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Table 3 Included studies—nonsurgical treatment of peri-implant mucositis: alternative or adjunctive measures for biofilm removal

From: Efficacy of alternative or adjunctive measures to conventional treatment of peri-implant mucositis and peri-implantitis: a systematic review and meta-analysis

Publication

Design

Population

Case definition

Period

Test

Control

Mean (SD) outcome

Ji et al. [15]

RCT, parallel

24 patients

PD ≥4 mm, BOP + no radiographic bone loss compared with baseline (i.e. immediately after prosthesis installation)

3 months

OHI + mechanical debridement (ultrasonic scaler with carbon fibre tips) + air abrasive device, glycine powder (sites with PD ≥4 mm)

OHI + mechanical debridement (ultrasonic scaler with carbon fibre tips)

Test

  

33 implants

   

BI: 1.4 (0.57) (BL) to 1.1 (0.58) (3 months, subject level)

  

Molar/premolar sites

    

BI: 1.7 (0.93) (BL) to 1.1 (0.98) (3 months, implant level)

  

1 implant system

    

Sites without bleeding: 29.3 %

       

PD: 3.6 (0.47) (BL) to 3.2 (0.48) mm (3 months, subject level)

       

Control

       

BI: 1.5 (0.65) (BL) to 1.0 (0.85) (3 months, subject level)

       

BI: 1.7 (1.0) (BL) to 0.9 (1.1) (3 months, implant level)

       

Sites without bleeding: 42 %

       

PD: 3.5 (0.5) (BL) to 3.1 (0.38) mm (3 months, subject level)

De Siena et al. [18]

CCT, parallel

30 patients

BOP or spontaneous bleeding with local swelling

6 months

OHI + mechanical debridement Teflon curettes, polishing) + air abrasive device, glycine powder

OHI + mechanical debridement Teflon curettes, polishing)

Test

  

No information on number and types of implants

PD ≤3.5 mm

   

PD: 3.0 (0.4) (BL) to 2.4 (0.5) mm (6 months, subject level)

   

Bone loss ≤ 3.0 mm

   

13 patients did not present bleeding at 6 months

       

Control

       

PD: 2.9 (0.4) (BL) to 3.0 (0.6) mm (6 months, subject level)

       

9 patients did not present bleeding at 6 months

       

BI and PD scores sign. lower in the test group at 6 months

Riben Grundström et al. [21]

RCT, parallel

37 patients

PD ≥4 mm, BOP + with or without suppuration

12 months

OHI + air abrasive device, glycine powder

OHI + mechanical debridement (ultrasonic scaler with plastic coated tips)

Test

  

One implant per subject used

Bone loss ≤2 mm from implant shoulder

 

Repeated treatment at 3 and 6 months

Repeated treatment at 3 and 6 months

BOP: 43.9 (7.3) (BL) to 12.1 (3.8) % (12 months, subject level)

  

Test N = 19

    

Number of diseased sites (pocket depth ≥4 mm with bleeding/suppuration)

  

Control N = 18

    

38 % (BL) to 8 % (12 months, subject level)

       

Control

       

BOP: 53.7 (7.9) (BL) to 18.6 (6.4) % (12 months, subject level)

       

Number of diseased sites (pocket depth ≥4 mm with bleeding/suppuration)

       

52 % (BL) to 17 % (12 months, subject level)

       

No significant differences between groups for either reduction of

       

BOP or of diseased sites

  1. BI bleeding index, BL baseline, BOP bleeding on probing, CCT non-randomized controlled clinical study, OHI oral hygiene instructions, PD probing pocket depth, RCT randomized controlled clinical study