Fluoroquinolones

Chapter 63


Fluoroquinolones






INDICATIONS


See Table 63-1 for specifics.



TABLE 63-1


Fluoroquinolone Indications with Dosages and Recommendations



















































































































Drug Bacteria Site/Disease Dosage and Administration
ciprofloxacin E. coli, Klebsiella, Proteus, Enterobacter Uncomplicated UTI 250 mg bid 3 days
  M. catarrhalis, H. influenzae, M. pneumoniae, Listeria, Legionella, Staphylococcus Cystitis (mild/moderate) 250 mg bid 7-14 days
  Shigella, Serratia, Salmonella Cystitis (severe) 500 mg bid 7-14 days
    Lower respiratory tract, skin, and skin structure 500-750 mg bid 7-14 days
    Sinusitis 500 mg q12h 10 days
    Infectious diarrhea; intraabdominal 500 mg bid 5-7 days (Salmonella)
      500 mg bid 3 days (Shigella)
      500 mg bid 7-14 days (intraabdominal)
norfloxacin Same as ciprofloxacin Uncomplicated UTI 400 mg q12h 3 days
levofloxacin Same plus GABHS, many gram negative Acute exacerbation of COPD 500 mg once daily 7 days
    CAP 500 mg once daily 7-14 days
    Sinusitis 500 mg once daily 10-14 days
    Skin, soft tissue 500 mg once daily 7-10 days
    Uncomplicated UTI 250 mg once daily 3 days
moxifloxacin Same as ciprofloxacin plus anaerobic activity (Bacteroides spp) Uncomplicated UTI 400 mg once daily 3 days
    Sinusitis 400 mg once daily 10 days
    Acute exacerbation of COPD 400 mg once daily 5 days
    CAP 400 mg once daily 7-14 days
    Skin and soft tissue (uncomplicated) 400 mg once daily 7 days
gemifloxacin Same plus GABHS, many gram negative CAP 320 mg po once daily 7 days
    Acute exacerbation of COPD 320 mg po once daily 5 days


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CAP, Community-acquired pneumonia; GABHS, group A β-hemolytic Streptococcus pyogenes.



Quinolones were discovered in 1962 as a byproduct of chloroquine synthesis. The earliest drugs were called quinolones. Later, a fluorine radical was added to the structure, and these newer drugs were called fluoroquinolones, to distinguish them from the earlier drugs. Currently, all quinolones on the market are fluoroquinolones. Many texts now use the terms quinolone and fluoroquinolone interchangeably.


The fluoroquinolones are a group of potent antibiotics with a wide spectrum of action against gram-positive and gram-negative organisms. The primary care provider should be familiar with ciprofloxacin, moxifloxacin, and levofloxacin. Fluoroquinolones have a good safety profile and excellent absorption after oral administration. Headache and dizziness occur in up to 11% of patients and are the most commonly reported adverse events. The newer fluoroquinolones offer expanded coverage of gram-positive pathogens, and one agent, moxifloxacin, is active against anaerobes. However, three fluoroquinolones introduced after 2001 have been taken off the market because of adverse events.


Quinolones are active against aerobic gram-negative bacilli, especially Enterobacteriaceae, Haemophilus, and gram-negative cocci such as Neisseria and Moraxella catarrhalis. They are active against Staphylococcus and Mycoplasma. Ciprofloxacin and levofloxacin are the only quinolones active against Pseudomonas aeruginosa.



Therapeutic Overview


Allergy


Allergic reactions occur in 0.5% to 3% of patients. Rashes are the most common allergic reaction. The newest fluoroquinolone, gemifloxacin, causes rashes in 14% of young women. More serious reactions such as anaphylaxis, drug fever, vasculitis, interstitial nephritis, and serum sickness have been uncommon. If patients demonstrate any of these reactions, it is recommended that they not take any of the fluoroquinolones.





Treatment Principles


Fluoroquinolones should not be considered first-line antibiotics for mild infection; however, they are often the agent of first choice for UTIs and pyelonephritis because of the frequency of resistant bacteria with these conditions. In general, they should be reserved for moderate infections and bacterial infections that are resistant to other antibiotics. Because fluoroquinolones have good tissue penetration, they provide effective treatment for skin, bone, and genital infections. CNS penetration, however, is poor and is not considered clinically effective. Always give fluoroquinolones orally when possible because oral absorption is excellent.


Fluoroquinolones are considered first-choice drugs for empirical treatment of complicated sinusitis, severe diarrhea, UTIs, pyelonephritis, and prostatitis. The CDC advises that fluoroquinolones should not be used any longer for gonorrhea. They are acceptable as an alternative treatment for dog bite, acute sinusitis, severe sinusitis, and chlamydia. Fluoroquinolones with enhanced activity via S. pneumoniae provide alternative therapy for acute exacerbation of COPD and pneumonia in adults.


