The Use of Rapid-Rate Transcranial Magnetic Stimulation (rTMS) in Refractory Depressed Patients

Between January 1996 and March 1997, 56 patients received a course of rTMS at Wesley Woods Geriatric Hospital/Emory University Medical Center. All 56 patients and their families gave informed consent to a protocol approved by the Human Investigations Committee of the Emory University School of Medicine and by the research committees of both hospitals. All 56 patients were referred to the Mood Disorders Clinic at Wesley Woods Geriatric Hospital. Forty-four of these patients had been referred for electroconvulsive therapy (ECT) and chose to receive rTMS prior to ECT. Fifty-three of the patients (94%) had received at least a 6-week trial of an antidepressant at a therapeutic dose (Table 1). Seventeen patients had a prior history of receiving ECT. There were 31 women and 25 men among the 56 patients who received rTMS. The patients ranged in age from 22 to 89, with a mean age of 60 years.

All patients met DSM-IV criteria for a major depressive episode (53 unipolar, 3 bipolar). All patients were rated at least moderately ill on the Clinical Global Impression Scale and had a pretreatment score on the 21-item Hamilton Rating Scale for Depression (Ham-D) of greater than 20 (mean score of 34). In addition, 4 patients had a DSM-IV diagnosis of dementia. All diagnoses were made by a physician (G.S.F.) using a DSM-IV checklist during a structured clinical interview. The Folstein Mini-Mental State Examination (MMSE) was administered to 54 of the 56 patients before they received rTMS administered by a member of the treatment team (J.A.-L.). Two patients were not able to perform the mental status examination because of the severity of their illness.

In general, patients were tapered off their psychotropic medications prior to beginning their course of rTMS. A few patients (n=6) were unable to be tapered off their medications because of the severity of their illness. In no case was a patient started on a new psychotropic medication during rTMS treatments. The patients who remained on psychotropic medications had been on these medications for several months. As a result, any change in these patients' clinical status during rTMS was not felt to be attributable to the concomitant use of the psychotropic medications.

Many (n=21) of the patients had a history of one or more of the following medical illnesses: hypertension and/or coronary artery disease (n=21), congestive heart failure (n=2), history of transient ischemic attacks (n=3), diabetes mellitus (n=6), or cerebral vascular accident (n=1). Patients with a history of a recent myocardial infarction, cardiac pacemaker, intracranial metallic objects, or an increased intracranial pressure were excluded from the study.

The patients were classified as responders according to the criteria of Sackeim et al.¹¹ They had to show a 60% reduction from their pretreatment Ham-D score, as well as a posttreatment Ham-D score of 16 points or less. In addition, patients had to be rated as moderately to markedly improved on a 7-point Clinical Global Impression Scale. These ratings were completed by the patient's clinical treatment team along with the physician on the rTMS service (G.S.F.). All ratings were obtained prior to beginning rTMS and within 48 hours after the fifth treatment.

All treatments were administered in the ECT laboratory, once daily for 5 consecutive weekdays. If there was no clinical response after 5 treatments, rTMS was stopped. Patients lay supine with the head elevated on a pillow. Continuous cardiac monitoring was performed, and blood pressure was taken every 60 seconds during stimulation.

High-speed rTMS was performed with a custom device, using a damped cosine pulse and a prototype iron-core magnetic coil. The latter induces electric fields similar in distribution to those from a Cadwell water-cooled figure-eight coil but is much smaller, quieter, and more efficient, requiring no special cooling. This coil also has an open port in the center for precisely marking and reproducing position on the head.

Relaxed motor threshold and the location of the right-hand motor area were identified over the left hemisphere as previously described.¹² During stimulation at a rate of 1.0 Hz, the magnetic coil was moved across the left central region and the stimulator output was gradually increased to locate the point of lowest-intensity activation, followed by the magnetic threshold at that site. This position was then labeled with a permanent marker. Determining motor threshold required only 5 to 10 minutes at the first treatment session, and less time on subsequent days because the location had been marked. The site of rTMS treatment was then measured 5 cm anteriorly from the hand motor area on a sagittal line.

For each rTMS treatment, the system output was set to 110% of relaxed motor threshold and a repetition rate of 10 Hz. Stimulation was delivered in ten trains of 5 seconds each, with trains 30 seconds apart. The coil was oriented so that electric fields were induced to a sagittal plane. Ear protection was worn throughout.

Data were stored on a Lotus program. Comparisons on parametric and nonparametric variables were made by using Student's t-tests and chi-square tests, respectively.

Fifty-six patients were recruited into the study, and 50 patients completed a course of 5 rTMS treatments. There were 21 responders (42%) and 29 nonresponders (58%; Table 2). Twenty-eight patients were less than age 65. Sixteen (56%) of these young patients responded to rTMS. However, only 5 (23%) of the 22 elderly (≥65 years of age) responded to rTMS (Table 2). Three of the 4 (75%) elderly depressed patients who had their first episode of depression prior to the age of 65 (early onset) responded to rTMS. However, only 2 (11%) of the 18 elderly patients with late-onset depression (first episode after the age of 65) responded to rTMS (Table 2). Individual scores fell by 60% or more in all responders and below 10 in 17 of the responders.

Patients who responded to rTMS differed significantly from those who did not respond with respect to age (P=0.038; Table 2) and pretreatment Ham-D scores (P=0.008). However, there was no difference in the pretreatment Ham-D scores between the young patients who responded to rTMS and those who did not. There was no gender difference between responders and nonresponders (P=0.5; Table 2). In addition, there was no significant difference in pre-rTMS MMSE scores between responders and nonresponders (P=0.2). Among patients with major depression (unipolar, recurrent), 17 of 39 (43.5%) were responders. Among patients with psychotic depression, 2 of 8 (25%) were responders (Table 2). Only 1 of 6 elderly patients with psychotic depression (17%) responded to rTMS. Two of 3 bipolar disorder patients (67%) and only 1 of 4 dementia patients (25%) responded to rTMS (Table 2). Sixteen patients reported a favorable response to ECT in the past; only 8 of these responded to rTMS. The only patient who reported an unfavorable response to ECT in the past likewise did not respond to rTMS.

Six of the 56 patients did not complete a course of rTMS. One 47-year-old man and a 33-year-old woman requested to stop after one rTMS treatment because of pain over the left frontal scalp area elicited during the treatment. In both cases, the pain stopped immediately with cessation of the rTMS treatment. Neither patient required an analgesic medication for the pain. A third patient was a 66-year-old man whose rTMS treatment was stopped because of brisk right upper extremity muscular contractions during the treatment. These muscular contractions ended immediately when the treatment was stopped. A fourth patient was a 44-year-old woman with preexisting motor tics of the right upper and lower extremity who had recurrence of these movements during her first rTMS treatment. Periodic limb flexion persisted for 20 minutes without change in speech or alertness; it could be quenched repeatedly with gentle pressure to the arm or leg. Movements ceased after 2 mg of lorazepam intravenously, without any subsequent complications. The fifth subject was a 45-year-old woman who developed a left body dysthesia 10 minutes after her first rTMS treatment. The dysthesia lasted approximately 48 hours and then resolved spontaneously. The patient's brain magnetic images, EEG, and neurologic examination were all within normal limits. Finally, a 77-year-old woman received one rTMS treatment without any complications. Six hours after her treatment she experienced a syncopal episode. Workup was negative, and the syncopal episode resolved without any complications. This patient did not experience any change in her blood pressure or heart rate during her rTMS treatment. It was not felt that the syncopal episode was related to the rTMS treatment. No patient developed a new onset of seizures during the course of rTMS. A 46-year-old woman, who was a responder to rTMS, initially reported that she had no history of epilepsy prior to beginning treatment. However, 2 weeks after starting treatment she reported apparent left focal motor seizures and admitted preexisting twitching of the left face. All episodes were remote from the times of rTMS by at least several hours. Complete neurological examination, EEG, and MRI were normal. Seizures continued despite therapeutic phenytoin levels and were highly correlated with attendance at church and funerals. After two episodes were witnessed in an outpatient psychiatry program, they were assessed as pseudoseizures. She was tapered off phenytoin without recurrence. Ten patients complained of mild headaches during the rTMS treatments. These headaches ended immediately after the treatments stopped. No patient required treatment with analgesics to control the headaches. All of these 10 patients completed their course of rTMS. No patients complained of any memory or cognitive side effects during rTMS. However, no formal cognitive testing was done in this study. rTMS had no effect on any patient's blood pressure or heart rate during the treatments.