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Association of thrombocytopenia and infection in patients with ST-elevation myocardial infarction undergoing percutaneous coronary intervention

BMC Cardiovascular Disorders volume 21, Article number: 404 (2021) Cite this article

Abstract

Background

The impact of thrombocytopenia on infection in patients with ST-elevation myocardial infarction (STEMI) remains poorly understood.

Aims

To evaluate the association between thrombocytopenia and infection in patients with STEMI.

Methods

Patients diagnosed with STEMI were identified from January 2010 to June 2016. The primary endpoint was in-hospital infection, and major adverse clinical events (MACE) and all-cause death were considered as secondary endpoints.

Results

A total of 1401 STEMI patients were enrolled and divided into two groups according to the presence (n = 186) or absence (n = 1215) of thrombocytopenia. The prevalence of in-hospital infection was significantly higher in the thrombocytopenic group (30.6% (57/186) vs. 16.2% (197/1215), p < 0.001). Prevalence of in-hospital MACE (30.1% (56/186) vs. 16.4% (199/1215), p < 0.001) and all-cause death (8.1% (15/186) vs. 3.8% (46/1215), p = 0.008) revealed an increasing trend. Multivariate analysis indicated that thrombocytopenia was independently associated with increased in-hospital infection (OR, 2.09; 95%CI 1.32–3.27; p = 0.001) and MACE (1.92; 1.27–2.87; p = 0.002), but not all-cause death (1.87; 0.88–3.78; p = 0.091). After a median follow-up of 2.85 years, thrombocytopenia was not associated with all-cause death at multivariable analysis (adjusted hazard ratio, 1.19; 95%CI 0.80–1.77; p = 0.383).

Conclusions

Thrombocytopenia is significantly correlated with in-hospital infection and MACE, and might be used as a prognostic tool in patients with STEMI.

Peer Review reports

Background

Infection is an uncommon (reported prevalence of 2.4%) but potentially devastating complication in patients with ST-elevation myocardial infarction (STEMI). Infection in these patients is usually associated with a significantly increased risk of mortality and morbidity, prolongs hospitalization, and increases healthcare costs [1,2,3]. Given most infections are considered preventable, there is an urgent need to identify STEMI patients at high risk of infection, and implement interventions to prevent infection.

Thrombocytopenia is a common laboratory abnormality in patients presenting with acute myocardial infarction (AMI) and always defined as a platelet count < 150 × 109/L [4]. Baseline thrombocytopenia showed strong predictive capacity for major adverse clinical events (MACE), ischemic target lesion revascularization and 1-year death among patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) [5]. Additionally, thrombocytopenia has been previously considered as a risk factor for worse outcomes and has been reported to be independently associated with in-hospital mortality in ACS patients [6]. However, few studies have explored the prognostic value of thrombocytopenia for infection in patients with STEMI. In terms of etiological factors, in addition to congenital thrombocytopenia and pseudothrombocytopenia, different acquired causes can be included. Of which, infectious agents play a crucial role for their contribution to a reduction in the platelet count by suppressing the bone marrow directly or increasing peripheral consumption of platelets [7,8,9].

Recent studies have reported that patients with coronavirus disease 2019 (COVID-19) exhibited severe thrombocytopenia [10], and Helicobacter pylori (H. pylori) infection was on the rise as a cause of immune thrombocytopenia (ITP) [11], while another research demonstrated that low platelet count was independently correlated with an increased risk of infection in patients with ITP [12], which indicated that infections were closely associated with thrombocytopenia. Furthermore, thrombocytopenia has been shown to be a poor prognostic risk factor for systemic infections among patients from medical, surgical, mixed, or trauma ICUs [13], and moderate thrombocytopenia (platelet count < 100 × 109/L) was a potential risk stratification tool for severe Clostridium difficile infection (CDI) [14].

Given the potential value of thrombocytopenia in the prediction of infection, and in order to improve risk stratification for these patients, we sought to investigate the association between thrombocytopenia and infection in patients with STEMI.

