keyword
https://read.qxmd.com/read/33264072/polysulfated-hyaluronan-gm-1111-inhibits-elastase-and-improves-rheology-in-cf-sputum
#61
JOURNAL ARTICLE
Apparao B Kummarapurugu, Shuo Zheng, Abigail Pulsipher, Justin R Savage, Jonathan Ma, Bruce K Rubin, Thomas P Kennedy, Judith A Voynow
Cystic fibrosis (CF) lung disease is marked by high concentrations of neutrophil elastase (NE) and DNA polymers; both factors contribute to airway disease. Although inhaled recombinant human dornase alfa reduces the frequency of CF pulmonary exacerbations, it also increases free NE activity in the sputum. There are no approved anti-NE therapies for patients with CF. We investigated whether synthetic, low molecular weight polysulfated hyaluronan (GM-1111) would be effective as an anti-NE drug using ex vivo CF sputum...
December 2, 2020: American Journal of Respiratory Cell and Molecular Biology
https://read.qxmd.com/read/33138807/the-cost-effectiveness-of-hypertonic-saline-inhalations-for-infant-bronchiolitis
#62
JOURNAL ARTICLE
Jefferson Antonio Buendía, Ranniery Acuña-Cordero
BACKGROUND: Pharmacological treatment for bronchiolitis is primarily supportive because bronchodilators, steroids, and antibiotics, show little benefit. Clinical studies have suggested that nebulized 3% hypertonic solution is useful for infants with bronchiolitis. This study aims to evaluate the cost-effectiveness of the HS inhalations in infant bronchiolitis in a tropical country. METHODS: Decision tree analysis was used to calculate the expected costs and QALYs...
November 2, 2020: BMC Health Services Research
https://read.qxmd.com/read/33098717/saline-in-dermatology-a-literature-review
#63
REVIEW
Heba Saed El-Amawy, Sameh Magdy Sarsik
BACKGROUND: Saline, with its different concentrations, is the most used crystalloid solution in medicine. In dermatology, no large studies investigated the benefits of saline. The aim of this article is to review the different possible uses of saline in dermatology, in order to give final recommendations based on the literature review and our experience. METHODS: We performed a literature search based on PubMed, EMBASE, WHO Global Health Library, Virtual Health Library, Web of Science, Scopus, Google Scholar, and Research gate...
July 2021: Journal of Cosmetic Dermatology
https://read.qxmd.com/read/33046287/the-efficacy-of-inhaled-hypertonic-saline-for-bronchiectasis-a-meta-analysis-of-randomized-controlled-studies
#64
REVIEW
Bingfeng Xie, Ping Liu, Qi Wu, Weineng Xiang
INTRODUCTION: The efficacy of inhaled hypertonic saline for bronchiectasis remains controversial. We conduct a systematic review and meta-analysis to explore the influence of inhaled hypertonic saline versus 0.9% isotonic saline for the treatment of bronchiectasis. METHODS: We have searched PubMed, EMbase, Web of science, EBSCO, and Cochrane library databases through April 2020 for randomized controlled trials (RCTs) assessing the efficacy of inhaled hypertonic saline versus 0...
December 2020: American Journal of Emergency Medicine
https://read.qxmd.com/read/33003557/use-of-hyaluronic-acid-ha-in-chronic-airway-diseases
#65
REVIEW
Luis Máiz Carro, Miguel A Martínez-García
Hyaluronic acid (HA) is a key component of the extracellular matrix of the lungs. A unique attribute of HA is its water-retaining properties, so HA has a major role in the regulation of fluid balance in the lung interstitium. Hyaluronic acid has been widely used in the treatment of eyes, ears, joints and skin disorders, but in the last years, it has been also proposed in the treatment of certain lung diseases, including airway diseases, due to its anti-inflammatory and water-binding capacities. Hyaluronic acid aerosol decreases the severity of elastase-induced emphysema in murine models, prevents bronchoconstriction in asthmatics and improves some functional parameters in chronic obstructive pulmonary disease (COPD) patients...
September 29, 2020: Cells
https://read.qxmd.com/read/32928154/exploring-the-efficacy-of-using-hypertonic-saline-for-nebulizing-treatment-in-children-with-bronchiolitis-a-meta-analysis-of-randomized-controlled-trials
#66
JOURNAL ARTICLE
Chia-Wen Hsieh, Chiehfeng Chen, Hui-Chuan Su, Kee-Hsin Chen
BACKGROUND: Inhaled hypertonic saline (HS) has shown benefit in decreasing airway edema in acute bronchiolitis which is the most common lower respiratory infection resulting in dyspnea among infants under 2 years old. The aim of this systematic review and meta-analysis was to evaluate the efficacy and safety of HS in the implementation of treatment with nebulized HS among children with bronchiolitis. METHODS: A systematic literature search was conducted using Cochrane Library, PubMed, EMBASE and Airiti Library (Chinese Database) for randomized controlled trials from inception to July 2019...
September 14, 2020: BMC Pediatrics
https://read.qxmd.com/read/32802823/effect-of-hypertonic-saline-on-mucociliary-clearance-and-clinical-outcomes-in-chronic-bronchitis
#67
JOURNAL ARTICLE
William D Bennett, Ashley G Henderson, Agathe Ceppe, Kirby L Zeman, Jihong Wu, Christine Gladman, Fred Fuller, Stephen Gazda, Brian Button, Richard C Boucher, Scott H Donaldson
Background: Mucus dehydration and impaired mucus clearance are common features of cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD). In CF, inhaled hypertonic saline (HS) improves lung function and produces sustained increases in mucociliary clearance (MCC). We hypothesised that administration of HS (7% NaCl) twice daily for 2 weeks would improve clinical outcomes and produce sustained increases in MCC in COPD subjects with a chronic bronchitis (CB) phenotype. Methods: Twenty-two CB subjects completed a double-blinded, crossover study comparing inhaled HS to a hypotonic control solution (0...
July 2020: ERJ Open Research
https://read.qxmd.com/read/32530559/hyaluronic-acid-for-the-treatment-of-airway-diseases-in-children-little-evidence-for-few-indications
#68
JOURNAL ARTICLE
Maria Di Cicco, Diego Peroni, Margherita Sepich, Maria Giulia Tozzi, Pasquale Comberiati, Renato Cutrera
BACKGROUND: Hyaluronic acid (HA) is major physiological component of the extracellular matrix, which, in its high molecular weight form (HMW-HA) has anti-inflammatory properties. The diffusion of many different medical devices for inhalation therapy containing HA has led to an increase in their prescription, also in children. Here, we systematically review the published evidence on the efficacy and safety of HA for the treatment of upper and lower airway diseases in childhood. METHODS: Relevant published studies (randomized controlled trials) for the efficacy of HA inhalation in children with upper airways diseases, asthma, cystic fibrosis (CF), and non-CF bronchiectasis were searched in Pubmed, Scopus, and Web of Knowledge databases by combining the adequate Medical Subject Headings terms and keywords, with no limit for the year of publication...
August 2020: Pediatric Pulmonology
https://read.qxmd.com/read/32431125/-hypertonic-saline-for-hospitalized-infants-with-acute-bronchiolitis-in-israel-in-2018
#69
JOURNAL ARTICLE
Aviv Goldbart, Inbal Golan-Tripto, Yaakov Schachter
INTRODUCTION: Inhalations of hypertonic saline is a known therapy for infants diagnosed with acute bronchiolitis. Recent meta-analysis has shown that it can reduce the length of hospitalization and decrease the chances of admission. AIMS: To assess the extent of use of hypertonic saline inhalations in the pediatric wards in Israel in 2018. METHODS: During October 2018 a detailed questionnaire was emailed to all the managers of pediatric wards in Israel...
May 2020: Harefuah
https://read.qxmd.com/read/32428154/conditions-of-vulnerability-to-the-inadequate-treatment-of-bronchiolitis
#70
JOURNAL ARTICLE
Kattia Cristina Neves, Sandra Elisabete Vieira
OBJECTIVE: To analyze clinical and demographic variables possibly associated with the prescriptions of non-recommended but routinely used therapies for infants with acute viral bronchiolitis. METHODS: A cross-sectional study included hospitalized infants with bronchiolitis caused by the respiratory syncytial virus. Those with other associated infections and/or morbidities were excluded. The data were collected from medical records. RESULTS: Among 120 cases, 90% used inhaled beta-agonists, 72...
May 15, 2020: Revista da Associação Médica Brasileira
https://read.qxmd.com/read/32359945/cystic-fibrosis-2019-year-in-review
#71
REVIEW
Iolo Doull
The evidence base for modulator therapies in cystic fibrosis (CF) has continued to expand, and it is likely that up to 90% of people with CF could benefit. Worldwide there are however marked inequalities of access to basic CF care and modulator therapies. For infants and young children there is now an evidence base for inhaled hypertonic saline. There is increasing evidence that structural lung disease in CF is not due purely to infection and that mucus retention and inflammation are also key, and further evidence of the value of azithromycin in those chronically infected with Pseudomonas aeruginosa...
