Treatment FAQ

which antibiotic should not be used for the treatment of an enterococcal urinary tract infection

by Mrs. Mae Sipes Published 2 years ago Updated 2 years ago

Which antibiotics are used in the treatment of enterococcal urinary tract infection (UTI)?

 · Macrolides, lincosamides, and streptogramin antibiotics inhibit protein synthesis by binding to the 50S subunit of the ribosome. Macrolides and lincosamides are not used to treat enterococcal infections, but resistance to them is nonetheless widespread (Jonas, Murray, & Weinstock, 2001). The most common form of acquired resistance to macrolides is production …

What is the best antibiotic for Enterococcus?

 · Isolates of E. faecalis are typically susceptible to ampicillin but resistant to quinupristin-dalfopristin, whereas most E. faecium isolates are resistant to ampicillin (minimum inhibitory concentration ≥16 mcg/mL) but susceptible to quinupristin-dalfopristin.

Which medications are used in the treatment of Enterococcus faecalis?

 · Commonly prescribed antibiotics to treat bacterial urinary tract infections and bladder infections include Levaquin (levofloxacin), Cipro, Proquin (ciprofloxacin), Keflex (cephalexin), Zotrim, Bactrim (trimethoprim/sulfamethoxazole), Macrobid, Furadantin (nitrofurantoin), Monurol (fosfomycin), Hiprex (methenamine.

Why is Enterococcus faecalis resistant to antibiotics?

Enterococcus species, a common cause of nosocomial urinary tract infection, have been identified, and susceptibilities to a range of antibiotics have been determined. In addition, isolates in 1988 were tested for breakpoint susceptibility to vancomycin and teicoplanin. Despite changes in the hospitals covered, isolation of Enterococcus species ...

What is the treatment for enterococcal infection?

Vancomycin is an antibiotic that doctors sometimes use to treat enterococci infections. Strains of enterococci that have become resistant to vancomycin are called VRE. Resistance means vancomycin can no longer kill these bacteria. VRE infections typically affect people who are already sick and in the hospital.

What antibiotics dont cover Enterococcus?

faecalis. Cell wall-active agents with limited or no activity against enterococci include nafcillin, oxacillin, ticarcillin, ertapenem, most cephalosporins, and aztreonam.

What antibiotics are sensitive to Enterococcus faecalis?

All isolated strains of E. faecalis (100%) were sensitive to glycopeptides (vancomycin and teicoplanin) and to nitrofurantoin, 96% strains were sensitive to penicillin, 43% to ciprofloxacin and 28% to tetracycline.

Can you treat Enterococcus with cephalosporins?

This spectrum of activity is reflected in the utility of these drugs for treatment, insofar as ampicillin remains an effective therapy for susceptible enterococcal infections, but cephalosporins are completely ineffective against enterococci.

Does ciprofloxacin treat Enterococcus?

Ciprofloxacin, considered to have only modest activity against enterococci,2 is not used as a drug of first choice but has been successfully employed in the treatment of enterococcal UTIs. A report by Perry et al. indicated problems associated with ciprofloxacin susceptibility testing with the enterococci.

Does metronidazole treat Enterococcus?

As with other antimicrobial agents, the use of metronidazole has resulted in the development of resistance in H. pylori[3]. Several independent studies show an association between metronidazole treatment and infection by vancomycin-resistant Enterococcus species [4–8].

Is Enterococcus sensitive to cephalexin?

Cephalexin does not have activity against Enterococcus faecalis, or Pseudomonas the virulent bugs that can cause dangerous hospital infections.

Is Enterococcus faecalis sensitive to ciprofloxacin?

Nevertheless, recent studies have indicated the presence of Enterococcus faecalis strains sensitive to vancomycin and ciprofloxacin (4). The available fluoroquinolones, including ciprofloxacin, are of limited interest in the treatment of infections by Enterococci, since they show moderate in vitro activity.

Does Augmentin treat Enterococcus faecalis?

All enterococci were fully sensitive to ampicillin and augmentin (amoxicillin-clavulanic acid).

Does nitrofurantoin treat Enterococcus faecalis?

