南方医科大学学报 ›› 2026, Vol. 46 ›› Issue (1): 104-112.doi: 10.12122/j.issn.1673-4254.2026.01.11
安建雄1,2,3(
), 迟智佳3, 赵彩群3, 李永祥3, 王若国3, 胡亚楠1,2(
)
收稿日期:2025-07-15
出版日期:2026-01-20
发布日期:2026-01-16
通讯作者:
胡亚楠
E-mail:anjianxiong@yeah.net;huyanan1998@yeah.net
作者简介:安建雄,教授,博士生导师,E-mail: anjianxiong@yeah.net
基金资助:
Jianxiong AN1,2,3(
), Zhijia CHI3, Caiqun ZHAO3, Yongxiang LI3, Ruoguo WANG3, Yanan HU1,2(
)
Received:2025-07-15
Online:2026-01-20
Published:2026-01-16
Contact:
Yanan HU
E-mail:anjianxiong@yeah.net;huyanan1998@yeah.net
摘要:
目的 比较多次电刺激下显著延长癫痫波发作的超级电休克(super ECT)对难治性抑郁的治疗疗效。 方法 基于人群的队列研究纳入2024年12月~2025年6月接受super ECT的难治性抑郁患者292例。根据一次super ECT中电击次数分为3组:E1组为一次ECT过程电击1次(n=88),E2组为一次ECT过程电击2次(n=89),E3组为一次ECT过程电击3次(n=39)。分析基线抑郁、焦虑和失眠量表评分之间的相关性。首次疗程后第1、3、6个月利用汉密尔顿抑郁量表-17(HAMD-17)评估抑郁症状,基于减分率比较3组治疗缓解率和反应率。比较6个月内治疗次数,再住院率和不良反应发生率。分析首次super ECT治疗时的脑电图(EEG)癫痫波发作持续时间。 结果 E1组74例(84.09%)、E2组76例(76.40%)、E3组32例(82.05%)患者在super ECT后6个月内达到缓解。在6个月内super ECT治疗疗程在E1组为2.13±1.44次,E2组为2.23±2.01次,E3组为2.41±2.15次。基线HAMA、HAMD-17和PSQI评分相关(P<0.001)。第1次癫痫波发作时间在E1组显著高于E2和E3组(P<0.001)。E2组3个月和6个月的再住院率高于E1组(P=0.012、0.026)。短期不良反应包括发热、头痛/头晕、全身痛和口干。 结论 super ECT作为该领域的技术创新方法在>180 s的发作时间下具备临床安全性和有效性。一次麻醉下电击次数对治疗效果无明显影响。
安建雄, 迟智佳, 赵彩群, 李永祥, 王若国, 胡亚楠. 超级电休克在难治性抑郁中应用的临床研究:一项回顾性研究[J]. 南方医科大学学报, 2026, 46(1): 104-112.
Jianxiong AN, Zhijia CHI, Caiqun ZHAO, Yongxiang LI, Ruoguo WANG, Yanan HU. Efficacy and safety of super electroconvulsive therapy for treatment-resistant depression: a retrospective analysis of 292 cases[J]. Journal of Southern Medical University, 2026, 46(1): 104-112.
| Index | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
| Age (year, Mean±SD) | 27.97±12.83 | 30.43±10.48 | 27.84±12.02 | 0.299 |
Gender [n (%)] Male Female | 43 (48.31) 45 (51.14) | 54 (60.67) 35 (39.33) | 18 (46.15) 21 (53.85) | 0.469 0.513 |
| BMI (kg/m2, Mean±SD) | 28.23±5.35 | 29.23±8.22 | 27.23±7.46 | 0.423 |
Education [n (%)] None ≤6 years >6 years | 13 (14.77) 10 (11.36) 65 (73.86) | 11 (12.36) 18 (20.22) 60 (67.42) | 3 (7.69) 7 (17.95) 29 (74.36) | 0.348 0.472 0.621 |
Medications [n (%)] Antidepressant Sleep medicine | 88 (100) 67 (76.14) | 89 (100) 70 (78.65) | 38 (97.43) 31 (79.48) | 0.989 0.863 |
Suicide attempt [n (%)] Within 1 year No | 62 (70.45) 26 (29.55) | 54 (60.67) 35 (39.33) | 30 (76.92) 9 (23.08) | 0.437 0.265 |
Diagnosis [n (%)] Without psychotic features With psychotic features | 56 (63.64) 32 (36.36) | 61 (68.54) 28 (31.46) | 27 (69.23) 12 (30.77) | 0.652 0.537 |
Anesthesia induction (Mean±SD) Scopolamine (mg) Propofol (mg) Remifentanil (μg) | 0.32±0.07 52.21±5.15 198.31±22.22 | 0.30±0.08 55.34±21.45 202.26±24.14 | 0.30±0.09 51.67±4.49 200.26±24.97 | 0.831 0.243 0.529 |
| Duration between propofol and electric stimulus (min) | 12.11±1.53 | 11.88±1.71 | 12.18±1.75 | 0.522 |
表1 3组一般资料
Tab.1 General characteristics of the patients in the 3 groups
| Index | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