April 9, 2020: Paediatric Respiratory Reviews
https://read.qxmd.com/read/32358807/inhaled-mannitol-for-cystic-fibrosis
#72
JOURNAL ARTICLE
Sarah J Nevitt, Judith Thornton, Clare S Murray, Tiffany Dwyer
BACKGROUND: Several agents are used to clear secretions from the airways of people with cystic fibrosis. Mannitol increases mucociliary clearance, but its exact mechanism of action is unknown. The dry powder formulation of mannitol may be more convenient and easier to use compared with established agents which require delivery via a nebuliser. Phase III trials of inhaled dry powder mannitol for the treatment of cystic fibrosis have been completed and it is now available in Australia and some countries in Europe...
May 1, 2020: Cochrane Database of Systematic Reviews
https://read.qxmd.com/read/32345761/2019-year-in-review-aerosol-therapy
#73
REVIEW
Ariel Berlinski
Relevant publications related to medicinal and toxic aerosols are discussed in this review. Treatment of COPD includes a combination of long-acting bronchodilators and long-acting muscarinic antagonists. A combination of aclidinium bromide and formoterol fumarate was approved in the United States. The combination was superior to its components alone, as well as tiotropium and a salmeterol-fluticasone combination. Increased risk of an asthma exacerbation was reported in children exposed to electronic nicotine delivery systems...
May 2020: Respiratory Care
https://read.qxmd.com/read/32312052/dried-blood-spot-based-metabolomic-profiling-in-adults-with-cystic-fibrosis
#74
JOURNAL ARTICLE
Wafa Al-Qahtani, Mai Abdel Jabar, Afshan Masood, Minnie Jacob, Imran Nizami, Majed Dasouki, Anas M Abdel Rahman
Mucoviscidosis of the respiratory, gastrointestinal, and genitourinary tracts is the major pathology in patients with cystic fibrosis (CF), a lethal monogenic panethnic and multisystemic disease most commonly identified in Caucasians. Currently, the measurement of immuno reactive trypsinogen in dry blood spots (DBSs) is the gold-standard method for initial newborn screening for CF, followed by targeted CF transmembrane regulator (CFTR) mutation analysis, and ultimate confirmation with abnormally elevated sweat chloride...
June 5, 2020: Journal of Proteome Research
https://read.qxmd.com/read/32152407/hypertonic-saline-enhances-the-efficacy-of-aerosolized-gentamicin-against-pseudomonas-aeruginosa
#75
JOURNAL ARTICLE
Hui-Ling Lin, Li-Chung Chiu, Gwo-Hwa Wan, Chung-Chi Huang, Zong-Tian Lee, Yun-Tzu Lin, Shan-Rong Wu, Chi-Shuo Chen
Aerosol inhalation is a promising strategy for the delivery of antibiotic agents. The efficacy of antibiotic treatment by aerosol inhalation is reduced by the formation of microbial biofilms in the respiratory system and excessive airway mucus build-up. Various approaches have been taken in order to overcome this barrier. In this in vitro study, we used hypertonic saline (7%, by weight), a low cost Food and Drug Administration-approved reagent, as an aerosol carrier to study its effects with the antibiotic, gentamicin, on the most common respiratory opportunistic pathogen, Pseudomonas aeruginosa, present in the mucus...
March 9, 2020: Scientific Reports
https://read.qxmd.com/read/32107770/timing-of-hypertonic-saline-inhalation-for-cystic-fibrosis
#76
JOURNAL ARTICLE
Mark Elkins, Ruth Dentice
BACKGROUND: Inhalation of hypertonic saline improves sputum rheology, accelerates mucociliary clearance and improves clinical outcomes of people with cystic fibrosis. This is an update of a previously published Cochrane Review. OBJECTIVES: To determine whether the timing of hypertonic saline inhalation (in relation to airway clearance techniques or in relation to time of day) has an impact on its clinical efficacy in people with cystic fibrosis. SEARCH METHODS: We identified relevant randomised and quasi-randomised controlled trials from the Cochrane Cystic Fibrosis Trials Register, the Physiotherapy Evidence Database (PEDro), and international cystic fibrosis conference proceedings...
