Skip to main content
. 2019 Aug;16(8):1024–1033. doi: 10.1513/AnnalsATS.201902-112OC

Table 1.

Patient and caregiver participant characteristics (n = 20)

Characteristics Patients (n = 10) Family Caregivers* (n = 10)
Demographic characteristics    
 Age, yr 60.4 ± 7.5 58.3 ± 8.7
 African American race, % 5 (50) 4 (40)
 Male sex, % 7 (70) 1 (10)
 Married, % 3 (30) 5 (50)
 Education (high school graduate), % 5 (50) 5 (50)
 Health insurance, %    
  Medicare 5 (50) 5 (50)
  Uninsured 3 (30) 1 (10)
 Current Smoking, % 5 (50) 4 (40)
 Religious preference    
  Protestant, % 1 (10) 3 (30)
  None, % 3 (30) 1 (10)
  Regularly attends religious services 1 (10) 7 (70)
  Ever prayed for own health 7 (70) 9 (90)
 Prior palliative care 1 (10) n/a
 Advanced directive 1 (10) n/a
 Identified surrogate decision maker 3 (30) n/a
Clinical characteristics    
 Charlson comorbidity index 1.5 ± 1.0 n/a
 GOLD Stage    
  GOLD II (moderate), % 3 (30) n/a
  GOLD III (severe), % 3 (30) n/a
  GOLD IV (very severe), % 4 (40) n/a
 FEV1 % predicted 37.4 ± 20.4 n/a
 Supplemental oxygen, % 8 (80) n/a
 ≥One severe exacerbations in the year prior, % 3 (30) n/a
 Prior cardiopulmonary rehabilitation, % 4 (40) n/a
 Severe dyspnea§ 8 (80) n/a

Definition of abbreviations: FEV1 = forced expiratory volume in 1 second; GOLD = Global Initiative for Chronic Obstructive Lung Disease.

*

Family caregivers represented the following relationships with patients: spouse (n = 4), ex-spouse (n = 2), significant other (n = 2), child (n = 1), and parent (n = 1).

Derived from 19 comorbidities; higher scores associated with higher mortality.

Moderate = 50% ≤ FEV1 < 80%; severe = 30% ≤ FEV1 < 50%; very severe = FEV1 < 30%.

§

≥2 on the Modified Medical Research Council scale for dyspnea.