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1.
Eur J Cancer Care (Engl) ; 28(2): e12991, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30628750

ABSTRACT

OBJECTIVE: About 14% of cancer patients live with dependent children. Healthcare professionals are well placed to help patients support their children as part of a patient-centred practice. Children tend to appreciate open communication during the course of illness, but patients often find this difficult. However, research is unclear about patients' preferences and their willingness to talk with healthcare professionals about their dependent children. METHODS: We conducted 15 in-depth interviews with patients from haematological (N = 11) and gynaecological oncology (N = 4). The interviews and subsequent analysis focused on patients' communicative preferences, taking the theoretical framework of "biographical disruption" as a starting point and using Jenkins' concept of identity as a social, relational and dynamic process. RESULTS: We identified two overall identities at stake for seriously ill patients with parental responsibility: "patient identity" and "parent identity." As "patients," patients were ambivalent about relating to their children, but as "parents" they wanted healthcare professionals to talk about their children. CONCLUSION: In order to be patient-centred, clinicians should, we suggest, acknowledge that patients have these conflicting perspectives and identities, which surface at various times and situations throughout their illness trajectories. Research is needed to further explore these findings in different illness groups and cultures.


Subject(s)
Communication , Genital Neoplasms, Female/psychology , Hematologic Neoplasms/psychology , Professional-Patient Relations , Adult , Attitude to Death , Child , Child Welfare/psychology , Child of Impaired Parents , Female , Humans , Male , Parent-Child Relations , Parents/psychology , Self Concept
2.
Psychooncology ; 26(12): 2162-2167, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28419731

ABSTRACT

OBJECTIVE: Research indicates that health personnel caring for seriously ill patients with dependent children aged 0 to 18 years often avoid discussing with them the challenges of being a family with a parent in treatment. Children of seriously ill patients risk serious trauma and emotional difficulty later in life and depend on adult support to minimize these consequences. Patients suffer anxiety about supporting their children during their illness. Because of their potentially pivotal role in supporting patients in enabling parent-child communication, we examined HP's structural and emotional barriers to communicating with patients about their children. METHODS: The study was based on 49 semi-structured, in-depth interviews with doctors and nurses working with haematology, gynaecological cancer, and neurointensive care. Both interviews and analysis addressed emotional and structural barriers, drawing on the theoretical framework of Maturana's domains. RESULTS: The study found structural barriers (eg, lack of space in the medical recording system, professional code, time pressure, and lack of training) and emotional barriers (eg, the painful nature of the situation and the perceived need of keeping professional distance). We found that emotional barriers tended to grow when structural barriers were not addressed. CONCLUSIONS: Our study indicates (1) the need to use templates and manual procedures to gather and process information about children in medical records; (2) the need for managerial backing for addressing children of seriously ill patients and time spent on it; and (3) the need for future HP training programmes to include how to implement procedures and how to address all barriers.


Subject(s)
Communication Barriers , Nurse-Patient Relations , Nurses/psychology , Physician-Patient Relations , Physicians/psychology , Adult , Attitude of Health Personnel , Child , Communication , Female , Health Care Surveys , Health Personnel , Humans , Interviews as Topic , Male , Middle Aged , Parents/psychology , Qualitative Research , Severity of Illness Index
3.
Epidemiology ; 24(4): 608-15, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23676260

ABSTRACT

BACKGROUND: Early parental death is one of the most stressful childhood life events and may influence subsequent psychological health. We investigated the association between early parental loss and risk of hospitalization for an affective disorder in adulthood. METHODS: Our nationwide register-based cohort study comprises 1,225,660 people born in Denmark in 1970-1990, of whom 138,893 experienced the death of a parent before the age of 30 years. Follow-up for hospitalization for an affective disorder in the period 1990-2009 yielded 15,261,058 person-years and 19,867 hospitalizations for affective disorder (bereaved n = 2,644; nonbereaved n = 17,223). A Cox proportional hazards model was used to assess hazard ratios (HRs) for hospitalization with an affective disorder according to early parental death. RESULTS: People who experienced early parental death had an increased risk of hospitalization for a unipolar disorder (men: HR= 1.33; 95% confidence interval [CI] = 1.23-1.44; women: 1.23; 1.17-1.30). Stronger associations were observed for parental death caused by suicide than for other causes. For bipolar affective disorder, an increased risk of hospitalization was observed only after suicide. CONCLUSIONS: People who had lost a parent had an increased risk of hospitalization for unipolar affective disorder. Although this was particularly true for bereavement due to parental suicide, it was also found for parental death from other causes. In contrast, an increased risk of hospitalization for bipolar affective disorder was observed only after parental suicide.