Our study has demonstrated that nitrofurantoin is active against E. faecium and E. faecalis. More importantly, nitrofurantoin retained its activity against vanA- and vanB-positive isolates.

Does levofloxacin cover Enterococcus?

In addition, levofloxacin is approved for the treatment of CBP caused by E. coli, E. faecalis, or Staphylococcus epidermidis.

Does doxycycline treat Enterococcus?

Conclusion: Enterococcus faecalis isolates were completely susceptible, in vitro, to amoxicillin, amoxicillin-clavulanic acid, vancomycin and moxifloxacin. Most isolates were susceptible to chloramphenicol, tetracycline, doxycycline or ciprofloxacin. Erythromycin and azithromycin were least effective.

What is the name of the drug that is used to treat bacteraemia?

Munita JM, Murray BE, Arias CA. Daptomycin for the treatment of bacteraemia due to vancomycin-resistant enterococci. Int J Antimicrob Agents 2014; 44:387.

Can enterococci cause bacteremia?

Enterococcal species can cause a variety of infections, including urinary tract infections, bacteremia, endocarditis, and meningitis. The antimicrobial agents available for treatment of enterococcal infection are reviewed here, followed by treatment approaches for clinical syndromes caused by enterococci. Other issues related to enterococci are discussed in detail separately. (See "Mechanisms of antibiotic resistance in enterococci"and "Vancomycin-resistant enterococci: Epidemiology, prevention, and control"and "Microbiology of enterococci".)

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Can enterococci be impermeable?

Enterococci are also relatively impermeable to aminoglycosides, and the serum concentrations of aminoglycosides required for bactericidal activity are much higher than can be achieved safely in humans. However, the simultaneous use of a cell wall-active agent raises the permeability of the cell so that an intracellular bactericidal aminoglycoside concentration can be achieved [1]. Bactericidal antimicrobial activity is warranted in clinical circumstances of life-threatening infection. (See 'Approach to specific infections'below.)

Does vancomycin kill enterococci?

Approach to susceptible strains — Enterococci are relatively resistant to penicillin and ampicillin (compared with most streptococci); even when these cell wall–active agents inhibit enterococci, they often do not kill them; vancomycin is even less bactericidal. E. faeciumclinical isolates are more resistant to penicillin than E. faecalis(minimum inhibitory concentration for 90 percent of strains [MIC90] >16 mg/mL versus 2 to 4 mcg/mL, respectively); MICs of ampicillin are usually 1 dilution lower than those of penicillin. Piperacillin activity is similar to that of penicillin, and imipenem generally is active against penicillin-susceptible E. faecalis. Cell wall-active agents with limited or no activity against enterococci include nafcillin, oxacillin, ticarcillin, ertapenem, most cephalosporins, and aztreonam.

Is E. faecalistend more virulent than Enterococcus fa

Infections due to Enterococcus faecalistend to be more virulent than infections due to Enterococcus faecium. In addition, bacteremia due to E. faecalisis more likely to be associated with endocarditis than bacteremia due to E. faecium. Clinical isolates of E. faecalistend to be considerably more susceptible to beta-lactam agents than clinical isolates of E. faecium. Isolates of E. faecalisare typically susceptible to ampicillin but resistant to quinupristin-dalfopristin, whereas most E. faeciumisolates are resistant to ampicillin (minimum inhibitory concentration ≥16 mcg/mL) but susceptible to quinupristin-dalfopristin.

Is tigecycline an antimicrobial?

Antimicrobial susceptibility among pathogens collected from hospitalized patients in the United States and in vitro activity of tigecycline, a new glycylcycline antimicrobial. Antimicrob Agents Chemother 2006; 50:3479.

What is the best treatment for enterococcal endocarditis?

The treatment of choice for enterococcal endocarditis is ampicillin or penicillin G plus gentamicin. faecalis, other combinations such as ampicillin plus imipenem or ampicillin plus ceftriaxone or ceftotaxime have been recommended.

Is Enterococcus faecalis gram positive?

