ABSTRACT
Depressive symptoms are highly prevalent yet undertreated in people living with HIV/AIDS (PLHAs). As part of a larger study of symptom self-management (N=1217), this study examined the prevalence, correlates, and characteristics (intensity, distress, and impact) of depressive symptoms, and the self-care strategies used to manage those symptoms in PLHAs in five countries. The proportion of respondents from each country in the total sample reporting depressive symptoms in the past week varied and included Colombia (44%), Norway (66%), Puerto Rico (57%), Taiwan (35%), and the USA (56%). Fifty-four percent (n=655) of the total sample reported experiencing depressive symptoms in the past week, with a mean of 4.1 (SD 2.1) days of depression. Mean depression intensity 5.4 (SD 2.7), distressfulness 5.5 (SD 2.86), and impact 5.5 (SD 3.0) were rated on a 1-10 scale. The mean Center for Epidemiologic Studies Depression Scale score for those reporting depressive symptoms was 27 (SD 11; range 3-58), and varied significantly by country. Respondents identified 19 self-care behaviors for depressive symptoms, which fell into six categories: complementary therapies, talking to others, distraction techniques, physical activity, medications, and denial/avoidant coping. The most frequently used strategies varied by country. In the US sample, 33% of the variance in depressive symptoms was predicted by the combination of education, HIV symptoms, psychological and social support, and perceived consequences of HIV disease.
Subject(s)
Depressive Disorder/therapy , HIV Infections/psychology , Self Care/methods , Adaptation, Psychological , Adult , Aged , Aged, 80 and over , Antidepressive Agents/therapeutic use , Colombia/epidemiology , Communication , Complementary Therapies/methods , Depressive Disorder/complications , Female , HIV Infections/diagnosis , HIV Infections/epidemiology , Humans , Male , Middle Aged , Norway/epidemiology , Puerto Rico/epidemiology , Severity of Illness Index , Social Support , Taiwan/epidemiology , United States/epidemiology , Young AdultABSTRACT
The prevalence of peripheral neuropathy is frequent in HIV disease and is often associated with antiretroviral therapy. Unhealthy behaviours, particularly substance-use behaviours, are utilized by many HIV-positive individuals to manage neuropathic symptoms. As part of a larger study on self-care for symptoms in HIV disease, this study analyzed the prevalence and characteristics of unhealthy behaviours to self-manage peripheral neuropathy in HIV disease. Sociodemographic and disease-related correlates and unhealthy behaviours were examined in a convenience sample of 1,217 respondents who were recruited from data collection sites in several US cities, Puerto Rico, Colombia, and Taiwan. Results of the study indicated that respondents with peripheral neuropathy (n=450) identified a variety of unhealthy self-care behaviours including injection drug use, oral drug use, smoking cigarettes and alcohol ingestion. Specific unhealthy behaviours that participants reported to alleviate peripheral neuropathy included use of marijuana (n=67), smoking cigarettes (n=139), drinking alcohol (n=81) and street drugs (n=30). A subset of those individuals (n=160), who identified high levels of neuropathy (greater than five on a scale of 1-10), indicated significantly higher use of amphetamines and injection drug use in addition to alcohol use and cigarette smoking. For participants from Norway, substance use (using alcohol: 56%) was one of the most frequent self-management strategies. Implications for clinical practice include assessment and education of persons with HIV for self-care management of the complex symptom of peripheral neuropathy.
Subject(s)
HIV Infections/psychology , Peripheral Nervous System Diseases/therapy , Risk-Taking , Self Care/methods , Adult , Aged , Aged, 80 and over , Alcohol Drinking/epidemiology , Anti-Retroviral Agents/adverse effects , Attitude to Health , Female , Humans , Male , Middle Aged , Norway/epidemiology , Peripheral Nervous System Diseases/chemically induced , Peripheral Nervous System Diseases/psychology , Prevalence , Puerto Rico/epidemiology , Risk Factors , Smoking/epidemiology , Substance-Related Disorders/epidemiology , Taiwan/epidemiology , United States/epidemiologyABSTRACT
Peripheral neuropathy is the most common neurological complication in HIV and is often associated with antiretroviral therapy. As part of a larger study on self-care for symptoms in HIV disease, this study analyzed the prevalence and characteristics of peripheral neuropathy in HIV disease, sociodemographic and disease-related correlates and self-care strategies. A convenience sample of 1,217 respondents was recruited from data collection sites in several US cities, Puerto Rico, Colombia and Taiwan. Results of the study indicated that respondents with peripheral neuropathy (n=450) identified 20 self-care behaviors including complementary therapies, use of medications, exercise and rest and/or elevation of extremities. Ratings of frequency and effectiveness were also included. An activities checklist summarized into five categories of self-care behaviors including activities/thoughts, exercise, medications, complementary therapies and substance was used to determine self-care behaviors. Taking a hot bath was the most frequent strategy used by those with peripheral neuropathy (n=292) and received the highest overall rating of effectiveness of any self-management strategies included in this study at 8.1 (scale 1-10). Other self-care strategies to manage this symptom included: staying off the feet (n=258), rubbing the feet with cream (n=177), elevating the feet (n=236), walking (n=262), prescribed anti-epileptic agent (n=80), prescribed analgesics (n=84), over-the-counter medications (n=123), vitamin B (n=122), calcium supplements (n=72), magnesium (n=48), massage (n=156), acupuncture (n=43), reflexology (n=23) and meditation (n=80). Several behaviors that are often deemed unhealthy were included among the strategies reported to alleviate peripheral neuropathy including use of marijuana (n=67), cigarette smoking (n=139), drinking alcohol (n=81) and street drugs (n=30).
