Bloodstream Infection and Endocarditis Caused by Staphylococcus aureus in Patients with Cancer: A Multicenter Cohort Study.

INTRODUCTION: In a large cohort of patients with Staphylococcus aureus bloodstream infection (SABSI), we aimed to analyze the incidence and risk factors for infective endocarditis (IE) among patients with active cancer (PAC) in comparison with those without cancer (PWC).
METHODS: Multicenter cohort study of patients with SABSI admitted to two tertiary care hospitals, from 2011 to 2019. PAC were defined as those with an active solid organ cancer or hematological malignancies. SABSI and S. aureus IE were compared between PAC and PWC.
RESULTS: Among 978 episodes of SABSI, 217 (22.2%) occurred in PAC. PAC were younger, had fewer comorbidities, carried cardiac devices less often, and had less community-acquired SABSI than PWC. Compared to PWC, PAC more frequently had catheter-related SABSI, less IE (2.8% vs 10.9%, p < 0.001) and osteoarticular infection (2.3% vs 14.3%, p < 0.001). Independent risk factors for IE were cardiopathy (aOR 4.392, 95% CI 2.719-7.094) and persistent bacteremia (aOR 3.545, 95% CI 2.159-5.820). Thirty-day mortality was high, and similar between groups (24.2% vs 25.5%, p = 0.282).
CONCLUSIONS: PAC with SABSI developed IE less frequently than PWC did. This finding seems related to the differences in baseline characteristics and may have significant clinical implications, such as transesophageal echocardiography in PAC without cardiopathy or persistent bacteremia.

Key Summary Points

Introduction

Staphylococcus aureus is one of the leading causes of bloodstream infection (BSI) worldwide [1]. Healthcare exposure and invasive procedures increase the burden of this disease [2]. Furthermore, S. aureus is ranked among the most important causes of bloodstream infection-associated death [3]. Mortality of patients with S. aureus bloodstream infection (SABSI) has been consistently associated with host and pathogen characteristics as well as with prompt source management and adequate antibiotic treatment [3]. One of the most important aspects among the host–pathogen interaction is the source of the infection. Among these, endocarditis and pneumonia are the ones with the highest associated mortality rates [3]. S. aureus causes around 25% of episodes of infective endocarditis (IE) [4]. In a recent Danish nationwide study including 69,000 bacteraemia episodes, IE was diagnosed in one of every 10 SABSI episodes [5], and it has also been identified as a strong risk factor for 30-day mortality in patients with SABSI [6, 7].

Cancer incidence and mortality are rapidly rising worldwide [8]. Bloodstream infection (BSI) entails an important risk of complications in patients with malignancy. Indeed, cancer is the most frequent comorbidity in patients with sepsis, described in 17% of cases [9]. BSI in patients with cancer may delay the start of chemotherapy, increase the length of hospitalization and costs, and raise morbidity and mortality rates [10]. SABSI is a serious complication in patients with cancer, and is a clear risk factor for mortality, with an odds ratio (OR) of 1.8 (95% CI 1.03–3.15) [11].

To date, few studies have specifically focused on SABSI in patients with cancer, even though it is the second leading cause of Gram-positive BSI [12]. SABSI has usually been associated with gastrointestinal mucositis and catheter-related infection [13, 14]. Nosocomial acquisition, urinary catheter, nasogastric tube, corticosteroids, skin and soft tissue infection, and pneumonia are also significantly associated with SABSI in patients with malignancy [11]. The incidence of IE in patients with cancer and SABSI seems to be lower than in patients without cancer, but this issue has not been explored in depth in the literature [15, 16]. To the best of our knowledge, no studies have focused on IE in this specific population. Nor have the characteristics of SABSI in patients with cancer been compared with those of SABSI in other patients, and it is not clear at present why patients with cancer appear to be less prone to IE than patients without malignancies.

In our large multicenter cohort of SABSI, we aimed to analyze the epidemiology, clinical characteristics, risk factors for IE, and outcomes of patients with active cancer (PAC) in comparison with those without malignancies (PWC).

Methods

Study Design, Setting, and Participants

The study design consisted in a retrospective cohort analyses of prospectively collected data of SABSI episodes in adult patients (at least 18 years old) hospitalized from January 2011 to December 2019 in two tertiary care hospitals in Barcelona, Spain: Bellvitge University Hospital, a 700-bed teaching hospital for adults, and Duran i Reynals Hospital, a 200-bed referral cancer center. Positive blood cultures were reported daily by members of the Microbiology Department. All patients were prospectively followed up by infectious disease specialists during hospital admission and for up to 90 days thereafter.

