4 research outputs found
Influence of thermo-light curing on the microhardness and fluoride release of glass-Ionomer cements
Glass ionomer cements (GICs) are important restorative materials that are frequently preferred in both primary and permanent teeth. The aim of this study was to investigate the effect of thermo-light curing on the surface microhardness and fluoride ion (F-) release of the materials during the curing reactions of high-viscosity GICs. In our study, Equia Fil (EQ-GC), Fuji IX GP Extra (FGP-GC), and Fuji IX Capsule (FC-GC) were prepared in accordance with the manufacturer's instructions, and for 60 and 90 seconds during curing Woodpecker LED-C (WL), GC D-Light Pro (GLC) and BlueLuxcer M-855 Halogen Curing Light (HALO) light instruments formed the experimental groups, and self-curing glass ionomer cement samples formed the control groups. VHN and F- release values of both groups were evaluated on 1st day, 1st week, 1st, 3rd, and 6th months. The Jamovi (Version 1.0.4) program was used for statistical analysis. Significant difference was analyzed by the Tukey's post hoc-test (a = 0.05). In the 1st month, EQ exhibited significantly higher microhardness than FC (p0.05). All materials exhibited higher microhardness during 1st day than in other periods (p0.05). Within the limitations of this study, it can be concluded that thermo-light application does not cause unacceptable long-term changes in the physical and chemical properties of materials
Effectiveness of Premedication Agents Administered Prior to Nitrous Oxide/Oxygen
Çocuk dis hekimliğinde kaygı, korku ya da davranıs
bozuklukları nedeniyle dis tedavileri gerçeklestirilemediğinde sedasyon
uygulamalarına ihtiyaç duyulmakta ancak bazı olgularda ilaç
uygulamasına rağmen istenilen düzeyde sedasyon elde edilememektedir.
Bu arastırmada Nitröz Oksit/Oksijen (N2O/O2) sedasyonu altında dis
tedavisi planlanan çocuklarda farklı ajanlarla yapılan oral
premedikasyonun etkinliğinin değerlendirilmesi amaçlanmıstır.
Çalısma; Gazi Üniversitesi Tıp Fakültesi Etik Kurul izni ve
bilgilendirilmis ebeveyn onayı alındıktan sonra 5-8 yas arası, ASA I-II
grubu, mental ve motor geriliği bulunmayan, en az iki seans dis tedavisine
ihtiyacı olan, daha önce sedasyon veya genel anestezi uygulanmamıs, dis
tedavisine uyum göstermeyen (Frankl Davranıs Skalası≥3) çocuklar
arasından randomize seçilen 60 çocuk üzerinde gerçeklestirilmistir.
Randomize olarak 4 esit gruba ayrılan olgulara, gruplara uygun olarak;
islemden 1 saat önce oral 1 mg/kg hidroksizin hidroklorür süspansiyon
(Atarax) (grup I, n=15), 15 dakika önce oral 0,7 mg/kg midazolam HCl
(Dormicum) (grup II, n=15), 15 dakika önce oral 3 mg/kg ketamin
hidroklorür (Ketalar)+0.25 mg/kg midazolam HCl (Dormicum) (grup III,
n=15) verilmistir. Tedavi srasında pulse oksimetre cihazı (TuffSAT,
Datex-Ohmeda) ile periferik oksijen satürasyonu (SpO2), kalp atım hızı
(KAH) ve bispektral indeks monitörü (BĐS® XP, Aspect) ile BĐS değerleri
monitorize edilmistir. Premedikasyon ardından tüm gruplara nazal maske
ile % 40 N2O/ % 60 O2 uygulanmıstır. Kontrol grubunda (grup IV, n=15)
oral premedikasyon uygulanmamıstır. Çocukların sedasyon derinliği
Ramsay Sedasyon Skalası (RSS) ve Houpth Sedasyon Skalası (HSS) ile
değerlendirilerek veriler 5 dakika aralıklarla kaydedilmistir. Herhangi bir
ölçüm zamanında RSS’nin (2, 3, 4, 5) olması ve tedavinin basarıyla
gerçeklestirilmesi basarılı sedasyon, RSS’nin (1, 2) olması ve tedavinin
güçlükle gerçeklestirilmesi orta derecede basarılı sedasyon ve RSS’nin (1)
olması ve tedavinin gerçeklestirilememesi basarısız sedasyon olarak
değerlendirilmistir. Đslem bitiminde olguların kaygı, sedasyon düzeyleri,
derlenme süreleri ile ebeveylerinin ve olguların tedaviden memnuniyetleri
kaydedilmistir.
Çalısma bulgularımız değerlendirildiğinde tüm gruplarda ciddi
bir komplikasyon ile karsılasılmadan dis tedavisi islemleri basarıyla
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tamamlanmıstır. Sedasyon basarısı; basarılı/ orta derecede basarılı/
basarısız olmak üzere aynı sıra ile grup I’de % 13,3/ 53,3/ 33,3, grup II’de
% 54/ 20/ 26, grup III’te % 33,3/ 33,3/ 33,3, grup IV’te % 6,7/ 60/ 33,3
olarak saptanmıstır. BĐS değerleri açısından BĐS sensörü takıldığı anda,
N2O/O2 grubunundaki olguların uyanık, en derin uyuyan grubun ise
ketamin hidroklorür+midazolam HCl grubu olduğu saptanmıstır. Bispektral
indeks ile RSS skorları arasındaki korelasyon değerlendirildiğinde,
sonuçların % 65 oranında örtüstüğü saptanmıs dis hekimliği sedasyon
uygulamalarında BĐS kullanımının, sedasyon güvenliği sınırlarını arttırdığı
bulgulanmıstır. Houpth sedasyon skalası ve RSS sonuçları
değerlendirildiğinde, en etkili ilacın 0,7 mg/kg midazolam HCl olduğu
saptanmıstır.
