Implementing Electronic Patient-Reported Outcomes for Patients With New Oral Chemotherapy Prescriptions at an Academic Site and a Community Site

被引:13
作者
Doolin, Jim W. [1 ]
Berry, Jonathan L. [1 ]
Forbath, Natalia S. [2 ]
Tocci, Noah X. [2 ]
Dechen, Tenzin [2 ]
Li, Stephanie [2 ]
Hartwell, Rebekah A. [3 ]
Espiritu, Jennifer K. [4 ]
Roberts, Daniel A. [4 ]
Zerillo, Jessica A. [1 ]
Shea, Meghan [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Div Hematol Oncol, 330 Brookline Ave, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Ctr Healthcare Deliver Sci, Boston, MA 02215 USA
[3] Clovis Oncol, Boulder, CO USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
来源
JCO CLINICAL CANCER INFORMATICS | 2021年 / 5卷
关键词
QUALITY; SAFETY;
D O I
10.1200/CCI.20.00191
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSE Oral chemotherapy challenges providers' abilities to safely monitor patients' symptoms, adherence, and financial toxicity. COVID-19 has increased the urgency of caring for patients remotely. Collection of electronic patient-reported outcomes (ePROs) has demonstrated efficacy for patients on intravenous chemotherapy, but limited data support their use in oral chemotherapy. We undertook a pilot project to assess the feasibility of implementing an ePRO system for patients starting oral chemotherapy at our cancer center, which includes both an academic site and a community site. METHODS Patients initiating oral chemotherapy were asked to participate. A five-question tool was built in REDCap. Concerning responses triggered outreach within one business day. The primary outcome was time to first symptom assessment. For comparison, we used a historical cohort of patients who had been prescribed oral chemotherapies by providers in the same disease groups at the cancer center. RESULTS Twenty-five of 62 (40%) patients completed ePRO assessments. Fifty historical charts were reviewed. Time to first symptom assessment was 7 days (IQR, 4-14 days) in the historical group compared with 3 days (IQR, 2-4 days) in the ePRO group. Time to clinical action was 14 days (7-35 days) in the historical group compared with 8 days (4-19 days) in the ePRO group. No statistically significant differences were detected in 30-day emergency department visit or hospitalization (12% for both groups) or 90-day emergency department visit or hospitalization rates (historical 28% and ePRO 20%). CONCLUSION An ePRO tool monitoring patient concerns about adherence, cost, and toxicities for patients with new oral chemotherapy regimens is feasible and improves time to symptom assessment. Further investigation is needed to improve patient engagement with ePROs and evaluate the long-term impacts for patients on oral chemotherapy.
引用
收藏
页码:631 / 640
页数:10
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