Devices in both groups performed regular, low-energy safety checks. After treatment, they were losing weight at a rate of. The suture and cinch elements were judged to be effective in the majority of cases. The gastric restrictive procedures include vertical banded gastroplasty accompanied by gastric banding which attempt to induce weight loss by creating an intake-limiting gastric pouch by segmenting the stomach along its vertical axis. But still pharmacists cannot dispense the item as a pharmaceutical benefit unless it has the necessary Authority code.
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Electrodes were implanted laparoscopically on both vagi near the esophago-gastric junction to provide electrical block. Patients were followed for 6 months for body weight, safety, electrocardiogram, dietary intake, satiation, satiety, and plasma pancreatic polypeptide PP response to sham feeding.
To specifically assess device effects alone, no diet or exercise programs were instituted. A total of 31 patients mean BMI of Mean EWL at 4 and 12 weeks and 6 months after implant was 7. There were no deaths or device-related serious adverse events AEs.
Three patients had serious AEs that required brief hospitalization, 1 each for lower respiratory tract, subcutaneous implant site seroma, and Clostridium difficile diarrhea.
The authors concluded that intermittent, intra-abdominal vagal blocking is associated with significant EWL and a desirable safety profile. A total of subjects were enrolled at 15 centers. Devices in both groups performed regular, low-energy safety checks. The authors concluded that VBLOC therapy to treat morbid obesity was safe, but weight loss was not greater in treated compared to controls; clinically important weight loss, however, was related to hours of device use.
Post-study analysis suggested that the system electrical safety checks low charge delivered via the system for electrical impedance, safety, and diagnostic checks may have contributed to weight loss in the control group. In an open-label study, Shikora et al evaluated the effect of intermittent vagal blocking VBLOC on weight loss, glycemic control, and blood pressure BP in obese subjects with diabetes mellitus type-2 DM2. One serious AE pain at implant site was easily resolved. The authors stated that additional long-term data and continued follow-up of the ReCharge study are needed to further characterize the safety and effectiveness profile of vBloc therapy.
Natural orifice transluminal endoscopic surgery NOTES is being explored for a variety of surgeries, including bariatric procedures. NOTES procedures are incisionless surgeries performed with an endoscope passed through the mouth. Tissue approximation and closure devices are being developed for use in conjunction with various endoscopic procedures, including NOTES. Restorative obesity surgery, endoluminal ROSE procedure is suggested for the treatment of weight regain following gastric bypass surgery due to a gradual expansion of the gastric pouch.
The stomach is accessed orally via an endoscope and reduced in size using an endoscopic closure device. Transoral gastroplasty TG , also referred to as vertical sutured gastroplasty or endoluminal vertical gastroplasty, is an incisionless procedure in which the stomach is purportedly restricted with staples or sutures by using endoscopic surgical tools guided through the mouth and esophagus.
Main outcome measure was technical feasibility. These researchers successfully used an endoscopic free-hand suturing system in 4 subjects, thus demonstrating the technical feasibility of a novel technique to mimic the anatomic manipulations created by surgical sleeve gastrectomy endoscopically. The authors concluded that endoscopic sleeve gastroplasty ESG for treatment of obesity is feasible. The main drawback of this study was that it was a pilot feasibility study with small number of subjects.
Sharaiha et al stated that novel endoscopic techniques have been developed as effective treatments for obesity. Recently, reduction of gastric volume via endoscopic placement of full-thickness sutures, termed ESG, has been described. These investigators evaluated the safety, technical feasibility, and clinical outcomes for ESG. Between August and May , ESG was performed on 10 patients using an endoscopic suturing device.
Their weight loss, waist circumference, and clinical outcomes were assessed. Mean patient age was There were no significant adverse events noted. The differences observed in mean BMI and waist circumference were 4. The authors concluded that ESG is effective in achieving weight loss with minimal adverse events.
They stated that this approach may provide a cost-effective out-patient procedure to add to the steadily growing armamentarium available for treatment of this significant epidemic. Lopez-Nava et al described the ESG used in 50 patients. The goal of this procedure is to reduce the gastric lumen into a tubular configuration, with the greater curvature modified by a line of sutured plications.
