PubMed Health⌕ Search

Biomedical subjects

B E Meyerowitz

Publications and source records attributed to B E Meyerowitz.

34 records · Page 2Linked to original sources

Reactions of asbestos-exposed workers to notification and screening.

In the wake of efforts to pass legislation mandating notification of workers at high risk of developing occupational disease, considerable controversy exists regarding the potential costs and benefits of such notification efforts. It has been suggested that individual notification would cause undue psychological distress, especially when primary prevention efforts are no longer possible. In this study, we assessed reactions of asbestos-exposed workers to a letter notifying them of their risk for asbestos-related illnesses and the availability of a medical screening program. Two hundred forty-seven workers who attended the screening program and 53 who chose not to attend completed a questionnaire that tapped reactions to notification. Workers reported neither undue psychological distress nor avoidance behavior in response to notification, and many respondents reported engaging in active and appropriate coping behaviors. Workers who first learned of their risk through the notification letter (33.7%) were no more likely to report distress or denial than were workers who had learned previously through other sources. Individuals who chose not to attend the screening program were less likely than attenders to report experiencing distress upon learning of their risk status, more likely to engage in minimization of risk, and less likely to have taken direct action. Our results suggest that the psychological costs of notifying workers of increased risk for asbestos-related illness appear to be outweighed by the benefits of notification and screening.

Asbestos↗

Helping patients cope with cancer.

Oncologists and oncology nurses are in a unique and important position to help patients cope with the many stressful aspects of cancer. Oncology professionals can provide tremendous help to patients and their families by: 1. Being aware of the emotional, cognitive, behavioral, and social problems that patients and their families commonly experience as they adjust to cancer; 2. Encouraging patients to communicate freely about their current problems and their fears for the future; 3. Listening to these concerns and providing information about the normalcy of these reactions; 4. Providing specific suggestions for coping, when needed, based on knowledge of the successful coping efforts of others; 5. Making referrals to mental health professionals when these more limited interventions fail to provide sufficient help. We summarize reactions and difficulties that are common among cancer patients at six stages of the disease and we suggest interventions that may be helpful to patients as they cope with and adjust to these difficulties.

Adaptation, Psychological↗

The derivation and validation of six Multidimensional Health Locus of Control Scale clusters.

The purpose of this research was twofold. First, to determine if eight Multidimensional Health Locus of Control types hypothesized by Wallston and Wallston (1982) existed. Second, to assess the reliability, validity, and clinical utility of the control types. Two investigations were conducted based on research procedures designed for the discovery of clusters. The first study involved the derivation and replication of MHLC clusters with a sample of 400 healthy undergraduate men and women. The results of Study 1 suggested the existence of six MHLC clusters: pure internal; double external; pure chance; yea sayer; nay sayer, and believer in control. The sample for Study 2 consisted of 90 female undergraduate and graduate students. The six-cluster solution was replicated in this second cross-validation study. Furthermore, construct validity of the clusters was established through computer simulation. Finally, relationships between clusters and the Krantz Health Opinion Survey suggested the clusters have a theoretical as well as a empirical foundation. The implications of these findings for clinical practice, for the development of the health locus of control construct, and for future research on the MHLC Scale are discussed.

Adolescent↗

The effect of message framing on breast self-examination attitudes, intentions, and behavior.

In this study we tested the framing hypothesis that a pamphlet stressing the negative consequences of not performing breast self-examination (BSE) would be more persuasive than a pamphlet emphasizing BSE's positive consequences. College-aged female subjects were exposed to a loss-frame pamphlet, a gain-frame pamphlet, or a no-arguments pamphlet, or they received no pamphlet describing the importance of and the techniques for performing BSE. Attitudes toward BSE and intentions to perform BSE were assessed immediately after this intervention and again 4 months later. The follow-up also assessed subjects' postexperimental BSE behavior. Consistent with predictions, subjects who read a pamphlet with arguments framed in loss language manifested more positive BSE attitudes, intentions, and behaviors than did subjects in the other three conditions. The greater impact of the loss pamphlet could not be attributed to greater fear arousal, better memory for pamphlet content, greater perceived susceptibility to breast cancer, or stronger beliefs in BSE's efficacy on the part of the loss subjects. Only measures of perceived self-efficacy in performing BSE were differentially affected by the framing manipulation, with loss subjects reporting the greatest levels of self-confidence. The results are discussed in terms of prospect theory's framing postulate and a simpler negativity-bias conceptualization, and underlying mechanisms such as differential salience and vividness are considered. Clinical implications of the findings are also explored.

