Abstract
Background Heart failure with preserved ejection fraction (HFpEF) is under-identified in primary care.
Aim The aim of this study was to determine what information is available in patients’ primary care practice records that would identify patients with HFpEF.
Design & setting Record review in two practices in east of England.
Method Practices completed a case report form on each patient on the heart failure register and sent anonymised echocardiography reports on patients with an ejection fraction (EF) >50%. Reports were reviewed and data analysed using SPSS (version 25).
Results One hundred and forty-eight patients on the heart failure registers with mean age 77 +12 years were reviewed. Fifty-three patients (36%) had possible HFpEF based on available information. These patients were older and multimorbid, with a high prevalence of overweight and obesity. Confirmation of diagnosis was not possible as recommended HFpEF diagnostic information (natriuretic peptides, echocardiogram parameters of structural heart disease and diastolic function) was widely inconsistent or absent in these patients.
Conclusion Without correct identification of HFpEF, patient management may be suboptimal or inappropriate, and lack the needed focus on comorbidities and lifestyle that can improve patient outcomes. This study describes in detail the characteristics of many of the patients who probably have HFpEF in a real-world sample, and the improvements and diagnostic information required to better identify them. Identifying more than the tip of the iceberg that is the HFpEF population will allow the improvement of the quality of their management, the prevention of ineffective health care, and the recruitment of patients into research.
How this fits in
Patients with HFpEF comprise half of the patients with heart failure but are under-identified in primary care. Patients with possible HFpEF seldom had natriuretic peptides measured, and lacked consistent echocardiographic measurement of relevant parameters for structural heart disease and diastolic function needed for diagnosis. The absence of relevant diagnostic information and interpretation in primary care hinders identification and appropriate management of patients with HFpEF.
Introduction
Heart failure affects 900 000 people in the UK and accounts for 2% of NHS expenditure, primarily due to emergency hospitalisations.1,2 Many clinicians in general practice may be surprised to know that approximately half of these patients have a type of heart failure called heart failure with a preserved ejection fraction (HFpEF), as very few of these patients ever receive a specific diagnosis.3–7 This really matters, as HFpEF patients need a different management strategy to patients with heart failure with reduced ejection fraction (HFrEF, where the heart ejects <40% of its volume of blood each time it contracts). Patients with HFpEF need a focus on regulation of fluid status with diuretics, self-management including diet and exercise, and control of comorbid conditions such as atrial fibrillation (AF) and hypertension, rather than drugs and devices which are the mainstay for HFrEF.8,9 Misdiagnosis also undermines quality improvement and research into HFpEF. Misdiagnosis would no longer be tolerated in fields such as diabetes and stroke, where specific diagnosis is understood to be vital for patient care, and should no longer be tolerated in the field of heart failure.
However, diagnosing heart failure without a reduced left ventricular ejection fraction (LVEF) is more complex and this complexity likely stems from an incomplete understanding of the exact pathophysiological processes leading to HFpEF, changes in and lack of agreement on diagnostic criteria, a heterogeneous population with HFpEF, a lack of specific evidence-based treatment, and a focus on HFrEF for whom evidence-based treatment exists.5,8,10–14 The recent European Society of Cardiology (ESC) guidelines on acute and chronic heart failure8 define HFpEF as symptoms and signs of heart failure, an LVEF >50%, elevated levels of natriuretic peptides (brain natriuretic peptide >35 picograms per millilitre [pg/mL] or N-terminal pro b-type natriuretic peptide [NT-ProBNP] >125 pg/mL) and at least one of the following additional criteria: relevant structural heart disease (left ventricular hypertrophy [LVH] and/or left atrial enlargement; or diastolic dysfunction. These criteria pose some challenges for primary care practitioners. Although recommended to rule out heart failure by the ESC and NICE, not all patients presenting with suspected heart failure in primary care have natriuretic peptides measured. LVH and left atrial enlargement are easily and frequently assessed but other recommended echocardiographic parameters for HFpEF are more technically challenging and require specialist interpretation. Diastolic dysfunction is defined by specific indices on echocardiogram measuring mitral valve early and late diastolic inflow, early diastolic tissue velocity, the ratio between early mitral inflow velocity and mitral annular early diastolic velocity and peak tricuspid regurgitation velocity.8,15 Although not a diagnostic parameter, elevated pulmonary artery systolic pressure (PASP) is common, and is an important indicator for prognosis and management. Recommendations for what to measure on echocardiogram and values considered abnormal differ between professional groups (Box 1).
