Literature DB >> 32410337

Prognostic impact of nutritional status and physical capacity in elderly patients with acute decompensated heart failure.

Kaori Yasumura1, Haruhiko Abe1, Yoshinori Iida1, Taishi Kato1, Masayuki Nakamura1, Chieko Toriyama1, Hiroki Nishida1, Akiko Idemoto1, Kazuya Shinouchi1, Tsuyoshi Mishima1, Masaki Awata1, Motoo Date1, Yasunori Ueda1, Masaaki Uematsu1, Yukihiro Koretsune1.   

Abstract

AIMS: Nutritional status as well as physical capacity is related to prognosis in patients with heart failure. The purpose of this study was to explore a simple prognostic indicator in patients with acute decompensated heart failure (ADHF) by including both nutritional status and physical capacity. METHODS AND
RESULTS: Patients hospitalized with ADHF (N = 203; mean age, 81 years) were enrolled. We evaluated the geriatric nutritional risk index (GNRI) on hospital admission and at discharge. A GNRI score < 92 was defined as malnutrition. Physical capacity was evaluated by simple walking test to determine if patients could walk 200 m, with a Borg scale score ≤ 13, without critical changes in vital signs. Primary endpoints were mortality and heart failure rehospitalization within 2 years. A total of 49% and 48% of patients showed malnutrition on admission and at discharge, respectively. Malnutrition at discharge was more strongly related to mortality [hazard ratio (HR) 3.382, 95% confidence interval (CI) 1.900-6.020, P < 0.0001)] than that on admission (HR 2.448, 95% CI 1.442-4.157, P = 0.001) by univariable analysis. Malnutrition at discharge was related to mortality (HR 2.370, 95% CI 1.166-4.814, P = 0.02), but malnutrition on admission was not related (HR 1.538, 95% CI 0.823-2.875, P = 0.18) by multivariable analysis. Almost half of patients (45%) could not walk 200 m, which was significantly related to mortality by univariable analysis (HR 3.303, 95% CI 1.905-5.727, P < 0.0001), but was not by multivariable analysis (HR 1.990, 95% CI 0.999-3.962, P = 0.05). The combined index including both GNRI and simple walking test was an independent and stronger predictor of mortality than either index alone by multivariable analysis (HR 2.249, 95% CI 1.362-3.716, P < 0.01). Neither malnutrition nor low physical capacity was related to heart failure rehospitalization by univariable analysis (HR 0.702, 95% CI 0.483-1.020, P = 0.06; HR 1.047, 95% CI 0.724-1.515, P = 0.81, respectively). Malnutrition at discharge significantly reduced heart failure rehospitalization by multivariable analysis (HR 0.431, 95% CI 0.266-0.698, P < 0.01). When patients were classified into Group G (both nutritional status and physical capacity at discharge were good), Group E (either was good), and Group B (both were bad), mortality rates were significantly different among the groups (log rank P < 0.0001).
CONCLUSION: A simple indicator including both nutritional status and physical capacity may predict 2 year mortality in elderly patients with ADHF.
© 2020 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology.

Entities:  

Keywords:  Acute decompensated heart failure; Elderly patients; Geriatric nutritional risk index; Simple walking test

Mesh:

Year:  2020        PMID: 32410337      PMCID: PMC7373881          DOI: 10.1002/ehf2.12743

Source DB:  PubMed          Journal:  ESC Heart Fail        ISSN: 2055-5822


Introduction

Malnutrition and reduced physical capacity are common in elderly patients with heart failure, and both have been associated with adverse outcomes. , Malnutrition exists in 20–42% of patients with heart failure. , Heart failure causes a low nutritional status due to malabsorption by intestinal oedema and hyperpermeability, along with anorexia, increased energy consumption, and anabolism. According to the cycle of frailty, malnutrition leads to sarcopenia. At the same time, reduced physical capacity occurs as a result of sarcopenia and frailty. , , However, the prognostic impact of an index incorporating both nutritional status and physical capacity in elderly patients with acute decompensated heart failure (ADHF) remains unknown. The purpose of this study was to explore a clinically feasible prognostic indicator in these patients by incorporating both nutritional status and physical capacity.

