What psychosocial issues do adolescent cystic fibrosis (CF) patients experi
ence after undergoing lung transplantation (Tx)? The aim of this study was
to determine, using an ethnographic study design, the common themes and emo
tional responses in post-lung transplant adolescent CF patients of the Card
iothoracic Transplant Clinic at the Childrens Hospital Los Angeles. Ninetee
n CF lung transplant recipients were studied (eight males, 11 females: mean
age at time of transplant, 15.7 +/- 2.7 yr). The mean time interval from T
x to interview was 25.4 months (range 1-58 months). Sixteen patients had li
ving donor lobar lung Tx while three patients received cadaveric lungs. A s
eries of 25 questions was used to assess the psychosocial impact of Tx, and
a semistructured interview focused on the following five domains: lifestyl
e, family functioning, social functioning, body image, and psychological fu
nctioning. The major themes identified by patients included: a strong desir
e to set and attain meaningful long-range goals, the need to control as man
y aspects of their lives as possible while dealing with parental over-prote
ctiveness, and the adjustment to a new lifestyle. Common emotional response
s included manageable fear/anxiety of lung rejection and uncertainty of the
future, impatience with disruptions of daily routines caused by post-trans
plant medical management and its effect on the attainment of set. goals, an
d frustration with parental over-protectiveness. In general, patients repor
ted a positive outlook on life, with greater emphasis on sought-after goals
as well as inter-personal relationships. This study demonstrates that adol
escent CF transplant recipients develop long-term goals and plans for indep
endence. By identifying and anticipating the emotional needs of this popula
tion, health care providers call assist patients in improving the quality o
f their lives from a physioiogical, as well as a psychological, viewpoint.