Literature DB >> 24779617

Predicting the occurrence of embolic events: an analysis of 1456 episodes of infective endocarditis from the Italian Study on Endocarditis (SEI).

Marco Rizzi1, Veronica Ravasio, Alessandra Carobbio, Irene Mattucci, Massimo Crapis, Roberto Stellini, Maria Bruna Pasticci, Pierangelo Chinello, Marco Falcone, Paolo Grossi, Francesco Barbaro, Angelo Pan, Pierluigi Viale, Emanuele Durante-Mangoni.   

Abstract

BACKGROUND: Embolic events are a major cause of morbidity and mortality in patients with infective endocarditis. We analyzed the database of the prospective cohort study SEI in order to identify factors associated with the occurrence of embolic events and to develop a scoring system for the assessment of the risk of embolism.
METHODS: We retrospectively analyzed 1456 episodes of infective endocarditis from the multicenter study SEI. Predictors of embolism were identified. Risk factors identified at multivariate analysis as predictive of embolism in left-sided endocarditis, were used for the development of a risk score: 1 point was assigned to each risk factor (total risk score range: minimum 0 points; maximum 2 points). Three categories were defined by the score: low (0 points), intermediate (1 point), or high risk (2 points); the probability of embolic events per risk category was calculated for each day on treatment (day 0 through day 30).
RESULTS: There were 499 episodes of infective endocarditis (34%) that were complicated by ≥ 1 embolic event. Most embolic events occurred early in the clinical course (first week of therapy: 15.5 episodes per 1000 patient days; second week: 3.7 episodes per 1000 patient days). In the total cohort, the factors associated with the occurrence of embolism at multivariate analysis were prosthetic valve localization (odds ratio, 1.84), right-sided endocarditis (odds ratio, 3.93), Staphylococcus aureus etiology (odds ratio, 2.23) and vegetation size ≥ 13 mm (odds ratio, 1.86). In left-sided endocarditis, Staphylococcus aureus etiology (odds ratio, 2.1) and vegetation size ≥ 13 mm (odds ratio, 2.1) were independently associated with embolic events; the 30-day cumulative incidence of embolism varied with risk score category (low risk, 12%; intermediate risk, 25%; high risk, 38%; p < 0.001).
CONCLUSIONS: Staphylococcus aureus etiology and vegetation size are associated with an increased risk of embolism. In left-sided endocarditis, a simple scoring system, which combines etiology and vegetation size with time on antimicrobials, might contribute to a better assessment of the risk of embolism, and to a more individualized analysis of indications and contraindications for early surgery.

Entities:  

Mesh:

Year:  2014        PMID: 24779617      PMCID: PMC4101861          DOI: 10.1186/1471-2334-14-230

Source DB:  PubMed          Journal:  BMC Infect Dis        ISSN: 1471-2334            Impact factor:   3.090


Background

Embolic events are common complications of infective endocarditis (IE) and are of prognostic importance [1-3]. Neurologic complications, mostly caused by embolic events, are frequent causes of intensive care unit admission, and embolism is a strong predictor of death for patients who have IE [4-8]. Small, clinically inapparent emboli probably occur in most patients who have IE, as demonstrated with positron-emission tomography and magnetic resonance imaging; silent cerebrovascular complications (including ischemia and microhemorrhage) may occur in up to 81% of patients [9-11]. Symptomatic embolism may occur in 13% to 46% of patients [6,12,13]. Many symptomatic emboli involve the central nervous system; clinical evidence of cerebrovascular embolic events is present in 12% to 40% of patients who have IE; the incidence may be higher in patients who are treated in referral centers, critically ill, or admitted to an intensive care unit [5,6,14]. Assessment of the embolic risk in individual patients is difficult, this having a major impact on clinical decisions regarding the indications for diagnostic procedures, antiaggregant and anticoagulant therapy and the timing of cardiac valve surgery [2,3,12,15-20]. Prevention of embolism is an established indication for surgery; in the Euro Heart Survey, vegetation size and previous embolism were reported as factors contributing to the surgical decision in, respectively, 48% and 18% of the patients who had surgery; in the French series recently published by Hubert et al. the presence of large vegetations (with or without previous embolism) was reported as an indication for surgery in 36% of the 493 patients who underwent surgery [3,21,22]. Most previous studies about the embolic complications of IE have been retrospective, with selection bias and limited numbers of patients. In addition, the epidemiology and standard of care of IE have clearly evolved over the years, and less recent observations may no more adequately represent the contemporary clinical profile of the disease [8,12,23-26]. The present study was based on data from a large prospective observational cohort; the retrospective analysis of the database had two main objectives: (1) to identify factors associated with the occurrence of embolic events and (2) to design a scoring system for the assessment of the risk of embolic complications.

