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1.
Br Dent J ; 234(3): 171-176, 2023 02.
Article in English | MEDLINE | ID: mdl-36765231

ABSTRACT

Background Competency-based education has led to the introduction of entrustable professional activities (EPAs) in health sciences education. EPAs are assessment tools that serve to certify a trainee's preparedness to conduct a given clinical activity. Objective Given its modest introduction into dental education, we sought to examine the current situation of EPAs in our field and identify possible barriers and facilitators. This review aimed to summarise evidence about EPA introduction in dental education programmes.Data sources A review of articles published between January 2005 and December 2021 was conducted using the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews methodology in three databases (PubMed, Cochrane and Embase).Data selection Keywords were 'entrustable professional activity' OR 'entrustable professional activities' AND 'dentistry' OR 'dental education'.Data extraction Eligibility criteria targeted papers published in English describing dental education EPA.Data synthesis Ten publications were selected: six reported on new EPAs, three discussed their relevance for dental education and one article described a process for developing validated EPAs. EPAs focused on clinical examination, health promotion, treatment planning, pain and/or anxiety control and topics related to a specific discipline or care procedures.Conclusion Topics covered by EPAs described in our study adequately reflect the specificities of today's dental professional. The benefits of EPAs will ensure tomorrow's dentists consistently meet societal expectations.


Subject(s)
Clinical Competence , Internship and Residency , Humans , Competency-Based Education/methods , Curriculum , Educational Measurement , Health Education
2.
Biomaterials ; 275: 120969, 2021 08.
Article in English | MEDLINE | ID: mdl-34157563

ABSTRACT

Dental pulp stem cells (DPSCs) are a promising cell source for regeneration of dental pulp. Migration is a key event but influence of the microenvironment rigidity (5 kPa at the center of dental pulp to 20 GPa for the dentin) is largely unknown. Mechanical signals are transmitted from the extracellular matrix to the cytoskeleton, to the nuclei, and to the chromatin, potentially regulating gene expression. To identify the microenvironmental influence on migration, we analyzed motility on PDMS substrates with stiffness increasing from 1.5 kPa up to 2.5 MPa. We found that migration speed slightly increases as substrate stiffness decreases in correlation with decreasing focal adhesion size. Motility is relatively insensitive to substrate stiffness, even on a bi-rigidity PDMS substrate where DPSCs migrate without preferential direction. Migration is independent of both myosin II activity and YAP translocation after myosin II inhibition. Additionally, inhibition of Arp2/3 complex leads to significant speed decrease for all rigidities, suggesting contribution of the lamellipodia in the migration. Interestingly, the chromatin architecture remains stable after a 7-days exposure on the PDMS substrates for all rigidity. To design scaffold mimicking dental pulp environment, similar DPSCs migration for all rigidity, leaves field open to choose this mechanical parameter.


Subject(s)
Dental Pulp , Stem Cells , Cell Differentiation , Cell Proliferation , Cells, Cultured , Extracellular Matrix
3.
Quintessence Int ; 50(10): 802-807, 2019.
Article in English | MEDLINE | ID: mdl-31559399

ABSTRACT

Over the past decades, the walking bleach technique using sodium perborate was considered a safe and effective method to bleach nonvital discolored teeth. However, sodium perborate has been classified as carcinogenic, mutagenic, and toxic for reproduction by European Union legislation. Its use is therefore prohibited since April 2015. The initially described inside/outside bleaching technique, combining internal and external application of 10% carbamide peroxide, is an alternative to the walking bleach technique using sodium perborate. While good esthetic results and low risks of external cervical resorptions have been associated with this technique, its main drawback is that the access cavity is left open. To overcome this disadvantage, the present authors propose to seal the bleaching agent in the access cavity instead of leaving the latter open. Through a clinical case, this paper presents and discusses several aspects of this protocol, including the clinical steps, the design of the bleaching tray, and the treatment of potential recurrences. The present authors believe that the protocol proposed in this article is easier to use for the patient. Moreover, it prevents the accumulation of food debris in the access cavity and avoids the colonization of coronary dentin by bacteria.


Subject(s)
Tooth Bleaching , Tooth Discoloration , Tooth, Nonvital , Carbamide Peroxide , Humans , Hydrogen Peroxide , Peroxides , Urea
4.
Quintessence Int ; 50(6): 494-502, 2019.
Article in English | MEDLINE | ID: mdl-31086855

ABSTRACT

Invasive cervical resorption (ICR) is a dental lesion starting in the cervical region and involving the loss of dental hard tissue as a result of odontoclastic action. Due to its localization and invasive pattern, this process represents a challenging clinical situation. When feasible, the major aim of an ICR treatment is to completely remove the pathologic tissue (specifically at the entry point of the lesion) and to seal the resulting defect, without compromising tooth rehabilitation. In this context, choosing how to access the resorptive lacuna is essential. Two main options have been described in the literature: an external approach, requiring the surgical exposure of the resorptive lacuna, and an internal approach, taking advantage of the endodontic access cavity. However, there are no guidelines that indicate which approach to choose for the treatment of an ICR. This article is based on four clinical cases. It aims to provide specific clinical and radiologic features that should be considered in order to take the most appropriate decision, when choosing between the internal and the external approaches. It is proposed to base the therapeutic strategy on the accessibility and the size of the portal of entry of the lesion. When the entry point is wide, its extension along the root must also be taken into account. Other important parameters are the circumferential and vertical extents of the lesion in the radicular dentin. Although it is not a determining factor, the pulpal involvement of the lesion can also be considered.


