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1.
Br J Dermatol ; 170(4): 824-31, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24641720

RESUMO

BACKGROUND: Psychosocial stress can be a risk factor for the maintenance and exacerbation of chronic inflammatory diseases, such as psoriasis and rheumatoid arthritis (RA). OBJECTIVES: To gain insight into the specificity of the psychophysiological stress response during chronic inflammation, we assessed autonomic and neuroendocrine responses to stress in different chronic inflammatory diseases. METHODS: Thirty patients with psoriasis (nine women, mean age 58·5 years ± 12·4), 34 patients with RA (16 women, mean age 60·8 years ± 9·2) and 25 healthy controls (16 women, mean age 55·6 years ± 8·7) underwent a standardized psychosocial stress task (Trier Social Stress Test). Salivary levels of α-amylase and cortisol and self-reported tension levels were measured before and after the stress test. RESULTS: The cortisol response to stress was heightened in patients with psoriasis compared with patients with RA and healthy controls, whereas there were no differences in the autonomic and self-reported measures. CONCLUSIONS: The altered neuroendocrine stress response in patients with psoriasis suggests that stressful events might have different physiological consequences for specific patient groups with chronic inflammatory conditions, possibly adversely affecting disease status.


Assuntos
Artrite Reumatoide/psicologia , Psoríase/psicologia , Estresse Psicológico/complicações , Adulto , Idoso , Idoso de 80 Anos ou mais , Antirreumáticos/uso terapêutico , Artrite Reumatoide/tratamento farmacológico , Estudos de Casos e Controles , Fármacos Dermatológicos/uso terapêutico , Feminino , Humanos , Hidrocortisona/metabolismo , Masculino , Pessoa de Meia-Idade , Psoríase/tratamento farmacológico , Fatores de Risco , Saliva/química , alfa-Amilases/metabolismo
2.
Br J Dermatol ; 167(2): 262-9, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22404598

RESUMO

BACKGROUND: Itch and pain are common symptoms in skin disease. It has been suggested that negative emotions may play a role in itch and pain. To date, however, the role of emotions has only been studied for pain in experimental studies, not yet for itch. OBJECTIVES: To investigate the effects of negative and positive emotions on the sensitivity to itch and pain. METHODS: Film fragments were used to induce a negative or positive emotional state in healthy women. Itch and pain were induced using the following somatosensory stimuli: electrical stimulation, histamine iontophoresis and the cold pressor test. RESULTS: Results showed that the scores for itch and pain evoked by histamine and the cold pressor test, respectively, were significantly higher in the negative than in the positive emotion condition, whereas tolerance thresholds to electrical stimulation and the cold pressor test, and stimulus unpleasantness scores did not differ between the two conditions. CONCLUSIONS: These findings for the first time indicate in an experimental design that emotions play a role in sensitivity to somatosensory sensations of both itch and pain.


Assuntos
Emoções , Dor/psicologia , Prurido/psicologia , Análise de Variância , Temperatura Baixa , Estimulação Elétrica , Feminino , Histamina/farmacologia , Agonistas dos Receptores Histamínicos/farmacologia , Humanos , Iontoforese , Medição da Dor , Autorrelato , Adulto Jovem
3.
Ann Rheum Dis ; 70(12): 2131-3, 2011 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-21926189

RESUMO

OBJECTIVES: Patients with fibromyalgia have diminished levels of physical fitness, which may lead to functional disability and exacerbating complaints. Multidisciplinary treatment comprising cognitive-behavioural therapy (CBT) and exercise training has been shown to be effective in improving physical fitness. However, due to the high drop-out rates and large variability in patients' functioning, it was proposed that a tailored treatment approach might yield more promising treatment outcomes. METHODS: High-risk fibromyalgia patients were randomly assigned to a waiting list control group (WLC) or a treatment condition (TC), with the treatment consisting of 16 twice-weekly sessions of CBT and exercise training tailored to the patient's cognitive-behavioural pattern. Physical fitness was assessed with two physical tests before and 3 months after treatment and at corresponding intervals in the WLC. Treatment effects were evaluated using linear mixed models. RESULTS: The level of physical fitness had improved significantly in the TC compared with the WLC. Attrition rates were low, effect sizes large and reliable change indices indicated a clinically relevant improvement among the TC. CONCLUSIONS: A tailored multidisciplinary treatment approach for fibromyalgia consisting of CBT and exercise training is well tolerated, yields clinically relevant changes, and appears a promising approach to improve patients' physical fitness. ClinicalTrials.gov ID NCT00268606.


