Literature DB >> 26135650

Prevention of esophageal stenosis after large endoscopic submucosal dissection: is there a better way to use steroids?

Mathieu Pioche1, Jérôme Rivory2.   

Abstract

Entities:  

Year:  2015        PMID: 26135650      PMCID: PMC4477018          DOI: 10.1055/s-0034-1391414

Source DB:  PubMed          Journal:  Endosc Int Open        ISSN: 2196-9736


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When an endoscopic resection involves more than 50 % to 75 % of the esophageal circumference, the risk of stenosis drastically increases to between 68 % and 90 %, respectively 1 2 3. In the past, a wait-and-see attitude was prevalent, and treatment was initiated only for patients with symptomatic stenosis. Treatment was based on endoscopic balloon dilation (EBD) conducted in several sessions, with a significant effect on the patient’s quality of life 3. Gradually, it became clear that a prophylactic strategy was essential to reduce the number of unfavorable issues. In parallel, either alone 4 or combined with EBD 5, steroids proved beneficial for the treatment of benign stenosis. Based on these results, it was naturally proposed that they be included in prophylactic strategies. As has been shown in many indications, these drugs are very effective for reducing inflammation and scarring, but they are associated with many severe adverse effects, such as metabolic disorders, infections, and osteoporosis, depending on the dose. The benefit-to-risk ratio is a key point in any preventive strategy for asymptomatic patients. Thus, two different approaches progressively emerged: local injections in the ulcer bed and oral intake of steroids. In the local approach, steroids are injected into the submucosa and edges of the resection bed. By reducing the synthesis of collagen and enhancing its breakdown, these local treatments have proved effective in reducing the incidence of stenosis 6 in corrosive esophagitis. For endoscopic resections involving up to 50 % of the circumference, three sessions of local injections (at 3, 7, and 10 days) of low doses of triamcinolone (between 18 and 62 mg) significantly reduced the incidence of stenosis from 75 % to 19 % 7. Furthermore, the mean number of balloon dilations for a patient with symptoms of stenosis was reduced from 6.6 to 1.7 procedures. In this experience, no side effects were reported, but in some studies injecting different drugs, severe issues were rarely encountered, including fatal mediastinitis, perforations, and pleural effusion 6 8. Thus, importance of reducing the dose and the number of procedures rapidly became apparent, and a single session of injection was tested with successful outcomes 9. Some patients with stenosis resistant to local injections underwent systemic steroid therapy with good outcomes, illustrating the superior power of repeated and high-dose systemic administration 10 11. Oral steroids appeared to be a compromise between local and systemic injections. Given to patients undergoing prophylactic balloon dilations for resections involving more than 50 % of the circumference, oral steroids reduced the incidence of stenosis from 32 % to 5 %, with a decrease in the mean number of dilations required from 15.6 to 1.7 procedures 5. Systematic balloon dilation entails its own morbidity inasmuch as the mucosal defect is recent, with a relatively high risk of perforation. Furthermore, steroid administration for 8 weeks, leading to a high cumulative dose of more than 1000 mg, is associated with well-known adverse effects on the bones and adrenal glands and the development of metabolic disorders and infections. At present, steroid-free alternative strategies are being evaluated and offer different solutions. Among them, local grafts of tissue-engineered cell sheets 12, amniotic membrane 13, or gastric mucosa 14 seem promising for reducing the number of cases of stenosis in small, preliminary preclinical reports. However, the real effectiveness and safety of these grafts are not yet known, and several large studies should be conducted before we can think of discontinuing steroid use. Steroids are the only effective option currently available for preventing stenosis after a large ESD in the esophagus, but the optimization of treatment with lower doses that are effective but safer appears necessary. In the present issue of Endoscopy International Open, Kataoka et al. report testing a short and low dose steroid treatment to prevent stenosis after esophageal ESD involving up to 50 % of the circumference. Although the two study groups were not treated during the same period, the same ESD technique was used. Furthermore, the investigators did not use systematic EBD after the ESD procedure, allowing the effects of steroids alone to be evaluated. With an average cumulative dose of 420 mg of prednisolone within 3 weeks, the incidence of stenosis was 17.6 %, whereas it was 68 % without prevention. In addition, the authors considered not only symptomatic stenosis but also the inability to pass a 9.2-mm gastroscope at 8 weeks after ESD. For the patients in whom stenosis developed, the mean number of EBDs required was 4.6 in the steroid group compared with 8.1 in the control group. In other words, low dose oral steroids reduced the number of cases of stenosis and its severity when it developed. No steroid-related adverse events occurred in the relatively short 12-month follow-up period. Although this work is not comparative and randomized, it introduces steroid dose reduction in the prevention of esophageal stenosis. In regard to steroid-related adverse events, the risk of bone fractures appears at doses of up to 7.5 mg per day during 3 months in the guidelines of the European League Against Rheumatism 15. Such treatment represents a cumulative dose of 675 mg, and the change from 1000 mg for 8 weeks in the current strategies to 420 mg for 3 weeks in this study is highly beneficial in preventing the induction of osteoporosis. We need comparative data on the effectiveness of the low dose and the high dose to support the reduced-dose strategy. As we await these evaluations, we have to remember to implement all the prophylactic measures needed for patients on steroid therapies, including calcium and vitamin D3 supplementation, bisphosphonate treatment (cumulative dose of > 675 mg) 15, physical activity, control of body weight, and a low fat and low salt diet. To summarize, post-ESD esophageal stenosis is a frequent issue, and prophylactic strategies in which steroids are used are effective and can be justified. The choice of steroid strategy – local injections or oral intake – is not clear, and comparative studies are needed. The present paper introduces a new concept for endoscopists – low dose oral intake – and demonstrates its effectiveness. This dose reduction is known to decrease the number of adverse events, in particular those involving the bones, and must be spread out. In the meantime, without comparative work, we must remember to implement all the prophylactic measures needed for patients taking steroids to minimize their negative effects.
  14 in total

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Authors:  J N Hoes; J W G Jacobs; M Boers; D Boumpas; F Buttgereit; N Caeyers; E H Choy; M Cutolo; J A P Da Silva; G Esselens; L Guillevin; I Hafstrom; J R Kirwan; J Rovensky; A Russell; K G Saag; B Svensson; R Westhovens; H Zeidler; J W J Bijlsma
Journal:  Ann Rheum Dis       Date:  2007-07-27       Impact factor: 19.103

2.  Fatal mediastinitis following botulinum toxin injection for esophageal spasm.

Authors:  Sophie Marjoux; Mathieu Pioche; Thomas Benet; Jean-Sébastien Lanne; Sabine Roman; Thierry Ponchon; François Mion
Journal:  Endoscopy       Date:  2013-11-27       Impact factor: 10.093

3.  Predictors of postoperative stricture after esophageal endoscopic submucosal dissection for superficial squamous cell neoplasms.

Authors:  S Ono; M Fujishiro; K Niimi; O Goto; S Kodashima; N Yamamichi; M Omata
Journal:  Endoscopy       Date:  2009-06-29       Impact factor: 10.093

4.  Endoscopic intralesional steroid injections in the management of refractory esophageal strictures.

Authors:  N N Zein; J M Greseth; J Perrault
Journal:  Gastrointest Endosc       Date:  1995-06       Impact factor: 9.427

5.  The efficacy of endoscopic triamcinolone injection for the prevention of esophageal stricture after endoscopic submucosal dissection.

Authors:  Satoru Hashimoto; Masaaki Kobayashi; Manabu Takeuchi; Yuichi Sato; Rintaro Narisawa; Yutaka Aoyagi
Journal:  Gastrointest Endosc       Date:  2011-12       Impact factor: 9.427

6.  Intralesional steroid injection to prevent stricture after endoscopic submucosal dissection for esophageal cancer: a controlled prospective study.

Authors:  N Hanaoka; R Ishihara; Y Takeuchi; N Uedo; K Higashino; T Ohta; H Kanzaki; M Hanafusa; K Nagai; F Matsui; H Iishi; M Tatsuta; Y Ito
Journal:  Endoscopy       Date:  2012-08-28       Impact factor: 10.093

7.  High dose intravenous methylprednisolone resolves esophageal stricture resistant to balloon dilatation with intralesional injection of dexamethasone.

Authors:  Nobuyuki Morikawa; Toshiro Honna; Tatsuo Kuroda; Koji Watanabe; Hideaki Tanaka; Hajime Takayasu; Akihiro Fujino; Hiroko Tanemura; Makoto Matsukubo
Journal:  Pediatr Surg Int       Date:  2008-10       Impact factor: 1.827

8.  Prevention of esophageal stricture after endoscopic submucosal dissection using tissue-engineered cell sheets.

Authors:  Takeshi Ohki; Masayuki Yamato; Masaho Ota; Ryo Takagi; Daisuke Murakami; Makoto Kondo; Ryo Sasaki; Hideo Namiki; Teruo Okano; Masakazu Yamamoto
Journal:  Gastroenterology       Date:  2012-05-03       Impact factor: 22.682

9.  Predictive factors for esophageal stenosis after endoscopic submucosal dissection for superficial esophageal cancer.

Authors:  H Mizuta; I Nishimori; Y Kuratani; Y Higashidani; T Kohsaki; S Onishi
Journal:  Dis Esophagus       Date:  2009-03-06       Impact factor: 3.429

10.  Amniotic membrane grafts for the prevention of esophageal stricture after circumferential endoscopic submucosal dissection.

Authors:  Maximilien Barret; Carlos Alberto Pratico; Marine Camus; Frédéric Beuvon; Mohamed Jarraya; Carole Nicco; Luigi Mangialavori; Stanislas Chaussade; Frédéric Batteux; Frédéric Prat
Journal:  PLoS One       Date:  2014-07-03       Impact factor: 3.240

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