Objective
To define the incidence, risk factors, and characteristics of bloodstream infections (BSIs) after invasive nonsurgical cardiologic procedures (ICPs).
Methods
Retrospective case-control study; multivariate analysis.
Results
Between January 1991 and December 1998, 22 006 ICPs were performed in our hospital and 25 BSIs were documented within 72 hours after ICP. Overall incidence of bacteremia was 0.11% (25 cases) (0.24% after percutaneous transluminal coronary angioplasty [14 cases of 5625 patients], 0.6% after diagnostic cardiac catheterization [9 cases of 14 034 patients], and 0.8% after electrophysiologic studies [2 cases of 2347 patients]). These 25 patients with bacteremia were compared with 50 controls randomly selected among patients who underwent an ICP but did not have BSIs. Patient-related risk factors for BSI were age older than 60 years (20 cases [80%] vs 28 controls [56%]), valvular disease (4 [16%] vs 1 [2%]), congestive heart failure (7 [28%] vs 1 [2%]), indwelling bladder catheter before the ICP (5 [20%] vs 1 [2%]), more than 1 puncture for the ICP (5 [20%] vs 3 [6%]), a prolonged procedure (83.7 vs 65.1 minutes); and/or more than 1 ICP performed (2 [8%] vs 0). Multivariate analysis identified the presence of congestive heart failure (odds ratio, 21; 95% confidence interval, 6.8-66.0) and age older than 60 years (odds ratio, 1.9; 95% confidence interval, 1.9-6.3) as independent risk factors for BSI after ICP. Bloodstream infection was detected a median of 1.7 days after the procedure. Gram-negative bacteremia accounted for 17 cases (68%) of the BSIs. Among the patients with BSI, the duration of hospital stay was significantly increased (21 vs 6 days). The overall mortality rate was 0.009% for patients who underwent an ICP (8.0% for the 25 patients with bacteremia documented within 72 hours after ICP).
Conclusions
Bloodstream infection should be included among the potential complications of ICP. Elderly patients with recent congestive heart failure episodes constitute a subgroup with a higher risk of postprocedure bacteremia. Therapy with antimicrobial agents against gram-positive and gram-negative bacteremia should be initiated after performing blood cultures in patients with signs suggestive of infection.
IN MODERN hospitals many invasive nonsurgical cardiologic procedures (ICPs) are performed every day. Although these techniques are safe, a wide array of systemic and local potential complications associated with these procedures have been reported. Systemic adverse effects include cerebrovascular accidents (0.07%-0.30%), myocardial infarction (0.06%-4.80%), and even death (0.10%-1.10%).1-8
Related infectious complications are not commonly reported, and local problems predominate.6,8-24 However, patients undergoing ICP may develop bloodstream infections (BSIs) that may cause death or significantly extend the hospital stay, which increases the cost.
An ICP-related BSI is an infrequent finding, and most of the available literature consists of isolated case reports that do not allow for an accurate definition of risk factors.14,16,17,19-22 Herein we report what is to our knowledge the largest case-control series of early BSI after ICP from a single center. Our objective was to define the incidence, risk factors, and clinical characteristics of early BSI in patients who have undergone ICP.
Population, materials, and methods
Our institution is a 2000-bed teaching hospital with a very active invasive cardiology department and heart transplantation program. The records of ICPs performed in the Cardiology Department were cross referenced with the records of BSI detected in the Clinical Microbiology Laboratory. Patients with BSI detected within 72 hours after ICP were selected as "cases." This period was chosen to maximize the likelihood of only including BSIs related to the ICPs. For each case subject with ICP-related BSI, 2 "control" subjects were elicited from a random number table from patients who had undergone ICP in the same period but had not developed a subsequent BSI.
