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Comparision of biofilm production and multiple drug resistance in ...

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M. Dheepa et al., Int J Pharm Biomed Sci 2011, 2(4), 103-107<br />

Table 5<br />

Antibiotic susceptibility pattern <strong>of</strong> the 50 A.baumannii isolates tested are<br />

given <strong>in</strong> this table<br />

Antibiotic<br />

Number (% sensitive)<br />

n=50<br />

Amikac<strong>in</strong> 30 µg 22<br />

Ceftazidime 30 µg 28<br />

Cipr<strong>of</strong>loxac<strong>in</strong> 5 µg 38<br />

Cefepime 30 µg 28<br />

Imipenem 10 µg 46<br />

Pipercill<strong>in</strong> 100 µg 28<br />

Ampicilll<strong>in</strong> + sulbactum 10 µg +10µg 44<br />

Gentamic<strong>in</strong> 10 µg 28<br />

Co-trimoxazole 1.25µg +23.75 µg 32<br />

Doxycyl<strong>in</strong>e 30 µg 52<br />

Piperacill<strong>in</strong> + tazobactum 100 µg + 10 µg 50<br />

Meropenem 10 µg 32<br />

Tobramyc<strong>in</strong> 10 µg 50<br />

Lev<strong>of</strong>loxac<strong>in</strong> 10 µg 62<br />

Aztreonam 30 µg 18<br />

Netilmyc<strong>in</strong> 30 µg 72<br />

Ofloxac<strong>in</strong> 5 µg 24<br />

Table 6<br />

Antibiotic susceptibility results (percentage) <strong>of</strong> A. baumannii isolates<br />

Antibiotics<br />

Resistance <strong>of</strong><br />

Bi<strong>of</strong>ilm positive<br />

isolates N=20<br />

Bi<strong>of</strong>ilm negative<br />

isolates N=30<br />

Amikac<strong>in</strong> 80 73.3 78<br />

Ceftazidime 95 86.6 72<br />

Cipr<strong>of</strong>lox 85 80 62<br />

Cefepime 95 86.6 72<br />

Imipenem 65 70 54<br />

Pipercill<strong>in</strong> 95 93.3 72<br />

Ampicilll<strong>in</strong> + sulbactum 55 66 56<br />

Gentamic<strong>in</strong> 70 70 72<br />

Co-trimoxazole 75 76 68<br />

Doxycyl<strong>in</strong>e 35 56 48<br />

Piperacill<strong>in</strong> + tazobactum 40 50 50<br />

Meropenem 70 66 68<br />

Tobramyc<strong>in</strong> 75 33 50<br />

Lev<strong>of</strong>lox 50 30 38<br />

Aztreonam 85 76.6 82<br />

Netilmyc<strong>in</strong> 20 20 28<br />

Ofloxoc<strong>in</strong> 60 76 76<br />

Table 7<br />

Multiple <strong>drug</strong> resistant patterns <strong>of</strong> A. baumannii<br />

Multiple <strong>drug</strong> comb<strong>in</strong>ations<br />

Number <strong>of</strong> isolates<br />

show<strong>in</strong>g <strong>resistance</strong><br />

Resistance<br />

<strong>of</strong> all<br />

isolates<br />

N =50<br />

Percent<br />

Ak, Ao, Cf, I, Of 31 62<br />

Ak, Ao, I 31 62<br />

Cf, I 33 66<br />

Ak, I, Of 30 60<br />

Ao, Cf, I 33 66<br />

Ak- amikac<strong>in</strong>, Ao- aztreonam, Cf- cipr<strong>of</strong>loxac<strong>in</strong>, I- imepenem, Of –<br />

<strong>of</strong>loxac<strong>in</strong><br />

chloramphenicol 94.7%, amoxicill<strong>in</strong>/clavul<strong>in</strong>ic acid 94.7%,<br />

netilmyc<strong>in</strong> 93.9%, ceftazidime 90.9%, gentamic<strong>in</strong> 87.9%,<br />

pipercill<strong>in</strong>/tazobactam 84.8%, nalidixic acid 84.2%,<br />

tobramyc<strong>in</strong> 75%, imipenem 7.2%, colist<strong>in</strong> 7.1% [10].<br />

106<br />

Another study done <strong>in</strong> Estonia showed 60 % <strong>of</strong> A.<br />

baumanii isolates sensitive to ampicill<strong>in</strong> + sulbactum, 95%<br />

to imepenem <strong>and</strong> meropenum <strong>and</strong> 70 % to amikac<strong>in</strong> [11]. In a<br />

study conducted <strong>in</strong> UK showed <strong>resistance</strong> to piperacill<strong>in</strong> +<br />

tazobactum 39%, imipenam 7%, cipr<strong>of</strong>loxac<strong>in</strong> 46%,<br />

meropenem 0.5%, ceftazidime 46%, pipercill<strong>in</strong> 72%,<br />

gentamic<strong>in</strong> 43%, amikac<strong>in</strong> 21% respectively [12]. Similar<br />

study conducted <strong>in</strong> Ankara <strong>in</strong> 2002 shows the <strong>resistance</strong><br />

rates were 31.2% for netilmic<strong>in</strong>, 44.6% for sulbactamcefoperazone,<br />

