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Original Research |
Xcenda, Palm Harbor, FL (JHJ, BN)
Section of Cardiology, Advocate Health Care, Chicago, IL (JS)
Austin Regional Clinic, TX (RK)
Department of Evidence-Based Medicine, Novartis Pharmaceuticals Corporation, East Hanover, NJ (KSW, FF-T)
Correspondence: Corresponding author: James H. Jackson, Senior Director, Xcenda, 4114 Woodlands Parkway, Suite 500, Palm Harbor, FL 34685 (E-mail: jay.jackson{at}xcenda.com)
| Abstract |
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Methods: This was a retrospective, time series analysis of 27 provider groups and managed care organizations from 1998 through 2006. Patients with hypertension were identified from more than 4000 physicians. Medical charts were collected and clinical data were evaluated using prevailing JNC criteria during the time period before and after JNC 7.
Results: A total of 19,258 patients were identified with hypertension: 15,258 included in the before-JNC 7 cohort and 4,000 in the after-JNC 7 cohort. BP control in the before-JNC 7 cohort was 40.8% compared with 49.3% in the after-JNC 7 cohort (P < .0001). After controlling for demographic and clinical covariates, patients in the before-JNC 7 cohort were 45% less likely to achieve BP control compared with the after-JNC 7 cohort (odds ratio, 0.551; P < .0001).
Conclusion: Although findings indicate BP control is improving, a significant need for further improvement remains.
Because hypertension is a precursor to multiple disease conditions, maintaining blood pressure (BP) control and adherence to goals are imperative to reducing morbidity and mortality, especially in patients with high risk.2,3 Since its first report in 1977, the Joint National Committee on the Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC) has guided the medical community in the awareness, prevention, and treatment of hypertension.4 Seven published reports (JNC 1 to JNC 7) define acceptable BP level and recommend treatment strategies based on a patient's comorbid disease states and level of BP control. Each successive report has been updated based on new clinical evidence about hypertension and its treatment.
The acceptable BP level has become more rigorous through the years, with normal diastolic blood pressure (DBP) defined as <90 mm Hg in JNC 1 versus <80 mm Hg in JNC 7; normal systolic blood pressure (SBP) was defined as <140 mm Hg in JNC 3 versus <120 mm Hg in JNC 7 (Figure 1). Until the 1980s, SBP was listed separately from DBP. However, beginning with JNC 5 (1993), hypertension was defined as a systolic/diastolic reading of at least 140/90. To better guide evaluation and treatment, in JNC 5 the categorization of BP ranges changed from a severity classification to a staging classification. JNC 7 reduced the staging categories from 3 to 2 but added "prehypertension," defined as those patients at risk of developing hypertension. Most notably, JNC 7 recognizes the increased risk of cardiovascular events in individuals with diabetes and chronic kidney disease and recommends more aggressive BP control (<130/80 mm Hg).
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Released in May 2003, the JNC 7 report focuses on greater awareness for at-risk patients, lower BP goals for people with diabetes, the use of multiple agents, and specialized treatment recommendations for compelling indications. For example, ACEIs and angiotensin II receptor blockers (ARBs) are recommended for patients with diabetes because they have been shown to also provide cardiovascular protection and slow the progression of nephropathy.5 Beta-blockers were moved to second-line treatment after results from a meta-analysis that demonstrated superiority of diuretics on all outcomes of cardiovascular heart disease, stroke, congestive heart failure, major cardiovascular events, and cardiovascular and total mortality. In addition, 2-drug combination therapy is recommended as initial therapy for patients with stage 2 hypertension.5,6
Despite significant JNC efforts, a majority of patients are not reaching their BP goals. A 2003 study conducted in 8 managed care organizations in the United States concluded that less than 50% of plan members diagnosed with hypertension met their BP goal (JNC 6). This conclusion held even after various educational and awareness campaigns were initiated.7 In addition, data from the National Health and Nutrition Examination Survey (NHANES) revealed that only 36.8% of patients (including those undiagnosed) were at their target BP.8
Given the significant changes in JNC 7 and the fact that the most recent data on BP control in the United States was obtained before its release, an updated investigation of hypertension treatment patterns and control after JNC 7 is warranted. This study was conducted to 1) assess improvements in BP control since publication of the JNC 7 guidelines, and 2) examine patterns of drug therapy regarding recommended best practices within the JNC guidelines.