Methods

Study population

Patients diagnosed with STEMI were enrolled from January 2010 to June 2016 in Guangdong Provincial People’s Hospital. STEMI was diagnosed if patients presented within 12 h from the onset of symptoms including typical chest pain lasting for ≥ 30 min, not responsive to nitrates, with ST-segment elevation of ≥ 0.2 mV in at least two contiguous leads, or left bundle-branch block [15]. The exclusion criteria were as follows: (a) with chronic inflammatory disease; (b) with chronic renal failure necessitating hemodialysis upon hospital admission; (c) undergoing cardiac surgery; (d) who died within 24 h after hospital admission; (e) without performing PCI; (f) without platelet count data and (g) receiving dual antiplatelet therapy (DAPT) or other medications potentially causing thrombocytopenia before admission. The study protocol was approved by Ethics Committee of our hospital. The study was carried out according to the Principles of the Declaration of Helsinki 1975 and its later amendments. Written informed consents were obtained from patients or their relatives.

Study endpoints and follow-up

Thrombocytopenia was defined as a platelet count < 150 × 109/L [4]. The primary endpoint was the development of infection during hospitalization, which was defined as infection requiring antibiotics (reflecting the clinical influence of infection compatible with the necessity for additional treatment) [16], and was determined in medical records in accordance with ICD-10-CM codes, including pneumonia (J18.9), pyelonephritis (N10), ureteritis (N28.86), urethritis (N34.1), cystitis (N30.90), and other infections (such as sepsis, A41.9; bacteremia, R78.81 or unspecified infectious disease, B99.9). Additionally, the types of infections included pulmonary, urinary, or other (including abdominal sepsis, primary bacteremia, and unidentified primary infection site) infections. The secondary endpoint was in-hospital MACE, including all-cause death, stroke, and any bleeding during hospitalization. Other endpoints were also documented, including all-cause death during hospitalization and follow-up. Patients were followed up through telephone-tracking methods or outpatient clinic interviews for ≥ 1 year by trained nurses.

Statistical analyses

Continuous variables with a normal distribution were presented as mean ± SD, and compared using two-sample t-tests. Continuous variables with a non-normal distribution were expressed as median and interquartile ranges, and analyzed using Wilcoxon rank sum tests. Categorical variables (which are presented as percentages) were compared using the chi-squared test or Fisher’s exact test (as appropriate). In-hospital outcomes and follow-up outcomes were calculated using a logistic regression model or Cox regression model in multivariable analysis. As for sample size consideration, we applied a rule of thumb, namely, that the number of events per variable should be 10 or greater. We expected about no more than 11 factors in the development model; thus, at least 110 infections were needed. According to the incidence of infections (10%) in the previous study [17], the final sample size of at least 1100 patients was needed. All tests were two-tailed, and p < 0.05 was considered significant. Data analyses were carried out using SAS v9.4 (SAS Institute, Cary, NC, USA).

Results

A total of 2283 patients with STEMI at our hospital were identified between January 2010 and June 2016; of these, 882 patients were excluded according to the exclusion criteria. Finally, 1401 patients (61.77 ± 12.37 years, 82.7% male) diagnosed with STEMI undergoing PCI were enrolled and analyzed in this study (Fig. 1). During hospitalization, 186 (13.3%) STEMI patients developed thrombocytopenia (platelet count < 150 × 109/L). The clinical characteristics of the study population at baseline are shown in Table 1. Patients with thrombocytopenia were older and more likely to be men, than those not suffering from thrombocytopenia. A higher serum level of creatinine, and lower levels of total cholesterol and hemoglobin, were found in thrombocytopenic patients. Furthermore, thrombocytopenic patients had a higher prevalence of myocardial infarction and new use of antibiotics compared with non-thrombocytopenia cases. However, left ventricular ejection fraction (LVEF), procedural characteristics, and the prevalence of hypertension, diabetes mellitus, chronic obstructive pulmonary disease (COPD), and hyperlipemia were not significantly different between the two groups.