53.6% for imipenem, 59.8% for amikac<strong>in</strong>,<br />

59.9% for tobramyc<strong>in</strong>, 74% for cipr<strong>of</strong>loxac<strong>in</strong>, 78% for<br />

gentamic<strong>in</strong>, 79.5% for sulbactam-ampicill<strong>in</strong>, 82.3% for<br />

cotrimoxazole, 84.8% for ticarcill<strong>in</strong>, 87.3% for piperacill<strong>in</strong>tazobactam,<br />

88.1% for ceftazidime <strong>and</strong> 92.1% for piperacill<strong>in</strong><br />

[13].<br />

Another study was conducted <strong>in</strong> USA regard<strong>in</strong>g the multi<br />

<strong>drug</strong> <strong>resistance</strong>. The results showed, about 79.5% (66/83)<br />

were multi-<strong>drug</strong> resistant (MDR) A. baumanii. Among these,<br />

62 were resistant to ceftazidime <strong>and</strong> 66 were resistant to<br />

imipenem. The imipenem resistant isolates (66/83) were also<br />

resistant to kanamyc<strong>in</strong>, amikac<strong>in</strong>, gentamic<strong>in</strong>, streptomyc<strong>in</strong>,<br />

tetracycl<strong>in</strong>e, cipr<strong>of</strong>loxac<strong>in</strong> <strong>and</strong> nalidixic acid [14].<br />

In a study conducted <strong>in</strong> India, Hyderabad Ac<strong>in</strong>etobacter<br />

baumannii showed 77% <strong>resistance</strong> to piperacill<strong>in</strong>-tazobactam<br />

[15]. In another study conducted <strong>in</strong> India, Pune 75% <strong>of</strong> the<br />

isolates were multi<strong>drug</strong> resistant (MDR) <strong>and</strong> <strong>resistance</strong> to<br />

aztreonam 60% <strong>and</strong> for imipenem 29% was noted [16].<br />

In our study bi<strong>of</strong>ilm producers showed <strong>in</strong>creased<br />

<strong>resistance</strong> to Ceftazidime 95%, Cefepime 95% <strong>and</strong> Pipercill<strong>in</strong><br />

95%. A recent study showed significantly higher <strong>resistance</strong> to<br />

cefotaxime, amikac<strong>in</strong>, cipr<strong>of</strong>loxac<strong>in</strong> <strong>and</strong> aztreonam among<br />

bi<strong>of</strong>ilm producers. Non-bi<strong>of</strong>ilm producers showed <strong>in</strong>creased<br />

<strong>resistance</strong> only for netill<strong>in</strong> <strong>and</strong> <strong>of</strong>loxac<strong>in</strong> [7].<br />

5. CONCLUSIONS<br />

In conclusion, cont<strong>in</strong>uous surveillance <strong>of</strong> the <strong>in</strong>-vitro<br />

antimicrobial susceptibility <strong>of</strong> Ac<strong>in</strong>etobacter baumannii<br />

isolates <strong>in</strong> various geographical areas are necessary <strong>in</strong> order<br />

to generate data useful for optimis<strong>in</strong>g empirical antimicrobial<br />

treatment <strong>of</strong> patients with <strong>in</strong>fections that are likely to be<br />

caused by this pathogen. Our <strong>in</strong>vestigation reveals a<br />

simultaneous emergence <strong>of</strong> <strong>resistance</strong> to many antimicrobial<br />

agents when the organisms produce bi<strong>of</strong>ilm <strong>and</strong> represents a<br />

severe threat <strong>in</strong> the treatment <strong>of</strong> hospitalized patients. It is a<br />

challenge to treat <strong>and</strong> also to eradicate this multi<strong>drug</strong><br />

resistant organism because the overall healthcare costs which<br />

are attributed to the treatment <strong>of</strong> bi<strong>of</strong>ilm associated <strong>in</strong>fections<br />

will be much higher. The high rate <strong>of</strong> <strong>in</strong>vitro antibiotic<br />

<strong>resistance</strong> <strong>of</strong> the Ac<strong>in</strong>etobacter baumanii stra<strong>in</strong>s <strong>in</strong>dicate the<br />

importance <strong>of</strong> controlled antibiotic usage <strong>and</strong> appliance <strong>of</strong><br />

hospital <strong>in</strong>fection control measures.<br />

©2011 PharmaInterScience Publishers. All rights reserved. www.pharma<strong>in</strong>terscience.com

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