IJMLR231704
IJMLR231704
IJMLR231704
2456-4400
Int J Med Lab Res 2017, 2(3): 19-25
Ramakrishna Pai Jakribettu1, 2, SurluVidya Rao2, 3, Ovine Loyster D’souza2,Valerian Sudeep Pinto2,
BrincyLoyalaD’souza2,LaveenaAgnisTellis2,Manjeshwar Shrinath Baliga4
1
Departments of Microbiology,
2
Hospital Infection Control,
3
Hospital Administration, Father Muller Medical College Hospital, Kankanady, Mangalore 575002,
Karnataka, India
4
Father Muller Research Centre, Kankanady, Mangalore 575002, Karnataka, India
KEY WORDS: Staphylococcus aureus; MRSA; Hospital Infection Control; Skin and soft tissue
infections.
Corresponding Author:
Dr Ramakrishna PaiJakribettu,
Infection Control Officer,Hospital Infection Control Division, Father Muller
Medical College Hospital, Mangalore, Karnataka, India, 575002
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considering the number of resistance possessed by to the antibiotics increased from 3.47±1.19 (in
each against each drug, as well as for the class the 2010) to 3.71±2.39 (in 2015) and was significant (p
antibiotic belonged to by using unpaired students t < 0.04) (Table 2).
test. A statistical value of p < 0.05 was considered
significant. DISCUSSION:
Innumerable data published from around the
RESULTS: world have equivocally shown that S. aureus,
The study indicates that a total of 735 and 776 especially the MRSA, is a major pathogen
S aureus organisms were isolated from the SSTIs especially amongst vulnerable at risk patients and
were isolated and tested against a panel of also that their characteristics are changing rapidly.23
antibiotics in accordance to the CLSI guidelines. The SSTIs are one of the most common infections
The most important observation was all the by S aureus and the emergence of MRSA has
organisms tested in both the years were sensitive to compelled the use of fusidic acid, cotrimoxazole,
vancomycin, linezolid and teicoplanin. The results clindamycin, tetracycline, rifampicin, quinolones,
of resistance to the various antibiotics and grouped chloramphenicol, vancomycin, teicoplanin and
in accordance to the chemical class are depicted in linezolid.24
Table 1 and 2. In this study it was observed that all the organisms
With respect to the data when analyzed from the tested in both the years were sensitive to
perspective of individual antibiotics, the results vancomycin, linezolid and teicoplanin. However
indicated that when compared to the year 2010 the drug resistant pattern changed significantly over
there was decrease in the percentage of S aureus a 5 year time period for most other antibiotics. The
resistant to A (87.21 vs 83.39), CP (45.85 vs incidence of S. aureus resistant to the antibiotics
14.93), CN (19.45 vs 14.93), CO (47.89 vs 30.75), like A, CP, CN, CO and G reduced while that for
G (32.78 vs 26.38) (P < 0.02 to 0.0001). On the AK, OF, LF, E and CD increased. Additionally
contrary, during the study time points there was from the chemical classification perspective, a
increase in the number of organisms resistant to AK decrease in the percentage of S aureus resistant was
(2.31 vs 7.07), OF (41.49 vs 62.16), LF (22.44 vs seen for beta lactams, folic acid inhibitors,
32.43), E (20.40 vs 42.59) and CD (3.67 vs 17.11) aminoglycoside, while on the contrary there was an
(P < 0.0001). The data are all represented in Table increase in resistance to fluoroquinolones and
1. macrolides (Table 1 and 2).
When the data was analyzed from the In our study it was observed that the pattern of drug
perspective of the class the antibiotics belonged to, resistance for S aureus was different in the two time
the results indicated that when compared to the year points (Table 1 and 2). The most important aspect
2010 there was decrease in the percentage of S to be observed is that there was a 23.24% decrease
aureus resistant to the beta lactams (p < 0.0001), in the incidence of MRSA and 35.79% reduction in
folic acid inhibitors (p < 0.0001), aminoglycoside resistance to the Folic acid inhibitor CO (Table 1,
(p < 0.6), while on the contrary there was a increase 2). With respect to aminoglycoside antibiotics there
in resistance to fluoroquinolones (p < 0.0001) and was a 19.53% reduction in resistance to G while for
macrolides (p < 0.0001). It was also observed that AK a 3.06 fold increase in the resistance was seen
there was a 23.24% reduction in the incidence of (Table 1). The reason for this change is that the
MRSA. However a cumulative analysis for all the Infection Control practices were implemented and
11 antibiotics tested indicated that when compared monitored by the committee through regular
to the year 2010, the number of organism resistant sensitization, teaching and evaluation programs.
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Table 1: Drug Sensitivity pattern of various antibiotics for S aureus tested in the year 2010 and
Folic
Amino Fluro
acid
Beta lactams Macrolides
inhibi
glycosides quninolones
tor
A AC CP CN CO G AK OF LF E CD
Resistant 641 191 337 143 352 241 17 305 165 150 27
2010
Sensitive 94 544 398 592 383 494 718 430 570 585 708
% Resistant 87.21 25.98 45.85 19.45 47.89 32.78 2.312 41.49 22.44 20.4 3.67
Resistant 648 294 116 116 239 205 55 483 252 331 133
2015
Sensitive 129 483 661 661 538 572 722 294 525 446 644
% Resistant 83.39 37.84 14.93 14.93 30.75 26.38 7.078 62.16 32.43 42.59 17.11
2 172.0
X value 4.36 172.09 5.45 46.56 7.45 18.91 64.65 19.12 85.75 72.16
9
0.000 0.000 0.000 0.000
P value 0.036 0.0001 0.019 0.0001 0.006 0.0001 0.0001
1 1 1 1
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ribosomes by inducing conformational changes of LF); and the macrolides (E and CD) increased. The
the bacterial binding site.30 For the macrolides like possible explanation for this is that in the recent
ketolides and azalides, resistant strains of S aureus past these drugs have been the cornerstone in
are reported to up regulate genes that mediate the treating infections and their rampant prescription
active efflux of antibiotics by the pumps on without having an antibiogram results by the
bacterial cell membrane.30 Additionally reports professionals and non-adherence to the dose and
also indicate that in some S aureus strains schedule, and over the counter prescription must
resistance is also conferred to macrolides by have led to the resistant strains. Efforts have
genetically coded inducible constitutive enzymes to already been initiated towards remedial measures
protect the ribosome from the macrolide attacks or and on adherence to the good practice guidelines
by 50s ribosome.30 With respect quinolones reports and antibiotic policy to minimize the evolution of
exists that S aureus develop drug resistance by drug resistant strains.
causing chromosomal mutations to the DNA gyrase
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