Methods

Subjects and study protocol

This retrospective and observational study enrolled 203 consecutive patients with ADHF at the National Hospital Organization Osaka National Hospital between April 2015 and January 2017. The investigation conformed to the principles outlined in the Declaration of Helsinki, and the National Hospital Organization Osaka National Hospital Institutional Review Board #2 approved the protocol (Approval No. 18026). Acute decompensated heart failure was defined as the rapid onset or worsening of clinical symptoms/signs of congestion and/or peripheral hypoperfusion according to European Society of Cardiology guidelines. We excluded 26 patients who did not undergo cardiac rehabilitation because their condition was serious at the time of admission; all 26 died during hospitalization. We also excluded patients in whom we could not calculate the geriatric nutritional risk index (GNRI) or if medical records had insufficient data. We evaluated GNRI at hospital admission and at discharge. A GNRI score < 92 was defined as a high risk of malnutrition. We performed simple walking test (SWT) at discharge. SWT <200 m was defined as reduced physical capacity. We also classified patients into three groups: Group G (both nutritional status and physical capacity at discharge were good), Group E (either variable was good), and Group B (both variables were bad) (Figure ). Patients were followed up until 1 September 2019. Survival data were obtained by physicians at the hospital or in the outpatient setting. The clinical endpoints were all‐cause mortality and heart failure rehospitalization within 2 years of discharge.
Figure 1

Study population. We divided patients into the three groups: Group G (both nutritional status and physical capacity at discharge were good), Group E (either variable was good), and Group B (both variables were bad).

Study population. We divided patients into the three groups: Group G (both nutritional status and physical capacity at discharge were good), Group E (either variable was good), and Group B (both variables were bad). We classified baseline heart diseases into dilated cardiomyopathy, hypertrophic cardiomyopathy, hypertensive heart disease, ischemic cardiomyopathy, valvular diseases, and other (sarcoidosis, amyloidosis, and cardiomyopathy based on arrhythmia). Each diagnosis was made by a cardiologist. Patients with more than moderate regurgitation and stenosis in the mitral or the aortic valves were classified as having valvular heart disease. Comorbidities were assessed based on medical records. Standard laboratory tests were assessed on hospital admission and at discharge. Echocardiography was performed at discharge. Left ventricular ejection fraction (EF) was evaluated by the modified Simpson method for patients with segmental asynergy and by the Teichholz method for patients without segmental asynergy. We also checked the number of previous hospitalizations for heart failure from medical records.

Nutritional assessment

Nutritional status was assessed by the GNRI. GNRI was calculated as 14.89 × serum albumin (g/dL) + 41.7 ×  [present body weight (kg)/height (m)2]/22 = 14.89 × serum albumin (g/dL) + 41.7 × body mass index (BMI)/22. A GNRI score ≥ 98 was considered normal, a score ≥92 to <98 represented a low risk of malnutrition, ≥82 to <92 represented a moderate risk, and <82 represented a severe risk. We defined patients with a GNRI score < 92 as the high‐risk nutritional group and those with a GNRI score ≥ 92 as the low‐risk nutritional group according to earlier reports. ,

Simple walking test

We evaluated physical capacity and ambulatory status according to SWT during cardiac rehabilitation. Patients hospitalized due to ADHF expanded their levels of activity using the following protocol: patients started with a stepping exercise. If a patient could step more than 20 times without critical changes in vital signs and with a Borg scale ≤13 for leg fatigue and shortness of breath, they were considered to have passed the activity level. The Borg scale is a simple method to evaluate subjective symptoms. Cardiac rehabilitation exercises in which patients perform exercise with a low to moderate intensity and achieve a Borg scale score of 11–13. , The next level of activity was walking in the patient room, and each time the patient passed the SWT, we gradually extended the walking distance to 50, 100, and 200 m. When they would walk 200 m without resting or critical changes in vital signs and with a Borg scale ≤13 regardless of speed, patients proceeded to bicycle ergometer exercise.

Statistical analysis

Continuous data are expressed as mean ± standard deviation (SD). Independent samples t‐tests were used for comparison of continuous variables, and χ 2 tests were used for categorical variables. Cox hazard univariable and multivariable analyses were performed to assess the predictive value of GNRI and SWT for all‐cause mortality and heart failure rehospitalization. For Cox hazard analysis of the combined index including both GNRI and SWT, analysis was performed with Groups B, E, and G as continuous variables 0, 1, and 2. The multivariable analysis model included well‐established major confounders, such as age, brain natriuretic peptide (BNP), haemoglobin, and C‐reactive protein. Event‐free survival after discharge was estimated using the Kaplan–Meier analysis and compared using the log‐rank test. A P value <0.05 was considered statistically significant. All statistical analyses were performed using MedCalc (version 18.2.1, Ostend, Belgium).

