scholarly journals Barriers and Facilitators to Effective Inpatient Palliative Care Consultations: A Qualitative Analysis of Interviews With Palliative Care and Nonpalliative Care Providers

2018 ◽  
Vol 36 (3) ◽  
pp. 191-199 ◽  
Author(s):  
Meghan McDarby ◽  
Brian D. Carpenter

Objective: To identify factors that hinder or facilitate the palliative care consultation team’s (PCCT) successful collaboration with other providers from the perspectives of both PCCT and nonpalliative specialists. Methods: Qualitative study, including semistructured interviews with PCCT and nonpalliative care providers from various specialties at 4 Midwestern hospitals. Interviews were audio-recorded and transcribed into written text documents for thematic analysis. Palliative care consultation team (n = 19) and nonpalliative care providers (n = 29) were interviewed at their respective hospital sites or via telephone. Palliative care consultation team providers included physicians, nurse practitioners, registered nurses, social workers, and one chaplain. Specialists included critical care physicians, surgeons, hospitalists, nephrologists, oncologists, and cardiologists. Results: Six themes emerged reflecting barriers to and facilitators of successful collaboration between the PCCT and other providers. Primary barriers included attitudes about palliative care, lack of knowledge about the role of the PCCT, and patient and family resistance. Facilitators included marketing of the palliative care service and education about the expertise of the PCCT. Conclusion: In order to engage in more effective collaboration with other specialty providers, the PCCT may consider strategies including structured educational interventions, increased visibility in the hospital, and active marketing of the utility of palliative care across disciplines.

Blood ◽  
2018 ◽  
Vol 132 (Supplement 1) ◽  
pp. 2242-2242
Author(s):  
Rika Kihara ◽  
Yumi Ishiguri ◽  
Norihiro Ueda ◽  
Yasuyuki Asai ◽  
Takuya Odagiri ◽  
...  

Abstract Previous research demonstrated that patients with hematologic malignancies have a high probability receiving intensive care at their end-of-life (EOL). In this study, we assessed EOL quality measures in patients with hematologic malignancies before and after starting the provision of a specialist palliative care service. We conducted a retrospective cohort study in Komaki City Hospital. Provision of the specialist palliative care service was started in our hospital on April 1, 2012. We reviewed the medical records of all adult patients who died of hematologic malignancies between April 1, 2007 and March 31, 2017. Patients who had been cared for in the Departments of Hematology and Palliative Care were included. This study was approved by the institutional review board of Komaki City Hospital. We assessed the prevalence and trends of multiple measures of intensive EOL care established in the peer-reviewed literature. Intensive EOL care was defined as the occurrence of at least one of the following acts: 1) cardiopulmonary resuscitation (CPR) in the last 30 days of life, 2) intubation in the last 30 days of life, 3) intensive care unit (ICU) admission in the last 30 days of life, 4) chemotherapy use within the last 14 days of life, 5) receiving red cell transfusions within the 7 days before death, and 6) receiving platelet transfusion within the 7 days before death. Analysis of frequencies was performed using Fisher's exact test for 2 x 2 tables. The Cochran-Armitage test was used to test for trends over time. A total of 351 consecutive patients who died from hematologic malignancies were identified: 176 before and 175 after April 1, 2012. The median age at death was 73 years old. These included 150 patients with non-Hodgkin lymphoma, 113 with acute myeloid leukemia, 63 with multiple myeloma, 11 with acute lymphoblastic leukemia, 8 with chronic lymphocytic leukemia, and 5 with Hodgkin lymphoma. A total of 69 (39%) received specialist palliative care consultation and 24 (14%) died in the palliative care unit (PCU) after April 2012. Deaths in the PCU increased from 1 (2%) in 2012 to 8 (27%) in 2016 (P for trend <0.001). The median time from palliative care referral to death was 26 days (interquartile range [IQR]: 10-49 days). The length of stay in the PCU was 16 days (IQR: 9.5-22.5 days). Cases of CPR in the last 30 days of life decreased from 4 (13%) in 2007 to 0 in 2016 (P for trend <0.001). Intubations in the last 30 days of life also decreased from 2 (6%) in 2007 to 1 (3%) in 2016 (P for trend 0.046). Platelet transfusions within 7 days before death decreased from 18 (56%) in 2007 to 14 (47%) in 2016 (P for trend 0.031). There were no significant decreases in ICU admissions in the last 30 days of life, chemotherapy use within the last 14 days of life, or receiving red cell transfusions within 7 days before death from 2007 to 2016. Patients receiving at least one act of intensive EOL care significantly decreased from 23 (72%) in 2007 to 19 (63%) in 2016 (P for trend 0.019). Compared with patients with acute leukemia (AL), those with malignant lymphoma (ML) were more likely to receive specialist palliative care consultation (49% vs. 27%, respectively; P=0.010) and die in the PCU (21% vs. 5%, respectively; P=0.007). In patients with ML, deaths in the PCU increased from 1 (5%) in 2012 to 7 (50%) in 2016 (P for trend <0.001). In patients with ML, cases of chemotherapy use within the last 14 days of life decreased from 5 (22%) in 2007 to 2 (14%) in 2016 (P for trend 0.030). Patients with ML who received palliative care consultation were less likely to receive platelet transfusion within 7 days before death compared with those who did not (28% vs. 51%, respectively; P=0.041). In patients with ML, those receiving at least one act of intensive EOL care significantly decreased from 11 (65%) in 2007 to 5 (35%) in 2016 (P for trend <0.001). In patients with AL, there was no significant difference in chemotherapy use within the last 14 days of life or receiving transfusions within 7 days before death between patients who received specialist palliative care and those who did not. All patients with AL received at least one act of intensive EOL care in 2016. These findings suggest that specialist palliative care improved the quality of EOL care in patients with hematologic malignancies, especially in those with ML. However, in patients with AL, EOL care is still suboptimal with the provision of specialist palliative care. Disclosures No relevant conflicts of interest to declare.


