• DOI:10.1001/ARCHDERM.136.3.323
• Corpus ID: 10332270

Toxic epidermal necrolysis and Stevens-Johnson syndrome: does early withdrawal of causative drugs decrease the risk of death?

@article{GarcaDoval2000ToxicEN,
  title={Toxic epidermal necrolysis and Stevens-Johnson syndrome: does early withdrawal of causative drugs decrease the risk of death?},
  author={Ignacio Garc{\'i}a-Doval and L Lecleach and H{\'e}l{\`e}ne Bocquet and X L Otero and Jean Claude Roujeau},
  journal={Archives of dermatology},
  year={2000},
  volume={136 3},
  pages={
          323-7
        }
}

• I. García-Doval, L. Lecleach, +2 authors J. Roujeau
• Published 1 March 2000
• Medicine
• Archives of dermatology

BACKGROUND
Withdrawal of the drug(s) that cause severe cutaneous adverse reactions is usually recommended without proof that it alters the course of those reactions.

OBJECTIVE
To determine whether the timing of causative drug withdrawal is related to the prognosis of patients with toxic epidermal necrolysis (TEN) or Stevens-Johnson syndrome (SJS).

DESIGN
A 10-year observational study (January 1, 1987, through October 30, 1997) of patients admitted to a dermatological intensive care unit, using binary logistic regression analysis.

SETTING
A single referral unit in a university hospital.

PATIENTS
Consecutive sample of 203 patients with TEN or SJS. Exclusion criteria included causative drug undetermined, lack of information on disease evolution, the date of causative drug(s) withdrawal, or the date when the first definite sign of TEN or SJS appeared.

MAIN OUTCOME MEASURE
Death before hospital discharge.

RESULTS
One hundred thirteen patients were included; 74 had TEN and 39 had SJS; 20 died. The drug causing TEN or SJS was withdrawn early in 64 patients and late (after the first definite sign of TEN or SJS) in 49 patients. After adjustment for confounding variables (age, maximum extent of detachment, admission year, human immunodeficiency virus status), our model showed that the earlier the causative drug was withdrawn, the better the prognosis (odds ratio, 0.69 for each day; 95% confidence interval, 0.53-0.89). Patients exposed to causative drugs with long half-lives had an increased risk of dying (odds ratio, 4.9; 95% confidence interval, 1.3-18.9). The variables did not interact.

CONCLUSIONS
Prompt withdrawal of drug(s) that are suspected to cause SJS or TEN may decrease mortality. Prompt withdrawal of causative drugs should be a priority when blisters or erosions appear in the course of a drug eruption.