ABSTRACT
OBJECTIVES: To explore factors related to sleep disturbance in patients with rheumatoid arthritis (RA). METHOD: Cross-sectional data from 986 patients in the Oslo RA Register (ORAR) collected in 2009 were included. Sleep problems were assessed by four measures: the Medical Outcomes Study (MOS) sleep disturbance scale, and the sleep components of the Rheumatoid Arthritis Impact of Disease (RAID) score, the Multi-Dimensional Health Assessment Questionnaire (MDHAQ), and the 15-dimensional quality of life questionnaire (15D). Patient-reported outcomes (PROs) were recorded using standard questionnaires for physical and mental function [the HAQ and the MOS 36-item Short-Form Health Survey (SF-36), disease activity (the RA Disease Activity Index, RADAI), utility (SF-6D), and visual analogue scales (VAS) for pain, fatigue, and disease activity]. Demographics including comorbidity were collected. Information on use of medication for RA and sleep disturbance was obtained using checklists. Multivariate analyses were used to identify factors independently associated with sleep problems by four different measures. RESULTS: The mean (standard deviation, SD) age of the patients was 59.4 (12.5) years, 76.9% were females, and the mean (SD) disease duration was 13.7 (10.7) years. The correlation between the various sleep measures was high (r2 = 0.71-0.78). Sleep disturbance was moderately correlated to pain (r2 = 0.41-0.61), fatigue (r2 = 0.44-0.58), physical function (r2 = 0.33-0.48), RADAI (r2 = 0.42-0.55), and utility (r2 = 0.49-0.61). RAID sleep demonstrated the highest correlation with other PROs. RADAI, fatigue, the mental component score of SF-36, physical function, body mass index (BMI), and use of Z-drugs/benzodiazepines were independently associated with two or more measures of sleep problems (all p < 0.001). CONCLUSIONS: Sleep disturbance measured by four different measures was independently related to other PROs including fatigue, pain, and disease activity in RA patients.
Subject(s)
Arthritis, Rheumatoid/complications , Fatigue/complications , Patient Reported Outcome Measures , Sleep Wake Disorders/etiology , Adult , Aged , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Pain/physiopathologyABSTRACT
OBJECTIVE: To examine changes in patient reported outcome measures (PROs) over 15â years in a representative population of patients with rheumatoid arthritis (RA), with a particular focus on gender differences. PATIENTS AND METHODS: Patients in the Oslo RA register filled in questionnaires including the Modified Health Assessment Questionnaire (MHAQ), the Short-Form 36 (SF-36) with physical (PCS) and mental component summaries and derived utility (SF-6D), visual analogue scales (VAS) for pain, patient global assessment of disease (PtGA) and fatigue, and checklists of medication commonly used in the treatment of RA. Data were collected at five time points during a 15-year period from 1994. Mixed model analyses were used to analyse longitudinal changes in PROs from 1994 to 1996, 2001, 2004 and 2009. RESULTS: Data were available from 829-1025 RA patients at each time point. PROs were statistically significantly improved from 1994 to 2009 (MHAQ, SF-36 PCS, SF-6D, pain VAS, PtGA VAS and fatigue VAS; all p<0.001), and also with clinically important improvement. Men reported significantly better health status than women in 1994, but women improved significantly more than men over 15â years with a reduction of the gender gap in 2009. Antirheumatic medication was increasingly used over 15â years with no gender differences. CONCLUSIONS: RA patients reported statistically significantly improved health status for most PROs from 1994 to 2009. Women improved most, and although they still reported higher disease impact than men, the gender differences were small at the final data collection in 2009.