Methods

Patients

The Italian Study on Endocarditis (Studio Endocarditi Italiano - SEI) working group was established in October 2003 in order to promote research on IE in Italy. Within this group, a prospective, observational, multicenter, open cohort study was designed. All consecutive episodes of IE diagnosed from January 2004 through December 2011 at 25 secondary and tertiary care institutions were included in the study. The diagnosis of IE was defined as possible or definite, in accordance with the modified Duke criteria [27]. Adult and pediatric patients were identified prospectively using institution-specific procedures, so as to ensure the consecutive enrollment of all the patients with IE observed at each participating institution. Echocardiography, diagnosis of embolic complications and treatment, were in accordance with current clinical practice (the study did not prescribe a standard diagnostic and therapeutic approach). At the time of clinical observation of each patient, clinical data were recorded in a form that was designed for the study and registered in an electronic data entry system. The SEI database was maintained at the Infectious Diseases Department, Bergamo Hospital; the study was approved by the ethics committee “Comitato di Bioetica dell'Azienda Ospedali Riuniti di Bergamo”, and patients consented to enrollment in the SEI cohort as required by local guidelines and procedures. Details on the SEI study have been previously published [28]. Here we present the results of a retrospective analysis of the SEI database, aimed at investigating factors associated with the occurrence of embolic events; all the episodes of possible and definite IE were included.

Clinical data

Available information included demographic data, predisposing conditions, anatomic site of disease, microbiology, echocardiographic findings (presence, number, location and maximal length of vegetations), antimicrobial and surgical treatment, complications (heart failure, embolic events, intracardiac abscess, persistent positive blood cultures and new cardiac conduction abnormalities) and clinical outcome (survival and New York Hearth Association functional class). Central nervous system embolic events were reported as transient ischemic attack, ischemic stroke or hemorrhagic stroke. Peripheral embolic events were reported with details of anatomic site. Mycotic aneurysms, meningitis, encephalopathy, cerebral abscesses, arthritis, spondylodiscitis and cutaneous complications were excluded. Infective endocarditis was classified as left-sided IE (LS-IE), left-sided native valve IE (LS-NVE), left-sided prosthetic valve IE (LS-PVE), right-sided IE (RS-IE) or IE associated with a cardiac implantable electronic device (CIED-IE).

Statistical analysis

Data analysis was performed with statistical software (Stata 13, StataCorp LP, College Station, TX). Comparisons were done using χ2 test (chi-square test) for proportions and Mann–Whitney test for ordered or continuous variables. Receiver operating characteristic (ROC) analysis was performed to determine the optimal vegetation size cut-off for the prediction of embolism. Cumulative incidence analysis was performed from the date of starting treatment to the date of embolism (uncensored) or discharge from the hospital (censored). Cardiac surgery was treated as a competing event. Univariate and multivariate analyses were performed with logistic regression. Variables that were statistically significant in univariate analysis, variables that were clinically meaningful and possible confounders, were selected for prognostic assessment. For LS-IE, a weight was assigned to each factor that was associated with embolism, in order to build a risk score. The Kaplan‒Meier method was used to estimate univariate cumulative incidence of embolism according to the risk score. All tests were 2-sided, and statistical significance was defined by p ≤ 0.05. The probability of the occurrence of embolic events for each risk category was calculated for each day on treatment (from day 1 through day 30).

Results

Clinical characteristics of patients and embolic events

During the study period, 1456 IE episodes were observed at the participating institutions (1297 definite and 159 possible episodes); 10 episodes (0.7%) involved pediatric patients (age <18 y); basic demographic and medical data are summarized in Table 1.
Table 1

Demographic and clinical characteristics of the cohort*

CharacteristicsAll episodesLS-NVELS-PVERS-IECIED-IE
Number of IE episodes
1456 (100)
967 (66.4)
339 (23.3)
89 (6.1)
61 (4.2)
Age (y)
65 (50 to 64)
64 (48 to 74)
70 (61 to 76)
48 (35 to 67)
67 (55 to 77)
Male
1018 (70)
688 (71)
221 (65)
61 (69)
48 (79)
Comorbidity and predisposing conditions
 
  Native valve disease
372 (26)
299 (31)
60 (18)
7 (8)
6 (10)
  Diabetes mellitus
268 (18)
164 (17)
79 (23)
10 (11)
15 (25)
  Chronic liver disease
262 (18)
169 (18)
49 (15)
38 (43)
6 (10)
  Cancer
175 (12)
131 (14)
28 (8)
10 (11)
6 (10)
  Chronic intravenous access
154 (11)
102 (11)
34 (10)
11 (12)
7 (12)
  Current intravenous drug abuse
131 (9)
81 (8)
14 (4)
34 (38)
2 (3)
  Previous IE
118 (8)
48 (5)
59 (17)
7 (8)
4 (7)
  Congenital heart disease
112 (8)
85 (9)
16 (5)
6 (7)
5 (8)
  Immunosuppressive therapy
86 (6)
70 (7)
11 (3)
2 (2)
3 (5)
  HIV infection
52 (4)
36 (4)
4 (1)
10 (11)
2 (3)
  Hemodialysis
29 (2)
21 (2)
4 (1)
2 (2)
2 (3)
Microbiology
 
