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Patient-level comparison of heart failure patients in clinical phenotype and prognosis from China and Sweden

Abstract

Background

Clinical phenotype and prognosis of heart failure (HF) may be variable among different racial populations. Therefore, a patient-level comparison of hospitalized HF patients in two university hospitals from China and Sweden was performed.

Methods and results

This study was a pooled data analysis of the patients prospectively enrolled in two single-center studies in China (n = 949) and Sweden (n = 1639) from 2011 to 2015. Clinical characteristics and 6-month all-cause mortality were collected. Higher systolic blood pressure (126.1 ± 20.3 vs. 114.2 ± 15.4 mmHg, p < 0.001) and NT-proBNP level (4540 vs. 3251 pg/mL, p = 0.013) were found in the Swedish cohort, also more patients with ischemic heart disease (32.0% vs. 19.2%), hypertension (64.2% vs. 36.8%), valvular heart disease (40.9% vs.31.6%) and atrial fibrillation (55.3% vs. 39.6%) (all p < 0.001). The use of ACEIs/ARBs (48.8% vs. 80.8%) or beta-blockers (58.8% vs. 86.5%) (both p < 0.001) was lower in Chinese cohort. Given younger age in Chinese cohort (61.6 vs. 76.4 years, p < 0.001), age-stratified analyses were conducted, as there were similar patient numbers in 50–74 years in Chinese (n = 550) and Swedish (n = 554) cohorts, therefore baseline characteristics and prognosis were further compared. The age- and sex-adjusted outcome (HR 0.80 [95% CI 0.55–1.19], p = 0.273) was comparable between the two populations. The NT-proBNP and eGFR independently predicted 6-month mortality in both Chinese (HR [95% CI] 1.006 [1.003–1.008], 0.986 [0.976–0.999]) and Swedish cohort (1.003 [1.000–1.007], 0.988 [0.976–0.999]).

Conclusions

Patient-level comparison of real-world HF populations from China and Sweden demonstrated different clinical phenotypes and therapy but similar prognosis and their predictors.

Peer Review reports

Introduction

Heart failure (HF) is a major worldwide health problem with a prevalence estimated to 0.9% in China [1] and even higher in European countries (1.5–2%) [2]. Although guideline-directed therapy has now been proven to reduce mortality and morbidity [3], HF remains the leading cause of hospitalization with a rate of death varying from about 10% after 1 year to about 50% after 5 years from diagnosis [4]. Therefore, it is a global public health concern and places a significant economic burden on the health care system in both developed and developing countries [5, 6].

Epidemiology, clinical profile, management and prognosis of HF have been well described in a number of clinical trials [7,8,9,10] and large registries [11,12,13,14,15,16] performed in developed countries like North America and Europe, however, there is limited information derived from the Chinese HF population [17,18,19,20,21,22]. Few data have suggested regional and ethnic heterogeneity between China and Western countries [23], and to what extent such discrepancies contribute to prognosis of HF patients in a real-world clinical setting remains largely unexplored. Therefore, we compared hospitalized HF patients of two single-center registries from China and Sweden, with regard to clinical characteristics, HF therapy and prognosis.

Methods

Study design, setting and populations

This study was a pooled data analysis of two different ethnic groups. The study population consisted of patients from two HF registries, one in China and the other in Sweden. The former was conducted in a large tertiary referral hospital in China (West China Hospital, Sichuan University, Chengdu), while the latter was established in a leading hospital (Sahlgrenska University Hospital/Östra Hospital, Sweden) of the Swedish Heart Failure Registry (SwedeHF) [24]. The two registries complied with the 2008 Declaration of Helsinki and were approved by the Chinese Ethics Committee of Registering Clinical Trials (West China Hospital) and the Ethics Committees of the University of Gothenburg. Informed consent was obtained from all participants or, if participants were dead, from a next of kin and/or legal guardian. Patients aged ≥ 18 years old hospitalized for HF were enrolled in the registries according to the diagnostic criteria of the guidelines prevailing at that time, without specific exclusion criteria. Only those who underwent coronary artery revascularization and valve intervention during the indexed hospitalization failed to be included in the Chinese registry. Both registries recorded variables regarding patient characteristics and therapy at discharge and prognosis at follow-up. As the overlapping period of enrollment in the two registries was from December, 2011 to December, 2015, patients registered within that time were selected for the current study.

Data collection

Variables included in both cohorts were matched based on unified definitions according to existing guidelines at the time of patient enrollment. Variables with more than 25% missing values were excluded.

The study population was divided into two subgroups with left ventricular ejection fraction (LVEF) either < 40% (HFrEF) or ≥ 40% (non-HFrEF) due to two reasons: 1) only in those with LVEF < 40% there are evidence-based lifesaving therapy, and 2) there was no uniform definition of those patients with HF with LVEF ≥ 40% during the study period. When the study was initiated in 2011, a preserved left ventricular ejection fraction (LVEF) was defined as > 40–50% [25] until 2012 thereafter LVEF was set to ≥ 50% and renamed uniformly as HFpEF [26]. Blood pressure was recorded in the right arm in the sitting position by a mercury sphygmomanometer, and heart rate was measured by 12-lead electrocardiography (ECG) in the supine position. Anemia was defined as hemoglobin level < 12 g/dL in women and < 13 g/dL in men [27]. The Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation was used to calculate the estimated glomerular filtration rate (eGFR), while renal dysfunction was defined as eGFR ≤ 60 ml/min/1.73m2 [28].

Follow up and end-points

All patients were followed-up for at least 6 months, and the primary outcome measure was 6-month all-cause mortality. It was obtained by phone call and/or review of the medical record in the Chinese cohort, whereas by the automatic linking of SwedeHF with the Cause of Death Registry of the National Board of Health and Welfare of Sweden every month in the Swedish cohort.

Statistical analyses

Normally distributed continuous data are presented as mean ± standard deviation (SD), whereas non-normally distributed variables are presented as median with interquartile ranges. Categorical data are presented as numbers and percentages. Comparisons between the two cohorts were performed by the independent-sample t test or Mann–Whitney U-test for continuous variables and the chi-square test for categorical variables. Missing data were handled by multiple imputation (n = 10), respectively in the two cohorts. Given a different age distribution between the two cohorts, age-stratified analyses of prognosis were conducted. Kaplan–Meier curves and log-rank tests were used to compare survival and Cox proportional models to explore the predictors of mortality. Statistics were performed using IBM SPSS Statistics 25.0 (IBM Corp, Armonk, NY, USA). A p value of < 0.05 (two tailed) was considered statistically significant.

Results

Between 2011 and 2015, 1047 patients from West China Hospital and 1842 patients from Sahlgrenska University Hospital/Östra Hospital were screened for eligibility of pooled analysis. Figure 1 depicts the enrollment. Finally, 949 patients in the Chinese cohort and 1639 patients in the Swedish cohort were studied.

Fig. 1
figure 1

Flow chart of the patient enrollment

Clinical phenotype

Patients in the Chinese cohort were younger (Median 64 [IQR] 52–73 vs. 79 [IQR] 69–86 years in the Swedish cohort, p < 0.001) (Table 1). Proportion of HFrEF (40.8% vs. 44.1%, p = 0.084) and non-HFrEF was similar in Chinese and Swedish cohort. Systolic (126.1 ± 20.3 vs. 114.2 ± 15.4 mmHg, p < 0.001) and diastolic (71.7 ± 11.3 vs 69.1 ± 10.1 mmHg, p < 0.001) blood pressure were higher in the Swedish patients, whereas heart rate was lower (72.2 + 14.3 vs.83.7 ± 20.9 beats/min, p < 0.001). N-termin pro-brain natriuretic peptide (NT-proBNP) level was higher in the Swedish cohort (Median 4540 vs. 3251 pg/mL, p = 0.013).

Table 1 Baseline characteristics of patients in the two cohorts

Comorbidities were significantly different between the two cohorts. In the Swedish cohort there were more patients with ischemic heart disease (32.0% vs. 19.2%, p < 0.001), hypertension (64.2% vs. 36.8%, p < 0.001), valvular heart disease (40.9% vs.31.6%, p < 0.001), atrial fibrillation/flutter (55.3% vs.39.6%, p < 0.001), pulmonary disease (21.5% vs. 12.4%, p < 0.001) and anemia (43.5% vs.37.9%, p = 0.005), whereas only dilated cardiomyopathy (25.8% vs. 7.1%, p < 0.001) was more common in the Chinese cohort.

The use of angiotensin converting enzyme inhibitors/angiotensin receptor blockers (ACEIs/ARBs) (48.8% vs. 80.8%, p < 0.001) and beta-blockers (BBs) (58.8% vs. 86.5%, p < 0.001) was lower, whereas that of mineralcorticoid receptor antagonists (MRAs) (66.6% vs. 30.6%, p < 0.001) and digitalis (39.9% vs. 13.1%, p < 0.001) was higher in the Chinese cohort than in the Swedish cohort. As shown in Fig. 2, the HFrEF group was more likely to receive medical therapy than the non-HFrEF group in both cohorts. In patients with HFrEF, 20.4% of the Chinese patients and 64.6% of the Swedish patients were on 50% guideline-directed medical therapy (GDMT) target ACEIs/ARBs dose; 6.4% of the Chinese patients and 56.9% of the Swedish patients were on 50% GDMT target BBs dose; 79.9% of the Chinese patients and 32.3% of the Swedish patients were on 50% GDMT target MRAs dose (Additional file 1: Fig. S1). The reasons for no use of selected GDMT in each cohort were demonstrated in Additional file 1: Fig. S2.

