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Clinical, microbiological, and immunological effects of 3- or 7-day systemic antibiotics adjunctive to subgingival instrumentation in patients with aggressive (Stage III/IV Grade C) periodontitis: A randomized placebo-controlled clinical trial.
Cosgarea, Raluca; Jepsen, Søren; Heumann, Christian; Batori-Andronescu, Ionela; Rosu, Alexandra; Bora, Raluca; Arweiler, Nicole B; Eick, Sigrun; Sculean, Anton.
Afiliación
  • Cosgarea R; Department of Periodontology, Operative and Preventive Dentistry, University of Bonn, Bonn, Germany.
  • Jepsen S; Department of Periodontology and Peri-implant Diseases, Philips University Marburg, Marburg, Germany.
  • Heumann C; Clinic for Prosthetic Dentistry, University Iuliu-Hatieganu, Cluj-Napoca.
  • Batori-Andronescu I; Department of Periodontology, Operative and Preventive Dentistry, University of Bonn, Bonn, Germany.
  • Rosu A; Department for Statistics, LMU Munich, Munich, Germany.
  • Bora R; Periodontal Private Practice Cosmedica, Cluj-Napoca, Romania.
  • Arweiler NB; Department of Periodontology, University Iuliu-Hatieganu, Cluj-Napoca, Romania.
  • Eick S; Clinic for Prosthetic Dentistry, University Iuliu-Hatieganu, Cluj-Napoca.
  • Sculean A; Periodontal Private Practice Cosmedica, Cluj-Napoca, Romania.
J Clin Periodontol ; 49(11): 1106-1120, 2022 11.
Article en En | MEDLINE | ID: mdl-35781888
AIM: To evaluate the clinical non-inferiority of a 3-day protocol of systemic antibiotics adjunctive to subgingival instrumentation (SI) compared with a 7-day-protocol in patients with Stage III/IV Grade C periodontitis. MATERIALS AND METHODS: Fifty systemically healthy patients (32.7 ± 4.3 years) with aggressive periodontitis (AgP; Stage III/IV Grade C periodontitis) were treated by SI and adjunctive amoxicillin and metronidazole and were randomly assigned to Group A: (n = 25) 500 mg antibiotics (AB) 3 times a day for 3 days, followed by placebo 3 times a day for 4 days, or Group B: (n = 25) 500 mg AB 3 times a day for 7 days. Clinical, microbial, and immunological parameters were assessed at baseline, 3 months, and 6 months, and patient-related outcomes were assessed after 2 weeks. The primary outcome variable was the number of residual sites with pocket depth (PD) ≥6 mm at 6 months. RESULTS: For the primary outcome variable (the number of residual sites with PD ≥6 mm at 6 months), the null hypothesis was rejected and non-inferiority of the 3-day AB protocol compared with the 7-day AB protocol was demonstrated (the upper limits of the 95% confidence interval for intention to treat analysis: [-2.572; 1.050] and per protocol analysis: [-2.523; 1.318] were lower than the assumed margin of Δ = 3.1). Comparable clinical improvements were obtained for all parameters with both antibiotic protocols (p > .05). All investigated periodontopathogens and pro-inflammatory host-derived markers were statistically significantly reduced without differences between the treatments (p > .05). CONCLUSIONS: These findings indicate that in patients with AgP (Stage III/IV Grade C periodontitis), a 3-day systemic administration of amoxicillin and metronidazole adjunctive to SI may lead to non-inferior clinical outcomes after 6-months with fewer adverse events compared with a 7-day-protocol.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Periodontitis Agresiva / Antibacterianos Tipo de estudio: Clinical_trials / Guideline Límite: Humans Idioma: En Revista: J Clin Periodontol Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Periodontitis Agresiva / Antibacterianos Tipo de estudio: Clinical_trials / Guideline Límite: Humans Idioma: En Revista: J Clin Periodontol Año: 2022 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos