Erythromycin is a macrolide antibiotic that was originally discovered in 1952. It can be used for treating various infections and also has an indication for a non-infectious pathology.
Traditionally, it has been used for various respiratory infections, prophylaxis of neonatal conjunctivitis and chlamydia. It is also FDA approved for treating skin infections, syphilis and pelvic inflammatory disease (PID). If mixed with tretinoin cream, it is effective for treating acne. During pregnancy, it can be used for the prevention of Group B streptococcal infection in the newborn. Although, some literature shows specific forms of erythromycin may not be fully safe in pregnant women. Erythromycin is also used off-label for treating gastroparesis; also known as delayed gastric emptying. However, treatment of gastroparesis is a non-FDA approved indication.
Erythromycin is active against gram-positive bacteria, gram-negative bacteria and several other organisms. The gram-positive bacteria include Streptococcus pneumoniae, Streptococcus pyogenes, Staphylococcus aureus, Listeria monocytogenes, Corynebacterium minutissimum, Corynebacterium diphtheria. The gram-negative bacteria include Legionella pneumophila, Neisseria gonorrhoeae, Haemophilus influenzae, and Bordetella pertussis. Other microorganisms that are covered by erythromycin include Chlamydia trachomatis, Entamoeba histolytica, Mycoplasma pneumoniae, Treponema pallidum, ureaplasma urealyticum.
Once erythromycin is orally administered, it is easily absorbed through the gastrointestinal system. It readily diffuses into most bodily fluids. Erythromycin is concentrated in the liver and is then later excreted in bile. Erythromycin can also be administered in intravenous form, topical form and ophthalmic form.
The side effect profile of erythromycin includes those commonly seen in most antibiotics: nausea, abdominal pain, and diarrhea. As all macrolide antibiotics cause QT prolongation; erythromycin causes the most significant prolongation of the QT interval. Rarely, serious rashes such as Stevens-Johnson syndrome may occur.
Erythromycin is a bacteriostatic antibiotic. This means it stops the further growth of bacteria rather than directly destroying it. This is achieved by inhibiting protein synthesis. Erythromycin binds to the 23S ribosomal RNA molecule in the 50S subunit of the bacterial ribosome. This causes a blockage in the exiting of the peptide chain that is growing. Given that humans have 40S and 60S subunits, and do not have 50S subunits, erythromycin does not affect protein synthesis in human tissues.
Resistance can develop against erythromycin. This occurs via modification of the 23S rRNA that is found in the 50S rRNA. The erythromycin cannot bind to the ribosome, and the bacteria can continue the process of protein synthesis.
Aside from being a bacteriostatic macrolide antibiotic, erythromycin is a pro-motility drug. It is an agonist to motilin which increases motility in the gut.
Once erythromycin is orally administered, it is readily deactivated by gastric acid. Oral tablets must either contain an ester or stable salt as part of the molecular structure or be enteric-coated. Once the drug is absorbed via the gastrointestinal system, it diffuses into various tissues and phagocytes. As phagocytes circulate the blood and induce phagocytosis of harmful bacteria, erythromycin is released during this process.
The liver metabolizes most of the administered erythromycin. It undergoes demethylation through the cytochrome P450 system; specifically the enzyme CYP3A4. It is then eliminated through bile. A very small percentage of the drug undergoes renal excretion.
Erythromycin has a half-life of 1.5 to 2 hours. Levels of the drug peak 4 hours after intake.
Erythromycin is available in oral form. It is also available in an intravenous form, topical form for the skin, and as an ophthalmic preparation for the eyes.
The oral form of the medication is available in 250-mg tablets and 500-mg tablets.
Optimal blood levels are achieved when it is taken in a fasted state.
All antibiotics carry a significant risk of nausea, vomiting, abdominal pain and diarrhea. Erythromycin is a motilin agonist, and this increases the likelihood of gastrointestinal side effects compared to other antibiotics.
All macrolide antibiotics cause QT prolongation. Azithromycin causes the least QT prolongation, usually clinically insignificant. Clarithromycin causes greater QT prolongation. Erythromycin is known to cause major prolongation of the QT interval and carries a risk of torsades de pointes. This arrhythmia may cease on its own, or it may degenerate into ventricular fibrillation, a deadly heart rhythm.
There also exists a risk of rash, allergic reaction, and reversible deafness. Rare side effects include Stevens-Johnson syndrome, toxic epidermal necrolysis, and cholestasis.
Erythromycin comes in various forms. Pregnant women should not use the form of erythromycin estolate as it may cause hepatotoxicity. It may also increase the risk of pyloric stenosis in the newborn.
Erythromycin is a cytochrome P450 inhibitor. This means it carries the potential to interact with broad ranges of medications. Given it is an inhibitor of CYP450, drugs that are metabolized via the cytochrome P450 system would have increased concentrations and hence carry risks of toxicity.
Patients who have a prolonged QT interval on an electrocardiogram (ECG) should not use erythromycin. A normal QTc interval would be <440ms in males and <460ms in females. Anyone using a medication that prolongs the QT interval should be very cautious and monitored if adding erythromycin. Similarly, patients who are diagnosed with long QT syndrome (LQTS) should not use erythromycin. Likewise, patients who have had an episode of torsades de pointes in the past should avoid QT prolonging drugs such as erythromycin.
As erythromycin may cause serious rashes in a small number of patients, anyone who has experienced similar symptoms in the past should avoid future use of the drug.
Pregnant women should avoid using erythromycin estolate as it may precipitate hepatotoxicity.
Erythromycin is a cytochrome P450 inhibitor which means it interacts with a very broad range of medications. Depending on the medication, dosage adjustment may be required. In some cases erythromycin should be avoided entirely as CYP450 inhibition may induce toxicity of the other medication.
Macrolide antibiotics have varying levels of cardiotoxicity. Erythromycin carries the most prominent risk of cardiotoxicity among the more commonly used macrolide antibiotics. It induces QT prolongation and increases the risk of the potentially deadly heart rhythm known as torsades de pointes. Careful monitoring of the QTc interval on the ECG is recommended to minimize risk. Patients at higher risk should also have their potassium, magnesium and calcium levels monitored.
There is no known reversal agent for erythromycin.