Publication | Design | Population | Case definition | Period | Test | Control | Mean (SD) outcome | Supportive therapy/comments |
---|---|---|---|---|---|---|---|---|
Alternative measures for biofilm removal | ||||||||
Schwarz et al. (2005) | RCT, parallel | 20 patients Test: 10, mean age: 48 years Control: 10, mean age: 51 years Smokers excluded 32 implants rough and medium-rough surfaces | PD ≥ 4 mm + BOP/SUPP + radiographic bone loss | 6 months | OHI + Er:YAG laser device (cone-shaped glass fiber tip) at 12.7 J/cm2 | OHI + mechanical debridement (plastic curettes), 0.2% CHX pocket irrigation and 0.2% CHX gel | Subject level BOP Test baseline: 83.2 (17.2)%, 6 months: 31.1 (10.1)%; p < 0.001 Control baseline: 81.3 (19.0)%, 6 months: 58.3 (16.9)%; p < 0.001 Between group comparison: p < 0.001 PD Test baseline: 5.4 (1.2) mm, 6 months: to 4.6 (1.1) mm; p < 0.001 Control baseline: 5.5 (1.5) mm, 6 months: 4.8 (1.4) mm; p < 0.001 Between group comparison: p > 0.05 ML (recession) Test baseline: 0.4 (0.6) mm, 6 months: 0.5 (0.6) mm Control baseline: 0.7 (0.8)mm, 6 months: 0.8 (0.8) mm | Er:YAG treatment results in statistically significantly higher reduction of BOP |
Schwarz et al. (2006) | RCT, parallel | 18 patients Test: 10; mean age: 56 (14) years Control: 8; mean age: 54 (11) years Smokers excluded 36 implants rough and medium-rough surfaces | PD ≥ 4 mm + BOP/SUPP + radiographic bone loss | 12 months | OHI + Er:YAG laser device (cone-shaped glass fiber tip) at 12.7 J/cm2 | OHI + mechanical debridement (plastic curettes), 0.2% CHX pocket irrigation and 0.2% CHX gel | Subject level Moderately deep sites (PD 4–6 mm) BOP Test baseline: 81.7 (6.7)%, 12 months: 35.0 (6.3) %; p < 0.01 Control baseline: 81.6 (5.2)%, 12 months: 53.3 (7.3) % Deep sites Test baseline: 79.9 (4.8)%, 12 months: 55.0 (6.5)% Control baseline: 88.3 (3.5)%, 12 months: 66.6 (5.5) % Significantly higher reduction in test group (p < 0.01) PD (PD > 7 mm) Moderately deep sites Test baseline: 4.5 (1.4) mm, 12 months: 4.0 (0.1) mm Control baseline: 4.4 (0.2) mm, 12 months: 4.3 (0.1) mm Deep sites Test baseline: 5.9 (0.1) mm, 12 months: 5.4 (0.1) mm Control baseline: 5.9 (0.3) mm. 12 months: 5.5 (0.2) mm No significant differences between groups | Er:YAG treatment results in significantly higher BOP reduction, however, its effectiveness seemed to be limited to a period of 6 months |
Renvert et al. (2009) | RCT, parallel | 31 patients Test: 14; mean age: 60.3(12.9) years; 7 female; 7 male; 2 patients current smokers Control: 17; mean age: 62.7(12.1) years; 7 female; 10 male; 3 current smokers; 31 implants machined and medium-rough surfaces | PD ≥ 4 mm + BOP/SUPP + bone loss < 2.5 mm | 6 months | OHI + ultrasonic device with hydroxyapatite fluid polish | OHI + mechanical debridement (titanium curettes) | Subject level BI Test baseline: 1.7 (0.6); 6 months: 1.2 (0.7) Control baseline: 1.7 (0.9); 6 months: 1.4 (1.0) No significant differences between groups PD Test baseline: 4.3 (0.6) mm, 6 months: 3.9 (0.8) mm Control baseline: 6.2 (1.6) mm; 6 months: 6.3 (2.2) mm No significant differences between groups | All patients received OHI at all study timepoints No group differences were found in the treatment outcomes |
Renvert et al. (2011) | RCT, parallel | 42 patients Tests: 21; mean age: 68.5 (6.4) years; Control: 21; mean age: 68.9 (12.5) years Smokers included 90 implants machined and medium-rough surfaces | PD ≥ 5 mm, BOP + and/or SUPP + bone loss > 3 mm | 6 months | OHI + air abrasive device with glycine powder | OHI + Er:YAG laser device (cone-shaped glass fiber tip, 12.7 J/cm2) | Implant level BOP 6 months Test: 25% of implant showed no bleeding Control: 30.9% of implant showed no bleeding Between-group comparison: p = 0.22 PD change Tests: 0.9 (0.8) mm Control: 0.8 (0.5) mm Between-group comparison: p = 0.55 RBL change: Test: − 0.3 (0.9)mm Control: − 0.1 (0.8)mm No significant differences between groups Positive treatment outcome (i.e., PD reduction ≥ 0.5 mm + no further bone loss): Test: 47% Positive treatment outcome: Control: 44% Between-group comparison: p = 0.84 | All patients received OHI at all study timepoints The clinical treatment results were limited and similar between the two methods compared with those in cases with severe peri-implantitis |
Sahm et al. 2011, John et al. (2011) | RCT, parallel | 30 patients Smokers excluded Test: 15 patients, 22 implants Control: 15 patients, 19 implants 8 implant systems 12 months 25 patients Test: 12 patients Control: 13 patients | PD ≥ 4 mm + BOP with SUPP + bone loss ≤ 33% | 12 months | OHI + air abrasive device with glycine powder | OHI + mechanical debridement (carbon curettes + 0.1% CHX) | Subject level BOP Test baseline: 99.0 (4.1)%, 12 months: 57.8 (30.7) % Control baseline: 94.7 (13.7)%, 12 months: 78.1 (30.0) %; Between-group comparison: p < 0.05 PD Test baseline: 3.7 (1.0) mm, 12 months: 3.2 (1.1)mm Control baseline: 3.9 (1.1) mm, 12 months: 3.5 (1.2) mm Between-group comparison: p > 0.05 ML (recession) Test baseline: 1.5 (1.4) mm, 12 months: 0.1 (0.9) mm Control baseline: 1.0 (1.1) mm, 12 months: 0.1 (0.7) mm; Between-group comparison: p > 0.05 | Supragingival professional implant/tooth cleansing and reinforcement of oral hygiene was performed at each follow-up visit: 2,4,6,8,10,12 and 24 weeks after the treatment Both treatment procedures results in comparable outcomes |
Adjunctive diode laser/aPDT therapy | ||||||||
Arisan et al. (2015) | CCT, parallel | 10 patients Patients with ongoing or history of periodontitis excluded 48 two piece, rough-surface implants | BOP + pain ± SUPP + PD 4–6 mm + marginal bone loss < 3 mm | 6 months | Suprastructures removed + mechanical debridement with plastic curette + diode laser (810 nm) 1 min + irrigation with sterile saline solution | Suprastructures removed + mechanical debridement with plastic curette + irrigation with sterile saline solution | Implant level BOP Test baseline: 100%; 6 months: 95.8% Control baseline: 100%, 6 months:100% PD Test baseline: 4.71 (0.67) mm, 6 months: 4.54 (0.74) mm Control baseline: 4.38 (0.42) mm, 6 months: 4.17 (0.41) mm RBL Test baseline: 2.12 (0.47) mm, 6 months: 2.79 (0.48) mm Control baseline: 2.35 (0.56), 6 months: 2.63 (0.53) mm No statistically significant difference between the groups | Adjunctive use of diode laser did not yield any additional positive influence compared with conventional scaling |