Blood cultures were ordered when the patients experienced fever, chills, or others signs suggestive of infection. Only significant bacteremic episodes were included, and all blood cultures were obtained through direct venipuncture rather than through an intravascular device. When a case of Staphylococcus epidermidis bacteremia was found, the episode was only included when at least 2 blood culture sets yielded the same microorganism and the patient showed clinical signs suggestive of infection. Blood samples were processed with an automated monitoring system (BACTEC NR; Becton, Dickinson and Company, Franklin Lakes, NJ). Isolates were identified with standard microbiological tests and automated methods (MicroScan; Dade International Inc, West Sacramento, Calif). None of the patients received prophylactic treatment, and ICPs were performed using standard sterile techniques and infection prevention measures.25 Femoral access was undertaken in all instances.
Data collected included age; sex; underlying diseases (diabetes mellitus, malignancy, central nervous system disorders, chronic renal failure, liver disease, human immunodeficiency virus, valvular heart disease, congestive heart failure in the previous 14 days, presence of intravascular prosthetic material, chronic obstructive pulmonary disease, and previous myocardial infarction); risk factors (alcoholism, current smoking, drug abuse, steroid treatment, central venous catheters, and indwelling urinary tract catheter); type of ICP (percutaneous transluminal coronary angioplasty [PTCA], diagnostic cardiac catheterization, or electrophysiologic studies); priority of the ICP (urgent or not); procedure variables (duration of the procedure, number of punctures, and number of days the sheath was left in place); complications and outcome during or after ICP (fever, chills, vascular lesion, neurologic lesion, hematoma at the site of puncture, primary BSI, catheter-related BSI, urosepsis, pneumonia, meningitis, endocarditis, shock, intensive care unit admission, and death); analytical data (white blood cell count, left deviation, platelet count); microorganism identified from blood cultures (gram-positive, gram-negative, or polymicrobial); duration of hospital stay; and empirical treatment (adequate or inadequate). Antimicrobial therapy was considered adequate if 1 or more antimicrobial agents with in vitro activity against the corresponding isolate were administered for a minimum of 5 days. Death was attributed to the infectious process if the patient died within 10 days of the bacteremic episode with a clinical course suggesting persistent infection; it was always attributed if the patient died during the phase of acute infection and death could not be clearly attributed to any other cause.
Assessment of significant risk factors for BSI was performed by univariate and multivariate analyses. Quantitative variable analysis was analyzed with the Mann-Whitney test. The study of qualitative variables was performed with the χ2 test with the Yates correction or the Fisher exact test (2-tailed) whenever possible. Adjusted risk ratios with 95% confidence intervals were assessed by stepwise logistic regression analysis (SPSS software; SPSS Inc, Chicago, Ill). Nonrelated variables identified as significant in the univariate analysis were entered into the logistic regression analysis. Statistical significance was defined as P<.05.
During the study period (January 1991 to December 1998), 68 patients had an episode of BSI among the 22 006 who underwent an ICP. Of these episodes, 25 occurred within 72 hours after the procedure, resulting in an overall incidence of 0.11%. Incidence of early BSI was significantly higher after PTCA: 14 (0.24%) of 5625 patients who underwent PTCA followed by 9 (0.06%) of 14 034 patients who underwent cardiac catheterization and 2 (0.08%) of 2347 patients who underwent electrophysiologic studies (P = .001). However, the type of cardiologic procedure was not an independent risk factor in the multivariable study.
Risk factors predisposing to BSI were grouped into those present before the procedure (the first group) and those related to the procedure itself (the second group) (Table 1). Among the first group, age older than 60 years (20 cases [80%] vs 28 controls [56%]), prior valvular disease (4 [16%] vs 1 [2%]), congestive heart failure (7 [28%] vs 1 [2%]), and indwelling bladder catheterization (5 [20%] vs 1 [2%]) were more common among patients with BSI. Among the second group, more than 1 ICP performed (2 [8%] vs 0), number of punctures needed (mean of 1.2 vs 1.05), duration of the procedure (mean of 83.7 vs 65.1 minutes), and development of inguinal hematoma (4 [16%] vs 1 [2%]) were associated with a higher risk of developing BSI in the univariate analysis. Multivariate analysis identified the presence of congestive heart failure (odds ratio [OR], 21; 95% confidence interval, 6.8-66.0) and age older than 60 years (OR, 1.9; 95% confidence interval, 1.9-6.3) as independent risk factors for BSI after ICP.
