Open access
Peer reviewed journal

www.actualgyn.com

Actual Gynecology
and Obstetrics

Very low incidence of infections after cesarean section with prophylactic antibiotics after cord clamping
Miroslav Gregor
Actual Gyn 2021, 13, 36-42
Publication date: 2021-08-18
Manuscript ID: 1321006
Number of views: 8099
How to cite this article: Gregor M. Very low incidence of infections after cesarean section with prophylactic antibiotics after cord clamping. Actual Gyn. 2021;13:36-42
Abstrakt

Objective: The optimal timing of prophylactic antibiotics in women undergoing cesarean section (CS) remains uncertain. Prophylactic antibiotics are beneficial for the mother, but it is proven that antibiotics given before cord clamping can affect the infant's gut bacterial flora, with the potential to impact systemic immune function. Additionally, prophylactic antibiotics may lead to increased drug resistant organisms. This study aimed to assess the effects of giving the antibiotics after the cord is clamped on the incidence of infections after CS. 

Methods: A prospective study involving pregnant woman who underwent CS from January to June 2013 at a tertiary referral center in the Czech Republic. The procedures were done in accordance with the criteria of the Center for Disease Control and Prevention with a follow-up period of 30 days. 

Results: Ten patients (3.3%) had a postcesarean infection. Nine infections were surgical site infections (SSIs) and one was non-surgical site infections (non-SSIs). SSIs included 4 superficial, no deep, and 5 organ/space SSIs. 80% were diagnosed after hospital discharge. One woman’s condition resolved without antibiotics, seven with antibiotics, and two required reoperation with antibiotics. 

Conclusion: In this study timing of administration of prophylactic antibiotics after cord clamping was safe for the baby and efficient for the mother with a low rates of postcesarean infections. 

Key words: infections after cesarean section, antibiotic resistance, prophylactic antibiotics

Introduction

Cesarean section (CS) is one of the most commonly

performed surgical procedures in hospitals and its incidence is rapidly increasing in the world (1). An infection after CS is the most frequent postcesarean complication and is associated with significant maternal morbidity and mortality, and increased health care costs (2,3). The incidence rate of infections after CS reported in literature ranges widely from 0% to 23.5% depending on monitoring methods and prevalence of risk factors (2,4-9).

The routine use of prophylactic antibiotics in women undergoing CS reduces the incidence of infections after CS by 60% to 70% (10). Both ampicillin and first generation cephalosporins appeared to have sufficient efficacy in reducing infections after CS (11). Usually a single dose intravenously is administered at the time of the procedure or multiple doses intravenously is administered over a short period of time. For CS, prophylactic antibiotics are administered either before or after the cord is clamped. Unfortunately, obstetricians prefer the administration before the cord is clamped. Because there is some data that antibiotics reaching the baby during SC, can affect the pattern of bacterial flora in the infant gut, with the potential to affect the baby’s developing immune system (12,13), it is important to assess the whether antibiotic prophylaxis should be given before or after the cord is clamped.
Because of the potential for adverse outcomes for the baby and the effect on maternal infectious complications, we performed this study to assess the effects of giving the antibiotics after the cord is clamped. In our prospectively designed study, we investigated postcesarean infections according to the CDC criterion, with complete follow-up data on both the infections diagnosed in hospital and postdischarge infections.

Materials and methods

In a prospective observational study at the Department of Gynecology and Obstetrics, University Hospital in Hradec Králové, Czech Republic, data were analyzed for all women undegoing SC between January 1, 2013 and June 30, 2013.
The University Hospital in Hradec Králové is a tertiary referral center for high-risk maternal and fetal medicine and performs approximately 2,500 deliveries a year.
Ethics committee approval was not required because the survey was a descriptive study and therefore did not influence either the diagnostic or therapeutic processes. Informed consent was also not required.

