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1.
Tijdschr Psychiatr ; 66(1): 19-23, 2024.
Article in Dutch | MEDLINE | ID: mdl-38380483

ABSTRACT

BACKGROUND: The Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) is a widely used semi structured clinician-rated interview to assess the presence and severity of obsessive-compulsive disorder (OCD). The scale is revised (Y-BOCS-II) to overcome several psychometric limitations, for example by extending the scoring for better discrimination within higher severity levels. AIM: To examine the responsiveness and other psychometric properties of the Y-BOCS-II in a Dutch clinical sample. METHOD: The Y-BOCS-II was translated into Dutch (Y-BOCS-II) and administered to 110 patients seeking therapy for OCD. This was done twice, before and after treatment. The original Y-BOCS was simultaneously rated. Self-report measures regarding depression, symptom severity and OCD symptoms were assessed. RESULTS: The Y-BOCS-II had a good internal consistency (Cronbach’s α = 0.84), test-retest (ICC = 0.81) and inter-rater reliability (ICC = 0.94). The construct validity proved to be modest to good. The responsiveness over time was in favour of the Y-BOCS-II, compared with the YBOCS-I, particularly in the severely affected OCD patients. CONCLUSION: The Y-BOCS-II severity scale is a reliable and valid instrument for accurately assessing the severity of OCD symptoms and for measuring treatment-induced change. This second version also has clinical and psychometric advantages over the YBOCS-I. When these findings are sufficiently replicated, use of the YBOCS-II as the new common standard seems recommendable.


Subject(s)
Obsessive-Compulsive Disorder , Humans , Psychometrics , Reproducibility of Results , Severity of Illness Index , Obsessive-Compulsive Disorder/diagnosis , Ethnicity , Psychiatric Status Rating Scales
2.
Eur Psychiatry ; 40: 38-44, 2017 02.
Article in English | MEDLINE | ID: mdl-27837671

ABSTRACT

BACKGROUND: Preliminary studies have shown that the addition of the partial NMDA-agonist d-cycloserine (DCS) might be promising in enhancing the results of exposure therapy in obsessive-compulsive disorder (OCD). We examined the effect of DCS addition to exposure therapy in a somewhat larger sample of OCD patients with special attention to subgroups, because of the heterogeneity of OCD. METHODS: A randomized, double-blind, placebo controlled trial was conducted in 39 patients with OCD. Patients received 6 guided exposure sessions, once a week. One hour before each session 125mg DCS or placebo was administered. RESULTS: Scores on the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) declined more in the DCS group than in the placebo group, but the difference did not reach statistical significance (P=0.076, partial η2=0.13). Response percentages also did not differ between the DCS and the placebo group (37% and 15% respectively). In the 'cleaning/contamination' subgroup a significant effect was found in favour of DCS (P=0.033, partial η2=0.297). CONCLUSIONS: The results of this study did not support the application of DCS to exposure therapy in OCD. Some specific aspects need further investigation: efficacy of DCS in a larger 'cleaning/contamination' (sub-)group, DCS addition only after successful sessions, interaction with antidepressants.


Subject(s)
Antidepressive Agents/administration & dosage , Cognitive Behavioral Therapy/methods , Cycloserine/administration & dosage , Obsessive-Compulsive Disorder/drug therapy , Adult , Combined Modality Therapy , Double-Blind Method , Female , Humans , Male , Middle Aged , Obsessive-Compulsive Disorder/therapy , Therapy, Computer-Assisted/methods , Treatment Outcome , Young Adult
3.
Tijdschr Psychiatr ; 52(5): 349-52, 2010.
Article in Dutch | MEDLINE | ID: mdl-20458682

ABSTRACT

Differentiating panic disorder form epilepsy can be a difficult task. In this case study the task was made more complicated because the patient was being treated with the selective serotonin reuptake inhibitor (SSRI) citalopram which evoked a partial response, thereby delaying the diagnosis of epilepsy. Research results demonstrate that ssris can have not only an antidepressive and calming effect, they can also have an anticonvulsant effect. However, there are also signs that, as this case illustrates, in the long term the anticonvulsant effect can actually convert to proconvulsant effect.


Subject(s)
Citalopram/adverse effects , Epilepsy/diagnosis , Panic Disorder/diagnosis , Selective Serotonin Reuptake Inhibitors/adverse effects , Adult , Citalopram/therapeutic use , Diagnosis, Differential , Humans , Male , Panic Disorder/drug therapy , Selective Serotonin Reuptake Inhibitors/therapeutic use
4.
Tijdschr Psychiatr ; 48(6): 461-6, 2006.
Article in Dutch | MEDLINE | ID: mdl-16956005