General anesthesia with endotracheal intubation is needed. An endoscopic suturing system requiring a specific double-channel endoscope delivers full-thickness sets of running sutures from the antrum to the fundus. Patients were admitted and observed, with discharge planned within 24 hours. Post-procedure out-patient care included diet instruction with intensive follow-up by a multi-disciplinary team.
Voluntary oral contrast and endoscopy studies were scheduled to evaluate the gastroplasty at 3, 6, and 12 months. The technique was applied in 50 patients 13 men with an average BMI of Procedure duration averaged 66 mins during which 6 to 8 sutures on average were placed. All patients were discharged in less than 24 hours. There were no major intra-procedural, early, or delayed adverse events. Weight loss parameters were satisfactory, mean BMI changes from Oral contrast studies and endoscopy revealed sleeve gastroplasty configuration at least until 1 year of follow-up.
The authors concluded that ESG is a safe, effective, and reproducible primary weight loss technique. Furthermore, a Cochrane review on "Surgery for weight loss in adults" Colquitt et al, as well as an UpToDate review on " Bariatric surgical operations for the management of severe obesity: Descriptions " Lim, do not mention endoscopic sleeve gastroplasty as a therapeutic option. In a pilot study, Sullivan and colleagues evaluated the use of endoscopic aspiration therapy for the treatment of obesity.
This method entails endoscopic placement of a gastrostomy tube A-Tube and the AspireAssist siphon assembly Aspire Bariatrics, King of Prussia, PA to aspirate gastric contents 20 minutes after meal consumption.
These researchers performed a study of 18 obese subjects who were randomly assigned 2: Lifestyle intervention comprised a session diet and behavioral education program; 10 of the 11 subjects who underwent aspiration therapy and 4 of the 7 subjects who underwent lifestyle therapy completed the 1st year of the study. After 1 year, subjects in the aspiration therapy group lost There were no AEs of aspiration therapy on eating behavior and no evidence of compensation for aspirated calories with increased food intake.
No episodes of binge eating in the aspiration therapy group or serious AEs were reported. The authors concluded that aspiration therapy appeared to be a safe and effective long-term weight loss therapy for obesity. These preliminary findings from a pilot study need to be validated by well-designed studies. Forssell and Noren evaluated the effectiveness of a novel device, the AspireAssist aspiration therapy system, for the treatment of obesity. After 4 weeks taking a very-low-calorie diet, 25 obese men and women BMI A low-profile valve was installed 14 days later and aspiration of gastric contents was performed approximately 20 minutes after meals 3 times per day.
Cognitive behavioral therapy was also started. At month 6, mean weight lost was The mean percentage EWL was No clinically significant changes in serum potassium or other electrolytes occurred.
The authors concluded that in this study, substantial weight loss was achieved with few complications using the AspireAssist system, suggesting its potential as an attractive therapeutic device for obese patients. A total of 25 obese subjects, mean age of 48 years range of 33 to 65 were included in this study. A custom gastrostomy tube A-tube was percutaneously inserted during a gastroscopy performed under conscious sedation.
Drainage and irrigation of the stomach were performed 3 times daily, 20 mins after each meal, for 1 to 2 years.
Efficient aspiration required thorough chewing of ingested food. Treatment included a cognitive behavioral weight loss program. Mean BMI at inclusion was Quality of life, as measured with EQ-5D, improved from 0.
After 2 years BMI was There were no serious AEs or electrolyte disorders. The authors concluded that aspiration therapy is a safe and efficient treatment for obesity, and weight reduction improves quality of life.
Excess weight was approximately halved in a year, with weight stability if treatment was continued; and long-term results remain to be investigated. It is unclear whether firm conclusions can be drawn from a person observational study.
This study only encompasses treatment during 1 to 2 years. Long-term patency is still unknown. It is our belief that once the desired weight goal is achieved many, if not most, patients will need to continue aspiration therapy, albeit possibly at a reduced frequency, to maintain weight stability. In this week clinical trial, a total of subjects with a BMI of A total of The most frequently reported AEs were abdominal pain and discomfort in the peri-operative period and peristomal granulation tissue and peristomal irritation in the post-operative period.
Serious AEs were reported in 3. On June 14, , the FDA approved the AspireAssist device to assist in weight loss in patients aged 22 and older who are obese, with a BMI of 35 to 55, and who have failed to achieve and maintain weight loss through non-surgical weight-loss therapy. Side effects related to use of the AspireAssist include occasional indigestion, nausea, vomiting, constipation and diarrhea.
The AspireAssist is contraindicated in those with certain conditions, including uncontrolled hypertension, diagnosed bulimia, diagnosed binge eating disorder, night eating syndrome, certain types of previous abdominal surgery, pregnancy or lactation, inflammatory bowel disease or stomach ulcers.
The AspireAssist is also contraindicated in patients with a history of serious pulmonary or cardiovascular disease, coagulation disorders, chronic abdominal pain or those at a high-risk of medical complications from an endoscopic procedure.
Furthermore, the AspireAssist device it is not indicated for use in short durations in those who are moderately overweight. In a post-market study, Nystrom and colleagues evaluated long-term safety and efficacy of aspiration therapy AT in a clinical setting in 5 European clinics. A total of participants, with BMI of Mean baseline BMI was Mean percent total weight loss at 1, 2, 3, and 4 years, respectively, was Clinically significant reductions in glycated hemoglobin HbA1C , triglycerides, and blood pressure were observed.
The authors concluded that the findings of this study established that AT is a safe, effective, and durable weight loss therapy in people with classes II and III obesity in a clinical setting. Kumar and associates noted that weight management is increasingly incorporating endoscopic bariatric therapy EBT. As the global burden of obesity and its co-morbidities has increased, it is evident that novel therapeutic approaches will be necessary to address the obesity epidemic.
EBTs offer greater efficacy than diet and lifestyle modification and lower invasiveness than bariatric surgery. The FDA has approved 2 intra-gastric balloons and aspiration therapy AT for the treatment of obesity: These devices have proven safe and effective in clinical trials and are gaining commercial acceptance in the USA; the Orbera has been used extensively outside the USA for over 20 years. These devices will need to be delivered in the context of a multi-disciplinary weight loss program, integrating comprehensive care of obesity.
Patient selection is important, and ensuring appropriate patient expectations and understanding of alternatives such as pharmacologic therapy and surgery is essential. With several EBTs on the horizon, patients with obesity will have an even broader array of safe and effective options for weight management in the future. The authors stated that AT addresses a broader BMI range and offers the potential for a significant and durable weight loss.
Pajot and co-workers stated that EBT is a rapidly developing area that has now seen FDA approval of 6 endoscopic bariatric devices and procedures and there are a number of other novel EBTs progressing through various stages of development with newly published findings.
This paper aimed to assist readers in either selecting an appropriate therapy for their patient or deciding to incorporate these therapies into their practice. This paper provided an updated review of the available data on EBTs, both FDA approved and not, with a particular focus on safety and effectiveness, as well as guidance for discussing with patients the decision to use endoscopic therapies.
The authors of a large meta-analysis of Orbera concluded its ideal balloon volume to be to ml. AspireAssist has had favorable effectiveness and safety data published in a large RCT. A large study of endoscopic sleeve gastroplasty has published findings at up to 24 months showing promising durability. Elipse, a swallowed intra-gastric balloon not requiring endoscopy for either insertion or removal, has had early favorable results published.
A magnet-based system for creation of a gastrojejunostomy has published favorable findings from its pilot study. The authors concluded that EBTs are safe and effective therapies for weight loss when used in conjunction with lifestyle changes and fill an important gap in the management of obesity.
These researchers stated that more study is needed to understand the role of EBTs used in combination or in sequence with medications and bariatric surgery.
