Leandro Slipczuk1, J Nicolas Codolosa2, Carlos D Davila3, Abel Romero-Corral2, Jeong Yun4, Gregg S Pressman2, Vincent M Figueredo5. 1. Department of Medicine, Einstein Medical Center, Philadelphia, Pennsylvania, United States of America ; Heart Institute, Cedars-Sinai Medical Center, Los Angeles, California, United States of America. 2. Einstein Institute for Heart and Vascular Health, Einstein Medical Center, Philadelphia, Pennsylvania, United States of America. 3. Department of Medicine, Einstein Medical Center, Philadelphia, Pennsylvania, United States of America. 4. Department of Medicine, Einstein Medical Center, Philadelphia, Pennsylvania, United States of America ; Pulmonary and Critical Care Medicine Division, Brigham and Women's Hospital, Boston, Massachusetts, United States of America. 5. Einstein Institute for Heart and Vascular Health, Einstein Medical Center, Philadelphia, Pennsylvania, United States of America ; Jefferson Medical College, Philadelphia, Pennsylvania, United States of America.
Abstract
AIMS: To Assess changes in infective endocarditis (IE) epidemiology over the last 5 decades. METHODS AND RESULTS: We searched the published literature using PubMed, MEDLINE, and EMBASE from inception until December 2011. DATA FROM: Einstein Medical Center, Philadelphia, PA were also included. Criteria for inclusion in this systematic review included studies with reported IE microbiology, IE definition, description of population studied, and time frame. Two authors independently extracted data and assessed manuscript quality. One hundred sixty studies (27,083 patients) met inclusion criteria. Among hospital-based studies (n=142; 23,606 patients) staphylococcal IE percentage increased over time, with coagulase-negative staphylococcus (CNS) increasing over each of the last 5 decades (p<0.001) and Staphylococcus aureus (SA) in the last decade (21% to 30%; p<0.05). Streptococcus viridans (SV) and culture negative (CN) IE frequency decreased over time (p<0.001), while enterococcal IE increased in the last decade (p<0.01). Patient age and male predominance increased over time as well. In subgroup analysis, SA frequency increased in North America, but not the rest of the world. This was due, in part, to an increase in intravenous drug abuse IE in North America (p<0.001). Among population-based studies (n=18; 3,477 patients) no significant changes were found. CONCLUSION: Important changes occurred in IE epidemiology over the last half-century, especially in the last decade. Staphylococcal and enterococcal IE percentage increased while SV and CN IE decreased. Moreover, mean age at diagnosis increased together with male:female ratio. These changes should be considered at the time of decision-making in treatment of and prophylaxis for IE.
AIMS: To Assess changes in infective endocarditis (IE) epidemiology over the last 5 decades. METHODS AND RESULTS: We searched the published literature using PubMed, MEDLINE, and EMBASE from inception until December 2011. DATA FROM: Einstein Medical Center, Philadelphia, PA were also included. Criteria for inclusion in this systematic review included studies with reported IE microbiology, IE definition, description of population studied, and time frame. Two authors independently extracted data and assessed manuscript quality. One hundred sixty studies (27,083 patients) met inclusion criteria. Among hospital-based studies (n=142; 23,606 patients) staphylococcal IE percentage increased over time, with coagulase-negative staphylococcus (CNS) increasing over each of the last 5 decades (p<0.001) and Staphylococcus aureus (SA) in the last decade (21% to 30%; p<0.05). Streptococcus viridans (SV) and culture negative (CN) IE frequency decreased over time (p<0.001), while enterococcal IE increased in the last decade (p<0.01). Patient age and male predominance increased over time as well. In subgroup analysis, SA frequency increased in North America, but not the rest of the world. This was due, in part, to an increase in intravenous drug abuse IE in North America (p<0.001). Among population-based studies (n=18; 3,477 patients) no significant changes were found. CONCLUSION: Important changes occurred in IE epidemiology over the last half-century, especially in the last decade. Staphylococcal and enterococcal IE percentage increased while SV and CN IE decreased. Moreover, mean age at diagnosis increased together with male:female ratio. These changes should be considered at the time of decision-making in treatment of and prophylaxis for IE.
Infective endocarditis (IE) extols a high cost for society worldwide, with a US incidence of 10,000 to 15,000 cases each year[1]. IE is associated with prolonged hospitalization, can require surgery[2], and impairs quality of life[3]. IE was initially described in 1885 by Osler[4] as a disease of patients with pre-existing valvular abnormalities. Since then, notable improvements in IE diagnosis and treatment have been made. However, in-hospital mortality is still close to 20 percent[5,6].Risk factors for IE have changed over time. There have been widespread changes in health-care delivery in the last five decades, which have impacted the clinical spectrum of IE. These include the use of intracardiac devices[7], prosthetic valves[8], hemodialysis[9], and an increase in the elderly population[10]. Furthermore, changes in antibiotics have led to alterations in patterns of infection and bacterial resistance in both the US[11,12] and Europe[13].In recent decades, several studies have noted an increase in the proportion of IE caused by staphylococcal species[14,15]. However, others have not[16]. A systematic review of population-based studies including 15 studies and 2,371 cases found no significant changes in the causative organism over time[17]. However, significant limitations were present in this study, including a low power to detect changes; nor did it cover the last decade. Moreover, to the best of our knowledge, there are no systematic reviews of hospital based studies.Proper understanding of IE epidemiology is paramount, as different organisms produce varied complications and may require different treatment and prophylaxis[18]. The objective of this research was to assess whether there have been changes in IE epidemiology globally over the last half century. Towards this end, we performed a systematic review of both population and hospital-based studies.
Methods
Data Sources and Searches
We searched, with no language restrictions, PubMed, OVID/MEDLINE and EMBASE electronic databases from their inception to December 2011, for studies reporting infective endocarditis microbiology. We used the term ‘infective endocarditis’ for the Mesh keyword. Date last search performed was December 1st, 2011. We supplemented the search with references from articles reviewed and correspondence with other researchers, including experts in the field. When a reference was deemed potentially suitable for inclusion, a full-text copy was obtained and reviewed according to predefined criteria (listed below). We followed the PRISMA guidelines for systematic reviews.