Assuntos
Terapia Cognitivo-Comportamental/métodos , Terapia por Exercício/métodos , Fibromialgia/reabilitação , Adulto , Terapia Combinada , Teste de Esforço/métodos , Feminino , Fibromialgia/fisiopatologia , Humanos , Masculino , Pessoa de Meia-Idade , Aptidão Física , Resultado do Tratamento
4.
Tijdschr Psychiatr ; 53(6): 333-42, 2011.
Artigo em Holandês | MEDLINE | ID: mdl-21674446

RESUMO

BACKGROUND: Up till now in the Netherlands no controlled studies haven been published regarding the effect of outpatient treatment of violent adolescents at a psychiatric clinic. AIM: To investigate in an explanatory study the results of group treatment of violent adolescents (aggression control therapy) performed at the forensic outpatient clinic 'het Dok' in Rotterdam. METHOD: First of all, personality traits and problem behaviours of the patients were compared with those of a group of secondary vocational students. Then we compared the traits and behaviour of those who completed the treatment with those of the patients who dropped out. In order to determine the therapy results, patients were measured at three moments; during uptake, at the beginning of treatment and at the end of treatment. RESULTS: Patients appeared to score significantly higher on the trait anger and on hostility than the secondary vocational students but significantly lower on social anxiety. Patients who completed the therapy scored significantly lower on psychopathy than the patients who dropped out early. During the waiting-list period there was no change in the problem behaviours of the patients. Patients who completed the therapy demonstrated significant decrease in physical aggression. However, the size effect appeared to be small. CONCLUSION: Aggression control therapy at a forensic psychiatric outpatient clinic seems to result in a significant decrease in self-reported physically aggressive behaviour in violent adolescents.


Assuntos
Comportamento do Adolescente/psicologia , Agressão/psicologia , Psiquiatria Legal , Psicoterapia de Grupo/métodos , Violência , Adolescente , Assistência Ambulatorial , Feminino , Humanos , Masculino , Países Baixos , Pacientes Desistentes do Tratamento/psicologia , Pacientes Desistentes do Tratamento/estatística & dados numéricos , Testes Psicológicos , Violência/prevenção & controle , Violência/psicologia , Adulto Jovem
5.
Arthritis Care Res (Hoboken) ; 63(6): 800-7, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21312345

RESUMO

OBJECTIVE: The heterogeneity of cognitive-behavioral patterns in patients with fibromyalgia (FM) has been proposed to underlie the variability in treatment outcomes. It has previously been shown that pain-avoidance and pain-persistence treatments tailored to the patient's pattern are effective in improving physical and psychological functioning and overall impact in high-risk patients with heightened psychological distress. In the present study, the cognitive-behavioral effects of these treatments were evaluated to provide insight into the main proposed mechanisms, specifically pain-avoidance behaviors and activity pacing in the pain-avoidance and pain-persistence treatments, respectively. METHODS: High-risk FM patients were classified into 2 groups, pain avoidance and pain persistence, and randomized in groups to the relevant treatment or waiting-list control condition. The pain-avoidance and pain-persistence treatments both comprised 16 twice-weekly sessions of cognitive-behavioral therapy and exercise training. Cognitive--behavioral factors assessed at pre- and posttreatment and 6 months of followup were evaluated using linear mixed models. RESULTS: A significant treatment effect was found for pain-avoidance behavior in the pain-avoidance treatment and for activity pacing in the pain-persistence treatment, showing improvements in the treatment condition relative to the controls. Furthermore, the effect on functioning was mediated by changes in pain-avoidance behavior in the pain-avoidance treatment and by changes in activity pacing in the pain-persistence treatment. Both treatments also showed significant improvements in other relevant cognitive-behavioral factors. CONCLUSION: Both the pain-avoidance and pain-persistence treatments are effective in improving cognitive-behavioral factors in high-risk FM patients. Pain-avoidance behavior and activity pacing might be important mediating mechanisms for beneficial outcomes in pain-avoidance and pain-persistence treatments, respectively.


