Hostname: page-component-586b7cd67f-t8hqh Total loading time: 0 Render date: 2024-11-25T20:14:26.608Z Has data issue: false hasContentIssue false

“Truly holistic?” Differences in documenting physical and psychosocial needs and hope in Portuguese palliative patients

Published online by Cambridge University Press:  25 June 2020

Miguel Julião*
Affiliation:
Equipa Comunitária de Suporte em Cuidados Paliativos de Sintra, Sintra, Portugal
Maria Ana Sobral
Affiliation:
Equipa Comunitária de Suporte em Cuidados Paliativos de Sintra, Sintra, Portugal
Paula Calçada
Affiliation:
Equipa Comunitária de Suporte em Cuidados Paliativos de Sintra, Sintra, Portugal
Bárbara Antunes
Affiliation:
Primary Care Unit - Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK Centro de Estudos e Investigação em Saúde da Universidade de Coimbra, Porto, Portugal Faculty of Medicine, University of Porto, Porto, Portugal King's College London, Department of Midwifery and Palliative Care, Florence Nightingale School of Nursing, London, UK
Baltazar Nunes
Affiliation:
Departamento de Epidemiologia, Instituto Nacional de Saúde Dr. Ricardo Jorge; Centro de Investigação em Saúde Pública, Escola Nacional de Saúde Pública, Universidade NOVA de Lisboa, Lisboa, Portugal
Ana Bragança
Affiliation:
Agrupamento de Centros de Saúde de Lisboa Central, Lisboa, Portugal
Daniela Runa
Affiliation:
Equipa Comunitária de Suporte em Cuidados Paliativos de Sintra, Sintra, Portugal
Paulo Faria de Sousa
Affiliation:
Equipa Comunitária de Suporte em Cuidados Paliativos de Sintra, Sintra, Portugal
Harvey Max Chochinov
Affiliation:
Department of Psychiatry, Research Institute of Oncology and Hematology, Cancer Care Manitoba, Manitoba, Canada
Eduardo Bruera
Affiliation:
Department of Palliative, Rehabilitation and Integrative Medicine, University of Texas MD Anderson Cancer Center, Houston, TX, USA
*
Author for correspondence: Miguel Julião, Equipa Comunitária de Suporte em Cuidados Paliativos de Sintra, Sintra, Portugal. E-mail: [email protected]

Abstract

Objective

Palliative care (PC) aims to improve patients' and families' quality of life through an approach that relieves physical, psychosocial, and spiritual suffering, although the latter continues to be under-assessed and under-treated. This study aimed to describe the prevalence of physical, psychosocial, and hope assessments documented by a PC team in the first PC consultation.

Method

The retrospective descriptive analysis of all first PC consultations registered in our anonymized database (December 2018–January 2020), searching for written documentation regarding (1) Edmonton Symptom Assessment Scale (ESAS) physical subscale (pain, tiredness, nausea, drowsiness, appetite, shortness of breath, constipation, insomnia, and well-being), (2) the single question “Are you depressed?” (SQD), (3) the question “Do you feel anxious?” (SQA), (4) feeling a burden, (5) hope-related concerns, (6) the dignity question (DQ), and (7) will to live (WtL).

Results

Of the 174 total of patients anonymously registered in our database, 141 PC home patients were considered for analysis; 63% were male, average age was 70 years, the majority had malignancies (82%), with a mean performance status of 52%. Evidence of written documentation was (1) ESAS pain (96%), tiredness (89%), nausea (89%), drowsiness (79%), appetite (89%), shortness of breath (82%), constipation (74%), insomnia (72%), and well-being (52%); (2) the SQD (39%); (3) the SQA (11%); (4) burden (26%); (5) hope (11%); (6) the DQ (33%); and (7) WtL (33%).

Significant differences were found between the frequencies of all documented items of the ESAS physical subscale (29%), and all documented psychosocial items (SQD + SQA + burden + DQ) (1%), hope (11%), and WtL (33%) (p = 0.0000; p = 0.0005; p = 0.0181, respectively).

Significance of results

There were differences between documentation of psychosocial, hope, and physical assessments after the first PC consultation, with the latter being much more frequent. Further research using multicenter data is now required to help identify barriers in assessing and documenting non-physical domains of end-of-life experience.

