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BRIEF RESEARCH REPORT article

Front. Cardiovasc. Med., 09 September 2024
Sec. Intensive Care Cardiovascular Medicine

Short term outcomes and resource utilization in de-novo versus acute on chronic heart failure related cardiogenic shock: a nationwide analysis

\r\nMary Quien
Mary Quien1*Ju Young BaeJu Young Bae1Sun-Joo JangSun-Joo Jang2Carlos Davila\r\nCarlos Davila2
  • 1Section of Cardiovascular Medicine, Department of Internal Medicine, Yale New Haven Health Bridgeport Hospital, Bridgeport, CT, United States
  • 2Section of Cardiovascular Medicine, Department of Internal Medicine, Yale New Haven Hospital, New Haven, CT, United States

Background: There has been growing recognition of non-ischemic etiologies of cardiogenic shock (CS). To further understand this population, we aimed to investigate differences in clinical course between acute on chronic heart failure related (CHF-CS) and de-novo CS (DN-CS).

Methods: Using the Nationwide Readmission Database, we examined 92,426 CS cases. Outcomes of interest included in-hospital and 30-day outcomes and use of advanced heart failure therapies.

Results: Patients with DN-CS had higher in-hospital mortality than the CHF-CS cohort (32.6% vs. 30.4%, p < 0.001). Mechanical circulatory support (11.9% vs. 8.6%, p < 0.001) was more utilized in DN-CS. Renal replacement therapy (13.8% vs. 15.5%, p < 0.001) and right heart catheterization (16.0% vs. 21.0%, p < 0.001) were implemented more in the CHF-CS cohort. The CHF-CS cohort was also more likely to undergo LVAD implantation (0.4% vs. 3.6%, p < 0.001) and heart transplantation (0.5% vs. 2.0%, p < 0.001). Over the study period, advanced heart failure therapy utilization increased, but the proportion of patients receiving these interventions remained unchanged. Thirty days after index hospitalization, the CHF-CS cohort had more readmissions for heart failure (1.1% vs. 2.4%, p < 0.001) and all causes (14.1% vs. 21.1%, p < 0.001) with higher readmission mortality (1.1% vs. 2.3%, p < 0.001).

Conclusion: Our findings align with existing research, demonstrating higher in-hospital mortality in the DN-CS subgroup. After the index hospitalization, however, the CHF-CS cohort performed worse with higher all-cause readmission rate and readmission mortality. The study also underscores the need for further investigation into the underutilization of certain interventions and the observed trends in the management of these CS subgroups.

Introduction

Cardiogenic shock (CS) is defined as severe myocardial functional impairment resulting in systemic hypoperfusion, reduced cardiac output, and hypoxemia. Traditionally, research has focused on the pathophysiology and management of CS resulting from acute myocardial infarction (AMI) due to its high mortality (1). However, heart failure related cardiogenic shock has emerged as a significant contributor to CS cases (2). One multicenter analysis of cardiac intensive care units in North America revealed that more than half of cases were unrelated to AMI (3).

To further understand non-AMI cardiogenic shock, studies have aimed to investigate differences in clinical course between acute on chronic heart failure related cardiogenic shock (CHF-CS) and newly diagnosed or “de-novo” cardiogenic shock (DN-CS). However, there are inconsistent findings with some studies demonstrating higher in-hospital mortality in DN-CS while another suggesting overall worse long-term outcomes in the acute on chronic heart failure population (36). In addition, mortality in CS patients has not significantly improved over time, and the use of advanced heart failure resources remains variable across the country given the lack of evidence-based guidelines for resource use in these groups.

Using the Nationwide Readmission Database (NRD), we aim to compare the clinical course and outcomes in patients with DN-CS and CHF-CS.

Method

This was a retrospective study using the data from the Nationwide Readmissions Database (NRD) between January 2016 and November 2019. The NRD is a large, publicly available, administrative database constructed using discharge data from Healthcare Cost and Utilization Project State Inpatient Databases in the United States. The NRD is developed through a Federal-State-Industry partnership sponsored by the Agency for Healthcare Research and Quality (AHRQ). Each record in the NRD contains information on the patient's diagnoses and procedures performed during the hospitalization, based on International Classification of Diseases, Tenth Revision-Clinical Modification (ICD-10-CM) codes or Procedure Coding System (ICD-10-PCS). We identified our study population, comorbidities, causes of readmissions and in-hospital outcomes using a combination of ICD-10-CM and ICD-10-PCS. Institutional Review Board approval and informed consent were not required for this study since all the data is de-identified and publicly available.

