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Books on the topic 'Acute mania'

Author: Grafiati

Published: 11 March 2023

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1

National Institute for Clinical Excellence., ed. Olanzapine and valproate semisodium in the treatment of acute mania associated with bipolar I disorder. London: National Institute for Clinical Excellence, 2003.

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2

Rowling, J. K. Harry Potter and the Order of the Phoenix. Waterville, ME, USA: Thorndike Press, 2003.

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3

Rowling, J. K. Harry Potter und der Orden des Phönix. Hamburg, Germany: Carlsen, 2003.

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4

(translator), Gemma Rovira Ortega. Harry Potter y la Orden del Fenix. Navarra, España: Salamandra Publicacions Y Edicions, S.L., 2004.

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5

Rowling, J. K. Harry Potter és a Főnix Rendje. 2nd ed. Budapest: Animus, 2005.

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6

Rowling, J. K. Harry Potter & Huoi Phưvong Hoàng. Thành phro Hso Chí Minh: NXB Trke, 2005.

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7

Rowling, J. K. Harry Potter and the Order of the Phoenix. New York, NY: Arthur A. Levine Books, 2003.

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8

Rowling, J. K. Harry Potter i l'orde del fènix. Barcelona, Spain: Editorial Empúries, 2004.

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9

Rowling, J. K. Harry Potter & Huoi Phưvong Hoàng. 3rd ed. TP. Hso Chí Minh, Viet Nam: NXB Trke, 2007.

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10

Rowling, J. K. হ্যারি পটার অ্যান্ড দ্য অর্ডার অব দ্য ফিনিক্স. Ḍhākā: Aṅkura Prakāśanī, 2007.

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11

Rowling, J. K. Harry Potter and the Order of the Phoenix. Vancouver, Canada: Raincoast Books, 2003.

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12

Rowling, J. K. Harry Potter and the Order of the Phoenix. London: Bloomsbury, 2007.

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13

Rowling, J. K. हैरी पॉटर और मायापंछी का समूह. Bhopal, India: Mañjula Pabliśiṅga Hāusa, 2008.

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14

Rowling, J. K. Harry Potter en de Orde van de Feniks. Amsterdam / Antwerp: De Harmonie / Standaard, 2003.

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15

Rowling, J. K. Harry Potter and the Order of the Phoenix. New York, USA: Scholastic, 2003.

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16

Rowling, J. K. Haeri P'ot'ŏ pulsajo kisadan. Kyŏnggi-do Pʹaju-si: Munhak Suchʹŏp, 2014.

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17

Rowling, J. K. Hary Potter i zakon feniksa. Poznan: Media Rodzina, 2004.

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18

Rowling, J. K. Гарри Поттер и Орден Феникса. Moskva, Russia: ROSMĖN, 2004.

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19

Rowling, J. K. Harry Potter et l'ordre du Phénix. Paris, France: Gallimard Jeunesse, 2003.

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20

Rowling, J. K. Harry Potter & Hội Phượng Hoàng. Thành phố Hồ Chí Minh: NXB Trẻ, 2005.

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21

Gamba, Daniela, ed. Harry Potter e l’Ordine della Fenice. Milan, Italy: Salani, 2009.

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22

Rowling, J. K. Harry Potter and the Order of the Phoenix. London, England: Bloomsbury, 2004.

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23

Rowling, J. K. הארי פוטר ומסדר עוף החול. Tel-Aviv, Israel: Yediʻot aḥaronot, 2008.

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24

Rowling, J. K. Harry Potter und der Orden des Phönix. Hamburg, Germany: Carlsen, 2003.

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25

Rowling, J. K. 哈利波特与凤凰社. Beijing, China: Ren min wen xue chu ban she, 2003.

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26

Managing Acute Mania. Science Press, 2003.

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27

Shorter, Edward, and Max Fink. Delirious Mania and Febrile Catatonia. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190881191.003.0008.

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The acute onset of excited, aggressive, and destructive states, often febrile, described as Bell’s mania and Stauder’s delirium are hallmarks in the literature. Death is frequent. Subjects are disoriented, and delirious with catatonia signs of mutism, posturing, and repetitive speech. Treatments were ineffective until multiple daily induced seizures (ECT) were shown to be life-saving. A syndrome of nostalgia was also described in French and German armies among subjects pining to death. Delirious mania and its fatal variants were a rock-solid part of traditional psychiatric diagnosis. By the 1960s, almost everywhere in the UK and Europe, fatal delirious mania or pernicious catatonia was an accepted part of psychiatric diagnostics that a clinician would ignore at the patient’s peril.

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28

Keck, Paul E., and Susan L. McElroy. Pharmacological Treatments for Bipolar Disorder. Oxford University Press, 2015. http://dx.doi.org/10.1093/med:psych/9780199342211.003.0008.

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The majority of clinical trials in patients with bipolar disorders have been conducted in groups with bipolar I illness, although a few trials have included patients with bipolar II disorder. Pharmacological management of bipolar disorder involves the treatment of acute manic, hypomanic, mixed, and depressive episodes, as well as the prevention of further episodes and subsyndromal symptoms. Lithium, divalproex, carbamazepine, haloperidol, risperidone, olanzapine, quetiapine, ziprasidone, aripiprazole, and asenapine have demonstrated efficacy in the treatment of acute mania in randomized controlled (type 1) trials. Although the pharmacological treatment of acute bipolar depression remains understudied, data from randomized controlled trials indicate that lithium, olanzapine, olanzapine-fluoxetine, quetiapine, lurasidone, tricyclics, monoamine oxidase inhibitors, and fluoxetine have efficacy in this phase of the illness. Lithium, lamotrigine, olanzapine, aripiprazole, quetiapine, and risperidone (long-acting, injectable) have been shown to have efficacy in relapse prevention. Less extensive data suggest that divalproex and carbamazepine are also efficacious for prevention.

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29

Hazell, Philip. The treatment of bipolar disorder in children and adolescents. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198748625.003.0021.

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The presentation of bipolar disorder in young people can be different from that of adults; therefore, the approach to treatment differs slightly. Treatment is described for early intervention, acute mania, bipolar depression, relapse prevention, and refractory bipolar disorder. A strong therapeutic alliance with the patient and engagement and involvement of the patient’s family is critical to successful intervention. The evidence informing treatment is limited, but there is emerging research focused on the management of acute mania favouring monotherapy with a second-generation antipsychotic (SGA) over a mood stabilizer. Preliminary data favour a combination of an SGA and antidepressant over monotherapy with an SGA for the treatment of bipolar depression. Guidelines endorse electroconvulsive therapy for refractory mania and bipolar depression but there is no clinical trial evidence to support this practice. The development of algorithms to guide the management of all phases of bipolar disorder is a work in progress.

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30

Owen, Gareth, Sir Simon Wessely, and Sir Simon Wessely, eds. Treatments. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199661701.003.0009.

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This chapter deals with treatment, especially early treatment. Psychosis, mania, catatonia, and severe depression are dealt with in a practical and evidence-based manner, and advice is also given on rapid tranquillization for acute behavioural disturbances. The medication details relate to adults and appendices giving further details on antipsychotic medications are referred to. The chapter also gives advice on prescribing in pregnancy and breastfeeding, on using ECT, and on treatments for alcohol and drug problems. The chapter finishes with outlining the main modalities of psychotherapy.

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31

Frye, Mark A., Paul E. Croarkin, Marin Veldic, Malik M. Nassan, Katherine M. Moore, Simon Kung, Susannah J. Tye, William V. Bobo, and Jennifer L. Vande Voort. Evidence-based treatment of bipolar depression. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198748625.003.0007.

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Despite the predominant illness burden, evidence-based treatment, and by extension regulatory approved, for acute bipolar depression is significantly less than evidence bases in acute mania and maintenance treatment. Complicating this deficit has been persistent use of unimodal antidepressant therapy without clear and convincing benefit. Successful regulatory-approved drug development has focused on atypical antipsychotic therapy. Evidence-based treatments also include lamotrigine and divalproex by meta-analyses and a number of manual-based psychotherapies. In contrast, unimodal antidepressants as a class for bipolar depressed patients as a group appear to provide substantial benefit and may pose risk for mood destabilization. Promising novel and neuromodulatory treatments while encouraging require further systematic investigation. Understanding unimodal antidepressant response and risk patterns in bipolar disorder has immediate clinical implications. Moreover, evidence-based guidelines will need to bridge more individualized or precision-based treatment interventions.