Results

A total of 203 patients were enrolled. Median follow‐up period was 948 days [interquartile range (IQR): 493–1195]. Twenty patients dropped out during follow‐up within 2 years from discharge. Mean GNRI on admission was 99 ± 12, and 49% patients had a GNRI score < 92. Mean BMI and albumin on admission were higher than that at discharge (mean BMI; 23.4 ± 5.1 vs. 21.5 ± 4.8 kg/m2, P < 0.0001, mean albumin; 3.7 ± 0.5 vs. 3.5 ± 0.5 g/l, P < 0.0001). On admission, mean BNP was 813 ± 941 pg/mL, mean haemoglobin was 11.3 ± 2.0 g/dL, mean estimated glomerular filtration rate (eGFR) was 41 ± 19 mL/min/1.73m2, and mean C‐reactive protein was 1.01 ± 5.06 mg/dL. Table shows the clinical characteristics of the patients. Patient mean age was 81 years, and there were 126 men (62%). EF was 50 ± 17%, and mean BNP was 276 pg/mL at discharge. A total of 85% of patients had chronic kidney disease (eGFR <60 mL/min/1.73m2) with an mean eGFR of 39 mL/min/1.73m2. Mean GNRI score at discharge was 93 ± 12, and 48% of patients had a GNRI score < 92. In the group with a GNRI score < 92 at discharge, the mean age was older, mean BNP and C‐reactive protein were higher, and mean haemoglobin was lower than the group with GNRI score ≥ 92 (P < 0.01). At discharge, 92 patients (45%) could not walk 200 m. In the group with SWT <200 m, the mean age was older (P < 0.01), mean BMI and haemoglobin were lower (P = 0.01, P < 0.01, respectively), mean EF and C‐reactive protein were higher (P = 0.03, P < 0.01, respectively), and more patients had chronic obstructive pulmonary disease when compared with the group with SWT ≥200 m (P = 0.01). Additionally, the group with SWT <200 m had a higher incidence of past hospitalizations for heart failure than the group with SWT ≥200 m (P < 0.01).
Table 1

Patient characteristics

VariablesTotal cohortGNRI <92GNRI ≥92 P valueSWT <200 mSWT ≥200 m P value
(n = 203)(n = 97)(n = 106)(n = 92)(n = 111)
Age (years)81 ± 984 ± 779 ± 9<0.0184 ± 1078 ± 9<0.01
Men (%)6252680.0252680.03
BMI (kg/m2)21.5 ± 4.818.5 ± 2.524.2 ± 4.7<0.0120.5 ± 4.822.3 ± 4.60.01
Comorbidities
Atrial fibrillation (%)4547420.4947420.53
Hypertension (%)6859750.0264700.35
Diabetes mellitus (%)3330360.3528380.15
COPD (%)9780.751340.01
DCM (%)8770.832110.02
HCM (%)5370.17550.99
HHD (%)3735370.7730410.11
ICM (%)2319250.2724210.59
Valvular disease (%)3240230.0133300.66
Other (%)2121220.7820220.71
Medication
ACEi/ARB (%)5955610.4549660.02
Beta blockers (%)6667630.5555720.01
Diuretics (%)9493930.9695910.33
Pimobendan (%)2529200.1130190.06
Laboratory variables
BNP (pg/mL)276 ± 334354 ± 434207 ± 186<0.01324 ± 416237 ± 2420.07
Haemoglobin (g/dL)11.5 ± 1.910.7 ± 1.712.1 ± 1.9<0.0111.0 ± 1.911.9 ± 1.8<0.01
Urea (mg/dL)32 ± 1632 ± 1532 ± 170.8333 ± 1531 ± 170.31
eGFR (mL/min/1.73m2)39 ± 1741 ± 1838 ± 170.1538 ± 1839 ± 190.79
Sodium (mEq/L)139 ± 6138 ± 8139 ± 50.50139 ± 4138 ± 80.27
C‐reactive protein (mg/dL)0.44 ± 0.710.59 ± 0.910.32 ± 0.44<0.010.59 ± 0.890.31 ± 0.49<0.01
Albumin (g/L)3.5 ± 0.53.3 ± 0.403.8 ± 0.36<0.013.4 ± 0.53.7 ± 0.4<0.01
Lymphocytes (mm3)1533 ± 5571373 ± 5131677 ± 558<0.011418 ± 5141628 ± 575<0.01
Echocardiography indices
EF (%)50 ± 1749 ± 1752 ± 180.2554 ± 1748 ± 170.03
LVDd (mm)52 ± 951 ± 953 ± 90.3251 ± 1053 ± 80.09
LVMI (g/m2)135 ± 49135 ± 45135 ± 520.97142 ± 60130 ± 390.17
RWT0.38 ± 0.100.37 ± 0.100.39 ± 0.100.200.39 ± 0.130.37 ± 0.070.37
E/A0.96 ± 0.700.88 ± 0.631.02 ± 0.770.390.81 ± 0.371.05 ± 0.840.12
E/E'17 ± 817 ± 817 ± 70.8119 ± 816 ± 70.08
TrPG (mmHg)30 ± 1229 ± 1031 ± 140.3132 ± 1129 ± 130.33
Prior HF hospitalizations (≥3 times) (%)3741340.304927<0.01

