Abstract
Background
Primary care physicians (PCPs) typically manage early chronic kidney disease (CKD), but recent guidelines recommend nephrology co-management for some patients with stage 3 CKD and all patients with stage 4 CKD. We sought to compare quality of care for co-managed patients to solo managed patients.
Methods
We conducted a retrospective cross-sectional analysis. Patients included in the study were adults who visited a PCP during 2009 with laboratory evidence of CKD in the preceding two years, defined as two estimated glomerular filtration rates (eGFR) between 15–59 mL/min/1.73 m2 separated by 90 days. We assessed process measures (serum eGFR test, urine protein/albumin test, angiotensin converting enzyme inhibitor or angiotensin receptor blocker [ACE/ARB] prescription, and several tests monitoring for complications) and intermediate clinical outcomes (mean blood pressure and blood pressure control) and performed subgroup analyses by CKD stage.
Results
Of 3118 patients, 11 % were co-managed by a nephrologist. Co-management was associated with younger age (69 vs. 74 years), male gender (46 % vs. 34 %), minority race/ethnicity (black 32 % vs. 22 %; Hispanic 13 % vs. 8 %), hypertension (75 % vs. 66 %), diabetes (42 % vs. 26 %), and more PCP visits (5.0 vs. 3.9; p < 0.001 for all comparisons). After adjustment, co-management was associated with serum eGFR test (98 % vs. 94 %, p = <0.0001), urine protein/albumin test (82 % vs 36 %, p < 0.0001), and ACE/ARB prescription (77 % vs. 69 %, p = 0.03). Co-management was associated with monitoring for anemia and metabolic bone disease, but was not associated with lipid monitoring, differences in mean blood pressure (133/69 mmHg vs. 131/70 mmHg, p > 0.50) or blood pressure control. A subgroup analysis of Stage 4 CKD patients did not show a significant association between co-management and ACE/ARB prescription (80 % vs. 73 %, p = 0.26).
Conclusion
For stage 3 and 4 CKD patients, nephrology co-management was associated with increased stage-appropriate monitoring and ACE/ARB prescribing, but not improved blood pressure control.
Keywords: Primary care, Nephrology, Quality of healthcare, Ambulatory care, Kidney diseases
Background
Twenty-six million Americans have chronic kidney disease (CKD). Approximately 90 % of CKD patients are in an early stage of the disease and are typically cared for by primary care physicians (PCPs). U.S. and international guidelines recommend that physicians monitor for progression, monitor for complications, prescribe medications to delay progression, and focus on cardiovascular risk modification, all of which are within a PCP’s scope of practice [1]. Recent international guidelines, however, recommend nephrology co-management for some patients with stage 3 CKD and all patients with stage 4 CKD, based on the assumption that co-management lessens complications, delays renal failure, and decreases mortality [2]. While nephrologist involvement is associated with decreased mortality for the small group of patients who progress to end stage renal disease and need renal replacement therapy [3, 4], we do not know whether co-management of a larger proportion of stage 3 patients and all stage 4 patients will improve quality of care. To assess the relationship between nephrology co-management and quality of care, we conducted a retrospective cross-sectional analysis of electronic health record (EHR) data for patients with stage 3 and 4 CKD, comparing co-managed patients to solo managed patients.
Methods
Study population and setting
After receiving approval from the Partners Healthcare Human Research Committee and being granted waiver of consent, we electronically screened all patients who had at least one visit to a PCP at one of 12 primary care clinics in the Brigham and Women’s Primary Care Practice Based Research Network during 2009. This network includes hospital-based and community-based clinics, two of which are federally qualified health centers. We included adult patients with stage 3 or 4 CKD, defined as two past estimated glomerular filtration rates (eGFR) between 15–60 mL/min/1.73 m2, separated by 90 days and collected during routine clinical care between January 1, 2007 to December 31, 2008 [5]. This approach allowed us to identify a cohort of patients who had CKD at the beginning of calendar year 2009. We excluded patients with documented end-stage renal disease.
Data source
Data sources were billing data and EHR data. The practices have used the home-grown, CCHIT-certified, Longitudinal Medical Record EHR since July 2000. We used billing data, rather than EHR data, to identify clinic visits because the EHR notes do not specify whether nephrologist consultations were inpatient or outpatient. For the outcomes, we used EHR data. We queried the EHR for laboratory results, medications, and blood pressure measurements from 2009. PCPs prescribed all medications through the EHR and medications which were not prescribed by PCPs were included on the medication list as well. All outpatient vital signs were recorded in the EHR. Covariates such as socio-demographic data were collected during registration and updated periodically in the EHR. Our data was collected in 2009 because a large-scale EHR intervention was implemented in 2010 to increase recognition of CKD [6].
