About Cystic Fibrosis
Cystic fibrosis (CF) is an inherited disease resulting from the amount or function of a cell protein called the cystic fibrosis transmembrane regulator (CFTR). Problems with CFTR alter how the body adjusts salt and water in certain tissues and body fluids. A signature of CF is a high salt concentration in the sweat. Mucus another fluid normally produced in several organ systems becomes thick and sticky. This leads to tissue damage as mucus builds up and interferes with the normal function of those organs. The lungs are primarily affected in most individuals with CF: thick mucus blocks the airways and allows for infection by various types of microbes. Thick mucus also impacts other organ systems including the gastrointestinal tract (pancreas, liver, gallbladder, and intestines), reproductive tract and the upper respiratory tract (sinuses). These result in other complications of CF such as difficulty digesting and absorbing nutrients from food, impaired intestinal motility, increased risk for diabetes, and problems with infertility. While CF is a chronic and usually progressive disease, advances in CF therapies and disease management in recent decades, have improved survival dramatically. Median survival of patients with CF is now in the late 30s, and many patients are living with CF in their 50s and beyond. Sustaining health by following daily self-care regimens and regular visits with an integrated Adult Cystic Fibrosis Care Team has enabled many individuals to grow into adulthood and live full lives.
UCSF Adult Cystic Fibrosis Program
Adults with cystic fibrosis have received care at UCSF for over thirty years. Many cystic fibrosis specialists throughout the State of California were trained by the Pulmonary Division of UCSF Department of Medicine.
The UCSF Adult Cystic Fibrosis Program is accredited by the Cystic Fibrosis Foundation and the State of California Department of Health. The Adult CF Program is led by adult lung specialists in the Division of Pulmonary and Critical Care Medicine (Mary Ellen Kleinhenz, MD). Individuals who are 18 years of age and older are seen, including many older individuals with CF. A team of experienced providers from nursing, nutrition, social work and respiratory therapy provide the expert care required by adults with CF in the ambulatory and inpatient settings. The Adult CF Care team also works closely with the pediatric CF care team at UCSF to help prepare patients for the transition from pediatric to adult CF Care. This integrated CF care team approach addresses and manages the needs and issues faced by CF patients and their families.
- Adult CF Program Director: Mary Ellen Kleinhenz, MD
- Nurse Practitioner: Diana Dawson, PNP
- Respiratory Therapist: Jeff Tarnow, RRT
- Nutritionist/Dietician: Evalyn Carbrey, RD
- CF Social Worker: Monica Eisenhardt, LCSW
In addition, CF patients who require hospitalization are cared for by adult pulmonologists on the Advanced Lung Disease Service who are experienced in caring for patients with CF.
The Adult Cystic Fibrosis Care team sees patients weekly on Wednesday mornings in the Chest Practice (5th Floor) of the UCSF Ambulatory Care Center, 400 Parnassus Avenue. Appointments can be scheduled at
- Initial appointments are made by referral from a patient’s primary care physician, pulmonologist or another CF Center. Current medical records will be requested and reviewed. Patients will be contacted with an appointment date and time. Patients will continue to see their primary care physician for health needs that are unrelated to cystic fibrosis.
- For patients who are transitioning from the UCSF Pediatric CF Center, the Adult CF team makes every effort to meet the patient and family prior to a first appointment in the Adult Clinic at Parnassus. This may take place in the hospital or pediatric clinic setting depending on circumstances.
- To meet special needs of young adults who are transferring to Adult CF Care while in college or living with family in the East Bay, we have initiated an “outreach” clinic in Pleasanton, CA staffed by our adult nurse practitioner, Diana Dawson, PNP. The “outreach” clinic is available to patients with stable health and an effective CF regimen. Patients attending this outreach clinic agree to be seen by Adult CF Team during CF Clinic on the Parnassus campus at least once each year.
- Follow-up visits 4 times a year are encouraged for all patients, as recommended by Cystic Fibrosis Foundation CF Care guidelines. For patients with limited travel resources, there may be assistance available from Medi-Cal or other programs. Patients are urged to contact the Adult CF Social Worker, Monica Eisenhardt, LCSW, for information. The Adult CF Care Team is highly vested in the care and well-being of our patients. In return, we expect patients will make every effort to participate responsibly in their medical care.