Clinical Study | Open Access
M. Alnawaiseh, N. Mihailovic, A. C. Wieneke, V. Prokosch, A. Rosentreter, R. L. Merté, N. Eter, "Long-Term Outcomes of External Dacryocystorhinostomy in the Age of Transcanalicular Microendoscopic Techniques", Journal of Ophthalmology, vol. 2016, Article ID 5918457, 4 pages, 2016. https://doi.org/10.1155/2016/5918457
Long-Term Outcomes of External Dacryocystorhinostomy in the Age of Transcanalicular Microendoscopic Techniques
Purpose. This study aimed to evaluate long-term results of external dacryocystorhinostomy (DCR) at a tertiary eye care center specializing in lacrimal duct surgery in Germany. Methods. The medical records of 1010 patients with acquired nasolacrimal duct obstruction (NLDO), who had undergone lacrimal duct surgery at a tertiary eye care center, were reviewed. Only adult patients who had undergone external DCR were included. The evaluation included the following parameters: age, gender, duration of symptoms, patient satisfaction, previous dacryocystitis, complication rates, and surgical outcome. Results. 154 eyes of 146 patients (14.5%) could be included in the study. The average age was years. 66.4% of patients were females and 33.6% were males. Acute or chronic dacryocystitis was found in 81 patients (55.5%). Overall, 82.8% of patients had full resolution of symptoms. The success rate of external DCR for patients with previous episodes of dacryocystitis was 82.7% compared to 83.4% for patients without dacryocystitis in their medical history. Conclusion. In cases in which transcanalicular microendoscopic techniques are contraindicated (e.g., after dacryocystitis) or in complex cases where microendoscopic procedures have failed (revision surgery), external DCR is still the surgical treatment of choice with very good postoperative success.
Dacryocystorhinostomy (DCR) is the standard treatment for nasolacrimal duct obstruction. There are two main types of DCR: external and endonasal. External DCR was first described by Toti in 1904 , and the procedure has been modified many times by different surgeons over the years . The endonasal technique was first described by West in 1910 .
However, since the early 1990s minimally invasive microendoscopic transcanalicular therapeutic techniques such as laser dacryoplasty (LDP) or microdrill dacryoplasty (MDP) have become more and more popular [5, 6]. These procedures allow the physiology of the lacrimal drainage system to be preserved intact and obviate the need for an external DCR. Thus, in specialized centers the number of external DCRs performed has decreased markedly, and external DCR is usually chosen only when transcanalicular microendoscopic techniques are contraindicated, such as in revision operations or in complicated or traumatic cases [5–8].
The purpose of the current study was to evaluate preoperative characteristics and postoperative outcomes of external DCR in this new and demanding indication area at a tertiary referral center specializing in lacrimal duct surgery in Germany.
2. Materials/Subjects and Methods
In this study we retrospectively reviewed the medical records of all patients who had undergone lacrimal surgery at a tertiary eye care center between 2009 and 2011. The retrospective study was approved by the local ethics committee and adhered to the tenets of the Declaration of Helsinki.
2.1. Inclusion Criteria
Inclusion criteria are as follows:(1)adult patients (age over 18 years);(2)patients with acquired NLDO;(3)patients s/p external DCR performed at our department between 2009 and 2011.The extracted data included patient demographics, side of obstruction, duration of symptoms, previous dacryocystitis, previous lacrimal duct surgery, postoperative complications, and surgical outcome.
2.2. Surgical Procedure
In our department external DCR is generally performed under general anesthesia. An incision was made medial to the angular vein at the level of the medial canthal ligament. An osteotomy with a mean diameter of 10 mm was created and the lacrimal sac opened. Posterior and anterior mucosal flaps were made and all patients were intubated with silicone tubes. The skin was closed with a 6-0 polypropylene suture. The silicon tubes were usually kept in place for 3–6 months.
Postoperative, long-term results regarding patient satisfaction and success rate were evaluated by telephone survey in October 2015. Success was defined as full resolution of symptoms and no postoperative dacryocystitis without additional postoperative lacrimal duct surgery. Regarding the analysis of long-term outcome, only the first side was included in bilateral cases. Patients were also asked to rate their satisfaction on a scale of 1 to 10 (1 = extremely dissatisfied to 10 = extremely satisfied).
Data management was performed with Microsoft Excel 2010. IBM SPSS® Statistics 22 for Windows (IBM Corporation, Somers, NY, USA) was used for statistical analyses. Fisher’s exact test was used to compare the results of DCR surgeries in the different subgroups.
