Dolmetsch Angela M, Gallon Marco A, Holds John B
Division of Orbital, Ophthalmic Plastic and Reconstructive Surgery, Clinica de Oftalmología de Cali, Hospital Universitario del Valle, Cali, Colombia, South America.
Ophthalmic Plast Reconstr Surg. 2008 Sep-Oct;24(5):390-3. doi: 10.1097/IOP.0b013e3181831f56.
To determine the outcome and safety of pediatric endonasal dacryocystorhinostomy with the use of adjunctive mitomycin C.
A prospective, nonrandomized and noncomparative interventional case series study was performed in 71 consecutive procedures. Sixty patients 16 years of age and younger underwent nonlaser endonasal dacryocystorhinostomy with the use of adjunctive mitomycin C. Eleven patients had a simultaneous bilateral procedure performed. All patients underwent a standardized procedure, with an endonasal approach to the lacrimal sac and surgical removal of nasal mucosa, lacrimal bone, and a fragment of the frontal process of the maxilla. The medial wall of the lacrimal sac was completely removed and a neurosurgical cottonoid soaked in mitomycin C at 0.5 mg/ml placed at the osteotomy site for 5 minutes. All patients underwent bicanalicular or monocanalicular silicone intubation.
The main outcome measures were the resolution of epiphora, lacrimal discharge, and patency of the ostium confirmed either by endoscopic visualization and/or irrigation at 6 months or a normal dye disappearance test. Thirteen patients' (18%) final evaluation was via telephone survey. The mean follow-up was 12.3 months. Nonlaser endonasal dacryocystorhinostomy with adjunctive mitomycin C was successful in 67 cases (94.4%). African descent was strongly associated with a higher rate of obstruction (p < 0.001). Infection at the time of surgery (p = 0.051) and less than 3 months intubation (p = 0.059) were also borderline significant. Previous trauma, gender, age, and side operated had no influence on the final outcome. No significant complications were encountered.
Nonlaser endonasal dacryocystorhinostomy with mitomycin C is a safe and successful procedure for the treatment of congenital nasolacrimal duct obstruction in children. It has the advantage of leaving no scar and of preserving the medial canthal structures. It can be successfully performed as a simultaneous bilateral procedure.
确定使用辅助性丝裂霉素C进行小儿鼻内镜下泪囊鼻腔造口术的疗效和安全性。
对连续71例手术进行前瞻性、非随机且非对照的干预性病例系列研究。60例16岁及以下患者接受了使用辅助性丝裂霉素C的非激光鼻内镜下泪囊鼻腔造口术。11例患者同时进行了双侧手术。所有患者均接受标准化手术,采用鼻内镜入路至泪囊,手术切除鼻黏膜、泪骨和上颌骨额突的一部分。完全切除泪囊内侧壁,将浸泡于0.5mg/ml丝裂霉素C的神经外科棉片置于截骨部位5分钟。所有患者均接受双泪小管或单泪小管硅胶插管。
主要观察指标为6个月时通过内镜观察和/或冲洗确认的溢泪、泪液分泌情况的改善以及造口通畅,或染料消失试验正常。13例患者(18%)通过电话调查进行最终评估。平均随访时间为12.3个月。使用辅助性丝裂霉素C的非激光鼻内镜下泪囊鼻腔造口术在67例患者(94.4%)中取得成功。非洲裔与更高的阻塞率密切相关(p<0.001)。手术时的感染(p=0.05)和插管时间少于3个月(p=0.059)也接近显著水平。既往外伤、性别、年龄和手术侧别对最终结果无影响。未出现明显并发症。
使用丝裂霉素C的非激光鼻内镜下泪囊鼻腔造口术是治疗儿童先天性鼻泪管阻塞的一种安全且成功的手术。它具有不留瘢痕和保留内眦结构的优点。可以成功地作为双侧同时手术进行。