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VPR/Kirk CarapezzaVermont towns flooded by Tropical Storm Irene, including Woodstock, are still on boil-water orders.
(Host)Homeowners in the flood zone whose wells or septic systems were inundated needto check the safety of their drinking water.
TheDepartment of Health says it will test wells for free. and at least one groupis offering a filter to help make water drinkable.
VPR’sKirk Carapezza reports from Bridgewater Corners.
(Carapezza)Jody Pindt laughs now, but whenTropical Storm Irene ripped through this small hamlet last week she actually calledTown Hall to see if it had sand bags. It didn’t.
VPR/Kirk CarapezzaJody Pindt on her porch in Bridgwater. Tropical Storm Irene floodwater filled with sewage rushed from the Ottauquechee River and swelled six feet above her private well.
(Pindt) “We watched all kinds of debrisfloat down the river.”
(Carapezza)Pindt stands on her back porch, and remembers how propane tanks rushed down thenorth branch of the Ottauquechee River through her backyard and into her barn.
(Prindt) “Trees, gigantic trees, weregoing sideways down the river with the root system still attached. Some wereshooting down like torpedoes.”
(Carapezza)Bridgewater was one of the communities along Routes 4 and 100 thatIrene slapped especially hard.
Irene’sfloodwaters swept away pieces of Bridgewater’s new bridge on Route 100A. Construction on thatbridge was supposed to be completed this month.
Butofficials are particularly concerned now about drinking water supplies. The floodwatersovercame the town’s sewage treatment plant. Raw sewage flowed into the river,though no one knows exactly how much.
JodyPindt’s well was covered by six feet of sewage-laden river water.
(Prindt)“When we took the well cap off wecould tell that water had gotten in.”
(Carapezza)The Natural Resources Agency says private wells that were flooded should betested repeatedly for bacterial contamination. Theagency says some wastewater systems will have to be repaired or even replaced. Untilthen, the agency says people in many of areas of the flood zone should filter and boil theirwater.
(Scott) “This will filter about two andhalf liters in two minutes.”
(Carapezza)Inside the old Bridgewater Grange Hall, Scott Tommola shows some residents howto use a filter that can clean up water from their wells.
(Scott) “We’ll pour it into thereservoir.”
(Carapezza)Tommola is a physical therapist from Rutland, which is just over the mountains from Bridgewater.
VPR/Kirk CarapezzaScott Tommola, founder of 802Relief, demonstrates to concerned residents at the Bridgewater Grange Hall how to filter their water.
Lastweek, shocked by Irene’s devastation, Tommola launched a nonprofit called 802Relief. He’s asking people to buy and donate these filters so thathe can distribute them to anyone in the flood zone who needs them.
Tommolaworries that amid all the other problems Vermont faces in rebuilding clean water remains a secondaryconcern.
(Scott) “I think it’s almost aninvisible crisis at this point. I think a lot of people are out there sayingthe power is coming back on. The well isworking again. It’s pumping water again,and it’s coming out clear. Just because it’s clear doesn’t mean it’s safe todrink.”
(JodyPindt) “This stuff is so thick.”
(Carapezza)Back at her barn, Jody Pindt says her first priority is digging herself out ofall the muck that the river left on her property. Thenshe’ll focus on her drinking water.
(Pindt) “I am a little concerned,although we did shock the system with enough chlorine to have killed anything.but it is a little discolored.”
(Carapezza) Pindt says she’ll be careful because she doesn’t have health insurance. Soshe’ll wait another month before drinking the water from her well.
ForVPR News, I’m Kirk Carapezza
Antimicrobial prophylaxis is commonly used by clinicians for the prevention of numerous Infectious diseases, Including herpes simplex infection, rheumatic fever, recurrent cellulitis, meningococcal disease, recurrent uncomplicated urinary tract infections in women, spontaneous bacterial peritonitis in patients with cirrhosis, influenza, infective endocarditis, pertussis, and acute necrotizing pancreatitis, as well as infections associated with open fractures, recent prosthetic joint placement, and bite wounds. Perioperative antimicrobial prophylaxis is recommended for various surgical procedures to prevent surgical site infections. Optimal antimicrobial agents for prophylaxis should be bactericidal, nontoxic, inexpensive, and active against the typical pathogens that can cause surgical site infection postoperatively. to maximize its effectiveness, intravenous perioperative prophylaxis should be administered within 30 to 60 minutes before the surgical incision. Antimicrobial prophylaxis should be of short duration to decrease toxicity and antimicrobial resistance and to reduce cost.