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32

Cavanna, Andrea E. Valproate. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198791577.003.0014.

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Valproate is a first-generation antiepileptic drug characterized by a wide range of antiepileptic indications, with an acceptable interaction profile in polytherapy. Valproate has a good behavioural tolerability profile, despite the existence of occasional reports of depression, irritability, and other behavioural symptoms in patients with encephalopathy. Valproate is also characterized by a wide range of psychiatric uses. Most importantly, valproate is an effective mood stabilizser, with a licensed indication for the treatment of acute mania in patients with bipolar affective disorder. Although it has no formal indication, it is also considered as a first-line agent for maintenance treatment in bipolar affective disorder.

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33

Sousa Alves, Gilberto, Felipe Kenji Sudo, and Johannes Pantel. The treatment of bipolar disorder in the elderly. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198748625.003.0022.

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Bipolar disorder (BD) is an extremely disabling condition characterized by mood switches, and cognitive and functional impairment. The current chapter discusses the updated review on pharmacological and non-pharmacological interventions targeting BD in the elderly. The risk of concurrent medical diseases (eg, metabolic syndrome) and relatively lower tolerability than young BD make the patient safety a major concern in most cases. Evidence-based guidelines, although useful for promoting rational and effective therapy, are generally lacking in elderly BD. Current recommendations for acute mania include atypical antipsychotics, careful use of lithium, and election of valproate as the gold-standard therapy. In acute BD depression, first-line agents in monotherapy may include lithium, lamotrigine, quetiapine, and quetiapine extended release (XR). Electroconvulsive therapy may be an option for severe/refractory cases. Family members or caregivers should be encouraged to support the patient, since potential ethical issues involving patrimony or profession may arise during the treatment.

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34

Cavanna, Andrea E. Carbamazepine, oxcarbazepine, and eslicarbazepine. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198791577.003.0003.

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Carbamazepine is a first-generation antiepileptic drug characterized by a good range of antiepileptic indications, with acceptable risk of interactions in polytherapy. Carbamazepine has a very good behavioural tolerability profile and is in widespread psychiatric use (indication for bipolar disorder—acute mania). Oxcarbazepine and eslicarbazepine are carbamazepine derivatives. Oxcarbazepine is a second-generation antiepileptic drug characterized by a good range of antiepileptic indications, with acceptable risk of interactions in polytherapy. Like carbamazepine, oxcarbazepine has a very good behavioural tolerability profile and potential for widespread psychiatric use. Eslicarbazepine is a third-generation antiepileptic drug for which clinical experience is still limited. Little is known about its positive and negative psychotropic properties and their implications for the management of behavioural symptoms in patients with epilepsy.

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35

Kittel-Schneider, Sarah. The treatment of bipolar mixed states. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198748625.003.0005.

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Definition of mixed episodes has changed in the Diagnostic and Statistical Manual of Mental Disorders (5th edition) (DSM-5). A mixed feature specifier can be added not only to major depressive episodes and manic episodes in bipolar patients but also to hypomanic episodes in bipolar II patients and major depressive episode in major depressive disorder. Atypical antipsychotics seem to be effective in acute treatment as well as valproate and carbamazepine. Regarding prophylaxis of mixed states, monotherapy with valproate, olanzapine and quetiapine seems to prevent mixed episodes. Adjunctive therapy with valproate or lithium to quetiapine has also proven to be effective in prophylaxis of mixed episodes. In patients who suffer from pharmacotherapy-resistant mixed episodes electroconvulsive therapy can lead to response/remission. There is a lack of randomized controlled clinical trials investigating pharmacological and non-pharmacological treatments with focus on mixed states of bipolar patients, especially according to the DSM-5 definition.