| Methods |
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Inclusion and Exclusion Criteria
Inclusion and exclusion criteria were the same for all patients regardless of the time frame sampled. Patients were identified using medical and pharmacy claims data obtained from participating health plans or from clinical data systems within the physician group practices. Patients were considered for inclusion if they had a medical claim with a diagnosis of hypertension (defined as an International Classification of Disease, 9th Revision, Clinical Modification, code of 401–404) or a pharmacy claim for an antihypertensive medication. If pharmacy claims data were available, antihypertensive agents were identified using the Generic Product Identifier, Universal System Classification, or American Hospital Formulary Service codes. Patients were required to be continuously enrolled in the health plan and/or seen by the medical provider group throughout the time frame of analysis.
Patients were excluded if they were younger than 18 years of age. To capture only those patients with a principal diagnosis of hypertension, patients identified by an antihypertensive pharmacy claim without a coexisting hypertension medical claim were excluded if any claim contained a diagnosis of congestive heart failure, benign prostatic hyperplasia, ischemic heart disease, arrhythmia, migraine, or lower extremity edema. Patients without documentation of hypertension in the medical chart were excluded.
Data Collection
Five hundred patients from each of the 27 participating sites were randomly selected for chart review. Data were collected by a nurse or pharmacist trained in standardized data abstraction methods. Data collected included age, gender, hypertension diagnosis, cardiovascular risk factors, relevant comorbidities, SBP and DBP measurements, and prescribing patterns. A hypertension diagnosis was confirmed when at least one of the following terms was found in the medical chart: hypertension, HTN, high blood pressure, high BP, HBP, or
BP. Consistent with the Health Care Effectiveness Data and Information Set, technical specifications for determining BP control, the representative BP reading documented for this study was the reading taken during the most recent visit within the time frame of interest, provided that the visit occurred after a diagnosis of hypertension was documented.9 If more than one BP reading was documented during a single visit, the lowest reading was recorded. If multiple positional readings were documented during a single visit, only the sitting measurement was recorded. If there were supine and standing BP readings, but not a sitting BP reading, the supine measurement was recorded. A standing BP measurement was recorded if it was the only one documented.5 BP control was evaluated in all patients with a hypertension diagnosis, regardless of status of treatment.
BP control was defined under the prevailing JNC criterion applicable for each time period. In the before-JNC 7 cohort, BP control was defined consistent with JNC 6 guidelines: <140/90 mm Hg in patients with hypertension and without diabetes and <130/85 mm Hg in patients with hypertension and diabetes or renal disease.6 In the after-JNC 7 cohort, BP control was defined as <140/90 mm Hg in patients with hypertension and without diabetes and <130/80 mm Hg in patients with hypertension and diabetes or chronic kidney disease.5
Best practice recommendations evaluated in this study included the use of an ACEI or ARB in patients with comorbid diabetes; the use of an ACEI, ARB, or beta-blocker in patients with comorbid congestive heart failure; and the use of beta-blockers in patients with a history of myocardial infarction.
Statistical Analysis
A secure relational database was used to validate and house all data collected from each site. Statistical analyses were performed using SAS software (version 8.2, SAS Institute, Inc, Cary, NC). Descriptive statistics, such as mean ± SD, frequency, and percentages, were generated for all demographic variables, clinical indicators, BP values, and prescribing metrics.
