CLINDAMYCIN

USES AND CONCERNS

Dr.T.V.Rao MD

DR.T.V.RAO MD

CLINDAMYCIN
Clindamycin rINN is a Lincosamides antibiotic. It is usually used to treat infections with anaerobic bacteria but can also be used to treat some protozoal diseases, such as malaria. It is a common topical treatment for acne and can be useful against some methicillin-resistant Staphylococcus aureus (MRSA) infections.
DR.T.V.RAO MD

ANTIBACTERIAL ACTIVITY Active against G+ cocci, including penicillin- resistant Staph. and many anaerobes, esp. Bacteroides sp. Not effective against G-ve aerobes.
DR.T.V.RAO MD

CLINDAMYCIN
Inhibits protein synthesis ( 50 s subunit )

Pharmacokinetics
May be given orally or parenterally Widely concentrated in tissues ( including bones ) & body fluids It diffuses across the placenta but not BBB 90% protein bound Metabolized in liver ( active )( enter hepatic circulation), 10 % excreted unchanged Excretion urine and bile
DR.T.V.RAO MD

CLINICAL USES
Staphylcoccal joint & bone infections such as osteomyelitis
Staph. Conjunctivitis ( eye drops )

Diabetic foot infections

Acne ( 1% topical gel & lotion )

Use Limited because of

pseudomembrano us colitis- can be fatal

DR.T.V.RAO MD

DR.T.V.RAO MD

TESTING FOR ANTIBIOTIC RESISTANCE IN CLINDAMYCIN'S DIFFERS FROM OTHER BACTERIA

The detection of its three resistance phenotypes (sensitive, resistant, inducible resistance) is crucial to guide antimicrobial therapy. Standard disk diffusion and broth micro dilution fail to detect inducible clindamycin resistance . Clinical and Laboratory Standards Institute (CLSI) recommends the double disk diffusion test (D-test) to detect the presence of inducible clindamycin resistance . Also, the incidence of clindamycin resistance varies with geographic area and therefore local statistics are crucial to guide empiric therapy
DR.T.V.RAO MD

CLINDAMYCIN-ERYTHROMYCIN DISCORDANT
Clindamycin-susceptible, erythromycin-resistant Staphylococcus aureus (clindamycin-erythromycin discordant) may develop clindamycin resistance. The erm gene product is a ribosome methylase whose expression is normally minimal. Erythromycin induces the production of this methylase, which is why these strains are erythromycin resistant, but mutations in the promoter region of erm allow production of methylase without an inducer

DR.T.V.RAO MD

TESTING FOR ERYTHROMYCIN AND CLINDAMYCIN RESISTANCE IS A PRIORITY

DR.T.V.RAO MD

THE D-TEST FOR MACROLIDE-INDUCIBLE RESISTANCE TO CLINDAMYCIN

A positive D test indicates the presence of macrolide-inducible resistance to clindamycin produced by an inducible methylase that alters the common ribosomal binding site for macrolides, clindamycin and the group B Streptogramins (Quinpristin) (Woods, 2009) . The cross-resistance, called the MLS-B phenotype, results from enzymatic methylation of an adenine residue of the 23S component of the 50S ribosomal subunit that these 3 drug groups bind to. The methylase is encoded by a plasmid-borne gene erm. This genotype has been associated with clinical reports of clindamycin failure. As a result the Clinical and Laboratory Standards Institute (a nonprofit standards organization) recommends that laboratories report Dtest+ isolates as resistant to clindamycin (NCCLS 2004; Woods, 2009).

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D TEST WILL IDENTIFY THE INDUCIBLE RESISTANCE

These mutants are stably erythromycin and clindamycin resistant. Since erythromycin resistance can occur with other mechanisms. (e.g., efflux pumps and enzymatic modification) the D-test identifies inducible resistance that might presage mutational clindamycin constitutive resistance.
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A NEGATIVE D- TEST
A negative D-test observed for an erythromycin-resistant culture of S. aureus. The small discs labeled E & C represent disks containing either 15 g erythromycin (E) or 2 g clindamycin (C) placed 15 to 20 mm apart on an agar plate that has been inoculated with the clinical isolate (indicated by the green background). The lack of a zone of inhibition around the erythromycin disc indicates bacterial resistance to macrolides The large clear zone of inhibition around the clindamycin disc indicates sensitivity to clindamycin
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A POSITIVE D- TEST
A positive D-test. Diffusion of erythromycin from the disc towards the clindamycin disc does not kill bacteria due to S. aureus resistance to macrolides. However, in this case the bacterial isolate contains a strain of S. aureus with an erythromycin-inducible methylase (iMLS-B) resulting in inhibited growth. The inhibition of bacterial growth in zone 2 but not zone 1 produces a D shape surrounding

