Using pharmacists to improve risk stratification and management of stage 3A chronic kidney disease: a feasibility study
Chang et al. BMC Nephrology (2016) 17:168
DOI 10.1186/s12882-016-0383-7
RESEARCH ARTICLE
Open Access
Using pharmacists to improve risk
stratification and management of stage 3A
chronic kidney disease: a feasibility study
Alex R. Chang1,2*, Michael Evans3, Christina Yule2, Larissa Bohn2, Amanda Young2, Meredith Lewis5,
Elisabeth Graboski2, Bethany Gerdy3, William Ehmann3, Jonathan Brady3, Leah Lawrence3, Natacha Antunes4,
Jamie Green1,2, Susan Snyder5, H. Lester Kirchner6, Morgan Grams7 and Robert Perkins8
Abstract
Background: Measurement of albuminuria to stratify risk in chronic kidney disease (CKD) is not done universally in
the primary care setting despite recommendation in KDIGO (Kidney Disease Improving Global Outcomes)
guidelines. Pharmacist medication therapy management (MTM) may be helpful in improving CKD risk stratification
and management.
Methods: We conducted a pragmatic, cluster-randomized trial using seven primary care clinic sites in the Geisinger
Health System to evaluate the feasibility of pharmacist MTM in patients with estimated glomerular filtration rate
(eGFR) 45–59 ml/min/1.73 m2 and uncontrolled blood pressure (≥150/85 mmHg). In the three pharmacist MTM
sites, pharmacists were instructed to follow a protocol aimed to improve adherence to KDIGO guidelines on testing
for proteinuria and lipids, and statin and blood pressure medical therapy. In the four control clinics, patients
received usual care. The primary outcome was proteinuria screening over a follow-up of 1 year. A telephone survey
was administered to physicians, pharmacists, and patients in the pharmacist MTM arm at the end of the trial.
Results: Baseline characteristics were similar between pharmacist MTM (n = 24) and control (n = 23) patients,
although pharmacist MTM patients tended to be younger (64 vs. 71 y; p = 0.06) and less likely to have diabetes
(17 % vs. 35 %; p = 0.2) or baseline proteinuria screening (41.7 % vs. 60.9 %, p = 0.2). Mean eGFR was 54 ml/min/1.
73 m2 in both groups. The pharmacist MTM intervention did not significantly improve total proteinuria screening at
the population level (OR 2.6, 95 % CI: 0.5–14.0; p = 0.3). However, it tended to increase screening of previously
unscreened patients (78.6 % in the pharmacist MTM group compared to 33.3 % in the control group; OR 7.3, 95 %
CI: 0.96–56.3; p = 0.05). In general, the intervention was well-received by patients, pharmacists, and providers, who
agreed that pharmacists could play an important role in CKD management. A few patients contacted the research
team to express anxiety about having a CKD diagnosis without prior knowledge.
Conclusions: Pharmacist MTM may be useful in improving risk stratification and management of CKD in the
primary care setting, although implementation requires ongoing education and multidisciplinary collaboration and
careful communication regarding CKD diagnosis. Future studies are needed to establish the effectiveness of
pharmacist MTM on slowing CKD progression and improvement in cardiovascular outcomes.
(Continued on next page)
* Correspondence:
1
Division of Nephrology, Geisinger Health System, 100 N Academy Ave,
Danville, PA 17821, USA
2
Kidney Health Research Institute, Geisinger Health System, 100 N Academy
Ave, Danville, PA 17821, USA
Full list of author information is available at the end of the article
© The Author(s). 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver
(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Chang et al. BMC Nephrology (2016) 17:168
Page 2 of 9
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Trial registration: ClinicalTrials.gov, NCT02208674
Registered August 1, 2014, first patient enrolled September 30, 2014
Keywords: Pharmacist medication therapy management, Chronic kidney disease, Albuminuria, Proteinuria,
Screening, KDIGO guidelines
Background
Chronic kidney disease (CKD) affects one in seven adults
in the U.S. and is estimated to account for more than
20 % of annual Medicare expenditures [1, 2]. Optimal
screening and treatment strategies for CKD have been recommended by KDIGO (Kidney Disease: Improving Global
Outcomes). For example, guidelines recommend using
both estimated glomerular filtration rate (eGFR) and
quantification of albuminuria (or proteinuria) to stratify
renal and cardiovascular risk in CKD patients [3–5]. For
patients with non-proteinuric CKD, KDIGO guidelines
recommend treatment to a blood pressure goal of ≤140/90.
For patients with proteinuric CKD, KDIGO guidelines
recommend a lower blood pressure goal of ≤130/80,and
the use of angiotensin converting enzyme inhibitors
(ACEIs) or angiotensin receptor blockers (ARBs) [3].
KDIGO guidelines also recommend treatment with statins
for all adults ≥ 50 years with CKD, regardless of proteinuria
status [3, 6].
Despite these recommendations, adherence to CKD
guidelines is low; for instance, proteinuria screening
rates in CKD patients range from 10 to 45 % across different health systems. [7–10] Similar deficiencies in
CKD guideline adherence have been reported for
achievement of optimal blood pressure goals [7–9], prescription of indicated ACEIs and ARBs [11–13], and prescription of statin therapy [14, 15]. Primary care
providers manage the majority of CKD patients and
often do not list CKD as a problem list diagnosis [8].
Thus, effective interventions, delivered in the primary
care setting, are needed to improve screening and treatment for CKD.
Pharmacist medication therapy management (MTM)
has been shown to be effective in treating hypertension
[16, 17], diabetes [18], and CKD-related anemia [19]. We
performed a pilot, cluster-randomized trial of outpatient
primary care clinics to examine the feasibility of using
pharmacist MTM to improve proteinuria screening and
CKD management in a large, integrated health system.
Methods
The pilot study was a prospective 2-arm, clusterrandomized pragmatic trial, funded by Geisinger Clinic.
We recruited participants from seven primary care clinic
sites at Geisinger, a large integrated health system that
includes 43 community practice clinic sites across
central and northeastern Pennsylvania and an extensive
pharmacist-led MTM program. The Geisinger Clinic
institutional review board (IRB Number 2014-0251)
approved the protocol. A modified informed consent
process was utilized, which entailed full disclosure and
explanation to eligible patients (delivered by mail) and
to participating providers (by email) at the primary care
sites. Eligible patients were asked to respond within
7 d (...truncated)