Multidisciplinary care in Stevens-Johnson syndrome

Author:

Shanbhag Swapna S.12,Chodosh James1,Fathy Cherie3,Goverman Jeremy4,Mitchell Caroline5,Saeed Hajirah N.6ORCID

Affiliation:

1. Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Boston, MA, USA

2. LV Prasad Eye Institute, Tej Kohli Cornea Institute, Hyderabad, Telangana, India

3. Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA

4. Department of Surgery, Massachusetts General Hospital, Sumner Redstone Burn Center, Boston, MA, USA

5. Department of Obstetrics and Gynecology, Massachusetts General Hospital, Boston, MA, USA

6. Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, 243 Charles St, Boston, MA 02114, USA

Abstract

Stevens-Johnson syndrome (SJS) and Toxic Epidermal Necrolysis (TEN) are potentially fatal mucocutaneous diseases that can involve many organ systems. Manifestations of SJS/TEN outside of the skin, eyes, and oral mucosa are not well defined or well recognized, and, therefore, are often not addressed clinically. As supportive care improves and mortality from SJS/TEN decreases, chronic complications in affected organ systems are becoming more prevalent. Recognition of the manifestations of SJS/TEN in the acute phase is critical to optimal care. In this review, we review the organ systems that may be involved in SJS/TEN, provide an overview of their management, and propose a list of items that should be communicated to the patient and family upon discharge. The organ systems discussed include the pulmonary, gastrointestinal/hepatic, oral, otorhinolaryngologic, gynecologic, genitourinary, and renal systems. In addition, the significant psychosocial, nutritional, and pain consequences and management of SJS/TEN are discussed.

Funder

National Eye Institute

Publisher

SAGE Publications

Subject

Medicine (miscellaneous)

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