Vk. Sharma et S. Dhar, CLINICAL-PATTERN OF CUTANEOUS DRUG ERUPTION AMONG CHILDREN AND ADOLESCENTS IN NORTH-INDIA, Pediatric dermatology, 12(2), 1995, pp. 178-183
Various types of cutaneous drug eruptions and the incriminating drugs
were analyzed in 50 children and adolescents up to 18 years of age (34
or 65% boys, 16 or 32% girls). Thirteen (26%) patients had a maculopa
pular rash, 11 (22%) a fixed drug eruption (FDE), 10 erythema multifor
me (EM), 6 (12%) toxic epidermal necrolysis (TEN), 5 (10%) Stevens-Joh
nson syndrome (SJS), 3 (6%) urticaria, and 2 (4%) erythroderma. The in
cubation period for maculopapular rashes, SJS and TEN due to commonly
used antibiotics and sulfonamides was short, a few hours to two to thr
ee days, reflecting reexposure, and for drugs used sparingly such as a
ntiepileptics and antituberculosis agents, was approximately one week
or more, suggesting a first exposure. Antibiotics were responsible for
cutaneous eruptions in 27 patients, followed by antiepileptics in 17,
analgin in 4, and metronidazole and albendazole in 1 each. Cotrimoxaz
ole, a combination of sulfamethoxazole and trimethoprim, was the most
common antibacterial responsible for eruptions (11 patients), followed
by penicillin and its semisynthetic derivatives (8 patients), sulfona
mide alone (3 patients), and other antibiotics (4 patients). Antiepile
ptics were the most frequently incriminated drugs in EM, TEN, and SJS.
The role of systemic corticosteroids in the management of SJS and TEN
is controversial. We administered prednisolone or an equivalent corti
costeroid 2 mg/kg/day for 7 to 14 days. With this dosage the mortality
rate in the combined patients with TEN and SJS was 18.2%. Our limited
experience suggests that these drugs might still have a role in the m
anagement of SJS and TEN in children and adolescents.