Abstract
Background:
The objective was to explore the
relationship between left ventricular
ejection fraction (LVEF) assessed during
hospitalization for acute myocardial
infarction (MI) and later health-related
quality of life (HRQoL).
Methods:
We used multivariable linear regression to assess the relationship between LVEF and HRQoL in 256 MI patients who responded to the Kansas City Cardiomyopathy Questionnaire (KCCQ), the EQ-5D Index, and the EuroQol Visual Analogue Scale (EQ-VAS) 2.5 years after the index MI.
Methods:
167 patients had normal LVEF (>50%), 56
intermediate (40%-50%), and 33 reduced
(<40%). The mean (SD) KCCQ clinical summary
scores were 85 (18), 75 (22), and 68 (21) (p
< 0.001) in the three groups, respectively.
The corresponding EQ-5D Index scores were
0.83 (0.18), 0.72 (0.27), and 0.76 (0.14) (p
= 0.005) and EQ-VAS scores were 72 (18), 65
(21), and 57 (20) (p = 0.001). In
multivariable linear regression analysis age
³ 70 years, known chronic obstructive
pulmonary disease (COPD), subsequent MI,
intermediate LVEF, and reduced LVEF were
independent determinants for reduced KCCQ
clinical summary score. Female sex,
medication for angina pectoris at discharge,
and intermediate LVEF were independent
determinants for reduced EQ-5D Index score.
Age ³ 70 years, COPD, and reduced LVEF were
associated with reduced EQ-VAS score.
Conclusion: LVEF measured during hospitalization for
MI was a determinant for HRQoL 2.5 years
later. Heart Views 2008;9(4):142-151.
Key words: ¨ myocardial infarction ¨ quality of life
¨ ejection fraction
Background
Left ventricular ejection fraction (LVEF) is
the single most used non-invasive measure of
cardiac function in clinical practice and is
an important prognostic factor for survival
after myocardial infarction (MI), in stable
coronary artery disease (CAD), and in heart
failure1-3. Health-related quality of life (HRQoL)
has also been identified as a predictor of
survival in patients with CAD and heart
failure4-7.
However, the relationship between LVEF and
HRQoL has not been settled and whether LVEF
can predict HRQoL is still controversial.
Some studies have observed an
association8-11 while others have not12-17.
Most of these studies reported on highly
selected heart patients enrolled in clinical
trials9,13,14, patients with known reduced
LVEF13,14, and patients with chronic heart
failure11,17. Only two previous studies
included unselected MI patients, of which
one observed an association between LVEF
measured at the time of the MI and later
HRQoL10,16.
Better understanding of the relationship
between cardiac function and quality of life
might contribute to tailor treatment that
would maintain or improve the patients daily
functioning. Evidently, more research on
this subject is needed.
Accordingly, our aim was to assess the
relationship between LVEF measured during
hospitalization for acute MI and HRQoL 2.5
years later in an unselected MI patient
population, using both a generic and a
disease-specific HRQoL measure.
Methods
Study design and sample
We established a cohort of hospitalized
patients with a discharge diagnosis of acute
MI, defined as codes I21 and I22 in ICD-10
(The International Statistical
Classification of Diseases and Related
Health Problems, tenth revision)18. We
wanted our cohort to be representative of
Norwegian patients with MI, and hence
recruited them from teaching and
non-teaching hospitals in different regions
of Norway. We included a total of 754
consecutive patients who were discharged
alive from 15 hospitals during a 3-month
period between August 1, 1999, and January
31, 2000. Before discharge, LVEF was
measured in 406 (54%) patients. The patient
population is described in Figure 1.
In 2002, we mailed a questionnaire to
patients who were still alive according to
hospital information systems and the
National Population Register of Statistics
Norway. The questionnaires were mailed from
the hospital of discharge, along with a
cover letter signed by the head of the
hospital s cardiology unit. After 4 weeks,
we sent a reminder to non-respondents.
At the time of the survey, 191 of the 754
patients had died, 8 had an unknown address,
and 7 were excluded for miscellaneous
reasons. Hence, we mailed the questionnaire
to the remaining 548 patients of whom 408
(74%) returned completed questionnaires. A
total of 256 of the 408 respondents (63%)
had data on LVEF (Figure 1).