Assuntos
Aprendizagem da Esquiva/fisiologia , Terapia Cognitivo-Comportamental/métodos , Fibromialgia/terapia , Manejo da Dor , Adulto , Feminino , Fibromialgia/psicologia , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Dor/psicologia , Medição da Dor/métodos , Resultado do Tratamento
6.
Br J Dermatol ; 163(5): 986-91, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20716227

RESUMO

BACKGROUND: Psychological stressors might contribute to the severity of chronic inflammatory diseases such as psoriasis by dysregulating hypothalamic-pituitary-adrenal (HPA) axis activity. OBJECTIVES: To evaluate the role of cortisol, a key component of the HPA axis, in reaction to psychological stress in patients with psoriasis. METHODS: Serum cortisol, clinical indicators of disease severity (Psoriasis Area and Severity Index) and self-report measures of daily stressors were measured monthly for 6 months in 62 patients with psoriasis. RESULTS: In addition to the previous findings in this sample showing that peak levels of daily stressors predicted an increase in disease severity a month later, the peak levels of daily stressors were also significantly associated with a lower cortisol level. Moreover, patients who persistently experienced higher levels of daily stressors had lower mean cortisol levels than patients who experienced lower levels of daily stressors. CONCLUSIONS: Results suggest that daily stressors influence disease outcome in patients with psoriasis by affecting cortisol levels at moments of high stress. Furthermore, patients with persistently high levels of stressors seem to have a specific psychophysiological profile of lowered cortisol levels and may be particularly vulnerable to the influence of stressors on their psoriasis.


Assuntos
Hidrocortisona/sangue , Psoríase/sangue , Psoríase/psicologia , Estresse Psicológico/sangue , Adulto , Idoso , Biomarcadores/sangue , Feminino , Humanos , Estudos Longitudinais , Masculino , Pessoa de Meia-Idade , Psoríase/diagnóstico , Índice de Gravidade de Doença , Estresse Psicológico/psicologia , Adulto Jovem
7.
Br J Dermatol ; 161(3): 542-6, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19538185

RESUMO

BACKGROUND: Narrow-band ultraviolet (UV) B phototherapy is an effective treatment for psoriasis. However, there is considerable variability in the number of treatment sessions needed to achieve psoriasis clearance. While several clinical and treatment-related factors predict time to clearance, the effect of itching and scratching on the number of irradiation sessions is insufficiently understood. OBJECTIVE: Predictors of the time to clearance were assessed in patients with psoriasis who were referred for UVB treatment in a randomized double-blind comparison of irradiation regimens for UVB phototherapy. METHODS: After randomization to either UVB irradiation with a suberythematogenic or an erythematogenic regimen, patients were irradiated with 20% and 40% incremental doses, respectively, three times weekly. The Psoriasis Area and Severity Index (PASI) score was measured at baseline and every 4 weeks, and itching and habitual scratching were measured at baseline. RESULTS: Among the 77 patients who achieved psoriasis clearance (90% reduction of PASI), itching and scratching were correlated with the number of irradiation sessions needed to achieve clearance, with higher levels of itch and scratching predicting more sessions. These effects remained significant after controlling for the initial PASI score, irradiation schemes, minimal erythema dose (MED), skin type, cumulative dose, protocol adjustments and lifestyle factors (smoking habits and alcohol consumption). CONCLUSIONS: Patients with higher levels of itch and scratching need more irradiation sessions to achieve clearance of psoriasis with UVB phototherapy. Systematic assessment of the severity of itch and scratching, followed by short-term itch-coping programmes for patients at risk, might be a cost-effective, adjunct to UVB therapy.


Assuntos
Prurido , Psoríase/radioterapia , Terapia Ultravioleta/métodos , Adulto , Idoso , Método Duplo-Cego , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Prurido/etiologia , Psoríase/complicações , Índice de Gravidade de Doença , Inquéritos e Questionários , Resultado do Tratamento
8.
Br J Dermatol ; 161(2): 295-9, 2009 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-19438455

RESUMO

BACKGROUND: There is increasing evidence that stressors contribute to the severity of chronic inflammatory diseases such as psoriasis. However, much less is known about possible individual differences between patients in their stress reactivity, particularly the role of cognitive and behavioural factors, such as the role of worrying or scratching behaviour, in reaction to itch. OBJECTIVES: To investigate the direct and moderating role of individual stress reactivity factors, particularly of cognitive and behavioural patterns of worrying and scratching, on the relationship between daily stressors and changes in disease severity [Psoriasis Area and Severity Index (PASI)] and itch in patients with psoriasis. METHODS: Patients were followed for 6 months through monthly clinical and self-reported measures of daily stressors, itch, disease severity and individual reactivity factors. Data from 62 patients were suitable for analysis. RESULTS: Cognitive and behavioural patterns of worrying and scratching were both independently related to an increase 4 weeks later in disease severity (PASI) and itch, at moments when patients experienced a high level of daily stressors. At these moments, stressors also interacted with vulnerability factors, showing that patients with more daily stress and high worrying and scratching had particularly worsened disease severity and itch. CONCLUSIONS: Patients with high levels of worrying and scratching are most vulnerable to the impact of stressors on their psoriasis, particularly at highly stressful periods.


