- 1Department of Nursing, College of Health Science, Debre Berhan University, Debre Berhan, Ethiopia
- 2Department of Clinical Medicine and Surgery—Section of Infectious Diseases, University of Naples “Federico II”, Via Sergio Pansini, Naples Berhan, Italy
- 3Department of Orthopedic and Trauma Surgery, Gondar, Ethiopia
Background: Surgical site infections (SSIs) are a leading cause of morbidity and mortality worldwide. Particularly, in low- and middle-income countries (LMICs), they are the most prevalent kind of healthcare-associated infection (HAI), and they play a role in the emergence of antibiotic resistance, which can result in serious illnesses. Therefore, this study aims to ascertain the burden and association of surgical site infection among patients on the surgical ward in resource-limited surgical setups.
Method: An institutional-based cross-sectional study was conducted in Wolaita Sodo University Comprehensive Specialized Hospital from March 1, 2022 to July 30, 2023. A systematic random sampling method was employed. Data management and statistical analysis were performed using SPSS version 25. An adjusted odds ratio (AOR) with 95% confidence interval was used to measure the association between dependent and independent variables. A p-value < 0.05 was used to determine the level of significance.
Result: This study included a total of 309 patients, of whom 198 (64.1%) were males. The average age of the participants was 42, and participants more than 42 years’ old totaled 156 (50.5%); the type of residence was found to be rural for 236 patients (84.6%). The magnitude of surgical site infection was calculated to be 29.1%. Predisposing factors for surgical site infection included male sex (AOR −4.9; 95%; 2.0–11.3), drainage use (AOR −4.46; 95%; 1.9–10.3), and abdominal surgery (AOR−4.3; 95%; 1.3–14.1), whereas protective factors included younger female sex, elective surgery, and a surgery duration of less than 2 h.
Background
Surgical site infections (SSIs) are a preventable consequence of surgery that pose a serious risk to public health, affecting not only patients but also the financial and human resources of the medical field (1). It' is one of the growing concerns in nosocomial infections. This issue is made worse by the steady rise in antibiotic resistance, the growing number of therapies, and the increasingly complex type of patients as a result of their comorbidities (2). The World Health Organization (WHO) states that there are 1.2–23.6 SSIs for every 100 surgical procedures worldwide (3), and its cumulative incidence ranged from 2.5% to 30.9% in Africa (4). According to reports, SSIs account for almost one-third of postoperative fatalities globally (5), and it annually endangers the lives of millions of people and fuels the development of antibiotic resistance (6).
An SSI is characterized by a surgical wound that exhibits localized infection symptoms and, in more severe cases, systemic symptoms such as fever or leukocytosis (7). It can develop within 30 days following a surgical procedure (or within 90 days for surgeries involving the implantation of prosthetic material) at the incision site and/or deeper underlying tissue spaces and organs. SSIs make up roughly 38% of all surgically related nosocomial infections (8).
According to a comprehensive assessment conducted in 2020, SSIs have a significant impact on LMICs, accounting for 38% of all deaths. LMICs saw a greater rate of SSIs than HICs in Europe, with the patient bearing the majority of the costs when medical expenses incurred as a result of the incident surpassed 10% of the household's yearly income (9–11). The SSI rate covered between 2% and 5% European countries (12), while the pooled prevalence rate in LMICs was 11.2% (13). In Sub-Saharan Africa, the rate of impact of SSIs ranged from 6.8% to 26% with a predominance in general surgery (14), and other studies showed that its rate of prevalence was about 2.5–30.9% (4, 15–17). In Tanzania, 22% of patients developed SSIs after open urologic surgery (18), and studies reported SSI rates of 19.4% and 24% in the district and tertiary hospitals of Tanzania, respectively (19). The rate was 16.4% in Uganda (20) and 13.0–22.05% in Nigeria (21). In Ethiopia, the pooled prevalence rate of SSIs was 12.3% (1) as reported in one study and 25.22% (22) as reported in another study.
