Hypersensitivity of the Exposed Root Surface after the Surgical Periodontal Treatment

Nishida, M; Murayama, Yoji; Nomura, Yoshio; Asano, Kiyokazu; Ujimoto, Fumikazu; Shinoda, Shuichi; Sakan, Junko; Uchida, Akitsugu; Katamsi, Dewi; Yokomizo, I

doi:10.2329/perio.18.502

Cited by 5 publications

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“…For example, four studies were predominantly female [ 9 , 15 , 41 , 45 ] whereas the other two studies were predominantly male [ 42 , 47 ]. However, some studies did not mention the gender distribution [ 39 , 40 , 44 ].…”

Section: Resultsmentioning

confidence: 99%

The Prevalence of Root Sensitivity following Periodontal Therapy: A Systematic Review

Lin

Gillam

2012

International Journal of Dentistry

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The reported prevalence of dentine/root (hyper)sensitivity (DH/RS) in the published literature varies, and this may be due in part to a) the different study populations and (b) the different methodologies employed in evaluating the pain response. According to von Troil et al. (2002) there are limited data available in terms of the prevalence and intensity of DH/RS following periodontal therapy. Objectives. The aim of the present study was therefore to review the literature in order to identify all relevant studies for inclusion and to determine whether there was any evidence of DH/RS following periodontal procedures in the published literature up to 31st December 2009 using an agreed search protocol. Methods. 840 papers were identified, from searching both electronic databases (PUBMED) and hand searching of relevant written journals. Twelve papers were subsequently accepted for inclusion. Results. The results of the present study would indicate that the reported prevalence for DH/RS (following nonsurgical therapy) was between 62.5% and 90% one day after treatment decreasing to approximately 52.6% to 55% after one week. The prevalence of DH/RS following surgical therapy was between 76.8% and 80.4% one day after treatment subsequently decreasing over time to 36.8% after 1 week, 33.4% after 2 weeks, 29.6% after 4 weeks, and 21.7% after 8 weeks. Conclusions. It is evident from reviewing the included studies that patients may suffer from mild discomfort following periodontal procedures although both the prevalence and intensity of DH/RS may vary depending on the duration and the type of procedure involved. Most of the studies included in this paper would tend to suggest that DH/RS may be relatively mild/moderate in nature and transient in duration.

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Section: Resultsmentioning

confidence: 99%

The Prevalence of Root Sensitivity following Periodontal Therapy: A Systematic Review

Lin

Gillam

2012

International Journal of Dentistry

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“…It has been reported that the hypersensitivity degree was related to the extent of the exposed root surface (Nishida et al. , Wallace & Bissada ). The absence of correlation between periodontal parameters and hypersensitivity demonstrated at 6 weeks in this study reinforces the importance of the in‐office arginine–calcium carbonate paste in the greater hypersensitivity reduction achieved in the test group.…”

Section: Discussionmentioning

confidence: 99%

Effectiveness of an in‐office arginine‐calcium carbonate paste on dentine hypersensitivity in periodontitis patients: a double‐blind, randomized controlled trial

Pepelassi

Rahiotis

Peponi

et al. 2014

J Clinic Periodontology

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“…The current clinical study tried to compare the clinical effectiveness of Gluma Desensitizer, Clearfil S 3 Bond (one-bottle self-etching adhesive), and placebo (distilled water) for CDS treatment after periodontal surgery in different evaluation times by using VAS. Several studies noted that the patient may encounter abrupt and severe dentin sensitivity after periodontal therapies [ 13 14 ]. Also, the occurrence and severity of CDS directly depend on the type of periodontal treatment and are greater after surgical procedures [ 15 ].…”

Section: Discussionmentioning

confidence: 99%

Comparing the effect of a desensitizing material and a self-etch adhesive on dentin sensitivity after periodontal surgery: a randomized clinical trial

et al. 2017

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ObjectivesThis double-blind randomized placebo-controlled clinical trial evaluated the ability of a desensitizing agent and a self-etch adhesive on cervical dentin sensitivity (CDS) after periodontal surgery.Materials and MethodsNinety hypersensitive teeth of 13 subjects were included in the study. After periodontal surgery, the teeth of each posterior sextant treated with one of the following materials: G1: Clearfil S3 Bond (Kuraray Dental), G2: Gluma Desensitizer (Heraeus Kulzer), and G3: placebo (water). The sensitivity was assessed using evaporative stimuli before treatment (baseline, T0), 1 day after treatment (T1), after 1 week (T2), and after 1 month (T3) according to visual analog scale (VAS).ResultsFollowing the treatment, all the 3 groups showed significant reduction of CDS in T1 compared to T0. Reduction of CDS between T1 and T2 was observed only in G1 but there was no significant difference between T2 and T3 in this group. Although we observed a significant difference in T3 compared to T1 and T2 in G2 and G3, comparison of treatment groups in each assessment time showed a significant difference only in T3. According to paired comparison, this was due to the difference between G2 and G3.ConclusionsDentin sensitivity following periodontal surgery will decrease spontaneously over time, but treating the sensitive teeth with Gluma Desensitizer and Clearfil S3 Bond can have some benefits.

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Hypersensitivity of the Exposed Root Surface after the Surgical Periodontal Treatment

Cited by 5 publications

References 0 publications

The Prevalence of Root Sensitivity following Periodontal Therapy: A Systematic Review

The Prevalence of Root Sensitivity following Periodontal Therapy: A Systematic Review

Effectiveness of an in‐office arginine‐calcium carbonate paste on dentine hypersensitivity in periodontitis patients: a double‐blind, randomized controlled trial

Comparing the effect of a desensitizing material and a self-etch adhesive on dentin sensitivity after periodontal surgery: a randomized clinical trial

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