Assuntos
Prurido/psicologia , Psoríase/psicologia , Estresse Psicológico/psicologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Prurido/tratamento farmacológico , Psoríase/tratamento farmacológico , Fatores de Risco , Índice de Gravidade de Doença
9.
Int J Behav Med ; 15(3): 211-20, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18696315

RESUMO

BACKGROUND: The heterogeneity of patients regarding pain-related cognitive-behavioral mechanisms, such as pain-avoidance and pain-persistence patterns, has been proposed to underlie varying treatment outcomes in patients with fibromyalgia (FM). PURPOSE: To investigate the validity of a screening instrument to discriminate between pain-persistence and pain-avoidance patterns in FM. METHOD: In a three-part study, a self-reported screening instrument that assesses pain-avoidance behavior was used to distinguish patients with pain-persistence and pain-avoidance patterns. The resultant groups were compared with regard to several pain-related cognitive-behavioral factors, performance on a physical fitness test, and with regard to the judgments of trained therapists based on a semi-structured interview. RESULTS: The validity of the screening instrument to distinguish between pain-avoidance and pain-persistence patterns was supported by other validated self-report questionnaires for pain-related cognitive-behavioral factors, physical exercise tests, as well as by a high correspondence with blinded therapist judgment after intake assessments. CONCLUSION: These findings suggest that a short self-report screening instrument can be used to distinguish between pain-avoidance and pain-persistence patterns within the heterogeneous population of FM patients, which offers promising possibilities to improve treatment efficacy by tailoring treatment to specific patient patterns.


Assuntos
Fibromialgia/psicologia , Medição da Dor/instrumentação , Medição da Dor/métodos , Dor/diagnóstico , Dor/psicologia , Adulto , Aprendizagem da Esquiva , Comportamento , Teste de Esforço , Feminino , Humanos , Entrevistas como Assunto , Masculino , Pessoa de Meia-Idade , Países Baixos , Medição da Dor/normas , Ensaios Clínicos Controlados Aleatórios como Assunto
10.
Patient Educ Couns ; 71(2): 308-14, 2008 May.
Artigo em Inglês | MEDLINE | ID: mdl-18187283

RESUMO

OBJECTIVE: To illustrate a multidisciplinary group treatment for patients with fibromyalgia (FM) tailored to the patient's cognitive-behavioral pattern. METHOD: In a case-study design the tailored treatment approaches of two FM patients were described. One patient characterized by avoidance behavior (pain-avoidance pattern) participated in a group treatment aimed at changing pain-avoidance mechanisms and one patient characterized by continuing with activities in spite of pain (pain-persistence pattern) participated in a group treatment aimed at changing pain-persistence mechanisms. Assessments were made at baseline, post-treatment and at 6-months follow-up. RESULTS: Comparison of the pretest, post-test and follow-up scores on pain, functional disability, fatigue and psychological distress showed clinically significant improvements for both patients. CONCLUSION: The heterogeneity of patients regarding pain-related cognitive-behavioral mechanisms has been proposed to underlie varying treatment outcomes in FM patients. These results demonstrate that a group treatment tailored to pain-avoidance and pain-persistence patterns is feasible and can result in clinically significant changes for FM patients. PRACTICE IMPLICATIONS: FM offers a great challenge for clinicians due to the lack of effective treatment options. These case studies suggests that tailored CBT and exercise training directed at specific patient patterns can contribute to the improvement of the care of FM patients.


