FIBRO-COVID: Pulmonary Fibrosis During Severe COVID-19 Pneumonia
Study Details
Study Description
Brief Summary
The COVID-19 pandemic is caused by the severe acute respiratory syndrome coronavirus 2 (SARS CoV-2), an emerging coronavirus, which has already infected 192 million people with a case fatality rate close to 2%. About 5% of patients infected with SARS CoV-2 have a critical form with organ failure. Among critical patients admitted to intensive care, about 70% of them will require ventilatory assistance by invasive mechanical ventilation (MV) with a mortality rate of 35% and a median MV duration of 12 days. The most severe lung damage resulting from SARS CoV-2 infection is the acute respiratory distress syndrome (ARDS). The virus infects alveolar epithelial cells and capillary endothelial cells leading to an activation of endothelium, hypercoagulability and thrombosis of pulmonary capillaries. This results in abnormal ventilation / perfusion ratios and profound hypoxemia. To date, the therapeutic management of severe SARS CoV-2 pneumonia lay on the early use of corticosteroids and Interleukin-6 (IL-6) receptor antagonist, which both reduce the need of MV and mortality. The risk factors of death in Intensive Care Unit (ICU) are: advanced age, severe obesity, coronary heart disease, active cancer, severe hypoxemia, and hepatic and renal failure on admission. Among MV patients, the death rate is doubled in those with both reduced thoracopulmonary compliance and elevated D-dimer levels. Patients with severe alveolar damage are at risk of progressing towards irreversible pulmonary fibrosis, the incidence of which still remain unknown. The diagnosis of pulmonary fibrosis is based on histology but there are some non-invasive alternative methods (serum or bronchoalveolar biomarkers, chest CT scan). We aim to assess the incidence of pulmonary fibrosis in patients with severe SARS CoV-2 related pneumonia. We will investigate the prognostic impact of fibrosis on mortality and the number of days alive free from MV at Day 90. Finally, we aim to identify risk factors of fibrosis.
Condition or Disease | Intervention/Treatment | Phase |
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Detailed Description
Medical charts of patients admitted at the Intensive Care Unit (ICU) of the European Hospital of Marseille between March 2020 and June 2021 will be collected retrospectively using electronic database. Data collected will focus on demography, clinical variables, biological analyses, lung biopsies, and chest CT scans performed during the hospital stay.
Our routine protocol for COVID-19 management follows the "Coronavirus Disease 2019 (COVID-19) Treatment Guidelines" including the early use of corticosteroids (Dexamethasone) and IL-6 receptor antagonist (Tocilizumab). Additionally, we routinely perform, on a weekly basis, measurements of SARS CoV-2 viral load by PCR, SARS CoV-2 antibodies production, and biomarkers of fibrosis including hyaluronic acid (HA) and amino-terminal type I (PINP) and type III (PIIINP) peptides of procollagen.
The present study aim to determine the proportion of patients encountering non-invasive criteria of pulmonary fibrosis as defined by either typical CT scan patterns (reticulation and/or bronchiectasia), or increased serum concentration of PIIINP above 16 µg/L, or increased bronchoalveolar lavage (BAL) concentration of PIIINP above 9 µg/L.
A definitive diagnosis of lung fibrosis will be established according to lung pathology findings in patients for whom a lung biopsy have been performed during the hospital stay.
Patients with a diagnosis of pulmonary fibrosis will be compared with those without fibrosis, both in the population of mechanically ventilated patients and in those remained spontaneously breathing.
The primary end-point will be the number of days alive and free from the ventilator (ventilator-free days) at Day 90. The others outcomes of interest will be the duration of mechanical ventilation, the duration of ICU stay, the ICU mortality, the in-hospital mortality, the Day 28 mortality, and the Day 90 mortality.
The present study also aims to determine the risk factors of pulmonary fibrosis occurence, focusing on mechanical ventilatory settings, daily dose of corticosteroids, and the occurence of nosocomial pneumonia with special attention to lung reactivation of herpesviridae.