Fig.1: Flow chart of study population. Study population stratified on patients with and without their left ventricular ejection fraction measured |
The mean time
from the index MI to questionnaire response
was 2.5 (SD = 0.2) years, range 2.1-3.1
years.bsp;
Review of medical records
Baseline characteristics were abstracted
from the patients medical records and
included previous medical history,
presenting features, in-hospital treatment,
and medication at discharge. Cardiovascular
morbidities from before the index MI were
categorized as previous MI, hypertension,
angina pectoris, heart failure, peripheral
vascular disease, or stroke. The diagnoses
were based on either previous ICD-codes or
explicit statements in the medical record.
The major indications for each
cardiovascular drug prescribed at discharge
were classified as secondary prevention,
hypertension, angina pectoris, heart
failure, or other. More details about
sampling and collection of data from the
patients medical records are available
elsewhere18.
Measurement of left ventricular ejection fraction
We measured LVEF by one of two methods:
Multiple gated-acquisition radionuclide
ventriculography (MUGA) in 129 (51%)
patients and echocardiography in 127 (49%)
patients. MUGA is a reliable reference
method, and the widely used
echocardiographic method correlates fairly
well with radionuclide imaging19,20. LVEF >
50% is considered to indicate normal left
ventricular function, while LVEF < 40%
indicates reduced function. According to
this classification we categorized LVEF as
normal (LVEF > 50%), intermediate (40-50%)
or reduced (< 40%).
Questionnaire
The questionnaire focused on HRQoL, using
the EQ-5D Index, the EQ-5D Visual Analogue
Scale (EQ-VAS), and the Kansas City
Cardiomyopathy Questionnaire (KCCQ). In
addition, we asked about subsequent cardiac
events and revascularization procedures
after hospital discharge for the index MI.
The KCCQ is a self-administered 23-item
questionnaire designed for measuring HRQoL
in patients with chronic heart failure. It
comprises six scales: Symptoms, Symptom
stability, Physical limitation, Social
limitation, Self-efficacy and Quality of
life21. Four of the scales, Symptoms,
Physical limitation, Social limitations and
Quality of life, are aggregated to an
overall score, the KCCQ clinical summary
score21. Each item is scored on a 5 to
7-point Likert scale22. Each scale score is
calculated as the mean of its item scores
and transformed to a 0-100 scale, with
higher score indicating higher level of
functioning. The KCCQ has been translated
into Norwegian, and its psychometric
properties have been documented in post MI
patients23. Change in KCCQ score of 5, 10,
and 15 points correspond with small,
moderate, and large clinical change
respectively24.
The EQ-5D is a self-administered HRQoL
instrument with 5 items: Mobility,
Self-care, Usual activities,
Pain/discomfort, and Anxiety/depression.
Each item is scored on a 3-point Likert
scale: no problems (score of 1), moderate
problems (2), and extreme problems (3).
Responses to these items can be converted to
a utility score, the EQ-5D Index, by
applying an algorithm derived from time
trade-off valuations of health status
obtained from the general population25. A
score of 1.0 represents perfect health and 0
represents dead. For the EQ-5D Index
negative utilities are possible,
representing states perceived to be worse
than dead. We used a UK time trade-off
tariff26. The EQ-5D Index has been used and
documented in post MI patients27-29. In
addition to the QE-5D Index the EQ-5D
questionnaire include the EQ-VAS, a visual
analogue scale ranging current overall
health by one single number on a scale from
0 (worst imaginable health state) to 100
(best imaginable health state)28. The EQ-VAS
has documented acceptable reliability and
validity in patients with CAD29-31.
Statistical analysis
We present descriptive statistics with means
and SDs, or proportions. For group
comparisons, we used the t-test, analysis of
variance, Kruskal-Wallis test for three
independent groups, Wilcoxon rank-sum test,
or chi-square test where appropriate.
We used multiple linear regression analysis
to identify determinants for KCCQ clinical
summary score, EQ-5D Index, and EQ-VAS at a
mean of 2.5 years after MI. To reduce
problems with multicollinearity, we checked
pairwise Pearson correlations (r) between
independent variables. However, none of the
pairwise correlations had
r > 0.70. Variables with p < 0.25 in
bivariable linear regression analysis were
included in multivariable modeling. In the
multivariable models, we first included age
at admission, sex, length of education in
years, and LVEF in the models, and then
added the other potential independent
determinant variables in a forward stepwise
fashion. In addition to age, sex, education,
and LVEF, we retained all independent
variables with p < 0.05 in multivavariable
linear regression in the final model. The
final models were checked for interactions.
The coefficient of determination (R-square)
is a measure of explained variance in
regression analysis. To determine the
marginal contribution of LVEF to R-square,
in KCCQ clinical summary score, EQ-5D Index
score, and EQ-VAS, we compared the R-square
in the final models adjusted for degrees of
freedom, with R-square in the final models
without LVEF.