ACEi, angiotensin‐converting‐enzyme inhibitor; ARB, angiotensin II receptor blocker; BMI, body mass index; BNP, brain natriuretic peptide; COPD, chronic obstructive pulmonary disease; DCM, dilated cardiomyopathy; EF, ejection fraction; eGFR, estimate glomerular filtration rate; GNRI, geriatric nutritional risk index; HCM, hypertrophic cardiomyopathy; HF, heart failure; HHD, hypertensive heart failure; ICM, ischemic cardiomyopathy; LVDd, left ventricular end diastolic diameter; LVMI, left ventricular mass index; RWT, relative wall thickness; SWT, simple walking test.

Patient characteristics ACEi, angiotensin‐converting‐enzyme inhibitor; ARB, angiotensin II receptor blocker; BMI, body mass index; BNP, brain natriuretic peptide; COPD, chronic obstructive pulmonary disease; DCM, dilated cardiomyopathy; EF, ejection fraction; eGFR, estimate glomerular filtration rate; GNRI, geriatric nutritional risk index; HCM, hypertrophic cardiomyopathy; HF, heart failure; HHD, hypertensive heart failure; ICM, ischemic cardiomyopathy; LVDd, left ventricular end diastolic diameter; LVMI, left ventricular mass index; RWT, relative wall thickness; SWT, simple walking test. Table shows data on patients on passing the activity level on the SWT. There were 10 patients with a severely low physical capacity, including four patients who were unable to walk. A total of 111 patients passed the 200 m walk. Mean time between admission and starting rehabilitation was 4 ± 3 days; rehabilitation was continued until discharge. Mean total length of hospitalization was 24 ± 14 days.
Table 2

Passing the activity level on the simple walking test

n Age (years)Men (%)GNRIEF (%)Hb (g/dL)
Walking within room1088 ± 42076 ± 947 ± 1710.9 ± 3.2
Walking within 50 m1786 ± 75387 ± 1055 ± 1510.9 ± 1.7
Walking within 100 m2385 ± 75294 ± 1354 ± 2210.7 ± 1.4
Walking within 200 m4284 ± 76092 ± 1254 ± 1511.2 ± 1.9
Walking over 200 m11178 ± 96897 ± 1148 ± 1711.9 ± 1.8

GNRI, geriatric nutritional risk index; EF, ejection fraction; Hb, haemoglobin..

