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1.
Eur J Dent Educ ; 27(3): 640-649, 2023 Aug.
Article in English | MEDLINE | ID: mdl-36039793

ABSTRACT

INTRODUCTION: Dentists educated outside the EU, EEA and Switzerland have the option to undergo proficiency testing to practice dentistry in Sweden. A standardised evidence-based procedure for proficiency tests is crucial. This paper explores if the standard setting of the theoretical examination in the Swedish proficiency test for foreign dentists is fit to differentiate candidates who meet the acceptable standard for licensure from those who do not, by analysis of inter-rater reliability and credibility of Angoff panels and the test's ability to differentiate candidates regarding learning outcomes and dental disciplines. MATERIALS AND METHODS: In a cohort study design, test results were collected from seven examinations during 2018-2019 (n = 316), combined with Angoff judgements and demographic data from The National Board of Health and Welfare. Intraclass correlation, Pearson correlation and linear regression were calculated. RESULTS: All exams demonstrated substantial judge inter-rater reliability using the Angoff procedure (0.65-0.82). Item difficulty predicted by the expert panels showed significant positive correlations with the item difficulty by candidate results (0.69-0.77). Candidates who did not meet the requirements for pass mark in the theoretical test revealed a significantly reduced performance overall in professional qualifications (i.e., learning outcomes) and reduced performance within dental disciplines. CONCLUSIONS: The results indicate that a modified Angoff method is a feasible, simple, and defensible method for setting the pass mark for the theoretical examinations. The standard setting appears to differentiate candidates who do not meet the requirements of the professional qualifications of the dental degree. Adjustments could be undertaken to further discriminate for competence within single dental disciplines.


Subject(s)
Education, Dental , Educational Measurement , Humans , Reproducibility of Results , Cohort Studies , Educational Measurement/methods , Clinical Competence , Dentists
2.
Swed Dent J ; 40(2): 133-142, 2016.
Article in English | MEDLINE | ID: mdl-28853785

ABSTRACT

The aim of the study was to evaluate the technical quality of endodontic treatment per- formed by postgraduate students in Karolinska Institutet, Stockholm, Sweden during the years (2008-2011) and to evaluate the treatment outcome. In addition, possible influencing factors to treatment outcome were analyzed. All maxillary first molars that received endo- dontic treatment between 2008 and 2011 were included in the study. Pre, post and follow up radiographs were collected.The apical status (PAI-score),the quality of the root canal treat- ment (RCT) and the treatment outcome were assessed. Analysis of the treatment outcome in relation to the quality of root canal treatment and other possible influencing variables was performed by Chi2 or Fisher's Exact test, and the statistical significance was set at P<0.05. A total of 73 teeth were included in the study. Out of these, sixty-three teeth (86,3 %) had periapical lesions at the time for RCT. An initial root canal treatment was performed in 46 teeth (63 %) and 27 teeth (37 %) were retreated.There was no significant as- sociation between the outcome and the type of treatment.The majority of the RCT's (58 %) had good seal and correct length. In total, the treatment outcome was successful in 59 (81 %) of the cases. The success rate was 88% in cases with high quality root fillings, compared to 71% in cases with less good quality.There was a non- significant trend (P =0.066) of an association between RCT quality and treatment outcome. In conclusion the association between the quality of the root filling and the treatment outcome was not verified with statistical significance, but the results indicate a trend that satisfactory root fillings are associated with a favorable outcome.This study was limited by its retrospective nature and a relatively small sample size.

3.
Community Dent Oral Epidemiol ; 41(2): 163-72, 2013 Apr.
Article in English | MEDLINE | ID: mdl-22963525

ABSTRACT

OBJECTIVES: The question of health risks associated with dental materials, especially dental amalgam, has long been controversial and remains unresolved. For the past 10 years, people in Sweden with perceived adverse reactions to dental restorative materials have been entitled to apply to their local county council for subsidized replacement of restorative materials. The aim of the study was to investigate symptoms, perceived health changes over time and health-related quality of life (HRQoL) in this population, comprising subjects with subjective health impairment, allegedly because of dental materials. A further aim was to compare their HRQoL with that of the general population. METHODS: A comprehensive questionnaire was sent to 515 people who had applied for subsidized replacement of dental restorations. The questionnaire covered general and oral symptoms, HRQoL, health ratings over time and dental restoration replacement. RESULTS: The response rate was 54.4% (n=280). Most (83.2%) answered that they had undergone replacement of restorative materials because of impaired health, perceived to be related to dental restorative materials. The most common symptoms were musculoskeletal pain (67.5%), sleep disturbance (60.0%) and fatigue (58.6%). The HRQoL of the study subjects was significantly lower than that of the Swedish population in general. CONCLUSIONS: Subjects who had undergone subsidized dental restoration replacement reported persistent subjective symptoms and low HRQoL. The results indicate that replacement of restorative materials alone is insufficient to achieve improved health in patients with symptoms allegedly attributable to dental restorations.


Subject(s)
Dental Materials/adverse effects , Dental Restoration, Permanent/adverse effects , Health Status , Quality of Life , Acrylic Resins/adverse effects , Aged , Attitude to Health , Ceramics/adverse effects , Chromium Alloys/adverse effects , Cohort Studies , Composite Resins/adverse effects , Dental Alloys/adverse effects , Dental Amalgam/adverse effects , Fatigue/etiology , Female , Gold Alloys/adverse effects , Humans , Male , Middle Aged , Muscle Weakness/etiology , Musculoskeletal Pain/etiology , Sleep Wake Disorders/etiology , Sweden , Titanium/adverse effects , Toothache/etiology , Xerostomia/etiology
4.
Acta Odontol Scand ; 69(2): 65-74, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21319941

ABSTRACT

OBJECTIVE: To evaluate the scientific evidence regarding laser technology for removal of carious tissue. MATERIAL AND METHODS: A search for literature on the effect of treatment and on economic aspects of laser technology identified 23 papers. No relevant studies on economic aspects were found. Regarding the effect of treatment, 16 papers were selected for assessment according to established criteria. RESULTS: Cavity preparation and caries excavation by erbium laser were evaluated in three studies of medium quality. The time required to remove carious tissue was evaluated in five studies assessed as being of medium quality for this outcome. In four studies the effect of laser treatment on the dental pulp was included as an outcome but, due to the short follow-up time, the quality was assessed as low. Two studies that included the longevity of the restoration as an outcome were also assessed as being of low quality because the follow-up time was inadequate. Patient response was evaluated in three studies, which were assessed as being of medium quality with respect to this outcome. CONCLUSIONS: There is limited scientific evidence that laser treatment is as effective as a rotary bur for removing carious tissue. Treatment time is prolonged. There is limited scientific evidence that adults prefer laser treatment. No conclusions can be drawn regarding biological or technical complications, children's perception of laser treatment or the cost-effectiveness of the method.


Subject(s)
Dental Caries/therapy , Laser Therapy/methods , Lasers, Solid-State/therapeutic use , Controlled Clinical Trials as Topic , Dental Cavity Preparation/methods , Humans , Time Factors , Treatment Outcome
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