Subject(s)
Affective Disorders, Psychotic/epidemiology , Hospitalization/statistics & numerical data , Parental Death/psychology , Parental Death/statistics & numerical data , Adult , Affective Disorders, Psychotic/therapy , Age Factors , Bereavement , Denmark/epidemiology , Female , Follow-Up Studies , Humans , Male , Registries , Risk Assessment , Stress, Psychological , Suicide/psychology
4.
Dan Med Bull ; 53(3): 342-8, 2006 Aug.
Article in English | MEDLINE | ID: mdl-17092453

ABSTRACT

INTRODUCTION: No studies have systematically asked larger groups of health professionals about their own experience as patients. This study estimated the level of satisfaction with hospital care among health professionals based on experience from their own hospital admission or that of a close family member. METHODOLOGY: A cross-sectional questionnaire study of 1995 doctors (41% women) and 1472 nurses (98% women) drawn randomly from union registers. Response rate: 70%. RESULTS: Twenty-seven percent had themselves been hospitalized within the preceding five years, and 31% had followed a hospital stay for a close relative during the preceding two years. At least 85% were satisfied with these conditions: information from the hospital, nursing staff, and doctors before admission; quality of the sickroom; level of smoke exposure; quality of breakfast, lunch, and beverages; nursing staff's and doctors' communication with the patient, and; doctors' treatment and diagnostics. Dissatisfaction above 15% was seen for several other factors associated with facilities, care, and treatment. One severe observation was related to the degree of treatment complications, reported by 23% of the patients. When reporting on behalf of an admitted relative a tendency was found to be slightly more critical. Generally, the results of this study are in agreement with previous Danish studies on patient satisfaction. CONCLUSION: The results of the present study indicate room for improvement in several respects in Danish hospital care: Better physical facilities, improved patient information, and a continuous quality surveillance to prevent treatment errors.


Subject(s)
Attitude of Health Personnel , Hospital Administration/standards , Nurses/psychology , Patient Satisfaction/statistics & numerical data , Physicians/psychology , Quality of Health Care , Adult , Cross-Sectional Studies , Denmark , Female , Hospital-Patient Relations , Housekeeping, Hospital , Humans , Male , Middle Aged , Multivariate Analysis , Noise , Nurses/statistics & numerical data , Physicians/statistics & numerical data , Physicians, Women/psychology , Physicians, Women/statistics & numerical data
6.
Environ Health Perspect ; 110(10): 991-5, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12361923

ABSTRACT

Our objective in this study was to evaluate the mortality of workers exposed to sulfur dioxide in the pulp and paper industry. The cohort included 57,613 workers employed for at least 1 year in the pulp and paper industry in 12 countries. We assessed exposure to SO(2) at the level of mill and department, using industrial hygiene measurement data and information from company questionnaires; 40,704 workers were classified as exposed to SO(2). We conducted a standardized mortality ratio (SMR) analysis based on age-specific and calendar period-specific national mortality rates. We also conducted a Poisson regression analysis to determine the dose-response relations between SO(2) exposure and cancer mortality risks and to explore the effect of potential confounding factors. The SMR analysis showed a moderate deficit of all causes of death [SMR = 0.89; 95% confidence interval (CI), 0.87-0.96] among exposed workers. Lung cancer mortality was marginally increased among exposed workers (SMR = 1.08; 95% CI, 0.98-1.18). After adjustment for occupational coexposures, the lung cancer risk was increased compared with unexposed workers (rate ratio = 1.49; 95% CI, 1.14-1.96). There was a suggestion of a positive relationship between weighted cumulative SO(2) exposure and lung cancer mortality (p-value of test for linear trend = 0.009 among all exposed workers; p = 0.3 among workers with high exposure). Neither duration of exposure nor time since first exposure was associated with lung cancer mortality. Mortality from non-Hodgkin lymphoma and from leukemia was increased among workers with high SO(2) exposure; a dose-response relationship with cumulative SO(2) exposure was suggested for non-Hodgkin lymphoma. For the other causes of death, there was no evidence of increased mortality associated with exposure to SO(2). Although residual confounding may have occurred, our results suggest that occupational exposure to SO(2) in the pulp and paper industry may be associated with an increased risk of lung cancer.