Christensen and colleagues noted that AT with AspireAssist is a novel endoscopic obesity treatment. AspireAssist was recently approved by the FDA, and it induced weight loss comparable to the weight loss observed after bariatric surgery, but with a lower risk of complications. The authors stated that few clinical studies about the safety and efficacy of AspireAssist have been carried out and published.
Thus, further intervention studies evaluating acute as well as long-term effects are needed. Smith et al examined if bariatric surgery prior to total hip arthroplasty THA or total knee arthroplasty TKA reduces the complication rates and improves the outcome following arthroplasty in obese patients. These researchers performed a systematic literature search of published and unpublished databases on the November 5, All papers reporting studies comparing obese patients who had undergone bariatric surgery prior to arthroplasty, or not, were included.
E ach study was assessed using the Downs and Black appraisal tool. From potential studies, 5 were considered to be eligible for inclusion in the study. A total of 23, patients who had undergone bariatric surgery, 22, who had not were analyzed. The evidence-base was moderate in quality. There was no statistically significant difference in outcomes such as superficial wound infection RR 1.
The authors concluded that for most peri-operative outcomes, bariatric surgery prior to THA or TKA did not significantly reduce the complication rates or improve the clinical outcome. They stated that the findings of this study questions the previous belief that bariatric surgery prior to arthroplasty may improve the clinical outcomes for patients who are obese or morbidly obese.
This finding is based on moderate quality evidence. Abdemur et al stated that laparoscopic sleeve gastrectomy LSG as a primary bariatric procedure has gained significant popularity.
Between January and August , a total of 1, patients underwent primary LSG for morbid obesity. Of the entire cohort of revisions, 9 0. Both the stricture and the leak patients were referred from outside institutions. The authors concluded that the most common reason for conversion was chronic leak. El Chaar et al noted that bariatric surgery is the only proven and effective long-term treatment for morbid obesity, with LSG being the most commonly performed weight loss procedure in the United States.
Descriptive outcomes were reported due to the small sample size. Median time from the initial surgery to conversion was 27 months range of 17 to Median operating room time was minutes range of to Median length of stay was 48 hours range of 24 to In a systematic review and meta-analysis, Dasari and colleagues examined if mesh prevents post-operative incisional hernia IH in open and laparoscopic bariatric surgery patients.
A total of 7 studies met inclusion criteria. These investigators abstracted data regarding post-operative IH development, surgical site infection, and seroma or wound leakage and performed a meta-analysis. The prophylactic mesh group had significantly decreased odds of developing IH than the standard closure group odds ratio, 0. No included studies evaluated outcomes after prophylactic mesh during laparoscopic bariatric surgery.
The authors concluded that prophylactic mesh during open bariatric surgery appeared to be beneficial in reducing post-operative IH without significant increasing the odds of surgical site infection or seroma or wound leakage. Moreover, they stated that higher quality studies, including those in laparoscopic patients, and cost-utility analysis, are needed to support routine use of this intervention.
Dimitrokallis and colleagues noted that single-incision laparoscopic surgery has attracted a great deal of interest in the surgical community in recent years, including bariatric surgery. Single-incision laparoscopic sleeve gastrectomy SILSG has been proposed as an alternative to the multi-port laparoscopic procedure; however, it has yet to meet wide acceptance and application. These researchers summarized existing data on SILSG and checked the procedure's feasibility, technical details, safety, and, if possible, outcomes.
They checked the most important databases for studies concerning SILSG and included all these that summarized the criteria placed and contained the data needed for this review.
They excluded case reports. A total of 19 studies 1, patients met the selection criteria of this review. Their mean age was In the majority of cases A wide variety of instruments had been used and mean operating time was One conversion to open surgery was reported and 7.
There was a complication rate of 7. Mean EWL for a follow-up of 1 year was achieved in A tendency for less analgesia and better wound satisfaction was reported. However, there is insufficient evidence to recommend it as the new gold standard for sleeve gastrectomy in the place of conventional laparoscopic sleeve gastrectomy.
