(Circulation. 1997;96:358-366.)
© 1997 American Heart Association, Inc.
Articles |
| Abstract |
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Participants An ad hoc writing group appointed by the American Heart Association for their expertise in endocarditis and treatment with liaison members representing the American Dental Association, the Infectious Diseases Society of America, the American Academy of Pediatrics, and the American Society for Gastrointestinal Endoscopy.
Evidence The recommendations in this article reflect analyses of relevant literature regarding procedure-related endocarditis, in vitro susceptibility data of pathogens causing endocarditis, results of prophylactic studies in animal models of endocarditis, and retrospective analyses of human endocarditis cases in terms of antibiotic prophylaxis usage patterns and apparent prophylaxis failures. MEDLINE database searches from 1936 through 1996 were done using the root words endocarditis, bacteremia, and antibiotic prophylaxis. Recommendations in this document fall into evidence level III of the US Preventive Services Task Force categories of evidence.
Consensus Process The recommendations were formulated by the writing group after specific therapeutic regimens were discussed. The consensus statement was subsequently reviewed by outside experts not affiliated with the writing group and by the Science Advisory and Coordinating Committee of the American Heart Association. These guidelines are meant to aid practitioners but are not intended as the standard of care or as a substitute for clinical judgment.
Conclusions Major changes in the updated recommendations include the following: (1) emphasis that most cases of endocarditis are not attributable to an invasive procedure; (2) cardiac conditions are stratified into high-, moderate-, and negligible-risk categories based on potential outcome if endocarditis develops; (3) procedures that may cause bacteremia and for which prophylaxis is recommended are more clearly specified; (4) an algorithm was developed to more clearly define when prophylaxis is recommended for patients with mitral valve prolapse; (5) for oral or dental procedures the initial amoxicillin dose is reduced to 2 g, a follow-up antibiotic dose is no longer recommended, erythromycin is no longer recommended for penicillin-allergic individuals, but clindamycin and other alternatives are offered; and (6) for gastrointestinal or genitourinary procedures, the prophylactic regimens have been simplified. These changes were instituted to more clearly define when prophylaxis is or is not recommended, improve practitioner and patient compliance, reduce cost and potential gastrointestinal adverse effects, and approach more uniform worldwide recommendations.
Key Words: cardiovascular disease endocarditis prevention AHA Medical/Scientific Statements antibiotic prophylaxis
| Introduction |
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Endocarditis usually develops in individuals with underlying structural cardiac defects who develop bacteremia with organisms likely to cause endocarditis. Bacteremia may occur spontaneously or may complicate a focal infection (eg, urinary tract infection, pneumonia, or cellulitis). Some surgical and dental procedures and instrumentations involving mucosal surfaces or contaminated tissue cause transient bacteremia that rarely persists for more than 15 minutes. Blood-borne bacteria may lodge on damaged or abnormal heart valves or on the endocardium or the endothelium near anatomic defects, resulting in bacterial endocarditis or endarteritis. Although bacteremia is common following many invasive procedures, only certain bacteria commonly cause endocarditis. It is not always possible to predict which patients will develop this infection or which particular procedure will be responsible.
There are currently no randomized and carefully controlled human trials in patients with underlying structural heart disease to definitively establish that antibiotic prophylaxis provides protection against development of endocarditis during bacteremia-inducing procedures. Further, most cases of endocarditis are not attributable to an invasive procedure. The following recommendations reflect analyses of relevant literature regarding procedure-related endocarditis, including in vitro susceptibility data of pathogens causing endocarditis, results of prophylactic studies in experimental animal models of endocarditis, and retrospective analyses of human endocarditis cases in terms of antibiotic prophylaxis usage patterns and apparent prophylaxis failures.