the clindamycin disk, which is considered a positive D-test.

(Adapted from Woods 2009).

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PERFORMING D- TEST
The D-test is performed by placing clindamycin and erythromycin disks at an edge-to-edge distance of 15 to 20 mm and looking for flattening of the clindamycin zone nearest the erythromycin disk . A positive D-test suggests the presence of an erm gene that could result in constitutive clindamycin resistance and clinical 14 failure.

DR.T.V.RAO MD

WHEN TO AVOID USE OF CLINDAMYCIN

Clindamycin may still be effective in some patients with this phenotype, the working assumption is that the isolate is presumed to be resistant based upon detection of inducible clindamycin resistance. For serious infections such as sepsis, pneumonia, or other invasive S. aureus infections, even the small risk of emergence of resistance to clindamycin as indicated by a positive D-test should lead to avoidance of use of clindamycin (Woods, 2009).

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CLINDAMYCIN IN MALARIA
Given with chloroquine or quinine, clindamycin is effective and well-tolerated in treating Plasmodium falciparum malaria; the latter combination is particularly useful for children, and is the treatment of choice for pregnant women who become infected in areas where resistance to chloroquine is common. Clindamycin should not be used as an antimalarial by itself, although it appears to be very effective as such, because of its slow action. Patient-derived isolates of Plasmodium falciparum from the Peruvian Amazon have been reported to be resistant to clindamycin as evidenced by in vitro drug susceptibility testing.[
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ADVERSE COMPLICATIONS WITH CLINDAMYCIN

Common adverse drug reactions (ADRs) associated with clindamycin therapy found in over 1% of patients include: diarrhea, pseudomembranous colitis, nausea, vomiting, abdominal pain or cramps, rash, and/or itch. High doses (both intravenous and oral) may cause a metallic taste, and topical application may cause contact dermatitis. Diarrhea, vomiting, and nausea are common if the individual lies down for an extended period of time within 30 minutes of taking clindamycin. In addition, severe heartburn can be expected for up to three days if the individual does not stay in an elevated position for at least 30 minutes.

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COLITIS IS A FEARED COMPLICATION

Clindamycin has been associated with colitis (inflammation of the bowel); this is caused by a toxin produced from an overgrowth of a bacterium, Clostridium difficile. Symptoms can range from mild watery Diarrhoea to severe, persistent Diarrhoea with fever, abdominal cramps and the passage of blood and mucus. It may be potentially serious. If significant Diarrhoea develops whilst taking clindamycin, the drug should be stopped. A stool test may show the presence of the toxin.
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PSEUDOMEMBRANOUS COLITIS IS A POTENTIALLY LETHAL CONDITION

Pseudomembranous colitis is a potentially lethal condition commonly associated with clindamycin, but which occurs with other antibiotics, as well. Overgrowth of Clostridium difficile, which is inherently resistant to clindamycin, results in the production of a toxin that causes a range of adverse effects, from diarrhea to colitis and toxic mega colon. Rarely in less than 0.1% of patients clindamycin therapy has been associated with anaphylaxis, blood dyscrasias, polyarthritis, jaundice, raised liver enzyme levels, and/or hepatotoxicity.

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PRECAUTIONS IN USE OF CLINDAMYCIN

The safety of use in pregnancy has not been established.

Clindamycin has been reported to appear in breast milk. If therapy is prolonged, liver and renal function tests may be monitored periodically. May enhance the action of neuromuscular blocking agents. May counteract the effects of erythromycin

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 Programme created by Dr.T.V.Rao MD for Medical and Health Care workers in the Developing world
Email

doctortvrao@gmail.com

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