We used a 5% significance level with
two-sided tests. Standard statistical
software was used for all analyses (SPSS
version 12.0, SPSS, Chicago, IL). The
Regional Committee for Medical Research
Ethics and the Norwegian Data Inspectorate
approved the study.
Demographics
Respondents (n = 408) were younger
than non-respondents (n = 140), comprised a
higher proportion of males, had less
cardiovascular morbidity at admission, and
fewer cardiovascular indications for
medication at discharge. Respondents and
non-respondents did not differ in the
proportion of patients with ST-segment
elevation at admission, Q-wave infarction,
or localization of the index MI. Respondents
who had their LVEF measured (n = 256) had
higher LVEF than non-respondents who had
their LVEF measured (n = 71) (normal,
intermediate, reduced: 65%, 22%, 13% vs 51%,
27%, 23%, p = 0.02). A more extensive
comparison of respondents and
non-respondents has been presented
elsewhere23.
Results
Respondents who had their LVEF measured (n = 256) during hospitalization for the index MI who had not (n = 152), had less cardiovascular morbidity at were younger than respondents admission, and a higher proportion were smokers. Further, a larger proportion of respondents who had their LVEF measured had ST-segment elevation MI, underwent acute revascularisation, and developed Q-wave MI, and a lower proportion had medication for angina pectoris at discharge (Table 1).
Table 1: Possible determinant
variables. |
Background variables, characteristics of the index myocardial infarction, treatment and subsequent events according to whether left ventricular ejection fraction (LVEF) was measured or not and in patients with normal (>50%), intermediate (40-50%), and reduced (<40%) LVEF. Numbers represent mean (SD) or percent.
an = 227; bn = 137; cn = 150; dn = 48; en = 29; MI, Myocardial Infarction |
Among respondents who had their h reduced LVEF were older and had increased prevalence of heart failure at admission. There was an increased prevalence of previous MI, anterior wall infarction, and use of medication on the indication heart failure with falling LVEF. Further a smaller proportion of respondents with reduced LVEF underwent acute revascularization or had subsequent percutaneous coronary intervention (Table 1).
Health-related quality of life
The mean score for all patients with LVEF
measured was 80 for the KCCQ clinical
summary scale, 0.80 for the EQ-5D Index, and
69 for the EQ-VAS. HRQoL scores differed
between patients with different levels of
LVEF both for the KCCQ clinical summary
score (p < 0.001) the EQ-5D Index (p =
0.005), and the EQ-VAS (p = 0.001) (Table
2).
Table 2: Health-related quality of life scores.
|
KCCQ clinical summary score, EQ-5D Index score, and EQ-VAS score according to left ventricular ejection fraction, mean (SD) KCCQ, Kansas City Cardiomyopathy Questionnaire; EQ-VAS, EuroQol Visual Analogue Scale . |
In multivariable linear regression analysis,
age ³ 70 years, a history of chronic
obstructive pulmonary disease (COPD),
subsequent MI, and intermediate or reduced
LVEF measured during hospitalization were
all independent determinants of lower KCCQ
clinical summary score 2.5 years after the
index MI (Table 3). Female sex, medication
for angina pectoris at discharge, and
intermediate LVEF were independent
determinants a lower EQ-5D Index score,
while a history of peripheral vascular
disease was associated with a higher EQ-5D
Index score (Table 3). Age 70 ? years, a
history of COPD, and reduced LVEF were
independent determinants of lower EQ-VAS
score (Table 3).
Table 3: Multivariable linear
regression analyses. |
Independent determinants of health-related quality of life 2.5 years after myocardial infarction in patients with left ventricular ejection fraction measured during index hospitalization. . |
In the final multivariable models, R-square
was 0.16 for both KCCQ clinical summary
score and EQ-5D Index, and 0.10 for the EQ-VAS
(Table 3). When excluding LVEF in the final
models, R-square was 0.09, 0.12, and 0.06
respectively, indicating that LVEF accounted
for 25% to 44% of the variation explained by
the final multivariable models.
One hospital measured LVEF routinely in all
MI patients, using MUGA (n = 101). When
applying our final multivariable models in
this subset of patients, the relationship
between LVEF and HRQoL was essentially the
same as in all patients with measured LVEF.