The incidence of endocarditis following most procedures in patients with underlying cardiac disease is low. A reasonable approach for endocarditis prophylaxis should consider the following: the degree to which the patients underlying condition creates a risk of endocarditis; the apparent risk of bacteremia with the procedure (as defined in these recommendations); the potential adverse reactions of the prophylactic antimicrobial agent to be used; and the cost-benefit aspects of the recommended prophylactic regimen. Failure to consider all of these factors may lead to overuse of antimicrobial agents, excessive cost, and risk of adverse drug reactions.
This statement provides guidelines for prevention of bacterial endocarditis. It is not intended as the standard of care or as a substitute for clinical judgment. The current recommendations are an update of those made by the committee in 19901 and incorporate new data and include opinions voiced by national and international experts at endocarditis meetings around the world.
| Cardiac Conditions |
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Table 1
2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 stratifies cardiac conditions
into high- and moderate-risk categories primarily on the basis of
potential outcome if endocarditis occurs.
High Risk
Individuals at highest risk are those who have prosthetic
heart valves, a previous history of endocarditis (even in the absence
of other heart disease), complex cyanotic congenital heart disease, or
surgically constructed systemic pulmonary shunts or
conduits.2 3 These individuals are at a much higher risk
for developing severe endocardial infection that is often associated
with high morbidity and mortality.
Moderate Risk
Individuals with certain other underlying cardiac defects are at
moderate risk for severe infection.2 3 4 Congenital cardiac
conditions listed in the moderate-risk category include the following
uncorrected conditions: patent ductus arteriosus,
ventricular septal defect, primum atrial septal defect,
coarctation of the aorta, and bicuspid aortic valve. Acquired valvar
dysfunction (eg, due to rheumatic heart disease or collagen vascular
disease) and hypertrophic cardiomyopathy are also
moderate-risk conditions.
Mitral valve prolapse (MVP) is common, and the need for prophylaxis for this condition is controversial. Only a small percentage of patients with documented MVP develop complications at any age.5 6 7 Mitral valve prolapse represents a spectrum of valvular changes and clinical behavior.5 6 7 In view of the controversy surrounding the need for prophylaxis of the individual patient with MVP, a detailed description of the spectrum of MVP is warranted.
Normal mitral valve leaflets close at or below the plane of the mitral annulus. This closure position is controlled by the lengths of the leaflets, their attached chordae and papillary muscles, and the systolic size of the ventricle. The closure position will shift beyond the annular plane toward the left atrium, or prolapse, if the lengths of the valve apparatus, which are constant, become too large for the size of the end-systolic ventricle, which is variable and dynamic. Dehydration and tachycardia are common causes of intermittent MVP. Abnormal motion of normal mitral valves is found on echocardiographic examination in a small percentage of the adult and adolescent ambulatory population. The high prevalence of such motion abnormalities in young adults underscores that MVP is often an abnormality of volume status, adrenergic state, or growth phase and not of valve structure or function. When normal valves prolapse without leaking, as in patients with one or more systolic clicks but no murmurs and no Doppler-demonstrated mitral regurgitation, the risk of endocarditis is not increased above that of the normal population.2 6 7 Antibiotic prophylaxis against bacterial endocarditis is therefore not necessary. This is because it is not the abnormal valve motion but the jet of mitral insufficiency that creates the shear forces and flow abnormalities that increase the likelihood of bacterial adherence on the valve during bacteremia.
