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full pdf of issue - Middle East Journal of Family Medicine

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ORIGINAL CONTRIBUTION AND CLINICAL INVESTIGATION<br />

T<strong>issue</strong> and plasma concentrations <strong>of</strong> meropenem in<br />

diabetic foot infected patients<br />

Mohammed Abdullah Ali (1)<br />

Nidhal AK Mohammed Ali (2)<br />

(1) Department <strong>of</strong> Pharmacology, College <strong>of</strong> Pharmacy,<br />

Hawler Medical University, Iraq<br />

(2) College <strong>of</strong> <strong>Medicine</strong>, Hawler Medical University, Iraq<br />

Correspondence:<br />

Nidhal AK Mohammed Ali<br />

Department <strong>of</strong> Pharmacology, College <strong>of</strong> Pharmacy,<br />

Hawler Medical University, Iraq<br />

Email: nabdulqader@yahoo.co.uk<br />

Abstract<br />

Objective: Meropenem is a broad<br />

antibacterial agent against most<br />

pathogens causing diabetic foot<br />

infections. The pharmacodynamics<br />

parameter, time during which<br />

antibiotic concentration remains<br />

above the MIC for the infecting<br />

pathogen (T>MIC) has been<br />

recommended for good efficacy.<br />

This study aimed to determine<br />

meropenem concentrations in<br />

plasma and foot infected t<strong>issue</strong>s<br />

in diabetic patients and relate<br />

these values with microbiological<br />

findings.<br />

Patients and Materials: Ten<br />

patients with diabetic foot infections<br />

were enrolled in the study.<br />

Microbiological examination and<br />

the minimum inhibitory concentration<br />

(MIC) were determined<br />

for foot infected samples. All<br />

patients received meropenem by<br />

intravenous infusion <strong>of</strong> 1000 mg<br />

for 30 minutes at 8 hourly intervals.<br />

Blood samples were taken<br />

after 1, 2, 4, and 8 hours <strong>of</strong> the<br />

last meropenem dose and<br />

the plasma meropenem concentration<br />

was analyzed by HPLC.<br />

Viable s<strong>of</strong>t t<strong>issue</strong> samples were<br />

obtained at time <strong>of</strong> amputation<br />

and meropenem concentration<br />

was determined by microbiological<br />

assay.<br />

Results: Meropenem attained<br />

high concentrations in foot<br />

t<strong>issue</strong>s in excess <strong>of</strong> the MICs<br />

<strong>of</strong> the isolated bacteria and the<br />

mean T>MIC% was 77.5± 19.45.<br />

Conclusion: The present data<br />

shows good t<strong>issue</strong> penetration <strong>of</strong><br />

meropenem in foot t<strong>issue</strong>s that<br />

permits its recommendation for<br />

the treatment <strong>of</strong> foot infections in<br />

diabetic patients.<br />

Key words: pharmacodynamics,<br />

meropenem, T>MIC.<br />

Introduction<br />

Pharmacodynamics <strong>of</strong> antimicrobials<br />

explore the relationship between the<br />

attained drug concentrations and the<br />

infecting organism with the clinical<br />

outcome (1, 2).<br />

Achieving therapeutic drug<br />

concentrations at the site <strong>of</strong> infection<br />

is one <strong>of</strong> the main goals <strong>of</strong> antibiotic<br />

therapy especially where peripheral<br />

vascular circulation is embedded in<br />

situations such as foot infections <strong>of</strong><br />

diabetic patients (2, 3).<br />

Some antibiotics when used in<br />

the treatment <strong>of</strong> diabetic foot<br />

infections, may attain adequate<br />

blood levels but may not achieve<br />

sufficient antimicrobial concentration<br />

in infected t<strong>issue</strong>s to combat<br />

the infection leading to more<br />

complication that may necessitate<br />

amputation (1, 4, 5).<br />

Choosing antibiotics for diabetic<br />

foot infections should include an<br />

agent active against staphylococci,<br />

Gram-negative bacilli, Enterococcus<br />

and anaerobic species especially in<br />

previously treated or severe cases<br />

as they are involved in diabetic foot<br />

infections (6, 7, 8).<br />

Meropenem is a broad-spectrum<br />

carbapenem antibiotic with excellent<br />

activity against many pathogens<br />

associated with complicated<br />

skin and s<strong>of</strong>t t<strong>issue</strong> infections<br />

(cSSTIs)(9).<br />

The optimal pharmacodynamic<br />

parameter predicting microbiologic<br />

efficacy is the time that the drug<br />

concentration in the blood remains<br />

above the MIC (T> MIC) (1, 10, 11).<br />

Pharmacokinetic studies revealed<br />

that meropenem penetrates rapidly<br />

and widely into a range <strong>of</strong> body<br />

fluids and t<strong>issue</strong>s (12, 13) resulting<br />

in sufficient T>MIC in body fluids<br />

enough to kill bacteria (11, 14) and a<br />

regimen which provides a T>MIC <strong>of</strong><br />

40% <strong>of</strong> the dosing interval has<br />

MIDDLE EAST JOURNAL OF FAMILY MEDICINE VOLUME 10 ISSUE 6<br />

MIDDLE EAST JOURNAL OF FAMILY MEDICINE • VOLUME 7, ISSUE 10 35

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