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This study investigates to which extent recommended nephroprotective measures are implemented in critically ill patients with moderate or severe acute kidney injury.
Acute kidney injury (AKI) is a global problem affecting more than 10% of all hospitalized patients and up to 50% of critically ill patients, with survival related not only to the severity,1 but also to the duration of renal dysfunction.2 Recent evidence suggests that two-thirds of patients with AKI resolve their renal dysfunction within 3-7 days whereas those in whom renal dysfunctions persist have dramatically reduced survival over the following year.2 Persistence of AKI is of grave importance in that it increases an individual's risk of developing chronic kidney disease (CKD) which is a major cause of morbidity and mortality. This link between AKI and CKD has been established over the last decade3 and specific recommendations for the management of patients with AKI have been proposed in order to potentially influence this transition.4 To date, there are no specific pharmacological options for preventing or treating AKI, which is why new approaches and intensive efforts are urgently needed to reduce the occurrence of AKI. The Kidney Disease: Improving Global Outcomes (KDIGO) clinical practice guidelines recommend implementing a bundle of different supportive measures, which, in theory, should be initiated in all patients with AKI in order to prevent disease progression. However, clinical practice and recent studies have shown that the implementation of the KDIGO bundle is still not standard clinical practice despite the fact that evidence suggest clear effectiveness in the reduction of AKI rates.5-9 Poor implementation of nephroprotective measures presents a major missed opportunity to reduce AKI-related morbidity and mortality and to improve long-term outcomes. To investigate the extent to which nephroprotective measures are implemented in patients with AKI can reduce the occurrence of persistent surgical AKI, a multi-center prospective cohort study will be performed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Critically ill patients |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Nephroprotective measures | Procedure | Due to the observational design of the study, no study specific interventions are performed. The treatment of the patients is completely guided by the responsible physicians. |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of patients in whom "Kidney Disease: Improving Global Outcomes (KDIGO)" guideline recommendations are successfully implemented for 48 hours, following the onset of moderate/ severe AKI (defined by KDIGO criteria) | 60 hours after onset of moderate/severe AKI |
| Measure | Description | Time Frame |
|---|---|---|
| Severity of Acute Kidney Injury | Severity of AKI (worst Acute Kidney Injury (AKI) stage according to Kidney Disease: Improving Global Outcomes (KDIGO) criteria, with stage 1 being the least and stage 3 being the most severe stage) | within 72 hours after diagnosis |
| Duration of AKI (Acute Kidney Injury) |
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with recovery of baseline renal function | recovery of baseline renal function measured by estimated glomerular filtration rate (eGFR) at hospital discharge | hospital discharge (up to 30 days) |
| Number of Participants with need for renal replacement therapy |
Inclusion Criteria:
Exclusion Criteria:
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Critically ill patients (intensive care unit of the participating study sites)
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Melanie Meersch-Dini, MD | Contact | +492518347255 | meersch@uni-muenster.de |
| Name | Affiliation | Role |
|---|---|---|
| Alexander Zarbock, MD | University Münster | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Universitätsklinik Innsbruck | Recruiting | Innsbruck | 6020 | Austria | ||
| University Hospital Münster; Department of Anesthesiology, Intensive Care Medicine and Pain Medicine |
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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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Blood plasma, urine
transient AKI (< 48 hours), persistent AKI (48 hours - 7 days) or acute kidney disease (AKD) (> 7 days) |
| from onset of AKI until follow-up day 30 |
defined as whether or not any kind of renal replacement therapy became necessary at any point |
| within 30 days of AKI onset |
| Free-days of mechanical ventilation | within 30 days of AKI onset |
| Length of hospital stay | at hospital discharge (up to 30 days) |
| Length of Intensive Care Unit stay | at hospital discharge (up to 30 days) |
| Number of Participants with renal replacement therapy | at day 90 |
| Mortality | at day 90 |
| Recruiting |
| Münster |
| 48149 |
| Germany |
|
| Radboud University medical cener | Recruiting | Nijmegen | 6500 | Netherlands |
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |