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Biomedical subjects

Conrad M. Swartz

Publications and source records attributed to Conrad M. Swartz.

23 records · Page 2Linked to original sources

Electroconvulsive Therapy-Induced Cortisol Release: Changes with Depressive State.

With administration of 2 mg of dexamethasone 9 h before, serum cortisol levels were determined for the times just before and 30 min after the first and last electroconvulsive therapies (ECTs) of a series of at least six sessions. Twelve drug-free patients with melancholic or psychotic depression completed the study. Response to treatment was taken as a fall in the value of the Carroll rating scale. The average cortisol elevation over baseline was by 575% with the first ECT, 10 times larger than other studies in the literature that were done without dexamethasone. With the final ECT the elevation was lower (p < 0.01), averaging 181%. Post-ECT cortisol levels (and elevations over baseline) were lower after the final ECT than after the initial ECT, with 10 of the 11 patients who responded to this treatment (p < 0.005 vs. 50%). Consistent with this, the lone nonresponder showed a large increase in serum cortisol level and elevation over baseline from the first to the last treatment. The one responder who went against this trend had an unusually high baseline cortisol level, 24.1 &mgr;g/dl, which can be considered to disqualify his inclusion. The near-unanimous fall of post-ECT cortisol levels with remission suggests that defects in cortisol regulation are much more prevalent (p < 0.01) than those detected by the dexamethasone suppression test (36% in this sample).

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Electroconvulsive Therapy and Prolactin Release: Relation to Treatment Response in Melancholia.

Serum prolactin levels 15 min after each of four consecutive electroconvulsive treatments (ECTs) in 16 male melancholics fell from the first to the fourth treatment. A larger mean prolactin response to ECT correlated with a slower treatment response, as measured by global outcome ratings after six ECTs and the total number of ECTs administered, both blind to prolactin levels. These findings were independent of baseline prolactin levels or treatment electrode placement; they are consistent with the hypothesis that ECT increases postsynaptic dopamine receptor sensitivity. Although intriguing, they await confirmation in a larger sample.

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Time Course of Post-Electroconvulsive Therapy Prolactin Levels.

Serum samples before and after electroconvulsive therapy (ECT) from eight women patients revealed that prolactin blood levels reached a peak about 11 min after the end of the seizure. On average, the peak elevation over baseline was 385%; this elevation correlated strongly (r = 0.6, p < 0.001) with baseline blood levels. Prolactin peaks after bilateral ECT were significantly (p < 10(-5)) higher than those after unilateral ECT, although seizure duration was not longer. Application of a mathematical model gave an estimate of 17.3 min for the half-life of prolactin elimination from the blood, close to published metabolic measurements. The rate of prolactin release into the blood was greater than the rate of its elimination from the blood.

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Electroconvulsive Therapy and Prolactin Release: Effects of Stimulus Parameters.

We report a study of electroconvulsive therapy (ECT) induced prolactin release in nine patients as a function of treatment electrode placement, stimulus energy, and seizure length. Only electrode placement differentially affected prolactin release, with bilateral ECT yielding larger increments over baseline than unilateral ECT.

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Characterization of the Total Amount of Prolactin Released by Electroconvulsive Therapy.

Many factors can obscure determination of the total hormone release induced by a course of electroconvulsive therapy (ECT). Not the least of these factors are the rates of hormone release and their elimination. A method of estimating the total amount of prolactin released during an ECT-induced seizure has been constructed by mathematical modeling. Using prolactin levels measured from patients undergoing ECT, this simulation indicates that the optimal times for sampling plasma prolactin are 5, 10, 20, and 45 min following the seizure, besides the baseline measurement.

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