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        <title>Annals of General Psychiatry - Latest Articles</title>
        <link>http://www.annals-general-psychiatry.com</link>
        <description>The latest research articles published by Annals of General Psychiatry</description>
        <dc:date>2010-07-29T00:00:00Z</dc:date>
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                                <rdf:li rdf:resource="http://www.annals-general-psychiatry.com/content/9/1/33" />
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/33">
        <title>The Factors Influencing Depression Endpoints Research (FINDER) study: final results of Italian patients with depression</title>
        <description>Background:
Factors Influencing Depression Endpoints Research (FINDER) is a 6-month, prospective, observational study carried out in 12 European countries aimed at investigating health-related quality of life (HRQoL) in outpatients receiving treatment for a first or new depressive episode. The Italian HRQoL data at 6 months is described in this report, and the factors associated with HRQoL changes were determined.
Methods:
Data were collected at baseline, 3 and 6 months of treatment. HRQoL was measured using components of the 36-item Short Form Health Survey (SF-36; mental component summary (MCS), physical component summary (PCS)) and the European Quality of Life-5 Dimensions (EQ-5D; visual analogue scale (VAS) and health status index (HSI)). The Hospital Anxiety and Depression Scale (HADS) was adopted to evaluate depressive symptoms, while somatic and painful physical symptoms were assessed by using the 28-item Somatic Symptom Inventory (SSI-28) and a VAS.
Results:
Of the initial 513 patients, 472 completed the 3-month observation and 466 the 6-month observation. The SF-36 and EQ-5D mean (&#177; SD) scores showed HRQoL improvements at 3 months and a further smaller improvement at 6 months, with the most positive effects for SF-36 MCS (baseline 22.0 &#177; 9.2, 3 months 34.6 &#177; 10.0; 6 months 39.3 &#177; 9.5) and EQ-5D HSI (baseline 0.4 &#177; 0.3; 3 months 0.7 &#177; 0.3; 6 months 0.7 &#177; 0.2). Depression and anxiety symptoms (HADS-D mean at baseline 13.3 &#177; 4.2; HADS-A mean at baseline 12.2 &#177; 3.9) consistently decreased during the first 3 months (8.7 &#177; 4.3; 7.5 &#177; 3.6) and showed a further positive change at 6 months (6.9 &#177; 4.3; 5.8 &#177; 3.4). Somatic and painful symptoms (SSI and VAS) significantly decreased, with the most positive changes in the SSI-28 somatic item (mean at baseline 2.4 &#177; 0.7; mean change at 3 months: -0.5; 95% CI -0.6 to -0.5; mean change at 6 months: -0.7; 95% CI -0.8 to -0.7); in &apos;interference of overall pain with daily activities&apos; (mean at baseline 45.2 &#177; 30.7; mean change at 3 months -17.4; 95% CI -20.0 to -14.8; mean change at 6 months -24.4; 95% CI -27.3 to -21.6) and in &apos;having pain while awake&apos; (mean at baseline 41.1 &#177; 29.0; mean change at 3 months -13.7; 95% CI -15.9 to -11.5; mean change at 6 months -20.2; 95% CI -22.8 to -17.5) domains. The results from linear regression analyses showed that the antidepressant switch within classes was consistently associated with a worsening in SF-36 MCS, EQ-5D VAS and HSI compared to non-switching treatment. Furthermore, between-group antidepressants (AD) switch was associated with a worse SF-36 MCS and EQ-5D HSI. MCS (P = 0.028), PCS (P = 0.036) and HSI (P = 0.002) were inversely related to the number of each previous additional depressive episode. PCS (P = 0.009) and HSI (P = 0.005) were also less improved in patients suffering from a chronic medical condition. Moreover, PCS (P = 0.044) and EQ-5D VAS (P &lt; 0.0001) worsening was consistently associated with the presence of a psychiatric illness in the 24 months before baseline. For every additional point on the SSI-somatic score and on the overall pain VAS score at baseline, HSI score were on average 0.062 (P &lt; 0.001) and 0.001 (P = 0.005) smaller, respectively.
