Evaluating an Intervention to Improve Communication between Oncology Clinicians and Patients with Life-Limiting Cancer

A Cluster Randomized Clinical Trial of the Serious Illness Care Program

Joanna Paladino, Rachelle Bernacki, Bridget A. Neville, Jane Kavanagh, Stephen P. Miranda, Marissa Palmor, Joshua Lakin, Meghna Desai, Daniela Lamas, Justin J. Sanders, Jonathon Gass, Natalie Henrich, Stuart Lipsitz, Erik Fromme, Atul A. Gawande, Susan D. Block

Research output: Contribution to journalEditorial

9 Citations (Scopus)

Abstract

Importance: Earlier clinician-patient conversations about patients' values, goals, and preferences in serious illness (ie, serious illness conversations) are associated with better outcomes but occur inconsistently in cancer care. Objective: To evaluate the efficacy of a communication quality-improvement intervention in improving the occurrence, timing, quality, and accessibility of documented serious illness conversations between oncology clinicians and patients with advanced cancer. Design, Setting, Participants: This cluster randomized clinical trial in outpatient oncology was conducted at the Dana-Farber Cancer Institute and included physicians, advanced-practice clinicians, and patients with cancer who were at high risk of death. Main Outcomes and Measures: The primary outcomes (goal-concordant care and peacefulness at the end of life) are published elsewhere. Secondary outcomes are reported herein, including (1) documentation of at least 1 serious illness conversation before death, (2) timing of the initial conversation before death, (3) quality of conversations, and (4) their accessibility in the electronic medical record (EMR). Results: We enrolled 91 clinicians (48 intervention, 43 control) and 278 patients (134 intervention, 144 control). Of enrolled patients, 58% died during the study (n=161); mean age was 62.3 years (95% CI, 58.9-65.6 years); 55% were women (n=88). These patients were cared for by 76 of the 91 enrolled clinicians (37 intervention, 39 control); years in practice, 11.5 (95% CI, 9.2-13.8); 57% female (n=43). Medical record review after patients' death demonstrated that a significantly higher proportion of intervention patients had a documented discussion compared with controls (96% vs 79%, P =.005) and intervention conversations occurred a median of 2.4 months earlier (median, 143 days vs 71 days, P <.001). Conversation documentation for intervention patients was significantly more comprehensive and patient centered, with a greater focus on values or goals (89% vs 44%, P <.001), prognosis or illness understanding (91% vs 48%, P <.001), and life-sustaining treatment preferences (63% vs 32%, P =.004). Documentation about end-of-life care planning did not differ between arms (80% intervention vs 68% control, P =.08). Significantly more intervention patients had documentation that was accessible in the EMR (61% vs 11%, P <.001). Conclusions and Relevance: This communication quality-improvement intervention resulted in more, earlier, better, and more accessible serious illness conversations documented in the EMR. To our knowledge, this is the first such study to demonstrate improvement in all 4 of these outcomes. Trial Registration: ClinicalTrials.gov identifier: NCT01786811.

Original languageEnglish (US)
JournalJAMA Oncology
DOIs
StatePublished - Jan 1 2019
Externally publishedYes

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Randomized Controlled Trials
Communication
Neoplasms
Documentation
Electronic Health Records
Quality Improvement
Terminal Care
Medical Records
Outpatients
Outcome Assessment (Health Care)
Physicians

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Cite this

Evaluating an Intervention to Improve Communication between Oncology Clinicians and Patients with Life-Limiting Cancer : A Cluster Randomized Clinical Trial of the Serious Illness Care Program. / Paladino, Joanna; Bernacki, Rachelle; Neville, Bridget A.; Kavanagh, Jane; Miranda, Stephen P.; Palmor, Marissa; Lakin, Joshua; Desai, Meghna; Lamas, Daniela; Sanders, Justin J.; Gass, Jonathon; Henrich, Natalie; Lipsitz, Stuart; Fromme, Erik; Gawande, Atul A.; Block, Susan D.

In: JAMA Oncology, 01.01.2019.