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36

Goldberg, Pablo H., Prerna Martin, Carolina Biernacki, and Moira A. Rynn. Treatments for Pediatric Bipolar Disorder. Oxford University Press, 2015. http://dx.doi.org/10.1093/med:psych/9780199342211.003.0009.

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The past two decades have seen significant advances in the development of evidence-based treatments for pediatric bipolar disorder. Practice guidelines recommend pharmacotherapy with mood stabilizers or second-generation antipsychotics (SGAs) as the first-line treatment. Lithium, risperidone, aripiprazole, quetiapine, and olanzapine are approved by the U.S. Food & Drug Administration for treating bipolar disorder in children and adolescents. The pharmacological literature suggests that SGAs are faster and more effective than mood stabilizers in treating acute manic or mixed episodes, but they have significant side effects and require careful monitoring. While mild to moderate bipolar disorder can be treated with monotherapy, combination pharmacotherapy with an SGA and a mood stabilizer is recommended for youth with severe bipolar disorder. A growing body of literature also suggests the efficacy of psychosocial interventions, with family psychoeducation and skills building as adjunct treatments to pharmacotherapy. More type 1 studies of pharmacotherapy and psychosocial treatments are needed.

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37

Hall, Dewey W., and Jillmarie Murphy, eds. Gendered Ecologies. Liverpool University Press, 2020. http://dx.doi.org/10.3828/liverpool/9781949979046.001.0001.

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Gendered Ecologies: New Materialist Interpretations of Women Writers in the Long Nineteenth Century is comprised of a diverse collection of essays featuring analyses of literary women writers, ecofeminism, feminist ecocriticism, and the value of the interrelationships that exist among human, nonhuman, and nonliving entities as part of the environs. The book presents a case for the often-disregarded literary women writers of the long nineteenth century, who were active contributors to the discourse of natural history—the diachronic study of participants as part of a vibrant community interconnected by matter. While they were not natural philosophers as in the cases of Sir Isaac Newton, Robert Boyle, and Michael Faraday among others, these women writers did engage in acute observations of materiality in space (e.g., subjects, objects, and abjects), reasoned about their findings, and encoded their discoveries of nature in their literary and artistic productions. The collection includes discussions of the works of influential literary women from the long nineteenth century—Mary Wollstonecraft, Mary Shelley, Caroline Norton, Charlotte Brontë, George Eliot, Mary Elizabeth Braddon, Jane Johnston Schoolcraft, Margaret Fuller, Susan Fenimore Cooper, Celia Thaxter, Laura Ingalls Wilder, Francis Wright, and Lydia Maria Child—whose multi-directional observations of animate and inanimate objects in the natural domain are based on self-made discoveries while interacting with the environs.

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38

Harry Potter and the Order of the Phoenix. Listening Library, 2003.

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39

Harry Potter and the Order of the Phoenix. London, England: Bloomsbury, 2014.

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40

'Harry Potter and the Order of the Phoenix. Gramedia Pustaka Utama, 2003.

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41

Harry Potter y la Orden del Fénix. Salamandra, 2012.

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42

Harry Potter and the Order of the Phoenix. scholastic, 2008.

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43

Rowling, J. K. Harry Potter and the Order of the Phoenix. Turtleback Books Distributed by Demco Media, 2004.

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44

Rowling, J. K. Harry Potter and the Order of the Phoenix. Bloomsbury Children's Books, 2016.

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45

Rowling, J. K. Harry Potter U-misdar Of Hachol. S.l, 2003.

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46

Rowling, J. K. Harry Potter and the Order of the Phoenix (Book 5). Arthur A. Levine Books, 2003.

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47

Rowling, J. K. Harry Potter og Fonixordenen. Gyldendal, 2003.

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48

Harry Potter and the Order of the Phoenix. Listening Library, 2003.

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49

Rowling, J. K. Harry Potter and the Order of the Phoenix - Gryffindor Edition. Bloomsbury Publishing Plc, 2020.

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50

Rowling, J. K. Harry Potter and the Order of the Phoenix Gryffindor. Bloomsbury Publishing Plc, 2020.

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