Mayo Clin Proc. 2011;86(7):686-701
AAOS = American Association of Orthopedic Surgeons; ADA = American Dental Association; ANP = acute necrotizing pancreatitis; AP = antimicrobial prophylaxis; AUA = American Urological Association; CP = chemoprophylaxis; FDA = US Food and Drug Administration; HlV = human immunodeficiency virus; IDSA = Infectious Diseases Society of America; IE = infective endocarditis; IS = Information Statement; MRSA = methicillin-resistant Staphylococcus aureus; PJl = prosthetic Joint Infection; PJR = prosthetic Joint replacement; RF = rheumatic fever; SBP = spontaneous bacterial peritonitis; SCIP = Surgical Care Improvement Project; Tdap = tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccine, adsorbed; UGI = upper gastrointestinal; UTI = urinary tract infection
On completion of this article, readers should be able to: (I) identify common surgical and nonsurgical indications for the use of antimicrobial prophylaxis in adults, (2) formulate selected surgical and nonsurgical antimicrobial prophylaxis regimens for adults, and (3) summarize the arguments for and against the use of antimicrobial prophylaxis in adults.
Antimicrobial prophylaxis (AP) can be used effectively to prevent infection, but its use should be limited to specific, well-accepted indications to avoid excess cost, toxicity, and antimicrobial resistance. Antimicrobial prophylaxis may be considered primary (prevention of an initial infection) or secondary (prevention of the recurrence or reactivation of an infection), or it may also be administered to prevent infection by eliminating a colonizing organism. This article reviews widely accepted indications for AP in nonsurgical and surgical patients and is an update of a previously published review of this topic.1 in selected situations, vaccination may be recommended as part of a prophylaxis regimen. This article is meant to be a point-ofcare overview topic for the busy clinician. Many of these recommendations are based on expert opinion rather than on prospective clinical trials. Most of the recommended antimicrobial agents are not approved by the US Food and Drug Administration (FDA) for prophylaxis. Current full prescribing information available in the package insert of each drug should be consulted before prescribing any product. Detailed information on individual topics can be found in the cited references.
The potential risks and benefits of AP should be discussed in detail with the patient. Potential risks include allergic reactions that may be severe or life-threatening as well as Clostridium difficile colitis with the use of antibacterial agents.2 Patients taking fluoroquinolones should be warned of the risk of developing tendinitis, including Achilles tendon rupture.3 For all antibiotic dosing recommended in this article, normal hepatic and renal function are assumed.
Rheumatic fever (RF), which is associated with tonsillopharyngitis caused by the group A ?-hemolytic streptococci, may result in carditis with or without valvulopathy. Primary prevention of RF involves prompt and appropriate antibiotic treatment of group A ?-hemolytic streptococcal pharyngitis with a penicillin (drug of choice) or alternative antibiotic.4 Continuous secondary AP prevents recurrent episodes of RF, which could otherwise lead to worsening of the severity of rheumatic heart disease that developed after the initial attack or the development of rheumatic carditis in those who did not develop carditis with the initial RF episode. Guidelines for secondary AP of RF have recently been updated (recommendations for AP regimens are summarized in Table I).4 Penicillins are the antibiotics of choice for secondary prophylaxis for RF, and intramuscular penicillin is superior to oral penicillins.25 Macrolides (eg, erythromycin, clarithromycin, azithromycin) should be reserved for patients who are allergic to both penicillin and sulfa antibiotics. the duration of secondary prophylaxis for RF is reviewed in detail elsewhere and is summarized in Table 2.4 Physicians should tailor the duration of secondary prophylaxis to the individual patient, taking into account the patient’s risk factors for RF recurrence, such as exposure to young children and the presence of carditis with or without underlying valvular disease. Antimicrobial prophylaxis should be considered for at least 10 years or until age 40 years (whichever is longer) for patients with carditis with persistent valvular disease. Prophylaxis should be continued in patients even after prosthetic valve replacement surgery. Antibiotic suppression for the prevention of RF is not adequate for infective endocarditis (IE) prophylaxis before dental procedures.
