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Aminoglycosides

By

Brian J. Werth

, PharmD, University of Washington School of Pharmacy

Last full review/revision May 2020| Content last modified May 2020
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Aminoglycosides (see table Aminoglycosides) have concentration-dependent bactericidal activity. These antibiotics bind to the 30S ribosome, thereby inhibiting bacterial protein synthesis. Spectinomycin is a bacteriostatic antibiotic chemically related to the aminoglycosides.

Table
icon

Aminoglycosides

Amikacin

Gentamicin

Kanamycin*

Neomycin*

Plazomicin

Streptomycin

Tobramycin

* Should be used topically or orally only.

Pharmacokinetics

Aminoglycosides are poorly absorbed orally but are well absorbed from the peritoneum, pleural cavity, joints , and from denuded skin.

Aminoglycosides are usually given IV but may be given IM if IV access is unavailable. Aminoglycosides are distributed well into extracellular fluid except for vitreous humor, cerebrospinal fluid, respiratory secretions, and bile (particularly in patients with biliary obstruction). Intravitreous injection is required to treat endophthalmitis. Intraventricular injection is often required to reach intraventricular cerebrospinal fluid levels high enough to treat meningitis.

Aminoglycosides are excreted by glomerular filtration and have a serum half-life of 2 to 3 hours; the half-life increases exponentially as the glomerular filtration rate falls (eg, in renal insufficiency, in older people).

Indications

Aminoglycosides are used for

Aminoglycosides are active against most gram-negative aerobic and facultative anaerobic bacilli but lack activity against anaerobes and most gram-positive bacteria, except for most staphylococci; however, some gram-negative bacilli and staphylococci are resistant.

Aminoglycosides that are active against P. aeruginosa include tobramycin (particularly), gentamicin, and amikacin. Streptomycin, neomycin, and kanamycin are not active against P. aeruginosa. Gentamicin and tobramycin have similar antimicrobial spectra against gram-negative bacilli, but tobramycin is more active against P. aeruginosa, and gentamicin is more active against Serratia marcescens. Amikacin is frequently active against gentamicin- and tobramycin-resistant pathogens.

Aminoglycosides are infrequently used alone, except when used for plague and tularemia. They are usually used with a broad-spectrum beta-lactam for severe infection suspected to be due to a gram-negative bacillary species. However, because of increasing aminoglycoside resistance, a fluoroquinolone can be substituted for the aminoglycoside in initial empiric regimens. If the pathogen is found to be susceptible to the accompanying antibiotic, the aminoglycoside can be stopped after 2 to 3 days unless an aminoglycoside-susceptible P. aeruginosa is identified.

Gentamicin or, less commonly, streptomycin may be used with other antibiotics to treat endocarditis due to streptococci or enterococci. Enterococcal resistance to aminoglycosides has become a common problem. Because treatment of enterococcal endocarditis requires prolonged use of a potentially nephrotoxic and ototoxic aminoglycoside plus a bacterial cell wall–active drug (eg, penicillin, vancomycin) to achieve bactericidal synergy, the choice of aminoglycoside must be based on special in vitro susceptibility testing. Susceptibility only to high levels of aminoglycosides in vitro predicts synergy when low-dose aminoglycoside therapy is combined with a cell wall–active drug. If the strain is susceptible to high levels of gentamicin and streptomycin, gentamicin is preferred because serum levels can be readily determined and toxicity is less. High-level enterococcal resistance to gentamicin in vitro does not rule out susceptibility of these strains to high levels of streptomycin; in such cases, streptomycin should be used if these strains are susceptible to high levels of streptomycin.

Few therapeutic options are available for endocarditis due to enterococci that are resistant to high levels of gentamicin and streptomycin; no synergistic cell wall–active drug/aminoglycoside combination exists for endocarditis due to such strains, but the combination of the cell wall–active drugs ampicillin and ceftriaxone has recently been shown to be effective and minimizes the risk of nephrotoxicity. Many clinicians have begun to use ampicillin plus ceftriaxone rather than ampicillin plus gentamicin for Enterococcus faecalis endocarditis, even for strains without aminoglycoside resistance, because efficacy is similar and toxicity is less.