Study Selection and Data Collection
Prospective and nonprospective studies reporting the frequency distribution of infective endocarditis in the last five decades were included in this systematic review. Two investigators had the protocol for study selection (LS and CD) and independently assessed the studies for eligibility. Inclusion criteria were: (1) a clear definition of the population studied; (2) a clear definition of the time period; (3) a clear definition of infective endocarditis; and (4) a clear description of the frequency distribution of the microbiology encountered. In order to avoid bias, we excluded studies limited to specific populations (e.g. HIV or intravenous drug users). When there was difference of opinion, a third investigator (NC) resolved the disagreement. The authors are fluent in English, Spanish, Portuguese, and Italian; papers in other languages were translated by collaborating physicians who were native speakers. When two studies reported data from the same cohort and time frame, only the most complete one was included. If a study reported data for various time frames, data were analyzed separately for each decade. Kappa (k) for inclusion was calculated from a sample of 10 randomly selected papers. Results were compared and inconsistencies were resolved by consensus. Dr. Andrew Wang from Duke University was consulted for reviewing the list of included studies for completeness.For each study included, the following information was extracted: first author’s last name, journal, year of publication, IE definition used, certainty (possible IE vs. definite IE), countries, time-frame, multi-center vs. single center, sample size, age, gender, mortality, intravenous drug abuse (IVDA), intracardiac device or prosthetic valve, Staphylococcus aureus (SA), coagulase-negative staphylococcus (CNS), enterococci, Streptococcus viridans (SV) and culture negative (CN) IE.We also included patients from Einstein Medical Center (EMC), a tertiary 440-bed city hospital in Philadelphia, PA, US; for the years 2000 - 2010. Data were retrospectively extracted per ICD code and then included only if patients met ‘definite’ or ‘possible’ modified Duke criteria[19]. Clinical characteristics were extracted for each patient as mentioned above. This data was added as one more study to the last decade. Sensitivity analyses showed that subtracting this data from the rest did not modify results significance.
Quality assessment
Two reviewers (LS and CD) independently assessed the quality of the manuscripts using the approaches recommended by Khan and colleagues[20] and Stroup and colleagues[21] for cohort studies. The main criteria were: (1) prospective study, (2) Duke or Von Reyn definition of IE, (3) definite IE, and (4) number of patients above 40. Quality was assigned as A, or excellent, with 4 points, B or good, with 2-3 points, and C, or suboptimal, with 0-1 points. Data was weighted for quality for SA and SV without affecting results statistical significance.
Statistical analysis
Data were extracted independently by two researchers (LS and CD) and collected on an Excel spreadsheet. Data were allocated to a decade according to the midpoint date for the time frame studied. For example if the time frame was 1979 to 1983, data was assigned to the 80s. Results are shown as mean +/- SD, percentages for each decade, and the 95% CI. Main variables studied were the frequency distribution of pathogens, patient age and gender, and in-hospital mortality. ANOVA and Chi2 test were used to compare studies by decades. Each group was compared to the rest using paired Students t-tests. Samples were weighted for size. Results from our own hospital were included in the last decade and weighted for size. Sensitivity analysis showed that subtracting this data did not affect results statistic significance. Moreover subtracting the biggest study by Murdoch et al. from the International Collaboration on Endocarditis did not affect statistical significance of results. Sub-analyses were performed for continent and IVDA. Correlation between IVDA and SA was performed using Spearman correlation test. Hospital-based studies and population-based studies were included. As both types of studies may be prone to bias (hospital-based studies to referral bias[22] and population-based studies to selection bias) hospital-based and population-based studies were analyzed separately. Sensitivity analyses were performed for size, single vs multi-center and quality without affecting significance of results. A p<0.05 was considered statistically significant. Analyses were performed using JMP version 10.0 (SAS Institute, Cary, NC, US).Data were presented in a graph as mean (in green, centerline of diamond) and variance (size of diamond) for each variable studied in each decade, with standard deviations (blue). Each dot in a column represents a particular study percentage. N below decades represents total number of patients in each decade. Every patient included in each study was diagnosed with IE as described above.
