International Journal of Infection Prevention

International Journal of Infection Prevention

International Journal of Infection Prevention

Current Issue Volume No: 1 Issue No: 1

Research Article Open Access Available online freely Peer Reviewed Citation

Surgical Site Infection in Cesarean Section Operation: Risk and Management

1Head of Oncology Department, Hospital Alemão Oswaldo Cruz - São Paulo/ Brazil

2medical student at Universidade São Camilo, São Paulo/ Brazil

3Head of Thoracic Surgery/ Hospital Paulistano, Americas Serviços Médicos São Paulo, United Health Group, Rua Martiniano de Carvalho

Abstract

Cesarean sections (CS) are one of the most commonly performed surgical procedures worldwide. There is great variability in the percentage of cesarean sections between countries, varying from 3% to 42.9%5. In the US, approximately 32% of deliveries occur through a cesarean section. Overall, a drastic increase in cesarean section rate has been reported reaching its highest level at the present time.

In Brazil, considering the types of births by live births from 2006 to 2016, the national percentage of cesarean section was 52.37%. The variability in this percentage can still be perceived within Brazilian territory. The highest cesarean rate occurred in the Southern region, representing 58.33% of births, while the lowest rate occurred in the Northern region, with 41.79%. It is possible to see the steady increase in the percentage of CS over time, from 45.01% in 2006 to 55.39% in 2016.

Author Contributions
Received 10 May 2019; Accepted 21 May 2019; Published 22 May 2019;

Academic Editor: El-Sabbagh AH, professor of plastic surgery, faculty of medicine, mansoura university, Egypt.

Checked for plagiarism: Yes

Review by: Single-blind

Copyright ©  2019 Riad N. Younes, et al.

License
Creative Commons License     This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Competing interests

The authors have declared that no competing interests exist.

Citation:

Riad N. Younes, Tayna F. Farias, Rodrigo A.S. Sardenberg (2019) Surgical Site Infection in Cesarean Section Operation: Risk and Management. International Journal of Infection Prevention - 1(1):16-24. https://doi.org/10.14302/issn.2690-4837.ijip-19-2842

Download as RIS, BibTeX, Text (Include abstract )

DOI 10.14302/issn.2690-4837.ijip-19-2842

 Introduction

Cesarean sections (CS) are one of the most commonly performed surgical procedures worldwide1, 2, 3, 4. There is great variability in the percentage of cesarean sections between countries, varying from 3% to 42.9%5. In the US, approximately 32% of deliveries occur through a cesarean section 2, 5, 6. Overall, a drastic increase in cesarean section rate has been reported 3, 5, 7, 8,reaching its highest level at the present time8.

In Brazil, considering the types of births by live births from 2006 to 2016, the national percentage of cesarean section was 52.37%. The variability in this percentage can still be perceived within Brazilian territory. The highest cesarean rate occurred in the Southern region, representing 58.33% of births, while the lowest rate occurred in the Northern region, with 41.79%. It is possible to see the steady increase in the percentage of CS over time, from 45.01% in 2006 to 55.39% in 2016 9.

Surgical site infection (SSI) is reported to be the most common hospital-associated infection in community hospital settings10. Moreover, in a recent well-designed multicentre study in England, SSI was estimated to be just under 10% and the readmission rate due to SSI following CS was 0.6% 11.

Like other surgical procedures, there are risks factors of complications associated with cesarean section1. Independent risk factors are not well documented in the literature. In a systematic review of the maternal intrinsic risk factors associated with SSI following CS, obesity and chorioamnionitis were identified as the most significant risk factors for overall SSI (incisional and organ/space)11, along with the following factors: lack or improper use of pre-operative prophylaxis antibiotics, duration of rupture of membranes, emergency CS, and CS accompanied by fetal distress 12.

The present study reviews the current literature related to SSI in CS, risk factors, and potential preventive measure to decrease incidence and severity of that complication.

Methods

References for this review were identified through searches of PubMed, EMBASE (Ovid), the Cochrane Central Register of Controlled Trials (CENTRAL), CINAHL, and World Health Organization for articles in English published from January 2006 to December 2018 by use of the terms “cesarean infection”, “cesarean surgical site infection” and “surgical site infection”. We included randomized controlled trials, meta-analysis registries, relevant systematic reviews, cross-sectional, case–control or cohort studies reporting the incidence of SSI following CS, or studies with enough data to allow the estimated information. All studies where the case definition for SSI-incisional and organ/space, met the CDC/National Healthcare Safety Network (NHSN) criteria. Studies which were not published in English, case reports, case-series, editorials, letters and commentaries, were excluded from this review.

