A 2-Week Course of Enteral Treatment with a Very Low-Calorie Protein-Based Formula for the Management of Severe Obesity

被引:6
|
作者
Castaldo, Giuseppe [1 ]
Monaco, Luigi [2 ]
Castaldo, Laura [1 ]
Sorrentino, Paolo [3 ]
机构
[1] AORN San Giuseppe Moscati, Clin Nutr Unit, I-83100 Avellino, Italy
[2] AORN San Giuseppe Moscati, Ultrasonog Unit, I-83100 Avellino, Italy
[3] AORN San Giuseppe Moscati, Liver Unit, I-83100 Avellino, Italy
关键词
SPARING-MODIFIED FAST; BETA-CELL FUNCTION; WEIGHT-REDUCTION; DIETS; FAT; PHARMACOLOGY; METAANALYSIS; RESPONSES;
D O I
10.1155/2015/723735
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Multiple weight loss failures among obese patients suggest the design of new therapeutic strategies. We investigated the role of 2-week course of enteral treatment with a very low-calorie protein-based formula in the management of severe obesity. Methods. We evaluated the feasibility, safety, and efficacy of 2-week continuous administration of a protein-based formula (1.2 g/kg of ideal body weight/day) by nasogastric tube in severely obese adults (body mass index (BMI) = 40 kg/m(2)). Results. In total, 364 patients (59% women; BMI = 46.6 +/- 7.2 kg/m(2)) were recruited. The intervention was discontinued within 48 hours in 26 patients, due to nasogastric tube intolerance. No serious adverse events occurred. During the first and the second week, 65% and 80% patients, respectively, reported no side effects. All biochemical safety parameters were affected by the intervention, particularly uric acid (+45%) and aminotransferases (+48%). In the other cases the change was negligible. We observed significant weight loss (5.7 +/- 2.3%) and improvement in blood pressure and glucose and lipid metabolism parameters (P < 0.001). Conclusions. A 2-week course of enteral treatment with a very low-calorie protein-based formula appeared a feasible, likely safe, and efficacious therapeutic option to be considered for inclusion into a composite weight loss program for the management of severe obesity. This trial is registered with ClinicalTrials.gov Identifier: NCT01965990.
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页数:10
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