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Research Article | Volume 14 Issue: 2 (March-April, 2024) | Pages 1481 - 1486
Incidence, Microbiological Profile, and Risk Factors for Surgical Site Infection Following Major Abdominal Surgery: A Prospective Observational Study
 ,
 ,
1
Associate Professor, Department of General Surgery, Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, Andhra Pradesh, India
2
Associate Professor, Department of General Surgery, Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, Andhra Pradesh, India.
3
Dean and Professor, Department of Pharmacology, Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, Andhra Pradesh, India
Under a Creative Commons license
Open Access
Received
Feb. 14, 2024
Revised
Feb. 26, 2024
Accepted
March 12, 2024
Published
March 16, 2024
Abstract

Background: Surgical site infection (SSI) remains an important complication of abdominal surgery. Local surveillance can describe infection patterns and guide further investigation of perioperative risk. Objectives: To describe SSI occurrence, microbiological findings, and the distribution of infection across potential risk factors in 100 patients undergoing major abdominal surgery. Methods: This is a prospective observational study at Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, Andhra Pradesh, India, from August 2023 to January 2024. Clinical and operative characteristics were compared descriptively between exposure categories. Results: The mean age was 49.6 ± 15.2 years; 62% were men. SSI was recorded in 20 patients (20.0%), comprising 12 superficial incisional, five deep incisional, and three organ/space infections. Eighteen of 20 specimens yielded bacterial growth. Escherichia coli accounted for six of 18 isolates (33.3%); Gram-negative organisms represented 66.7%. SSI proportions were higher with diabetes (40.0% versus 11.4%), hypoalbuminaemia (40.0% versus 13.3%), emergency surgery (35.0% versus 10.0%), contaminated or dirty/infected wounds (40.0% versus 9.2%), and prophylaxis outside the specified interval (45.0% versus 13.8%). Conclusion: The study describe a 20.0% SSI proportion with predominantly Gram-negative isolates. Exposure-specific differences are descriptive and do not establish independent risk factors. 

Keywords
INTRODUCTION

Surgical site infection (SSI) is an infection involving an operative incision or an organ or anatomical space accessed during surgery. Standard definitions distinguish superficial incisional infection, deep incisional infection, and organ/space infection, allowing surveillance to reflect the anatomical extent of disease.[1] These categories also prevent clinically different complications from being combined without adequate explanation. Reliable classification requires clinical assessment alongside relevant microbiological, operative, or imaging findings. Culture results support characterization of infection but do not substitute for a consistent case definition. Established prevention guidance therefore places surveillance within a broader programme of perioperative infection control.[2]

 

Major abdominal surgery presents a diverse infection risk because procedures involve different organs, degrees of microbial exposure, and underlying diseases. Elective operations undertaken after preparation differ substantially from emergency procedures performed in the presence of obstruction, perforation, or existing infection. International prospective evidence demonstrates that SSI occurrence varies across healthcare settings and levels of intraoperative contamination.[3] Consequently, an overall institutional infection proportion should be interpreted together with operative case mix and wound classification. Local reporting can identify where infections cluster, while comparisons between hospitals require compatible definitions, surveillance periods, and ascertainment procedures.

 

Patient characteristics contribute additional variation. A systematic review identified an association between diabetes mellitus and SSI across several surgical specialties.[4] Preoperative hypoalbuminaemia has also been associated with infection following gastrointestinal procedures, although albumin reflects inflammation and disease severity as well as nutritional status.[5] Age, anaemia, obesity, and smoking deserve evaluation within the clinical context rather than automatic designation as independent predictors. Operative duration is another relevant exposure; a systematic review found increasing infection risk with longer procedures.[6] These relationships can overlap because complex operations often involve greater contamination, longer operating times, and patients with more severe illness.