All patients who underwent CS during the study period were included. Women who had an active infection within 1 week of admission or during CS were excluded. 99.5% of patients were caucasian. All care was provided free of charge. A CS was defined as elective if the procedure was performed at least 24 h after the decision was made to operate and the woman had intact membranes. A CS performed within 30 minutes of the decision was classified as an urgent operation, whereas all other instances of CS were defined as emergency procedures. All surgical interventions were performed jointly by an attending consultant and a resident. Our standard operative procedure, after abdomen disinfection with povidone– iodine 10% prior to incision, is the Joel Cohen incision followed by a transverse incision on the lower uterine segment. The abdomen is closed with a continuous single layer suture of the uterotomy and the fascia along with intradermal suturing of the skin. All sutures are resorbable. The prophylactic antibiotic cefuroxim (1.5 g) was given to all women undergoing CS as a single intravenous dose following umbilical cord clamping. Women presumed to be allergic to cefuroxim were instead given 900 mg of clindamycin as a single intravenous dose after umbilical cord clamping.

Data on demographic characteristics, medical and obstetric history, course of labor, indications for SC, and surgical data were prospectively collected on each patient using a standardized questionnaire. The information was then entered into an electronic database (Tab. 1). In-hospital infectious complications were diagnosed by a physician and recorded on the standardized questionnaire. All women were contacted by telephone 40-50 days after CS and were asked about the development of any signs and symptoms of infection. There were up to five attempts to contact each patient before designating them lost to follow-up. In cases of readmission, monitoring was expanded using hospital databases. The treatment and outcomes of infections for both in-hospital and post-discharge patients were recorded.

The main outcome in our study was any infection after CS defined as an infection diagnosed in-hospital or post-discharge within 30 days after CS. The infection was diagnosed according to the criteria of the Centers for Disease Control and Prevention, Atlanta, USA (14), with infections categorized as surgical site infections (SSIs) or non-surgical site infections (non- SSIs). SSIs were categorized as superficial, deep, or organ/space. Non-SSIs were categorized as urinary tract infection, respiratory tract infection, gastrointestinal tract infection, skin and soft tissue infection, bloodstream infection, arterial or venous infection, or mastitis.

The data were analyzed via NCSS version 8 (NCSS Statistical Software, Kaysville, Utah, USA). Baseline characteristics were described using absolute numbers, percentages, and relative frequencies. A univariate analysis was used to compare categorical data of included and lost patients. Univariate associations among categorical variables of both included and lost patients with a P value of 0.15 or smaller were explored using the χ2 or Fisher exact test. Multivariable logistic regression was used to identify risk factors associated with the infection for variables that were significant in a univariate analysis. Results are reported with a 95% confidence interval (CI).

Results

A total of 1,125 deliveries were performed during the study period, 768 by the vaginal route and 357 (31.7%) by CS (Fig. 1). 13 women were excluded from the analysis because of an active infection within one week of admission or during CS.
Of these women, eight intraamniotic inflammations, two respiratory tract infections, one gastrointestinal tract infection, and two infections of unknown origin were diagnosed. From the remaining 344 CSs, 299 were followed up for 30 days and 45 excluded as a result of being designated lost to follow-up.

Table 1 lists demographic data and clinical characteristics of followed and lost patients. A univariate analysis was used to compare data in both groups
(Tab. 1).

Univariate associations among categorical variables of followed and lost patients with a P value of 0.15 or smaller were explored using the χ2 or Fisher exact test. We found a statistically significant difference in seven variables between followed and lost patients (Tab. 2).

Of the 299 patients who were followed up 30 days, ten were diagnosed with a postoperative infection, giving an incidence rate of 3.3%. Out of all infections, nine were SSIs and one was non-SSI (Fig. 2). These SSIs included four superficial, no deep, and five organ/ space SSIs. The organ/space SSIs were all cases of endometritis and simultaneously one peritonitis. One non-SSI was a urinary tract infection. All infections occurred between the 2nd and 30th day postoperatively, with a median time of occurrence of 14 days. 8 cases (80%) were diagnosed after hospital discharge.

Univariate analysis and multivariate logistic regression analysis were conducted for variables expected to be related to postoperative infection. Obesity was the only independent risk factor for postoperative infection identified in this study. From seven significant different variables among both the followed and lost patients, none were determined to be independent risk factors.

Discussion

The overall postcesarean infection rate of 3.3% in our center is lower than rates from other studies. Despite the fact that prophylactic antibiotics were administered after umbilical cord clamping, our incidence was very low. A study from England identified high rates of postcesarean infections (9.6%) but only SSI, and follow-up data were available on only a third of the women at 30 postoperative days (4). In a Danish study, 458 of 2,492 patients developed postcesarean infections such as SSI and non-SSI, yielding a rate of 18.4%, with postdischarge monitoring of 30 days (15).