Assuntos
Terapia Cognitivo-Comportamental/organização & administração , Fibromialgia/prevenção & controle , Fibromialgia/psicologia , Planejamento de Assistência ao Paciente/organização & administração , Equipe de Assistência ao Paciente/organização & administração , Autocuidado , Atividades Cotidianas , Adaptação Psicológica , Adulto , Atitude Frente a Saúde , Aprendizagem da Esquiva , Fadiga/etiologia , Medo , Estudos de Viabilidade , Feminino , Fibromialgia/complicações , Fibromialgia/diagnóstico , Seguimentos , Comportamentos Relacionados com a Saúde , Humanos , Pessoa de Meia-Idade , Avaliação das Necessidades , Medição da Dor , Autocuidado/métodos , Autocuidado/psicologia , Estresse Psicológico/etiologia , Resultado do Tratamento
11.
Br J Dermatol ; 158(1): 101-8, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17999699

RESUMO

BACKGROUND: In dermatological research and clinical practice, there is a need for comprehensive self-report instruments that assess a broad spectrum of health implications of chronic skin diseases, including generic and skin-specific aspects of disease-related quality of life. The advantages of dermatology-specific, multidimensional instruments over generic instruments or single-dimensional quality-of-life measures are in the detailed and specific information they provide about health areas that are affected by the skin condition and that may change through therapeutic intervention. OBJECTIVES: The development of a multidimensional health status inventory for chronic skin diseases (Impact of Chronic Skin Disease on Daily Life, ISDL) is described. The dermatology-specific part of the inventory assesses dimensions of physical functioning, more specifically skin status, physical symptoms of itch, pain and fatigue and scratching responses as well as disease-related stressors like stigmatization. The generic part gauges dimensions of psychological functioning, disease-related impact, illness cognitions and social support by means of existing scales validated for other chronic diseases. METHODS: Reliability and validity of the questionnaire were studied in various samples of patients with psoriasis and atopic dermatitis. RESULTS: The ISDL showed high reliability and test-retest reliability in both patient groups. Convergent validity was indicated by moderate to strong correlations with other validated questionnaires. The scales proved sensitive to change both for dermatological ultraviolet B radiation therapy and cognitive behavioural treatment for itching. CONCLUSION: With its convincing results for reliability and validity the present evaluation supports the usefulness and applicability of the instrument for different chronic skin diseases.


Assuntos
Indicadores Básicos de Saúde , Qualidade de Vida , Dermatopatias/reabilitação , Atividades Cotidianas , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Doença Crônica , Fadiga/etiologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Dor/etiologia , Prurido/etiologia , Reprodutibilidade dos Testes , Dermatopatias/complicações , Dermatopatias/psicologia
12.
J Eur Acad Dermatol Venereol ; 21(9): 1187-92, 2007 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17894703

RESUMO

BACKGROUND: Physicians are frequently confronted with patients reporting severe itch and pain. Particularly in patients suffering from persistent itch and pain, central and peripheral sensitization processes are assumed to be involved in the long-term maintenance and aggravation of the symptoms. The present study explores generalized and symptom-specific sensitization processes in patients suffering from persistent itch and pain. Specifically, it examines whether patients with chronic itch and pain are more sensitive to somatosensory stimuli (generalized sensitization) and simultaneously perceive somatosensory stimuli as a symptom of their main physical complaint, e.g. pain in chronic pain patients (symptom-specific sensitization). METHODS: Thresholds for different mechanical and electrical sensory stimuli of Quantitative Sensory Testing were determined in 15 female patients suffering from chronic itch associated with atopic dermatitis, 15 female chronic pain patients diagnosed with fibromyalgia, and 19 female healthy controls. Intensities of itch and pain sensations were rated on a visual analogue scale. RESULTS: As expected, the patient groups had significantly lower tolerance thresholds for the somatosensory stimuli applied than the healthy controls, supporting generalized sensitization. Moreover, patients with chronic itch consistently reported more itch, while patients with chronic pain partly reported more pain in response to analogous somatosensory stimuli than the healthy controls and the other patient group, indicating symptom-specific sensitization. CONCLUSION: The present study provides preliminary support that both generalized and symptom-specific sensitization processes play a role in the regulation and processing of somatosensory stimulation of patients with chronic itch and pain.


Assuntos
Dermatite Atópica/fisiopatologia , Fibromialgia/fisiopatologia , Dor/fisiopatologia , Prurido/fisiopatologia , Adulto , Análise de Variância , Estudos de Casos e Controles , Doença Crônica , Dermatite Atópica/complicações , Estimulação Elétrica , Feminino , Fibromialgia/complicações , Humanos , Dor/etiologia , Medição da Dor , Limiar da Dor , Estimulação Física , Prurido/etiologia , Limiar Sensorial
13.
Br J Dermatol ; 156(6): 1346-9, 2007 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-17535233