Conclusions:
After starting AD treatment, HRQoL improvements at 3 and 6 months were observed. However, several factors can negatively influence HRQoL, such as the presence of somatic and painful symptoms, the presence of any chronic medical condition or previous psychiatric illness.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/33</link>
                <dc:creator>Rosangela Caruso</dc:creator>
                <dc:creator>Andrea Rossi</dc:creator>
                <dc:creator>Alessandra Barraco</dc:creator>
                <dc:creator>Deborah Quail</dc:creator>
                <dc:creator>Luigi Grassi</dc:creator>
                <dc:creator>On behalf of the Italian FINDER study group</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:33</dc:source>
        <dc:date>2010-07-29T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-33</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>33</prism:startingPage>
        <prism:publicationDate>2010-07-29T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/32">
        <title>The combined effect of gender and age on post traumatic stress disorder: do men and women show differences in the lifespan distribution of the disorder?</title>
        <description>Background:
The aim of the study was to examine the combined effect of gender and age on post traumatic stress disorder (PTSD) in order to describe a possible gender difference in the lifespan distribution of PTSD.
Methods:
Data were collected from previous Danish and Nordic studies of PTSD or trauma. The final sample was composed of 6,548 participants, 2,768 (42.3%) men and 3,780 (57.7%) women. PTSD was measured based on the Harvard Trauma Questionnaire, part IV (HTQ-IV).
Results:
Men and women differed in lifespan distribution of PTSD. The highest prevalence of PTSD was seen in the early 40s for men and in the early 50s for women, while the lowest prevalence for both genders was in the early 70s. Women had an overall twofold higher PTSD prevalence than men. However, at some ages the female to male ratio was nearly 3:1. The highest female to male ratio was found for the 21 to 25 year-olds.
Conclusions:
The lifespan gender differences indicate the importance of including reproductive factors and social responsibilities in the understanding of the development of PTSD.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/32</link>
                <dc:creator>Daniel Ditlevsen</dc:creator>
                <dc:creator>Ask Elklit</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:32</dc:source>
        <dc:date>2010-07-21T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-32</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>32</prism:startingPage>
        <prism:publicationDate>2010-07-21T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/31">
        <title>The &apos;antisocial&apos; person: an insight in to biology, classification and current evidence on treatment</title>
        <description>Background:
This review analyses and summarises the recent advances in understanding the neurobiology of violence and empathy, taxonomical issues on defining personality disorders characterised by disregard for social norms, evidence for efficacy of different treatment modalities and ethical implications in defining &apos;at-risk&apos; individuals for preventive interventions.
Methods:
PubMed was searched with the keywords &apos;antisocial personality disorder&apos;, &apos;dissocial personality disorder&apos; and &apos;psychopathy&apos;. The search was limited to articles published in English over the last 10 years (1999 to 2009)
Results:
Both diagnostic manuals used in modern psychiatry, the Diagnostic and Statistical Manual published by the American Psychiatric Association and the International Classification of Diseases published by the World Health Organization, identify a personality disorder sharing similar traits. It is termed antisocial personality disorder in the diagnostic and statistical manual and dissocial personality disorder in the International Classification of Diseases. However, some authors query the ability of the existing manuals to identify a special category termed &apos;psychopathy&apos;, which in their opinion deserves special attention. On treatment-related issues, many psychological and behavioural therapies have shown success rates ranging from 25% to 62% in different cohorts. Multisystemic therapy and cognitive behaviour therapy have been proven efficacious in many trials. There is no substantial evidence for the efficacy of pharmacological therapy. Currently, the emphasis is on early identification and prevention of antisocial behaviour despite the ethical implications of defining at-risk children.
