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.com

Volume 8

Journal of Gastrointestinal & Digestive System

ISSN: 2161-069X

Bariatric Surgery 2018 & Gastro 2018

March 15-16, 2018

JOINT EVENT

12

th

Global Gastroenterologists Meeting

3

rd

International Conference on Metabolic and Bariatric Surgery

&

March 15-16, 2018 Barcelona, Spain

Long term outcome after Biliopancreatic diversion in Prader-Willi syndrome

Antonino Crino, Danilo Fintini, Alessio Convertino, Sarah Bocchini

and

Graziano Grugni

Bambino Gesu Hospital, Italy

Background:

Improvement in weight control remains the most important goal of any treatment program in Prader-Willi syndrome

(PWS). To date, bariatric surgery experience in Prader-Willi syndrome (PWS) is limited, and different procedures have been used

with varying success. Malabsorptive procedures, such as biliopancreatic diversion (BPD), are not always recommended for PWS due

to lack of safety data and can involve long-term complications.

Patients & Methods:

We report 10 severely obese patients (6 males) with genetically confirmed PWS (7 del15, 3 UPD15) who

underwent Scopinaro’s BPD after inability to control food intake with the classical approaches. Surgery was performed on patients

aged 18.8±3 yrs. (mean±SD) (range: 15.4-24.4) and the BMI (kg/m2) was ≥40 in all cases (49.9±6.7). At baseline, severe co-morbidities

were present, such as obstructive sleep apnea (OSAS), type 2 diabetes mellitus (T2DM), hypertension, metabolic syndrome and/or

steatohepatitis.

Results:

No perioperative complications were observed. After a follow-up period of 13.9±7.3 yrs. (range 4.8-27; mean age at follow-

up: 32.5±6.8 yrs) the maximum weight loss % (MWL%) was 30.7±10 (10.1-52.6). Following BPD, BMI decreased in six patients,

stable in three subjects and increased in one individual. The mean BMI at the last visit was 40.5±8.8 (28.9-51.6). After BPD, appetite

was reduced in seven cases; eight subjects had hypochromic anemia and seven had diarrhea; OSAS were present in 5 patients and

osteoporosis/osteopenia in all individuals. T2DM disappeared and behavioral problems improved in some cases. One patient

suddenly died at the age of 37.3 yrs. After surgery all patients received medical therapy to prevent nutritional deficiency.

Conclusion:

The long-term outcome of BPD in our PWS seems to be favorable, with a significant reduction of weight excess in the

majority of subjects. Thus, BPD seems to be a good option in the presence of severe comorbility and in selected PWS patients, with co-

operating families, when other classical approaches have failed. Due to the presence of specific side effects of the procedure, however,

a careful long-term multidisciplinary follow-up is always necessary.

Recent Publications

1.

S Bocchini, D Fintini, G Grugni, A Boiani, A Convertino and A Crinò (2017) Congenital hypothyroidism due to ectopic

sublingual thyroid gland in Prader-Willi syndrome: a case report. Ital J Pediatr. 43(1):87.

2.

Maltese P E, Iarossi G, Ziccardi L, Colombo L, Buzzonetti L, Crinò A, Tezzele S and Bertelli M (2017) A next generation

sequencing custom gene panel as first line diagnostic tool for atypical cases of syndromic obesity: application in a case of

Alström syndrome. Eur J Med Genet. 61(2):79-83.

3.

Rigamonti A E, Crinò A, Bocchini S, Convertino A, Bidlingmaier M, Haenelt M, Tamini S, Cella S G, Grugni G and Sartorio

A (2017) GHRH plus arginine and arginine administration evokes the same ratio of GH isoforms levels in young patients

with Prader-Willi syndrome. Growth Horm IGF Res. pii: S1096-6374(17)30108-9.

4.

Brunetti G, Grugni G, Piacente L, Delvecchio M, Ventura A, Giordano P, Grano M, D’Amato G, Laforgia D, Crinò A and

Faienza M (2018) Analysis of circulating mediators of bone remodelling in Prader-Willi syndrome. Calcif Tissue Int. doi:

10.1007/s00223-017-0376-y.

5.

S Allas, A Caixàs, C Poitou, M Coupaye, D Thuilleaux, F Lorenzini, G Diene, A Crinò, F Illouz, G Grugni, Diane Potvin, S

Bocchini, T Delale, T Abribat and M Tauber (2018) AZP-531, an unacylated ghrelin analog, improves food-related behavior

in patients with Prader-Willi syndrome: A randomized placebo-controlled trial. PLoS One 13(1):e0190849.

Antonino Crino et al., J Gastrointest Dig Syst 2018, Volume 8

DOI: 10.4172/2161-069X-C1-064