Copyright © 2017 Wolters Kluwer Health, Inc. Unauthorized reproduction of this article is prohibited.
Tor et al Journal of ECT • Volume 00, Number 00, Month 2017
depression (20.4%), and mania (6.8%) being the other major examined 2 outcomes for symptomatic response, as defined by
indications. (1) change in BPRS scores pre- and post-ECT across the patients
Patients were referred to the ECT service by psychiatrists who and (2) the proportion of patients who showed an improvement of
diagnosed schizophrenia using clinical assessments based on 40% or more from pretreatment scores based on the psychotic
Diagnostic and Statistical Manual of Mental Disorders, Fourth/Fifth symptom subscale.2,33,34 The primary cognitive outcome was
Edition (DSM-IV/DSM-V) or International Statistical Classification performance on the Montreal Cognitive Assessment (MoCA
of Diseases, 10th Revision (ICD-10) criteria. Patients were typically Singaporean versions of the MoCA35,36 in the local languages
referred for treatment of psychotic symptoms, which had not [English, Chinese, Malay, and Tamil] were used). Alternate
responded adequately to pharmacological treatment and as a result, forms of the English MoCA forms were used for post-ECT
were too unwell for discharge back to the community. The number of testing. We examined the change in total MoCA scores from
sessions of ECT prescribed was determined by the treating psychiatrist pre- to post-ECT. Changes in anterograde memory were
based on the patient's clinical response. Data from patients with additionally reported using the MoCA delayed recall subtest.
schizoaffective disorder or substance-induced psychosis were not The BPRS ratings were completed by ECT medical officers
examined. who underwent rating training using standardized training videos
under the supervision of P.C.T. Intraclass correlation, as defined
Electroconvulsive Therapy by (MSrater − MSerror)/[MSrater + (average number of patients per
Before 2015, standard ECT treatment at IMH consisted of rater − 1)*MSerror], between the BPRS raters was 0.77, where MS
indicates mean square. The MoCA was administered by
bitemporal ECT administered 3 times per week, using disposable
adhesive type electrodes; dosing was determined by the refer-ring ECT nurses. These nurses were trained by P.C.T and D.M., a
psychiatrist using an “age minus 10% (50.4 mC)” dosing registered neuropsychologist.
29 The following baseline clinical and demographic variables were
method. Increases in dosing were made based on reductions in extracted from the electronic patient records: type of ECT (BT-AB,
seizure duration or electroencephalogram quality, which usu-ally RUL-ST, BT-ST, and BF-ST), initial seizure threshold, daily dose of
meant a 5% to 10% machine power increase in energy levels. concurrent antipsychotic treatment (expressed as chlorpromazine
A revamp of ECT services in 2015 consisted of several major
equivalents) given during ECT,37 lifetime duration of illness (months),
changes. Individualized dosing based on each patient's empiri-
cally determined seizure threshold was used, rather than the age- age, sex, and post-ECT MoCA and BPRS scores. The duration of
29 current episode of schizophrenia is known to cor-relate with response
based (age − 10%) dosing method. Electroconvulsive therapy
to ECT38 but was not available for analysis.
continued to be delivered using a Thymatron System IV
(Somatics, LLC) and used either a bitemporal, right unilateral Ethics approval for data access, analysis, and report was
30 31 ob-tained from the local institutional research ethics board.
(d’Elia position ), or bifrontal electrode positioning. Bitemporal
ECT was delivered at 0.5 millisecond pulse width, and Bifrontal
ECTwas delivered at 1.0 millisecond pulse width, both at 1.5 Statistics
times seizure threshold. The longer pulse width was selected for To test for differences in clinical and demographic
bifrontal ECT compared with bitemporal ECT, because of baseline data between the groups receiving different types of
1
demonstrated efficacy in previous studies (Phutane et al ). Right ECT, analyses of variance was performed.
unilateral ECT was delivered at 0.5 millisecond pulse width at 5 Mixed analysis of covariance (ANCOVA) examined (1) whether
times seizure threshold. The anesthetic used was propofol, which completing an ECT course affected symptom (BPRS scores) or
was dosed at 1 mg/kg. cognitive outcomes (MoCA scores) and (2) whether the change in
After the revamp in 2015, the type of ECT treatment was outcomes differed depending on the type of ECT administered (BT-
changed, although at any one time the default treatment protocol was AB, RUL-ST, BT-ST, and BF-ST). Between-subjects factor was ECT
1 type of ECT for all patients. In the first change, the default type of type (BT-AB, RUL-ST, BT-ST, and BF-ST) and within-subjects factor
ECT was switched from bitemporal age-based dosage (BT-AB; 0.5 was time (pre-ECT and post-ECT). Covariates were age, sex, duration
millisecond pulse width) to right unilateral seizure threshold–based of illness, antipsychotic dose, and number of ECT sessions. For
dosage (RUL-ST; 0.5 millisecond pulse width) due to the well- analysis of MoCA scores, post-ECT BPRS was an additional
established cognitive benefits of RUL-ST over bitemporal ECT. 14 An covariate. Where the ANCOVAs yielded signif-icant results, follow-
interim analysis of effectiveness showed a trend for RUL-ST to be less up tests examined where the between-group differences occurred.
effective than BT-AB ECT. Hence, the ECT modality for Paired-samples t tests also examined changes in symptom and
schizophrenia was changed to bitemporal seizure threshold–based cognitive outcomes across the course of ECT, within each type of
dosing (BT-ST; 0.5 millisecond pulse width). Subsequently, the ECT ECT modality. The proportion of patients in each ECT group who had
modality was changed to bifrontal seizure threshold–based dosing 40% or more improvement in BPRS psychotic subscale (“responders”)
(BF-ST; 1.0 millisecond pulse width) after the team became aware of was compared using a χ2 test. Only available data were analyzed, and
a recent trial suggesting superiority of BF-ST over BT-ST in missing data was not imputed.
schizophrenia.1 Data were reported from December 2014 to May Significance was set at a threshold of P value less than
2016, and each type of ECT was the default protocol at the hospital for 0.05, and all analyses were completed using the Statistical
approximately 4 months. Program for Social Sciences Version 14 (SPSS; Chicago, IL).
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Journal of ECT • Volume 00, Number 00, Month 2017 ECT in Schizophrenia: A Naturalistic Study
TABLE 1. Patient Demographic, Clinical, and Treatment Variables for the Sample by Type of ECT
Overall (N = 62), BT-AB (n = 25), RUL-ST (n = 15), BT-ST (n = 11), BF-ST (n = 11),
mean (SD) mean (SD) mean (SD) mean (SD) mean (SD) P*
Age, y 43.74 (14.02) 47.04 (10.82) 43.93 (14.84) 39.91 (14.92) 39.82 (18.07) 0.388
Age range, y 15–69 20–65 21–69 19–66 15–68 NA
Sex 0.588
Male, n (%) 26 (41.9) 8 (32.0) 8 (53.3) 5 (45.5) 5 (45.5)
Female, n (%) 36 (58.1) 17 (68.0) 7 (46.7) 6 (54.5) 6 (54.5)
Duration of illness, mo 112.7 (90.7) 112.6 (87.8) 102.4 (78.1) 120.8 (124.2) 118.9 (86.5) 0.956
CPZ equivalent, mg 670.5 (436.3) 826.5 (575.9) 574.4 (314.9) 584.8 (234.9) 532.7 (259.4) 0.140
No. ECT 9.8 (3.4) 9.5 (3.4) 8.0 (3.3)† 11.3 (1.9) 11.6 (3.8)† 0.021
Initial ECT seizure threshold 19.0 (15.8) NA 9.6 (3.1)† 17.2 (7.9)‡ 33.2 (20.6)†‡ 0.001
(% machine energy)
Initial ECT dosage (% machine energy) 42.0 (21.9) 39.5 (18.3) 48.7 (10.9)† 27.8 (10.9)†‡ 50.0 (38.3)‡ 0.048
Final ECT dosage (% machine energy) 53.5 (24.1) 51.9 (21.5) 59.7 (18.0) 33.3 (12.9) 59.1 (34.9) 0.116
Propofol dosage (mg) 55.4 (11.9) 52.7 (9.4) 55.7 (8.6) 62.2 (19.2) 54.6 (12.1) 0.249
Suxamathonium dosage, mg 29.5 (10.2) 29.5 (9.9) 28.7 (9.5) 35.0 (15.0) 25.9 (4.9) 0.253
Copyright © 2017 Wolters Kluwer Health, Inc. Unauthorized reproduction of this article is prohibited.