Conclusions:
Further research is needed in the areas of neuroendocrinological associations of violent behaviour, taxonomic existence of psychopathy and efficacy of treatment modalities.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/31</link>
                <dc:creator>Chaturaka Rodrigo</dc:creator>
                <dc:creator>Senaka Rajapakse</dc:creator>
                <dc:creator>Gamini Jayananda</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:31</dc:source>
        <dc:date>2010-07-06T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-31</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>31</prism:startingPage>
        <prism:publicationDate>2010-07-06T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/30">
        <title>Assessment of the emotional responses produced by exposure to real food, virtual food and photographs of food in patients affected by eating disorders</title>
        <description>Background:
Many researchers and clinicians have proposed using virtual reality (VR) in adjunct to in vivo exposure therapy to provide an innovative form of exposure to patients suffering from different psychological disorders. The rationale behind the &apos;virtual approach&apos; is that real and virtual exposures elicit a comparable emotional reaction in subjects, even if, to date, there are no experimental data that directly compare these two conditions. To test whether virtual stimuli are as effective as real stimuli, and more effective than photographs in the anxiety induction process, we tested the emotional reactions to real food (RF), virtual reality (VR) food and photographs (PH) of food in two samples of patients affected, respectively, by anorexia (AN) and bulimia nervosa (BN) compared to a group of healthy subjects. The two main hypotheses were the following: (a) the virtual exposure elicits emotional responses comparable to those produced by the real exposure; (b) the sense of presence induced by the VR immersion makes the virtual experience more ecological, and consequently more effective than static pictures in producing emotional responses in humans.
Methods:
In total, 10 AN, 10 BN and 10 healthy control subjects (CTR) were randomly exposed to three experimental conditions: RF, PH, and VR while their psychological (Stait Anxiety Inventory (STAI-S) and visual analogue scale for anxiety (VAS-A)) and physiological (heart rate, respiration rate, and skin conductance) responses were recorded.
Results:
RF and VR induced a comparable emotional reaction in patients higher than the one elicited by the PH condition. We also found a significant effect in the subjects&apos; degree of presence experienced in the VR condition about their level of perceived anxiety (STAI-S and VAS-A): the higher the sense of presence, the stronger the level of anxiety.
Conclusions:
Even though preliminary, the present data show that VR is more effective than PH in eliciting emotional responses similar to those expected in real life situations. More generally, the present study suggests the potential of VR in a variety of experimental, training and clinical contexts, being its range of possibilities extremely wide and customizable. In particular, in a psychological perspective based on a cognitive behavioral approach, the use of VR enables the provision of specific contexts to help patients to cope with their diseases thanks to an easily controlled stimulation.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/30</link>
                <dc:creator>Alessandra Gorini</dc:creator>
                <dc:creator>Eric Griez</dc:creator>
                <dc:creator>Anna Petrova</dc:creator>
                <dc:creator>Giuseppe Riva</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:30</dc:source>
        <dc:date>2010-07-05T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-30</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>30</prism:startingPage>
        <prism:publicationDate>2010-07-05T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/29">
        <title>Serum glutamine, set-shifting ability and anorexia nervosa</title>
        <description>Background:
Set-shifting is impaired in people with anorexia nervosa (AN), but the underlying physiological and biochemical processes are unclear. Animal studies have established that glutamatergic pathways in the prefrontal cortex play an important role in set-shifting ability. However, it is not yet understood whether levels of serum glutamatergic amino acids are associated with set-shifting performance in humans. The aim of this study was to determine whether serum concentrations of amino acids related to glutamatergic neurotransmission (glutamine, glutamate, glycine, l-serine, d-serine) are associated with set-shifting ability in people with acute AN and those after recovery.
Methods:
Serum concentrations of glutamatergic amino acids were measured in 27 women with current AN (AN group), 18 women recovered from AN (ANRec group) and 28 age-matched healthy controls (HC group). Set-shifting was measured using the Wisconsin Card Sorting Test (WCST) and the Trail Making Task (TMT). Dimensional measures of psychopathology were used, including the Eating Disorder Examination Questionnaire (EDEQ), the Maudsley Obsessive-Compulsive Inventory (MOCI) and the Hospital Anxiety and Depression Scale (HADS).
