Chan H L, Stern R S, Arndt K A, Langlois J, Jick S S, Jick H, Walker A M
Department of Dermatology, Beth Israel Hospital and Harvard Medical School, Boston, MA 02215.
Arch Dermatol. 1990 Jan;126(1):43-7.
We carried out a study to estimate the incidence of erythema multiforme (EM), Stevens Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN) requiring hospitalization and to determine which drug therapies were associated with these reactions. We reviewed the clinical records of all patients who were hospitalized with these discharge diagnoses at Group Health Cooperative (GHC) of Puget Sound, Seattle, Wash, from 1972 through 1986. During this 14-year period, an average of about 260,000 persons, with demographic characteristics similar to those of the general population, received their care from GHC, and there were about 25,000 admissions to hospitals per year at the GHC hospitals. Based on International Classification of Diseases-Adapted coding, a total of 61 suspect cases of EM, SJS, or TEN were identified from the computerized hospital discharge file. Based on record review and the application of a uniform set of diagnostic criteria, a total of 37 patients (61%) were classified as having EM, SJS, or TEN. Of these, 16 cases (43%) were attributed to drugs administered to these patients prior to hospitalization. The overall incidence of hospitalization for EM, SJS, or TEN due to all causes was 4.2 per 10(6) person-years. The incidence of TEN alone due to all causes was 0.5 per 10(6) person-years. The incidence of EM, SJS, or TEN associated with drug use were 7.0, 1.8, and 9.0 per 10(6) person-years, respectively, for persons younger than 20 years of age, 20 to 64 years of age, and 65 years of age and older. Drug therapies with reaction rates in excess of 1 per 100,000 exposed individuals include phenobarbital (20 per 100,000), nitrofurantoin (7 per 100,000), sulfamethoxazole and trimethoprim, and ampicillin (both 3 per 100,000), and amoxicillin (2 per 100,000). Overall, our data suggest that cases of EM, SJS, and TEN sufficiently severe to require hospitalization are infrequent among outpatients using well-established drug therapies. A continuing challenge is the evaluation of these severe cutaneous reactions that are associated with newly marketed or less frequently prescribed drug therapies.
我们开展了一项研究,以估计需要住院治疗的多形红斑(EM)、史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死松解症(TEN)的发病率,并确定哪些药物治疗与这些反应相关。我们回顾了1972年至1986年期间在华盛顿州西雅图市普吉特海湾集团健康合作社(GHC)因这些出院诊断而住院的所有患者的临床记录。在这14年期间,平均约有26万人在GHC接受治疗,其人口统计学特征与普通人群相似,GHC医院每年约有2.5万例住院病例。根据国际疾病分类适应性编码,从计算机化的医院出院档案中总共识别出61例疑似EM、SJS或TEN的病例。基于记录审查和一套统一的诊断标准应用,共有37例患者(61%)被归类为患有EM、SJS或TEN。其中,16例(43%)归因于这些患者住院前使用的药物。所有原因导致的EM、SJS或TEN的住院总体发病率为每10^6人年4.2例。所有原因导致的单独TEN的发病率为每10^6人年0.5例。对于年龄小于20岁、20至64岁以及65岁及以上的人群,与药物使用相关的EM、SJS或TEN的发病率分别为每10^6人年7.0例、1.8例和9.0例。暴露个体反应率超过十万分之一的药物治疗包括苯巴比妥(十万分之二十)、呋喃妥因(十万分之七)、磺胺甲恶唑和甲氧苄啶以及氨苄西林(均为十万分之三)和阿莫西林(十万分之二)。总体而言,我们的数据表明,在使用成熟药物治疗的门诊患者中,严重到需要住院治疗的EM、SJS和TEN病例并不常见。一个持续的挑战是评估与新上市或使用频率较低的药物治疗相关的这些严重皮肤反应。