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<title>MED: Psychiatry Papers</title>
<link>http://hdl.handle.net/2144/2455</link>
<description/>
<pubDate>Wed, 27 Mar 2013 01:29:05 GMT</pubDate>
<dc:date>2013-03-27T01:29:05Z</dc:date>
<item>
<title>The Physician Clinical Support System-Buprenorphine (PCSS-B): A Novel Project to Expand/Improve Buprenorphine Treatment</title>
<link>http://hdl.handle.net/2144/3411</link>
<description>The Physician Clinical Support System-Buprenorphine (PCSS-B): A Novel Project to Expand/Improve Buprenorphine Treatment
Egan, James E.; Casadonte, Paul; Gartenmann, Tracy; Martin, Judith; McCance-Katz, Elinore F.; Netherland, Julie; Renner, John A.; Weiss, Linda; Saxon, Andrew J.; Fiellin, David A.
Opioid dependence is largely an undertreated medical condition in the United States. The introduction of buprenorphine has created the potential to expand access to and use of opioid agonist treatment in generalist settings. Physicians, however, often have limited training and experience providing this type of care. Some physicians believe having a mentoring relationship with an experienced provider during their initial introduction to the use of buprenorphine would ease implementation. Our goal was to describe the development, implementation, resources, and evaluation of the Physician Clinical Support System-Buprenorphine (PCSS-B), a federally funded program to improve access to and quality of treatment with buprenorphine. We provide a description of the PCSS-B, a national network of 88 trained physician mentors with expertise in buprenorphine treatment and skills in clinical education. We provide information regarding the use the PCSS-B core services including telephone, email and in-person support, a website, clinical guidances, a warmline and outreach to primary care and specialty organizations. Between July 2005 and July 2009, 67 mentors and 4 clinical experts reported providing mentoring services to 632 participants in 48 states, Washington DC and Puerto Rico. A total of 1,455 contacts were provided through email (45%), telephone (34%) and in-person visits (20%). Seventy-six percent of contacts addressed a clinical issue. Eighteen percent of contacts addressed a logistical issue. The number of contacts per participant ranged from 1–125. Between August 2005 and April 2009 there were 72,822 visits to the PCSS-B website with 179,678 pages viewed. Seven guidances were downloaded more than 1000 times. The warmline averaged more than 100 calls per month. The PCSS-B model provides support for a mentorship program to assist non-specialty physicians in the provision of buprenorphine and may serve as a model for dissemination of other types of care.
</description>
<pubDate>Tue, 11 May 2010 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/2144/3411</guid>
<dc:date>2010-05-11T00:00:00Z</dc:date>
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<title>Prolonged Grief Disorder: Psychometric Validation of Criteria Proposed for DSM-V and ICD-11</title>
<link>http://hdl.handle.net/2144/3412</link>
<description>Prolonged Grief Disorder: Psychometric Validation of Criteria Proposed for DSM-V and ICD-11
Prigerson, Holly G.; Horowitz, Mardi J.; Jacobs, Selby C.; Parkes, Colin M.; Aslan, Mihaela; Goodkin, Karl; Raphael, Beverley; Marwit, Samuel J.; Wortman, Camille; Neimeyer, Robert A.; Bonanno, George; Block, Susan D.; Kissane, David; Boelen, Paul; Maercker, Andreas; Litz, Brett T.; Johnson, Jeffrey G.; First, Michael B.; Maciejewski, Paul K.
Holly Prigerson and colleagues tested the psychometric validity of criteria for prolonged grief disorder (PGD) to enhance the detection and care of bereaved individuals at heightened risk of persistent distress and dysfunction. 

BACKGROUND. 

Bereavement is a universal experience, and its association with excess morbidity and mortality is well established. Nevertheless, grief becomes a serious health concern for a relative few. For such individuals, intense grief persists, is distressing and disabling, and may meet criteria as a distinct mental disorder. At present, grief is not recognized as a mental disorder in the DSM-IV or ICD-10. The goal of this study was to determine the psychometric validity of criteria for prolonged grief disorder (PGD) to enhance the detection and potential treatment of bereaved individuals at heightened risk of persistent distress and dysfunction. 

METHODS AND FINDINGS. 

