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Social-Interaction Knowledge Translation for In-Home Management of Urinary Incontinence and Chronic Care*

Published online by Cambridge University Press:  24 September 2013

Lynn Jansen*
Affiliation:
College of Nursing, University of Saskatchewan
Carol L. McWilliam
Affiliation:
Arthur Labatt Family School of Nursing, University of Western Ontario
Dorothy Forbes
Affiliation:
Faculty of Nursing, University of Alberta
Cheryl Forchuk
Affiliation:
Arthur Labatt Family School of Nursing, University of Western Ontario
*
Correspondence and requests for offprints should be sent to / La correspondance et les demandes de tirés-à-part doivent être adressées à: Lynn Jansen, R.N., Ph.D. University of Saskatchewan College of Nursing 4400 4th Avenue Regina, SK S4T OH8 (lynn.jansen@usask.ca)

Abstract

Although urinary incontinence (UI) can be managed conservatively, it is a principal reason for the breakdown of in-home family care. This study explored the social interaction processes of knowledge translation (KT) related to how UI management knowledge might be translated within in-home care. In-depth interview data were collected from a theoretical sample of 23 family caregivers, older home care recipients, and home care providers. Constant comparison and Glaser’s analysis criteria were used to create translating knowledge through relating, a substantive theory with 10 subthemes: living with the problem; building experiential knowledge; developing comfort; easing into a working relationship; nurturing mutuality; facilitating knowledge exchange; building confidence; fine-tuning knowledge; putting it all together; and managing in-home care. Findings inform both theory and practice of in-home UI KT, illuminating how intersubjectivity and bi-directional relational interactions are essential to translating in-home chronic care knowledge, which is largely tacit and experiential in nature.

Résumé

Bien que l’incontinence urinaire peut être géré d’une manière conservatrice, c’est une cause principale de la dégradation des soins de famille dans la maison. Cette étude a examiné les processus d’interaction sociale et de l’application des connaissances (AC) se rapportant à la façon dont la gestion de l’incontinence urinaire (IU) peut être traduit dans les soins à domicile. Les données provenant des entretiens approfondis ont été receuillies auprès d’un échantillon théorique des 23 aidants familiaux, des beneficiaires âgés et des prestataires de soins à domicile. Les comparaisons constantes et les critères d’analyse de Glaser ont été utilisés pour arriver à traduire les connaissances à travers une théorie de fond. Dix sous-themes sont inclus: comment vivre avec le problème; le renforcement de connaissances expérientielles; le développement du confort; l’assouplissement dans une relation de travail; la mutualité nourricière; facilitant l’échange de connaissances; le renforcement de la confiance; l’affinage de connaissances; mettant tous ensemble, et la gestion de soins à domicile. Les résultats sont instructifs pour l’AC au sujet d’IU à la fois dans la théorie et la pratique des soins à domicile, grâce à avoir éclairé comment l’intersubjectivité et les interactions bi-directionelles sont indispensables à l’application des connaissances des soins à domicile chroniques, ce qui sont largement tacites et empiriques.

Type
Articles
Copyright
Copyright © Canadian Association on Gerontology 2013 

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Footnotes

*

This research was supported by a Social Sciences and Humanities Research Council Doctoral Fellowship and University of Western Ontario Faculty of Health Sciences Scholarship and Dr. Jansen’s doctoral supervisors, Dr. McWilliam, Dr. Forbes and Dr. Forchuk.