Streptomycin has limited uses because of resistance and toxicity. It is used to treat tularemia and plague and, with other antibiotics, to treat tuberculosis.

Because of toxicity, neomycin and kanamycin are limited to topical use in small amounts. Neomycin is available for eye, ear, oral, and rectal use and as a bladder irrigant. Oral neomycin is used topically against intestinal flora to prepare the bowel before surgery and to treat hepatic coma.

Contraindications

Aminoglycosides are contraindicated in patients who are allergic to them.

Use During Pregnancy and Breastfeeding

With aminoglycosides, there is evidence of risk to the fetus (eg, auditory toxicity), but clinical benefits may outweigh risk. If an aminoglycoside is used during pregnancy or if the patient becomes pregnant while taking an aminoglycoside, she should be apprised of the potential hazard to the fetus.

Aminoglycosides enter breast milk but are not well absorbed orally. Thus, they are considered compatible with use during breastfeeding.

Adverse Effects

All aminoglycosides cause

  • Renal toxicity (often reversible)

  • Vestibular and auditory toxicity (often irreversible)

  • Prolongation of effects of neuromuscular blockers

Symptoms and signs of vestibular damage are vertigo and ataxia.

Risk factors for renal, vestibular, and auditory toxicity are

  • Frequent or very high doses

  • Very high blood levels of the drug

  • Long duration of therapy (particularly > 3 days)

  • Older age

  • A preexisting renal disorder

  • Coadministration of vancomycin, cyclosporine, amphotericin B, iodinated contrast agents, or other nephrotoxins

  • For auditory toxicity, a genetic predisposition, preexisting hearing problems, and coadministration of loop diuretics

High doses given over a long period of time typically cause more concern about renal toxicity, but even low doses given for a short time can worsen renal function.

Patients receiving aminoglycosides for > 2 weeks and those at risk of vestibular and auditory toxicity should be monitored with serial audiography. At the first sign of toxicity, the drug should be stopped (if possible), or dosing should be adjusted.

Aminoglycosides can prolong the effect of neuromuscular blockers (eg, succinylcholine, curare-like drugs) and worsen weakness in disorders affecting neuromuscular transmission (eg, myasthenia gravis). These effects are particularly likely when the drug is given too rapidly or serum levels are excessively high. The effects sometimes resolve more rapidly if patients are given neostigmine or IV calcium. Other neurologic effects include paresthesias and peripheral neuropathy.

Hypersensitivity reactions are uncommon except for contact dermatitis due to topical neomycin. High oral doses of neomycin can cause malabsorption.

Dosing Considerations

Because toxicity depends more on duration of therapeutic levels than on peak levels and because efficacy is concentration-dependent rather than time-dependent, frequent doses are avoided. Once/day IV dosing is preferred for most indications except enterococcal endocarditis. IV aminoglycosides are given slowly (30 minutes for divided daily dosing or 30 to 45 minutes for once/day dosing).

In patients with normal renal function, once/day dosing is

  • Gentamicin or tobramycin: 5 mg/kg (7 mg/kg if patients are critically ill) every 24 hours

  • Amikacin: 15 mg/kg every 24 hours

If patients respond to the 7-mg/kg dose of gentamicin clinically and renal function continues to be normal, the once/day dose can be reduced to 5 mg/kg after the first few days of treatment.

In critically ill patients, peak serum levels should be determined after the first dose. In all patients, peak and trough levels are measured after the 2nd or 3rd dose (when the daily dose is divided) or when therapy lasts > 3 days, as well as after the dose is changed. Serum creatinine is measured every 2 to 3 days, and if it is stable, serum aminoglycoside levels do not need to be measured again. Peak concentration is the level 60 minutes after an IM injection or 30 minutes after the end of a 30-minute IV infusion. Trough levels are measured during the 30 minutes before the next dose.

