Mobile therapy that works.1,2,3
The Monarch® Airway Clearance System is a high frequency chest wall oscillation (HFCWO) therapeutic device with revolutionary new technology. The therapy combines mobility with targeted kinetic energy and airflow to thin and mobilize secretions from the airways. By allowing patients to move about freely during therapy, it empowers them to take control of their therapy – and their lives.
Powered by POD technology.
The Monarch® System is used to aid mobilization of secretions from the airways to help improve airway health. This is achieved by the placement of eight pulmonary oscillating discs (PODs) containing magnets, over the upper and lower lobes of the lungs. The PODs oscillate and provide a targeted kinetic energy to the lungs. This therapy generates airflow to help thin and mobilize mucus from the small airways to the large airways, where it can be coughed out or suctioned.
Mobile and connected.
The Monarch® System helps motivate and empower patients to collaborate in their therapy by offering key attributes:
- Enabled with either LTE or WiFi connectivity.
- Connects patients wirelessly to their care team via the VisiView® Health Portal.
- Provides access to patient therapy session feedback.
- Encourages adherence through collaboration between patient and physician.
Sportswear-inspired design is made for freedom of mobility
Its quiet operation enables easy conversation.3 Fun colors and patterns let patients personalize their device.
Powers therapy on the move
Are intuitive and simple to use.
Used with Bluetooth® connectivity, streamlines device operation for patients.
Handy rolling case
With retractable handle and backpack straps, looks like ordinary luggage and makes it easy to travel with the device.
The man behind the Monarch® System
Marten De Vileger and his sister, both Cystic Fibrosis patients, grew up with their mother manually performing CPT to help clear their airways. With a vision for more independence, Marten created a mobile therapeutic device for airway clearance. This novel device gave him the freedom to travel and live his adventurous, kite-surfing life while raising a family. Wanting others to experience this flexibility and control, he partnered with Hill-Rom to develop the Monarch® Airway Clearance System.
Hill-Rom YouTube channel.
Monarch 3D Animation Video
Indications and Important Safety Information
Indications for Use4
The Monarch Airway Clearance System is intended to provide Airway Clearance Therapy and promote bronchial drainage where external manipulation of the thorax is the physician’s choice of treatment. It is indicated for patients having difficulty with secretion clearance, or the presence of atelectasis caused by mucus plugging. The Monarch Airway Clearance System is intended to be used in the Home Care environment by patients,15 years and older.
If any patient conditions exist that could cause the use of Monarch Airway Clearance System, Model 1000 to present a risk to the patient, do not use the unit except as directed by a physician. Death or serious injury could occur.
Monarch Airway Clearance System, Model 1000 is contraindicated if these conditions are present:
- Patients who have any of the following active implantable medical devices, due to the presence of the magnetic field created by the Monarch device, whether it is turned on or off:
- Infusion Pumps
- Circulatory Support Devices
- Implantable Cardioverter Defibrillators (ICDs)
- Cochlear Implants
- Head and/or neck injury that has not yet been stabilized.
- Active hemorrhage with hemodynamic instability.
The Monarch Airway Clearance System warnings include:
- Patients that may have difficulty clearing secretions from the upper airway (such as those with DMD or other advanced neuromuscular or neurological disorders) may require specialized therapy regiments involving manually or mechanically assisted coughing or other techniques in conjunction with Monarch Airway Clearance System. Please consult your physician to determine if additional therapy is appropriate.
- The Monarch System has been prescribed by your physician for your use only. No one else should ever try on your device, whether it is on or off. It should never be worn by someone with an active implantable medical device due to the presence of the magnetic field created by the Monarch Pulmonary Oscillating Discs (PODs).
For a complete list of Warnings or to obtain a copy of the User Manual, please call us at 800-426-4224.
1. Bench testing conducted in 2017. Testing was performed at the following therapy settings: The Vest® System Model 105 and the MonarchTM System Model 1000 with intensity/pressure set at 10, frequencies settings at 5, 14, and 20 Hz; the AffloVest® System was tested at the “Vibration” setting at “Low”, Medium” and “High” settings, which according to the AffloVest® web site operate at 5Hz, 13Hz, and 20Hz respectively. The AffloVest® Systems used were labeled as REF 8200 and 8300. Testing consisted of measuring impulse force, or applied force over a timeframe of 30 seconds, via 4 force sensors placed on a mannequin in upper and lower chest locations. Comparisons are not based on head to head clinical efficacy or safety studies.
2. Independent lab testing conducted in 2017. Data was analyzed and compared average pulse airflows at the mouth generated by high frequency chest wall oscillation (HFCWO) therapy in 10 human subjects using home care garments. Airflows were measured via pneumotachometer at settings of the following: The Vest® System Model 105 and the MonarchTM System Model 1000 with intensity/pressure set at 10, frequencies settings at 5, 10, 15, and 20 Hz; the AffloVest® System was tested at the “Vibration” setting at “Low”, Medium” and “High” settings, which according to the AffloVest® web site operate at 5Hz, 13Hz, and 20Hz respectively. The AffloVest® Systems used were labeled as REF 8200 and 8300. Comparisons are not based on head to head clinical efficacy or safety studies. Airflow test subjects were adult males with healthy lung function. Results for female subjects and patients with lung disease may vary from those in this study.
3. Sound testing per International Standard IEC 60601-1, 3rd Edition at a distance of 30 cm. Sound testing results found the Monarch System operates at a level at or below that considered as a “normal conversation”; reference https://www.nidcd.nih.gov/health/noise-induced-hearing-loss.
4. The Monarch Airway Clearance System Model 1000 User Manual (195292).
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