Format

Send to

Choose Destination
BMC Nephrol. 2017 Apr 12;18(1):132. doi: 10.1186/s12882-017-0541-6.

Implementation of a pragmatic randomized trial of screening for chronic kidney disease to improve care among non-diabetic hypertensive veterans.

Author information

1
San Francisco VA Medical Center, 4150 Clement St., 111A1, San Francisco, CA, 94121, USA. carmenalicia.peralta@ucsf.edu.
2
San Francisco VA Medical Center, 4150 Clement St., 111A1, San Francisco, CA, 94121, USA.
3
University of California, San Francisco, 533 Parnassus Avenue, San Francisco, CA, 94117, USA.
4
University of California, San Francisco, 533 Parnassus Ave, UC Hall, San Francisco, CA, 94143, USA.
5
San Francisco General Hospital, 1001 Potrero Ave, SFGH 100, San Francisco, CA, 94110, USA.

Abstract

BACKGROUND:

Whether screening for chronic kidney disease (CKD) can improve the care of persons at high risk for complications remains uncertain. We describe the design and early implementation experience of a pilot, cluster-randomized pragmatic trial to evaluate the feasibility, implementation, and effectiveness of a "triple marker" CKD screening program (creatinine, cystatin C and albumin to creatinine ratio) for improving care among hypertensive veterans seen in primary care at one Veterans Administration Hospital.

METHODS/DESIGN:

Non-diabetic hypertensive veterans age 18-80 without known CKD were randomized in clusters determined by primary care provider (unit of randomization) into three arms. Usual care will be compared with two incrementally intensified treatment strategies: (1) screen for CKD followed by patient and provider education or (2) screen-educate plus a clinical pharmacist-led CKD and BP management program. The primary clinical outcome is systolic blood pressure (BP) change from baseline. Secondary clinical outcome is BP control. The primary process outcomes is triple marker screening (across three arms), and secondary process outcomes include use of inhibitors of the renin-angiotensin system (ACE/ARB) overall and in persons with albuminuria, CKD recognition by PCP, use of non-steroidal anti-inflammatory drugs (NSAIDs) and NSAID education by PCP. The design uses the Veterans Health Administration electronic health record (EHR) to identify participants, deliver the interventions and ascertain study outcomes. Assessment of the program implementation will use the Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) framework. Study duration is 12 months.

RESULTS:

A total of 1,819 patients have been randomized within 41 provider clusters. The median age (interquartile range) is 68 years (61-72), and 99% of participants are male. Approximately 16% are Black, and 5% Hispanic. In the first 6 months of the trial, 434 triple marker screening tests have been ordered, and 217(50%) have been tested. A total of 48 new CKD cases have been identified among those tested, for a preliminary yield of 22%.

CONCLUSION:

We have successfully implemented a pragmatic protocol that uses the EHR to identify and characterize eligible participants, deliver the intervention, and ascertain study outcomes with high rates of participation by providers and patients. Results from this study can guide design of pragmatic trials in the field of CKD.

TRIAL REGISTRATION:

NCT01978951 ; Date or Registration: 1/17/2014.

KEYWORDS:

Blood pressure; Chronic kidney disease; Hypertension; Screening

PMID:
28399844
PMCID:
PMC5389143
DOI:
10.1186/s12882-017-0541-6
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for BioMed Central Icon for PubMed Central
Loading ...
Support Center