Type
Original Article
Copyright
Copyright © The Author(s), 2020. Published by Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Adler, ED, Goldfinger, JZ, Kalman, J, et al. (2000) Palliative care in the treatment of advanced heart failure. Circulation 120(25), 25972606.CrossRefGoogle Scholar
Ahluwalia, SC, Levin, JR, Lorenz, KA, et al. (2012) Missed opportunities for advance care planning communication during outpatient clinic visits. Journal of General Internal Medicine 27(4), 445451.CrossRefGoogle ScholarPubMed
Bernacki, RE and Block, SD (2014) Communication about serious illness care goals: A review and synthesis of best practices. JAMA Internal Medicine 174(12), 19942003.CrossRefGoogle ScholarPubMed
Bernardo, A (2005) Avaliação de Sintomas em Cuidados Paliativos (MSc thesis). Lisboa: Faculdade de Medicina da Universidade de Lisboa.Google Scholar
Bjørn, P, Burgoyne, S, Crompton, V, et al. (2009) Boundary factors and contextual contingencies: Configuring electronic templates for healthcare professionals. European Journal of Information Systems 18(5), 428441.CrossRefGoogle Scholar
Bostwick, D, Wolf, S, Samsa, G, et al. (2017) Comparing the palliative care needs of those with cancer to those with common non-cancer serious illness. Journal of Pain and Symptom Management 53(6), 10791084.e1.CrossRefGoogle ScholarPubMed
Breitbart, W (1995) Identifying patients at risk for, and treatment of major psychiatric complications of cancer. Support Care Cancer 3, 4560.CrossRefGoogle ScholarPubMed
Breitbart, W, Pessin, H, Rosenfeld, B, et al. (2018) Individual meaning-centered psychotherapy for the treatment of psychological and existential distress: A randomized controlled trial in patients with advanced cancer. Cancer 1, 124. (15), 3231–3239.Google Scholar
Capelas, M, Coelho, P, Murinello, AN, et al. (2019) Relatório de Outono 2019, Secçao Atividade Assistencial das Equipas/ Serviços de Cuidados Paliativos [Internet] (37 p.) Observatório Português dos Cuidados Paliativos. Available at: https://ics.lisboa.ucp.pt/asset/2751/file (accessed February 2020).Google Scholar
Chochinov, HM, Wilson KG, Enns, M, et al. (1995) Desire for death in the terminally ill. Amercian Journal of Psychiatry 152, 11851191.Google ScholarPubMed
Chochinov, HM, Wilson, KG, Enns, M, et al. (1997) Are you depressed?” Screening for depression in the terminally ill. Amercian Journal of Psychiatry 154(5), 674–6.Google ScholarPubMed
Chochinov, HM, McClement, S, Hack, T, et al. (2015) Eliciting personhood within clinical practice: Effects on patients, families, and health care providers. Journal of Pain and Symptom Management 49, 974–80.CrossRefGoogle ScholarPubMed
Csikai, EL and Weisenfluh, S (2013) Hospice and palliative social workers’ engagement in life review interventions. American Journal of Hospice and Palliative Medicine 30(3), 257263.CrossRefGoogle ScholarPubMed
Ferreira, F, Pinto, A, Laranjeira, A, et al. (2010) Validação da escala de Zarit: Sobrecarga do cuidador em cuidados paliativos domiciliários para população portuguesa. Cad Saúde 3, 13–9.Google Scholar
Foley, G, Timonen, V and Hardiman, O (2012a) Patients’ perceptions of services and preferences for care in amyotrophic lateral sclerosis: A review. Amyotrophic Lateral Sclerosis 13(1), 1124.CrossRefGoogle Scholar
Foley, G, Timonen, V and Hardiman, O (2012b) Experience of services as a key outcome in amyotrophic lateral sclerosis (ALS) care: The case for a better understanding of patient experiences. American Journal of Hospice and Palliative Medicine 29(5), 362367.CrossRefGoogle Scholar
Girgis, A, Johnson, C, Currow, D, et al. (2006) Palliative Care Needs Assessment Guidelines. Newcastle, NSW: The Centre for Health Research & Psycho-oncology.Google Scholar
Gore, JM, Brophy, CJ and Greenstone, MA (2000) How well do we care for patients with end stage chronic obstructive pulmonary disease (COPD)? A comparison of palliative care and quality of life in COPD and lung cancer. Thorax 55(12), 10001006.CrossRefGoogle ScholarPubMed
Granek, L, Nakash, O, Ariad, S, et al. (2019) Strategies and barriers in addressing mental health and suicidality in patients with cancer. Oncology Nursing of Forum 46(5), 561571.CrossRefGoogle ScholarPubMed
Greenberg, DB (2004) Barriers to the treatment of depression in cancer patients. JNCI Monographs 32, 127135.CrossRefGoogle Scholar
Holland, JC and Alici, Y (2010) Management of distress in cancer patients. Journal of Supportive Oncology 8, 412.Google ScholarPubMed
Hotopf, M, Chidgey, J, Addington-Hall, J, et al. (2002) Depression in advanced disease: A systematic review. Part 1. Prevalence and case finding. Palliative Medicine 16, 8197.CrossRefGoogle ScholarPubMed
Hui, D and Bruera, E (2016) Integrating palliative care into the trajectory of cancer care. Nature Reviews Clinical Oncology 13(3), 159–71.CrossRefGoogle ScholarPubMed
