22 results match your criteria: "Center for Respiratory Biology and Therapeutics[Affiliation]"

Baseline-dependent improvement in CF studies, plausibility of bias.

Contemp Clin Trials Commun

December 2024

University of Washington, Departments of Pediatrics and Biostatistics Seattle Children's Research Institute, Center for Respiratory Biology and Therapeutics, United States of America.

Background: It has been commonly reported that therapeutic treatments in cystic fibrosis (CF) have ceiling effects, such that their efficacy is diminished for persons with high pre-treatment health (Montgomery et al., 2012 and Newsome et al., 2019).

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Background: Treatment of pediatric craniopharyngioma requires a multidisciplinary approach to counsel patients and families on the spectrum of treatment options, including biopsy, radiation, and/or resection. Gross-total resection can avoid radiation and its long-term comorbidities. In very young patients, this is of particular importance but is especially challenging because of anatomical considerations.

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High-frequency jet ventilation in ELBW infants: A review and update.

Semin Fetal Neonatal Med

December 2024

Respiratory Therapy Department, Seattle Children's Hospital, Seattle, WA, USA; Center for Respiratory Biology and Therapeutics, Seattle Children's Research Institute, Seattle, WA, USA.

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Background: Public health interventions delivered by community health workers (CHWs) have been proven effective in improving health outcomes across multiple fields, particularly in populations that are underserved by traditional health care systems. To date, little research is available about how CHW-led interventions could be successfully delivered virtually, despite many other health care services being offered via telehealth.

Objective: This paper details a scoping review protocol that aims to assess the existing literature on CHW-led interventions using videoconferencing technology.

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A survey of cystic fibrosis physicians' views on lung transplant referral in the era of elexacaftor/tezacaftor/ivacaftor.

Pediatr Pulmonol

December 2024

Division of Pulmonary, Critical Care, and Sleep Medicine, Department of Medicine, University of Washington, Seattle, Washington, USA.

Article Synopsis
  • In 2015, a survey indicated gaps in cystic fibrosis (CF) physicians' knowledge about lung transplant (LTx) referrals, prompting the creation of new referral guidelines and the introduction of elexacaftor/tezacaftor/ivacaftor (ETI) treatment for many patients.
  • A survey of CF center directors revealed that while many physicians recognize key indicators for LTx, a significant number still delay referrals for patients who qualify based on their lung function.
  • Despite improvements in understanding transplant criteria, many physicians express uncertainty about the best timing for referrals, especially for patients on ETI, indicating a need for updated guidelines as more data on ETI's long-term effects are available.
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Purpose: Surfactant therapy incorporates liquid bolus instillation via endotracheal tube catheter and a mechanical ventilator in preterm neonates with respiratory distress syndrome (RDS). Aerosolized surfactants have generated interest and conflicting data on the efficacy of phospholipid (PL) dose requirements. We developed and characterized a synthetic lung surfactant excipient enhanced growth (SLS-EEG) dry powder aerosol product.

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Purpose: Improving the deep lung delivery of aerosol surfactant therapy (AST) with a dry powder formulation may enable significant reductions in dose while providing improved efficacy. The objective of Part I of this two-part study was to present the development of a new dry powder aerosol synthetic lung surfactant (SLS) product and to characterize performance based on aerosol formation and realistic in vitro airway testing leading to aerosol delivery recommendations for subsequent in vivo animal model experiments.

Methods: A new micrometer-sized SLS excipient enhanced growth (EEG) dry powder formulation was produced via spray drying and aerosolized using a positive-pressure air-jet dry powder inhaler (DPI) intended for aerosol delivery directly to intubated infants with respiratory distress syndrome (RDS) or infant-size test animals.

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Background: We undertook a human-centered design approach to design the OUTREACH study of home spirometry as a CF clinical trial endpoint. We conducted a qualitative needs assessment to elicit the perspectives of people with CF (PwCF) and research coordinators (RCs) about home spirometry in the research setting and co-produced written and video home spirometry instructions in partnership with representatives from these stakeholder groups.

Methods: We conducted 7 focus groups of PwCF (N = 27), caregivers of children with CF (N = 6), or RCs (N = 24) to elicit current experiences, barriers and facilitators of home spirometry across 6 target areas, followed by discussion and prioritization.

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In Vitro Comparison of Aerosol Delivery in High-Frequency Assisted Airway Clearance Devices With Integrated Nebulizers.

Respir Care

September 2024

Center for Respiratory Biology and Therapeutics, Seattle Children's Research Institute, Seattle, Washington. Respiratory Therapy Department, Seattle Children's Hospital, Seattle, Washington.

Background: High-frequency assisted airway clearance systems combine positive expiratory pressure or oscillatory positive airway pressure with integrated nebulizers to improve the delivery of aerosols and assist with airway clearance. This aerosol study evaluated lung delivery efficiency during positive expiratory pressure and oscillatory positive airway pressure therapy of 2 high-frequency assisted airway clearance/nebulizer systems.

