Weight Loss Balloon

Weight Loss Balloon
Weight Loss Balloon

References: 1. Reshape the patient Portal Data. The data file to the. Establish Medical, Inc.

It Is Important To Form Integrated Dual Balloon System Security Information

Indications: establishing Integrated Dual Balloon System is indicated for weight loss when used in conjunction with diet and exercise, against the patient’s obesity with a body mass index (BMI) 30 – 40 kg/m2 and one or more obesity-related a State of komorbiditas. It is indicated for use against adult patients who’ve failed the reduction of weight by diet and exercise alone.

Contraindications: establishing Integrated Dual Balloon system is not recommended for patients with a State that is able to increase the risk of a bad outcome (for example, before going to surgery channel cerna with sequelae, before going to open or laparoscopic Bariatric Surgery, inflammatory diseases of the gastrointestinal tract, the potential of upper GI bleeding), who are willing to participate in setting up medical supervised diet and behavior modification programs that are already an alcohol or drug addiction, which receives daily Healing with prescribed aspirin, anti-inflammatory, anticoagulant or other irritation of the stomach, or the pas is the middle or perhaps pregnant or breastfeeding.

Warning: the maximum period of the placement to form Integrated Dual Balloon is 6 months. Intragastrik balloon deflation risks and obstruction of the bowel (and therefore perhaps the complications associated with bowel obstruction) were significantly higher when the balloon was left in place for more than 6 months. The presence of blue-green urine or suddenly lose a sense of satiety, increasing hunger and/or weight gain perhaps gestures of balloon deflation. Patients who experience symptoms of acute pancreatitis (eg, acute abdominal pain, nausea, or vomiting) need to seek treatment immediately. The failure of patients to take over the daily prescribed proton pump inhibitors-medications that increase the risk of gastric ulceration or perforation.

Side effects: the placement of the form the Integrated Dual Balloon requires endoscopy with action for anesthesia. Potential risk of the subject with endoscopy and sedation had an adverse reaction to sedation (headache, muscle pain, nausea), infections, pneumonia, and breathing problems. Potential risk of the subject by forming Integrated Dual Balloon like acute pancreatitis, ulceration, and perforation, significant bleeding stomach, gastric outlet obstruction, aspiration pneumonia, abdominal pain, nausea, vomiting, bloating, belching, pain solar plexus, dehydration, and sore throat. This complication can afford adequate for initial removal requires a chronic Form Integrated Dual balloon. Although the Form of Dual Balloon designs provide anti-Migration feature, there is a potential risk of bowel obstruction and migration. Risk of bowel obstruction increases if the device is not removed after 6 months. If migration occurs, bowel surgery or endoscopic removal is probably needed. (05-26-2017)

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