Subject(s)
Dental Caries , Root Resorption , Tooth Resorption , Dental Pulp , Humans , Tooth Cervix
5.
Sci Rep ; 8(1): 12655, 2018 08 23.
Article in English | MEDLINE | ID: mdl-30140058

ABSTRACT

Mechanical properties of the cellular environment are known to influence cell fate. Chromatin de-condensation appears as an early event in cell reprogramming. Whereas the ratio of euchromatin versus heterochromatin can be increased chemically, we report herein for the first time that the ratio can also be increased by purely changing the mechanical properties of the microenvironment by successive 24 h-contact of the cells on a soft substrate alternated with relocation and growth for 7 days on a hard substrate. An initial contact with soft substrate caused massive SW480 cancer cell death by necrosis, whereas approximately 7% of the cells did survived exhibiting a high level of condensed chromatin (21% heterochromatin). However, four consecutive hard/soft cycles elicited a strong chromatin de-condensation (6% heterochromatin) correlating with an increase of cellular survival (approximately 90%). Furthermore, cell survival appeared to be reversible, indicative of an adaptive process rather than an irreversible gene mutation(s). This adaptation process is associated with modifications in gene expression patterns. A completely new approach for chromatin de-condensation, based only on mechanical properties of the microenvironment, without any drug mediation is presented.


Subject(s)
Adaptation, Biological/genetics , Cellular Reprogramming , Chromatin Assembly and Disassembly , Euchromatin/metabolism , Heterochromatin/metabolism , Tumor Microenvironment , Cell Differentiation , Cell Line, Tumor , Cell Movement/genetics , Cell Survival/genetics , Elasticity , Gene Expression Regulation, Neoplastic , Humans
6.
Sci Rep ; 8(1): 9235, 2018 06 18.
Article in English | MEDLINE | ID: mdl-29915284

ABSTRACT

The excessive use of antifungal agents, compounded by the shortage of new drugs being introduced into the market, is causing the accumulation of multi-resistance phenotypes in many fungal strains. Consequently, new alternative molecules to conventional antifungal agents are urgently needed to prevent the emergence of fungal resistance. In this context, Cateslytin (Ctl), a natural peptide derived from the processing of Chromogranin A, has already been described as an effective antimicrobial agent against several pathogens including Candida albicans. In the present study, we compared the antimicrobial activity of two conformations of Ctl, L-Ctl and D-Ctl against Candida albicans. Our results show that both D-Ctl and L-Ctl were potent and safe antifungal agents. However, in contrast to L-Ctl, D-Ctl was not degraded by proteases secreted by Candida albicans and was also stable in saliva. Using video microscopy, we also demonstrated that D-Ctl can rapidly enter C. albicans, but is unable to spread within a yeast colony unless from a mother cell to a daughter cell during cellular division. Besides, we revealed that the antifungal activity of D-Ctl could be synergized by voriconazole, an antifungal of reference in the treatment of Candida albicans related infections. In conclusion, D-Ctl can be considered as an effective, safe and stable antifungal and could be used alone or in a combination therapy with voriconazole to treat Candida albicans related diseases including oral candidosis.


Subject(s)
Antifungal Agents/pharmacology , Candida albicans/drug effects , Candidiasis, Oral/drug therapy , Chromogranin A/pharmacology , Peptide Fragments/pharmacology , Cell Division/drug effects , Cell Line , Humans , Microbial Sensitivity Tests , Peptides/pharmacology , Voriconazole/pharmacology
7.
Sci Rep ; 7(1): 15199, 2017 11 09.
Article in English | MEDLINE | ID: mdl-29123174

ABSTRACT

The rise of antimicrobial resistant microorganisms constitutes an increasingly serious threat to global public health. As a consequence, the efficacy of conventional antimicrobials is rapidly declining, threatening the ability of healthcare professionals to cure common infections. Over the last two decades host defense peptides have been identified as an attractive source of new antimicrobials. In the present study, we characterized the antibacterial and mechanistic properties of D-Cateslytin (D-Ctl), a new epipeptide derived from L-Cateslytin, where all L-amino acids were replaced by D-amino acids. We demonstrated that D-Ctl emerges as a potent, safe and robust peptide antimicrobial with undetectable susceptibility to resistance. Using Escherichia coli as a model, we reveal that D-Ctl targets the bacterial cell wall leading to the permeabilization of the membrane and the death of the bacteria. Overall, D-Ctl offers many assets that make it an attractive candidate for the biopharmaceutical development of new antimicrobials either as a single therapy or as a combination therapy as D-Ctl also has the remarkable property to potentiate several antimicrobials of reference such as cefotaxime, amoxicillin and methicillin.


Subject(s)
Anti-Infective Agents/pharmacology , Antimicrobial Cationic Peptides/pharmacology , Chromogranin A/pharmacology , Escherichia coli/drug effects , Peptide Fragments/pharmacology , Anti-Infective Agents/chemical synthesis , Anti-Infective Agents/toxicity , Antimicrobial Cationic Peptides/chemical synthesis , Antimicrobial Cationic Peptides/toxicity , Caco-2 Cells , Cell Membrane/drug effects , Cell Survival/drug effects , Cell Wall/drug effects , Chromogranin A/chemical synthesis , Chromogranin A/toxicity , Drug Synergism , Epithelial Cells/drug effects , Firmicutes/drug effects , Humans , Microbial Sensitivity Tests , Microbial Viability/drug effects , Peptide Fragments/chemical synthesis , Peptide Fragments/toxicity , Permeability/drug effects , Prevotella intermedia/drug effects
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