European Society of Cardiology clinical practice guidelines on acute and chronic heart failure 20163 |
Relevant structural heart disease
|
American Society of Echocardiography and the European Association of Cardiovascular Imaging 20169 |
Annular e’ velocity
Left atrium maximum volume index (>34 mL/m2) Peak tricuspid regurgitation velocity >2.8 m/sec Note: LV diastolic function is normal if more than half of the variables do not meet the cut-off for identifying abnormal function. |
cm/sec = centimetres per second. E = early mitral diastolic inflow. e’ = early diastolic tissue velocity. E/A = ratio between peak early (E) and late (A) diastolic filling velocities. E/e’ = ratio between early mitral inflow velocity and mitral annular early diastolic velocity. g/m2 = grams per metre squared. LV = left ventricle. m/sec = metres per second. mL/m2 = millilitres per metre squared. MV = mitral valve.
Primary care provides sole or shared care for all patients with heart failure in the UK, and maintains registers of heart failure patients as mandated by the Quality Outcomes Framework (QOF). QOF also requires that an echocardiogram is done to confirm or refute the heart failure diagnosis. The aim of this study was to determine what information was available in patients’ full primary care practice records to identify patients with HFpEF from within practice heart failure patient registers.
Method
Two primary care practices in the east of England were recruited for the study; one urban and one in a smaller town accessing echocardiography services run by different hospitals. Each practice completed a simple case report form (CRF) on each patient on the heart failure register of the practice requesting brief demographic and clinical information. Data were collected during 2016–17, but included patients on heart failure registers regardless of when diagnosed. Practices were asked to send anonymised echocardiography reports on all patients with an EF >50%, or those patients with LVEF labelled as ‘normal, preserved, or near-normal’. The echocardiography reports or letters detailing echocardiographic information were scrutinised for parameters measured and assessment of left ventricular diastolic function.
Data were entered into an SPSS (version 25) database by the research nurse and re-checked by the principal investigator. The principal investigator and a consultant cardiologist reviewed the data and echocardiographic reports and letters on each patient. Patients were divided into three groups based on EF as defined by the ESC:8 EF <40% (HFrEF or LVSD), EF 40–49% as heart failure with a mid-range EF (HFmrEF), and EF >50% (HFpEF). Patients were included in the HFrEF category if their systolic function was described as severely impaired even if a numeric value was not provided. Similarly, patients were included in the HFpEF category if their EF was described as normal, near-normal, or preserved. A fourth group comprised those patients for whom echocardiographic data were missing or not clear enough for categorisation. This final group included those with descriptions of mild, moderate, or mild–moderate systolic dysfunction as there was uncertainty regarding matching these descriptors to a specific numerical LVEF. These groups were compared on demographic and clinical characteristics.
Results
The two practices participating in this study differed in size and socioeconomic deprivation of the practice area. The urban practice had a list size of 7890, with 48 patients on the heart failure register, and was in the least deprived decile for socioeconomic status. The town practice had a list size of 13 229 with 100 patients on the heart failure register, and was in the fifth most deprived decile. The proportion of patients aged ≥65 were similar (15–17%) and both practices had predominantly white patients. Non-white ethnicity ranged from 5% (in the smaller town practice) to 19% (urban).
