Pituitary disease - perspectives of patients and partners

Aim. To explore experiences of pituitary disease of people with pituitary disease (PD) and their partners (PT).

Background. Pituitary disease encompasses a range of hormonal abnormalities that produce a variety of signs and symptoms depending on the underlying cause.

Design. A triangulated exploratory study.

Methods. The study was conducted in three phases: (a) non-participant monitoring of an Internet pituitary chat room over four months; (b) in-depth structured interviews with PD attending a pituitary outpatient clinic (n = 8) and PT (n = 6), (c) focus groups (n = 12). Data were collected in 2005.

Results. Four themes emerged from the discussion in each phase: 'need to be normal', 'emotional merry-go-round', 'damage to the self', and 'doctor ignorance'. Symptoms of pituitary disease were often mistaken for sinusitis, 'getting old before my time', hypochondria, stress, and 'something sinister changing the way I look'. Time to diagnosis varied from four weeks to 15 years. PD felt included in decision-making but partners relied on PD for information. Body image changes were significant making PD feel like a 'freak show for medical students' and the emotional distress persisted after treatment and 'cure'. The word 'tumour' caused significant stress and anxiety and depression was common. PD and PT felt general practitioners (GP) lacked information about pituitary disease.

Conclusions. Pituitary disease has a major impact on psychological well-being. PD but not PT felt involved in decisions about their management. GPs may need more education about pituitary disease. The study adds important information about the emotional effects of pituitary disease and its treatment.

Relevance to clinical practice. Pituitary disease is a generic term encompassing a range of underlying disease processes that often produce vague symptoms, often attributed to other causes, which delays diagnosis and treatment. Pituitary disease has a significant under recognised impact on people's mental and physical wellbeing and self-concept. Although the underlying hormonal imbalances associated with pituitary disease are largely reversible (cured), emotional distress persists. Regular monitoring of emotional wellbeing as well as medical and hormone status is warranted.

Psychometric properties of a scale to measure investment in the sick role : the Illness Cognitions Scale

Rationale, aims and objectives A person’s beliefs about their illness may contribute to recovery and prognosis. Some degree of acceptance of illness and its impact is necessary to integrate the presence of a chronic disorder into one’s lifestyle and adhere to necessary components of illness management; however, some individuals can become ‘stuck’ and have difficulty adjusting out of the sick role. Inventories exist to measure illness cognitions, attitudes and behaviours as they relate to hypochondria and psychosomatic illness, but there is no extant measure of sick role inertia.We describe the psychometric properties of a new scale, the Illness Cognitions Scale (ICS), a metric of investment in the sick role.

Methods The ICS was administered to 97 individuals with bipolar or schizoaffective disorder, and the psychometric properties of the scale measured. Dimensionality was assessed using Principal Components Analysis with Oblimin rotation.

Results The scale has a strong internal consistency, with a Cronbach’s alpha of 0.858. Results of a factor analysis suggested the presence of one main factor, with three other smaller, related sub-factors, capturing aspects of maladaptive illness beliefs.

Conclusion The ICS is a 17-item, internally validated scale measuring difficulty adjusting out of the sick role. The scale predominantly measures a single construct. Further research on external validity of the ICS is required as well as determination of the clinical significance and patient acceptability of the scale.

Reflexions sur les affections vaporeuses ou Examen du traité des vapeurs des deux sexes /

Mode of access: Internet.

Observations on the nature, causes, and cure of those disorders which have been commonly called nervous hypochondriac, or hysteric : to which are prefixed some remarks on the sympathy of the nerves /

Signatures: pi⁸ A-2I⁸ K⁴.

Acceptance of relapse fears in breast cancer patients: effects of an act-based abridged intervention

Objective: Relapse fear is a common psychological scar in cancer survivors. The aim of this study is to assess the effects of an abridged version of Acceptance and Commitment Therapy (ACT) in breast cancer patients.Method: An open trial was developed with 12 non-metastatic breast cancer patients assigned to 2 conditions, ACT and waiting list. Interventions were applied in just one session and focused on the acceptance of relapse fears through a ‘defusion’ exercise. Interference and intensity of fear measured through subjective scales were collected after each intervention and again 3 months later. Distress, hypochondria and ‘anxious preocupation’ were also evaluated through standardized questionnaires.Results: The analysis revealed that ‘defusion’ contributed to decrease the interference of the fear of recurrence, and these changes were maintained three months after intervention in most subjects. 87% of participants showed clinically significant decreases in interference at follow-up sessions whereas no patient in the waiting list showed such changes. Statistical analysis revealed that the changes in interference were significant when comparing pre, post and follow-up treatment, and also when comparing ACT and waiting list groups. Changes in intensity of fear, distress, anxious preoccupation and hypochondria were also observed.Conclusions: Exposure through ‘defusion’ techniques might be considered a useful option for treatment of persistent fears in cancer patients. This study provides evidence for therapies focusing on psychological acceptance in cancer patients through short, simple and feasible therapeutic methods.

Riesgo de trastornos de la conducta alimentaria, composición corporal y gasto energético en chicas adolescentes de la Comunidad de Madrid

La alimentación está controlada por muchos factores, incluyendo el apetito, la disponibilidad de alimentos, la familia, los compañeros, la cultura, ... En la actualidad, los trastornos de la conducta alimentaria (en lo sucesivo, TCA) forman parte de nuestra cultura, aunque la familiaridad con estos términos es muy reciente. Las primeras referencias sobre casos de restricción alimentaria se remontan a la literatura religiosa antigua. El primer registro médico se atribuye a Richard Morton en 1689 quien publicó su libro “Phthisiologia, seu Exercitaciones de Phthisi” considerándose la primera referencia médica sobre anorexia nerviosa. Morton, la describe como un “consumo nervioso causado por la tristeza y las preocupaciones ansiosas”. La traducción al inglés de su libro, “Phthisiologia, or, a Treatise of Consumptions” (traducido en 1694) describe el caso de dos pacientes, una mujer de 18 años y un varón de 16 que comenzaron su enfermedad dos años antes de pedir ayuda a Morton y en el que describe con detalle los procesos patológicos que causan la pérdida de tejido corporal. Otros casos similares se encuentran descritos por Robert Whytt en 1767 y por De Valangin en 1768. Un siglo después, en 1759, el psiquiatra Louis-Victor Marcé, publicó un informe titulado “Note sur one Forme de Deliré Hypochondria que Consécutive aux Dyspesies et Caractérisée Principalement par le Refusd'Aliments” (“Una nota sobre el delirio hipocondríaco, consecutivo a la dispepsia y principalmente caracterizado por el rechazo a la comida”). En este informe, describe esta patología, dejando claro que la enfermedad era de origen psiquiátrico y no físico, y su psicopatología compleja...