Fig. 2
figure 2

Guideline-directed medical therapy in the two cohorts

Age stratified clinical characteristics and 6-month prognosis

The 6-month crude all-cause mortality was lower in the Chinese cohort than in the Swedish cohort (9.8% vs. 20.7%, p < 0.001). In the age group of age < 50 years, 50–74 years and ≥ 75 years, the mortality was 10.7%, 8.7% and 9.3% respectively in Chinese patients, in contrast to 0, 11.0% and 27.2% in Swedish patients.

There were 205 out of 949 Chinese patients (21.6%) and 69 out of 1639 Swedish patients (4.2%) in the age group < 50 years. The three most common comorbidities were dilated cardiomyopathy (40.5%), valvular disease (34.1%), atrial fibrillation/flutter (33.2%) in the Chinese cohort. HFrEF was noted in 53.7% of the patients and the median level of NT-proBNP was 3622 (IQR 1730–6793) pg/mL. The three most common comorbidities of the Swedish cohort included valvular disease (33.3%), hypertension (29.0%) and dilated cardiomyopathy (29.0%). HFrEF was diagnosed in 44.9% of the patients and the median level of NT-proBNP was 1100 (222–3699) pg/mL.

There were 194 (20.4%) Chinese patients and 1026 (62.6%) Swedish patients in the age group ≥ 75 years. Median age of this Chinese cohort was 79 (IQR 76–82) years. The five most prevalent comorbidities were hypertension (64.4%), renal dysfunction (60.3%), anemia (55.7%), diabetes (43.8%) and atrial fibrillation/flutter (40.7%). In this cohort 21.6% of Chinese patients had HFrEF and the median value of NT-proBNP was 3665 (IQR 1436–8742) pg/mL. In the Swedish cohort, median age of the patients was 84 (IQR 80–89) years, and approximately half of the deceased were older than 80 years. The five most prevalent comorbidities were hypertension (71.7%), renal dysfunction (65.9%), AF (63.7%), valvular disease (46.7%) and anemia (49.5%). 59.1% of Swedish patients had HFrEF and the median value of NT-proBNP was 4978 (IQR 2209–9741) pg/mL.

There were 550 (58.0%) Chinese patients and 554 (33.2%) Swedish patients in the age group 50–74 years. Figure 3 illustrates the age- and sex-adjusted Cox regression survival analysis between the two cohorts (HR 0.80 [95% CI 0.55–1.19], p = 0.273). Differences between the two study populations were obvious in terms of demographics, medical history, physical examination, lab tests and treatment, as shown in Table 2. The Swedish cohort had more patients with ischemic heart disease or hypertension, as well as more patients treated with ACEIs/ARBs or beta-blockers. Higher systolic and diastolic blood pressure with lower resting heart rate were also present in this cohort.

Fig. 3
figure 3

Age- and sex-adjusted Kaplan–Meier survival curves in patients aged 50–74 years

Table 2 Baseline characteristics of patients aged 50–74 years in the two cohorts

Predictors of 6-month mortality

In the age group of 50–74 years, multivariate Cox regression model was established for predictors of 6-month all-cause mortality in the Chinese cohort and the Swedish cohort, respectively. By including common clinical parameters as shown in Table 3, higher NT-proBNP and lower eGFR were independent predictors of higher mortality in both cohorts. Besides, older age, lower systolic blood pressure and prolonged QRS duration were associated with increased death rate in the Swedish cohort.

Table 3 Predictors of 6-month mortality in patients aged 50–74 years

Discussion

This patient-level comparison of hospitalized HF cohorts in China and Sweden revealed several main findings: (a) Clinical phenotype of HF population was distinct from each other. Swedish patients were 15 years older with more comorbidities while Chinese patients had lower blood pressure and NT-proBNP level; (b) Utilization of guideline-directed medical therapy was more frequent in Swedish patients with more prescription of ACEIs/ARBs and/or beta blockers but more Chinese patients were given MRAs and/or digitalis; (c) Overall 6-month mortality was higher in the Swedish cohort because of higher age, while the mortality was similar in patients of 50–75 years; (d) NT-proBNP and eGFR were independent predictors of 6-month mortality in both cohorts.

