Mineur, majeur sous sauvegarde de justice, sous curatelle ou encore sous tutelle, malade mental admis en soins psychiatriques libres ou sous contrainte, le patient doit pouvoir, dans un contexte de démocratie sanitaire, aspirer à un irréductible respect de son autonomie. Situées aux confins de la médecine, de l’éthique et du droit, l’opportunité et la part d’autonomie à concéder à ces personnes au discernement diminué procèdent néanmoins d’une décision médicale devant tantôt privilégier la volonté du patient vulnérable, tantôt préserver ses intérêts. Parce que le rejet de la légendaire figure juridique du contrat médical est, à n’en pas douter, définitivement acquis, le colloque singulier appelle, en ces temps modernes, l’édification d’un nouveau modèle, celui de la décision médicale. Pour l’heure, la situation d’incapacité de ces patients fait, dans une large mesure, l’objet d’une approche cloisonnée entre d’un côté les prescriptions du Code civil et de l’autre, celles du Code de la santé publique. Il s’agit donc, à travers la présente analyse, de relever et de mettre en exergue les faiblesses du système juridique actuel. Les causes de dysfonctionnements qui se trouvent à l’origine d’une instrumentalisation de l’autonomie de ces patients mentalement affaiblis ou encore qui se dressent comme des obstacles structurels à leur autonomie invitent à proposer des pistes de réflexion en faveur de l’élaboration d’une théorie de la décision médicale / Minor, major under protection of law, under guardianship or trusteeship, mentally ill person admitted to psychiatric care free or constrained, the patient must be able, in a context of health democracy, aspire to an irreducible respect for her autonomy. Located on the borders of medicine, ethics and law, timeliness and the degree of autonomy to be granted to such persons shall nevertheless declined to discernment of medical decision making in favor sometimes the will of the patient vulnerable, sometimes preserve its interests. Because the rejection of the legendary figure of the medical contract is legal, to no doubt, definitely acquired, the conference called singular, in these modern times, building a new model, that of the medical decision. For now, the situation of disability of these patients is, in large measure, the subject of a compartmentalized approach from one side to the rules of the Civil Code and the other, those of the Health Code public. It is therefore, through this analysis, to identify and highlight the weaknesses of the current legal system. The causes of failures that are the source of an instrumentalisation of autonomy of mentally impaired patients or that stand as obstacles to their structural autonomy invited to offer food for thought for the development of a theory of medical decision making

Bakgrund: ACT- modellen växte fram under 70 och 80-talet i samband med att många psykiatriska kliniker stängdes i USA. Den ursprungliga ACT- modellen kan ses som en fullservicemodell men har sedan modifierats och anpassats efter samhällets och sjukvårdens rådande förhållanden. Som det ser ut idag så har flera modeller utvecklats med utgångspunkt från ACT-modellen men kan särskiljas av vilka komponenter som ingår. Modellen har visat positiva resultat avseende patienters delaktighet och återhämtning. Sjuksköterskan har en bred yrkesbakgrund och anses ha en viktig roll i teamet. Med sin kompetens har de grundläggande kunskaper för att utföra medicinsk och psykiatrisk omvårdnad men flera studier har visat att det finns ett behov av specialistutbildade sjuksköterskor då många av patienterna är svårt sjuka. Syfte: Syftet var att beskriva psykiatriska specialistsjuksköterskors erfarenheter av sin kompetens och roll i team som arbetar enligt ACT-modellen Metod: En kvalitativ design har valts. Datainsamling skedde med semi-strukturerade intervjuer. En kvalitativ innehållsanalys med induktiv ansats användes för att bearbeta materialet. Resultat: Innehållsanalysen resulterade i två huvudkategorier, Kompetensen med in i teamet samt Den mångsidiga sjuksköterskan, med tillhörande sex underkategorier. Diskussion: Resultatet diskuterades utifrån de två huvudkategorierna Kompetensen med in i teamet och Den mångsidiga sjuksköterskan. Som stöd i diskussionen användes till ämnet relevanta artiklar och litteratur samt Phil Barkers tio förpliktelser som utgångspunkt. / Background: The ACT model developed in the 70's and 80's when many psychiatric clinics were closed in the United States. The original ACT model can be seen as a full service model but has since been modified and adapted to the current conditions of society and health care. As it appears today, several models have been developed based on the ACT model but can be distinguished by which components are included. The model has shown positive results regarding patient participation and recovery. The nurse has a wide professional background and is considered to be an important part of the team. With their skills, they have the basic knowledge to perform medical and psychiatric care, but several studies have shown that there is a need for specialist educated nurses, as many of the patients are severely ill. Aim: The aim of this study was to describe the psychiatric specialist nurse's experience of their competence and role in teams working under the ACT model. Method: A qualitative design has been selected. Data collection was done with semi-structured interviews. A qualitative content analysis with inductive approach was used to process the material. Results: The content analysis resulted in two main categories, skills in the team and the versatile nurse, with six associated subcategories. Discussions: The result was discussed based on the two main categories, skills in the team and the versatile nurse. In support of the discussion, relevant topics and literature were used as well as Phil Barker's ten obligations as a starting point.

Bakgrund: Forskning visar att ökad delaktighet leder till en högre vårdkvalitet, men studier visar på brister i patientdelaktigheten. Syfte: Syftet med denna studie var att beskriva patienters upplevelse av delaktighet inom rättspsykiatrisk heldygnsvård. Metod: Examensarbetet har en kvalitativ metod med induktiv ansats och analyserades utifrån en kvalitativ innehållsanalys. Sju patienter med erfarenheter av att vårdas inom rättspsykiatrisk heldygnsvård intervjuades genom semistrukturerade intervjuer. Resultat: Analysen resulterade i tre slutkategorier; ”Att ingen lyssnar och informerar”, ”Att vara fast i en miljö styrd av lagar och regler”, ”Att tillitsfulla relationer ger styrka”. Det som hindrar delaktighet beskrivs av deltagarna som att inte känna sig lyssnad på, inte bli bemötta utifrån den person de är och att vara fast i en miljö som styrs av lagar och regler. De känner sig begränsade i vården och tycker det är svårt att ta sig framåt. Det som underlättar delaktighet upplevs kopplat till tillitsfulla relationer som avgörande för att kunna känna att man har kontroll och makt över sitt liv. Slutsats: Resultatet bidrar med en fördjupad förståelse av betydelsen av delaktighet i rättspsykiatrisk vård, och vad som kan hindra och underlätta den. Delaktighet är något som patienterna inte tar för givet och vården behöver utveckla förståelse för relationens betydelse som är helt avgörande för vilka möjligheter patienten får till delaktighet och återhämtning. Den rättspsykiatriska vården skulle kunna utvecklas i en riktning mot ökad delaktighet med hjälp av personcentrerad vård.

This thesis deals with the Czech and international ideas applied in the "Strategy of Reform of Psychiatric Care" issued in 2013 by the Ministry of Health of the Czech Republic. The main starting point of this work is the fact that the care of people with mental illness in Czech and international environment is oriented on the biological treatment of the patient with psycho- pharmaceuticals and that there is a deficit in the area of psychosocial treatment. International and Czech mental health policy seeks to promote a bio-psycho-social approach to patient's care. However, current psychiatry continues to be involved in conducting clinical research focused on the efficiency of psycho-pharmaceuticals. These studies are driven and sponsored mainly by the pharmaceutical industry. But international and Czech policies are still not able to adequately reflect this situation within the field of psychiatry. The Czech Republic has not so far paid attention to mental health issues and has lagged behind the other developed countries in this area. The empirical part of this work is divided into two parts. The first part of the research focuses on the Czech and international ideas applied in the "Strategy of Reform of Psychiatric Care" issued in 2013 by Ministry of Health. The methods used here are - content...

The main goal of the Strategy for the Reform of Psychiatric Care, published in 2013 by the Ministry of Health of the Czech republic, was to improve the quality of life of people suffering from mental illness. One of the results of this strategy was the emergence of new mental health centres. These mental health centres are meant to provide individualized social and health care to people with mental illness in order to prevent or minimize their hospitalization. The service is ensured by multidisciplinary teams which include professionals such as psychiatrists, psychologists, psychiatric nurses, and social workers. Case management is supposed to be a dominant form of the service provided. The theoretical part of the thesis describes the historical context of the case management and its recent exploitation in the mental health centres in the Czech republic. The empirical part focuses on a particular multidisciplinary team applying the case management method. Through qualitative research, it aims to identify the different parts of the case management and the constraints and obstacles of its application. The analysis of the data collected brings the definition of the key problem areas the team is facing. The final part of the thesis provides recommendations for further development and proposes steps...

