parental obesity.  N Engl J Med. 1997;337(13):869-8739302300PubMedGoogle ScholarCrossref
13.
Fontaine KR, Redden DT, Wang C, Westfall AO, Allison DB. Years of life lost due to obesity.  JAMA. 2003;289(2):187-19312517229PubMedGoogle ScholarCrossref
14.
Tsai AG, Williamson DF, Glick HA. Direct medical cost of overweight and obesity in the USA: a quantitative systematic review.  Obes Rev. 2011;12(1):50-6120059703PubMedGoogle ScholarCrossref
15.
McNiece KL, Poffenbarger TS, Turner JL, Franco KD, Sorof JM, Portman RJ. Prevalence of hypertension and pre-hypertension among adolescents.  J Pediatr. 2007;150(6):640.e1-644.e117517252PubMedGoogle Scholar
16.
Din-Dzietham R, Liu Y, Bielo MV, Shamsa F. High blood pressure trends in children and adolescents in national surveys, 1963 to 2002.  Circulation. 2007;116(13):1488-149617846287PubMedGoogle ScholarCrossref
17.
Field AE, Cook NR, Gillman MW. Weight status in childhood as a predictor of becoming overweight or hypertensive in early adulthood.  Obes Res. 2005;13(1):163-16915761176PubMedGoogle ScholarCrossref
18.
Ford CA, Nonnemaker JM, Wirth KE. The influence of adolescent body mass index, physical activity, and tobacco use on blood pressure and cholesterol in young adulthood.  J Adolesc Health. 2008;43(6):576-58319027646PubMedGoogle ScholarCrossref
19.
Li L, Law C, Power C. Body mass index throughout the life-course and blood pressure in mid-adult life: a birth cohort study.  J Hypertens. 2007;25(6):1215-122317563534PubMedGoogle ScholarCrossref
20.
Cook S, Weitzman M, Auinger P, Nguyen M, Dietz WH. Prevalence of a metabolic syndrome phenotype in adolescents: findings from the third National Health and Nutrition Examination Survey, 1988-1994.  Arch Pediatr Adolesc Med. 2003;157(8):821-82712912790PubMedGoogle ScholarCrossref
21.
Pinhas-Hamiel O, Dolan LM, Daniels SR, Standiford D, Khoury PR, Zeitler P. Increased incidence of non-insulin-dependent diabetes mellitus among adolescents.  J Pediatr. 1996;128(5, pt 1):608-6158627431PubMedGoogle ScholarCrossref
22.
Duncan GE. Prevalence of diabetes and impaired fasting glucose levels among US adolescents: National Health and Nutrition Examination Survey, 1999-2002.  Arch Pediatr Adolesc Med. 2006;160(5):523-52816651496PubMedGoogle ScholarCrossref
23.
Pacifico L, Nobili V, Anania C, Verdecchia P, Chiesa C. Pediatric nonalcoholic fatty liver disease, metabolic syndrome and cardiovascular risk.  World J Gastroenterol. 2011;17(26):3082-309121912450PubMedGoogle Scholar
24.
Centers for Disease Control and Prevention (CDC).  Prevalence of abnormal lipid levels among youths—United States, 1999-2006 [published correction appears in MMWR Morb Mortal Wkly Rep. 2010;59(3):78].  MMWR Morb Mortal Wkly Rep. 2010;59(2):29-3320094024PubMedGoogle Scholar
25.
Mark AL. Dietary therapy for obesity: an emperor with no clothes.  Hypertension. 2008;51(6):1426-1434, discussion 143418474832PubMedGoogle ScholarCrossref
26.
Kramer FM, Jeffery RW, Forster JL, Snell MK. Long-term follow-up of behavioral treatment for obesity: patterns of weight regain among men and women.  Int J Obes. 1989;13(2):123-1362663745PubMedGoogle Scholar
27.