RESUMO

BACKGROUND: Physical symptoms of skin diseases have been shown to negatively affect patients' wellbeing. Although insight into physical symptoms accompanying skin diseases is relevant for the management and treatment of skin diseases, the prevalence of physical symptoms among patients with skin diseases is a rather unexplored territory. OBJECTIVES: The goal of the present study was to examine the prevalence of physical symptoms of itch, pain and fatigue in patients with skin diseases. METHODS: On the basis of a systematic morbidity registration system in primary care, questionnaires were sent to 826 patients with skin diseases. Eventually, questionnaires from 492 patients were suitable for our analyses. RESULTS: Results indicated that patients with skin diseases particularly experience symptoms of itch and fatigue. Approximately 50% of all patients report experiencing these symptoms and about 25% experience these symptoms as relatively severe. Pain was relatively less frequently reported by 23% of all patients, and was on average somewhat less intense. The physical symptoms showed relatively strong correlations with disease-related quality of life and self-reported disease severity. In contrast, only moderate correlations were found with comorbidity and demographic variables, which suggests that the physical symptoms of itch, pain and fatigue are consequences of the skin diseases. CONCLUSIONS: Itch and fatigue and, to a somewhat lesser extent, pain have a high prevalence among patients with skin diseases. Clinicians should be encouraged to carefully assess itch, pain and fatigue in patients with skin diseases, and where appropriate focus treatment to these symptoms.


Assuntos
Fadiga/epidemiologia , Dor/epidemiologia , Prurido/epidemiologia , Dermatopatias/epidemiologia , Adulto , Medicina de Família e Comunidade/estatística & dados numéricos , Fadiga/psicologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Países Baixos/epidemiologia , Dor/psicologia , Prurido/psicologia , Qualidade de Vida/psicologia , Dermatopatias/psicologia , Inquéritos e Questionários
14.
J Eur Acad Dermatol Venereol ; 21(5): 662-8, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17447981

RESUMO

BACKGROUND: Skin diseases are a substantial part of the problems dealt with by general practitioners. Although the psychosocial consequences of skin diseases in secondary care has been extensively studied, little is known about the psychosocial well-being of patients with skin diseases in primary care. OBJECTIVE: To investigate the psychosocial well-being of patients with skin diseases in primary care. PATIENTS/METHODS: Questionnaires about the psychosocial consequences of skin diseases were sent to patients with a skin disease who were registered within a research network (continuous morbidity registration) of general practices that continuously have recorded morbidity data since 1971. Questionnaires completed by 532 patients were eventually suitable for analyses. RESULTS: Compared with the general population, patients with skin diseases reported significantly lower scores for psychosocial well-being. Furthermore, a lower psychosocial wellbeing was significantly related with higher levels of disease-severity, lower disease-related quality of life, longer disease duration, more comorbidity and more physical symptoms of itch, pain and fatigue. After demographic variables and comorbidity were controlled for, sequential regression analyses showed that disease duration, disease severity and physical symptoms (itch, pain and fatigue) were significant predictors of psychosocial well-being. CONCLUSION: The psychosocial well-being of patients with skin diseases in primary care is lower than that of the general population. Special attention has to be directed to those patients with lowered psychosocial well-being who might be at risk of developing severe psychosocial impairments such as clinical depression.


Assuntos
Medicina de Família e Comunidade , Dermatopatias/psicologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Países Baixos/epidemiologia , Qualidade de Vida , Sistema de Registros , Análise de Regressão , Dermatopatias/epidemiologia , Inquéritos e Questionários
15.
Ann Rheum Dis ; 66(5): 571-81, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-16916856

RESUMO

This review provides an overview of the effects of non-pharmacological treatments for patients with fibromyalgia (FM), including cognitive-behavioural therapy, exercise training programmes, or a combination of the two. After summarising and discussing preliminary evidence of the rationale of non-pharmacological treatment in patients with FM, we reviewed randomised, controlled trials for possible predictors of the success of treatment such as patient and treatment characteristics. In spite of support for their suitability in FM, the effects of non-pharmacological interventions are limited and positive outcomes largely disappear in the long term. However, within the various populations with FM, treatment outcomes showed considerable individual variations. In particular, specific subgroups of patients characterised by relatively high levels of psychological distress seem to benefit most from non-pharmacological interventions. Preliminary evidence of retrospective treatment analyses suggests that the efficacy may be enhanced by offering tailored treatment approaches at an early stage to patients who are at risk of developing chronic physical and psychological impairments.