From January 2016 to November 2019, patients with cardiogenic shock were identified using ICD-10-CM codes for cardiogenic shock as the primary or secondary diagnosis (Figure 1). Patient variables were obtained from the database and included in our analysis as baseline characteristics. Since NRD prohibits linking patients across years, patients whose index hospitalization was in December were excluded in order to allow for completeness of data on thirty days of follow-up after discharge, similar to other prior studies examining the NRD (79). Patients were excluded if they carried a diagnosis of prior myocardial infarction, percutaneous coronary intervention, coronary artery bypass graft (CABG), or aortic valve replacement, tricuspid valve replacement, mitral valve replacement, or any valvular heart disease. Patients deemed to have an “elective admission” were also excluded. Patients were then divided into 2 groups: DN-CS or CHF-CS based on whether or not they carried a prior diagnosis of heart failure. The ICD codes used for the inclusion and exclusion criteria can be found in the Supplementary Material.

Figure 1
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Figure 1. Flowchart of study population.

The primary outcome of interest was in-hospital outcomes and used of advanced heart failure therapies, over the course of 2016–2019. The secondary outcomes were thirty-day outcomes, excluding in-hospital death, after index hospitalization for cardiogenic shock. For thirty-day readmissions, only the first readmission within thirty days of the discharge was included. Transfer to another hospital was not included in the analysis since same-day readmissions and transfers are combined in a single variable in the NRD, and it does not specify if the transfer is to a higher or lower level of care.

All statistical analyses were performed using R statistical software, version 4.3.2, with its package “survey”. Discharge weight and stratum provided by NRD were used for all analyses and thus all the reported numbers are weighted national estimates. Domain analysis was used for accurate variance calculations for subgroup analyses. All analyses accounted for NRD sampling design by including hospital-year fixed effects based on hospital identification number. Categorical variables are presented as frequencies and analyzed by the Rao-Scott chi-square test. Continuous variables are shown as mean with standard error or median with interquartile range and are tested by either the Mann–Whitney–Wilcoxon test or a survey-specific linear regression test. All tests were two-sided with p value < 0.05 considered statistically significant.

Results

Over the course of 2016–2019, there were 92,426 patients who presented with cardiogenic shock. 18,138 (19.6%) were determined to have DN-CS and 74,288 (80.4%) to have CHF-CS. The average age was 65 ± 0.1 years in the CHF-CS group and 62.6 ± 0.2 years (p < 0.001) in the DN-CS group. 56.3% of patients in the DN-CS group were male, compared to 63.6% of patients in the CHF-CS group. The CHF-CS group had significantly more comorbidities than the DN-CS group, including diabetes (31.2% vs. 42.0%, p < 0.001), pulmonary hypertension (12.8% vs. 24.0%, p < 0.001), chronic pulmonary disease (25.7% vs. 32.1%, p < 0.001), obesity (19.1% vs. 24.6%, p < 0.001), and chronic kidney disease (28.8% vs. 53.7%, p < 0.001). Further characteristics of each group are described in Table 1.

Table 1
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Table 1. Patient and hospital characteristics for patients hospitalized with cardiogenic shock.

For in-hospital outcomes (Table 2), patients with DN-CS had overall higher in-hospital mortality than the CHF-CS cohort (32.6% vs. 30.4%, p < 0.001) and were more likely to present with cardiac arrest during the index hospitalization (8.4% vs. 5.6%, p < 0.001). In-hospital mortality was significantly higher in patients with DN-CS than patients with CHF-CS especially in 2019. Renal replacement therapy (RRT) (13.8% vs. 15.5%, p < 0.001) and right heart catheterization (RHC) (16.0% vs. 21.0%, p < 0.001) were implemented more in the CHF-CS cohort than in the DN-CS cohort, whereas mechanical circulatory support (MCS) (11.9% vs. 8.6%, p < 0.001) was more utilized in the DN-CS than in the CHF-CS group. The CHF-CS cohort was more likely to undergo LVAD implantation (0.4% vs. 3.6%, p < 0.001) and heart transplantation (0.5% vs. 2.3%, p < 0.001) than the DN-CS cohort. The absolute number of heart failure resources increased over time, but the proportion of patients who received these resources did not appear to significantly change.

Table 2
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Table 2. In-hospital outcomes for patients hospitalized with cardiogenic shock.

Analysis of thirty days after index hospitalization (Table 3) revealed that the CHF-CS cohort had significantly higher incidence of readmissions for heart failure (1.1% vs. 2.4%, p < 0.001) and all causes (14.1% vs. 21.1%, p < 0.001) and higher readmission mortality (1.1% vs. 2.3%, p < 0.001) than the DN-CS cohort.

Table 3
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Table 3. Thirty-day outcomes (excluding in-hospital death) for patients hospitalized with cardiogenic shock.

Discussion

Using a large administrative database, we found key differences in the outcomes of patients presenting with CS with DN-CS and CHF-CS. Compared to the CHF-CS cohort, the DN-CS cohort had a worse in-hospital mortality rate. However, the CHF-CS cohort was found to have a significantly higher thirty-day readmission rate of any kind and a higher readmission mortality rate. Our findings overall align with those elucidated by other studies that investigated similar cohorts. First, we found that the CHF-CS cohort made up the majority of CS cases, comprising about 82% of total cases of CS every year. Although this is greater than the percentages quoted by the studies done by the Critical Care Cardiology Trials Network Registry and the Cardiogenic Shock Working Group registry, which was closer to 70%, we were unable to differentiate primary ventricular failure from other etiologies such as severe valvular disease, incessant arrhythmia, and tamponade, which may account for this difference (5, 6).