A majority of postoperative infections are detected after patients are discharged from hospital (15-19). During postdischarge monitoring in our study, 80% of infections were detected. The data suggest the necessity to perform postdischarge monitoring to obtain more accurate infection rates. It is recommended that when the rate is being calculated, it is advisable to use the number of followed patients rather than the number of the total sample. The patients in our study were contacted by telephone, a feasible and effective method. Weinberg et al demonstrate reducing infections among women undergoing CS in Colombia by means of continuous quality improvement methods in two hospitals from 10.5% to 0% and from 6.1% to 4.4% but postdischarge surveillance was not performed (5).
Despite studies have not shown an increase in maternal infectious outcomes when the antibiotic prophylaxis was administered after clamping of the cord (8,20-22), several meta-analyses have presented that there was significant evidence that antibiotics given before cord clamping improves maternal infectious complications compared with administration after the cord was clamped (23,24). However, it has been proven that antibiotics given before cord clamping can affect the infant’s gut bacterial flora, with the potential to impact mucosal and systemic immune function (12,13,25). Additionally, prophylactic antibiotics may lead to increased drug resistant organisms which may cause serious hospital-acquired drug resistant infections (26).
There is missing data on the adverse effects of antibiotics on the baby, making the assessment of overall benefits and harms difficult. No studies have systematically collected the reported adverse infant outcomes nor the effect of antibiotics on the developing infant immune system. Prophylactic antibiotics given to women undergoing CS are beneficial for the mother but there is uncertainty about the consequences for the baby (10,23,25). It has been suggested that institutions with a low levels of baseline postcesarean infections may see no impact of antibiotics on the baby and currently good effects of antibiotics on maternal infectious complications when the antibiotic prophylaxis was administered after clamping of the cord (8,22). In this study, we assess whether antibiotics given after cord clamping are effective in preventing infection in women having CS. The results seen are clinically important when the postcesarean infection rate of 3.3% was sufficiently low and the timing of administering antibiotics was safe to the baby.
The limitation of this study includes the potential for overestimating the postoperative infection rate. The patient population in our study was not representative of the typical obstetrics population in our tertiary referral center. There was a higher percentage of women with pregnancy pathology and a higher prevalence of women who were obese. The major strengths of this study were the prospective approach and method of monitoring according to CDC criteria with including complete follow-up 30 days after CS. The unique merits of our study were the exclusion of women with an active infection before or during CS (for fear of overestimating the postoperative infection incidence) and the exclusion of patients lost to follow-up (for fear of underestimating the postoperative infection rate).

Conclusion. Prophylactic antibiotics after umbilical cord clamping were sufficient in our center. We believe the very low postcesarean infection incidence in the present study to be the true incidence, and comes as a result of following the CDC criteria and 30 day monitoring period. This study supports the suggestion that prophylactic antibiotics given after cord clamping can be efficient for the mother and safe for the baby on obstetric units with a low rates of postcesarean infections.