These investigators stated that RCTs are needed to analyze the results and the possible benefits of this technique. Zaveri et al noted that the increase in the prevalence of obesity and gastro-esophageal reflux disease GERD has paralleled one another. Laparoscopic fundoplication LF Nissen or Toupet is a minimally invasive form of anti-reflux surgery. The duodenal switch DS is a highly effective weight loss surgery with a proven record of long-term weight loss success.
However, fundoplication alone does not give satisfactory results when used for GERD in morbidly obese patients. The variables collected were age, sex, height, weight, intra-operative and post-operative complications, length of stay, operative time, and estimated blood loss. All revisions were excluded. Descriptive statistics such as mean and standard deviation were used to analyze the data.
The total sample size of the study was 5 patients, with a mean age of Weight loss patterns were the same as those without LF. All 5 patients had resolution or improvement in their GERD symptoms within 6 months. Mitzman et al stated that although the DS has been the most effective weight loss surgical procedure, it is a small minority of the total bariatric surgical cases performed.
Modifications that can make the operation technically simpler and reduce a long-term risk of short bowel syndrome would be of benefit. Data from patients who underwent a primary SIPS procedure performed by 2 surgeons at 2 centers from January to August were retrospectively analyzed. All revisions of prior bariatric procedures were excluded. Regression analyses were performed for all follow-up weight loss data.
The mean BMI was The authors concluded that modification of the classic DS to one with a single anastomosis and a longer common channel had effective weight loss results.
Morbidity appeared comparable to other stapling reconstructive procedures. Moreover, they stated that future analyses are needed to determine whether a SIPS procedure reduces the risk of future small bowel obstructions and micronutrient deficiencies. Cottam and colleagues stated that in bariatric surgery, the procedure with the highest average weight loss is the bilio-pancreatic diversion with duodenal switch BPDDS. Additionally, co-morbidity resolution, nutritional data, and complications were also compared.
Data were analyzed using both descriptive and comparative statistics. There also was no difference in nutritional data between the 2 procedures pre- and post-op.
Complication rates were lower in SIPS however, due to the small sample sizes this is not statistically significant. However, there are fewer complications with SIPS.
The main drawbacks of this study were its retrospective design and small sample size. To convert pounds to kilograms, multiply pounds by 0. To convert inches to meters, multiply inches by 0. For a simple and rapid calculation of BMI, please click below and it will take you to the Obesity Education Initiative.
Clinical Policy Bulletin Notes. Links to various non-Aetna sites are provided for your convenience only. Clinically significant obstructive sleep apnea i.
BMI exceeding 40 with one or more of the following serious co-morbidities: Medically refractory hypertension; or Dyslipidemias; or Nonalcoholic steatohepatitis; or Venous stasis disease; or Significant impairment in activities of daily living; or Intertriginous soft-tissue infections; or Stress urinary incontinence; or Gastroesophageal reflux disease; or Weight-related arthropathies that impair physical activity; or Obesity-related psychosocial distress.
Physician-supervised nutrition and exercise program: This physician-supervised nutrition and exercise program must meet all of the following criteria Member's participation in a physician-supervised nutrition and exercise program must be documented in the medical record by an attending physician who supervised the member's participation. The nutrition and exercise program may be administered as part of the surgical preparative regimen, and participation in the nutrition and exercise program may be supervised by the surgeon who will perform the surgery or by some other physician.
A physician's summary letter is not sufficient documentation. Documentation should include medical records of physician's contemporaneous assessment of patient's progress throughout the course of the nutrition and exercise program. For members who participate in a physician-administered nutrition and exercise program e. Behavior modification program supervised by qualified professional; and Consultation with a dietician or nutritionist; and Documentation in the medical record of the member's participation in the multi-disciplinary surgical preparatory regimen at each visit.
Records must document compliance with the program; the member must not have a net gain in weight during the program. A physician's summary letter, without evidence of contemporaneous oversight, is not sufficient documentation.