Similar to these studies, we also confirmed a higher in-hospital mortality rate with the DN-CS cohort. As proposed by the aforementioned studies, this could be attributed to a greater severity of shock at presentation due to lack of chronic adaptation to low flow states (5). Although the NRD is unable to provide specific clinical details, this idea is supported by the higher rate of cardiac arrest found in our DN-CS cohort as well as the higher utilization of MCS devices. Interestingly, after the index hospitalization, the CHF-CS cohort performed worse than the DN-CS cohort, with a higher all cause readmission rate, including heart failure, and readmission mortality. The CHF-CS cohort was overall a more debilitated group compared to the DN-CS cohort with a significantly higher number of comorbidities. This places the CHF-CS cohort at higher risk of persistent organ dysfunction and complications during and after the index hospitalization.

In terms of resource utilization, the CHF-CS cohort was more likely to undergo RRT, RHC, LVAD placement, and heart transplant compared to the DN-CS cohort. This difference is similar to other studies and likely multifactorial (5, 6). CHF-CS patients had more comorbidities that may have precluded them from MCS use but were more likely to have had prior evaluations for advanced therapies. The increased medical complexity of the CHF-CS cohort may have also prompted the increased use of RHC to garner more information, especially since this cohort had a higher prevalence of known pulmonary hypertension, suggesting a more complicated hemodynamic profile. Given the varying practices of RHC utilization at different institutions, the exact rationale for its use is difficult to pinpoint. Other studies have also shown that the DN-CS cohort may have greater multi-organ dysfunction in the acute setting that precludes them from consideration of LVAD or heart transplant (6).

Interestingly, despite an increase in heart failure therapies from 2016 to 2019, the proportion of CS patients who received these therapies appears largely unchanged. The lack of RHC utilization is most surprising since several studies have suggested that the use of RHC have led to improved outcomes and suggest possible mortality benefits (10, 11). Moreover, societies such as the European Society of Cardiology specifically have recommended RHC for patients with severe heart failure who are being evaluated for MCS or transplant (12). Further studies may be needed to discover why RHC are underutilized in the management of CS patients and whether some types of CS benefit from RHC more than others. The lack of increase in MCS does differ from a study that showed increases in temporary MCS use after the revised UNOS system took place in 2018 (13). However, the study showed this was mainly the case in transplant centers, which may not be reflected in our study that looks at all centers across the United States. It is also possible that there is simply a lack of available resources to accommodate the growing number of CS patients.

There are several limitations to this study. First, this study is limited by its retrospective design. Second, since data was extracted from an administrative database, we are unable to derive further detail from patient cases. As described above, this does not allow us to explore the clinical variables that may have played a role in the differences in outcomes between these two cohorts from other studies. Lastly, the NRD is only able to provide the occurrence of procedures but cannot relay the timing. The timing of RHC specifically has been shown to lead to shorter length of stay and lower readmission rates but needs to be further validated in future studies (11). The results from the study by Hernandez-Montfort and others also suggest that there is heterogeneity in the use and timing of MCS use in this patient population that needs further exploration (6).

This study underscores a paradox where, despite CHF-CS patients experiencing better in-hospital outcomes, their thirty-day results, including readmissions and readmission mortality, are worse. Our study brings attention to a high-risk population and possible underutilization of resources that could positively affect its clinical course.

Data availability statement

Publicly available datasets were analyzed in this study. This data can be found here: https://hcup-us.ahrq.gov/nrdoverview.jsp.

Ethics statement

Ethical approval was not required for the study involving humans in accordance with the local legislation and institutional requirements. Written informed consent to participate in this study was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and the institutional requirements.

Author contributions

MQ: Conceptualization, Writing – original draft, Writing – review & editing. JB: Writing – original draft, Writing – review & editing. S-JJ: Conceptualization, Data curation, Formal Analysis, Methodology, Writing – review & editing. CD: Supervision, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcvm.2024.1454884/full#supplementary-material

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Keywords: cardiogenic shock, de novo heart failure, critical care cardiology, chronic heart failure, advanced heart failure

Citation: Quien M, Bae JY, Jang S-J and Davila C (2024) Short term outcomes and resource utilization in de-novo versus acute on chronic heart failure related cardiogenic shock: a nationwide analysis. Front. Cardiovasc. Med. 11:1454884. doi: 10.3389/fcvm.2024.1454884

Received: 25 June 2024; Accepted: 26 August 2024;
Published: 9 September 2024.

Edited by:

Sascha Treskatsch, Charité University Medicine Berlin, Germany

Reviewed by:

Götz Schmidt, University of Giessen, Germany
Thomas Simon Zajonz, University Hospital Giessen, Germany

Copyright: © 2024 Quien, Bae, Jang and Davila. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Mary Quien, mmquien@gmail.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.