Fig. 1
figure 1

Flowchart showing patient selection

Full size image
Table 1 Clinical characteristics of the study cohort
Full size table

As shown in Table 2, thrombocytopenic patients were more likely to develop infection (30.6% (57/186) vs. 16.2% (197/1215), p < 0.001), with no significant differences in various types of infection (p = 0.804), as well as in-hospital MACE (30.1% (56/186) vs. 16.4% (199/1215), p < 0.001) than non-thrombocytopenia cases during hospitalization. The thrombocytopenia group also had a higher proportion of in-hospital death (8.1% (15/186) vs. 3.8% (46/1215), p = 0.008) and longer hospital stay (11.41 ± 10.17 vs. 8.43 ± 6.80 days, p < 0.001) than the non-thrombocytopenia group (Table 2). Additionally, subgroup analysis revealed that 50 ≤ PLT < 150 was prominently associated with an increased risk of infection (odds ratio (OR), 2.21; 95% confidence interval (CI) 1.55–3.12; p < 0.001), but not severe thrombocytopenia defined as PLT < 50 (OR, 5.02; 95% CI 0.20–127.28; p = 0.255) due to the small sample size possibly (Additional file 1: Table S1). Conversely, an obvious negative correlation between normal platelet count and infection was discovered (OR, 0.20; 95% CI 0.17–0.23; p < 0.001) (Additional file 1: Table S1).

Table 2 In-hospital adverse events of the study cohort
Full size table

Univariate analysis suggested that thrombocytopenia was significantly associated with an elevated risk of infection (OR, 2.28; 95%CI 1.61–3.22; p < 0.001). After adjustment for potential confounding factors (including age, Killip classification, diabetes, MI, stroke, serum albumin, WBC, hemoglobin, serum creatinine and LVEF), multivariate analysis showed that thrombocytopenia remained a significant predictor of infection risk in such patients (OR, 2.09; 95%CI 1.32–3.27; p = 0.001) (Table 3). Similar results were observed for the prevalence of in-hospital MACE (OR, 1.92; 95%CI 1.27–2.87; p = 0.002) but not all-cause death (OR, 1.87; 95%CI 0.88–3.78; p = 0.091) (Table 3).

Table 3 Adjusted OR and 95% CI of thrombocytopenia for infection, MACE and all-cause death at multivariate analysis
Full size table

After a median follow-up of 2.85 years, univariate Cox proportional hazard regression analyses showed that thrombocytopenia was independently associated with increased all-cause death (hazard ratio (HR), 1.52; 95%CI 1.04–2.20; p = 0.029). However, upon fully adjusted multivariate Cox regression analysis, this significant association disappeared (adjusted HR, 1.19; 95%CI 0.80–1.77; p = 0.383) (Table 4).

Table 4 Cox proportional hazards regression analysis of factors associated with all-cause death
Full size table

Discussion

The present study investigated, for the first time, the relationship between thrombocytopenia and infection in patients with STEMI undergoing PCI. We found that thrombocytopenia was associated with a significantly increased risk of in-hospital infection, in-hospital MACE but not all-cause death. These findings suggested that serial monitoring of platelet counts was essential to identify patients with STEMI at high risk of adverse outcomes.

Platelets are anucleate blood cells that play a crucial role in the maintenance of hemostasis [18]. Thrombocytopenia has been evaluated in various cardiovascular procedures [19, 20], and been proven to be associated with worse short-term and long-term outcomes in patients with ACS [5]. Williamson and colleagues reported that critically ill patients with thrombocytopenia had an increased risk of death compared with patients with a normal platelet count [21]. An increased risk of death, ischemic events, and bleeding has also been reported in thrombocytopenic patients with ACS without ST elevation upon electrocardiography [22]. In patients suffering from sepsis, thrombocytopenia reflected proinflammatory stimuli and pro-hemostatic mechanisms [23], which suggested that the more the pronounced infectious stimulus, the greater the risk of thrombocytopenia. Additionally, as reported previously, acute and chronic infectious diseases were common causes of thrombocytopenia [24]. However, the prognostic value of thrombocytopenia for infection remains unclear.

