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Books on the topic 'Systemic counselling'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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1

Jim, Downey, ed. Brief therapeutic consultations: An approach to systemic counselling. Chichester: Wiley, 1996.

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2

Riva, Miller, and Goldman Eleanor, eds. Theory and practice of HIV counselling: A systemic approach. New York: Brunner/Mazel, 1993.

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3

Riva, Miller, and Goldman Eleanor, eds. Theory and practice of HIV counselling: A systemic approach. London: Cassell, 1992.

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4

Solution-focused therapy with children: Harnessing family strengths for systemic change. New York: Guilford Press, 1997.

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5

VanZandt, Zark. Developing your school counseling program: A handbook for systemic planning. Australia: Brooks/Cole, 2001.

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6

Hill, Andrew. Counselling older people: A systematic review. Rugby: British Association for Counselling and Psychotherapy, 2004.

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7

Workplace counselling: A systematic approach to employee care. London: Thousand Oaks, Calif., 1996.

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8

Harris, Belinda. Research on counselling children and young people: A systematic scoping review. Rugby: British Association for Counselling and Psychotherapy, 2004.

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9

John, McLeod. Counselling in the workplace: The facts : a systematic study of the research evidence. Rugby: British Association for Counselling and Psychotherapy, 2001.

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10

McLeod, John. Counselling in the workplace: the facts: A systematic study of the research evidence. Rugby: BACP, 2001.

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11

Robert, Bor, ed. AIDS: A guide to clinical counselling. London: Science Press, 1988.

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12

Miller, Riva. AIDS: A guide to clinical counselling. London: Science Press, 1988.

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13

Wright, Barry. Intervention and support for parents and carers of children and young people on the autism spectrum: A resource for trainers. London: Jessica Kingsley Publishers, 2007.

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14

T, Fogle Paul, ed. Counseling skills for speech-language pathologists and audiologists. Australia: Thomson Delmar Learning, 2004.

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15

Brown, Erica. Supporting the child and the family in paediatric palliative care. London: Jessica Kingsley Publishers, 2007.

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16

Mary, Burgess, and British Psychological Society, eds. Communication in cancer care. Malden, MA: BPS Blackwell, 2002.

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17

Interacting Selves: Systemic Solutions for Personal and Professional Development in Counselling and Psychotherapy. Routledge, 2016.

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18

Hedges, Fran. Introduction to Systemic Therapy with Individuals: A Social Constructionist Approach (Basic Texts in Counselling and Psychotherapy). Palgrave Macmillan, 2005.

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19

Solution-Focused Therapy with Children: Harnessing Family Strengths for Systemic Change. The Guilford Press, 2002.

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20

Developing Your School Counseling Program: A Handbook for Systemic Planning. Wadsworth Publishing, 2000.

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21

Ajithkumar, Thankamma, Ann Barrett, Helen Hatcher, and Natalie Cook. Concepts of multidisciplinary management. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199235636.003.0003.

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Cancer prevention 18Cancer screening 22Cancer genetics 24Genetic counselling 28Principles of cancer diagnosis and management 32Principles of surgical oncology 38Radiotherapy 42Principles of systemic therapy 46Carcinogenesis is a multistep process consisting of progressive molecular and cellular changes leading to early invasive cancer and finally to distant metastasis and death. The initiation and progression of cancer usually takes years. Attempts are being made to reverse the molecular and cellular changes at an early state of cancer initiation or progression. The World Health Organization (WHO) estimates that at least one-third of all cancers are preventable and cancer prevention is the most cost-effective long-term strategy for the control of cancer....
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22

Wiles, Kate, Kate Bramham, and Catherine Nelson-Piercy. Kidney disease. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198713333.003.0044.