Dis tedavileri planlanan çocuklarda N2O/O2 sedasyonu
öncesi oral premedikasyon amacıyla 0,7 mg/kg dozunda uygulanan
midazolam HCl’nin, 3 mg/kg ketamin hidroklorür+0,25 mg/kg midazolam
HCl ve 1 mg/kg hidroksizin hidroklorüre göre daha etkin sedasyon
sağladığı kanısına varılmıstır.In pediatric dentistry, sedation procedures are required when
there is no possibility to carry out dental treatments because of anxiety,
dental fear or behavioral impairments. However, sedation at the desired
level might not be achieved despite administration of various agents. The
present study aims to evaluate the effectiveness of oral premedication with
different agents on children scheduled for dental treatment under nitrous
oxide/oxygen (N2O/O2) sedation.
This research was approved by Gazi University Faculty of
Medicine Ethical Committee. 60 children aged between 5-8 years,
corresponding to ASA I or II, having no mental or motor retardation,
requiring at least 2 visit-dental treatment, having no sedation or general
anesthesia experience and incompliant with dental treatment (Frankl
Behavior Scale≥3) were enrolled to the study after obtaining informed
parental consent. Then the children were randomly assigned to 1 of 4
groups. The treatment regime according to the study groups was as
follows: oral administration of 1 mg.kg-1 hydroxizine hydrochloride
suspension (Atarax) 1 hour preoperatively (group I, n=15), oral
administration of 0.7 mg.kg-1 midazolam HCl (Dormicum) 15 minutes
preoperatively (group II, n=15), oral administration of 3 mg.kg-1 ketamine
(Ketalar)+0.25 mg.kg-1 midazolam HCl (Dormicum) 15 minutes
preoperatively (group III, n=15) and no oral premedication was
administered to the control group (group IV, n=15). Peripheral oxygen
saturation (SpO2) and heart rate (HR) were monitored with pulse oximeter
(TuffSAT, Datex-Ohmeda) during treatment. Sedation level was
monitored with BIS (BIS® XP, Aspect). Following premedication, 40 % N2O
and 60 % O2 were administered to all groups with nasal hood. Sedation
depth was evaluated using Ramsay Sedation Scale (RSS) and data were
recorded at 5-minute intervals. The children’s sedation success during
dental treatment was classified as: satisfactory (If RSS at any evaluation
point was 2, 3 or 4 and dental treatment was performed successfully),
middle level satisfactory (If RSS at any evaluation point 1, 2, 3 and
treatment was performed with difficulty) or unsatisfactory (If RSS at any
evaluation point 1 or 2 and dental treatment could not be performed due to
agitation). Sedation success, and other sedation related events were
recorded. Anxiety and sedation levels, recovery time of children in addition
to satisfaction of parents and children were recorded postoperatively.
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The evaluation of the findings of this study revealed that
treatment procedures were achieved without any serious complications.
Achievement of sedation in terms of satisfactory/ middle level satisfactory/
unsatisfactory was as follows respectively: 13.3 % / 53.3 % / 33.3 % in
group I, 54 % / 20 % / 26 % in group II, 33.3 % / 33.3 % / 33.3 % in group
III and 6.7 % / 60 % / 33.3 % in group IV. With respect to BIS values, it
was found that the subjects at N2O/O2 group were more awake and the
deepest sleep was observed at ketamine+midazolam HCl group at the
moment BIS sensor was placed. when the correlation between BIS and
RSS scores was evaluated, it was concluded that the use of BIS in dental
sedation practice increased the confidence level of sedation taking the
65% correlation into account. HSS and RSS results revealed that the most
effective medication was 0.7 mg.kg-1 midazolam HCl.
It is concluded that 0.7 mg.kg-1 midazolam HCl is more
effective than 0.25 mg.kg-1 midazolam+3 mg.kg-1 ketamine and 1 mg.kg-1
hydroxizine hydrochloride in terms of oral premedication prior to N2O/O2
sedation in children scheduled for dental treatments
Effects of Different Pediatric Drugs on the Color Stability of Various Restorative Materials Applicable in Pediatric Dentistry
Background. The chronic recommendation of pediatric drugs could exhibit erosive and cariogenic problems. Objective. To evaluate the effects of different pediatric drugs on the color stability of various restorative materials. Methods. Five specimens (1mm x 3 mm) were prepared and immersed in ten different pediatric drugs and agitated every 8 hours daily for 2 min up to 1 week. Between immersion periods, the samples were stored in artificial saliva. After 1-week period, Delta Epsilon(*) values were calculated. Two-way ANOVA and Fisher's LSD test were used for statistical analysis at a level of p< 0.05. Results. Delta Epsilon(*) values were only significantly influenced by restorative material factor (p< 0.001) and varied in the range of 2.08 and 6.55 units for all drugs/estorative materials. The highest Delta Epsilon(*) was found in Ferrosanol B-composite (6.55 +/- 1.38) and the lowestonewas found inDolven-glass ionomer (2.08 +/- 0.40) pairwise. The most prominent Delta Epsilon(*) value elevations were obtained in composite material compared to the compomer and/or glass ionomers inMacrol, Ferrosanol B, and Ventolin (p < 0.001; for all) and also for other drugs (p< 0.05). Dolven exhibited significantly higher values compared to Augmentin (p - 0.021), Macrol (p - 0.018), and Ventolin (p - 0.013) in compomer group. Conclusion. The clinically perceptible color changes for tested composite/pediatric drug pairwise can be more problematic than compomer and glass ionomers in pediatric dentistry