Clinical presentation of bsi after an icp
Bloodstream infection was detected a median of 1.7 days after ICP (range, 0-3 days); 9 (36%) of them were detected in the first 24 hours after ICP and 21 (84%) in the first 48 hours. The main clinical signs of BSI were fever (25 [100%]) and chills (16 [64%]), which were both only present in patients with BSI. One patient developed endocarditis, which was possibly related to an episode of Staphylococcus aureus BSI after an electrophysiologic study. However, it was not included in this analysis because the BSI occurred 7 days after the procedure. None of the patients with both bacteremia and valvular heart lesions who were included in this study developed endovascular infection. No local infection was documented in this series.
Microorganisms responsible for BSI are listed in Table 2. Of the episodes, 17 (68%) were caused by gram-negative microorganisms. None of them were polymicrobial and no grouping of cases was detected. Our 4 patients with previous valvular heart lesions had a gram-negative bacteremia (Pseudomonas cepacia, Klebsiella pneumoniae, Enterobacter cloacae, and Escherichia coli), and none of them had endocarditis or endarteritis. The origins of the bacteremia in the patients with an indwelling bladder catheter were S aureus in 2; Enterococcus faecalis in 1; Serratia marcescens in 1; and E coli in 1.
Antimicrobial therapy was considered adequate in 75% of cases. Five patients did not receive therapy (1 patient died before treatment was initiated, and the other 4 had already been released from the hospital or were asymptomatic when the results were available). All of them survived, and the origins of these bacteremias were Klebsiella oxytoca in 2; E faecalis in 1; and E coli in 1.
Three patients (12%) developed septic shock, and 2 of them died (the overall mortality was 12%, and the related mortality was 8% for the 25 patients with bacteremia that was detected within 72 hours after ICP). The median hospital stay was significantly longer for patients with bacteremia (21 vs 6 days) (Table 1).
The use of ICP has experienced a rapid expansion in recent years, and a large number of patients undergo these procedures every day. More than 300 000 PTCAs were performed in the United States in 199023 and more than 600 000 in 1999.
Although infectious complications are uncommon, the great number of procedures performed every year implies that even a low incidence of infection may have significant consequences. We are reporting what is to our knowledge the largest series of early BSIs after ICP. In our hospital, 0.11% of all patients who had undergone an ICP had a clinically significant procedure-related BSI in the following 3 days. Incidence of BSI was significantly higher among patients who underwent PTCA (0.24%), although the type of procedure was not an independent risk factor in our multivariate model. In the literature, incidence of bacteremia after PTCA ranges from 0.20 to 0.80,9-11,19 although the study by Samore et al11 includes bacteremias that were detected in the first 7 weeks following PTCA.
To identify patients with a higher risk of severe infectious complications who would require a closer follow-up or even prophylaxis, we performed a case-control study and literature review. Risk factors proposed in previous studies (all but 2 were derived from series with less than 6 patients with bacteremia) are summarized in Table 3.
Congestive heart failure was the most significant risk factor in our multivariate model (OR, 21; 95% confidence interval, 6.8-66.0). This factor was also identified by Samore et al11 in the only other comparative series of patients with bacteremia after PTCA (OR, 43.3). The reason for this association is not clear. In our series, patients with bacteremia and previous congestive heart failure were younger than those without BSI (median age, 61 vs 71 years; P = .04), had a greater incidence of valvular diseases (3 cases [42%] vs 1 control [5%]; P = .02) and diabetes mellitus (4 [57%] vs 1 [5%]; P = .003), were more commonly receiving mechanical ventilation (2 [28%] vs 0; P = .01), required more central venous catheters (3 [43%] vs 1 [5%]; P = .02), and needed more than 1 puncture for the ICP (4 [57%] vs 1 [5%]; P = .03).
