Open Access Open Access  Restricted Access Subscription Access

From reactive to proactive basic palliative hospital care. Evaluation of one-nurse-based telephone follow-up and bedside consultation to advanced gastrointestinal cancer patients and informal caregivers: A quasi-experimental study

Lisbeth Soelver, Marianne Krogsgaard

Abstract


Rationale and aim: Organizational and staff-related barriers need to be overcome in order to integrated early palliative care and develop its supporting infrastructure. We aimed to evaluate the use of a one-nurse-staffed telephone line and bedside consultations on a surgical ward.

Method: Advanced gastrointestinal cancer patients and their relatives are offered at diagnosis telephone contact with a nurse with a specialism experience and expertise in the field of palliative care – the contact is lifelong. A proactive holistic approach is taken, including individual needs assessment, guidance, regulation of medication and a tight follow-up. The nurse also acts as a sparring advice partner for colleagues and facilitates complex situations and process. Contacts are described qualitatively in a logbook and the effect on the incidence of hospital admissions and hospital deaths was investigated using a quasi-experimental design with a historical control group. Data were processed using descriptive statistics and Chi-squared (x 2) test.

Results: Over 9 month 131 patients and 427 consultations were registred. Outgoing telephone calls to patients, caregivers and professionals (40%). Incoming phone calls (31%) and in-person meeting with patients and families during hospitalization or outpatient visits (29%). Over 15 month intervention and control period the test showed a significant reduction in the short-term admissions of  < 2 days, and a significant reduction in the number of patients who died during hospitalization.

Conclusion: The telephone follow-up and bedside consultations by one qualified nurse, is an interface that supports continuity and cooperation and could underpine more effective basic palliative care.


Full Text:

PDF

References


Radbruch, L., Payne, S. and EAPC Board of Directors (2009) White Paper on Standards and norms for hospice and palliative care in Europe: part 1. European Journal of Palliative Care, 16(6), 278-302.

Murray, S.A., Kendall, M., Boyd, K., Sheikh, A. (2005) Ilness trajectories and palliative care. British Medical Journal, 330(7498), 1007-1011.

Klint, A., Engholm, G., Storm, H.H., Tryggvadôttir, L., Gislum, M., Hakulinen, T., Bray, F. (2010) Trends in survival of patients diagnosed with cancer of the digestive organs in the Nordic countries 1964-2003 followed up to the end of 2006. Acta Oncologica, 49(5), 578-607.

Uitdehaag, M.J., Verschuur, E.M.L., van Eijck, C.H.J., van der Gaast, A., van der Rijt, C.C.D., de Man, R.A., Steyerberg, E.,W., Kuipersa, E.J., Siersema, P.D. (2015) Problems and Needs in Patients With Incurable Esophageal and Pancreaticobiliatry Cancer. Gastroenterology Nursing, 38(1), 42-54.

WHO. National Cancer Programmes (2002) Policies and manageria guidelines. 2nd ed. Geneva: World Health Organization.

Penrod, J. (2007) Living with uncertainty: concept advancement. Journal of Advanced Nursing, 57(6), 658-667.

Brant, J.M. (2010) Palliative Care for Adults Across the Cancer Trajectory: From Diagnosis to End of Life. Seminars in Oncology Nursing, 26(4), 222-230.

Haggerty, J.L., Reid, R.J., Freeman, G.K., Starfield, B.H., Adair, C.E., McKendry, R. (2003) Continuity of care: a multidisciplinary review. British Medical Journal, 327(7425), 1219-1221.

Centeno, C., Clark, D., Lynch, T., Rocafort, J., Praill, D., De Lima, L., Greenwood, A., Flores, L.A., Brasch, S., Giordan, A. (2007) Facts and indicators on palliative care development in 52 countries of the WHO European region: results of an EAPC Task Force. Palliative Medicine, 21(6), 463-471.

Ahmedzai, S.H, Costa, A., Blengini, C., Bosch, A., Sanz-Ortiz, J., Ventafridda, V., Verhagen, S.C. (2004) A new international framework for palliative care. European Journal of Cancer, 40(15), 2192-2200.

Beernaert, K., Deliens, L., De Vleminck, A., Devroey, D., Pardon, K., Van den Block, L., Cohen, J. (2014) Early identification of palliative care needs by family physicians: A qualitative study of barriers and facilitators freom the perspective of family physiciens, community nurses, and patients. Palliative Medicine, 28(6), 480-490.

Aabom, B., Pfeiffer, P. (2009) Why are some patients in treatment for advanced cancer reluctant to consult their GP? Scandinavian Journal of Primary Health Care, 27, 58-62.

