1. Background
2. Objectives
3. Methods
| Items | Answers |
|---|---|
| Type of the underlying disease regarding the need for cognitive assessment in ECT-candidate patients | Mood disorder, Psychosis, Catatonia, Other |
| Need for initial cognitive assessment in patients receiving ECT | Yes/No |
| The referral rate for initial cognitive assessment in patients receiving ECT | Yes/No |
| Recommended intervals for cognitive assessment | At the baseline before ECT; After each ECT session; After the end of the second session; After the end of the third session; After the end of the fourth session; After the termination of ECT; 1 month after the termination of ECT; 2 months after the termination of ECT; 3 months after the termination of ECT; 6 months after the termination of ECT; 12 months after the termination of ECT |
| Recommended duration for cognitive assessment | 30 minutes; 60 minutes; 90 minutes; 120 minutes |
| Recommended tools for cognitive evaluation | Trail Making Test; Delis-Kaplan Executive Function System; Rey Auditory Verbal Learning Test; Wechsler Memory Scale-Revised; Color Word Interference Test; Controlled Oral Word Association Test; Kopelman’s Autobiographical; Memory Interview; Montreal Cognitive Assessment Test |
| Recommended intervention in case of severe cognitive impairment after receiving ECT | ECT continuation; ECT cession; Decreased dose and interval of ECT; Depending on the severity and patient’s condition |
| Recommended treatment in case of post-ECT cognitive impairment | Modafinil; Cholinesterase inhibitors; Cognitive rehabilitation |
| Barriers related to patient’s cognitive assessment | Failure to complete the test due to the patient’s psychiatric symptoms; Patient noncooperation due to the duration of the evaluation; Lack of examiner’s expertise; Lack of proper guidelines for cognitive assessment; Lack of sensitive tests for cognitive screening |
Abbreviation: ECT, electroconvulsive therapy.
4. Results
4.1. Previous Experience of Research Projects and Clinical Observations Related to Cognitive Assessment and ECT
4.2. Type of Underlying Disease Regarding the Need for Cognitive Assessment in ECT-Candidate Patients
4.3. Preferred Cognitive Tools for Cognitive Assessment
| Recommended Batteries | Professors | Residents | Nurses | Total | P-Value |
|---|---|---|---|---|---|
| Trail Making Test | 1 (7.7) | 7 (41.2) | N-O | 8 (13.8) | 0.002 |
| Delis-Kaplan Executive Function System | 4 (33.3) | 8 (47.1) | 3 (15.8) | 15 (25.9) | 0.128 |
| Rey Auditory Verbal Learning Test | 1 (7.7) | 3 (17.6) | 8 (42.1) | 12 (20.7) | 0.061 |
| Wechsler Memory Scale-Revised | 6 (46.2) | 10 (58.8) | 9 (47.4) | 25 (43.1) | 0.727 |
| Color Word Interference Test | N-O | N-O | 1 (5.3) | 1 (1.7) | 0.447 |
| Controlled Oral Word Association Test | 1 (7.7) | N-O | 1 (5.3) | 2 (3.4) | 0.542 |
| Kopelman’s Autobiographical Memory Interview | 2 (15.4) | 1 (5.9) | 6 (31.6) | 9 (15.5) | 0.132 |
| Montreal Cognitive Assessment Test | 1 (1.7) |
Abbreviation: N-O, none observed.
aValues are expressed as No. (%).
4.4. Recommended Duration for Cognitive Assessment
| Professors | Residents | Nurses | Total | P-Value | |
|---|---|---|---|---|---|
| Recommended duration for cognitive assessment | 0.062 | ||||
| 30 minutes | 12 (92.3) | 16 (76.2) | 10 (50.0) | 38 (65.5) | |
| 60 minutes | N-O | 2 (9.5) | 8 (40.0) | 10 (17.2) | |
| 90 minutes | N-O | 2 (9.5) | 1 (5.0) | 3 (5.2) | |
| 120 minutes | 1 (7.7) | 1 (4.8) | N-O | 2 (3.4) | |
| No recommendation | 5 (6.8) |
Abbreviation: N-O, none observed.
aValues are expressed as No. (%).
4.5. Proposed Interval for Cognitive Assessment
4.6. Recommended Approach in Case of Severe Cognitive Impairment After Receiving ECT
| Cognitive Assessment Interval | Professors | Residents | Nurses | Total | P-Value |
|---|---|---|---|---|---|
| At the baseline | 14 (93.3) | 15 (75) | 7 (35.0) | 36 (62.1) | 0.001 |
| After each electroshock session | 3 (20.0) | 6 (30.0) | 6 (30.0) | 15 (25.9) | 0.760 |
| After the end of the second session | N-O | 3 (15) | 1 (5.0) | 4 (6.9) | 0.212 |
| After the end of the third session | 5 (33.3) | 3 (15) | 3 (15) | 11 (19) | 0.318 |
| After the end of the fourth session | N-O | 3 (15) | 1 (5.0) | 4 (6.9) | 0.212 |
| After the end of the electroshock | 7 (46.7) | 6 (30.0) | 6 (30.0) | 19 (32.8) | 0.512 |
| 1 month after the end of the electroshock | 2 (13.3) | 2 (10.0) | 5 (25) | 9 (15.5) | 0.410 |
| 2 months after the end of the electroshock | 2 (13.3) | 2 (10.0) | 1 (5.0) | 5 (8.6) | 0.687 |
| 3 months after the end of the electroshock | 5 (33.3) | 3 (15.0) | 1 (5.0) | 9 (15.5) | 0.079 |
| 6 months after the end of the electroshock | 6 (40.0) | 9 (45.0) | N-O | 15 (25.9) | 0.003 |
| 12 months after the end of the electroshock | 1 (6.7) | 7 (35.0) | N-O | 8 (13.8) | 0.004 |
Abbreviation: N-O, none observed
aValues are expressed as No. (%).
4.7. Recommended Intervention in Case of Post-ECT Cognitive Impairment
4.8. Limitations in Patient’s Cognitive Assessment
| Professors | Residents | Nurses | Total | P-Value | |
|---|---|---|---|---|---|
| Failure to complete the test due to patient’s psychiatric problems | 12 (85.7) | 17 (81.0) | 9 (45.0) | 38 (65.5) | 0.013 |
| Lack of sensitive tests | 6 (42.9) | 5 (23.8) | 5 (25.0) | 16 (27.6) | 0.421 |
| Patient noncooperation due to the duration of the evaluation | 7 (50.0) | 14 (66.7) | 9 (45.0) | 30 (51.7) | 0.351 |
| Lack of cooperation of the responsible physician | N-O | 1 (4.8) | N-O | 1 (1.7) | - |
| Lack of proper guidelines | N-O | 1 (4.8) | N-O | 1 (1.7) | - |
Abbreviation: N-O, none observed
aValues are expressed as No. (%).