| Age (year, Mean±SD) | 27.97±12.83 | 30.43±10.48 | 27.84±12.02 | 0.299 |
Gender [n (%)] Male Female | 43 (48.31) 45 (51.14) | 54 (60.67) 35 (39.33) | 18 (46.15) 21 (53.85) | 0.469 0.513 |
| BMI (kg/m2, Mean±SD) | 28.23±5.35 | 29.23±8.22 | 27.23±7.46 | 0.423 |
Education [n (%)] None ≤6 years >6 years | 13 (14.77) 10 (11.36) 65 (73.86) | 11 (12.36) 18 (20.22) 60 (67.42) | 3 (7.69) 7 (17.95) 29 (74.36) | 0.348 0.472 0.621 |
Medications [n (%)] Antidepressant Sleep medicine | 88 (100) 67 (76.14) | 89 (100) 70 (78.65) | 38 (97.43) 31 (79.48) | 0.989 0.863 |
Suicide attempt [n (%)] Within 1 year No | 62 (70.45) 26 (29.55) | 54 (60.67) 35 (39.33) | 30 (76.92) 9 (23.08) | 0.437 0.265 |
Diagnosis [n (%)] Without psychotic features With psychotic features | 56 (63.64) 32 (36.36) | 61 (68.54) 28 (31.46) | 27 (69.23) 12 (30.77) | 0.652 0.537 |
Anesthesia induction (Mean±SD) Scopolamine (mg) Propofol (mg) Remifentanil (μg) | 0.32±0.07 52.21±5.15 198.31±22.22 | 0.30±0.08 55.34±21.45 202.26±24.14 | 0.30±0.09 51.67±4.49 200.26±24.97 | 0.831 0.243 0.529 |
| Duration between propofol and electric stimulus (min) | 12.11±1.53 | 11.88±1.71 | 12.18±1.75 | 0.522 |
图2 基于HAMA、HAMD-17及PSQI基线评分评估其相关性
Fig.2 Correlation among HAMA, HAMD-17, and PSQI scores of the patients at baseline. A: 3-D scatterplot of the relation among HAMA, HAMD-17 and PSQI scores. B: Correlation between HAMA and HAMD-17 scores. C: Correlation between PSQI and HAMD-17 scores.
| Variables | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
EEG seizure duration (s) Total First Second Third | 235.3±123.79 235.3±123.79† - - | 208.76±72.99 77.85±27.50* 112.26±62.01 - | 231.85±93.34 50.56±22.99* 64.33±13.20 115.15±75.08 | 0.171 <0.001 0.185 - |
| Super ECT sessions | 2.13±1.44 | 2.23±2.01 | 2.41±2.15 | 0.759 |
Race of hospitalizations [n(%)] 1 month 3 months 6 months | 44 (50.00) 8 (9.09) 13 (14.77) 19 (21.59) | 43 (48.31) 14 (15.73) 28 (31.46)* 32 (35.96)* | 17 (43.59) 7 (17.95) 10 (25.64) 11 (28.21) | 0.383 0.470 0.012 0.026 |
表2 癫痫波发作时间分析和治疗情况
Tab.2 Seizure duration analysis and treatment conditions
| Variables | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
EEG seizure duration (s) Total First Second Third | 235.3±123.79 235.3±123.79† - - | 208.76±72.99 77.85±27.50* 112.26±62.01 - | 231.85±93.34 50.56±22.99* 64.33±13.20 115.15±75.08 | 0.171 <0.001 0.185 - |
| Super ECT sessions | 2.13±1.44 | 2.23±2.01 | 2.41±2.15 | 0.759 |
Race of hospitalizations [n(%)] 1 month 3 months 6 months | 44 (50.00) 8 (9.09) 13 (14.77) 19 (21.59) | 43 (48.31) 14 (15.73) 28 (31.46)* 32 (35.96)* | 17 (43.59) 7 (17.95) 10 (25.64) 11 (28.21) | 0.383 0.470 0.012 0.026 |
图3 EEG癫痫波发作时间分析
Fig.3 EEG seizure duration analysis. A, B: Correlation between the first and second seizure duration in E2 group. C-E: Correlation between the first, second and third seizure duration in E3 group. **P<0.01.
