A randomized trial comparing the cost-effectiveness of 2 approaches for treating unilateral nasolacrimal duct obstruction.

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Abstract

Objective: To compare the cost-effectiveness of 2 approaches for treating unilateral nasolacrimal duct obstruction (NLDO).

Methods: One hundred sixty-three infants aged 6 to less than 10 months with unilateral NLDO were randomly assigned to receive immediate office-based nasolacrimal duct probing (n = 82) or 6 months of observation/nonsurgical management (n = 81) followed by probing in a facility for persistent symptoms.

Main outcome measures: Treatment success was defined as the absence of clinical signs of NLDO (epiphora, increased tear lake, mucous discharge) on masked examination at age 18 months. Cost of treatment between randomization and age 18 months included costs for all surgical procedures and medications.

Results: In the observation/deferred facility-probing group, NLDO resolved within 6 months without surgery in 44 of the 67 patients (66%; 95% CI, 54% to 76%) who completed the 6-month visit. Twenty-two (27%) of the 81 patients in the observation/deferred facility-probing group underwent surgery, 4 of whom were operated on within the initial 6 months. At age 18 months, 69 of 75 patients (92%) in the immediate office-probing group were treatment successes, compared with 58 of 71 observation/deferred facility-probing group patients (82%) (10% difference in success; 95% CI, -1% to 21%). The mean cost of treatment was $562 in the immediate office-probing group compared with $701 in the observation/deferred facility-probing group (difference, -$139; 95% CI, -$377 to $94). The immediate office-probing group experienced 3.0 fewer months of symptoms (95% CI, -1.8 to -4.0).

Conclusions: The immediate office-probing approach is likely more cost-effective than observation followed by deferred facility probing if needed. Adoption of the immediate office-probing approach would result in probing in approximately two-thirds of infants whose obstruction would have resolved within 6 months of nonsurgical management, but would largely avoid the need for probing under general anesthesia.

Application to clinical practice: Although unilateral NLDO often resolves without surgery, immediate office probing is an effective and potentially cost-saving treatment option.

Trial registration: clinicaltrials.gov Identifier: NCT00780741.

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一项随机试验,比较治疗单侧鼻泪管阻塞的两种方法的成本效益。
目的:比较治疗单侧鼻泪管阻塞(NLDO)的两种方法的成本效益:比较治疗单侧鼻泪管阻塞(NLDO)的两种方法的成本效益:方法:随机分配163名年龄在6个月至10个月以下的单侧鼻泪管阻塞婴儿,让他们立即接受诊室鼻泪管探查术(n = 82)或6个月的观察/非手术治疗(n = 81),然后在出现持续症状时到医疗机构接受探查:治疗成功的定义是:18 个月大时,在蒙面检查中未发现 NLDO 的临床症状(外窥、泪湖增加、粘液分泌物)。随机化至 18 个月大期间的治疗费用包括所有手术和药物费用:在观察/延迟设施-探查组中,67 名完成 6 个月访视的患者中有 44 人(66%;95% CI,54% 至 76%)的 NLDO 在 6 个月内得到缓解,无需手术。观察/推迟设施检查组的81名患者中有22人(27%)接受了手术,其中4人在最初的6个月内接受了手术。18 个月大时,即时诊室检查组的 75 名患者中有 69 名(92%)治疗成功,而观察/延迟设施检查组的 71 名患者中有 58 名(82%)治疗成功(成功率相差 10%;95% CI,-1% 至 21%)。即时诊室探查组的平均治疗费用为 562 美元,而观察/延迟设施探查组为 701 美元(差异为-139 美元;95% CI 为-377 美元至 94 美元)。即时诊室检查组的症状月数减少了 3.0 个月(95% CI,-1.8 到 -4.0):结论:立即进行诊室探查的方法可能比先观察,然后在必要时推迟设施探查的方法更具成本效益。在临床实践中的应用:对临床实践的应用:尽管单侧 NLDO 通常无需手术即可解决,但立即进行诊室探查是一种有效且可能节省成本的治疗方案。试验注册:clinicaltrials.gov Identifier:试验注册:clinicaltrials.gov Identifier:NCT00780741。
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Archives of ophthalmology
Archives of ophthalmology 医学-眼科学
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