Results
Candidate studies included 24,415 articles identified in PubMed, 10,421 in Medline, and 4,528 in EMBASE; one hundred sixty studies met all inclusion criteria (see flow diagram in Figure 1). Of these, 142 were hospital-based, including a total of 23,606 patients (Table 1), and 18 were population-based, including a total of 3,477 patients (Table 2). Investigators (LS and CD) were in agreement on which articles were to be included (k=1).
Figure 1
Flowchart of the selection process.
Table 1
Characteristics of hospital-based studies included.
Author
N
De
Definition
Cert
Age
Male
SA
SV
CNS
Ent
CN
Mort
IVDA
Prosthetic
Year
Country
Quality
Agüero[33]
25
R
Pelletier
NR
NR
NR
12
40
12
77-80
Chile
C
AIPEI[34]
390
P
Duke
Def
60
71
23
16
6
7
5
17
6
16
99
France
A
Ako[35]
69
R
Duke
Pos
55
72
15
38
10
25
19
0
33
90-99
Tokyo
B
Ako[35]
125
R
Duke
Pos
46
70
6
45
6
25
0
16
80-90
Japan
B
Allal[36]
101
R
Other
N/A
56
70
18
11
9
17
4
66-82
France
C
Al-Tawfiq[37]
54
R
Mod Duke
Def
60
68
43
17
7
22
29
19
95-08
Saudi Arabia
B
Auger[38]
50
R
Pelletier
Pos
43
6
28
14
69-77
Canada
C
Avanekar[39]
600
P
Mod Duke
NR
63
67
22
32
7
10
34
80-98
USA
B
Bailey[40]
210
R
Hickie
N/A
43
70
14
25
30
31
0
8
62-71
Australia
C
Barrau[41]
170
P
Mod Duke
Def
65
74
13
18
7
10
11
3
41
14-00
France
A
Bennis[42]
157
R
Other
N/A
28
63
4
11
22
4
83-94
Morocco
C
Bishara[43]
252
R
Mod Duke
Pos
62
54
24
32
11
6
25
16
0
23
87-96
Israel
B
Borer[44]
71
R
Duke
Pos
50
55
4
18
18
8
17
1
27
80-94
Israel
B
Bouramoue[45]
32
R
Von Reyn
Pos
19
41
76-89
Congo
B
Bouza[46]
109
P
VReyn/Steckelberg/Duke
Pos
50
73
45
9
14
9
10
36
17
94-96
Spain
B
Braun[47]
261
P
Von Reyn/Duke
Pos
49
69
18
31
10
23
16
28
80-99
Chile
B
Buchholtz[48]
235
P
Mod Duke
Pos
61
70
22
9
18
12
15
6
25
02-05
Denmark
B
Cabell[49]
329
P
Duke
Pos
57
54
40
11
9
10
10
8
27
93-99
USA
B
Casabe[50]
294
P
Duke
Pos
51
70
26
31
2
11
20
24
14
9
92-93
Argentina
B
Cecchii[51]
147
P
Mod Duke
Def
19
18
8
25
14
10
25
00-01
Italy
A
Cetinkaya[52]
189
R
Mod Duke/Von Reyn
NR
36
66
12
8
5
6
50
0
20
74-99
Turkey
B
Chao[53]
88
R
Duke
Pos
41
67
32
17
2
3
20
25
24
8
90-97
Taiwan
B
Chen[54]
58
R
Duke
Def
41
79
21
55
9
3
5
87-98
Taiwan
B
Chen[55]
178
R
Von Reyn
Pos
62
39
27
6
25
79-91
Australia
B
Cheng[56]
101
R
Other
Pos
39
8
53
4
14
79-87
Taiwan
C
Choudhury[57]
190
R
Other
N/A
25
70
17
8
3
2
54
25
1
81-91
India
C
Chu[58]
65
R
Duke
Pos
68
29
31
25
2
5
23
20
23
97-02
NZ
B
Cicalini[59]
151
R
Duke
Def
44
69
42
19
8
7
17
60
11
92-03
Italy
B
Cicalini[59]
132
R
Duke
Def
36
65
44
23
6
5
15
58
12
80-91
Italy
B
Corral[60]
550
R
Mod Duke
Pos
51
73
44
15
12
5
8
41
85-02
Spain
B
Couturier[61]
66
R
Duke/Von Reyn
Def
57
65
26
6
20
5
14
92-98
France
B
Deprele[62]
80
R
Duke
NR
65
70
7
21
6
11
11
10
95-01
France
B
Di Salvo[63]
178
R
Duke
Def
57
75
5
12
11
3
26
93-00
France
B
Durack[64]
204
R
Duke
Def
48
51
37
23
7
7
3
21
28
31
85-92
USA
B
Dwyer[65]
193
R
Von Reyn
Pos
51
65
39
26
5
5
10
9
22
79-92
Australia
B
Dyson[66]
128
R
Other
N/A
53
70
11
38
15
13
5
17
0
39
87-96
UK
C
Fedorova[67]
112
R
Duke
NR
51
65
23
4
41
26
15
3
00-07
Russia
B
Fefer[68]
108
R
Duke/Von Reyn
Pos
57
56
13
31
7
11
18
11
31
90-99
Israel
B
Ferreiros[69]
390
P
Mod Duke
Def
59
70
28
25
6
10
11
25
4
16
01-02
Argentina
A
Finland[70]
78
R
Other
N/A
31
18
9
60-64
USA
C
Garvey[71]
165
R
Other
N/A
56
14
32
6
16
30
7
20
68-73
USA
C
Gergaud[72]
53
R
Von Reyn
Pos
66
66
11
19
4
11
15
13
17
83-90
France
B
Giannitsioti[73]
195
P
Mod Duke
Pos
64
65
17
21
10
20
10
20
7
22
00-04
Greece
B
Gossius[74]
46
R
Von Reyn
Pos
37
20
13
4
20
17
72-81
Norway
B
Gotsman[75]
100
R
Duke
Def
55
55
17
22
5
4
12
8
1
24
91-00
Israel
B
Gracey[76]
49
R
Other
N/A
39
14
49
60-65
Australia
C
Haddy[77]
23
R
Cherubin
N/A
39
0
73-79
USA
C
Haddy[77]
43
R
Cherubin
N/A
7
16
64-73
USA
C
Hammami[78]
72
R
Duke
Def
32
56
18
17
6
1
67
97-00
Tunisia
B
Heiro[79]
95
R
Duke
Pos
55
70
33
20
8
6
18
26
16
00-04
Finland
B
Heiro[79]
125
R
Duke
Pos
58
72
24
22
10
6
29
11
5
20
90-99
Finland
B
Heiro[79]
106
R
Duke
Pos
51
56
13
19
9
14
34
0
26
80-89
Finland
B
Heper[80]
74
R
Other
N/A
25
66
14
19
15
10
18
14
95-99
Turkey
C
Hermida Amej[81]
87
R
Mod Duke
Def
55
76
44
18
7
8
2
30
89-03
Spain
B
Hill[82]
203
P
Mod Duke
Def
67
60
31
12
11
17
11
1
34
00-04
Belgium
A
Hricak[83]
190
P
Duke/Von Reyn
Pos
16
6
33
02-06
Slovakia
B
Hricak[83]
339
P
Duke/Von Reyn
Pos
15
7
41
91-01
Slovakia
B
Hricak[83]
75
P
Duke/Von Reyn
Pos
15
12
11
0
84-90
Slovakia
B
Hsu[84]
315
R
Mod Duke
Pos
51
59
22
6
5
20
4
8
95-03
Taiwan
B
Huang[85]
72
R
Mod Duke
Pos
58
50
35
4
3
25
30
19
4
03-06
Taiwan
B
Husebye[86]
68
R
Duke
Def
58
69
38
21
4
3
12
34
10
18
88-94
Norway
B
Jaffe[87]
70
R
Other
N/A
47
57
34
26
3
9
10
10
29
16
83-88
USA
C
Jain[88]
247
R
Mod Duke
Pos
71
57
19
5
4
5
15
75
3
96-03
USA
B
Jalal[89]
466
R
Other
N/A
23
59
12
10
2
0
68
1
82-97
India
C
Julander[90]
217
R
Other
N/A
39
23
2
4
27
65-80
Sweden
C
Kanafani[91]
89
R
Mod Duke
Pos
48
64.
