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Biomedical subjects

B B Germino

Publications and source records attributed to B B Germino.

13 recordsLinked to original sources

Psychosocial and educational intervention trials in prostate cancer.

OBJECTIVES: To describe the nature and focus of published educational intervention trials in prostate cancer in the last 10 years and to examine the state of the research in this particular area of knowledge. DATA SOURCES: Health science and psychosocial electronic databases were searched for studies reporting trials of educational or psychosocial interventions for men with prostate cancer and for the partners or families of these men. CONCLUSIONS: Interventions were characterized by the aspect of the illness trajectory that was targeted. The majority of the studies focused on managing the disease, treatments, and side effects. IMPLICATIONS FOR NURSING PRACTICE: Psychosocial stressors and uncertainty are pervasive throughout the prostate cancer trajectory. Knowledge of psychosocial and educational interventions that have been tested is critical for nurses working with these patients and their families.

Adaptation, Psychological↗

When a chronic illness becomes terminal.

Patients with ESRD and their families experience a variety of transitions across the trajectory of this chronic illness. A major transition occurs when patients who have been perceived as chronically ill become terminally ill, as changes and complications limit options for treatment. These changes are very disruptive, characterized by uncertainty and disturbances in the patients' prior view of themselves. In order to restructure a new reality, patients must acknowledge the losses and changes that have occurred. Several kinds of trigger events may facilitate this process. Patient responses to the transition include a variety of strategies such as seeking information, normalizing, comparing themselves to others, and finding their identity in continuing activities or substitutes that make them feel competent. Nephrology nurses knowledgeable about this transition process, because of their longstanding relationships with ESRD patients and their families, are in an excellent position to take advantage of opportunities to provide presence, understanding, and guidance in negotiating this difficult transition.

Chronic Disease↗

Survey of nephrology nurses' interest in graduate education.

OBJECTIVE: The purpose of the survey was to determine interest in a Master's nephrology nursing program among ANNA members residing in North Carolina, South Carolina, and Virginia. DESIGN: Needs assessment. SAMPLE/SETTING: 153 ANNA members residing in South Carolina, North Carolina, and Virginia. METHOD: Mailed survey. RESULTS: Response rate was 27%; 54 (35%) expressed interest in attending such a program, with 62 others (41%) interested "depending." Part-time study was the most commonly desired program option. Almost half (48%) were not currently baccalaureate prepared, a requirement for admission. CONCLUSIONS: Enrollment was inadequate to support the program despite numerous marketing efforts, bringing into question the adequacy of needs surveys for program planning.

Attitude of Health Personnel↗

Cancer and the partner relationship: what is its meaning?

When cancer occurs, it is an illness that has meaning for the lives of all members of the family. This article focuses on the meaning and significance of the illness for the partner relationship, both the individuals within the relationship and the dyad. Results of two studies are presented: one study is based on in-depth interviews with 50 individuals who were newly diagnosed with cancer and their partners, and the other study used questionnaires from 412 patients and 175 partners to obtain statistical data. Findings pointed to the importance of meaning in the adjustment of individuals, as well as the dyad. Interview data indicated that patients and their partners searched for meaning in the illness that would decrease its threat, and statistical analyses showed the significance of meaning as it applies to specific aspects of adjustment. The importance of considering meaning in care that is directed toward the prevention of problems within the dyad, which can occur as a result of coping with the stress of cancer are emphasized, and some specific recommendations are made.

Adaptation, Psychological↗

What makes oncology nursing special? Walking the road together.

PURPOSE: To identify the factors that influence oncology nurses' decisions to enter nursing and specialize in oncology and to describe the role dimensions of oncology nursing practice. DESIGN: Multi-institutional, descriptive, qualitative. SETTING: Six sites in different regions of the United States; rural and urban cancer and noncancer centers. SAMPLE: 38 oncology nurses (mean age = 35 years; average time in nursing = 10 years and in oncology = 7 years; 47% bachelor's degree in nursing, 29% diploma, 13% associate degree in nursing, and 11% master's prepared). METHODS: Phenomenological; content analysis of interviews. MAIN RESEARCH VARIABLES: Life events, career decision-making, personal and professional rewards, role dimensions of practice, caring behaviors. FINDINGS: Nurses said that their decisions to specialize in oncology were based on family experiences with cancer, the challenges of administering sophisticated cancer therapies, and influential role models. They reported that professional rewards are derived from valuing each patients as a 'whole person' and providing family-centered care. Nurses find that personal rewards and career survivorship are embedded in several ongoing discoveries: work offers a unique laboratory for learning about life in general, distancing maneuvers are necessary for self-preservation, and the fuzzy boundary between work and personal life must be constantly renegotiated. CONCLUSIONS: Oncology nurses find the best in the worst of situations, live fully the cancer experience by embracing their patients' heartaches and triumphs, share a collective sense of pride in their specialty, and report a high level of job satisfaction. IMPLICATIONS FOR NURSING PRACTICE: Caring for the dying person with cancer is the most difficult aspect of oncology nursing practice and being with--being present in the moment, no matter what the outcome--is the most rewarding and ubiquitous caring behavior of oncology nurses.

Adult↗

Impact of a parent's cancer on adult children: role and relationship issues.

The diagnosis and initial treatment of a parent for cancer is a highly stressful process that generates a variety of concerns for adult children. This study describes the initial effect of a parent's cancer on adult children. Adult children's concerns about role and relationship issues emerged as major themes in the content analysis of their interviews.

