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Data on cost-effectiveness, based on the assumption of EEG based treatment discontinuation, will be presented.
The reason for each discontinuation will be registered.
The exact date and reason for discontinuation will be registered.
The outcome of complete discontinuation will be assessed using Cox-proportional hazards.
Study completion or discontinuation will be documented with the reason for any discontinuation.
Reasons for switching to another OC or discontinuation will be requested if applicable.
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Finally, the prevalence and severity of an antidepressant discontinuation syndrome will be measured in those who withdraw from medication using the Discontinuation-Emergent Signs and Symptoms (DESS) Scale [ 35].
In the current economic evaluation, costs and health outcomes of discontinuation strategy will be compared with the results of maintenance treatment in patients with remitted first episode psychosis.
At the final visit, a patient discontinuation form will be completed for each patient.
In case of study discontinuation data will be extinguished, except the patient affirms explicitly the further analysis of his data.
If the patient is not willing to continue in the study, or does not appear at appointments, or dies, a research discontinuation form will be completed.
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