Assuntos
Terapia Cognitivo-Comportamental/métodos , Terapia por Exercício/métodos , Fibromialgia/terapia , Terapia Combinada/métodos , Feminino , Fibromialgia/psicologia , Humanos , Masculino , Ensaios Clínicos Controlados Aleatórios como Assunto , Fatores de Tempo , Resultado do Tratamento
16.
Hum Reprod Update ; 13(1): 27-36, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-16940360

RESUMO

This review provides an overview of how women adjust emotionally to the various phases of IVF treatment in terms of anxiety, depression or general distress before, during and after different treatment cycles. A systematic scrutiny of the literature yielded 706 articles that paid attention to emotional aspects of IVF treatment of which 27 investigated the women's emotional adjustment with standardized measures in relation to norm or control groups. Most studies involved concurrent comparisons between women in different treatment phases and different types of control groups. The findings indicated that women starting IVF were only slightly different emotionally from the norm groups. Unsuccessful treatment raised the women's levels of negative emotions, which continued after consecutive unsuccessful cycles. In general, most women proved to adjust well to unsuccessful IVF, although a considerable group showed subclinical emotional problems. When IVF resulted in pregnancy, the negative emotions disappeared, indicating that treatment-induced stress is considerably related to threats of failure. The concurrent research reviewed, should now be underpinned by longitudinal studies to provide more information about women's long-term emotional adjustment to unsuccessful IVF and about indicators of risk factors for problematic emotional adjustment after unsuccessful treatment, to foster focused psychological support for women at risk.


Assuntos
Fertilização in vitro/psicologia , Infertilidade Feminina/terapia , Estresse Psicológico/etiologia , Ansiedade/etiologia , Depressão/etiologia , Feminino , Humanos , Infertilidade Feminina/psicologia
17.
Br J Dermatol ; 152(6): 1275-81, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15948993

RESUMO

BACKGROUND: Chronic skin diseases, such as atopic dermatitis and psoriasis, are known to affect quality of life by heightening psychological distress. Knowledge about factors contributing to psychological distress is essential for supporting physicians in diagnostic and multidisciplinary treatment options for patients psychologically at risk. OBJECTIVES: To examine whether generic physical, psychological and social factors relevant to patients with chronic diseases might contribute to psychological distress in adults with psoriasis and atopic dermatitis. METHODS: Self-report data on clinical skin status, physical symptoms of itching and fatigue, impact of the disease on daily life, illness cognitions and social support were collected from 128 patients with psoriasis and 120 patients with atopic dermatitis (aged over 16 years). RESULTS: For patients with either skin disease, clinical status and physical symptoms of itching scarcely affected psychological distress. Instead, higher levels of fatigue, perceived helplessness and less social support best predicted psychological distress in patients with both skin diseases in multiple regression analyses. CONCLUSIONS: Results demonstrate that generic physical, psychological and social aspects play a role in chronic skin diseases and suggest that multidisciplinary care for patients with psoriasis and atopic dermatitis can be greatly improved by integrating common screening and treatment components for chronic diseases.


Assuntos
Dermatopatias/psicologia , Estresse Psicológico/etiologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Análise de Variância , Dermatite Atópica/psicologia , Fadiga/psicologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Psoríase/psicologia , Análise de Regressão , Apoio Social , Inquéritos e Questionários , Urticária/psicologia
18.
Hum Reprod ; 20(8): 2253-60, 2005 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-15817584

RESUMO

BACKGROUND: A longitudinal study into the course of the emotional response to IVF from pre-treatment to 6 months post-treatment and factors that contributed to that course. METHODS: A total of 148 IVF patients and 71 partners completed self-report questionnaires on anxiety, depression, personality characteristics, meaning of fertility problems, coping, marital relationship and social support at pre-treatment. Assessments of anxiety and depression were repeated immediately following the final treatment cycle and again 6 months later (follow-up). RESULTS: Women showed an increase of both anxiety and depression after unsuccessful treatment and a decrease after successful treatment. Men showed no change in anxiety and depression either after successful or after unsuccessful treatment. In the 6 months after unsuccessful treatment, women showed no recovery. At follow-up, >20% of the women showed subclinical forms of anxiety and/or depression. Personality characteristics, meaning of the fertility problems, and social support determined the course of the emotional response. CONCLUSIONS: Most women adjusted well to unsuccessful treatment, but at follow-up, a considerable proportion still showed substantial emotional problems. Personality characteristics, pre-treatment meaning of the fertility problems and social support have demonstrated the adjustment to unsuccessful IVF in women. This allows early identification of women at risk as well as tailored interventions.