Wang et al. (2019) | RCT, parallel | 131 patients Patients with long history of smoking excluded Test: 66; mean age: 42.6 (13.0) years; patients with history of smoking: 21 Control: 65; mean age: 42; mean age: 44.1(9.8) years; patients with history of smoking: 13 | PD ≥ 6 mm + BOP + radiographic bone loss | 6 months | OHI/full mouth cleansing 2 weeks prior to the therapy + subgingival air abrasive device with glycine powder + irrigation with sterile saline + aPDT (toluidine blue photosensitized application for 3 min.) + 19 s. light emitting didoe lidht (LED) | OHI/full mouth cleansing 2 weeks prior to the therapy + subgingival air abrasive device with glycine powder + irrigation with sterile saline | Subject level SBI Test baseline: patients with no bleeding 0%, 6 months: 93.8% Grade 1 Control baseline: patients with no bleeding 0%, 6 months: 81.8% Grade 3; Significantly higher reduction in the test group (p < 0.001) PD Test baseline: 4.93 (1.07); 6 months: 3.06 (0.29), p < 0.001 Control baseline: 5.07 (0.72), 6 months: 4.62 (0.45), p < 0.001. Significantly higher reduction in the test group (p < 0.001) | Adjunctive aPDT significantly improved PD and SBI values |
Adjunctive local antiseptic/antibiotic therapy | ||||||||
Renvert et al. (2006) | RCT, parallel | 32 patients Test: 16; mean age: 65.5 (8.6) years; female: 7; male: 9; present smokers: 5; former smokers: 6 Control: 14; mean age: 61.1 (8.6) years; 11 female; 3 male; present smokers: 3; former smokers: 7 1–5 (test)/1–6 (control) implants per patient machined surfaces | PD ≥ 4 mm + BOP + SUPP + bone loss ≤ 3 threads | 12 months | OHI + mechanical debridement (scalers + rubber cup + polishing) + 1 mg minocycline microspheres | OHI + mechanical debridement (scalers + rubber cup + polishing) + 1.0% CHX gel | Subject level BOP Test baseline: 88 (12)%, 12 months: 71 (22) % Control baseline: 86 (14)%, 12 months: 78 (13) % No significant difference between the groups PD Test baseline: 3.9 (0.7) mm, 12 months: 3.6 (0.6) mm Control baseline: 3.9 (0.3) mm, 12 months: 3.9 (0.4) mm Significantly higher reduction in the test group (p < 0.001) | Use of local antibiotics as an adjunct to mechanical treatment og incipient peri-implantitis lesions demonstrated improvements in PD values that were sustained over 12 months |
Renvert et al. (2008) | RCT, parallel | 32 patients Test: 17; mean age: 60.82 (12.72) years; female: 13, male: 4; present smokers: 2; former smokers: 8 Control: 15; mean age: 62.40 (7.72) years; 9 female, 6 male; present smokers: 5; former smokers: 3 95 implants machined surfaces | PD ≥ 4 mm + BOP + SUPP + bone loss ≤ 3 threads | 12 months | OHI + mechanical debridement + 1 mg minocycline microspheres Treatment was repeated at days 30 and 90 | OHI + mechanical debridement + 0.5 ml of 1.0% CHXgel Treatment was repeated at days 30 and 90 | Implant level BOP Test baseline: 86.5 (20.1)%, 12 months: 48.1 (20.7) %; p < 0.001 Control baseline: 89.2 (17.2)%, 12 months: 63.5 (19.2) %; p < 0.001 Significantly higher reduction in test group PD Test baseline: 3.85 (1.04) mm, 12 months: 3.55 (0.98) mm; p < 0.001 Control baseline: 3.87 (1.16) mm, 12 months: to 3.72 (1.02) mm; p < 0.001 No significant difference between the groups RBL Test baseline: 0.77 (0.85) Mm, 12 months: 0.7 (0.85)mm Control baseline: 0.41 (0.7) mm, 12 months: 0.46 (0.76) mm No significant difference between groups | The use of repeated local antibiotics as an adjunct to mechanical treatment of peri-implantitis lesions demonstrated significant improvements in BOP values |