2017 ◽  
Vol 32 (1) ◽  
pp. 36-45 ◽  
Author(s):  
Caroline Shulman ◽  
Briony F Hudson ◽  
Joseph Low ◽  
Nigel Hewett ◽  
Julian Daley ◽  
...  

Background: Being homeless or vulnerably housed is associated with death at a young age, frequently related to medical problems complicated by drug or alcohol dependence. Homeless people experience high symptom burden at the end of life, yet palliative care service use is limited. Aim: To explore the views and experiences of current and formerly homeless people, frontline homelessness staff (from hostels, day centres and outreach teams) and health- and social-care providers, regarding challenges to supporting homeless people with advanced ill health, and to make suggestions for improving care. Design: Thematic analysis of data collected using focus groups and interviews. Participants: Single homeless people ( n = 28), formerly homeless people ( n = 10), health- and social-care providers ( n = 48), hostel staff ( n = 30) and outreach staff ( n = 10). Results: This research documents growing concern that many homeless people are dying in unsupported, unacceptable situations. It highlights the complexities of identifying who is palliative and lack of appropriate places of care for people who are homeless with high support needs, particularly in combination with substance misuse issues. Conclusion: Due to the lack of alternatives, homeless people with advanced ill health often remain in hostels. Conflict between the recovery-focused nature of many services and the realities of health and illness for often young homeless people result in a lack of person-centred care. Greater multidisciplinary working, extended in-reach into hostels from health and social services and training for all professional groups along with more access to appropriate supported accommodation are required to improve care for homeless people with advanced ill health.


2009 ◽  
Vol 8 (1) ◽  
Author(s):  
Carlos Centeno ◽  
María Angustias Portela ◽  
Antonio Noguera ◽  
Antonio Idoate ◽  
Álvaro Sanz Rubiales

2020 ◽  
Vol 73 (6) ◽  
Author(s):  
Magda Aparecida dos Santos Silva ◽  
Marcio Augusto Diniz ◽  
Ricardo Tavares de Carvalho ◽  
Toshio Chiba ◽  
Cibele Andrucioli de Mattos-Pimenta

ABSTRACT Objective: To compare the relief of symptoms provided by palliative care consultation team (PCCT) compared to the traditional care team (TC), in patients with advanced cancer in the first 48 hours of hospitalization. Method: Allocated to PCCT Group and TC Group, this study assessed 290 patients according to the Edmonton Symptom Assessment System (ESAS) within the first 48 hours of hospitalization. The main outcome was a minimum 2-point reduction in symptom intensity. Results: At 48 hours, the PCCT Group had a 2-point reduction in the mean differences (p <0.001) in pain, nausea, dyspnea, and depression; and TC Group, on nausea and sleep impairment (p <0.001). Multiple Logistic Regression found for the PCCT Group a greater chance of pain relief (OR 2.34; CI 1.01-5.43; p = 0.049). Conclusion: There was superiority of the PCCT Group for pain relief, dyspnea and depression. There is a need for more studies that broaden the understanding of team modalities.


2013 ◽  
Vol 28 (4) ◽  
pp. 312-317 ◽  
Author(s):  
Amy Chang ◽  
Indrany Datta-Barua ◽  
Beth McLaughlin ◽  
Barbara Daly

2017 ◽  
Vol 31 (4) ◽  
pp. 378-386 ◽  
Author(s):  
Peter May ◽  
Melissa M Garrido ◽  
J Brian Cassel ◽  
Amy S Kelley ◽  
Diane E Meier ◽  
...  

Background: Studies report cost-savings from hospital-based palliative care consultation teams compared to usual care only, but drivers of observed differences are unclear. Aim: To analyse cost-differences associated with palliative care consultation teams using two research questions: (Q1) What is the association between early palliative care consultation team intervention, and intensity of services and length of stay, compared to usual care only? (Q2) What is the association between early palliative care consultation team intervention and day-to-day hospital costs, compared to a later intervention? Design: Prospective multi-site cohort study (2007–2011). Patients who received a consultation were placed in the intervention group, those who did not in the comparison group. Intervention group was stratified by timing, and groups were matched using propensity scores. Setting/participants: Adults admitted to three US hospitals with advanced cancer. Principle analytic sample contains 863 patients ( nUC = 637; nPC EARLY = 177; nPC LATE = 49) discharged alive. Results: Cost-savings from early palliative care accrue due to both reduced length of stay and reduced intensity of treatment, with an estimated 63% of savings associated with shorter length of stay. A reduction in day-to-day costs is observable in the days immediately following initial consult but does not persist indefinitely. A comparison of early and late palliative care consultation team cost-effects shows negligible difference once the intervention is administered. Conclusion: Reduced length of stay is the biggest driver of cost-saving from early consultation for patients with advanced cancer. Patient- and family-centred discussions on goals of care and transition planning initiated by palliative care consultation teams may be at least as important in driving cost-savings as the reduction of unnecessary tests and pharmaceuticals identified by previous studies.


2008 ◽  
Vol 11 (2) ◽  
pp. 191-197 ◽  
Author(s):  
Navneet Dhillon ◽  
Scott Kopetz ◽  
Be Lian Pei ◽  
Egidio Del Fabbro ◽  
Tao Zhang ◽  
...  

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