TY - JOUR
T1 - Child neurology telemedicine
T2 - Analyzing 14 820 patient encounters during the first year of the COVID-19 pandemic
AU - CHOP Neuroscience Center - Telemedicine Research Group
AU - Kaufman, Michael C.
AU - Xian, Julie
AU - Galer, Peter D.
AU - Parthasarathy, Shridhar
AU - Gonzalez, Alexander K.
AU - McKee, Jillian L.
AU - Prelack, Marisa S.
AU - Fitzgerald, Mark P.
AU - Helbig, Ingo
AU - Ruggiero, Sarah Mckeown
AU - Craig, Sansanee
AU - Rametta, Salvatore C.
AU - Molisani, Sara E.
AU - Sharif, Uzma
AU - Melamed, Susan E.
AU - Digiovine, Marissa
AU - Fried, Lawrence
AU - Malcolm, Marissa P.
AU - Kessler, Sudha Kilaru
AU - Chadehumbe, Madeline
AU - Szperka, Christina L.
AU - Chuo, John
AU - Caffee, Laurel
AU - Stephenson, Donna J.
AU - Banwell, Brenda L.
AU - Goldberg, Ethan
AU - Abend, Nicholas S.
AU - Helbig, Katherine
N1 - Publisher Copyright:
© 2022 Mac Keith Press.
PY - 2023/3
Y1 - 2023/3
N2 - Aim: To determine the long-term impact of telemedicine in child neurology care during the COVID-19 pandemic and with the reopening of outpatient clinics. Method: We performed an observational cohort study of 34 837 in-person visits and 14 820 telemedicine outpatient visits across 26 399 individuals. We assessed differences in care across visit types, time-period observed, time between follow-ups, patient portal activation rates, and demographic factors. Results: We observed a higher proportion of telemedicine for epilepsy (International Classification of Diseases, 10th Revision G40: odds ratio [OR] 1.4, 95% confidence interval [CI] 1.3–1.5) and a lower proportion for movement disorders (G25: OR 0.7, 95% CI 0.6–0.8; R25: OR 0.7, 95% CI 0.6–0.9) relative to in-person visits. Infants were more likely to be seen in-person after reopening clinics than by telemedicine (OR 1.6, 95% CI 1.5–1.8) as were individuals with neuromuscular disorders (OR 1.6, 95% CI 1.5–1.7). Self-reported racial and ethnic minority populations and those with highest social vulnerability had lower telemedicine participation rates (OR 0.8, 95% CI 0.8–0.8; OR 0.7, 95% CI 0.7–0.8). Interpretation: Telemedicine continued to be utilized even once in-person clinics were available. Pediatric epilepsy care can often be performed using telemedicine while young patients with neuromuscular disorders often require in-person assessment. Prominent barriers for socially vulnerable families and racial and ethnic minorities persist.
AB - Aim: To determine the long-term impact of telemedicine in child neurology care during the COVID-19 pandemic and with the reopening of outpatient clinics. Method: We performed an observational cohort study of 34 837 in-person visits and 14 820 telemedicine outpatient visits across 26 399 individuals. We assessed differences in care across visit types, time-period observed, time between follow-ups, patient portal activation rates, and demographic factors. Results: We observed a higher proportion of telemedicine for epilepsy (International Classification of Diseases, 10th Revision G40: odds ratio [OR] 1.4, 95% confidence interval [CI] 1.3–1.5) and a lower proportion for movement disorders (G25: OR 0.7, 95% CI 0.6–0.8; R25: OR 0.7, 95% CI 0.6–0.9) relative to in-person visits. Infants were more likely to be seen in-person after reopening clinics than by telemedicine (OR 1.6, 95% CI 1.5–1.8) as were individuals with neuromuscular disorders (OR 1.6, 95% CI 1.5–1.7). Self-reported racial and ethnic minority populations and those with highest social vulnerability had lower telemedicine participation rates (OR 0.8, 95% CI 0.8–0.8; OR 0.7, 95% CI 0.7–0.8). Interpretation: Telemedicine continued to be utilized even once in-person clinics were available. Pediatric epilepsy care can often be performed using telemedicine while young patients with neuromuscular disorders often require in-person assessment. Prominent barriers for socially vulnerable families and racial and ethnic minorities persist.
UR - http://www.scopus.com/inward/record.url?scp=85138181001&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85138181001&partnerID=8YFLogxK
U2 - 10.1111/dmcn.15406
DO - 10.1111/dmcn.15406
M3 - Article
C2 - 38767061
AN - SCOPUS:85138181001
SN - 0012-1622
VL - 65
SP - 406
EP - 415
JO - Developmental medicine and child neurology
JF - Developmental medicine and child neurology
IS - 3
ER -