20
20
8
3
22
18
0
20
86-01
Lebanon
B
Kazanjian[92]
60
P
Pelletier/Von Reyn
NR
62
57
27
15
10
8
5
28
7
84-89
USA
B
Khanal[93]
46
NR
Duke
Def
26
57
11
13
2
40
2
95-97
India
B
Kim[94]
56
R
Von Reyn
Pos
52
71
14
47
5
4
20
7
23
75-87
USA (HI)
B
King[95]
30
R
Pelletier
Pos
45
60
10
23
17
10
80-82
USA
C
King[95]
13
R
Pelletier
Pos
44
46
8
54
15
0
70-72
USA
C
Kiwan[96]
60
P
Other
N/A
28
12
32
7
85-88
Kuwait
B
Knudsen[97]
51
P
Mod Duke
NR
58
75
25
31
8
16
8
16
6
6
00-01
Denmark
B
Knudsen[97]
121
P
Mod Duke
NR
64
78
25
25
15
15
9
22
3
45
05-06
Denmark
B
Koegelenberg[98]
60
P
Duke
Pos
38
58
2
10
3
2
65
0
167
97-00
South Africa
B
Koga[99]
55
R
Other
N/A
9
22
11
36
20
75-83
Japan
C
Krecki[100]
69
R
Duke
Def
52
59
10
7
41
39
10
92-05
Poland
B
Kurland[101]
154
R
Other
N/A
54
44
27
24
7
7
23
14
4
12
83-92
Sweden
C
Leblebicioglu[102]
112
P
Mod Duke
Pos
45
50
35
29
15
16
16
8
17
00-04
Turkey
B
Lederman[103]
123
R
Mod Von Reyn
NR
42
55
23
34
6
6
6
10
29
10
72-84
USA
B
Leitersdorf[104]
92
R
Pelletier
NR
43
14
37
5
21
33
70-80
Israel
C
Letaief[105]
440
P
Mod Duke
Pos
32
55
12
11
6
4
50
21
0
17
91-00
Tunisia
B
Lien[106]
72
R
Pelletier/Von Reyn
Prob
55
58
21
33
4
4
18
0
10
73-84
Norway
C
Lode[107]
103
P
Other
N/A
46
54
12
12
3
9
71-81
Germany
B
Lopez-Dupla[108]
120
R
Mod Duke
Pos
51
68
33
24
10
6
13
19
25
6
90-04
Spain
B
Lou[109]
120
R
Duke
NR
43
66
37
97-07
China
B
Loupa[110]
101
P
Duke
Pos
55
70
22
19
16
3
18
3
31
97-00
Greece
B
Lowes[111]
60
R
Other
N/A
60
7
52
2
12
25
2
3
66-75
UK
C
Lupis[112]
36
R
Mod Duke
Def
54
56
8
11
58
8
03-06
Italy
B
Manzano[113]
586
P
Duke
NR
18
16
16
8
14
5
39
95-05
Spain
B
Math[114]
104
P
Mod Duke
Def
24
71
7
7
5
66
26
0
23
04-06
India
A
Meirino[115]
131
R
Other
N/A
35
51
14
45
28
2
33
90-94
Mexico
C
Mesa[116]
145
R
Other
N/A
42
62
25
20
12
24
24
37
78-87
Spain
C
Mills[117]
144
R
Vogler
N/A
45
66
24
36
1
7
17
30
19
63-71
USA
C
Morelli[118]
13
R
Other
N/A
58
62
0
46
0
23
31
8
8
31
91-93
Italy
C
Mouly[119]
90
R
Duke
Pos
60
67
31
8
13
8
12
20
8
25
97-98
France
B
Murdoch[120]
2781
P
Mod Duke
Def
58
68
31
17
11
10
10
18
10
22
00-05
Multicenter
A
Nadji[121]
310
P
Duke
Def
60
74
23
7
10
19
13
90-03
France
A
Nakamura[122]
93
R
Other
N/A
34
58
8
47
24
76-81
Japan
C
Nashmi[123]
47
R
Mod Duke
Def
32
59
24
11
17
13
26
9
4
21
93-03
S. Arabia
B
Netzer[124]
125
R
Duke
Pos
24
10
35
7
14
13
17
88-95
Switzerland
B
Netzer[124]
87
R
Duke
Pos
21
26
12
9
16
7
17
80-87
Switzerland
B
Nigro[125]
18
R
Duke
Pos
43
72
22
11
28
33
96-99
Italy
C
Nihoyannopoulos[126]
109
R
Other
N/A
43
55
16
14
29
68-82
UK
C
Nunes[127]
62
P
Mod Duke
Pos
45
63
21
10
10
36
31
31
01-08
Brazil
B
Okada[128]
28
R
Duke
Def
45
46
0
50
0
11
7
7
87-97
Japan
B
Olaison[129]
161
P
Duke/Von Reyn
NR
60
50
27
23
5
7
22
10
4
16
84-88
Sweden
B
Olds[130]
43
R
Von Reyn
Pos
61
17
17
5
7
24
85-89
USA
B
Ordonez[131]
85
P
Duke
Def
43
71
22
6
28
32
24
92-96
Spain
A
Pachirat[132]
160
R
Duke
Pos
39
66
16
23
6
38
25
8
5
90-99
Thailand
B
Pazdernik[133]
117
R
Mod Duke
Def
60
73
31
9
7
13
18
19
1
18
98-06
Czech Rep
B
Peat[134]
78
R
Von Reyn
Pos
50
54
21
53
6
1
24
21
76-86
NZ
B
Pelletier[135]
125
R
Pelletier
Pos
43
77
30
5
10
10
15
10
63-72
USA
C
Proenca[136]
65
R
Duke
Def
54
3
15
2
23
72
2
88-98
Portugal
B
Quenzer[137]
72
R
Other
N/A
10
26
6
7
24
33
69-72
USA
C
Roca[138]
54
R
Duke
NR
62
61
20
15
13
6
19
20
22
99-04
Spain
B
Romero-Vivas[139]
100
R
Von Reyn
40
23
30
8
7
24
77-82
Spain
C
Rostagno[140]
86
P
Duke
NR
59
65
20
5
13
27
12
35
03-06
Italy
B
Ruiz[141]
168
R
Duke
Pos
38
64
27
16
4
5
39
21
13
92-97
Brazil
B
Sanabria[142]
112
R
Other
N/A
40
7
13
12
5
81-86
USA
C
Sandre[143]
135
R
Duke/Von Reyn
Pos
65
27
4
10
6
10
11
31
85-93
Canada
B
Sarli-Issa[144]
703
P
Pelletier
N/A
36
66
19
7
11
6
31
78-98
Brazil
B
Seibaek[145]
69
R
Other
N/A
51
70
13
12
6
29
83-92
Denmark
C
Sekido[146]
38
R
Duke
Def
43
66
13
34
8
32
16
3
86-96
Japan
B
Shinebourne[147]
63
R
Other
N/A
69
3
40
10
11
56-65
UK
C
Shively [148]
16
P
Other
N/A
38
19
6
23
18
88-89
USA
C
Siddiq[149]
182
P
Other
N/A
46
63
57
21
3
7
4
9
67
9
90-93
USA
B
Singhman[150]
101
R
Other
N/A
59
14
43
24
23
1
68-77
Malaysia
C
Slipczuk
261
R
Mod Duke
Pos
60
49
48
10
7
20
4
25
15
11
00-10
USA
B
Strate[151]
30
R
Other
N/A
51
33
20
37
7
10
13
0
10
75-84
Denmark
C
Sucu[152]
72
R
Mod Duke
Def
45
57
17
17
10
4
36
15
29
04-07
Turkey
B
Svanbom[153]
41
P
Other
Prob
53
22
32
2
7
5
67-71
Sweden
B
Sy[154]
273
R
Mod Duke
Pos
55
68
43
19
4
8
15
23
19
20
96-06
Australia
B
Tariq[155]
66
R
Mod Duke
Pos
24
67
5
18
8
2
48
27
2
8
97-01
