4.3 Article

Changing epidemiology of the respiratory bacteriology of patients with cystic fibrosis-data from the European cystic fibrosis society patient registry

期刊

JOURNAL OF CYSTIC FIBROSIS
卷 19, 期 3, 页码 376-383

出版社

ELSEVIER
DOI: 10.1016/j.jcf.2019.08.006

关键词

Cystic fibrosis; Pseudomonas aeruginosa; Registry; Staphylococcus aureus; Epidemiology

向作者/读者索取更多资源

Background: Monitoring changes in the epidemiology of cystic fibrosis (CF) pathogens is essential for clinical research, quality improvement, and clinical management. Methods: We analyzed data reported to the European Cystic Fibrosis Society Patient Registry (ECFSPR) from 2011 to 2016 to determine the overall and the age-specific annual prevalence and incidence of selected CF pathogens and their trends during these years. The ECFSPR collects data on three chronic infections: Pseudomonas aeruginosa (PsA), Burkholderia cepacia complex Species (BCC) and Staphylococcus aureus (SA), as well as on the occurrence of non-tuberculous mycobacteria (NTM) and Stenotrophomonas maltophilia (SM). The same analyses were performed for different country groups, according to their gross national income (GNI). Results: The pathogens with the highest prevalence were SA and PsA, with prevalence, in 2016, equal to 38.3% and 29.8% respectively, followed by SM (8.1%). The pathogens with the lowest prevalence were NTM (3.3%) and BCC (3.1%). The overall prevalence and incidence significantly decreased for PsA; they also decreased for BCC, while they increased significantly for SA. The overall prevalence of NTM and SM increased significantly. The most considerable prevalence changes were observed for PsA, which decreased across all income country groups and all age strata (with the exception of 0-1 years) The prevalence and incidence of pathogens differed significantly according to GNI. Conclusions: The epidemiology of CF pathogens in Europe has changed; epidemiologic data differ significantly among countries with different socio-economic status. The causes of these observations are multifactorial and include improvements in clinical care and infection control. (C) 2019 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Respiratory System

Disease severity of people with cystic fibrosis carrying residual function mutations: Data from the ECFS Patient Registry

Meir Mei Zahav, Annalisa Orenti, Andreas Jung, Elpis Hatziagorou, Hanne Vebert Olesen, Eitan Kerem

Summary: Patients with residual function (RF) mutations in cystic fibrosis experience a decline in pulmonary function with age and shortened life spans. The study emphasizes the importance of standard of care therapies and CFTR function augmentation to improve the survival and quality of life for these patients.

JOURNAL OF CYSTIC FIBROSIS (2023)

Article Allergy

Physical activity and quality of life in children with well-controlled asthma

Pauline Peftoulidou, Maria Gioulvanidou, Elissavet-Anna Chrysochoou, Elpis Hatziagorou

Summary: This study aimed to assess the association between lung function, physical activity, and quality of life (QoL) in children with well-controlled asthma. The results showed a significant correlation between QoL and both lung function and physical activity levels. However, despite reasonable asthma control, the children exhibited low physical activity levels, which negatively impacted their QoL.

JOURNAL OF ASTHMA (2023)

Article Respiratory System

Prevalence, trends and outcomes of long-term inhaled antibiotic treatment in people with cystic fibrosis without chronic Pseudomonas aeruginosa infection-A European cystic fibrosis patient registry data analysis

Annalisa Orenti, Meir Mei-Zahav, Patrizia Boracchi, Anders Lindblad, Michal Shteinberg

Summary: Many patients with cystic fibrosis without chronic Pseudomonas aeruginosa infection receive long-term treatment with inhaled antibiotics, despite a lack of support from clinical trials or practice guidelines. Factors such as PA infection, severe genotype, diabetes, and pancreatic insufficiency are associated with inhaled antibiotic treatment, but no improvement in outcomes was observed.

JOURNAL OF CYSTIC FIBROSIS (2023)

Article Respiratory System

European survey of newborn bloodspot screening for CF: opportunity to address challenges and improve performance

Anne Munck, Daria Berger, Kevin W. Southern, Carla Carducci, Karin M. de Winter-de Groot, Silvia Gartner, Nataliya Kashirskaya, Barry Linnane, Marijke Proesmans, Dorota Sands, Olaf Sommerburg, Carlo Castellani, Juerg Barben

Summary: The study aimed to assess the current status and performance of newborn bloodspot screening (NBS) for CF in Europe. A survey was conducted among representatives of NBS programs across Europe, and performance was evaluated using a previously developed framework. The results showed that in 2022, there were 22 national and 34 regional NBS programs in Europe. The integration of DNA analysis into the NBS protocol improved the positive predictive value, but also led to increased carrier and CFSPID recognition.

JOURNAL OF CYSTIC FIBROSIS (2023)

Article Respiratory System

Clinical outcomes associated with Achromobacter species infection in people with cystic fibrosis

Eitan Kerem, Annalisa Orenti, Anna Zolin, Luigi Annicchiarico, Pavel Drevinek

Summary: This study analyzed data from European cystic fibrosis patients and found that Achromobacter infection has a similar impact on lung disease severity as Pseudomonas aeruginosa infection. The co-infection of both bacteria is associated with a more severe disease outcome.