Passing the activity level on the simple walking test GNRI, geriatric nutritional risk index; EF, ejection fraction; Hb, haemoglobin.. All‐cause death occurred in 58 patients within 2 years of discharge, including cardiovascular death (n = 17; 14 heart failure, 2 cerebral haemorrhage, 1 aortic dissection) and non‐cardiovascular death (n = 41; 19 infection, 6 senility, 2 haemorrhagic shock, 14 unknown). Heart failure rehospitalization occurred in 115 patients. Table shows findings on the univariable and multivariable Cox hazard analysis for mortality adjusted for the combined index, age, BNP, haemoglobin, and C‐reactive protein. Only the combined index was an independent predictor of all‐cause mortality [hazard ratio (HR) 2.249, 95% confidence interval (CI) 1.362–3.716, P < 0.01)].
Table 3

Univariable and multivariable Cox hazard model for mortality

Univariable analysisMultivariable analysis
HR (95% CI) P valueHR (95% CI) P value
Age (years)1.071 (1.033–1.109)<0.011.024 (0.979–1.072)0.31
BNP (pg/mL)1.001 (1.000–1.001)<0.011.001 (0.999–1.001)0.13
Haemoglobin (g/dL)0.803 (0.695–0.928)<0.010.954 (0.811–1.123)0.57
C‐reactive protein (mg/dL)1.310 (0.980–1.751)0.071.144 (0.839–1.561)0.39
combined index (GNRI + SWT)3.005 (2.051–4.404)<0.00012.249 (1.362–3.716)<0.01

BNP, brain natriuretic peptide; CI, confidence interval; GNRI, geriatric nutritional risk index; HR, hazard ratio; SWT, simple walking test.

Univariable and multivariable Cox hazard model for mortality BNP, brain natriuretic peptide; CI, confidence interval; GNRI, geriatric nutritional risk index; HR, hazard ratio; SWT, simple walking test. Table shows Cox hazard univariable and multivariable analysis for mortality and heart failure rehospitalization adjusted for age, BNP, haemoglobin, and C‐reactive protein. A GNRI score < 92 at discharge was more strongly related to mortality (HR 3.382, 95% CI 1.900–6.020, P < 0.0001) than that on admission (HR 2.448, 95% CI 1.442–4.157, P = 0.001) by univariable analysis. GNRI score < 92 at discharge was related to mortality (HR 2.370, 95% CI 1.166–4.814, P = 0.02), but the score on admission was not related (HR 1.538, 95% CI 0.823–2.875, P = 0.18) by multivariable analysis. SWT <200 m and the combined index including both GNRI and SWT were also significantly related to mortality by univariable analysis (HR 3.303, 95% CI 1.905–5.727, P < 0.0001; HR 3.005, 95% CI 2.051–4.404, P < 0.0001, respectively). The combined index was a stronger predictor of the prognosis than either index alone by multivariable analysis (HR 2.249, 95% CI 1.362–3.716, P < 0.01). On the other hand, neither GNRI score < 92 nor SWT <200 m at discharge was related to heart failure rehospitalization by univariable analysis (HR 0.702, 95% CI 0.483–1.020, P = 0.06; HR 1.047, 95% CI 0.724–1.515, P = 0.81, respectively). Furthermore, GNRI score < 92 at discharge reduced heart failure rehospitalization by multivariable analysis (HR 0.431, 95% CI 0.266–0.698, P < 0.01).
Table 4

Cox hazard model for mortality and heart failure rehospitalization

Univariable analysisMultivariable analysis
HR (95% CI) P valueHR (95% CI) P value
Mortality (n = 58)
GNRI < 92 at admission2.448 (1.442–4.157)0.0011.538 (0.823–2.875)0.18
GNRI < 92 at discharge3.382 (1.900–6.020)<0.00012.370 (1.166–4.814)0.02
SWT < 200 m3.303 (1.905–5.727)<0.00011.990 (0.999–3.962)0.05
Combined index (GNRI + SWT)3.005 (2.051–4.404)<0.00012.249 (1.362–3.716)<0.01
Rehospitalization (n = 115)
GNRI < 92 at admission0.776 (0.518–1.161)0.220.585 (0.362–0.946)0.03
GNRI < 92 at discharge0.702 (0.483–1.020)0.060.431 (0.266–0.698)<0.01
SWT < 200 m1.047 (0.724–1.515)0.810.950 (0.617–1.464)0.82
Combined index (GNRI + SWT)0.859 (0.660–1.118)0.260.673 (0.488–0.927)0.02

The multivariable analysis model included age, brain natriuretic peptide, haemoglobin and C‐reactive protein.

BNP, brain natriuretic peptide; CI, confidence interval; GNRI, geriatric nutritional risk index; HR, hazard ratio; SWT, simple walking test.