CRFs were completed on 148 patients aged 40–99 years. Patients had a mean age of 77 +12 years with multiple comorbid conditions and a high prevalence of overweight and obesity (Table 1). Echocardiogram reports or letters were unavailable or did not provide enough information to characterise 31 patients (21%) by EF. This 21% included patients placed on the heart failure register prior to the QOF requirement for echocardiographic confirmation of heart failure, patients awaiting echocardiography, echocardiograms reported as technically difficult with limited data, and a few with unknown reasons for lack of echocardiogram reports. Sixty-nine of the patients (56% of those with an echocardiogram) had a numeric EF provided, and the other reports used verbal descriptions (for example, preserved or moderately impaired) to describe systolic function and EF.
Grouping patients by EF resulted in 43 patients (29%) with EF <40% or labelled severe systolic dysfunction or severely impaired EF; 21 (14%) with EF 40–49%; 53 (36%) with EF >50% or described as having normal, near-normal, or preserved EF; and 31 (21%) missing or unable to be categorised. Small sample sizes in the groups precluded finding significant differences in characteristics by EF group except for a lower recorded prevalence of atrial fibrillation in patients for whom echocardiographic data were missing or unclear (Table 2). Patients with EF >50% had a mean age of nearly 80, 83% had hypertension, 81% were overweight or obese, 65% had more than 3 comorbid conditions, half had chronic kidney disease, 45% were women, and nearly one-third had diabetes. Although not significant, there were trends toward older age, a higher proportion of women, greater prevalence of obesity and multiple comorbidities, and lower rates of ischaemic heart disease in patients with EF >50% compared to those with EF <40%. Only 9% of the total sample had natriuretic peptides (specifically NT-ProBNP) results available in the record. Six of the 53 patients with an EF >50% had natriutric peptides measured, with 5 of these being elevated well above the ESC guideline recommended level for considering a diagnosis of heart failure (NT-ProBNP >125 pg/mL).7 Seven of the 43 patients with EF <40% had NT-ProBNP results. The mean NT-ProBNP for those with EF >50% was 2699 +2138 pg/mL, compared to 4858 +6479 pg/mL for those with EF <40%.
Echocardiographic data
Of the 53 patients with documented EF >50%, 39 were found to have echocardiographic reports that included at least one of the parameters recommended for diagnosing HFpEF and diastolic dysfunction (Table 3). Left ventricular size and mass were commented on in 35 and left atrial size and volume were discussed in 33. Sixteen of 35 patients (46%) had at least some degree of LVH, and the left atrium was dilated in 28 of 33 patients (85%). Only in seven of the 39 patients (18%) were both the left atrium and left ventricle normal. At least one measure of diastolic function was available in 24 patients and 17 had at least one abnormal measure. Comments about diastolic function were found in reports of 12 patients, with 11 of these patients having some degree of diastolic dysfunction noted, and one with elevated filling pressures. However measurements of specific indices of diastolic function were not documented in five patients with diastolic dysfunction noted on the report.
In total 24 patients had both measures of relevant structural heart disease and diastolic function, and 15 patients had abnormal values of both of these. Seven patients had pulmonary hypertension (PH) or possible PH documented, and PASPs were available in 9 patients. Differences on echocardiogram reports in measurements and information provided for patients with possible HFpEF differed by individual echocardiographers, more so than by the service. This finding was independent of reports of technical or other difficulties in performing the echocardiogram.
Diagnosis
Very few patients would have met the ESC diagnostic criteria for HFpEF given the lack of recommended measurements. Although 73.5% of the 53 patients with possible HFpEF had at least one measure of structural heart disease and/or diastolic function assessed, there was a lack of consistency in which indices were measured and how many were reported. Natriuretic peptide levels were available in <10% of all of the patients.
Discussion
Summary
In two primary care registers of heart failure patients, this study found that patients with possible HFpEF comprised 36% of the patients. This group of patients were on average a few years older than the other heart failure patient groups, and had a high comorbidity burden including the highest prevalence of being overweight or obese. Confirmation of diagnosis was not possible as precise HFpEF diagnostic information was widely inconsistent or absent in these patients. Echocardiographic indices related to diastolic function (and to a less extent structural heart disease), and interpretation of findings related to HFpEF were extremely limited or missing. An additional 21% of patients had missing echocardiograms or were unable to be categorised by EF, and this may include additional patients with HFpEF. Natriuretic peptide results were also infrequently available.