Enterococcus faecalis is a gram-positive bacterium that can cause a variety of noso comial infections of which urinary tract infections are the most common. These infections can be exceptionally difficult to treat because of drug resistance of many E. faecalis to cause disease in the urinary tract.

What are the antibiotics that enterococci are resistant to?

Enterococci are intrinsically resistant to cephalosporins, clindamycin, aminoglycosides, and trimethoprim-sulfamethoxazole. [6] They also gain antibiotic resistance through their ability to acquire and transfer resistance-related mobile genetic elements (MGE) via various mechanisms like plasmids, conjugation, and transposons. [1] This latter property is believed to be due to the absence of CRISPR-Cas gene loci, which usually limits invading harmful DNA.

What is the most common infection caused by enterococci?

Urinary tract infections (UTI) are the most common infections caused by enterococci, usually occurring in chronically ill patients in the nosocomial setting associated with obstruction, urinary catheterization, or instrumentation. [46] They can also cause complicated UTIs such as pyelonephritis, perinephric abscesses, and chronic prostatitis, which can all act as sources for bacteremia.

What are the virulence factors that enterococci secrete?

Enterococci secrete virulence factors like bacteriocins, hemolysin/cytolysin, gelatinase, and serine protease. [1] Moreover, they are also capable of producing toxic oxygen metabolites, leading to cell injury.

Can antibiotics cause VRE?

The risk of VRE colonization and infections is associated with previous antibiotic exposure disrupting normal gut microbiomes, especially vancomycin and cephalosporins use. In addition, prolonged hospitalization, ICU stays, residence in long term care (LTC) facilities, hemodialysis patients, diabetes, cancer, and transplant patients, stomach acid suppression, use of invasive devices, and exposure to contaminated surfaces including shared medical equipment can also predispose individuals to get enterococci/VRE infections. [12] [13] [14]

What is the main predisposing factor for severe infections?

Enterococcal colonization of the GI tract is the main predisposing factor for severe infections, which occur through gut translocation. Enterococci are phagocytosed and transported across the intestinal wall and resist killing by the lymph system. [11]

Can enterococci survive disinfectant?

Enterococci are highly resilient and can survive various difficult conditions like common antiseptics and disinfectants, promoting their widespread persistence on ordinary hospital inanimate items. [1] [4] More importantly, they are found in the hands of healthcare workers (HCW), accounting for their easy transmission. [10]

Where are enterococci found?

Enterococci are found in the soil, water, food, sewage, plants, human skin, the oral cavity, and the large intestine, constituting less than 1% of the total microbiota. [3] [5]

What is the best treatment for enterococci?

Such infections may be treated with a number of antimicrobial agents including ampicillin, nitrofurantoin and vancomycin. Ciprofloxacin, considered to have only modest activity against enterococci,2 is not used as a drug of first choice but has been successfully employed in the treatment of enterococcal UTIs.

What is the best treatment for enterococcal endocarditis?

The treatment of choice for enterococcal endocarditis is ampicillin or penicillin G plus gentamicin. faecalis, other combinations such as ampicillin plus imipenem or ampicillin plus ceftriaxone or ceftotaxime have been recommended.

What is the treatment for E. faecalis?

E. faecalis infections are treated with antibiotics. One challenge is that these bacteria have become resistant to many types of antibiotics.

How many UTIs are caused by enterococci?

Each year in the United States, Enterococci are the culprit for 110,000 urinary tract infections (UTIs), 40,000 wound infections, 25,000 cases of bacteremia, and 1,100 cases of endocarditis. Most of these infections take place in hospitals. Here’s some more information on each infection:

What is the most common type of enterococci?

Enterococcus faecalis (also called E. faecalis) is one of the most common species of Enterococci and is the leading cause of enterococcal infections. However, researchers aren’t sure what factors lead to a higher presence of this bacteria in certain people and body parts.

What is the best medicine for endocarditis?

One course of treatment involves combining a wall-active drug — such as penicillin, ampicillin, amoxicillin, piperacillin, or vancomycin — with what’s called an aminoglycoside — such as gentamicin or streptomycin. However, skin infections and endocarditis often require different combinations.

