Research Article

Clinical Features and Treatment Outcomes among Children with Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis: A 20-Year Study in a Tertiary Referral Hospital

Table 3

Treatment and treatment outcomes of patients with Stevens-Johnson syndrome and overlap-toxic epidermal necrolysis.

SJS, N = 20Overlap-TEN, N = 16Overall, N = 36P value

Treatment, N (%)
 Specific treatment16 (80.0)75.077.80.720
 Supportive treatment only4 (20.00)25.022.20.720

Duration of hospital stay (d) (mean ± SD)7.1 ± 4.117.7 ± 13.111.8 ± 10.6<0.001

Comorbidities/short-term complication, N (%)
 Skin10 (50.0)16 (100.00)26 (72.2)0.001
  Dyspigmentation10 (50.0)16 (100.00)26 (72.2)0.001
  Nail change04 (25.00)4 (11.1)0.018
 Eye10 (50.0)14 (87.5)24 (66.7)0.018
  Conjunctivitis8 (40.0)9 (56.3)17 (47.2)0.332
  Corneal epithelial defects2 (10.0)4 (25.0)6 (16.7)0.230
  Synechiae/symblepharon2 (10.0)4 (25.0)6 (16.7)0.248
  Pseudomembrane3 (15.0)3 (18.8)6 (16.7)0.764
 Superinfection3 (15.0)7 (43.8)10 (27.8)0.053
 Vaginal adhesion03 (18.8)3 (8.3)0.043
 Pneumonia1 (5.0)1 (6.2)2 (5.6)0.871
 Pancreatitis01 (6.2)1 (2.8)0.257
 Adrenal insufficiency01 (6.2)1 (2.8)0.257

Long-term sequel, N (%)
 Skin5 (25.0)14 (87.5)19 (52.8)0.001
 Eye4 (20.0)9 (56.3)13 (36.1)0.042
 GI (transaminitis)2 (10.0)6 (37.5)8 (22.2)0.124

Recurrence, N (%)1 (5.0)01 (2.8)0.364

Mortality rate, N (%)000

Significant values are shown in bold.