Exposure, outcomes, and covariates
We defined the exposure, nephrology co-management, as at least one outpatient visit with a nephrologist over the course of the year 2009 according to billing data. The quality of care outcomes were derived from nationally accepted guidelines [5, 7]. We examined the following outcomes: 1) annual serum eGFR test (a measurement during the year 2009, in addition to the two measurements over 2007–2008 that were used for inclusion), 2) annual urine albumin/protein test, 3) an angiotensin converting enzyme inhibitor or angiotensin receptor blocker (ACE/ARB) prescription, 4) annual LDL test, 5) annual serum hemoglobin/hematocrit test, 6) annual serum calcium test, 7) annual serum phosphorus test, 8) annual serum parathyroid test for patients with stage 4 CKD, 9) mean blood pressure (BP; using last value for SBP and last value for DBP), and 10) BP control.
For the urine protein monitoring outcome, we included several tests: urine total protein, microalbumin, and albumin-to-creatinine ratio. We used medication list data to determine whether an ACE/ARB was listed as an active medication during 2009. We used the most recent recorded BP for BP outcomes. We examined hypertension by assessing mean BP and BP control according to two definitions: blood pressure ≤ 130/80 mmHg and ≤ 140/90 mmHg, due to differing opinions about the appropriate target for non-diabetic kidney disease in the absence of proteinuria [7–10].
We stratified CKD patients into stage 3 (two measurements of eGFR 30–59 mL/min/1.73 m2) and stage 4 (two measurements of eGFR 16–29 mL/min/1.73 m2). We examined tests to monitor for complications of CKD differently for stage 3 and stage 4 patients [11–14]. For stage 3 patients we examined 1) annual serum hemoglobin test, 2) annual serum calcium test and 3) annual serum phosphorus test. For stage 4 patients, we additionally examined annual serum parathyroid hormone test.
We examined several potential confounders of the relationship between co-management and outcomes by first assessing association between the potential confounder and co-management. We examined socio-demographic variables (age, gender and race), severity of disease as measured by eGFR, and co-morbid diabetes and hypertension, and the frequency of PCP visits. We hypothesized that PCP diagnosis of CKD could be related to, or on the causal pathway to, referral and so we examined the impact of adjusting for this variable in fully adjusted models.
Statistical analysis
We examined the association of nephrology co-management and outcomes for stage 3 and stage 4 CKD patients and then performed subgroup analyses stratified by CKD stage.
We first analyzed the data assuming that the outcome was independent and then repeated the analyses accounting for clustering by PCP. Since we found similar results, we present all results accounting for clustering by PCP. We used multivariable logistic and linear regression to adjust for potential confounders and to produce weighted estimates (weighted to adjust for covariates and to account for clustering using the LSMEANS feature of the GENMOD procedure in SAS, SAS Institute, Cary, NC).
Results and discussion
Patient characteristics
Of the 79,605 patients who made a visit to a PCP in 2009, we identified 3,118 patients (4 %) with stage 3 or 4 CKD. Patients had a mean age of 74 years and were predominantly female (Table 1). Race/ethnicity rates were 67 % White, 23 % Black, 8 % Hispanic, and 1.5 % Asian. The average eGFR was 46 mL/min/1.73 m2, 27 % had diabetes, 67 % had hypertension, and, on average, patients saw their PCP 4 times during the year.
Table 1.
Characteristics of stage 3 and stage 4 CKD patients and association with nephrology co-management
| Patient characteristics | Total (N = 3118) | Nephrology co-management (n = 341) | Solo PCP management (n = 2777) | p value |
|---|---|---|---|---|
| Age, mean (SD) | 74 (12) | 69 (13) | 74 (12) | P <0.0001 |
| Male gender, N (%) | 1108 (36 %) | 155 (46 %) | 953 (34 %) | P <0.0001 |
| Race/Ethnicity, N (%) | P <0.0001 | |||
| White | 2060 (67 %) | 177 (53 %) | 1883 (69 %) | |
| Black | 716 (23 %) | 108 (32 %) | 608 (22 %) | |
| Hispanic | 253 (8 %) | 45 (13 %) | 208 (8 %) | |
| Asian | 46 (2 %) | 7 (2 %) | 39 (1 %) | |
| Serum Creatinine, mean (SD) | 1.46 (0.8) | 2.28 (1.3) | 1.36 (0.6) | P <0.0001 |
| eGFR (average of 2 values), mean (SD) | 46.0 (9.89) | 35.6 (11.1) | 47.3 (8.92) | P <0.0001 |
| CKD Stage, N (%) (based on average of 2 values) | ||||
| 3a (eGFR 45–59 mL/min/1.73 m2) | 1929 (62 %) | 80 (23 %) | 1849 (67 %) | |
| 3b (eGFR 30–44 mL/min/1.73 m2) | 926 (30 %) | 144 (42 %) | 782 (28 %) | |
| 4 (eGFR 15–29 mL/min/1.73 m2) | 255 (8 %) | 117 (34 %) | 138 (5 %) | |
| Serum Hematocrit, mean (SD) | 37.2 (4.6) | 35.6 (4.9) | 37.4 (4.6) | P <0.0001 |
| Diabetes on problem list, N (%) | 851 (27 %) | 143 (42 %) | 708 (26 %) | P <0.0001 |
| Hypertension on problem list, N (%) | 2099 (67 %) | 254 (75 %) | 1845 (66 %) | P = 0.003 |
| Tobacco Use, N (%) | P = 0.02 | |||
| Current | 179 (8 %) | 33 (12 %) | 146 (7 %) | |
| Former | 960 (41 %) | 107 (38 %) | 853 (41 %) | |
| Never | 1224 (52 %) | 143 (51 %) | 1081 (52 %) | |
| Insurance status, N (%) | P = 0.002 | |||
| Public | 2391 (77 %) | 252 (74 %) | 2139 (77 %) | |
| Private | 620 (20 %) | 66 (19 %) | 554 (20 %) | |
| Self Pay | 107 (4 %) | 23 (7 %) | 84 (3 %) | |
| PCP visits yearly, mean (SD) | 4.0 (2.9) | 5.0 (3.6) | 3.9 (2.8) | P <0.0001 |
| Nephrology visits yearly, mean (SD) | N/A | 2.3 (1.5) | N/A | N/A |
Nephrology co-management
Of the 3,118 stage 3 and 4 CKD patients, 341 (11 %) had at least one visit with a nephrologist during 2009 [191 (7.5 %) of stage 3 patients and 94 (50 %) of stage 4 patients]. On average, patients saw nephrology twice during the year (Table 1). Nephrology co-management was associated with younger age, male gender, Black or Hispanic race/ethnicity, hypertension, diabetes, and more frequent PCP visits (Table 1). Within the stage 4 CKD subgroup, the only covariates associated with nephrology co-management were younger age and more frequent PCP visits.
Outcome measures
Patients co-managed with nephrology were more likely to have received tests monitoring for progression: serum eGFR and urine protein/albumin (Table 2). We found no evidence that PCP diagnosis of early CKD was responsible for these differences.
Table 2.
Association of nephrology co-management with quality of care for pooled stage 3 and stage 4 CKD patients
| Unadjusted estimatesa | Adjusted estimatesb | |||||
|---|---|---|---|---|---|---|
| Outcome | Nephrology co-management (n = 341) | Solo PCP management (n = 2777) | p value | Nephrology co-management | Solo PCP management | p value |
| Serum eGFRc | 100 % | 93 % | P < 0.0001 | 98 % | 94 % | P < 0.0001 |
| Urine protein | 87 % | 37 % | P <0.0001 | 82 % | 36 % | P < 0.0001 |
| ACE/ARB prescription | 81 % | 65 % | P < 0.0001 | 77 % | 69 % | P = 0.03 |
| BP <140/90 | 68 % | 72 % | P = 0.15 | 70 % | 73 % | P = 0.41 |
| BP <130/80 | 47 % | 45 % | P = 0.40 | 47 % | 46 % | P = 0.68 |
| Mean | Mean | Weighted estimate | Weighted estimate | |||
| Systolic, mmHg | 133.1 | 132.4 | P = 0.54 | 132.6 | 130.8 | P = 0.15 |
| Diastolic, mmHg | 70.9 | 72.1 | P = 0.13 | 69.0 | 70.2 | P = 0.12 |
aAll estimates account for clustering by PCP
bWeighted percentage and p value estimated by multivariate model accounting for clustering by PCP and adjusting for age, gender, race/ethnicity, eGFR, hypertension, diabetes, and number of PCP visits
cLinear model due to 100 % rate in co-management group
Patients who were co-managed were more likely to receive an ACE/ARB prescription (Table 2). The mean BP was 133/72 mmHg. There were no significant associations between nephrology co-management and mean BP before or after adjustment (Table 2). With a BP goal of 140/90 mmHg, 71 % were under control and the likelihood of being under control was not associated with nephrology co-management. With a BP goal of 130/80 mmHg, 45 % were under control and the likelihood of BP being under control was not associated with nephrology co-management.