An SSI is associated with a number of risk factors, including identifiable intrinsic and extrinsic factors. Modifiable inherent risk factors include diabetes, respiratory conditions and other preexisting illness (19, 23, 24), smoking, steroid use, alcoholism, obesity, immunocompromised individuals, albumin levels <3.5 mg/dl, and anemia and bilirubin levels >1.0 mg/dl. Age, type of surgery, and recent radiation therapy (25, 26) are non–modifiable risk factors. Clean wounds are usually closed, are free of infection, and show no symptoms of inflammation. Clean-contaminated wounds are wounds that have a low level of contamination, while contaminated wounds have a high level of contamination and typically result from a breach in sterile techniques or leakage from the gastrointestinal tract. Dirty wounds are grossly infected and usually occur because of an inadequate treatment of traumatic wounds, gross purulence, and evident infections (1, 20, 27, 28). An American Society of Anesthesiologists (ASA) Score III or IV (27, 29), non-use of prophylactic antibiotics, (30) presence of hypovolemia (19, 31), longer duration of operation (19, 23, 30), and longer preoperative (23, 30) and postoperative hospital stay (23, 28) are common determinants of SSIs across studies. SSIs continue to be a significant contributor to hospital-acquired infections even with advances in operating room procedures, equipment sterilization techniques, and surgical techniques and varies from setup to setup. Therefore, this study aims to ascertain the burden and associated factors of SSIs in peripheral teaching hospitals in resource-limited settings.
Method
A retrospective institutional-based cross-sectional study was conducted between August 1 and 30, 2023, at Wolaita Sodo University Comprehensive Specialized Hospital (WSUCSH) located in Wolaita Zone, Ethiopia, among patients who were operated upon and admitted to the surgical ward March 01, 2022 to July 30, 2023. The hospital serves as a teaching institution for health science students and surgical residents and provides 24-hour comprehensive services for more than 6 million people with different demographic and socioeconomic backgrounds from in and around the southern part of the country. It offers general surgery, internal medicine, neurology, orthopedics, neurosurgery, obstetrics and gynecology, pediatrics, radiology, dermatology, pathology, oncology, anesthesiology, and neonatal care specialty services in the respective departments for the entire population of southern Ethiopia.
Source and study population
All patients were operated upon and admitted to the WSUCSH surgery department during the period of the study in both private and public wards.
Inclusion criteria
Adult patients who were operated upon and admitted to the surgery department and had a complete medical record.
Exclusion criteria
Patients with lost or incomplete charts or those who underwent obstetric or gynecological surgery.
Sample size determination and sampling technique
The sample size for the first objective was calculated using a single population proportion formula considering p 24.6% taken from a study done in Hawassa, with 95% CI and a margin of error of 5%. This gave a sample size of 285. Then, if a 10% non-response rate was added, the final sample size became 314.
n = 285
where
n = desired sample sizes
Zα/2 == critical value at 95% CI, which equals to 1.96 P = proportion of SSI at Hawasa 0.246,.
d = margin of error (0.05).
The sample size for the second objective was calculated with Open Epi using an assumption of power of 80%, 95% CI, and an exposed/unexposed ratio of 1:1. Therefore, for the maximum sample size is the sample size required for the first objective. Then the final sample size becomes 314. A systematic random sampling method was employed to select the study subjects.
Dependent variable: surgical site infection
Data collection tools and methods
Data were collected using a validated, pretested, and structured data extraction checklist adopted from relevant literature and modified to the study variables. First, the operation theatre and admission records were reviewed to prepare lists of patients operated upon and admitted to the surgical ward between August 1, 2023 and August 30, 2023. Then, data were extracted from the medical registrations of patients taken from the examination room on arrival, operating room records, postsurgical evaluation and monitoring sheets, and intensive care and discharge records. Data were collected by trained data collectors and supervisors through a review of the medical records of the patients.
Data quality management
A pretested validated structured data collection tool prepared in simple English after a review of related literature was used to ensure data quality. One day of training was given to data collectors and supervisors on the purpose of the study, the contents of the data collection tool, where to find the records, and how to extract the required data from the medical records and record data appropriately. A pretest was conducted on 5% of the sample size before the actual data collection period to check for the reliability and validity of the data collection tool. The questionnaires were reviewed and checked for completeness, accuracy, and consistency by the principal investigator and amended accordingly based on the pretest results. Supervisors and the principal investigator carefully checked the collected data for completeness, accuracy, and consistency daily. Two individuals performed double data entry to minimize errors.
