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1.
Occup Environ Med ; 80(12): 694-701, 2023 Nov 23.
Artigo em Inglês | MEDLINE | ID: mdl-37984917

RESUMO

OBJECTIVES: This study aims to present an overview of the formal recognition of COVID-19 as occupational disease (OD) or injury (OI) across Europe. METHODS: A COVID-19 questionnaire was designed by a task group within COST-funded OMEGA-NET and sent to occupational health experts of 37 countries in WHO European region, with a last update in April 2022. RESULTS: The questionnaire was filled out by experts from 35 countries. There are large differences between national systems regarding the recognition of OD and OI: 40% of countries have a list system, 57% a mixed system and one country an open system. In most countries, COVID-19 can be recognised as an OD (57%). In four countries, COVID-19 can be recognised as OI (11%) and in seven countries as either OD or OI (20%). In two countries, there is no recognition possible to date. Thirty-two countries (91%) recognise COVID-19 as OD/OI among healthcare workers. Working in certain jobs is considered proof of occupational exposure in 25 countries, contact with a colleague with confirmed infection in 19 countries, and contact with clients with confirmed infection in 21 countries. In most countries (57%), a positive PCR test is considered proof of disease. The three most common compensation benefits for COVID-19 as OI/OD are disability pension, treatment and rehabilitation. Long COVID is included in 26 countries. CONCLUSIONS: COVID-19 can be recognised as OD or OI in 94% of the European countries completing this survey, across different social security and embedded occupational health systems.


Assuntos
COVID-19 , Doenças Profissionais , Exposição Ocupacional , Humanos , COVID-19/epidemiologia , Síndrome de COVID-19 Pós-Aguda , Europa (Continente)/epidemiologia , Doenças Profissionais/epidemiologia , Doenças Profissionais/terapia , Ocupações , Exposição Ocupacional/efeitos adversos
3.
Am J Respir Crit Care Med ; 189(6): 707-17, 2014 Mar 15.
Artigo em Inglês | MEDLINE | ID: mdl-24568568

RESUMO

RATIONALE: Primary ciliary dyskinesia (PCD) is a genetically heterogeneous recessive disorder of motile cilia, but the genetic cause is not defined for all patients with PCD. OBJECTIVES: To identify disease-causing mutations in novel genes, we performed exome sequencing, follow-up characterization, mutation scanning, and genotype-phenotype studies in patients with PCD. METHODS: Whole-exome sequencing was performed using NimbleGen capture and Illumina HiSeq sequencing. Sanger-based sequencing was used for mutation scanning, validation, and segregation analysis. MEASUREMENTS AND MAIN RESULTS: We performed exome sequencing on an affected sib-pair with normal ultrastructure in more than 85% of cilia. A homozygous splice-site mutation was detected in RSPH1 in both siblings; parents were carriers. Screening RSPH1 in 413 unrelated probands, including 325 with PCD and 88 with idiopathic bronchiectasis, revealed biallelic loss-of-function mutations in nine additional probands. Five affected siblings of probands in RSPH1 families harbored the familial mutations. The 16 individuals with RSPH1 mutations had some features of PCD; however, nasal nitric oxide levels were higher than in patients with PCD with other gene mutations (98.3 vs. 20.7 nl/min; P < 0.0003). Additionally, individuals with RSPH1 mutations had a lower prevalence (8 of 16) of neonatal respiratory distress, and later onset of daily wet cough than typical for PCD, and better lung function (FEV1), compared with 75 age- and sex-matched PCD cases (73.0 vs. 61.8, FEV1 % predicted; P = 0.043). Cilia from individuals with RSPH1 mutations had normal beat frequency (6.1 ± Hz at 25°C), but an abnormal, circular beat pattern. CONCLUSIONS: The milder clinical disease and higher nasal nitric oxide in individuals with biallelic mutations in RSPH1 provides evidence of a unique genotype-phenotype relationship in PCD, and suggests that mutations in RSPH1 may be associated with residual ciliary function.


Assuntos
Proteínas de Ligação a DNA/genética , Síndrome de Kartagener/genética , Mutação , Adolescente , Adulto , Criança , Cílios/fisiologia , Análise Mutacional de DNA , Exoma , Feminino , Estudos de Associação Genética , Marcadores Genéticos , Testes Genéticos , Homozigoto , Humanos , Síndrome de Kartagener/fisiopatologia , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Mucosa Nasal/fisiologia , Análise de Sequência de DNA , Adulto Jovem
6.
J Public Health Policy ; 44(1): 138-146, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-36646883

RESUMO

We strive to increase public (PH) and occupational health (OSH) inter-linkages by building a collaborative framework. Besides Covid-19 pandemic, recent approaches such as Human Exposome and Total Worker Health TM, have led to a shift to improving health of working population and consequently the total population. These health objectives can be best realised through primary care actors in specific contexts. Work, school, home and leisure are the four multi-stakeholder contexts in which health and healthcare (goal-oriented care) objectives needs to be set and defined. PH policy makers need to establish a shared decision-making process involving employees, employers and OSH representatives to set PH goals and align with OSH goals. The policy making process in OSH can serve as a potential way forward, as the decisions and policies are being decided centrally in consultation with social partners and governments. This process can then be mirrored on company level to adopt and implement.


Assuntos
COVID-19 , Saúde Ocupacional , Humanos , Saúde Pública , Pandemias , COVID-19/epidemiologia , Atenção à Saúde
8.
Occup Med (Lond) ; 66(3): 260, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26965841
9.
Occup Med (Lond) ; 66(1): 1, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26732789
13.
Occup Med (Lond) ; 64(3): 145, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24706464
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