TY - JOUR
T1 - A controlled study of use of patient-reported outcomes to improve assessment of late effects after treatment for head-and-neck cancer
AU - Kjaer, Trille Kristina
AU - Dalton, Susanne Oksbjerg
AU - Andersen, Elo
AU - Karlsen, Randi V
AU - Nielsen, Anni Linnet
AU - Hansen, Merete Kjaer
AU - Frederiksen, Kirsten
AU - Johansen, Christoffer
N1 - Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.
PY - 2016/5
Y1 - 2016/5
N2 - BACKGROUND AND PURPOSE: To test the effect of longitudinal feedback on late effects reported by survivors of head-and-neck cancer (HNC) to clinicians during regular follow-up.MATERIAL AND METHODS: A total of 266 participants were sequentially assigned to either control or intervention group and filled in electronic versions of the EORTC QLQ C-30, H&N35, HADS and a study-specific list of symptoms at up to two consecutive follow-up visits. Participants' symptoms displayed according to severity were provided to the clinician for the intervention group but not for the control group. Linear mixed-effects models were used to examine the number of symptoms assessed by clinicians (primary outcome). Multivariate linear regression models examined participants' long-term symptom control and QoL (secondary outcome).RESULTS: More symptoms were assessed by clinicians in the intervention group at all three visits (P<0.001, <0.001, and P=0.04). No effect was observed on most patient outcomes. When prompted by patient-reported outcomes at consultations, clinicians and patients were in better agreement about the occurrence of severe symptoms at all three visits.CONCLUSION: Timely patient-reported outcomes to clinicians in routine follow-up of HNC survivors enhanced clinicians' rates of assessment of late symptoms. Giving reports of patient-reported outcome to clinicians had limited impact on participants' QoL or symptom burden.
AB - BACKGROUND AND PURPOSE: To test the effect of longitudinal feedback on late effects reported by survivors of head-and-neck cancer (HNC) to clinicians during regular follow-up.MATERIAL AND METHODS: A total of 266 participants were sequentially assigned to either control or intervention group and filled in electronic versions of the EORTC QLQ C-30, H&N35, HADS and a study-specific list of symptoms at up to two consecutive follow-up visits. Participants' symptoms displayed according to severity were provided to the clinician for the intervention group but not for the control group. Linear mixed-effects models were used to examine the number of symptoms assessed by clinicians (primary outcome). Multivariate linear regression models examined participants' long-term symptom control and QoL (secondary outcome).RESULTS: More symptoms were assessed by clinicians in the intervention group at all three visits (P<0.001, <0.001, and P=0.04). No effect was observed on most patient outcomes. When prompted by patient-reported outcomes at consultations, clinicians and patients were in better agreement about the occurrence of severe symptoms at all three visits.CONCLUSION: Timely patient-reported outcomes to clinicians in routine follow-up of HNC survivors enhanced clinicians' rates of assessment of late symptoms. Giving reports of patient-reported outcome to clinicians had limited impact on participants' QoL or symptom burden.
KW - Female
KW - Follow-Up Studies
KW - Head and Neck Neoplasms
KW - Humans
KW - Male
KW - Middle Aged
KW - Patient Reported Outcome Measures
KW - Quality of Life
KW - Research Design
KW - Surveys and Questionnaires
KW - Survivors
KW - Journal Article
KW - Research Support, Non-U.S. Gov't
U2 - 10.1016/j.radonc.2016.04.034
DO - 10.1016/j.radonc.2016.04.034
M3 - Journal article
C2 - 27178143
SN - 0167-8140
VL - 119
SP - 221
EP - 228
JO - Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
JF - Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
IS - 2
ER -