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Treatment of peri-i...
Treatment of peri-implantitis: clinical outcome of chloramine as an adjunctive to non-surgical therapy, a randomized clinical trial
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- Roos‐Jansåker, Ann‐Marie (författare)
- Department of Periodontology, Public Dental Health Service, Kristianstad, Swed
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- Almhöjd, Ulrica S. (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för odontologi,Institute of Odontology,Department of Cariology, Institute of Odontology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
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- Jansson, Henrik (författare)
- Jönköping University,Malmö högskola,Odontologiska fakulteten (OD),Oral Health Centre of Expertise in Eastern Norway, Oslo, Norway,HHJ, Avdelningen för naturvetenskap och biomedicin,Adult
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(creator_code:org_t)
- 2015-05-26
- 2017
- Engelska.
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Ingår i: Clinical Oral Implants Research. - : Wiley. - 0905-7161 .- 1600-0501. ; 28:1, s. 43-48
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https://doi.org/10.1...
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https://urn.kb.se/re...
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Abstract
Ämnesord
Stäng
- PurposeTo evaluate the adjunctive clinical effects of a chloramine to non-surgical treatment of peri-implantitis. Material and methodsEighteen individuals diagnosed with peri-implantitis (clinical signs of inflammation and progressive bone loss) on at least two implants were included. Clinical variables; plaque accumulation (Pl), probing depth (PD), clinical attachment level (CAL) and bleeding on probing (BoP), were recorded at baseline and at 3-month follow-up. Primary clinical efficacy variable was the change in the number of sites with BoP. The implants were randomized into two different treatment groups: test and control. Both implants received supra- and submucosal debridement by ultrasonic instrumentation supplemented with hand instruments. The implants assigned to the test group first received local applications of a chloramine gel (Perisolv; RLS Global AB, Gothenburg, Sweden) followed by mechanical instrumentation. The oral hygiene was checked at 6weeks. ResultsAfter 3months, implants of both groups showed statistically significant reduction (P<0.001) in the number of BoP-positive sites compared with baseline. The reduction of BoP-positive sites in the test group changed from 0.97 (SD0.12) to 0.38 (SD +/- 0.46), and in the control group from 0.97 (SD +/- 0.12) to 0.31 (SD +/- 0.42). Between-group comparisons revealed no statistically significant differences at baseline and after 3months, for BoP or any of the other variables. ConclusionIn the present randomized clinical trial of peri-implantitis therapy; non-surgical mechanical debridement with adjunctive use of a chloramine is equally effective in the reduction of mucosal inflammation as conventional non-surgical mechanical debridement up to 3months.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Odontologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Dentistry (hsv//eng)
Nyckelord
- chloramine
- non-surgical therapy
- peri-implantitis
- surface decontamination
- local-drug delivery
- periodontal therapy
- osseointegrated implants
- prevalence
- system
- carisolv(tm)
- topography
- diseases
- dentin
- Dentistry
- Oral Surgery & Medicine
- Engineering
- chloramine
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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