Relevant bibliographies by topics / Impact biopsychosocial

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Impact biopsychosocial'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Impact biopsychosocial"

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Tripp, Dean A., Phylicia Verreault, Steven Tong, Jason Izard, Angela Black, and D. Robert Siemens. "Biopsychosocial impact of prostate cancer and androgen-deprivation therapy." Canadian Urological Association Journal 11, no. 10 (2017): 338–43. http://dx.doi.org/10.5489/cuaj.4499.

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Introduction: Prostate cancer is the most non-cutaneous malignancy in men, and androgen-deprivation therapy (ADT) is a cornerstone of management in advanced disease. The aim of this study was to evaluate the association of ADT with changes in depression and mental and physical quality of life (QoL) within a prospective patient cohort design.Methods: Patients were prospectively recruited and consented at a single academic health sciences centre in Ontario, Canada. Inclusion criteria included those men with adenocarcinoma of the prostate and either on watchful waiting or initiating ADT as pallia
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Laher, Nazeefah, Sara Bocchinfuso, Madeline Chidiac, Claire Doherty, Alexandra Persson, and Emma Warren. "The Biopsychosocial Impact of COVID-19 on Older Adults." Gerontology and Geriatric Medicine 7 (January 2021): 233372142110342. http://dx.doi.org/10.1177/23337214211034274.

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COVID-19 has spread rapidly around the world and taken over 2.6 million lives. Older adults experience disproportionate morbidity and mortality from the disease because increasing age and the presence of comorbidities are important predictors of negative outcomes. Lasting effects of COVID-19 have been described after recovery from the acute illness despite eradication of the virus from the body. The impact of COVID-19 on a person’s biological health post-infection is observed in multiple systems including respiratory, cardiac, renal, haematological, and neurological. Psychological dysfunction
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Van Wijck-Warnaar, A., M. J. M. C. Van Opstal, K. Exelmans, K. Schaekers, G. Thomas, and F. I. C. R. S. de Jong. "Biopsychosocial Impact of Voicing and General Coping Style in Teachers." Folia Phoniatrica et Logopaedica 62, no. 1-2 (2010): 40–46. http://dx.doi.org/10.1159/000239062.

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Hagen, Martina, Taara Madhavan, and John Bell. "Combined analysis of 3 cross-sectional surveys of pain in 14 countries in Europe, the Americas, Australia, and Asia: impact on physical and emotional aspects and quality of life." Scandinavian Journal of Pain 20, no. 3 (2020): 575–89. http://dx.doi.org/10.1515/sjpain-2020-0003.

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AbstractBackground and aimsRecognition of the biopsychosocial aspects of pain is important for a true understanding of the burden of pain and the necessity of pain management. Biopsychosocial aspects of pain may differ between countries and cultures. Market research methods can be well suited and effective for assessing patient perspectives of pain and biopsychosocial differences. We conducted and combined 3 cross-sectional, international surveys to document the impact of pain on physical and emotional aspects of life, as well as quality of life (QOL).MethodsOnline panelists from 24 countries
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Moseley, Lorimer. "Chronic Pain-related Disability: Current Scientific Rationale and Recommendations for Practice." Australian Journal of Rehabilitation Counselling 5, no. 1 (1999): 9–22. http://dx.doi.org/10.1017/s1323892200001186.

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The present paper concerns the prevention and management of disability due to chronic pain. The problem of disabling chronic pain is presented and the impact on the community is highlighted. The scientific rationale for current approaches to management is discussed and the available empirical evidence reviewed. In particular, the present paper advocates application of the biopsychosocial model for the prevention and management of chronic pain-related disability. As such, the components of the biopsychosocial model are reviewed and recommendations for rehabilitation counselling practice are pre
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McLaren, Niall. "The Biopsychosocial Model: The End of a Reign of Error." Ethical Human Psychology and Psychiatry 22, no. 2 (2020): 71–82. http://dx.doi.org/10.1891/ehpp-d-20-00016.

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Four decades after the publication of the concept of Engel's “biopsychosocial model” for medicine and its subsequent enthusiastic embrace by psychiatry, it is widely accepted as a valid alternative to the reductionism of biological psychiatry. However, unlike models in mainstream science, the original model has not been developed or expanded. Despite widespread efforts to “talk it up,” Engel's “biopsychosocial model” has failed to have any lasting impact on psychiatry. The reason is simply that it doesn't exist. The logical flaws in Engel's original concept are explored, and some consequences
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Ali Jadoo, Saad Ahmed. "COVID -19 pandemic is a worldwide typical Biopsychosocial crisis." Journal of Ideas in Health 3, no. 2 (2020): 152–54. http://dx.doi.org/10.47108/jidhealth.vol3.iss2.58.

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Since December 2019, the world has been stunned by the speed of the spread of the COVID-19. All the possibilities were likely, except that people would hide in their homes for fear of contracting the disease, as it was very unlikely. The lockdown was imposed severely, and people panicked, and their interest has limited to providing food and caring for health and family. The effect of isolation and the prevention of social interaction was apparent in the individuals' psychological behavior. Unfortunately, the incidence of depression, anxiety, and domestic violence increased, which negatively im
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Grimwood, Samuel, Kaz Stuart, Ruth Browning, Elaine Bidmead, and Thea Winn-Reed. "The perception of biopsychosocial impacts of COVID-19 during lockdown restrictions over time in the UK – a mixed methods study." Journal of Ideas in Health 4, Special2 (2021): 402–14. http://dx.doi.org/10.47108/jidhealth.vol4.issspecial2.131.

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Background: The COVID-19 pandemic has profoundly impacted the health of individuals physically, mentally, and socially. This study aims to gain a deeper understanding of this impact across the pandemic from a biopsychosocial stance.
 Methods: A survey created by the research team was employed between November 2020 and February 2021 across social media, relevant organizations, and networks. The survey incorporated 5-time points across the different stages of the pandemic, covering biological, psychological, and social. There were 5 items for each survey (Very Positive affect to Very Negati
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Frankenhaeuser, Marianne. "A Biopsychosocial Approach to Work Life Issues." International Journal of Health Services 19, no. 4 (1989): 747–58. http://dx.doi.org/10.2190/01dy-ud40-10m3-cky4.

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This article is based on research carried out in the author's laboratory during the past decades. The central theme is the study of how environmental factors influence health and behavior. The approach is multidisciplinary, focusing on the dynamics of stressful person-environment interactions, viewed from social, psychological, and biomedical perspectives. A biopsychosocial framework for the study of stress and coping at the workplace is outlined. Key notions in the biopsychosocial approach are that endocrine responses to the psychosocial environment reflect its impact on the individual and se
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Menkes, Lena. "Assessing the Impact of Biopsychosocial Factors on Adolescent Survivors of Extremity Tumors." American Journal of Occupational Therapy 72, no. 4_Supplement_1 (2018): 7211500045p1. http://dx.doi.org/10.5014/ajot.2018.72s1-po6002.

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Dissertations / Theses on the topic "Impact biopsychosocial"

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Su, Ying-hwa. "Biopsychosocial impact of parental cancer on schoolagers." Connect to this title online, 2004. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1103543803.

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Thesis (Ph. D.)--Ohio State University, 2004.<br>Title from first page of PDF file. Document formatted into pages; contains xi, 170 p.; also includes graphics (some col.) Includes bibliographical references (p. 158-170).
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Su, Ying-hwa. "Biopsychosocial impact of parental cancer on schoolagers." The Ohio State University, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=osu1103543803.

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Escande-Arnas, Anne-Marie. "Etude de la charge supportee par les familles dans les demences de type alzheimer." Toulouse 3, 1990. http://www.theses.fr/1990TOU31083.

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Vas, Venessa Firmin. "The biopsychosocial impact of hearing loss on people with hearing loss and their communication partners." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/47506/.

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Hearing loss is a prevalent condition that can have negative implications on the day-to-day lives of those with hearing loss, and their communication partners. Several reviews have identified numerous questionnaires that explore the impact of hearing loss, with little consensus among researchers as to their preference. One reason for this is a lack of an agreed framework concerning exactly what is the impact of hearing loss, and what is important to those who live with the condition. To address this gap in understanding, the experiences of those living with hearing loss or with someone that ha
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Agnafors, Sara. "A Biopsychosocial and Long Term Perspective on Child Behavioral Problems : Impact of Risk and Resilience." Doctoral thesis, Linköpings universitet, Avdelningen för neuro- och inflammationsvetenskap, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-124209.