ABSTRACT

BACKGROUND: In certain disorders the boundaries between thoughts, obsessions, overvalued ideas and delusions are not always clearly delineated. AIM: To find out whether delusions can be distinguished from the convictions that often accompany anorexia nervosa, obsessive compulsive disorder (OCD), body dysmorphic disorder (BDD) and hypochondriasis, all of which apparently may involve impaired reality testing. METHOD: The literature was reviewed with the help of PubMed, using as key words 'delusions' in combination with 'hypochodriasis', 'anorexia nervosa', 'body image', 'obsessive compulsive disorder' or 'body dysmorphic disorder'. We also searched the Tijdschrift voor Psychiatrie and references of the literature we used. RESULTS: A number of disorders can probably be classified on a spectrum ranging from non-psychotic to psychotic. For instance, OCD, hypochondriasis, BDD and to a lesser degree anorexia nervosa can all be particularized as 'with good insight', 'with poor insight' or 'with psychotic features'. CONCLUSION: Current practice in DSM-IV is to classify OCD, BDD or hypochondriasis and a delusional disorder as separate entities; this way of classifying seems to be an artefact. Our findings indicate that a dimensional system of classifying psychotic systems is preferable to a categorised system.


Subject(s)
Delusions/psychology , Feeding and Eating Disorders/psychology , Hypochondriasis/psychology , Obsessive-Compulsive Disorder/psychology , Psychotic Disorders/psychology , Somatoform Disorders/psychology , Body Image , Delusions/classification , Feeding and Eating Disorders/classification , Humans , Hypochondriasis/classification , Obsessive-Compulsive Disorder/classification , Psychiatric Status Rating Scales , Somatoform Disorders/classification , Thinking
5.
Psychopharmacology (Berl) ; 126(4): 339-44, 1996 Aug.
Article in English | MEDLINE | ID: mdl-8878350

ABSTRACT

The effects of the CCKB-receptor agonist pentagastrin, a synthetic analogue of the cholecystokinin tetrapeptide (CCK-4), were studied in seven patients suffering from obsessive compulsive disorder (OCD) and seven healthy controls. All subjects were challenged with an IV dose of 0.6 micrograms/kg pentagastrin or placebo under double blind placebo controlled conditions, on two separate occasions, with a minimum interval of 1 week. Six (86%) out of seven OCD patients experienced a panic-like reaction after pentagastrin administration, against only two (29%) in the control group. These differences failed to reach statistical significance, probably due to the small sample size. No increases were observed in obsessions or compulsive behaviors as assessed with the Yale-Brown Obsessive Compulsive Challenge Scale, neither in the pentagastrin, nor in the placebo condition. These findings suggest that pentagastrin has panic-inducing properties in OCD patients, without affecting the core symptoms. The panic-inducing properties of pentagastrin are not specific for panic disorder patients, which might be indicative of a common neurobiological dysfunction in panic disorder and OCD at the level of CCK-B receptors.


Subject(s)
Obsessive-Compulsive Disorder/drug therapy , Panic Disorder/chemically induced , Pentagastrin/adverse effects , Adult , Affect/drug effects , Double-Blind Method , Female , Humans , Hydrocortisone/blood , Male , Methoxyhydroxyphenylglycol/blood , Pentagastrin/therapeutic use , Prolactin/blood
6.
Int Clin Psychopharmacol ; 9 Suppl 4: 47-52, 1995 Jan.
Article in English | MEDLINE | ID: mdl-7622824

ABSTRACT

The selective serotonin reuptake inhibitor (SSRI) fluvoxamine has been used in an attempt to understand whether there is a biological distinction among anxiety disorders. A comparison of fluvoxamine with the specific noradrenaline reuptake inhibitor maprotiline in patients with panic disorder showed fluvoxamine to be a potent anti-panic agent, whereas maprotiline had no effect on the frequency of panic attacks. This result supported the hypothesis of serotonergic involvement in the pathogenesis of panic disorder. In a second study, unlike fluvoxamine, the 5-HT2A/2C antagonist ritanserin had no effect on the number of panic attacks, or phobic avoidance. This suggested that the efficacy of antidepressants in panic disorder was not a result of down-regulation of postsynaptic 5-HT2 receptors. Most studies suggest that the efficacy of antidepressants in obsessive-compulsive disorder (OCD) is not related to their antidepressant or mood-enhancing effects. Fluvoxamine has also been shown to reduce general and phobic anxiety in social phobia patients. In conclusion, serotonergic systems are implicated in the pathophysiology of global anxiety irrespective of the nosological background, and SSRIs, exemplified by fluvoxamine, appear to be effective in panic disorder, OCD and probably also social phobia.


Subject(s)
Anxiety Disorders/drug therapy , Fluvoxamine/therapeutic use , Selective Serotonin Reuptake Inhibitors/therapeutic use , Fluvoxamine/pharmacology , Humans , Maprotiline/pharmacology , Obsessive-Compulsive Disorder/drug therapy , Panic/drug effects , Receptors, Serotonin/physiology , Ritanserin/pharmacology , Selective Serotonin Reuptake Inhibitors/pharmacology , Time Factors
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