Subject(s)
Acquired Immunodeficiency Syndrome/complications , Peripheral Nervous System Diseases/therapy , Self Care/methods , Adult , Aged , Aged, 80 and over , Alcohol Drinking/therapy , Attitude to Health , Colombia/epidemiology , Exercise , Female , Humans , Male , Middle Aged , Nonprescription Drugs/therapeutic use , Peripheral Nervous System Diseases/epidemiology , Prevalence , Puerto Rico/epidemiology , Smoking/therapy , Taiwan/epidemiology , United States/epidemiologyABSTRACT
PURPOSE: To record symptoms experienced by people with HIV/AIDS, and describe useful self-care strategies and how symptoms impact on daily life. METHOD: A questionnaire was used with self-reported answers and descriptions of how symptoms impact on daily activities and suggestions for useful self-care strategies. Four hundred and twenty-two (n = 422) HIV-positive persons from seven sites in the USA and one site in Norway (n = 20) answered the questionnaire. RESULTS: In this article subjective symptom descriptions from the Norwegian sample are presented along with self-care strategies and their effectiveness. Findings revealed the Norwegian sample to be a little older, maybe less anxious and depressed, than participants in the larger study. This difference might be explained by the structure of the national social and health care system in Norway, where treatments, medications and social services are available to all citizens without cost. Respondents described a number of related symptoms as well as their subjective explanations of what triggered the symptoms. Most of the self-care strategies were learnt by trial and error. RECOMMENDATIONS: Community health providers, nurses and physicians should become more knowledgeable about the symptoms that infected persons struggle with, as well as the impact these symptoms have on routine daily self-care activities and a person's quality of life. There is need for more research about helpful self-care strategies to assist HIV-positive persons to manage their symptoms and to disseminate these to community health providers and support groups for HIV infected persons.
Subject(s)
HIV Infections/therapy , Self Care , Adult , Aged , Female , HIV Infections/complications , HIV Infections/psychology , Humans , Male , Middle Aged , Norway , Quality of LifeABSTRACT
The study presented in this article is based on field observations over one year on a critical care unit in Norway. Data were analysed according to Glaser's grounded theory and generated a theory of hidden and emerging drama in the context of ambiguity while the nurses routinized the handling of complex technology. To the untrained eye the unit presented a picture of calm competence, while under the surface one finds hidden drama full of difficult interacting clinical and ethical problems. The nurses identified six ethical dilemmas: (1) end of life issues; (2) whether there should be an age limit for coronary surgery; (3) distributing limited resources; (4) resource allocation in terms of better staffing; (5) situations in which is it more harmful than beneficial to continue treatment; and (6) transferring patients to other facilities. The six problems overlap and have clinical as well as ethical components, but it was the ethical dimensions that the nurses identified and discussed. The significance for nursing is the importance of well-educated and well-qualified nurses and how they find viable solutions to complex ethical and clinical problems.
Subject(s)
Critical Care/ethics , Ethics, Nursing , Intensive Care Units/ethics , Nurse's Role , Nursing Staff, Hospital/ethics , Adult , Clinical Competence/standards , Critical Care/standards , Ethics, Institutional , Female , Humans , Intensive Care Units/standards , Male , Norway , Nursing Methodology Research , Nursing Staff, Hospital/standards , Surveys and QuestionnairesABSTRACT
Following the analysis of about 150 hours of field observation on a critical care unit in Norway a theory was generated to explain the actual ethical decision-making process. This was grounded in the empirical reality of physicians, nurses and family. The core theme in this study was a delayed clarification in assessing the prognosis of accident victims with neurosurgical traumas. The physicians, nurses and family had to wait for the clinical picture to clarify, during which time there was an exchange and emergence of information. Exchanging information, a subprocess to delayed clarification, involved a continuous flow of collecting and dispersing information about the clinical status of the patient. The nurses engaged in two useful strategies: grading information to family when the patient prognosis was poor, and providing grieving strategies for themselves, colleagues and family members. The core variable, delayed clarification has three dimensions: clinical, psychological and ethical. The nurses participated in the decision-making process to discontinue treatment as passive participants, they did not engage in collegial deliberations with the physicians. Ethical dilemmas were end of life questions, resource allocations, and questions of justice and organ transplants.