This study was approved by the Clinical Research Ethics Committee of Bellvitge University Hospital (PR326/21). The informed consent form and information sheet were waived because of the retrospective nature of the study. Patient data were anonymized for the purposes of the analysis. Information that could identify patients was protected according to the national normative approach.

Some parts of the methodologies and analyses used in this study were similar to those published in some of our previous studies, reported elsewhere [17, 18].

Variables and Data Sources

Demographic, epidemiological, clinical, and microbiological data were prospectively collected from patients with SABSI. For each patient, the following data were recorded: age, sex, comorbidities, functional and immunological status, history of contact with healthcare providers or prior antibiotic therapy, implanted foreign bodies or devices, clinical data at the BSI onset (grade of severity of illness at presentation, source of infection, and the presence of septic emboli), diagnostic and therapeutic interventions, antibacterial therapy, and outcomes. Follow-up information for up to 90 days after BSI was obtained by reviewing the patients’ electronic clinical charts, in order to assess the mortality and microbiological failure rates.

Bias

All consecutive episodes of SABSI detected during the study period were included in the initial analysis with the objective of minimizing selection bias.

Definitions

SABSI was defined as at least one positive blood culture obtained from a patient with clinical signs and symptoms of infection (namely fever, chills, malaise, specific signs or symptoms of infection, e.g., phlebitis, cellulitis, septic emboli). The presence of underlying diseases was assessed by the Charlson comorbidity index [19]. BSI acquisition categories were considered in three mutually exclusive classes, community-acquired, nosocomial, and healthcare-related, based on the criteria from Friedman et al. [20]. Sepsis was assessed with the quick Sequential Organ Failure Assessment (qSOFA) score, and was defined as a score of at least 2 points [21].

The source of infection was defined as the infective focus possibly responsible for the BSI, based on the clinical presentation, physical examination, and complementary results. The sources of infection included eight groups: vascular catheter-related infections; infective endocarditis (according to the modified Duke criteria) [22]; skin and soft tissue infections; pneumonia; osteoarticular infections (with or without prosthetic devices); urinary tract infections; unknown; and other sources (including abdominal, head and neck, and central nervous system sources). IE was considered for both source of infection and complication of BSI from another source.

Platelet count was assessed at the time of hospitalization and confirmed with a second blood count performed 48–72 h after hospital admission. Previous or concomitant use (for at least 3 months before SABSI) of antiplatelet and anticoagulant drugs was recorded. Echocardiography was performed in all patients except those who presented rapid clearance of bacteremia.

Persistent bacteremia was considered when follow-up blood cultures after more than 2 days of treatment were positive. Cases of positive blood culture after negative follow-up blood cultures were considered recurrent bacteremia. We considered consecutive episodes where bacteremia occurred after the 90-day follow-up and after clear resolution of the previous episode. Source control refers to all the physical procedures used to control a focus of infection, including drainage of liquid/purulent abscesses, debridement of necrotic tissues, removal of indwelling catheters and potentially infected devices, and we considered this achieved if performed within the first 72 h from BSI.

Cardiopathy was defined as the presence of one or more of the following conditions: previous predisposing factor for IE heart conditions such as valvular heart disease and/or presence of cardiac devices. Valvulopathy or valvular heart disease was defined as the presence of previous damage in any cardiac valve. Patients with active cancer (PAC) were defined as those with active solid organ cancer or hematological malignancies, who underwent chemotherapy/radiotherapy and/or hematopoietic stem cell transplant in the previous 3 months or who had metastatic cancer. SABSI and S. aureus IE in PAC were compared with patients without cancer (PWC). Mortality was defined as all-cause death and was evaluated 30 days after bacteremia onset.

Microbiological Studies

Blood cultures were processed in a BD BACTEC™ FX blood culture system (Becton Dickinson, Barcelona, Spain) at the Department of Microbiology of Bellvitge University Hospital. In the first 2 years of the study (2011–2012), S. aureus was identified by latex agglutination tests (Pastorex Staph-plus, Bio-Rad Laboratories, Madrid, Spain) and DNase production (DNase test agar, bioMérieux, Marcy l’Etoile, France). From 2013 onwards, identification was carried out by MALDI-TOF (MALDI Biotyper; Bruker Daltonics, Spain). Antimicrobial susceptibility was determined by microdilution using commercially available panels (MicroScan, Beckman Coulter, Barcelona, Spain) and according to the EUCAST guidelines [23]. To rapidly assess methicillin resistance, following positivity of the blood culture and the confirmation of S. aureus isolation, Xpert® MRSA/SA Blood Culture (Cepheid, Sunnyvale, CA) was used.

Statistical Methods

To calculate the incidence of SABSI and IE, we divided the number of episodes of SABSI and IE, respectively, by the annual hospital discharges. Categorical variables are presented as numbers of episodes and percentages, and continuous variables as means and standard deviation or medians and interquartile range (IQR). Continuous variables were compared using the Student’s t test or Mann–Whitney U test as appropriate. Fisher exact test or Pearson χ2 test was applied to assess the relationship between categorical variables. All consecutive episodes of SABSI detected during the study period were included in the analysis in order to minimize selection bias.

Multivariate logistic regression analysis was then used to assess factors potentially associated with IE and with 30-day mortality, and included all significant variables identified in the univariate analysis along with the relevant ones according to the literature. The goodness of fit of the model was assessed by the Hosmer–Lemeshow test. Relative risks are expressed as adjusted odds ratios (aORs) and 95% confidence intervals. Statistical significance was established at α = 0.05. All reported p values are two tailed.

Results

Participants and Descriptive Data

During the study period, 978 episodes of SABSI were recorded and followed up. Of these, 761 (77.8%) occurred in PWC and 217 (22.2%) in PAC. Among PAC, 104 (47.9%) had solid organ cancer and 113 (52.1%) had hematological malignancies. Among solid organ cancer, patients had more frequently head and neck (13.4%), breast (9.6%), and colorectal cancer (8.6%). The hematological malignancies most frequently identified were myeloid acute leukemia (23%), multiple myeloma (14%), diffuse large B cell lymphoma (8%), and T cell lymphomas (8%). Seventeen patients (15%) had previously undergone hematopoietic stem cell transplantation. Seventy PAC (32.2%) presented neutropenia  (neutrophil level less than 500/µL) at SABSI presentation, while in five (2.3%) citomegalovirus infection was documented and seven patients presented invasive fungal infection (3.2%). The incidences of SABSI are shown in Fig. 1: the incidence of SABSI was higher in PAC than in PWC (7.3/1000 hospital discharges/year vs. 2.9/1000 hospital discharges/year, p < 0.001).

Fig. 1

Incidence of S. aureus bloodstream infection. SABSI Staphylococcus aureus bloodstream infection, PWC patients without cancer, PAC patients with active cancer

Baseline characteristics and differences between PAC and PWC are shown in Table 1. Overall, there were 647 men (66.3%), mean age was 64.6 years, and the patients had a mean Charlson comorbidity index of 5.4 points. PAC were younger, had fewer chronic comorbidities, and they were less likely to receive antiplatelet drugs. Acquisition of SABSI was different between PAC and PWC (p < 0.001): community-acquired SABSI was more common in PWC than in PAC (7.4% vs 28.0%), while PAC had more healthcare-related (54.4% vs 41.7%) and nosocomial SABSI (38.2% vs 30.4%). Catheter-related infection was more often diagnosed in PAC (41.5% vs 25.4%, p < 0.001), although IE (2.8% vs 10.9%, p < 0.001) and osteoarticular infections (2.3% vs 14.3%, p < 0.001) were less frequent in these patients. PAC were less likely to have indwelling foreign material in place, such as osteoarticular prosthesis (1.8% vs 10.5%, p < 0.001) and cardiac devices (0.5% vs 7.4%, p < 0.001). PAC presented more thrombocytopenia, and less sepsis, persistent bacteremia, and metastatic infections. Echocardiography was performed more often in PWC (43.7% vs 75.8%, p < 0.001).

