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J Penrod

Publications and source records attributed to J Penrod.

27 records · Page 2Linked to original sources

Predicting the short term direct medical costs incurred by patients with rheumatoid arthritis.

OBJECTIVE: With increasing interest in revising the mechanisms of health care funding, the ability to anticipate patients' medical expenditures as well as to identify potentially modifiable predictors would be informative for health care providers, payers, and policy makers. METHODS: Eight hundred fifty-eight patients with rheumatoid arthritis from 2 Canadian centers reported semi-annually on their health services utilization and health status for up to 12 years. Annual direct costs were calculated using 1994 Canadian prices. Regression models for the variation in total direct costs and the individual resource components (i.e., physicians, tests, medications, acute and non-acute hospital care) were estimated using previous values of age, sex, disease duration, education, methotrexate availability, employment status, global well being, pain, duration of morning stiffness, and functional disability as predictor variables. The models were developed using all available data except the last 2 observations (i.e., data collected on the last 2 self-report questionnaires) from each patient, which were reserved for model validation. The predictive abilities of the models were assessed by comparing the most recent costs with those predicted by the model using values of the predictor variables from the previous time period. Further, to assess whether the models conferred any advantage over cost estimates based only on previous costs, most recent observed costs were also compared with costs observed in the preceding time period. RESULTS: Self-reported indices of either global well being, pain, or functional disability predicted total direct costs as well as the costs of the 5 individual resource components. Being younger, female, disabled from the work force, having shorter disease duration, and receiving more formal education also predicted higher costs in at least on health resource category. However, being older predicted higher acute and non-acute care hospital costs. Regression models incorporating longitudinal data did not perform better than average costs in the preceding time period in predicting future short term costs. CONCLUSION: Global well being, pain, functional disability, and previous costs are the most important predictors of short term direct medical costs. Although we have demonstrated that regression models do not perform better than previous costs in predicting future short term costs, previous costs are a much less informative predictor than health status variables. Variables such as functional disability and pain identify potentially modifiable disease features and suggest interventions that may improve patient well being and reduce costs.

Aged↗

An international perspective on the well being and health care costs for patients with systemic lupus erythematosus. Tri-Nation Study Group.

OBJECTIVE: To compare health care expenditure and health status for patients with systemic lupus erythematosus (SLE) between nations with distinct mechanisms for funding and delivering health care services. METHODS: Seven hundred eight patients with SLE from 2 centers in each of 3 countries (Canada 229, United States 268, United Kingdom 211) underwent physician assessment of disease activity and damage and reported on physical and psychosocial well being, satisfaction, social support, and health resource utilization. To compare overall utilization, constant prices (1997 Canadian dollars) were applied across countries for each service, enabling diverse resources to be collapsed into a single expression. RESULTS: After adjusting for important patient covariates, Canadian, compared to American and British patients, reported significantly superior health status in 3 of 8 Medical Outcome Survey Short Form-36 (SF-36) subscales, the SF-36 physical component summary score, and the visual analog scale of general health status. There was no consistent trend in patient satisfaction. Overall annual resource utilization did not vary significantly, with mean annual per patient expenditures (adjusted for demographics, disease duration, activity, damage, social support, health status, patient satisfaction, and age and sex adjusted country-specific SF-36 general population norms) totalling $4853, $5285, and $4760 for Canada, US, and the UK, respectively. However, within each resource category, differences were observed. Canadians saw more specialists than the British, the British more generalists. Canadians and Americans were more frequent users of the emergency room; Americans of laboratory/imaging procedures. Canadians had higher hospital costs than Americans. CONCLUSION: After adjustment, Canadian patients reported better well being than their counterparts. Despite considerable differences in the mechanisms of health care funding and service mixture, overall resource utilization did not vary significantly between the countries, although there was a trend towards more intense use of inpatient services in Canada and outpatient services in the United States.

Adult↗

Caregivers' experiences in making placement decisions.

Demographic trends indicate a growth in the older adult population, and in turn, are affecting the availability and use of health services. Although placement of an older adult charge into nursing home care is often described as a logical progression through the continuum of available services, informal caregivers often view placement as a last resort or as an indication of failure. This qualitative study used grounded theory methods to explore the experiences of caregivers actively involved in the process of placing an older adult in a long-term care facility upon discharge from acute care. Four themes (uncertainty, surrendering to the system, urgency, and validating) were interwoven throughout caregivers' perspectives of the conflictive decision to use nursing home care after hospitalization.

Adult↗

Developing reciprocal trust in the caregiving relationship.

A summer camp for ventilator-dependent children provided a natural laboratory in which to explore the development of a caregiver-child relationship. The campers' routine treatments were "downplayed" to create a more "normal" camp experience while ensuring that the children had a safe environment and maintained a stable medical condition. Campers who normally had consistent home caregivers were observed as they were cared for by new caregivers. Using grounded theory methods, a model describing four types of relationships--tentative, familiar, mutually protective, and connected--was developed. Strategies used by caregiver-camper dyads to sustain a relationship or to progress to a more intense relationship were identified. Developing reciprocal trust was the basic social process that enabled the caregiver and child to reach the goal of becoming connected. Previous camp experience and caregiver contact had an impact on the initial degree of trust between camper and caregiver, and subsequently, it influenced the development of the relationship. This study provides important information about the role of trust in establishing effective caregiving relationships.

Adolescent↗

Strategies for assessing and fostering hope: the hope assessment guide.

PURPOSE/OBJECTIVES: To detail behavioral manifestations of hope and to present the Hope Assessment Guide with stage-specific nursing strategies to foster the development of hope. DATA SOURCES: Previous research and a concept analysis of hope, including interviews with survivors of breast cancer, people awaiting heart transplants, breast-feeding mothers returning to work, and patients with spinal cord injuries. Criteria for inclusion included empirical validity of the conceptual framework, power of the autobiographic data to illustrate theoretical fit, and usefulness of the theory in assessing hope and devising clinical strategies. DATA SYNTHESIS: Behavioral manifestations within reported breast cancer experiences demonstrated theoretical fit. From this, the researchers extracted assessment factors and identified clinical strategies based on reported experiences and strategies found helpful at various stages of the hope development process. CONCLUSIONS: The conceptual model provides structure for assessing and responding to developing hopefulness in a stage-specific manner. IMPLICATIONS FOR NURSING PRACTICE: By becoming aware of the processes of developing hope, nurses are better prepared to clinically assess this dynamic process and to devise highly individualized clinical interventions in cases in which hope needs to be supported or modified.

Breast Neoplasms↗

Volatility in Medicare AAPCC rates: 1990-1997.

As Medicare beneficiary enrollment in managed care plans increases, and as Congress considers relying on capitation for achieving savings in the program, the question of finding a fair and equitable formula for determining the monthly payment to managed care plans has become increasingly salient. This DataWatch focuses on one dimension of using previous expenditures to determine annual capitation rates: the effects of historic volatility in total expenditures. Annual changes in adjusted average per capita cost (AAPCC) rates are especially dramatic in rural counties, with those not adjacent to urban areas experiencing the greatest volatility. This pattern of annual change may discourage managed care organizations from entering markets, even when the rate in any given year may appear to be favorable for accepting risk.

Capitation Fee↗

Going it alone: the experiences of spouses of critically ill patients.

Spouses of critically ill patients are faced with major changes in responsibilities while their spouse is in the intensive care unit. Using grounded theory methods, this qualitative study investigated the changes in responsibilities and the impact these additional responsibilities (such as financial decision making and child care) had on patients' spouses. Patients' spouses need help to meet their needs and alleviate some stress so they can "be there" for their critically ill partner.

Critical Illness↗