Robinson, J., Gott, M., Gardiner, C., Ingleton, C. (2015) A qualitative study exploring the benefits of hospital admissions from the perspectives of patients with palliative care needs. Palliative Medicine, 29(8), 703-710.

Jarlbaek, L., Timm, H. (2013) Hospitalernes palliative indsats på basalt niveau. En landsdækkende kortlægning blandt afdelingsledelser. Palliativt Videnscenter. [Basic palliative hospital care in Denmark mapping 2011-2013. Danish Knowledge Center for Palliative Care].

Christiansen, A.H., Lipczak, H. (2014) Kræftpatienters sikkerhed i sundhedsvæsnet efter kræftbehandling. En analyse af rapporter fra Dansk Patientsikkerhedsdatabase. Kræftens Bekæmpelse.[Patient safety after cancer treatment. The Danish Cancer Society]. www. cancer dk/rapporter.

Dietz, I., Borasio, G.D., Molnar, C., Müller-Busch, C., Plog, A., Schneider, G., Jox, R.J. (2013) Errors in Palliative Care: Kinds, Caused Consequences: A Pilot Survey of Experiences and Attitudes of Palliative Care Professionals. Journal of Palliative Medicine, 16(1), 74-81.

Johnsen, A.T., Petersen, M.A., Pedersen, L., Houman, L.J., Groenvold, M. (2013) Do advanced cancer patients in Denmark receive the help they need? A nationally representative survey of the need related to 12 frequent symptoms/problems. Psycho-Oncology, 22(8), 1724-1730.

Laugsand, E.A., Jakobsen, G. Kaasa, S., Klepstad, P. (2011) Inadequate symptom control in advanced cancer patients across Europe. Supportive Care in Cancer, 19(12), 2005-2014.

Sandgren, A., Fridlund, B., Nyberg, P., Strang, P., Petersson, K., Thulesius, H. (2010) Symptoms, care needs and diagnosis in palliative cancer patients in acute care hospital: a 5-year follow-up survey. Acta Oncologica, 49(4), 460-466.

Aabom, B., Kragstrup, J., Vondeling, H., Bakketeig, L., Støvring, H. (2005) Population-based study of place of death of patients with cancer:implications for GPs. British Journal of General Practice, 55(518), 684-689.

Dalgaard, K.M., Bergenholtz, H., Nielsen, M.E., Timm, H. (2014) Early integration of palliative care in hospitals: A systematic review on methods, barriers, and outcome. Palliative and Supportive Care,12(6),495-513.

Soelver, L., Rydahl-Hansen, S., Oestergaard, B., Wagner, L. (2014) Identifying factors significant to continuity in basic palliative hospital care - from the perspective of patients with advanced cancer. Psycho-Oncology, 32, 167-188.

Lund, L., Ross, L., Petersen, M., Groenvold, M. (2015) The interaction between informal cancer caregivers and health care professionals: a survey of caregivers' experiences of problems and unmet neds. Supportive Care in Cancer, 23, 1719-1733.

Schwartz, D., Lellouch J. (2009) Explanatory and Pragmatic Attitudes in Therapeutical Trials. Journal of clinical epidemiology, 62, 499-505.

Meleis, A.I., Sawyer, L.M., Eun-Ok, I., Hilfinger, M.D.K., Schumacher, K. (2000) Experiencing transitions: an Emerging Middle-Range Theory. Advances in Nursing Science, 23(1), 12-28.

Honneth, A. (2003) Usynlighed - om 'anerkendelsens' erkendelsesteori. Behovet for anerkendelse. [Die soziale Dynamik von Missachtung Zur Ortsbestimmung einer kritischen Gesellschaftstheorie] pp. 98-117. Denmark: Hans Reitzels Forlag.

Zhou, M., Holden, L., Bedard, G., Zeng, L., Lam, H., Chu, D., Lao, N., Lauzon, N., Chow, E. (2012) The utilization of telephone follow-up in the advanced cancer population: a review of the literature. Comparative Effectiveness Research, 1(6), 509-517.

Danish National Board of Health (Sundhedsstyrelsen) (1998) Bekendtgørelse om information og samtykke og videregivelse af helbredsoplysninger m.v. Bek. nr. 665 [Executive order regarding information and consent and disclosure of health information]. Available at: https://www.retsinformation.dk/. Accessed 10. Oktober, 2015.

World Health Organization. International Classification of Diseases (ICD) Information Sheet: Available at: http://www.who.int/classifications/icd/factsheet/en/. Accessed 23. November, 2015.

