Abstract
Objective:
To compare the intraoperative and postoperative outcomes of using oxidized regenerated cellulose (Surgicel®) versus absorbable gelatin sponge (Spongostan®) for supporting graft material in endoscopic tympanoplasty.
Methods:
We retrospectively analyzed 92 patients who underwent endoscopic type 1 tympanoplasty between 2020 and 2024. Patients were divided into 2 groups based on the supporting graft material used: 47 received Surgicel® and 45 received Spongostan®. Primary outcome measures included intraoperative hemostasis quality, duration of graft placement, postoperative graft success, graft lateralization, and hearing outcomes at 6 and 12 months.
Results:
Hemostasis during graft placement was better in the Surgicel® group (P = .017), and shorter graft placement duration was observed (P = .047). At ≥ 6 months, graft success rates were comparable between the groups (89.4% for Surgicel® vs 82.2% for Spongostan®; P = .380). However, graft lateralization was significantly less frequent in the Surgicel® group (2.1%) compared to the Spongostan® group (15.6%; P = .029). While the Spongostan® group showed significantly better hearing results at 6 months (mean ABG 16.9 dB vs 28.6 dB; P < .001), hearing outcomes were similar by 12 months.
Conclusion:
Both Spongostan® and Surgicel® are effective supporting graft materials in endoscopic tympanoplasty. However, Surgicel® was associated with certain intraoperative advantages, including superior hemostasis and shorter operative time, along with a significantly lower risk of postoperative graft lateralization. These benefits suggest Surgicel® may be a preferable option for enhancing surgical efficiency and optimizing outcomes in endoscopic ear surgery.
Keywords
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