How does E. faecalis spread?

This is mainly because hospitalized patients often have weakened immune systems. For the most part, the bacteria are transmitted by people who work at the hospital, some of whom carry the E. faecalis in their gut. Other times, enterococci are transmitted through medical devices.

What are the symptoms of bacteremia?

faecalis, such as UTIs or wound infections. The symptoms of bacteremia include: Fever and chills. Nausea and/or vomiting.

What is a UTI?

A UTI is an infection of any part of your urinary system, which includes your bladder, kidneys, uterus, and urethra. If you’re a woman, you have a higher risk of getting a UTI. The symptoms include:

Can antibiotics be used to treat a bacterial infection?

Such infections can often be difficult to treat, as ordinary doses of antibiotics typically aren’t strong enough to effectively treat them. In other words, the bacteria are highly drug-resistant.

What is the best antibiotic for bacteria?

How it works: Ciprofloxacin and levofloxacin are antibiotics that keep bacteria from copying their DNA and multiplying. These types of antibiotics work slightly better than amoxicillin/potassium clavulanate, cefdinir, and cephalexin, but the risk of serious side effects is higher. Most healthcare providers will avoid prescribing these types of antibiotics for minor UTIs.

How do antibiotics kill bacteria?

All three antibiotics kill bacteria by destroying one of its most important components: the cell wall, which normally keeps bacteria structurally intact.

Can you take amoxicillin if you have a penicillin allergy?

If you have a penicillin allergy, your healthcare provider won’t prescribe amoxicillin/clavulanate. They may or may not prescribe cefdinir or cephalexin since there is a small chance ( <5%) that a person with a penicillin allergy may also be allergic to these two.

What are the side effects of a ten antibiotic?

Notable side effects: Diarrhea, nausea, vomiting, and rash are common side effects of these antibiotics. In rare cases, all three have the potential to cause the dangerous skin reactions, SJS and TEN.

What class of antibiotics is amoxicillin?

How it Works: Amoxicillin/potassium clavulanate is another combination drug that belongs to the penicillin class of antibiotics. Cefdinir and cephalexin belong to a different class of antibiotics that’s closely related to penicillins.

What are the side effects of nitrofurantoin?

Notable side effects: Loss of appetite, nausea, and vomiting are common side effects of nitrofurantoin. More serious potential side effects include liver conditions like jaundice — yellowing of the skin and eyes — and hepatitis (inflammation of the liver).

How does Nitrofurantoin work?

How it works: Nitrofurantoin is an antibiotic that’s used specifically to treat UTIs and not much else since it only works well in urine. Nitrofurantoin keeps bacteria from making the DNA and proteins they need to survive.

What antibiotics are used for enterococci?

In addition, enterococci have acquired resistance to a wide-range of antibiotic classes, including aminoglycosides, β-lactams, fluoroquinolones, lincosamides, macrolides, oxazolidinones (linezolid), quinupristin/dalfopristin, rifampin, tetracyclines, and vancomycin. Thus, effective directed therapy for any severe enterococcal infection requires susceptibility testing by experienced microbiology laboratories, with therapy adjusted based on the results. However, even when enterococcus appears susceptible to trimethoprim-sulfamethoxazole in vitro, it should not be used in therapy because clinical failures have been reported secondary to the ability of enterococci to utilize exogenous folate. Recently, there has been increasing isolation of E. faecium strains with intrinsic resistance to penicillins. Importantly, E. faecalis is intrinsically resistant to quinupristin/dalfopristin, which therefore should not be used in therapy for infections caused by this species. However, most E. faecalis strains remain susceptible to ampicillin and the related piperacillin, in contrast to most E. faecium strains, which are resistant to ampicillin. Optimal therapy for most infections includes intravenous ampicillin, penicillin, or vancomycin. Given the resistance or tolerance to cell wall–targeting antibiotics, including penicillins and vancomycin, standard therapy with these antibiotics, except in UTIs, should include the addition of a synergistic aminoglycoside (i.e., streptomycin or gentamicin), as long as high-level resistance is not detected. This strategy of two-drug therapy has been associated with improved outcomes. If the VRE strains are known to be susceptible, potential therapy in these infections includes linezolid, quinupristin/dalfopristin, and daptomycin. Although daptomycin is not approved by the U.S. Food and Drug Administration (FDA) to treat VRE, it has been used to treat skin and soft tissue infections and bacteremia. Newly licensed tigecycline is FDA approved to treat complicated skin and soft tissue infections and complicated intra-abdominal infections caused by vancomycin-susceptible isolates of E. faecalis. Quinupristin/dalfopristin use is associated with myalgias and arthralgias, and linezolid use is associated with bone marrow suppression including thrombocytopenia; both have only bacteriostatic activity against the enterococci. Linezolid, when used in combination with selective serotonin reuptake inhibitors, can be associated with serotonin syndrome ( Chapter 442 ). Given the complexity of enterococcal infections, an infectious disease consult should be considered for therapeutic guidance.