Comparison of HF patients from developing versus developed countries has been described by few studies [8,9,10]. Almost exclusively, HF patients from Asian areas or low- and middle-income countries were generally younger than those from Europe or high-income countries as observed in the current study. Apart from the age gap in this study, the Swedish cohort seemed to have “sicker” patients with heavier comorbidity burdens and more death than the Chinese cohort and the proportion of patients with dilated cardiomyopathy also varied enormously. It may indicate not only aging population in Sweden, but also different healthcare system between the two countries where Sweden has stricter referral criteria to tertiary care and higher thresholds of hospitalization [4, 29]. On the other hand, it may be explained by that more younger patients with dilated cardiomyopathy in China tend to seek medical service in the tertiary hospital but those patients with worsening HF are not routinely hospitalized in the tertiary settings, particularly the elderly with lower standard of living and poorer educational level from remote rural areas [30].

Sweden is one of the leading countries that early investigated and implemented neurohormonal suppression therapy in HF patients. Use of both renin-angiotensin system (RAS) antagonists and beta blockers in patients with EF < 30% were approximately 90% already in 2003 and remained constant over time [31]. In contrast, previous studies showed relatively worse performance in prescribing these medicines and guideline adherence when China was compared with European countries [17, 32,33,34], and the treatment with RAS antagonists and beta blockers never exceeded 80% [35]. Even if the underuse of ACEI/ARBs and beta blockers in the Chinese cohort of this study could partially be explained by contraindicated blood pressure in some patients (the Chinese cohort presented lower BP), there is still room for improvement in utilization of these drugs. On the contrary, more prescriptions of digitalis in the Chinese cohort may reflect the difference in the clinical practice of its good acceptance by Chinese doctors in terms of symptom relief and low cost, which might be also associated with reimbursement patterns of the countries.

Given unmatched age of the two populations, age-stratified analysis helped us to understand that senior patients with multiple diseases contributed to higher mortality in the Swedish cohort. Within the age group < 50 or ≥ 75 years, it is rational not to perform further comparison except descriptive analysis because of so big difference in sample size. Interestingly, similar to the China-HF registry that showed higher in-hospital mortality in younger (< 40 years) than older adults [17], the current study observed higher 6-month mortality in younger age group (< 50 years) of the Chinese cohort. It is in contrast to the established concept that death increases with age in HF population; but might be explained by an underestimated mortality in the senior age group due to fewer referrals of seriously ill old patients to tertiary hospitals [30]. In the Swedish cohort, there was no death in the youngest age group, < 50 years, that may be only attributed to the limited number of patients. A previous study reported an unadjusted 6-month mortality of about 10% among those aged ≤ 54 years and about 20% among those ≥ 55 years during 2002–2006 [36].

What is most interesting is when both cohorts were compared when they were in the similar age, aged 50–74 years, even if the mean age was 1.7 years higher in the Swedish cohort. In this case, the mortality was similar between cohorts though clinical characteristics and heart failure therapy differed. The question is why different phenotypes and different therapy were associated with similar mortality in two cohort in similar age? One possible explanation is that factors affecting survival were balanced between cohorts. For instance, in the Chinese cohort dilated cardiomyopathy was more frequent than that in the Swedish cohort, and vice versa for ischemic heart disease. It is known that dilated cardiomyopathy has better prognosis than ischemic heart disease. In the meantime, Swedish patients received optimal treatment with ACEIs/ARBs and beta blockers. In our study, a similar mortality was associated with similar NT-proBNP levels between cohorts. In accordance with previous reports [37, 38], increased NT-proBNP and decreased eGFR, common risk factors in both cohorts, independently predicted 6-month mortality. Nevertheless, some predictors tested in previous studies such as age and systolic blood pressure were only significant in the Swedish cohort, the reasons for that were not well illustrated.

This study had several limitations. First, a pooled data analysis was not equal to a pre-defined multi-center prospective study, though the difference was minimized by including those parameters with unified definitions acceptable to both sides. Second, different age distribution of the entire two cohorts and unmatched patient numbers in two age groups (< 50 years and ≥ 75 years) resulted in that head-to-head comparison was only conducted in the age group of 50–74 years. Third, the information obtained from patients enrolled in single-center registries may not be generalized and representative of the Chinese and Swedish HF patients who were admitted to tertiary referral hospitals. Besides, the present study focused on the only outcome of 6-month all-cause mortality but other concerned outcomes such as cardiovascular mortality, rehospitalization were lacking. Some previous reported important variables associated with the prognosis of HF such as New York Heart Association functional class, body mass index and coronary revascularization failed to be included into analysis because of their substantial missing values (> 25%) and also some parameters have not been collected either in Chinese or Swedish study when the registry initiated. Those factors which were not adjusted for might affect the difference in mortality between the cohorts.

