RESUMO
GOALS: To determine whether the perceived impact of ulcerative colitis (UC) on activities of living (illness intrusiveness) is greater for people who are not living in a married or common-law relationship. BACKGROUND: In general, social and occupational achievement is not greatly impaired by UC, yet patients, especially young adults, often have interpersonal concerns. METHODS: One hundred fifty-five outpatients with UC were assessed for disease activity, and completed self-reports of marital status, income, social support and illness intrusiveness. RESULTS: Fifty-one patients (32.9%) were single, separated or divorced, and 104 patients (67.1%) were married or in common-law relationships. Compared with those who were married or in common-law relationships, single or separated patients were younger, had a lower household income, had lived with UC for fewer years and were less satisfied with social support. Among 135 patients in remission, marital status was significantly associated with illness intrusiveness, controlling for age, income and perceived social support (F=5.73; P=0.02). Low social support (F=4.94; P=0.03) and younger age (F=7.24; P=0.008) were independently associated with illness intrusiveness. Single patients in remission reported illness intrusiveness of similar severity to that reported by patients with active disease. CONCLUSIONS: The perceived impact of UC on the lives of patients is greater in those who are not married or living in common-law relationships. Youth, single status and lower social support commonly coexist, and exert additive effects on the functional impact of UC. Resources to improve social support should be directed toward this group of patients.
Assuntos
Colite Ulcerativa/psicologia , Qualidade de Vida , Pessoa Solteira , Atividades Cotidianas , Adolescente , Adulto , Fatores Etários , Humanos , Renda , Estado Civil , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Apoio Social , Inquéritos e QuestionáriosRESUMO
Although psychiatric aftercare has received increased attention, little is known about patients' needs for community resources or about predischarge referral patterns. The authors interviewed hospital staff about needs and referrals for each of 747 patients about to be discharged. Nearly all patients had needs in the medical/therapeutic area and most received referrals. In three other nonmedical aftercare areas needs were identified for a much lower percentage of patients, and identified need was two to three times greater than referrals made. The authors discuss the implications of these findings for the provision of aftercare services.
Assuntos
Assistência ao Convalescente , Transtornos Mentais/reabilitação , Encaminhamento e Consulta , Adulto , Serviços Comunitários de Saúde Mental , Demografia , Feminino , Humanos , Masculino , Pessoa de Meia-IdadeRESUMO
The authors interviewed 162 widows 1, 6, 12, and 24 months after bereavement to determine which sociodemographic, prebereavement, and response variables and circumstances of the husband's death were related to distress level, as measured by the General Health Questionnaire (GHQ). The most important variable associated with high distress at 1 month was the woman's perception that she was seeing old friends less than before her husband's death. At 2 years it was possible to predict distress levels with 86% accuracy by means of a multiple regression analysis using 10 variables, including 1-month GHQ score, short final illness of the husband, and satisfaction with available help.
Assuntos
Adaptação Psicológica , Pesar , Casamento , Adulto , Idoso , Atitude , Feminino , Humanos , Entrevista Psicológica , Acontecimentos que Mudam a Vida , Masculino , Pessoa de Meia-Idade , Satisfação Pessoal , Inventário de Personalidade , Fatores Sexuais , Ajustamento Social , Estresse Psicológico/psicologia , Inquéritos e Questionários , Fatores de TempoRESUMO
In a four-week study, a comparison was made of oxazepam, flurazepam and chloral hydrate as hypnotic sedatives in 17 geriatric patients. Each drug was given alone for six nights, with a two-night placebo interval following each phase. Each patient completed an additional placebo phase (up to six nights) before each drug phase. The number of awakenings per night and the sleep latency (time required to fall asleep) were determined from the patients' reports and from the reports of a nurse-observer. Only for oxazepam was the number of patient-reported awakenings per night significantly less than for placebo, although with both oxazepam and flurazepam the awakenings were fewer than with chloral hydrate. According to the patient-reports, sleep latency was significantly lower with flurazepam than with placebo; for oxazepam and chloral hydrate the latencies were not significantly different from those for flurazepam or placebo. Only for oxazepam were the patients' ratings of sleep quality significantly greater than for placebo. The objective assessment of sleep by the nurse-observer usually confirmed the patients' assessments. Morning drowsiness was the most common side effect, reported equally for placebo and for the active drugs. Drowsiness during the day was reported less frequently for oxazepam than for flurazepam, chloral hydrate or placebo. It is concluded that oxazepam is safe and efficacious for the short-term management of insomnia in the elderly.
Assuntos
Ansiolíticos/farmacologia , Hidrato de Cloral/farmacologia , Flurazepam/farmacologia , Hipnóticos e Sedativos , Oxazepam/farmacologia , Idoso , Ensaios Clínicos como Assunto , Método Duplo-Cego , Feminino , Humanos , Hipnóticos e Sedativos/efeitos adversos , Masculino , Placebos , Fases do SonoRESUMO
Findings in family burden research suggest that, in families with a mentally ill relative, patterns of family interaction develop in response to the onset of major mental illness and result from the burden experienced by family members in coping with illness. The present study focused on instrument development and validation of the Perceived Family Burden Scale (PFBS), a measure of those patient behaviors associated with schizophrenia and the impact of these behaviors on relatives. The PFBS was found to be a valid and reliable instrument which demonstrated greater predictive power for early symptomatic relapse in schizophrenia than another measure of family interaction, expressed emotion.
Assuntos
Cuidadores/psicologia , Efeitos Psicossociais da Doença , Família/psicologia , Inventário de Personalidade/estatística & dados numéricos , Esquizofrenia/terapia , Psicologia do Esquizofrênico , Adolescente , Adulto , Emoções Manifestas , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Psicometria , Reprodutibilidade dos Testes , Esquizofrenia/diagnósticoRESUMO
OBJECTIVE: This study examined the 7-year developmental and academic outcome of speech/language-impaired and control children selected from a community sample. METHOD: Speech/language and psychiatric measures were administered to the children at ages 5 and 12.5 years. Using children's age 5 speech/language test results, a cluster analysis was performed to ascertain whether specific linguistic subgroups would emerge. The long-term consistency of these subgroups was explored. The association between time 1 speech/language clusters and linguistic, cognitive and academic measures at time 2 were examined. RESULTS: Four groups were identified in the cluster analysis: high overall, poor articulation, poor comprehension, and low overall. Children with pervasive language problems continued to perform poorly on linguistic, cognitive, and academic measures, while those with comprehension problems fared slightly better but still had more difficulties than those with normal language. The poor articulation cluster had few articulation errors at follow-up. CONCLUSIONS: Empirically supported speech/language classifications identified as early as age 5 continued to be relevant into late childhood. Pervasive speech/language impairment in early childhood was associated with increased risk of poor linguistic and academic outcome at follow-up, while isolated articulatory problems improved over time. These findings reveal the urgent need for early intervention among children with pervasive speech/language impairment.
Assuntos
Escolaridade , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Distúrbios da Fala/diagnóstico , Criança , Pré-Escolar , Feminino , Seguimentos , Humanos , Transtornos do Desenvolvimento da Linguagem/psicologia , Transtornos do Desenvolvimento da Linguagem/terapia , Testes de Linguagem , Deficiências da Aprendizagem/diagnóstico , Deficiências da Aprendizagem/psicologia , Deficiências da Aprendizagem/terapia , Masculino , Distúrbios da Fala/psicologia , Distúrbios da Fala/terapiaRESUMO
OBJECTIVE: This study examined the 7-year behavioral, emotional, and social outcome of speech/language-impaired and control children selected from a community sample. METHOD: Speech/language and psychosocial measures were administered to the children at ages 5 and 12.5 years. Using children's age 5 speech/language test results, a cluster analysis was performed to ascertain whether specific linguistic subgroups would emerge. The association between speech/language cluster at age 5 and psychosocial functioning at age 12.5 was examined. RESULTS: Children with receptive and pervasive speech/language problems at age 5 demonstrated greater behavioral disturbance than children without such impairment. Controlling for initial behavioral status, early childhood language profile was still associated with behavioral and social competence ratings, 7 years later. Children without receptive language problems showed superior social adjustment. CONCLUSIONS: Empirically supported speech/language classifications identified as early as age 5 were associated with behavioral disturbance in late childhood. Receptive and pervasive speech/language impairment in early childhood was associated with the greatest risk at follow-up. Early auditory comprehension problems may be a specific risk factor for later aggressive and hyperactive symptoms. These findings identify the need for effective intervention with speech/language-impaired children.