Rosenbaum M, Leibel RL, Hirsch J. Obesity.  N Engl J Med. 1997;337(6):396-4079241130PubMedGoogle ScholarCrossref
28.
Dansinger ML, Tatsioni A, Wong JB, Chung M, Balk EM. Meta-analysis: the effect of dietary counseling for weight loss.  Ann Intern Med. 2007;147(1):41-5017606960PubMedGoogle Scholar
29.
Wilfley DE, Stein RI, Saelens BE,  et al.  Efficacy of maintenance treatment approaches for childhood overweight: a randomized controlled trial.  JAMA. 2007;298(14):1661-167317925518PubMedGoogle ScholarCrossref
30.
Tsai AG, Wadden TA. Systematic review: an evaluation of major commercial weight loss programs in the United States.  Ann Intern Med. 2005;142(1):56-6615630109PubMedGoogle Scholar
31.
 Methods for voluntary weight loss and control: NIH Technology Assessment Conference Panel: Consensus Development Conference, 30 March to 1 April 1992.  Ann Intern Med. 1993;119(7, pt 2):764-7708363212PubMedGoogle Scholar
32.
Mark AL. Dietary therapy for obesity is a failure and pharmacotherapy is the future: a point of view.  Clin Exp Pharmacol Physiol. 2006;33(9):857-86216922821PubMedGoogle ScholarCrossref
33.
Maier IB, Stricker L, Ozel Y, Wagnerberger S, Bischoff SC, Bergheim I. A low fructose diet in the treatment of pediatric obesity: a pilot study.  Pediatr Int. 2011;53(3):303-30820831653PubMedGoogle ScholarCrossref
34.
Spieth LE, Harnish JD, Lenders CM,  et al.  A low-glycemic index diet in the treatment of pediatric obesity.  Arch Pediatr Adolesc Med. 2000;154(9):947-95110980801PubMedGoogle Scholar
35.
Willi SM, Oexmann MJ, Wright NM, Collop NA, Key LL Jr. The effects of a high-protein, low-fat, ketogenic diet on adolescents with morbid obesity: body composition, blood chemistries, and sleep abnormalities.  Pediatrics. 1998;101(1, pt 1):61-679417152PubMedGoogle ScholarCrossref
36.
Dietz WH Jr. Childhood obesity: susceptibility, cause, and management.  J Pediatr. 1983;103(5):676-6866631594PubMedGoogle ScholarCrossref
37.
Rogovik AL, Chanoine JP, Goldman RD. Pharmacotherapy and weight-loss supplements for treatment of paediatric obesity.  Drugs. 2010;70(3):335-34620166770PubMedGoogle ScholarCrossref
38.
Butryn ML, Wadden TA, Rukstalis MR,  et al.  Maintenance of weight loss in adolescents: current status and future directions.  J Obes. 2010;2010:78928021274275PubMedGoogle Scholar
39.
Kanekar A, Sharma M. Pharmacological approaches for management of child and adolescent obesity.  J Clin Med Res. 2010;2(3):105-11121629521PubMedGoogle Scholar
40.
Berkowitz RI, Wadden TA, Tershakovec AM, Cronquist JL. Behavior therapy and sibutramine for the treatment of adolescent obesity: a randomized controlled trial.  JAMA. 2003;289(14):1805-181212684359PubMedGoogle ScholarCrossref
41.
Chanoine JP, Hampl S, Jensen C, Boldrin M, Hauptman J. Effect of orlistat on weight and body composition in obese adolescents: a randomized controlled trial.  JAMA. 2005;293(23):2873-288315956632PubMedGoogle ScholarCrossref
42.
Savoye M, Shaw M, Dziura J,  et al.  Effects of a weight management program on body composition and metabolic parameters in overweight children: a randomized controlled trial.  JAMA. 2007;297(24):2697-270417595270PubMedGoogle ScholarCrossref
43.