Patients with lymphedema or severe venous insufficiency of their extremities are at increased risk of recurring ?-streptococcal cellulitis. Common scenarios for recurrent cellulitis of the lower extremity include patients with venous insufficiency after saphenous vein graft harvesting or pelvic lymphadenectomy. Recurrent cellulitis has been observed in the upper extremity after lymphadenectomy performed at the time of mastectomy for breast cancer. Antimicrobial prophylaxis may be a useful addition to the control of lymphedema with local measures and treatment of concurrent tinea pedis in the prevention of recurrent cellulitis. However, this recommendation is based on small, uncontrolled studies.26″28 Typically, more than 2 or 3 episodes per year should occur before AP is initiated. Recommended prophylactic antibiotics for recurrent cellulitis are summarized in Table 1. Oral penicillin V (Phenoxymethylpenicillin) is a reasonable first choice, but optimal dosing of this agent is not well established.5″7 although monthly administration of 1.2 MU of intramuscular benzathine penicillin is recommended as an alternative to oral penicillin V, this dosing regimen was shown to be effective only in those patients not at risk of cellulitis recurrence.28 some experts recommend intramuscular administration of benzathine penicillin every 2 to 3 weeks for individuals who break through once-monthly intramuscular benzathine penicillin regimens.5
Recurrent pyogenic skin infections caused by Staphylococcus aureus, including methicillin-resistant S aureus (MRSA), may be managed by encouraging good personal hygiene, the avoidance of shared personal items, and the diligent cleaning of high-touch environmental surfaces. if a patient is found to be colonized by S aureus , nasal decolonization with mupirocin for 5 to 10 days with or without a topical body decolonization with a skin antiseptic solution such as 4% Chlorhexidine for 5 to 14 days may be reasonable in an attempt to decolonize the patient.8 Antimicrobial prophylaxis options are listed in Table 1 for recurrent methicillin-susceptible S aureus skin infections.9,29Long-term oral AP of recurrent MRSA skin infections is not well studied, and formal recommendations for this situation were not included in recently published MRSA treatment guidelines.8
MENINGOCOCCAL DISEASE
Antimicrobial prophylaxis for meningococcal diseases should be offered to close contacts of sporadic cases of Neisseria meningitidis infection (Table 1). Close contacts include household members, day care center staff, and any person directly exposed to an infected person’s oral secretions (for example, through kissing, mouth-to-mouth resuscitation, endotracheal intubation, or endotracheal tube management).11 Public health authorities may recommend population-based prophylaxis in the event of an outbreak. Prophylaxis should be offered as soon as possible. Close contacts should be offered meningococcal vaccination if the outbreak strain is one that is contained in the currently available meningococcal tetravalent conjugate vaccine.30
Penicillin prophylaxis is recommended in children during the first few years after splenectomy to prevent overwhelming Streptococcus pneumoniae sepsis.31 French and American authorities have advocated this form of prophylaxis (eg, 250 mg of oral penicillin V or amoxicillin twice daily) in adults for 1 to 2 years after splenectomy, although data showing the efficacy of this approach are lacking.3133 Haemophilus influenzae type B, meningococcal, and pneumococcal vaccinations should be current in asplenic adults.
URINARY TRACT INFECTION
Several prophylactic antibiotic options are available to nonpregnant women with recurrent (?3 per year), uncomplicated urinary tract infections (TJTIs)13 (Table 1). Continuous low-dose AP and patient-initiated treatment after onset of symptoms are both effective.13?14 During AP, monthly urine cultures should be performed to monitor for bacteriuria and the development of antibiotic resistance.34 Structural abnormality of the urinary tract, renal involvement with infection, or chronic prostatitis (in men) should be considered in the setting of recurrent VTIs. Methenamine hippurate (dosage, 1 g twice daily) has been approved by the FDA for UTI prophylaxis. A recent Cochrane review concluded that methenamine hippurate may be effective for short-term prophylaxis (^l week) in patients without known renal tract abnormalities.35 the typical duration of an initial trial of continuous AP is 6 months. Patients with prolonged exposure to nitrofurantoin should be counseled about the rare but serious complications associated with this agent, including hepatitis, pulmonary reactions, and neuropathy. Cranberries contain 2 substances that prevent fimbriated Escherichia coli from adhering to uroepithelial cells.36 Clinical studies have shown that cranberry juice and cranberry products may reduce the recurrence of UTIs in women. A recent Cochrane review noted limitations in these studies, including variable cranberry products and dosing used in the various studies, as well as high study participant dropout rates.37 other patients who may be considered for prophylaxis of frequent UTIs include pregnant women, persons with spinal cord injuries, persons with neurogenic bladders, renal transplant recipients, and men with chronic bacterial prostatitis.13?34 Postcoital regimens may be appropriate for female patients with UTIs temporally related to sexual intercourse.15?38 Patients who use postcoital regimens should be informed that only 1 dose per day is recommended, regardless of the frequency of intercourse. Postcoital AP in pregnancy can be managed with a single dose of either cephalexin (250 mg) or nitrofurantoin (50 mg).34 Tetracyclines and fluoroquinolones should be avoided during pregnancy, and sulfonamides should be avoided during the last weeks of gestation to minimize the risk of hyperbilirubinemia and kernicterus in the newborn. Topical vaginal estrogen therapy has been shown to reduce the risk of recurrent UTIs in postmenopausal women; it may be a consideration for postmenopausal women who are not receiving estrogen replacement therapy and who have no contraindications to estrogen therapy.39
