HARTFORD NOMOGRAM PDF

The Hartford nomogram was one of the first published extended-interval Unlike other nomograms, it uses the highest dose of gentamicin/tobramycin (7 mg/kg. Printable extended-interval aminoglycoside nomograms. The Hartford nomogram suggests dividing an amikacin concentration by 2 to plot onto this. Gentamicin is monitored using the Hartford nomogram which relates observ ed concentration to the time post dose within a given concentration range.

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There are a number of proposed benefits to extended-interval dosing compared to conventional dosing: Once daily aminoglycoside therapy.

The duration of this effect 2 harhford 8 hours depends on several factors, chief among them the height of the preceding aminoglycoside peak. Right hand Right arm below elbow Right arm whole arm Right foot Right leg below knee Right leg above knee. Daily dosage of aminoglycosides.

Drawn min after the start of the infusion. This aminoglycoside calculator uses a variety of published pharmacokinetic equations and principles to estimate an appropriate aminoglycoside regimen. Interval is based on creatinine clearance. The parameters are found in the drug model database and are fully user-editable.

Some pk studies have shown that the pharmacokinetics of aminoglycosides at high doses differ significantly from those at traditional doses. The calculations utilized to arrive at these dosages as well as the rationale for each dosing strategy are described below. The following criteria are used by this calculator to determine an aminoglycoside dosing weight:.

Although definitive evidence is still lacking, animal and human studies strongly suggest that once-daily dosing is less nephrotoxic. Infusion time of 60 minutes This level represents the first aminoglycoside dose The level is drawn 6 to 14 hours after the start of the aminoglycoside infusion.

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Hartford Nomogram 3 The Hartford nomogram was one of the first published extended-interval nomograms.

BB-K8, kanamycin, and gentamicin. It is important to note that this method relies on an accurate creatinine clearance; therefore, this method may not be appropriate in patients with unstable nomogran function or those with difficult-to-estimate creatinine clearance.

Furthermore, some have questioned the validity of all ODA nomograms because they are based on one-compartment parameters derived from nmogram of traditional dosing methods. Comparative in vitro activity of three aminoglycosidic antibiotics: For more information, read more about IDMS.

Regardless, a conservative conclusion is that extended-interval dosing is at least as beneficial and safe, if not better, than conventional dosing. The authors of the Hartford nomogram then flattened these decay curves to simplify the nomogram. Although the Barnes-Jewish nomogram has not been hwrtford published, it is commonly used as an extended-interval nomogram. Most institutions are using IDMS by this point, but you should contacting your laboratory if you are unsure of your assay.

Assumptions of this level: Is it less toxic than multiple daily doses and how should it be monitored? This phenomenon “adaptive post-exposure resistance” is observed as an apparent increase in hartfrd MIC90 i. In addition to the well-known risk factors age, volume depletion, liver disease, co-administration of certain drugs, etc. The following patient populations should be excluded from the high-dose, extended-interval dosing and conventional dosing should be used: The nomogram is no longer available as a webpage via the Barnes-Jewish Hospital St.

Barnes-Jewish 4 Although the Barnes-Jewish nomogram has not been formally published, it is commonly used as an extended-interval nomogram. Dosed mg IV Q hrs.

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There have been numerous clinical trials published attempting to determine whether extended-interval dosing is superior in efficacy or safety harttford conventional dosing. Click this icon button to either include or ignore the patient’s dose for the calculation.

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Adjust maintenance dose using the 1-compartment Bayesian algorithm. Aminoglycosides exhibit a significant PAE against aerobic gram- negative bacteria. You can tailor each drug model to fit your patient population, or you can create your own models.

Minimize nephrotoxicity by administering larger, less frequent doses and potentially decreasing renal cortical aminoglycoside concentrations. Aminoglycoside uptake into renal tubule cells and the inner ear appears to be saturated at relatively low serum levels, suggesting that higher peaks do not necessarily result in a greater risk of toxicity.

– Aminoglycoside Dosing Calculator

This calculator uses the above equation to estimate aminoglycoside clearance. In vitro studies indicate that more frequent dosing of aminoglycosides tends to reduce their uptake into the bacterial cell of aerobic GNB. The Hartford nomogram was one of the first published extended-interval nomograms. Updated November 10, Obtain a mid-interval drug level 6 to 16 hours after the initial dose, then evaluate the interval based on the dosage adjustment nomogram.

The Urban-Craig nomogram was developed with an option for Q12h dosing, which is especially useful in younger patients with high aminoglycoside clearance who may have an inappropriately long interval of subtherapeutic drug levels. Utilize the post-antibiotic effect PAEdefined as a recovery period before organisms can resume growth after drug removal. You may select a specific nomogram by clicking the “Config” icon in the top, right-hand corner of this webpage.

Accessed December 31, Louis, MObut harrtford is available as an appendix in a meta-analysis that was published from the same institution.

Home Academy Blog Nomogtam. Drawn min prior to the next dose. The rationale for high-dose extended-interval dosing of aminoglycosides is rooted in the following observations:

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