Cox hazard model for mortality and heart failure rehospitalization The multivariable analysis model included age, brain natriuretic peptide, haemoglobin and C‐reactive protein. BNP, brain natriuretic peptide; CI, confidence interval; GNRI, geriatric nutritional risk index; HR, hazard ratio; SWT, simple walking test. Figure shows the Kaplan–Meier survival analysis for all‐cause mortality among the three groups. The 2 year mortality rate of Group G (both nutritional status and physical capacity at discharge were good) was 9%, that of Group E (either variable was good) was 27%, and that of Group B (both variables were bad) was 57%. Mortality rates were significantly different among the groups (log rank P < 0.0001).
Figure 2

Kaplan–Meier curves for survival probability among the three groups. Group G, both nutritional status and physical capacity at discharge were good; Group E, either variable was good; Group B, both variables were bad.

Kaplan–Meier curves for survival probability among the three groups. Group G, both nutritional status and physical capacity at discharge were good; Group E, either variable was good; Group B, both variables were bad.

Discussion

The results from this study indicate that (i) malnutrition and reduced physical capacity were frequently observed in elderly patients with ADHF; (ii) malnutrition and reduced physical capacity were predictors of all‐cause mortality; (iii) the combined index incorporating both nutritional status and physical capacity was an independent predictor of prognosis in elderly patients with ADHF, and it was a stronger predictor than either index alone.

Nutritional status

In our study, 48% of patients had malnutrition (GNRI <92) at discharge. This ratio was similar to that reported in an earlier study. The Academy of Nutrition and Dietetics and American Society for Parenteral and Enteral Nutrition and the European Society of Clinical Nutritional and Metabolism recommend that a diagnosis of malnutrition should not be made based on biochemical data, because inflammation is considered the major reason for reduced serum albumin. , They reported that the relevance of laboratory tests of acute phase protein levels as indicators of malnutrition is limited. , In this study, GNRI was calculated using albumin; thus, a low GNRI score may not represent only malnutrition. In fact, C‐reactive protein in group with GNRI score < 92 was higher than that of GNRI score ≥ 92. Malnutrition in heart failure has been related to cardiac cachexia. Mechanisms of cardiac cachexia are multifactorial, involving neurohormonal disorders, overexpression of proinflammatory cytokines, increased oxidative stress, and an imbalance between anabolic and catabolic states. Diagnostic criteria of cardiac cachexia from the Cachexia Consensus Working Group include elevated C‐reactive protein and decreased haemoglobin. In our study, inflammation and anaemia were found in the group with a GNRI score < 92. Malnutrition was related to mortality in this study, which is similar to findings in another study. One study used data on admission for the measurement of GNRI, and another study used data at discharge for GNRI. Thus, in terms of nutritional status on admission and at discharge in these studies, it was unclear which value was more relevant in the prediction of mortality. We assessed GNRI on admission and at discharge in this study and showed that malnutrition at discharge was more strongly related to mortality than that on admission. In one study, malnutrition was related not only to the mortality but also to heart failure rehospitalization. However, in our study, malnutrition reduced heart failure rehospitalization by multivariable analysis. Several factors could explain these findings. For example, it is possible that patients without malnutrition in this study did not comply with salt and water restrictions, which are a common cause of heart failure rehospitalization in patients with chronic heart failure. Alternatively, many patients with malnutrition died from non‐cardiovascular events. In addition, patient characteristics may also be different from the earlier studies. In fact, many old patients with advanced renal dysfunction were included in this study.

Physical capacity

Almost half of patients (45%) could not walk 200 m mostly because of sarcopenia and sometimes because of tachycardia and hypoxia. In patients with chronic obstructive pulmonary disease, dyspnoea and hypoxia were the main causes of inability to walk 200 m. Patients with heart failure commonly report reduced physical capacity, and reduced physical capacity in patients with heart failure has been associated with worse prognosis. Peak oxygen uptake on the cardiopulmonary exercise test (CPX) is the gold standard for the assessment of exercise capacity. However, the CPX is not always applicable to patients with ADHF, especially during hospitalization. The walking test is useful to evaluate physical capacity in such conditions, because there is no need for special equipment, and it is applicable to all patients even if they cannot perform the ergometer exercise because of extremely decreased exercise capacity. The 6‐min walking test (6MWT) is a widely used measure of physical capacity, and it was reported that the 6MWT provides prognostic utility comparable with the CPX. Curtis et al. showed that a 6MWT score < 200 m could identify patients with heart failure who are at markedly increased risk of death. In our study, we performed SWT, and we showed that SWT <200 m predicted mortality. However, inability to walk 200 m was not related to heart failure rehospitalization. Patients with inability to walk 200 m had significantly more heart failure hospitalizations in the past than those who could walk more than 200 m. It is well known that repeated hospitalizations lead to gradual loss of physical capacity and death. Many patients who were unable to walk 200 m had repeated hospitalizations for heart failure before admission, and had likely reached the end stage of heart failure.

