Dataset Information

Power output from 12 brands of contemporary LED light-curing units measured using 2 brands of radiometers.

ABSTRACT:

Background

Given the increasing use of photo-activated resins in dentistry, dentists and researchers need a user-friendly dental radiometer to measure the power output from dental light-curing units (LCUs).

Objective

Our goal was to measure the accuracy of two brands of dental radiometers in reporting the power (mW) from twelve brands of contemporary LCUs compared to a 'gold standard' (GS) reference value obtained from an integrating sphere attached to a fiberoptic spectroradiometer.

Methods

The power output was measured from two units of 12 brands of LCUs, five times on the ''GS" system, five times on two Bluephase Meter II dental radiometers, and five times on two Mini Gig hand-held spectroradiometers. The emission spectrum was also recorded using the 'GS' integrating sphere. The power values reported by each meter were subjected to t-tests to compare the two examples of each LCU, and 3-way ANOVA followed by Bonferroni's post-hoc tests. Regression analyses were also performed to determine the relationship between the data from the hand-held radiometers and the 'GS' integrating sphere.

Results

There was a large difference in the power values (mW) and the emission spectra from the 12 brands of LCUs on their standard-settings (p<0.001). Except for one LCU (Dental Spark @ 15.1%), the differences between the two LCUs of the same brand were less than 5.3% when measured using the 'GS' integrating sphere. Regression analyses showed a highly significant agreement between the power values reported from the two brands of radiometers and the 'GS' integrating sphere (R2 > 98%).

Conclusion

We concluded that the power values reported from both brands of dental radiometers we tested were accurate, provided that the light source did not emit wavelengths of light that were beyond the radiometer's detection limit.

SUBMITTER: Maucoski C

PROVIDER: S-EPMC9269870 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Similar Datasets

Project description:BackgroundRetrospective studies conducted in psychiatric wards have indicated a shorter duration of stay for depressed inpatients in bright compared to dim daylight-exposed rooms, pointing to a possible antidepressant effect of daylight conditions. Dynamic LED lighting, aiming to mimic daylight conditions, are currently been installed in several hospitals, but their feasibility is poorly investigated.MethodsTo investigate the feasibility of these systems, we developed and installed a LED-lighting system in four rooms in a psychiatric inpatient ward. The system could function statically or dynamically regarding light intensity and colour temperature. The system consisted of (A) a large LED luminaire built into the window jamb mimicking sunlight reflections, (B) two LED light luminaires in the ceiling and (C) a LED reading luminaire. In the static mode, the systems provided constant light from A and B. In the dynamic mode, the system changed light intensity and colour temperature using A, B and C. Patients with unipolar or bipolar depression were randomised to dynamic or static LED lighting for 4 weeks, in addition to standard treatment. Primary outcome was the rate of patients discontinuing the trial due to discomfort from the lighting condition. Secondary outcomes were recruitment and dropout rates, visual comfort, depressive symptoms and suicidal ideation.ResultsNo participants discontinued due to discomfort from the LED lighting. Recruitment rate was 39.8%, dropout from treatment rates were 56.3% in the dynamic group and 33.3% in the static group. 78.1% in the dynamic group were satisfied with the lighting compared with 71.8% in the static group. Discomfort from the light (glare) was reported by 11.5% in the dynamic group compared to 5.1% in the static group. Endpoint suicidal scores were 16.8 (10.4) in the dynamic and 16.3 (14.9) in the static group. The lighting system was 100% functional. The light sensor system proved unstable.ConclusionDropout from treatment was high primarily due to early discharge and with a lack of endpoint assessments. The feasibility study has influenced an upcoming large-scale dynamic lighting efficacy trial where we will use a shorter study period of 3 weeks and with more emphasis on endpoint assessments. The lighting was well tolerated in both groups, but some found intensity too low in the evening. Thus, we will use higher intensity blue-enriched light in the morning and higher intensity amber (blue-depleted) light in the evening in the upcoming study. The light sensor system needs to be improved.Trial registrationClinicalTrials.gov: NCT03363529.