Sexualidad de personas con acromegalia y síndrome de Cushing; experiencias y aspectos psicosociales relacionados / Sexuality in people with acromegaly and Cushing's syndrome; experiences and related psychosocial aspects

Antecedentes: aunque la literatura documenta que la acromegalia y el síndrome de Cushing pueden producir dificultades sexuales, los estudios sobre el tema son escasos, especialmente desde la perspectiva de los sujetos. Objetivo: describir el impacto de la acromegalia y el síndrome de Cushing sobre la sexualidad y algunos aspectos psicosociales relacionados, desde la perspectiva de personas con estas enfermedades. Métodos: estudio descriptivo, retrospectivo, cualitativo, con 12 mujeres y 8 varones, atendidos en Instituto Nacional de Endocrinología, Cuba. Se utilizaron entrevistas en profundidad y técnicas psicológicas proyectivas. La información fue transcrita, codificada, interpretada y triangulada. Se consideraron los aspectos éticos. Resultados: las manifestaciones clínicas, corporales y psíquicas de la enfermedad impactaron la sexualidad de la mayoría de los sujetos. Los roles de género y la estética corporal jugaron un rol importante, especialmente en mujeres. La pareja se estructuró como apoyo ante las dificultades sexuales, especialmente en varones. Aparecieron tres perfiles de experiencias sexuales: 1) un grupo refirió que la enfermedad impactó negativamente su sexualidad en forma de dificultades con la erección (varones) y el deseo sexual (mujeres), e incidió en la pareja; 2) otro grupo refirió similares cambios sexuales, pero vividos con menor impacto psicoemocional debido al apoyo de la pareja; 3) un tercer grupo no refirió cambios en la sexualidad ni en la pareja. Se discuten factores relacionados. Conclusiones: las experiencias sexuales de los sujetos son diversas, relacionadas con representaciones sobre pareja, sexualidad, cuerpo y enfermedad. Mujeres y varones muestran diferencias en la influencia del impacto estético y psicoemocional de la enfermedad sobre la sexualidad. Las representaciones (genéricas, corporales, sexuales) más flexibles se relacionan con menor impacto sexual de la enfermedad(AU)

Background: although literature documents that acromegaly and Cushing's syndrome may cause sexual difficulties, the number of studies about the topic is low, mainly from the subjects' perspective. Objective: to describe the impact of acromegaly and Cushing's syndrome on the sexuality and some related psychosocial aspects from the perspective of people living with these diseases. Methods: retrospective, descriptive and qualitative study of 12 women and 8 men who were seen at the National Institute of Endocrinology of Cuba. In depth interviews and projective psychological techniques were used. The collected information was transcripted, coded, construed and triangled. Ethical aspects were taken into consideration. Results: the clinical, body and psychical manifestations of the disease had an impact on the sexuality of most of subjects. The gender role and the body image played significant roles mainly in women. The couple was formed as a support to face sexual difficulties, particularly in men. There were three profiles of sexual experiences: 1) a group stated that the disease had a negative impact on their sexuality regarding difficulties in erection (men) and sexual desire (women) and this influenced on the couple; 2) this group mentioned similar sexual changes but experienced lower psychoemotional impact due to the support of the sexual partner; and 3) the third group did not mention any change in sexuality or in the couple. Related factors were also discussed. Conclusions: sexual experiences of the subjects were varied and related to representations about couple, sexuality, body and disease. Women and men showed differences in the effect of the esthetic and psycho-emotional impact of the disease on sexuality. The most flexible representations (generic, body, sexual) were related to lower sexual impact of disease(AU)

Sexualidad de personas con acromegalia y síndrome de Cushing; experiencias y aspectos psicosociales relacionados / Sexuality in people with acromegaly and Cushing's syndrome; experiences and related psychosocial aspects

Antecedentes: aunque la literatura documenta que la acromegalia y el síndrome de Cushing pueden producir dificultades sexuales, los estudios sobre el tema son escasos, especialmente desde la perspectiva de los sujetos. Objetivo: describir el impacto de la acromegalia y el síndrome de Cushing sobre la sexualidad y algunos aspectos psicosociales relacionados, desde la perspectiva de personas con estas enfermedades. Métodos: estudio descriptivo, retrospectivo, cualitativo, con 12 mujeres y 8 varones, atendidos en Instituto Nacional de Endocrinología, Cuba. Se utilizaron entrevistas en profundidad y técnicas psicológicas proyectivas. La información fue transcrita, codificada, interpretada y triangulada. Se consideraron los aspectos éticos. Resultados: las manifestaciones clínicas, corporales y psíquicas de la enfermedad impactaron la sexualidad de la mayoría de los sujetos. Los roles de género y la estética corporal jugaron un rol importante, especialmente en mujeres. La pareja se estructuró como apoyo ante las dificultades sexuales, especialmente en varones. Aparecieron tres perfiles de experiencias sexuales: 1) un grupo refirió que la enfermedad impactó negativamente su sexualidad en forma de dificultades con la erección (varones) y el deseo sexual (mujeres), e incidió en la pareja; 2) otro grupo refirió similares cambios sexuales, pero vividos con menor impacto psicoemocional debido al apoyo de la pareja; 3) un tercer grupo no refirió cambios en la sexualidad ni en la pareja. Se discuten factores relacionados. Conclusiones: las experiencias sexuales de los sujetos son diversas, relacionadas con representaciones sobre pareja, sexualidad, cuerpo y enfermedad. Mujeres y varones muestran diferencias en la influencia del impacto estético y psicoemocional de la enfermedad sobre la sexualidad. Las representaciones (genéricas, corporales, sexuales) más flexibles se relacionan con menor impacto sexual de la enfermedad(AU)