Pakinstan
B
Terpenning[156]
154
R
Von Reyn
Prob
36
26
9
10
3
22
18
76-85
USA
B
Thalme[157]
192
R
Duke
Pos
52
55
36
21
10
10
14
9
31
15
94-00
Sweden
B
Thornton[158]
139
R
Other
N/A
41
61
24
36
1
13
3
13
69-79
USA
C
Tornos[159]
104
P
Mod Duke
Pos
57
70
33
13
14
14
8
26
01
Europe
B
Tran[160]
136
R
Duke
Pos
54
61
24
28
9
12
18
15
13
21
98-00
Denmark
B
Tugcu[161]
68
R
Mod Duke
Pos
51
59
28
13
13
2
21
25
0
56
97-07
Turkey
B
Venezio[162]
40
R
Other
N/A
15
35
3
15
72-80
USA
C
Verheul[163]
141
R
Von Reyn
Pos
45
74
18
68
66-91
Netherlands
B
Vlessis[164]
140
R
Von Reyn
Pos
57
65
21
5
9
11
22
82-92
USA
B
Von Reyn[165]
104
R
Von Reyn
Pos
51
25
34
3
7
5
4
21
70-77
USA
B
Wang[166]
70
R
Duke
x
36
54
33
7
40
11
88-00
China
C
Watanakukakorn[167]
210
R
Other
N/A
65
55
47
14
5
16
14
80-90
USA
C
Wells[168]
102
R
Von Reyn
NR
52
64
27
43
3
4
5
27
4
9
79-86
NZ
B
Welsby[169]
91
R
Other
N/A
53
65
4
18
1
11
59-74
UK
C
Weng[170]
109
R
Duke
Pos
38
73
15
22
1
2
49
5
9
84-94
China
B
Werner[171]
106
R
Duke
Def
59
18
28
14
17
13
20
5
26
89-93
Germany
B
Witchitz[172]
228
NR
Von Reyn
Prob
36
9
81-88
France
B
Witchitz[172]
257
NR
Von Reyn
Prob
30
13
9
9
22
73-80
France
B
Wong[173]
57
R
Mod Duke
Pos
66
77
28
7
10
12
28
02-07
NZ
B
Zamorano[174]
151
NR
Duke
Def
51
66
31
13
21
27
33
91-03
Spain
B
Frequency distribution for pathogens, male, in-hospital mortality and, IVDA and prosthetic valve are expressed as percentage of total. De=Design. Cert= Diagnosis certainty. SA= Staphylococcus aureus. SV Strepcococcus viridans. CNS= Coagulase-negative Staphylococcus. Ent= Enterococci. CN= Culture negative. Mort= In-hospital mortality. IVDA= Intravenous drug abuse IE. Prosthetic= Prosthetic valve IE. P= Prospective. R=Retrospective. Def= Definite. Pos= Possible. Prob= Probable. NR= Not reported. N/A= Not applicable.
Table 2
Characteristics of population-based studies included.
Author
N
De
Definition
Cert
Incidence
Case find
Age
Male
SA
SV
CNS
Ent
Cn
Mort
IVDA
Prosth
Year
Country
Quality
Benes[175]
134
P
Mod Duke
Pos
3.4cases/100K/year
MD report hospital
69
60
30
13
8
8
34
8
8
07-08
Czech Rep
B
Benn[176]
62
R
Von Reyn
NR
27 cases/millon/year
D/c statistics
55
58
34
21
5
15
8
5
13
84-93
Denmark
B
Correa de Sa[177]
40
P
Mod Duke
Pos
5.0 to 7.9 cases/100K/year
Registry
71
50
30
30
20
8
5
18
01-06
USA
B
Delahaye[178]
401
P
Von Reyn
Pos
22.4cases/millon/year
Questionnaire
56
64
18
27
5
10
9
21
5
22
90-91
France
B
Goulet[179]
288
P
Von Reyn
Pos
18cases/millon/year
Survey
50
12
37
6
20
10
15
82-83
France
B
Griffin[180]
37
R
Von Reyn
Pos
3.9 cases/millon/year
Registry
33
35
6
3
70-81
USA
C
Griffin[180]
21
R
Von Reyn
Pos
3.3 cases/millon/year
Registry
38
43
10
0
60-69
USA
C
Hoen[181]
390
P
Duke
Def
31 cases/million/year
Survey
60
71
23
16
6
7
5
16
6
16
99
France
A
Hogevik[182]
127
P,R
Mod Von Reyn
Pos
6.2 cases/100K/year
MD report hospital
69
36
31
22
6
5
9
23
7
15
84-88
Sweden
B
King[183]
75
P
Pelletier/Von Reyn
Pos
1.7 cases/100K/year
MD report hospital
48
56
35
25
4
9
3
17
19
85-86
USA
B
Nakatani[184]
848
R
Other
N/A
NR
Survey
55
61
17
32
9
7
12
00-01
Japan
C
Schnurr[185]
70
R
Other
N/A
NR
Registry and hospitand records
61
20
45
7
7
6
73-76
Scotland
C
Scudeller[186]
254
P
Mod Duke
Pos
4.21 cases/100K/year
MD report hospital
67
67
18
17
19
19
2
32
04-08
Italy
B
Smith[187]
78
R
Other
NA
16 cases/million/year
Registry
56
18
24
20
69-72
Scotland
C
Steckelberg[22]
68
NR
Mod Von Reyn
NR
4.2 cases/100K/year
Registry and hospital records
29
40
7
3
12
28
3
35
70-87
USA
B
Tleyjeh[16]
48
P
Mod Duke
Pos
6.3-6.5 cases/100K/year
Registry and hospital records
64
71
29
42
4
8
0
6
25
90-00
USA
B
Tleyjeh[16]
34
P
Mod Duke
Pos
5.0-7.0 cases/100K/year
Registry and hospital records
57
71
20
47
15
6
0
29
80-90
USA
B
Tleyjeh[16]
25
P
Mod Duke
Pos
5.3 - 6.0 cases/100K/year
Registry and hospital records
61
80
28
44
0
0
4
4
70-79
USA
B
Van der Meer[188]
406
P
Von Reyn
Pos
15 cases/million/year
Survey
52
66
20
40
5
1
20
7
20
86-88
Netherla
B
Whitby[189]
71
R
Von Reyn
NR
NR
Registry, MD report and medical records
51
68
13
42
4
9
17
76-81
UK
B
Frequency distribution for pathogens is expressed as percentage of total. De=Design. Cert= Diagnosis certainty. SA= Staphylococcus aureus. SV Strepcococcus viridans. CNS= Coagulase-negative Staphylococcus. Ent= Enterococci. CN= Culture negative. Mort= In-hospital mortality. IVDA= Intravenous drug abuse IE. Prosth= Prosthetic valve IE. P= Prospective. R=Retrospective. Def= Definite. Pos= Possible. NR= Not reported. N/A= Not applicable.