References

Abrams, P., Cardozo, L., Fall, M., Griffiths, D., Rossier, P., Ulmsten, U., et al. (2003). The standardisation of terminology in lower urinary tract function: Report from the Standardisation Sub-committee of the International Continence Society. Urology, 61, 3749.Google Scholar
Benzein, E., Johansson, B., & Saveman, B. (2004). Families in home care: A resource or a burden? District nurses’ beliefs. Journal of Clinical Nursing, 7, 867875.CrossRefGoogle Scholar
Boreus, K. A. (2006). Typology. European Journal of Social Theory, 9, 405424.Google Scholar
Brittain, K. R., & Shaw, C. (2007). The social consequences of living with and dealing with incontinence: A carer’s perspective. Social Science & Medicine, 65, 12741283.CrossRefGoogle Scholar
Buber, M. (1958). I and thou (2nd ed.). New York, NY: Charles Scribner’s Sons.Google Scholar
Canadian Continence Foundation. (2007). About the Canadian continence foundation. Retrieved January 9, 2013, from http://www.canadiancontinence.ca/pdf/Research_paper_August2007.pdf.Google Scholar
Canadian Institute for Health Information (CIHI). (2010). Home care reporting system (HCRS) – analysis in brief. Supporting informal caregivers: The heart of home care. Ottawa, ON: Author.Google Scholar
Canadian Institute of Health Research. (2009). About knowledge translation. Retrieved January 2, 2013, from http://www.cihr-irsc.gc.ca/e/29418.html.Google Scholar
Caroline, H. (1993). Exploration of close friendship: A concept analysis. Archives of Psychiatric Nursing, 4, 236243.CrossRefGoogle Scholar
Colling, J., Owen, T. R., McCreedy, M., & Newman, D. (2003). The effects of a continence program on frail community-dwelling elderly persons. Urologic Nursing, 23(2), 117–122, 127131.Google Scholar
Doane, G. H. (2002). Beyond inter-personal communication: The significance of relationship in health promoting practice. In Young, L., & Hayes, V. (Eds.), Transforming health promotion practice. Concepts, issues, and applications (pp. 4958). Philadelphia, PA: F.A. Davis.Google Scholar
Doane, G. H., & Varcoe, C. (2008). Knowledge translation in everyday nursing: From evidenced-based to inquiry-based practice. Advances in Nursing Science, 31, 283295.CrossRefGoogle Scholar
Du Moulin, M. F., Hamers, J. P., Ambergen, A. W., Janssen, M. A., & Halfens, R. J. (2008). Prevalence of urinary incontinence among community-dwelling adults receiving home care. Research in Nursing and Health, 31, 604612.Google Scholar
DuBeau, C. E., Kuchel, G. A., Johnson, T., Palmer, M. H., & Wagg, A. (2009). Incontinence in the frail elderly. In Abrams, P., Cardozo, L., Khoury, S., & Wein, S.. (Eds.), Incontinence (4th ed.) (pp. 9611024). Paris: Health Publications Ltd.Google ScholarPubMed
Egnew, T. R. (2009). Suffering, meaning, and healing: Challenges of contemporary medicine. Annals of Family Medicine, 7, 170175.CrossRefGoogle ScholarPubMed
Fader, M., Bliss, D., Cottenden, A., Moore, K., & Norton, C. (2010). Continence products: Research priorities to improve the lives of people with urinary and/or fecal leakage. Neurourology and Urodynamics, 29, 640644.CrossRefGoogle ScholarPubMed
Farage, M. A., Miller, K. W., Berardesca, E., & Maibach, H. I. (2007). Incontinence in the aged: Contact dermatitis and other cutaneous consequences. Contact Dermatitis, 57(4), 211217.CrossRefGoogle ScholarPubMed
Ferlie, E., & Dopson, S. (2005). Studying complex organizations in healthcare. In Dopson, S. & Fitzgerald, L. (Eds.), Knowledge to action? Evidence-based health care in context (pp. 826).New York, NY: Oxford University Press.Google Scholar
Forbes, D., Montague, P., Gibson, M., Hirdes, J., & Clark, K. (2011). Social support deficiency in home care clients. Perspectives: Journal of the Gerontological Nursing Association, Spring. Retrieved from http://findarticles.com/p/articles/mi_7546/is_201110/ai_n57626414/pg_2/?tag=content;col1.Google Scholar