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Mental health has become a prominent issue in society. Yet, much remains unknown about the etiology of psychiatric disorders. The aim of the present thesis was to investigate the association between biological, psychological and social factors of risk and resilience and behavioral problems in a birth cohort of Swedish children. 1723 mothers and their children were followed from birth to the age of 12 as part of the South East Sweden Birth Cohort Study (the SESBiC study). Information was gathered through register data, standardized questionnaires and DNA samples. In study I, stability of matern
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Collins, Megan A. S. "Art’s Ability to Illuminate the Biopsychosocial-Cultural-Spiritual Impact of Living with a Chronic Medical Disease." Digital Commons at Loyola Marymount University and Loyola Law School, 2012. https://digitalcommons.lmu.edu/etd/98.

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This study sought to examine art’s ability to illuminate the biopsychosocial-cultural- spiritual impact of chronic medical disease. Chronic disease participants were self- selected and consisted of clinical supervisors, staff, and psychotherapy interns at a community-based mental health clinic in Los Angeles. Quantitative questionnaire data and art-based response data, both imagery and word descriptions, were examined. Data analysis combined with the synthesized literature revealed the complex biopsychosocial- cultural-spiritual interactions and interdependencies with chronic disease managemen
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Knott, Linda. "Exploring the acceptability and usefulness of the Impact of Symptoms Questionnaire (IoSQ)." Thesis, University of Exeter, 2013. http://hdl.handle.net/10871/15089.

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Background: Clinical and physiotherapy professional guidelines advocate enquiry into, and documentation of the impact of musculoskeletal pain on a range of psychosocial and functional aspects of life. However, there is no clinical tool to assist this process. The Impact of Symptoms Questionnaire (IoSQ) is patient-completed and was developed to meet the needs of outpatient physiotherapists. It explores the impact of health conditions on patients’ beliefs/concerns and their ability to undertake work/caring responsibilities and activities of daily living; and to enjoy their usual hobbies or activ
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Kuehne, Jan (Jan Cavan). "The impact of materialistic monism and suffering on medical students :a critique of the biomedical and biopsychosocial model of medical schools." Thesis, Stellenbosch : Stellenbosch University, 2007. http://hdl.handle.net/10019.1/18209.

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Thesis (MPhil)--University of Stellenbosch, 2007.<br>ENGLISH ABSTRACT: On entry to medical school, students are confronted with a worldview that can be typified as materialistic monism. The student progressively becomes a materialistic monist, not only because of the teaching, but also because medical schools fail to address the question of suffering. One would expect the biopsychosocial model to surmount the limitations of the biomedical model, but it in itself has to deal with both suffering and materialistic monism. Suffering cements the collapse into materialistic monism in the way the stu
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Douglas, Clint. "The impact of pain on the quality of life of people with multiple sclerosis." Queensland University of Technology, 2007. http://eprints.qut.edu.au/16523/.

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This thesis was concerned with determining the scope, nature and impact of pain on quality of life (QOL) among a community-based sample of people with multiple sclerosis (MS). An analysis of the research literature on pain in MS reveals that pain is a significant problem which has historically been underinvestigated and is currently poorly understood. The vast majority of the published literature consists of prevalence studies, descriptive research and clinical reports. Where available, empirical data are often limited by methodological and analytical problems such that substantive conclusions
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Lynch, Kimberly Vandermark. "Narratives of Men Living with Systemic Lupus Erythematosus." ScholarWorks, 2017. https://scholarworks.waldenu.edu/dissertations/3704.

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While systemic lupus erythematosus (SLE) has been traditionally viewed as a woman's disease, SLE impacts men as well. Although most research on SLE has concentrated on how it affected women, little is known about how it impacts men. The purpose of this phenomenological study was to examine how men who live with SLE perceive its psychological impact. Using the lens of the biopsychological theory, common themes were examined pertaining to how men with SLE perceive the impact that SLE has on their cognitive and emotional functioning. Data were collected via interviews with 9 men with SLE, and the
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Books on the topic "Impact biopsychosocial"

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Price, Julie R., Micah J. Price, and Marc A. Huntoon. Psychology of Pain. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190217518.003.0004.