Results:
Serum glutamine concentrations in the AN group (1,310.2 &#177; 265.6 &#956;M, mean &#177; SD) were significantly higher (by approximately 20%) than those in the HC group (1,102.9 &#177; 152.7 &#956;M, mean &#177; SD) (F(2, 70) = 6.3, P = 0.003, 95% CI 61.2 to 353.4). Concentrations of serum glutamine were positively associated with markers of the illness severity: a negative correlation was present between serum glutamine concentrations and body mass index (BMI) and lowest BMI and a positive correlation was found between duration of illness and EDEQ. The AN group showed significantly impaired set shifting in the WCST, both total errors, and perseverative errors. In the AN group, there were no correlations between serum glutamine concentrations and set shifting.
Conclusions:
Serum concentrations of glutamine may be a biomarker of illness severity in people with AN. It does not appear to be directly associated with changes in executive function.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/29</link>
                <dc:creator>Michiko Nakazato</dc:creator>
                <dc:creator>Kenji Hashimoto</dc:creator>
                <dc:creator>Ulrike Schmidt</dc:creator>
                <dc:creator>Kate Tchanturia</dc:creator>
                <dc:creator>Iain Campbell</dc:creator>
                <dc:creator>David Collier</dc:creator>
                <dc:creator>Masaomi Iyo</dc:creator>
                <dc:creator>Janet Treasure</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:29</dc:source>
        <dc:date>2010-06-25T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-29</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>29</prism:startingPage>
        <prism:publicationDate>2010-06-25T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/28">
        <title>Sigma-1 receptor agonist fluvoxamine for postoperative delirium in older adults: report of three cases</title>
        <description>Background:
Postoperative delirium is a topic of great importance in the geriatric surgical specialty. Although antipsychotic drugs are the medications most frequently used to treat this syndrome, these drugs are associated with a variety of adverse events, including sedation, extrapyramidal side effects, and cardiac arrhythmias. Drug treatment for postoperative delirium requires careful consideration of the balance between the effective management of symptoms and potential adverse effects.
Methods:
We report on a Japanese woman (an 86-year-old (open reduction and internal fixation of the right femoral neck fracture), and two Japanese men (an 86-year-old (abdominal aortic aneurysm stent grafting), and a 77-year-old (right upper lobectomy due to lung tumour)) in which the selective serotonin reuptake inhibitor and sigma-1 receptor agonist fluvoxamine was effective in ameliorating the postoperative delirium of these patients.
Results:
Delirium Rating Scale scores in these patients dramatically decreased after treatment with fluvoxamine.
Conclusions:
Doctors should consider fluvoxamine as an alternative approach to treating postoperative delirium in older patients in order to avoid the risk of side effects and increased mortality by antipsychotic drugs.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/28</link>
                <dc:creator>Tsutomu Furuse</dc:creator>
                <dc:creator>Kenji Hashimoto</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:28</dc:source>
        <dc:date>2010-06-24T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-28</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>28</prism:startingPage>
        <prism:publicationDate>2010-06-24T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
    </item>
        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/27">
        <title>A randomised, double-blind, placebo-controlled trial of tropisetron in patients with schizophrenia</title>
        <description>Background:
Cognitive deficits in schizophrenia are associated with psychosocial deficits that are primarily responsible for the poor long-term outcome of this disease. Auditory sensory gating P50 deficits are correlated with neuropsychological deficits in attention, one of the principal cognitive disturbances in schizophrenia. Our studies suggest that the &#945;7 nicotinic acetylcholine receptor (&#945;7 nAChR) agonist tropisetron might be a potential therapeutic drug for cognitive deficits in schizophrenia. Therefore, it is of particular interest to investigate the effects of tropisetron on the cognitive deficits in patients with schizophrenia.
