N‐terminal pro‐B‐type natriuretic peptide testing patterns in patients with heart failure with reduced ejection fraction

Introduction

Heart failure (HF) is a serious health problem with high risks of hospitalization and mortality as well as poor quality of life and high economic burden.1, 2 HF with reduced ejection fraction (HFrEF) is a major form of the HF diagnosis and is accompanied by a high risk for cardiovascular events, particularly when the disease course is progressive.3 Patients with HFrEF who experience a worsening HF event (WHFE) have poorer outcomes, with a 2 year mortality rate of ~22.5% and a 30 day readmission rate of 56%.4

B-type natriuretic peptide (BNP) and N-terminal pro-B-type natriuretic peptide (NT-proBNP) are released by the heart in response to transmural wall stress and neurohormonal stimulation. BNP and NT-proBNP are commonly used biomarkers in HF for diagnosis and prognostication,5 and concentrations of NT-proBNP are associated with important physiological measures in HFrEF such as left ventricular ejection fraction, left atrial volume index, and diastolic function.6 Increases in the concentration of NT-proBNP over time are associated with deleterious left ventricle remodelling, worse quality of life, and higher risk for death or hospitalization.7 Recent predictive models identified NT-proBNP as one of the most important predictors of hospital readmission and mortality8, 9 Therefore, clinical practice documents acknowledge the utility of BNP and NT-proBNP as important biomarkers for both diagnosis of HF and assessment of clinical deterioration in HF10-12 and advise that BNP or NT-proBNP values should be a regular component of an HF patient's medical record and should be updated periodically.12 Additionally, NT-proBNP has also been used as an important inclusion criterion in pivotal trials of HFrEF treatments to ensure a correct diagnosis and enrich for cardiovascular outcome events.13-17

In human plasma and serum, NT-proBNP concentrations are typically higher, likely because of its slower clearance from the circulation.17 Because NT-proBNP immunoassays use the same antibody for detection, whereas BNP assays use different antibodies, standardization is better for NT-proBNP.17 Furthermore, age-stratified thresholds of NT-proBNP for HF diagnosis have been verified in clinical trials.18 We therefore focused on NT-proBNP testing in this study, although we also present results on prevalence of BNP testing.

Patterns and results of NT-proBNP testing in patients with HFrEF in clinical practice are not well characterized, with few studies reporting testing rates or full distributions of NT-proBNP concentrations, especially following a WHFE. The objective of this study was to examine the prevalence of NT-proBNP testing and the distribution of NT-proBNP concentrations in patients with HFrEF, both overall and after a WHFE. A secondary objective was to identify patient characteristics associated with receiving NT-proBNP testing.

Methods Study design and data sources

This was a retrospective cohort study analysing two sources: (i) the de-identified Humana Research Database (Louisville, KY, USA) and (ii) the Veradigm PINNACLE Registry®. The de-identified Humana Research Database includes claims data for all of Humana's fully insured commercial and Medicare Advantage/Part D membership. The database includes Humana member enrolment and medical, pharmacy, and laboratory data and captures inpatient, outpatient, home care, long-term care, and other care settings. Patients from the de-identified Humana Research Database are referred to in the succeeding text as being from ‘all settings’.

The PINNACLE Registry is part of the American College of Cardiology's National Cardiovascular Data Registry® and is the largest outpatient quality improvement registry in the USA, capturing data on coronary artery disease, hypertension, HF, and atrial fibrillation. The PINNACLE Registry collects information on patient demographics, payers, cardiovascular events, vital signs, laboratory orders and results, and medications on a voluntary basis with patients selected at the physicians' discretion. The database used in this study contains HF patients only, and it is linked with Symphony Health's Integrated Dataverse (IDV) pharmacy and medical claims data, which contains physician office medical claims, hospital claims, and pharmacy claims. The medical and hospital claims are pre-adjudicated and are submitted by providers to different types of payers including commercial, Medicare, and Medicaid. The pharmacy claims are final paid claims. Note in the analysis of the PINNACLE/IDV database, NT-proBNP testing and concentrations were only available in the PINNACLE Registry, not in IDV claims, so NT-proBNP values from the PINNACLE/IDV database were from the outpatient setting. Thus, patients from the PINNACLE Registry are referred to in the succeeding text as being from ‘the outpatient setting’.