Schär et al. 2012, Bassetti et al. (2013) | RCT, parallel | 40 patients Test: 20; 10 female; mean age: 59 (range: 27–78); 18 patients with history of periodontitis Control: 20; 10 female; mean age: 57 (range: 29–75) Smokers excluded 40 implants medium rough surfaces | PD 4–6 mm + BOP + bone loss = 0.5–2 mm | 12 months | OHI + mechanical debridement (titanium curettes + glycine powder air polishing, pocket irrigation using 3% H2O2) + aPDT (660 nm, phenothiazine chloride dye) | OHI + mechanical debridement (titanium curettes + glycine powder air polishing, pocket irrigation using 3% H2O2) + minocycline microsphere | Subject level BOP change Test: 57% Control: 65% PD change Test: 0.56 mm Control: 0.11 mm Complete resolution of mucosal inflammation Test: 31.6% Control: 35% No significant differences between groups | Oral hygiene reinforcement at 1,2,3,8 weeks. In the presence of BOP at implant sites after 3 and 6 months, additional treatment procedures equivalent to initial therapy was provided Mechanical debridement with aPDT was equally effective in reducing mucosal inflammation as with adjunctive delivery of local antibiotics |
Machtei et al. (2012) | Multicentre RCT, parallel | 60 patients 77 implants Test: 30 patients; 40 implants; mean age: 57.42 (10.5) years; 20 female; current smokers: 5, former smokers: 7 Control: 30 patients; 37 implants; mean age: 60.95(7.9) years; 15 female; current smokers: 5, former smokers: 6 | PD 6–10 mm + BOP + radiographic bone loss | 6 months | OHI + ultrasonic debridement + matrix containing 2.5-mg CHX chips (i.e., up to 4 per implant site) Repeated application at sites with PD ≥ 6 mm at 2, 4, 6, 8, 12 and 18 weeks | OHI + ultrasonic debridement + biodegradable crosslinked gelatin matrix chip Repeated application at sites with PD ≥ 6 mm at 2, 4, 6, 8, 12 and 18 weeks | Subject level BOP Test baseline: 100 (0.0)%, 6 months: 42.5 (50.0) % Control baseline: 100 (0.0)%, 6 months: 54.5 (50.5) % PD Test baseline: 7.6 (1.1), 6 months: 5.47 (1.86)mm Control baseline: 7.21 (1.08) mm, 6 months: 5.48 (1.25) mm BOP and PD reductions not significantly different between groups | At 12 weeks, supragingival debridement was performed Treatment in both groups results in a substantial improvement |
Machtei et al. (2020) | Multicentre RCT, parallel | 290 patients Test: 146; mean age: 62.5 (11.2) years; female: 91; current smokers: 15; former smokers: 51 Control: 144; mean age: 62.6 (11.6) years; female: 81; current smokers: 14; former smokers: 55 386 implants Test: 197 Control: 189 10 centers | PD 5–8 mm + BOP/SUPP + radiographic bone loss at least 3 mm from implant shoulder | 6 months | OHI + subgingival debridement at baseline and 3 months + matrix containing 2.5-mg CHX chips (i.e., up to 2 per implant site) Repeated supragingival plaque removal and CHX chips application for 12 weeks every 2nd week | OHI + subgingival debridement at baseline and 3 months Repeated supragingival plaque removal for 12 weeks every 2nd week | Subject level BOP Test baseline: 100%, 6 months: 50.31% Control baseline: 100%, 6 months: 55.21% PD Test baseline: 6.16 (1.0) mm, 6 months: 4.40 (1.25) mm Control baseline: 6.06 (0.92), 6 months: 4.52 (1.27) mm. Significantly higher reduction in test group (p = 0.01) ML (recession) Test baseline: 0.51 (0.99) mm, 6 months: 0.80 (1.21)mm Control baseline: 0.26 (0.72), 6 months: 0.42 (0.85) mm. Significantly higher change in test group (p = 0.0017) | Test group showed significantly greater improvements in PD values |
Merli et al. (2020) | RCT, parallel | 58 patients Patients with intreated periodontitis excluded 58 implants Test 1 (adjunctive desiccant material): 15; mean age: 60.3(10.7) years; female: 12; smokers: 4 Test 2 (adjunctive air-flow): 13; mean age: 66.4(9.4) years; 9 female; 2 smokers Test 3 (air-flow + desiccant material): 14; mean age: 60.3(8.5) years; 10 female; 4 smokers Control: 16; mean age: 64.5(8.3) years; smokers: 3; female: 9 | PD 5–8 mm + BOP/SUPP + bone loss beyond initial bone remodeling + infraosseous defect component (radiographic) ≤ 5 mm + radiographic suprabobe component of defect ≤ 4 mm | 6 months | OHI + supragingival/supramucosal debridement prior to treatment Removal of prosthetic reconstruction + mechanical debridement with ultrasonic scaler + Test 1: application of desiccant material (gel of concentrated mixture of hydroxybenzenesulphonic and hydromethyloxybenzene acids and sulphuric acid (HybenX)) in peri-implant pocket for 30 s. followed by saline rinsing Test 2: + air polishing with glycine powder Test 3: Test 2 + Test 1 + 0.12% CHX mouthrinse twice a day, 15 days | OHI + supragingival/supramucosal debridement prior to treatment Removal of prosthetic reconstruction + mechanical debridement with ultrasonic scaler | Subject level BOP (number of sites per implant with bleeding) Test 1 baseline: 2.9 (1.3); 6 months: 2.5 (1.7) Test 2 baseline: 3.6 (0.8); 6 months: 2.8 (1.3) Test 3 baseline: 3.6 (0.8); 6 months: 2.7 (1.3) Control baseline: 3.3 (0.8); 6 months: 2.9 (0.8) No significant difference between groups PD Test 1 baseline: 5.0 (1.2) mm; 6 months: 4.5 (1.2) mm Test 2 baseline: 5.1 (1.5) mm; 6 months: 4.8 (1.3) mm Test 3 baseline: 4.9 (1.1) mm; 6 months: 4.0 (1.2) mm Control baseline: 4.4 (1.1) mm; 6 months: 4.2 (1.3) mm Reduction was higher in patients treated with desiccant material ML (recession) Test 1 baseline: 0.4 (0.5) mm; 6 months: 0.3 (0.5) mm Test 2 baseline: 0.2 (0.9) mm; 6 months: 0.3 (0.7) mm Test 3 baseline: 0.1 (0.2) mm; 6 months: 0.2 (0.4) mm Control baseline: 0.1 (0.1) mm; 6 months: 0.1 (0.2) mm No significant difference between groups Radiographic mean bone defect Test 1 baseline: 3.9 (1.2) mm; 6 months: 4.0 (1.8) mm Test 2 baseline: 3.6 (1.7) mm; 6 months: 4.0 (1.8) mm Test 3 baseline: 3.6 (1.7) mm; 6 months: 3.5 (1.0) mm Control baseline: 3.3 (1.2) mm; 6 months: 3.1 (1.5) mm No significant difference between groups Treatment success (no PD ≥ 5 mm with BOP/SUPP + no further bone loss): Test 1: 3 (25%) Test 2: 2 (14%) Test 3: 6 (43%) Control: 6 (37%) No significant difference between groups | Patients were seen at 1 wee, 1 month, 3 and 6 months for maintenance with supragingival prophylaxis Pocket reduction was more pronounced in groups treated with adjunctive desiccant material |
Adjunctive systemic antibiotics | ||||||||