  Staphylococcus aureus
283 (19)
181 (19)
53 (16)
35 (39)
14 (23)
  Viridans group streptococci
217 (15)
172 (18)
29 (9)
8 (9)
8 (13)
  Enterococcus species
182 (13)
117 (12)
53 (16)
8 (9)
4 (7)
  Coagulase-negative staphylococci
147 (10)
74 (8)
55 (16)
4 (5)
14 (23)
  Streptococcus bovis
142 (10)
105 (11)
29 (9)
7 (8)
1 (2)
  Other streptococci
59 (4)
46 (5)
7 (2)
3 (3)
3 (5)
  Other microorganisms
61 (4)
36 (4)
20 (6)
2 (2)
3 (5)
  Polymicrobial
51 (4)
34 (4)
10 (3)
4 (5)
3 (5)
  Fungi
20 (1)
12 (1)
8 (2)
0 (0)
0 (0)
  HACEK
3 (0.2)
0 (0)
2 (0.6)
1 (1)
0 (0)
  Microbiology negative291 (20)190 (20)73 (22)17 (19)11 (18)

*Data reported as number, median (interquartile range), or number (% patients).

Abbreviations:CIED-IE infective endocarditis associated with a cardiac implantable electronic device, HACEKHaemophilus species, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, and Kingella kingae, HIV human immunodeficiency virus, LS-NVE left-sided native valve endocarditis, LS-PVE left-sided prosthetic valve endocarditis, RS-IE right-sided infective endocarditis.

Demographic and clinical characteristics of the cohort* *Data reported as number, median (interquartile range), or number (% patients). Abbreviations:CIED-IE infective endocarditis associated with a cardiac implantable electronic device, HACEKHaemophilus species, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, and Kingella kingae, HIV human immunodeficiency virus, LS-NVE left-sided native valve endocarditis, LS-PVE left-sided prosthetic valve endocarditis, RS-IE right-sided infective endocarditis. Embolization occurred in 499 IE episodes (34.3%), with more than one embolic event in 135 episodes (9.3%), and a cumulative number of 700 embolic events (Table 2). In 121/499 IE episodes (24.2%) the first embolic event occurred in the days preceding the diagnosis of IE and the start of antimicrobial therapy; in 77 cases (15.4%) on the same day of diagnosis. After the starting of antimicrobial therapy, most embolic events occurred early (15.5 episodes per 1000 patient days during the first week of therapy; 3.7 episodes per 1000 patient days during the second week of therapy) (Figure 1). In 93 IE episodes, the disease was complicated by both CNS and peripheral embolism; in 25 of these episodes CNS embolism was preceded by overt peripheral embolism.
Table 2

Type and anatomic site of embolic events*

CharacteristicsAll IE episodesLS-NVELS-PVERS-IECIED-IE
Number of IE episodes
1456
967
339
89
61
Embolic events
700
436
166
74
24
CNS emboli
249 (36)
174 (40)
68 (41)
3 (4)
4 (17)
  Ischemic stroke
176 (25)
126 (29)
45 (27)
2 (3)
3 (13)
  Transient ischemic attack
42 (6)
26 (6)
14 (8)
1 (1)
1 (4)
  Hemorrhagic stroke
31 (4)
22 (5)
9 (6)
0 (0)
0 (0)
Peripheral emboli
451 (64)
262 (60)
98 (59)
71 (96)
20 (83)
  Pulmonary
122 (17)
26 (6)
25 (15)
57 (84)
14 (58)
  Splenic
117 (17)
90 (21)
23 (14)
3 (4)
1 (4)
  Limbs
95 (14)
70 (16)
15 (9)
7 (10)
3 (13)
  Other117 (17)76 (17)35 (21)4 (6)2 (8)

*Data reported as number or number (% of embolic events).

Abbreviations: CIED-IE infective endocarditis associated with a cardiac implantable electronic device, LS-NVE left-sided native valve endocarditis, LS-PVE left-sided prosthetic valve endocarditis, RS-IE right-sided infective endocarditis.

Figure 1

Timing of embolic events. Negative values represent days before the beginning of the antibiotic therapy; zero represents the day of the beginning of antibiotic therapy; positive values represent the days after the beginning of the antibiotic therapy.

