Publications by authors named "Erik Fromme"

Article Synopsis
  • - Dashboards in health systems help track and improve serious illness conversation (SIC) quality indicators, but the effectiveness and challenges of these dashboards are still not fully understood.
  • - Interviews with palliative care leaders revealed that while dashboards can enhance data transparency and support clinician practice changes, they rely heavily on structured documentation that clinicians don't always use effectively.
  • - Key challenges include ensuring the reliability of data, securing necessary resources for dashboard maintenance, and integrating patient-centered outcome measures, which may hinder the overall effectiveness of these tools in practice.
View Article and Find Full Text PDF
Article Synopsis
  • Interventions aimed at improving care for seriously ill patients often do not reach marginalized communities, including racialized, indigenous, and rural populations, despite their demonstrated benefits.
  • The study focused on understanding the implementation of the Serious Illness Care Program in healthcare systems that primarily serve these underserved groups by conducting qualitative interviews and focus groups with healthcare team members.
  • Three main themes were identified regarding implementation factors: patient-related challenges, specific elements of the intervention, and the health system's context; notable barriers include resource limitations and mistrust in healthcare, while mission-driven efforts and interprofessional collaboration were seen as supportive factors.
View Article and Find Full Text PDF

The Serious Illness Care Program was developed to support goals and values discussions between seriously ill patients and their clinicians. The , that is, the essential clinical conversation skills that are described as requisite for effective serious illness conversations (SICs) in practice, have not yet been explicated. This integrative systematic review aimed to identify core competencies for SICs in the context of the Serious Illness Care Program.

View Article and Find Full Text PDF

Objectives: POLST is widely used in the care of seriously ill patients to document decisions made during advance care planning (ACP) conversations as actionable medical orders. We conducted an integrative review of existing research to better understand associations between POLST use and key ACP outcomes as well as to identify directions for future research.

Design: Integrative review.

View Article and Find Full Text PDF
Article Synopsis
  • The study evaluated a patient-friendly Workbook designed to help seriously ill patients and their caregivers engage in important conversations about their care.
  • Twenty-nine participants provided feedback through surveys and in-depth interviews, highlighting the Workbook's safety, acceptability, and ease of use, with ratings indicating generally positive responses.
  • The findings suggest that the Workbook is most effective when introduced by a trusted individual, emphasizing the importance of context and rapport in discussions about serious illness.
View Article and Find Full Text PDF

Background: Serious illness communication is a key element of high-quality care, but it is difficult to implement in practice. The Serious Illness Care Program (SICP) is a multifaceted intervention that contributes to more, earlier, and better serious illness conversations and improved patient outcomes. This qualitative study examined the organizational and implementation factors that influenced improvement in real-world contexts.

View Article and Find Full Text PDF

Objective: Communication about patients' values, goals, and prognosis in serious illness (serious illness communication) is a cornerstone of person-centered care yet difficult to implement in practice. As part of Serious Illness Care Program implementation in five health systems, we studied the clinical culture-related factors that supported or impeded improvement in serious illness conversations.

Methods: Qualitative analysis of semi-structured interviews of clinical leaders, implementation teams, and frontline champions.

View Article and Find Full Text PDF

Background: Ariadne Labs' Serious Illness Care Program (SICP), inclusive of the Serious Illness Conversation Guide (SICG), has been adapted for use in a variety of settings and among diverse population groups. Explicating the core elements of serious illness conversations could support the inclusion or exclusion of certain components in future iterations of the programme and the guide.

Aim: This integrative systematic review aimed to identify and describe core elements of serious illness conversations in relation to the SICP and/or SICG.

View Article and Find Full Text PDF

Advance Care Planning (ACP) in the US is complex due in part to a lack of a unified health care system, though more recent policy changes permitting reimbursement for ACP conversations offer some hope. One key barrier to ACP is public perceptions of ACP, made worse by a historical focus on messaging that is unappealing and does not meet people's need to focus on the present before contemplating the future. As we learn more about how to engage the public, there is also increasing recognition that the previous focus on making very specific decisions about the future needs to shift to a focus on preparing people for communication and decision making.