Humana data were accessed for the years 2015–18 (the 2015 data were only used for the baseline characteristics in the analysis of factors associated with receiving NT-proBNP testing) and PINNACLE/IDV data from 1 July 2013 to 30 September 2017. All data were de-identified, and this study was exempt from institutional review board approval.

Study population

Study subjects were identified based on an index diagnosis of HFrEF during the respective study periods. For the de-identified Humana Research Database, inclusion criteria were a diagnosis of HFrEF, age ≥18 years on the diagnosis date, and enrolment in the health plan for at least 30 days both before and after the index diagnosis. HFrEF was defined as (i) at least one inpatient claim or two outpatient claims with International Classification of Diseases, Tenth Revision (ICD-10) codes (I50.2X or I50.4X) or (ii) one outpatient claim with an HF diagnosis using ICD-10 codes (I50.1, I50.2X, I50.3X, I50.4X, I50.8X, I50.9, or I11.0) plus one outpatient claim with an HFrEF diagnosis using ICD-10 codes I50.2X or I50.4X (Supporting Information, Table S1). For the PINNACLE Registry data, inclusion criteria were a diagnosis of HFrEF, age ≥18 years on the diagnosis date, and ≥1 medical claim and ≥1 pharmacy claim at least 30 days before and after the diagnosis date. HFrEF was defined as (i) a diagnosis of HF in the PINNACLE Registry plus (ii) an ejection fraction <40% or at least two claims showing an HFrEF diagnosis using the ICD-10 codes I50.2X or I50.4X or ICD-9 code 428.2X in the IDV claims (Supporting Information, Table S1). In both data sources, patients with clinical trial participation, a heart transplant, a left ventricular assist device, adult congenital heart disease, or amyloidosis were excluded. Subjects were followed for at least 30 days after the diagnosis, until either death or the end of the study period. For the analysis of patient characteristics associated with the receipt of NT-proBNP testing, eligible patients needed to have a 1 year baseline period.

In each data source, a subgroup of patients with a WHFE was identified, where a WHFE was defined as an HF-related hospitalization or receipt of intravenous diuretics after the index diagnosis date. HF-related hospitalization was defined as a claim for hospital admission with HF or any inpatient claim with a diagnosis of HF using ICD-10 codes I50.1, I50.2x, I50.3x, I50.4x, I50.8x, I50.9, or I11.0, or ICD-9 codes 402.01, 402.11, 402.91, 428.XX, 404.01, 404.03, 404.11, 404.13, 404.91, or 404.93. Intravenous diuretics were identified by either registry records or procedure codes in claims (J1205, J1940, J3265, S0171, and S9361).

Variable measurement

We assessed the prevalence of NT-proBNP and BNP testing, as well as trends in testing over the course of the study period. Testing was confirmed by the presence of a laboratory result. The NT-proBNP testing around the HFrEF diagnosis was determined within 30 days before and after the index diagnosis. Among those with a post-diagnosis test, the duration from the diagnosis to the first post-diagnosis test and the number of NT-proBNP tests performed after the diagnosis were also measured.

N-terminal pro-B-type natriuretic peptide concentrations were determined for each cohort; these analyses were stratified by age (18–65 and >65 years), sex, inpatient status (for cohorts from all settings), estimated glomerular filtration rate (eGFR; ≤30, >30 to <60, and ≥60 mL/min/1.73 m2), and New York Heart Association (NYHA) classification (I–II or III–IV; for cohorts from the outpatient registry). If multiple NT-proBNP values were available, the one closest to the first diagnosis date was used for the general HFrEF cohorts and the one closest to the worsening event date was used for patients with a WHFE. Also, for patients with a WHFE, only NT-proBNP testing on or within 365 days following the worsening event date was considered. The analysis by inpatient status applied only to the Humana data because PINNACLE is an outpatient registry. In this analysis, an inpatient was defined as a subject with an NT-proBNP test any time from 2 days before hospital admission to 2 days following discharge. All other subjects were classified as ‘non-inpatients’.

