Randomized, Placebo-Controlled Pilot Study of Naproxen During Dental Implant Osseointegration

IF 1.7 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Clinical and Experimental Dental Research Pub Date : 2025-01-05 DOI:10.1002/cre2.70065
Hattanas Kumchai, Daniel I. Taub, Ryan E. Tomlinson
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Abstract

Objectives

Nonsteroidal anti-inflammatory drugs (NSAIDs) are often prescribed following the placement of dental implants, but the effects of these drugs on the osseointegration process are poorly understood. We designed a randomized, placebo-controlled pilot study to quantitatively assess the effect of NSAIDs during early implant osseointegration.

Materials and Methods

Subjects receiving a maxillary dental implant were randomized to take naproxen or placebo for 7 days after the surgery. Implant osseointegration was quantified using Resonance Frequency Analysis device. Implant-Stability-Quotient (ISQ) measurement was performed at the time of surgery and at follow-up visits 1, 4, and 16 weeks after surgery. Periapical radiographs were taken to measure the marginal bone level. Separately, a questionnaire of NSAIDs usage was provided to subjects presenting with early implant failure.

Results

After 4 weeks, ISQ values increased modestly ( + 1%) in subjects receiving naproxen whereas subjects receiving placebo had a much larger increase in ISQ value (+41%). We observed 55% more marginal bone loss at 4 weeks, and 52% at 16 weeks in the naproxen group compared to the placebo group. These results were not found to have statistically significant between groups (p ≥ 0.05). These effect sizes and variance were used to conduct a power analysis to determine the necessary sample size for future studies. Furthermore, our separate questionnaire study revealed that 68% of our patients with early failed dental implants reported a history of NSAIDs usage after the surgery.

Conclusion

In conclusion, this pilot study provides effect sizes and sample size estimates for future studies to definitively determine recommendations regarding NSAID usage following dental implant surgery. Nonetheless, our study did not observe any statistically significant differences in ISQ value or marginal bone loss after up to 16 weeks of follow-up between subjects from naproxen and placebo groups.

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萘普生在种植体骨整合中的随机、安慰剂对照试验研究。
目的:非甾体抗炎药(NSAIDs)通常在种植体植入后使用,但这些药物对骨整合过程的影响尚不清楚。我们设计了一项随机、安慰剂对照的初步研究,定量评估非甾体抗炎药在早期种植体骨整合中的作用。材料和方法:接受上颌种植体的受试者在术后7天随机服用萘普生或安慰剂。采用共振频率分析仪定量种植体骨整合。植体稳定性商数(ISQ)测量在手术时和术后1、4和16周的随访中进行。采用根尖周围x线片测量边缘骨水平。另外,向出现早期种植失败的受试者提供非甾体抗炎药使用问卷。结果:4周后,接受萘普生治疗的受试者的ISQ值略有增加(+ 1%),而接受安慰剂治疗的受试者的ISQ值增加幅度要大得多(+41%)。我们观察到,与安慰剂组相比,萘普生组4周时的边缘骨质流失多55%,16周时多52%。各组间差异无统计学意义(p≥0.05)。这些效应量和方差被用来进行功效分析,以确定未来研究所需的样本量。此外,我们的单独问卷研究显示,68%的早期种植牙失败的患者报告术后使用非甾体抗炎药的历史。结论:本初步研究为未来研究提供了效应量和样本量估计,以明确确定种植牙手术后使用非甾体抗炎药的建议。尽管如此,我们的研究并没有观察到在长达16周的随访后,萘普生组和安慰剂组的受试者在ISQ值或边缘骨质流失方面有任何统计学上的显著差异。
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来源期刊
Clinical and Experimental Dental Research
Clinical and Experimental Dental Research DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.30
自引率
5.60%
发文量
165
审稿时长
26 weeks
期刊介绍: Clinical and Experimental Dental Research aims to provide open access peer-reviewed publications of high scientific quality representing original clinical, diagnostic or experimental work within all disciplines and fields of oral medicine and dentistry. The scope of Clinical and Experimental Dental Research comprises original research material on the anatomy, physiology and pathology of oro-facial, oro-pharyngeal and maxillofacial tissues, and functions and dysfunctions within the stomatognathic system, and the epidemiology, aetiology, prevention, diagnosis, prognosis and therapy of diseases and conditions that have an effect on the homeostasis of the mouth, jaws, and closely associated structures, as well as the healing and regeneration and the clinical aspects of replacement of hard and soft tissues with biomaterials, and the rehabilitation of stomatognathic functions. Studies that bring new knowledge on how to advance health on the individual or public health levels, including interactions between oral and general health and ill-health are welcome.
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