Type and anatomic site of embolic events* *Data reported as number or number (% of embolic events). Abbreviations: CIED-IE infective endocarditis associated with a cardiac implantable electronic device, LS-NVE left-sided native valve endocarditis, LS-PVE left-sided prosthetic valve endocarditis, RS-IE right-sided infective endocarditis. Timing of embolic events. Negative values represent days before the beginning of the antibiotic therapy; zero represents the day of the beginning of antibiotic therapy; positive values represent the days after the beginning of the antibiotic therapy. IE episodes complicated by embolic events had a higher in-hospital mortality (OR 1.84; 95% CI 1.36 – 2.49, p ≤ 0.0001); no significant difference was observed in the rate of cardiac surgical procedures when comparing IE episodes complicated by embolism with uncomplicated IE episodes (OR 0.98; 95% CI 0.79 – 1.23, p ns) (Additional file 1: Appendix 1 and Additional file 2: Appendix 2).

Factors associated with embolic events

In the total cohort (including LS-IE, RS-IE, and CIED-IE), univariate analysis showed that embolism was associated with younger patient age, HIV infection, absence of cancer, presence of chronic liver disease, current intravenous drug abuse, RS-IE, larger vegetation size, S. aureus and Enterococcus species etiology (Table 3). The ROC curve analysis showed that a vegetation size ≥ 13 mm was significantly associated with the occurrence of emboli (Figure 2). Anticoagulant therapy at the onset of the IE episode was not associated with a significant difference in the frequency of embolic events; the same was true for antiaggregant therapy (Table 3). Multivariate analysis showed that the only independent predictors of embolism were prosthetic valve involvement, right-side localization, vegetation size (13 mm cut-off value) and S. aureus etiology (Table 4).
Table 3

Total cohort: univariate analysis of factors associated with embolism*

Characteristics
IE episodes
IE episodes
p ≤ †
 
with embolic
without embolic
 
 eventsevents 
Number of episodes of IE
499
957
 
Age (y)
62 (28 to 81)
67 (31 to 84)
0.0002
Male
361 (72)
657 (69)
NS
Hemodialysis
10 (2)
19 (2)
NS
Diabetes mellitus
86 (17)
182 (19)
NS
HIV infection
29 (6)
23 (2)
0.004
Cancer
46 (9)
129 (13)
0.03
Chronic liver disease
115 (23)
147 (15)
0.0005
Current intravenous drug abuse
74 (15)
57 (6)
0.0001
Previous IE
38 (8)
80 (8)
NS
Chronic intravenous access
59 (12)
95 (10)
NS
Congenital heart disease
38 (8)
74 (8)
NS
Native valve predisposition
132 (26)
270 (28)
NS
Nosocomial IE
29 (6)
50 (5)
NS
Health care associated IE
107 (21)
227 (24)
NS
Community-acquired IE
363 (73)
680 (71)
NS
Native vs prosthetic valve
385 vs 114
732 vs 225
NS
Site of IE (n = 1282)
 
  Mitral vs aortic valve
166 vs 161
329 vs 359
NS
  Bivalvular involvement (mitral and aortic)
39 (8)
78 (8)
NS
Right-sided IE
60 (12)
29 (3)
0.0001
CIED-IE
21 (4)
40 (4)
NS
Vegetations (n = 710)‡
 
  Size of all vegetations (mm)
14 (6 to 30)
10 (4 to 26)
0.0001
  ≥ 10 mm
228 (79)
264 (63)
0.0001
  ≥ 15 mm
142 (49)
145 (35)
0.0001
  ≥ 20 mm
74 (26)
78 (19)
0.03
Concomitant therapy at onset of IE
 
  Anticoagulants
102 (20)
228 (24)
NS
  Antiaggregants
68 (14)
103 (11)
NS
Microbiology
 
 
 
   Staphylococcus aureus
141 (28)
142 (15)
0.0001
  Viridans group streptococci
66 (13)
151 (16)
NS
  Coagulase-negative staphylococci
52 (10)
95 (10)
NS
   Enterococcus species
45 (9)
137 (1)
0.004
  Streptococcus bovis
44 (9)
98 (10)
NS
  Polymicrobial
19 (4)
32 (3)
NS
  Other microorganisms
16 (3)
45 (6)
NS
  Other streptococci
16 (3)
43 (5)
NS
  Fungi/yeasts
7 (1)
13 (1)
NS
  HACEK
1 (0.2)
2 (0.2)
NS
  Microbiology negative92 (18)199 (21)NS

*Total cohort, N = 1456 episodes of infective endocarditis. Data reported as number, median (range, 5th to 95th percentile), or number (%). Abbreviations:CIED-IE infective endocarditis associated with a cardiac implantable electronic device, HACEKHaemophilus species, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, and Kingella kingae, HIV human immunodeficiency virus, IE infective endocarditis.

†NS, not significant (p > 0.05).

‡ IE episodes with vegetations of known size: 710 episodes (290 episodes with embolism and 420 episodes without embolism).