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The role of psychosocial variables in the understanding, diagnosis, and treatment of pain has grown significantly in the past 30 years. Pain is no longer dichotomously thought of as either a purely psychological or physiological condition (mind–body dualism) but, rather, as a combination of biopsychosocial factors and experiences. The questions in this chapter consider the changing role of these psychosocial factors by exploring the fifth edition of the Diagnostic and Statistical Manual of Mental Disorders and other pain-related assessments and psychodiagnostics; cognitive–behavioral, acceptan
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Onishi, Hideki, and Mayumi Ishida. Psycho-oncology and psychosocial aspects of gynaecological cancer. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198749547.003.0010.

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Patients with gynaecological cancer encounter, everyday, various problems in their family lives, jobs, and finances, in addition to the direct effects of the cancer itself. They also face problems concerning a loss of femininity, such as those related to the menopause, their reproductive function, and sexual activity that is brought about by the effects of the disease and its management. Hence, problems are not only limited to the biological aspect of cancer, but also to its impact on psychosocial aspects, thereby increasing the level of stress in these patients. Hence, when considering the pr
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Rosen, David H., and Uyen B. Hoang. The Doctor–Patient Relationship. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190628871.003.0004.

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This chapter examines the doctor–patient relationship. It underscores the key nature of the human bond between the healthcare worker and the patient as a partnership, which is essential to the healing process. The doctor–patient relationship is anchored by the language of medicine to facilitate effective communication skills and to support ongoing cooperation. Because young doctors are socialized into a frequently dehumanized system, which can erode compassion and empathy, they are not helped to cope with the emotional impact of their work. The education of these future physicians must include
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Bullock, Kim, and John J. Barry. Psychiatric Factors. Edited by Barbara A. Dworetzky and Gaston C. Baslet. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190265045.003.0003.

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Psychogenic nonepileptic seizures (PNES) is a multifactorial illness requiring a personalized biopsychosocial (BPS) formulation across the lifespan to understand its causes. This chapter reviews the current evidence focusing on predisposing, precipitating, perpetuating, and prognostic variables (4P’s), merging them into a chronologically based 4P-BPS model. Positive PNES randomized controlled trials suggest that self-efficacy and illness beliefs, avoidance behaviors, trigger sensitization, and comorbid psychiatric disorders are important etiological variables to target during treatment. Epidem
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Cohen, Mary Ann, Anna L. Dickerman, and Harold W. Goforth. Distress in Persons with HIV and AIDS. Edited by Mary Ann Cohen, Jack M. Gorman, Jeffrey M. Jacobson, Paul Volberding, and Scott Letendre. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199392742.003.0022.

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Persons with HIV have multifactorial and multidimensional sources of distress. Distress has a profoundly negative impact on persons with HIV and their loved ones. While the term distress is more acceptable to patients and does not carry with it the stigma of a specific psychiatric diagnostic disorder, the anguish and suffering associated are still painful. This chapter explores the sources for distress utilizing a comprehensive biopsychosocial approach and presents ways to recognize distress. Related tools in assessing HIV-related distress include the Distress Thermometer (DT), Hospital Anxiet
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Thompson, Amanda L., and Molly A. Gardner. Gender Considerations in Adolescents and Young Adults with Cancer (DRAFT). Edited by Youngmee Kim and Matthew J. Loscalzo. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190462253.003.0009.

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Literature on adolescents and young adults (AYA) with cancer has largely focused on the biopsychosocial challenges of this developmental period, with limited attention paid to the role of gender or to gender differences in adjustment and outcomes. Differences have been found in the self-reported needs of AYA patients both during and after treatment, as well as in the information received regarding fertility preservation, psychological distress, positive growth, and benefit-finding and the role of social support in adjustment. Methodological limitations, however, impact our ability to draw robu
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Cohen, Mary Ann, Harold Goforth, Joseph Lux, et al. Handbook of AIDS Psychiatry. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195372571.001.0001.