Subject(s)
Air Pollutants/adverse effects , Lung Neoplasms/etiology , Lung Neoplasms/mortality , Occupational Exposure , Sulfur Dioxide/adverse effects , Cohort Studies , Humans , Industry , Leukemia/etiology , Leukemia/mortality , Lymphoma, Non-Hodgkin/etiology , Lymphoma, Non-Hodgkin/mortality , Odds Ratio , Paper
7.
J Occup Environ Med ; 44(6): 579-84, 2002 Jun.
Article in English | MEDLINE | ID: mdl-12085486

ABSTRACT

We studied the mortality from lung and pleural cancers in a cohort of 62,937 male workers employed for at least 1 year in the pulp and paper industry in 13 countries during 1945 to 1996. Mill departments were classified according to probability and level of exposure to asbestos on the basis of available dust measurements and mill-specific information on exposure circumstances. Thirty-six percent of workers were classified as ever exposed to asbestos. Standardized mortality ratios of lung cancer were 0.99 (95% confidence interval [CI], 0.90 to 1.08) among unexposed and 1.00 (95% CI, 0.90 to 1.11) among ever exposed workers. The number of pleural cancer deaths among unexposed workers was 10; that among exposed workers was 14, most of which occurred among maintenance workers. In internal analyses, a trend in mortality from either neoplasm was suggested for estimated cumulative exposure to asbestos, weighted for the individual probability of exposure within the department and for duration of exposure (relative risk for lung cancer for 0.78+ f/cc-years, as compared with < or = 0.01 f/cc-years: 1.44; 95% CI, 0.85 to 2.45; corresponding relative risk for pleural cancer: 2.43; 95% CI, 0.43 to 13.63). Despite a possible nondifferential misclassification of exposure and outcome, this study suggests that the carcinogenic effect of asbestos can be detected among workers employed in industries such as the pulp and paper industry, in which it is not considered to be a major hazard.


Subject(s)
Air Pollutants, Occupational/adverse effects , Asbestos/adverse effects , Industry , Lung Neoplasms/mortality , Occupational Diseases/mortality , Paper , Pleural Neoplasms/mortality , Cause of Death , Cohort Studies , Humans , Lung Neoplasms/etiology , Occupational Diseases/etiology , Pleural Neoplasms/etiology , Risk
8.
Bioethics ; 5(3): 250-6, 1991 Jul.
Article in English | MEDLINE | ID: mdl-11659342

ABSTRACT

... The allocation of resources can indirectly control science by defining areas undesirable for research from the point of view of society. In the United States federal funds are not available for research on human embryos. The European experience represents a new approach to control of scientific research. The project is neither prohibited nor accepted in accordance with certain ethical rules, but is followed throughout the project. This new approach originates from the complexity of the human genome project and its unpredictable consequences for man.


Subject(s)
Human Genome Project , Social Control, Formal , Advisory Committees , Denmark , Europe , European Union , Genetic Testing , Germany , Humans , International Cooperation , Internationality , Public Policy , Risk , Risk Assessment , Science
9.
Bioethics ; 4(3): 232-6, 1990 Jul.
Article in English | MEDLINE | ID: mdl-11651988

ABSTRACT

KIE: Denmark is the only Western European country that has not changed the criterion of death from one based on the cessation of cardiac function to one based on the irreversible loss of all brain function. The Danish Council of Ethics, at the behest of the political establishment, launched an educational campaign to promote public debate on brain death before proceeding to legislation. National surveys conducted before and during the campaign and the debate to measure public knowledge of death criteria revealed that knowledge had increased but that there was still much misunderstanding of the current criterion of death, of brain death, of the persistent vegetative state, and of criteria for organ harvesting. Rix concludes that increased education targeted at specific groups is worthwhile to increase trust in the definition of death and in organ donation.^ieng


Subject(s)
Brain Death , Cognition , Community Participation , Comprehension , Death , Heart , Public Opinion , Public Policy , Reference Standards , Advisory Committees , Data Collection , Denmark , Humans , Information Dissemination , Information Services , Jurisprudence , Mass Media , Persistent Vegetative State , Tissue Donors , Tissue and Organ Procurement , Trust
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