Documentation should include medical records of the physician's initial assessment of the member, and the physician's assessment of the member's progress at the completion of the multi-disciplinary surgical preparatory regimen. Aetna considers open or laparoscopic vertical banded gastroplasty VBG medically necessary for members who meet the selection criteria for obesity surgery and who are at increased risk of adverse consequences of a RYGB due to the presence of any of the following co-morbid medical conditions: Demonstrated complications from extensive adhesions involving the intestines from prior major abdominal surgery, multiple minor surgeries, or major trauma; or Hepatic cirrhosis with elevated liver function tests; or Inflammatory bowel disease Crohn's disease or ulcerative colitis ; or Poorly controlled systemic disease American Society of Anesthesiology ASA Class IV see Appendix ; or Radiation enteritis.
Experimental and Investigational Bariatric Surgical Procedures: Aetna considers each of the following procedures experimental and investigational because the peer-reviewed medical literature shows them to be either unsafe or inadequately studied: Gastrointestinal liners endoscopic duodenal-jejunal bypass, endoscopic gastrointestinal bypass devices; e.
Background These criteria were adapted from the NIH Consensus Conference on Surgical Treatment of Morbid Obesity which state that obesity surgery should be reserved only for patients who have first attempted medical therapy: Contraindications to Obesity Surgery: Requirement that Obesity be Persistent: Obesity Surgery in Children and Adolescents: Requirement for Psychological Evaluation: Oliveira et al stated that pathogenesis of non-alcoholic fatty liver disease NAFLD remains incompletely known, and oxidative stress is one of the mechanisms incriminated.
The aim of this study was to evaluate the role of liver oxidative stress in NAFLD affecting morbidly obese patients.
Female gender was dominant Histology showed fatty liver in Liver cirrhosis was present in Liver biochemical variables were normal in The authors concluded that non-alcoholic steatosis, steatohepatitis and cirrhosis were identified in substantial numbers of morbidly obese patients; and concentration of hydroperoxides was increased in steatohepatitis, consistent with a pathogenetic role for oxidative stress in this condition.
Bariatric Surgery and Pregnancy: Huang et al noted that the laparoscopic adjustable gastric band has been widely accepted as 1 of the safest bariatric procedures to treat morbid obesity. However, because of variations in the results and the complications that tend to arise from port adjustment, alternative procedures are needed.
These investigators enrolled 26 patients from May to August Laparoscopic adjustable gastric banded plication was performed using 5-port surgery. They placed Swedish bands using the pars flaccida method, divided the greater omentum, and performed gastric plication below the band to 3 cm from the pylorus using a single-row continuous suture.
The data were collected and analyzed pre- and post-operatively. The average post-operative hospitalization was 1. The mean excess weight loss at 1, 3, 6, 9, and 12 months after surgery was The mean follow-up time was 8.
Sclerotherapy for Dilated Gastrojejunostomy: Gersin et al examined the effects of an endoscopic DJBL for pre-operative weight loss in bariatric surgery candidates. A total of 21 obese subjects in the DJBL arm and 26 obese subjects in the sham arm composed the intent-to-treat population.
The subjects in the sham arm underwent an esophagogastroduodenoscopy and mock implantation. Both groups received identical nutritional counseling. The primary endpoint was the difference in the percentage of EWL at week 12 between the 2 groups. A total of 13 DJBL arm subjects and 24 sham arm subjects completed the week study. Total weight change in the DJBL arm was None had further clinical symptoms after DJBL explantation.
The authors concluded that the DJBL achieved endoscopic duodenal exclusion and promoted significant weight loss beyond a minimal sham effect in candidates for bariatric surgery. The main drawbacks of this study were: The OverStitch Suturing Device: Laparoscopic Greater Curvature Plication: Transoral Mucosal Excision Sutured Gastroplasty: Bariatric Surgery for Type-2 Diabetes: Interventions were implantation of either vBloc or sham devices and weight management counseling.
Most weight regain preceded unblinding. The authors concluded that weight loss with vBloc was sustained through 18 months, while sham regained weight between 12 and 18 months.
They stated that vBloc is effective with a low rate of serious complications. This study had several drawbacks: The authors noted that this study has several drawbacks: However, the baseline and demographic characteristics of the randomized, enrolled, and completer populations were analyzed for homogeneity and were not different in the AspireAssist and Lifestyle Counseling groups.
