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1.
Patient Educ Couns ; 101(3): 414-421, 2018 03.
Article in English | MEDLINE | ID: mdl-28964559

ABSTRACT

OBJECTIVE: First, to describe communication of home hospice nurse visits to cancer patient-caregiver dyads. Second, to assess change in communication related to domains of care over the course of visits. METHODS: Multi-site prospective observational longitudinal study of audio-recorded home hospice visits (N=537 visits; 101 patient-caregiver dyads; 58 nurses). Communication was coded using the Roter Interaction Analysis System to describe content and process. Conversation representing three care domains (physical, psychosocial/daily life, and emotional) was calculated from RIAS categories across speakers and analyzed to assess change in communication over time. RESULTS: On average, nurses spoke 54% of total utterances, caregivers 29%, and patients 17%. For all participants, the predominant conversational focus was on physical care. Linear mixed effects models indicated that combined participant emotional talk showed a small systematic decrease over time; however, the results for all domains indicated variability unexplained by time or speaker effects. CONCLUSIONS: Home hospice conversations are predominantly focused on physical care. Systematic change in communication versus responsiveness to the dynamic effects of patient death and family response over time are discussed. PRACTICE IMPLICATIONS: Communication strategies already in use by hospice nurses could be leveraged and expanded upon to better facilitate family competence and confidence.


Subject(s)
Caregivers/psychology , Communication , Hospice Care/psychology , Neoplasms/nursing , Nursing Staff/psychology , Professional-Family Relations , Professional-Patient Relations , Terminal Care/psychology , Aged , Aged, 80 and over , Emotions , Female , Humans , Longitudinal Studies , Male , Middle Aged , Neoplasms/psychology , Prospective Studies , Tape Recording
2.
Patient Educ Couns ; 101(4): 631-638, 2018 04.
Article in English | MEDLINE | ID: mdl-29241975

ABSTRACT

OBJECTIVE: Little is known about positive emotion communication (PEC) in end-of-life care. This study aims to identify types and patterns of PEC among hospice nurses, caregivers, and patients. METHODS: A coding system based on positive psychology theory was applied as a secondary analysis to audio recordings of hospice nurse home visits with cancer patients and family caregivers, collected as part of a prospective longitudinal study. Eighty recordings (4 visits from 20 triads) were coded for humor, connection, praise, positive focus, gratitude, taking joy/savoring, and perfunctory statements. RESULTS: Descriptive statistics revealed the greatest proportion of PEC was made by nurses. Humor was most frequently used across all speakers. Cluster analysis revealed four PEC visit types: Savor/Take Joy; Humor; Perfunctory; and Other-focused Expressions of Positive Emotions. Linear mixed effect regression was used to estimate the trajectory of PEC over time, but no significant change was found. CONCLUSION: We found that positive emotions are common in nurse, caregiver and patient communication at end-of-life and do not decline closer to death. PRACTICE IMPLICATION: This study is among the first to explore PEC at end-of-life, and offers a way to bring strengths-based approaches into end of life communication research.


Subject(s)
Caregivers/psychology , Communication , Emotions , Hospice Care/psychology , Hospice and Palliative Care Nursing/methods , House Calls , Neoplasms/nursing , Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Neoplasms/psychology , Nurse-Patient Relations , Prospective Studies , Tape Recording , Terminal Care
3.
Am J Hosp Palliat Care ; 35(1): 52-59, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28273753

ABSTRACT

BACKGROUND: Differences in end-of-life (EOL) care preferences (eg, location of death, use of life-sustaining treatments, openness to hastening death, etc) based on hypothetical death scenarios and associated physical and/or cognitive losses have yet to be investigated within the palliative care literature. AIM: The purpose of this study was to explore the multidimensional EOL care preferences in relation to 3 different hypothetical death scenarios: pancreatic cancer (acute death), Alzheimer disease (gradual death), and congestive heart failure (intermittent death). DESIGN: General linear mixed-effects regression models estimated whether multidimensional EOL preferences differed under each of the hypothetical death scenarios; all models controlled for personal experience and familiarity with the disease, presence of an advance directive, religiosity, health-related quality of life, and relevant demographic characteristics. SETTING/PARTICIPANTS: A national sample of healthy adults aged 50 years and older (N = 517) completed electronic surveys detailing their multidimensional preferences for EOL care for each hypothetical death scenario. RESULTS: The average age of the participants was 60.1 years (standard deviation = 7.6), 74.7% were female, and 66.1% had a college or postgraduate degree. Results revealed significant differences in multidimensional care preferences between hypothetical death scenarios related to preferences for location of death (ie, home vs medical facility) and preferences for life-prolonging treatment options. Significant covariates of participants' multidimensional EOL care preferences included age, sex, health-related quality of life, and religiosity. CONCLUSION: Our hypothesis that multidimensional EOL care preferences would differ based on hypothetical death scenarios was partially supported and suggests the need for disease-specific EOL care discussions.


Subject(s)
Patient Preference/psychology , Terminal Care/methods , Terminal Care/psychology , Advance Directives/psychology , Age Factors , Aged , Aged, 80 and over , Alzheimer Disease/physiopathology , Alzheimer Disease/psychology , Attitude to Death , Chronic Disease , Cross-Sectional Studies , Euthanasia, Active, Voluntary/psychology , Female , Heart Failure/physiopathology , Heart Failure/psychology , Humans , Life Support Care/psychology , Male , Middle Aged , Pancreatic Neoplasms/physiopathology , Pancreatic Neoplasms/psychology , Quality of Life , Sex Factors , Socioeconomic Factors
4.
Psychooncology ; 26(12): 2285-2293, 2017 Dec.
Article in English | MEDLINE | ID: mdl-28029712

ABSTRACT

OBJECTIVE: Few studies have examined the triadic communication between patients, spouse caregivers, and nurses in the home hospice setting. Thus, little is known about the types of communication patterns that unfold. The goals of the study were to, first, identify common patterns of communication in nurse-patient-caregiver home hospice visits and, second, to identify nurse, caregiver-patient dyad, and visit characteristics that predict visit communication patterns. METHOD: Nurses (N = 58) and hospice cancer patient and spouse caregiver dyads (N = 101; 202 individuals) were recruited from 10 hospice agencies. Nurses audio recorded visits to patient/caregiver homes from study enrollment until patient death. All patient, caregiver, and nurse utterances from the audio recordings were coded using an adapted Roter interaction analysis system. Using identified codes, cluster analysis was conducted to identify communication patterns within hospice visits. Logistic regression was used with demographic variables to predict visit communication patterns. RESULTS: Six visit communication patterns were identified and were defined largely by 2 dimensions: (1) either the patient, the caregiver, or the patient and caregiver dyad interacting with the nurse and (2) the relatively high or low expression of distress during the visit. Time until death significantly predicted several clusters. CONCLUSION: This study leads the way in outlining triadic communication patterns in cancer home hospice visits. Our findings have implications for nursing education, letting future nurses know what to expect, and lays the foundation for future research to determine effectiveness and interventions to improve health care communication.


Subject(s)
Caregivers/psychology , Communication , Hospice Care/psychology , Hospice and Palliative Care Nursing/methods , Neoplasms/nursing , Nurse-Patient Relations , Adult , Aged , Female , Humans , Logistic Models , Longitudinal Studies , Male , Middle Aged , Neoplasms/psychology , Stress, Psychological/psychology
5.
Public Health Genomics ; 17(3): 141-8, 2014.
Article in English | MEDLINE | ID: mdl-24713606

