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Table 1 Participant characteristics

From: How can we improve the experiences of patients and families who request medical assistance in dying? A multi-centre qualitative study

Patient characteristics (n = 24)

 Gender, n(%)

Female 11 (46%)

Male 13 (54%)

 Age Range, n(%)

41–50, 1 (4%)

51–60, 4 (17%)

61–70, 6 (25%)

71–80, 5 (21%)

81–90, 5 (21%)

> = 91, 3 (12%)

 Diagnoses, n(%)

Cancer 15 (63%)

Amyotrophic lateral sclerosis 3 (12%)

Cardiovascular/Respiratory 4 (17%)

Other neurological 1 (4%)

Other (hotel) 1 (4%)

 Current location, n(%)

Hospital 18 (75%)

Home 5 (21%)

Other 1 (4%)

 European Cooperative Oncology Group Functional Status, n(%)

0, 1: 0

2: 3 (12%)

3: 8 (32%)

4: 8 (32%)

Unreported/unsure: 5 (20%)

 Preferred location of assisted dying, n(%)

Home 6 (24%)

Hospice 1 (4%)

Hospital 12 (50%)

No preference 3 (12%)

Other 2 (18%)

 Preferred route of medications for assisted dying, n(%)

Oral medications 1 (4%)

Intravenous 17 (71%)

No preference 6 (25%)

 Preferred timing of assisted dying, n(%)

Within one week 10 (42%)

One week to one month 4 (17%)

Greater than one month 5 (21%)

No preference 5 (21%)

Family member characteristics (n = 17)

 Gender, n(%)

Male 3 (18%)

Female 13 (76%)

Declined to answer 1 (6%)

 Age Range, n(%)

21–30, 1 (6%)

31–40, 0

41–50, 1 (6%)

51–60, 3 (18%)

61–70, 9 (53%)

71–80, 2 (12%)

81–90, 1 (6%)

 Location, n(%)

Ontario, 15 (88%)

British Columbia, 1 (6%)

Nova Scotia, 1 (6%)

 Relationship to patient, n(%)

Spouse/partner 6 (35%)

Child 7 (41%)

Sibling 2 (12%)

Friend 2 (12%)