TY - JOUR
T1 - Comprehensive survival analysis of a cohort of patients with Stevens-Johnson syndrome and toxic epidermal necrolysis
AU - Sekula, Peggy
AU - Dunant, Ariane
AU - Mockenhaupt, Maja
AU - Naldi, Luigi
AU - Bouwes Bavinck, Jan Nico
AU - Halevy, Sima
AU - Kardaun, Sylvia
AU - Sidoroff, Alexis
AU - Liss, Yvonne
AU - Schumacher, Martin
AU - Roujeau, Jean Claude
N1 - Funding Information:
We are indebted to all patients whose participation made this study possible, as well as to their treating physicians for the great cooperation. We also thank Alexander Hellmer (Germany; data management), Esther Lai A Fat (The Netherlands; data acquisition), Batya Davidovici (Israel; data acquisition), Martine Grosber (Germany; data acquisition), Jean-Paul Fagot (France, data acquisition), and Malika Bounoua (France, data acquisition) for their contributory assistance in the study. Between 2003 and 2007, the RegiSCAR study was funded by unrestricted grants from the European Commission (QLRT-2002-01738), GIS-Institut des Maladies Rares and INSERM (4CH09G) in France, and by a consortium of pharmaceutical companies (Bayer Vital, Boehringer-Ingelheim, Cephalon, GlaxoSmithKline, MSD Sharp and Dohme, Merck, Novartis, Pfizer, Roche, Sanofi-Aventis, Servier). MM received the Else Kröner Memorial Stipendium for support of clinical research through Else Kröner-Fresenius-Foundation. Methodological considerations were partly supported by Deutsche Forschungsgemeinschaft (FOR 534).
PY - 2013/1/1
Y1 - 2013/1/1
N2 - Stevens-Johnson syndrome and toxic epidermal necrolysis are severe cutaneous adverse reactions that are of major concern because of high mortality rates. On the basis of data collected in the RegiSCAR study, the aim was to assess risk factors (including modalities of patient management) for mortality, regardless of the cause, up to 1 year after the reaction. Within this cohort, the mortality rate was 23% (95% confidence interval (CI) 19-27%) at 6 weeks and 34% (95% CI 30-39%) at 1 year. Severity of reaction was a risk factor for mortality only in the first 90 days after onset, whereas serious comorbidities and age influenced mortality beyond 90 days and up to 1 year after onset of reaction. The risk of death for patients with identified drug cause was borderline lower than for patients with a reaction of unknown cause (hazard ratio 0.66, 95% CI 0.45-0.96). The study could not provide conclusive evidence regarding patient management. This large-scale population-based follow-up study of such patients confirmed high in-hospital mortality and revealed a remarkable number of deaths after discharge, which could mainly be attributed to severe comorbidities and older age, whereas the impact of severity of reaction on the risk of death was limited to the first few weeks.
AB - Stevens-Johnson syndrome and toxic epidermal necrolysis are severe cutaneous adverse reactions that are of major concern because of high mortality rates. On the basis of data collected in the RegiSCAR study, the aim was to assess risk factors (including modalities of patient management) for mortality, regardless of the cause, up to 1 year after the reaction. Within this cohort, the mortality rate was 23% (95% confidence interval (CI) 19-27%) at 6 weeks and 34% (95% CI 30-39%) at 1 year. Severity of reaction was a risk factor for mortality only in the first 90 days after onset, whereas serious comorbidities and age influenced mortality beyond 90 days and up to 1 year after onset of reaction. The risk of death for patients with identified drug cause was borderline lower than for patients with a reaction of unknown cause (hazard ratio 0.66, 95% CI 0.45-0.96). The study could not provide conclusive evidence regarding patient management. This large-scale population-based follow-up study of such patients confirmed high in-hospital mortality and revealed a remarkable number of deaths after discharge, which could mainly be attributed to severe comorbidities and older age, whereas the impact of severity of reaction on the risk of death was limited to the first few weeks.
UR - http://www.scopus.com/inward/record.url?scp=84876679035&partnerID=8YFLogxK
U2 - 10.1038/jid.2012.510
DO - 10.1038/jid.2012.510
M3 - Article
C2 - 23389396
AN - SCOPUS:84876679035
SN - 0022-202X
VL - 133
SP - 1197
EP - 1204
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 5
ER -