 

Infection prevention depends on coordinated measures before, during, and after surgery. Hospital guidance emphasizes appropriate antimicrobial prophylaxis, aseptic practice, patient preparation, and systematic review of outcomes.[7] The Centers for Disease Control and Prevention guideline additionally supports perioperative practices directed at reducing avoidable infection.[8] Microbiological surveillance complements these measures by documenting recovered organisms. However, organism frequencies alone cannot determine antibiotic effectiveness or local resistance patterns. Interpretation requires the number of specimens, culture-positive cases, isolates, and any polymicrobial infections to be reported with clear denominators.

 

The objectives of this study were to estimate SSI occurrence following major abdominal surgery at Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, Andhra Pradesh, India; describe the anatomical categories and microbiological profile of infection; and examine its distribution across demographic, clinical, and operative factors. This observational assessment covers August 2023 to January 2024 and a cohort of 100 patients.

MATERIALS AND METHODS

Study design and setting

The specified design was a prospective observational study at Konaseema Institute of Medical Sciences and Research Foundation, Amalapuram, Andhra Pradesh, India, during August 2023 to January 2024. This study has 100 patients.

 

Participants and study size

The described cohort comprised patients undergoing major abdominal procedures, including elective and emergency operations. Principal operative categories were small-bowel, colorectal, gastric or duodenal, hepatobiliary or pancreatic, and other abdominal surgery. The available sample comprised 100 patients.

 

Clinical and operative variables

Variables available in the summary were age, sex, diabetes, hypertension, preoperative anaemia, hypoalbuminaemia, obesity, and current smoking. Obesity was categorized as body mass index ≥30 kg/m². Operative variables included urgency, principal procedure category, wound classification, duration, and antibiotic prophylaxis timing. Duration was grouped at 120 minutes. Prophylaxis categories require the actual drug-specific timing interval, informed by established guidance.[9]

 

Outcome definition and follow-up

The principal outcome was the proportion developing SSI during postoperative surveillance. Infections were grouped as superficial incisional, deep incisional, or organ/space, with each affected patient assigned once to the deepest category.[1,2] The calculation 20/100 represents cumulative incidence only when the denominator has adequate surveillance over the specified interval.

 

Microbiological assessment

The study described specimens from 20 SSI cases, including 18 positive cultures and two without growth. Organism percentages used 18 recovered isolates as the denominator.

 

Statistical analysis and reporting

Continuous and categorical variables were summarized using mean ± standard deviation and number with percentage, respectively. Exposure-specific SSI proportions used the number of patients in each category as denominator. Recruitment and ascertainment procedures require documentation to address bias and complete STROBE reporting.[10]

 

Ethical considerations

Necessary Permissions were obtained before starting the study.

RESULTS

Baseline demographic and clinical characteristics

The cohort comprised 100 patients with a mean age of 49.6 ± 15.2 years. Men constituted 62.0%, and the largest age category was 46–60 years (35.0%). Diabetes, preoperative anaemia, and hypoalbuminaemia were recorded in 30%, 35%, and 25%, respectively (Table 1).

 

Table 1. Baseline demographic and clinical characteristics (N = 100)

Characteristic

Number (%) or mean ± SD

Age, years

49.6 ± 15.2

Age group, years

 

18–30

14 (14.0)

31–45

26 (26.0)

46–60

35 (35.0)

>60

25 (25.0)

Sex

 

Male

62 (62.0)

Female

38 (38.0)

Clinical characteristics

 

Diabetes mellitus

30 (30.0)

Hypertension

28 (28.0)

Preoperative anaemia

35 (35.0)

Hypoalbuminaemia

25 (25.0)

Obesity, BMI ≥30 kg/m²

18 (18.0)

Current smoking

24 (24.0)

SD: standard deviation; BMI: body mass index.

 

Operative characteristics

Sixty patients underwent elective surgery and 40 underwent emergency procedures. Small-bowel and colorectal operations represented 28% and 25% of cases. Clean-contaminated wounds accounted for 55%. Forty operations exceeded 120 minutes, and prophylaxis was outside the specified interval in 20 cases (Table 2).

