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Adjunctive antibiotics in peri-implantitis surgery reduce bleeding on probing but not other outcomes

Adjunctive antibiotics in peri-implantitis surgery reduce bleeding on probing but not other outcomes
Photo by ClinicalPulse / Unsplash
Key Takeaway
Interpret isolated BOP reduction with adjunctive antibiotics cautiously; no broader clinical benefit was demonstrated.

This single-blind randomized controlled trial evaluated 59 patients with peri-implantitis and no, one-wall, or two-wall bony defects. Patients were randomized to receive either access-flap peri-implantitis surgery supplemented with systemic amoxicillin and metronidazole (n=29) or the same surgery without systemic antibiotics (n=30), with follow-up at 3, 6, 9, and 12 months postoperatively.

The primary outcomes were mean peri-implant probing pocket depth and mean peri-implant bleeding on probing. The test group showed significantly lower bleeding on probing at 9 months (β = -10.57%, 95% CI: -20.17 to -0.97, p=0.03) and 12 months (β = -14.47%, 95% CI: -25.9 to -3.04, p=0.01). However, no statistically significant differences were found between groups for probing pocket depth, disease resolution (composite outcome of residual probing depths ≤5 mm, no BOP in one or more sites, and no suppuration), suppuration on probing, or radiographic marginal bone levels at any timepoint.

Safety and tolerability data were not reported. Key limitations include the single-blind design, short-term 1-year follow-up, and the isolated effect on BOP that did not translate into broader or sustained clinical benefit. The clinical implications should be interpreted with caution, as the isolated short-term BOP reduction must be weighed against the risks associated with systemic antibiotic use without evidence of improvement in other important clinical parameters.

Study Details

Study typeRct
Sample sizen = 29
EvidenceLevel 2
Follow-up12.0 mo
PublishedApr 2026
View Original Abstract ↓
AIM: To analyse the effect of systemic amoxicillin and metronidazole on surgical peri-implantitis treatment with a follow-up period of 1 year. MATERIALS AND METHODS: Fifty-nine patients were randomly assigned to receive peri-implantitis surgery supplemented with (29 patients; test) or without (30 patients; control) systemic amoxicillin and metronidazole, in cases with no, one-wall or two-wall bony defects. Primary outcomes were mean peri-implant probing pocket depth (PPD) and mean peri-implant bleeding on probing (BOP); secondary outcomes included disease resolution (composite treatment outcome: residual probing depths ≤ 5 mm; no BOP in one or more probing site; no suppuration on probing), suppuration on probing (SOP) and radiographic marginal bone levels (MBLs), evaluated 3, 6, 9 and 12 months postoperatively (T3, T6, T9, T12). Linear and logistic mixed-effects models were employed. RESULTS: Between-group analyses showed that BOP was significantly lower in the test group compared to the control group at T9 (β = -10.57%, 95% CI: -20.17 to -0.97, p = 0.03) and T12 (β = -14.47%, 95% CI: -25.9 to -3.04, p = 0.01). No other parameters in the mixed-effects models showed statistically significant differences between groups at any timepoint. CONCLUSION: Access-flap peri-implantitis surgery supplemented with systemic amoxicillin and metronidazole led to a statistically significant reduction in peri-implant BOP after 1 year, whereas no other parameters showed statistically significant differences between groups at any timepoint. The clinical implications of these differences should be interpreted with caution, as the isolated short-term effect does not translate into broader or sustained clinical benefit and must be weighed against the risks associated with systemic antibiotic use.
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