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1.
Cancer Pract ; 7(2): 86-92, 1999.
Article in English | MEDLINE | ID: mdl-10352066

ABSTRACT

PURPOSE: Although support groups are offered to many patients who have received a diagnosis of cancer, a majority of patients choose not to participate. This article reports the results of a study comparing the behavior of men diagnosed with prostate cancer and women diagnosed with breast cancer in their responses to invitations to participate in support groups. DESCRIPTION OF STUDY: One hundred thirty women with breast cancer and 87 men with prostate cancer completed a structured telephone interview. The interview included questions about the patients' choices about support group participation. RESULTS: Interview findings showed that men are less likely to join a support group, but those men who do join attend meetings for about 1 year, as do the women who join. Men and women cite essentially the same reasons for participation: to learn more about their diagnosis, to share their, concerns to compare their physical and emotional progress with other individuals. CLINICAL IMPLICATIONS: These results indicate the need for further exploration of effective interventions for men and women who have been diagnosed with prostate and breast cancer, respectively, in an effort to offer support for the difficult psychological and emotional issues associated with their diagnoses. Although more women than men join support groups, the majority of both populations (67% for women, 87% for men) do not attend any support group meetings. Innovative approaches are needed to encourage participation in existing support groups or to design alternative interventions.


Subject(s)
Breast Neoplasms/psychology , Men/psychology , Patient Acceptance of Health Care/psychology , Prostatic Neoplasms/psychology , Self-Help Groups/statistics & numerical data , Women/psychology , Aged , Breast Neoplasms/diagnosis , Decision Making , Female , Health Knowledge, Attitudes, Practice , Humans , Male , Middle Aged , Motivation , Prostatic Neoplasms/diagnosis , Sex Factors , Surveys and Questionnaires
2.
Lancet ; 349(9048): 309-13, 1997 Feb 01.
Article in English | MEDLINE | ID: mdl-9024373

ABSTRACT

BACKGROUND: Data about the frequency of adverse events related to inappropriate care in hospitals come from studies of medical records as if they represented a true record of adverse events. In a prospective, observational design we analysed discussion of adverse events during the care of all patients admitted to three units of a large, urban teaching hospital affiliated to a university medical school. Discussion took place during routine clinical meetings. We undertook the study to enhance understanding of the incidence and scope of adverse events as a basis for preventing them. METHODS: Ethnographers trained in qualitative observational research attended day-shift, weekday, regularly scheduled attending rounds, residents' work rounds, nursing shift changes, case conferences, and other scheduled meetings in three study units as well as various departmental and section meetings. They recorded all adverse events during patient care discussed at these meetings and developed a classification scheme to code the data. Data were collected about health-care providers' own assessments about the appropriateness of the care that patients received to assess the nature and impact of adverse events and how health-care providers and patients responded to the adverse events. FINDINGS: Of the 1047 patients in the study, 185 (17.7%) were said to have had at least one serious adverse event; having an initial event was linked to the seriousness of the patient's underlying illness. Patients with long stays in hospital had more adverse events than those with short stays. The likelihood of experiencing an adverse event increased about 6% for each day of hospital stay, 37.8% of adverse events were caused by an individual, 15.6% had interactive causes, and 9.8% were due to administrative decisions. Although 17.7% of patients experienced serious events that led to longer hospital stays and increased costs to the patients, only 1.2% (13) of the 1047 patients made claims for compensation. INTERPRETATION: This study shows that there is a wide range of potential causes of adverse events that should be considered, and that careful attention must be paid to errors with interactive or administrative causes. Healthcare providers' own discussions of adverse events can be a good source of data for proactive error prevention.


Subject(s)
Hospitals, Teaching/standards , Hospitals, Urban/standards , Iatrogenic Disease/epidemiology , Quality of Health Care/statistics & numerical data , Female , Health Services Research/methods , Hospitals, Teaching/statistics & numerical data , Hospitals, Urban/statistics & numerical data , Humans , Length of Stay , Male , Middle Aged , Prospective Studies , Severity of Illness Index , United States/epidemiology
3.
New Dir Ment Health Serv ; (41): 11-9, 1989.
Article in English | MEDLINE | ID: mdl-2654608

ABSTRACT

An overview of the legal and administrative issues involved in dealing with impaired physicians is presented from the perspective of an attorney experienced in hospital law.


Subject(s)
Medical Staff, Hospital/legislation & jurisprudence , Physician Impairment/legislation & jurisprudence , Constitution and Bylaws , Humans , Professional Staff Committees/organization & administration , Substance-Related Disorders/psychology , United States
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