Normal mitral valves with normal motion often have minimal leaks detectable by Doppler examination. This does not appear to increase the risk of endocarditis. In contrast, the regurgitation that occurs with structurally normal but prolapsing valves originates from larger regurgitant orifices and creates broader areas of turbulent flow. Patients with prolapsing and leaking mitral valves, evidenced by audible clicks and murmurs of mitral regurgitation or by Doppler-demonstrated mitral insufficiency, should receive prophylactic antibiotics.7 8 9 10 11 This is supported by formal cost-benefit analysis.12
Mitral valve prolapse also occurs in the setting of myxomatous degeneration of the mitral valve. This is a progressive disorder that has a spectrum of manifestations.13 14 The mitral leaflets of these patients appear thickened on the echocardiogram, due to accumulations of proteoglycan deposits.15 The amount of thickening is variable and may increase with age.16 There is a range of valve motion in these patients as well: they may prolapse continuously or only with changes in heart rate or volume. Further, when prolapse occurs, it may or may not create valvular insufficiency. In patients of any age, myxomatous mitral valve degeneration with regurgitation is an indication for antibiotic prophylaxis.11 17 18
Anterior mitral valve thickening is commonly found in both competent and insufficient myxomatous mitral valves, but its presence increases the likelihood of significant mitral regurgitation.16 Those with significant regurgitation were older and more likely to be men.16 Other studies have shown that male sex and age older than 45 years represent increased risk for developing endocarditis.8 10 11 19 Patients with thickened valves that do not leak on resting examination often develop regurgitation with exercise. These patients with exercise-induced mitral insufficiency have been shown to constitute a higher-risk subset for common complications (syncope, congestive heart failure, progressive regurgitation requiring valve replacement); endocarditis and cerebral embolic events, occurring far less frequently, were not demonstrated to be increased in this small series.20 Men older than 45 years with MVP, without a consistent systolic murmur, may warrant prophylaxis even in the absence of resting regurgitation.12 19
Some experts feel that an audible nonejection click even without a murmur may identify patients with a potential for intermittent regurgitation and therefore a risk of developing endocarditis. While there are insufficient data on this issue, an isolated click may be an indication for more thorough evaluation of valve morphology and function, including Doppler-echocardiographic imaging or auscultation during maneuvers that elicit or augment mitral regurgitation.
While children and adolescents with MVP may have the same symptoms as adults, such as palpitations or syncope, the development of symptoms in childhood is relatively unusual. The vast majority of children with chest pain or fatigue do not have any form of heart disease, including MVP. Careful evaluation is nevertheless required in children who have isolated clinical findings, such as nonejection systolic click, since this may be the only indicator of important mitral valve abnormality requiring prophylaxis.21 In the most recent series of reports, MVP has emerged as an important underlying diagnosis associated with endocarditis in the pediatric age group.3 21
A clinical approach to determination of the need for prophylaxis in individuals with suspected MVP is given in the Figure.23
Negligible Risk
Although endocarditis may develop in any individual,
including persons with no underlying cardiac defect, the
negligible-risk category lists cardiac conditions in which the
development of endocarditis is not higher than in the general
population. Whereas in pediatric patients innocent heart murmurs may be
clearly defined on auscultation, in the adult population other studies
such as echocardiography may be necessary to
confirm that a murmur is innocent. Individuals with innocent heart
murmurs have structurally normal hearts and do not require
prophylaxis.
| Bacteremia-Producing Procedures |
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| Dental and Oral Procedures |
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Antiseptic mouth rinses applied immediately prior to dental procedures may reduce the incidence or magnitude of bacteremia.24 Agents include chlorhexidine hydrochloride and povidone-iodine. Fifteen milliliters of chlorhexidine can be given to all at-risk patients via gentle oral rinsing for about 30 seconds prior to dental treatment; gingival irrigation is not recommended. Sustained or repeated frequent interval use is not indicated as this may result in the selection of resistant micro-organisms.24
Antibiotic prophylaxis for at-risk patients is recommended for dental
and oral procedures likely to cause bacteremia (Table 2
22 24 25 26 28 29 30 31 ). In general, prophylaxis
is recommended for procedures associated with significant bleeding from
hard or soft tissues, periodontal surgery, scaling, and professional
teeth cleaning. Similarly, antimicrobial prophylaxis is recommended for
tonsillectomy or adenoidectomy. It is recognized that unanticipated
bleeding may occur on some occasions. In such an event, data from
experimental animal models suggest that antimicrobial prophylaxis
administered within 2 hours following the procedure will provide
effective prophylaxis.32 Antibiotics administered more
than 4 hours after the procedure probably have no
prophylactic benefit. Procedures for which antimicrobial
prophylaxis is not recommended are also listed (Table 2
).
