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Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies

Background and objectives: Procedural sedation for bone marrow examination (BME) and intrathecal chemotherapy (ITC) is necessary for pediatric patients with hematological malignancies. There has been no report on adverse events after discharge from the recovery room. This retrospective study evaluat...

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Autores principales: Joo, Jin, Yu, Sanghyuck, Koh, Hyun Jung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501634/
https://www.ncbi.nlm.nih.gov/pubmed/36143885
http://dx.doi.org/10.3390/medicina58091208
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author Joo, Jin
Yu, Sanghyuck
Koh, Hyun Jung
author_facet Joo, Jin
Yu, Sanghyuck
Koh, Hyun Jung
author_sort Joo, Jin
collection PubMed
description Background and objectives: Procedural sedation for bone marrow examination (BME) and intrathecal chemotherapy (ITC) is necessary for pediatric patients with hematological malignancies. There has been no report on adverse events after discharge from the recovery room. This retrospective study evaluated the types and incidences of delayed adverse events among pediatric patients scheduled for BME or ITC under deep sedation in a single center for 3 years. Materials and Methods: The patients were divided into two groups: inpatients (group I) and outpatients (group O). All patients were managed during the procedures and the recovery period. In total, 10 adverse events were assessed; these occurred 2 h (T1, acute), 12 h (T2, early), and 24 h (T3, delayed) after the procedure. The duration of each adverse event was also recorded and was classified as 2 h (D1), 12 h (D2), or 24 h (D3). The data of 263 patients (147 inpatients and 116 outpatients) who met the inclusion criteria were analyzed. Results: The overall incidence of adverse events was statistically significant difference: 48.3% in group I and 33.6% in group O (p = 0.011). The rates of adverse events at T1 and T2 were significantly different between groups I and O (42.8% vs. 11.2% and 7.5% vs. 20.7%, respectively) (p < 0.001). The adverse events were mostly of D1 or D2 duration in both groups. Patients with a higher proportion of ketamine in a propofol–ketamine mixture had a significantly higher proportion of adverse events at T1 (34.6%), as compared with those with a mixture with a lower proportion of ketamine (21.1%) or propofol alone (17.9%) (p = 0.012). Conclusions: The most common adverse events were dizziness or headache; typically, they did not last longer than 12 h. The propofol-ketamine combination with a higher proportion of ketamine seems to produce more adverse events within 2 h after the procedure. Nevertheless, all sedative types appear safe to use without additional management.
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spelling pubmed-95016342022-09-24 Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies Joo, Jin Yu, Sanghyuck Koh, Hyun Jung Medicina (Kaunas) Article Background and objectives: Procedural sedation for bone marrow examination (BME) and intrathecal chemotherapy (ITC) is necessary for pediatric patients with hematological malignancies. There has been no report on adverse events after discharge from the recovery room. This retrospective study evaluated the types and incidences of delayed adverse events among pediatric patients scheduled for BME or ITC under deep sedation in a single center for 3 years. Materials and Methods: The patients were divided into two groups: inpatients (group I) and outpatients (group O). All patients were managed during the procedures and the recovery period. In total, 10 adverse events were assessed; these occurred 2 h (T1, acute), 12 h (T2, early), and 24 h (T3, delayed) after the procedure. The duration of each adverse event was also recorded and was classified as 2 h (D1), 12 h (D2), or 24 h (D3). The data of 263 patients (147 inpatients and 116 outpatients) who met the inclusion criteria were analyzed. Results: The overall incidence of adverse events was statistically significant difference: 48.3% in group I and 33.6% in group O (p = 0.011). The rates of adverse events at T1 and T2 were significantly different between groups I and O (42.8% vs. 11.2% and 7.5% vs. 20.7%, respectively) (p < 0.001). The adverse events were mostly of D1 or D2 duration in both groups. Patients with a higher proportion of ketamine in a propofol–ketamine mixture had a significantly higher proportion of adverse events at T1 (34.6%), as compared with those with a mixture with a lower proportion of ketamine (21.1%) or propofol alone (17.9%) (p = 0.012). Conclusions: The most common adverse events were dizziness or headache; typically, they did not last longer than 12 h. The propofol-ketamine combination with a higher proportion of ketamine seems to produce more adverse events within 2 h after the procedure. Nevertheless, all sedative types appear safe to use without additional management. MDPI 2022-09-02 /pmc/articles/PMC9501634/ /pubmed/36143885 http://dx.doi.org/10.3390/medicina58091208 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Joo, Jin
Yu, Sanghyuck
Koh, Hyun Jung
Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies
title Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies
title_full Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies
title_fullStr Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies
title_full_unstemmed Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies
title_short Delayed Adverse Events after Procedural Sedation in Pediatric Patients with Hematologic Malignancies
title_sort delayed adverse events after procedural sedation in pediatric patients with hematologic malignancies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501634/
https://www.ncbi.nlm.nih.gov/pubmed/36143885
http://dx.doi.org/10.3390/medicina58091208
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