Results

A population-based study between 1988 and 2013 showed 41.375 CS performed during the study period, 1.521 (3.7%) were complicated with SSI 21. SSI rates significantly decreased over the years, from 7.4% in 1988 to 1.5% in 2012. Using a multivariable regression model, the following independent risk factors for SSI were identified: obesity (OR 2.0; 95% CI, 1.6–2.5); previous cesarean delivery (OR 1.8; 95% CI, 1.6–2.0); hypertensive disorders (OR 1.4; 95% CI, 1.2–1.6); premature rupture of membranes (OR 1.3; 95% CI, 1.1–1.6); gestational diabetes mellitus (GDM, OR 1.2; 95% CI, 1.1–1.4); and recurrent pregnancy losses (OR 1.2; 95% CI, 1.1–1.5) 21.

The skin preparation with antiseptic agents has the potential to reduce the SSI risk and is part of a standard operative protocol 2, 6, 7, 13. Although skin preparation is a well-established recommendation, there is no consensus of the ideal solution 7, 14. Chlorhexidine and povidine-iodine are the antiseptic agents most commonly used in abdominal surgeries 13, 14. Regarding the results of current studies, in order to evaluate the superiority of certain antiseptics to reduce the rate of SSI in CS, they are divergences. The more recently published clinical trials compared the more widely used and effective antiseptics for skin preparation (chlorhexidine in alcoholic solution x iodopovidone, chlorhexidine in alcoholic solution x iodinated alcohol, chlorhexidine in aqueous solution x iodopovidone)2, 6, 15, 16. Only one demonstrated the reduction of the SSI rate when using alcoholic chlorhexidine compared to iodinated alcohol 2. Of the three observational studies analyzed, the results also differed, while one showed a superiority of alcoholic chlorhexidine in decreasing the SSI rate, further to reduce the rate of long stay and readmissions to emergency services after cesarean section17, the other two showed no difference between the types of antiseptics compared 18, 19. Table 1 summarizes the comparative analysis of these studies.

Table 1. Comparative analysis of the result of the last studies analyzing skin preparing and surgical site infection in cesarean deliveries
Year Title Authors Type of Study SSI Rates
Control Group Intervention Group
2012 Chlorhexidine-alcohol compared with povidone-iodine for surgical-site antisepsis in cesarean deliveries. Menderes et al18 Retrospective Cohort Review (n=1000) Povidone-Iodine =5.8% Chlorhexidine-Alcohol = 5%
P = 0.58
2013 Can we reduce the surgical site infection rate in cesarean sections usinga chlorhexidine-based antisepsis protocol? Amer-Alshiek et al17 Retrospective Study (n=362) Povidone-iodine + Povidone-iodine in alcoholic solution = 10.4% Chlorhexidine + Alcohol = 3.07%
P = 0.008
2014 Chlorhexidine gluconate versus povidone iodine at cesarean delivery: a randomized controlled trial Kunkle et al.15 Single-center. Randomized Controlled Trial (n=60) Povidone-iodine = 4.5% Chlorhexidine Gluconate = 9.5%
P = 0.60
2015 Skin Preparation for Prevention of Surgical Site Infection After Cesarean Delivery: A Randomized Controlled Trial. Ngai et al16 Prospective. Randomized Clinical Trial (N=1404) Povidone-iodine with alcohol = 4.6%Chlorhexidine with alcohol = 4.5% Povidone-iodine with alcohol + Chlorhexidine with alcohol = 3.9%
P = 0.85
2016 A Randomized Trial Comparing Skin Antiseptic Agents at Cesarean Delivery Tuuli et al2 Single-center. Randomized Controlled Trial (n=1147) Iodine-Alcohol = 7.7% Chlorhexidine Alcohol = 4.3%
P = 0.02
2017 A Randomized Open-Label Controlled Trial of Chlorhexidine-Alcohol versus Povidone-Iodine for Cesarean Antisepsis: The CAPICA Trial. Springel et al.6 Randomized Open-Label Controlled Trial (n=932) Povidine-iodine = 7% Chlorhexidine-alcohol = 6.3%
P = 0.38
2018 Chlorhexidine–alcohol versus povidone–iodine forskin preparation before elective cesarean section: a prospective observational study Elshamy et al.19 Prospective Observational Study (n=1424) Povidine-iodine = 4.6% Chlorhexidine-alcohol = 3.7%
P = 0.35

As main studies carried out on the issue have compared alcoholic chlorhexidine with other products, it is uncertain if the good results are solely due to chlorhexidine, alcohol, or to both. Current guidelines tend to recommend alcohol-soluble antiseptics 2, 20.

