A three-year prospective cohort study evaluating implant stability utilising the osstell® and periotest™ devices

IF 1.5 Q3 DENTISTRY, ORAL SURGERY & MEDICINE Frontiers in dental medicine Pub Date : 2023-03-13 DOI:10.3389/fdmed.2023.1139407
I. Reynolds, L. Winning, I. Polyzois
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引用次数: 2

Abstract

Objectives To investigate implant stability measurements from two different devices and at three different time points in order to determine their level of correlation. To also evaluate the influence of a range of clinical characteristics on the values produced by the devices at these three time points. Materials & Methods Measurements were recorded at implant placement (T1), implant exposure (T2) and at 3 years from implant placement (T3). A range of clinical data was collected including patient demographics and site characteristics. Stability measurements and clinical characteristics were recorded for 29 patients and 68 dental implants at T1, subsequent stability measurements were recorded for 67 implants at T2 and 58 implants at T3. Correlation testing between the Osstell® and Periotest™ devices was carried out utilising Spearman's rank correlation for each time point. Analysis of the difference between clinical factors and stability measurements was compared using Krushal-Wallis test for each variable and time point. Results A single dental implant failed shortly after 2nd stage surgery for an overall survival rate of 98% during the study timeline. The median ISQ value was 73.25 (IQR 67–75) at T1 and 74 (IQR 70.5–77) at T3. The median Periotest value was −4 (IQR −6, −2) at T1 and −6 (IQR −7, −5) at T3. The range of ISQ values observed was 50 (39–89) ISQ at T1 and decreased to 21 (61–82) ISQ at T3. The Periotest values ranged from 37 (29 to −8) at T1 and decreased to 6 (−2 to −8) at T3. A weak to moderate correlation was observed between mean ISQ and Periotest values across time-points T1, T2 and T3, (r = −0.26, p = 0.05), (r = −0.35, p < 0.01) and (r = −0.28, p = 0.04) respectively. Conclusions Based on the results of this study there was a weak to moderate level of correlation between values recorded between the two measurement devices at implant placement, implant exposure and three years following placement. For both the Osstell® and Periotest™ a narrowing of the range of stability values was observed from T1 to T3. In general, Periotest™ seemed to be more sensitive in highlighting differences in measurements affected by local conditions.
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一项利用osstell®和periotest™装置评估种植体稳定性的为期三年的前瞻性队列研究
目的研究两种不同装置在三个不同时间点进行的植入物稳定性测量,以确定其相关性水平。还评估一系列临床特征对这三个时间点设备产生的值的影响。材料和方法在植入物放置(T1)、植入物暴露(T2)和植入物放置后3年(T3)记录测量结果。收集了一系列临床数据,包括患者人口统计和部位特征。在T1时记录了29名患者和68个牙种植体的稳定性测量和临床特征,随后在T2时记录了67个种植体和T3时记录了58个种植体的稳定测量。Osstell®和Periotest之间的相关性测试™ 设备是利用Spearman的秩相关性对每个时间点进行的。使用Krushal Wallis检验对每个变量和时间点的临床因素和稳定性测量之间的差异进行比较。结果在第二阶段手术后不久,单个牙种植体失败,在研究时间内,总生存率为98%。中位ISQ值在T1时为73.25(IQR 67-75),在T3时为74(IQR 70.5-77)。Periotest中值在T1时为−4(IQR−6,−2),在T3时为−6(IQR–7,−5)。观察到的ISQ值范围在T1为50(39–89)ISQ,在T3降至21(61–82)ISQ。Periotest值在T1时为37(29至−8),在T3时降至6(−2至−8。在时间点T1、T2和T3的平均ISQ和Periotest值之间观察到弱到中等的相关性,(r = −0.26,p = 0.05),(r = −0.35,p < 0.01)和(r = −0.28,p = 0.04)。结论根据本研究的结果,在植入物放置、植入物暴露和植入后三年,两种测量设备之间记录的值之间存在弱到中等程度的相关性。对于Osstell®和Periotest™ 观察到稳定性值的范围从T1到T3变窄。一般来说,Periotest™ 在强调受当地条件影响的测量差异方面似乎更为敏感。
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2.10
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审稿时长
13 weeks
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