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Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial
In COVID-19-induced acute respiratory distress syndrome, the lungs are incapable of filling with sufficient air, leading to hypoxemia that results in high mortality among hospitalized patients. In clinical trials, low-molecular-weight heparin was administered via a specially designed soft-mist inhal...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618458/ https://www.ncbi.nlm.nih.gov/pubmed/34834183 http://dx.doi.org/10.3390/pharmaceutics13111768 |
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author | Erelel, Mustafa Kaskal, Mert Akbal-Dagistan, Ozlem Issever, Halim Dagistanli, Ahmet Serhan Balkanci, Hilal Oguz, Merve Sinem Qarayeva, Aygun Culha, Meltem Erturk, Aybige Basarir, Nur Sena Sahin, Gokben Uresin, Ali Yagiz Araman, Ahmet Ogul Medetalibeyoglu, Alpay Tukek, Tufan Oncul, Mustafa Oral Yildiz-Pekoz, Ayca |
author_facet | Erelel, Mustafa Kaskal, Mert Akbal-Dagistan, Ozlem Issever, Halim Dagistanli, Ahmet Serhan Balkanci, Hilal Oguz, Merve Sinem Qarayeva, Aygun Culha, Meltem Erturk, Aybige Basarir, Nur Sena Sahin, Gokben Uresin, Ali Yagiz Araman, Ahmet Ogul Medetalibeyoglu, Alpay Tukek, Tufan Oncul, Mustafa Oral Yildiz-Pekoz, Ayca |
author_sort | Erelel, Mustafa |
collection | PubMed |
description | In COVID-19-induced acute respiratory distress syndrome, the lungs are incapable of filling with sufficient air, leading to hypoxemia that results in high mortality among hospitalized patients. In clinical trials, low-molecular-weight heparin was administered via a specially designed soft-mist inhaler device in an investigator initiated, single-center, open-label, phase-IIb clinical trial. Patients with evidently worse clinical presentations were classed as the “Device Group”; 40 patients were given low-molecular-weight heparin via a soft mist inhaler at a dose of 4000 IU per administration, twice a day. The Control Group, also made up of 40 patients, received the standard therapy. The predetermined severity of hypoxemia and the peripheral oxygen saturation of patients were measured on the 1st and 10th days of treatment. The improvement was particularly striking in cases of severe hypoxemia. In the 10-day treatment, low-molecular-weight heparin was shown to significantly improve breathing capability when delivered via a soft-mist inhaler. |
format | Online Article Text |
id | pubmed-8618458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86184582021-11-27 Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial Erelel, Mustafa Kaskal, Mert Akbal-Dagistan, Ozlem Issever, Halim Dagistanli, Ahmet Serhan Balkanci, Hilal Oguz, Merve Sinem Qarayeva, Aygun Culha, Meltem Erturk, Aybige Basarir, Nur Sena Sahin, Gokben Uresin, Ali Yagiz Araman, Ahmet Ogul Medetalibeyoglu, Alpay Tukek, Tufan Oncul, Mustafa Oral Yildiz-Pekoz, Ayca Pharmaceutics Article In COVID-19-induced acute respiratory distress syndrome, the lungs are incapable of filling with sufficient air, leading to hypoxemia that results in high mortality among hospitalized patients. In clinical trials, low-molecular-weight heparin was administered via a specially designed soft-mist inhaler device in an investigator initiated, single-center, open-label, phase-IIb clinical trial. Patients with evidently worse clinical presentations were classed as the “Device Group”; 40 patients were given low-molecular-weight heparin via a soft mist inhaler at a dose of 4000 IU per administration, twice a day. The Control Group, also made up of 40 patients, received the standard therapy. The predetermined severity of hypoxemia and the peripheral oxygen saturation of patients were measured on the 1st and 10th days of treatment. The improvement was particularly striking in cases of severe hypoxemia. In the 10-day treatment, low-molecular-weight heparin was shown to significantly improve breathing capability when delivered via a soft-mist inhaler. MDPI 2021-10-22 /pmc/articles/PMC8618458/ /pubmed/34834183 http://dx.doi.org/10.3390/pharmaceutics13111768 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Erelel, Mustafa Kaskal, Mert Akbal-Dagistan, Ozlem Issever, Halim Dagistanli, Ahmet Serhan Balkanci, Hilal Oguz, Merve Sinem Qarayeva, Aygun Culha, Meltem Erturk, Aybige Basarir, Nur Sena Sahin, Gokben Uresin, Ali Yagiz Araman, Ahmet Ogul Medetalibeyoglu, Alpay Tukek, Tufan Oncul, Mustafa Oral Yildiz-Pekoz, Ayca Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial |
title | Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial |
title_full | Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial |
title_fullStr | Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial |
title_full_unstemmed | Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial |
title_short | Early Effects of Low Molecular Weight Heparin Therapy with Soft-Mist Inhaler for COVID-19-Induced Hypoxemia: A Phase IIb Trial |
title_sort | early effects of low molecular weight heparin therapy with soft-mist inhaler for covid-19-induced hypoxemia: a phase iib trial |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618458/ https://www.ncbi.nlm.nih.gov/pubmed/34834183 http://dx.doi.org/10.3390/pharmaceutics13111768 |
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