Assuntos
Sintomas Afetivos/diagnóstico , Transtornos do Comportamento Infantil/diagnóstico , Transtornos do Desenvolvimento da Linguagem/diagnóstico , Ajustamento Social , Distúrbios da Fala/diagnóstico , Sintomas Afetivos/psicologia , Sintomas Afetivos/terapia , Criança , Transtornos do Comportamento Infantil/psicologia , Transtornos do Comportamento Infantil/terapia , Pré-Escolar , Feminino , Seguimentos , Humanos , Controle Interno-Externo , Transtornos do Desenvolvimento da Linguagem/psicologia , Transtornos do Desenvolvimento da Linguagem/terapia , Testes de Linguagem , Masculino , Determinação da Personalidade , Distúrbios da Fala/psicologia , Distúrbios da Fala/terapiaRESUMO
OBJECTIVE: This study examined the 7-year outcome of speech/language (S/L) impaired and control children selected from a community sample at age 5 years. METHOD: Two hundred fifteen children completed a variety of speech and language tests at age 12 years. Children with S/L impairment were further classified as "speech only," "language only," or "speech and language impaired." RESULTS: More than 72% of children who had S/L impairment at age 5 remained impaired at age 12. Children with both speech and language problems were most likely to remain S/L impaired; 81% had some kind of S/L impairment at follow-up. Similarly, children with both expressive and receptive language impairment were more likely to show expressive or receptive impairment at follow-up than children with expressive impairment alone. One third of time 1 controls had S/L problems at follow-up, and of these 82% had speech impairment only. CONCLUSIONS: S/L impairment identified at age 5 has long-lasting effects. More pervasive problems were associated with poorer outcomes. Screening at age 5 may be useful, as most serious S/L problems that emerged by middle childhood could be identified at age 5. The effects of S/L treatment require further study.
Assuntos
Transtornos da Linguagem/epidemiologia , Distúrbios da Fala/epidemiologia , Adolescente , Canadá/epidemiologia , Criança , Feminino , Seguimentos , Humanos , Transtornos da Linguagem/terapia , Masculino , Distúrbios da Fala/terapia , Resultado do TratamentoRESUMO
Six hundred and eight women were treated with 200 microgram of ethinylestradiol and 2 mg of dl-norgestrel, administered in two divided doses, as a postcoital contraceptive. Criteria for entry into the study included definite unprotected coital exposure within the previous 72 hours and the absence of any contraindications to the use of estrogen/progestin-containing compounds. Women with coital exposures outside of the 72-hours-to-treatment time frame were excluded. Four hundred and sixty-four of the patients were cycling regularly and, of these, 152 were exposed at midcycle. Only one patient became pregnant as a result of probable method failure as compared with the minimal estimated number of 12 to 30 pregnancies.