N-terminal pro-B-type natriuretic peptide concentrations were also assessed as binary (above vs. below) frequency distributions around cut-offs of 125, 300, 3000, 4000, 5000, and 8000 pg/mL. The cut-off values were derived from guideline-recommended diagnostic cut-offs and previous studies showing a difference in cardiovascular outcomes for patients with NT-proBNP values above vs. below these levels.9, 12, 19-22 Among subjects with >1 NT-proBNP test, patterns of test results were defined in terms of these cut-offs with respect to the initial test result. Stable patterns were defined as remaining below (low) or above (high) the cut-off after the first test result. Increased values were below the cut-off initially and above it thereafter. Decreased values were above the cut-off initially and below it thereafter. Fluctuating values varied from below to above the cut point, or vice versa, across three or more test results.

To identify patient characteristics associated with receiving NT-proBNP testing, we used bivariate and multivariate analyses. For this analysis, eligible patients were required to have a 1 year baseline period, and the receipt of NT-proBNP testing was assessed from 30 days before the diagnosis date to any time after diagnosis in the study period. Independent variables included sociodemographic variables [age, gender, and insurance type (commercial and Medicare)], clinical data (heart rate; blood pressure; eGFR; serum levels of sodium, potassium, haemoglobin, HbA1c, low-density and high-density lipoprotein cholesterol, total cholesterol, and creatinine; and BNP testing), co-morbidities (anaemia, atrial fibrillation, chronic kidney disease, chronic obstructive pulmonary disease, asthma, coronary artery disease, valvular heart disease, pulmonary hypertension, depression, type 2 diabetes, hyperlipidaemia, hypertension, myocardial infarction, peripheral artery disease, sleep apnoea, stroke, and cancer), medical procedures (cardiac resynchronization therapy, coronary artery bypass grafting, cardiac valve surgery, cardioverter-defibrillator implantation, percutaneous coronary intervention, heart transplantation, and left ventricular assist device implantation), pharmacological treatments for HF (angiotensin-converting enzyme inhibitors, angiotensin receptor blockers, mineralocorticoid receptor antagonist, beta-blocker, digoxin, diuretics, hydralazine, ivabradine, and sacubitril/valsartan) and treatment regimens (monotherapy, dual therapy, triple therapy, other, and none), and healthcare resource utilization (inpatient, outpatient, and emergency room visits). The dependent variable was receipt of NT-proBNP testing within 30 days before the HFrEF diagnosis and any time after the diagnosis date. These analyses were conducted only in the de-identified Humana Research Database because of the comparatively small number of patients receiving an NT-proBNP test in the PINNACLE Registry data and the large number of missing values for some patient characteristics of interest.

Statistical analysis

Prevalence of NT-proBNP testing, overall and around the diagnosis date, and distributions of NT-proBNP concentrations are presented as numbers and percentages. NT-proBNP concentrations are presented as medians and inter-quartile ranges (IQRs). The number of days to the first post-diagnosis test was assessed as both a mean with its standard deviation and a median with its range. The number of NT-proBNP tests in Years 1–3 after diagnosis is presented as the mean and standard deviation.

In stratified analyses of NT-proBNP concentrations, the comparison of NT-proBNP values across groups was based on a Wilcoxon rank-sum test or non-parametric one-way ANOVA. Patient characteristics were assessed for association with receiving NT-proBNP testing using bivariate and multivariate analyses. Bivariate analyses were compared by Student's t-tests for continuous variables and by χ2 tests for categorical variables. Multiple logistic regression was utilized for multivariate analyses. Because of the large number of missing values for laboratory results, these clinical variables were not included in the multivariate analyses.

Because the de-identified Humana Research Database only captures laboratory data from part of their laboratory and data vendors, we also conducted sensitivity analyses using the subset of patients with one or more laboratory claims in the study period.

All analyses were conducted using SAS 9.4 (SAS Institute, Cary, NC, USA). P values <0.05 were considered statistically significant.

Results Proportion of patients receiving N-terminal pro-B-type natriuretic peptide testing

Of the 249 238 patients with HFrEF from all settings, 22 830 (9.2%) had an NT-proBNP test during 2016–18; 10.8% of patients with a WHFE received a test in the study period (Table 1). When restricted to patients with at least one laboratory claim, 11.3% of patients with HFrEF and 13.2% of those with a WHFE received NT-proBNP testing (data not shown). In the outpatient registry cohort, all patients with HFrEF and the subset of patients with a WHFE both received NT-proBNP testing at a rate of 2.3% (Table 1). Testing prevalence increased by 1–2 percentage points over the 3 year analysis period in all of these cohorts (Figure 1). For the purposes of comparison, the testing prevalence and trends for BNP are shown in Table 1 and Figure 1.

