Volume 34, Issue 4 , Pages 585-590, April 2008
Multistate outbreak of toxic anterior segment syndrome, 2005
Purpose
To present the findings of an outbreak of toxic anterior segment syndrome (TASS).
Setting
Six states, 7 ophthalmology surgical centers, United States.
Methods
Cases were identified through electronic communication networks and via reports to a national TASS referral center. Information on the procedure, details of instrument reprocessing, and products used during cataract surgery were also collected. Medications used during the procedures were tested for endotoxin using a kinetic assay.
Results
The search identified 112 case patients (median age 74 years) from 7 centers from July 19, 2005, through November 28, 2005. Common presenting clinical features included blurred vision (60%), anterior segment inflammation (49%), and cell deposition (56%). Of the patients, 100 (89%) had been exposed to a single brand of balanced salt solution manufactured by Cytosol Laboratories and distributed by Advanced Medical Optics as AMO Endosol. Two patients continued to have residual symptoms. There were no reports of significant breaches in sterile technique or instrument reprocessing. Of 14 balanced salt solution lots, 5 (35%) had levels exceeding the endotoxin limit (0.5 EU/mL). Based on these findings, the balanced salt solution product was withdrawn, resulting in a termination of the outbreak.
Conclusions
This is the first known report of an outbreak of TASS caused by intrinsic contamination of a product with endotoxin. Ophthalmologists and epidemiologists should be aware of TASS and its common causes. To facilitate investigations of adverse outcomes such as TASS, those performing cataract surgeries should document the type and lot numbers of products used intraoperatively.
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No author has a financial or proprietary interest in any material or method mentioned.
Institution at which work was performed: Centers for Disease Control and Prevention (CDC), Atlanta, Georgia. The findings and conclusions in this article are those of the authors and do not necessarily represent the views of the CDC. Use of trade names and commercial sources is for identification purpose only and does not imply endorsement by the Public Health Service or the U.S. Department of Health and Human Services.
Keren Z. Landman, MD, Centers for Disease Control and Prevention, Department of Health and Human Services; Mary Spayne, MPH, Vermont Department of Health; Walter I. Fried, PhD, MD, Surevision Eye Centers of Lake County, Gurnee, Illinois; and Dean Carlson, MD, Eye Associates of Colorado Springs, Colorado Springs, Colorado, helped prepare this paper. Mark Iverson, MD, Copley Hospital; Laura Ure, CGRN, Rocky Mountain Laser and Surgical Center, Pueblo, Colorado; and Sue MeKenna provided technical and/or clinical assistance.
Presented at the 17th Annual Scientific Meeting of the Society for Healthcare Epidemiology of America, Baltimore, Maryland, USA, April 2007.
PII: S0886-3350(08)00048-5
doi:10.1016/j.jcrs.2007.11.037
© 2008 ASCRS and ESCRS. Published by Elsevier Inc. All rights reserved.
Volume 34, Issue 4 , Pages 585-590, April 2008