Subject(s)
Activities of Daily Living , Arthritis, Rheumatoid/physiopathology , Health Status , Patient Outcome Assessment , Registries , Sex Factors , Antirheumatic Agents/therapeutic use , Arthritis, Rheumatoid/drug therapy , Female , Humans , Male , Middle Aged , Norway , Quality of Life , Severity of Illness Index , Surveys and QuestionnairesSubject(s)
Abdominal Pain/etiology , Anti-Inflammatory Agents, Non-Steroidal/adverse effects , Arthritis, Rheumatoid/drug therapy , Cyclooxygenase 2 Inhibitors/adverse effects , Mental Health , Abdominal Pain/epidemiology , Abdominal Pain/physiopathology , Aged , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Arthritis, Rheumatoid/epidemiology , Arthritis, Rheumatoid/physiopathology , Cyclooxygenase 2 Inhibitors/therapeutic use , Female , Follow-Up Studies , Humans , Male , Middle Aged , Norway , Pain Measurement , Registries , Risk Assessment , Self-Assessment , Sickness Impact Profile , Surveys and QuestionnairesABSTRACT
Managed care is becoming a significant force shaping the development of contemporary mental health treatment. In order to understand how the HMO affects practice style, 294 psychotherapists (psychologists, psychiatrists, social workers, and others) responded to objective and open-ended questions about psychotherapy models, psychotherapy orientation, practice habits, quality of work, work conditions, stresses, burnout and its prevention, graduate training, evolution of practice style and the development of self as a person. A tentative "composite sketch" of the typical HMO therapist is developed. Practical applications of the findings are discussed, and advice and recommendations are offered to the beginning HMO therapist.
Subject(s)
Health Maintenance Organizations/organization & administration , Mental Health Services/organization & administration , Psychotherapy/organization & administration , Adult , Attitude of Health Personnel , Evaluation Studies as Topic , Female , Health Maintenance Organizations/statistics & numerical data , Humans , Job Satisfaction , Male , Mental Health Services/statistics & numerical data , Psychotherapy/statistics & numerical data , Surveys and Questionnaires , United StatesABSTRACT
This article describes the "Wisdom Group," a therapy devised for the psychotherapeutic treatment of elderly persons. Preliminary work was done with five men of advanced age who were psychiatric in-patients with diagnoses of organicity and depression. The approach was effective in eliciting interaction during the meetings with each other and the group leader. The potential use of this intervention with a greater variety of elderly persons is discussed.
Subject(s)
Adaptation, Psychological , Dementia/therapy , Depressive Disorder/therapy , Hospitalization , Psychotherapy, Group/methods , Activities of Daily Living/psychology , Aged , Dementia/psychology , Depressive Disorder/psychology , Female , Humans , MaleABSTRACT
The psychological symptoms of patients diagnosed as having epidemic neuromyasthenia were investigated using the Minnesota Multiphasic Personality Inventory, the Social Readjustment Rating Scale, the Mehrabian Achieving Tendency Scale for Females, a personal data questionnaire, and a subjective anxiety rating. Twenty-five women with epidemic neuromyasthenia were compared with 25 women who were not ill. Multivariate analysis using the Hotelling T-test on the group data indicated that the patient and non-patient groups differed significantly (P less than 0.001) in respect of psychological characteristics. Stress as a possible predisposing factor in the illness was supported (P less than 0.001). The data do not support the concept of epidemic neuromyasthenia as being 'mass hysteria' as mentioned by McEvedy and Beard, but rather seem to support the suggestion that diagnosis can be made by use of a combination of logical, objective medical and physiological measures. The use of biofeedback as a possible treatment is also proposed.
Subject(s)
Fatigue Syndrome, Chronic/psychology , Personality , Achievement , Adult , Anxiety , Female , Humans , MMPI , Middle Aged , Psychological Tests , Stress, PsychologicalSubject(s)
Hospitals, Psychiatric , Patient Discharge , Professional-Patient Relations , Adolescent , Adult , Female , Humans , MaleSubject(s)
Beauty , Esthetics , Mental Disorders/psychology , Social Adjustment , Adult , Female , Humans , Male , Mental Disorders/rehabilitation , Middle Aged , Prospective Studies , Social DesirabilitySubject(s)
Attitude , Child Abuse , Foster Home Care/psychology , Parent-Child Relations , Adolescent , Adult , Child , Child Abuse/prevention & control , Child, Preschool , Female , Humans , Infant , MaleSubject(s)
Parent-Child Relations , Puberty, Precocious/psychology , Child , Child, Preschool , Female , HumansABSTRACT
The intake records of a selected sample of children adopted in early infancy are reviewed and their presenting symptoms categorized. A majority of the children's symptoms fell into the first 5 of 15 categories: Oppositional Behavior, Aggressive Behavior, Anti-social Acting Out, Academic Problems and Problems with Peers. While these symptoms are not uncommon in non-adoptive clinic cases, the authors note an emphasis on the adoptive parents' disappointment and accusatory attitude to toward these children as well as high incidence of symptoms indicative of interpersonal difficulties and problems in developing solid parental attachments and self-control.