Gomi et al. (2015) | RCT, parallel | 20 patients; 11 female; mean age: 67.6 (5.3) years (range: 55–78) All patients periodontally compromised Smokers excluded | PD > 5 mm + BOP + bone loss > 2 mm | 12 months | Azithromycin® 500 mg 3 days before treatment + mechanical full-mouth scaling (implants with plastic curettes and plastic ultrasonic scaler) | Mechanical full-mouth scaling (implants with plastic curettes and plastic ultrasonic scaler) | Subject level BOP Test baseline: 27.9 (4.3)%, 6 months: 4.4 (0.3)% Control baseline: 25.7 (4.3)%, 6 months: 19.8 (5.7) %; Between-group comparison: p < 0.001 PD Test baseline: 4.28 (0.85) mm, 6 months: 4.35 (0.22) mm Control baseline: 5.7 (0.8) mm; 6 months: 4.22 (0.29) mm; Between-group comparison: p = 0.002 | All clinical parameters showed better improvements in test group |
Shibli et al. (2019) | CCT, parallel | 40 patients; 29 female; mean age: 58.5 (11.1) years Current smokers excluded | PD > 5 mm + bone loss > 4 mm + BOP | 12 months | Mechanical debridement with teflon curettes + metronidazole 400 mg and amoxicillin 500 mg three times a day, 14 days | Mechanical debridement with teflon curettes | Subject level BOP Test baseline: 90.0 (31.6)%, 12 months: 39.0 (48.8%), p < 0.05 Control baseline: 97.0 (34.5)%, 12 months: 50.0 (53.5%); p < 0.05; Between-group comparison: p > 0.05 PD Test baseline: 9.9 (2.6)mm, 12 month: 5.1 (1.8), p < 0.05 Control baseline: 7.6 (1.8) mm, 12 months: 3.8 (1.6), p < 0.05; Between-group comparison: p > 0.05 | Periodontal supragingival maintenance therapy every 3 months Addition of systemic antibiotics to the mechanical treatment of severe peri-implantitis did not improve clinical outcomes |
Adjunctive probiotics | ||||||||
Tada et al. (2017) | RCT, parallel | 30 patients Test: 15; mean age: 68.80 (7.46) years; 3 smokers Control: 15; mean age: 65.87 (8.84) years; 1 smokers | PD > 4 mm and < 7 mm + BOP/SUPP + bone loss > 2 mm | 6 months | OHI + supragingival scaling + Azithromycin® 500 mg once a day for 3 days + after 1 week probiotic tablets (L. reuteri two strains; ProDentis) once a day for 6 months | OHI + supragingival scaling + Azithromycin® 500 mg once a day for 3 days | Subject level mBI Test baseline: 3.20 (1.26), 6 months: 1.53 (1.41), p = 0.235 Control baseline: 3.67 (1.59), 6 months: 2.33 (1.95), p = 0.375 PD Test baseline: 3.90 (0.60), 6 months: 3.21 (0.84), p = 0.033 Control baseline: 4.04 (1.14) mm, 6 months: 3.47 (0.95) mm, p = 1 | PDs were significantly reduced only in test group |
Laleman et al. (2019) | RCT, parallel | 19 patients Smokers and patients with uncontrolled periodontitis excluded Test: 9; 4 female; mean age: 64 (11) Control: 10; 6 female; mean age: 69 89) | PD ≥ 4 mm + BOP + bone loss at least 1 mm compared to the baseline | 6 months | OHI + mechanical debridement (titanium curettes + scaler) + Air polishing + topical application of probiotic drops containing L. reuteri two stains + probiotic tablets (BioGaia) for 6 months | OHI + mechanical debridement (titanium curettes + scaler) + Air polishing + topical application of placebo drops + placebo tablets for 6 months | Subject level BOP (number of bleeding sites pro implants 0 to 6) Test baseline: 87 (23)%, 6 months: 59 (32), p < 0.01 Control baseline: 87 (22), 6 months: 53 (39), p < 0.01 Between-group comparison: p = 0.876 PD Test baseline: 5.17 (0.92), 6 months: 4.15 (0.96), p < 0.01 Control baseline: 5.45 (1.20), 6 moths: 4.18 (1.26), p < 0.01 Between-group comparison: p = 0.801 | No adjunctive effects of the use of L. reuteri probiotics were found |