SPONTANEOUS BACTERIAL PERITONITIS
Spontaneous bacterial peritonitis (SBP) in patients with cirrhosis is associated with increased morbidity and mortality. Aerobic gram-negative organisms and streptococci are the most frequent causes of this infection. in a recent Cochrane review of 12 treatment trials, empirical oral or parenteral antimicrobial treatment of patients with cirrhosis and upper gastrointestinal (UGI) bleeding reduced the incidence of bacterial infections and was associated with shortened hospital stays and reduced rates of overall mortality, mortality from bacterial infections, and rebleeding.40 no one antibiotic regimen or route of administration was found to be superior. On the basis of these data, 7 days of empirical antibiotics are recommended for patients with ascites and UGI bleeding16 (Table 1). in prospective randomized clinical trials, primary prophylaxis in high-risk patients and secondary prophylaxis after an initial episode of SBP have been shown to be effective in preventing SBP.41″44 A recent Cochrane review of 7 trials of empirical AP to prevent SBP in cirrhotic patients with ascites without UGI bleeding revealed a pooled reduction in SBP and mortality but noted issues with trial methodology and findings suggestive of systematic bias in publication and design.45 A 1998 analysis concluded that prophylaxis in high-risk patients (serum bilirubin level 2.5 mg/dL [to convert to umol/L, multiply by 17.104]; ascitic fluid protein level, 1 g/dL) is cost-effective.46 the American Association for the Study of Liver Diseases has published guidelines that recommend long-term daily AP for patients with previous SBP and for primary prophylaxis in those with an ascitic fluid protein level of less than 1 .5 g/dL and at least 1 of the following criteria: a serum creatinine level of 1.2 mg/dL or higher (to convert to ?p???/L, multiply by 88.4), a blood urea nitrogen level of 25 mg/dL or higher (to convert to mmol/L, multiply by 0.357), a serum sodium level of 130 mEq/L or less (to convert to mmol/L, multiply by 1), or a Child-Pugh score of 9 points or higher with a bilirubin level of 3 mg/dL or higher16 (Table 1). Before initiation of AP, SBP should be ruled out in all patients with ascites at hospital admission and in cirrhotic patients with ascites with signs, symptoms, or laboratory abnormalities suggestive of infection.16
ACUTE NECROTIZING PANCREATITIS
Severe pancreatitis with necrosis is associated with an overall mortality rate of 17% and a mortality rate of 25% to 30% with infected necrosis. Debate is ongoing as to whether AP in the setting of acute necrotizing pancreatitis (ANP) leads to improved outcomes (some consider the use of antibiotics in this setting preemptive).47 A recent Cochrane database review of 7 randomized studies concluded that patients randomized to receive AP for ANP had no statistically significant reduction in infections.48 Recent practice guidelines published by the American College of Gastroenterology do not recommend AP for ANP.49 if AP is initiated, a broadspectrum ?-lactam such as imipenem-cilastatin is often recommended and should be limited to computed tomographydocumented pancreatic necrosis involving 30% or more of the pancreas for 14 days or less.50
Five percent of dog bites and 30% of cat bites become secondarily infected because these wounds are highly contaminated by microorganisms present in the oral cavity of these animals. these infections can lead to septic arthritis, tenosynovitis, severe soft tissue infection, or sepsis.51 the microbiology of dog and cat bite infections is typically polymicrobial and includes Pasteurella species as the most common isolate, followed by staphylococci, streptococci, and anaerobes.52 although AP for animal bites remains controversial, a meta-analysis of 8 clinical trials by Cummings53 found that AP significantly protects against subsequent wound infection. Antimicrobial prophylaxis of a contaminated wound may be more accurately considered expectant therapy to prevent the development of a wound infection in a contaminated but not yet infected wound. no clinical trials have shown superiority of one antibiotic regimen over another; choices should be based on the likely microbiology of dog and cat bite infections.54 Antimicrobial prophylaxis for bite wounds has recently been reviewed and should be offered to all patients who are thought to have an increased risk of infection17 (Table 1). High-risk situations include, but are not limited to, bites to body areas where deeper structures (tendons and bones) can become easily injured, bites to the hand(s) or close to a bone or joint, crush injuries, puncture wounds (difficult to clean), bites in which treatment is delayed more than 8 to 10 hours, wounds requiring closure, bites in compromised persons (diabetic patients, persons with no spleen, immunocompromised patients), bites in persons with indwelling prosthetic devices, and all cat bites.17?18 Consideration for hospitalization and intravenous antibiotics may be reasonable for patients in the setting of fever, sepsis, spread of cellulitis, significant edema or crush injury, loss of function, compromised immunity, or patient nonadherence to treatment.19 All dog and cat bites should be appropriately irrigated and d?brided, and rabies prophylaxis should be administered, if indicated. Delayed primary closure of heavily contaminated wounds should be considered to decrease the risk of wound infection.
Human bite wounds, including clenched fist injuries, are considered to be at high-risk of infection with organisms such as Streptococcus anginosus, S aureus, Eikenella corrodens, and anaerobes. Recommended AP is similar to that for animal bite wounds17?55 (Table 1). Patients who have sustained human bites should be assessed for human immunodeficiency virus (HTV) and hepatitis B infection risk, and prophylaxis should be offered as indicated according to published guidelines. Tetanus immune globulin and tetanus toxoid should be administered to patients who have not been immunized or tetanus toxoid alone to any patient who has not received a tetanus booster within the past 5 years.