Picot J, Jones J, Colquitt JL,  et al.  The clinical effectiveness and cost-effectiveness of bariatric (weight loss) surgery for obesity: a systematic review and economic evaluation.  Health Technol Assess. 2009;13(41):1-190, 215-357, iii-iv19726018PubMedGoogle Scholar
44.
O’Brien PE, Dixon JB, Laurie C,  et al.  Treatment of mild to moderate obesity with laparoscopic adjustable gastric banding or an intensive medical program: a randomized trial.  Ann Intern Med. 2006;144(9):625-63316670131PubMedGoogle Scholar
45.
Nguyen NT, Masoomi H, Magno CP, Nguyen XM, Laugenour K, Lane J. Trends in use of bariatric surgery, 2003-2008.  J Am Coll Surg. 2011;213(2):261-26621624841PubMedGoogle ScholarCrossref
46.
Schilling PL, Davis MM, Albanese CT, Dutta S, Morton J. National trends in adolescent bariatric surgical procedures and implications for surgical centers of excellence.  J Am Coll Surg. 2008;206(1):1-1218155562PubMedGoogle ScholarCrossref
47.
Woolford SJ, Clark SJ, Gebremariam A, Davis MM, Freed GL. To cut or not to cut: physicians' perspectives on referring adolescents for bariatric surgery.  Obes Surg. 2010;20(7):937-94220401742PubMedGoogle ScholarCrossref
48.
Iqbal CW, Kumar S, Iqbal AD, Ishitani MB. Perspectives on pediatric bariatric surgery: identifying barriers to referral.  Surg Obes Relat Dis. 2009;5(1):88-9318996760PubMedGoogle ScholarCrossref
49.
 Gastrointestinal surgery for severe obesity: National Institutes of Health Consensus Development Conference Statement.  Am J Clin Nutr. 1992;55:(2 suppl)  615S-619S1733140PubMedGoogle Scholar
50.
Pratt JS, Lenders CM, Dionne EA,  et al.  Best practice updates for pediatric/adolescent weight loss surgery.  Obesity (Silver Spring). 2009;17(5):901-91019396070PubMedGoogle ScholarCrossref
51.
Ibele AR, Mattar SG. Adolescent bariatric surgery.  Surg Clin North Am. 2011;91(6):1339-1351, x22054157PubMedGoogle ScholarCrossref
52.
Brandt ML, Harmon CM, Helmrath MA, Inge TH, McKay SV, Michalsky MP. Morbid obesity in pediatric diabetes mellitus: surgical options and outcomes.  Nat Rev Endocrinol. 2010;6(11):637-64520842181PubMedGoogle ScholarCrossref
53.
Rubino F, R'bibo SL, del Genio F, Mazumdar M, McGraw TE. Metabolic surgery: the role of the gastrointestinal tract in diabetes mellitus.  Nat Rev Endocrinol. 2010;6(2):102-10920098450PubMedGoogle ScholarCrossref
54.
Xanthakos SA, Daniels SR, Inge TH. Bariatric surgery in adolescents: an update.  Adolesc Med Clin. 2006;17(3):589-612, abstract x17030281PubMedGoogle Scholar
55.
Byrne TK. Complications of surgery for obesity.  Surg Clin North Am. 2001;81(5):1181-1193, vii-viii11589251PubMedGoogle ScholarCrossref
56.
Lawson ML, Kirk S, Mitchell T,  et al; Pediatric Bariatric Study Group.  One-year outcomes of Roux-en-Y gastric bypass for morbidly obese adolescents: a multicenter study from the Pediatric Bariatric Study Group.  J Pediatr Surg. 2006;41(1):137-14316410123PubMedGoogle ScholarCrossref
57.
Sugerman HJ, Sugerman EL, DeMaria EJ,  et al.  Bariatric surgery for severely obese adolescents.  J Gastrointest Surg. 2003;7(1):102-107, discussion 107-10812559191PubMedGoogle ScholarCrossref
58.
Cameron JLCA. Current Surgical Therapy. 10th ed. Philadelphia, PA: Elsevier Saunders; 2011
59.
