Lamotrigine Emerging as a Driver of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: An 8-Year Retrospective Study.

Allergic drug reaction Anticonvulsants Lamotrigine SJS/TEN overlap syndrome Stevens-Johnson syndrome Toxic epidermal necrolysis

Journal

Burns : journal of the International Society for Burn Injuries
ISSN: 1879-1409
Titre abrégé: Burns
Pays: Netherlands
ID NLM: 8913178

Informations de publication

Date de publication:
20 Jul 2024
Historique:
received: 08 11 2023
revised: 16 04 2024
accepted: 04 07 2024
medline: 11 8 2024
pubmed: 11 8 2024
entrez: 10 8 2024
Statut: aheadofprint

Résumé

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) represent severe manifestations of a potentially life-threatening spectrum defined by a desquamating rash of the skin and mucous membranes. This study was prompted by the observed increase in the off-label use of lamotrigine as a causal agent in SJS/TEN in our regional burn center. A retrospective cohort of 48 patients presenting to the Connecticut Burn Center from 2015-2022 with suspicion for SJS/TEN were reviewed for age, sex, causative drug, presenting symptoms, hospital course, biopsy confirmation, length of stay, comorbidities, and 30-day mortality. Descriptive statistical analysis was conducted to identify trends in causative agent, clinical presentation, and mortality. Thirty patients in our cohort received a final diagnosis of SJS/TEN. While antibiotics remain the most frequent cause of SJS/TEN across the study period (33.3 %, n = 10), the incidence of cases attributable to lamotrigine increased from 1 case between 2015 and 2018 (6.7 %) to 6 cases between 2019 and 2022 (40 %). In 2020 alone, 50 % of all cases were attributable to lamotrigine (n = 4). Of the patients where lamotrigine was implicated, 71.4 % (n = 5) were prescribed lamotrigine for off-label use in the treatment of non-bipolar mood disorders. The average lamotrigine-associated SJS/TEN patient was younger (p < 0.001), had fewer comorbidities, and was more likely to be female than the general SJS/TEN population. Off-label use of lamotrigine is emerging as a major driver of SJS/TEN with notable changes in patient demographics. Further research is necessary to understand how changing trends in the patient population will impact clinical course and optimal management.

Sections du résumé

BACKGROUND BACKGROUND
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) represent severe manifestations of a potentially life-threatening spectrum defined by a desquamating rash of the skin and mucous membranes. This study was prompted by the observed increase in the off-label use of lamotrigine as a causal agent in SJS/TEN in our regional burn center.
METHODS METHODS
A retrospective cohort of 48 patients presenting to the Connecticut Burn Center from 2015-2022 with suspicion for SJS/TEN were reviewed for age, sex, causative drug, presenting symptoms, hospital course, biopsy confirmation, length of stay, comorbidities, and 30-day mortality. Descriptive statistical analysis was conducted to identify trends in causative agent, clinical presentation, and mortality.
RESULTS RESULTS
Thirty patients in our cohort received a final diagnosis of SJS/TEN. While antibiotics remain the most frequent cause of SJS/TEN across the study period (33.3 %, n = 10), the incidence of cases attributable to lamotrigine increased from 1 case between 2015 and 2018 (6.7 %) to 6 cases between 2019 and 2022 (40 %). In 2020 alone, 50 % of all cases were attributable to lamotrigine (n = 4). Of the patients where lamotrigine was implicated, 71.4 % (n = 5) were prescribed lamotrigine for off-label use in the treatment of non-bipolar mood disorders. The average lamotrigine-associated SJS/TEN patient was younger (p < 0.001), had fewer comorbidities, and was more likely to be female than the general SJS/TEN population.
CONCLUSION CONCLUSIONS
Off-label use of lamotrigine is emerging as a major driver of SJS/TEN with notable changes in patient demographics. Further research is necessary to understand how changing trends in the patient population will impact clinical course and optimal management.

Identifiants

pubmed: 39127578
pii: S0305-4179(24)00202-X
doi: 10.1016/j.burns.2024.07.006
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 Elsevier Ltd and International Society of Burns Injuries. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors report no funding sources or conflict of interest concerning the materials or methods used in this study or the findings specified in this study.

Auteurs

Joshua Zev Glahn (JZ)

Division of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, United States.

Mariana N Almeida (MN)

Division of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, United States.

Alejandro Kochen (A)

Division of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, United States.

Olivier Noel (O)

Division of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, United States.

Viola Stogner (V)

Division of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, United States; Department of Plastic, Aesthetic, Hand and Reconstructive Surgery, Hannover Medical School, Hannover, Germany.

Henry C Hsia (HC)

Division of Plastic and Reconstructive Surgery, Yale School of Medicine, New Haven, CT, United States.

Alisa Savetamal (A)

Department of Surgery, Connecticut Burn Center, Bridgeport Hospital, Bridgeport, CT, United States. Electronic address: alisa.savetamal@bpthosp.org.

Classifications MeSH