 

Table 2. Operative characteristics (N = 100)

Characteristic

Number (%)

Nature of surgery

 

Elective

60 (60.0)

Emergency

40 (40.0)

Principal operative category

 

Small-bowel surgery

28 (28.0)

Colorectal surgery

25 (25.0)

Gastric or duodenal surgery

17 (17.0)

Hepatobiliary or pancreatic surgery

15 (15.0)

Other major abdominal procedures

15 (15.0)

Wound classification

 

Clean

10 (10.0)

Clean-contaminated

55 (55.0)

Contaminated

25 (25.0)

Dirty/infected

10 (10.0)

Operative duration

 

≤120 minutes

60 (60.0)

>120 minutes

40 (40.0)

Antibiotic prophylaxis timing

 

Within the specified interval

80 (80.0)

Outside the specified interval

20 (20.0)

 

SSI occurrence and classification

SSI was recorded in 20 patients, corresponding to 20.0% of the cohort. This represents cumulative incidence only if adequate postoperative surveillance is confirmed for all 100 patients. Superficial incisional infection affected 12 patients; deep incisional and organ/space infections affected five and three, respectively (Table 3).

 

Table 3. SSI occurrence and anatomical classification

Outcome

Number

All patients (%)
N = 100

SSI cases (%)
n = 20

Any SSI

20

20.0

100.0

Superficial incisional SSI

12

12.0

60.0

Deep incisional SSI

5

5.0

25.0

Organ/space SSI

3

3.0

15.0

No SSI

80

80.0

—

Each affected patient was classified once according to the deepest infection category.

 

Microbiological profile

Of 20 specimens from SSI cases, 18 yielded bacterial growth (90.0%). Escherichia coli accounted for six of the 18 isolates (33.3%). Klebsiella pneumoniae and Staphylococcus aureus each accounted for four isolates (22.2%). Gram-negative and Gram-positive organisms represented 12 (66.7%) and six (33.3%) isolates, respectively (Table 4).

 

 

 

 

 

 

Table 4. Culture results and recovered organisms

Finding

Number

Percentage

Culture results among SSI cases (n = 20)

 

 

Culture positive

18

90.0

No growth

2

10.0

Organisms among recovered isolates (n = 18)

 

 

Escherichia coli

6

33.3

Klebsiella pneumoniae

4

22.2

Staphylococcus aureus

4

22.2

Pseudomonas aeruginosa

2

11.1

Enterococcus species

2

11.1

Organism percentages assume one recovered isolate per culture-positive patient; this requires confirmation. Rounded organism percentages total 99.9%.

 

SSI distribution according to potential risk factors

SSI proportions were higher with diabetes (40.0% versus 11.4%), anaemia (34.3% versus 12.3%), and hypoalbuminaemia (40.0% versus 13.3%). Emergency surgery had a higher proportion than elective surgery (35.0% versus 10.0%). Contaminated or dirty/infected wounds had a proportion of 40.0%, compared with 9.2% for clean or clean-contaminated wounds. Exposure-specific findings are presented in Table 5.

 

Table 5. SSI occurrence according to potential risk factors (N = 100)

Factor

Category

Total patients

SSI, n (%) within category

Age

>60 years

25

8 (32.0)

 

≤60 years

75

12 (16.0)

Sex

Male

62

13 (21.0)

 

Female

38

7 (18.4)

Diabetes mellitus

Present

30

12 (40.0)

 

Absent

70

8 (11.4)

Preoperative anaemia

Present

35

12 (34.3)

 

Absent

65

8 (12.3)

Hypoalbuminaemia

Present

25

10 (40.0)

 

Absent

75

10 (13.3)

Obesity

Present

18

7 (38.9)

 

Absent

82

13 (15.9)

Current smoking

Present

24

8 (33.3)

 

Absent

76

12 (15.8)

Nature of surgery

Emergency

40

14 (35.0)

 

Elective

60

6 (10.0)

Wound classification

Contaminated or dirty/infected

35

14 (40.0)

 

Clean or clean-contaminated

65

6 (9.2)

Operative duration

>120 minutes

40

13 (32.5)

 

≤120 minutes

60

7 (11.7)

Antibiotic prophylaxis timing

Outside the specified interval

20

9 (45.0)

 

Within the specified interval

80

11 (13.8)

Percentages use the total within each exposure category. Comparisons are descriptive; statistical significance and independent prediction were not established.