图4 基于HAMD-17评分的反应率分析
Fig.4 Response to super ECT assessed according to HAMD-17 scores relative to the baseline during the initial 6 months. A: HAMD-17 scores in E1 group. B: HAMD-17 scores in E2 group. C: HAMD-17 scores in E3 group. *P<0.05.
| Variables | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
Total response 1 month 3 months 6 months | 74 (84.09) 72 (81.82) 74 (84.09) | 84 (88.76) 81 (79.78) 76 (76.40) | 31 (79.48) 31 (79.48) 32 (82.05) | 0.634 0.863 0.790 |
Recovered 1 month 3 months 6 months | 5 (5.68) 5 (5,68) 30 (34.09) | 6 (6.74) 9 (10.11) 28 (31.46) | 2 (5.13) 4 (10.26) 10 (25.64) | 0.781 0.632 0.459 |
Significant improved 1 month 3 months 6 months | 56 (63.64) 40 (45.45) 42 (47.73) | 52 (58.43) 43 (48.31) 30 (33.71) | 23 (58.97) 18 (46.15) 20 (51.28) | 0.702 0.693 0.764 |
Improved 1 month 3 months 6 months | 13 (14.77) 27 (30.68) 2 (2.27) | 21 (23.59) 19 (21.35) 10 (11.24) | 6 (15.38) 9 (23.08) 2 (5.13) | 0.603 0.534 0.357 |
Ineffective 1 month 3 months 6 months | 2 (2.27) 4 (4.55) 2 (2.27) | 2 (2.25) 5 (5.62) 1 (1.12) | 2 (5.13) 2 (5.13) 1 (2.56) | 0.913 0.893 0.796 |
表3 首次治疗后1、3、6个月内基于HAMD-17减分率的疗效分析
Tab.3 Treatment response based on the reduction rate of HAMD-17 scores in 1 month, 3 months, and 6 months [n(%)]
| Variables | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
Total response 1 month 3 months 6 months | 74 (84.09) 72 (81.82) 74 (84.09) | 84 (88.76) 81 (79.78) 76 (76.40) | 31 (79.48) 31 (79.48) 32 (82.05) | 0.634 0.863 0.790 |
Recovered 1 month 3 months 6 months | 5 (5.68) 5 (5,68) 30 (34.09) | 6 (6.74) 9 (10.11) 28 (31.46) | 2 (5.13) 4 (10.26) 10 (25.64) | 0.781 0.632 0.459 |
Significant improved 1 month 3 months 6 months | 56 (63.64) 40 (45.45) 42 (47.73) | 52 (58.43) 43 (48.31) 30 (33.71) | 23 (58.97) 18 (46.15) 20 (51.28) | 0.702 0.693 0.764 |
Improved 1 month 3 months 6 months | 13 (14.77) 27 (30.68) 2 (2.27) | 21 (23.59) 19 (21.35) 10 (11.24) | 6 (15.38) 9 (23.08) 2 (5.13) | 0.603 0.534 0.357 |
Ineffective 1 month 3 months 6 months | 2 (2.27) 4 (4.55) 2 (2.27) | 2 (2.25) 5 (5.62) 1 (1.12) | 2 (5.13) 2 (5.13) 1 (2.56) | 0.913 0.893 0.796 |
| Variables | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
Side effects [n (%)] Fever Headache/dizziness General pain Dry mouth Nausea | 13 (14.77) 27 (30.68) 18 (20.45) 20 (22.73) 18 (20.45) | 21 (23.59) 28 (31.46) 9 (10.11) 17 (19.10) 19 (21.35) | 6 (15.38) 17 (43.58) 12 (30.76) 4 (10.26) 9 (23.08) | 0.764 0.213 0.179 0.452 0.812 |
Cognitive function assessment (Mean±SD) MMSE in pre-treatment MMSE in post-treatment | 27.13±1.24 27.3±3.79 | 26.83±2.03 26.76±2.99 | 27.41±2.15 26.85±3.73 | 0.559 0.794 |
表4 不良反应发生率和认知功能评估
Tab.4 Evaluation of the side effects of the treatment and cognitive function of the patients
| Variables | E1 (n=88) | E2 (n=89) | E3 (n=39) | P |
|---|---|---|---|---|
Side effects [n (%)] Fever Headache/dizziness General pain Dry mouth Nausea | 13 (14.77) 27 (30.68) 18 (20.45) 20 (22.73) 18 (20.45) | 21 (23.59) 28 (31.46) 9 (10.11) 17 (19.10) 19 (21.35) | 6 (15.38) 17 (43.58) 12 (30.76) 4 (10.26) 9 (23.08) | 0.764 0.213 0.179 0.452 0.812 |
Cognitive function assessment (Mean±SD) MMSE in pre-treatment MMSE in post-treatment | 27.13±1.24 27.3±3.79 | 26.83±2.03 26.76±2.99 | 27.41±2.15 26.85±3.73 | 0.559 0.794 |
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