In this subset, using KCCQ clinical summary
score as the dependent variable, the
unstandardized regression coefficient (B)
and 95% confidence interval (CI) for
patients with intermediate LVEF and reduced
LVEF were -10.4 (-21.0 to 0.3) (p = 0.06)
and -13.6 (-26.9 to -0.4) (p = 0.04)
respectively. With EQ-5D Index as dependent
variable B and 95% CI were -0.13 (-0.25 to
-0.02) (p = 0.02) and -0.02 (-0.16 to 0.12)
(p = 0.7).
Discussion
In this study LVEF measured during
hospitalization for the index MI was a
determinant of HRQoL 2.5 years later, with
poorer HRQoL in patients with reduced LVEF.
This relationship persisted after adjusting
for comorbidities, sociodemographic
variables, and variables related to the
index MI. The summary score of the
condition-specific KCCQ questionnaire, which
has been validated in an earlier study23,
and the EQ-VAS showed a trend of falling
scores with falling LVEF, while the EQ-5D
Index only captured a difference between
patients with normal and intermediate LVEF.
A difference in score for the KCCQ clinical
summary score between patients with normal
LVEF and intermediate or reduced LVEF of 10
and17 points respectively, indicates a
moderate to large clinical difference
between the groups of patients with
different LVEF24.
The observed falling HRQoL scores with
falling LVEF both for KCCQ clinical summary
score and EQ-VAS indicate that the level of
systolic heart function is a determinant for
HRQoL. However, some influence from the mere
fact that an MI has occurred cannot be ruled
out since also patients with normal LVEF
tend to have reduced EQ-5D scores compared
to US norms32. If so, it is possible that
other cardiac pathophysiological mechanisms
or psychological mechanisms are involved.
An understanding of the way LVEF may
influence HRQoL can be provided from a
conceptual model outlined by Wilson and
Cleary33. In their model biological and
physiological variables influence symptoms,
that is, patients with reduced LVEF may
experience symptoms such as fatigue,
dyspnoea, and sleep disturbances. These
symptoms can in turn affect the patients
functional status, general health, and
overall quality of life. The impact on
individual patients is further modified by
psychological and socioeconomic variables33.
In our study the level of LVEF immediately
after the index MI had a statistically
significant impact on later HRQoL and in
accordance with the usual interpretation of
the KCCQ the clinical importance was
moderate to large24. However, the observed
absolute change in R-square was small
indicating that the amount of variation in
HRQoL scores explained by LVEF was moderate.
A moderate amount of variation in HRQoL
score explained by a single clinical
variable can be expected if Wilson and
Cleary s model is valid, as other
interrelated variables intervene between
pathophysiology of the heart and quality of
life33.
Three previous studies have observed an
association between LVEF and HRQoL in
patients with CAD8-10. However, two of these
studies reported on patients not comparable
to those in the present study. One reported
on patients admitted to hospital with acute
chest pain, thus including patients with
acute MI, unstable angina, and chest pain of
other reasons8. The second study presented
results from patients enrolled in a clinical
trial of thrombolysis, thus representing a
highly selected group of MI patients9. In
the third study Ecochard et al. showed that
LVEF < 46% measured by ventricular
angiography within a month after the index
MI was associated with reduced function on
the Physical mobility dimension of the
Nottingham Health Profile (NHP) assessed at
one year10. However, they did not observe
any association between LVEF and the five
other dimensions of the NHP (Energy level,
Sleep, Pain, Emotional reactions, and Social
isolation).
By contrast, we found a relationship between
LVEF and composite HRQoL scales covering
physical, emotional, and social aspects of
the HRQoL concept. Furthermore, we observed
falling HRQoL scale scores with falling LVEF
for the KCCQ clinical summary score and the
EQ-VAS. Ecochard et al. did not find a
similar fall by use of NHP, neither did we
by use of the EQ-5D Index10. The
dissimilarities might be due to the fact
that both NHP and EQ-5D Index are generic
instruments and thus supposed to be less
sensitive to smaller changes in health
status and disease severity than the
disease-specific KCCQ34.
Another reason why reduced LVEF was not
independently associated with lower EQ-5D
Index score in our study was the reduced
statistical power due to low number of
respondents with LVEF < 40%.
Studies that did not find an association
between LVEF and later HRQoL also varied
with regard to inclusion criteria and most
of them reported on selective groups of
patients and not on unselected acute MI
patients as we did12-16. One reported on
patients 65 years of age or older with
CAD12, two on clinical trials of post MI
patients with reduced LVEF13,14, and one on
patients with their first MI receiving
thrombolysis15. McBurney et al. did not
detect any difference in HRQoL between
patients with LVEF < 40% and patients with
normal and sub-normal LVEF in a patient
sample comparable to ours16. However, they
used a generic questionnaire, the short form
12 (SF-12) which probably is less sensitive
to changes in health status and disease
severity34.