Attitude to Health↗

Factors associated with active participation in a Cancer Prevention Clinic.

To investigate factors that influence individuals at higher than average risk for cancer to seek preventive care, we studied 78 people by questionnaires designed to assess a variety of psychological, familial, and personal demographic variables. Twenty-six of these subjects (probands) had actively sought the services provided by a Cancer Prevention Clinic whereas the other subjects (nonprobands) did not initiate contact with the clinic. The results of a discriminant analysis indicate that prior involvement in cancer preventive activities, interest in cancer-specific information, and level of perceived susceptibility to cancer all contributed significantly to active participation in the Cancer Prevention Clinic. Level of psychological discomfort was found to be associated with cancer-specific variables, but did not contribute significantly to proband status. Involvement in preventive behaviors and perceived cancer susceptibility were most highly associated with familial factors, such as the proportion of first-degree relatives with cancer, whereas interest in cancer information was primarily related to perceived risk level.

Adult↗

Psychosocial findings in radial keratotomy patients two years after surgery.

In a psychosocial study of patients who participated in an evaluation of the visual, refractive and keratometric results of radial keratotomy, respondents stated that their primary reasons for electing the operation related to anticipated changes in vision. Improving appearance was not reported as a primary reason for seeking radial keratotomy by these patients. When asked two years after surgery if their vision had improved, remained the same, or worsened, 94.3% reported improvement over preoperative vision. About 40% still wear corrective lens, 26% full time and 14% only part of the time. Most patients (84.1%) reported overall satisfaction with the surgical outcome. Patient satisfaction was strongly related to perceived improvement of vision after surgery, and not to patient self-esteem, to changes in appearance or lifestyle brought about by the operation, or to having a particular physician perform the surgery.

Adaptation, Psychological↗

Psychosocial implications of adjuvant chemotherapy. A two-year follow-up.

Thirty-five women, who had received adjuvant chemotherapy after surgery for Stage II breast carcinoma, were interviewed approximately 21 months after treatment ended. Patients were asked to describe any continuing psychosocial effects of adjuvant chemotherapy in five life areas. All patients had responded to similar interviews 2 1/2 years earlier, while they were receiving chemotherapy. A comparison of first and second interview ratings for disease-free patients indicated that significant improvements in quality of life were reported in four of the five life areas. However, patients did report some continuing disruption in general activity level. Forty-four percent of the patients reported long-term disruption in at least one area, and 56% described continuing physical problems related to chemotherapy. When asked what they would suggest to help other patients adjust to receiving adjuvant chemotherapy, over 50% of the respondents recommended "staying busy" and "getting information." The implications of these findings are discussed.

Antineoplastic Combined Chemotherapy Protocols↗

A comparison of black and white children's WISC/WISC-R differences.

Administered the WISC and WISC-R to 20 white child psychiatric out-patients in a counterbalanced design. The white Ss' WISC/WISC-R differences were compared to equivalent data obtained from black children (Munford, 1978). For the white Ss, no differences were found between WISC and WISC-R Verbal, Performance, and Full Scale IQs, whereas black children scored significantly lower on the WISC-R than on the WISC on all three IQ measures. These findings indicate increased cultural bias in the WISC-R, despite apparent efforts to produce contrary results. A possible reason for this seemingly paradoxical outcome is offered, and future research possibilities are suggested.

Adolescent↗

Adjuvant chemotherapy for breast carcinoma: psychosocial implications.

Fifty women receiving adjuvant chemotherapy after surgery for Stage II breast carcinoma were interviewed in an effort to describe the psychosocial effect of the treatment. Perceptions of emotional distress and behavioral disruption were rated in five areas, yielding a rating of overall level of disruption and distress. Results showed that all women experienced adverse changes while receiving adjuvant treatments. Of the 50 women, 88% described a decrease in activities related to the effects of adjuvant chemotherapy; 54% reported an increased financial burden; and 41% claimed that their family and/or sexual life had been adversely affected. Despite these adverse changes, 74% of these patients "would definitely" recommend the treatment to friends in a similar situation. Results from this preliminary study may provide useful information to potential participants in adjuvant trials and to the physicians who conduct such trials.