Conclusions

This study investigated patient-level comparison from single-center HF registries in China and Sweden, which revealed different clinical phenotype but similar prognosis between the two cohorts beyond age.

Availability of data and materials

The datasets used and/or analyzed during the study is available from the corresponding author on reasonable request.

References

  1. Weiwei C, Runlin G, Lisheng L, Manlu Z, Wen W, Yongjun W, Zhaosu W, Huijun L, Zhe Z, Lixin J, Shengshou H. Outline of the report on cardiovascular diseases in China, 2014. Eur Heart J Suppl. 2016;18:F2-f11.

  2. Ponikowski P, Voors AA, Anker SD, Bueno H, Cleland JG, Coats AJ, Falk V, Gonzalez-Juanatey JR, Harjola VP, Jankowska EA, Jessup M, Linde C, Nihoyannopoulos P, Parissis JT, Pieske B, Riley JP, Rosano GM, Ruilope LM, Ruschitzka F, Rutten FH, van der Meer P. 2016 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure: the Task Force for the diagnosis and treatment of acute and chronic heart failure of the European Society of Cardiology (ESC). Developed with the special contribution of the Heart Failure Association (HFA) of the ESC. Eur J Heart Fail. 2016;18:891–975.

    Article  Google Scholar 

  3. Mozaffarian D, Benjamin EJ, Go AS, Arnett DK, Blaha MJ, Cushman M, Das SR, de Ferranti S, Despres JP, Fullerton HJ, Howard VJ, Huffman MD, Isasi CR, Jimenez MC, Judd SE, Kissela BM, Lichtman JH, Lisabeth LD, Liu S, Mackey RH, Magid DJ, McGuire DK, Mohler ER 3rd, Moy CS, Muntner P, Mussolino ME, Nasir K, Neumar RW, Nichol G, Palaniappan L, Pandey DK, Reeves MJ, Rodriguez CJ, Rosamond W, Sorlie PD, Stein J, Towfighi A, Turan TN, Virani SS, Woo D, Yeh RW, Turner MB. Executive summary: heart disease and stroke statistics—2016 update: a report from the American Heart Association. Circulation. 2016;133:447–54.

    Article  Google Scholar 

  4. Zarrinkoub R, Wettermark B, Wändell P, Mejhert M, Szulkin R, Ljunggren G, Kahan T. The epidemiology of heart failure, based on data for 2.1 million inhabitants in Sweden. Eur J Heart Fail. 2013;15:995–1002.

    Article  Google Scholar 

  5. Savarese G, Lund LH. Global public health burden of heart failure. Card Fail Rev. 2017;3:7–11.

    Article  Google Scholar 

  6. Ambrosy AP, Fonarow GC, Butler J, Chioncel O, Greene SJ, Vaduganathan M, Nodari S, Lam CSP, Sato N, Shah AN, Gheorghiade M. The global health and economic burden of hospitalizations for heart failure: lessons learned from hospitalized heart failure registries. J Am Coll Cardiol. 2014;63:1123–33.

    Article  Google Scholar 

  7. Dewan P, Jhund PS, Shen L, Petrie MC, Abraham WT, Atif Ali M, Chen CH, Desai AS, Dickstein K, Huang J, Kiatchoosakun S, Kim KS, Kb L, Lai WT, Liao Y, Mogensen UM, Oh BH, Packer M, Rouleau JL, Shi V, Sibulo AS, Solomon SD, Sritara P, Swedberg K, Tsutsui H, Zile MR, McMurray JJV. Heart failure with reduced ejection fraction: comparison of patient characteristics and clinical outcomes within Asia and between Asia, Europe and the Americas. Eur J Heart Fail. 2019;21:577–87.

    Article  CAS  Google Scholar 

  8. Greene SJ, Fonarow GC, Solomon SD, Subacius H, Maggioni AP, Böhm M, Lewis EF, Zannad F, Gheorghiade M. Global variation in clinical profile, management, and post-discharge outcomes among patients hospitalized for worsening chronic heart failure: findings from the ASTRONAUT trial. Eur J Heart Fail. 2015;17:591–600.

    Article  Google Scholar 

  9. Kristensen SL, Martinez F, Jhund PS, Arango JL, Bĕlohlávek J, Boytsov S, Cabrera W, Gomez E, Hagge AA, Huang J, Kiatchoosakun S, Kim KS, Mendoza I, Senni M, Squire IB, Vinereanu D, Wong RC, Gong J, Lefkowitz MP, Rizkala AR, Rouleau JL, Shi VC, Solomon SD, Swedberg K, Zile MR, Packer M, McMurray JJ. Geographic variations in the PARADIGM-HF heart failure trial. Eur Heart J. 2016;37:3167–74.