As previously reported, in relation to cesarean sections, studies do not show an advantage of alcoholic chlorhexidine in the surgical preparation of the skin, despite several randomized clinical trials in general surgery does. It is believed that this result should not be directly extrapolated to obstetric surgery due to the polymicrobial type of the infection and the physiological immune modulation associated with pregnancy, which may alter the response against infection2, 7.

In the most recent controlled trial published comparing antiseptic solutions in the preparation of skin on cesarean sections - CAPICA trial, the rate of 7% of SSI was observed when povidine-iodine was used versus 6.3% when using chlorhexidine, showing no statistically significant difference between the infection rate and the level of the infection between the two solutions (RR = 0.90, 95% CI 0.00-1.35, p = 0.38).

Discussion

SSI is the infection that occurs in the skin and subcutaneous tissue at the incision site and can occur within 30 days after the procedure 13. The rate of infection varies according to the patient's risk factors, team ability and hospital infrastructure 5. SSI affects approximately 5-12% of cesareans 2, 3, 6, 7, 22. In limited resource areas, the prevalence of SSI can range from 4-70%5. These epidemiological estimates are probably underestimated because infections outside the hospital environment are not considered, even though they are included in the definition 23. SSI is related to the contamination index of surgeries. (Table 2).

Table 2. Infection according to wound classification
Clean Non-traumatic, elective surgery, GI, respiratory and GU tract not entered Mastectomy, vascular, hernias 2%
Clean-contaminated Respiratory, GI,GU tract entered with minimal contamination Gastrectomy, hysterectomy < 10%
Contaminated Open, fresh, traumatic wounds, uncontrolled spillage, miner break in sterile Technique Rupture app, emergent bowel resect 20%
Dirty Open, traumatic, dirty wounds; traumatic perforation of hollow viscus, frank pus in the field Intestinal fistula resection 28-70%

SSI, as well as others operative wound complications, generate problems for the patient, family, and healthcare services 8, 22, 24. This condition results in increased physical and emotional burden, as well as maternal postpartum morbidity and mortality 4, 7, 24. Due to other factors as physical pain, psychological stress, interference in the mother-baby relationship, impact on the onset and continuation of breastfeeding, delayed return to routine activities, chronic pelvic pain, depression and extra costs, CS represent a concern in public health. For the health system, the financial burden stands out for prolonging maternal hospitalization, care costs and need for readmission1, 4, 7, 25. An American study has shown that this financial burden has an average of an additional USD 3,529 per patient with SSI, attributed to readmission and treatment, extra expenses with medical staff, use of pharmaceutical supplies, and an increase in hospitalization time 6, 13, 22.

The surgical site is at contamination risk by skin pathogens, which are the main source[2,7,14]. Staphylococcus aureus is the most commonly isolated microorganism in SSI, accounting for 15-20% of cases 7.

Wound infection, which presents with erythema, discharge, and induration of the incision, complicates 2-7% of patients and generally develops 4 to 7 days after CS 26, 27, 28. When wound infection develops within 48h of the CS, the offending organisms usually are groups A or B-hemolytic Streptococcus. Other common pathogens involved in wound infections are Ureaplasmaurealyticum, Staphylococcus epidermidis, Enterococcus facialis, Staphylococcusaureus, Escherichia coli, and Proteus mirabilis29, 30.

Some maternal risk factors for SSI were identified in studies such as high BMI, diabetes mellitus, pre-existing infection (eg.: chorioamnionitis), ASA score> 3, nulliparity, high intraoperative blood loss, tobacco use in pregnancy, incision size > 16.6 cm, limited pre-natal care, corticosteroids use, subcutaneous tissue thickness > 3 cm, prolonged second stage of the delivery, hypertensive disease/preeclampsia, premature rupture of membranes and emergency surgery 3, 13, 31. A possible explanation for higher SSI rates in the emergency CS is the possible shorter contact duration between the skin and the surgical preparation3. Several preventive methods are investigated in an attempt to reduce the infection rate of surgical site, with the proper preparation of the skin playing an important role 1, 3, 13.