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This chapter describes the physiological adaptations to pregnancy in women with and without renal disease, reports pregnancy outcomes in women with both acute kidney injury and chronic kidney disease, and discusses a management strategy for antenatal and peripartum care. Acute kidney injury (AKI) is difficult to define in pregnancy because of the physiological increase in glomerular filtration. A normal creatinine can mask renal injury in pregnancy. This chapter considers important causes of AKI in pregnancy including pre-eclampsia, HELLP syndrome, thrombotic microangiopathy, acute fatty liver of pregnancy, systemic lupus erythematosus, urinary tract infection, and obstruction. The trend in the developed world for delaying pregnancy and the increasing prevalence of obesity mean that greater numbers of pregnancies will be complicated by chronic kidney disease. Maternal and fetal complications increase with worsening prepregnancy renal function including the development of pre-eclampsia, fetal growth restriction, premature delivery, and fetal loss. Prepregnancy counselling and the intrapartum management for women with lupus nephritis, immunoglobulin A nephropathy, polycystic kidney disease, and diabetic nephropathy are discussed. Renal replacement therapies in pregnancy including both dialysis and renal transplantation are considered, and practical guidance on renal biopsy, anaesthesia, and the pharmacology of renal disease in pregnancy is offered.
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23

Janice, Connell, ed. A systematic scoping review of the research on counselling in higher and further education. Rugby: British Association for Counselling & Psychotherapy, 2006.

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24

MacLean, Allan B. Vulval pain. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198749547.003.0009.

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Vulval pain or pain involving the vulval tissue is discussed in Chapter 9. It becomes chronic when lasting for at least three months. Vulvodynia is a subset of chronic vulval pain, once known causes (infective, inflammatory, neoplastic, neurological, traumatic, iatrogenic and hormone deficiencies) are excluded. It reportedly affects one in six women at some stage of their lives. Uncertain terminology has hampered understanding. Even the latest classification from the International Society for the Study of Vulvovaginal Disease has deficiencies but it allows the discarding of previously used unhelpful terms. Differentiating features between provoked (entry dyspareunia), and unprovoked, localised and generalised, overlap, both in diagnosis and management. Older theories on causation included infection, irritation and inflammation but laboratory-based research has not supported these. Hormonal and neural mechanisms seem more likely to cause the pain, while the interplay of biological, psychological, and social factors has recently gained credence. Publications on successful management demonstrate a powerful placebo effect. The role of specially designated vulval pain clinics, multidisciplinary approaches, and team working is emphasised. General measures in vulval care, such as wearing clothes made of natural fibre, using emollients or carrying out pelvic floor exercises besides reducing stress, can minimise the pain. Topical anaesthetic creams or systemic treatments with antidepressants or anti-epileptics have advocates. Treatment is most effective when careful selection, adequate counselling, and ongoing psychosomatic evaluation address all the interactive factors that initiate, and maintain vulval pain besides modulating patient response. Case scenarios illustrate the complexities of diagnosis and management.
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25

Archer, Nick, and Nicky Manning. History and examination. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199230709.003.0004.

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History 42Examination 44As in any area of medicine, assessment of the fetal cardiovascular system should begin with sufficient accurate information to allow a proper assessment and relevant counselling to be carried out. Aspects of the history are considered under 3 headings of information that should be available before investigation is performed and, in some cases, before referral to a fetal cardiac clinic. Much of the information should be available in maternity notes but some specific details often need clarifying....
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26

Perry, Kathryn Nicholson, and Mary Burgess. Communication in Cancer Care (Communication and Counselling in Health Care). British Psychological Society, 2003.

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27

Speck, Peter, and Christopher Herbert. Communication issues in pastoral care and chaplaincy. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198736134.003.0050.

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The remit of those involved in pastoral care and chaplaincy is not confined to patients of a particular faith or belief system. However, it differs from counselling, since the encounter takes place within the context of a belief system held by the pastoral carer, and which may or may not be shared by the recipient of care. The diagnosis of a life-threatening illness will trigger a range of emotional responses, which may include questions of an existential nature relating to causality, the meaning of the illness, and fears for the future. The essence of communication in pastoral care and chaplaincy is the creation of a safe space within which the person can explore issues of importance to them within the context of their own spirituality.
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28

Gerard, McMeel. Part V Deposit-Taking and Consumer Credit Conduct of Business, 17 Regulation of Consumer Credit Business by the Financial Conduct Authority. Oxford University Press, 2014. http://dx.doi.org/10.1093/law/9780198705956.003.0017.

