Lincomycin
derivatives
Because of its high potential for causing
serious adverse effects, clindamycin
is an-other antibacterial prescribed only when there’s no therapeutic
alternative. It’s used for many gram-pos-itive and anaerobic organisms.
Less
from lincomycin
Lincomycin is less effective than clindamycin andis
rarely used. Lincomycin shouldn’t be used in the treatment of minor infections
but would be used to treat serious respiratory or skin infections in the
patient who’s al-lergic to other antibiotics indicated for the infection.
When taken orally, clindamycin is absorbed
well and distributed widely throughout the body. It’s metabolized by the liver
and ex-creted by the kidneys and biliary pathways. About 20% to 30% of
lincomycin, when taken orally, is absorbed from the GI tract; food delays its
absorption. Lincomycin is partially metabolized in the liver and is excreted in
the urine, stool, and bile.
Clindamycin and lincomycin inhibit bacterial
protein synthesis by inhibiting the binding of bacterial ribosomes. At
therapeutic con-centrations, clindamycin is primarily bacteriostatic against
most organisms.
Because of their potential for causing serious
toxicity and pseudomembranous colitis (characterized by severe diarrhea,
ab-dominal pain, fever, and mucus and blood in stool), these drugs are limited
to a few clinical situations in which safer alternative antibacterials aren’t
available.
§ Clindamycin is potent against most aerobic
gram-positive organ-isms, including staphylococci, streptococci (except Enterococcusfaecalis), and pneumococci.
§ Clindamycin is effective against most
clinically important anaer-obes and is used primarily to treat anaerobic
intraabdominal, pleural, or pulmonary infections caused by Bacteroides fragilis. It’s also used as an alternative to
penicillin in treating Clostridiumperfringens
infections.
§ Clindamycin and lincomycin may be used as
alternatives to penicillin in treating staphylococcal infections in a patient
who’s allergic to penicillin
Clindamycin and lincomycin have neuromuscular
blocking prop-erties and may enhance the neuromuscular blocking action of
neuromuscular blockers. This can lead to profound respiratory de-pression. (See
Adverse reactions to clindamycin.)
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