View Article and Find Full Text PDF

Objective: In 2019, the Danish parliament issued legislation requiring Danish physicians to clarify and honor seriously ill patients' treatment preferences. The American POLST (Physician Orders for Life-Sustaining Treatment) document could be a valuable model for this process. The aim of the study was to examine patients' preferences for life-sustaining treatment and participant assessment of a Danish POLST form.

View Article and Find Full Text PDF
Article Synopsis
  • - Serious illness conversations are designed to better align medical treatment with what patients value and prefer, but effective methods to identify patients in need of these conversations are not well-studied or compared across different settings.
  • - A scoping review analyzed literature from 2014 to 2021 and found that common methods for identifying patients include clinical triggers, the 'surprise question', or a combination of methods, with contributions from various healthcare staff and automated tools.
  • - The study highlighted both facilitative factors and barriers in the patient identification process, suggesting that future research should evaluate how to improve identification methods and better understand clinicians' decision-making in this area.
View Article and Find Full Text PDF

Objectives: The Serious Illness Care Programme (SICP) is a multicomponent evidence-based intervention that improves communication about patients' values and goals in serious illness. We aim to characterise implementation strategies for programme delivery and the contextual factors that influence implementation in three 'real-world' health system SICP initiatives.

Methods: We employed a qualitative thematic framework analysis of field notes collected during the first 1.

View Article and Find Full Text PDF

Objective: To explore patients' and physicians' perspectives on a decision-making conversation for life-sustaining treatment, based on the Danish model of the American Physician Orders for Life Sustaining Treatment (POLST) form.

Design: Semi-structured interviews following a conversation about preferences for life-sustaining treatment.

Setting: Danish hospitals, nursing homes, and general practitioners' clinics.

View Article and Find Full Text PDF
Article Synopsis
  • Medically frail and chronically ill patients in Denmark often lack documented preferences for care upon hospital admission, potentially leading to inappropriate treatment decisions.
  • The study aimed to develop and pilot a Danish version of the POLST form, inspired by a similar American model, to effectively record patients' wishes regarding life-sustaining treatment through discussions with healthcare providers.
  • Feedback from 25 patients indicated that the Danish POLST form was generally readable and helpful, with 93% of participants finding it effective for discussions about their treatment preferences, highlighting the importance of clear communication surrounding patient wishes.
View Article and Find Full Text PDF

Context: Simplifying medication regimens by tapering and/or withdrawing unnecessary drugs is important to optimize quality of life and safety for patients with serious illness. Few resources are available to educate clinicians, patients and family caregivers about this process.

Objective: To describe the development of an educational program called Shared Medication PLanning In (SIMPLIfy) Home Hospice.

View Article and Find Full Text PDF

Context: There are concerns that policies aimed to prevent opioid misuse may unintentionally reduce access to opioids for patients at end-of-life.

Objective: We assessed trends in opioid prescribing among patients on discharge from the hospital to hospice care.

Methods: This was a retrospective cohort study among adult (age ≥18 years) patients discharged from a 544-576 bed, academic medical center to hospice care between January 1, 2010 to December 31, 2018.

View Article and Find Full Text PDF

The COVID-19 pandemic has exposed the medical and social vulnerability of an unprecedented number of people. Consequently, there has never been a more important time for clinicians to engage patients in advance care planning (ACP) discussions about their goals, values, and preferences in the event of critical illness. An evidence-based communication tool-the Serious Illness Conversation Guide-was adapted to address COVID-related ACP challenges using a user-centered design process: convening relevant experts to propose initial guide adaptations; soliciting feedback from key clinical stakeholders from multiple disciplines and geographic regions; and iteratively testing language with patient actors.

View Article and Find Full Text PDF

Context: Many consider goal-concordant care (GCC) to be the most important of advance care planning and palliative care. Researchers face significant challenges in attempting to measure this outcome. We conducted a randomized controlled trial to assess the effects of a system-level intervention to improve serious illness communication on GCC and other outcomes.

View Article and Find Full Text PDF

Serious illness conversations are part of advance care planning (ACP) and focus on prognosis, values, and goals in patients who are seriously ill. To be maximally effective, such conversations must be documented accurately and be easily accessible. The two coprimary objectives of the study were to assess concordance between written documentation and recorded audiotaped conversations, and to evaluate adherence to the Serious Illness Conversation Guide questions.

View Article and Find Full Text PDF