Fluoroquinolones are active against many gram-positive organisms; gram-negative organisms, including M. catarrhalis, Haemophilus influenzae, E. coli, chlamydia, and Mycoplasma pneumoniae; and anaerobes. They are not active against Clostridium difficile.


Warnings have been issued for the fluoroquinolone antibiotics for the increased risk of tendon ruptures. Ruptures have occurred unilaterally and bilaterally, and have involved the Achilles tendon; however, ruptures in the shoulder joint, hand, biceps, thumb, and other tendons sites have been reported. The risk of tendon rupture is further increased in those over age 60, those receiving concomitant steroid therapy, and in kidney, heart, and lung transplant recipients. Reasons for tendon ruptures also include physical activity or exercise, kidney failure, and tendon problems in the past. These ruptures may occur during therapy or up to several months after discontinuation of drugs. There also may be rare risk for serious and potentially fatal adverse events that may occur after repeated doses. Some tendonitis and tendon rupture requires surgical repair or results in prolonged disability. A significant number of cases have been reported, including cases in the United States. Discontinue ciprofloxacin at the first sign of tendon inflammation or tendon pain, as these are symptoms that may precede rupture of the tendon. The products identified with increased risk are second-generation quinolone ciprofloxacin (Cipro, tablets or oral suspension), intravenous injection (Cipro IV), and extended-release tablets (Cipro XR), as well as ofloxacin (Floxin tablets) and the third-generation quinolone levofloxacin (Levaquin tablets, oral solution, injection, and injection in 5% dextrose).


There is the risk for serious and occasionally fatal hypersensitivity reactions that may occur after the first dose of a quinolone. These have included cardiovascular collapse, hypotension or shock, seizure, loss of consciousness, tingling, angioedema, airway obstruction, dyspnea, urticaria, and other serious skin reactions. There is a rare risk for serious and sometimes fatal events after multiple doses. Clinical manifestations may include one or more of the following: fever, rash, or severe dermatologic reactions (e.g., toxic epidermal necrolysis and Stevens-Johnson syndrome); vasculitis, arthralgia, myalgias, and serum sickness; allergic pneumonitis; interstitial nephritis and acute renal insufficiency or failure; hepatitis, jaundice, and acute hepatic necrosis or failure; and anemia (including hemolytic and aplastic), thrombocytopenia (including thrombocytopenic purpura), leukopenia, agranulocytosis, pancytopenia, and other hematologic abnormalities. Treatment should be discontinued at the first sign of a skin rash, jaundice, or any other sign of hypersensitivity, and supportive measures should be instituted.


Treatment with a fluoroquinolone can alter the colon’s normal flora, leading to overgrowth of C. difficile and subsequent release of toxins A and B that contribute to the development of c. difficile acute diarrhea (CDAD). Nearly all antibiotics have been implicated in CDAD, which may range in severity from mild diarrhea to fatal colitis. Because hypertoxin-producing strains of C. difficile can be refractory to antimicrobial therapy, they are associated with increased morbidity and mortality and may require colectomy. The FDA advises that CDAD be considered in all patients who present with diarrhea after antibiotic use. Careful examination of medical history is required because of the potential for late-onset disease; cases of CDAD have been reported more than 2 months after completion of an antimicrobial course of therapy. The FDA notes that current antibiotic therapy for the primary infection may need to be discontinued in patients with known or suspected CDAD. Appropriate fluid and electrolyte management, protein supplementation, antibiotic therapy for C. difficile, and surgical evaluation also may be required.


In a recently published case-controlled study, it was found that levofloxacin and moxifloxacin, two commonly used fluoroquinolones, are tied to higher odds of hospitalization among older adults for idiosyncratic liver injury. Researchers said the chance of hospital admission is greater with the drugs compared with clarithromycin. It is not clear yet whether these drugs will be given regulatory warnings by the FDA.



How to Monitor




• Monitor renal, hepatic, and hematopoietic function during prolonged therapy.


• Patients on warfarin anticoagulation should be monitored closely for prothrombin times and INR at baseline—daily for the first week of therapy, and weekly thereafter. The patient should be instructed to report immediately any sign of bleeding.


• Patients on any theophylline product (e.g., theophylline, oxtriphylline, aminophylline) should have serum theophylline levels monitored because theophylline clearance may be decreased with concomitant fluoroquinolone use.


• Evaluate renal and hepatic function at baseline and every 6 weeks if therapy is to be continued.


• Monitor hematology parameters periodically for evidence of leukopenia, hemolytic anemia, and thrombocytopenia.


• Monitor for CNS side effects such as headache, weakness, shaking, dizziness, drowsiness, and confusion.

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Jul 22, 2016 | Posted by in PHARMACY | Comments Off on Fluoroquinolones

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