Edentulous patients may develop bacteremia from ulcers caused by ill-fitting dentures. Denture wearers should be encouraged to have periodic examinations or to return to the practitioner if discomfort develops. When new dentures are inserted, it is advisable to have the patient return to the practitioner to correct any problems that could cause mucosal ulceration.
If a series of dental procedures is required, it may be prudent to observe an interval of time between procedures to both reduce the potential for the emergence of resistant organisms and allow repopulation of the mouth with antibiotic susceptible flora. Various studies have suggested an interval of 933 to 1434 days. If possible, a combination of procedures should be planned within the same period of prophylaxis.
| Respiratory, Gastrointestinal, and Genitourinary Tract Procedures |
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The risk of endocarditis as a direct result of an endoscopic procedure is small. Transient bacteremia may occur during or immediately after endoscopy; however, there are few reports of infective endocarditis attributable to endoscopy.35 36 37 38 39 40 41 42 43 For most gastrointestinal endoscopic procedures, the rate of bacteremia is 2% to 5%, and the organisms typically identified are unlikely to cause endocarditis.44 45 The rate of bacteremia does not increase with mucosal biopsy, polypectomy, or sphincterotomy.46 47 48 There are no data to indicate that deep biopsy, as may be performed in the rectum or stomach, leads to a higher rate of bacteremia.
Some gastrointestinal procedures are associated with a higher
rate of transient bacteremia; for these procedures, antimicrobial
prophylaxis is recommended, particularly for patients in the high-risk
category (Table 3
). Esophageal stricture dilation has been associated
with bacteremia rates as high as 45%.44 However, this
number is an average result of several clinical studies in which the
rate of bacteremia ranged from 0% to 100%.49 50 51 52 In only
one study was the oropharynx the documented source of
infection.52 These studies were performed with differing
methods and involved relatively small numbers of patients. Until more
data documenting the true rate of bacteremia associated with stricture
dilation become available, it is prudent to consider this procedure as
one potentially associated with an increased risk of transient
bacteremia.
The bacteremia rate associated with sclerotherapy of esophageal varices is approximately 31%.44 Bacteremia appears to be most associated with increased sclerosant volumes, as can occur with emergency sclerosis for active bleeding, and with relatively longer injection needles. The bacteremia rate is lessened with the use of shorter injection needles and sterile water.53 54 Endoscopic ligation of varices, or banding, is not associated with increased rates of transient bacteremia.55
An obstructed biliary tree, due to benign or malignant disease, may be colonized with a variety of organisms. A prime risk factor for dissemination of infection from an obstructed biliary tree is instrumentation of the obstructed region without provision of adequate drainage. The bacteremia rates for endoscopic retrograde cholangiography in the absence of ductal obstruction are approximately equal to most other endoscopic procedures. Prophylaxis should be considered primarily in cases in which biliary obstruction is known or suspected.
In biliary tract surgery, or in any operative procedure that involves the intestinal mucosa, there is a potential for bacteremia with organisms known to cause endocarditis. It is therefore prudent to provide prophylaxis for patients at high risk to develop endocarditis.
Surgery, instrumentation, or diagnostic procedures
that involve the genitourinary tract may cause bacteremia. Although the
risk that any particular patient will develop endocarditis is low, the
genitourinary tract is second only to the oral cavity as a portal of
entry for organisms that cause endocarditis. The rate of bacteremia
following urinary tract procedures is high in the presence of urinary
tract infection (UTI). Sterilization of the urinary tract with
antimicrobial therapy in patients with bacteriuria should be attempted
prior to elective procedures, including lithotripsy. Results of a
preprocedure urine culture will allow the practitioner to
choose antibiotics appropriate to the recovered organisms. Procedures
for which antimicrobial prophylaxis is or is not recommended are listed
in Table 3
.
