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Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome
AIM: To study the effects of infusion of atrial natriuretic peptide (ANP) versus the inhalation of nitric oxide (NO) in patients with an early acute respiratory distress syndrome (ARDS). METHODS: Ten patients with severe ARDS were studied in a crossover study design, within 72 hours after starting m...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC31579/ https://www.ncbi.nlm.nih.gov/pubmed/11353932 |
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author | Bindels, Alexander JGH van der Hoeven, Johannes G Groeneveld, Paul HP Frölich, Marijke Meinders, Arend E |
author_facet | Bindels, Alexander JGH van der Hoeven, Johannes G Groeneveld, Paul HP Frölich, Marijke Meinders, Arend E |
author_sort | Bindels, Alexander JGH |
collection | PubMed |
description | AIM: To study the effects of infusion of atrial natriuretic peptide (ANP) versus the inhalation of nitric oxide (NO) in patients with an early acute respiratory distress syndrome (ARDS). METHODS: Ten patients with severe ARDS were studied in a crossover study design, within 72 hours after starting mechanical ventilation. We studied the effects of ANP infusion (10 ng/kg/min for 1 hour) and of inhalation of NO (20 ppm for 1 hour) on hemodynamic and respiratory patient parameters, as well as the effects on plasma levels of ANP, guanosine 3',5'-cyclic monophosphate, nitrate and endothelin-1. RESULTS: Despite an approximate 50% increase in mixed venous ANP plasma concentration (from 86 ± 21 to 123 ± 33 ng/l, P < 0.05) during ANP infusion, there were no changes in mean pulmonary artery pressure, pulmonary vascular resistance index, extravascular lung water index, or in pulmonary gas exchange. NO inhalation, in contrast, lowered mean pulmonary artery pressure (from 26 ± 1.9 to 23.9 ± 1.7 mmHg, P < 0.01), pulmonary vascular resistance index (from 314 ± 37 to 273 ± 32 dynes/cm(5)/m(2), P < 0.05) and central venous pressure (from 8.2 ± 1.2 to 7.3 ± 1.1 mmHg, P < 0.02). Furthermore, NO inhalation improved pulmonary gas exchange, reflected by a decrease in alveolar-arterial oxygen gradient (from 41.9 ± 3.9 to 40.4 ± 3.6 kPa, P < 0.05), a small increase in oxygenation (PaO(2)/FiO(2) from 17.7 ± 1.4 to 19.7 ± 1.1 kPa, P = 0.07) and a small decrease in venous admixture (Q(s)/Q(t) from 35.7 ± 2.0 to 32.8 ± 2.7%, P = 0.11). CONCLUSION: This study shows that, in contrast to NO inhalation, infusion of ANP neither improves oxygenation nor attenuates pulmonary hypertension or pulmonary edema in patients with severe ARDS. |
format | Text |
id | pubmed-31579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-315792001-05-18 Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome Bindels, Alexander JGH van der Hoeven, Johannes G Groeneveld, Paul HP Frölich, Marijke Meinders, Arend E Crit Care Primary Research AIM: To study the effects of infusion of atrial natriuretic peptide (ANP) versus the inhalation of nitric oxide (NO) in patients with an early acute respiratory distress syndrome (ARDS). METHODS: Ten patients with severe ARDS were studied in a crossover study design, within 72 hours after starting mechanical ventilation. We studied the effects of ANP infusion (10 ng/kg/min for 1 hour) and of inhalation of NO (20 ppm for 1 hour) on hemodynamic and respiratory patient parameters, as well as the effects on plasma levels of ANP, guanosine 3',5'-cyclic monophosphate, nitrate and endothelin-1. RESULTS: Despite an approximate 50% increase in mixed venous ANP plasma concentration (from 86 ± 21 to 123 ± 33 ng/l, P < 0.05) during ANP infusion, there were no changes in mean pulmonary artery pressure, pulmonary vascular resistance index, extravascular lung water index, or in pulmonary gas exchange. NO inhalation, in contrast, lowered mean pulmonary artery pressure (from 26 ± 1.9 to 23.9 ± 1.7 mmHg, P < 0.01), pulmonary vascular resistance index (from 314 ± 37 to 273 ± 32 dynes/cm(5)/m(2), P < 0.05) and central venous pressure (from 8.2 ± 1.2 to 7.3 ± 1.1 mmHg, P < 0.02). Furthermore, NO inhalation improved pulmonary gas exchange, reflected by a decrease in alveolar-arterial oxygen gradient (from 41.9 ± 3.9 to 40.4 ± 3.6 kPa, P < 0.05), a small increase in oxygenation (PaO(2)/FiO(2) from 17.7 ± 1.4 to 19.7 ± 1.1 kPa, P = 0.07) and a small decrease in venous admixture (Q(s)/Q(t) from 35.7 ± 2.0 to 32.8 ± 2.7%, P = 0.11). CONCLUSION: This study shows that, in contrast to NO inhalation, infusion of ANP neither improves oxygenation nor attenuates pulmonary hypertension or pulmonary edema in patients with severe ARDS. BioMed Central 2001 2001-04-20 /pmc/articles/PMC31579/ /pubmed/11353932 Text en Copyright © 2001 Bindels et al, licensee BioMed Central Ltd |
spellingShingle | Primary Research Bindels, Alexander JGH van der Hoeven, Johannes G Groeneveld, Paul HP Frölich, Marijke Meinders, Arend E Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome |
title | Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome |
title_full | Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome |
title_fullStr | Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome |
title_full_unstemmed | Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome |
title_short | Atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome |
title_sort | atrial natriuretic peptide infusion and nitric oxide inhalation in patients with acute respiratory distress syndrome |
topic | Primary Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC31579/ https://www.ncbi.nlm.nih.gov/pubmed/11353932 |
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