topical desiccant agent in association with manual

1
Copyright © 2017, Giorgio Lombardo ([email protected]), Caterina Signoretto ([email protected]), Alessia Pardo ([email protected]), Giovanni Corrocher ([email protected]), Jacopo Pighi ([email protected]), Annarita Signoriello ([email protected]),Pier Francesco Nocini ([email protected]) G. Lombardo 1 , C. Signoretto 1 , A. Pardo 1 , G. Corrocher 1 , J. Pighi 1 , A. Signoriello 1 , P. F. Nocini 1 1 Department of Surgery, Dentistry, Paediatrics and Gynaecology, Section of Dentistry and Maxillo-facial Surgery, University of Verona, Verona, Italy Background & Aim Limited data exist regarding the treatment of peri-implant mucositis and current treatment protocols for this condition are still unpredictable [1]. The aim of this randomized study was to evaluate the clinical effects of the adjunctive administration of a locally delivered desiccant liquid with molecular hygroscopic properties (HYBENX® Oral Tissue decontaminant TM ; HBX) in association with manual scaling and root planning (SRP) in the treatment of peri-implant mucositis. EuroPerio9 (June 20-23 2018, Amsterdam) TOPICAL DESICCANT AGENT IN ASSOCIATION WITH MANUAL DEBRIDEMENT IN THE INITIAL TREATMENT OF PERI-IMPLANT MUCOSITIS: A CLINICAL PROSPECTIVE STUDY Results Between T0 and T3 examinations, both groups presented a statistically significant reduction in m-BI: 1,63±1.02 for the Test group; 1,29±1,20 for the Control group. Furthermore, the SRP+HBX group showed a significantly (p<0.05) greater PPD reduction (concerning the deepest PPD site), compared to SRP+CHX group. Despite an increased percentage of sites showing a complete disease resolution (9/16 sites BOP+, 56%, in the Test group; 6/14 sites BOP+, 43% in the Control group), comparisons failed to demonstrate statistically significant differences among groups. Better performances in microbiological analysis were revealed by SRP+CHX group, which exhibitied a validated and targeted effect on anaerobic bacteria. Methods 12 patients presenting at least one implant with a probing depth (PPD) 4 mm combined with bleeding and/or exudate on probing, were included in the study. At baseline (T0) subjects were randomly assigned to: the Test group SRP+HBX (6 subjects and 16 implants), which received local administration of HBX before SRP; Discussion and Conclusion Similarly to other studies concerning different agents [2,3], both groups were effective in reducing inflammatory signs on the short term, but failed to achieve a References [1] Renvert, S., Roos-Jansaker, A. M. & Claffey, N.(2008). Non- surgical treatment of peri-implantmucositis and peri-implantitis: a literature review. Journal of Clinical Periodontology. 35(8):305– 315; [2] Renvert, S., Lessem, J., Dahlen, G., Renvert, H., & Lindahl, C. (2008). Mechanical and Repeated Antimicrobial Therapy Using a Local Drug Delivery System in the Treatment of Peri-Implantitis: A Randomized Clinical Trial. Journal of Periodontology. 79(5):836-44. [3] Lombardo, G., Signoretto, C., Corrocher, G., Pardo, A., Pighi, J., Rovera, A., Caccuri, F. & Nocini, P. F. (2015). A topical desiccant agent in association with ultrasonic debridement in the initial treatment of chronic periodontitis: a clinical and microbiological study. New Microbiologica. 38(3):393-407. Treatment was repeated after 2 and 4 weeks (T1 and T2). Follow-up examinations were conducted at 3 months (T3). Visible plaque index (VPI), modified plaque index (mPLI), bleeding on probing (BOP), modified bleeding index (mBI) and peri-implant probing depths (PPD) were clinically detected to estimate soft tissues conditions. mBI reduction was the main outcome. 0 20 40 60 80 100 BOP+ T0 BOP+ T3 100% 44% 100% 57% QUALIFYING SITES BOP+ (%) SRP+HBX (16 SITES) SRP+CHX (14 SITES) 0 1 2 3 4 5 6 PPD T0 PPD T3 4,8 3,7 5,6 4,9 QUALIFYING SITES PPD (mm) SRP+HBX (16 SITES) SRP+CHX (14 SITES) Anaerobic bacterial count SRP+HBX (16 sites) SRP+CHX (14 sites) T0 9.40E+06 4.51E+05 T3 1.40E+06 1.23E+05 or to the Control group SRP+CHX (6 subjects and 14 implants), which received Chlorhexidine Digluconate Corsodyl TM Dental Gel 1% (CHX) after debridement. complete disease resolution. Greater results were found in T-HBX group, with a statistically significant difference in PPD. On the contrary, T-CHX group revealed superior microbiological outcomes, especially among anaerobic bacteria.

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Page 1: TOPICAL DESICCANT AGENT IN ASSOCIATION WITH MANUAL

Copyright © 2017, Giorgio Lombardo ([email protected]), Caterina Signoretto ([email protected]), Alessia Pardo ([email protected]), Giovanni Corrocher ([email protected]), Jacopo Pighi ([email protected]), Annarita Signoriello

([email protected]),Pier Francesco Nocini ([email protected])

G. Lombardo1, C. Signoretto1, A. Pardo1, G. Corrocher1, J. Pighi1, A. Signoriello1, P. F. Nocini1

1 Department of Surgery, Dentistry, Paediatrics and Gynaecology, Section of Dentistry and Maxillo-facial Surgery, University of Verona, Verona, Italy

Background & AimLimited data exist regarding the treatment of peri-implant mucositis and current treatment protocols for this condition are still

unpredictable [1]. The aim of this randomized study was to evaluate the clinical effects of the adjunctive administration of a locally

delivered desiccant liquid with molecular hygroscopic properties (HYBENX® Oral Tissue decontaminantTM; HBX) in association with

manual scaling and root planning (SRP) in the treatment of peri-implant mucositis.

EuroPerio9 (June 20-23 2018, Amsterdam)

TOPICAL DESICCANT AGENT IN ASSOCIATION WITH MANUAL DEBRIDEMENT IN THE INITIAL TREATMENT OF PERI-IMPLANT MUCOSITIS: A CLINICAL

PROSPECTIVE STUDY

ResultsBetween T0 and T3 examinations, both groups presented a statistically

significant reduction in m-BI: 1,63±1.02 for the Test group; 1,29±1,20 for the

Control group. Furthermore, the SRP+HBX group showed a significantly

(p<0.05) greater PPD reduction (concerning the deepest PPD site), compared to

SRP+CHX group. Despite an increased percentage of sites showing a completedisease resolution (9/16 sites BOP+, 56%, in the Test group; 6/14 sites BOP+,

43% in the Control group), comparisons failed to demonstrate statistically

significant differences among groups. Better performances in microbiological

analysis were revealed by SRP+CHX group, which exhibitied a validated and

targeted effect on anaerobic bacteria.

Methods12 patients presenting at least one implant with a probing depth (PPD) ≥4 mm

combined with bleeding and/or exudate on probing, were included in the study. At

baseline (T0) subjects were randomly assigned to: the Test group SRP+HBX (6

subjects and 16 implants), which received local administration of HBX before SRP;

Discussion and ConclusionSimilarly to other studies concerning different agents [2,3], both groups were

effective in reducing inflammatory signs on the short term, but failed to achieve a

References[1] Renvert, S., Roos-Jansaker, A. M. & Claffey, N.(2008). Non-

surgical treatment of peri-implantmucositis and peri-implantitis: a

literature review. Journal of Clinical Periodontology. 35(8):305–

315; [2] Renvert, S., Lessem, J., Dahlen, G., Renvert, H., &

Lindahl, C. (2008). Mechanical and Repeated AntimicrobialTherapy Using a Local Drug Delivery System in the Treatment of

Peri-Implantitis: A Randomized Clinical Trial. Journal of

Periodontology. 79(5):836-44. [3] Lombardo, G., Signoretto, C.,

Corrocher, G., Pardo, A., Pighi, J., Rovera, A., Caccuri, F. &

Nocini, P. F. (2015). A topical desiccant agent in association withultrasonic debridement in the initial treatment of chronic

periodontitis: a clinical and microbiological study. New

Microbiologica. 38(3):393-407.

Treatment was repeated after 2 and 4 weeks (T1 and T2). Follow-up

examinations were conducted at 3 months (T3). Visible plaque index (VPI),

modified plaque index (mPLI), bleeding on probing (BOP), modified bleeding

index (mBI) and peri-implant probing depths (PPD) were clinically detected to

estimate soft tissues conditions. mBI reduction was the main outcome.

0

20

40

60

80

100

BOP+ T0 BOP+ T3

100%

44%

100%

57%

QUALIFYING SITES BOP+ (%)

SRP+HBX (16 SITES) SRP+CHX (14 SITES)

0123456

PPD T0 PPD T3

4,83,7

5,64,9

QUALIFYING SITES PPD (mm)

SRP+HBX (16 SITES) SRP+CHX (14 SITES)

Anaerobicbacterial

count

SRP+HBX (16 sites)

SRP+CHX (14 sites)

T0 9.40E+06 4.51E+05T3 1.40E+06 1.23E+05

or to the Control group SRP+CHX (6 subjects and 14 implants), which received

Chlorhexidine Digluconate Corsodyl TM Dental Gel 1% (CHX) after

debridement.

complete disease resolution. Greater results were found in T-HBX group, with a statistically

significant difference in PPD. On the contrary, T-CHX group revealed superior microbiological

outcomes, especially among anaerobic bacteria.