Home About Us Contact Us

 

Table of Content - Volume 19 Issue 1- July 2021


 

A Study of antibiotic susceptibility pattern of bacteria isolated from cases of skin and soft tissue infections of infants at tertiary health care center

 

Ravidas Arjun Vasave1*, Shripad Taklikar2, Sujata Baveja3

 

1Assistant Professor, Department of Microbiology, Government Medical College, Nandurbar, Maharashtra, INDIA.

2Assistant Professor, 3Professor, Department of Microbiology, Lokmanya Tilak municipal Medical College Sion, Mumbai, Maharashtra, INDIA.

Email: ravidas.vasave.rv@gmail.com

 

Abstract              Background: Skin and soft tissue infections (SSTIs) can be defined as an inflammatory microbial invasion of the epidermis, dermis and subcutaneous tissues. With knowledge of likely causative organisms causing SSTIs and their sensitivity pattern, the most suitable antibiotic can be started without waiting for the result. Therefore, present study was aimed to study antibiotic susceptibility pattern of bacteria isolated from cases of skin and soft tissue infections of infants at tertiary health care center. Material and Methods: Present study was hospital based observational study, conducted in children less than one year of age with clinical features suggestive of skin and soft tissue infection presented in the Out Patient Department (OPD) or In Patient Department (IPD) under Paediatric Surgery unit. Results: In present study 250 children were studied. Majority of them were male. Most common risk factor in this study was daily massage with oils (94.8%). Other risk factors were trauma (79.6%), body piercing (19.2%) and previous hospitalization (14%). Heat 248 (99.2%), redness 246 (98.4%) and localized swelling 240 (96%) were the commonest clinical signs present. Out of 152 bacterial isolates, 59 (38.81%) were Staphylococcus aureus, 25 (16.44%) were Escherichia coli, 14 (9.21%) were Enterobacter spp. and 13 (8.55%) were Pseudomonas aeruginosa. All gram negative bacteria other than Pseudomonas aeruginosa and Acinetobacter spp. were sensitive meropenem (96.92%), amikacin (70.76%) and imipenem (63.07%). Among Pseudomonas aeruginosa isolates were sensitive to imipenem (92.30%), netilmycin and meropenem (75% each). All Acinetobacter spp. were sensitive to higher antibiotics such as imipenem, meropenem, colistin, tigecycline and netilmycin. All the Staphylococcus aureus isolates were sensitive to higher antibiotics such as netilmycin, linezolid and vancomycin. Conclusion: All the Staphylococcus aureus isolates were sensitive to higher antibiotics such as netilmycin, linezolide and vancomycin. Streptococcus spp. were susceptible to linezolide and vancomycin. All gram-negative bacteria other than Pseudomonas aeruginosa and Acinetobacter spp. were sensitive to meropenem (96.92%), amikacin (70.76%) and imipenem (63.07%).

Keywords: SSTIs, Staphylococcus aureus, gram negative enteric organisms. Linezolide, meropenem

 

INTRODUCTION

Skin and soft tissue infections (SSTIs) can be defined as an inflammatory microbial invasion of the epidermis, dermis and subcutaneous tissues.1 The practice guidelines of the Infectious Diseases Society of America (IDSA) for the diagnosis and management of skin and soft tissue infections2 classifies SSTIs into five categories, comprising superficial uncomplicated infection (includes impetigo, erysipelas and cellulitis), necrotizing infection, infections associated with bites and animal contact, surgical site infections and infections in the immune-compromised host. Human skin serves as the first line of defense against microbial infection as a physical barrier; by secreting low pH, sebaceous fluid and fatty acids to inhibit growth of pathogens; and by possessing its own normal flora, thus deterring colonization by other pathogenic organisms.3 Unfortunately, having penetrated the integumentary barrier, infecting organisms may cause tissue damage and may incite an inflammatory response. Once the proper diagnosis is made, the next important step is selecting the most appropriate therapy. With this knowledge of likely causative organisms causing SSTIs and their sensitivity pattern, the most suitable antibiotic can be started without waiting for the result. This would help in avoiding unnecessary medication with ineffective antibiotics and prevent development drug resistance. Therefore, present study was aimed to study antibiotic susceptibility pattern of bacteria isolated from cases of skin and soft tissue infections of infants at tertiary health care center.

              

MATERIAL AND METHODS

Present study was hospital based observational study, conducted at Department of Microbiology, Lokmanya Tilak municipal Medical College Sion Mumbai, over a period of 1 year 6 months. Study was approved by institutional ethical committee.

 

 

Inclusion Criteria: Children less than one year of age with clinical features suggestive of skin and soft tissue infection presented in the Out Patient Department (OPD) or In Patient Department (IPD) under Paediatric Surgery unit

Exclusion Criteria: Patients with Hospital Acquired Infections occurring after 48 hours of admission.

A written informed consent was taken from parents. Skin and soft tissue infection was clinical. Pus or exudate was collected from the depth of the lesion by either aspiration or using at least two sterile cotton swabs after cleaning the wound with sterile normal saline and surrounding skin with alcohol. For blood culture, venipuncture site was prepared with 70% alcohol and 2% tincture iodine and 1-5 ml blood was drawn with sterile needle and syringe and transferred into the bottle containing 10-50 ml of brain heart infusion broth under aseptic precautions. Identification of isolates was done by cultural characteristics and standard biochemical tests.4 The isolates were subjected for antibiotic susceptibility testing by employing Kirby Bauer disc diffusion technique as recommended by Clinical and Laboratory Standards Institute (CLSI)59. Patients were observed till discharge from the hospital in case admitted for the procedure for removal of pus.

Data was entered into Microsoft excel data sheet Statistical analysis was done using descriptive statistics.


RESULTS

In present study 250 children were studied. Majority of them were male (Most common risk factor in this study was daily massage with oils (94.8%). Other risk factors were trauma (79.6%), body piercing (19.2%) and previous hospitalization (14%). Heat 248 (99.2%), redness 246 (98.4%) and localized swelling 240 (96%) were the commonest clinical signs present.

Table 1: General-wise distribution

Sex

No. of cases

Percentage

Male

143

57.2

Female

107

42.8

Risk factor

No. of cases

Percentage

Animal bite

3

1.2

Trauma

199

79.6

Body piercing

48

19.2

Daily massage with oil

237

94.8

Previous hospitalization

35

14

Clinical signs

No. of cases

Percentage

Heat

248

99.2

Redness

246

98.4

Localized swelling

240

96

Localized tenderness

209

83.6

Purulent discharge

177

70.8

Fever

170

68

Abscess

74

29.6

CRP was positive in 38 (15.2%) cases and negative in majority, i.e., 212 (84.8%) of the cases. The blood culture was positive in only 32 (12.8%) cases whereas in remaining 218 (87.2%) cases it was negative. Pus culture was positive in 145 (58%) cases and there was no growth in 105 (42%) samples. In one case (0.4%) acid fast bacilli were seen. Out of 152 infections in the cases of SSTIs in present study, 74 (48.68%) were gram positive and 78 (51.31%) were gram negative bacteria. Polymicrobial infection was noted in 4 cases.

Table 2: Laboratory findings

Laboratory signs

Normal range

Mean

SD

Blood culture Positive

32

12.8

 

Pus culture Positive

145

58

 

AFB positive

1

0.4

 

Gram reaction

 

 

 

Gram positive

74

48.68

 

Gram negative

78

51.31

 

Out of 152 bacterial isolates, 59 (38.81%) were Staphylococcus aureus, 25 (16.44%) were Escherichia coli, 14 (9.21%) were Enterobacter spp. and 13 (8.55%) were Pseudomonas aeruginosa. Of the 74 gram positive organisms, 59 (79.72%) were Staphylococcus aureus, 5 (6.75%) were Streptococcus spp., 6 (8.13%) were Micrococci, 3 (4.05%) were Diphtheroids and one (1.35%) was Enterococcus spp Among all the gram negative organisms (n=78) isolated, Escherichia coli were the commonest (32.05%) followed by Enterobacter spp. (17.94%), Pseudomonas aeruginosa (16.66%), Klebsiella pneumoniae. and Acinetobacter spp. (14.10% each) and Citrobacter spp., Proteus mirabilis and Serratia spp. (1.28% each). The Micrococci and Diphtheroids were considered as commensals and not processed further.

 

Table 3: Frequency of Microorganisms isolated

Organisms

Frequency

Percentage

Gram positive (n=74)

Staphylococcus aureus

59

79.72

MRSA

33

55.93

MSSA

26

44.06

Streptococcus spp.

05

6.75

Enterococcus spp.

01

1.35

Micrococcus

06

8.13

Diphtheroids

03

4.05

Gram negative (n=78)

Escherichia coli

25

32.05

Enterobacter spp.

14

17.94

Pseudomonas aeruginosa

13

16.66

Klebsiella pneumoniae.

11

14.10

Acinetobacter spp.

11

14.10

Citrobacter spp.

01

1.28

Proteus mirabilis

01

1.28

Serratia spp.

01

1.28

Mixed growth

04

5.12

All gram negative bacteria other than Pseudomonas aeruginosa and Acinetobacter spp. were sensitive to higher antibiotics such as colistin and tigecycline. Majority of the isolates were sensitive to meropenem (96.92%), amikacin (70.76%) and imipenem (63.07%). Amoxycillin-clavulanic acid (4.61%) and piperacillin (13.84%) were the least susceptible antibiotics.

 

Table 4: Antibiotic susceptibility pattern of Gram Negative organisms (n=65) (except Pseudomonas aeruginosa and Acinetobacter spp.)

Antibiotics

Sensitive

Resistant

Amikacin

46 (70.76%)

19 (29.23%)

Amoxycillin-clavulanic acid

03 (4.61%)

62 (95.38%)

Ciprofloxacin

25 (38.46%)

40 (61.53%)

Cefotaxime

12 (18.46%)

50 (76.92%)

Cefazolin

10 (15.38%)

55 (84.61%)

Piperacillin

09 (13.84%)

56 (86.15%)

Meropenem

63 (96.92%)

02 (3.07%)

Piperacillin-tazobactam

16 (24.61%)

49 (75.38%)

Netilmycin

33 (50.76%)

32 (49.23%)

Imipenem

41 (63.07%)

24 (36.92%)

Cefepime

21 (32.30%)

44 (67.69%)

Colistin

65 (100%)

00 (0%)

Tigecycline

65 (100%)

00 (0%)

Among the 13 isolates of Pseudomonas aeruginosa, 12 (92.30%) isolates were sensitive to imipenem. Higher antibiotics such as netilmycin and meropenem were susceptible to most of the strains (75% each).

Table 5: Antibiotic susceptibility pattern of Pseudomonas aeruginosa isolates(n=13)

Antibiotics

Sensitive

Resistant

Gentamicin

7 (53.84%)

6 (46.15%)

Ceftazidime

6 (46.15%)

7 (53.84%)

Ofloxacin

7 (53.84%)

6 (46.15%)

Piperacillin

8 (61.53%)

5 (38.46%)

Imipenem

12 (92.30%)

1 (7.69%)

Piperacillin-tazobactam

2 (50%)

2 (50%)

Netilmycin

3 (75%)

1 (25%)

Meropenem

3 (75%0

1 (25%)

Aztreonam

1 (25%)

3 (75%)

All Acinetobacter spp. were sensitive to higher antibiotics such as imipenem, meropenem, colistin, tigecycline and netilmycin. Among other antibiotics the isolates were sensitive to piperacillin-tazobactam (63.63%) followed by ampicillin-sulbactam and cefepime (54.54% each). The isolates were resistant to amoxicillin-clavulanic acid, Cefotaxime, ceftazidime and co-trimoxazole. They were least sensitive to amikacin and ciprofloxacin (18.18% each).

 

Table 6: Antibiotic susceptibility pattern of Acinetobacter spp. isolates (n=11)

Antimicrobial agents

Sensitive

Resistant

Amikacin

02 (18.18%)

09 (81.81%)

Amoxycillin-clavulanic acid

00 (0%)

11 (100%)

Ciprofloxacin

02 (18.18%)

09 (81.81%)

Cefotaxime

00 (0%)

11 (100%)

Ceftazidime

00 (0%)

11 (100%)

Piperacillin

01 (9.09%)

10 (90.90%)

Meropenem

11 (100%)

00 (100%)

Piperacillin-tazobactam

07 (63.63%)

04 (36.36%)

Netilmycin

11 (100%)

00 (0%)

Imipenem

11 (100%)

00 (0%)

Cefepime

06 (54.54%)

05 (45.45%)

Ampicillin-sulbactam

06 (54.54%)

05 (45.45%)

Co-trimoxazole

00 (0%)

11 (100%)

Colistin

11 (100%)

00 (0%)

Tigecycline

11(100%)

00 (0%)

All the Staphylococcus aureus isolates were sensitive to higher antibiotics such as netilmycin, linezolid and vancomycin. Majority of the isolates were sensitive to clindamycin (83.05%) followed by gentamicin (76.27%), erythromycin (61.01%) and ciprofloxacin (44.06%).

Table 7: Antibiotic susceptibility pattern of Staphylococcus aureus isolates (n=59)

Antimicrobial agents

Sensitive

Resistant

Gentamicin

45 (76.27%)

14 (23.72%)

Penicillin-G

03 (5.08%)

56 (94.91%)

Cefoxitin

26 (44.06%)

33 (55.93%)

Ciprofloxacin

34 (57.62%)

25(42.37%)

Co-trimoxazole

24 (40.67%)

35 (59.32%)

Erythromycin

36 (61.01%)

23 (38.98%)

Clindamycin

49 (83.05%)

10 (16.94%)

Linezolid

59 (100%)

00 (0%)

Vancomycin

59 (100%)

00 (0%)

Netilmycin

59 (100%)

00 (0%)

All the five isolates of Streptococcus spp. were susceptible to linezolid and vancomycin. Penicillin-G (20%), erythromycin (20%) and clindamycin (40%) were the least susceptible antibiotics.

Table 8: Antibiotic susceptibility pattern of Streptococcus spp.

Antimicrobial

Sensitive

Resistant

Penicillin-G

1 (20%)

4 (80%)

Erythromycin

1 (20%)

4 (80%)

Clindamycin

2 (40%)

3 (60%)

Cefotaxime

3 (60%)

2 (40%)

Vancomycin

5 (100%)

0 (0%)

Linezolid

5 (100%)

0 (0%)


DISCUSSION

Skin and soft tissue infections (SSTIs) are suppurative microbial invasions of the epidermis, dermis and subcutaneous tissues characterized by induration, erythema, warmth, and pain or tenderness. Local manifestations may be accompanied by systemic signs and symptoms, such as fever, chills, malaise and, at times, haemodynamic instability. Systemic signs include hypotension and associated findings consistent with severe sepsis/septic shock including mental obtundation, cardiovascular and/or pulmonary collapse among other organ system failures. Emergency department (ED) visits for skin and soft tissue infections in children have increased dramatically in the last decade.5 Accordingly, from 1997 to 2009, hospital admission for pediatric patients with skin and soft tissue infections increased from 1.9 to 3.4 million annually.6 During that same time, pediatric patients requiring incision and drainage have doubled. 6 This growing volume of patients is thought to be largely due to the emergence of community-acquired methicillin-resistant Staphylococcus aureus (CA-MRSA). In the present study, majority of patients were male. In several other studies conducted by Ghadage DP et al.7 and Andrews RM et al.8 similar pattern of gender distribution was found. In present study most common risk factor was daily massage with oils (94.8%). Other risk factors were trauma (79.6%), body piercing (19.2%) and previous hospitalization (14%). None of the case had history of attending day care center, diabetes or presence of some other risk factor. Natural vegetable or plant oils (for example, mustard, sunflower, sesame, coconut, olive, and soybean oils) have emollient properties and in many low- and middle-income countries application of these to the newborn infant's whole body surface is a widespread traditional practice. 9 But, topical application of oils has not been shown to reduce the risk of infection or its associated morbidity or mortality, and may increase the risk of infection with coagulase-negative staphylococci in a study by Cleminson et al.9 Out of 156 cases, 152 (97.43%) were monomicrobial and 4 (2.56%) were polymicrobial infections. Among 152 monomicrobial infections, 74 (48.68%) were gram positive and 78 (51.31%) were gram negative bacteria. In a study by Rani et al.10 90% cases yielded growth of bacteria, out of which 71.85% were monomicrobial and 28.14% were polymicrobial infections. Of the 152 bacterial isolates in present study, 59 (38.81%) were Staphylococcus aureus, 25 (16.44%) were Escherichia coli, 14 (9.21%) were Enterobacter spp. and 13 (8.55%) were Pseudomonas aeruginosa. Mohanty et al.11 reported Staphylococcus aureus(38.05%), Escherichia coli(17.39%) and Pseudomonas aeruginosa(11.82%) as the top three isolates in their study. They have reported incidence of Enterobacter spp. as 2.80% in their study. Zargar et al.12 from India and Rennie et al.13 and Sader et al.14 also reported these organisms among top five pathogens isolated from skin and soft tissue infections in hospitalized patients. In present study, resistance to methicillin was detected in 33 (55.93%) of Staphylococcus aureus isolates. MRSA is on the rise in SSTIs in children both in the hospital setup (HA-MRSA) and in the community. Prevalence of MRSA was found to be consistent with studies by Gupta et al.(54.5%)15,Anupurba et al.(54.8%)16 and by Roveta et al.(53%)17. All the Staphylococcus aureus isolates (n=59) were sensitive to higher antibiotics such as netilmycin, linezolid and vancomycin. Majority of the isolates were sensitive to clindamycin (83.05%) followed by gentamicin (76.27%), erythromycin (61.01%) and ciprofloxacin (44.06%), whereas, maximum resistance was seen to penicillin (95%). This is in correlation with the study of Thind et al.18 where Staphylococcus aureus showed 100% resistance to penicillin and 100% sensitivity to vancomycin, teicoplanin and linezolid. Ramana et al.19, Nagaraju et al.20, Patil et al.21 and Singh et al.22 observed a similar high resistance of Staphylococcus aureus to penicillin. All gram negative bacteria other than Pseudomonas aeruginosa and Acinetobacter spp. were sensitive to higher antibiotics such as colistin and tigecycline. Majority of the isolates were sensitive to meropenem (96.92%), amikacin (70.76%) and imipenem (63.07%). Amoxycillin-clavulanic acid (4.61%) and piperacillin (13.84%) were the least susceptible antibiotics. Resistance of Gram negative organisms was minimum against meropenem, imipenem and amikacin which is similar to other studies.23,24 The susceptibility data collected in this study suggests that the most common organisms likely to be encountered in soft tissue infections are gram-positive cocci, notably Staphylococcus aureus, many of them methicillin-resistant. Thus, any first line antibiotic treatment should be primarily directed against this pathogen. For coverage of gram negative bacteria, aminoglycosides, meropenem and imipenem would be more useful. Use of mono drug therapy with cephalosporins, aminoglycosides and fluoroquinolones need to be guided by the sensitivity report. Lastly, continued monitoring of susceptibility pattern need to be carried out in individual settings so as to detect the true burden of antibiotic resistance in organisms and prevent their further emergence by judicious use of drugs.

 

CONCLUSION

In present study the main pathogens involved in these infections are Staphylococcus aureus and gram negative enteric organisms. All the Staphylococcus aureus isolates were sensitive to higher antibiotics such as netilmycin, linezolide and vancomycin. Streptococcus spp. were susceptible to linezolide and vancomycin. All gram negative bacteria other than Pseudomonas aeruginosa and Acinetobacter spp. were sensitive to meropenem (96.92%), amikacin (70.76%) and imipenem (63.07%). Increasing antibacterial resistance is becoming a major problem in the treatment of these infections worldwide. Continued monitoring of susceptibility pattern need to be carried out in individual settings so as to detect the true burden of antibiotic resistance in organisms.

 

REFEREssNCES

  1. Dryden MS. Skin and soft tissue infection: microbiology and epidemiology. Int J Antimicrob Agents 2009;33Suppl3:2–7.
  2. Stevens DL,Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft tissue infections: 2014 update by the Infectious Diseases Society of America. Clin Infect Dis 2014; 59:e10.
  3. McAdam AJ, Sharpe AH. Infectious diseases – bacterial infections. In: Kumar V, Abbas AK, Fausto N, editors. Robbins andCotran Pathologic Basis of Disease. Philadelphia: Elsevier Inc; 2005. pp. 371–96.
  4. Collee JG, Fraser AG, Marmion BP, Simmons A, editors. Mackie and McCartney Practical medical microbiology. 14th edn. Edinburg: Churchill Livingstone. 1996:245- 261.
  5. Pallin DJ, Espinola JA, Leung DY, et al. Epidemiology of dermatitis and skin infections in United States physicians’ offices, 1993–2005. Clin Infect Dis 2009;49:901-907.
  6. Lopez MA, Cruz AT, Kowalkowski MA, Raphael JL. Trends in resource utilization for hospitalized children with skin and soft tissue infections. Pediatrics 2013;131:e718-725.
  7. Ghadage DP, Sali YA. Bacteriological study of pyoderma with special reference to antibiotic susceptibility to newer antibiotics. Indian J Dermatol Venereol Leprol. 1999;65:177-81.
  8. Andrews RM, Kearns T, Connors C, Parker C, Carville KA. Regional initiative to reduce skin infections amongst aboriginal children living in remote communities of the Northern Territory, Australia. PLoS Negl Trop Dis 2009;3(11):e554.
  9. Cleminson J, McGuire W. Topical emollient for preventing infection in preterm infants. Cochrane Database of Systematic Reviews 2016, Issue 1. Art. No.: CD001150.
  10. Rani SR, Jayalekha B, Sreekumary PK. Bacteriological profile of pyoderma in a tertiary care centre in Kerala, India. Int J Res Dermatol 2016;2:1-11.
  11. Mohanty S, Kapil A, Dhawan B, Das BK. Bacterilogical and antimicrobial susceptibility profile of soft tissue infections from northern India. Indian J Med Sci 2004;58:10-15.
  12. Zargar AH, Masoodi SR, Laway BA, Wani AL, Bashir MI. Ciprofloxacin in the management of soft tissue infections in diabetes mellitus. J Assoc Phys India 2000;48:757-8.
