Global Assessment of Acute and Chronic Kidney Disease Incidence and Outcomes in Patients With COVID-19 Infection

Sponsor
University of California, San Diego (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04491227
Collaborator
(none)
2,000
12
34.8
166.7
4.8

Study Details

Study Description

Brief Summary

The coronavirus (COVID-19) pandemic has created a significant strain on health care resources across the world for managing critically ill patients. Emerging reports from China, South Korea and Italy have reported varying incidence of acute kidney (AKI) ranging from 5-15% with a mortality of 60-80% however there is no systematic assessment of the risk factors, recognition, course and outcomes in patients with and without kidney disease whose course is complicated by AKI1-4. Patients with underlying CKD, immunosuppressed patients with renal transplants and ESKD patients are at high risk for COVID-19 infection and there is limited information on the effect of COVID-19 on the course and outcomes of these patients. The requirement for renal support including IHD, CRRT and sorbent based therapies has been variable and has contributed to the intense pressure on the nephrology and critical care providers for delivering these therapies. As the COVID-19 pandemic expands in the USA and abroad, there is an intense need to understand the epidemiology of the disease and the resources needed for renal support to inform clinical management and public health interventions.

In this study, the investigators aim to investigate health care facilities across the world (hospital wards, ICU, outpatient clinics, nursing homes, healthcare centers) to draw a global picture of incidence, risk factors, resources available for treatment and prognosis of acute and chronic kidney disease in patient with COVID 19 confirmed infection. The aim is to identify trends in patients with acute and chronic kidney disease, determine its incidence, treatment and outcomes in different settings across the world. This information will be used to develop and implement educational tools and resources to prevent deaths from AKI and progression of CKD in this and following pandemics.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Acute and Chronic kidney diseases are important causes of mortality and morbidity worldwide. The associated socioeconomic burden of kidney disease and AKI, as in some cases recovery is incomplete and chronic kidney disease (CKD) can arise, is a growing problem around the world. During the COVID 19 pandemic the incidence of AKI has been reported to be as low as 0.5% to as high as 23%. AKI was reported to develop at a median of 15 days in one study, and another study reported that most AKI developed within 7 days of admission. The data on acute kidney injury (AKI) in patients with COVID-19 is mostly from patients who are hospitalized, and in some studies limited to critically ill patients in the ICU. In ICU patients the requirement for renal support and mortality is reported to be high, however is a lack of epidemiological studies specifically designed to determine the impact of COVID 19 on kidney outcomes.

    The mortality rate of patients with kidney dysfunction varies widely and is inversely related to country income and percentage of gross domestic product spent on total health expenditure. Several initiatives will be very insightful and identified important gaps in knowledge, more effort is required to understand this problem affecting all regions of the globe. In order to eventually implement resources and tools to help prevent, diagnose and treat patients with COVID 19 infection and kidney dysfunction, the investigators need to understand its incidence, risk factors, available resources and barriers to diagnosis and treatment.

    This project will collect data on kidney function progression in patients infected with COVID 19 across the world. The study will open to individual physicians across the world who agreed to participate by providing de-identified clinical and lab data of patients with confirmed COVID 19 infection with acute and chronic kidney dysfunction.

    Primary Objectives:
    1. Establish incidence and outcomes of acute kidney injury (AKI) in different settings worldwide during the COVID 19 pandemic.
    Secondary Objectives:
    1. Compare risk factors, etiologies, diagnosis, management and outcomes of acute and chronic kidney dysfunction in COVID 19 patients in different countries

    2. Determine resources available for recognition, non-dialytic and dialytic management and follow up of patients with acute and chronic kidney dysfunction and COVID 19 infection in different settings and countries.

    3. Determine long term outcomes, 6 months and 1 year, of patients with acute and chronic kidney dysfunction and COVID 19 infection in different settings.

    4. Evaluate barriers preventing access to the standard treatments of acute and chronic kidney dysfunction and COVID 19 infection across different countries.

    5. Determine the impact of COVID 19 infection on the progression of acute and chronic kidney disease in patient with native and transplanted kidney.

