1.Pain and quality of life related to suture removal after 3 or 7 days at the extraction sites of impacted lower third molars.
Pirasut RODANANT ; Kannika WATTANAJITSEREE ; Binit SHRESTHA ; Natthamet WONGSIRICHAT
Journal of Dental Anesthesia and Pain Medicine 2016;16(2):131-136
BACKGROUND: This study aimed to evaluate the patient's pain and quality of life after suture removal at either 3 or 7 days following the bilateral surgical extraction of impacted lower third molars. METHODS: This study was a prospective, randomized controlled clinical trial carried out in 30 patients, who acted as their own control. Each patient required the bilaterally impacted mandibular third molars to be extracted. The impacted teeth were removed and the wound margins were approximated and sutured with black braided silk. The suture material was removed on day 3 on one side and on day 7 on the other. Each participant was asked to complete a questionnaire after the removal of the suture material on each designated day. RESULTS: Regarding overall clinical symptoms, the mean VAS scores of male and female participants on day 3 were not significantly different from those on day 7. A significant difference was found in female participants, in that overall daily activity was better on day 7. There were significant differences in the ability to smile and laugh in both sexes and the ability to chew in the male participants was better on day 7. CONCLUSIONS: There were no significant differences in the patient's pain and quality of life between suture removal on day 3 or on day 7 following surgery to remove impacted lower third molars.
Female
;
Humans
;
Male
;
Molar, Third*
;
Patient Satisfaction
;
Prospective Studies
;
Quality of Life*
;
Silk
;
Suture Techniques
;
Sutures*
;
Tooth, Impacted
;
Trismus
;
Wounds and Injuries
2.Pain and quality of life related to suture removal after 3 or 7 days at the extraction sites of impacted lower third molars.
Pirasut RODANANT ; Kannika WATTANAJITSEREE ; Binit SHRESTHA ; Natthamet WONGSIRICHAT
Journal of Dental Anesthesia and Pain Medicine 2016;16(2):131-136
BACKGROUND: This study aimed to evaluate the patient's pain and quality of life after suture removal at either 3 or 7 days following the bilateral surgical extraction of impacted lower third molars. METHODS: This study was a prospective, randomized controlled clinical trial carried out in 30 patients, who acted as their own control. Each patient required the bilaterally impacted mandibular third molars to be extracted. The impacted teeth were removed and the wound margins were approximated and sutured with black braided silk. The suture material was removed on day 3 on one side and on day 7 on the other. Each participant was asked to complete a questionnaire after the removal of the suture material on each designated day. RESULTS: Regarding overall clinical symptoms, the mean VAS scores of male and female participants on day 3 were not significantly different from those on day 7. A significant difference was found in female participants, in that overall daily activity was better on day 7. There were significant differences in the ability to smile and laugh in both sexes and the ability to chew in the male participants was better on day 7. CONCLUSIONS: There were no significant differences in the patient's pain and quality of life between suture removal on day 3 or on day 7 following surgery to remove impacted lower third molars.
Female
;
Humans
;
Male
;
Molar, Third*
;
Patient Satisfaction
;
Prospective Studies
;
Quality of Life*
;
Silk
;
Suture Techniques
;
Sutures*
;
Tooth, Impacted
;
Trismus
;
Wounds and Injuries
3.In vitro antimicrobial effects of grape seed extract on peri-implantitis microflora in craniofacial implants.
Binit SHRESTHA ; M L Srithavaj THEERATHAVAJ ; Sroisiri THAWEBOON ; Boonyanit THAWEBOON
Asian Pacific Journal of Tropical Biomedicine 2012;2(10):822-825
OBJECTIVETo determine the antimicrobial effects of grape seed on peri-implantitis microflora.
METHODSThe grape seed extract was tested against peri-implantitis microflora most commonly found in craniofacial implants including reference strains of Staphylococcus aureus (S. aureus), Escherichia coli (E. coli), Candida albicans (C. albicans) and clinical strains of S. aureus, Klebsiella pneumonia (K. pneumonia) and Candida parapsilosis (C. parapsilosis) by disk diffusion test. Minimum inhibitory concentrations (MIC) and minimum cidal concentrations (MCC) were determined using modified agar dilution millpore method. The extract was further combined with polyethylene glycol and propylene glycol, and was tested for antimicrobial effects.
RESULTSGrape seed extract showed positive inhibitory effects with S. aureus at MIC of 0.625 mg/mL and MCC of 1.25 mg/mL respectively. However the extracts showed minimal or no reactivity against strains of E. coli, K. pneumonia, C. parapsilosis and C. albicans. The use of grape seed extract in combination with polyethylene glycol and propylene glycol also showed dose dependent inhibitory effect on S. aureus.
CONCLUSIONSThe results of the study showed that grape seed has potential antimicrobial effects which can be further studied and developed to be used in the treatment of infected skin-abutment interface of craniofacial implants.
Anti-Infective Agents ; pharmacology ; Bacteria ; drug effects ; Craniofacial Abnormalities ; surgery ; Disk Diffusion Antimicrobial Tests ; Grape Seed Extract ; pharmacology ; Humans ; Microbial Sensitivity Tests ; Prostheses and Implants ; adverse effects ; Prosthesis-Related Infections ; drug therapy ; microbiology
4.In vitro effects of Salvia officinalis L. essential oil on Candida albicans.
Tularat SOOKTO ; Theerathavaj SRITHAVAJ ; Sroisiri THAWEBOON ; Boonyanit THAWEBOON ; Binit SHRESTHA
Asian Pacific Journal of Tropical Biomedicine 2013;3(5):376-380
OBJECTIVETo determine the anticandidal activities of Salvia officinalis L. (S. officinalis) essential oil against Candida albicans (C. albicans) and the inhibitory effects on the adhesion of C. albicans to polymethyl methacrylate (PMMA) resin surface.
METHODSDisc diffusion method was first used to test the anticandidal activities of the S. officinalis L. essential oil against the reference strain (ATCC 90028) and 2 clinical strains of C. albicans. Then the minimal inhibitory concentration (MIC) and minimal lethal concentration (MLC) were determined by modified membrane method. The adhesion of C. albicans to PMMA resin surface was assessed after immersion with S. officinalis L. essential oil at various concentrations of 1×MIC, 0.5×MIC and 0.25×MIC at room temperature for 30 min. One-way ANOVA was used to compare the Candida cell adhesion with the pretreatment agents and Tukey's test was used for multiple comparisons.
RESULTSS. officinalis L. essential oil exhibited anticandidal activity against all strains of C. albicans with inhibition zone ranging from 40.5 mm to 19.5 mm. The MIC and MLC of the oil were determined as 2.780 g/L against all test strains. According to the effects on C. albicans adhesion to PMMA resin surface, it was found that immersion in the essential oil at concentrations of 1×MIC (2.780 g/L), 0.5×MIC (1.390 g/L) and 0.25×MIC (0.695 g/L) for 30 min significantly reduced the adhesion of all 3 test strains to PMMA resin surface in a dose dependent manner (P<0.05).
CONCLUSIONSS. officinalis L. essential oil exhibited anticandidal activities against C. albicans and had inhibitory effects on the adhesion of the cells to PMMA resin surface. With further testing and development, S. officinalis essential oil may be used as an antifungal denture cleanser to prevent candidal adhesion and thus reduce the risk of candida-associated denture stomatitis.
Antifungal Agents ; chemistry ; pharmacology ; Candida albicans ; drug effects ; Disk Diffusion Antimicrobial Tests ; Microbial Sensitivity Tests ; Oils, Volatile ; chemistry ; pharmacology ; Salvia officinalis ; chemistry