Forfori F, Ferro B, Mancini B,  et al.  Role of thrombolestagrophy in monitoring perioperative coagulation status and effect of thromboprophylaxis in bariatric surgery.  Obes Surg. 2011;22(1):113-11821611876PubMedGoogle ScholarCrossref
60.
Inge TH, Krebs NF, Garcia VF,  et al.  Bariatric surgery for severely overweight adolescents: concerns and recommendations.  Pediatrics. 2004;114(1):217-22315231931PubMedGoogle ScholarCrossref
61.
Angrisani L, Favretti F, Furbetta F,  et al.  Obese teenagers treated by Lap-Band System: the Italian experience.  Surgery. 2005;138(5):877-88116291388PubMedGoogle ScholarCrossref
62.
Treadwell JR, Sun F, Schoelles K. Systematic review and meta-analysis of bariatric surgery for pediatric obesity.  Ann Surg. 2008;248(5):763-77618948803PubMedGoogle ScholarCrossref
63.
Holterman AX, Browne A, Tussing L,  et al.  A prospective trial for laparoscopic adjustable gastric banding in morbidly obese adolescents: an interim report of weight loss, metabolic and quality of life outcomes.  J Pediatr Surg. 2010;45(1):74-78, discussion 78-7920105583PubMedGoogle ScholarCrossref
64.
Nadler EP, Youn HA, Ren CJ, Fielding GA. An update on 73 US obese pediatric patients treated with laparoscopic adjustable gastric banding: comorbidity resolution and compliance data.  J Pediatr Surg. 2008;43(1):141-14618206472PubMedGoogle ScholarCrossref
65.
Widhalm K, Fritsch M, Widhalm H,  et al.  Bariatric surgery in morbidly obese adolescents: long-term follow-up.  Int J Pediatr Obes. 2011;6:(suppl 1)  65-6921905819PubMedGoogle ScholarCrossref
66.
Campos GM, Rabl C, Roll GR,  et al.  Better weight loss, resolution of diabetes, and quality of life for laparoscopic gastric bypass vs banding: results of a 2-cohort pair-matched study.  Arch Surg. 2011;146(2):149-15521339424PubMedGoogle ScholarCrossref
67.
Naef M, Mouton WG, Naef U, Kummer O, Muggli B, Wagner HE. Graft survival and complications after laparoscopic gastric banding for morbid obesity—lessons learned from a 12-year experience.  Obes Surg. 2010;20(9):1206-121420524156PubMedGoogle ScholarCrossref
68.
Boza C, Gamboa C, Awruch D, Perez G, Escalona A, Ibañez L. Laparoscopic Roux-en-Y gastric bypass versus laparoscopic adjustable gastric banding: five years of follow-up.  Surg Obes Relat Dis. 2010;6(5):470-47520702146PubMedGoogle ScholarCrossref
69.
Frezza EE, Chiriva-Internati M, Wachtel MS. Analysis of the results of sleeve gastrectomy for morbid obesity and the role of ghrelin.  Surg Today. 2008;38(6):481-48318516524PubMedGoogle ScholarCrossref
70.
Cottam D, Qureshi FG, Mattar SG,  et al.  Laparoscopic sleeve gastrectomy as an initial weight-loss procedure for high-risk patients with morbid obesity.  Surg Endosc. 2006;20(6):859-86316738970PubMedGoogle ScholarCrossref
71.
Till HK, Muensterer O, Keller A,  et al.  Laparoscopic sleeve gastrectomy achieves substantial weight loss in an adolescent girl with morbid obesity.  Eur J Pediatr Surg. 2008;18(1):47-4918302070PubMedGoogle ScholarCrossref
72.
Landau Z, Karplus G, Hanukoglu A, Abiri S, Levy A, Serour F. Laparoscopic sleeve gastrectomy (LSG) in adolescents with morbid obesity [in Hebrew].  Harefuah. 2011;150(10):765-768, 816, 81522111118PubMedGoogle Scholar
73.
