Safe Kidney Care Cohort Study

This study is currently recruiting participants. (see Contacts and Locations)
Verified June 2012 by University of Maryland
Sponsor:
Collaborator:
Information provided by (Responsible Party):
Jeffrey C Fink, University of Maryland
ClinicalTrials.gov Identifier:
NCT01407367
First received: April 26, 2011
Last updated: June 4, 2012
Last verified: June 2012
  Purpose

Chronic kidney disease (CKD) is common, but it is often over-looked in patients with this disease when they are getting medical treatment. Patients with CKD have special needs for their medical treatment. When these special needs are not considered their medical care may lead to unintended harm (called safety events) which can cause hospitalization, more kidney problems, and even death.

This research study has two purposes. The first purpose is to determine how participants feel about wearing a medical alert bracelet or necklace that alerts health care workers that the user of the bracelet or necklace has decreased kidney function. Medical alert bracelets are often recommended for people who have other medical problems, such as diabetes. This medical alert bracelet or necklace has an address to an informational website about the safe care of patients with kidney problems. The investigators think that alerting health care workers that a person has decreased kidney function may decrease their chances of having a medical injury and improve the safety of their care.

The second purpose of this research study is to track how often people with kidney problems may be exposed to medicines, tests, or procedures that might increase their chance of having an accidental medical injury or safety event. Though some medical injuries can not be prevented, the investigators want to find out what medical events in patients with kidney problems might be preventable. The investigators also want to find out if other things might increase a patient's chances of getting a medical injury, such as physical weakness or medical instructions that might be confusing.


Condition
Chronic Kidney Disease

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Does Under-recognition of Kidney Disease Affect Patient Safety?

Resource links provided by NLM:


Further study details as provided by University of Maryland:

Primary Outcome Measures:
  • The discrete incidence of any of the chronic kidney disease patient safety indicators (CKD-PSIs) endorsed by the consensus expert panel [ Time Frame: at the end of study (up to 4.25 years, depending on participant enrollment date) ] [ Designated as safety issue: No ]

    The discrete incidence of any of the following CKD-PSIs endorsed by the consensus expert panel:

    1. Incidence of usage of medications or agents to be avoided in CKD
    2. Incidence of improperly dosed medications in CKD
    3. Incidence of hyperkalemia detected at annual study visits
    4. Incidence of hypoglycemia detected at annual visits
    5. Incidence of adverse events related to medical care or medicines:

    5a. Falling 5b. Bleeding 5c. Edema 5d. Angioedema 5e. Confusion or altered mental status 5f. Rhabdomyolysis



Secondary Outcome Measures:
  • Rate of all-cause hospitalization [ Time Frame: at the end of study (up to 4.25 years, depending on participant enrollment date) ] [ Designated as safety issue: No ]
    Hospitalizations (following enrollment); including length of stay and safety events during hospitalization until time of end of study.

  • Change in renal function from baseline [ Time Frame: at the end of study (up to 4.25 years, depending on participant enrollment date) ] [ Designated as safety issue: No ]
    Renal function with estimated glomerular filtration rate (eGFR) based on serum creatinine measured annually until time of end of study.

  • Incidence rate of end-stage renal disease (ESRD) defined as need for renal replacement therapy (dialysis or transplant) [ Time Frame: at the end of study (up to 4.25 years, depending on participant enrollment date) ] [ Designated as safety issue: No ]
    ESRD defined as the need for renal replacement therapy with either dialysis (hemodialysis or peritoneal) for 3 months or more; or renal transplantation up until the time of end of study.

  • Incidence rate of all-cause Death [ Time Frame: at the end of study (up to 4.25 years, depending on participant enrollment date) ] [ Designated as safety issue: No ]
    determined until time of end of study.


Biospecimen Retention:   Samples Without DNA

At each yearly research clinic visit (up to 4), 30 cc (6 teaspoons) of blood will be processed and stored for future assays related to kidney function.

At first research clinic visit, 9 cc urine will be processed and stored for future assays related to kidney function.

At each yearly research clinic visit, 1 swab of both nares, 1 pharyngeal swab and 1 skin swab will be obtained, processed and stored with future testing for multiple antibiotic resistant (MAR) organisms.


Estimated Enrollment: 350
Study Start Date: April 2011
Estimated Study Completion Date: June 2015
Estimated Primary Completion Date: June 2015 (Final data collection date for primary outcome measure)
Groups/Cohorts
Phase I and Phase II

Phase I (First 100 participants):

Medical alert bracelet/necklace, Medical event diary, Medical event ascertainment, Repeated measurement of renal function and other electrolytes, Review for CKD-PSIs

Phase II (Next 250 participants):

Medical event diary, Medical event ascertainment, Repeated measurement of renal function and other electrolytes, Review for CKD-PSIs


Detailed Description:

Chronic kidney disease not requiring dialysis (CKD) is common, but under-recognized, among patients who frequent the health care system, where improving patient safety is a high priority. Poor recognition of the disease and several other features unique to CKD make it a high-risk condition for adverse, patient-safety incidents (PSIs). In this context, PSIs refer to events of unintended harm or injury related to medications or medical care. These adverse safety events may include those usually cited for the general population (PSI), but also, CKD-specific unsafe practices (CKD-PSI) all of which, in turn, can lead to frequent hospitalization, accelerated loss of kidney function, increased risk of end-stage renal disease (ESRD), and death - all common outcomes in CKD. CKD-PSIs have been established in prior work by the investigators of this study with the help of an expert panel but it is not known how commonly PSIs or CKD-PSIs occur or how to measure these reliably in the CKD population. Furthermore, it is not known what role poor disease recognition plays in the occurrence of such safety events. Finally, it remains to be determined whether CKD-PSIs contribute to the high frequency of adverse outcomes so common in this disease. If CKD-PSIs are common and account for a significant portion of the adverse events so common in this population, then it is possible that by reducing the incidence of CKD-PSIs, through increased disease recognition, outcomes can be improved in this patient population.

In this study, the investigators will enroll volunteers from the population with pre-dialysis CKD for the purpose of observing the frequency of CKD-PSI in the target population detected over time. The participants will be assessed annually for events that relate to CKD-PSI. The first 100 participants (Phase I) will be provided with a standard medical alert accessory (bracelet or necklace) which is commonly used to alert doctors and other providers of a patient's disease state. In this case the medical alert accessory will state "Decreased Kidney Function. For My Care, Please Visit www.safekidneycare.org" Participants are asked to log onto the website using unique 4-digit ID assigned by the PI to track the participant's use of the website and to further improve the website. Since all information on the website is available to the public, participants are not required to use the ID to access the content of the website. The website does not collect or store patient health information, except for the IP address which provides limited information on the location of the computer used to access the website (city, state, zip, and area code).

The volunteers in Phase I will be tracked over time as to whether they use and tolerate this medical alert bracelet/necklace and for their incidence of CKD-PSI. Enrollment will continue after Phase I in Phase II (n = 250) with participants tracked on an identical study schedule for detection of CKD-PSI. All study procedures are the same for Phase II except for the medical alert accessory. The overall goal of this study will be to determine: the frequency of CKD-PSI in the target population, the acceptability of an alert device (Phase I only) intended to increase the recognition of CKD, and the contribution of CKD-PSI to the high incidence of adverse outcomes in CKD

  Eligibility

Ages Eligible for Study:   21 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Participants will be recruited from a variety of chronic kidney disease (CKD) management and primary care setting. Some participants will be self-referrals.

Criteria

Inclusion Criteria:

  • estimated glomerular filtration rate (eGFR) < 60 ml/min/1.73m2 (using Modified Diet in Renal Disease (MDRD) equation) based on the 2 out-patient serum creatinines obtained within the last 18 months and at least 90 days apart

Exclusion Criteria:

  • < 21 years of age,
  • Expected to need dialysis within 12 months after time of enrollment,
  • Expected to die within 12 months after time of enrollment,
  • Unable to provide informed consent, or is a
  • Prisoner
  • Skin sensitivity or allergy to stainless steel and sterling silver (Phase 1 only)
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01407367

Contacts
Contact: Jeffrey C Fink, MD, MS 410-605-7000 ext 5280 jfink@medicine.umaryland.edu
Contact: Wanda Fink, RN, BSN, MS 410-706-6559 wfink@medicine.umaryland.edu

Locations
United States, Maryland
Baltimore VA Medical Center Recruiting
Baltimore, Maryland, United States, 21201
Contact: Jeffrey C Fink, MD MS    410-605-7000 ext 5280    jfink@medicine.umaryland.edu   
University of Maryland Medical System Recruiting
Baltimore, Maryland, United States, 21201
Contact: Jeffrey C Fink, MD, MS    410-605-7000 ext 5280    jfink@medicine.umaryland.edu   
Contact: Wanda Fink, RN, BSN, MS    410-706-6559    wfink@medicine.umaryland.edu   
Principal Investigator: Jeffrey C Fink, MD, MS         
Sub-Investigator: Clarissa Diamantidis, MD, MHS         
Sub-Investigator: Matthew Weir, MD         
Sub-Investigator: Min Zhan, PhD         
Sponsors and Collaborators
University of Maryland
Investigators
Principal Investigator: Jeffrey C Fink, MD, MS University of Maryland, Baltimore County
  More Information

No publications provided by University of Maryland

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Jeffrey C Fink, Associate Professor, Nephrology, University of Maryland
ClinicalTrials.gov Identifier: NCT01407367     History of Changes
Other Study ID Numbers: HP-00048532, R01DK084017
Study First Received: April 26, 2011
Last Updated: June 4, 2012
Health Authority: United States: Institutional Review Board
United States: Federal Government

Keywords provided by University of Maryland:
patient safety
chronic kidney disease
medical errors

Additional relevant MeSH terms:
Kidney Diseases
Renal Insufficiency, Chronic
Urologic Diseases
Renal Insufficiency

ClinicalTrials.gov processed this record on August 28, 2014