Tor et al Journal of ECT • Volume 00, Number 00, Month 2017
Overall (N = 62), BT-AB (n = 25), RUL-ST (n = 15), BT-ST (n = 11), BF-ST (n = 11)
mean (SD) mean (SD) mean (SD) mean (SD) M (SD)
Pre-ECT BPRS 45.7 (11.8) 47.4 (12.8) 44.1 (11.4) 42.4 (12.2) 47.3 (10.1)
Post-ECT BPRS 31.7 (8.1)* 32.0 (7.6)* 29.2 (8.0)* 29.4 (4.1)* 36.9 (10.7)*
Improvement in BPRS 13.9 (13.6) 15.4 (13.2) 14.9 (14.9) 13.0 (12.1) 10.4 (15.4)
Pre-ECT psychotic subscale 10.7 (6.4) 10.0 (6.5) 10.9 (6.1) 10.5 (6.3) 12.0 (7.1)
Post-ECT psychotic subscale 5.3 (4.1)* 4.9 (2.8)* 5.3 (4.5)* 4.8 (3.6)* 6.8 (6.1)*
Response to ECT (40% improvement)† 40 (64.5%) 15 (60%) 10 (66.7%) 8 (72.7%) 7 (63.6%)
Response to ECT (20% improvement)‡ 47 (75.8%) 19 (76%) 12 (80%) 8 (72.7%) 8 (72.7%)
Pre-ECT Depression subscale 5.5 (5.4) 5.4 (6.9) 6.3 (4.4) 4.9 (4.2) 5.4 (4.3)
Post-ECT depression subscale 3.7 (2.7)* 3.0 (2.3)* 4.5 (2.4) 3.1 (1.8) 4.7 (4.2)
Pre-ECT negative subscale 8.9 (4.1) 9.6 (4.0) 8.6 (4.1) 8.6 (4.5) 7.8 (4.0)
Post-ECT negative subscale 6.2 (2.7) 6.9 (2.8)* 5.1 (2.3)* 5.5 (1.4) 7.1 (3.3)
Pre-ECT paranoid subscale 4.2 (1.5) 4.7 (2.5) 3.8 (1.9) 4.2 (1.8) 3.5 (1.8)
Post-ECT paranoid subscale 2.5 (1.5) 2.6 (1.7)* 2.5 (1.4)* 1.9 (0.7)* 2.9 (1.6)
Pre-ECT mania subscale 4.7 (2.1) 4.9 (2.4) 4.7 (1.9) 4.3 (1.7) 4.6 (2.2)
Post-ECT mania subscale 3.5 (1.4)* 3.5 (1.7)* 3.7 (1.7) 3.1 (0.3) 3.5 (0.9)
*Post-ECT scores that were statistically significantly different from pre-ECT scores within the same ECT group at P = 0.05.
†40% decrease in psychotic subscale.