Pertussis (whooping cough), an upper respiratory tract infection caused by Bordetella pertussis, is associated with prolonged bouts of coughing that may last 1 to 6 weeks. Numerous pertussis outbreaks have occurred in the United States during the past 6 years among adolescents and adults as immunity from childhood vaccination has waned. because pertussis is spread by aerosolized respiratory droplets, it is recommended that all household and other close contacts of infected patients who did not use respiratory precautions while in contact with an infected patient receive AP, regardless of age or immunization status20 (Table 1).
The first tetanus toxoid, reduced diphtheria toxoid, and acellular pertussis vaccine, adsorbed (Tdap) licensed for adults was approved by the FDA in 2005 (ADACEL; Sanofi Pasteur; Swiftwater, PA [US Headquarters]; Lyon, France [Global Headquarters]) as a single-dose booster vaccine for persons aged 1 1 to 64 years to provide protection against tetanus, diphtheria, and pertussis. Tdap was initially recommended to replace the next adult booster dose of tetanus- and diphtheria-toxoid vaccines in patients whose last tetanus booster was 10 years or more earlier. the interval between the most recent tetanus vaccination and Tdap for persons with contact with infants, child care providers, or health care professionals with direct patient contact could be as short as 2 years or less.56 given the poor adult pertussis vaccine coverage (5.9% in 200857), and in the setting of increasing numbers of pertussis cases in the United States (16,858 cases in 2009, including 14 infant deaths58), the Pertussis Vaccine Working Group of the Advisory Committee on Immunization Practices59 recommends the administration of a single Tdap (either ADACEL or BOOSTRTX [GlaxoSmithKline Biologicals; Morrisville, NC]), when indicated, for any adult, at any interval since the previous tetanus-diphtheria vaccination. A single Tdap should be considered for adults 65 years or older who have or anticipate having close contact with an infant younger than 12 months as well as for children aged 7 through 10 years who are not fully vaccinated against pertussis. Tdap is not licensed for revaccination. A provisional recommendation from the Advisory Committee on Immunization Practices (February 23, 2011) states that the data on the need for postexposure AP for Tdap-vaccinated health care professionals are inconclusive.60 in view of this, Tdap-vaccinated health care professionals may still be at risk of acquiring pertussis and should be considered for chemoprophylaxis (CP) after a significant pertussis exposure, particularly if they are likely to be exposed to a patient at risk of severe pertussis, such as hospitalized neonates and pregnant women.
INFECTIVE ENDOCARDITIS
Infective endocarditis is a relatively rare endocardial infection that can lead to catastrophic complications and death. Guidelines for the prevention of LE have been published by the American Heart Association for more than 50 years. the first 9 guidelines (1955-1997) were based on low-level evidence; more recently, guidelines have been stratified according to the lifetime risk of LE. the recommendations of the most recent (2007) guidelines reflected a new reticence about using AP for LE based on the following premises: (1) cumulative bacteremia risk is much greater with daily activities than dental procedures; (2) antibiotics do not eliminate bacteremia or clearly reduce IE risk; (3) there are no prospective, placebo-controlled AP trials; and (4) even if 100% effective, antibiotics would prevent only rare cases of TE.61 the 2007 AP guidelines for LE from the American Heart Association and the Infectious Diseases Society of America (LDSA) recommend AP only for patients at highest risk of complications of LE (Table 3) and only for selected dental procedures (Table 4). Administration of prophylactic antibiotics is no longer stratified according to lifetime LE risk. the antibiotics that are recommended for TE prophylaxis before dental procedures are fisted in Table 5. Patients receiving a penicillin for RF prophylaxis should not receive a penicillin for LE dental prophylaxis.