From the medical records of a total of 1010 patients who had undergone lacrimal duct surgery () from January 2009 to December 2011, 154 eyes of 146 patients (14.5%) were included according to the previously mentioned inclusion criteria. Mean preoperative age was years; 97 patients (66.4%) were females and 49 patients (33.6%) males. Demographics of the study population are summarized in Table 1. 81 patients (55.5%) were older than 65 years (Figure 1). 138 had unilateral DCR (right side, 75 (51.4%); left side, 63 (43.2%)), and 8 patients had bilateral DCR.
Figure 2 shows the duration of symptoms. The majority of the patients showed a duration of symptoms prior to first presentation at our department of more than one year (Figure 2). 78.8% () patients complained of epiphora, and 55.5% () of patients had previously had acute or chronic dacryocystitis.
97 of the 146 patients (66.4%) underwent DCR as the initial lacrimal duct surgery. 33.6% of patients () had had previous lacrimal duct surgery at another institution.
Telephone interviews could be performed in 87 patients (59.6%). The follow-up period ranged from 42 months to 80 months (mean months). The success rate of DCR in different subgroups is summarized in Table 2. The success rate of external DCR for patients with previous episodes of dacryocystitis was 82.7%, compared to 83.4% for patients without previous episodes of dacryocystitis. The difference was not statistically significant (). The success rate in patients without previous lacrimal duct surgery was 88.5% compared to 74.3% for patients with previous lacrimal duct surgery. The difference was also not statistically significant ().
Patient satisfaction with the surgical outcome is summarized in Figure 3. Significant postoperative hemorrhage was observed in 2 cases (1.4%).
The relative number of external DCR procedures in relation to the total number of all forms of lacrimal duct surgery performed at our department (14.5%) agrees with results from other centers specializing in lacrimal duct surgery [5, 7]. Due to the development of microendoscopic transcanalicular techniques (MDP and LDP) over the last 10 years, the relative number of external DCR procedures performed has decreased markedly [5–7]. The minimally invasive, scarless endoscopic techniques have an acceptable success rate of up to 80% and are highly suitable for use as an initial treatment (first-step procedure) [5–7]. In recent years external DCR at our department has been performed mainly following dacryocystitis, as a secondary procedure after prior lacrimal duct surgery, or where transcanalicular microendoscopic techniques were contraindicated [5–8].
66.4% of the patients were females, which is comparable with reports in the literature [1, 2, 9]. The majority of patients were older than 65 years. As DCR has a better success rate than transcanalicular microendoscopic techniques [1, 6, 7, 9–12], we applied DCR more frequently in elderly multimorbid patients to minimize the risk of revision surgery and further general anesthesia.
About 50% of patients showed duration of symptoms of less than one year prior to first presentation at the clinic. Some patients with chronic symptoms and a history of different forms of lacrimal duct surgery reported their symptoms to have lasted for several years.
Comparing success rates of lacrimal duct surgery is a difficult task because different studies use different success criteria (anatomic patency, improvement in tearing, or full resolution of symptoms) and the follow-up time varies widely. Evidence of anatomic patency to irrigation does not provide any information about the physiologic function of the DCR or patient satisfaction and can overestimate surgical success [18–20]. In this study only patients who became completely asymptomatic following DCR, with a minimum follow-up time of 3.5 years after surgery, were rated as successes. A further important aspect to take into consideration is the type of study population. This study investigated success rates of external DCR in some completely new and demanding indication areas: elderly patients (55.5% were older than 65 years), patients after dacryocystitis (55.5%), or patients after previous lacrimal duct surgery (33.6%).
In this study 55.5% of the patients had had a previous episode of dacryocystitis; there was no significant difference in the success rate of external DCR in patients with or without a previous episode of dacryocystitis. These findings are consistent with other studies in the literature .
Our study is limited by its retrospective design. However, the relatively large sample size with a long follow-up (mean follow-up of months) and the unusual study population (reflecting real-life data from a tertiary referral center specializing in lacrimal duct surgery) do add value to this study.
In conclusion, with the rapid development and progress achieved in minimally invasive microendoscopic lacrimal duct surgery, the relative number of external DCRs performed as first-line treatment has decreased markedly and the indication area has changed completely over the last 10 years. However, external DCR is still the surgical treatment of choice with very good postoperative success rate in special indication fields.
The authors declare no competing interests.
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