Table 1. Prevalence of NT-proBNP and BNP testing Patients with HFrEF from all settingsa (N = 249 238) Patients with a WHFE from all settingsa (N = 166 892) Patients with HFrEF from the outpatient settingb (N = 91 444) Patients with a WHFE from the outpatient settingb (N = 50 093) NT-proBNP testing, N (%) 22 830 (9.2%) 18 015 (10.8%) 2108 (2.3%) 1141 (2.3%) BNP testing, N (%) 48 088 (19.3%) 36 794 (22.0%) 7649 (8.4%) 3847 (7.7%) BNP, B-type natriuretic peptide; HFrEF, heart failure with reduced ejection fraction; NT-proBNP, N-terminal pro-B-type natriuretic peptide; WHFE, worsening heart failure event. image

Trends in N-terminal pro-B-type natriuretic peptide (NT-proBNP) and B-type natriuretic peptide (BNP) testing. The data points show the percentages of patients with heart failure with reduced ejection fraction (HFrEF) and the subgroup of patients with a worsening heart failure event (WHFE) with an NT-proBNP or BNP test in years (A) 2016–18 for cohorts from the de-identified Humana Research Database (all settings) and (B) 2014–16 for cohorts from the PINNACLE Registry (outpatient setting).

Proportions of patients undergoing N-terminal pro-B-type natriuretic peptide testing at different time points

In both data sources, about one-third of patients with an NT-proBNP test received it around the time of their HFrEF diagnosis (36.9% in the all-setting cohort and 30.6% in the outpatient registry cohort), but the majority received the test after the diagnosis (90.4% and 88.0%, respectively; Table 2).

Table 2. Proportion of patients undergoing NT-proBNP testing at different time points and number of tests at different time points Patients with HFrEF from all settingsb (N = 22 830) Patients with a WHFE from all settingsb (N = 18 015) Patients with HFrEF from the outpatient settingc (N = 2108) Patients with a WHFE from the outpatient settingc (N = 1141) Within 30 days before and after the HFrEF diagnosis, n (%) 8426 (36.9%) 6733 (37.4%) 644 (30.6%) 304 (26.6%) After HFrEF diagnosis, n (%) 20 640 (90.4%) 16 625 (92.3%) 1855 (88.0%) 1052 (92.2%) Days to first post-diagnosis test, mean (SD)d 236.5 (274.6) 231.0 (271.7) 230.3 (270.6) 245.6 (274.7) Days to first post-diagnosis test, mediand 118 111 118 133 NT-proBNP tests in Year 1, mean (SD) 2.1 (2.2) 2.3 (2.3) 1.7 (1.4) 1.8 (1.5) NT-proBNP tests in Year 2, mean (SD) 2.0 (2.1) 2.2 (2.2) 1.5 (1.1) 1.5 (1.1) NT-proBNP tests in Year 3, mean (SD) 2.0 (2.2) 2.1 (2.3) 1.5 (1.1) 1.5 (1.0) HFrEF, heart failure with reduced ejection fraction; NT-proBNP, N-terminal pro-B-type natriuretic peptide; SD, standard deviation; WHFE, worsening heart failure event.

For those who had NT-proBNP testing after the HFrEF diagnosis, the median number of days from diagnosis to NT-proBNP testing was 118 for both cohorts, and patients received an average of 1.7–2.1 tests in the first year across both cohorts. This number slightly decreased in the second and third years following the diagnosis. Results for subgroups with a WHFE were not substantially different.

N-terminal pro-B-type natriuretic peptide concentrations and distribution

Figure 2 shows the distribution of NT-proBNP concentrations in both data sources. Most patients with HFrEF from all settings had NT-proBNP concentrations >1000 pg/mL, whereas most patients with HFrEF from the outpatient setting had concentrations <1000 pg/mL.

image

N-terminal pro-B-type natriuretic peptide (NT-proBNP) value distribution. (A) All eligible patients with heart failure with reduced ejection fraction (HFrEF) in the de-identified Humana Research Database, and the subgroup with a worsening heart failure event (WHFE). (B) All patients with HFrEF in the PINNACLE Registry, and the subgroup with a WHFE.