Many procedures involving the urethra and prostatic bed are associated with high rates of bacteremia. The incidence of bacteremia was studied in 300 patients undergoing one of four different urologic procedures: transurethral resection (TUR) of the prostate, cystoscopy, urethral dilation, and urethral catheterization.56 Bacteremia was most frequent after TUR of the prostate, occurring in 31% of the patients. In the other procedures, bacteremia occurred in 24% following urethral dilatation, in 17% following cystoscopy, and in 8% following urethral catheterization. Bacteremia was significantly associated with both prostatitis on histological examination of resected prostate and prior UTI following TUR and with prior UTI following urethral dilatation and cystoscopy. Preexisting UTI was the major source of organisms causing the bacteremia following TUR but was the source in only about one third of patients following the other procedures. Enterococci and Klebsiella were the most frequent organisms. Although bacteremia due to gram-negative bacilli is unlikely to cause endocarditis unless a prosthetic valve is present, it may nevertheless cause life-threatening sepsis. Therefore, an antimicrobial regimen effective against the infective urinary pathogen, eg, enteric gram-negative bacilli, in addition to the enterococcus, should be administered before the invasive genitourinary procedures.
Bacteremia follows uncomplicated vaginal delivery in only 1% to 5% of procedures, usually with various types of streptococci22 ; well-documented cases of endocarditis after normal vaginal delivery are uncommon.57 Therefore, antibiotic prophylaxis for normal vaginal delivery is not recommended. If an unanticipated bacteremia is suspected during vaginal delivery, intravenous antibiotics can be administered at that time. No bacteremia has been detected in studies following cervical biopsy or manipulation of an intrauterine device (IUD) in the absence of obvious infections.22 Bacteremia following removal of an infected IUD is unresolved58 but would seem possible and should warrant prophylaxis, as would other genitourinary procedures in the presence of infection.
| Prophylactic Regimens |
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Practitioners must exercise their own clinical judgment in determining the choice of antibiotics and number of doses that are to be administered in individual cases or special circumstances. Furthermore, because endocarditis may occur in spite of appropriate antibiotic prophylaxis, physicians and dentists should maintain a high index of suspicion regarding any unusual clinical events (such as unexplained fever, night chills, weakness, myalgia, arthralgia, lethargy, or malaise) following dental or other surgical procedures in patients who are at risk for developing bacterial endocarditis.
Regimens for Dental, Oral, Respiratory Tract, or Esophageal Procedures
Streptococcus viridans (
-hemolytic
streptococci) is the most common cause of endocarditis following dental
or oral procedures, certain upper respiratory tract procedures,
bronchoscopy with a rigid bronchoscope, surgical procedures that
involve the respiratory mucosa, and esophageal procedures. Prophylaxis
should be specifically directed against these organisms. The same
regimens are recommended for all these procedures (Table 4
1 22 59 60 61 ). The recommended standard
prophylactic regimen for all these procedures is a single
dose of oral amoxicillin. The antibiotics amoxicillin, ampicillin, and
penicillin V are equally effective in vitro against
-hemolytic
streptococci; however, amoxicillin is recommended because it is better
absorbed from the gastrointestinal tract and provides higher and more
sustained serum levels. Previously the recommended dose was 3.0 g
1 hour before a procedure and then 1.5 g 6 hours after the initial
dose.1 Recent comparisons of 2.0-g and 3.0-g dosing
indicate that a 2.0-g dose results in adequate serum levels for several
hours and causes less gastrointestinal adverse effects.59
The newly recommended adult dose is 2.0 g of amoxicillin
(pediatric dose is 50 mg/kg not to exceed the adult dose) to be
administered 1 hour before the anticipated procedure. A second dose is
not necessary, both because of the prolonged serum levels above the
minimal inhibitory concentration of most oral
streptococci59 and the prolonged serum
inhibitory activity induced by amoxicillin against such
strains (6 to 14 hours).60 For individuals who are unable
to take or unable to absorb oral medications, a parenteral agent may be
necessary. Ampicillin sodium is recommended because parenteral
amoxicillin is not available in the United States. Individuals who are
allergic to penicillins (such as amoxicillin, ampicillin, or
penicillin) should be treated with the provided alternative oral
regimens. Clindamycin hydrochloride is one recommended alternative.