JOURNAL OF CYSTIC FIBROSIS (2023)

Article Respiratory System

Treatment effects of Elexacaftor/Tezacaftor/Ivacaftor in people with CF carrying non-F508del mutations

Galit Livnat, Adi Dagan, Moshe Heching, Einat Shmueli, Dario Prais, Karin Yaacoby-Bianu, Nili Stein, Meir Mei-Zahav, Michal Gur, Malena Cohen-Cymberknoh, Michal Shteinberg

Summary: This study demonstrates the clinical efficacy of ETI in patients with CF carrying non-F508del mutations, supporting its routine use in this patient group. ETI treatment resulted in reduced sweat chloride concentration, decreased pulmonary exacerbations, and improvements in nutritional status and lung function.

JOURNAL OF CYSTIC FIBROSIS (2023)

Article Health Care Sciences & Services

Tight control in patients with rheumatoid arthritis treated with targeted therapies across the COVID-19 pandemic era

Angela Flavia Luppino, Gilberto Cincinelli, Annalisa Orenti, Patrizia Boracchi, Ennio Giulio Favalli, Roberto Caporali, Francesca Ingegnoli

Summary: This study analyzed the impact of different patterns of healthcare delivery on remission of RA patients treated with targeted therapies during the pandemic. The results showed that the different healthcare delivery strategies did not significantly affect the remission rate of RA patients, including difficult-to-treat patients.

JOURNAL OF TELEMEDICINE AND TELECARE (2023)

Article Pediatrics

High flow nasal cannula therapy in the pediatric home setting

Shay Ehrlich, Inbal Golan Tripto, Moran Lavie, Michal Cahal, Tommy Shonfeld, Dario Prais, Hagit Levine, Meir Mei-Zahav, Ophir Bar-On, Yulia Gendler, Jonatan Zalcman, Eahab Sarsur, Micha Aviram, Aviv Goldbart, Patrick Stafler

Summary: A retrospective study conducted in three pediatric centers in Israel showed that home high-flow nasal cannula (HFNC) therapy was well tolerated and safe for a variety of indications, leading to improved weight gain, reduced hospitalization days, and high parental satisfaction.

PEDIATRIC PULMONOLOGY (2023)

Article Health Care Sciences & Services

Association of Oxygen Therapy with the Natural Disease Progression of Cystic Fibrosis: A Multi-State Model of the European Cystic Fibrosis Society Patient Registry

Simone Gambazza, Annalisa Orenti, Giovanna Pizzamiglio, Anna Zolin, Carla Colombo, Dario Laquintana, Federico Ambrogi, ECFSPR

Summary: This study aimed to understand the prognosis for people with cystic fibrosis (pwCF) on oxygen therapy (OT), evaluating the probability of lung transplantation (LTx) and death in pwCF with and without OT. The study found that OT is strongly associated with poor survival in pwCF, highlighting the importance of harmonizing CF care throughout European countries and minimizing the onset of pulmonary gas exchange abnormalities.

THERAPEUTICS AND CLINICAL RISK MANAGEMENT (2023)

Article Pediatrics

Mannitol Challenge to Assess Therapy Response in Asthmatic Children: An Interventional Cohort Study

Nikolaos Karantaglis, Fotios Kirvassilis, Elpis Hatziagorou, Antonios Gkantaras, Kalliopi Kontouli, John Tsanakas, Maria Emporiadou

Summary: Bronchial provocation tests, such as the mannitol challenge, can help identify and measure the severity of bronchial hyperresponsiveness in asthmatic patients. This study aimed to compare the bronchial hyperresponsiveness to mannitol in treatment-naive asthmatic children before and after receiving asthma prophylaxis. The results showed that the provocative dose of mannitol increased significantly after treatment, suggesting that bronchial hyperresponsiveness to mannitol could be a potential monitoring tool in pediatric asthmatic patients.

CHILDREN-BASEL (2023)

Article Respiratory System

Risk factors for forced expiratory volume in 1 s decline in European patients with cystic fibrosis: data from the European Cystic Fibrosis Society Patient Registry

Elpis Hatziagorou, Steffen Fieuws Annalisa Orenti, Lutz Naehrlich, Uros Krivec, Meir Mei-Zahav, Andreas Jung, Kris De Boeck

Summary: This study used data from the European Cystic Fibrosis Society patient registry to examine the trajectory of forced expiratory volume in 1 second (FEV1) from 2008 to 2016. Risk factors for FEV1 decline were evaluated, and it was found that age and age at diagnosis were significant factors. Males had a higher %FEV1 but experienced a higher yearly %FEV1 loss during adolescence. Patients from low-income countries had a faster decline in %FEV1 compared to those from middle- and high-income countries.

ERJ OPEN RESEARCH (2023)

Article Pediatrics

Low-frequency oscillometry indices to assess ventilation inhomogeneity in CF patients

Sotirios Fouzas, Christos Kogias, Maria Gioulvanidou, Aris Bertzouanis, Elisavet-Anna Chrysochoou, Michael B. Anthracopoulos, John Tsanakas, Elpis Hatziagorou

Summary: The study investigates the utility of lower-frequency forced oscillations technique (FOT) in assessing ventilation inhomogeneity in cystic fibrosis (CF) patients. The specific respiratory conductance (sGrs) at 5 Hz was found to be strongly correlated with the lung clearance index (LCI) and unaffected by lung hyperinflation.

PEDIATRIC PULMONOLOGY (2023)

暂无数据