Literature DB >> 10635613

Treatment of severe drug eruptions.

J C Roujeau1.   

Abstract

Severe drug eruptions are rare, life-threatening events. The management begins with the withdrawal of the suspect drug(s). We recently confirmed that an earlier withdrawal of drugs with short elimination half-life was associated with a better survival of patients with Stevens-Johnson syndrome (SJS) or toxic epidermal necrolysis (TEN). In cases of "acute skin failure" (exfoliative dermatitis, extensive SJS or TEN), management of patients must be undertaken in specialized intensive care units or in burn units. The main principles of symptomatic therapy are the same as for major burns: warming of the environment, correction of electrolyte disturbances, high caloric intake, and prevention of sepsis. The suspected immunologic orgin of drug eruptions prompted the use of corticosteroids, immunosuppressive drugs, and anti-cytokines. Systemic corticosteroids are useful in "hypersensitivity syndrome" when visceral lesions depend on infiltration by activated cosinophils. Systemic corticosteroids were shown to be deleterious in cases of advanced TEN. Their potential usefulness at earlier stages of SJS or TEN remains controversial. High intravenous doses of cyclophosphamide or oral cyclosporin have been administered to a few patients with TEN, most often following ineffective treatment with corticosteroids for 1 to 5 days. It remains doubtful that the progression of the lesions was shortened. A few patients appeared to benefit from treatment with pentoxifyllin, a drug suppressing the production of TNF. Thalidomide, another suppressor of TNF production, significantly increased the death rate when tested in a double-blind placebo controlled trial in patients with early TEN. High dose intravenous immunoglobulins were used in 10 patients with TEN on the basis of their ability to inhibit fas-fas ligand mediated apoptosis. The potential benefit of this treatment needs confirmation by further studies. Patients and their first degree relatives should be advised to avoid the responsible drug and chemically related compounds. Regulatory agencies should be notified of such cases.

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Year:  1999        PMID: 10635613     DOI: 10.1111/j.1346-8138.1999.tb02082.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  7 in total

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Authors:  Anusha Shanbhag; E Ryan Pritchard; Kshitij Chatterjee; Drayton A Hammond
Journal:  Hosp Pharm       Date:  2017-07-18

Review 2.  Immunological principles of adverse drug reactions: the initiation and propagation of immune responses elicited by drug treatment.

Authors:  D J Naisbitt; S F Gordon; M Pirmohamed; B K Park
Journal:  Drug Saf       Date:  2000-12       Impact factor: 5.606

Review 3.  DRESS syndrome: a case report and literature review.

Authors:  Cláudia Sofia Cardoso; Ana Margarida Vieira; Ana Paula Oliveira
Journal:  BMJ Case Rep       Date:  2011-06-03

4.  Stevens-Johnson Syndrome: A Case Study.

Authors:  Matthew Smelik
Journal:  Perm J       Date:  2002

5.  Causality assessment of cutaneous adverse drug reactions.

Authors:  Young-Min Son; Jong-Rok Lee; Joo-Young Roh
Journal:  Ann Dermatol       Date:  2011-11-03       Impact factor: 1.444

6.  A Case of the Drug Reaction with Eosinophilia and Systemic Symptom (DRESS) Following Isoniazid Treatment.

Authors:  Jin-Yong Lee; Yun-Jae Seol; Dong-Woo Shin; Dae-Young Kim; Hong-Woo Chun; Bo-Young Kim; Shin-Ok Jeong; Sang-Hyok Lim; An-Soo Jang
Journal:  Tuberc Respir Dis (Seoul)       Date:  2015-01-29

7.  Drug Reaction with Eosinophilia and Systemic Symptom Syndrome Induced by Lamotrigine.

Authors:  Song Hee Han; Min Seok Hur; Hae Jeong Youn; Nam Kyung Roh; Yang Won Lee; Yong Beom Choe; Kyu Joong Ahn
Journal:  Ann Dermatol       Date:  2017-03-24       Impact factor: 1.444

  7 in total

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