Individuals who can tolerate first-generation cephalosporins
(cephalexin or cefadroxil) may receive these agents, provided they have
not had an immediate, local, or systemic IgE-mediated anaphylactic
allergic reaction to penicillin. Azithromycin or clarithromycin are
also acceptable alternative agents for the penicillin-allergic
individual,61 although they are more expensive than the
other regimens. When parenteral administration is needed in an
individual who is allergic to penicillin, clindamycin phosphate is
recommended; cefazolin may be used if the individual does not have an
immediate type local or systemic anaphylactic hypersensitivity to
penicillin. The previous recommendations from this committee listed
erythromycin as an alternate agent for the penicillin-allergic patient.
Erythromycin is no longer included because of gastrointestinal upset
and complicated pharmacokinetics of the various
formulations.62 Practitioners who have
successfully used erythromycin for prophylaxis in individual patients
may choose to continue with this antibiotic. The regimen is included in
our previous recommendations.1
Regimens for Genitourinary and Nonesophageal Gastrointestinal Procedures
Bacterial endocarditis that occurs following genitourinary and
gastrointestinal tract surgery or instrumentation is most often caused
by Enterococcus faecalis (enterococci). Although
gram-negative bacillary bacteremia may follow these procedures,
gram-negative bacilli are only rarely responsible for endocarditis.
Thus, antibiotic prophylaxis to prevent endocarditis that occurs
following genitourinary or gastrointestinal procedures should be
directed primarily against enterococci.
Table 5
1 22 outlines the recommended
regimens for prophylaxis for genitourinary or gastrointestinal tract
procedures (excluding esophageal procedures). The committee continues
to recommend parenteral antibiotics, particularly in high-risk
patients. In medium-risk patients requiring prophylaxis, a parenteral
(ampicillin) or oral (amoxicillin) regimen is provided. For procedures
in which prophylaxis is not routinely recommended, physicians may
choose to administer prophylaxis in high-risk patients.
| Specific Situations and Circumstances |
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Procedures Involving Infected Tissues
Incision and drainage or other procedures involving infected
tissues may result in bacteremia with the same organism causing the
infection. In individuals at risk for endocarditis (the high- and
moderate-risk categories in Table 1
), it is advisable to administer
antimicrobial prophylaxis before the procedure. Prophylaxis should be
directed at the most likely pathogen causing the infection. For nonoral
soft tissue infections (cellulitis), or bone and joint infections
(osteomyelitis and pyogenic arthritis), an antistaphylococcal
penicillin or first-generation cephalosporin is an appropriate choice.
For patients who are allergic to penicillins, clindamycin is an
acceptable alternative. For those unable to take oral antibiotics or
who are known to have methicillin sodiumresistant
Staphylococcus aureus bacteremia, vancomycin is the regimen
of choice. For UTI, agents active against enteric gram-negative bacilli
(such as aminoglycosides or third-generation cephalosporins) are
advisable.
Patients Who Receive Anticoagulants
Intramuscular injections for endocarditis prophylaxis should be
avoided in patients who receive heparin. The use of warfarin sodium is
a relative contraindication to intramuscular injections.
Intravenous or oral regimens should be used whenever
possible.
Patients Who Undergo Cardiac Surgery
A careful preoperative dental evaluation is recommended so that
required dental treatment can be completed before cardiac surgery
whenever possible. Such measures may decrease the incidence of late
postoperative endocarditis.
