elastin and Respiratory-Distress-Syndrome

elastin has been researched along with Respiratory-Distress-Syndrome* in 5 studies

Trials

1 trial(s) available for elastin and Respiratory-Distress-Syndrome

ArticleYear
Elastin fibers and the diagnosis of bacterial pneumonia in the adult respiratory distress syndrome.
    Critical care medicine, 1995, Volume: 23, Issue:11

    It has been inferred from previous work that 40% potassium hydroxide preparations of lower respiratory tract secretions that demonstrate elastin fibers have a 100% specificity and positive predictive value in diagnosing bacterial pneumonia in intubated, mechanically ventilated patients without the adult respiratory distress syndrome (ARDS). Our aim was to assess the specificity of 40% potassium hydroxide preparations in diagnosing bacterial pneumonia in patients with ARDS and suspected pneumonia.. Prospective, case-referral clinical study.. Referral hospital.. Of 24 patients with ARDS who were intubated and mechanically ventilated with suspected bacterial pneumonia, 22 were assessable and evaluated for this report.. Tracheo-bronchial aspirates were obtained from all patients and analyzed for elastin fibers using 40% potassium hydroxide.. Of the 22 assessable patients, ten patients did not have a complicating bacterial pneumonia. Six of these ten patients had potassium hydroxide preparations that demonstrated elastin fibers (false positives). The other four patients had preparations that did not demonstrate elastin fibers (true negatives). Specificity was 40%.. Elastin fiber preparations are not specific for diagnosing bacterial pneumonia in patients with ARDS.

    Topics: Adult; Bronchi; Bronchoalveolar Lavage Fluid; Case-Control Studies; Elastin; Humans; Hydroxides; Pneumonia, Bacterial; Potassium Compounds; Predictive Value of Tests; Prospective Studies; Respiration, Artificial; Respiratory Distress Syndrome; Sensitivity and Specificity

1995

Other Studies

4 other study(ies) available for elastin and Respiratory-Distress-Syndrome

ArticleYear
Role of matrix metalloprotease-9 in hyperoxic injury in developing lung.
    American journal of physiology. Lung cellular and molecular physiology, 2008, Volume: 295, Issue:4

    Matrix metalloprotease-9 (MMP-9) is increased in lung injury following hyperoxia exposure in neonatal mice, in association with impaired alveolar development. We studied the role of MMP-9 in the mechanism of hyperoxia-induced functional and histological changes in neonatal mouse lung. Reduced alveolarization with remodeling of ECM is a major morbidity component of oxidant injury in developing lung. MMP-9 mediates oxidant injury in developing lung causing altered lung remodeling. Five-day-old neonatal wild-type (WT) and MMP-9 (-/-) mice were exposed to hyperoxia for 8 days. The lungs were inflation fixed, and sections were examined for morphometry. The mean linear intercept and alveolar counts were evaluated. Immunohistochemistry for MMP-9 and elastin was performed. MMP-2, MMP-9, type I collagen, and tropoelastin were measured by Western blot analysis. Lung quasistatic compliance was studied in anaesthetized mice. MMP-2 and MMP-9 were significantly increased in lungs of WT mice exposed to hyperoxia compared with controls. Immunohistochemistry showed an increase in MMP-9 in mesenchyme and alveolar epithelium of hyperoxic lungs. The lungs of hyperoxia-exposed WT mice had less gas exchange surface area and were less compliant compared with room air-exposed WT and hyperoxia-exposed MMP-9 (-/-) mice. Type I collagen and tropoelastin were increased in hyperoxia-exposed WT with aberrant elastin staining. These changes were ameliorated in hyperoxia-exposed MMP-9 (-/-) mice. MMP-9 plays an important role in the structural changes consequent to oxygen-induced lung injury. Blocking MMP-9 activity may lead to novel therapeutic approaches in preventing bronchopulmonary dysplasia.

    Topics: Animals; Animals, Newborn; Body Weight; Elastin; Hyperoxia; Lung; Matrix Metalloproteinase 9; Mice; Pulmonary Alveoli; Respiratory Distress Syndrome; Respiratory Function Tests

2008
Use of elastin fibres detected in non-directed low volume bronchial lavage in ventilated ICU patients.
    Anaesthesia and intensive care, 2007, Volume: 35, Issue:2

    Elastin fibres in sputum have been described as a more sensitive marker of pulmonary necrosis than plain chest X-rays. This study aimed to determine the prevalence of elastin fibres using non-directed non-protected mini-bronchoalveolar lavage (BM-BAL) in mechanically ventilated patients in the intensive care unit. Patients admitted to the general intensive care unit of a tertiary referral hospital requiring more than 48 hours of mechanical ventilation had surveillance BM-BAL performed on admission and were then examined weekly using potassium hydroxide wet preparations for the presence of elastin fibres. All positive and a random selection of 16 negative preparations from patients with acute respiratory distress syndrome or pneumonia were fixed and examined using Weigert's staining method for elastin. Of 412 patients enrolled, 130 (32%) had pneumonia on admission, 50 (12%) developed 58 episodes of ventilator-associated pneumonia and acute respiratory distress syndrome was diagnosed in 86 patients (21%). No chest X-ray showed cavitating infiltrates. Of 985 specimens examined, only seven had elastin fibres. Elastin fibres are uncommonly found using BM-BAL in general screening, acute respiratory distress syndrome or pneumonia in the intensive care unit, the incidence too low to be a useful indicator of pulmonary necrosis.

