Affiliation:
1. Department of Pharmacology, Sri Manakula Vinayagar Medical college and hospital, Puducherry-605017, India
2. Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry-605006, India
3. Department of Clinical Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry-605006, India
Abstract
Background and Objective:
Identification of the offending drug is crucial and challenging
in cases of severe cutaneous adverse drug reactions (CADR) like Stevens-Johnson syndrome
(SJS) and toxic epidermal necrolysis (TEN). Poor reproducibility and varying levels of agreement
have been observed among different causality assessment tools (CATs) in assessing severe CADRs.
This study was conducted to examine the agreement among four different CATs in assessing
cases of drug-induced SJS, TEN and SJS/TEN overlap.
Methods:
All cases of drug-induced SJS, TEN and SJS/TEN overlap, which were reported between
January 2012 and January 2020, were identified from the ADR register at an ADR monitoring
centre. Causality assessment was done in these reported cases using the following CATs: The
World Health Organization–Uppsala Monitoring Centre (WHO–UMC) scale, Naranjo algorithm,
Liverpool algorithm and Algorithm of drug causality for epidermal necrolysis (ALDEN). Weighted
kappa (κw) test was used to evaluate the agreement among four CATs.
Results:
A total of 30 cases of drug-induced SJS, TEN and SJS/TEN overlap were included in our
analyses. The most common offending groups of drugs were anticonvulsants (46.7%), antimicrobials
(40%) and nonsteroidal anti-inflammatory drugs (13.3%). Of the anticonvulsants, phenytoin
(13.3%), carbamazepine (10%), and valproate (10%) were the commonly reported offending drugs.
Poor agreement was observed among the four different causality assessment scales.
Conclusion:
Discrepancies were observed among four different CATs in assessing drug-induced
SJS and TEN. A CAT, which is more specific to drug-induced SJS and TEN, simple, user-friendly
with limited subjective interpretation, incorporating new immunological and pharmacogenetic
markers, is necessary.
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology (medical),Pharmacology,Toxicology
Cited by
1 articles.
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1. Multiple drugs;Reactions Weekly;2023-01-07