Methods:
A randomised, placebo-controlled trial of tropisetron in patients with schizophrenia was performed. A total of 40 patients with chronic schizophrenia who had taken risperidone (2 to 6 mg/day) were enrolled. Subjects were randomly assigned to a fixed titration of tropisetron (n = 20, 10 mg/day) or placebo (n = 20) in an 8-week double-blind trial. Auditory sensory gating P50 deficits and Quality of Life Scale (QLS), Cambridge Neuropsychological Test Automated Battery (CANTAB), and Positive and Negative Syndrome Scale (PANSS) scores were measured.
Results:
In all, 33 patients completed the trial. Tropisetron was well tolerated. Administration of tropisetron, but not placebo, significantly improved auditory sensory gating P50 deficits in non-smoking patients with schizophrenia. The score on the rapid visual information processing (sustained visual attention) task of CANTAB was significantly improved by tropisetron treatment. Total and subscale scores of PANSS were not changed by this trial. QLS scores in the all patients, but not non-smoking patients, were significantly improved by tropisetron trial.
Conclusions:
This first randomised, double-blind, placebo-controlled trial supports the safety and efficacy of adjunctive tropisetron for treatment of cognitive deficits in schizophrenia.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/27</link>
                <dc:creator>Akihiro Shiina</dc:creator>
                <dc:creator>Yukihiko Shirayama</dc:creator>
                <dc:creator>Tomihisa Niitsu</dc:creator>
                <dc:creator>Tasuku Hashimoto</dc:creator>
                <dc:creator>Taisuke Yoshida</dc:creator>
                <dc:creator>Tadashi Hasegawa</dc:creator>
                <dc:creator>Tadashi Haraguchi</dc:creator>
                <dc:creator>Nobuhisa Kanahara</dc:creator>
                <dc:creator>Tetsuya Shiraishi</dc:creator>
                <dc:creator>Mihisa Fujisaki</dc:creator>
                <dc:creator>Goro Fukami</dc:creator>
                <dc:creator>Michiko Nakazato</dc:creator>
                <dc:creator>Masaomi Iyo</dc:creator>
                <dc:creator>Kenji Hashimoto</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:27</dc:source>
        <dc:date>2010-06-24T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-27</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>27</prism:startingPage>
        <prism:publicationDate>2010-06-24T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/26">
        <title>Collaboration between general hospitals and community health services in the care of suicide attempters in Norway: a longitudinal study</title>
        <description>Background:
The aim of this paper was to study the collaboration between emergency departments (EDs) in general hospitals and community health services (CHS) in Norway when providing psychosocial care and aftercare to patients treated in EDs following a suicide attempt. We wanted to explore the extent to which quality indicators at the hospital level measured in 1999 and 2006 could predict the presence or absence of a chain of care structure in the CHS in 2006.
Methods:
Data were collected through structured interviews with informants from 95% of all general hospitals in Norway in 1999 and 2006, and informants from CHS, in a stratified sample of Norwegian municipalities in 2006 (n = 47).
Results:
In 15 of the 47 municipalities (32%), the CHS reported having a chain of care structure in 2006. A discriminant function analysis revealed that the hospitals that in 1999 had: (a) a collaboration agreement with aftercare providers, and (b) written guidelines, including a quality assurance system, were significantly more likely to have municipalities with a chain of care structure in their catchment area in 2006.