    Article  Google Scholar 

  10. Metra M, Mentz RJ, Hernandez AF, Heizer GM, Armstrong PW, Clausell N, Corbalan R, Costanzo MR, Dickstein K, Dunlap ME, Ezekowitz JA, Howlett JG, Komajda M, Krum H, Lombardi C, Fonarow GC, McMurray JJ, Nieminen MS, Swedberg K, Voors AA, Starling RC, Teerlink JR, O’Connor CM. Geographic differences in patients in a global acute heart failure clinical trial (from the ASCEND-HF Trial). Am J Cardiol. 2016;117:1771–8.

    Article  Google Scholar 

  11. Cleland JG, Swedberg K, Follath F, Komajda M, Cohen-Solal A, Aguilar JC, Dietz R, Gavazzi A, Hobbs R, Korewicki J, Madeira HC, Moiseyev VS, Preda I, van Gilst WH, Widimsky J, Freemantle N, Eastaugh J, Mason J. The EuroHeart Failure survey programme—a survey on the quality of care among patients with heart failure in Europe. Part 1: patient characteristics and diagnosis. Eur Heart J. 2003;24:442–63.

    Article  CAS  Google Scholar 

  12. Adams KF Jr, Fonarow GC, Emerman CL, LeJemtel TH, Costanzo MR, Abraham WT, Berkowitz RL, Galvao M, Horton DP. Characteristics and outcomes of patients hospitalized for heart failure in the United States: rationale, design, and preliminary observations from the first 100,000 cases in the Acute Decompensated Heart Failure National Registry (ADHERE). Am Heart J. 2005;149:209–16.

    Article  Google Scholar 

  13. Fonarow GC, Abraham WT, Albert NM, Stough WG, Gheorghiade M, Greenberg BH, O’Connor CM, Sun JL, Yancy CW, Young JB. Influence of beta-blocker continuation or withdrawal on outcomes in patients hospitalized with heart failure: findings from the OPTIMIZE-HF program. J Am Coll Cardiol. 2008;52:190–9.

    Article  CAS  Google Scholar 

  14. Nieminen MS, Brutsaert D, Dickstein K, Drexler H, Follath F, Harjola VP, Hochadel M, Komajda M, Lassus J, Lopez-Sendon JL, Ponikowski P, Tavazzi L. EuroHeart Failure Survey II (EHFS II): a survey on hospitalized acute heart failure patients: description of population. Eur Heart J. 2006;27:2725–36.

    Article  Google Scholar 

  15. Maggioni AP, Dahlstrom U, Filippatos G, Chioncel O, Leiro MC, Drozdz J, Fruhwald F, Gullestad L, Logeart D, Metra M, Parissis J, Persson H, Ponikowski P, Rauchhaus M, Voors A, Nielsen OW, Zannad F, Tavazzi L. EURObservational Research Programme: the Heart Failure Pilot Survey (ESC-HF Pilot). Eur J Heart Fail. 2010;12:1076–84.

    Article  Google Scholar 

  16. Yancy CW, Lopatin M, Stevenson LW, De Marco T, Fonarow GC. Clinical presentation, management, and in-hospital outcomes of patients admitted with acute decompensated heart failure with preserved systolic function: a report from the Acute Decompensated Heart Failure National Registry (ADHERE) Database. J Am Coll Cardiol. 2006;47:76–84.

    Article  Google Scholar 

  17. Zhang Y, Zhang J, Butler J, Yang X, Xie P, Guo D, Wei T, Yu J, Wu Z, Gao Y, Han X, Zhang X, Wen S, Anker SD, Filippatos G, Fonarow GC, Gan T, Zhang R. Contemporary epidemiology, management, and outcomes of patients hospitalized for heart failure in China: results from the China Heart Failure (China-HF) Registry. J Card Fail. 2017;23:868–75.

    Article  Google Scholar 

  18. Sakata Y, Shimokawa H. Epidemiology of heart failure in Asia. Circ J. 2013;77:2209–17.

    Article  Google Scholar 

  19. Guo L, Guo X, Chang Y, Yang J, Zhang L, Li T, Sun Y. Prevalence and risk factors of heart failure with preserved ejection fraction: a population-based study in Northeast China. Int J Environ Res Public Health. 2016;13:770.

    Article  Google Scholar 

  20. Yu SB, Cui HY, Qin M, Kong B, Liu T, Zhao QY, Huang H, Yang B, Huang CX. Characteristics of in-hospital patients with chronic heart failure in Hubei province from 2000 to 2010. Zhonghua Xin Xue Guan Bing Za Zhi. 2011;39:549–52.

