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Riley Cystic Fibrosis Center Home Flu Update from our CF Center Director School/Daycare Information on CF |
Riley Hospital for Children/Indiana University is one of more than 115 care centers across the country accredited by the Cystic Fibrosis Foundation. We work closely as a team and with the CF Foundation to continue to improve care and the quality of life for our patients. Since the CF Foundation was established in 1955, we've all made great strides in treating this disease. Today, the predicted median age of survival for people with CF is 38 years. We are proud of this progress. And, we're always striving to improve. It is our desire and our responsibility to provide the best possible care to you and/or your child. In December 2007, the CF Foundation took another significant step in quality improvement by publicly reporting health outcomes data for all care centers on their web site: www.cff.org. The CF Foundation is providing this information proactively to accelerate the quality of care for individuals with CF – and to further strengthen the relationship between persons with CF, their families, and the care center. The data shows center-specific health outcomes results, how they compare to national averages and aggressive national goals established by medical experts. It includes four measures vital to the health of people with CF:
We encourage you to review the public reports on the web site. We also have our center's data available in clinic. Keep in mind the numbers posted on the web site are only part of the story. The outcomes relate in part to your follow through on the treatment plan that we have discussed in clinic. If you are having trouble following your treatment plan, please let us know so we can work with you to adapt the care plan. Our center has implemented standardized prescribing practices. Standardized prescribing practices assist in making all therapies available to all who may benefit from available therapies. We are focusing on areas that promote optimal lung health. Our goal is to work with you to provide the best long-term outcome for you and/or your child. The Cystic Fibrosis Foundation is recommending a Body Mass Index (weight in relation to height) for all persons with cystic fibrosis to be at least at the 50th percentile. New studies have shown that persons with CF who are well nourished tend to have better lung function. On the day of your visit, body mass index of all patients scheduled for clinic that day have been calculated by the dietitian and provided to your CF pulmonologist. At each patient's annual screen, growth charts as well as body mass index percentiles and weight goals are provided to each family. If there is a concern about weight, please feel free to discuss the treatment options to improve nutritional status with your CF health care providers. As a Center, we remain committed to the Seven Worthy Goals instituted by the CF Foundation and look forward to you and your family joining in our mission to achieve the best possible care plan for our patients. These goals are as follows:
If you have questions or suggestions, please call your physician or a member of the care team or make an appointment to see us in clinic. We want to work with you to improve both your care and health outcomes and our center's care and health outcomes. We look forward to seeing you soon. |