Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patient

Valproic acid (VPA) is a commonly used antiepileptic drug (AED). Aplastic crisis is defined as acute arrest of hematopoiesis. Stevens-Johnson syndrome (SJS) is a fatal cutaneous adverse drug reaction. We herein report a rare case of aplastic crisis and SJS in a single pediatric patient that were pro...

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Main Authors: Wei-Jian Yang, Zhen-Hui Chen, Yi-Nan Zheng
Format: Article
Language:English
Published: Elsevier 2023-01-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844022037495
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author Wei-Jian Yang
Zhen-Hui Chen
Yi-Nan Zheng
author_facet Wei-Jian Yang
Zhen-Hui Chen
Yi-Nan Zheng
author_sort Wei-Jian Yang
collection DOAJ
description Valproic acid (VPA) is a commonly used antiepileptic drug (AED). Aplastic crisis is defined as acute arrest of hematopoiesis. Stevens-Johnson syndrome (SJS) is a fatal cutaneous adverse drug reaction. We herein report a rare case of aplastic crisis and SJS in a single pediatric patient that were probably caused by VPA. A 2-year-old girl was involved in a car accident. She was diagnosed with skull fractures, cerebral contusions, pulmonary contusions, and fractures of the left iliac bone by computed tomography. VPA was administered as prophylaxis for post-traumatic epilepsy. From day 13, she developed repeated high fevers, and multiple antibiotics were ineffective; she was then transferred to our pediatric intensive care unit. After transfer, she developed liver function impairment, decreased peripheral blood cell counts, and skin damage. After withdrawal of the VPA and administration of prednisone, intravenous immunoglobulin, local skin care, and nutritional support, her body temperature normalized and her hematopoietic function and skin lesions successively resolved. She was transferred out of the pediatric intensive care unit on day 56 and discharged on day 70. At the 6-month follow-up, a blood examination was normal, and repeat computed tomography revealed multiple softening foci of the bilateral brain and less subdural effusion than before. To our knowledge, no report to date has described aplastic crisis and SJS in a single patient. The purpose of this paper is to increase clinicians’ knowledge in the treatment of adverse drug reactions (ADRs) and emphasize the importance of standardized application and strict monitoring of VPA in patients with post-traumatic brain trauma.
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spelling doaj.art-85a31dffdd6b4b90b5bec576c8fcde1d2023-02-03T04:58:22ZengElsevierHeliyon2405-84402023-01-0191e12461Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patientWei-Jian Yang0Zhen-Hui Chen1Yi-Nan Zheng2Pediatric Intensive Care Unit, Guangdong Women And Children Hospital, Guangzhou, Guangdong, ChinaDepartment of Clinical Laboratory, Guangdong Women And Children Hospital, Guangzhou, Guangdong, ChinaPediatric Intensive Care Unit, Guangdong Women And Children Hospital, Guangzhou, Guangdong, China; Corresponding author.Valproic acid (VPA) is a commonly used antiepileptic drug (AED). Aplastic crisis is defined as acute arrest of hematopoiesis. Stevens-Johnson syndrome (SJS) is a fatal cutaneous adverse drug reaction. We herein report a rare case of aplastic crisis and SJS in a single pediatric patient that were probably caused by VPA. A 2-year-old girl was involved in a car accident. She was diagnosed with skull fractures, cerebral contusions, pulmonary contusions, and fractures of the left iliac bone by computed tomography. VPA was administered as prophylaxis for post-traumatic epilepsy. From day 13, she developed repeated high fevers, and multiple antibiotics were ineffective; she was then transferred to our pediatric intensive care unit. After transfer, she developed liver function impairment, decreased peripheral blood cell counts, and skin damage. After withdrawal of the VPA and administration of prednisone, intravenous immunoglobulin, local skin care, and nutritional support, her body temperature normalized and her hematopoietic function and skin lesions successively resolved. She was transferred out of the pediatric intensive care unit on day 56 and discharged on day 70. At the 6-month follow-up, a blood examination was normal, and repeat computed tomography revealed multiple softening foci of the bilateral brain and less subdural effusion than before. To our knowledge, no report to date has described aplastic crisis and SJS in a single patient. The purpose of this paper is to increase clinicians’ knowledge in the treatment of adverse drug reactions (ADRs) and emphasize the importance of standardized application and strict monitoring of VPA in patients with post-traumatic brain trauma.http://www.sciencedirect.com/science/article/pii/S2405844022037495Aplastic crisisStevens-Johnson syndromeAntiepileptic drugsAdverse drug reactionsMetagenomic next-generation sequencing
spellingShingle Wei-Jian Yang
Zhen-Hui Chen
Yi-Nan Zheng
Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patient
Heliyon
Aplastic crisis
Stevens-Johnson syndrome
Antiepileptic drugs
Adverse drug reactions
Metagenomic next-generation sequencing
title Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patient
title_full Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patient
title_fullStr Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patient
title_full_unstemmed Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patient
title_short Valproic acid induced aplastic crisis and Stevens-Johnson syndrome in a single pediatric patient
title_sort valproic acid induced aplastic crisis and stevens johnson syndrome in a single pediatric patient
topic Aplastic crisis
Stevens-Johnson syndrome
Antiepileptic drugs
Adverse drug reactions
Metagenomic next-generation sequencing
url http://www.sciencedirect.com/science/article/pii/S2405844022037495
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