Subject(s)
Critical Care/standards , Decision Making , Medical Futility , Patient Care Team , Trauma, Nervous System/diagnosis , Bereavement , Ethics, Medical , Freedom , Humans , Intensive Care Units , Norway , Physician-Nurse Relations , Professional-Family Relations , Prognosis , Time Factors , Tissue and Organ Harvesting , Trauma, Nervous System/nursing , Trauma, Nervous System/surgeryABSTRACT
This article reports findings from Phase 1 of a replicated study conducted in Norway. The study is part of a cross-national study developing an ethnically sensitive instrument to assess quality of life for people with advanced HIV/AIDS. Interpretive data generated from interviews with 10 men and 3 significant others, a total of 19 interviews, shows that they learn to live with the virus but that after crossing over (the time when AIDS was diagnosed), they became aware that there was no turning around. Useful strategies for maintaining quality of life were controlling, hoping, talking, and reminiscing. Reminiscing was like a sentimental journey into the past, not looking to the future, letting go while planning and preparing to die. Comparing findings from the Norwegian study replication with the San Francisco study shows that similar themes were of concern to the subjects but they were played out differently.
Subject(s)
Adaptation, Psychological , HIV Infections/psychology , Quality of Life , Adult , Cross-Sectional Studies , HIV Infections/ethnology , Humans , Male , Middle Aged , Morale , Norway , Nursing Assessment , Nursing Methodology Research , Surveys and QuestionnairesABSTRACT
Norway's National Health Care system guarantees all citizens a right to health care within a decentralized system based on values like solidarity and equality. Seventy-five per cent of people with HIV/AIDS live and are treated in Oslo, the capital. Local home care agencies have minimal, if any experience working with AIDS patients residing in the community. Therefore a home care team with two nurses employed by the hospital was established as a 2-year trial project to establish a home care system for AIDS patients. In March 1993 a post hoc evaluation of the project for AIDS patients was completed, based on descriptive data. Results seem to indicate that a prerequisite for patients to live at home is someone to do chores like cleaning, laundry and shopping. The home care nurses functioned as vital links between the hospital, the outpatient clinic and the local home agency.
Subject(s)
Acquired Immunodeficiency Syndrome/nursing , Community Health Nursing/organization & administration , Home Care Services/organization & administration , Adult , Aged , Humans , Middle Aged , Norway , Nursing Audit , Nursing Evaluation Research , Program Evaluation , Surveys and QuestionnairesABSTRACT
One explanation for nurses' reticence about becoming involved in money issues is that they often mistakenly associate economics with cutting costs or cost containment. Another is nursing's European heritage, where the nurses' morale obligation has historically been to the patient. However, if nursing as a service is to continue, nurses must learn to plan their nursing resources, cost their services and document their effectiveness in terms of interventions and patient outcomes. To help nurse administrators gather more and better data for resource planning, below is a look at a framework suggested by Martha Quivey and the future directions to be taken.
Subject(s)
Health Care Rationing , Health Planning , Nurse Administrators , Budgets , Cost Control , Cost-Benefit Analysis , Health Care Costs , Health Care Rationing/organization & administration , Health Planning/organization & administration , Humans , Norway , Organizational Objectives , Patient AdvocacyABSTRACT
The purpose of this descriptive study was by means of a questionnaire to obtain data on how 13 nursing schools, offering a postgraduate specialization in psychiatric nursing in Norway, have incorporated a public health perspective into their curricula. Since the mid-1980s, national health policies and Health for All by A.D. 2000 have placed emphasis on decentralization of all health care services, including services for the mentally ill. The Community Health Law of 1984 guarantees all Norwegian citizens such services in their local communities. The schools have traditionally emphasized curative services in hospitals, rather than health promotion and preventive measures at community level. Are the new graduates prepared for psychiatric work at community level? A content analysis of a semistructured questionnaire revealed that a social psychiatric perspective has indeed been incorporated in today's curricula. This was supported by reviewing the required reading lists for each of the 13 schools. Roughly one can say that the schools represent two perspectives: 1) those focusing primarily on relational aspects, and 2) those focusing on relational aspects within a social psychiatric framework.