Bakgrund: Självmord är brett representerat över hela världen och berör många miljoner människor direkt eller indirekt. Psykiatriskt sjukdomstillstånd och andra sociala och biologiska tillstånd ligger som grund då en människa tar sitt liv. Omvårdnaden vid självmordsproblematik är central och sjuksköterskors inställning och den vårdrelation som finns mellan sjuksköterska och patient är viktig vid omvårdanden av självmordsnära patienter. Syfte: Syftet med studien var att utifrån sjuksköterskor inom psykiatrisk vård och självmordsnära patienter beskriva omvårdnad som kan vara betydelsefull samt svårigheter som kan föreligga. Metod: Litteraturstudie med 12 artiklar där kvalitativ, kvantitativ och mixad metod användes. Data analyserades med Thomas och Hardens tematiska syntes. Resultat: Resultatet bildade två huvudteman; ”Förutsättningar för att bedriva ändamålsenlig omvårdnad för självmordsnära patienter” och ”Sjuksköterskors känslor – En utmaning vid omvårdnaden av självmordspatienter”. Underteman för respektive huvudteman beskriver ”Observation och säkerhet”, ”Bedömning”, ”Teamarbete”, ”Kommunikation”, ”Kunskap och stöd” samt ”Tid” och för huvudtema två ”Osäkerhet”, ”Sjuksköterskors förhållningssätt: Empati – icke empati” samt ”Medkänsla och sjuksköterskans ingjutande av hopp hos patienten”. Diskussion: Resultatet diskuteras utifrån Joyce Travelbees teoretiska utgångspunkt och belyser den unika människan och den mellanmänskliga relationen, hoppets betydelse för den lidande människan och hur vi förstår andras upplevelser genom tid och kommunikation. / Background: Suicide is widely represented all over the world and affects many millions of people directly or indirectly. Psychiatric disease states and other social and biological conditions lie as a basis when a person takes one’s life. Nursing in suicide problems is central and nurses' attitude and the care relationship between nurse and patient is important in nursing suicidal thinking patients. Aim: The purpose of the study was to describe nursing care that may be significant as well as difficulties that may exist from nurses in psychiatric care and suicidal patients. Method: Literature review with 12 articles using qualitative, quantitative and mixed methodology. Data was analyzed by Thomas and Hardens thematic synthesis. Results: The result formed two main themes; "Prerequisites for proper care for suicidal patients" and "Nursing feelings – A challenge in nursing of suicide patients". Subtopics for the respective main themes describes "Observation and Security", "Assessment", "Teamwork", "Communication", "Knowledge and Support" and "Time" and for the main theme two "Uncertainty", "Nurse’s approach: Empathy - Empathy" and "Compassion and nurse’s initiation of hope for the patient". Discussions: The result is discussed based on Joyce Travelbee's theoretical theory and highlighting the unique human and interpersonal relationship, the significance of the hope for the suffering person, and how we understand the experiences of others through time and communication.

The thesis is based on three months of participant observation in a long-term care facility in 2010 and interviews conducted during next three years. It draws from a perspectives of medical anthropology and anthropology of institutions. The focus is on an ethnography of institution for clients with chronic mental disease, dementia and substance abuse. The thesis is mapping institution's components and actors, their social life and relationships in the institution. The analyses is based upon the concept of total institution by Erving Goffman, and draws from thoughts of Josef Pieper, Martin Buber, Emanuel Lévinas and Michel Foucault. A long-term facility is an institution, which shares clients and some of problems with classical examples of total institutions, but recent reforms aimed to minimalize features of total institutions. Still it does not seem to be a vital institution and new aspects of social situation of staff and clients are recognized. Among new problems is non-existence of therapy for the inhabitants, their marginalization through poor financial situation in an institution, where lot of services are paid and little continuity to other forms of care of more community and ambulant character. Key words: total institution, long-term facility, psychiatric care, medical anthropology,...