Methods: Aerosol delivery was evaluated during positive expiratory pressure therapy of 10 cm HO and oscillatory positive airway pressure therapy of 20 cm HO with the BiWaze Clear and the Volara high-frequency assisted airway clearance/nebulizer systems.

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Altered circadian gene expression in primary human airway epithelial cells in asthma.

ERJ Open Res

July 2024

Center for Respiratory Biology and Therapeutics, Seattle Children's Research Institute, Seattle Children's Hospital, Department of Pediatrics, Pulmonary and Sleep Medicine, University of Washington, Seattle, WA, USA.

https://bit.ly/3v9lOC6.

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Article Synopsis
  • The study investigated how effectively different aerosol delivery systems (aerosol adapter vs. aerosol circuit) deliver bronchodilators through high-flow nasal cannula (HFNC) across neonatal, pediatric, and adult models.
  • Inhaled lung doses varied by age group, with adults receiving the highest doses, while neonates showed similar results between systems, but the aerosol circuit was slightly better for older children and adults.
  • The findings highlight that current aerosol delivery methods have low lung doses (1-5%) and suggest a need for improved systems to enhance treatment efficacy for patients on HFNC.*
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Background: Newborn screening (NBS) for cystic fibrosis (CF) is universal in the United States. Protocols vary but include an immunoreactive trypsinogen (IRT) level and CFTR variant panel. California CF NBS has a 3-step screening: IRT level, variant panel, and CFTR sequencing if only one variant identified on panel.

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Epithelial cells secrete chloride to regulate water release at mucosal barriers, supporting both homeostatic hydration and the "weep" response that is critical for type 2 immune defense against parasitic worms (helminths). Epithelial tuft cells in the small intestine sense helminths and release cytokines and lipids to activate type 2 immune cells, but whether they regulate epithelial secretion is unknown. Here, we found that tuft cell activation rapidly induced epithelial chloride secretion in the small intestine.

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Genetic variation in severe cystic fibrosis liver disease is associated with novel mechanisms for disease pathogenesis.

Hepatology

November 2024

Marsico Lung Institute/UNC CF Research Center, School of Medicine, Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

Article Synopsis
  • - The study aims to uncover genetic factors contributing to severe cystic fibrosis liver disease (CFLD) since it affects only about 7% of individuals with cystic fibrosis (CF).
  • - Researchers analyzed whole-genome sequencing data from over 4,000 CF patients, finding significant associations with specific genetic variants related to CFLD, including the Z allele of SERPINA1 and several other genes.
  • - The findings suggest that severe CFLD is linked to various biological pathways, such as inflammation, immune response, and liver cell signaling, potentially leading to better understanding and treatment methods for the condition.
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Inter-alpha-trypsin inhibitor (IαI) and hyaluronan modifications enhance the innate immune response to influenza virus in the lung.

Matrix Biol

February 2024

Center for Lung Biology, the University of Washington at South Lake Union, Seattle, WA, USA; Department of Comparative Medicine, University of Washington, Seattle, WA, USA; Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, University of Washington, Seattle, WA, USA.

The inter-alpha-trypsin inhibitor (IαI) complex is composed of the bikunin core protein with a single chondroitin sulfate (CS) attached and one or two heavy chains (HCs) covalently linked to the CS chain. The HCs from IαI can be transferred to hyaluronan (HA) through a TNFα-stimulated gene-6 (TSG-6) dependent process to form an HC•HA matrix. Previous studies reported increased IαI, HA, and HC•HA complexes in mouse bronchoalveolar lavage fluid (BALF) post-influenza infection.

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Endoscopy is the gold standard for characterizing pediatric airway disorders, however, it is limited for quantitative analysis due to lack of three-dimensional (3D) vision and poor stereotactic depth perception. We utilize structure from motion (SfM) photogrammetry, to reconstruct 3D surfaces of pathologic and healthy pediatric larynges from monocular two-dimensional (2D) endoscopy. Models of pediatric subglottic stenosis were 3D printed and airway endoscopies were simulated.

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Objective: To investigate a novel servo pressure (SP) setting during high-frequency jet ventilation (HFJV) for a lung protective strategy in a neonatal model of acute respiratory distress.

Study Design: Comparison of efficacy between variable (standard) and fixed SP settings in a randomized animal study using rabbits (n = 10, mean weight = 1.80 kg) with surfactant deficiency by repeated lung lavages.

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Aerosolized lung surfactant therapy during nasal continuous positive airway pressure (CPAP) support avoids intubation but is highly complex, with reported poor nebulizer efficiency and low pulmonary deposition. The study objective was to evaluate particle size, operational compatibility, and drug delivery efficiency with various nasal CPAP interfaces and gas humidity levels of a synthetic dry powder (DP) surfactant aerosol delivered by a low-flow aerosol chamber (LFAC) inhaler combined with bubble nasal CPAP (bCPAP). A particle impactor characterized DP surfactant aerosol particle size.

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