Daveson, B., Harding, R., Shipman, C., et al. (2014) The Real-World Problem of Care Coordination: A Longitunal Qualitative Study with Patients Living with Advanced Progressive Illness and Their Unpaid Caregivers. PLOS ONE, 9(5), 1-12.

Thorne, S., Kuo, M., Armstrong, A., Mcpherpson, G., Harris, S., Hislop, T. (2005) 'Being known': Patients' perspectives of the dynamics of human connection in cancer care. Psycho-Oncology,14, 887-898.

Freeman, H., Rodriguez, R. (2011) History and Principles of Patient Navigation. Cancer, 3539-3542.

May, M., Woldhuis, C., Taylor, W.K., McCahill, L.E. (2014) Gastrointestinal Nurse Navigation: Implementation of a Novel Role. Clinical Journal of Oncology Nursing, 18(2), 193-199.

Thygesen, M.K., Pedersen, B.D., Kragstrup, J., Wagner, L., Mogensen, O. (2012) Benefits and challenges perceived by patients with cancer when offered a nurse navigator. International Journal of Integrated Care, 12, 168.

Gagnon, J., Duggleby, W. (2014)The provision of end-of-life care by medical-surgical nurses working in acute care: A literature review. Palliative and Supportive Care, 12, 393-408.

Parry, R., Land, V., Seymour, J. (2014) How to communicate with patients about future illness progression and end of life: a systematic review. BMJ Suppportive & Palliative Care, 4, 331-341.

Gittell, J. (2002) Coordinating mechanisms in care provider groups: Relational coordination as a mediator and input uncertainty as a moderator of performance effects. Management Science, 48(11), 1408-1426.

Gott, M., Frey, R., Robinson, J., Boyd, M., O'Callaghan, A., Richards, N., Snow, B. (2013) The nature of, and reasons for, inappropriate' hospitalisations among patients with palliative care needs: A qualitative exploration of the views of generalist palliative care providers. Palliative Medicine, 27(8), 747-756.

Grim, R.D., McElwain, D., Hartmann, R., Hudak, M., Yuoung, S. (2010) Evaluating Causes for Unplanned Hospital Readmissions of Palliative Care Patients. American Journal of Hospice & Palliative Medicine, 27(8), 526-531.

Paris, J., Morrison, R.S. (2014) Evaluating the Effects of Inpatient Palliative Care Consultations on Subsequent Hospice Use and Place of Death in Patients With Advanced GI Cancer. Journal of Oncology Practice, 10(3), 177.

Brogaard, T., Neergaard, M.A., Sokolowski, I., Olesen, F., Jensen, A.B. (2013) Congruence between preferred and actual place of care and death among Danish cancer patients. Palliative Medicine, 27(2), 155-164.

Barnes, K., Barlow, C., Harrington, J., Ornadel, K., Tookman, A., King, M., Jones, L. (2011) Advance care planning discussions in advanced cancer: Analysis of dialogues between patients and care planning mediators. Palliative and Supportive Care, 9, 73-79.

Bakitas, M.A., Tosteson, T.D., Li ,Z., et al. (2015) Early Versus Delayed Initiation of Concurrent Palliative Oncology Care: Patient Outcomes in the ENABLE III Randomized Controlled Trial. Journal of Clinical Oncology,33(13), 1438-1445.

Starks, H., Diehr P., Curtis, J.R. (2009) The Challenge of Selection Bias and Confounding in Palliative Care Research. Palliative Medicine, 12(2), 181-187.

Kirkwood, B.R., Sterne, A.C. (2006) Medical Statistics. Second ed. Oxford UK: Blackwell Science Ltd.

Simon, S., Higginso, I. (2009) Evaluation of hospital palliative care teams: strengths and weaknesses of the before-after study design and strategies to improve it. Palliative Medicine, 23, 23-29.

Sturmberg, J., Topolski, S. (2014) For every complex problem, there is an answer that is clear, simple and wrong. Journal of Evaluation in Clinical Practice, 20, 1017-1025.

Craig, P., Dieppe, P., MaCintyre, S., Mitchi, S., Nazareth, I., Petticrew, M. (2008) Developing and evaluating complex interventions: the new Medical Research Council guidance. British Medical Journal, 337, 979-983.

Datta, J., Petticrew, M. (2013) Challenges to evaluating complex interventions: a content analysis of published papers. BMC Public Health, 13, 568.




DOI: http://dx.doi.org/10.5750/ejpch.v4i2.1141

Refbacks

  • There are currently no refbacks.