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The Handbook of AIDS Psychiatry is a practical guide for AIDS psychiatrists and other mental health professionals as well as for other clinicians who work with persons with HIV and AIDS and a companion book to the Comprehensive Textbook of AIDS Psychiatry (Cohen and Gorman, 2008). The Handbook provides insights into the dynamics of adherence to risk reduction and medical care in persons with HIV and AIDS as well as strategies to improve adherence using a biopsychosocial approach. Psychiatric disorders can accelerate the spread of the virus by creating barriers to risk reduction. Risky sexual b
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Forstein, Marshall, Farah Ahmad-Stout, and Gaddy Noy. Young Adulthood and Serodiscordant Couples. Edited by Mary Ann Cohen, Jack M. Gorman, Jeffrey M. Jacobson, Paul Volberding, and Scott Letendre. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199392742.003.0034.

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Advances in HIV medical care and antiretroviral therapy transformed AIDS from a rapidly devastating fatal illness into a chronic illness for persons with access to care, leading to vast changes in the health of individuals, couples, their children, extended families, and social networks. In addition, adherence to antiretroviral therapy and viral suppression have reduced the likelihood of transmission of HIV, and the use of pre-exposure prophylaxis (PrEP) in an HIV-negative partner offers an additional option to prevent seroconversion. Significant biopsychosocial challenges remain, however, for
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Ryff, Carol D., and Robert F. Krueger, eds. The Oxford Handbook of Integrative Health Science. Oxford University Press, 2018. http://dx.doi.org/10.1093/oxfordhb/9780190676384.001.0001.

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This handbook signals a paradigm shift in health research. Population-based disciplines have employed large national samples to examine how sociodemographic factors contour rates of morbidity and mortality. Behavioral and psychosocial disciplines have studied the factors that influence these domains using small, nonrepresentative samples in experimental or longitudinal contexts. Biomedical disciplines, drawing on diverse fields, have examined mechanistic processes implicated in disease outcomes. The collection of chapters in this handbook embraces all such prior approaches and, via targeted qu
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Horan Fisher, Jacqueline, Sara Becker, Molly Bobek, and Aaron Hogue. Substance-Related and Addictive Disorders. Edited by Thomas H. Ollendick, Susan W. White, and Bradley A. White. Oxford University Press, 2018. http://dx.doi.org/10.1093/oxfordhb/9780190634841.013.29.

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Significant developmental changes in adolescence typically lead to increased risky behavior, including substance use. Survey data indicated that adolescent alcohol and drug use has declined in recent years, with the exception of marijuana use, which has remained consistent, and e-cigarette use, which is on the rise. This chapter provides a summary of prevalence rates, trends, and maladaptive consequences of adolescent substance use. Etiological models of adolescent substance use are discussed, including dual-process and biopsychosocial models. Current literature on evidence-based screening, co
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Book chapters on the topic "Impact biopsychosocial"

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Martins, Gabriella Di Girolamo, Veronica Vidotto Caricati, Beatriz Cortese Barbugli, et al. "The Biopsychosocial Impact of Abusive Use of Digital Media." In Drugs and Human Behavior. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-62855-0_33.

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Manda, Charles B. "Biopsychosocial impact of trauma." In HTS Religion & Society Series. AOSIS, 2019. http://dx.doi.org/10.4102/aosis.2019.bk107.02.

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Džamonja Ignjatović, Tamara. "Services for Children with Disabilities and Their Families: The Impact on the Family’s Life Quality." In Quality of Life - Biopsychosocial Perspectives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.86750.

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Veras, Samuel, Verônica Kozmhinsky, Paulo Goes, and Mônica Heimer. "Behavioral and Psychosocial Factors as Mediators of the Oral Health Impact on Adolescents Quality of Life." In Quality of Life - Biopsychosocial Perspectives. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.89567.

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Arnstein, Paul, and Megan Keating. "Impact of Pain on the Individual and Others." In Pain Care Essentials, edited by Mark Schumacher and Beth B. Hogans. Oxford University Press, 2019. http://dx.doi.org/10.1093/med/9780199768912.003.0004.