SSI rates are high not only in CS, but also in surgical procedures in general. Currently, researches focus on use of different resources and at various operative moments, to supplement already established and scientifically proven measures for the prevention of infection. One conception that has been explored in recent years is the irrigation of the operative site with numerous solutions to prevent contamination and SSI.

Prophylactic intra-operative wound irrigation (PIOWI) is defined as promoting the flow of a solution across the wound surface to achieve tissue hydration, removing and diluting body fluids, metabolic wastes, bacteria, blood clots, and necrotic cell debris from the surgical field prior to closure 1, 32, 33. This would be a good measure to reduce local bacterial contamination 34, concomitant with the facilitation of the healing process, as well as to promote a better visualization and evaluation by the surgeon of the affected area, immediately before the end of the surgery35.

The healing stages of the wound include hemostasis, inflammation, epithelization, fibroplasia and maturation. Failure or modification of some point in this sequential process can lead to noninfectious complications such as hematoma, bruise and dehiscence, in addition to SSI 1. Whether bacteria and residual debris remain in the surgical site, healing will be affected with prolonged and excessive inflammatory phase, with late or inappropriate angiogenesis and excess granulation of the tissue, which increases SSI risk and possible complications such as sepsis 35.

Contamination can also alter collagen synthesis, cause tissue anoxia, and decrease phagocytic cell function35. PIOWI would be a method easily performed by professionals, as well as being an economically accessible option to reduce the risks of SSI 1, 33, 34. This approach have already being used in clinical practice by some surgeons according to individual preference or hospital protocols 34, although, there is no standardization regarding patient population, application surface, technique and solutions applied 32, 35. Studies with PIOWI show mixed, and often, divergent results due to different methodologies applied, so no convincing evidence of irrigation effectiveness exist, becoming, therefore, a practice not widely accepted35.

International guidelines such as the NICE (National Institute for Health and Care Excellence - UK) do not recommend irrigation of operative wound (OW) with saline solutions containing antibiotics or antiseptics due to potential adverse effects such as tissue toxicity and systemic side effects, without proven efficacy with any irrigated solution36. The WHO 37 and CDC 20 guidelines concluded that PIOWI with saline solution isolated is not efficient and that solutions containing antiseptics such as povidone-iodine may have potential benefit in preventing SSI.

About the solution used to perform PIOWI in cesarean sections, saline solution (sodium chloride 0.9%) is the most commonly used because of its safety, but there are limited data on its effect1. Three clinical trials have been conducted in recent years to evaluate OW irrigation in cesarean sections. Güngördük et al. compared the incidence of wound infection between irrigation with saline versus non-irrigation and did not obtained a significant difference 38. Aslan et al. recently also made the same comparison between saline irrigation vs. no irrigation and reached the same result 1.

Corroborating with the previous results, Al-Ramahi et al. conducted a study evaluating the efficacy of saline irrigation in the incidence of OW infection after gynecological surgeries, showing no difference in infection rate, stating that saline solution lavage did not reduce OW contamination 39

Using a distinct solution, Mahomed, Ibiebele and Buchanan (2016) compared a group irrigated with aqueous solution of povidine-iodine (PI) versus a group receiving no irrigation prior to wound closure, desiring to assess the incidence of SSI in both groups. The result was similarity between the incidence, making it clear that PI did not prevent or decrease SSI40.

Since cesareans are considered clean-contaminated surgeries, OW irrigation can hydrate the bed, allow better visualization, remove clots, tissue remains, and organic fluids, but it does not affect the bacteria, thus not influencing the rate of infections 38. To further support this hypothesis, a systematic review and meta-analysis by Mueller et al. with the objective of determining the current knowledge regarding PIOWI, showed that non-colorectal surgeries, ie clean or contaminated clean, did not have a beneficial effect on SSI with any solution used in irrigation, regardless whether it was performed with saline, antiseptics or antibiotics 34.