Assuntos
Adaptação Psicológica , Fertilização in vitro/psicologia , Infertilidade/psicologia , Adulto , Ansiedade/epidemiologia , Ansiedade/psicologia , Depressão/epidemiologia , Depressão/psicologia , Emoções , Feminino , Fertilização in vitro/estatística & dados numéricos , Seguimentos , Humanos , Infertilidade/epidemiologia , Infertilidade/terapia , Estudos Longitudinais , Masculino , Casamento , Paridade , Estudos Prospectivos , Fatores de Risco , Apoio Social
19.
Ned Tijdschr Geneeskd ; 146(49): 2363-6, 2002 Dec 07.
Artigo em Holandês | MEDLINE | ID: mdl-12510401

RESUMO

OBJECTIVE: Determination of the emotional burden of the first IVF or ICSI treatment cycle, the effect of the treatment on the marital relationship, and the course of the treatment following a failed and a successful first attempt. DESIGN: Descriptive longitudinal study with repeated measures before and after the first treatment cycle. METHOD: 240 women and 219 men filled in questionnaires both before and after the first treatment cycle in the area of anxiety, depression, and the marital relationship (as measured with the 'Spielberger state trait anxiety inventory' (STAI), the 'Beck depression inventory for primary care' (BDI-PC) and the 'Maudsley marital questionnaire' (MMQ), respectively), as well as their plans for further treatment. RESULTS: After a first failed treatment cycle, both women and men showed an increase in depression, while women also showed increased anxiety. No differences were found between pre- and post-treatment levels of anxiety and depression after a successful treatment. After the first failed cycle, almost 13% of the women showed clinically relevant forms of depression. There was an increase in dissatisfaction with the sexual relationship in both men and women regardless of the success of the treatment. Before the start of the first treatment cycle, 2% of the couples had no intention to undergo further treatment if the first cycle failed; none of these couples started a new cycle. Ultimately, 18% of the couples refrained from further treatment following a failed first treatment cycle. CONCLUSION: After a failed first treatment cycle the couples showed an increase in depression and one in eight women had a clinically relevant form of depression. More than one out of every 6 couples decided to refrain from further treatment after a failed first cycle.


Assuntos
Ansiedade/etiologia , Transtorno Depressivo/etiologia , Inseminação Artificial/psicologia , Ansiedade/psicologia , Transtorno Depressivo/psicologia , Feminino , Humanos , Estudos Longitudinais , Masculino , Casamento , Escalas de Graduação Psiquiátrica , Injeções de Esperma Intracitoplásmicas/psicologia , Estresse Psicológico/etiologia , Estresse Psicológico/psicologia , Inquéritos e Questionários , Falha de Tratamento
20.
Fertil Steril ; 76(3): 525-31, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11532476

RESUMO

OBJECTIVE: To determine differences in emotional status (anxiety and depression) and marital satisfaction in pregnant and nonpregnant women before and after their first cycle of IVF and intracytoplasmic sperm injection (ICSI). DESIGN: Repeated measurement. SETTING: Fertility department at a university and a regional hospital. PATIENT(S): Women entering their first treatment cycle of IVF or ICSI. INTERVENTION(S): Questionnaires on psychological factors were administered 3 to 12 days before the start of their first treatment cycle and repeated 3 weeks after the pregnancy test. MAIN OUTCOME MEASURE(S): State anxiety, depression, mood, and marital satisfaction. RESULT(S): At pretreatment, the women who became pregnant showed lower levels of depression than those who did not. Higher levels of depression in the pregnant women after the first cycle were due to higher scores on vital aspects of depression, related to signs of early pregnancy. Higher levels of depression in the nonpregnant women were due to a higher score on cognitive aspects of depression. CONCLUSION(S): Differences in emotional status between pregnant and nonpregnant women were present before treatment and became more apparent after the first IVF and ICSI cycle. There were no differences in emotional status between the women who underwent IVF and those who underwent ICSI.


Assuntos
Afeto , Fertilização in vitro/psicologia , Casamento/psicologia , Gravidez/psicologia , Injeções de Esperma Intracitoplásmicas/psicologia , Estresse Psicológico , Adulto , Ansiedade , Depressão/etiologia , Emoções , Feminino , Humanos , Masculino , Análise Multivariada , Reprodutibilidade dos Testes , Comportamento Sexual , Inquéritos e Questionários , Falha de Tratamento
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