Adult↗

Understanding the cancer patient's search for meaning.

The period following a cancer diagnosis has been described as a time when concerns about life and death predominate. However, little is understood about how persons recently diagnosed with cancer deal with such issues as finding meaning in their lives, their illness, and their impending death. The purpose of this study is to describe what is involved in the process of the personal search for meaning conducted by the patient who has been recently diagnosed with breast, lung, or colorectal cancer. Six major themes were identified from interviews of 30 patients: seeking an understanding of the personal significance of the diagnosis; looking at the consequences of the cancer diagnosis; reviewing life; change in outlook toward self, life, others; living with the cancer; and hope. Two significant factors were found--faith and social support. With an understanding of the components in an individual's search for meaning of life, the nurse can facilitate the process by which patients explore what the cancer means for their lives.

Adaptation, Psychological↗

Uncertainty in prostate cancer. Ethnic and family patterns.

PURPOSE: Prostate cancer occurs 37% more often in African-American men than in white men. Patients and their family care providers (FCPs) may have different experiences of cancer and its treatment. This report addresses two questions: 1) What is the relationship of uncertainty to family coping, psychological adjustment to illness, and spiritual factors? and 2) Are these patterns of relationship similar for patients and their family care givers and for whites and African-Americans? DESCRIPTION OF STUDY: A sample of white and African-American men and their family care givers (N = 403) was drawn from an ongoing study, testing the efficacy of an uncertainty management intervention with men with stage B prostate cancer. Data were collected at study entry, either 1 week after post-surgical catheter removal or at the beginning of primary radiation treatment. Measures of uncertainty, adult role behavior, problem solving, social support, importance of God in one's life, family coping, psychological adjustment to illness, and perceptions of health and illness met standard criteria for internal consistency. Analyses of baseline data using Pearson's product moment correlations were conducted to examine the relationships of person, disease, and contextual factors to uncertainty. RESULTS: For family coping, uncertainty was significantly and positively related to two domains in white family care providers only. In African-American and white family care providers, the more uncertainty experienced, the less positive they felt about treatment. Uncertainty for all care givers was related inversely to positive feelings about the patient recovering from the illness. For all patients and for white family members, uncertainty was related inversely to the quality of the domestic environment. For everyone, uncertainty was related inversely to psychological distress. Higher levels of uncertainty were related to a poorer social environment for African-American patients and for white family members. For white patients and their family members, higher levels of uncertainty were related to lower scores on adult role behavior (shopping, running errands). For white family members, higher levels of uncertainty were related to less active problem solving and less perceived social support. Finally, higher levels of uncertainty were related to the importance of God for white patients and family care providers. CLINICAL IMPLICATIONS: The clearest finding of the present study is that there are ethnic differences in the relationship of uncertainty to a number of quality-of-life and coping variables. This has immediate implications for the assessment of psychosocial responses to cancer and cancer treatment. Much of what is in curricula is based on clinical and research experience primarily with white individuals. The experience of uncertainty related to cancer and its treatment is influenced by the cultural perspectives of patients and their families. To assist patients and families with the inevitable uncertainties of the cancer experience, healthcare providers need to reconsider their ethnocentric assumptions and develop more skill in assessing patient and family beliefs, values, cultural perspectives, and the influence of these on patient and family uncertainties.

Adaptation, Psychological↗

Helping women and their families cope with the impact of gynecologic cancer.

The impact of gynecologic cancer on the woman and her family depends on psychosocial factors and cancer-specific factors. Family assessments determine how the family is adapting to the woman's illness. Nursing interventions that families say are helpful include providing physical care, providing information, and giving support. Strategies used by families to cope with the stress and emotional strain of caregiving include taking time for themselves, maintaining a sense of humor, and focusing on the present.

Adaptation, Psychological↗

Prostate cancer treatment decisions: a focus group exploration.

PURPOSE/OBJECTIVES: To explore the decision-making process as retrospectively described by patients with prostate cancer and their spouses and to test the feasibility of a larger scale prospective examination of decision making in this same population. DESIGN: A qualitative study using focus group methodology. SAMPLE/SETTING: Twelve patients with prostate cancer and six spouses were recruited purposefully from a newly organized prostate cancer support group in an urban North Carolina community. METHODS: Using an interview guide, an experienced facilitator conducted two 90-minute focus groups. Sessions were audiotaped, transcribed verbatim, and analyzed using thematic content analysis techniques. MAIN RESEARCH VARIABLES: Decision making, prostate cancer treatment, spousal participation. FINDINGS: Six themes were derived from the data: (a) Finding Out, (b) Prostate Specific Antigen Talk, (c) (Getting the Story, (d) Who Decides, (e) Treatment Options, and (f) Looking Back. The data corroborated American Cancer Society findings that national cancer resources are not being used effectively by this population and reinforced the need for a multidisciplinary approach to the management of prostate cancer. CONCLUSIONS: Additional prospective studies are needed to explore the decision process from a family perspective. Studies focusing on the unique needs of older patients with prostate cancer and their spouses also are needed. IMPLICATIONS FOR NURSING PRACTICE: Nurses must assess informal information sources and work toward a more comprehensive presentation of treatment options. Misconceptions about surgery and radiotherapy hamper informed decision making. Nurses are in a unique position to educate families regarding prostate cancer treatment options.

Aged↗