Peak levels in serum of at least 10 times the minimum inhibitory concentration (MIC) are desirable. Dosing is adjusted to ensure a therapeutic peak serum level (to facilitate concentration-dependent activity) and nontoxic trough levels (see table Dosing for Aminoglycosides in Adults). In critically ill patients, who are likely to have expanded volumes of distribution and who are given higher initial doses, target peak serum levels are 16 to 24 mcg/mL for gentamicin and tobramycin and 56 to 64 mcg/mL for amikacin. For gentamicin and tobramycin, trough levels should be < 1 mcg/mL at 18 to 24 hours after the first dose with once/day dosing and between 1 and 2 mcg/mL with divided daily dosing.

For patients with renal insufficiency, the loading dose is the same as that for patients with normal renal function; usually, the dosing interval is increased rather than the dose decreased. Guidelines for maintenance doses based on serum creatinine or creatinine clearance values are available (see table Dosing for Aminoglycosides in Adults), but they are not precise, and measurement of blood levels is preferred.

If patients are taking a high dose of a beta-lactam (eg, piperacillin, ticarcillin) and an aminoglycoside, the high serum levels of the beta-lactam can inactivate the aminoglycoside in vitro in serum specimens obtained to determine drug levels unless the specimen is assayed immediately or frozen. If patients with renal failure are concurrently taking an aminoglycoside and a high-dose beta-lactam, the serum aminoglycoside level may be lower because interaction in vivo is prolonged.

Table
icon

Dosing for Aminoglycosides in Adults

1. Choose loading dose in mg/kg for peak serum levels in the range listed below for the aminoglycoside being used. If the patient’s actual weight is > 20% higher than ideal weight* because of obesity, the weight used for dosing equals ideal weight plus 40% of excess body weight (actual weight minus ideal weight). If actual weight exceeds ideal weight because of ascites or edema, the weight used for dosing is the actual weight.

Aminoglycoside

Usual Loading Doses

Expected Peak Serum Levels

Target Serum Trough Levels

Gentamicin

Tobramycin

1.5–2.0 mg/kg

4–10 mcg/mL (gentamicin 8.36–20.90 micromol/L; tobramycin 8.56–21.39 micromol/L)

1–2 mcg/mL (gentamicin 2.09–4.18 micromol/L; tobramycin 2.14–4.28 micromol/L)

Amikacin

5.0–7.5 mg/kg

15–30 mcg/mL (25.62–51.24 micromol/L)

5–10 mcg/mL (8.54–17.08 micromol/L)

2. Choose maintenance dose (as percentage of chosen loading dose) to maintain peak serum levels indicated above based on the selected dosing interval and the patient’s corrected creatinine clearance†:

Percentage of Loading Dose Required for Dosage Interval Selected

Creatinine clearance (mL/minute)‡

8 hours (%)

12 hours (%)

24 hours (%)

90

84

70

76

88

50

65

79

30

48

63

86

20

37

50

75

15

31

42

67

10

24

34

56

5

16

23

41

0

8

11

21

* Ideal body weight = 50 kg (men) or 45.5 kg (women) at a height of 152 cm; 0.9 kg is subtracted for each cm of height < 152 cm or is added for each cm > 152 cm.

† CrCl(c) for men = (140 – age)wt in kg/70 × serum creatinine.

CrCl(c) for women = 0.85 × CrCl(c) for men.

‡ If CrCl(c) is 90 mL/minute, serum levels should be measured to help determine dosing.

CrCl(c) = corrected creatinine clearance.

Modified from Sarubbi FA Jr, Hull JH: Amikacin serum concentrations: Prediction of levels and dosage guidelines. Annals of Internal Medicine 89:612–618, 1978.

Drugs Mentioned In This Article

Drug Name Select Trade
ANECTINE, QUELICIN
No US brand name
NEORAL, SANDIMMUNE
ROCEPHIN
BLOXIVERZ
TOBI, TOBREX
GENOPTIC
VANCOCIN
NEO-FRADIN
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