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Chapter 3 describes how pain is a powerful stressor that aids in surviving an injury and how the resultant physiologic stressors put vulnerable patients at risk for pulmonary, renal, gastrointestinal, metabolic, and psychosocial complications. The timeliness and efficacy of pain control contribute to health outcomes. Of the estimated 30% of adults who develop chronic pain, these individuals face increased risk for an impoverished, premature death. Pain is a biopsychosocial experience that undermines health, activities, and enjoyment of life. Unless assessed and treated properly, pain devalues important things in the life of the sufferer, often leading down a path to disability and despair. Pain is always a combined physical, mental, and social experience that often partially responds to properly targeted therapy. Disparities are common in the way pain is managed and may relate to factors at the patient, provider, organizational, or payer levels. Thus, healthcare professionals who interact with people experiencing pain have a duty to dampen the biopsychosocial impact of pain to help them think, feel, and do better. Given potential harm related to analgesics or invasive treatments, ethical practices involve advocating for delivering personalized treatments, with vigilant monitoring to avoid potential harm.
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Cohen, Mary Ann, and Harold W. Goforth. "A Biopsychosocial Approach to Treatment." In Handbook of AIDS Psychiatry. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195372571.003.0015.

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The care of persons with HIV and AIDS presents clinicians, caregivers, families, and loved ones with special biopsychosocial challenges posed by the infectious nature of HIV, the specific modes of HIV transmission, the particular way HIV affects the brain, the age of onset, and the complex stigma of HIV. These challenges differentiate AIDS from other severe and complex illnesses, causes, have significant clinical and public health implications, and necessitate early recognition and treatment. The multifactorial nature of these challenges is summarized in Table 11.1, and some unique aspects of AIDS are briefly summarized in Table 11.2. AIDS psychiatrists, psychosomatic medicine psychiatrists, physicians trained in both medicine and psychiatry, and other mental health clinicians can play a vital role the care of persons with HIV and AIDS, in the prevention of HIV transmission, and in training of other clinicians to alleviate distress, reduce ongoing high-risk behavior and nonadherence, provide support for patients and families, and improve patients’ quality of life. In this chapter, we will review the biopsychosocial aspects of AIDS and suggest strategies to address the unique challenges of this devastating and complex illness. Although the AIDS epidemic was first described in the medical literature in 1981, it was not until 1983 that the first articles were published about the psychosocial or psychiatric aspects of AIDS. The first article was not written by a psychiatrist. This article, written by Holtz and colleagues (1983), was essentially a plea for attention to the psychosocial aspects of AIDS. They stated that “noticeably absent in the flurry of publications about the current epidemic of acquired immune deficiency syndrome (AIDS) is reference to the psychosocial impact of this devastating new syndrome.” The authors deplored ostracism of persons with AIDS by both their families and their medical systems of care. These authors were the first to describe the profound withdrawal from human contact as the “sheet sign” observed when a person with AIDS drew a bed sheet over his or her face and head, essentially withdrawing and hiding from visitors.
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Glover, Jonathan. "Psychiatry, folk psychology, and the impact of neuroscience—a response to Steven Hyman’s Loebel Lectures." In Psychiatry Reborn: Biopsychosocial psychiatry in modern medicine, edited by Julian Savulescu, Rebecca Roache, Will Davies, and J. Pierre Loebel. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198789697.003.0019.

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This chapter reflects on Steven Hyman's Loebel Lectures, which revolve around a contrast between folk psychology and what neuroscience is starting to reveal. Folk psychology is the unscientific picture of what goes on in people’s minds when they perceive, remember, think, feel, decide, and act. It is based on introspection and on intuitive ‘reading’ of other people. In contrast to folk psychology is the fine structure neuroscience is starting to reveal: the brain mechanisms underlying perception, memory, thought, emotion, decision, and action. Hyman says that mapping out this fine structure has the promise of changing the understanding and treatment of psychiatric disorders. Out of this emerges Hyman’s philosophical claim that neuroscience radically challenges the status of folk psychology. Folk psychology, being in conflict with neuroscience, is largely false.
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Welch, Killian A., and Mansur A. Kutlubaev. "The impact of fatigue on neurorehabilitation." In Oxford Textbook of Neurorehabilitation, edited by Volker Dietz, Nick S. Ward, and Christopher Kennard. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198824954.003.0026.