Table 1

Baseline characteristics of patients with S. aureus bloodstream infection

Variables	Total (n = 978)	No malignancy (n = 761)	Malignancy (n = 217)	p values
Age, years, mean (SD)	64.6 (15.9)	66.1 (15.8)	59.5 (15.2)	0.001
Age > 65 years	521 (53.3)	441 (58.0)	80 (36.9)	< 0.001
Male sex	647 (66.3)	504 (66.4)	143 (65.9)	0.890
Comorbidities
Charlson comorbidity index
Mean (SD)	5.4 (2.89)	5.3 (2.8)	5.9 (3.2)	0.007
Charlson > 6 points	338 (34.6)	249 (32.7)	89 (41.0)	0.023
Cardiopathy	191 (19.5)	171 (22.5)	20 (9.2)	< 0.001
Valvulopathy	155 (16.7)	136 (18.9)	19 (9.1)	0.001
Diabetes mellitus	327 (33.4)	296 (38.9)	31 (14.3)	< 0.001
COPD	190 (19.9)	164 (22.2)	26 (12.0)	0.001
Chronic renal failure	217 (22.7)	202 (27.4)	15 (6.9)	< 0.001
Neurological disorders	122 (12.8)	115 (15.6)	7 (3.2)	< 0.001
Previous corticosteroids	177 (19.1)	97 (13.5)	80 (37.9)	< 0.001
Antiplatelet drugs	238 (24.7)	220 (29.3)	18 (8.5)	< 0.001
Anticoagulant drugs	141 (16.4)	128 (17.1)	13 (11.9)	0.176
Acquisition
Community acquired	229 (23.4)	213 (28.0)	16 (7.4)	< 0.001
Healthcare related	435 (44.5)	317 (41.7)	118 (54.4)	< 0.001
Nosocomial	314 (32.1)	231 (30.3)	83 (38.2)	< 0.001
MRSA	207 (21.2)	170 (22.3)	37 (17.1)	0.093
Source of bloodstream infection
Catheter-related infection	283 (28.9)	193 (25.4)	90 (41.5)	< 0.001
Infective endocarditis	89 (9.1)	83 (10.9)	6 (2.8)	< 0.001
Ostheoarticular infection	114 (11.7)	109 (14.3)	5 (2.3)	< 0.001
SSTI	148 (15.1)	109 (14.3)	39 (18.0)	0.186
Urinary tract infection	55 (5.6)	45 (5.9)	10 (4.6)	0.462
Unknown	136 (13.9)	100 (13.1)	36 (16.6)	0.195
Indwelling foreign materials
Ostheoarticular prosthesis	84 (8.6)	80 (10.5)	4 (1.8)	< 0.001
Cardiac device	57 (5.8)	56 (7.4)	1 (0.5)	< 0.001
Thrombocytopenia < 100,000/µL	179 (18.3)	78 (10.3)	101 (46.1)	< 0.001
Thrombocytopenia < 50,000/µL	85 (8.7)	21 (2.8)	64 (29.5)	< 0.001
Thrombocytopenia < 20,000/µL	34 (3.5)	2 (0.3)	32 (14.7)	< 0.001
Severity illness
Sepsis or septic shock	317 (32.4)	276 (36.3)	41 (18.9)	< 0.001
Metastatic infection	127 (13.0)	119 (15.6)	8 (3.7)	< 0.001
Infection management
Echocardiography	484 (67.2)	405 (75.8)	79 (42.5)	< 0.001
Source control (< 72 h)	423/651 (65.0)	382/590 (64.7)	41/61 (67.2)	0.701
Outcomes
Persistent bacteremia	172/856 (20.1)	143/663 (21.6)	29/193 (15.0)	0.026
30-day mortality	242/978 (24.7)	189/761 (25.5)	53/217 (24.2)	0.282

Data are presented as no. (%), unless otherwise specified

Statistically significant differences are marked in bold

SD standard deviation, COPD chronic obstructive pulmonary disease, MRSA methicillin-resistant S. aureus, SSTI skin and soft tissues infection

Risk Factors for Infective Endocarditis

Eighty-nine patients (9.1%) were diagnosed with IE. Among them, six (6.7%) were PAC, four with hematological malignancy and two with solid cancer. Clinical characteristics of PAC with IE are detailed in Table 1 of the supplementary material.

Compared with patients with other sources of BSI in the univariate analysis, patients with IE had more previous cardiopathy (49.4% vs 16.5%, p < 0.001), valvulopathy (37.5% vs 14.5%, p < 0.001), cardiac devices (21.3% vs 4.3%, p < 0.001), and presented more sepsis at presentation (44.9% vs 31.2%, p = 0.008), whereas they had less often an underlying malignant disease (6.7% vs 23.7%, p < 0.001). In the multivariate analysis, the presence of previous cardiopathy (aOR 4.392; 95% CI 2.719–7.094, p < 0.001) and persistent bacteremia (aOR 3.545, 95% CI 2.159–5.820, p < 0.001) were the only risk factors independently associated with IE, whereas active cancer was identified as a protective factor (aOR 0.338, 95% CI 0.142–0.806, p = 0.011) (Table 2). Goodness of fit, assessed by the Hosmer–Lemeshow test, was 0.277. This protective effect was also observed when solid organ cancer and hematological malignancies were analyzed separately (data not shown). As shown in Table 2 of the supplementary material, no significant differences were observed between PWC and PAC with IE.

