3 results on '"Verboom, Diana"'
Search Results
2. Age-dependent differences in pulmonary host responses in ARDS: a prospective observational cohort study
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Schouten, Laura R., van Kaam, Anton H., Kohse, Franziska, Veltkamp, Floor, Bos, Lieuwe D., de Beer, Friso M., van Hooijdonk, Roosmarijn T., Horn, Janneke, Straat, Marleen, Witteveen, Esther, Glas, Gerie J., Wieske, Luuk, van Vught, Lonneke A., Wiewel, Maryse A., Ingelse, Sarah A., Cortjens, Bart, van Woensel, Job B., Bos, Albert P., Walther, Thomas, Schultz, Marcus J., Wösten-van Asperen, Roelie M., Hoogendijk, Arie J., Huson, Mischa A., van der Poll, Tom, Scicluna, Brendon, Bonten, Marc J., Cremer, Olaf L., Frencken, Jos F., van de Groep, Kirsten, Klein Klouwenberg, Peter M., Koster-Brouwer, Maria E., Ong, David S., Verboom, Diana M., Amsterdam Reproduction & Development (AR&D), Internal medicine, Division 1, Pediatric surgery, Amsterdam Neuroscience - Brain Imaging, Neurology, Neonatology, ARD - Amsterdam Reproduction and Development, Graduate School, AII - Inflammatory diseases, Intensive Care Medicine, ACS - Heart failure & arrhythmias, ANS - Neuroinfection & -inflammation, Anesthesiology, ANS - Amsterdam Neuroscience, APH - Quality of Care, ACS - Diabetes & metabolism, APH - Health Behaviors & Chronic Diseases, Center of Experimental and Molecular Medicine, Medical Microbiology and Infection Prevention, Paediatric Intensive Care, AGEM - Digestive immunity, AGEM - Endocrinology, metabolism and nutrition, General Paediatrics, Infectious diseases, Epidemiology and Data Science, APH - Personalized Medicine, ACS - Pulmonary hypertension & thrombosis, and ACS - Microcirculation
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medicine.medical_specialty ,ARDS ,Aging ,Critical Care and Intensive Care Medicine ,Gastroenterology ,Pathophysiology ,Endothelial activation ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Epidemiology ,medicine ,Journal Article ,Host response ,medicine.diagnostic_test ,biology ,business.industry ,Research ,lcsh:Medical emergencies. Critical care. Intensive care. First aid ,Interleukin ,030208 emergency & critical care medicine ,Angiotensin-converting enzyme ,lcsh:RC86-88.9 ,medicine.disease ,3. Good health ,Bronchoalveolar lavage ,030228 respiratory system ,biology.protein ,business ,Angiotensin converting enzyme ,Biomarkers ,Cohort study - Abstract
Background Results from preclinical studies suggest that age-dependent differences in host defense and the pulmonary renin–angiotensin system (RAS) are responsible for observed differences in epidemiology of acute respiratory distress syndrome (ARDS) between children and adults. The present study compares biomarkers of host defense and RAS in bronchoalveolar lavage (BAL) fluid from neonates, children, adults, and older adults with ARDS. Methods In this prospective observational study, we enrolled mechanical ventilated ARDS patients categorized into four age groups: 20 neonates ( 65 years of age). All patients underwent a nondirected BAL within 72 h after intubation. Activities of the two main enzymes of RAS, angiotensin converting enzyme (ACE) and ACE2, and levels of biomarkers of inflammation, endothelial activation, and epithelial damage were determined in BAL fluid. Results Levels of myeloperoxidase, interleukin (IL)-6, IL-10, and p-selectin were higher with increasing age, whereas intercellular adhesion molecule-1 was higher in neonates. No differences in activity of ACE and ACE2 were seen between the four age groups. Conclusions Age-dependent differences in the levels of biomarkers in lungs of ARDS patients are present. Especially, higher levels of markers involved in the neutrophil response were found with increasing age. In contrast to preclinical studies, age is not associated with changes in the pulmonary RAS. Electronic supplementary material The online version of this article (10.1186/s13613-019-0529-4) contains supplementary material, which is available to authorized users.