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Fatigue is common in neurological disease and associated with substantial disability. Aetiology is generally multifactorial, meaning an individualized, patient-specific understanding of relevant contributors is central to effective management. Primary factors may include brain injury, endocrine changes, or inflammation; medications, deconditioning, psychiatric disorders, pain, and unhelpful beliefs about activity are potential secondary factors. Heterogeneity of causation makes a unifying theory of fatigue elusive, but convergent data across neurological conditions suggest dysfunction in the striatal-thalamic-frontal system is important. Computational neuroscience models suggest fatigue could arise from metacognitive recognition of failure of homeostatic process, then perpetuated by fatigue expectation altering neurocomputational processes during preparation and monitoring of effortful activity. Treatment is guided by biopsychosocial formulation, with emphasis on maintaining factors. Exercise has best evidence, ideally delivered through individually tailored exercise programmes. Cognitive behavioural therapy (CBT) can be helpful in more cognitively able patients. Evidence for pharmacological treatments is weak, though amantadine is generally first choice.
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Cecil, Charlotte A. M. "Biopsychosocial pathways to mental health and disease across the lifespan: The emerging role of epigenetics." In Psychiatry Reborn: Biopsychosocial psychiatry in modern medicine, edited by Julian Savulescu, Rebecca Roache, Will Davies, and J. Pierre Loebel. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198789697.003.0012.

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The biopsychosocial (BPS) model of psychiatry has had a major impact on our modern conceptualization of mental illness as a complex, multi-determined phenomenon. Yet, interdisciplinary BPS work remains the exception, rather than the rule in psychiatry. It has been suggested that this may stem in part from a failure of the BPS model to clearly delineate the mechanisms through which biological, psychological, and social factors co-act in the development of mental illness. This chapter discusses how epigenetic processes that regulate gene expression, such as DNA methylation, are fast emerging as a candidate mechanism for BPS interactions, with potentially widespread implications for the way that psychiatric disorders are understood, assessed, and, perhaps in future, even treated.
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Gustafson, Kathryn E., and Melanie J. Bonner. "Biopsychosocial and Developmental Issues in Sickle Cell Disease." In Comprehensive Handbook of Childhood Cancer and Sickle Cell Disease. Oxford University Press, 2006. http://dx.doi.org/10.1093/oso/9780195169850.003.0032.

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As advances in health care have prolonged and improved the quality of life of children with chronic illnesses such as sickle cell disease (SCD), psychologists have sought to understand the impact of the illnesses on children and their families and to formulate effective interventions to enhance adaptation. These efforts have been informed by a biopsychosocial conceptual approach such that the biomedical, psychological, and social-ecological processes associated with successful adaptation and effective intervention have been explored (Thompson &amp; Gustafson, 1996). Moreover, it has been recognized that chronic childhood illness occurs within the ongoing context of the child’s cognitive and socioemotional development. Development occurs as a consequence of the transactions between the innate qualities of the biological organism and life experiences occurring in a psychosocial context (Thompson, 1985). There is a continuous and mutual influence of the child and the child’s environment, and the implications of the chronic illness for the child’s cognitive, social and emotional development will vary depending on the impact of the disease at each stage of development (Perrin &amp; Gerrity, 1984). The child’s interactions with the environment can be affected by SCD or other chronic illness both directly and indirectly (Thompson &amp; Gustafson, 1996). There can be a direct effect in terms of the biological processes of the disease on systems of the body that result in cognitive, motor, sensory, or other functional impairments. SCD, for example, is a hematological disorder but poses a risk to cognitive processes through central nervous system (CNS) stroke. There can also be an indirect effect of the chronic illness in terms of the effects of the disease on the child’s attainment of normative psychosocial developmental tasks that arise during phases of the life course. The pain crises that are associated with SCD, for example, may interfere with a child’s developmental tasks, including gaining autonomy, participating fully in school, interacting with peers, and forming an integrated sense of self-identity (e.g., Robinson, 1999; Sexson &amp; Dingle, 1997). This chapter reviews the biopsychosocial and developmental issues that are relevant to SCD. Because subsequent chapters in this volume also review the neuropsychological and psychosocial issues in detail, this review is not meant to be exhaustive.
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Conference papers on the topic "Impact biopsychosocial"

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Ünal, E., E. D. Batu Akal, E. H. Sönmez, et al. "AB1447-HPR Biopsychosocial status of jia patients: perspectives of daily living activities, disease activity and family impact." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.7248.