Bold numbers represent statistically significant differences.

Figure 2

Total cohort: size of vegetation. Receiver operating characteristic analysis for the prediction of embolic events, based on vegetation size.

Table 4

Total cohort: multivariate analysis of factors associated with embolism*

 Odds ratio95% CIp ≤ †
Age
1.0
1.0 – 1.0
NS
HIV infection
0.8
0.3 – 2.0
NS
Cancer
1.10
0.7 – 1.9
NS
Chronic liver disease
1.4
0.9 – 2.2
NS
Mitral vs aortic valve
1.0
0.7 – 1.3
NS
Prosthetic vs native valve
1.8
1.2 – 2.9
0.011
Righ-sided IE
3.9
2.0 – 7.7
<0.0001
Size of vegetation ≥ 13 mm
1.9
1.32.6
<0.0001
Staphylococcus aureus
2.2
1.53.4
<0.0001
Coagulase-negative staphylococci
1.6
1.0 – 2.6
NS
Enterococcus spp.
0.8
0.4 – 1.4
NS
Anticoagulant therapy0.80.5 – 1.3NS

*N = 1456 IE episodes. Abbreviation:HIV human immunodeficiency virus.

†NS, not significant (p > 0.05).

Bold numbers represent statistically significant differences.

Total cohort: univariate analysis of factors associated with embolism* *Total cohort, N = 1456 episodes of infective endocarditis. Data reported as number, median (range, 5th to 95th percentile), or number (%). Abbreviations:CIED-IE infective endocarditis associated with a cardiac implantable electronic device, HACEKHaemophilus species, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, and Kingella kingae, HIV human immunodeficiency virus, IE infective endocarditis. †NS, not significant (p > 0.05). ‡ IE episodes with vegetations of known size: 710 episodes (290 episodes with embolism and 420 episodes without embolism). Bold numbers represent statistically significant differences. Total cohort: size of vegetation. Receiver operating characteristic analysis for the prediction of embolic events, based on vegetation size. Total cohort: multivariate analysis of factors associated with embolism* *N = 1456 IE episodes. Abbreviation:HIV human immunodeficiency virus. †NS, not significant (p > 0.05). Bold numbers represent statistically significant differences. In LS-IE, univariate analysis showed that embolism was associated with younger patient age, current intravenous drug abuse, larger vegetation size, S. aureus and Enterococcus species etiology (Additional file 3: Table S1). The ROC curve analysis showed that a vegetation size ≥ 13 mm was significantly associated with the occurrence of emboli (Additional file 4: Figure S1). Multivariate analysis showed that in LS-IE the only independent predictors of embolism were vegetation size (13 mm cut-off value; OR 2.1; 95% CI 1.5 – 2.8, p = 0.0001) and S. aureus etiology (OR 2.1; 95% CI 1.5 – 3.1, p = 0.0001) There were no significant differences in the frequency of embolism between mitral and aortic valves or between native and prosthetic valves. (Additional file 5: Table S2).

Risk score

The two risk factors for LS-IE embolism that were identified with multivariate analysis (vegetation size ≥ 13 mm and Staphylococcus aureus etiology) were combined for designing the risk score. Because there was no marked difference in the odds ratios of the 2 prognostic variables, 1 point was assigned for the presence of each factor (total risk score range: minimum 0 points; maximum 2 points), this resulting in a three-tiered score: •low risk category (no poor prognostic factor: etiology other than S. aureus, and vegetations size <13 mm); •intermediate risk category (1 poor prognostic factor: S. aureus etiology or vegetations size ≥ 13 mm); •high risk category (2 poor prognostic factors: S. aureus etiology and vegetations size ≥ 13 mm). •The 30-day cumulative incidence of embolism varied significantly across the different risk categories: 11.8% (95% CI 7.2 – 19.2) in the low risk category, 24.5% (95% CI 20.3 – 37.0) in the intermediate risk category, 37.7 (95% CI 22.1 – 64.9) in the high risk category. Kaplan-Meier plots showed that the 3 risk categories differed significantly from each other by log-rank test and test for trend (p ≤ 0.001) (Figure 3, Table 5).
Figure 3

Left-sided IE: Kaplan-Meier plots of failure rates (embolic events) for different risk categories. Bold numbers: number of patients at risk at any given time. Numbers in parentheses: number of embolic events that occurred in each time interval.

Table 5

Left-sided IE: 30-day probability (%) of embolic events per risk category

Time from start of therapy (d)Low (0) Intermediate (1) High (2)
0
11.78
24.54
37.73
1
7.90
20.82
34.79
2
6.61
18.95
25.97
3
4.88
16.13
25.97
4
4.01
14.70
25.97
5
4.01
12.78
25.97
6
3.14
11.34
25.97
7
2.71
8.95
22.81
15
0.48
5.02
3.46
300.000.000.00

Note: numbers represent the probability (%) of embolism at the end of a given time interval. Time 0 values include embolic events occurred on the first calendar day of therapy; day 1 values represent the risk at the end of the first calendar day of therapy.