DISCUSSION

The study described SSI in 20 of 100 patients, with superficial incisional infections constituting 60.0% of affected cases. This numerical pattern requires validation against patient records and the actual surveillance window. For context, Huda and colleagues reported SSI in 16 of 112 patients undergoing elective laparotomy, corresponding to 14.29%.[11] Their retrospective elective cohort differs from the present description, which includes 40% emergency procedures. International prospective evidence likewise demonstrates substantial variation by setting and intraoperative contamination.[3] Differences in operative mix and outcome ascertainment therefore limit direct comparisons of crude infection proportions.

Eighteen specimens yielded growth, and Gram-negative organisms accounted for two-thirds of the 18 isolates. Escherichia coli was the leading organism, followed by Klebsiella pneumoniae and Staphylococcus aureus. Huda and colleagues also identified E. coli as the predominant isolate.[11] In contrast, Ratnesh and colleagues reported S. aureus as the most frequently recovered bacterium in an Indian abdominal SSI series.[12] Such differences support institution-specific microbiological surveillance. The current counts do not establish resistance patterns, and no antimicrobial recommendation can be derived from species frequencies alone. Specimen quality, previous antibiotic exposure, and the detection of mixed infections also influence culture interpretation.

SSI proportions were higher among patients with diabetes, hypoalbuminaemia, and anaemia. The diabetes comparison, 40.0% versus 11.4%, is directionally consistent with the association identified by Martin and colleagues.[4] Similarly, Hennessey and colleagues linked preoperative hypoalbuminaemia with SSI after gastrointestinal surgery.[5] These published findings provide context rather than validation of the example values. Albumin should not be interpreted as a standalone nutritional diagnosis. Current smokers also had a higher descriptive infection proportion, 33.3% versus 15.8%, consistent with published evidence linking smoking to impaired surgical healing and infection.[13] Overlap between exposures remains unresolved.

Emergency procedures and contaminated or dirty/infected wounds had higher SSI proportions than their respective comparison categories. This pattern agrees with the importance of contamination in international gastrointestinal surveillance.[3] Operations exceeding 120 minutes also showed more infections, consistent with the literature on prolonged operative duration.[6] Nevertheless, urgency, contamination, duration, and physiological severity are interrelated. The present category counts cannot determine whether any factor independently predicts infection. With only 20 events, an extensively parameterized multivariable model would require particular caution.

Prophylaxis outside the specified timing interval was accompanied by a 45.0% SSI proportion, compared with 13.8% within the interval. A systematic review by de Jonge and colleagues supports careful attention to prophylaxis timing.[14] Interpretation here depends on confirming the antibiotic, administration time, incision time, and treatment-versus-prophylaxis distinction. The draft supports further assessment of perioperative processes using verified records. It does not demonstrate that changing a single practice would reduce infection, nor establish statistically significant or causal relationships.

Limitations

This single-centre description includes 100 patients and only 20 infections, restricting precision and adjusted analysis. Susceptibility findings and postoperative outcome measures were unavailable. Descriptive exposure comparisons remain vulnerable to confounding, and the reported organism distribution does not capture unconfirmed polymicrobial, anaerobic, or fungal infections.

CONCLUSION

The study describe surgical site infection in 20 of 100 patients undergoing major abdominal surgery. Superficial incisional infections predominated, and Escherichia coli was the most frequent recovered organism. Higher infection proportions accompanied diabetes, hypoalbuminaemia, emergency procedures, contaminated or dirty/infected wounds, longer operations, and prophylaxis outside the specified interval.

