Cystic Fibrosis Clinic
At the Pediatric Cystic Fibrosis Clinic at BBCH, we’re here to help young patients and their families meet these challenges – and live a full and happy life. Despite the seriousness of their disease, children with Cystic Fibrosis (CF) can still do the things that most kids do, like go to school and participate in activities with their friends. We are here to help children with CF enjoy a good quality of life while taking care of their health.
We are also a CF Foundation Therapeutic Development Network (TDN) Center. The TDN is a nationwide network of nearly 80 CF clinical research centers specializing in clinical trials to evaluate the safety and effectiveness of new CF therapies. The TDN is currently involved in trials for gene therapy, protein-assist therapy, anti-infective drugs and other treatments – giving children with CF in Maine and New Hampshire access to the same promising new treatments at any other top CF Center in the country. We notify families of any trial in our clinic that they qualify for to give them the choice to participate in clinical research.
Learn more about what to expect at the clinic and understand diagnosis and treatment options.
The Pediatric CF Clinic is held weekly and the entire CF team is available to see each patient. We have a daily pulmonary clinic for emergency care and pulmonary nurses taking phone calls every day to answer your questions. The CF Foundation recommends that individuals with CF be seen in clinic at least four times a year. This not only ensures optimal care, but it also gives us the opportunity to really know our patients as individuals, tailor the care we provide to meet their unique needs and, ultimately, help them to live full lives.
Once each year, we’ll perform a comprehensive evaluation and exam. This includes lab tests, lung function tests and a chest x-ray. We’ll review these test results on the day of your child’s appointment. Following each visit, we’ll provide an updated care plan to you and your child’s primary care physician. We also encourage parents to coordinate their child’s vaccinations, routine medical care and non-CF related health issues with their primary care physician.
In accordance with State of Maine recommendations, all infants born in Maine are screened at birth for CF if the family agrees. Genetic counseling is available to parents of infants who screen positive for CF or who are carriers of the CF gene. We work closely with the state newborn screening laboratory to make sure we serve as a resource to these families during the difficult time of the initial CF diagnosis and we strive to see families within 24 hours of a CF diagnosis to answers the families questions and relieve their fears. Learn more about the CF screening process here.
If an abnormal screening is found, the sweat test is the standard test for diagnosing CF. The sweat test is a simple and painless procedure that measures the amount of salt in the sweat. A high salt level indicates CF. The CF Foundation recommends that the sweat test be performed at a CF Foundation-accredited care center such as ours which has strict guidelines to ensure accurate results. Genetic testing can also be used as necessary to diagnose CF.
Besides providing expert care for people with CF, we collect data from all our patients the national CF Foundation Patient Registry, which is a rich resource for parents, health care professionals and CF researchers to track the health of people living with CF in the U.S. Our data can be seen on the CF Foundation website.