Left-sided IE: Kaplan-Meier plots of failure rates (embolic events) for different risk categories. Bold numbers: number of patients at risk at any given time. Numbers in parentheses: number of embolic events that occurred in each time interval. Left-sided IE: 30-day probability (%) of embolic events per risk category Note: numbers represent the probability (%) of embolism at the end of a given time interval. Time 0 values include embolic events occurred on the first calendar day of therapy; day 1 values represent the risk at the end of the first calendar day of therapy.

Discussion

Embolism is a common complication of infective endocarditis. The cumulative incidence of clinically overt embolic events in our series (34.3%) is within the range observed in most published series, notwithstanding differences in definitions and enrollment criteria between studies [6,7,12,13,22,26,29,30]. More in detail, the incidence of embolization observed in our study in LS-NVE (31.4%), LS-PVE (33.6%), RS-IE (67%), CIED-IE (34.4%) is similar to what has been reported from most contemporary studies: a high incidence of embolic events in RS-IE, and an incidence in the range 20-33% for CIED-associated IE; it has to be noted that in our study, in contrast with other published series, we did not observe significant differences in the frequency of embolic events between mitral and aortic valve localization, and between LS-NVE and LS-PVE [8,15]. It is well known that embolic episodes occur early in the course of the disease, often before the diagnosis of IE is established and antimicrobial therapy is started; our findings confirm this, with a large part of the embolic events (39.6%) occurring in the days preceding the diagnosis or on the day of diagnosis [3,8,15]. The present study confirms that the risk of embolism decreases markedly after the first week of antimicrobial therapy; this seems to support previous recommendations against stroke prevention as the only indication for valvular surgery after 1 week of therapy [15]. An embolic event may predict the risk of further embolic events and neurologic complications, and this may have an effect on decision making [3,14]. In our series, central nervous system embolism was preceded by symptomatic peripheral embolism in just 25 patients, this apparently limiting the utility of peripheral embolism as a predictor for CNS embolic complications. These 25 patients might point to a missed opportunity for surgical prevention of embolism, but it has to be noted that in the SEI study data regarding the possible presence of major contraindications for surgery were not systematically collected. Many papers have reported on the characteristics of vegetations which are predictive of the risk of embolism [1,3,7,12,25,26,31]; lacking a standardized echocardiographic study of our patients, the analysis was restricted to the size of the vegetations, which is a major determinant of the embolic risk, as underlined by two meta-analyses [32,33]. The cut-off value of 13 mm derived by our cumulative analysis (and confirmed by an analysis restricted to the LS-IE episodes) is within the range commonly discussed in the literature (10 mm or 15 mm for LS-IE, and 20 mm for RS-IE) [3,7,12,25,26,31]. S. aureus has been associated with an increased risk of embolic events; our data clearly confirm this, with an OR for S. aureus versus all other microbial agents of 2.2 [3,7,8,15,34]. A few papers have also reported on a higher incidence of embolic complications in Streptococcus bovis IE: our analysis of 142 S. bovis IE episodes did not confirm these findings; it has to be noted that in the report by Pergola et al. (40 S. bovis episodes), a significant difference was observed when comparing S. bovis with other streptococci, but not when comparing S. bovis with other pathogens; and Tripodi et al. found a significant difference when comparing S. bovis IE (30 episodes) with IE due to other etiological agents (p = 0.002 at univariate analysis); however, patients with S. bovis IE were older and had a higher rate of bivalvular involvement [7,35,36]. High rates of embolic events have been described in fungal endocarditis (43% in 21 cases of PVE-IE reported by Boland); in our series (20 fungal episodes) we did not observe a significant difference when comparing fungal IE episodes with episodes due to other pathogens [37-39]. In our series age, sex and a number of predisposing and comorbidity conditions were not found to be associated with the occurrence of embolic events, and were not included in the score; this is in contrast with what has recently been proposed by Hubert et al., which included in their risk calculator not only vegetation size (10 mm cut-off) and S. aureus etiology, but also age, diabetes, previous embolism and atrial fibrillation [3]. Despite the large sample size in the present study, only 2 factors were significantly associated with the occurrence of embolic events in LS-IE: vegetation size ≥ 13 mm and S. aureus etiology. These variables were incorporated into a 3-tiered risk score; the 3 categories of the scoring system were associated with clinically relevant differences in the risk of developing embolic events. Combining the risk category with the number of days on antimicrobials could be used to assess the probability of embolism (as shown in Table 5), in order to compare the embolic risk with the risks associated with surgery, making it possible to individualize a patient’s evaluation, especially during the crucial first days of the clinical course. However, differences in patient populations, clinical settings, and models of care may affect the predictive value of the score. Therefore, the clinical use of the scoring system will be possible only following successful external validation. Our study has inherent limitations: firstly, the participant centers were secondary and tertiary care units, where a major interest in the field of IE had developed; yet, patients with IE are admitted all over the country to Infectious Diseases, Internal Medicine, Cardiology, Cardiac Surgery wards and to intensive care units, and a referral bias has to be taken in account; in fact, our data do not represent the wide range of clinical conditions and patterns of treatment which are observed across Italy, and there is clearly the need for large, population-based studies, which could better describe the full spectrum of the disease, as currently observed and treated in our country. Secondly, echocardiographic evaluation was left to local expertise, without a centralized standardization or supervision: this may have limited our ability to identify characteristics of the vegetations that may be associated with the occurrence of embolic events. Finally, embolization was diagnosed at the different institutions in accordance with current clinical practice, and therefore differences in the diagnostic approach may have reduced the discriminatory power of our analysis.

