TY - JOUR
T1 - Risk factors for near-miss events and safety incidents in pediatric radiation therapy
AU - Baig, Nimrah
AU - Wang, Jiangxia
AU - Elnahal, Shereef
AU - McNutt, Todd
AU - Wright, Jean
AU - DeWeese, Theodore
AU - Terezakis, Stephanie A
N1 - Funding Information:
J. Wang reports grants from the National Institutes of Health during the conduct of this study. S. Terezakis reports a grant from Elekta Industries outside the submitted work. N. Baig, S. Elnahal, T. McNutt, J. Wright, and T. DeWeese have no relevant disclosures to report.
Funding Information:
We would like to acknowledge support for the statistical analysis from the National Center for Research Resources and the National Center for Advancing Translational Sciences ( NCATS ) of the National Institutes of Health through Grant Number 1UL1TR001079 .
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/5
Y1 - 2018/5
N2 - Background and purpose: Factors contributing to safety- or quality-related incidents (e.g. variances) in children are unknown. We identified clinical and RT treatment variables associated with risk for variances in a pediatric cohort. Materials and methods: Using our institution's incident learning system, 81 patients age ≤21 years old who experienced variances were compared to 191 pediatric patients without variances. Clinical and RT treatment variables were evaluated as potential predictors for variances using univariate and multivariate analyses. Results: Variances were primarily documentation errors (n = 46, 57%) and were most commonly detected during treatment planning (n = 14, 21%). Treatment planning errors constituted the majority (n = 16 out of 29, 55%) of near-misses and safety incidents (NMSI), which excludes workflow incidents. Therapists reported the majority of variances (n = 50, 62%). Physician cross-coverage (OR = 2.1, 95% CI = 1.04–4.38) and 3D conformal RT (OR = 2.3, 95% CI = 1.11–4.69) increased variance risk. Conversely, age >14 years (OR = 0.5, 95% CI = 0.28–0.88) and diagnosis of abdominal tumor (OR = 0.2, 95% CI = 0.04–0.59) decreased variance risk. Conclusions: Variances in children occurred in early treatment phases, but were detected at later workflow stages. Quality measures should be implemented during early treatment phases with a focus on younger children and those cared for by cross-covering physicians.
AB - Background and purpose: Factors contributing to safety- or quality-related incidents (e.g. variances) in children are unknown. We identified clinical and RT treatment variables associated with risk for variances in a pediatric cohort. Materials and methods: Using our institution's incident learning system, 81 patients age ≤21 years old who experienced variances were compared to 191 pediatric patients without variances. Clinical and RT treatment variables were evaluated as potential predictors for variances using univariate and multivariate analyses. Results: Variances were primarily documentation errors (n = 46, 57%) and were most commonly detected during treatment planning (n = 14, 21%). Treatment planning errors constituted the majority (n = 16 out of 29, 55%) of near-misses and safety incidents (NMSI), which excludes workflow incidents. Therapists reported the majority of variances (n = 50, 62%). Physician cross-coverage (OR = 2.1, 95% CI = 1.04–4.38) and 3D conformal RT (OR = 2.3, 95% CI = 1.11–4.69) increased variance risk. Conversely, age >14 years (OR = 0.5, 95% CI = 0.28–0.88) and diagnosis of abdominal tumor (OR = 0.2, 95% CI = 0.04–0.59) decreased variance risk. Conclusions: Variances in children occurred in early treatment phases, but were detected at later workflow stages. Quality measures should be implemented during early treatment phases with a focus on younger children and those cared for by cross-covering physicians.
KW - Incidents
KW - Near-misses
KW - Patient safety
KW - Pediatrics
KW - Quality
KW - Variances
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U2 - 10.1016/j.radonc.2018.04.002
DO - 10.1016/j.radonc.2018.04.002
M3 - Article
C2 - 29776675
AN - SCOPUS:85047201121
SN - 0167-8140
VL - 127
SP - 178
EP - 182
JO - Radiotherapy and Oncology
JF - Radiotherapy and Oncology
IS - 2
ER -