Prophylaxis is no longer recommended for uncomplicated gastrointestinal bronchoscopy without incision of the respiratory mucosa and for urinary procedures. if the urine is colonized or infected before an elective cystoscopy, antibiotic therapy to eradicate the infection before the urologie manipulation is recommended. if an urgent cystoscopy is to be performed in the setting of colonized or infected urine, then an antibiotic with activity against enterococci should be administered. Ampicillin or amoxicillin are the preferred agents in this setting; vancomycin should be used in the setting of severe penicillin intolerance. Urinary tract colonization or infection with enterococci known or suspected to be resistant (including those resistant to vancomycin) may require a consultation with an infectious diseases expert.61
Although many respiratory tract procedures reportedly cause bacteremia involving a wide variety of microorganisms, no published data conclusively demonstrate a link between these procedures and LE. Antimicrobial prophylaxis (for regimens, see Table 5) is thought to be reasonable for patients at highest risk of complications from LE (Table 3) who undergo invasive procedures of the respiratory tract that involve incision or biopsy of the respiratory mucosa (eg, tonsillectomy, adenoidectomy). Patients at highest risk of complications from TE who undergo an invasive respiratory tract procedure to treat an established infection, such as drainage of an abscess or empyema, should receive an antibiotic that is active against the viridans group streptococci. if an infection is known or suspected to be caused by S aureus, the antibiotic regimen should contain an antistaphylococcal penicillin or a cephalosporin for patients who are unable to tolerate a penicillin. Vancomycin should be used in those in whom an infection is known or suspected to be caused by a metWcilfin-resistant strain of S aureus or in those who have a history of a severe reaction to ?-lactam antibiotics.61
PROSTHETIC JOINT INFECTIONS
Despite the lack of data supporting AP before dental procedures, many surveys of health care professionals have shown that a substantial number of them recommend AP before dental procedures in patients with a PJR.71?72 Antimicrobial prophylaxis for patients with a prosthetic joint undergoing a dental procedure or other invasive medical procedure has been controversial for decades.67?71?73″75 Consensus guidelines for this practice were initially published in 1997 and affirmed in 2003 by the American Dental Association (ADA) and the American Association of Orthopedic Surgeons (AAOS) on the basis of low-level evidence.69?76 It was proposed that AP be administered before dental procedures thought most likely to be associated with bacteremia for patients who were considered to be at highest risk of bacteremia-associated PJI. High-risk patients are thought to include all patients during the first 2 years after joint replacement, immunocompromised or immunosuppressed patients, patients with comorbid conditions (eg, diabetes, obesity, HTV infection, smoking), and patients with inflammatory arthropathies (eg, rheumatoid arthritis), systemic lupus erythematosus, medication- or radiation-induced immunosuppression, previous PJI, malnourishment, hemophilia, HTV infection, insulin-dependent (type 1) diabetes, megaprosthesis, or malignancy. More recently (February 2009), the Patient Safety Committee of the AAOS posted an Information Statement (IS) advising that “clinicians consider antibiotic prophylaxis for… all total joint replacement patients prior to any invasive procedure that may cause bacteremia.”77 the ADA no longer supports the 2003 AAOS/ADA Guidelines and refers patients and health care professionals to the AAOS IS (Karen London, American Dental Association, written communication, March 28, 201 1).77 although specific dental procedures that may cause bacteremia are not listed in the AAOS IS, the ADA lists the dental procedures that may cause bacteremia in the AAOS/ ADA 2003 guidelines.76?77 the antibiotics recommended in the AAOS IS to be administered to patients with PJR before dental procedures include 2 g of oral cephalexin, cephradine, or amoxicillin 1 hour before dental procedures. the AAOS IS makes no mention of parenteral antibiotic options or antibiotic alternatives for penicillin-allergic patients. the 2003 AAOS/ADA advisory statement recommended 1 g of intravenous cefazolin or ampicillin as parenteral antibiotic alternatives or 600 mg of clindamycin (intravenous or oral) for penicillin-allergic patients, to be administered 1 hour before the dental procedure; in our opinion, these remain valid antibiotic alternatives.76
A panel that included representatives from the ADA, AAOS, and LDSA was recently convened with the goal of producing an evidence-based antimicrobial guideline for patients with PJR before dental procedures (D.R.O. is a member of the working group). It is hoped that this will lead to a simpler consensus guideline for patients and health care professionals. Good dental health before and after total joint replacement and prompt treatment of active oral infection should be encouraged for all patients with PJR.
Antimicrobial prophylaxis in patients undergoing invasive gastrointestinal procedures is not recommended by the American Society of Colon and Rectal Surgeons78 or the American Society for Gastrointestinal Endoscopy.79 if clinicians elect to recommend AP for the prevention of hematogenous PJI in these patients, they should discuss with them the possibility of life-threatening adverse reactions (rare) and the more common drug toxicities. if used, antimicrobial agents should be chosen on the basis of the expected flora at the site of the procedure.
The American Urological Association (AUA) and the AAOS first published consensus- and expert opinion-based AP guidelines in 2003 for patients with total joint replacement who were undergoing urologie procedures.80 Antimicrobial prophylaxis is recommended for patients at increased risk of hematogenous PJI who undergo urologie procedures associated with an increased risk of bacteremia. the details of these recommendations can be found in the 2007 AUA best Practice Policy Statement on Urologie Surgery Antimicrobial Prophylaxis, which is available on the AUA Web site.80?81 the guidelines assume that the urine is sterile preoperatively. if bacteriuria is present, it should be treated with appropriate antibacterial agents before manipulation of the urinary tract.