In stage 3 patients, nephrology co-management was associated with tests monitoring for progression (serum eGFR and urine protein/albumin), tests monitoring for complications (serum hemoglobin, serum calcium, and serum phosphorus), both before and after adjustment for potential confounders (Table 3). Co-management was associated with serum LDL testing before adjustment only. Patients who were co-managed were more likely to receive an ACE/ARB prescription. There were no differences in BP outcomes.
Table 3.
Association of nephrology co-management with quality of care measures for CKD patients, stage 3 only
| Unadjusted estimatesa | Adjusted estimatesb | |||||
|---|---|---|---|---|---|---|
| Outcome | Nephrology co-management (n = 191) | Solo PCP management (n = 2363) | p value | Nephrology co-management | Solo PCP management | p value |
| Serum eGFRc | 100 % | 93 % | P < 0.0001 | 98 % | 94 % | P < 0.0001 |
| Urine protein | 88 % | 36 % | P < 0.0001 | 85 % | 34 % | P < 0.0001 |
| ACE/ARB prescription | 84 % | 65 % | P < 0.0001 | 79 % | 69 % | P = 0.02 |
| BP <140/90 mmHg | 71 % | 71 % | P = 0.93 | 71 % | 72 % | P = 0.68 |
| BP <130/80 mmHg | 48 % | 45 % | P = 0.36 | 46 % | 45 % | P = 0.96 |
| Serum LDL | 83 % | 77 % | P = 0.02 | 79 % | 78 % | P = 0.74 |
| Serum Hemoglobin or Hematocrit | 96 % | 79 % | P < 0.0001 | 96 % | 83 % | P < 0.0001 |
| Serum Calcium | 99 % | 91 % | P < 0.0001 | 99 % | 93 % | P = 0.0002 |
| Serum Phosphorus | 81 % | 18 % | P < 0.0001 | 76 % | 17 % | P < 0.0001 |
| Mean | Mean | Weighted estimate | Weighted estimate | |||
| Systolic, mmHg | 132.8 | 132.5 | P = 0.81 | 133.8 | 132.1 | P = 0.21 |
| Diastolic, mmHg | 72.7 | 72.1 | P = 0.57 | 71.9 | 72.1 | P = 0.84 |
aAll estimates account for clustering by PCP
bPercentage and p value estimated by multivariate model accounting for clustering by PCP and adjusting for age, gender, race/ethnicity, eGFR, hypertension, diabetes, and number of PCP visits
cLinear model due to 100 % rate in co-management group
In stage 4 patients, nephrology co-management was associated with a higher rate of one test monitoring for progression (urine protein/albumin), and tests monitoring for complications (serum hemoglobin, serum phosphorus, and serum parathyroid hormone), both before and after adjustment for potential confounders (Table 4). Co-management was associated with serum calcium testing before adjustment only (p = 0.04). Co-management was associated with mean diastolic blood pressure after adjustment only (p = 0.0007). Nephrology co-management was not associated with ACE/ARB prescription, mean systolic blood pressure, or blood pressure control.
Table 4.
