ntibiotic
administration during the perioperative period has
recently been proposed as a quality metric.1
Anesthesiologists are frequently responsible for
ensuring the timely administration of antibiotics
for surgical site infection and infective endocarditis
(IE) prophylaxis in the operating room or procedure
suite. Knowledge of the indications and appropriate
antibiotics and dose are necessary for appropriate
prophylactic antimicrobial therapy.
In the United States, 15,000 new patients each year
are diagnosed with IE.2
Despite advances in diagnosis and treatment, IE
remains associated with significant morbidity and
mortality. The vast majority of IE cases (~85 percent)
are caused by streptococci, enterococci or staphylococci.3
Risk factors for developing IE have changed over
time, from rheumatic valve lesions and congenital
cardiac abnormalities to myriad other risk factors,
including intravenous drug abuse, prosthetic valves,
degenerative valve disease and bacteremia associated
with invasive procedures. Since 1955, the American
Heart Association (AHA) has periodically published
guidelines for the prevention of IE, most recently
in October 2007.4
These latest guidelines were revised for several
reasons. IE is now thought more likely to result
from frequent bacteremias associated with daily
activities than from bacteremia caused by dental,
gastrointestinal (GI) or genitourinary (GU) tract
procedures or skin incision. For example, maintenance
of optimal oral health and hygiene can reduce the
incidence of bacteremia and thereby have a more
important role than prophylactic antibiotics in
reducing the risk of IE. Furthermore, there is little
evidence to suggest that prophylactic antibiotic
administration prevents IE. Finally, even if 100-percent
effective, universal antibiotic prophylaxis would
prevent a minimal number of IE cases. Consequently,
it was the opinion of the AHA guideline panel that
the risk of antibiotic-associated adverse events
exceeded the potential benefit of routine prophylactic
therapy, except in high-risk individuals undergoing
high-risk procedures (see below).
Compared to previous guidelines, the 2007 AHA IE
prevention guidelines have been greatly simplified.
Several important concepts summarize the current
recommendations:
1. The need for IE antibiotic prophylaxis is
based not only on the risk of developing IE but
also on the severity of outcome if IE were to
occur. Highest-risk patients include those with:
a. Presence of a prosthetic cardiac valve;
b. Previous IE;
c. Unrepaired cyanotic congenital heart disease
(including palliative shunts and conduits);
d. Completely repaired congenital heart defects
with prosthetic material or device, whether
placed by surgery or by percutaneous catheter
intervention, during the six months after the
procedure;
e. Repaired congenital heart disease with residual
defects at the site, or adjacent to the site,
of a prosthetic patch or prosthetic device (which
inhibit endothelialization); and
f. Previous cardiac transplantation with subsequent
cardiac valvulopathy (substantial leaflet pathology
and regurgitation).
It is noteworthy that highest-risk patients no
longer include those with common valvular lesions,
including bicuspid aortic valve, acquired aortic
or mitral valve disease (including mitral valve
prolapse with an audible click or murmur) or hypertrophic
cardiomyopathy.
2. Highest-risk patients who undergo dental procedures
that involve manipulation of gingival tissue or
the periapical region of teeth or perforation
of the oral mucosa should receive antibiotic prophylaxis.
Almost all dental procedures are included except:
a. Routine anesthetic injections through noninfected
tissue;
b. Dental radiographs;
c. Placement of removable prosthodontic or orthodontic
appliances;
d. Placement or adjustment of orthodontic appliances;
e. Shedding of deciduous teeth; and
f. Bleeding from trauma to the lips or oral
mucosa.
In addition to dental procedures, excluding those
listed above, highest-risk patients should receive
IE antibiotic prophylaxis prior to procedures
that involve incision or biopsy of respiratory
tract mucosa, such as tonsillectomy, adenoidectomy
or biopsies. Antibiotic prophylaxis is not recommended
for endotracheal intubation or routine bronchoscopy.
3. Antibiotic prophylaxis for dental and respiratory
tract procedures in highest-risk patients is focused
against viridans group streptococci and consists
of a single pre-procedure dose. No repeat dosing
is advised. Recommended drugs and dosages are
listed in Table 1.
4. Antibiotic prophylaxis solely to prevent IE
is no longer recommended for GI or GU procedures.
These procedures include diagnostic esophagogastroduodenoscopy,
colonoscopy, vaginal delivery and hysterectomy.
However, patients with established or suspected
GI or GU infections undergoing a GI or GU procedure
should receive, as part of routine infection management,
an antibiotic active against enterococci. In these
scenarios, IE prophylaxis is redundant. Infectious
disease consultation is recommended if an infection
is known or suspected to be caused by a resistant
strain of enterococcus.
5. In highest-risk patients, antibiotic prophylaxis
is recommended to prevent IE in procedures involving
infected skin, skin structure or musculoskeletal
tissue. Despite the polymicrobial nature of these
infections, only staphylococci and beta-hemolytic
streptococci are likely to cause IE; thus therapeutic
antibiotic regimens need to be active against
these pathogens, in addition to other potential
site-specific organisms.
These changes may violate longstanding expectations
of patients and practice patterns of physicians
and dentists. As previous guidelines contained
inconsistencies and were based on minimal published
data, conflicting interpretations among patients,
health care providers and attorneys often resulted.
In the past, various interpretations may have
resulted in unnecessary treatment by physicians
and dentists who felt an obligation (professionally
and legally) to protect their patients from IE.
In summary, the updated 2007 AHA Guidelines for
Prevention of Infective Endocarditis recommend antibiotic
prophylaxis for a decreased number of indications
in fewer patients. These simplified guidelines are
based on the best available, albeit minimal, data
and should result in less confusion regarding appropriate
therapy. Future studies will be necessary to monitor
the effects of these changes.
References:
1. American Medical Association Web site. Available
at www.ama-assn.org/ama1/pub/upload/mm/370/perioperativews1206.pdf.
Accessed on February 11, 2008.
2. Mylonakis E, Calderwood SB. Infective endocarditis
in adults. N Engl J Med. 2001; 345:1318-1330.
3. Hoen B. Epidemiology and antibiotic treatment
of infective endocarditis: An update. Heart.
2006; 92:1694-1700.
4. Wilson W, Taubert KA, Gewitz M, et al. Prevention
of infective endocarditis: Guidelines from the American
Heart Association. Circulation. 2007; 116:1736-1754.
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James
A. Onigkeit, M.D., is a Fellow, Division of
Critical Care Medicine, Department of Anesthesiology,
Mayo Clinic, Rochester, Minnesota. |
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Daniel
R. Brown, M.D., Ph.D., F.C.C.M., is Chair, Division
of Critical Care Medicine, Department of Anesthesiology,
Mayo Clinic, Rochester, Minnesota. |
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