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使用 rhFGF-2 联合脱蛋白牛骨矿物质或单独使用 rhFGF-2 治疗骨内牙周缺损:一项 6 个月的随机对照试验。

Treatment of intrabony periodontal defects using rhFGF-2 in combination with deproteinized bovine bone mineral or rhFGF-2 alone: A 6-month randomized controlled trial.

机构信息

Department of Periodontology, Tokyo Dental College, Tokyo, Japan.

出版信息

J Clin Periodontol. 2019 Mar;46(3):332-341. doi: 10.1111/jcpe.13086.

DOI:10.1111/jcpe.13086
PMID:30758076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6899590/
Abstract

AIM

To evaluate the use of recombinant human fibroblast growth factor (rhFGF)-2 in combination with deproteinized bovine bone mineral (DBBM) compared with rhFGF-2 alone, in the treatment of intrabony periodontal defects.

MATERIALS AND METHODS

Patients with periodontitis who had received initial periodontal therapy and had intrabony defects of ≥ 3 mm in depth were enrolled. Sites were randomly assigned to receive a commercial formulation of 0.3% rhFGF-2 + DBBM (test) or rhFGF-2 alone (control). Clinical parameters and a patient-reported outcome measure (PROM) were evaluated at baseline and at 3 and 6 months postoperatively.

RESULTS

Twenty-two sites in each group were evaluated. A significant improvement in clinical attachment level (CAL) from baseline was observed in both groups at 6 months postoperatively. CAL gain was 3.16 ± 1.45 mm in the test group and 2.77 ± 1.15 mm in the control group, showing no significant difference between groups. Radiographic bone fill was significantly greater in the test group (47.2%) than in the control group (29.3%). No significant difference in PROM between groups was observed.

CONCLUSIONS

At 6 months, no significant difference in CAL gain or PROM between the two treatments was observed, although combination therapy yielded an enhanced radiographic outcome.

摘要

目的

评估与单独使用重组人成纤维细胞生长因子(rhFGF-2)相比,rhFGF-2 联合脱蛋白牛骨矿物质(DBBM)在治疗骨内牙周缺损中的应用。

材料和方法

纳入接受初始牙周治疗且具有≥3mm 深度骨内缺损的牙周炎患者。将这些位点随机分配接受 0.3%rhFGF-2+DBBM(试验组)或单独 rhFGF-2(对照组)的商业化制剂治疗。在基线、术后 3 个月和 6 个月评估临床参数和患者报告的结果测量(PROM)。

结果

每组 22 个位点。两组在术后 6 个月时均观察到临床附着水平(CAL)有显著改善。试验组的 CAL 增益为 3.16±1.45mm,对照组为 2.77±1.15mm,两组间无显著差异。试验组的放射骨填充明显大于对照组(47.2%对 29.3%)。两组间 PROM 无显著差异。

结论

在 6 个月时,两种治疗方法在 CAL 增益或 PROM 方面没有显著差异,尽管联合治疗产生了增强的放射学结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b71c/6899590/a572abf67ba3/JCPE-46-332-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b71c/6899590/fa3e99ede680/JCPE-46-332-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b71c/6899590/a5e869bf4ffd/JCPE-46-332-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b71c/6899590/a572abf67ba3/JCPE-46-332-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b71c/6899590/fa3e99ede680/JCPE-46-332-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b71c/6899590/a5e869bf4ffd/JCPE-46-332-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b71c/6899590/a572abf67ba3/JCPE-46-332-g003.jpg

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