Assuntos
Anticoncepcionais Pós-Coito/farmacologia , Etinilestradiol/farmacologia , Norgestrel/farmacologia , Adolescente , Adulto , Comportamento Contraceptivo , Esquema de Medicação , Etinilestradiol/administração & dosagem , Etinilestradiol/efeitos adversos , Feminino , Fertilização/efeitos dos fármacos , Humanos , Menstruação , Náusea/induzido quimicamente , Norgestrel/administração & dosagem , Norgestrel/efeitos adversos , Gravidez , Fatores de TempoRESUMO
Depression, the most common form of psychological distress among university students, is often serious enough to warrant professional help but only a minority of depressed students seek formal help. This paper reports on the characteristics which differentiate two groups of depressed students--the help-seekers from the non-help-seekers. A university psychiatric clinic population (N = 183) was compared with a non-clinic sample (N = 55). Data about depressive symptoms, social supports, the use of medical, psychiatric and other helping services, sources of referral and the usual demographic and sociocultural information were obtained. The Beck Depression Inventory was used as the measure of depression. Severity of depression was the single most important predictor of use of the psychiatric service. In addition, being female was also an important predictor. After controlling for severity and sex, the demographic factors which distinguished help-seekers from non-help-seekers were as follows: The help-seekers were more likely to be graduate students, older, living away from family and/or to use a non-psychiatric physician. Contrary to expectation, having a confidant was not related to help-seeking, suggesting that the presence of a confidant may be preventive but does not necessarily decrease the need for professional help once a student has become depressed. A depressed student's decision to seek help may be influenced by four factors: the severity of the problem; the individual's propensity to seek help; the availability of alternate resources; and the accessibility of psychiatric services. The findings are discussed in the light of these factors.
Assuntos
Depressão/psicologia , Aceitação pelo Paciente de Cuidados de Saúde , Estudantes/psicologia , Adolescente , Adulto , Tomada de Decisões , Feminino , Humanos , Masculino , Serviços de Saúde Mental/estatística & dados numéricos , Ambulatório Hospitalar/estatística & dados numéricos , Unidade Hospitalar de Psiquiatria/estatística & dados numéricos , Serviços de Saúde para Estudantes/estatística & dados numéricosRESUMO
Difficulties experienced by nurses in treating a total of 249 patients in four short-stay psychiatric units were examined using a rating scale that assessed such factors as overall extent of treatment difficulty, patients' problem behaviors, adequacy of treatment resources, and staff members' affective responses. Data from each site were analyzed separately using stepwise hierarchical regression. The findings indicated that patient problem behaviors and treatment resources were comparable between settings. Except for patient violence, none of the problems were consistently related to overall treatment difficulty across settings. The results suggest that treatment difficulty is related to the unique combination of patient characteristics, resource deficits, and treatment philosophies in particular treatment settings and that efforts to reduce treatment difficulty should address setting-specific issues.
Assuntos
Atitude do Pessoal de Saúde , Transtornos Mentais/enfermagem , Relações Enfermeiro-Paciente , Admissão do Paciente , Psicoterapia Breve , Canadá , Feminino , Humanos , Masculino , Transtornos Mentais/psicologia , Transtornos do Humor/enfermagem , Transtornos do Humor/psicologia , Unidade Hospitalar de Psiquiatria , Escalas de Graduação Psiquiátrica , Esquizofrenia/enfermagem , Psicologia do Esquizofrênico , Resultado do Tratamento , Violência/prevenção & controle , Violência/psicologiaRESUMO
OBJECTIVE: Violence by patients in psychiatric settings is frequently associated with the quality of staff-patient interactions. Impulsivity has been identified as a high risk factor for anger and aggression. This study was designed to test the influence of nurses' limit-setting styles on anger among psychiatric inpatients grouped by high or low levels of impulsivity. METHODS: Ninety-seven patients with various diagnoses and either high or low levels of impulsivity participated in role-play scenarios in which nurse actors played out six limit-setting styles, ranging from belittlement to explanations of rules to empathy linked with a presentation of an alternative course of action. Patients' level of anger in response to the acted scenario was assessed using the Spielberger State-Trait Anger Scale. RESULTS: Patients' level of anger was highest in response to unempathic limit-setting styles, moderate for explanations, and lowest for empathic styles. Impulsive subjects were more likely to respond with anger than nonimpulsive patients, regardless of the limit-setting style. CONCLUSIONS: Although many current intervention programs focus on reducing patients' anger after it occurs, the study results suggest that it may be possible to prevent some of patients' anger by improving nurses' limit-setting styles.
