Patient and physician perceptions of palliative care during transplant

Definitions of palliative care can vary and the term is often subject to stigma due to associations with hospice and end-of-life care. In the context of patients undergoing hematopoietic stem cell transplantation (HSCT), palliative care can help patients to manage their symptoms and allow for advance care planning. However, perceptions of what palliative care is can vary between patients and physicians.

Here, we summarize two studies from the perspective of patient’s experiences with palliative care; one presented as a poster at the 2022 Society of Hematologic Oncology (SOHO) Annual Meeting by Melody et al.¹ and one published by Gemmell et al.² In addition, we summarize a study by Santivasi et al.³, which focusses on physician perspectives of palliative care.

Patient perceptions

In the study by Melody et al.¹, 32 patients who were undergoing evaluation for allogeneic HSCT were also referred for a palliative care consultation and asked to fill out a pre- and post-visit questionnaire. Results from two questions in this questionnaire are shown in Figure 1 and Figure 2. These figures highlight changes in patient knowledge and opinion of palliative care after a consultation.

*Data from Melody, et al.¹

 

*Data from Melody, et al.¹

In the study by Gemmell et al.², 12 patients were interviewed, and four patients took part in a focus group (used to survey patients pre- and post-transplant). These were semi-structured and used the idea of themes to identify patient thoughts about palliative care, which are illustrated in Figure 3. Physician knowledge of patient thoughts about palliative care and what they require from their care could potentially improve communication between patients and physicians and increase uptake of palliative care. It is important to note that all 12 interview patients had no experience with palliative care and two of the focus group patients had direct experience with palliative care during transplant.

HCPs, healthcare professionals; HSCT, hematopoietic stem cell transplantation; PC, palliative care.
*Data from Gemmell, et al.²

Physician perceptions

In the study by Santivasi et al.³, 1,000 palliative care physicians were emailed a survey about comfort discussing prognosis with patients, palliative care, and relationships with hematologists. The response rate of the survey was 55.5%. Figure 4 and Figure 5 illustrate some results from the survey, focused on prognosis discussion and the factors that can influence a patient receiving a palliative care consultation. Overall, physicians reported feeling less comfortable in providing symptom management, discussing prognosis, and understanding disease trajectory for patients undergoing HSCT compared to patients with leukemia, lymphoma, or multiple myeloma.

*Adapted from Santivasi, et al.³

 

PC, palliative care; PS, performance status.
*Adapted from Santivasi, et al.³

Key findings

• Patient knowledge of what palliative care is increased after a palliative care consultation. Prior to a palliative care consultation, 28% of patients reported having “good” or “excellent” knowledge of palliative care. After a consultation, 78% of patients reported having “good” or “excellent” knowledge of palliative care (13 out of 32 patients said “good” and 12 out of 32 patients said “excellent”).¹
• After a consultation, patients feel more comfortable about palliative medicine and are more likely to continue to use it during transplant.¹
• As Figure 3 shows, patients who have not had experience with palliative care could benefit from receiving it to help them manage symptoms and to feel that they are part of the decision-making process of their care. However, stigma around palliative care may have prevented them from utilizing it in the past.²
• Figure 4 highlights that palliative care physicians may not always feeling comfortable discussing prognosis with their patients, with some suggesting a multidisciplinary approach involving hematologists would be favorable.³
• There are many factors that may affect a patient’s ability to access palliative care, meaning some patients may not be benefiting from treatment that could improve their quality of life during transplant. Patients with uncertain prognosis are less likely to be offered palliative care than patients with an end-of-life prognosis.³

Conclusion

As shown in these three studies, patient and physician perceptions of what palliative care can offer may differ. Transplant patients with no direct experience with palliative care may not understand what it can offer in terms of symptom management and advance care planning. However, as patients are more likely to utilize palliative care during their transplant after receiving a consultation, increasing knowledge of palliative care in transplant patients may result in a wider uptake. Ending the stigma around palliative care and improving the relationship between healthcare professionals and their patients could also mean more patients becoming accepting of palliative care. In addition, the quality of palliative care consultations could be improved by increasing physician comfort in explaining diagnoses; this could be done by increasing clinical experience with HSCT and promoting relationships between palliative care physicians and hematologists.