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| Name | Class |
|---|---|
| University Hospital Muenster | OTHER |
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This research aims to investigate the role of daily measurement of urinary cell cycle arrest markers and other serum and urinary biomarkers to predict the development of acute kidney injury in critically ill patients with COVID-19 and acute respiratory disease.
COVID-19 is a rapidly evolving pandemic with approximately 5% of all patients requiring admission to an intensive care unit. In critically ill patients with COVID-19, acute respiratory disease and acute kidney injury (AKI) are very common. Patients with AKI have an increased risk of mortality, especially renal replacement therapy (RRT) is required. The latest Intensive Care National Audit & Research Centre (ICNARC) report shows a 77% ICU mortality in patients with COVID-19 who require mechanical ventilation and RRT.
COVID-19 associated AKI is still poorly understood. The exact underlying pathophysiology remains unknown. Furthermore, there are no specific strategies to prevent or treat AKI. Management is supportive consisting of fluid and haemodynamic optimization, discontinuation of nephrotoxic drugs and prevention of nephrotoxic exposures. Ideally, AKI needs to be recognized as early as possible for these supportive measures to be effective.
Early prediction of AKI may be valuable to optimize management and improve outcomes. In critically ill patients without COVID-19, the two cell-cycle arrest markers, tissue inhibitor of metalloproteinases-2 (TIMP-2) and insulin-like growth-factor binding protein 7 (IGFBP7), have been shown to predict the development of AKI. Whether these new biomarkers also predict the development of AKI in critically ill patients with COVID-19 is unknown.
The aim of this project is to explore whether urinary cell cycle arrest markers and other renal biomarkers have a role in predicting AKI in critically ill patients with COVID-19 and acute respiratory disease. The results will advance the understanding of this disease and serve to develop strategies for individualized management of this high-risk group.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| COVID-19 patients with acute respiratory disease | Adult patients with COVID-19 and moderate or severe respiratory disease |
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| Measure | Description | Time Frame |
|---|---|---|
| Any stage of acute kidney injury | As defined by Kidney Diseases: Improving Global Outcome | 7 days |
| Measure | Description | Time Frame |
|---|---|---|
| need for RRT in first 7 days | Renal replacement therapy requirement at the clinicians' discretion | 7 days |
| Mortality | ICU mortality | 7 and 28 days |
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Inclusion Criteria:
Exclusion Criteria:
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COVID-19 patients with moderate or severe respiratory disease
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Marlies Ostermann, MD, PhD | Contact | 0044 207 188 3038 | 83036 | Marlies.Ostermann@gstt.nhs.uk |
| Nuttha Lumlertgul, MD, PhD | Contact | 0044 207 188 3038 | 83036 | Nuttha.Lumlertgul@gstt.nhs.uk |
| Name | Affiliation | Role |
|---|---|---|
| Marlies Ostermann, MD, PhD | Guy's and St Thomas' NHS Foundation Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Guy's & St Thomas' Hospital | Recruiting | London | SE1 7EH | United Kingdom |
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| ID | Term |
|---|---|
| D058186 | Acute Kidney Injury |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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The investigators will collect blood and urine samples for biomarker measurement at the following time points: at the time point of study inclusion, 12h, 24h, 36h, 48h, 60h, and 72h after inclusion.
| Duration of mechanical ventilation | Duration | 7 and 28 days |
| Duration of vasopressor support | Duration | 7 and 28 days |
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |