Remote Monitoring for Cystic Fibrosis
At Keva Health, we understand the challenges of managing Cystic Fibrosis. Our advanced remote patient monitoring program uses devices like pulse oximeters and spirometers to track vital signs and lung function between office visits, ensuring continuous care and timely interventions.
The platform monitors breathing difficulties, flare-ups, oxygen levels, airway clearance routines, and medication adherence with real-time alerts—helping you gain deeper insights, act early, and support better long-term disease management from anywhere.
Keva365 Platform for COPD Patients
With Keva Health’s program, patients can manage their symptoms more proactively, with personalized insights and seamless care coordination.
Platform Features
Log Daily Symptoms
With Cystic FIbrosis monitoring on Keva365, patients record breathlessness, cough, and flare-ups daily to build a complete picture of trends over time.
Receive Alerts
Access to real-time notifications about any changes helps patients respond to issues quickly.
Enhanced Communication
Keva365 allows patients to share their health data with your care team, supporting timely decisions and more personalized Cystic FIbrosis management.
Monitor Lung Function
Track your spirometer readings and oxygen levels to stay on top of your lung function and detect early signs of decline.
Personalized Care Plans
Get access to your remote patient monitoring report, then share it with your physician to create your personalized care plan.
Virtual Care 24/7
Patients may access the platform and get personalized tips at anytime.
Are you a patient with Cystic FIbrosis?
Fill out this form to request more information or contact us! We can get in touch with your doctor to set up the program.
Keva365 Platform for Providers
Keva365 is a Physician’s tool for Cystic FIbrosis management and monitoring optimization in between visits.
HIPAA Compliant Solution
Our HIPAA-compliant and secured SaaS platform allows you to collect patient data in between clinic visits.
Home Spirometry Access
Bluetooth devices (pulse oximeter and spirometer) allow patients to monitor respiratory health.
Personalized Workflows
Treatment pathway decision making for patients and their stratification through workflows made easy.
2-Way Communication
Get regular reports to track patient progress, manage care between visits, and use customizable alerts to save time while delivering quality care.
What is Cystic FIbrosis?
Cystic fibrosis (CF) is a genetic condition that affects a protein in the body. People with cystic fibrosis have a faulty protein that affects the body’s cells, its tissues, and the glands that make mucus and sweat. People with CF may face persistent cough that produces thick mucus (sputum), wheezing, exercise intolerance, repeated lung infection, inflamed nasal passages or a stuffy nose, recurrent sinusitis.
Why Monitoring Matters
Cystic Fibrosis symptoms can change quickly, and without consistent monitoring, early signs of worsening lung function or infection may go unnoticed until they become serious. Continuous symptom tracking, lung function monitoring, airway clearance, and medication adherence are critical to managing the condition effectively.