Strengths and limitations
The strength of the study was in the thorough review of anonymised echocardiographic reports and cCRFs from patients on the heart failure registers of two primary care practices in different areas, and comparison with recommended criteria for diagnosing HFpEF. However the study did not include a search for patients with heart failure who may not have been on the heart failure registers. Heart failure registers have been found to have varying levels of accuracy (Audit British Heart Foundation, Bury Heart Failure Audit, unpublished data, 2010) and patients may be placed on the heart failure register prior to confirmation. A further limitation of the study is that there were a limited number of patients and both practices were in the east of England with limited ethnic diversity.
Comparison with existing literature
Patients with HFpEF comprise half of the patients with heart failure, and epidemiological analyses have shown an increasing prevalence of patients with HFpEF especially among those referred to acute services from the community.16 Given the mean age of the patients on the two heart failure registers (77 years) in this study, a higher proportion of patients with possible HFpEF would be expected. A pooled analysis of 105 studies with 196 105 patients with undifferentiated heart failure recruited from general practice indicated that the predominant phenotype was an older woman with hypertension rather than ischaemic heart disease,17 which would be suggestive of a high prevalence of HFpEF. The patients with possible HFpEF in the current analysis had a non-significant trend toward older age, a higher proportion of women, and multiple comorbidities. The increasing prevalence of HFpEF among older patients suggests that only the tip of a potential iceberg of patients with HFpEF in primary care is being identified.
Both underdiagnosis and overdiagnosis of heart failure in primary care have been found in other studies.6,18,19 Various routes to diagnosis of heart failure in patients in UK primary care have been documented, with nearly 80% of patients being diagnosed in secondary care, and less than one quarter following the recommended NICE diagnostic pathway.20 A recent survey found that most GPs (84%) did not diagnose HFpEF, and only 7% were very confident in their ability to do so.21 Although echocardiography is an essential tool for determining the diagnosis and type of heart failure it has been found to be underused in general practice. In a study of 683 patients with a heart failure diagnosis in 30 general practices, only 45.2% had undergone an echocardiogram at the start of the study in 2010–2011.18 Munoz and colleagues22 analysed records from 8376 patients with diagnoses of heart failure in 52 primary care practices in Barcelona 2009–2012. The majority of patients (91.5%) did not have an available EF. Most of the patients in the present analysis had an echocardiogram done, which may be due to the influence of the QOF criteria. However many GPs in the UK lack confidence in interpretation of echocardiography reports from open access services, especially in regards to HFpEF.21
Although echocardiogram reports or letters describing results were available for the majority of patients in our study, data on echocardiographic indices to diagnose HFpEF were inconsistently and infrequently measured in patients with possible HFpEF. Guidelines such as the ESC specify what needs to be measured for HFpEF assessment, but disagreement regarding criteria exists. The ESC guidelines8 do not specify how many measures of diastolic function need to be abnormal to establish a diagnosis of diastolic dysfunction, but the American Society of Echocardiography and the European Association of Cardiovascular Imaging15 require at least half of 5 recommended parameters to be abnormal. The British Society of Echocardiography (BSE) minimum dataset includes a few parameters related to diastolic function, and they have also published a practical guide on assessment and grading of diastolic dysfunction. The BSE noted that confidence in assessing and grading diastolic dysfunction increases with increasing numbers of corroborative parameters but does not specify how many.23,24 The inconsistency in reports seen in this analysis could also reflect local and regional practice and guidance, limited time for echocardiography appointments in busy services, and limited patient information provided in referral. The inconsistency in reporting specific parameters varied by echocardiographers within the two services rather than by service.
