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. Author manuscript; available in PMC: 2023 Feb 21.
Published in final edited form as: BMJ Support Palliat Care. 2019 Aug 31;12(e2):e281–e284. doi: 10.1136/bmjspcare-2019-001819

Table 1.

Demographic and clinical characteristics of a convenience sample of adults with cystic fibrosis (N = 165)

Characteristic n (%)
Pulmonary impairment
 Mild (FEV1 ≥80%) 42 (25)
 Moderate (50%–79%) 58 (35)
 Severe or very severe (<49%) 65 (39)
Gender
 Male 92 (56)
 Female 73 (44)
Race
 Caucasian 161 (98)
 African-American 1 (1)
 Other or multiple races 3 (2)
Religiosity (importance of religion)
 Not at all important 34 (21)
 Not too important 36 (22)
 Fairly important 46 (28)
 Very important 49 (30)
Religious affiliation
 Protestant Christian 30 (18)
 Roman Catholic 44 (27)
 Other Christian 30 (18)
 Jewish 2 (1)
 Buddhist 1 (1)
 Agnostic/atheist/no religion 21 (13)
 Other 37 (22)
Age in years
 Median (range) 29 (18–66)
 18–29 84 (51)
 30–39 56 (34)
 40–49 14 (8)
 50+ 11 (7)
Education
 Some high school or less 4 (2)
 High school diploma/GED 52 (32)
 Vocational school 2 (1)
 Some college 32 (19)
 College degree 58 (35)
 Professional or graduate degree 17 (10)
Financial status
 Money left over 75 (45)
 Just enough money to make ends meet 69 (42)
 Not enough money to make ends meet 21 (13)
Relationship status
 Single 102 (62)
 Partnered/married 63 (38)
BMI (kg/m2)
 Median (range) 21.3 (15.2–43.0)
Transplant status
 Not evaluated or listed 159 (96)
 Awaiting transplant 5 (3)
 Post-transplant 1 (1)
CF-related diabetes
 No 100 (61)
 Yes 65 (39)
Pulmonary exacerbations in prior 12 months
 Median (range) 0 (0–21)
Hospitalisations in prior 12 months
 Median (range) 1 (0–36)
Health status
 Excellent 20 (12)
 Good 62 (38)
 Fair 63 (38)
 Poor 20 (12)

BMI, body mass index; CF, cystic fibrosis; FEV1, forced expiratory volume in 1 s.