Data processing and analysis
The collected data were validated for completeness and accuracy and categorized, coded, and analyzed using Statistical Package for Social Sciences (SPSS) software version 25.0. Descriptive statistics were used for frequency, mean/median, standard deviation, and percentage. The results were summarized using graphs, charts, and tables. The interpretations of data using summaries were done according to the main finding in the study objective. Thus, variables having a P-value < 0.25 at a 95% confidence interval (CI) became the candidates for the final multivariate logistic regression. Hence, the features included in the final model were age, sex, hemodynamic status, preoperative sepsis, residence, GI contamination, surgical site infection, postoperative cough and/or vomiting, and duration of surgery. Logistic regression analyses were utilized, and a P-value < 0.05 was considered statistically significant with a confidence interval (CI) of 95%.
Ethical considerations
The Institutional Health Research and Ethics Review Committee (IHRERC) at Wolaita Sodo University's College of Health and Medical Sciences granted ethical approval for the study. To obtain administrative approval, a formal letter of collaboration was presented in writing to the WSUCSH before the start of data collection. The hospital and department chiefs gave their informed, voluntary consent after being made aware of the goals, objectives, and advantages of the study. Throughout the process of gathering data and disseminating information, confidentiality of information was upheld.
Result
This study included a total of 309 patients. Out of these, 198 (64.1%) were male patients and 35.9% female. The age of the participants was >42 years old for 156 patients (50.5%), and the type of residence was found to be rural for 236 (84.6%) patients among the subjects and/or participants incorporated in the study. Moreover, the evidence indicates that 31 (10%) patients had a history of hospitalization, and 249 (80.6%) patients were managed in public wards, which contrasts with an individual private room per patient with a single bed, as shown in Table 1.
An SSI affected a total of 90 (29.1%) patients incorporated in the study. For these patients, an SSI developed from a clean wound affected 30/180 (16.6%), from a clean-contaminated wound affected 26/83 (31.3%), a contaminated wound affected 20/30 (66.6%), and a dirty wound affected 14/16 (87.5%). Based on the type of SSI, 80/90 (88.8%) were superficial incisional SSIs, 8/90 (8.8%) deep incisional SSIs, and 2/90 (2.22%) organ/space SSIs. This study incorporated 184 (59.5%) patients from elective surgery and the operation site was abdominal for 219 (70.5%), neck 31 (10%), extremities 20 (6.5%), and the remaining 12.6% was thoracic and other procedures. The type of anesthesia given was spinal for 156 (51.7%) patients, and for the remaining it was general anesthesia, while prophylaxis antibiotics was given for 300 (97.1%) patients; prophylactic antibiotics was given at the induction stage for 200 (67%) patients Table 2). Furthermore, wound class was clean for 180 (58.3%) patients; the total duration of hospital stay was less than or equal to 8 days for 193 (62.4%) patients, and the time of SSI diagnosis was ≤7 days for 60 (66.7%) patients (Table 2).
A bivariate logistic regression was carried out to identify candidate-independent features in this study. Bivariate logistic regression variables with a P-value of less than 0.25 were considered candidate features for a final multivariate logistic regression. Thus, the candidate features for the multivariate logistic regression were age, sex, type of surgery, preoperative hemoglobin level, drainage usage, operation site, wound type, presence of comorbidities, history of hospital admission, and duration of surgery and were used to determine the factors for SSI at our study setup. Then, after controlling for confounders, a multivariate logistic regression analysis was done. Belonging to the male sex with an AOR of −4.9; 95% (2.0–11.3), drainage usage with an AOR of −4.46; 95% (1.9–10.3), and abdominal surgery with an AOR of −4.3; 95% (1.3–14.1) were predisposing factors for SSI, while younger female sex, elective surgery, and a duration of surgery of less than 2hr were protective factors for SSI. See Table 3 for associated factors for SSI in our study area.
Discussion
This study included a total of 309 patients, of whom 198 (64.1%) were male patients and 39.5% were females. The age of the participants was >42 years old in 156 (50.5%) patients, and the type of residence was found to be rural for 236 (84.6%) patients. In our study group, 24 (7.8%) patients had comorbidities and the commonest of these were malignancy in 8 (33.3%), DM in 7 (29.2%), hypertension in 6 (25%), and others made up the remaining share. Prophylactic antibiotics was given to 300 (97.1%) patients, out of whom 200 (66.6%) consumed them during the induction of anesthesia and 98 (32.6%) took them 30 min before operation. Based on carefully thought-out prospective clinical investigations, the selection of parenteral prophylactic antibiotic medicines, as well as the timing and method of administration, has been standardized. It is typically advised that anesthesia staff give a single intravenous dose of cephalosporin shortly before incision in clean, elective surgical operations involving a foreign body and in clean-contaminated surgeries (2).