Assuntos
Agressão/psicologia , Ira , Terapia Comportamental , Transtornos Mentais/enfermagem , Relações Enfermeiro-Paciente , Encenação , Adulto , Idoso , Feminino , Humanos , Comportamento Impulsivo/enfermagem , Comportamento Impulsivo/psicologia , Masculino , Transtornos Mentais/psicologia , Pessoa de Meia-Idade , Inventário de Personalidade , Unidade Hospitalar de Psiquiatria , Desempenho de Papéis , Esquizofrenia/reabilitação , Psicologia do EsquizofrênicoRESUMO
The grid test for schizophrenic thought disorder was administered to a sample of 149 psychiatric patients. This sample was drawn from a population with a known base rate of schizophrenia and an estimated base rate of thought disorder, thus allowing for the calculation of population specific cutting scores for the grid test. The grid test, using these data along with others from previous grid test studies, was then analysed for diagnostic efficiency using conditional probability formulae. The conclusion reached is that the grid test for schizophrenic thought disorder is unsatisfactory as a diagnostic instrument.
Assuntos
Esquizofrenia/diagnóstico , Psicologia do Esquizofrênico , Pensamento , Diagnóstico Diferencial , Humanos , Testes Psicológicos , PsicometriaRESUMO
Staff from 3 Toronto hospitals were surveyed for knowledge, attitudes and concerns about AIDS. 70% of the 1,366 respondents had direct clinical experience with persons with AIDS. Data were analyzed according to hospital setting and professional group: physicians, nurses, technologists and supervisory staff. No setting difference was observed and although statistically significant differences (at the .001 level) were observed between professional groups, these differences are small and have little practical importance. In general, subjects answered 68% of the knowledge questions correctly. All attitudes and concerns were inversely associated to knowledge (Pearson r range was -.31 to -.20). Multivariate analysis demonstrated that knowledge and concern about contagion are important mediating variables (multiple r = .40) for other attitudes and concerns.
Assuntos
Síndrome da Imunodeficiência Adquirida/transmissão , Conhecimentos, Atitudes e Prática em Saúde , Recursos Humanos em Hospital/psicologia , Feminino , Humanos , Masculino , Corpo Clínico Hospitalar/psicologia , Análise Multivariada , Recursos Humanos de Enfermagem Hospitalar/psicologiaRESUMO
BACKGROUND: The relationship of psychological stress to relapse in ulcerative colitis (UC) is inconsistent. This may be due to a failure to identify patient characteristics, such as social support, which moderate the transduction of stress from the central nervous system to the immune system. In this study we tested the hypothesis that social support enhances parasympathetic modulation of heart rate in UC. METHODS: An indirect measure of autonomic function (heart rate variability; HRV) was measured in 108 patients with UC in remission during a standard protocol involving periods of stress, paced breathing, and relaxation. Social support was measured with the Social Support Questionnaire. RESULTS: After controlling for age, which is strongly related to HRV, both satisfaction with social support (F = 5.7, significance = 0.002) and its interaction with age (F = 7.8, significance <0.001) were associated with high-frequency HRV, which measures parasympathetic modulation of heart rate. Social support was associated with higher levels of high-frequency HRV at almost all points in the stress protocol. Neither age nor social support was associated with differences in the LF/HF ratio, which measures sympathetic modulation of heart rate. CONCLUSIONS: Social support is related to parasympathetic activity in UC. Given previous evidence of an antiinflammatory role for the parasympathetic nervous system, this suggests that autonomic function could serve as a mediating link between social support and reduced inflammatory activity.