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Rodriguez-Rabassa, Mary, Ruthmarie Hernandez, Zindie Rodriguez, et al. "Abstract A042: Impact of a natural disaster on access to care and biopsychosocial outcomes among Hispanic/Latino cancer patients." In Abstracts: Twelfth AACR Conference on the Science of Cancer Health Disparities in Racial/Ethnic Minorities and the Medically Underserved; September 20-23, 2019; San Francisco, CA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7755.disp19-a042.

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Zamzam, Maki, Didik Gunawan Tamtomo, and Vitri Widyaningsih. "Biopsychosocial Determinants of Quality of Life in Post Stroke Patients: A Multiple Logistic Regression Analysis." In The 7th International Conference on Public Health 2020. Masters Program in Public Health, Universitas Sebelas Maret, 2020. http://dx.doi.org/10.26911/the7thicph.01.35.

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ABSTRACT Background: The impact of stroke on health may be disastrous. Stroke can affect multiple domains of quality of life. The purpose of this study was to examine biopsychosocial determinants of quality of life in post stroke patients. Subjects and Method: A cross sectional study was conducted at Surakarta hospital, Central Java, from September to October 2019. A sample of 200 post stroke patients was selected for this study purposively. The dependent variable was quality of life. The independent variables were age, gender, empoyment, income, family income, marital status, history of strok
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Nurvitasari, Rahsunji Intan, Didik Gunawan Tamtomo, and Yulia Lanti Retno Dewi. "Biopsychosocial and Economic Factors Affecting the Quality of Life in Patients with Type II Diabetes Mellitus." In The 7th International Conference on Public Health 2020. Masters Program in Public Health, Universitas Sebelas Maret, 2020. http://dx.doi.org/10.26911/the7thicph.01.65.

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Background: Type 2 diabetes mellitus (DM) is a chronic metabolic disease that has a major impact on the quality of life (QoL). The type 2 DM patients to know their capacity to manage the disease and maintain their health and well-being. This study aims to determine biological, psychological, social and economic factors on the quality of life in type 2 DM patients. Subjects and Method: A cross-sectional study was conducted in Surakarta, Central Java. A sample of 100 type 2 DM patients was selected by purposive random sampling. The dependent variable was quality of life. The independent variable
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Retnaningsih, Isna Rahmawati, Argyo Demartoto, and Eti Poncorini. "CASE STUDY ON THE BIOPSYCHOSOCIAL IMPACTS AND COPING BEHAVIORS AMONG VICTIMS OF FEMALE SEXUAL VIOLENCE IN SUKOHARJO, CENTRAL JAVA." In International Conference on Public Health. Masters Program in Public Health, Sebelas Maret University, 2017. http://dx.doi.org/10.26911/theicph.2017.067.

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Khalifah, Intan Noor, Argyo Demartoto, and Harsono Salimo. "HEALTH BELIEF MODEL AND LABELLING THEORY IN THE ANALYSIS OF PREVENTIVE BEHAVIORS TO ADDRESS BIOPSYCHOSOCIAL IMPACTS OF SEXUAL VIOLENCE AMONG STREET CHILDREN IN YOGYAKARTA." In THE 2ND INTERNATIONAL CONFERENCE ON PUBLIC HEALTH. Masters Program in Public Health, Graduate School, Sebelas Maret University Jl. Ir Sutami 36A, Surakarta 57126. Telp/Fax: (0271) 632 450 ext.208 First website:http//: pasca.uns.ac.id/s2ikm Second website: www.theicph.com. Email: theicph2017@gmail.com, 2017. http://dx.doi.org/10.26911/theicph.2017.109.

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