Conclusions

Embolism occurs early in the course of IE; the steep decline of the risk of embolization immediately after antibiotics initiation allows only a narrow time window for the surgical prophylaxis of embolic complications. In this challenging clinical context, the simple score system described in the present study, if externally validated, might contribute to a timely and individualized assessment of the embolic risk.

Competing interests

No financial support was obtained for this work. The authors declare that they have no competing interests.

Authors’ contributions

MR designed the study; VR managed the database; AC performed all statistical analyses; MR prepared the initial draft of the manuscript; MBP, EDM, and AP, revised the manuscript and made important content contributions; all authors were involved in manuscript review and editing; all authors, with the exception of AC, contributed to pts’ enrolment, and to the implementation of the SEI study. All authors read and approved the final manuscript.

Pre-publication history

The pre-publication history for this paper can be accessed here: http://www.biomedcentral.com/1471-2334/14/230/prepub

Additional file 1

Embolic events and in-hospital mortality. Click here for file

Additional file 2

Embolic events and surgery. Click here for file

Additional file 3: Table S1

Left-sided IE: univariate analysis of factors associated with embolism. Click here for file

Additional file 4: Figure S1

Left-sided IE: size of vegetation. Receiver operating characteristic analysis for the prediction of embolic events, based on vegetation size. Click here for file

Additional file 5: Table S2

Left-sided IE: multivariate analysis of factors associated with embolism. Click here for file
  38 in total

1.  Proposed modifications to the Duke criteria for the diagnosis of infective endocarditis.

Authors:  J S Li; D J Sexton; N Mick; R Nettles; V G Fowler; T Ryan; T Bashore; G R Corey
Journal:  Clin Infect Dis       Date:  2000-04-03       Impact factor: 9.079

2.  The risk of stroke and death in patients with aortic and mitral valve endocarditis.

Authors:  C H Cabell; K K Pond; G E Peterson; D T Durack; G R Corey; D J Anderson; T Ryan; A S Lukes; D J Sexton
Journal:  Am Heart J       Date:  2001-07       Impact factor: 4.749

3.  The ability of vegetation size on echocardiography to predict clinical complications: a meta-analysis.

Authors:  M D Tischler; P T Vaitkus
Journal:  J Am Soc Echocardiogr       Date:  1997-06       Impact factor: 5.251

4.  Neurologic complications and outcomes of infective endocarditis in critically ill patients: the ENDOcardite en REAnimation prospective multicenter study.

Authors:  Romain Sonneville; Mariana Mirabel; David Hajage; Florence Tubach; Philippe Vignon; Pierre Perez; Sylvain Lavoué; Achille Kouatchet; Olivier Pajot; Armand Mekontso Dessap; Jean-Marie Tonnelier; Pierre-Edouard Bollaert; Jean-Pierre Frat; Jean-Christophe Navellou; Hervé Hyvernat; Ali Ait Hssain; Alexis Tabah; Jean-Louis Trouillet; Michel Wolff
Journal:  Crit Care Med       Date:  2011-06       Impact factor: 7.598

5.  Echocardiography predicts embolic events in infective endocarditis.

Authors:  G Di Salvo; G Habib; V Pergola; J F Avierinos; E Philip; J P Casalta; J M Vailloud; G Derumeaux; J Gouvernet; P Ambrosi; M Lambert; A Ferracci; D Raoult; R Luccioni
Journal:  J Am Coll Cardiol       Date:  2001-03-15       Impact factor: 24.094

6.  Epidemiology, characteristics, and outcome of infective endocarditis in Italy: the Italian Study on Endocarditis.

Authors:  S Leone; V Ravasio; E Durante-Mangoni; M Crapis; G Carosi; P G Scotton; N Barzaghi; M Falcone; P Chinello; M B Pasticci; P Grossi; R Utili; P Viale; M Rizzi; F Suter
Journal:  Infection       Date:  2012-06-19       Impact factor: 3.553

