Nasolacrimal Stenting: Toward Improving Outcomes with a Simple Modification of the Song Stent
Autor: | Miguel Perea, Rufo Rodriguez-Merlo, Silvia De Miguel, Carlos Lanciego, Lorenzo García-García, Manuel Padilla |
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Rok vydání: | 2006 |
Předmět: |
Adult
Male medicine.medical_specialty Percutaneous Adolescent Secondary patency medicine.medical_treatment Polyurethanes Technical success Nose Asymptomatic Stent removal medicine Humans Radiology Nuclear Medicine and imaging Chronic dacryocystitis Aged Aged 80 and over Lacrimal Apparatus Diseases business.industry Stent Equipment Design Middle Aged equipment and supplies Surgery Treatment Outcome Etiology Female Stents medicine.symptom Cardiology and Cardiovascular Medicine business |
Zdroj: | CardioVascular and Interventional Radiology. 29:586-594 |
ISSN: | 1432-086X 0174-1551 |
DOI: | 10.1007/s00270-004-0297-9 |
Popis: | The purpose of this study was to evaluate, in a prospective, single-center study, the effectiveness of Song’s polyurethane stents, modified “in-house,” in the percutaneous management of epiphora. Patients (n = 170; age range 18–83, mean = 64; 50 male, 120 female) with severe epiphora had the modified stents inserted (183 eyes/195 stents) to treat unilateral/bilateral and complete/partial obstruction of the nasolacrimal system. The etiology of the obstruction was idiopathic in 119 cases (61%) and chronic dacryocystitis in 76 (39%). The set designed by Song was used in all patients but modified by us such that the extreme end is cone-shaped. The original technique was slightly modified by us and the procedure was conducted on an outpatient basis. The initial technical success rate of stent placement was 97%. Resolution of epiphora was complete in 180 eyes and partial in 3. On follow-up (mean = 18 months; range: 2 days to 24 months), 165 of 195 stents (85%) remained patent. Primary patency rates at follow-up were 86%, 84%, 84%, and 79% in the first 6 months, second and third 6 months, and the present (24 months), respectively. Stents became obstructed in 30 patients, but all but 2 were easily withdrawn and 20 of these patients remained asymptomatic for a mean of 14 months (secondary patency of 67%). Following stent removal, the withdrawn stent was replaced with a new stent in the same intervention on 14 occasions. In another six cases, patency was re-established without the need of a second stent. The procedure is simple and safe, both in stent insertion as well as in mechanical de-blocking and withdrawal when occluded. Success was >80 % in the short term (1-year follow-up). Stenting failure does not preclude other treatment because with the modification that we had introduced, the extreme end of the stent becomes more accessible to mechanical de-blocking, withdrawal, and relocation. The levels of primary and secondary patencies are promising and warrant more extensive investigation. |
Databáze: | OpenAIRE |
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