The second independent risk factor was age older than 60 years, which was also suggested in previous works.11 In our series, patients older than 60 years were more commonly heavy smokers (10 [50%] vs 0; P = .04). In the literature, cohorts of older patients who underwent PTCA include more women, more patients with unstable angina, and more patients with left ventricular dysfunction and congestive heart failure. Age older than 75 years was reported to be an independent risk factor for death, acute myocardial infarction, need for transfusion, and need for arterial repair after PTCA.3
In contrast to the results of Samore et al,11 we could not find a correlation between the risk of bacteremia and any of the factors related to the procedure itself, although some of them were significant in the univariate analysis (Table 1). Samore et al found that duration of the procedure (OR, 6.8), number of catheterizations in the same site (OR, 4.0), difficult vascular access (OR, 15.0), and length of time the sheath was left in place (OR, 6.8) increased the risk of bacteremia. The significantly lower incidence of bacteremia after PTCA in our study compared with that of Samore et al11 (14 cases [0.24%] vs 27 cases [0.64%]; P = .003) may be justified by technical factors. For example, 20 (80%) of our patients vs 12 (44%) of the patients required just 1 puncture, the duration of the procedure in our center was less than 1 hour in 36% vs 11% of the cases, and the sheath always remained in place less than 24 hours (mean time, 7.28 hours), while in the study by Samore et al11 the sheath remained in place less than 24 hours in only 7 cases (26%). In another series, duration of the procedure was also not found to be a significant risk factor.9
Retention of the sheath (40 vs 22 hours) and bleeding around the insertion site (43% vs 9% transfusion rate) were risk factors for infection in a prospective series of 500 patients who underwent angioplasty with 6 related infections (4 bacteremias).10 These factors were not found to increase the risk of bacteremia in our series, but both our transfusion rate (4%) and the length of time the sheath was left in place are significantly less than those reported in the series by McHenry et al10.
Early repuncture of the ipsilateral femoral artery or repeated procedures through a previously traumatized femoral access site have been proposed as risk factors in some short series, mainly for local complications.16,19-21,24 However, these findings were not confirmed by others.6,12 Two of our 25 patients with bacteremia underwent a second cardiologic procedure, but this factor was not independently related to a higher risk of bacteremia.
Local infections are very uncommon8; there were none in our series, probably because we had focused on the early onset of bacteremia. Blood cultures may remain negative even after severe local infections,18 and femoral endarteritis may be associated with osteoarticular metastases and peripheral emboli.22,23
Fever after ICP has been correlated with the use of contrast medium2 or with the introduction of bacterial endotoxin from the surface of the catheter or from the skin.12,24 However, the change to single-use pyrogen-free catheters has virtually eliminated these problems as well as the potential for BSI due to unsterile catheters. In our study, fever 25 (100%) of the cases vs none of the controls; P<.001) and chills were the most constant symptoms of BSI after ICP. The association of fever after an ICP with real infection has also been indicated by some authors (50% of cases vs 4% of controls).10
Gram-negative microorganisms were more commonly identified in our study (17 [68%]). This finding has also been observed by other authors,15,26,27 while gram-positive bacteria (mainly Staphylococcus species) predominated in other reports.9,11,19 In a series of 7 cases of bacteremia after coronary stenting, 3 episodes were caused by S aureus, 2 by E cloacae, and 1 each by Proteus mirabilis and S marcescens.15 Gram-negative bacteria are well-known colonizers of perineal and groin skin, mainly in patients with indwelling bladder catheters. However, this was not the only reason, since 3 of our 5 cases with indwelling bladder catheter had gram-positive bacteremia.
Other potential reasons for the importance of gram-negative bacteremia in our series is that our population was severely ill and older (mean age, 66.6 years), both well-recognized risk factors for colonization by gram-negative bacteria. In some of the published series in which gram-positive bacteremia predominated, blood cultures were obtained from the femoral catheter or from the vessel from which the catheter had just been removed. Thus, some of these isolates may represent contamination by skin pathogens.12 This practice is not useful for the diagnosis of BSI unless lysis centrifugation techniques are used and another blood culture is obtained through the vein.
The overall mortality rate related to the bloodstream infection was 0.09 per 1000 ICPs (8% of the 25 patients with bacteremia that was detected within 72 hours after ICP). In other series, 1.7% of the deaths were caused by a related infection (0.16 per 1000 PTCAs).2 Patients with bacteremia had a much more prolonged hospital stay (21 vs 6 days), which also increased the cost.
Bloodstream infection complicates 0.11% of ICPs. Elderly patients with recent congestive heart failure episodes constitute a subgroup with a higher risk of postprocedure bacteremia. Antimicrobial agents against gram-positive and gram-negative bacteria should be initiated after blood cultures are performed in patients with signs suggestive of infection. The selection of a subgroup of patients with a high risk of infection who could benefit from antimicrobial prophylaxis merits further study.
Accepted for publication February 12, 2001.
The authors are grateful for the help of the staff of the Cardiac Catheterization Department and Microbiology Laboratory of the Hospital General Universitario "Gregorio Marañón."
Corresponding author and reprints: Patricia Muñoz, MD, PhD, Servicio de Microbiología, Hospital General Universitario "Gregorio Marañón," Doctor Esquerdo 47, Madrid 28006, Spain (e-mail: pmunoz@micro.hggm.es).
1.Grossman
W Cardiac catheterization. Braunwald
Eed.
Heart Diseases A Textbook of Cardiovascular Medicine 4th ed. Philadelphia, Pa WB Saunders Co1992;
Google Scholar 2.Malenka
DJO'Rourke
DMiller
M
et al. Northern New England Cardiovascular Disease Study Group, Cause of in-hospital death in 12,232 consecutive patients undergoing percutaneous transluminal coronary angioplasty.
Am Heart J. 1999;137632- 638
Google ScholarCrossref 3.Lindsay
JReddy
VMPinnow
EELittle
TPichard
AD Morbidity and mortality rates in elderly patients undergoing percutaneous coronary transluminal angioplasty.
Am Heart J. 1994;128697- 702
Google ScholarCrossref 4.Davis
KKennedy
JWKemp
HGJudkins
MPGosselin
AJKillip
T Complications of coronary arteriography from the Collaborative Study of Coronary Artery Surgery (CASS).
Circulation. 1979;591105- 1111
Google ScholarCrossref 5.Dorros
GCowley
MJSimpson
J
et al. Percutaneous transluminal coronary angioplasty: report of complications from the National Heart, Lung, and Blood Institute PTCA Registry.
Circulation. 1983;67723- 730
Google ScholarCrossref 6.Hannan
ELArani
DTJohnson
LWKemp
HGLukacik
G Percutaneous transluminal coronary angioplasty in New York State: risk factors and outcomes.
JAMA. 1992;2683092- 3097
Google ScholarCrossref 7.Wennberg
DEMalenka
DJSengupta
A
et al. Percutaneous transluminal coronary angioplasty in the elderly: epidemiology, clinical risk factors and in-hospital outcomes.
Am Heart J. 1999;137639- 654
Google ScholarCrossref 8.Bredlau
CERoubin
GSLeimgruber
PPDouglas Jr
JSKing III
SBGruentiz
AR In-hospital morbidity and mortality in patients undergoing elective coronary angioplasty.
Circulation. 1985;721044- 1052
Google ScholarCrossref 9.Szela
JMcHenry
PGrines
CBand
J Infectious complications associated with percutaneous transluminal coronary angioplasty (PTCA) [abstract].
Program and Abstracts of the 32nd Interscience Conference on Antimicrobial Agents and Chemotherapy (Anaheim) Washington, DC American Society for Microbiology1992;248
Google Scholar 10.McHenry
PSzela
JMendelson
SGrines
CBand
J Infectious complications associated with interventional cardiovascular procedures: a prospective analysis [abstract].
Program and Abstracts of the 33rd Interscience Conference on Antimicrobial Agents and Chemotherapy (New Orleans) Washington, DC American Society for Microbiology1993;415
Google Scholar 11.Samore
MHWessolossky
MALewis
SMShubrooks
SJKarchmer
W Frequency, risk factors, and outcome for bacteremia after percutaneous transluminal coronary angioplasty.
Am J Cardiol. 1997;79873- 877
Google ScholarCrossref 12.Shea
KWSchwartz
RKGambino
ATMarzo
KPCunha
BA Bacteriemia associated with percutaneous transluminal coronary angioplasty.
Cathet Cardiovasc Diagn. 1995;365- 9
Google ScholarCrossref 13.Sande
MLevinson
MELukas
DSKaye
D Bacteremia associated with cardiac catheterization.
N Engl J Med. 1969;2811104- 1106
Google ScholarCrossref 14.Deshpande
SSBremmer
SSra
JS
et al. Ablation of left free-wall accessory pathways using radiofrequency energy at the atrial insertion site: transseptal versus transaortic approach.
J Cardiovasc Electrophysiol. 1994;3219- 231
Google ScholarCrossref 15.James
EBroadhurst
PSimpson
ADas
S Bacteraemia complicating coronary artery stenting.
J Hosp Infect. 1998;38154- 155
Google ScholarCrossref 16.Evans
BHGoldstein
EJC Increased risk of infection after repeat percutaneous transluminal coronary angioplasty.
Am J Infect Control. 1987;15125- 126
Google ScholarCrossref 17.Guerin
JMLeibinger
FMofredj
A Invasive staphylococcal infection complicating coronary angiography without angioplasty.
Clin Infect Dis. 1996;22886- 887
Google ScholarCrossref 18.Cleveland
KOGelfand
MS Invasive staphylococcal infections complicating percutaneous transluminal coronary angioplasty: three cases and review.
Clin Infect Dis. 1995;2193- 96
Google ScholarCrossref 19.Malanoski
GJSamore
MHPefanis
AKarchmer
AW
Staphylococcus aureus catheter-associated bacteremia: minimal effective therapy and unusual infectious complications associated with arterial sheath catheters.
Arch Intern Med. 1995;1551161- 1166
Google ScholarCrossref 20.Wiener
RSOng
LS Local infection after percutaneous transluminal coronary angioplasty: relation to early repuncture of ipsilateral femoral artery.
Cathet Cardiovasc Diagn. 1989;16180- 181
Google ScholarCrossref 21.Frazee
BWFlaherty
JP Septic endarteritis of the femoral artery following angioplasty.
Rev Infect Dis. 1991;13620- 623
Google ScholarCrossref 22.Brummitt
CFKravitz
GRGranrud
GAHerzog
CA Femoral endarteritis due to
Staphylococcus aureus complicating percutaneous transluminal coronary angioplasty.
Am J Med. 1989;86822- 824
Google ScholarCrossref 23.Topol
EJEllis
SGCosgrove
DM
et al. Analysis of coronary angioplasty practice in the United States with an insurance-claims data base.
Circulation. 1993;871489- 1497
Google ScholarCrossref 24.McCready
RASiderys
HPittman
JN
et al. Septic complications after cardiac catheterization and percutaneous transluminal coronary angioplasty.
J Vasc Surg. 1991;14170- 174
Google ScholarCrossref 25.Heupler Jr
FHeisler
MKeys
TFSerkey
JSociety for Cardiac Angiography and Interventions Laboratory Performance Standards Committee, Infection prevention guidelines for cardiac catheterization laboratories.
Cathet Cardiovasc Diagn. 1992;25260- 263
Google ScholarCrossref 26.Leroy
OMartin
EPrat
A
et al. Fatal infection of coronary stent implantation.
Cathet Cardiovasc Diagn. 1996;39168- 170
Google ScholarCrossref 27.Timsit
JFWolff
MABédos
JPLucet
JCDécre
D Cardiac abscess following percutaneous transluminal coronary angioplasty.
Chest. 1993;103639- 641
Google ScholarCrossref