Antibacterial agents have been shown to decrease the risk of travelers’ diarrhea by up to 84%.8284 Antimicrobial agents are not routinely recommended for the prevention of travelers’ diarrhea because antibiotic self-treatment is so rapidly effective. the traveler may be instructed to carry a supply of an antibiotic (often a 1- to 3-day course of a fluoroquinolone for travel to Central or South America or Africa or of azithromycin when traveling to Asia or the Indian subcontinent) to be taken on an as-needed basis.12 in certain circumstances (riskaverse travelers, athletes, persons taking antacids, or persons with diabetes, an elevated gastric pH, or inflammatory bowel disease), a daily oral antibiotic regimen may be considered on a short-term basis (ideally 2-3 weeks) to prevent travelers’ diarrhea. Fluoroquinolones may be less effective in areas with quinolone-resistant Campylobacter species infections (eg, India, Southeast Asia), so an agent such as azithromycin (250 mg once daily) may be considered, although this has not been studied. in a 14-day study among travelers to Mexico, rifaxirnin (200 mg 1-3 times daily) was 72% effective in preventing travelers’ diarrhea.23 Bismuth subsalicylate prophylaxis (Pepto-Bismol [Proctor & Gamble; Cincinnati, OH]: two 262-mg chewable tablets 4 times daily, with meals and once in the evening) is less effective (62%-65% effective) than antibiotics, is inconvenient to take, contains a salicylate (to be avoided if receiving anticoagulant therapy or high-dose salicylates), causes a black tongue, and may interfere with the absorption of medications such as doxycycline.12 Probiotics containing Lactobacillus GG or Saccharomyces boulardii are of limited efficacy (0%-60% effective) in the prevention of travelers’ diarrhea and generally are not recommended for this purpose.85,86
Open fractures, particularly Gustilo grade 3 fractures, are at an increased risk of infection.87 the key to infection avoidance of open class LTJ fractures is wound irrigation, surgical debridement of devitalized tissue, and delayed wound closure. A recent Surgical Infection Society Guideline recommended AP with a first-generation cephalosporin after open fracture until 24 to 48 hours after wound closure.88 some groups recommend adding gram-negative coverage for class UI open fractures.89
HERPES SIMPLEX VIRAL INFECTION
Frequent recurrent genital herpes simplex viral infections (5-6 episodes per year) are amenable to prophylaxis with continuous acyclovir (400 mg twice daily), famciclovir (250 mg twice daily), or valacyclovir (500-1000 mg once daily).90?91 Famciclovir may be less effective for suppression of viral shedding, and 500 mg of valacyclovir once daily might be less effective than other valacyclovir or acyclovir dosing regimens in patients who have very frequent recurrences (ie, ?10 episodes per year).91 Patients should be counseled regarding consistent condom use and avoidance of sexual activity during recurrences in addition to suppressive antiviral therapy.
Chemoprophylaxis of influenza A and B infection with a neuraminidase inhibitor (zanamivir [inhaled] or oseltamivir [oral]) is 70% to 90% effective92?93 (Table 1). these agents are particularly useful for prophylaxis after exposure in unvaccinated high-risk patients and unvaccinated health care professionals in an outbreak setting in a medical institution or community. Chemoprophylaxis is recommended for persons who are at high risk of influenza complications (Table 6) and those who are hospitalized or have severe, complicated, or progressive illness.94 Lowrisk, healthy persons who are not in contact with high-risk patients do not typically require CP. Adults for whom antiviral CP should be considered during periods of increased influenza activity in the community are listed in Table 7. Zanamivir and oseltamivir are classified as category C (risk cannot be ruled out) for use during pregnancy. Influenza CP should be considered as an adjunct to influenza vaccination. Chemoprophylaxis should not be administered 48 hours before or 2 weeks after administration of the intranasal live-attenuated FluMist influenza vaccine (Medlmmune, Gaithersburg, MD); CP has no effect on the inactivated influenza vaccine.21 Chemoprophylaxis may be stopped 10 days after exposure for household contacts and 7 days after other exposures.94 For control of outbreaks in long-term care facilities and hospitals, the Centers for Disease Control and Prevention recommends CP for a minimum of 2 weeks, even for vaccinated persons, up to 1 week after the last known case was identified.22?94 in patients who are unable to receive influenza vaccination and who are at high risk of complications, treatment should be continued for the duration of the influenza season in the community. Oseltamivir- and zanamivir-resistant influenza A strains have been reported; one should monitor the Centers for Disease Control and Prevention influenza Web site ( cdc.gov/flu) for seasonal updates. the adamantanes (amantadine and rimantadine) are active only against influenza A; with the emergence of adamantane resistance in most seasonal A H3N2 and pandemic 2009-2010 A HlNl strains, these agents are no longer recommended for CP.