Median (IQR) NT-proBNP concentrations around the HFrEF diagnosis were 1399 (423–4087) pg/mL in patients with HFrEF from all settings and 394 (142–688) pg/mL in patients with HFrEF from the outpatient setting (Table 3). Median (IQR) NT-proBNP concentrations tested following the event in patients with a WHFE were higher than the concentrations for HFrEF patients tested around diagnosis: 2209 (740–5894) in the all-setting cohort and 464 (174–783) pg/mL in the outpatient registry cohort (Table 3). In patients with HFrEF from all settings, 91.6%, 80.7%, 32.0%, 25.5%, 21.1%, and 13.4% had NT-proBNP concentrations above 125, 300, 3000, 4000, 5000, and 8000 pg/mL, respectively (Table 3). At each cut-off, the percentage of patients with a WHFE from all settings was higher (95.8%, 89.0%, 41.7%, 34.2%, 28.6%, and 18.9%, respectively). Few patients with HFrEF from the outpatient setting had NT-proBNP concentrations above the higher cut-offs (3000, 4000, 5000, and 8000 cut-offs: 3.4%, 2.7%, 2.3%, and 1.0%, respectively), but the percentage of patients was again higher in the subgroup of patients with a WHFE (3000, 4000, 5000, and 8000 cut-offs: 7.1%, 6.0%, 5.1%, and 2.5%, respectively; Table 3).

Table 3. NT-proBNP concentrations and distribution Patients with HFrEF from all settingsb (N = 22 830) Patients with a WHFE from all settingsb (N = 9787) Patients with HFrEF from the outpatient settingc (N = 2108) Patients with a WHFE from the outpatient settingc (N = 553) Median (IQR) NT-proBNP (pg/mL) 1399 (423–4087) 2209 (740–5894) 394 (142–688) 464 (174–783) NT-proBNP distribution, N (%) >125 pg/mL 20 918 (91.6) 9373 (95.8) 1619 (76.8) 432 (78.1) >300 pg/mL 18 426 (80.7) 8709 (89.0) 1235 (58.6) 355 (64.2) >3000 pg/mL 7312 (32.0) 4084 (41.7) 72 (3.4) 39 (7.1) >4000 pg/mL 5820 (25.5) 3349 (34.2) 57 (2.7) 33 (6.0) >5000 pg/mL 4811 (21.1) 2802 (28.6) 49 (2.3) 28 (5.1) >8000 pg/mL 3058 (13.4) 1851 (18.9) 22 (1.0) 14 (2.5) HFrEF, heart failure with reduced ejection fraction; IQR, inter-quartile range; NT-proBNP, N-terminal pro-B-type natriuretic peptide; WHFE, worsening heart failure event.

Stratified analyses of patients with HFrEF and the WHFE subgroup from all settings showed that NT-proBNP concentrations were higher in older patients (>65 vs. 18–64 years), inpatients (vs. non-inpatients), and in patients with lower eGFR (all P < 0.001; Supporting Information, Table S2). In patients with HFrEF from the outpatient setting, higher NT-proBNP concentrations were observed in HFrEF patients with older age, higher NYHA functional class (III–IV vs. I–II), and lower eGFR (Supporting Information, Table S3). Similar trends were observed in the WHFE subgroup from the outpatient setting except that NYHA functional class was no longer significant.

Among patients from all settings who had NT-proBNP tested, inpatient status was assigned to 53.0% of all patients with HFrEF and 65.2% of patients with a WHFE (Supporting Information, Table S2). Among these inpatients, NT-proBNP concentrations were higher at admission than at discharge, which was observed in both the overall population with HFrEF and the subgroup with a WHFE (Supporting Information, Table S4).

Patterns of test results

In patients with HFrEF from all settings, most patients had an initial test result below 4000 pg/mL and maintained concentrations below this cut-off in subsequent tests (57.7%; Table 4). However, a small proportion of this cohort had NT-proBNP concentrations consistently above this cut-off over multiple tests (15.7%) or concentrations that increased from the initial test to subsequent tests (9.9%; Table 4). At each cut-off, stable high NT-proBNP concentrations were more frequent among patients with a WHFE than the overall population of patients with HFrEF, but still the majority of patients with a WHFE had stable low NT-proBNP concentrations. Almost all patients with HFrEF from the outpatient setting were stably below the 8000 pg/mL cut-off (96.5%), while only about three-fourths (73.9%) of patients with HFrEF from all settings were classified this way. The majority of patients with a WHFE had NT-proBNP concentrations consistently below 8000 pg/mL (68.2% in the all-setting cohort and 94.2% in the outpatient cohort).