Patients who have cardiac conditions that predispose them to endocarditis are at risk for developing bacterial endocarditis when undergoing open heart surgery. Similarly, patients who undergo surgery for placement of prosthetic heart valves or prosthetic intravascular or intracardiac materials are also at risk for the development of bacterial endocarditis. Because the morbidity and mortality of endocarditis in such patients are high, perioperative prophylactic antibiotics are recommended. Endocarditis associated with open heart surgery is most often caused by S aureus, coagulase-negative staphylococci, or diphtheroids. Streptococci, gram-negative bacteria, and fungi are less common. No single antibiotic regimen is effective against all these organisms. Furthermore, prolonged use of broad-spectrum antibiotics may predispose to superinfection with unusual or resistant micro-organisms. Prophylaxis at the time of cardiac surgery should be directed primarily against staphylococci and should be of short duration. First-generation cephalosporins are most often used, but the choice of an antibiotic should be influenced by the antibiotic susceptibility patterns at each hospital. For example, high prevalence of infection by methicillin-resistant S aureus in a particular inpatient unit should prompt consideration of vancomycin for perioperative prophylaxis. It should be noted, however, that although the majority of nosocomial coagulase-negative staphylococci exhibit the methicillin-resistance phenotype in vitro, endocarditis prophylaxis with first-generation cephalosporins is effective for most patients undergoing cardiac valve surgery.63 Prophylaxis with the chosen antibiotic should be started immediately before the operative procedure, repeated during prolonged procedures to maintain levels intraoperatively, and continued for no more than 24 hours postoperatively to minimize emergence of resistant micro-organisms. The effects of cardiopulmonary bypass and compromised postoperative renal function on antibiotic levels in the serum should be considered and doses timed appropriately before and during the procedure.
Status Following Cardiovascular Procedures
Many reparative cardiac procedures do not modify the
patients long-term risk for infective endocarditis, which continues
indefinitely (Table 1
). In the case of prosthetic valve
replacement, the risk of endocarditis increases postoperatively. In
other conditions, such as closure of ventricular septal
defect or patent ductus arteriosus without residual leak, the risk of
endocarditis diminishes to the level of the general population after a
6-month healing period. Data are insufficient to make recommendations
for prophylactic therapy after closure of these lesions by
transcatheter devices. There is no evidence that
coronary artery bypass graft surgery introduces a risk for
endocarditis. Therefore, antibiotic prophylaxis is not needed for
individuals who have previously undergone this procedure.
Noncoronary vascular grafts may merit antibiotic prophylaxis
for the first 6 months after implantation.
There are insufficient data to support recommendations for patients who have had heart transplants. However, such patients are at risk of acquired valvular dysfunction, especially during episodes of rejection. Because of this, and the continuous use of immunosuppression in such patients, most transplant physicians administer prophylaxis according to regimens for the moderate-risk category
| Other Considerations |
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The use of prophylactic antibiotics to prevent infection of joint prostheses during potentially bacteremia-inducing procedures is not within the scope of issues addressed by this committee.
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| Acknowledgments |
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| Footnotes |
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A single reprint is available by calling 800-242-8721 (US only) or writing the American Heart Association, Public Information, 7272 Greenville Avenue, Dallas, TX 75231-4596. Ask for reprint No. 71-0117. To purchase additional reprints: up to 999 copies, call 800-611-6083 (US only) or fax 413-665-2671; 1000 or more copies, call 214-706-1466, fax 214-691-6342, or
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R. O. Bonow, B. Carabello, A. C. de Leon Jr, L. H. Edmunds Jr, B. J. Fedderly, M. D. Freed, W. H. Gaasch, C. R. McKay, R. A. Nishimura, P. T. O'Gara, et al. Guidelines for the Management of Patients With Valvular Heart Disease : Executive Summary: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Committee on Management of Patients With Valvular Heart Disease) Circulation, November 3, 1998; 98(18): 1949 - 1984. [Full Text] [PDF] |
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