The common patient factors that predispose for SSIs found in the study are older age, presence of comorbidities, and existing infection, which are consistent with those of other literature (32). The physiologic factors that predispose for SSIs found in our study are that the preoperative hemoglobin level is less than 10 mg/dl (which was the case for 47(15.2%) patients) and surgical risk factors like prolonged procedure time also had a higher association with SSIs. Independent risk factors like abdominal surgery (219/309 (70.9%) patients, of whom 83/209 (39.7%) developed SSI) and wound class are found to predictors in our study, which is consistent with the literature (32, 33).
The magnitude of SSIs in this study was found to be 29.1It is within the upper range reported in studies conducted in different parts of Sub-Saharan Africa, which varies from 6.8% to 26%. (3). Our study finding is relatively higher than the reports from Rwanda 10.9% (34), Nigeria 27.6% (35), Tanzania 10%–26% (36, 37) and the pooled prevalence of Ethiopia 12.3–25.22% (1, 22). It is also lower than in studies done for Niger 74.9% (38) and Nepal 80% (39) and a rural tertiary hospital in Nigeria 70.1% (40) and Tigrai (75%) (41). These differences may be due to differences in setup and SSI prevention strategies used, method of diagnosis, types of wound class, and inclusion of obstetric procedures.
Our study found that being male is associated with an approximate five times higher likelihood of developing an SSI, with an AOR of 4.9; 95% CI (2.13–11.3), although male sex is seen as a controversial risk factor for SSI. This is consistent with a study done in Germany, where the occurrence of SSI was significantly lower in women, with a rate of 2.92/100, while men developed SSIs in 4.37/100 of cases (42). Another study from Korea showed that being male is an independent risk factor for SSIs, with an AOR 1.67; 95%(1.09–2.58) (43). But there are also other multiple other studies that have reported no correlation between SSIs and gender (13, 44). Drainage tube usage is also associated with SSIs in our study, with an AOR 4.46; 95% CI (1.9–10.3), and this is consistent with studies done in Korea (45), India (46), and Switzerland (47), which stated that the presence of drainage tubes is related to a higher risk for developing SSIs. The presence of drains can serve as a conduit for bacteria, facilitating the entry of microbes into the surgical site (48).
In our study, abdominal surgery was associated with a fourfold higher risk of developing SSI, with an AOR of 4.3 (95% CI: 1.3–14.1). Many studies have shown that abdominal operations involve higher risk in terms of developing an SSI compared with other surgical site locations (49–51). Because of the intricate gastrointestinal tract microbiota, microbial variables play a crucial role in abdominal surgery. Surgery can cause dysbiosis, or an imbalance of microbial communities, which can result in an overabundance of harmful bacteria like Proteobacteria, which includes E. coli, a common culprit in surgical site infections (52). Patients who had surgery for less than two hours had an 81.4% (p-value = 0.00) lower chance of developing SSI than those who had surgery for more than two hours. This is consistent with multiple studies (50, 53, 54). This is due to increased microbial exposure in the operating field: longer surgical times would increase the risk of surgical wound contamination (55) and, because of the prolonged surgical process and significant blood loss that leads to tissue hypoxia, it also increases the extent of tissue trauma. An estimate would be that infection rate nearly doubles with each hour of surgery. Moreover, guidelines advised reducing the duration of surgical procedures because, the longer the incision is left open, the greater the chance is that bacteria may enter the surgical site (56).
Our findings showed a 68.7% (p-value _0.01) lower risk of surgical site infection for those who underwent elective surgery. This is consistent with most studies (57–59). This is due to inadequate preoperative preparation, lack of proper control of other medical comorbidities, and higher risks for contamination in emergency surgeries. In our study, compared to clean wounds, which were considered protective, contaminated/dirty wounds were 78.1% less likely (p-value: 0.04) and clean-contaminated wounds were 85.6% less likely (p-value: 0.00) to acquire SSI. The risk of surgical site infection increases as the percentage of contamination rises. This is consistent with literature from different studies all over the world (35, 60–62). A trend toward higher rates of postoperative SSIs was observed when progressing from clean to dirty wound procedures. Greater contamination during surgery is indicated by a higher wound class, which means that there are more bacteria in the wound area, the surgeons are more likely to use drainage, and a stoma is likely if abdominal surgery is being carried out. This greatly increases the risk of surgical site infection.