7.  Staphylococcus aureus endocarditis: a consequence of medical progress.

Authors:  Vance G Fowler; Jose M Miro; Bruno Hoen; Christopher H Cabell; Elias Abrutyn; Ethan Rubinstein; G Ralph Corey; Denis Spelman; Suzanne F Bradley; Bruno Barsic; Paul A Pappas; Kevin J Anstrom; Dannah Wray; Claudio Q Fortes; Ignasi Anguera; Eugene Athan; Philip Jones; Jan T M van der Meer; Tom S J Elliott; Donald P Levine; Arnold S Bayer
Journal:  JAMA       Date:  2005-06-22       Impact factor: 56.272

8.  Clinical presentation, etiology, and outcome of infective endocarditis in the 21st century: the International Collaboration on Endocarditis-Prospective Cohort Study.

Authors:  David R Murdoch; G Ralph Corey; Bruno Hoen; José M Miró; Vance G Fowler; Arnold S Bayer; Adolf W Karchmer; Lars Olaison; Paul A Pappas; Philippe Moreillon; Stephen T Chambers; Vivian H Chu; Vicenç Falcó; David J Holland; Philip Jones; John L Klein; Nigel J Raymond; Kerry M Read; Marie Francoise Tripodi; Riccardo Utili; Andrew Wang; Christopher W Woods; Christopher H Cabell
Journal:  Arch Intern Med       Date:  2009-03-09

9.  Risk factors for "major" embolic events in hospitalized patients with infective endocarditis.

Authors:  Emanuele Durante Mangoni; Luigi E Adinolfi; Marie-Francoise Tripodi; Augusto Andreana; Michele Gambardella; Enrico Ragone; Davide F Precone; Riccardo Utili; Giuseppe Ruggiero
Journal:  Am Heart J       Date:  2003-08       Impact factor: 4.749

10.  Impact of cerebrovascular complications on mortality and neurologic outcome during infective endocarditis: a prospective multicentre study.

Authors:  Franck Thuny; Jean-François Avierinos; Christophe Tribouilloy; Roch Giorgi; Jean-Paul Casalta; Loïc Milandre; Amel Brahim; Georges Nadji; Alberto Riberi; Frédéric Collart; Sebastien Renard; Didier Raoult; Gilbert Habib
Journal:  Eur Heart J       Date:  2007-03-15       Impact factor: 29.983

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  18 in total

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Authors:  Luca Longobardo; Concetta Zito; Scipione Carerj; Giuseppe Caracciolo; Matt Umland; Bijoy K Khandheria
Journal:  Curr Cardiol Rep       Date:  2018-10-11       Impact factor: 2.931

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Authors:  Trine K Lauridsen; Lawrence Park; Steven Y C Tong; Christine Selton-Suty; Gail Peterson; Enrico Cecchi; Luis Afonso; Gilbert Habib; Carlos Paré; Syahidah Tamin; Stuart Dickerman; Arnold S Bayer; Magnus C Johansson; Vivian H Chu; Zainab Samad; Niels E Bruun; Vance G Fowler; Anna Lisa Crowley
Journal:  Circ Cardiovasc Imaging       Date:  2015-07       Impact factor: 7.792

3.  Risk Factors and Outcomes of Endocarditis Due to Non-HACEK Gram-Negative Bacilli: Data from the Prospective Multicenter Italian Endocarditis Study Cohort.

Authors:  Marco Falcone; Giusy Tiseo; Emanuele Durante-Mangoni; Veronica Ravasio; Francesco Barbaro; Maria Paola Ursi; Maria Bruna Pasticci; Matteo Bassetti; Paolo Grossi; Mario Venditti; Marco Rizzi
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Journal:  Tex Heart Inst J       Date:  2016-08-01

5.  Association of Vegetation Size With Embolic Risk in Patients With Infective Endocarditis: A Systematic Review and Meta-analysis.

Authors:  Divyanshu Mohananey; Ashley Mohadjer; Gosta Pettersson; Jose Navia; Steven Gordon; Nabin Shrestha; Richard A Grimm; L Leonardo Rodriguez; Brian P Griffin; Milind Y Desai
Journal:  JAMA Intern Med       Date:  2018-04-01       Impact factor: 21.873

6.  Haemophilus parainfluenzae Mural Endocarditis: Case Report and Review of the Literature.

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7.  Time-sensitive predictors of embolism in patients with left-sided endocarditis: Cohort study.

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8.  A Spiral in the Heart: Mitral Valve Endocarditis with Unusual Vegetation Shape Potentially Affecting Effectiveness of Antibiotic Therapy.

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9.  Multiple systemic embolism in infective endocarditis underlying in Barlow's disease.

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