Frequency distribution for pathogens, male, in-hospital mortality and, IVDA and prosthetic valve are expressed as percentage of total. De=Design. Cert= Diagnosis certainty. SA= Staphylococcus aureus. SV Strepcococcus viridans. CNS= Coagulase-negative Staphylococcus. Ent= Enterococci. CN= Culture negative. Mort= In-hospital mortality. IVDA= Intravenous drug abuse IE. Prosthetic= Prosthetic valve IE. P= Prospective. R=Retrospective. Def= Definite. Pos= Possible. Prob= Probable. NR= Not reported. N/A= Not applicable.Frequency distribution for pathogens is expressed as percentage of total. De=Design. Cert= Diagnosis certainty. SA= Staphylococcus aureus. SV Strepcococcus viridans. CNS= Coagulase-negative Staphylococcus. Ent= Enterococci. CN= Culture negative. Mort= In-hospital mortality. IVDA= Intravenous drug abuse IE. Prosth= Prosthetic valve IE. P= Prospective. R=Retrospective. Def= Definite. Pos= Possible. NR= Not reported. N/A= Not applicable.
Hospital-based Studies
Among hospital-based studies, IE epidemiology changed over the last 5 decades (Figure 2). Patients were significantly older (Figure 2A; 1980s: mean age 45.3, CI 40.2- 50.5 vs 2000s: mean age 57.2, CI 54.7- 59.7, p<0.001), and more were men (Figure 2B; 1970s: 58.6%, CI 54.3- 63.0 vs 2000s: 66.3%, CI 63.6- 69.0, p<0.01). The percentage of IE cases occurring on prosthetic valves increased over time though with borderline statistical significance (Figure 2C; 1960s: 8.4%, CI -3.8- 20.5 vs 2000s: 22.9%, CI 19.1 - 26.7, p=0.05).
Figure 2
Epidemiology of Infective Endocarditis.
Figure shows age (A), male percentage (B) or prosthetic valve IE (C) of patients in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). Each dot in column represents a particular study mean. N below decades represents total number of patients in each decade. A) IE patients are older in the last two decades. B) Male to female ration increased in the last decade. C) No significant changes were found on prosthetic valve IE. However a trend towards an increase can be seen. *= p<0.05; **=p<0.01; ***=p<0.001.
Epidemiology of Infective Endocarditis.
Figure shows age (A), male percentage (B) or prosthetic valve IE (C) of patients in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). Each dot in column represents a particular study mean. N below decades represents total number of patients in each decade. A) IE patients are older in the last two decades. B) Male to female ration increased in the last decade. C) No significant changes were found on prosthetic valve IE. However a trend towards an increase can be seen. *= p<0.05; **=p<0.01; ***=p<0.001.Changes in microbiology percentage over time are summarized in Figure 3 and shown in e- Figure 1 for individual organisms. There were significant increases in frequency distribution of Staphylococcus aureus (SA, Figure 4A) IE (1960s: 18.1% CI 9.4- 26.7 vs 2000s: 29.7%, CI 26.2- 33.3, p<0.05) and coagulase-negative staphylococcus (CNS, Figure 4B) IE (1960s: 2.4%, CI 0.8-5.5 vs 2000s: 10.0%, CI 8.6-11.3, p<0.01). Enterococcal IE percentage increased significantly over the last decade (Figure 4C, 1980s: 6.8%, CI 5.4- 8.2 vs 2000s: 10.5%, CI 8.9- 12.1, p<0.001) while culture negative IE decreased in that time period (Figure 4D, 1980s: 23.1%, CI 15.0- 31.3 vs 2000s: 14.2% CI 9.9- 18.2; p=0.01). Streptococcus viridans (SV) IE markedly decreased in percentage over time span of the study (Figure 4E, 1960s: 27.4%, CI 18.4-36.4 vs 2000s: 17.6%, CI 15.7-19.5, p<0.05).
Figure 3
Summary of Worldwide Microbiology of Infective Endocarditis.
Bars represent percentage of Staphylococcus
aureus (SA) (light green), Streptococcus viridans (SV, dark green), enterococci (Entero, light blue), coagulase-negative staphylococcus (CNS, dark blue), and Culture negative (CN, white) endocarditis in each decade. *= p<0.05; **=p<0.01; ***=p<0.001.
Figure 4
Microbiology of Infective Endocarditis.
Figure shows percentage of Staphylococcus
aureus (SA) IE (A), coagulase-negative staphylococcus (CNS, B), enterococci (C), Culture negative (D) and Streptococcus viridans (SV, E) of patients in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). Each dot in column represents a particular study mean. N below decades represents total number of patients in each decade. A) SA increased in the last decade. B) CNS increased over time. C) enteroccoci increased in the last decade. D) Culture negative endocarditis decreased in the last decade. E) SV decreased over time. *= p<0.05; **=p<0.01; ***=p<0.001.