Association of nephrology co-management with quality of care measures for CKD patients, stage 4 only
| Unadjusted estimatesa | Adjusted estimatesb | |||||
|---|---|---|---|---|---|---|
| Outcome | Nephrology co-management (n = 94) | Solo PCP management (n = 95) | p value | Nephrology co-management | Solo PCP management | p value |
| Serum eGFRc | 100 % | 97 % | P = 0.08 | 100 % | 97 % | P = 0.09 |
| Urine protein | 86 % | 60 % | P < 0.0001 | 88 % | 56 % | P < 0.0001 |
| ACE/ARB prescription | 77 % | 72 % | P = 0.41 | 80 % | 73 % | P = 0.26 |
| BP <140/90 mmHg | 64 % | 69 % | P = 0.51 | 64 % | 70 % | P = 0.52 |
| BP <130/80 mmHg | 46 % | 47 % | P = 0.97 | 48 % | 44 % | p = 0.59 |
| Serum LDL | 76 % | 73 % | P = 0.59 | 77 % | 80 % | P = 0.69 |
| Serum Hemoglobin or Hematocritc | 99 % | 91 % | P = 0.01 | 99 % | 91 % | P = 0.04 |
| Serum Calciumc | 100 % | 96 % | P = 0.04 | 100 % | 96 % | P = 0.05 |
| Serum Phosphorus | 90 % | 49 % | P < 0.0001 | 91 % | 50 % | P < 0.0001 |
| Serum PTH | 92 % | 32 % | P < 0.0001 | 92 % | 33 % | P < 0.0001 |
| Mean | Mean | Weighted estimate | Weighted estimate | |||
| Systolic, mmHg | 132.3 | 131.7 | P = 0.85 | 130.6 | 130.0 | p = 0.84 |
| Diastolic, mmHg | 67.7 | 71.2 | P = 0.06 | 64.6 | 69.9 | P = 0.0007 |
aAll estimates account for clustering by PCP
bPercentage and p value estimated by multivariate model accounting for clustering by PCP and adjusting for age, gender, race/ethnicity, eGFR, hypertension, diabetes, and number of PCP visits. Race/ethnicity categories were collapsed to White, Black, Other due to inability to perform logistic regression with small cells
cLinear model due to 100 % rate in co-management group
Discussion
We found that only a small proportion (8 %) of stage 3 CKD patients and half of stage 4 CKD patients were co-managed by nephrology. Co-management was associated with socio-demographic differences, particularly in stage 3 CKD patients for whom co-management was associated with younger age, male gender and minority race/ethnicity. Co-management was associated with diabetes, hypertension, and more frequent PCP visits. After controlling for these potential confounders, co-management was associated with monitoring tests, both for progression and for complications. Co-management was associated with higher rates of ACE/ARB prescription in stage 3 CKD, but not in stage 4 CKD. Co-management was not associated with higher rates of cardiovascular risk modification through lipid monitoring or blood pressure control.
Our finding of a difference between the two groups for ACE/ARB prescription in stage 3, though not in stage 4, is in concert with another recently published study from the Chronic Renal Insuffiency Cohort (CRIC) [15]. One explanation for the higher impact of nephrology co-management in stage 3 CKD as compared to stage 4 CKD is low PCP recognition of CKD in stage 3. As we showed in a prior study, PCPs are more likely to diagnose CKD in patients with more advanced disease [16].
Co-management was associated with age, gender, and race/ethnicity. These associations align with patients who have higher muscle mass. This may indicate PCPs are still using serum creatinine levels rather than eGFR to judge severity of CKD in early disease. The only socio-demographic characteristic associated with nephrology referral in stage 4 CKD was younger age. PCPs were more likely to refer patients with diabetes in the stage 3 subgroup, which may reflect a higher rate of urine albumin screening and appropriate subsequent referral of albuminuric patients [16]. Patients who saw their PCP less often were less likely to be referred, which may reflect competing demands during office visits [17, 18]. We saw a similar dose–response relationship between the number of primary care visits and CKD documentation in our prior study [16] and the AVENIR study found a dose–response relationship between the number of nephrology visits and quality of care [19].
Other primary care CKD studies have revealed suboptimal urine protein testing, serum phosphorus testing, serum parathyroid hormone testing, prescription of ACE/ARB, and blood pressure control [16, 20–22]. The AVENIR nephrology clinic study reported low rates, similar to ours, of urine protein testing at 50 % and ACE/ARB prescription at 67 %, in addition to a BP control rate of 14 % (<130/80 mmHg), lower than ours [19]. One U.S. study designed to examine the impact of automated eGFR reporting also compared co-managed and solo managed patients (in stage 3b and 4, or eGFR 15–45 mL/min/1.73 m2). They found a significant difference in serum hemoglobin testing, serum phosphorus testing, and serum PTH testing, but neither urine protein testing (with a rate of <30 % overall) nor ACE/ARB prescribing (with a rate of <60 % overall) [23]. Ours is the first study to examine blood pressure outcomes in a similar manner.
There are several limitations to this study. There is a potential for type II error when we conclude that there is no difference in BP control between groups because co-managed patients may be sicker than solo managed patients. An analysis of anti-hypertensive regimens would help to elucidate any difference in management. There may be other patient level confounders for which we were unable to adjust. ACE/ARB prescriptions were assessed in all CKD patients, though these are only recommended for patients with either hypertension, diabetic kidney disease, or proteinuria. Our laboratory uses the MDRD equation to calculate eGFR without accounting for race. Generalizability is limited by the fact that the population is limited to one primary care network. We were unable to measure clinical outcomes such as progression to ESRD and mortality.
