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[The treatment of the resistant obsessive-compulsive disorder: an update].

Although the majority of patients with obsessive compulsive disorder (OCD) can be helped significantly by modern pharmacotherapy with serotonin uptake inhibitors (SUIs), usually in combination with behavioral techniques of exposure and response prevention, complete cure occurs infrequently and some remain very ill and refractory to treatment. In open-label reports, the addition of agents that enhance serotonin neurotransmission, such as lithium, tryptophan, fenfluramine, buspirone, clonazepam and other SUIs or tricyclic antidepressants to ongoing treatment in SUI-refractory patients has yielded encouraging results. However, the anti-obsessive efficacy of SRI-lithium and SRI-buspirone has not been confirmed in recent controlled trials. Preliminary evidence suggests that addition of low-dose dopamine antagonists appears to be a potentially useful strategy for the specific subgroup of OCD patients with a comorbid chromic tic disorder and possibly for those with concurrent psychotic spectrum disorders. Mono Amino oxidase Inhibitors (MAOIs) have also had promising results in open studies. New and experimental drugs are briefly reviewed. Other biological approaches (e.g., electroconvulsive therapy and psychosurgery) are considered in terms of their narrowly defined roles in the treatment of patients with SRI-resistant OCD.

Antidepressive Agents, Tricyclic↗

Treatment-resistant depression: clinical significance, concept and management.

Depression is a common disorder which causes intense personal suffering and socio-occupational dysfunction. It also imposes a heavy economic burden on society. It has been shown that between 29% and 46% of depressed patients fail to respond adequately to antidepressant medication. Treatment-resistant depression may contribute to the morbidity and mortality associated with affective illness. When treatment resistance is suspected, the patient's history should be reevaluated particularly regarding diagnostic subtypes and comorbidity. An assessment of treatment adequacy in terms of dose, duration and compliance should also be made. Treatment strategies for treatment-resistant depression should be systematic and empirically grounded because of the risk of increased resistance and loss of time in case of a random trial-and-error approach, and the inherent risks in certain novel strategies. A stepped care approach to treatment-resistant depression involves optimization of the current drug under trial, augmentation with drugs such as lithium and triiodothyronine, and switching to other somatic therapies such as electroconvulsive therapy and monoamine inhibitors. Only if these strategies fail, should novel treatments such as the use of venlafaxine, antidepressant combinations and augmentation with sleep deprivation be considered. Experimental strategies such as the use of antiglucocorticoids and sex hormones, which carry considerable risk, should be restricted to research settings. Somatotherapy should be combined in all cases with depression-specific psychotherapy. Psychosurgery should be considered only in truly intractable cases. Rational and energetic treatment can adequately help a large majority of patients with treatment-resistant depression.

Adolescent↗