Surgical site infections account for 14% to 18% of all health care infections and are the third most frequently reported nosocomial infection.96?97 Factors that may increase the risk of surgical site infection include those related to the patient (age, nutritional status, diabetes, smoking status, obesity, coexisting infections at a remote site, colonization with a pathogenic microorganism, altered immune response, and length of preoperative stay) and the operative procedure (duration of surgical scrub, skin antisepsis, preoperative shaving, preoperative skin preparation, duration of operation, AP, operating room ventilation, inadequate sterilization of instruments, foreign material at the surgical site, surgical drains, and surgical technique).98 the risk of surgical site infection also depends on whether the surgical procedure is clean, clean-contaminated, contaminated, or dirty-infected based on standard definitions of these terms.98 Improvements in operating room ventilation, sterilization methods, barriers, and surgical technique as well as the use of perioperative topical, oral, and intravenous AP have been important in decreasing the incidence of surgical site infection.98,99
Perioperative antimicrobial surgical prophylaxis is recommended for operative procedures that have a high rate of postoperative wound infection, when foreign material is implanted, or when the wound infection rate is low but the development of a wound infection results in a disastrous event.98100 Prophylactic antimicrobial agents should be bactericidal, nontoxic, and inexpensive and have in vitro activity against the common organisms that cause postoperative wound infection after a specific surgical procedure. Consensus panels most often recommend cefazolin and other cephalosporins because they meet the aforementioned criteria.98?100 Broad-spectrum antibiotics (eg, ertapenem) should be avoided for surgical prophylaxis.100,101 Perioperative antimicrobial surgical prophylaxis regimens for various surgical procedures adapted from the published recommendations of 2 consensus panels are summarized in Table 8.99,100,102 the use of vancomycin for prophylaxis is appropriate in the event of true type I hypersensitivity or other serious reaction to penicillin or when the incidence of surgical site infection is high due to methicillin-resistant staphylococci.132 Adherence to this practice will help to avoid the emergence of vancomycinresistant organisms and vancomycin-related toxicity.133136 Prophylactic antimicrobial agents should be administered not more than 30 to 60 minutes before surgery, including cesar?an sections.100?112?137?138 Exceptions to this include oral administration of antimicrobial agents before colonic and urologie procedures (Table 8). Infusions should be completed before the tourniquet is placed with orthopedic surgeries. Vancomycin and fluoroquinolone infusions should be started 90 to 120 minutes before surgical incision because these require at least 1 hour to infuse. Therapeutic concentrations of antimicrobial agents should be present in the tissue throughout the period that the wound is open. Additional antibiotic doses may need to be administered intraoperatively for prolonged procedures or with antimicrobial agents with short half-lives.102?139 Initiating intravenous antimicrobial therapy before the perioperative period provides no benefit. Prolonged postoperative AP should be discouraged because of the possibility of added antimicrobial toxicity, selection of resistant organisms, and unnecessary expense. the duration of AP for most procedures should not exceed 24 hours, with the exception of cardiac surgeries, in which antibiotics may be continued for up to 48 hours.99?100?102?103?140 the duration of antibiotic therapy for ophthalmic procedures has not been established. an advisory statement for AP in dermatologie surgery has been published recently.141 the LDSA, American Society of Health-System Pharmacists (ASHP), Society for Healthcare Epidemiology of America, and Surgical Infection Society are currently in the process of revising the 1999 ASHP Antimicrobial Prophylaxis in Surgery Guideline.99
In 2002, the Center for Medicaid and Medicare Services implemented a quality initiative project, currently entitled the Surgical Care Improvement Project (SCLP), in an attempt to decrease postoperative surgical site infections.140 As part of the SCLP, medical institutions are being graded on 3 surgical AP performance measures with cardiothoracic, vascular, colon, hip/knee, and vaginal or abdominal hysterectomy surgeries: (1) the proportion of patients who have parenteral AP initiated within 1 hour before surgical incision, (2) the proportion of patients who are provided an antibiotic agent that is consistent with currently published guidelines, and (3) the proportion of patients whose prophylactic antibiotic is discontinued within 24 hours after the end of the operation (48 hours for cardiothoracic surgery). the most up-to-date list of approved antibiotics for various surgeries is posted on the SCLP Web site.140
The use of AP has led to the prevention of a large number and variety of infections and to substantial declines in surgical site infections. Antimicrobial prophylaxis should be limited to specific, well-accepted indications to avoid excess cost, toxicity, and antimicrobial resistance. Patients should understand the potential risks and benefits of any AP regimen. although some AP practices are evidence-based, many are based on low-level evidence or expert opinion. More studies in the area of AP are needed.
Mark J. Enzler, MD; Elie Berbari, MD; and Douglas R. Osmon, MD, MPH
From the Division of Infectious Diseases, Mayo Clinic, Rochester, MN.
Address correspondence to Mark J. Enzler, MD, Division of Infectious Diseases, Mayo Clinic, 200 First St SW, Rochester, MN 55905 (). Individual reprints of this article and a bound reprint of the entire Symposium on Antimicrobial Therapy will be available for purchase from our Web site mayoclinicproceedings.com.