Table 2

Univariate and multivariate analyses for risk factors for endocarditis

Variable	Patients without endocarditis (n = 889)	Patients with endocarditis (n = 89)	p value	OR	95% CI	p value
Age > 65 years	471 (53.0)	50 (56.2)	0.564
Cardiopathy	147 (16.5)	44 (49.4)	< 0.001	4.392	2.719–7.094	< 0.001
Cardiac devices	38 (4.3)	19 (21.3)	< 0.001
Valvulopathy	122 (14.5)	33 (37.5)	< 0.001
Malignancy	211 (23.7)	6 (6.7)	< 0.001	0.338	0.142–0.806	0.014
Charlson > 6	311 (35.0)	27 (30.3)	0.38
Antiplatelet drug	212 (24.3)	26 (29.2)	0.305
Platelet < 50,000/μL	80 (9.0)	5 (5.6)	0.191
Platelet < 20,000/μL	33 (3.7%)	1 (1.1)	0.167
Sepsis	277 (31.2)	40 (44.9)	0.008	1.371	0.838–2.242	0.209
MRSA	196 (22.0)	11 (12.4)	0.033
Persistent bacteremia	130 (14.8)	41 (46.1)	< 0.001	3.545	2.159–5.820	< 0.001

Data are presented as no. (%), unless otherwise specified

Statistically significant differences are marked in bold

OR odds ratio, CI confidence interval, MRSA methicillin-resistant S. aureus

Outcomes

All-cause 30-day mortality among 978 episodes of SABSI was 24.6%. No differences were found between PWC and PAC. After multivariate analysis, risk factors that remained independently associated with 30-day mortality were age > 65 years, Charlson > 6 points (aOR 1.881; 95% CI 1.265–2.797; p = 0.002), unknown source of infection (aOR 2.759; 95% CI 1.650–4.611, p < 0.001), sepsis (aOR 7.578; 95% CI 5.177–11.090, p < 0.001), infection due to methicillin-resistant S. aureus (MRSA) strain (aOR 1.619; 95% CI 1.006–2.608, p = 0.047), and persistent bacteremia (aOR 5.666; 95% CI 3.314–9.687; p < 0.001) (Table 3 in the supplementary material).

Among PAC, patients who died within 30 days were older, more often had solid organ cancer, unknown source of BSI, MRSA infection, sepsis and persistent bacteremia, while they had less frequently catheter-related infection and prompt source control. In the multivariate analysis, risk factors independently associated with 30-day mortality were solid organ cancer (aOR 3.239, 95% CI 1.557–6.739, p = 0.002), unknown source of infection (aOR 5.566; 95% CI 2.146–14.443, p < 0.001), and MRSA infection (aOR 4.240, 95% CI 1.808–9.943, p = 0.001) (Table 4 in the supplementary material). No PAC had SABSI relapse, while it occurred in seven PWC.

Discussion

The present study, the first cohort study to compare SABSI and IE in patients with cancer and the general population, found IE to be significantly less frequent in PAC, probably because of notable differences in the source of SABSI, baseline comorbidities, and site of acquisition between the groups.

In agreement with previous work, we found a higher incidence of SABSI in PAC than in PWC [24]. PAC are highly susceptible to SABSI as a result of their frequent hospital admissions, chemotherapy administration, common use of long-term indwelling catheters, and other invasive procedures [25]. In fact, in our cohort, PAC had more catheter-related BSI and a higher rate of healthcare-related or nosocomial SABSI acquisition, showing a clear relationship of this population with healthcare exposure.