Literature

  1. Organization for Economic Co-operation and Development (OECD). Health at a Glance 2019: OECD Indicators [Internet]. Paris: OECD Publishing; 2019 [cit. 2021-05-14]. Available from: www.oecd.org/health/health-systems/health-at -a-glance-19991312.htm
  2. Leth RA, Møller JK, Thomsen RW, et al. Risk of selected postpartum infections after cesarean section compared with vaginal birth: a five-year cohort study of 32,468 women. Acta Obstet Gynecol Scand. 2009;88(9):976-83
  3. Koroukian SM. Relative risk of postpartum complications in the Ohio Medicaid population: vaginal versus cesarean delivery. Med Care Res Rev. 2004;61(2):203-24
  4. Wloch C, Wilson J, Lamagni T, et al. Risk factors for surgical site infection following caesarean section in England: results from a multicentre cohort study. BJOG. 2012;119(11):1324-33
  5. Weinberg M, Fuentes JM, Ruiz AI, et al. Reducing infections among women undergoing cesarean section in Colombia by means of continuous quality improvement methods. Arch Intern Med. 2001;161(19):2357-65
  6. Kittur ND, McMullen KM, Russo AJ, et al. Longterm effect of infection prevention practices and case mix on cesarean surgical site infections. Obstet Gynecol. 2012;120(2):246-51
  7. Opøien HK, Valbø A, Grinde-Andersen A, et al. Post-cesarean surgical site infections according to CDC standards: rates and risk factors. A prospective cohort study. Acta Obstet Gynecol Scand. 2007;86(9):1097-102
  8. Ben Shoham A, Bar-Meir M, Ioscovich A, et al. Timing of antibiotic prophylaxis in cesarean section: retrospective, difference-in-differences estimation of the effect on surgical-site-infection. J Matern Fetal Neonatal Med. 2019;32(5):804-808
  9. Schneid-Kofman N, Sheiner E, Levy A, et al. Risk factors for wound infection following cesarean deliveries. Int J Gynaecol Obstet. 2005;90(1):10-5
  10. Smaill FM, Grivell RM. Antibiotic prophylaxis versus no prophylaxis for preventing infection after cesarean section. Cochrane Database Syst Rev. 2014;(10):CD007482
  11. Gyte GML, Dou L, Vazquez JC. Different classes of antibiotics given to women routinely for preventing infection at caesarean section. Cochrane Database of Syst Rev. 2014;11:CD008726
  12. Mueller NT, Whyatt R, Hoepner L, et al. Prenatal exposure to antibiotics, cesarean section and risk of childhood obesity. Int J Obes (Lond). 2015;39(4):665-70
  13. Lee SY, Yu J, Ahn KM, et al. Additive effect between IL-13 polymorphism and cesarean section delivery/prenatal antibiotics use on atopic dermatitis: a birth cohort study (COCOA). PLoS One. 2014;9(5):e96603
  14. Horan TC, Andrus M, Dudeck MA. CDC/NHSN monitoring definition of health care-associated infection and criteria for specific types of infections in the acute care setting. Am J Infect Control. 2008;36(5):309-32
  15. Leth RA, Uldbjerg N, Nørgaard M, et al. Obesity, diabetes, and the risk of infections diagnosed in hospital and post-discharge infections after cesarean section: a prospective cohort study. Acta Obstet Gynecol Scand. 2011;90(5):501-9
  16. Cardoso Del Monte MC, Pinto Neto AM. Postdischarge monitoring following cesarean section: the incidence of surgical site infection and associated factors. Am J Infect Control. 2010;38(6):467-72
  17. Corcoran S, Jackson V, Coulter-Smith S, et al. Surgical site infection after cesarean section: implementing 3 changes to improve the quality of patient care. Am J Infect Control. 2013;41(12):1258-63.
  18. Daneman N, Ma X, Eng-Chong M, et al. Validation of administrative population-based data sets for the detection of cesarean delivery surgical site infection. Infect Control Hosp Epidemiol. 2011;32(12):1213-5
  19. Johnson A, Young D, Reilly J. Caesarean section surgical site infection surveillance. J Hosp Infect. 2006;64(1):30-5
  20. Cunningham FG, Leveno KJ, DePalma RT, et al. Perioperative antimicrobials for cesarean delivery: before or after cord clamping? Obstet Gynecol. 1983;62(2):151-4
  21. Gordon HR, Phelps D, Blanchard K. Prophylactic cesarean section antibiotics: maternal and neonatal morbidity before or after cord clamping. Obstet Gynecol. 1979;53(2):151-6
  22. Winther A, Axelsson PB, Clausen TD, et al. Prophylactic antibiotics in caesarean delivery before or after cord clamping - protecting the mother at the expense of the infant‘s microbiota? BJOG. 2020;127(2):203-206
  23. Baaqeel H, Baaqeel R. Timing of administration of prophylactic antibiotics for caesarean section: a systematic review and meta-analysis. BJOG. 2013;120(6):661-9
  24. Costantine MM, Rahman M, Ghulmiyah L, et al. Timing of perioperative antibiotics for cesarean delivery: a metaanalysis. Am J Obstet Gynecol. 2008;199(3):301.e1-6
  25. Wong WSW, Sabu P, Deopujari V, et al. Prenatal and peripartum exposure to antibiotics and cesarean section delivery are associated with differences in diversity and composition of the infant meconium microbiome. Microorganisms. 2020;8(2):179
  26. Dancer SJ. How antibiotics can make us sick: the less obvious adverse effects of antimicrobial chemotherapy. Lancet Infect Dis. 2004;4(10):611-9