The presence of comorbidity had no significant association with SSIs in our study finding. But studies conducted in Tanzania (19), East and West Gojjam hospitals (24), and systemic reviews and meta-analyses done at the national level in Ethiopia (1) have shown significant associations with SSIs. For example, uncontrolled hyperglycemia impairs leukocyte function and lowers immunity, rendering them unable to fight off invasive microbes. Even innocuous bacteria have the ability to spread swiftly and cause major health problems (63, 64). Hyperglycemia, especially from stress, has been linked to an increased risk of SSI, according to studies. Therefore, research suggested that perioperative blood sugar levels should be less than 200 mg/dl and HbA1C < 8% in order to maximize treatment for patients with diabetes mellitus and lower the risk of complications (3, 56). Patients with preoperative HGB ≤10 mg/dl had no significant association with surgical site infection in our study, although studies conducted in Uganda (20) and Nepal (65) showed that low hemoglobin predisposes a patient for SSIs. This is because low hemoglobin concentrations hinder tissue repair and cause tissue hypoxia, which increases the risk of SSIs. Previous history of hospitalization was not significantly associated with surgical site infection in our study. But other studies, such as reports from and meta-analyses done in Ethiopia, showed patients with previous hospitalization were significantly associated with SSIs (1, 66). This could be because the probability of infection is increased by previous exposure to resistant germs (57, 58). These differences may be due to sample differences, set up, or statistical issues.
Conclusions and recommendations
The magnitude of SSIs in this study was found to be 29.1%, which is very high. Overall drainage usage, abdominal surgery, and male sex are significantly associated with surgical site infection. While drains can be beneficial in certain contexts, their use should be carefully considered, weighing the potential benefits against the increased risk of SSIs. The decision to use drains should be individualized based on the patient's risk factors and the specific surgical context, as it has high association with surgical site infection. Optimization of patient, anticipating infection and acting accordingly either by prophylaxis or therapeutic antibiotics for wounds based on classes, and taking measures which reduce surgical site infection for abdominal surgery is recommended.
Limitations of the study
This study had some limitations. First, a retrospective document review was used, which may miss some variables and lacks detailed explanations. Also, due to the nature of the retrospective study design used, it was not easy to establish the cause-effect relationship between the study variables and to make other statistical inferences. The type of drainage used, the number of drainage tubes, and the duration of drainage in situ was not detailed in our study due to a lack of full documentations.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving humans were approved by WOLAITA SODO UNIVERSITY INTITUTIONAL REVIEW BOARD. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
SZ: Writing – original draft, Writing – review & editing, Conceptualization, Methodology, Supervision. AD: Formal analysis, Methodology, Software, Writing – original draft, Writing – review & editing. AA: Conceptualization, Methodology, Validation, Writing – review & editing. ZA: Methodology, Supervision, Writing – review & editing. HE: Methodology, Writing – review & editing. AB: Methodology, Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research and/or publication of this article.
Acknowledgments
We want to express our gratitude to data collectors and supervisors. Also, we would like to thank the study participants for their willingness and participation.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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The author(s) declare that no Generative AI was used in the creation of this manuscript.
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Keywords: surgical site infection, surgical ward, burden, resource-limited setup, factors
Citation: Zewdu S, Daniel A, Abebe A, Abraham Z, Elias H and Belete A (2025) The burden of surgical site infection and associated factors among patients admitted to the surgical ward in resource-limited countries: an institutional-based cross-sectional study. Front. Surg. 12:1571033. doi: 10.3389/fsurg.2025.1571033
Received: 4 February 2025; Accepted: 29 July 2025;
Published: 28 August 2025.
Edited by:
Gabriel Sandblom, Karolinska Institutet (KI), SwedenReviewed by:
Juan Antonio del Moral Luque, Madrid City Council, SpainKusumakshi Nayak, MCHP, MAHE, India
Copyright: © 2025 Zewdu, Daniel, Abebe, Abraham, Elias and Belete. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Abel Daniel, YWJlbGt1Y2hlMjAxNEBnbWFpbC5jb20=