In our analyses, we demonstrated that the prevalence of thrombocytopenia in STEMI patients was 13.3%, while previous studies have reported the incidence of thrombocytopenia in patients with ACS varied from 1.6 to 13% [25, 26]. The mechanisms of platelet loss in such patients have not been illustrated explicitly because patients with thrombocytopenia are frequently excluded from large clinical trials [27]. However, anti-platelet agents and anticoagulation, especially heparin, are employed after surgical as well as conservative treatment, and may cause heparin-induced thrombocytopenia when antibodies react with complexes of heparin molecules and platelet factor-4 [28]. Furthermore, scholars have reported ischemic necrosis in patients presenting with myocardial dysfunction, was able to facilitate inflammation at the cellular level, and subsequently increased platelet clearance by macrophages as well as became the dominant stimulus for thrombocytopenia [26].

With regard to the predictive value of thrombocytopenia for infection and the underlying mechanisms of the association between them, some factors might be notable. First, patients with thrombocytopenia receive many transfusions of red blood cells and platelets in necessity, both of these interventions are proinflammatory [29, 30]. Second, infectious agents, with their prominent role in the causes of thrombocytopenia, help to decrease the platelet number by suppressing bone marrow directly or increasing peripheral consumption of platelets [8, 9]. Thus, to some extent, thrombocytopenia is able to reflect infection indirectly. Third, studies have demonstrated that platelets have a crucial role in response to infection by promoting translocation of immune cells to inflamed areas and releasing cytokines and other molecular mediators. Therefore, thrombocytopenia might inhibit platelet effects against infection by reducing the number of platelets and their function, which might be conducive to increasing the prevalence of in-hospital infection [31, 32]. Furthermore, platelets could inhibit macrophage-dependent inflammation, or enhance interleukin-10 secretion and reduce tumor necrosis factor-α (TNF-α) secretion during infectious and noninfectious systemic inflammation [33, 34]. Finally, in gram-negative pneumonia–derived sepsis in mice, thrombocytopenia was associated with a strongly impaired host defense via enhancing proinflammatory cytokine release and bacterial growth, and disrupting vascular integrity and activating endothelial cell [35].

In addition to thrombocytopenia, our study firstly found that the levels of serum albumin and hemoglobin was independently associated with the risk of infection. Leonardi and colleagues reported that declining hemoglobin content, with or without overt bleeding, was independently associated with heightened risk of 1-year mortality among patients with ACS managed invasively [36]. Plakht et al. demonstrated that decreased serum albumin level on admission was an independent prognostic marker of increased long-term all-cause mortality in patients with AMI [37], while hypoalbuminemia was also found to be significantly associated with worse in-hospital outcomes in patients with ACS [38]. However, we did not find that the levels of serum albumin and hemoglobin were associated with the risk of all-cause death, which might be attributed to the little sample size and low incidence of all-cause death in our study.

Our study highlights the notion that thrombocytopenia is infrequent in patients diagnosed with STEMI, but is associated with a markedly increased prevalence of infection and in-hospital MACE, and should not be underestimated. Early identification of thrombocytopenia is essential for appropriate clinical care of STEMI patients. Hence, dynamic monitoring of platelet count might be encouraged for cardiologists among high-risk patients to avoid complications.

This study also had several main limitations. First, the causes of thrombocytopenia were not elucidated clearly, and the diagnosis of thrombocytopenia according to one complete blood count (CBC) test might be not sufficient while minor variation might occur and platelet agglutination might result in technical CBC diagnosis of thrombocytopenia. Second, our study was carried out at a single center with a relatively small study cohort. Third, we evaluated a cohort of Chinese patients, so caution is needed when trying to apply our conclusions to another population. Fourth, we failed to collect the information about blood product transfusion, which might be a potential confounding factor. Finally, because of a lack of studies investigating the outcome of infection in thrombocytopenia patients, the potential molecular mechanisms could not be explored.

Conclusions

In summary, the present study indicated that thrombocytopenia during hospitalization was independently associated with an increased prevalence of infection and in-hospital MACE in patients with STEMI. Thrombocytopenia could be used as a simple prognostic tool for these patients.