Activities of Daily Living↗

The multi-centre assessment of quality of life: the Interdisciplinary Group for Cancer Care Evaluation (GIVIO) experience in Italy.

One of the main issues to be considered in conducting clinical trials concerns the presence of missing data. This aspect is particularly relevant in oncology longitudinal studies, characterized by a long follow-up, and especially in quality of life studies where there is still little knowledge about patients' characteristics that predict loss of data. Since the middle of the 1980s the GIVIO (Interdisciplinary Group for Cancer Care Evaluation) co-operative group has been involved in conducting quality of life assessment studies, also focusing on the development of some strategies aimed at the minimization of missing data. In this paper we report on the results of two trials, which are now completed, concerning the quality of life assessment in a sample of breast and colon cancer patients. In order to cope with the problem of missing data, in both the trials the strategy of follow-up mailing was adopted, which proved to be an effective way to increase the response rate by nearly 50 per cent at each time point.

Adenocarcinoma↗

Sexuality following breast cancer.

This article provides sex and marital therapists with detailed, multifaceted descriptions of sexuality after breast cancer based on survey responses from 863 breast cancer survivors. One third of women reported that breast cancer had had a negative impact on her sex life, and most reported negative changes in at least some areas. Nonetheless, breast cancer survivors did not differ from age-matched, healthy women on a standard measure of sexuality. Women who were most likely to report a negative impact on sexuality from cancer were those who had experienced changes in hormonal status, problems in their relationships, and difficulties with vaginal dryness. On the basis of these findings, we offer suggestions for health professionals and therapists treating breast cancer survivors.

Breast Neoplasms↗

Quality of life among mastectomy patients using external breast prostheses.

BACKGROUND: Most women who undergo mastectomy for breast cancer use external breast prostheses. Yet, little is known about patterns of use, satisfaction levels, and quality of life associated with their use as compared to other options. PATIENTS AND METHODS: We report longitudinal, self-report questionnaire data regarding prosthetic use from 592 Italian mastectomy patients. Women who report satisfaction with their prostheses are compared on medical, demographic, and quality of life variables to a matched sample of women who report dissatisfaction. We also compare matched samples of women who do not use prostheses and women who had reconstruction to prosthetic users. RESULTS: Most women used and were satisfied with their prostheses. However, there was a small group of women who were dissatisfied. These women reported greater disruption to their sense of feminility and worse quality of life in some areas. We found few differences between prosthetic users and women who used either of the other two options available following mastectomy-taking no action to restore the appearance of the amputated breast or having reconstructive surgery. CONCLUSIONS: No one technique for restoring the appearance of the mastectomized breast is necessary to optimize quality of life for all women. Physicians should describe the options to women, along with the average satisfaction rates for women choosing those options, and help women to make the best personal decisions.

Body Image↗

Quality of life and coping in patients awaiting heart transplantation.

The psychosocial adaptation of patients awaiting heart transplantation has not been defined. Forty-one patients (36 men, 5 women; mean age, 48 years) completed standardized questionnaires before transplantation to assess quality of life, physical symptoms, marital/social adjustment, psychiatric morbidity, coping, and compliance to medical regimens. Also, data were obtained from spouses/partners and the transplantation nurse coordinator. Unlike previously reported findings with patients after transplantation, those awaiting transplantation report moderate dissatisfaction with quality of life. Patients report physical symptoms, functional disabilities, sexual dysfunction, and psychological distress. Nonetheless, reported levels of compliance with the medical regimens and of social support were high, and both patients and spouses/partners provided marital adjustment ratings on the Dyadic Adjustment Scale that were comparable to those of well-adjusted, happily married couples. High levels of coping also were recorded. Having a positive attitude and seeking social support were the most common coping strategies, whereas confrontation, acceptance, and escapism were relatively uncommon. In conclusion, patients awaiting heart transplantation, although dissatisfied with quality of life, maintain positive psychological and social adjustment.

Adaptation, Psychological↗