Summary of Worldwide Microbiology of Infective Endocarditis.
Bars represent percentage of Staphylococcusaureus (SA) (light green), Streptococcus viridans (SV, dark green), enterococci (Entero, light blue), coagulase-negative staphylococcus (CNS, dark blue), and Culture negative (CN, white) endocarditis in each decade. *= p<0.05; **=p<0.01; ***=p<0.001.
Microbiology of Infective Endocarditis.
Figure shows percentage of Staphylococcusaureus (SA) IE (A), coagulase-negative staphylococcus (CNS, B), enterococci (C), Culture negative (D) and Streptococcus viridans (SV, E) of patients in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). Each dot in column represents a particular study mean. N below decades represents total number of patients in each decade. A) SA increased in the last decade. B) CNS increased over time. C) enteroccoci increased in the last decade. D) Culture negative endocarditis decreased in the last decade. E) SV decreased over time. *= p<0.05; **=p<0.01; ***=p<0.001.Subgroup analyses, by continent, were performed. The increase in overall SA frequency was driven by an increase in North America (Figure 5A; 1960s: 25.3%, CI 13.9- 36.6 vs 2000s: 52.4%, CI 42.4- 62.3, p=0.001). SA percentage in Europe remained stable over the last 4 decades (Figure 5B; 1970s: 25.1%, CI 18.2- 32.1 vs 2000s: 23.5%, CI 19.1- 28.0, p=0.70). No significant differences were found in SA IE frequency in Asia, Africa, Latin America, or Oceania.
Figure 5
Regional Differences for Staphylococcus Aureus and Intravenous Drug Abuse.
Figure shows percentage of Staphylococcus
aureus (Staph, SA) IE in North America (A) or Europe (B) and intravenous drug abuse related IE in North America (C) and Europe (D), of patients in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). N below decades represents total number of patients in each decade. A) SA increased markedly over last half century in North America B) No changes in SA were found in Europe. C) IVDA related IE frequency increased in North America. D) IVDA related IE percentage decreased in Europe in the last decade. *= p<0.05; **=p<0.01; ***=p<0.001.
Regional Differences for Staphylococcus Aureus and Intravenous Drug Abuse.
Figure shows percentage of Staphylococcusaureus (Staph, SA) IE in North America (A) or Europe (B) and intravenous drug abuse related IE in North America (C) and Europe (D), of patients in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). N below decades represents total number of patients in each decade. A) SA increased markedly over last half century in North America B) No changes in SA were found in Europe. C) IVDA related IE frequency increased in North America. D) IVDA related IE percentage decreased in Europe in the last decade. *= p<0.05; **=p<0.01; ***=p<0.001.Counterbalancing the increase in SA IE percentage in North America was a decrease in SV IE frequency (1970s: 33.5%, CI 25.8- 41.3 vs 2000s: 14.4%, CI 5.6- 23.2, p<0.01). SV IE frequency distribution also decreased significantly in Asia (1970s: 41.5%, CI 28.7- 54.4 vs 2000s: 10.1%, CI -8.9- 29.2, p<0.01) while in Europe there was a decrease that did not reach statistical significance (p=0.06). No significant changes were seen in Latin America and Oceania (p=0.9, p=0.32, respectively). Insufficient data were available from Africa for separate analysis.Subgroup analyses for changes in IVDA IE percentage are shown in Figure 5. No significant changes were seen on a global basis. However, a significant increase in IVDA related IE frequency distribution was observed in North America in the last decade (Figure 5C; 1980s: 17.3%, CI 10.7- 23.9 vs 2000s: 50.7%, CI 28.5- 73.0, p<0.05). Conversely, we observed a significant decrease in IVDA related IE percentage in Europe in the last decade (Figure 5D; 1990s: 21.1%, CI 12.3- 29.8 vs 2000s: 6.8%, CI 3.5- 10.2, p<0.01). We found a positive correlation between SA IE and IVDA. Interestingly, this correlation lost strength in the last decade (1990s rs=0.82, p=0.001 vs 2000s rs=0.40 p=0.05; 1990s vs 2000s, Fisher r-to-z transformation, p<0.001). We further analyzed the studies that reported microbiology for the IVDA IE group. Twenty-five studies and 1288 patients were included in this sub-analysis. No significant temporal trends in IVDA IE microbiology were found. In this subset of patients, SA represented the main pathogen (1970s: 69.89 CI 31.40- 108.38, 1980s: 72.72 CI 57.98- 93.45, 1990s: 61.78 CI 47.87- 75.68 and 2000s: 65.99 CI 55.12- 76.86) and SV represented a small percentage of cases (1970s: 16.66 CI 3.87- 29.45, 1980s: 8.87 CI 2.79- 14.95, 1990s: 7.37 CI 3.57- 11.19, 2000s: 10.01 CI 7.21- 12.81).In-hospital mortality rate due to IE decreased following the 1960s and remained stable thereafter (Figure 6; 1960s: 30.6%, CI 24.4- 36.8 vs 2000s: 19.7%, CI 17.8- 21.6, p=0.01). On subgroup analysis by continent, no regional differences were observed.
Figure 6
In-Hospital Mortality of Infectious Endocarditis.
Figure shows percentage of in-hospital mortality of Infectious Endocarditis in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). Each dot in column represents a particular study mean. N below decades represents total number of patients in each decade. In-hospital mortality decreased after the 1960s and remained stable thereafter. ∗∗=p<0.01.
In-Hospital Mortality of Infectious Endocarditis.
Figure shows percentage of in-hospital mortality of Infectious Endocarditis in each decade (mean in green, centerline of diamond) and variance (as size of diamond) plus standard deviation (blue). Each dot in column represents a particular study mean. N below decades represents total number of patients in each decade. In-hospital mortality decreased after the 1960s and remained stable thereafter. ∗∗=p<0.01.
Population-based Studies
Among population-based studies, no significant trends were observed regarding IE microbiology as shown in Table 3 (SA p=0.82; SV p=0.14; enterococci p=0.33). These studies included populations in the US and Europe primarily. Only one study was from Asia. Of note, the majority of data from the US is from Olmstead County, Minnesota.
Table 3
Microbiology of Infective Endocarditis from Population-based Studies.