The consistency of study results by using different statistical analyses further indicated that withdrawals did not bias the results, this report included only 1-year results, and hence did not provide longer term safety and effectiveness of the AspireAssist therapy.
The placement and management of the A-tube was similar to percutaneous endoscopic gastrostomy tubes, which have been used in clinical practice for more than 35 years, so the short-term and long-term complications of this device are already well known, and the study population contained a high percentage of female participants, which is a common problem of weight loss studies.
Thus, these findings might not necessarily apply to men with obesity. Single-Incision Laparoscopic Sleeve Gastrectomy: This study had 2 main drawbacks: Consequently predicting its widespread applicability to all bariatric patients with reflux is premature and awaits larger trials, these researchers could not evaluate endoscopy or pH testing post-operatively in their patients, which is fundamental to evaluate the effect of anti-reflux surgery.
In addition to indicating underlying ASA status I - V , any patient undergoing an emergency procedure is indicated by the suffix "E". For example, a fundamentally healthy patient undergoing an emergency procedure is classified as I-E. If the patient is undergoing an elective procedure, the "E" designation is not used. CPT codes covered if selection criteria are met: Sleeve gastrectomy with SIPS - no specific code: S Adjustment of gastric band diameter via subcutaneous port by injection or aspiration of saline S Weight management classes, non-physician provider, per session S Exercise classes, non-physician provider, per session S Nutrition classes, non-physician provider, per session ICD codes covered if selection criteria are met: K30 Functional dyspepsia [dilated gastrojejunostomy] K Gastrointestinal surgery for severe obesity.
Consensus Development Conference Panel. Jones KB, et al. An effective anti-reflux procedure. Prospective hematologic evaluation of gastric exclusion surgery for morbid obesity.
Laparoscopic gastric banding; Preliminary series. The effect of gastric banding on weight loss in patients with morbid obesity. A review of seven years' experience with silicone gastric banding. Gastric banding for morbid obesity: Some patients may qualify for a care plan which can be arranged by your GP. You may apply to the Department of Human Services DHS for early release of superannuation funds to help cover the cost of weight loss surgery. Details of this may be found on the following DHS website:.
You may be eligible for an early release of superannuation to pay for necessary medical treatment or medical transport expenses for yourself or your dependant if either of you have:.
You will need the Adobe Reader to view and print these documents. Scientific Evidence for Obesity. Please use the following Out Of Pocket fees as a guide: Your initial consulatation is a very detailed discussion with Dr Hatzifotis, specifically tailored to you, and covers your medical and dietary history, and a comprehensive discussion around the weightloss procedure you decide upon. He will discuss in detail all of the advantages and disadvantages of your chosen procedure and the various risks involved, as well as answer any questions you may have.
Michael Hatzifotis you will be charged a Health Management fee. For privately insured patients this fee will cover: After the first 12 months, appointments are then annually. All band adjustments including needles and consumables Any further procedures should any complications arise.
Administration fee The Professional Health Management fees, for privately insured patients, are as follows: OPTIFAST VLCD Shake Chocolate Sachet 53g Pack of 18 is part of a nutritionally complete, very low calorie diet program, which contains all of the nutrients required for safe and effective weight loss, including protein to help you preserve lean muscle mass while you lose fat stores.
This great tasting Chocolate Shake is a satisfying, convenient and easy to prepare product that can be enjoyed for breakfast, lunch or dinner. The online support will help you set up you weight loss goals, meal plans and help you track your progress.
Very Low Energy Diet. Take an additional two litres of calorie-free fluid each day. Very Low Energy Diet: Additionally, consume a minimum of two litres of calorie-free fluid and at least two cups of low starch vegetables with one teaspoon of vegetable oil per day. A program of regular light exercise enhances wellbeing and the likelihood of success.
Contains Milk, Soy and Fish. Stir, blend or shake to dissolve. Do not use boiling water. All prepared products should be tightly covered and consumed within 6 hours at room temperature or within 24 hours if refrigerated. Do not change proportions.