Research output: Contribution to journalEditorial

Paladino, J, Bernacki, R, Neville, BA, Kavanagh, J, Miranda, SP, Palmor, M, Lakin, J, Desai, M, Lamas, D, Sanders, JJ, Gass, J, Henrich, N, Lipsitz, S, Fromme, E, Gawande, AA & Block, SD 2019, 'Evaluating an Intervention to Improve Communication between Oncology Clinicians and Patients with Life-Limiting Cancer: A Cluster Randomized Clinical Trial of the Serious Illness Care Program', JAMA Oncology. https://doi.org/10.1001/jamaoncol.2019.0292
Paladino, Joanna ; Bernacki, Rachelle ; Neville, Bridget A. ; Kavanagh, Jane ; Miranda, Stephen P. ; Palmor, Marissa ; Lakin, Joshua ; Desai, Meghna ; Lamas, Daniela ; Sanders, Justin J. ; Gass, Jonathon ; Henrich, Natalie ; Lipsitz, Stuart ; Fromme, Erik ; Gawande, Atul A. ; Block, Susan D. / Evaluating an Intervention to Improve Communication between Oncology Clinicians and Patients with Life-Limiting Cancer : A Cluster Randomized Clinical Trial of the Serious Illness Care Program. In: JAMA Oncology. 2019.
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abstract = "Importance: Earlier clinician-patient conversations about patients' values, goals, and preferences in serious illness (ie, serious illness conversations) are associated with better outcomes but occur inconsistently in cancer care. Objective: To evaluate the efficacy of a communication quality-improvement intervention in improving the occurrence, timing, quality, and accessibility of documented serious illness conversations between oncology clinicians and patients with advanced cancer. Design, Setting, Participants: This cluster randomized clinical trial in outpatient oncology was conducted at the Dana-Farber Cancer Institute and included physicians, advanced-practice clinicians, and patients with cancer who were at high risk of death. Main Outcomes and Measures: The primary outcomes (goal-concordant care and peacefulness at the end of life) are published elsewhere. Secondary outcomes are reported herein, including (1) documentation of at least 1 serious illness conversation before death, (2) timing of the initial conversation before death, (3) quality of conversations, and (4) their accessibility in the electronic medical record (EMR). Results: We enrolled 91 clinicians (48 intervention, 43 control) and 278 patients (134 intervention, 144 control). Of enrolled patients, 58{\%} died during the study (n=161); mean age was 62.3 years (95{\%} CI, 58.9-65.6 years); 55{\%} were women (n=88). These patients were cared for by 76 of the 91 enrolled clinicians (37 intervention, 39 control); years in practice, 11.5 (95{\%} CI, 9.2-13.8); 57{\%} female (n=43). Medical record review after patients' death demonstrated that a significantly higher proportion of intervention patients had a documented discussion compared with controls (96{\%} vs 79{\%}, P =.005) and intervention conversations occurred a median of 2.4 months earlier (median, 143 days vs 71 days, P <.001). Conversation documentation for intervention patients was significantly more comprehensive and patient centered, with a greater focus on values or goals (89{\%} vs 44{\%}, P <.001), prognosis or illness understanding (91{\%} vs 48{\%}, P <.001), and life-sustaining treatment preferences (63{\%} vs 32{\%}, P =.004). Documentation about end-of-life care planning did not differ between arms (80{\%} intervention vs 68{\%} control, P =.08). Significantly more intervention patients had documentation that was accessible in the EMR (61{\%} vs 11{\%}, P <.001). Conclusions and Relevance: This communication quality-improvement intervention resulted in more, earlier, better, and more accessible serious illness conversations documented in the EMR. To our knowledge, this is the first such study to demonstrate improvement in all 4 of these outcomes. Trial Registration: ClinicalTrials.gov identifier: NCT01786811.",
author = "Joanna Paladino and Rachelle Bernacki and Neville, {Bridget A.} and Jane Kavanagh and Miranda, {Stephen P.} and Marissa Palmor and Joshua Lakin and Meghna Desai and Daniela Lamas and Sanders, {Justin J.} and Jonathon Gass and Natalie Henrich and Stuart Lipsitz and Erik Fromme and Gawande, {Atul A.} and Block, {Susan D.}",
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T1 - Evaluating an Intervention to Improve Communication between Oncology Clinicians and Patients with Life-Limiting Cancer

T2 - A Cluster Randomized Clinical Trial of the Serious Illness Care Program

AU - Paladino, Joanna

AU - Bernacki, Rachelle

AU - Neville, Bridget A.

AU - Kavanagh, Jane

AU - Miranda, Stephen P.

AU - Palmor, Marissa

AU - Lakin, Joshua

AU - Desai, Meghna

AU - Lamas, Daniela

AU - Sanders, Justin J.

AU - Gass, Jonathon

AU - Henrich, Natalie

AU - Lipsitz, Stuart

AU - Fromme, Erik

AU - Gawande, Atul A.

AU - Block, Susan D.

PY - 2019/1/1

Y1 - 2019/1/1

N2 - Importance: Earlier clinician-patient conversations about patients' values, goals, and preferences in serious illness (ie, serious illness conversations) are associated with better outcomes but occur inconsistently in cancer care. Objective: To evaluate the efficacy of a communication quality-improvement intervention in improving the occurrence, timing, quality, and accessibility of documented serious illness conversations between oncology clinicians and patients with advanced cancer. Design, Setting, Participants: This cluster randomized clinical trial in outpatient oncology was conducted at the Dana-Farber Cancer Institute and included physicians, advanced-practice clinicians, and patients with cancer who were at high risk of death. Main Outcomes and Measures: The primary outcomes (goal-concordant care and peacefulness at the end of life) are published elsewhere. Secondary outcomes are reported herein, including (1) documentation of at least 1 serious illness conversation before death, (2) timing of the initial conversation before death, (3) quality of conversations, and (4) their accessibility in the electronic medical record (EMR). Results: We enrolled 91 clinicians (48 intervention, 43 control) and 278 patients (134 intervention, 144 control). Of enrolled patients, 58% died during the study (n=161); mean age was 62.3 years (95% CI, 58.9-65.6 years); 55% were women (n=88). These patients were cared for by 76 of the 91 enrolled clinicians (37 intervention, 39 control); years in practice, 11.5 (95% CI, 9.2-13.8); 57% female (n=43). Medical record review after patients' death demonstrated that a significantly higher proportion of intervention patients had a documented discussion compared with controls (96% vs 79%, P =.005) and intervention conversations occurred a median of 2.4 months earlier (median, 143 days vs 71 days, P <.001). Conversation documentation for intervention patients was significantly more comprehensive and patient centered, with a greater focus on values or goals (89% vs 44%, P <.001), prognosis or illness understanding (91% vs 48%, P <.001), and life-sustaining treatment preferences (63% vs 32%, P =.004). Documentation about end-of-life care planning did not differ between arms (80% intervention vs 68% control, P =.08). Significantly more intervention patients had documentation that was accessible in the EMR (61% vs 11%, P <.001). Conclusions and Relevance: This communication quality-improvement intervention resulted in more, earlier, better, and more accessible serious illness conversations documented in the EMR. To our knowledge, this is the first such study to demonstrate improvement in all 4 of these outcomes. Trial Registration: ClinicalTrials.gov identifier: NCT01786811.

AB - Importance: Earlier clinician-patient conversations about patients' values, goals, and preferences in serious illness (ie, serious illness conversations) are associated with better outcomes but occur inconsistently in cancer care. Objective: To evaluate the efficacy of a communication quality-improvement intervention in improving the occurrence, timing, quality, and accessibility of documented serious illness conversations between oncology clinicians and patients with advanced cancer. Design, Setting, Participants: This cluster randomized clinical trial in outpatient oncology was conducted at the Dana-Farber Cancer Institute and included physicians, advanced-practice clinicians, and patients with cancer who were at high risk of death. Main Outcomes and Measures: The primary outcomes (goal-concordant care and peacefulness at the end of life) are published elsewhere. Secondary outcomes are reported herein, including (1) documentation of at least 1 serious illness conversation before death, (2) timing of the initial conversation before death, (3) quality of conversations, and (4) their accessibility in the electronic medical record (EMR). Results: We enrolled 91 clinicians (48 intervention, 43 control) and 278 patients (134 intervention, 144 control). Of enrolled patients, 58% died during the study (n=161); mean age was 62.3 years (95% CI, 58.9-65.6 years); 55% were women (n=88). These patients were cared for by 76 of the 91 enrolled clinicians (37 intervention, 39 control); years in practice, 11.5 (95% CI, 9.2-13.8); 57% female (n=43). Medical record review after patients' death demonstrated that a significantly higher proportion of intervention patients had a documented discussion compared with controls (96% vs 79%, P =.005) and intervention conversations occurred a median of 2.4 months earlier (median, 143 days vs 71 days, P <.001). Conversation documentation for intervention patients was significantly more comprehensive and patient centered, with a greater focus on values or goals (89% vs 44%, P <.001), prognosis or illness understanding (91% vs 48%, P <.001), and life-sustaining treatment preferences (63% vs 32%, P =.004). Documentation about end-of-life care planning did not differ between arms (80% intervention vs 68% control, P =.08). Significantly more intervention patients had documentation that was accessible in the EMR (61% vs 11%, P <.001). Conclusions and Relevance: This communication quality-improvement intervention resulted in more, earlier, better, and more accessible serious illness conversations documented in the EMR. To our knowledge, this is the first such study to demonstrate improvement in all 4 of these outcomes. Trial Registration: ClinicalTrials.gov identifier: NCT01786811.

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