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Escherichia Coli (E Coli) Infections Medication - Antibiotics200
Escherichia Coli (E Coli) Infections Medication - Antibiotics200
Escherichia Coli (E Coli) Infections Medication - Antibiotics200
MEDICATION
Medication Summary
E coli meningitis requires antibiotics, such as third-generation cephalosporins (eg, ceftriaxone).
E coli pneumonia requires respiratory support, adequate oxygenation, and antibiotics, such as third-
generation cephalosporins or fluoroquinolones.
For E coli intra-abdominal abscess, antibiotics also must include anaerobic coverage (eg, ampicillin
and sulbactam or cefoxitin). In severe infection, piperacillin and tazobactam, imipenem and cilastatin,
or meropenem may be used. Combination therapy with antibiotics that cover E coli plus an
antianaerobe can also be used (eg, levofloxacin plus clindamycin or metronidazole).
E coli enteric infections require fluid replacement with solutions containing appropriate electrolytes.
Antimicrobials known to be useful in cases of traveler's diarrhea include doxycycline,
trimethoprim/sulfamethoxazole (TMP/SMZ), fluoroquinolones, and rifaximin. They shorten the duration
of diarrhea by 24-36 h. Antibiotics are not useful in enterohemorrhagic E coli (EHEC) infection and
may predispose to development of HUS. Antimotility agents are contraindicated in children and in
persons with enteroinvasive E coli (EIEC) infection.
Uncomplicated E coli cystitis can be treated with a single dose of antibiotic or 3-d course of a
fluoroquinolone, TMP/SMZ, or nitrofurantoin.
Recurrent E coli cystitis (ie, >2 episodes/y) is treated with continuous or postcoital prophylaxis with a
fluoroquinolone, TMP/SMZ, or nitrofurantoin.
Patients with complex cases (eg, those with diabetes, >65 y, or recent history of UTI) are treated with
a 7- to 14-d course of antibiotics (eg, levofloxacin, third-generation cephalosporins, or aztreonam).
https://emedicine.medscape.com/article/217485-medication 1/2
6/6/2018 Escherichia coli (E coli) Infections Medication: Antibiotics
E coli sepsis requires at least 2 wk of antibiotics and identification of the source of bacteremia based
on imaging study results.
McGannon et al found that antibiotics that target DNA synthesis, such as ciprofloxacin (CIP) and
TMP/SMZ, showed increased Shiga toxin production, whereas antibiotics that target the cell wall,
transcription, or translation did not. [6] Remarkably, high levels of Shiga toxin were detected even
when growth of O157:H7 was completely suppressed by CIP. In contrast, azithromycin significantly
reduced Shiga toxin levels even when O157:H7 viability remained high.
Since the late 1990s, multidrug-resistant Enterobacteriaceae (mostly E coli) that produce extended-
spectrum beta-lactamases (ESBLs), such as the CTX-M enzymes, have emerged within the
community setting as an important cause of UTIs. These bacteria are resistant to the groups of
antibiotics that are commonly used to treat these types of infections (penicillins, cephalosporins) and
to antibiotics normally reserved for more severe infections (eg, fluoroquinolones, gentamicin).
The spread of CTX-M–positive bacteria considerably changes how the treatment of community-
acquired infections is approached and limits the oral antibiotics that may be administered. This finding
has major implications for treating individuals who do not clinically respond to first-line antibiotics. [7]
In one study, mortality following bacteremic infection caused by ESBL producing E coli was
significantly higher than non–ESBL-producing E coli. These findings have serious implications for
antibiotic prescription, as cephalosporins are ineffective treatment for many E coli infections. [8]
https://emedicine.medscape.com/article/217485-medication 2/2