I'm interested in learning how your CF center is handling the transition from pediatric to adult CF care. We are served by a clinic that has a very small CF population. The number of patients becoming adults can be counted on one and a half hands.
There are 3 doctors involved in the clinic, the director (peds), a doc who sees adults, and a new doc who refuses to see patients over 18 because she feels that they belong in the "adult" program. [Whatever the heck that is!]
Another factor effecting this is that the adult program will admit to the adult hospital rather that the children's hospital. One of the problems I see with this is that the CF nursing expertise is deep and extraordinarily competent and caring on the peds side. Can you imagine the adult nursing staff dealing with just a few adult CF patients showing up periodically? The peds nurses know every CFer by name, condition, medical needs, etc.
The new "adult" program was instituted without a single word of input from the CFers transitioning to adult care.
Remember this is a program that has produced a handful of adult CFers. It does not have an adult population of dozens.
I'm tempted to write to the center director to express my displeasure on how the how division of care was artificially created, the complete lack of patient input, and the potential for substandard care under the new arrangement.
I would be very interested in learning about the pedi to adult transition in centers with a population less than 200 or so.
I would also welcome your thoughts in general on this topic.
There are 3 doctors involved in the clinic, the director (peds), a doc who sees adults, and a new doc who refuses to see patients over 18 because she feels that they belong in the "adult" program. [Whatever the heck that is!]
Another factor effecting this is that the adult program will admit to the adult hospital rather that the children's hospital. One of the problems I see with this is that the CF nursing expertise is deep and extraordinarily competent and caring on the peds side. Can you imagine the adult nursing staff dealing with just a few adult CF patients showing up periodically? The peds nurses know every CFer by name, condition, medical needs, etc.
The new "adult" program was instituted without a single word of input from the CFers transitioning to adult care.
Remember this is a program that has produced a handful of adult CFers. It does not have an adult population of dozens.
I'm tempted to write to the center director to express my displeasure on how the how division of care was artificially created, the complete lack of patient input, and the potential for substandard care under the new arrangement.
I would be very interested in learning about the pedi to adult transition in centers with a population less than 200 or so.
I would also welcome your thoughts in general on this topic.