How to diagnose enterococcus?

The diagnosis of an Enterococcus infection is made by isolating the organism through culture of a sterile site, such as blood culture or urine culture. The diagnosis and differential diagnosis of specific conditions are the same as discussed for UTIs ( Chapter 292) and endocarditis ( Chapter 76 ).

What is the best treatment for endocarditis?

Combination therapy (intravenous penicillin, ampicillin, or vancomycin plus an aminoglycoside) is the standard therapy for enterococcal endocarditis. Doses and durations are found in Chapter 76. Importantly, the aminoglycoside is used to provide synergistic killing of the organism. Duration of therapy is typically 4 weeks, with 6-week duration given to patients who had prolonged symptoms before seeking therapy, prosthetic valve infection, or relapsed after initial treatment. If the causative enterococcal strain is highly resistant to both gentamicin and streptomycin, then alternative agents and durations must be explored, and surgery to excise infected valves should be considered. Optimal therapy of VRE strains that are resistant to ampicillin is not known but includes combination therapy under the guidance of an infectious disease consultant. Several newly approved agents, including quinupristin/dalfopristin, linezolid, and daptomycin, could be considered if the strain is found to be susceptible. VRE endocarditis may require early surgery because outcomes with antibiotic therapy can be poor. Careful microbiologic and clinical assessment of all patients with enterococcal endocarditis and VRE in particular is helpful in deciding when surgery is necessary. If repeated blood cultures grow for more than 7 days after the initiation of medical therapy or other signs of uncontrolled infection (persistent fever or leukocytosis) are present, surgical repair of the valve or valve replacement should be considered early in the treatment course if there are no absolute contraindications for surgery.

Is E. faecium resistant to penicillin?

Enterococcus faecium is typically high-level penicillin and ampicillin resistant and this type of resistance has been reported as a significant predictor of lack of cure. 58,65 Therapy of enterococcal infections caused by vancomycin-resistant E. faecium is very difficult because these organisms are usually resistant to alternative antibiotics currently available. 58 The newly developed streptogramins (quinupristin and dalfopristin), oxazolidinones (linezolid), daptomycin and tigecycline appeared promising against vancomycin-resistant enterococci. 66 Nitrofurantoin is active against many strains of vancomycin-resistant enterococci and should be useful for urinary tract infections. 65

Can antibiotics be used for enterococcal infections?

Antimicrobial therapy for enterococcal infections is complicated because most antibiotics are not bactericidal at clinically relevant concentrations. Combination therapy with a cell wall agent plus an aminoglycoside improves the outcome of enterococcal endocarditis and probably of enterococcal meningitis, but may not improve the outcome in bacteremia.65 High-level aminoglycoside resistance, vancomycin resistance and high-level ampicillin resistance are increasing in prevalence. 25,58,65

How to prevent VRE?

Preventing the transmission of VRE by placing patients in isolation or grouping patients with VRE together, wearing gown and gloves (which need to be removed inside the patient's room), and washing hands immediately after working with an infected patient

When to initiate contact precautions with microbiology laboratory?

Timely communication between the microbiology laboratory and appropriate personnel to initiate contact precautions as soon as VRE is detected

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