Our findings have implications for the following: 1) PCP solo management, 2) nephrology co-management, and developing a systematic approach to referral to nephrology.
First, PCPs should improve solo management in stage 3 CKD through monitoring for complications, monitoring for progression of disease, and intervening to delay progression. One successful approach is through point-of-care EHR alerts that remind the physician of the diagnosis and recommended management of stage 3 CKD. Such reminders have improved urine protein testing [24]. A second approach which addresses the lack of time in primary care visits is population management by a non-physician. Nurse-led population management has improved quality of care for diabetes and hypertension [25, 26]. A study in one of our practices combined EHR alerts and population management to successfully improve PCP management of CKD [27].
Second, quality of care for co-managed patients could improve as well. Co-management did not increase the likelihood of cardiovascular risk modification in stage 3 or stage 4 CKD. PCPs and nephrologists working together should be able to control patients’ blood pressure, yet we saw no difference in this measure between solo managed and co-managed patients. Both EHR alerts and population management are likely to be part of the answer [26, 28], but to date, there have been no successful systems-level interventions for uncontrolled blood pressure in a CKD population. Ideally, we will develop EHR alerts that are sophisticated enough to track management over time and to consider previous medication regimens and drug allergies [29, 30]. Perhaps more importantly, we should routinely employ effective patient-centered interventions to improve medication adherence [31, 32].
Third, and just as critical as the first (i.e. improving PCP solo management) and the second (i.e. improving co-management), is developing a systematic approach to referral. The current approach relies on creatinine-based estimates of kidney function that do not accurately predict whether and when patients might progress [38, 39]; many patients do not progress.
That being said, two studies showed a slowing of progression in stage 3 CKD when nephrologists monitored patients electronically and gave advice to PCPs [40, 41]. At this point, we only have two studies to answer the important question of whether we can delay or prevent progression to ESRD through comanagement in stage 3 CKD. Further studies would be welcome. A potentially better approach would take into account the fact that nephrology referral has a mortality benefit when done 12 to 72 months before initiating dialysis [33–37]. PCPs may be aided by risk estimation models such as one validated by Tangri and colleagues that incorporates additional metabolic parameters beyond serum creatinine in order to predict how likely a patient is to progress to renal failure within a five years [42]. Such prediction models could encourage PCPs to increase appropriate referrals to nephrology based on length of time before renal replacement therapy is needed, rather than stage-based referral.
Conclusions
In conclusion, early CKD is commonly managed in primary care, but patients who are co-managed by nephrology receive better monitoring for progression and complications. Improving the quality of PCP solo management will help to close this gap. In addition, about one-quarter of early CKD patients have uncontrolled blood pressure whether they have been referred to a nephrologist or not. We should study interventions to improve co-management of blood pressure and to decrease cardiovascular events. These interventions should include population management, EHR tools, and patient-centered interventions. Finally, we have sophisticated tools to risk-stratify patients with CKD and we must learn how best to employ these tools in primary care practices to systematize referral of high-risk patients.
Acknowledgements
We would like to acknowledge Julie Fiskio, MS for data retrieval, Stuart Lipsitz, PhD for assistance with statistical techniques to adjust for clustering, and Julia Whelan, MS AHIP, for literature retrieval.
The corresponding author affirms that all people contributing significantly to the work have been acknowledged. Written permission has been obtained from all persons named in the acknowledgment.
Research reported in this publication was supported by the National Institute of Diabetes And Digestive And Kidney Diseases of the National Institutes of Health under Award Number K23DK097187. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Abbreviations
- CKD
Chronic kidney disease
- PCP
Primary care physician
- EHR
Electronic health record
- eGFR
Estimated glomerular filtration rate
- ACE
Angiotensin converting enzyme inhibitor
- ARB
Angiotensin receptor blocker
- BP
Blood pressure
Footnotes
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
LS conceived of the study, collected the data, performed the analysis, and drafted the manuscript. AW assisted in data collection and revised the manuscript. SSW assisted in data collection and revised the manuscript. JAL assisted in study design, analytic methods, and manuscript revision. All authors read and approved the final manuscript.
Authors’ information
Not applicable.
Contributor Information
Lipika Samal, Email: lsamal@partners.org.
Adam Wright, Email: awright@partners.org.
Sushrut S. Waikar, Email: swaikar@partners.org
Jeffrey A. Linder, Email: jlinder@partners.org
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