All ex-DCRs were performed by the same surgeon under local anesthesia using 2% lidocaine containing 0.0125 mg/mL epinephrine (Astra Zeneca K.K., Osaka, Japan). A skin incision was made at 2 mm from the medial canthus. Orbicularis muscle fibers were separated bluntly to expose the periosteum overlying the anterior lacrimal crest and the medial canthal tendon. A periosteum incision was made inferomedial to the insertion of the medial canthal tendon. A square-shaped osteotomy of approximately 10 × 10 mm called a bony window was made by a drill with a diamond-coated 2-mm round tip (Tact Medical, Inc., Tokyo, Japan). The bony window was extended to the nasal mucosa. The nasal mucosa was then removed along the bony window. For accurate lacrimal sac incision, 1% purified methylrosanilinium chloride (Wako Pure Chemical Industries, Ltd., Osaka, Japan) diluted to 0.01% with saline solution was injected into the lacrimal sac through the upper canaliculus for mucosal epithelium staining. In all cases of ex-DCR, a one-flap anastomosis was made; posterior flap using the lacrimal sac was fixed by electrocoagulation, and then a bicanalicular silicone stent (Nunchaku-style tubing [NST]; Kaneka Medix, Corp., Osaka, Japan) was inserted for all of the patients. After confirmation of hemostasis, the orbicularis muscle was closed with 6-0 polyglactin absorbable sutures. Finally, the skin was closed with 6-0 monofilament suture. 0.01% fluorometholone (Santen Pharmaceutical Co., Ltd., Osaka, Japan) and 0.5% tranilast (Kissei Phamaceutical Co., Ltd., Nagano, Japan) were used for suppression of granulation tissue four times per day after surgery, and 0.5% levofloxacin (Santen Pharmaceutical Co., Ltd.) hydrate was also administered four times per day after surgery for antibiotic prophylaxis. Fluorometholone was used for 4 months postoperatively. Tranilast and levofloxacin hydrate were used during the study period. Postoperative follow-up visits were performed after surgery at 2 weeks and monthly. Each visit included evaluation of TM with slit-lamp examination and AS-OCT, and then evaluation of the patency of the created passage by lacrimal irrigation. Nunchaku-style tubing (Kaneka Medix, Corp.) was used for all subjects and removed after examinations at 2 months after surgery. In three eyes of two patients, mild symptoms and findings of dry eye were observed postoperatively, and purified sodium hyaluronate (Santen Pharmaceutical Co., Ltd.) four times per day was used for these eyes.