Forchuk, C., & Reynolds, W. (2001). Clients’ reflections on relationships with nurses: Comparisons from Canada and Scotland. Journal of Psychiatric and Mental Health Nursing, 8, 4551.CrossRefGoogle ScholarPubMed
Forchuk, C., Westwell, J., Martin, M. L., Bamber-Azzapardi, W., Kosterewa-Tolman, D., & Hux, M. (2000). The developing nurse-client relationship: Nurses’ perspectives. Journal of the American Psychiatric Nurses Association, 6(1), 310. doi: 10.1177/107839030000600102.Google Scholar
Gagliardi, A. R., Légaré, F., Brouwers, M. C., Webster, F., Wiljer, D., Badley, E., et al. (2011). Protocol: Developing a conceptual framework of patient mediated knowledge translation, systematic review using a realist approach. Implementation Science, 6(25). doi: 10.1186/1748-5908-6-25.CrossRefGoogle ScholarPubMed
Gantert, T. W., McWilliam, C., Ward-Griffin, C., & Allen, N. (2009). Working it out together: Family caregivers’ perceptions of relationship-building with in-home service providers. The Canadian Journal of Nursing Research, 41(3), 4463.Google ScholarPubMed
Giddens, A. (1991). Modernity and self-identity. Self and society in the late modern age. Cambridge, UK: Polity.Google Scholar
Glaser, B., & Strauss, A. (1967). The discovery of grounded theory. Chicago, IL: Aldine.Google Scholar
Glaser, B. (1978). Theoretical sensitivity. Mill Valley, CA: The Sociology Press.Google Scholar
Graetz, F., & Smith, A. (2009). Duality theory and organizing forms in change management. Journal of Change Management, 9(1), 925.CrossRefGoogle Scholar
Graham, I., Logan, J., Harrison, M., Straus, S., Tetroe, T., Caswell, W., et al. (2006). Lost in knowledge translation: Time for a map? The Journal of Continuing Education in the Health Professions, 26, 1324.CrossRefGoogle ScholarPubMed
Guberman, N., Lavoie, J. P., Pepin, J., Lauzon, S., & Motejo, M. E. (2006). Formal service practitioners’ views of family caregivers’ responsibilities and difficulties. Canadian Journal on Aging, 25(1), 4353.CrossRefGoogle ScholarPubMed
Heinrich, M., Neufeld, A., & Harrison, M. (2003). Seeking support: Caregiver strategies for interacting with health personnel. Canadian Journal of Nursing Research, 35(4), 3856.Google ScholarPubMed
Hu, T. W., Wagner, T. H., Bentkover, J. D., Leblanc, K., Zhou, S. Z., & Hunt, T. (2004). Costs of urinary incontinence and overactive bladder in the United States: A comparative study. Urology, 63, 461465.CrossRefGoogle ScholarPubMed
Jansen, L. (2008). Collaborative and interdisciplinary health care teams: Ready or not? Journal of Professional Nursing, 24(4), 218227.Google Scholar
Jansen, L., & Forbes, D. (2006). The psychometric testing of a urinary incontinence nursing assessment instrument. Journal of Wound Ostomy and Continence Nursing, 33(1), 6976.CrossRefGoogle ScholarPubMed
Jansen, L., McWilliam, C., Forbes, D., & Forchuk, C. (2012). An exploration of in-home urinary incontinence management knowledge translation amongst family caregivers, homecare providers, and clients. Retrieved from http://ir.lib.uwo.ca/cgi/viewcontent.cgi?article=1573&context=etd.Google Scholar
Kothari, A., & Armstrong, R. (2011). Community-based knowledge translation: Unexplored opportunities. Implementation Science, 6(59). doi: 10.1186/1748-5908-6-59.CrossRefGoogle ScholarPubMed
Lussier, M., & Richard, C. (2008). Because one shoe doesn’t fit all. Canadian Family Physician, 54, 10891092.Google ScholarPubMed
Mahoney, E. K., Trudeau, S. A., Penyack, S. E., & MacLeod, C. E. (2006). Challenges to intervention implementation: Lessons learned in the bathing persons with Alzheimer’s disease at home study. Nursing Research, 55(2 Suppl), S10S16.Google Scholar
McWilliam, C. L. (2009). Patients, persons or partners? Involving those with chronic disease in their care. Chronic Illness, 4, 277292.CrossRefGoogle Scholar
