Can topical mitomycin prevent laryngotracheal stenosis?

被引:100
作者
Eliashar, R
Eliachar, I
Esclamado, R
Gramlich, T
Strome, M
机构
[1] Cleveland Clin Fdn, Dept Otolaryngol & Communicat Disorders A 71, Cleveland, OH 44195 USA
[2] Cleveland Clin Fdn, Dept Anat Pathol, Cleveland, OH 44195 USA
[3] Hadassah Univ Hosp, Dept Otolaryngol Head & Neck Surg, IL-91120 Jerusalem, Israel
关键词
laryngotracheal stenosis; pathogenesis; treatment; prevention; subglottic stenosis; mitomycin;
D O I
10.1097/00005537-199910000-00009
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Objectives/Hypothesis: Early topical application of mitomycin to a laryngotracheal lesion may prevent or reduce laryngotracheal stenosis (LTS), Study Design: Prospective controlled animal study, Methods: LTS was induced in 60 dogs randomly assigned to four groups. Controls received an immediate topical application of normal saline. The suction-control group received an immediate application of normal saline followed by suction of secretions on day 2, The mitomycin group received immediate application of 0.7 mt mitomycin (0.2 mg/mL), The repeat-mitomycin group received an immediate application of mitomycin and a second application on day 2, after secretions were suctioned, The laryngeal lumens were measured endoscopically at baseline, day 12, and day 21, Animals were euthanatized if stenosis approximated 95% or at day 21, Results: All dogs in the mitomycin groups survived to day 21, compared with 12 in the suction group and only 2 controls. No side effects of mitomycin were observed. At day 21, surviving controls had 85% and 95% stenosis, In the mitomycin group, median stenosis was 27% (interquartile range, 29% to 42%); in the repeat-mitomycin group, 30% (22% to 40%); and in the suction-control group, 84.5% (72.5% to 93.5%). The mitomycin group differed significantly from controls on day 12 (median difference = 85%, 95% CI = 80%-94%, P <.0001) and day 21 (difference 63.9%, 95% CI = 58%-85%, P =.031), Conclusion: A single topical application of mitomycin significantly reduces the severity of LTS in dogs. Reapplication after 2 days does not improve results. Prospective clinical studies are warranted to assess the efficacy in humans.
引用
收藏
页码:1594 / 1600
页数:7
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