  13. Rennie RP, Jones RN, Mutnick AH, and the SENTRY Program Study Group (North America). Occurrence and antimicrobial susceptibility patterns of pathogens isolated from skin and soft tissue infections: report from the SENTRY Antimicrobial Surveillance Program (United States and Canada, 2000) Diagn Microbiol Infect Dis 2003;45:287-93.
  14. Sader HS, Jones RN, Silva JB. Skin and soft tissue infections in Latin American medical centers: four-year assessment of the pathogen frequency and antimicrobial susceptibility patterns. Diagn Microbiol Infect Dis 2002; 44: 281-8.
  15. Gupta M, Singh NP, Kumar A, Kaur IR. Cefoxitin disk diffusion test - Better predictor of methicillin resistance in Staphylococcus aureus. Indian J Med Microbiol 2009;27:379-80.
  16. Anupurba S, Sen MR, Nath G, Sharma BM, Gulati AK, Mohapatra TM. Prevalence of methicillin resistant Staphylococcus aureus in a tertiary referral hospital in Eastern Uttar Pradesh. Ind J Med Microbiol 2003;21(1):49-51.
  17. Roveta S, Tonoli E, Marchese A, Schito GC. Epidemiology of methicillin resistance among staphylococcal strains isolated in risk units and effects of the vancomycin on the expression of methicillin resistance. Infect med 2001;9(2):82-89.
  18. Thind P, Prakash KS, Wadhwa A, Garg VK, Pati B. Bacteriological profile of community-acquired pyodermas with special reference to methicillin resistant Staphylococcus aureus. Indian J Dermatol Venereol Leprol 2010;76(5):572-4.
  19. Ramana KV, Mohanty SK, Kumar A. In-vitro activities of current antimicrobial agents against isolates of pyoderma. Indian J Dermatol Venereol Leprol 2008;74(4):430-2.
  20. Nagaraju U, Bhat G, Kuruvila M, Pai GS, Jayalakshmi, Babu RP. Methicillin-resistant Staphylococcus aureus in community-acquired pyoderma. Indian J Dermatol Venerol Leprol. 2004; 43:412-4.
  21. Patil R, Baveja S, Nataraj G, Khodpur U. Prevalence of methicillin-resistant Staphylococcus aureus (MRSA) in community-acquired primary pyoderma. Indian J Dermatol Venerol Leprol. 2006;72:126-8.
  22. Singh A, Gupta LK, Khare AK, Mittal A, Kuldeep CM, Balai M. A clinico-bacteriological study of pyodermas at a tertiary health center in southwest Rajasthan. Indian J Dermatol. 2015;60:479-84.
  23. Sah P,Khanal R, Upadhaya S. Skin and soft tissue infections: Bacteriological profile and antibiotic resistance pattern of the isolates. J Universal College of Medical Science 2013 ;18-21.
  24. Soumya K, Jaya S.Prevalence and antimicrobial susceptibility patterns of bacteria isolated from skin and wound infections. J Microbiol Biotech Res 2014; 4 :39-45.






























 








 




 








 

 









Policy for Articles with Open Access
Authors who publish with MedPulse International Journal of Anesthesiology (Print ISSN:2579-0900) (Online ISSN: 2636-4654) agree to the following terms:
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.
Authors are permitted and encouraged to post links to their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work.