Table 4. Patterns of NT-proBNP test results Patients with HFrEF from all settingsb (N = 11 893) Patients with a WHFE from all settingsb (N = 4693) Patients with HFrEF from the outpatient settingc (N = 932) Patients with a WHFE from the outpatient settingc (N = 223) Cut point: 125 pg/mL Stable low 322 (2.7) 66 (1.4) 114 (12.2) 20 (9.0) Increased 422 (3.6) 78 (1.7) 51 (5.5) 8 (3.6) Decreased 301 (2.5) 88 (1.9) 71 (7.6) 18 (8.1) Stable high 10 466 (88.0) 4388 (93.5) 631 (67.7) 165 (74.0) Fluctuated 382 (3.2) 73 (1.6) 65 (7.0) 12 (5.4) Cut point: 300 pg/mL Stable low 1010 (8.5) 223 (4.8) 242 (26.0) 46 (20.6) Increased 795 (6.7) 134 (2.9) 99 (10.6) 18 (8.1) Decreased 552 (4.6) 213 (4.5) 104 (11.2) 29 (13.0) Stable high 8780 (73.8) 3945 (84.1) 401 (43.0) 117 (52.5) Fluctuated 756 (6.4) 178 (3.8) 86 (9.2) 13 (5.8) Cut point: 3000 pg/mL Stable low 5992 (50.4) 2011 (42.9) 849 (91.1) 188 (84.3) Increased 1216 (10.2) 376 (8.0) 15 (1.6) 4 (1.8) Decreased 858 (7.2) 469 (10.0) 15 (1.6) 5 (2.2) Stable high 2498 (21.0) 1423 (30.3) 28 (3.0) 20 (9.0) Fluctuated 1329 (11.2) 414 (8.8) 25 (2.7) 6 (2.7) Cut point: 4000 pg/mL Stable low 6867 (57.7) 2367 (50.4) 860 (92.3) 195 (87.4) Increased 1174 (9.9) 384 (8.2) 16 (1.7) 3 (1.3) Decreased 751 (6.3) 425 (9.1) 12 (1.3) 5 (2.2) Stable high 1866 (15.7) 1104 (23.5) 22 (2.4) 17 (7.6) Fluctuated 1235 (10.4) 413 (8.8) 22 (2.4) 3 (1.3) Cut point: 5000 pg/mL Stable low 7519 (63.2) 2648 (56.4) 877 (94.1) 200 (89.7) Increased 1111 (9.3) 381 (8.1) 14 (1.5) 4 (1.8) Decreased 650 (5.5) 381 (8.1) 8 (0.9) 5 (2.2) Stable high 1477 (12.4) 896 (19.1) 15 (1.6) 10 (4.5) Fluctuated 1136 (9.6) 387 (8.3) 18 (1.9) 4 (1.8) Cut point: 8000 pg/mL Stable low 8794 (73.9) 3200 (68.2) 899 (96.5) 210 (94.2) Increased 912 (7.7) 330 (7.0) 13 (1.4) 3 (1.3) Decreased 466 (3.9) 299 (6.4) 6 (0.6) 3 (1.3) Stable high 843 (7.1) 533 (11.4) 2 (0.2) 1 (0.4) Fluctuated 878 (7.4) 331 (7.1) 12 (1.3) 6 (2.7) HFrEF, heart failure with reduced ejection fraction; NT-proBNP, N-terminal pro-B-type natriuretic peptide; WHFE, worsening heart failure event. Patient characteristics associated with receiving N-terminal pro-B-type natriuretic peptide testing

Patient characteristics (sociodemographic variables, clinical data, co-morbidities, medical procedures, pharmacological treatments for HF and treatment regimens, and healthcare resource utilization) associated with NT-proBNP testing in bivariate analyses are shown in Supporting Information, Table S5. Multiple logistic regressio

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