Receiving a heart failure diagnosis can be difficult, but you’re not alone. More people than ever are living longer and improving their quality of life with today’s heart failure management options.
The CardioMEMS™ HF System enables earlier and more proactive treatment to slow down your heart failure progression and keep you out of the hospital.
The CardioMEMS HF System is the leading remote heart failure monitoring system with 25,000+ patients using the system and it is now approved for even more patients in earlier stages of heart failure.
Ask your doctor how the CardioMEMS HF System can help you LIVE MORE and WORRY LESS.
Pulmonary artery (PA) pressure monitoring provides early detection of worsening heart failure, long before symptoms such as weight gain or blood pressure. Daily pressure readings from home can proactively inform your care team of any needed adjustments to your medications and/or lifestyle without a hospital or clinic visit.
Find a heart failure clinic near you that offers the CardioMEMS HF System or call 1-855-4-CMEMSHF
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Brief Summary: Prior to using these devices, please review the Instructions for Use for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.
CardioMEMS™ HF System Indications and Usage: The CardioMEMS HF System is indicated for wirelessly measuring and monitoring pulmonary artery pressure and heart rate in NYHA Class II or III heart failure patients who either have been hospitalized for heart failure in the previous year and/or have elevated natriuretic peptides. The hemodynamic data are used by physicians for heart failure management with the goal of controlling pulmonary artery pressures and reducing heart failure hospitalizations.
CardioMEMS™ HF System Contraindications: The CardioMEMS™ HF System is contraindicated for patients with an inability to take dual antiplatelet or anticoagulants for one month post implant.
CardioMEMS™ HF System Potential Adverse Events: Potential adverse events associated with the implantation procedure include, but are not limited to, the following: air embolism, allergic reaction, infection, delayed wound healing, arrhythmias, bleeding, hemoptysis, hematoma, nausea, cerebrovascular accident, thrombus, cardiovascular injury, myocardial infarction, death, embolization, thermal burn, cardiac perforation, pneumothorax, thoracic duct injury and hemothorax.
myCardioMEMS™ Mobile App Limitations: Patients must use their own Apple‡ or Android‡ mobile device to receive and transmit information to the myCardioMEMS™ Mobile App. To do so the device must be powered on, app must be installed and data coverage (cellular or Wi-Fi‡) available. The myCardioMEMS™ Mobile App can provide notification of medication adjustments and reminders, requests for lab work and acknowledgement that the PA pressure readings have been received. However, there are many internal and external factors that can hinder, delay, or prevent acquisition and delivery of the notifications and patient information as intended by the clinician. These factors include: patient environment, data services, mobile device operating system and settings, clinic environment, schedule/configuration changes, or data processing.
Refer to the Instructions for Use for detailed indications, contraindications, warnings, precautions and potential adverse events.
MAT-2002896 v8.0
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Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company.
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The following pages are intended for medical professionals and provide information on the proper use of products (medical devices, etc.) of Abbott Medical Japan GK.
The information provided here is not intended to provide information to patients and the general public.
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