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- 2019
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3. Estimated dead space fraction and the ventilatory ratio are associated with mortality in early ARDS
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Morales-Quinteros, Luis, Schultz, Marcus J., Bringué, Josep, Calfee, Carolyn S., Camprubí, Marta, Cremer, Olaf L., Horn, Janneke, van der Poll, Tom, Sinha, Pratik, Artigas, Antonio, Bos, Lieuwe D., de Beer, Friso M., Glas, Gerie J., Hoogendijk, Arie J., van Hooijdonk, Roosmarijn T., Huson, Mischa A., Scicluna, Brendon, Schouten, Laura R., Straat, Marleen, van Vught, Lonneke A., Wieske, Luuk, Wiewel, Maryse A., Witteveen, Esther, Bonten, Marc J., Frencken, Jos F., van de Groep, Kirsten, Klein Klouwenberg, Peter M., Koster-Brouwer, Maria E., Ong, David S., Varkila, Meri R., Verboom, Diana M., Intensive Care Medicine, ANS - Neuroinfection & -inflammation, Center of Experimental and Molecular Medicine, Infectious diseases, ACS - Heart failure & arrhythmias, Anesthesiology, Graduate School, ACS - Diabetes & metabolism, APH - Quality of Care, Epidemiology and Data Science, APH - Health Behaviors & Chronic Diseases, APH - Personalized Medicine, Medical Microbiology and Infection Prevention, AII - Inflammatory diseases, ARD - Amsterdam Reproduction and Development, ACS - Pulmonary hypertension & thrombosis, and ACS - Microcirculation
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medicine.medical_specialty ,ARDS ,medicine.medical_treatment ,Dead space ,Respiratory Dead Space ,Prognostication ,Critical Care and Intensive Care Medicine ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,law ,Internal medicine ,Journal Article ,medicine ,Acute respiratory distress syndrome (ARDS) ,Intensive care unit ,Mortality ,Respiratory dead space ,Mechanical ventilation ,Acute respiratory distress syndrome ,business.industry ,Research ,lcsh:Medical emergencies. Critical care. Intensive care. First aid ,Ventilatory ratio ,030208 emergency & critical care medicine ,lcsh:RC86-88.9 ,Odds ratio ,medicine.disease ,030228 respiratory system ,Breathing ,Cardiology ,Prediction ,business ,Cohort study - Abstract
Background Indirect indices for measuring impaired ventilation, such as the estimated dead space fraction and the ventilatory ratio, have been shown to be independently associated with an increased risk of mortality. This study aimed to compare various methods for dead space estimation and the ventilatory ratio in patients with acute respiratory distress syndrome (ARDS) and to determine their independent values for predicting death at day 30. The present study is a post hoc analysis of a prospective observational cohort study of ICUs of two tertiary care hospitals in the Netherlands. Results Individual patient data from 940 ARDS patients were analyzed. Estimated dead space fraction and the ventilatory ratio at days 1 and 2 were significantly higher among non-survivors (p VD/VT phys] and the ventilatory ratio at day 2 showed independent association with mortality at 30 days (odds ratio 1.28 [95% CI 1.02–1.61], p p VD/VT HB] and Penn State [VD/VT PS] estimations were not associated with mortality. The predicted validity of the estimated dead space fraction and the ventilatory ratio improved the baseline model based on PEEP, PaO2/FiO2, driving pressure and compliance of the respiratory system at day 2 (AUROCC 0.72 vs. 0.69, p Conclusions Estimated methods for dead space calculation and the ventilatory ratio during the early course of ARDS are associated with mortality at day 30 and add statistically significant but limited improvement in the predictive accuracy to indices of oxygenation and respiratory system mechanics at the second day of mechanical ventilation.
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- 2019
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