Nutritional status and physical capacity

Only the combined index including both GNRI and SWT was an independent predictor of all‐cause mortality in the multivariable Cox hazard analysis, after adjustment for other parameters reported to predict heart failure mortality in a previous study. We showed that the combined index including both GNRI and SWT was a stronger predictor of the prognosis than either index alone. Group G (both nutritional status and physical capacity at discharge were good) showed the lowest mortality among the groups. It is interesting to speculate that achievement of a GNRI score ≥ 92 and the ability to walk 200 m at discharge may reduce mortality in these patients. Further prospective studies are needed to confirm these findings.

Limitations

First, this is a single‐centre study with a limited sample size. Second, our study population included only elderly patients with heart failure. Therefore, further research is needed to determine if results can be extended to a younger population. Third, we did not examine sex differences, which might have an impact on prognosis, particularly in elderly patients with heart failure with preserved EF. Fourth, this study was a retrospective and observational study. Thus, it is not clear whether interventions for nutrition status and physical capacity improve prognosis.

Conclusions

It was feasible to perform both GNRI and SWT in elderly patients with ADHF. The simple indicator including both nutritional status and physical capacity may predict 2 year mortality in elderly patients with ADHF.

Conflict of interest

Haruhiko Abe has received grants from Nippon Boehringer Ingelheim. Yasunori Ueda has received grants from Nihon Kohden. Masaaki Uematsu has received grants from Nippon Boehringer Ingelheim, Daiichi Sankyo Co Ltd. Yukihiro Koretsune has received remuneration from Daiichi Sankyo Co Ltd. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Funding

None.
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Authors:  T Cederholm; I Bosaeus; R Barazzoni; J Bauer; A Van Gossum; S Klek; M Muscaritoli; I Nyulasi; J Ockenga; S M Schneider; M A E de van der Schueren; P Singer
Journal:  Clin Nutr       Date:  2015-03-09       Impact factor: 7.324

7.  Prognostic value of simple frailty and malnutrition screening tools in patients with acute heart failure due to left ventricular systolic dysfunction.

Authors:  S Sze; J Zhang; P Pellicori; D Morgan; A Hoye; A L Clark
Journal:  Clin Res Cardiol       Date:  2017-02-15       Impact factor: 5.460

8.  Sarcopenia in Asia: consensus report of the Asian Working Group for Sarcopenia.

Authors:  Liang-Kung Chen; Li-Kuo Liu; Jean Woo; Prasert Assantachai; Tung-Wai Auyeung; Kamaruzzaman Shahrul Bahyah; Ming-Yueh Chou; Liang-Yu Chen; Pi-Shan Hsu; Orapitchaya Krairit; Jenny S W Lee; Wei-Ju Lee; Yunhwan Lee; Chih-Kuang Liang; Panita Limpawattana; Chu-Sheng Lin; Li-Ning Peng; Shosuke Satake; Takao Suzuki; Chang Won Won; Chih-Hsing Wu; Si-Nan Wu; Teimei Zhang; Ping Zeng; Masahiro Akishita; Hidenori Arai
Journal:  J Am Med Dir Assoc       Date:  2014-02       Impact factor: 4.669

9.  Cachexia: a new definition.

Authors:  William J Evans; John E Morley; Josep Argilés; Connie Bales; Vickie Baracos; Denis Guttridge; Aminah Jatoi; Kamyar Kalantar-Zadeh; Herbert Lochs; Giovanni Mantovani; Daniel Marks; William E Mitch; Maurizio Muscaritoli; Armine Najand; Piotr Ponikowski; Filippo Rossi Fanelli; Morrie Schambelan; Annemie Schols; Michael Schuster; David Thomas; Robert Wolfe; Stefan D Anker
Journal:  Clin Nutr       Date:  2008-08-21       Impact factor: 7.324

10.  Geriatric nutritional risk index predicts functional dependency and mortality in patients with heart failure with preserved ejection fraction.