‡20% decrease in psychotic subscale.
cognitive advantage of RUL ECT was no longer apparent. An- the 4 periods, there was no demographic difference between the
other consideration is whether the equivalence of cognitive out- patients receiving the 4 types of ECT, and the cohorts of patients
comes was observed because BT-ST ECT was more effective, assigned to different types of ECT were from the same referral base
with cognitive improvements associated with symptom improve- and treated relatively closely in time (over a 17-month period).
ment leading to overall superior outcomes. However, results do Nevertheless, there could have been a positive rater bias as the raters
not support this interpretation, because there was no difference in were aware that the patients were receiving ECT. Another major
symptom efficacy between RUL-ST and BT-ST ECT. limitation is that because of incomplete longitudinal data, the sample
The lack of superiority in cognitive outcomes of BF-ST over size for each type of ECT was small with just over 10 patients in some
1
BT-ST, as might have been expected given the results of, is most groups, which means that our study may have been underpowered for
likely explained by the longer pulse width used for BF-ST (1.0 detecting differences between the 4 types of ECT in symptomatic and
millisecond) compared with BT-ST (0.5 millisecond) in this study. cognitive outcomes. Information on years of education for subjects
Shorter pulse widths potentially allow for more focused was not available and could not be included as a covariate. Further
46 47
stimulation and lesser cognitive adverse effects. On the other studies, ideally randomized controlled trials of different ECT
hand, one may have expected greater symptom reduction with BF- modalities with a larger sample size, will be required to substantiate
ST compared with BT-ST given the previous results of Phutane et our findings.
1
al. The reasons for this discrepancy are not clear, and may reflect
a lack of power in this study to detect differences.
There are several limitations to this naturalistic study, the CONCLUSIONS
most important being that data on outcomes of the 4 types of ECT In conclusion, ECT is an effective treatment for treatment-
studied were collected in sequential cohorts. Notwithstand-ing, we resistant schizophrenia, resulting in symptomatic improvement
note that there was no selection bias for the type of ECT received, and global cognitive benefits in some patients. In this study, there
as at any 1 point in time only 1 type of ECT was used to treat was no difference in outcomes between the 4 types of ECT
schizophrenia for all patients, the same small team of doctors and assessed. Almost two thirds of patients with schizophrenia
nurses conducted the ECT and assessments across responded to ECT after approximately 10 treatments.
Overall (n = 48), BT-AB (n = 17), RUL-ST (n = 10), BT-ST (n = 10), BF-ST (n = 11),
mean (SD) mean (SD) mean (SD) mean (SD) mean (SD)
Pre-ECT MoCA (n = 48) 16.8 (9.1) 15.9 (7.9) 16.2 (9.0) 16.3 (11.0) 19.5 (10.0)
Post-ECT MoCA 20.7 (6.0)* 17.5 (3.6) 18.8 (8.5) 24.0 (5.0)* 24.5 (3.3)
Improvement in MoCA post-ECT 3.9 (9.2) 1.5 (7.8) 2.6 (9.4) 7.7 (9.3) 5.0 (10.7)
Pre-ECT recall (MoCA) 2.20 (2.09) 1.88 (1.93) 1.81 (2.09) 2.63 (2.13) 2.80 (2.44)
Post-ECT recall (MoCA) 1.89 (1.96) 0.59 (1.12)* 1.80 (2.10) 3.25 (1.39) 3.10 (2.02)
*Post-ECT scores that were statistically significantly different from pre-ECT scores within the same ECT group at P = 0.05.
Copyright © 2017 Wolters Kluwer Health, Inc. Unauthorized reproduction of this article is prohibited.
Journal of ECT • Volume 00, Number 00, Month 2017 ECT in Schizophrenia: A Naturalistic Study
19. Wessels WH. A comparative study of the efficacy of bilateral and
unilateral electroconvulsive therapy with thioridazine in acute
Because these results are derived from a naturalistic real- schizophrenia. S Afr Med J. 1972;46:890–892.
world sample, they must be considered preliminary until a ran-
domized controlled trial can be conducted to compare the effects © 2017 Wolters Kluwer Health, Inc. All rights reserved.
of different ECT modalities on cognitive and symptom outcomes
in schizophrenia. While awaiting such results, it seems prudent to
choose the type of ECT for schizophrenia based on the patient's
treatment needs. Patients with poorer pretreatment cognitive func-
tioning might best avoid BT-AB ECT.
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