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1.
J ECT ; 29(1): 15-7, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23291701

ABSTRACT

OBJECTIVES: To compare the minimum charge to elicit a seizure using 2 different pulse widths, the brief pulse (0.5 milliseconds [ms]) and the ultrabrief pulse (0.3 ms). METHODS: We compared retrospectively the last 30 patients in our ECT unit whose seizure thresholds were titrated using a pulse width of 0.5 ms to the last 30 patients whose seizure thresholds were titrated using a pulse width of 0.3 ms. The former were regular clinical patients, and the latter were participating in a clinical trial on the use of ultrabrief pulse treatment. All titrations were performed with right unilateral electrode positioning. Most patients continued to use psychotropic medications. RESULTS: Initial seizure threshold (as measured in millicoulombs [mC]) for the brief pulse group (0.5 ms) was 16 (n = 1); 32 (n = 21), and 64 (n = 8); whereas for the ultrabrief pulse group (0.3 ms), it was 9.2 (n = 3), 38.4 (n = 21), 19.2 (n = 3), 76.8 (n = 2), and 307.2 (n = 1). Excluding the outlier, there was no statistical difference between mean seizure thresholds. CONCLUSIONS: If we exclude the outlier from the ultrabrief group (seizure threshold [ST], 307 mC), we can observe that most of the patients in both groups had an ST between 30 and 40 mC. No patient in the brief pulse group showed a lower ST than 16 mC, probably because this was the first step of titration for this group. The data suggest that the difference between 0.3 and 0.5 ms may not be big, although randomized prospective studies with a more precise and similar steps used for titration are needed. Clinical efficacy was not compared in the present study.


Subject(s)
Electroconvulsive Therapy/methods , Functional Laterality/physiology , Adult , Aging/physiology , Electroconvulsive Therapy/instrumentation , Electrodes , Electroencephalography , Female , Humans , Male , Middle Aged , Psychotropic Drugs/adverse effects , Psychotropic Drugs/therapeutic use , Retrospective Studies , Seizures/physiopathology , Sex Characteristics , Treatment Outcome
3.
Braz. J. Psychiatry (São Paulo, 1999, Impr.) ; 30(2): 149-151, jun. 2008. tab
Article in English | LILACS | ID: lil-485243

ABSTRACT

OBJECTIVES: To compare post anesthetic time for patient recovery after electroconvulsive therapy, as measured by the post anesthetic Recovery Score of Aldrete and Kroulik, using three different types of hypnotic drugs (propofol, etomidate and thiopental). METHOD: Thirty patients were randomized to receive one of the three drugs (n = 10 in each group), during a course of electroconvulsive therapy treatment. Patients and raters were blinded to which drug was received. Main treatment characteristics were recorded (as total electric charge received seizure threshold, number of treatments, and the mean time for recovery) along the whole treatment. RESULTS: Thiopental and propofol were associated with a significance increase in charge needed to induce a seizure (p < 0.0001) when compared to etomidate, as well as a significant decrease of time for recovery (p = 0.042). CONCLUSIONS: These findings suggest that, although there seems to be no difference in the clinical outcome across these three drugs, propofol offers the best recovery profile. However, it makes a higher mean electric charge necessary.


OBJETIVOS: Comparar o tempo de recuperação dos pacientes após eletroconvulsoterapia avaliada com a escala de recuperação pós-anestésica de Aldrete e Kroulik, utilizando três tipos de medicações anestésicas (propofol, etomidato and tiopental). MÉTODO: Trinta pacientes foram randomizados para receber uma das medicações (n = 10 em cada grupo) durante uma série de tratamentos com eletroconvulsoterapia. Os pacientes e o examinador ficaram cegos para o tipo de anestésico utilizado. As principais características do tratamento foram avaliadas (como carga total de eletricidade recebida, limiar convulsivo, número de sessões e o tempo médio para recuperação) ao longo de toda a série de tratamentos. RESULTADOS: Tiopental e propofol se associaram a um aumento significativo na carga elétrica total utilizada (p < 0,0001) quando comparados com etomidato, bem como uma diminuição significativa no tempo de recuperação pós-anestésica (p = 0,042). CONCLUSÕES: Estes achados sugerem que, apesar de não haver diferença na evolução clínica entre os três grupos estudados, a droga propofol oferece o melhor perfil de recuperação apesar de requerer uma carga elétrica média maior.


Subject(s)
Adult , Female , Humans , Male , Anesthesia, Intravenous , Electroconvulsive Therapy , Etomidate , Hypnotics and Sedatives , Propofol , Thiopental , Anesthesia Recovery Period , Double-Blind Method , Logistic Models , Time Factors
4.
Braz J Psychiatry ; 30(2): 149-51, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18470404

ABSTRACT

OBJECTIVES: To compare post anesthetic time for patient recovery after electroconvulsive therapy, as measured by the post anesthetic Recovery Score of Aldrete and Kroulik, using three different types of hypnotic drugs (propofol, etomidate and thiopental). METHOD: Thirty patients were randomized to receive one of the three drugs (n = 10 in each group), during a course of electroconvulsive therapy treatment. Patients and raters were blinded to which drug was received. Main treatment characteristics were recorded (as total electric charge received seizure threshold, number of treatments, and the mean time for recovery) along the whole treatment. RESULTS: Thiopental and propofol were associated with a significance increase in charge needed to induce a seizure (p < 0.0001) when compared to etomidate, as well as a significant decrease of time for recovery (p = 0.042). CONCLUSIONS: These findings suggest that, although there seems to be no difference in the clinical outcome across these three drugs, propofol offers the best recovery profile. However, it makes a higher mean electric charge necessary.