In our study on MI patients, age ³ 70 years
was associated with lower KCCQ clinical
summary score. This contrasts with previous
results on heart failure patients in which
increased age independently correlated with
higher KCCQ Quality of life scale score35.
One possible explanation for this
discrepancy is that the KCCQ clinical
summery score, which we used as an HRQoL
measure in our study, is an overall scale
including, in addition to the KCCQ Quality
of life scale, scales on symptoms, physical
limitations, and social limitations. Another
possible explanation is that in our sample
of patients with previous MI, increasing age
is associated with more advanced CAD and age
might act as a surrogate for disease
severity36. This might not be the case in a
sample of patients with heart failure as the
underlying cause in younger patients with
heart failure more commonly is dilated
cardiomyopathy or other cardiomyopathies
rather than CAD35. We did not observe an
association of age with EQ-5D Index scores
even though EQ-5D Index US norms report a
small decrease in scores with increasing age
32.
We identified sex as an independent
determinant of EQ-5D Index score, but not of
KCCQ clinical summary score. A difference in
score between men and women who are
otherwise comparable might be less likely
when applying a disease specific instrument
than a generic instrument which has a
broader perspective. Thus, the EQ-5D Index
US norms have reported a small difference
between men and women with poorer score in
women32. Our observations are in agreement
with these observations.
Our study showed that the presence of COPD
was associated with reduced HRQoL after MI.
COPD and CAD share some causal risk factors,
and might to some extent present with
similar symptoms, for example dyspnoea.
Therefore, it is not surprising that
patients with COPD who suffer an MI are at
increased risk of impaired HRQoL.
Similarly, medication for angina pectoris
was associated with reduced EQ-5D Index
score, and presumably, the reason for this
is the fact that such medication reflects
enhanced disease severity. In our study the
presence of peripheral vascular disease was
associated with higher EQ-5D Index score.
However, this finding is based on only 11
patients with peripheral vascular disease,
and therefore should be interpreted with
caution.
Due to the rather long time from the MI to
measuring of HRQoL in our study, the
association between LVEF and HRQoL could
have been distorted. Although the patients
reported on intervening major cardiac
events, such as new MI or coronary
revascularization procedures, other major
life events, worsening or improvement of
illness not reported in our study, might
have had an effect on current HRQoL. We
addressed this issue by entering the time
between the index MI and HRQoL assessment as
a variable in the multivariable analyses.
This factor was not, however, independently
associated with HRQoL.
In the context of study limitations the
representativeness of the sample should be
discussed. The eligible patients were
representative of survivors of an unselected
MI population. Three quarters of the
patients responded to the survey, and LVEF
was measured in two thirds of the
respondents, thus we completed our analysis
on approximately half of the eligible
patients. This might have skewed the
representativeness. However, results from a
sub-group analysis of patients in one
hospital in which all MI patients had their
LVEF measured, were largely in line with the
overall results, indicating that the main
results pertains to unselected MI patients.
Another limitation is the uncertainty of
whether the clinicians categorizing the
indications for drugs prescribed at
discharge did assign the most important
indication for each drug, as the protocol
instructed. Cardiovascular drugs may have
more than one indication for use, and we did
not assess the reliability and validity of
this classification. However, the
classification was undertaken by experienced
physicians, most of them cardiologists
ensuring the best possible assessment.
Conclusion
LVEF measured during hospitalization for
acute MI is an independent determinant for
later HRQoL also after taking
sociodemographic and clinical variables into
account. The magnitude of the difference in
HRQoL score between patients with normal,
intermediate, and reduced LVEF was of
clinical importance. As expected, in
accordance with theoretical models, only a
moderate amount of the observed variation in
HRQoL score was explained by the level of
LVEF.
Restoration of myocardial function after an
MI is, in addition to being important for
life expectancy, also crucial for long-term
daily functioning after the event.¨
Acknowledgements:
We thank the following
physicians for participating in the study:
E. Anker, T. Dahl, H.P. D?rum, T. Gr?nvold,
J. H?rem, T. Indreb?, K. Knutsen, K.T.
Lappeg?rd, A. Mangschau, C. Platou, J.
Vegsundv?g, A. von der Lippe, K. Waage, and
A. Zalmai.
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