2 and t tests were performed to assess any between-group differences in these variables individually. Because of the difference in sample size between the cohorts, tests for equal variances were conducted and accounted for statistically. A binomial logistic regression model was developed to assess differences in BP control between the 2 independent cohorts. To account for differences in cohort characteristics, the covariates of age, gender, ethnicity, geographic location, risk factors, comorbidities, and treatment were included in the model.
| Results |
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| Discussion |
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Other research indicates that reported levels of BP control can vary greatly depending on the study population, methods, and time frame. For instance, data reported from NHANES suggest that 36.8% of patients in the United States with hypertension had controlled BP during 2003 and 2004.8 The difference in this estimate and the 49.3% reported here (after JNC 7) may be explained by the fact that NHANES includes respondents who are undiagnosed, uninsured, and less likely to be treated. Similarly, Andros et al11 conducted a retrospective observational study of BP control in an insured diabetic population. In that population, the BP control rate (defined by JNC 7) was 28%, similar to the 29.4% reported here.
Rates of BP control reported in clinical trials have ranged from 45% to 66%.12,13 Because clinical trials typically represent a motivated, closely controlled, and monitored patient population, control rates would be expected to be higher than those observed in the general population.
Results from this study suggest that prescribers may increasingly be following the JNC 7 drug therapy recommendations, especially those related to compelling indications. Increase in the use of diuretics in the after-JNC 7 cohort follows the recommendation of thiazide-type diuretics as the preferred initial agent in patients without compelling indications. Similarly, fixed-dose combination therapy had the largest absolute percent increase in prescribed therapy after the release of the JNC 7 guidelines. Fixed-dose combination products provide patients with a more convenient once-daily medication regimen, which has been shown to improve medication adherence.14 The significant increase in the use of ACEIs and ARBs coincides with the JNC 7 recommendation for their use in patients with diabetes and/or congestive heart failure. Data reported here do not, however, suggest that improvements have been made with respect to treating patients with beta-blockers after a myocardial infarction.
Limitations
Several factors must be considered when interpreting the results of this study. First, the 2 study cohorts were different in several important characteristics. Patients in the after-JNC 7 cohort were typically older, more likely to be women, and more likely to have diabetes, hyperlipidemia, angina, nephropathy, or a family history of cardiovascular disease. Likewise, there was a greater percent of Africa-Americans in the after-JNC 7 cohort. In contrast, there was a higher percent of smokers in the before-JNC 7 cohort. Even accounting for these differences, patients in the after-JNC 7 cohort had a greater likelihood of achieving their target BP goal. Because this study included independent samples from multiple sites and geographic locations, sampling bias may have influenced the results.
Because of the retrospective design of the study, some data were not available or not able to be determined during the data collection process (Tables 1 and 2). Although missing data were accounted for during calculations, the possibility exists that certain patient characteristics, conditions, and risk factors were over- or under-represented.
The naturalistic design of this study limits inferences of causality. For instance, there was no ability to control for universal changes that may have occurred independent of any influences from JNC 7, including the introduction of new branded products (and any associated promotion), the generic availability of established market leaders, or any quality improvement initiatives that may have been implemented in participating sites. In addition, because of the study design, we were unable to follow within-patient trends over time. Likewise, the data used for this study was limited by provider documentation. As a result, the presence of concomitant medications or disease states may have been over- or under-reported. In addition, a provider may have prescribed a medication that was never filled or taken by the patient.
| Conclusions |
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| Notes |
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Funding: The study and the development of this manuscript were supported by a research grant from Novartis Pharmaceuticals Corporation.
Conflict of interest: Drs. Jackson and Nightengale are employees of Xcenda, a healthcare consulting firm that provides services to pharmaceutical companies. Xcenda was contracted by Novartis Pharmaceuticals to perform research related to this manuscript. Drs. Wong and Frech-Tamas are employees of Novartis Pharmaceuticals.
See Related Commentary on Page 487.
Received for publication February 1, 2008. Revision received June 2, 2008. Accepted for publication June 10, 2008.
| References |
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