Assuntos
Sistema Nervoso Autônomo/fisiopatologia , Colite Ulcerativa/psicologia , Apoio Social , Estresse Psicológico/psicologia , Adulto , Sistema Nervoso Autônomo/fisiologia , Colite Ulcerativa/fisiopatologia , Feminino , Frequência Cardíaca/fisiologia , Humanos , Masculino , Pessoa de Meia-Idade , Estresse Psicológico/fisiopatologiaRESUMO
OBJECTIVE: Characteristics attributed by nurses and by psychiatric residents to difficult-to-treat inpatients in a short-stay setting were compared to determine whether discipline-specific perceptions of such patients existed. METHODS: A total of 117 patients consecutively admitted to a short-stay inpatient unit were assessed by both psychiatric residents and nurses during the third week of hospitalization using subscales of the Hospital Treatment Rating Scales. The degree of management difficulty presented by each patient in 28 areas was rated, and an overall rating was calculated. Two separate regression analyses were used to examine characteristics of patients rated difficult. RESULTS: Self-harm behaviors, violence toward others, and behaviors that sabotage treatment were identified by both nurses and residents as characteristics of difficult patients, although these characteristics contributed less to residents' perceptions of patient difficulty than to nurses'. For nurses, the most important additional characteristics contributing to treatment difficulty were related to patients' inability to form a therapeutic alliance. For residents, by far the most significant contributor to overall treatment difficulty was lack of response to medication. CONCLUSIONS: The discipline-specific differences in perceptions of difficult-to-treat patients were associated with differences in professional roles. Communication problems between physicians and nurses may be due in part to their different perceptions of treatment and management difficulty.
Assuntos
Atitude do Pessoal de Saúde , Internato e Residência , Transtornos Mentais/psicologia , Relações Enfermeiro-Paciente , Relações Médico-Paciente , Adulto , Idoso , Contratransferência , Transtorno Depressivo/psicologia , Transtorno Depressivo/terapia , Feminino , Hospitais de Ensino , Humanos , Masculino , Transtornos Mentais/terapia , Pessoa de Meia-Idade , Determinação da Personalidade , Transtornos da Personalidade/psicologia , Transtornos da Personalidade/terapia , Agitação Psicomotora/psicologia , Agitação Psicomotora/terapia , Transtornos Psicóticos/psicologia , Transtornos Psicóticos/terapia , Suicídio/psicologia , ViolênciaRESUMO
Clinical empathy research has been plagued with conceptual and methodological difficulties. This paper describes a model of the empathic process that enables clinicians, teachers, and researchers to examine specific components of the model and to determine the influence of particular mediators on the empathic process. Empathy is conceptualized as a three-phase time-sequenced process rather than as a multidimensional or multicomponent phenomenon. Stripped of detail, the empathic process reveals an inducement phase, a matching phase, and a participatory-helping phase. By examining these phases, it becomes possible to distinguish empathy from closely related concepts such as sympathy. Each of the phases reveals numerous mediating variables that influence the outcome of the phase, i.e., whether the process of empathy continues or an alternate terminal point is reached. Many of these mediators are derived from existing conceptual and empirical work on empathy. Particular attention is paid to situational or contextual mediators of empathy. Contextual mediators have only recently been acknowledged as an important variable in the empathic process. For clinicians, identification of contextual variables that may be responsive to intervention is a critical step in the modification of the clinical environment. We would suggest that clinical empathy research is largely the study of these mediating influences and should be recognized as such.
Assuntos
Empatia , Modelos Psicológicos , Contratransferência , Humanos , Identificação Psicológica , Relações Profissional-Paciente , Psicoterapia , Pesquisa , EnsinoRESUMO
A prospective study of 47 married women who met RDC for major depressive disorder investigated the relationship between the social support provided by the husbands and the post-hospital symptom course of the women. Separate taped semistructured interviews were held with the patient and husband at the time of admission. Six months later, symptom course was rated using the LIFE psychiatric status schedule. Only 51% of the sample recovered in the six months. Few demographic or clinical factors were related to symptom course. Recovery was predicted by the depressed woman's ratings of the current marital relationship and by the husband's rating of the pre-morbid relationship but not by the husband's level of expressed criticism or his ratings of the current relationship.