Till H, Blüher S, Hirsch W, Kiess W. Efficacy of laparoscopic sleeve gastrectomy (LSG) as a stand-alone technique for children with morbid obesity.  Obes Surg. 2008;18(8):1047-104918459015PubMedGoogle ScholarCrossref
74.
Hutter MM, Schirmer BD, Jones DB,  et al.  First report from the American College of Surgeons Bariatric Surgery Center Network: laparoscopic sleeve gastrectomy has morbidity and effectiveness positioned between the band and the bypass.  Ann Surg. 2011;254(3):410-420; discussion 420-41221865942PubMedGoogle ScholarCrossref
75.
Angrisani L, Cutolo PP, Buchwald JN,  et al.  Laparoscopic reinforced sleeve gastrectomy: early results and complications.  Obes Surg. 2011;21(6):783-79321494813PubMedGoogle ScholarCrossref
76.
Bobowicz M, Lehmann A, Orlowski M, Lech P, Michalik M. Preliminary outcomes 1 year after laparoscopic sleeve gastrectomy based on Bariatric Analysis and Reporting Outcome System (BAROS).  Obes Surg. 2011;21(12):1843-184821491136PubMedGoogle ScholarCrossref
77.
Stroh C, Birk D, Flade-Kuthe R,  et al; Bariatric Surgery Working Group.  Results of sleeve gastrectomy-data from a nationwide survey on bariatric surgery in Germany.  Obes Surg. 2009;19(5):632-64019184256PubMedGoogle ScholarCrossref
78.
Xanthakos SA. Bariatric surgery for extreme adolescent obesity: indications, outcomes, and physiologic effects on the gut-brain axis.  Pathophysiology. 2008;15(2):135-14618585904PubMedGoogle ScholarCrossref
79.
Rand CS, Macgregor AM. Adolescents having obesity surgery: a 6-year follow-up.  South Med J. 1994;87(12):1208-12137973919PubMedGoogle ScholarCrossref
80.
Buchwald H, Williams SE. Bariatric surgery worldwide 2003.  Obes Surg. 2004;14(9):1157-116415527627PubMedGoogle ScholarCrossref
81.
Rao RS, Kini S. Diabetic and bariatric surgery: a review of the recent trends.  Surg Endosc. 2012;26(4):893-90321993947PubMedGoogle ScholarCrossref
82.
Marceau P, Marceau S, Biron S,  et al.  Long-term experience with duodenal switch in adolescents.  Obes Surg. 2010;20(12):1609-161620835899PubMedGoogle ScholarCrossref
83.
Papadia FS, Adami GF, Marinari GM, Camerini G, Scopinaro N. Bariatric surgery in adolescents: a long-term follow-up study.  Surg Obes Relat Dis. 2007;3(4):465-46817400517PubMedGoogle ScholarCrossref
84.
Serrot FJ, Dorman RB, Miller CJ,  et al.  Comparative effectiveness of bariatric surgery and nonsurgical therapy in adults with type 2 diabetes mellitus and body mass index <35 kg/m2.  Surgery. 2011;150(4):684-69122000180PubMedGoogle ScholarCrossref
85.
Adams TD, Gress RE, Smith SC,  et al.  Long-term mortality after gastric bypass surgery.  N Engl J Med. 2007;357(8):753-76117715409PubMedGoogle ScholarCrossref
86.
Barnett SJ. Contemporary surgical management of the obese adolescent.  Curr Opin Pediatr. 2011;23(3):351-35521572387PubMedGoogle ScholarCrossref
87.
Frank P, Crookes PF. Short- and long-term surgical follow-up of the postbariatric surgery patient.  Gastroenterol Clin North Am. 2010;39(1):135-14620202586PubMedGoogle ScholarCrossref
88.
