Tekin Görkem, Türedi Sena Özkiriş
Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Eskişehir Osmangazi University, Eskişehir, Türkiye.
BMC Oral Health. 2025 May 26;25(1):804. doi: 10.1186/s12903-025-06257-y.
Alveolar osteitis(AO) is an inflammatory and painful condition that occurs due to distruption of the fibrin matrix within the extraction socket following tooth extraction. This study investigates the effectiveness of I-PRF in reducing pain in AO patients compared to conventional treatment.
This prospective randomized controlled study included patients experiencing localized AO treated at the Oral, Dental, and Maxillofacial Surgery clinic between October 2024 and February 2025. Sixty patients diagnosed with AO were randomly assigned to two groups. The control group (Group 1) received standard treatment consisting of socket curettage followed by saline irrigation. The I-PRF group (Group 2) received I-PRF application after curettage and irrigation. Pain levels were assessed using the Visual Analog Scale (VAS) on postoperative days 3 and 7.
The study included 60 patients (28 males, 32 females) aged between 19 and 68 (mean 37.40 ± 12.81). There was no significant difference in preoperative VAS scores between the groups (p>0.05). On postoperative day 7, the I-PRF group showed a significant reduction in VAS scores compared to the control group (1.27 vs. 2.27, p<0.05). Our results show that I-PRF significantly reduces pain levels, offering a promising alternative to traditional therapies.
I-PRF significantly reduces pain in AO patients compared to conventional treatment. These findings suggest that I-PRF could be a valuable addition to clinical practice, but further studies are needed to confirm its long-term effectiveness.
Clinical Trials.gov Registration ID NCT06761001. Registered 30/12/ 2024- Retrospectively registered.
干槽症(AO)是一种炎症性疼痛病症,由于拔牙后拔牙窝内纤维蛋白基质遭到破坏而发生。本研究调查了与传统治疗相比,富血小板纤维蛋白(I-PRF)在减轻干槽症患者疼痛方面的有效性。
这项前瞻性随机对照研究纳入了2024年10月至2025年2月期间在口腔、牙科和颌面外科诊所接受局部干槽症治疗的患者。60名被诊断为干槽症的患者被随机分为两组。对照组(第1组)接受标准治疗,包括牙槽窝刮治,随后用生理盐水冲洗。富血小板纤维蛋白组(第2组)在刮治和冲洗后应用富血小板纤维蛋白。在术后第3天和第7天使用视觉模拟量表(VAS)评估疼痛程度。
该研究纳入了60名年龄在19至68岁之间(平均37.40±12.81)的患者(28名男性,32名女性)。两组术前VAS评分无显著差异(p>0.05)。在术后第7天,富血小板纤维蛋白组的VAS评分与对照组相比显著降低(1.27对2.27,p<0.05)。我们的结果表明,富血小板纤维蛋白显著降低了疼痛程度,为传统治疗提供了一种有前景的替代方法。
与传统治疗相比,富血小板纤维蛋白显著减轻了干槽症患者的疼痛。这些发现表明,富血小板纤维蛋白可能是临床实践中有价值的补充,但需要进一步研究来证实其长期有效性。
ClinicalTrials.gov注册编号NCT06761001。于2024年12月30日注册——回顾性注册。