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This chapter discusses the Financial Conduct Authority's (FCA) regulation of the consumer credit industry. It begins with an introduction to the consumer credit regime. It then details the scope of regulated credit-related activities, covering the rules for entering into a regulated credit agreement; entering into a regulated consumer hire agreement; operating an electronic system in relation to lending; credit broking; and debt adjusting, debt-counselling, debt-collecting and debt administration. This is followed by discussions of the authorisation, supervision, and enforcement of credit-related activities and credit firms by the FCA; conduct of business standards; and the rights of action and complaints to the Ombudsman.
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29

United Nations. Economic Commission for Africa. Public Administration, Human Resources, and Social Development Division., ed. The Role of mass media in promoting guidance and counselling services in career development. [Addis Ababa]: United Nations, Economic Commission for Africa, Public Administration, Human Resources and Social Development Division, 1989.

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30

Brugha, Traolach S. Approaches to treatment and care. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198796343.003.0012.

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Sharing with the patient and their carers the results of an assessment in autism and of what that means and the principles of post diagnostic support is covered. Conventional medically orientated ways of thinking about the treatment of autism including considerations of approaches to evaluating treatments are discussed. Also covered are the sought after targets of treatment, the role of patients, carers, and the public in choosing what their wishes and objectives are, uses of medication, structured psychological interventions including those focusing on adaptive and social skills, the limited role of genetic counselling, the role of guidelines and recent systematic reviews of the evidence base, and the treatment of comorbidities. Future prospects for treatment development are also touched on. Armed with a complete assessment and treatment recommendations, duties in relation to legal aspects of the psychiatry of autism are introduced.
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31

Graves, Tracey. Neurogenetic disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0223.

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There are many genetic diseases which affect the nervous system. Although some of these are extremely rare, several are quite common and, as a group, they comprise a significant proportion of neurological disease. Almost all clinical neurological syndromes can have a genetic cause. Not all of these have been genetically elucidated, but some have been extensively characterized in terms of clinical phenotype, molecular genetics, and cellular pathophysiology. Given the improvement in laboratory techniques and subsequent reduction in the cost of direct DNA sequencing, there is likely to be a rapid expansion over the next decade in the identification of causative genes and hence the availability of genetic tests. Thus, all clinicians should have a basic understanding about genetic disease; inheritance patterns; availability of genetic tests; genetic counselling; and ethics. Particular subspeciality areas where neurogenetic disease is common include neuromuscular disease and movement disorders.
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32

Vester, Udo, and Stefanie Weber. Townes–Brocks syndrome. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0359.

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Townes–Brocks syndrome (TBS) is an autosomal dominant disease with variable expression. Classical features are imperforate anus, dysplastic ears with congenital hearing deficit, and triphalangeal thumbs in most cases. A variety of other malformations (renal, genitourinary, heart, central nervous system, eyes) or hypothyroidism has been described. Mutations in SALL1 have been identified in patients with TBS and genetic testing allows confirmation of the diagnosis. Familiar and sporadic forms (caused by de novo mutations) seem to be equally distributed. Renal involvement in TBS is not uncommon and includes renal agenesis, hypo-/dysplasia, and renal cysts and may eventually lead to chronic renal failure. As renal function may not deteriorate before adulthood, renal function should be monitored in all patients. As cases with TBS can be oligosymptomatic, TBS should be suspected in every case with unexplained renal failure, minor abnormalities, or indicative family history. Genetic counselling is mandatory in identified cases.
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33

Edenborough, Frank P. Fertility, contraception, and pregnancy. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780198702948.003.0012.