Conclusions:
Hospitals&apos; and municipalities&apos; self-reported provision of aftercare services for patients treated after a suicide attempt was markedly below the recommendations given in national standards. Systems at the hospital level for the management and care of patients admitted after a suicide attempt and systematic collaboration between hospitals and aftercare providers seem to be important elements in the long-term maintenance of continuity of care for suicide attempters.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/26</link>
                <dc:creator>Erlend Mork</dc:creator>
                <dc:creator>Lars Mehlum</dc:creator>
                <dc:creator>Elin Anita Fadum</dc:creator>
                <dc:creator>Ingeborg Rossow</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:26</dc:source>
        <dc:date>2010-06-11T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-26</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>26</prism:startingPage>
        <prism:publicationDate>2010-06-11T00:00:00Z</prism:publicationDate>
                <prism:versionidentifier>XML</prism:versionidentifier>
                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/25">
        <title>Human depression: a new approach in quantitative psychiatry
</title>
        <description>The biomolecular approach to major depression disorder is explained by the different steps that involve cell membrane viscosity, Gs&#945; protein and tubulin. For the first time it is hypothesised that a biomolecular pathway exists, moving from cell membrane viscosity through Gs&#945; protein and Tubulin, which can condition the conscious state and is measurable by electroencephalogram study of the brain&apos;s &#947; wave synchrony.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/25</link>
                <dc:creator>Massimo Cocchi</dc:creator>
                <dc:creator>Lucio Tonello</dc:creator>
                <dc:creator>Mark Rasenick</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:25</dc:source>
        <dc:date>2010-06-03T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-25</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>25</prism:startingPage>
        <prism:publicationDate>2010-06-03T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.annals-general-psychiatry.com/content/9/1/24">
        <title>Predicting hospital admission and discharge with symptom or function scores in patients with schizophrenia: pooled analysis of a clinical trial extension</title>
        <description>Background:
The purpose of this analysis was to evaluate relationships between hospital admission or discharge and scores for symptom or functioning in patients with schizophrenia.
Methods:
Data were from three 52-week open-label extensions of the double-blind pivotal trials of paliperidone extended-release (ER). Symptoms and patient function were measured every 4 weeks using the Personal and Social Performance (PSP) scale and the Positive and Negative Syndrome Scale (PANSS). The intent-to-treat analysis set was defined as open-label patients who had at least one post-baseline PSP and PANSS measurement. Time until first hospitalization was evaluated using the Cox proportional hazard model with categorical time-dependent measures for the PSP (1 to 30, 31 to 70, 71 to 100) or PANSS (&lt; 75, &#8805; 75 to &lt; 95, &#8805; 95), as well as age, gender, schizophrenia duration, and country. Similar analyses were performed for time to discharge.
Results:
Of the 1,077 enrolled patients, 1,028 (95.5%) met study criteria; of these, 382 (37.2%) were hospitalized at open-label baseline. Compared with patients with PSP &#8805; 71 group, the hazard for new hospitalization was 8.351 times greater (P = 0.0001) for patients with the poorest functioning (PSP 1 to 30) and 1.977 times greater (P = 0.0295) for patients with PSP of 31-70 compared to the &#8805; 71 group. The hazard for new hospitalization was 5.457 times greater (P &lt; 0.0001) for patients PANSS &#8805; 95 and 2.316 times greater (P = 0.0027) for the &#8805; 75 to &lt; 95 group compared with the &lt; 75 group. For patients hospitalized at baseline, the PANSS &#8805; 95 patients had a discharge hazard that was 0.456 times lower than for the &lt; 75 patients (P &lt; 0.0001). The hazard for discharge was 0.646 times lower (P = 0.0012) for the PANSS &#8805; 75 to &lt; 95 group compared with the &lt; 75 group. A patient&apos;s country was a significant predictor variable, with US patients being admitted and discharged faster.
Conclusions:
Better functioning or being less symptomatic is associated with reduced risk for hospitalization and greater chance for early discharge. Treatments or programs that reduce symptoms or improve function decrease the risk of hospitalization in community patients or increase the chance of discharge for hospitalized patients.</description>
        <link>http://www.annals-general-psychiatry.com/content/9/1/24</link>
                <dc:creator>Chris Kozma</dc:creator>
                <dc:creator>Riad Dirani</dc:creator>
                <dc:creator>Carla Canuso</dc:creator>
                <dc:creator>Lian Mao</dc:creator>
                <dc:source>Annals of General Psychiatry 2010, 9:24</dc:source>
        <dc:date>2010-06-02T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/1744-859X-9-24</dc:identifier>
        <prism:publicationName>Annals of General Psychiatry</prism:publicationName>
        <prism:issn>1744-859X</prism:issn>
        <prism:volume>9</prism:volume>
        <prism:startingPage>24</prism:startingPage>
        <prism:publicationDate>2010-06-02T00:00:00Z</prism:publicationDate>
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