1960s
1970s
1980s
1990s
2000s
p
SA
38 % [-1%-77%]
22% [12%-31%]
21% [15%-26%]
21% [14%-27%]
19% [13%-24%]
0.82
SV
43% [-9%-95%]
37% [24%-50%]
34% [27%-42%]
23% [14%-31%]
27% [19%-33%]
0.14
Entero
56% [-3%-14%]
13% [8%-19%]
8% [3%-13%]
9% [5%-13%]
0.33
Among population-based studies, no significant changes were observed regarding infectious endocarditis microbiology incidence over last five decades. Note that percentages are weighted by size and therefore sum of each decade may exceed 100%.
Among population-based studies, no significant changes were observed regarding infectious endocarditis microbiology incidence over last five decades. Note that percentages are weighted by size and therefore sum of each decade may exceed 100%.
2000s data from Einstein Medical Center, Philadelphia, PA, US
We identified a total of 261 cases from 2000 to 2010 (Table 4). Mean age was 59 and 49% were male. In-hospital mortality rate was 25⋅3%. Prosthetic IE represented 10.7% and IVDA 14.6%. SA was the primary IE microorganism seen causing 48.3% of IE [25.3% Methicillin-sensitive Staphylococcus aureus (MSSA) and 23.0% Methicillin-resistant Staphylococcus aureus (MRSA)] while CNS was seen in 6.9% of the cases. Enterococcus was the IE etiology in 19.2% and SV 9.6%. Culture negative IE represented 3.8%. Removal of this data did not modify overall results.
Table 4
Data from Einstein Medical Center from 2000-2010.
Cases
261
Time frame
2000-2010
Age
59.8
Male
49.4%
In-hosp mort
25.3%
Prosthetic
10.7%
IVDA
14.6%
Staph aureus
48.3%
MSSA
25.3%
MRSA
23.0%
Enterococci
19.2%
Strep viridans
9.6%
Coag Neg Staph
6.9%
Culture neg
3.8%
Discussion
The main finding of this study is that the epidemiology of IE has changed worldwide over the last half century. Furthermore, the observed changes in IE microbiology varied by continent. These findings stemmed from analyses of hospital-based reports. In a separately analyzed smaller group of population-based studies (most of them from the US), no consistent changes in IE microbiology frequency distribution over time were observed.Most notably, the global percentage of SA IE has nearly doubled in the last five decades (18% in the 1960s to nearly 30% in the 2000s). When analyzed by continent this increase was largely due to an increased frequency of SA in North America (from 25% in the 1960s to 52% in the 2000s) with no significant change among reports from other continents. This finding has important implications as SA infections are associated with longer length of stay, higher death rates[23], increase hospitalizations[24], and elevated costs[24]. An increase in IVDA IE percentage in North America as compared to Europe may partially explain these changes in SA frequency distribution. However, the number of studies in the last decade in this analysis is small and therefore this finding should be studied further. Other potential contributors include increases in the elderly population[10], increased numbers of chronically-ill patients[25], increased contacts with the health-care system[26,27], and increasing use of intracardiac and vascular devices. Benito and colleagues[27] found a high percentage of health-care associated infections (related to catheters, dialysis, or immunosuppressive therapy) among US patients with native valve IE; SA was the most common organism isolated. Though the present study was not able to specifically track cardiac device implantation, another recent study found an increased prevalence of staphylococcal IE in these patients[28]. In absolute numbers Bor et al, reported an incidence of infective endocarditis in the US close to 40,000 cases/year [29]. Furthermore, at least when measured by ICD codes the total number of SA cases seems to be increasing in the US [15]. In addition, certain subgroups may behave differently; a well-designed population based study found that SA frequency has increased in Europe in patients without previously known valve disease[5]. It is important to clarify that changes in individual countries may not necessarily follow the trends at a continent level.The present study also documents a substantial decline in the frequency of SV IE over the last five decades (27.4% in the 1960s to 17.6% in the 2000s). This finding was statistically significant for North America and Asia with a strong trend in Europe. Therefore, it appears that changes in the epidemiology of this organism are more widespread than for SA.Paralleling the increase in SA IE frequency, there was also an increase in CNS IE percentage over time. It is known that CNS infections are often related to the use of intravascular catheters and prosthetic vascular grafts[30]. Thus, the rise in CNS IE may well be health-care related.Enterococcal IE frequency increased in the last decade of the study. Enterococcal infections typically affect elderly patients and those with prior valvular damage, diabetes mellitus, indwelling catheters, or who are on hemodyalisis[31]. This finding is extremely important given the high prevalence of multidrug resistant enterococci and therefore the implications on treatment options. Lastly, culture negative endocarditis percentage decreased in the last decade. This is likely because of improved laboratory techniques and culture methods.Worldwide, the present study found increases in age among IE patients. This has important implications for treatment and use of health care resources as elderly patients have more comorbidities and may be more prone to infection with certain organisms, such as enterococci. Consistent with the general perception[18], the present study found that in-hospital mortality rate of IE remains high with no significant decrease observed since the 1960s.A limitation of the present study is the lack of individual patient level data. This data was not available from older studies and including it for only the last decades would have changed one bias for another one, without adding accuracy. Another limitation is that most of the findings come from hospital-based studies, whereas no significant changes were seen in the population based-studies over time. One possible explanation for this is a lack of power (18 population-based studies covering 3,477 patients vs 142 hospital-based studies covering 23,606 patients). Population-studies are also subject to sample bias: the population studied may not truly represent the general population. They can be subject to underreporting, as many times they rely on surveys. Moreover, population-studies of IE in the US are mainly from the Olmstead County, a population that is unlikely to represent the total US population. Hospital-based studies can suffer from referral bias as well, with sicker patients being referred to specialized centers. Thus, these results might not apply to community hospitals. However, Kanafani and colleagues[32] found only a slight difference between referred and non-referred patients, with higher SA IE in the non-referred patients. Thus, had this played a role in the present study, it would have likely decreased SA frequency. Therefore, it is unlikely to explain our findings. Finally, the definition of IE has changed over time, as well as culture quality, which could have caused heterogeneity in the cases included.
Conclusion
The present study represents the largest systematic review of IE epidemiology to date. Important findings include an increase in staphylococcal IE frequency over the last half-century, particularly in North America, and a worldwide decrease in SV IE percentage. In the last decade SA IE and enterococci IE frequencies have increased while culture negative IE has decreased. Patients with IE are getting older and the male to female ratio is increasing. Mortality has changed little in the last four decades.(DOC)Click here for additional data file.
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