Subject(s)
Anesthesia, Intravenous , Electroconvulsive Therapy , Etomidate , Hypnotics and Sedatives , Propofol , Thiopental , Adult , Anesthesia Recovery Period , Double-Blind Method , Female , Humans , Logistic Models , Male , Time Factors
5.
J Clin Psychiatry ; 68(10): 1528-32, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17960967

ABSTRACT

OBJECTIVE: To study the therapeutic effects on auditory hallucinations refractory to clozapine with 1-Hz repetitive transcranial magnetic stimulation (rTMS) applied on the left temporoparietal cortex. METHOD: Eleven patients with schizophrenia (DSM-IV) experiencing auditory hallucinations (unresponsive to clozapine) were randomly assigned to receive either active of rTMS (N = 6) or sham stimulation (N = 5) (with concomitant use of clozapine) using a double-masked, sham-controlled, parallel design. A total of 160 minutes of rTMS (9600 pulses) was administered over 10 days at 90% motor threshold. The study was conducted from January 2003 to December 2005. RESULTS: There was a reduction in hallucination scores in both groups, which persisted during follow-up in the active group for the items reality (p = .0493) and attentional salience (p = .0360). Both groups showed similar patterns of symptomatic changes on subscales (negative symptoms, general psychopathology) and total scores of the Positive and Negative Syndrome Scale, Clinical Global Impressions scale, and Visual Analog Scale. CONCLUSION: Active rTMS in association with clozapine can be administered safely to treat auditory hallucinations, although its clinical utility is still questionable. No significant clinical effects were observed in the sample studied, possibly because it was too small and/or due to its high refractoriness.


Subject(s)
Clozapine/therapeutic use , Drug Resistance , Hallucinations/drug therapy , Hallucinations/etiology , Schizophrenia/diagnosis , Schizophrenia/therapy , Schizophrenic Psychology , Transcranial Magnetic Stimulation/methods , Adult , Demography , Diagnostic and Statistical Manual of Mental Disorders , Double-Blind Method , Female , Hallucinations/epidemiology , Humans , Male , Severity of Illness Index , Treatment Outcome
6.
J ECT ; 23(1): 6-8, 2007 Mar.
Article in English | MEDLINE | ID: mdl-17435563

ABSTRACT

Cardiovascular alterations during electroconvulsive therapy (ECT) are a major concern for this treatment. Although several studies have been performed to compare the effects of anesthetics on these alterations, the results are mixed and doubt still exists regarding the choice of the best drug. We conducted a randomized, double-blind clinical trial to compare the effects of 3 anesthetics used in ECT: etomidate, propofol, and thiopental. Patients (N=30) were randomized to receive one of these drugs as the anesthetic for the ECT procedure. Cardiovascular evaluation consisted of the measurement of blood systolic and diastolic pressure and heart rate before and immediately after the end of the seizure for each patient during a course of ECT. The results showed that etomidate, propofol, and thiopental were associated with similar cardiovascular effects.


Subject(s)
Anesthetics, Intravenous/administration & dosage , Cardiovascular System/drug effects , Depressive Disorder, Major/therapy , Electroconvulsive Therapy , Etomidate/administration & dosage , Propofol/administration & dosage , Thiopental/administration & dosage , Adult , Anesthesia, Intravenous , Anesthetics, Intravenous/adverse effects , Dose-Response Relationship, Drug , Double-Blind Method , Etomidate/adverse effects , Female , Humans , Logistic Models , Male , Middle Aged , Propofol/adverse effects , Thiopental/adverse effects , Treatment Outcome
7.
J ECT ; 22(4): 237-9, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17143152

ABSTRACT

The use of right unilateral electrode placement for electroconvulsive therapy (ECT) is one of the most important developments on the technique because it is considered to spare cognition. Nevertheless, the best way to determine the charge to be given to the individual patient is still controversial. We present an open study on the use of right unilateral ECT using the technique of method of limits and giving treatments with 6 times the seizure threshold. Of 30 patients, there was a response/remission rate of 53.33%, as measured by the Hamilton Depression Rating Scale, after a mean of 8 sessions. Half of the nonresponders (n = 7) received subsequent bilateral ECT, with improvement on 4. The data suggest that it is a good practice to start the treatment with unilateral ECT and, if no response is achieved, to switch to bilateral placement.


Subject(s)
Depressive Disorder, Major/therapy , Electric Stimulation Therapy , Electroconvulsive Therapy/methods , Adult , Anesthetics/therapeutic use , Electroconvulsive Therapy/standards , Electrodes/standards , Female , Functional Laterality , Humans , Male , Titrimetry , Treatment Outcome
8.
J ECT ; 22(4): 265-6, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17143158

ABSTRACT

Accidental induction of convulsions by using repetitive transcranial magnetic stimulation (rTMS) has been reported to have occurred in 6 normal voluntary subjects, in 1 patient with depression and in 1 patient who had temporal lobe epilepsy, with secondary generalization. In addition, 3 other cases have been published relating its use with seizure induction and in 1 case, using 1-Hz stimulation. In this paper, we report a patient who was participating in a protocol for the use of rTMS in chronic pain, with stimulation in the motor cortex, who developed a generalized seizure in the fifth application. Intertrain interval was within safety guidelines, but the combination of 10 Hz for 10 seconds was excessive and must be considered the main cause for the episode. No further complication has been noted after she was withdrawn from the study protocol.


Subject(s)
Motor Cortex/physiopathology , Seizures/etiology , Transcranial Magnetic Stimulation/adverse effects , Adult , Female , Humans , Seizures/physiopathology
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