February 28, 2020: Cochrane Database of Systematic Reviews
https://read.qxmd.com/read/32072797/effectiveness-of-chest-physiotherapy-and-pulmonary-rehabilitation-in-patients-with-non-cystic-fibrosis-bronchiectasis-a-narrative-review
#77
REVIEW
Sara Annoni, Angela Bellofiore, Elena Repossini, Marta Lazzeri, Antonello Nicolini, Paolo Tarsia
Respiratory physiotherapy and rehabilitation are important therapeutic options in non-cystic fibrosis bronchiectasis (NCFB). The aims of this review of clinical trials were to evaluate the safety and the effects on physiologic and clinical outcomes of airway clearance techniques (ACTs) and rehabilitation in NCFB patients, in comparison to usual care. The search was performed on March 2018 by using PubMed and PeDro databases. 33 studies were selected. The use of ACTs for NCFB were effective in increasing sputum volume although no benefit in quality of life (QoL) or pulmonary exacerbations were observed...
February 12, 2020: Monaldi Archives for Chest Disease
https://read.qxmd.com/read/31994896/intravital-microscopic-optical-coherence-tomography-imaging-to-assess-mucus-mobilizing-interventions-for-muco-obstructive-lung-disease-in-mice
#78
JOURNAL ARTICLE
Mario Pieper, Hinnerk Schulz-Hildebrandt, Marcus A Mall, Gereon Hüttmann, Peter König
Airway mucus obstruction is a hallmark of chronic lung diseases such as cystic fibrosis, asthma, and COPD, and the development of more effective mucus-mobilizing therapies remains an important unmet need for patients with these muco-obstructive lung diseases. However, methods for sensitive visualization and quantitative assessment of immediate effects of therapeutic interventions on mucus clearance in vivo are lacking. In this study, we determined whether newly developed high-speed microscopic optical coherence tomography (mOCT) is sensitive to detect and compare in vivo effects of inhaled isotonic saline, hypertonic saline, and bicarbonate on mucus mobilization and clearance in Scnn1b -transgenic mice with muco-obstructive lung disease...
March 1, 2020: American Journal of Physiology. Lung Cellular and Molecular Physiology
https://read.qxmd.com/read/31812839/current-evaluation-and-management-of-plastic-bronchitis-in-the-pediatric-population
#79
JOURNAL ARTICLE
Youjin Li, Ryan J Williams, Natasha D Dombrowski, Karen Watters, Kevin P Daly, Alexandria L Irace, Gary A Visner, Reza Rahbar, Francis Fynn-Thompson
OBJECTIVE: To describe a multidisciplinary approach for the treatment of plastic bronchitis (PB) in children. METHODS: Retrospective chart review of children with PB between 1997 and 2017. Data regarding clinical presentation, diagnosis, management, and outcomes were analyzed. RESULTS: Of 34 patients presenting with PB, 24 had single ventricle (SV) heart disease, 9 had pulmonary disease, and one had no underlying disease. Median (IQR: interquartile range) age at the time of PB diagnosis was 5...
March 2020: International Journal of Pediatric Otorhinolaryngology
https://read.qxmd.com/read/31765597/airway-mucus-hyperconcentration-in-non-cystic-fibrosis-bronchiectasis
#80
COMPARATIVE STUDY
Kathryn A Ramsey, Alice C H Chen, Giorgia Radicioni, Rohan Lourie, Megan Martin, Amy Broomfield, Yong H Sheng, Sumaira Z Hasnain, Graham Radford-Smith, Lisa A Simms, Lucy Burr, David J Thornton, Simon D Bowler, Stephanie Livengood, Agathe Ceppe, Michael R Knowles, Peadar G Noone, Scott H Donaldson, David B Hill, Camille Ehre, Brian Button, Neil E Alexis, Mehmet Kesimer, Richard C Boucher, Michael A McGuckin
Rationale: Non-cystic fibrosis bronchiectasis is characterized by airway mucus accumulation and sputum production, but the role of mucus concentration in the pathogenesis of these abnormalities has not been characterized. Objectives: This study was designed to: 1 ) measure mucus concentration and biophysical properties of bronchiectasis mucus; 2 ) identify the secreted mucins contained in bronchiectasis mucus; 3 ) relate mucus properties to airway epithelial mucin RNA/protein expression; and 4 ) explore relationships between mucus hyperconcentration and disease severity...
March 15, 2020: American Journal of Respiratory and Critical Care Medicine
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