The incidence of IE in patients with cancer and SABSI ranges between 1.6% and 6% [15, 16]. Despite the higher incidence of SABSI in PAC, in our cohort few patients (6/217, 2.7%) in this group developed infective IE. A number of reasons may explain this finding. First of all, PAC with SABSI presented different epidemiological and clinical characteristics with respect to PWC: PAC were younger, had less comorbidity (including cardiopathy and cardiac or orthopedic devices), and had more catheter-related, healthcare-associated, and nosocomial SABSI. Indeed, PAC with SABSI exhibited a faster clearance of bacteremia than PWC. All these features have previously been found to be associated with a lower risk of IE [26, 27]. Second, an appealing pathogenic explanation of the lower frequency of IE could be the higher prevalence of thrombocytopenia in PAC. Platelet aggregation has a fundamental role in the formation of the vegetation. It has recently been demonstrated that activation of endothelial cells stimulates the release of von Willebrand factor multimers which bind circulating platelets as well as S. aureus [28]. Moreover, the presence of platelets increases the adhesion of S. aureus to collagen under flow conditions, overcoming shear stress [28, 29]. Of note, thrombocytopenia was present in half of the PAC in our cohort using a cutoff of 100,000/µL, and it was more frequent in this group even when more restrictive cutoff values were used (50,000/µL or 20,000/µL). Although thrombocytopenia may have a protective role in PAC, we did not find this factor to be independently associated to the risk of developing IE. Moreover, previous studies in experimental models of IE have demonstrated that antiplatelet treatment may also hinder vegetation formation [30]. Recently, the use of dabigatran was also associated with a lower risk of SABSI in a large cohort of patients and with a lower risk of IE in an animal model [30, 31]. Nevertheless, we were not able to demonstrate the use of either antiplatelet agents or anticoagulant as a protective factor for IE.

Regarding the diagnostic approach to SABSI in PAC, and as a result of the low incidence of IE in this group, the question of whether these patients should undergo systematic transesophageal echocardiography (TEE) is controversial. In a recent study of the role of echocardiography in patients with cancer and SABSI, the authors did not find any additional infective IE after performing subsequent TEE [16]. Our study suggests that TEE is not mandatory in all PAC with SABSI and individualized indication should be carried out.

In our cohort, the 30-day mortality rate in PAC with SABSI was 24.2%, a figure higher than reported in previous studies, typically between 16.7% and 21.2% [12, 15]. Importantly, although PAC presented more low-risk SABSI, 30-day mortality in this group was as high as in PWC. Unlike a previous study that reported hematological malignancies as a risk factor for mortality in SABSI [15], we found that patients with solid organ cancer and unknown source of infection had a higher risk for 30-day mortality. Various explanations might be proposed for the higher mortality rate observed in patients with solid organ cancer. First, our cohort also included patients admitted to palliative care units, mostly with solid tumors. Second, the higher mortality rate might reflect more severe disease, given that the hospitals in our study are tertiary referral centers in Catalonia. Third, patients with hematological malignancy were younger and had less comorbidity than patients with solid organ cancer, features inversely associated with mortality.

This study has some strengths and limitations. It is, to the best of our knowledge, the first to compare SABSI and IE in PAC with those in patients without malignancy, and also the first to report the clinical characteristics and risk factors for S. aureus IE in this population. Although the study was conducted at two different centers, the large cohort of patients included increases the external validity of its results. The main limitation of this study was its retrospective design, although the patients were prospectively followed by infectious disease specialists. The low prevalence of IE in patients with cancer also hampered the multivariate analysis of risk factor for IE in this specific group. Because PAC were closely monitored, SABSI could be detected, diagnosed, and treated earlier in the course of the disease in PAC than in PWC and it could therefore be prone to selection bias.

Conclusions

PAC showed a higher incidence of SABSI and IE was detected less frequently than in PWC. Relevant differences in sources of SABSI, baseline comorbidities, and site of acquisition could explain the differential risk observed between populations. Thirty-day mortality was high in both groups of patients, underlying the importance of prompt source control and optimal antibiotic treatment. Our study suggests that PAC without previous cardiopathy and with rapid clearance of bacteremia have a low risk of developing IE. Thus, it is necessary to individualize the evaluation of the necessity of TEE in selected patients. This may reduce costs, length of stay, and avoid possible complications.

Below is the link to the electronic supplementary material.

Supplementary file1 (PDF 842 KB)

The incidence of S. aureus endocarditis was lower in patients with cancer compared to patients without cancer.

Risk factors for endocarditis were previous cardiopathy and persistent bacteremia.

Key baseline differences explain lower incidence of endocarditis in patients with cancer.

Transesophageal echocardiography could be avoided in patients with cancer without cardiopathy or persistent bacteremia.