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Biomarkers; Bronchoalveolar Lavage; Bronchoalveolar Lavage Fluid; Elastin; Female; Humans; Intensive Care Units; Lung Diseases; Male; Middle Aged; Necrosis; Pneumonia; Pneumonia, Ventilator-Associated; Respiration, Artificial; Respiratory Distress Syndrome

2007
Time course of lung parenchyma remodeling in pulmonary and extrapulmonary acute lung injury.
    Journal of applied physiology (Bethesda, Md. : 1985), 2006, Volume: 100, Issue:1

    The aim of this study is to test the hypothesis that the early changes in lung mechanics and the amount of type III collagen fiber do not predict the evolution of lung parenchyma remodeling in pulmonary and extrapulmonary acute lung injury (ALI). For this purpose, we analyzed the time course of lung parenchyma remodeling in murine models of pulmonary and extrapulmonary ALI with similar degrees of mechanical compromise at the early phase of ALI. Lung histology (light and electron microscopy), the amount of elastic and collagen fibers in the alveolar septa, the expression of matrix metalloproteinase-9, and mechanical parameters (lung-resistive and viscoelastic pressures, and static elastance) were analyzed 24 h, 1, 3, and 8 wk after the induction of lung injury. In control (C) pulmonary (p) and extrapulmonary (exp) groups, saline was intratracheally (it; 0.05 ml) instilled and intraperitoneally (ip; 0.5 ml) injected, respectively. In ALIp and ALIexp groups, mice received Escherichia coli lipopolysaccharide (10 microg it and 125 microg ip, respectively). At 24 h, all mechanical and morphometrical parameters, as well as type III collagen fiber content, increased similarly in ALIp and ALIexp groups. In ALIexp, all mechanical and histological data returned to control values at 1 wk. However, in ALIp, static elastance returned to control values at 3 wk, whereas resistive and viscoelastic pressures, as well as type III collagen fibers and elastin, remained elevated until week 8. ALIp showed higher expression of matrix metalloproteinase-9 than ALIexp. In conclusion, insult in pulmonary epithelium yielded fibroelastogenesis, whereas mice with ALI induced by endothelial lesion developed only fibrosis that was repaired early in the course of lung injury. Furthermore, early functional and morphological changes did not predict lung parenchyma remodeling.

    Topics: Adaptation, Physiological; Animals; Collagen; Elastin; Extracellular Matrix; Lung; Mice; Mice, Inbred BALB C; Recovery of Function; Respiratory Distress Syndrome; Respiratory Mechanics; Time Factors

2006
Elastin fiber analysis in acute diffuse lung injury caused by smoke inhalation.
    The Journal of trauma, 1995, Volume: 38, Issue:3

    The evaluation of various techniques to diagnose or exclude ventilator-associated bacterial pneumonia has been a focus of much research. One such technique involves elastin fiber detection. It has been inferred from previous work that 40% potassium hydroxide preparations of respiratory secretions that demonstrate elastin fibers have a 100% specificity in diagnosing bacterial pneumonia in intubated, mechanically ventilated patients without acute diffuse lung injury. The purpose of this investigation was to ascertain if elastin fibers might be detected in respiratory secretions in acute, diffuse lung injury in the absence of pneumonia (i.e., assess specificity).. An animal model using a standardized smoke inhalation protocol to cause acute, diffuse lung injury was used.. Respiratory secretions collected from the endotracheal tubes from eight sheep that underwent the standardized smoke inhalation protocol and were examined with 40% potassium hydroxide. Histologic data were obtained from autopsy to diagnose or exclude lung injury and pneumonia.. We found six (false) positive elastin fiber preparations in the absence of histologic pneumonia. Specificity was 0.25.. We concluded that seeing these results, given a true specificity of 0.99 inferred from previous work, is highly improbable with a probability of 2.74 x 10(-7). Thus, elastin fiber analysis is likely to be highly nonspecific for diagnosing pneumonia in the setting of acute diffuse lung injury.

    Topics: Acute Disease; Animals; Disease Models, Animal; Elastin; False Positive Reactions; Lung; Pneumonia, Bacterial; Respiratory Distress Syndrome; Sensitivity and Specificity; Sheep; Smoke Inhalation Injury

1995