ABSTRACT

BACKGROUND/OBJECTIVES: Studies have shown that the general public is supportive of newborn screening (NBS) and supportive of the storage and use of residual bloodspots for quality assurance and biomedical research. However, the attitudes of parents of children with serious health conditions have not been assessed. In this study, we assessed attitudes of parents with children who have phenylketonuria (PKU) and leukemia towards NBS and storage and use of residual bloodspots for research. METHODS: A total of 49 individuals were recruited and responded to a validated 41-item survey regarding NBS and the retention and use of residual bloodspots. Of these participants, 22 had a child with PKU and 27 had a child with leukemia. We compared their responses to those of 1,927 individuals from the general public obtained in a previous study using the same survey instrument. RESULTS/CONCLUSIONS: We found that parents of children with a serious health condition had higher levels of support than the general public towards the use of residual NBS samples for research but similar attitudes regarding choice and privacy protections. It is important to assess the attitudes of various stakeholders for policy development.


Subject(s)
Attitude to Health , Biomedical Research/methods , Dried Blood Spot Testing/statistics & numerical data , Neonatal Screening/methods , Neonatal Screening/statistics & numerical data , Parents/psychology , Adult , Age Factors , Child , Data Collection , Female , Genetic Predisposition to Disease/genetics , Humans , Infant, Newborn , Leukemia/genetics , Male , Middle Aged , Neonatal Screening/psychology , Phenylketonurias/diagnosis , Privacy/psychology , Public Opinion , Reproducibility of Results , Specimen Handling
6.
Patient Educ Couns ; 84(3): 294-302, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21733653

ABSTRACT

OBJECTIVE: This study evaluated variables thought to influence patient's perceptions of patient-centeredness. We also compared results from two coding schemes that purport to evaluate patient-centeredness, the Measure of Patient-Centered Communication (MPCC) and the 4 Habits Coding Scheme (4HCS). METHODS: 174 videotaped family practice office visits, and patient self-report measures were analyzed. RESULTS: Patient factors contributing to positive perceptions of patient-centeredness were successful negotiation of decision-making roles and lower post-visit uncertainty. MPCC coding found visits were on average 59% patient-centered (range 12-85%). 4HCS coding showed an average of 83 points (maximum possible 115). However, patients felt their visits were highly patient-centered (mean 3.7, range 1.9-4; maximum possible 4). There was a weak correlation between coding schemes, but no association between coding results and patient variables (number of pre-visit concerns, attainment of desired decision-making role, post-visit uncertainty, patients' perception of patient-centeredness). CONCLUSIONS: Coder inter-rater reliability was lower than expected; convergent and divergent validity were not supported. The 4HCS and MPCC operationalize patient-centeredness differently, illustrating a lack of conceptual clarity. PRACTICE IMPLICATIONS: The patient's perspective is important. Family practice providers can facilitate a more positive patient perception of patient-centeredness by addressing patient concerns to help reduce patient uncertainty, and by negotiating decision-making roles.


Subject(s)
Communication , Expert Testimony , Family Practice/methods , Patient-Centered Care/methods , Physician-Patient Relations , Adolescent , Adult , Aged , Aged, 80 and over , Decision Making , Female , Humans , Male , Middle Aged , Primary Health Care , Psychometrics , Reproducibility of Results , Self Report , Statistics as Topic , Time Factors , Uncertainty , Verbal Behavior , Videotape Recording , Young Adult
7.
Health Commun ; 26(7): 667-75, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21660793

