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1.
Midwifery ; 85: 102669, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32120330

RESUMO

OBJECTIVE: To describe how front-line managers of maternity wards provide support to midwives as second victims in the aftermath of an adverse incident. DESIGN: A qualitative study using critical incident technique and a content analytic approach of semi-structured in-depth interviews. SETTING: Maternity wards in 10 Norwegian hospitals with more than 200 registered births annually were included in the study. PARTICIPANTS: A purposeful sample of 33 midwives with more than two years' working experience described 57 adverse incidents. FINDINGS: Maternity ward managers utilised four types of practices to support midwives after critical incidents: management, transformational leadership, distributed leadership and laissez-faire leadership. KEY CONCLUSIONS AND IMPLICATIONS FOR PRACTICE: The study shows that proactive managers who planned for how to handle critical incidents provided midwives with needed individual support and learning. Proactive transformational leadership and delegating roles for individual support should be promoted when assisting second victims after critical incidents. Managers can limit the potential harm to second victims by preparing for the eventuality of a crisis and institute follow-up practices.


Assuntos
Assistência ao Convalescente/métodos , Erros Médicos/psicologia , Enfermeiros Obstétricos/psicologia , Adulto , Assistência ao Convalescente/psicologia , Feminino , Humanos , Entrevistas como Assunto/métodos , Erros Médicos/enfermagem , Noruega , Gravidez , Pesquisa Qualitativa , Análise e Desempenho de Tarefas
2.
Nat Commun ; 11(1): 229, 2020 01 13.
Artigo em Inglês | MEDLINE | ID: mdl-31932607

RESUMO

Lysosomes are membrane-surrounded cytoplasmic organelles filled with a powerful cocktail of hydrolases. Besides degrading cellular constituents inside the lysosomal lumen, lysosomal hydrolases promote tissue remodeling when delivered to the extracellular space and cell death when released to the cytosol. Here, we show that spatially and temporally controlled lysosomal leakage contributes to the accurate chromosome segregation in normal mammalian cell division. One or more chromatin-proximal lysosomes leak in the majority of prometaphases, after which active cathepsin B (CTSB) localizes to the metaphase chromatin and cleaves a small subset of histone H3. Stabilization of lysosomal membranes or inhibition of CTSB activity during mitotic entry results in a significant increase in telomere-related chromosome segregation defects, whereas cells and tissues lacking CTSB and cells expressing CTSB-resistant histone H3 accumulate micronuclei and other nuclear defects. These data suggest that lysosomal leakage and chromatin-associated CTSB contribute to proper chromosome segregation and maintenance of genomic integrity.


Assuntos
Catepsina B/metabolismo , Cromatina/metabolismo , Segregação de Cromossomos , Lisossomos/metabolismo , Mitose , Animais , Catepsina B/antagonistas & inibidores , Catepsina B/genética , Linhagem Celular , Núcleo Celular/genética , Núcleo Celular/patologia , Segregação de Cromossomos/genética , Feminino , Inativação Gênica , Histonas/metabolismo , Humanos , Membranas Intracelulares/metabolismo , Lisossomos/enzimologia , Metáfase , Camundongos , Mitose/genética , Permeabilidade , Telômero/metabolismo
3.
PLoS One ; 8(9): e74601, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24058597

RESUMO

Primary Failure of tooth Eruption (PFE) is a non-syndromic disorder which can be caused by mutations in the parathyroid hormone receptor 1 gene (PTH1R). Traditionally, the disorder has been identified clinically based on post-emergent failure of eruption of permanent molars. However, patients with PTH1R mutations will not benefit from surgical and/or orthodontic treatment and it is therefore clinically important to establish whether a given failure of tooth eruption is caused by a PTH1R defect or not. We analyzed the PTH1R gene in six patients clinically diagnosed with PFE, all of which had undergone surgical and/or orthodontic interventions, and identified novel PTH1R mutations in all. Four of the six mutations were predicted to abolish correct mRNA maturation either through introduction of premature stop codons (c.947C>A and c.1082G>A), or by altering correct mRNA splicing (c.544-26_544-23del and c.989G>T). The latter was validated by transfection of minigenes. The six novel mutations expand the mutation spectrum for PFE from eight to 14 pathogenic mutations. Loss-of-function mutations in PTH1R are also associated with recessively inherited Blomstrand chondrodysplasia. We compiled all published PTH1R mutations and identified a mutational overlap between Blomstrand chondrodysplasia and PFE. The results suggest that a genetic approach to preclinical diagnosis will have important implication for surgical and orthodontic treatment of patients with failure of tooth eruption.


Assuntos
Mutação/genética , Receptor Tipo 1 de Hormônio Paratireóideo/genética , Doenças Dentárias/genética , Adolescente , Adulto , Sequência de Bases , Criança , Análise Mutacional de DNA , Exostose Múltipla Hereditária/genética , Família , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Dados de Sequência Molecular , Osteocondrodisplasias/genética , Linhagem , Radiografia Panorâmica , Doenças Dentárias/diagnóstico por imagem , Adulto Jovem
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