Risk of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Associated With Antibiotic Use : A Case-Crossover Study
Copyright © 2023 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved..
BACKGROUND: Evidence is lacking on the association between antibiotic use and risk of Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) in Asians.
OBJECTIVE: We assessed the risk of SJS/TEN associated with different antibiotic classes in Japanese.
METHODS: We conducted a case-crossover study using a claims database. Firth conditional logistic regression was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) of SJS/TEN associated with antibiotic use in a 56-day hazard period versus 3 control periods. We created 18 cohorts for each antibiotic class and calculated 56-day cumulative incidence per 100,000 new users. The association between antibiotic class and SJS/TEN was also evaluated in each case using the ALgorithm of Drug causality for Epidermal Necrolysis (ALDEN).
RESULTS: Our case-crossover study included 170 SJS/TEN cases. Increased ORs were observed for lincomycins (OR, 33.00 [95% CI, 3.74-4332.05]), trimethoprim-sulfamethoxazole (21.20 [6.73-105.98]), penicillins (14.39 [6.95-34.21]), glycopeptides (14.37 [3.17-136.10]), cephalosporins (7.06 [4.25-12.21]), aminoglycosides (6.55 [1.97-26.84]), quinolones (5.98 [3.34-11.20]), fosfomycin (5.40 [1.20-30.97]), carbapenems (5.09 [1.85-15.64]), tetracyclines (4.95 [1.78-15.27]), and macrolides (3.78 [2.13-6.83]). Cumulative incidence of SJS/TEN was 67.4 for trimethoprim-sulfamethoxazole, 86.2 for glycopeptides, and below 10.0 for the others. Despite the high incidence, only 2 cases had a probable causal relationship with glycopeptides.
CONCLUSION: Some antibiotic classes, including lincomycins, glycopeptides, aminoglycosides, fosfomycin, and carbapenems, were newly suggested to be associated with risk of SJS/TEN; considered together with the high incidence for trimethoprim-sulfamethoxazole and glycopeptides, these findings warrant caution in clinical practice.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:11 |
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Enthalten in: |
The journal of allergy and clinical immunology. In practice - 11(2023), 11 vom: 07. Nov., Seite 3463-3472 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Fukasawa, Toshiki [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 13.11.2023 Date Revised 20.11.2023 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1016/j.jaip.2023.07.012 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM359605869 |
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500 | |a Date Revised 20.11.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2023 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved. | ||
520 | |a BACKGROUND: Evidence is lacking on the association between antibiotic use and risk of Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) in Asians | ||
520 | |a OBJECTIVE: We assessed the risk of SJS/TEN associated with different antibiotic classes in Japanese | ||
520 | |a METHODS: We conducted a case-crossover study using a claims database. Firth conditional logistic regression was used to estimate odds ratios (ORs) and 95% confidence intervals (CIs) of SJS/TEN associated with antibiotic use in a 56-day hazard period versus 3 control periods. We created 18 cohorts for each antibiotic class and calculated 56-day cumulative incidence per 100,000 new users. The association between antibiotic class and SJS/TEN was also evaluated in each case using the ALgorithm of Drug causality for Epidermal Necrolysis (ALDEN) | ||
520 | |a RESULTS: Our case-crossover study included 170 SJS/TEN cases. Increased ORs were observed for lincomycins (OR, 33.00 [95% CI, 3.74-4332.05]), trimethoprim-sulfamethoxazole (21.20 [6.73-105.98]), penicillins (14.39 [6.95-34.21]), glycopeptides (14.37 [3.17-136.10]), cephalosporins (7.06 [4.25-12.21]), aminoglycosides (6.55 [1.97-26.84]), quinolones (5.98 [3.34-11.20]), fosfomycin (5.40 [1.20-30.97]), carbapenems (5.09 [1.85-15.64]), tetracyclines (4.95 [1.78-15.27]), and macrolides (3.78 [2.13-6.83]). Cumulative incidence of SJS/TEN was 67.4 for trimethoprim-sulfamethoxazole, 86.2 for glycopeptides, and below 10.0 for the others. Despite the high incidence, only 2 cases had a probable causal relationship with glycopeptides | ||
520 | |a CONCLUSION: Some antibiotic classes, including lincomycins, glycopeptides, aminoglycosides, fosfomycin, and carbapenems, were newly suggested to be associated with risk of SJS/TEN; considered together with the high incidence for trimethoprim-sulfamethoxazole and glycopeptides, these findings warrant caution in clinical practice | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Adverse drug reaction | |
650 | 4 | |a Antibiotics | |
650 | 4 | |a Asia | |
650 | 4 | |a Incidence | |
650 | 4 | |a Japan | |
650 | 4 | |a Pharmacoepidemiology | |
650 | 4 | |a Real-world evidence | |
650 | 4 | |a Stevens-Johnson syndrome | |
650 | 4 | |a Toxic epidermal necrolysis | |
650 | 4 | |a Trimethoprim-sulfamethoxazole | |
650 | 7 | |a Anti-Bacterial Agents |2 NLM | |
650 | 7 | |a Trimethoprim, Sulfamethoxazole Drug Combination |2 NLM | |
650 | 7 | |a 8064-90-2 |2 NLM | |
650 | 7 | |a Fosfomycin |2 NLM | |
650 | 7 | |a 2N81MY12TE |2 NLM | |
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650 | 7 | |a Carbapenems |2 NLM | |
650 | 7 | |a Glycopeptides |2 NLM | |
700 | 1 | |a Urushihara, Hisashi |e verfasserin |4 aut | |
700 | 1 | |a Takahashi, Hayato |e verfasserin |4 aut | |
700 | 1 | |a Okura, Takayuki |e verfasserin |4 aut | |
700 | 1 | |a Kawakami, Koji |e verfasserin |4 aut | |
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