Finally, the relation between antibodies production and viral clearance (defined as the time to the first negative SARS CoV-2 PCR) or ICU survival will be investigated.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
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Patients with pulmonary fibrosis All ICU patients for which one of the non-invasive criteria of pulmonary fibrosis is reached : Typical CT scan patterns (reticulation and/or bronchiectasia) Serum PIIINP above 16 µg/L BAL PIIINP above 9 µg/L |
Diagnostic Test: Aminoterminal type III peptide of procollagen
Serial Measurement of PIIINP in serum and/or BAL
Other Names:
Diagnostic Test: Lung computed tomography
Screening for the presence of reticulation or bronchiectasia within lung parenchyma
Other Names:
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Patients without pulmonary fibrosis All ICU patients for which none of the non-invasive criteria of pulmonary fibrosis are reached. |
Diagnostic Test: Aminoterminal type III peptide of procollagen
Serial Measurement of PIIINP in serum and/or BAL
Other Names:
Diagnostic Test: Lung computed tomography
Screening for the presence of reticulation or bronchiectasia within lung parenchyma
Other Names:
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Outcome Measures
Primary Outcome Measures
- Ventilator-free days [Day 90]
Number of days alive and free from mechanical ventilation
Secondary Outcome Measures
- Day 90 mortality [Day 90]
Mortality at Day 90
- Day 28 mortality [Day 28]
Mortality at Day 28
- ICU Mortality [From date of ICU admission until the date of ICU liberation, assessed up to 6 months]
Death from any cause during the ICU stay
- In-hospital Mortality [From date of hospital admission until the date of hospital liberation, assessed up to 12 months]
Death from any cause during the Hospital stay
- Length of MV [From date of ICU admission until the date of ICU liberation, assessed up to 6 months]
Duration of mechanical ventilation during the ICU stay
- Length of ICU stay [From date of ICU admission until the date of ICU liberation, assessed up to 6 months]
Duration of ICU stay
- Length of hospital stay [From date of hospital admission until the date of hospital liberation, assessed up to 12 months]
Duration of hospital stay
- Time to viral clearance [From date of first symptom until the date of ICU liberation, assessed up to 6 months]
Time from first symptom to the first negative SARS CoV-2 PCR
- Corticosteroid dose [From date of ICU admission until the date of ICU liberation, assessed up to 6 months]
Daily corticosteroid dose (methylprednisolone equivalent)
- Lung herpesviridae reactivation [From date of ICU admission until the date of ICU liberation, assessed up to 6 months]
Presence on BAL of at least one Herpesviridae (Cytomegalovirus, Epstein-Barr Virus, Herpes simplex virus, Human herpes virus-6)
- Blood herpesviridae reactivation [From date of ICU admission until the date of ICU liberation, assessed up to 6 months]
Presence on serum of at least one Herpesviridae (Cytomegalovirus, Epstein-Barr Virus, Herpes simplex virus, Human herpes virus-6)
Eligibility Criteria
Criteria
Inclusion Criteria:
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Acute hypoxemic respiratory failure
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Positive SARS CoV-2 PCR on nasopharyngeal swab or distal airway sampling
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ICU admission during the hospital stay
Exclusion Criteria:
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Chronic respiratory failure (Oxygen or NIPPV at home)
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Patients with "Do Not Resuscitate" order at ICU admission
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Admission from an other ICU with a stay > 2 days
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Transfer to an another ICU during the ICU stay
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Hopital Europeen Marseille | Marseille | France | 13003 |
Sponsors and Collaborators
- Hôpital Européen Marseille
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Additional Information:
- World Health Organization Coronavirus (COVID-19) Dashboard
- Coronavirus Disease 2019 (COVID-19) Treatment Guidelines
Publications
- Burnham EL, Hyzy RC, Paine R 3rd, Kelly AM, Quint LE, Lynch D, Curran-Everett D, Moss M, Standiford TJ. Detection of fibroproliferation by chest high-resolution CT scan in resolving ARDS. Chest. 2014 Nov;146(5):1196-1204. doi: 10.1378/chest.13-2708.
- COVID-ICU Group on behalf of the REVA Network and the COVID-ICU Investigators. Clinical characteristics and day-90 outcomes of 4244 critically ill adults with COVID-19: a prospective cohort study. Intensive Care Med. 2021 Jan;47(1):60-73. doi: 10.1007/s00134-020-06294-x. Epub 2020 Oct 29.
- Forel JM, Guervilly C, Hraiech S, Voillet F, Thomas G, Somma C, Secq V, Farnarier C, Payan MJ, Donati SY, Perrin G, Trousse D, Dizier S, Chiche L, Baumstarck K, Roch A, Papazian L. Type III procollagen is a reliable marker of ARDS-associated lung fibroproliferation. Intensive Care Med. 2015 Jan;41(1):1-11. doi: 10.1007/s00134-014-3524-0. Epub 2014 Oct 30.
- Grasselli G, Tonetti T, Protti A, Langer T, Girardis M, Bellani G, Laffey J, Carrafiello G, Carsana L, Rizzuto C, Zanella A, Scaravilli V, Pizzilli G, Grieco DL, Di Meglio L, de Pascale G, Lanza E, Monteduro F, Zompatori M, Filippini C, Locatelli F, Cecconi M, Fumagalli R, Nava S, Vincent JL, Antonelli M, Slutsky AS, Pesenti A, Ranieri VM; collaborators. Pathophysiology of COVID-19-associated acute respiratory distress syndrome: a multicentre prospective observational study. Lancet Respir Med. 2020 Dec;8(12):1201-1208. doi: 10.1016/S2213-2600(20)30370-2. Epub 2020 Aug 27.
- Wiersinga WJ, Rhodes A, Cheng AC, Peacock SJ, Prescott HC. Pathophysiology, Transmission, Diagnosis, and Treatment of Coronavirus Disease 2019 (COVID-19): A Review. JAMA. 2020 Aug 25;324(8):782-793. doi: 10.1001/jama.2020.12839. Review.
- 2021_06_02_JAS