Growth of Airways and Lung Parenchyma in Normal Infants

正常婴儿气道和肺实质的生长

• 批准号: 7368051
• 负责人: Robert S. Tepper
• 金额: $ 40.16万
• 依托单位: INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS
• 依托单位国家: 美国
• 财政年份: 1996
• 资助国家: 美国
• 起止时间: 1996-03-01 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7368051
• 关键词: Adult; Age; Age-Years; Alveolar; Alveolus; Animals; Area; Arts; Autopsy; Birth; Borderline Personality Disorder; Bronchopulmonary Dysplasia; Cell Proliferation; Childhood; Chronic; Clinical; Clinical Trials; Computer Simulation; Conflict (Psychology); Continuous Positive Airway Pressure; Data; Delivery Rooms; Development; Diffuse; Diffusion; Early treatment; Effectiveness; Enrollment; Environmental air flow; Excision; Ferrets; Functional disorder; Gases; Growth; Growth and Development function; Heterogeneity; Human; Image; Infant; Institution; Intervention; Knowledge; Laboratories; Life; Living Wills; Lung; Lung diseases; Maintenance; Measurement; Measures; Mechanical ventilation; Mechanics; Methodology; Morphologic artifacts; Motion; National Institute of Child Health and Human Development; Neonatal; Noble Gases; Numbers; Oryctolagus cuniculus; Outcome; Pattern; Peripheral; Physiological; Pregnancy; Premature Birth; Premature Infant; Property; Pulmonary Diffusing Capacity; Range; Research; Research Personnel; Resolution; Respiratory distress; Respiratory physiology; Role; Staging; Structure; Structure of parenchyma of lung; Surface; Techniques; Therapeutic; Thick; Time; Tissues; Toddler; Uncertainty; Vital capacity; Week; X-Ray Computed Tomography; age effect; age group; airway obstruction; density; design; experience; improved; in vivo; infancy; lung development; lung injury; lung volume; premature lungs; programs; prophylactic; rapid growth; respiratory; size; surfactant; three dimensional structure; two-dimensional

This proposal will apply state-of-the-arttechniques to assess normal growth and development of the lung parenchyma in infants and toddlers, an important and difficult age group to evaluate. Understanding lung growth early in life is critical for designing therapeutic strategies to promote lung growth in infants with lung disease. We will also evaluate the chronic pulmonary sequelae related to premature birth, as well as compare the effects upon lung structure and function of two different strategies for ventilatory support of very premature infants. Our laboratory developed the methodology to assess forced expiratory maneuvers in infants, and we have adapted this technique to measure single-breath diffusing capacity in infants, as an in- vivo assessment of surface area for gas exchange. In addition, a technique to obtain high resolution CT images in infants at elevated lung volumes without artifactsfrom respiratory motion, we will obtain in-vivo quantitative measurements of the lung parenchyma! tissue density, as well as airway size and wall thickness. Ventilation inhomogeneity within the lung will also be assessed from washout studies of inert gases with differing diffusivity. Lastly, we will extend our computational model of the conducting airways to include the acinar structure, which will assist in interpreting the physiologic data and mechanisms contributing to pulmonary dysfunction in infants born prematurely. SPECIFIC AIM # 1: Determine the relationship between parenchymal tissue and alveolar volume with normal lung growth early in life. We hypothesize that during the first two years of life that parenchymal surface area and alveolar volume increase with somatic growth; however, the ratio of surface area to volume remains constant, while ventilation within the lung becomes more homogenous. SPECIFIC AIM # 2: Determine the pulmonary sequelae of premature birth and assessthe effectivenessof early treatment strategies upon the pulmonary sequelae. We hypothesize that premature birth impedes growth and development of the lung parenchyma and the airways at a corrected-age of 1-year. In addition, initiating continuous positive airway pressure (CPAP) and a permissive ventilatory strategy in very premature infants at birth will improve lung growth and lung function compared to treatment with early surfactant and conventional ventilation.

这项建议将应用最先进的技术来评估肺的正常生长和发育。 婴幼儿脑实质是一个重要且难以评估的年龄段。了解肺 生命早期发育对于设计促进肺部发育的治疗策略至关重要。 疾病。我们还将评估与早产有关的慢性肺部后遗症，以及 两种不同呼吸机支持策略对VERS患者肺结构和功能的影响 早产儿。我们的实验室开发了评估用力呼气动作的方法学 我们已经将这项技术应用于测量婴儿的单次呼吸弥散能力，作为一种 气体交换表面积的活体评估。此外，一种获得高分辨率CT的技术 没有呼吸运动伪影的婴儿肺容量增加的图像，我们将获得活体图像 肺实质的定量测量！组织密度，以及呼吸道大小和壁厚。 肺内通风的不均一性也将通过对惰性气体的冲刷研究进行评估 不同的扩散系数。最后，我们将扩展我们的传导通道的计算模型以包括 腺泡结构，这将有助于解释生理数据和机制有助于 早产儿的肺功能障碍。 具体目标1：确定实质组织和肺泡体积之间的关系 生命早期的正常肺生长。 我们假设在生命的头两年，肺实质表面积和肺泡体积 随着体细胞的生长而增加，但表面积与体积的比率保持不变，而 肺内的通风变得更加均匀。 具体目标2：确定早产的肺部后遗症并评估其疗效 肺部后遗症的早期治疗策略。 我们假设早产会阻碍肺实质的生长和发育，而 航空公司的更正年龄为1岁。此外，启动持续气道正压(CPAP)和 极早产儿出生时的允许性呼吸策略将改善肺生长和肺功能 与早期使用表面活性物质和常规机械通气治疗相比。