Another resource that has been explored as a measure to prevent SSI is the intra-abdominal irrigation. Two studies have not demonstrated a reduction of SSIs with intra-abdominal irrigation of normal saline 41, 42. In a randomized controlled trial of 236 women undergoing CS, intra- abdominal irrigation did not demonstrate decreased OW infection risks and endometritis, but was associated with intra-operative nausea (RR 1.62; 95% CI 1.15, 2.28)41. Similarly in a randomized controlled trial of 196 women undergoing CS, intra-abdominal irrigation by normal saline did not reduce intrapartum or postpartum maternal morbidity 42. Evidence does not support use of routine intra-abdominal irrigation. One study compared irrigation of the abdominal cavity prior to closure with saline solution versus low molecular weight povidone-iodine solution diluted with normal saline ("Betadine group"). Postoperative infections were statistically significantly lower in "Betadine group" - endometritis were 3.7% in "Betadine group" versus 5.9% in "No Betadine group" and wound infections 2.3% in "Betadine group" versus 6.3% in "No Betadine group", both with p value <0.05. As the only study comparing these groups, the authors concluded that the results are promising, but they should be considered preliminary 43.

As mentioned above, cesareans present an SSI rate of approximately 5-12%, and extensive efforts have been made to reduce these rates, including the following methods: use of preoperative prophylactic drugs such as intravenous antibiotics, use of antiseptic solutions in preparation of the skin, pre and postoperative vaginal cleaning with antiseptics, skin incision techniques, different forms of placental removal, closure with layer sutures, subcutaneous drainage and use of pressure dressings 1, 38, 40.

Hauk et al. 44conducted a prospective randomized study on 1,504 patients, and their demographic information, risk factors and surgical indications were recorded. Postoperatively, patients were monitored for signs of SSI. Out of 1,504 patients, 13% developed SSI, - prolonged hospital stay, wound class, ASA class, antibiotic prophylaxis and type of caesarean showed significant association with SSI. They concluded that the reasons for SSI were higher than developed countries were tertiary care hospital dealing with high risk pregnancies, late referrals from peripheries, prolonged hospital stay, heavy rush of attendants, faulty supervision where dose of antibiotics is actually missed, and no proper segregation of cases.

Conclusions

SSI following CS represent complex clinical situations and are caused by many factors such as patient characteristics and peri-operative management. In addition, SSI represents significant financial burden to health care systems. Creating bundles of evidence-based elements may decrease the rates of post-CS SSI, as has been demonstrated in non-obstetric patients.

Literature strongly recommend each hospital to consider the evidence-based information presented in creating its own surgical bundle to decrease the rates of SSI after CS. Independent risk factors for post-cesarean SSI include obesity, gestational diabetes mellitus, hypertensive disorders of pregnancy, premature rupture of membranes, and recurrent pregnancy losses. Information regarding higher rates of SSI and preventative measures should be provided to these high-risk women prior to surgery.