Hui, D and Bruera, E (2017) The Edmonton Symptom Assessment System 25 years later: Past, present, and future developments. Journal of Pain and Symptom Management 7(53), 630643.CrossRefGoogle Scholar
Julião, M, Barbosa, A, Oliveira, F, et al. (2013) Efficacy of dignity therapy for depression and anxiety in terminally ill patients: Early results of a randomized controlled trial. Palliative Support Care 11(6), 481–9.CrossRefGoogle ScholarPubMed
Julião, M, Oliveira, F, Nunes, B, et al. (2014) Efficacy of dignity therapy on depression and anxiety in Portuguese terminally ill patients: A phase II randomized controlled trial. Journal of Palliative Medicine 17(6), 688–95.CrossRefGoogle ScholarPubMed
Julião, M, Nunes, B, Sobral, MA, et al. (2016) Is it useful to ask “Está deprimido?” (“Are you depressed?”) to terminally-ill Portuguese patients? Results from outpatient research. Palliative Support Care 14(2), 138–41.CrossRefGoogle ScholarPubMed
Julião, M, Oliveira, F, Nunes, B, et al. (2017) Effect of dignity therapy on end-of-life psychological distress in terminally ill Portuguese patients: A randomized controlled trial. Palliative Support Care 15(6), 628637.CrossRefGoogle ScholarPubMed
Julião, M, Courelas, C, Costa, MJ, et al. (2018) The Portuguese versions of the This Is ME Questionnaire and the Patient Dignity Question: Tools for understanding and supporting personhood in clinical care. Annals of Palliative Medicine 7(Suppl. 3), S187S195.CrossRefGoogle ScholarPubMed
Julião, M, Antunes, B, Nunes, B, et al. (2020) Measuring total suffering and will to live in an advanced cancer patient using a patient-centered outcome measure: A follow-up case study. Journal of Palliative Medicine.23.5.733737.CrossRefGoogle Scholar
Kelly, B, McClement, S and Chochinov, HM (2006) Measurement of psychological distress in palliative care. Palliative Medicine 20(8), 779–89.CrossRefGoogle ScholarPubMed
Kristeller, JL, Zumbrun, CS and Schilling, RF (1999) ‘I would if I could:’ How oncologists and oncology nurses address spiritual distress in cancer patients. Psychooncology 8(5), 451–58.3.0.CO;2-3>CrossRefGoogle Scholar
Maguire, P (1985) Improving the detection of psychiatric problems in cancer patients. Social Science & Medicine 20, 819823.CrossRefGoogle ScholarPubMed
Mathioudakis, A, et al. (2016) How to keep good clinical records. Breathe 12, 371375.CrossRefGoogle ScholarPubMed
Meakin, CJ (1992) Screening for depression in the medically ill. The future of paper and pencil tests. British Journal of Psychiatry 160, 212216.CrossRefGoogle ScholarPubMed
Møller, NH and Bjørn, P (2011) Layers in sorting practices: Sorting out patients with potential cancer. Computer Supported Cooperative Work 20(3), 123153.CrossRefGoogle Scholar
Mørck, P, Langhoff, TO, Christophersen, M, et al. (2018) Variations in oncology consultations: How dictation allows variations to be documented in standardized ways. Computer Supported Cooperative Work 27, 539568.CrossRefGoogle Scholar
Murillo, M and Holland, JC (2004) Clinical practice guidelines for the management of psychosocial distress at the end of life. Palliative Support Care 2, 6577.CrossRefGoogle ScholarPubMed
Nakash, O, Levav, I, Aguilar-Gaxiola, S, et al. (2014). Comorbidity of common mental disorders with cancer and their treatment gap: Findings from the World Mental Health Surveys.Google Scholar
Palliative Care Needs Assessment Guidance (2014) The National Clinical Programme for Palliative Care, HSE Clinical Strategy and Programmes Division [Internet] (13 p.). Available at: www.hse.ie/palliativecareprogramme (revised January 2016; accessed February 2020).Google Scholar
Rankin, NM, Butow, PN, Thein, T, et al. (2015) Everybody wants it done but nobody wants to do it: An exploration of the barrier and enablers of critical components towards creating a clinical pathway for anxiety and depression in cancer. BMC Health Services Research 15, 28.CrossRefGoogle Scholar
Riba, MB, Donovan, KA, Andersen, B, et al. (2019) Distress management, version 3.2019, NCCN clinical practice guidelines in oncology. Journal of the National Comprehensive Cancer Network: JNCCN 17(10), 12291249.CrossRefGoogle Scholar
Saracino, RM, Rosenfeld, B, Breitbart, W, et al. (2019) Psychotherapy at the end of life. American Journal of Bioethics 19(12), 1928.CrossRefGoogle ScholarPubMed
Steinhauser, KE, Christakis, NA, Clipp, EC, et al. (2000) Factors considered important at the end of life by patients, family, physicians, and other care providers. JAMA 284(19), 24762482.CrossRefGoogle ScholarPubMed
van der Eijk, M, Faber, MJ, Al Shamma, S, et al. (2011) Moving towards patient-centered healthcare for patients with Parkinson's disease. Parkinsonism and Related Disorders 17(5), 360364.CrossRefGoogle ScholarPubMed
Wenger, NS, Solomon, DH, Roth, CP, et al. (2003) The quality of medical care provided to vulnerable community-dwelling older patients. Annals of Internal Medicine 139(9), 740747.CrossRefGoogle ScholarPubMed