The aim of the presented work is to present problematic aspects of the work of peer consultants in the field of mental health care, i.e., in psychiatric hospitals, social services and leisure clubs. The theoretical part will present the context from which the position grows and comes- the concept of mental illness and stigmatization of mental illness, as well as the project of deinstituonalization of the mental health care system. The theoretical part of the work is then concluded with an introduction to the position of the peer consultant. In the practical part I deal with the problematic aspects themselves by the means of semi-structured interviews. Aspects such as the scope of work of the peer consultant, experience with colleagues and clients, requirements for the position, the topic of the future and the work procedure and finally also the issue of the legislative anchoring of this position. Key words: mental illness, stigmatization, peer support, peer mentor, social works, psychiatric care, Centre for mental health care development, deinstitutionalisation

In my thesis I am going to focus on one of the areas of community care for people with mental illness and thus on the area of employment. The main focus of the thesis is on a description of current situation in the provision of the employment support for people with mental illness. The focus is also on the formulation of the specifics of the Employment Support Program for people with mental illness. Another part of my thesis contains empirical investigations focusing on the sustainability and the perspective of the Employment Support Program for people with mental illness. The goal of my thesis is to set up an updated oveview study on the issue of providing employment support for people with metal illness. Powered by TCPDF (www.tcpdf.org)

Le régime juridique des soins psychiatriques sans consentement et les dispositions légales qui l’entourent sont le fruit de la longue évolution de la collectivité à prendre en charge les personnes atteintes de troubles psychiques. Cette maturation, qui témoigne de l’équilibre fragile entre le respect des libertés fondamentales et les impératifs d’ordre public, explique en grande partie la reconnaissance tardive de ces patients vulnérables comme véritables sujets de droit. A travers la loi n°2011-803 du 5 juillet 2011 et la loi n°2013-869 du 27 septembre 2013, le législateur a conservé le système médico-administratif des soins sans consentement qu’il a érigé au XIXe siècle. Néanmoins, via ces deux dernières réformes, il l’a atténué en introduisant un contrôle obligatoire du Juge des libertés et de la détention et a élargi ces prises en charge aux soins ambulatoires. Ce système est caractérisé par une dualité des modalités d’admission : les soins à la demande du représentant de l’Etat (S.D.R.E.) d’une part, et les soins à la demande d’un tiers (S.D.T.) d’autre part. Ces deux blocs sont eux-mêmes subdivisés en une pluralité de mesures, chacune justifiée pour des motifs divers : urgence, absence de tiers, circonstances de fait, existence d’un trouble grave à l’ordre public ou à la sûreté des personnes… Si le régime juridique des soins sans consentement est censé prévoir une prise en charge adaptée à chaque situation particulière, en réalité, ces orientations sont souvent prises pour des raisons d’opportunité et ne correspondent pas toujours à la réalité. Les contentieux issus de ce régime juridique d’exception témoignent des nombreuses atteintes aux droits subies par les patients qui en font l’objet. Pour ces raisons, un toilettage de fond peut être envisagé. Il passerait par la fusion des deux blocs d’admission en un seul, par le prononcé des mesures par le juge et par un renforcement de la protection des droits et des libertés, dispositions qui devront s’entourer de garanties plus effectives et de contrôles plus appuyés. / The legal regime of the psychiatric care without consent, and the relevant legal provisions that surround it, are the direct consequence of the long-term development of the society in managing the mentally disabled people. This process of maturing, which reflects the delicate balance between the respect for fundamental freedoms and the imperatives of public order, mainly explains the rather belated recognition of these vulnerable patients as real subjects of rights. Through the law n°2011-803 of 5 July 2011 and the law n°2013-869 of 27 September 2013, the legislator maintained the model of care and medical administrative system without consent, dating from the nineteenth century. Nevertheless, through these last two reforms, the system has been attenuated by the introduction of a mandatory control of the liberty and custody judge and expanded these medical cares at the ambulatory. This system is characterised by its own duality in terms of admission rules: the request for care on demand of the representative of State (S.D.R.E.) on the one hand, and of a third party (S.D.T.) on the other hand. These two sets of procedures themselves are subdivided in a plurality of actions, each one justified on various purposes: urgency, absence of a third party, factual circumstances, existence of a serious public disorder or threat to the safety of individuals… Even if the legal regime for the medical care without consent is supposed to provide an appropriate care for each and every specific situations, often these policies are actually set for opportunistic reasons and do not always match reality. The disputes resulting from this exception legal regime demonstrate the many human rights violations suffered by the concerned patients. For these reasons, some tidying up can be envisaged. The latter would involve the merging of the two sets of procedures, the issuance of measures by the judge himself and a strengthening of the protection of civil rights and freedoms, provisions which will have to be surrounded by more effective safeguards and stronger controls.