References

  1. 1.Aslan Çetin B, Aydogan Mathykb B, Barut S. (2018) The impact of subcutaneous irrigation on wound complications after cesarean sections: A prospective randomised study. European Journal of Obstetrics & Gynecology and Reproductive Biology.227: 67-70.
  1. 2.Tuuli M G, Liu J, Stout M J. (2016) 18). A Randomized Trial Comparing Skin Antiseptic Agents at Cesarean Delivery.NEnglJ Med. 374(7), 647-55.
  1. 3.El-Achi V, Wan K M, Brown J. (2018) Readmissions for surgical site infections following caesarean section.AustNZJ.ObstetGynaecol.58(5):. 582-585.
  1. 4.Temming L A, Raghuraman N, Carter E B. (2017) . Impact of Evidence-Based Interventions on Wound Complications after Cesarean,AmericanJournalofObstetricsandGynecology,217(4): 449-1.
  1. 5.Sood G, Argani C, Ghanem K G. (2018) . Infections complicating cesarean delivery.CurrOpinInfect Dis,31(4): 368-376.
  1. 6.Springel E H, Wang X-Y, Sarfoh V M. (2017) A Randomized Open-Label Controlled Trial of Chlorhexidine-Alcohol versus Povidone-Iodine for Cesarean Antisepsis: The CAPICA Trial.AmericanJournalofObstetricsandGynecology.217(4):. 463-1.
  1. 7.Zuarez-Easton S, Zafran N, Garmi G. (2017) Postcesarean wound infection: prevalence, impact, prevention, and management challenges. , Int J Womens Health 17(9), 81-88.
  1. 8.KBM Saeed, Greene R A, Corcoran P. (2017) Incidence of surgical site infection following caesarean section: a systematic review and meta-analysis protocol.BMJ Open,7:e013037.
  1. 9.de Departamento.Informática do SUS-DATASUS (TABNET), Brasil: Ministério da Saúde-1991-Localizador de Estatísticas Vitais: banco de dados. Disponível em &lt; http://tabnet.datasus.gov.br/cgi/deftohtm.exe?sinasc/cnv/nvuf.def&gt;
  1. 10.Lewis S S, Moehring R W, Chen L F. (2013) Assessing the relative burden of hospital-acquired infections in a network of community hospitals. , Infect Control Hosp Epidemiol 34, 1229-30.
  1. 11.Wloch C, Wilson J, Lamagni T. (2012) Risk factors for surgical site infection following caesarean section in England: results from a multicentre cohort study.BJOG,119:. 1324-33.
  1. 12.TCF Farret, Dalle J, V da Silva Monteiro. (2015) Risk factors for surgical site infection following caesarean section in a Brazilian Women’s Hospital: a case–control study.Braz J Infect Dis,19:. 113-17.
  1. 13.Pierson R C, Scott N P, Briscoe K E. (2018) A review of post-caesarean infectious morbidity: how to prevent and treat.Journal of Obstetrics and. 38(5), 591-597.
  1. 14.Huang H, Li G, Wang H. (2017) Optimal skin antiseptic agents for prevention of surgical site infection in cesarean section: A metaanalysis with trial sequential analysis.TheJournalofMaternal-Fetal&NeonatalMedicine.31(24):. 3267-3274.
  1. 15.Kunkle C M, Marchan J, Safadi S. (2014) Chlorhexidine gluconate versus povidone iodine at cesarean delivery: a randomized controlled trial.JMaternFetalNeonatalMed,28(5):. 573-7.
  1. 16.Ngai I M, A Van, Govindappagari S. (2015) Skin Preparation for Prevention of Surgical Site Infection After Cesarean Delivery,Obstet Gynecol,126(6):. 1251-7.
  1. 17.Amer-Alshiek J, Alshiek T, Almog B. (2013) Can we reduce the surgical site infection rate in cesarean sections using a chlorhexidine-based antisepsis protocol?.Jmatern,Fetal,NeonatalMed.26(17):. 1749-52.
  1. 18.Menderes G, Athar Ali N, Aagaard K. (2012) Chlorhexidine-alcohol compared with povidone-iodine for surgical-site antisepsis in cesarean deliveries.ObstetGynecol. 120(5), 1037-44.
  1. 19.Elshamy E, YZA Ali, Khalafallah M. (2018) Chlorhexidine-alcohol versus povidone-iodine for skin preparation before elective cesarean section: a prospective observational study. , J Matern Fetal Neonatal Med 18, 1-5.
  1. 20.Berríos-Torres S I, Umscheid C A, Bratzler D W. (2017) . Centers for Disease Control and Prevention Guideline for the Prevention of Surgical Site Infection.Jama Surgery,152(8): 784-791.
  1. 21.KriegerY WalfischA, SheinerE. (2017) Surgical site infection following cesarean deliveries: trends and risk factors.The. , Journal of Maternal-Fetal & Neonatal Medicine 30(1), 8-12.
  1. 22.Martin E K, Beckmann M M, Barnsbee L N. (2018) Best practice perioperative strategies and surgical techniques for preventing caesarean section surgical site infections: a systematic review of reviews and. 125(8), 956-964.
  1. 23.Liu Z, Dumville J C, Norman G. (2018) Intraoperative interventions for preventing surgical site infection: an overview of Cochrane Reviews.Cochrane Database of Systematic Reviews. 6(2), 012653.
