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Table 2 Clinicians’ Approaches to Major Depressive Disorder in People with Very Poor Prognoses Versus Better Prognoses

From: Caring for depression in the dying is complex and challenging – survey of palliative physicians

INTERVENTION

RESPONSE

PALLIATIVE PHYSICIANS

(n = 70)

[counts (%)]

a. Non-pharmacological interventions (e.g. supportive psychotherapy / counselling, cognitive therapy)

I don’t use

2 (2.9)

Less likely (cumulative)

26 (37.1)

No difference

26 (37.1)

More likely (cumulative)

12 (17.1)

No response

4 (5.7)

b. Typical antidepressant

I don’t use

3 (4.3)

Less likely (cumulative)

36 (51.4)

No difference

18 (25.7)

More likely (cumulative)

9 (12.9)

No response

4 (5.7)

c. Psychostimulant (e.g. methylphenidate, modafinil)

I don’t use

18 (25.7)

Less likely (cumulative)

3 (4.3)

No difference

4 (5.7)

More likely (cumulative)

18 (25.7)

No response

27 (38.6)

d. Atypical antipsychotics (e.g. risperidone, olanzapine)

I don’t use

26 (37.1)

Less likely (cumulative)

6 (8.6)

No difference

14 (20)

More likely (cumulative)

20 (28.6)

No response

4 (5.7)

e. Benzodiazepine

I don’t use

28 (40.0)

Less likely (cumulative)

2 (2.9)

No difference

12 (17.1)

More likely (cumulative)

24 (34.3)

No response

4 (5.7)

f. Novel medication / experimental trials (e.g. ketamine, esketamine nasal spray)

I don’t use

49 (70)

Less likely (cumulative

4 (5.7)

No difference

1 (1.4)

More likely (cumulative)

12 (17.1)

No response

4 (5.7)

g. Electroconvulsive therapy

I don’t use

51 (72.9)

Less likely (cumulative)

10 (14.3)

No difference

4 (5.7)

More likely (cumulative)

1 (1.4)

No response

4 (5.7)

  1. ≠ Due to a technical fault, the survey item exploring psychostimulant use was initially not accessible to the first 28 Australian and New Zealand Society of Palliative Medicine (ANZSPM) respondents