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Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome

OBJECTIVE: To describe inpatient resource use in the 2 years following infantile epileptic spasms syndrome (IESS) diagnosis, examine the association between clinical/demographic variables and incidence of readmission, and identify risk factors/reasons for frequent readmissions. METHODS: Retrospectiv...

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Autores principales: Harini, Chellamani, Yuskaitis, Christopher J., Singh, Avantika, McHugh, Trevor, Liu, Shanshan, DeLeo, Michelle, Gupta, Nishtha, Marti, Candice, Zhang, Bo, Libenson, Mark H., Berry, Jay G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235577/
https://www.ncbi.nlm.nih.gov/pubmed/36790214
http://dx.doi.org/10.1002/epi4.12711
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author Harini, Chellamani
Yuskaitis, Christopher J.
Singh, Avantika
McHugh, Trevor
Liu, Shanshan
DeLeo, Michelle
Gupta, Nishtha
Marti, Candice
Zhang, Bo
Libenson, Mark H.
Berry, Jay G.
author_facet Harini, Chellamani
Yuskaitis, Christopher J.
Singh, Avantika
McHugh, Trevor
Liu, Shanshan
DeLeo, Michelle
Gupta, Nishtha
Marti, Candice
Zhang, Bo
Libenson, Mark H.
Berry, Jay G.
author_sort Harini, Chellamani
collection PubMed
description OBJECTIVE: To describe inpatient resource use in the 2 years following infantile epileptic spasms syndrome (IESS) diagnosis, examine the association between clinical/demographic variables and incidence of readmission, and identify risk factors/reasons for frequent readmissions. METHODS: Retrospective cohort analysis of readmissions (scheduled/unscheduled) within the first 2 years following IESS diagnosis, details of readmissions (number/time between rehospitalizations, and length of stay), demographic/clinical variables, and reasons for readmissions were collected. Negative binomial regression analysis evaluated associations between incidence of readmissions (both scheduled/unscheduled and unscheduled alone) and demographic/clinical factors. Logistic regression assessed the risk of having recurrent readmissions (≥5 readmissions). RESULTS: Among 93 (60% males) new‐onset IESS patients, there were 394 readmissions (56% scheduled and 44% unscheduled) within 2‐years following IESS diagnosis. Mean length of stay was 3.5 days (SD: 5.9). Readmissions occurred in 82 patients (88%) and 37 (40%) experienced ≥5 readmissions. On multivariate regression analysis, readmissions were increased with use of multiple first‐line treatments for IESS (P = 0.006), technology assistance (P ≤ 0.001), and multispecialty care (P = 0.01); seizure freedom (P = 0.015) and known etiology (P = 0.011) lowered the incidence of readmissions. Examining unscheduled readmissions separately, increased readmissions occurred with public insurance (P = 0.013), technology use (P ≤ 0.0.001), and multispecialty care (P = 0.013); seizure freedom decreased unscheduled readmissions (P = 0.006). Technology assistance (G‐tube, NG tube, VP shunt, and tracheostomy use) increased the odds (P = 0.007) for recurrent readmissions. Reasons for readmissions included EEG monitoring (protocol driven for verification of IESS remission/characterization of events/EEG surveillance/presurgical monitoring) (51%), acute medical issues (21%), and seizure exacerbation (15%). Protocol‐driven readmissions declined an estimated 52% following protocol modification during the study. SIGNIFICANCE: In the 2 years following IESS diagnosis, there is substantial inpatient resource use with nearly 40% experiencing ≥5 readmissions (mostly epilepsy related). Since readmissions are increased by intrinsic patient characteristics such as medical complexity (technology use and multispecialty care) or epilepsy‐related issues, the preventability of readmissions is uncertain, except for protocol‐driven ones.
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spelling pubmed-102355772023-06-03 Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome Harini, Chellamani Yuskaitis, Christopher J. Singh, Avantika McHugh, Trevor Liu, Shanshan DeLeo, Michelle Gupta, Nishtha Marti, Candice Zhang, Bo Libenson, Mark H. Berry, Jay G. Epilepsia Open Original Articles OBJECTIVE: To describe inpatient resource use in the 2 years following infantile epileptic spasms syndrome (IESS) diagnosis, examine the association between clinical/demographic variables and incidence of readmission, and identify risk factors/reasons for frequent readmissions. METHODS: Retrospective cohort analysis of readmissions (scheduled/unscheduled) within the first 2 years following IESS diagnosis, details of readmissions (number/time between rehospitalizations, and length of stay), demographic/clinical variables, and reasons for readmissions were collected. Negative binomial regression analysis evaluated associations between incidence of readmissions (both scheduled/unscheduled and unscheduled alone) and demographic/clinical factors. Logistic regression assessed the risk of having recurrent readmissions (≥5 readmissions). RESULTS: Among 93 (60% males) new‐onset IESS patients, there were 394 readmissions (56% scheduled and 44% unscheduled) within 2‐years following IESS diagnosis. Mean length of stay was 3.5 days (SD: 5.9). Readmissions occurred in 82 patients (88%) and 37 (40%) experienced ≥5 readmissions. On multivariate regression analysis, readmissions were increased with use of multiple first‐line treatments for IESS (P = 0.006), technology assistance (P ≤ 0.001), and multispecialty care (P = 0.01); seizure freedom (P = 0.015) and known etiology (P = 0.011) lowered the incidence of readmissions. Examining unscheduled readmissions separately, increased readmissions occurred with public insurance (P = 0.013), technology use (P ≤ 0.0.001), and multispecialty care (P = 0.013); seizure freedom decreased unscheduled readmissions (P = 0.006). Technology assistance (G‐tube, NG tube, VP shunt, and tracheostomy use) increased the odds (P = 0.007) for recurrent readmissions. Reasons for readmissions included EEG monitoring (protocol driven for verification of IESS remission/characterization of events/EEG surveillance/presurgical monitoring) (51%), acute medical issues (21%), and seizure exacerbation (15%). Protocol‐driven readmissions declined an estimated 52% following protocol modification during the study. SIGNIFICANCE: In the 2 years following IESS diagnosis, there is substantial inpatient resource use with nearly 40% experiencing ≥5 readmissions (mostly epilepsy related). Since readmissions are increased by intrinsic patient characteristics such as medical complexity (technology use and multispecialty care) or epilepsy‐related issues, the preventability of readmissions is uncertain, except for protocol‐driven ones. John Wiley and Sons Inc. 2023-03-30 /pmc/articles/PMC10235577/ /pubmed/36790214 http://dx.doi.org/10.1002/epi4.12711 Text en © 2023 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Harini, Chellamani
Yuskaitis, Christopher J.
Singh, Avantika
McHugh, Trevor
Liu, Shanshan
DeLeo, Michelle
Gupta, Nishtha
Marti, Candice
Zhang, Bo
Libenson, Mark H.
Berry, Jay G.
Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
title Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
title_full Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
title_fullStr Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
title_full_unstemmed Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
title_short Hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
title_sort hospital readmissions in children with new‐onset infantile epileptic spasms syndrome
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235577/
https://www.ncbi.nlm.nih.gov/pubmed/36790214
http://dx.doi.org/10.1002/epi4.12711
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