REFERENCES
  1. Horan TC, Gaynes RP, Martone WJ, Jarvis WR, Emori TG. CDC definitions of nosocomial surgical site infections, 1992: a modification of CDC definitions of surgical wound infections. Infect Control Hosp Epidemiol. 1992;13(10):606-8.
  2. Mangram AJ, Horan TC, Pearson ML, Silver LC, Jarvis WR. Guideline for prevention of surgical site infection, 1999. Hospital Infection Control Practices Advisory Committee. Infect Control Hosp Epidemiol. 1999;20(4):250-278. doi: 10.1086/501620.
  3. GlobalSurg Collaborative. Surgical site infection after gastrointestinal surgery in high-income, middle-income, and low-income countries: a prospective, international, multicentre cohort study. Lancet Infect Dis. 2018;18(5):516-525. doi: 10.1016/S1473-3099(18)30101-4.
  4. Martin ET, Kaye KS, Knott C, Nguyen H, Santarossa M, Evans R, et al. Diabetes and Risk of Surgical Site Infection: A Systematic Review and Meta-analysis. Infect Control Hosp Epidemiol. 2016;37(1):88-99. doi: 10.1017/ice.2015.249.
  5. Hennessey DB, Burke JP, Ni-Dhonochu T, Shields C, Winter DC, Mealy K. Preoperative hypoalbuminemia is an independent risk factor for the development of surgical site infection following gastrointestinal surgery: a multi-institutional study. Ann Surg. 2010;252(2):325-9. doi: 10.1097/SLA.0b013e3181e9819a.
  6. Cheng H, Chen BP, Soleas IM, Ferko NC, Cameron CG, Hinoul P. Prolonged Operative Duration Increases Risk of Surgical Site Infections: A Systematic Review. Surg Infect (Larchmt). 2017;18(6):722-735. doi: 10.1089/sur.2017.089.
  7. Anderson DJ, Podgorny K, Berríos-Torres SI, Bratzler DW, Dellinger EP, Greene L, et al. Strategies to prevent surgical site infections in acute care hospitals: 2014 update. Infect Control Hosp Epidemiol. 2014;35(6):605-27. doi: 10.1086/676022.
  8. Berríos-Torres SI, Umscheid CA, Bratzler DW, Leas B, Stone EC, Kelz RR, et al. Centers for Disease Control and Prevention Guideline for the Prevention of Surgical Site Infection, 2017. JAMA Surg. 2017;152(8):784-791. doi: 10.1001/jamasurg.2017.0904.
  9. Bratzler DW, Dellinger EP, Olsen KM, Perl TM, Auwaerter PG, Bolon MK, et al. Clinical practice guidelines for antimicrobial prophylaxis in surgery. Am J Health Syst Pharm. 2013;70(3):195-283. doi: 10.2146/ajhp120568.
  10. von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP; STROBE Initiative. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. PLoS Med. 2007;4(10):e296. doi: 10.1371/journal.pmed.0040296.
  11. Huda F, Shasheendran S, Basu S, Kumar N, Rajput D, Singh SK, et al. Risk factors of surgical site infection in elective laparotomy in a tertiary care center: an observational study. Int J Burns Trauma. 2022;12(3):106-113.
  12. Ratnesh K, Jha S, Arya A. Clinical and bacteriological profile of abdominal surgical site infections in an Indian Hospital. Bioinformation. 2022;18(10):962-967. doi: 10.6026/97320630018962.
  13. Sørensen LT. Wound healing and infection in surgery. The clinical impact of smoking and smoking cessation: a systematic review and meta-analysis. Arch Surg. 2012;147(4):373-83. doi: 10.1001/archsurg.2012.5.
  14. de Jonge SW, Gans SL, Atema JJ, Solomkin JS, Dellinger PE, Boermeester MA. Timing of preoperative antibiotic prophylaxis in 54,552 patients and the risk of surgical site infection: A systematic review and meta-analysis. Medicine (Baltimore). 2017;96(29):e6903. doi: 10.1097/MD.0000000000006903.
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