    PubMed  Google Scholar 

  21. Liu X, Yu H, Pei J, Chu J, Pu J, Zhang S. Clinical characteristics and long-term prognosis in patients with chronic heart failure and reduced ejection fraction in China. Heart Lung Circ. 2014;23:818–26.

    Article  Google Scholar 

  22. Lam CS, Teng TK, Tay WT, Anand I, Zhang S, Shimizu W, Narasimhan C, Park SW, Yu CM, Ngarmukos T, Omar R, Reyes EB, Siswanto BB, Hung CL, Ling LH, Yap J, MacDonald M, Richards AM. Regional and ethnic differences among patients with heart failure in Asia: the Asian sudden cardiac death in heart failure registry. Eur Heart J. 2016;37:3141–53.

    Article  Google Scholar 

  23. Dokainish H, Teo K, Zhu J, Roy A, AlHabib KF, ElSayed A, Palileo-Villaneuva L, Lopez-Jaramillo P, Karaye K, Yusoff K, Orlandini A, Sliwa K, Mondo C, Lanas F, Prabhakaran D, Badr A, Elmaghawry M, Damasceno A, Tibazarwa K, Belley-Cote E, Balasubramanian K, Islam S, Yacoub MH, Huffman MD, Harkness K, Grinvalds A, McKelvie R, Bangdiwala SI, Yusuf S, Investigators I-C. Global mortality variations in patients with heart failure: results from the International Congestive Heart Failure (INTER-CHF) prospective cohort study. Lancet Glob Health. 2017;5:e665–72.

    Article  Google Scholar 

  24. Jonsson A, Edner M, Alehagen U, Dahlstrom U. Heart failure registry: a valuable tool for improving the management of patients with heart failure. Eur J Heart Fail. 2010;12:25–31.

    Article  Google Scholar 

  25. Dickstein K, Cohen-Solal A, Filippatos G, McMurray JJ, Ponikowski P, Poole-Wilson PA, Stromberg A, van Veldhuisen DJ, Atar D, Hoes AW, Keren A, Mebazaa A, Nieminen M, Priori SG, Swedberg K. ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2008: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2008 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association of the ESC (HFA) and endorsed by the European Society of Intensive Care Medicine (ESICM). Eur Heart J. 2008;2008(29):2388–442.

    Google Scholar 

  26. McMurray JJ, Adamopoulos S, Anker SD, Auricchio A, Bohm M, Dickstein K, Falk V, Filippatos G, Fonseca C, Gomez-Sanchez MA, Jaarsma T, Kober L, Lip GY, Maggioni AP, Parkhomenko A, Pieske BM, Popescu BA, Ronnevik PK, Rutten FH, Schwitter J, Seferovic P, Stepinska J, Trindade PT, Voors AA, Zannad F, Zeiher A. ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure 2012: the Task Force for the Diagnosis and Treatment of Acute and Chronic Heart Failure 2012 of the European Society of Cardiology. Developed in collaboration with the Heart Failure Association (HFA) of the ESC. Eur Heart J. 2012;33:1787–847.

    Article  Google Scholar 

  27. Blanc B, Finch C, Hallberg L, et al. Nutritional anaemias. Report of a WHO scientific group. World Health Organ Tech Rep Ser. 1968;405:5–37.

    Google Scholar 

  28. Levey AS, Stevens LA, Schmid CH, Zhang YL, Castro AF 3rd, Feldman HI, Kusek JW, Eggers P, Van Lente F, Greene T, Coresh J. A new equation to estimate glomerular filtration rate. Ann Intern Med. 2009;150:604–12.

    Article  Google Scholar 

  29. Kroneman M, Siegers JJ. The effect of hospital bed reduction on the use of beds: a comparative study of 10 European countries. Soc Sci Med. 2004;59:1731–40.

    Article  Google Scholar 

  30. Atherton JJ, Hayward CS, Wan Ahmad WA, Kwok B, Jorge J, Hernandez AF, Liang L, Kociol RD, Krum H. Patient characteristics from a regional multicenter database of acute decompensated heart failure in Asia Pacific (ADHERE International-Asia Pacific). J Card Fail. 2012;18:82–8.

    Article  Google Scholar 

  31. Thorvaldsen T, Benson L, Dahlstrom U, Edner M, Lund LH. Use of evidence-based therapy and survival in heart failure in Sweden 2003–2012. Eur J Heart Fail. 2016;18:503–11.