ABSTRACT

The profession of genetic counseling has received limited guidance from theoretical models in how to communicate complex health information so that clients can actively use the information. In this study of a national sample of 145 genetic counselors conducting sessions with simulated clients, we apply two different approaches for analyzing and describing verbal health communication. The Roter interaction analysis system (RIAS) and linguistic inquiry word count (LIWC) were used to identify evidence of communication behaviors consistent with tenets of the social cognitive processing model (SCPM). These tools revealed descriptive evidence of counselor facilitation of client emotional processing and, to a lesser extent, facilitation of client cognitive processing and understanding. Conversely, descriptive analysis of client communication revealed evidence of cognitive processing, but less affective processing. Second, we assessed whether genetic counselor facilitative communication predicted simulated client responses consistent with the cognitive and emotional processing inherent in SCPM. These analyses revealed that counselor attempts to promote emotional expression and client insight were positively associated with client word usage indicative of expression of negative affect and cognitive processing. This study is the first to our knowledge to apply RIAS and LIWC in tandem and gives us a description of current practices within genetic counseling within a theoretical framework. Additionally, it provides suggestions for education and communication goals to improve providers' responses to patient emotions as well as skills to engender patient understanding and personal meaning-making of complex medical information.


Subject(s)
Cognition , Communication , Emotions , Genetic Counseling/psychology , Adult , Aged , Amniocentesis/psychology , Breast Neoplasms/genetics , Breast Neoplasms/psychology , Female , Humans , Male , Middle Aged , Ovarian Neoplasms/genetics , Ovarian Neoplasms/psychology , Patient Simulation , Pregnancy , Time Factors
8.
Clin Toxicol (Phila) ; 49(4): 316-23, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21563908

ABSTRACT

CONTEXT. The communication demands faced by specialists in poison information (SPI) are unique in the health-care context. OBJECTIVES. (1) To describe SPI communication patterns for the highest risk poison exposure calls using cluster analysis, and (2) to describe variation in communication patterns or clusters. METHODS. A sample of 1 year of poison exposure calls to a regional poison control center with SPIs' perceived severity rating of major or moderate perceived was collected. Digital voice recordings were linked with medical records and were coded using the Roter Interaction Analysis System. Descriptive analyses were applied, and cluster-analytic techniques were used to assess variation in call communication and factors associated with that variation. RESULTS. Cases were described, and four communication styles were identified. The informational cluster represents calls with relatively high levels of SPI clinical information and caller questions. The Facilitative cluster represents calls with a pattern of relatively high SPI questions and caller information provision. The Planning cluster represents calls with relatively high levels of SPI relationship talk. The Emotional cluster represents calls with relatively high caller and SPI emotion. Further analyses revealed relationships between call characteristics, SPI identity, and cluster membership. CONCLUSION. This study provides a beginning step to understanding SPI communication behaviors. Our results suggest that SPIs are able to use a range of communication strategies that often involve not only information but also emotional responsiveness and rapport building. Findings also point to the opportunity for future communication training for SPIs to meet the needs of the heterogeneous caller population.


Subject(s)
Communication , Information Services , Poison Control Centers , Adolescent , Adult , Aged , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Male , Middle Aged , Retrospective Studies
9.
J Forensic Nurs ; 6(1): 3-14, 2010.
Article in English | MEDLINE | ID: mdl-20201911

ABSTRACT

UNLABELLED: Two groups now constitute the fastest growing segment of the U.S. prison population: women and persons with mental illness. Few large-scale studies have explored associations among serious mental illness (SMI), gender, and recidivism, or compared factors such as illness severity and clinical history as these construct notably different situations for incarcerated women and men. We report on our recent study comparing prison recidivism rates, severity of mental illness, and clinical history for women and men released from Utah State Prison 1998-2002. IMPLICATIONS: While women generally have better recidivism outcomes than men, we find that SMI related factors have a greater negative effect on the trajectories of women in this sample as compared with the men. This suggests that programs and policies focused on the SMI-specific risks and needs of women could significantly reduce prison recidivism and increase community tenure for this group, with far-reaching effects for families and communities.


Subject(s)
Crime/psychology , Mental Disorders/epidemiology , Prisoners/psychology , Rehabilitation , Adult , Case-Control Studies , Crime/statistics & numerical data , Female , Forensic Nursing , Humans , Proportional Hazards Models , Severity of Illness Index , Sex Factors , Survival Analysis , Utah/epidemiology
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