Background: although literature documents that acromegaly and Cushing's syndrome may cause sexual difficulties, the number of studies about the topic is low, mainly from the subjects' perspective. Objective: to describe the impact of acromegaly and Cushing's syndrome on the sexuality and some related psychosocial aspects from the perspective of people living with these diseases. Methods: retrospective, descriptive and qualitative study of 12 women and 8 men who were seen at the National Institute of Endocrinology of Cuba. In depth interviews and projective psychological techniques were used. The collected information was transcripted, coded, construed and triangled. Ethical aspects were taken into consideration. Results: the clinical, body and psychical manifestations of the disease had an impact on the sexuality of most of subjects. The gender role and the body image played significant roles mainly in women. The couple was formed as a support to face sexual difficulties, particularly in men. There were three profiles of sexual experiences: 1) a group stated that the disease had a negative impact on their sexuality regarding difficulties in erection (men) and sexual desire (women) and this influenced on the couple; 2) this group mentioned similar sexual changes but experienced lower psychoemotional impact due to the support of the sexual partner; and 3) the third group did not mention any change in sexuality or in the couple. Related factors were also discussed. Conclusions: sexual experiences of the subjects were varied and related to representations about couple, sexuality, body and disease. Women and men showed differences in the effect of the esthetic and psycho-emotional impact of the disease on sexuality. The most flexible representations (generic, body, sexual) were related to lower sexual impact of disease(AU)

Bioethical dimensions of cultural psychosomatics: the need for an ethical research approach.

Contemporary psychosomatics is a research-based technical discipline and its social power depends on how scientific knowledge is obtained and applied in practice, considering cultural contexts. This article presents the view that the dialogical principles on which bioethical discourse is based are more inclusive than professional ethics and philosophical reflection. The distinction is advanced between rule-guided behavior and norm-justifiable acts (substantiation and justification). The practical implications of good practices in the generation of valid, reliable, generalizable and applicable knowledge are emphasized. For practitioners and researchers, the need to reflect on the distinction between patient and research participant can avoid the therapeutic misunderstanding, a form of abuse of the doctor-patient relationship. In addition, in resource-poor settings, the dilemma presented by the know-do gap (inapplicability of research results due to financial or social constraints) is part of the ethics' realm of the profession. Future prospects include a wider use of research results in practice, but avoidance of the know-do gap (the disparity between what is known and what can be done, particularly in settings with limited resources) requires a synthetic and holistic approach to medical ethics, combining moral reflection, theoretical analysis and empirical data.

'I'm more sick than my doctors think': ethical issues in managing somatization in developing countries.

Several ethical issues confront the healthcare professional who is managing somatization in developing countries where cost constraints, low literacy, poverty, poor nutrition and infections and inadequate access to healthcare are common. The paper discusses these in the context of the ethical principles of autonomy, beneficence, non-maleficence and justice. Some of the ethical issues in managing somatization include being influenced by patient distress rather than rational medical decision-making, inadequate attention to the cultural meaning of symptoms, psychologizing versus medicalizing, the ethics of nomenclature and labels, communicating ethically with patients, and managing them adequately given lack of evidence and training. An ethical approach to managing somatization in this context would include using an integrated and simultaneous medical and psychiatric approach. To ensure patient beneficence, the medical, psychological and social assessment should be undertaken side-by-side as much as possible and should be cost effective. Respecting patient autonomy by using adequate communication methods and the patient's cultural model of the illness as part of management is also integral to ethical practice. In the developing world, issues of equity are also an important ethical concern. When more serious illnesses are the health priority, functional syndromes may not get equal importance or resources.

Indigenous measures of personality assessment in Asian countries: a review.

This article reviews attempts to develop multidimensional personality measures in Asia and their applications in clinical assessment. Indigenous personality assessment measures in India, Korea, Japan, the Philippines, and Taiwan are examined. These early attempts have not yielded a comprehensive personality measure that integrates a theoretical framework and an empirical program of validation. The Chinese Personality Assessment Inventory (CPAI) is cited as an example to illustrate the process of developing an indigenous measure that meets the testing standards of established assessment instruments. On the basis of the research findings from the CPAI, the authors discuss the relevance of indigenous measures in clinical assessment in native cultures as well as in informing mainstream personality assessment.