Inge TH, Jenkins TM, Zeller M,  et al.  Baseline BMI is a strong predictor of nadir BMI after adolescent gastric bypass.  J Pediatr. 2010;156(1):103.e1-108.e119775700PubMedGoogle Scholar
89.
Nadler EP, Youn HA, Ginsburg HB, Ren CJ, Fielding GA. Short-term results in 53 US obese pediatric patients treated with laparoscopic adjustable gastric banding.  J Pediatr Surg. 2007;42(1):137-141; discussion 141-13217208554PubMedGoogle ScholarCrossref
90.
Nadler EP, Reddy S, Isenalumhe A,  et al.  Laparoscopic adjustable gastric banding for morbidly obese adolescents affects android fat loss, resolution of comorbidities, and improved metabolic status.  J Am Coll Surg. 2009;209(5):638-64419854406PubMedGoogle ScholarCrossref
91.
Inge TH, Miyano G, Bean J,  et al.  Reversal of type 2 diabetes mellitus and improvements in cardiovascular risk factors after surgical weight loss in adolescents.  Pediatrics. 2009;123(1):214-22219117885PubMedGoogle ScholarCrossref
92.
Teeple EA, Teich S, Schuster DP, Michalsky MP. Early metabolic improvement following bariatric surgery in morbidly obese adolescents.  Pediatr Blood Cancer. 2012;58(1):112-11622021118PubMedGoogle ScholarCrossref
93.
Zitsman JL, Digiorgi MF, Marr JR, Witt MA, Bessler M. Comparative outcomes of laparoscopic adjustable gastric banding in adolescents and adults.  Surg Obes Relat Dis. 2011;7(6):720-72621429814PubMedGoogle ScholarCrossref
94.
Vander Wal JS, Mitchell ER. Psychological complications of pediatric obesity.  Pediatr Clin North Am. 2011;58(6):1393-1401, x22093858PubMedGoogle ScholarCrossref
95.
Järvholm K, Olbers T, Marcus C,  et al.  Short-term psychological outcomes in severely obese adolescents after bariatric surgery.  Obesity (Silver Spring). 2012;20(2):318-32321996668PubMedGoogle ScholarCrossref
96.
Zeller MH, Reiter-Purtill J, Ratcliff MB, Inge TH, Noll JG. Two-year trends in psychosocial functioning after adolescent Roux-en-Y gastric bypass.  Surg Obes Relat Dis. 2011;7(6):727-73221497142PubMedGoogle ScholarCrossref
97.
Xanthakos SA, Inge TH. Nutritional consequences of bariatric surgery.  Curr Opin Clin Nutr Metab Care. 2006;9(4):489-49616778582PubMedGoogle ScholarCrossref
98.
Fullmer MA, Abrams SH, Hrovat K,  et al.  Nutritional strategy for adolescents undergoing bariatric surgery: report of a working group of the Nutrition Committee of NASPGHAN/NACHRI.  J Pediatr Gastroenterol Nutr. 2012;54(1):125-13521857247PubMedGoogle ScholarCrossref
99.
Shankar P, Boylan M, Sriram K. Micronutrient deficiencies after bariatric surgery.  Nutrition. 2010;26(11-12):1031-103720363593PubMedGoogle ScholarCrossref
100.
Towbin A, Inge TH, Garcia VF,  et al.  Beriberi after gastric bypass surgery in adolescence.  J Pediatr. 2004;145(2):263-26715289782PubMedGoogle ScholarCrossref
101.
Kaulfers AM, Bean JA, Inge TH, Dolan LM, Kalkwarf HJ. Bone loss in adolescents after bariatric surgery.  Pediatrics. 2011;127(4):e956-e96121444596PubMedGoogle ScholarCrossref
102.
Michalsky M, Kramer RE, Fullmer MA,  et al.  Developing criteria for pediatric/adolescent bariatric surgery programs.  Pediatrics. 2011;128:(suppl 2)  S65-S7021885647PubMedGoogle ScholarCrossref
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