Abstract:
BACKGROUND:Recommendations on drug dose adjustment in patients with renal impairment may vary between the references. It is often unknown which approach the dosing schemes were based on and what drug exposure is likely to be achieved. OBJECTIVE:To develop a simple method to evaluate recommended dosing schemes for patients with renal impairment, to apply this method to selected antibacterial drugs in order to evaluate expected drug concentrations using dosing schemes recommended for patients with severe infections, and to evaluate the expected consequences. SETTING:This was a theoretical study, which was based on data from published clinical trials. METHODS:Clinically established dosing schemes for 46 antibacterial drugs, as recommended for patients with renal impairment in the Summary of Product Characteristics, were analysed using a newly developed graphical method. Consistency of the dosing schemes with two general dose adjustment rules, the proportional rule and the eliminated fraction rule, was determined and drug exposure was predicted. MAIN OUTCOME MEASURE:Predicted drug exposure. Consistency of recommended dosing schemes with the general dose adjustment rules. RESULTS:Only 30% of the recommended dosing schemes were associated with similar average concentrations as expected in patients with normal renal function (44 % were associated with higher and 26% with lower concentrations). The highest median exposure was found in beta-lactams (170%, range 58-443%, for creatinine clearance of <15 ml/min, and 155%, range 54-232%, for creatinine clearance of 15 to <30 ml/min), where the medians were significantly different from 100% (P < 0.02). Consistency with a dosing rule was found in 59% of the dosing schemes (proportional rule 46%, eliminated fraction rule 50%, both rules 4%). CONCLUSIONS:Relative low exposure was found for several drugs, including ceftazidime, cefotaxime, imipenem, erythromycin, ciprofloxacin, levofloxacin, and teicoplanin, where dosing schemes should be reconsidered or used only in clinical situations where a lower than maximum exposure appears adequate. General application of the proportional rule for calculating drug dose adjustments would lead to lower than clinically established dose practice for 44% of drugs.
journal_name
Int J Clin Pharmjournal_title
International journal of clinical pharmacyauthors
Czock D,Spitaletta M,Keller Fdoi
10.1007/s11096-015-0141-0subject
Has Abstractpub_date
2015-10-01 00:00:00pages
906-16issue
5eissn
2210-7703issn
2210-7711pii
10.1007/s11096-015-0141-0journal_volume
37pub_type
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journal_title:International journal of clinical pharmacy
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journal_title:International journal of clinical pharmacy
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pub_type: 杂志文章
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更新日期:2017-12-01 00:00:00
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journal_title:International journal of clinical pharmacy
pub_type: 杂志文章
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更新日期:2015-12-01 00:00:00
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journal_title:International journal of clinical pharmacy
pub_type: 杂志文章
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journal_title:International journal of clinical pharmacy
pub_type: 杂志文章
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更新日期:2015-06-01 00:00:00
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