McWilliam, C. L., Kothari, A., Ward-Griffin, C., Forbes, D., Leipert, B., & South West Community Care Access Centre Home Care Collaboration (SW-CCAC). (2009). Evolving the theory and praxis of knowledge translation through social interaction: A social phenomenological study. Implementation Science, 4, 26.CrossRefGoogle ScholarPubMed
McWilliam, C. L., Stewart, M., Brown, J. B., McNair, S., Desai, K., Patterson, M. L., et al. (1997). Creating empowering meaning: An interactive process of promoting health with chronically ill older Canadians. Health Promotion International, 12(2), 111123.CrossRefGoogle Scholar
Meijers, J. M., Janssen, M. A., Cummings, G. G., Wallin, L., Estabrooks, C. A., & Halfens, R. (2006). Assessing the relationships between contextual factors and research utilization in nursing: Systematic literature review. Journal of Advanced Nursing, 55, 622635.CrossRefGoogle ScholarPubMed
Nutley, S., Walter, I., & Davies, H. T. O. (2003). From knowing to doing: A framework for understanding the evidence-into-practice agenda. Evaluation, 9(2), 125148.Google Scholar
O’Rourke, N., Cappeliez, P., & Guindon, S. (2003). Depressive symptoms and physical health of caregivers of persons with cognitive impairment: Analysis of reciprocal effects over time. Journal of Aging and Health, 15, 688712.CrossRefGoogle ScholarPubMed
Peplau, H. (1997). Peplau’s theory of interpersonal relations. Nursing Science Quarterly, 10(4), 162167.CrossRefGoogle ScholarPubMed
Rycroft-Malone, J., Harvey, G., Seers, K., Kitson, A., McCormack, B., & Titchen, A. (2004). An exploration of the factors that influence the implementation of evidence into practice. Journal of Clinical Nursing, 13, 913924.Google Scholar
Sales, A. E., Estabrooks, C. A., & Valente, T. W. (2010). The impact of social networks on knowledge transfer in long-term care facilities: Protocol for a study. Implementation Science. 5(49), 549. doi: 10.1186/1748-5908.CrossRefGoogle ScholarPubMed
Schumacher, K. L., Koresawa, S., West, C., Hawkins, C., Johnson, C., Wais, E., et al. (2002). Putting cancer pain management regimens into practice at home. Journal of Pain and Symptom Management, 23, 369382.CrossRefGoogle ScholarPubMed
Scott-Findlay, S., & Pollock, C. (2004). Evidence, research, knowledge: A call for conceptual clarity. Worldviews on Evidence-Based Nursing, 1(2), 9297.CrossRefGoogle Scholar
Sims-Gould, J., & Martin-Matthews, A. (2010). We share the care: Family caregivers’ experiences of their older relative receiving home support services. Health and Social Care in the Community, 18, 415423.CrossRefGoogle ScholarPubMed
Stoltz, P., Lindholm, M., Uden, G., & Willman, A. (2006). The meaning of being supportive for family caregivers as narrated by registered nurses working in palliative homecare. Nursing Science Quarterly, 19, 163173.CrossRefGoogle ScholarPubMed
Van den Brink, Y. (2003). Diversity in care values and expressions among Turkish family caregivers and Dutch community nurses in the Netherlands. Journal of Transcultural Nursing, 14(2), 146154.Google Scholar
Ward-Griffin, C. (2001). Negotiating care of frail elders: Relationships between community nurses and family caregivers. The Canadian Journal of Nursing Research, 33(2), 6381.Google ScholarPubMed
Welch, M. (2005). Pivotal moments in the therapeutic relationship. International Journal of Mental Health Nursing, 14, 161165.CrossRefGoogle ScholarPubMed
Yorks, L. (2005). Adult learning and the generation of new knowledge and meaning: Creating liberating spaces for fostering adult learning through practitioner-based collaborative action inquiry. Teachers College Record, 107, 12171244.CrossRefGoogle Scholar
Zoffmann, V., & Kirkevold, M. (2005). Life versus disease in difficult diabetes care: Conflicting perspectives disempower patients and professionals in problem solving. Qualitative Health Research, 5, 750765.CrossRefGoogle Scholar