The Bravo™ reflux recorder is designed to record reflux data and patient activity for up to 96 hours.
The Bravo™ monitoring system is intended to be used for gastroesophageal pH measurement and monitoring of gastric reflux in adults and children from four years of age. The Bravo™ capsule can be attached following either endoscopy or manometry. The reflux/AccuView software application is intended to record, store, view, and analyze gastroesophageal pH data.
Patients with bleeding diathesis, strictures, severe esophagitis, varices, obstructions, pacemakers, or implantable cardiac defibrillators are contraindicated.
Patients are restricted from undergoing an MRI study for 30 days from the start of a pH study. The Bravo™ reflux testing system is not compatible for use in an MRI magnetic field. Use of the Bravo™ reflux testing system in an MRI magnetic field will result in damage to the system and possible patient injury .
Potential complications include, but are not limited to:
Potential complications include, but are not limited to the following:
The Bravo™ pH capsule with delivery device is a single-use, disposable device. Reuse or any other misuse of a Bravo™ pH capsule with delivery device (such as sharp bending or kinking) results in an increased potential for damage to the delivery device and capsule, and possible patient injury.
Prior to use, all equipment for the pH study should be examined carefully to verify proper function.
Unauthorized maintenance by inadequately trained personnel would result in an unacceptable risk (e.g., excessive temperatures, fire, or explosion).
A thorough understanding of the technical principles, clinical applications, and risks associated with the Bravo™ recorder is necessary before using this product. Read the entire manual before using the system for the first time.
No modification of this equipment is allowed.
Patients are restricted from undergoing an MRI study within 30 days of the pH study.
The Bravo™ capsule contains a trocar needle that is made of stainless steel. Use caution in patients with known sensitivities or allergies to the metals that are contained including chromium, nickel, copper, cobalt, and iron. Tests last from 48 to 96 hours.
Prior to the pH study, the patient should not eat or drink for a minimum of six hours.
If excretion of the Bravo™ pH capsule from the patient has not been positively verified, and the patient develops unexplained post-procedure abdominal pain, vomiting, or other symptoms of obstruction, the patient should contact the physician for evaluation and possible abdominal X-ray.
Undergoing an MRI while the Bravo™ pH capsule is inside the patient’s body may result in serious damage to the patient’s intestinal tract or abdominal cavity. If the patient did not positively verify the excretion of any Bravo™ pH capsule, the patient should contact the physician for evaluation and possible abdominal X-ray before undergoing an MRI examination.
Find more information, including other available configurations, for Bravo™ reflux recorder.
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