    6. Evaluate the treatment strategies of patient with ESKD on hospitalized patients with COVID 19.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    2000 participants
    Observational Model:
    Cohort
    Time Perspective:
    Retrospective
    Official Title:
    Global Assessment of Acute and Chronic Kidney Disease Incidence and Outcomes in Patients With COVID-19 Infection
    Actual Study Start Date :
    May 5, 2020
    Anticipated Primary Completion Date :
    Apr 30, 2022
    Anticipated Study Completion Date :
    Mar 31, 2023

    Arms and Interventions

    Arm Intervention/Treatment
    Kidney disease in COVID-19

    Chronic Kidney Disease (CKD): Known diagnosis of chronic kidney disease; prior evidence of markers of kidney damage for 3 months (microalbuminuria, proteinuria >300mg/24 hrs or abnormalities in imaging tests) or the presence of glomerular filtration rate (GFR) <60 mL/min/1.73 m2 for 3 months calculated with CKD-EPI equation, with or without other signs of kidney damage as described above. ESKD: Patients that are dialysis dependent. Suspected AKI: Oliguria (<200 mL/6 hours) and any AKI-related clinical signs or symptoms (see table 1) or urinalysis/dipstick abnormality. All suspected AKI cases must be confirmed prior to enrollment. Confirmed AKI: Meeting of at least one of the modified KDIGO Criteria Increase or decrease in serum creatinine >0.3 mg/dl from reference in 48 hours Increase or decrease in serum creatinine > 50% from reference in 7 days Urine output < 400 ml/day Functioning Kidney transplant:

    Outcome Measures

    Primary Outcome Measures

    1. AKI incidence [from hospital admission through hospital discharge upto 24 weeks]

      Meeting of at least one of the modified KDIGO Criteria Increase or decrease in serum creatinine >0.3 mg/dl from reference in 48 hours Increase or decrease in serum creatinine > 50% from reference in 7 days Urine output < 400 ml/day

    2. Dialysis requirement [through study completion upto 1 year from enrollment]

      initiation of intermittent hemodialysis, continuous hemodialysis or peritoneal dialysis during the hospital stay

    3. hospital mortality [through study completion within 1 year]

      Deaths during primary hospitalization

    Secondary Outcome Measures

    1. Renal functional recovery [Assessed at at 3, 6 and 12 months from enrollment at hospital admission]

      C-Complete: SCr < 0.3 mg/dL from reference P-Partial: Requires no dialysis but not complete recovery N-No recovery: Dialysis dependent C-Complete: SCr < 0.3 mg/dL from reference P-Partial: Requires no dialysis but not complete recovery N-No recovery: Dialysis dependent Percentage of patinets with renal functioanl recovery based on serum creatinien levels classfied as C-Complete: SCr < 0.3 mg/dL from reference P-Partial: Requires no dialysis but not complete recovery N-No recovery: Dialysis dependent

    2. Functional status [questionnaires to be completed at 3, 6 and 12 months from enrollment at hospital admission]

      EQL5D scale and SH8 scales completed at 3, 6 and 12 months post enrollment

    3. Resource utilization [Within 1 year of enrollment for primary hospitalization]

      Number of days patient is in the hospital and ICU and is managed with ventilators, dialysis or other extracorporeal organ support e.g. ECMO during the hospital stay

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patients with confirmed infection with COVID 19

    • Patients with Acute Kidney injury (AKI) or Chronic kidney disease (CKD) or need for dialysis

    • Patients receiving Chronic dialysis (hemo or peritoneal dialysis)

    • Renal transplant recipients

    Exclusion Criteria:
    • • Patients < 18 yrs age

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Alabama, Birmingham Birmingham Alabama United States 35294
    2 University of California, San Diego San Diego California United States 92103
    3 University of Colorado Aurora Colorado United States 80045
    4 St. Peter's Hospital Albany New York United States 12208
    5 Jacobi Medical Center New York New York United States 10461
    6 Hospital Obrero #2 Cochabamba Bolivia
    7 Hopital Sacre Coeur & Universite de Montreal Montreal Quebec Canada
    8 Universidad de Los Andes Santiago Chile
    9 Postgraduate Institute of Research, Chandigarh Chandigarh India
    10 Royal Free Hospital London United Kingdom NW3 2QG
    11 Guy's & St Thomas's Hospital London United Kingdom SE1 7EH
    12 University of Nottingham Nottingham United Kingdom NG7 2RD

    Sponsors and Collaborators

    • University of California, San Diego

    Investigators

    • Principal Investigator: Ravindra L Mehta, University of California, San Diego

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ravindra Mehta, Recall Faculty, University of California, San Diego
    ClinicalTrials.gov Identifier:
    NCT04491227
    Other Study ID Numbers:
    • 000295
    First Posted:
    Jul 29, 2020
    Last Update Posted:
    Jul 29, 2020
    Last Verified:
    Jul 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ravindra Mehta, Recall Faculty, University of California, San Diego
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 29, 2020