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在阻塞性乳突切除术中使用博来霉素:解剖学结果和临床结果。

Use of bonalive in obliterative mastoidectomy: anatomical results and clinical outcome.

机构信息

Division of Otorhinolaryngology, Department of Surgical Sciences, A. O. Ordine Mauriziano di Torino, Largo Turati 62, 10128, Turin, Italy.

出版信息

Eur Arch Otorhinolaryngol. 2023 Aug;280(8):3577-3583. doi: 10.1007/s00405-023-07850-z. Epub 2023 Mar 14.

Abstract

PURPOSE

To investigate safety and efficacy of mastoid obliteration in canal-wall-down tympanoplasty performed for cholesteatoma using bioactive glass (BAG). The authors routinely adopt CWD tympanoplasty in case of massive cholesteatoma or revision surgery, performing obliteration with BAG to reduce the mastoid cavity and related disadvantages. We assessed anatomical results, infection control and cholesteatoma recurrence in obliterative mastoidectomy using BAG.

METHODS

The authors evaluated 66 patients treated with obliterative mastoidectomy using BAG during the period 2010-2021. 48.5% of the cases had first diagnosis of cholesteatoma, 48.5% had cholesteatoma recidivisms, and two patients underwent obliteration to improve clinical outcome. BAG granules were always moistened with venous blood to enhance their adhesion and reduce the risk of dispersion. Anatomical results were evaluated in otomicroscopy and infection control was assessed during follow-up visits. Periodical otomicroscopy was performed to check recurrent cholesteatoma. MRI-DWI was indicated only in case of clinical suspect of cholesteatoma.

RESULTS

Authors followed 66 patients during a mean of 23 months. No post-operative wound infections occured. The mean re-epithelialization time was 45 days. At the last visit, control of infection was achieved in 97% of patients and a clinical stable anatomical cavity in all patients. No clinical suspect for recurrent cholesteatoma was found.

CONCLUSIONS

The use of bioactive glass is safe and effective as obliteration material in cholesteatoma surgery. Authors pay a particular attention to obliterate only patients without suspect of epithelial residual, to correctly calibrate the ear canal and to completely cover the granules with graft.

摘要

目的

研究使用生物活性玻璃(BAG)进行胆脂瘤型中耳炎乳突根治术后鼓室成形术的安全性和疗效。作者常规采用 CWD 乳突根治术治疗巨大胆脂瘤或翻修手术,使用 BAG 进行填塞以缩小乳突腔并减少相关弊端。我们评估了 BAG 填塞乳突术的解剖学结果、感染控制和胆脂瘤复发情况。

方法

作者评估了 2010 年至 2021 年间使用 BAG 进行填塞乳突术的 66 例患者。48.5%的病例首次诊断为胆脂瘤,48.5%的病例为胆脂瘤复发,2 例患者进行填塞以改善临床结果。BAG 颗粒始终用静脉血湿润,以增强其附着力并降低分散风险。通过耳内镜评估解剖学结果,通过随访评估感染控制情况。定期进行耳内镜检查以检查胆脂瘤复发情况。仅在临床怀疑胆脂瘤的情况下进行 MRI-DWI。

结果

作者平均随访 66 例患者 23 个月。无术后伤口感染。平均上皮再上皮化时间为 45 天。最后一次随访时,97%的患者感染得到控制,所有患者的解剖腔均稳定。未发现胆脂瘤复发的临床可疑迹象。

结论

生物活性玻璃作为胆脂瘤手术中的填塞材料是安全有效的。作者特别注意仅在没有上皮残留可疑的患者中进行填塞,正确校准耳道并将颗粒完全用移植物覆盖。

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