A total of 291 bereaved respondents were interviewed three times, grouped as 0–6, 6–12, and 12–24 mo post-loss. Item response theory (IRT) analyses derived the most informative, unbiased PGD symptoms. Combinatoric analyses identified the most sensitive and specific PGD algorithm that was then tested to evaluate its psychometric validity. Criteria require reactions to a significant loss that involve the experience of yearning (e.g., physical or emotional suffering as a result of the desired, but unfulfilled, reunion with the deceased) and at least five of the following nine symptoms experienced at least daily or to a disabling degree: feeling emotionally numb, stunned, or that life is meaningless; experiencing mistrust; bitterness over the loss; difficulty accepting the loss; identity confusion; avoidance of the reality of the loss; or difficulty moving on with life. Symptoms must be present at sufficiently high levels at least six mo from the death and be associated with functional impairment.

CONCLUSIONS. 

The criteria set for PGD appear able to identify bereaved persons at heightened risk for enduring distress and dysfunction. The results support the psychometric validity of the criteria for PGD that we propose for inclusion in DSM-V and ICD-11.
</description>
<pubDate>Tue, 04 Aug 2009 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/2144/3412</guid>
<dc:date>2009-08-04T00:00:00Z</dc:date>
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<item>
<title>Prevalence and Predictors of Health Service Use among Iraqi Asylum Seekers in the Netherlands</title>
<link>http://hdl.handle.net/2144/3413</link>
<description>Prevalence and Predictors of Health Service Use among Iraqi Asylum Seekers in the Netherlands
Laban, Cornelis J.; Gernaat, Hajo B. P. E.; Komproe, Ivan H.; De Jong, Joop T. V. M.
BACKGROUND. A long asylum procedure is associated with higher prevalence rates of psychiatric disorders, lower quality of life, higher disability and more physical health problems. Additional knowledge about health seeking behavior is necessary to guide governments and health professionals in their policies. OBJECTIVE. To measure service use among one of the biggest asylum seekers population in the Netherlands and to assess its relationships with predisposing and need variables (including post-migration living problems). METHOD. Two groups were randomly selected: Group 1 (n = 143), less than 6 months and Group 2 (n = 151), more than 2 years in the Netherlands. Respondents were interviewed with fully structured, culturally validated, translated questionnaires, which contained instruments to measure psychiatric disorders, quality of life, disability, physical health and post-migration living problems. Use of preventive and curative (physical and mental) health services was measured and the relationship with predisposing and need risk factors was estimated with univariate and multivariate logistic regression analyses. RESULTS. A long asylum procedure is not associated with higher service use, except for mental health service use and drug use. Use of mental health services is, however, low compared to the prevalence of psychiatric disorders. Low quality of perceived general health and functional disability are the most important predictors of services use. Psychopathology predicts use of a medical specialist (non-psychiatrist), but does not predict mental health service use. CONCLUSION. A high percentage of asylum seekers with a psychiatric disorder is not getting adequate treatment. There is a mismatch between the type of health problem and the type of health service use. The various health services should work together in education, detection, referral and care in order to provide help to this group of patients.
</description>
<pubDate>Fri, 03 Aug 2007 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/2144/3413</guid>
<dc:date>2007-08-03T00:00:00Z</dc:date>
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<title>Development of a Multi-Layered Psychosocial Care System for Children in Areas of Political Violence</title>
<link>http://hdl.handle.net/2144/3410</link>
<description>Development of a Multi-Layered Psychosocial Care System for Children in Areas of Political Violence
Jordans, Mark JD; Tol, Wietse A; Komproe, Ivan H; Susanty, Dessy; Vallipuram, Anavarathan; Ntamatumba, Prudence; Lasuba, Amin C; de Jong, Joop TVM
Few psychosocial and mental health care systems have been reported for children affected by political violence in low- and middle income settings and there is a paucity of research-supported recommendations. This paper describes a field tested multi-layered psychosocial care system for children (focus age between 8-14 years), aiming to translate common principles and guidelines into a comprehensive support package. This community-based approach includes different overlapping levels of interventions to address varying needs for support. These levels provide assessment and management of problems that range from the social-pedagogic domain to the psychosocial, the psychological and the psychiatric domains. Specific intervention methodologies and their rationale are described within the context of a four-country program (Burundi, Sri Lanka, Indonesia and Sudan). The paper aims to contribute to bridge the divide in the literature between guidelines, consensus &amp; research and clinical practice in the field of psychosocial and mental health care in low- and middle-income countries.
</description>
<pubDate>Wed, 16 Jun 2010 00:00:00 GMT</pubDate>
<guid isPermaLink="false">http://hdl.handle.net/2144/3410</guid>
<dc:date>2010-06-16T00:00:00Z</dc:date>
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