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This chapter describes the physiological effect of CFTR dysfunction on the development of the reproductive system. Young people with CF and their parents are poorly educated regarding sexual function and becoming parents themselves. They often wish to learn this from their CF teams. Male and female potency, reproductive genetics, and the need for genetic and general counselling before embarking on pregnancy are covered. Contraception, emphasizing the need to avoid unwanted pregnancy and sexually transmitted diseases, and assisted reproductive techniques are described. We discuss the evolving medical and obstetric management of pregnancy, including the likely need for optimizing drug treatment or escalating to more intensive treatment for intercurrent infection. Optimal delivery in the context of maternal health, fetal risks, and longer term maternal outcomes are discussed. Pregnancy post transplantation and termination of unwanted pregnancy or where the mother is too poorly to continue conclude the chapter.
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34

Elliott, Perry, Pier D. Lambiase, and Dhavendra Kumar, eds. Inherited Cardiac Disease. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198829126.001.0001.

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Every year, thousands of people die or suffer chronic disability as the result of inherited diseases of the cardiovascular system. In many cases, diagnosis of inherited disease is delayed or missed owing to a lack of awareness, and an even greater number of relatives are exposed to unnecessary risk. This new edition of Inherited Cardiac Disease provides a comprehensive summary of the aetiology, presentation, and management of genetic disorders of the cardiovascular system. Fully updated to reflect the advances in molecular genetic technologies and the publication of national guidelines for the management of families with inherited cardiac diseases, it retains the first edition’s broad scope and applicability to all members of the multidisciplinary team, from specialists in cardiology and clinical genetics, to genetic counsellors, paediatricians, nurse specialists, and GPs who may come into contact with families presenting with inherited cardiac diseases. After chapters on the general principles of cardiovascular genetics, genetic testing and counselling, individual disorders are then examined in detail, each account featuring a clinical summary, diagnostic tests and special investigations, and treatments relevant to each inherited cardiac disease. Written in the succinct bullet-point style of the Oxford Specialist Handbooks, this new edition of Inherited Cardiac Disease delivers key information in an accessible manner, and is an invaluable guide to anyone who works with patients who are affected by inherited diseases of the cardiovascular system in their practice.
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35

Choon, Francis Chin Kuok, and Phua Dong Haur. Management of radiation poisoning. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0331.

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In radiation poisoning, a distinction between exposure and contamination should be made. Decontamination by removing clothes, washing of skin, and removal of debris can remove up to 90% of external contaminated radiation. Treatment of acute life-threatening injuries takes priority over treatment of radiation poisoning. Triage of severely exposed patients can give an indication of dose and severity of the radiation dose absorbed. Survival is related to dose absorbed. Identification of the radiation source should be made by the radiation characteristics to determine the shielding necessary for protection of hospital staff and the antidote required. Early gastric lavage and specific antidotes for ingested radiation poisoning should be used with caution. Death is mainly due to infection and haemorrhage. Acute radiation syndrome (ARS) is a manifestation of haematopoietic, gastrointestinal, cardiovascular, central nervous system, and cutaneous syndromes. Those receiving whole body doses of 1–5 Gy may recover easily with appropriate medical management; those with doses of 6–10 Gy may survive with intensive management; and those with doses of >10 Gy seldom survive. Treatment of ARS is supportive with the use of antibiotics, colony-stimulating factors, blood products, and stem cell transplants. Protection of the staff is by reducing time exposed, increasing distance from source and proper shielding. Psychological counselling should be available to patient or staff if required.
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36

Wright, Barry, and Chris Williams. Intervention and Support for Parents and Carers of Children and Young People in the Autistic Spectrum: A Resource for Trainers (Jkp Resource Materials). Jessica Kingsley Publishers, 2007.

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37

Flasher, Lydia V., and Paul T. Fogle. Counseling Skills for Speech-Language Pathologists and Audiologists. Singular, 2003.

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38

(Foreword), Sheila Shribman, ed. Supporting the Child and the Family in Pediatric Palliative Care. Jessica Kingsley Publishers, 2007.

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39

Perry, Kathryn Nicholson, and Mary Burgess. Communication in Cancer Care. Wiley & Sons, Incorporated, John, 2008.

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