Authors:  Yoshiharu Kinugasa; Masahiko Kato; Shinobu Sugihara; Masayuki Hirai; Kensaku Yamada; Kiyotaka Yanagihara; Kazuhiro Yamamoto
Journal:  Circ J       Date:  2012-11-25       Impact factor: 2.993

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  7 in total

1.  Prognostic value of DCTA scoring system in heart failure.

Authors:  Tian-Jun Zhao; Qian-Kun Yang; Li-Dan Bi; Jie Li; Chun-Yu Tan; Zhi-Lin Miao
Journal:  Herz       Date:  2020-10-21       Impact factor: 1.443

2.  Association Between Prognostic Nutritional Index and Prognosis in Patients With Heart Failure: A Meta-Analysis.

Authors:  Mei-Yu Chen; Jiang-Xiong Wen; Mei-Ting Lu; Xiang-Yu Jian; Xiao-Liang Wan; Zhi-Wen Xu; Jian-Qiu Liang; Jian-Di Wu
Journal:  Front Cardiovasc Med       Date:  2022-06-10

3.  Prognostic Value of Geriatric Nutritional Risk Index in Esophageal Carcinoma: A Systematic Review and Meta-Analysis.

Authors:  Jianfeng Zhou; Pinhao Fang; Xiaokun Li; Siyuan Luan; Xin Xiao; Yinmin Gu; Qixin Shang; Hanlu Zhang; Yushang Yang; Xiaoxi Zeng; Yong Yuan
Journal:  Front Nutr       Date:  2022-03-25

4.  Appetite loss at discharge from acute decompensated heart failure: Observation from KCHF registry.

Authors:  Erika Yamamoto; Takao Kato; Hidenori Yaku; Takeshi Morimoto; Yasutaka Inuzuka; Yodo Tamaki; Neiko Ozasa; Yusuke Yoshikawa; Takeshi Kitai; Ryoji Taniguchi; Moritake Iguchi; Masashi Kato; Mamoru Takahashi; Toshikazu Jinnai; Tomoyuki Ikeda; Kazuya Nagao; Takafumi Kawai; Akihiro Komasa; Ryusuke Nishikawa; Yuichi Kawase; Takashi Morinaga; Mitsunori Kawato; Yuta Seko; Masayuki Shiba; Mamoru Toyofuku; Yutaka Furukawa; Yoshihisa Nakagawa; Kenji Ando; Kazushige Kadota; Satoshi Shizuta; Koh Ono; Yukihito Sato; Koichiro Kuwahara; Takeshi Kimura
Journal:  PLoS One       Date:  2022-05-05       Impact factor: 3.752

5.  Prognostic impact of nutritional status and physical capacity in elderly patients with acute decompensated heart failure.

Authors:  Kaori Yasumura; Haruhiko Abe; Yoshinori Iida; Taishi Kato; Masayuki Nakamura; Chieko Toriyama; Hiroki Nishida; Akiko Idemoto; Kazuya Shinouchi; Tsuyoshi Mishima; Masaki Awata; Motoo Date; Yasunori Ueda; Masaaki Uematsu; Yukihiro Koretsune
Journal:  ESC Heart Fail       Date:  2020-05-14

6.  Relationship between Nutritional Status and Clinical and Biochemical Parameters in Hospitalized Patients with Heart Failure with Reduced Ejection Fraction, with 1-year Follow-Up.

Authors:  Marta Kałużna-Oleksy; Helena Krysztofiak; Jacek Migaj; Marta Wleklik; Magdalena Dudek; Izabella Uchmanowicz; Maciej Lesiak; Ewa Straburzyńska-Migaj
Journal:  Nutrients       Date:  2020-08-04       Impact factor: 5.717

7.  Prognostic Value of the Geriatric Nutritional Risk Index in Non-Small Cell Lung Cancer Patients: A Systematic Review and Meta-Analysis.

Authors:  Haoyu Wang; Cui Li; Ruiyuan Yang; Jing Jin; Dan Liu; Weimin Li
Journal:  Front Oncol       Date:  2022-01-18       Impact factor: 6.244

  7 in total

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