Keep the magnet at least 15 cm (6 inches) away from items sensitive to magnetic fields, including the ICM device when the magnet is not being used to initiate communication between the device and the patient or clinic app. It can also permanently disable some magnetic strip cards.

The magnet provided with the ICM system may cause interference with devices sensitive to magnetic fields such as hearing aids, pacemakers, and other implanted devices. Use of any other magnets has not been tested and could result in failure to initiate communication with the device. Magnet model 6386 has been tested for use with the ICM system. In situations where the risks are known, always interrogate the device and save data before the procedure, and check device function afterwards. The influence of medical equipment on implanted devices varies considerably according to the type of unit and energy levels employed. The interaction of diathermy therapy with an insertable cardiac monitor can damage the device and cause patient injury. To help prevent undesirable interactions, test the ICM system when used in combination with the co-implanted device.ĭo not expose a patient with an ICM system to diathermy. Verify sensing configuration, operation modes, surgical considerations and existing placement of all involved devices prior to any co-implant. Electromagnetic interference (EMI) or therapy delivery from the co-implanted device can interfere with ICM sensing and/or rate assessment, resulting in failure to monitor or record when needed. LATITUDE Clarity is contraindicated for use with any device other than a compatible Boston Scientific device.Ĭoncomitant use of the ICM system and implanted electro-mechanical devices can result in interactions that could compromise the function of the ICM, the co-implanted device, or both. However, the patient’s particular medical condition may dictate whether or not they can tolerate a subcutaneous, chronically- inserted device. There are no known contraindications for the insertion of the LUX-Dx insertable cardiac monitor. The LUX-Dx has not been tested specifically for pediatric use. The LUX-Dx is indicated for use in patients that have a known heart condition and are at risk of developing an abnormal heart rhythm, or have symptoms that may suggest a cardiac arrhythmia, such as dizziness, palpitations, syncope, chest pain, and/or shortness of breath. The recorded S-ECG is used for the clinical evaluation and diagnosis of cardiac arrhythmias. The LUX-Dx™ Insertable Cardiac Monitor (ICM) is intended to monitor and record subcutaneous electrocardiogram (S-ECG). Prior to use, please see the complete “User’s Manual” for more information on Indications, Contraindications, Warnings, Adverse Events, and Operator’s Instructions. LUX-Dx™ Insertable Cardiac Monitor System CAUTION: Federal law (USA) restricts this device to sale by or on the order of a physician. Medical Device ID Cards - Pacemaker, ICD, & CRT devices.Transcatheter Aortic Valve Replacement (TAVR).Cardiac Resynchronization Therapy (CRT) Devices.

Heart monitor implant side effects