Other important characteristics and prognostic indicators such as pulmonary artery pressures were also infrequently documented in this sample of patients. In a community sample of 244 patients with HFpEF, elevated PASPs were found in 83% of patients,25 and higher PASP was associated with mortality (age-adjusted hazard ratio 1.22 per 10 mm Hg; P<0.005). Another analysis (1663 patients with heart failure) found an elevated PASP >40 mm Hg to be an independent predictor of survival in patients with heart failure and an EF >40% with a hazard ratio of 2.27 (95% confidence intervals = 1.58 to 3.26; P<0.001).26
Implications for practice
The lack of consistent and relevant information and interpretation of findings from echocardiography and other diagnostic tests for patients with suspected heart failure could lead to misdiagnosis and inappropriate treatment. Patients with HFpEF may have reason to be on similar medications to those with HFrEF for control of hypertension and other cardiac conditions, but these should not be prescribed automatically as HFpEF-specific treatment due to lack of efficacy in improving mortality and morbidity. Some healthcare professionals may argue that, until there are evidence-based treatments for management of HFpEF, a formal diagnosis of HFpEF is unnecessary. However there is a clear message that HFrEF and HFpEF are not the same, that clinicians must treat HFpEF now by managing comorbidities, and that the greatest reductions in mortality and morbidity may result from treating comorbidities.9,14 In the CHARM clinical trial with over 1000 patients with HFpEF, the burden of non-cardiac conditions accounted for a greater proportion of risk for death than cardiac burden (population attributable risk 49% versus 15%; P<0.05).27 Comorbid conditions have a greater impact on functional class and physical health status in HFpEF, and hospitalisations and readmissions for non-cardiac causes are higher in patients with HFpEF compared to HFrEF.28,29 An analysis of over 43 000 patients hospitalised for HFpEF in the US found a 1-year composite of mortality and all-cause readmission to be 74%.30
Patients with HFpEF will also benefit from a focus on self-management and lifestyle factors. Physical activity has been shown to improve fitness and quality of life in patients with HFpE,31 and emerging evidence indicates that weight loss may also improve outcomes in obese patients.32 Patients experiencing problems with fluid overload may benefit from restrictions in fluid and salt intake. Diet non-compliance was shown to be a precipitating factor in hospitalisation for heart failure regardless of LVEF, and in another analysis patients with HFpEF who received sodium-restriction dietary instruction at time of hospital discharge had significantly lower risk of 30-day combined readmission and death.33,34
In conclusion, the findings of this study have highlighted that there is a deficit in identification of patients with HFpEF. The implications for this are that without correct identification, patient management may be suboptimal or inappropriate, and lack the needed focus on comorbidities and lifestyle that can improve patient outcomes. Furthermore, without correct identification patients cannot be recruited into clinical trials and other studies that could develop and test HFpEF-specific therapies. The authors have described in detail the characteristics of many of the patients who probably have HFpEF in a real-world sample, and the improvements and diagnostic information (comprehensive echocardiogram reports and natriuretic peptides) required to better identify them. Identifying more than the tip of the iceberg that is the HFpEF population will allow the improvement of the quality of their management, the prevention of ineffective health care, and the recruitment of patients into research.
Funding
This study presents independent research funded by the National Institute for Health Research School for Primary Care Research (NIHR SPCR). The views expressed are those of the author(s) and not necessarily those of the NIHR, the NHS, or the Department of Health.
Ethical approval
The study was approved by the Northwest-Preston Research Ethics Committee (16/NW/0444).
Provenance
Freely submitted; externally peer reviewed.
Acknowledgements
The authors would like to thank the two practices that participated in this study, and acknowledge the support of the East of England NIHR Clinical Research Network.
Notes
Competing interests
The authors declare that no competing interests exist.
- Received May 21, 2018.
- Accepted May 25, 2018.
- Copyright © The Authors 2018
This article is Open Access: CC BY license (https://creativecommons.org/licenses/by/4.0/)