    Article  CAS  Google Scholar 

  32. MacDonald MR, Tay WT, Teng TK, Anand I, Ling LH, Yap J, Tromp J, Wander GS, Naik A, Ngarmukos T, Siswanto BB, Hung CL, Richards AM, Lam CSP. Regional variation of mortality in heart failure with reduced and preserved ejection fraction across Asia: outcomes in the ASIAN-HF Registry. J Am Heart Assoc. 2020;9:e012199.

    PubMed  Google Scholar 

  33. Dokainish H, Teo K, Zhu J, Roy A, AlHabib KF, ElSayed A, Palileo-Villaneuva L, Lopez-Jaramillo P, Karaye K, Yusoff K, Orlandini A, Sliwa K, Mondo C, Lanas F, Prabhakaran D, Badr A, Elmaghawry M, Damasceno A, Tibazarwa K, Belley-Cote E, Balasubramanian K, Yacoub MH, Huffman MD, Harkness K, Grinvalds A, McKelvie R, Yusuf S. Heart failure in Africa, Asia, the Middle East and South America: the INTER-CHF study. Int J Cardiol. 2016;204:133–41.

    Article  Google Scholar 

  34. Chang HY, Wang CC, Wei J, Chang CY, Chuang YC, Huang CL, Chong E, Lin JL, Mar GY, Chan KC, Kuo JY, Wang JH, Chen ZC, Tseng WK, Cherng WJ, Yin WH. Gap between guidelines and clinical practice in heart failure with reduced ejection fraction: results from TSOC-HFrEF registry. J Chin Med Assoc. 2017;80:750–7.

    Article  Google Scholar 

  35. Wang H, Li YY, Chai K, Zhang W, Li XL, Dong YG, Zhou JM, Huo Y, Yang JF. Contemporary epidemiology and treatment of hospitalized heart failure patients in real clinical practice in China. Zhonghua Xin Xue Guan Bing Za Zhi. 2019;47:865–74.

    CAS  PubMed  Google Scholar 

  36. Barasa A, Schaufelberger M, Lappas G, Swedberg K, Dellborg M, Rosengren A. Heart failure in young adults: 20-year trends in hospitalization, aetiology, and case fatality in Sweden. Eur Heart J. 2014;35:25–32.

    Article  Google Scholar 

  37. Santaguida PL, Don-Wauchope AC, Oremus M, McKelvie R, Ali U, Hill SA, Balion C, Booth RA, Brown JA, Bustamam A, Sohel N, Raina P. BNP and NT-proBNP as prognostic markers in persons with acute decompensated heart failure: a systematic review. Heart Fail Rev. 2014;19:453–70.

    Article  CAS  Google Scholar 

  38. Zamora E, Lupon J, Vila J, Urrutia A, de Antonio M, Sanz H, Grau M, Ara J, Bayes-Genis A. Estimated glomerular filtration rate and prognosis in heart failure: value of the Modification of Diet in Renal Disease Study-4, chronic kidney disease epidemiology collaboration, and cockroft-gault formulas. J Am Coll Cardiol. 2012;59:1709–15.

    Article  Google Scholar 

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Acknowledgements

We thank all local investigators from West China Hospital and Sahlgrenska University Hospital for accurate data collection and entry.

Funding

This work was financially supported by the Science and Technology Project of Sichuan Province (Grant Number 2020YFS0241).

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Authors and Affiliations

Authors

Contributions

QZ, MF, and XC contributed to the conception or design of the work. YF and XC analyzed the data and drafted the article. QZ, MF and MS revised the text critically for important intellectual content. All authors gave final approval and agree to be accountable for all aspects of the work ensuring integrity and accuracy. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Qing Zhang.

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Ethics approval and consent to participate

This is a retrospective data analysis of two registries which were approved by the Chinese Ethics Committee of Registering Clinical Trials (West China Hospital) and the Ethics Committees of the University of Gothenburg. Informed consent was obtained from all participants or, if participants were dead, from a next of kin and/or legal guardian. The present study does not involve personal privacy. The study protocol was approved by Ethics Committee of West China Hospital (2017Y-480), all methods were carried out in accordance with relevant guidelines and regulations.

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Not applicable.

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The authors have no conflicts of interest to disclose. All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest, or non-financial interest in the subject matter or materials discussed in this manuscript.

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Supplementary Information

Additional file 1.

Fig. S1. Patients with HFrEF on 50% GDMT target dose. Fig. S2. Reasons for no use of selected GDMT (A ACEIs/ARBs; B beta-blockers) in patients with HFrEF.

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Feng, Y., Chen, X., Schaufelberger, M. et al. Patient-level comparison of heart failure patients in clinical phenotype and prognosis from China and Sweden. BMC Cardiovasc Disord 22, 91 (2022). https://doi.org/10.1186/s12872-022-02540-w

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