  1. 24.Troughton R, Birgand G, Johnson A P. (2018) Mapping national surveillance of surgical site infections (SSIs) to national needs and priorities: an assessment of England’s surveillance landscape.Journal of Hospital Infection,100(4):. 378-385.
  1. 25.Jenks P J, Laurent M, McQuarry S. (2014) Clinical and economic burden of surgical site infection (SSI) and predicted financial consequences of elimination of SSI from an English hospital. , J Hosp Infect 86, 24-33.
  1. 26.Haas D M, Pazouki F, Smith R R. (2010) Vaginal cleansing before cesareandelivery to reduce postoperative infectious morbidity: a randomized, controlled trial. , Am J Obstet Gynecol 202(3), 310-16.
  1. 27.Costantine M M, Rahman M, Ghulmiyah L. (2008) Timing of perioperativeantibiotics for cesarean delivery: a metaanalysis.AmJObstetGynecol,199(3):. 301-16.
  1. 28.Blumenfeld Y J, El-Sayed Y Y, Lyell D J. (2015) Risk factors for prolonged postpartum length of stay following cesarean delivery. , Am J Perinatol 32(9), 825-32.
  1. 29.Martens M G, Kolrud B L, Faro S. (1995) Development of wound infection or separation after cesarean delivery. Prospective evaluation of 2,431 cases. , J Reprod Med 40, 171-5.
  1. 30.Roberts S, Maccato M, Faro S, Pinell P. (1993) The microbiology of post-cesarean wound morbidity. , Obstet Gynecol 81, 383-6.
  1. 31.Kawakita, Landy. (2017) Surgical site infections after cesarean delivery: epidemiology, prevention and treatment. Maternal Health, Neonatology, and Perinatology. 3-12.
  1. 32.de Jonge SW, QJJ Boldingh, Solomkin J S. (2017) Systematic Review and Meta-Analysis of Randomized Controlled Trials Evaluating Prophylactic Intra-Operative Wound Irrigation for the Prevention of Surgical Site Infections.Surgical Infections,18(4):. 508-519.
  1. 33.Edmiston CE Jr, Spencer M, Leaper D. (2018) Antiseptic Irrigation as an Effective Interventional Strategy for Reducing the Risk of Surgical Site Infections.Surgical Infections,19(8):. 774-780.
  1. 34.Mueller T C, Loos M, Haller B. (2015) Intra-operative wound irrigation to reduce surgical site infections after abdominal surgery: a systematic review and meta-analysis.Langenbecks Arch Surg,400(2):. 167-81.
  1. 35.Edmiston CE Jr, Leaper D J. (2016) Intra-Operative Surgical Irrigation of the Surgical Incision: What Does the Future Hold—Saline, Antibiotic Agents, or Antiseptic Agents?.Surgical Infections,17(6):. 656-664.
  1. 36.National Institute (2008) for Health and Clinical Excellence (NICE). Surgical Site Infection—Prevention and Treatment of Surgical Site Infection. NICE Clinical Guideline nº74 , London: RCOG .
  1. 37. (2016) Global guidelines for the prevention of surgical site infection. Geneva: World Health Organization;.
  1. 38.Güngörduk K, Asicioglu O, Celikkol O. (2010) Does saline irrigation reduce the wound infection in caesarean delivery?.Journalof Obstetrics and Gynaecology,30(7):. 662-6.
  1. 39.Al-Ramahi M, Bata M, Sumreen I. (2006) Saline irrigation and wound infection in abdominal gynecologic surgery.International. , Journal of Gynecology and 94(1), 33-6.
  1. 40.Mahomed K, Ibiebele I, Buchanan J. (2016) The Betadine trial – antiseptic wound irrigation prior to skin closure at caesarean section to prevent surgical site infection: A randomized controlled trial.Australian and New Zealand. , Journal of Obstetrics and 56(3), 301-6.
  1. 41.Viney R, Isaacs C, Chelmow D. (2012) Intraabdominal irrigation at cesarean delivery: a randomized controlled trial. , Obstet Gynecol 120, 708.
  1. 42.Harrigill K M, Miller H S, Haynes D E. (2003) The effect of intraabdominal irrigation at cesarean delivery on maternal morbidity: a randomized trial. , Obstet Gynecol 101(1), 80-5.
  1. 43.Marino R, Capriglione S, Morosetti G. (2018) May intraperitoneal irrigation with Betadine improve cesarean delivery outcomes? Results of a 6 years’ single centre experience. , The Journal of Maternal-Fetal & Neonatal Medicine 31(5), 670-676.
  1. 44.P N Rauk. (2010) Educational intervention, revised instrument sterilization methods, and comprehensive preoperative skin preparation protocol reduce caesarean section surgical site infections. , American Journal of Infection Control 38(4), 319-323.

Cited by (1)

  1. 1.Gan Aditya, Khursheed Romana, Savanur Mahadevi, Dalal Anita, Maldar Arif, 2024, The Impact of an Evidence-Based Bundle on Cesarean Section-Related Surgical Site Infections: A Randomized Clinical Trial, Maternal-Fetal Medicine, (), 10.1097/FM9.0000000000000220