Availability of data and materials

The datasets used and/or analyzed in this study are available from the corresponding author on reasonable request.

Abbreviations

STEMI:

ST-elevation myocardial infarction

AMI:

Acute myocardial infarction

ACS:

Acute coronary syndrome

PCI:

Percutaneous coronary intervention

MACE:

Major adverse clinical events

ITP:

Immune thrombocytopenia

DAPT:

Dual antiplatelet therapy

TNF-α:

Tumor necrosis factor-α

SBP:

Systolic blood pressure

DBP:

Diastolic blood pressure

COPD:

Chronic obstructive pulmonary disease

TC:

Total cholesterol

CABG:

Coronary artery bypass grafting

LDL-C:

Low-density lipoprotein cholesterol

LVEF:

Left ventricular ejection fraction

CCB:

Calcium channel blockers

CBC:

Complete blood count

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Acknowledgements

The concise abstract was presented previously at the Great Wall International Congress of Cardiology 2020 (GW-ICC 2020) for academic communication.

Funding

This study was supported by a grant from the Shuangqing Talent Program Project of Guangdong Provincial people's Hospital (No. KJ012019095 and KJ012019084), the first clinical research training course “seed fund” of Guangdong Provincial people's Hospital (No.2018lcpx04), Bureau of Education of Jiangxi province (No. GJJ180814) and Key projects of Gannan Medical University (No. ZD201807). The funders had no role in the study design, data collection and analysis, the decision to publish, or the preparation of the manuscript. The work was not funded by any industry sponsors.

Author information

Author notes

  1. Litao Wang, Weijiang Su and Jinhua Xue have contributed equally to this work

Authors and Affiliations

  1. Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial Key Laboratory of Coronary Heart Disease Prevention, Guangdong Provincial People’s Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510100, China

    Litao Wang, Yining Dai, Jiyan Chen, Ling Xue, Pengcheng He, Yuanhui Liu & Ning Tan

  2. Guangdong Provincial People’s Hospital, School of Medicine, South China University of Technology, Guangzhou, 510100, China

    Litao Wang, Pengcheng He & Ning Tan

  3. Department of Cardiology, The People’s Hospital of Dianbai District, Maoming, 525400, China

    Weijiang Su

  4. Department of Physiology, School of Basic Medical Sciences, Key Laboratory of Prevention and Treatment of Cardiovascular and Cerebrovascular Diseases of Ministry of Education, Gannan Medical University, Ganzhou, 341000, China

    Jinhua Xue

  5. School of Public Health, Guangdong Pharmaceutical University, Guangzhou, 510006, China

    Xiao Gong

  6. The Second School of Clinical Medicine, Southern Medical University, Guangzhou, 510515, China

    Pengcheng He & Ning Tan

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Contributions

Conception/Design: NT, YHL, PCH. Collection and/or assembly of data: LTW, YHL, WJS, JHX, YND. Data analysis and interpretation: YHL, LTW, WJS, JHX, XG, YND. Manuscript writing: LTW, YHL. Manuscript revising: NT, YHL, PCH, LX, JYC. Final approval of the version to be published: All authors. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Yuanhui Liu or Ning Tan.

Ethics declarations

Ethics approval and consent to participate

This research was approved by the Ethics Committee of Guangdong Provincial People’s Hospital (GDREC2016378H). The written informed consent was obtained from almost all of the patients before the procedure, and some informed consents were acquired from their next of kin for patients who could not sign informed consent themselves due to the chest pain or other reasonable causes.

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Not applicable.

Competing interests

The authors declare that they have no competing interests.

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Supplementary Information

Additional file 1: Table S1.

Association of platelet count on infection after multivariable adjustment.

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Wang, L., Su, W., Xue, J. et al. Association of thrombocytopenia and infection in patients with ST-elevation myocardial infarction undergoing percutaneous coronary intervention. BMC Cardiovasc Disord 21, 404 (2021). https://doi.org/10.1186/s12872-021-02210-3

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  • DOI: https://doi.org/10.1186/s12872-021-02210-3

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BMC Cardiovascular Disorders

ISSN: 1471-2261

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