Prophylactic antibacterials for caesarean section reduce infection rate and costs

InPharma ◽  
1989 ◽  
Vol 712 (1) ◽  
pp. 4-4
2010 ◽  
Vol 2 ◽  
pp. 104-109
Author(s):  
Agnieszka Szlagatys-Sidorkiewicz ◽  
Magdalena Słomińska-Frączek ◽  
Anna Borkowska ◽  
Mariusz Sroka ◽  
Grzegorz Krzykowski ◽  
...  

2020 ◽  
Vol 7 (1) ◽  
pp. 107-112
Author(s):  
Ekta Jaiswal ◽  
Paban Sharma ◽  
Alka Singh

Introduction: Would infection following caesarean delivery adds physical, psychological, and health burden to individual and health care system. This hospital based study aim to determine the rate of infection, the risk factors, pathogens and antibiotic sensitivity. Method: A prospective study was carried out to analyze the wound infection in women following caesarean delivery in the Department of Obstetrics and Gynecology, Patan Hospital, Nepal, between January 2018 to December 2018. The study was approved from the institutional review committee. Clinicodemographic data during perinatal period of caesarean delivery were descriptive analyzed in relation to wound infection. Result: Wound infection occurred in 102 (3.1%)of 3285 caesarean section (of total 7131 deliveries during the study period. The caesarean SSI rate was 3.1%, all were incisional SSI (84 superficial and 18 deep) and there were no organ-space SSI. Majority (81.3%) SSI cases were detected in emergency LSCS. Coagulase Negative Staphylococci was the most common organism isolated from wound swab. Routine postoperative antibiotics did not have a major impact in reducing wound infection rate. Multiple per vaginal examinations, prolonged rupture of membrane and staples for skin closure were more commonly associated with SSI. Conclusion: Reduction in caesarean rate is the major key factor for decreasing the post caesarean wound infection. Protocol should be developed and strictly implemented by all the health care professionals in order to minimize and prevent the infection rate after caesarean section.


EP Europace ◽  
2001 ◽  
Vol 2 (Supplement_1) ◽  
pp. A77-A77
Author(s):  
F. Zanon ◽  
E. Baracca ◽  
C. Bilato ◽  
S. Aggio ◽  
A.S. Abbasciano ◽  
...  

2018 ◽  
Vol 46 (6) ◽  
pp. S72
Author(s):  
ShihYin Yen ◽  
ChenChun Kuo ◽  
FuChieh Chang ◽  
ChinChen Lin ◽  
ChangPan Liu

2019 ◽  
Author(s):  
Jie Chen ◽  
Yineng Zhou ◽  
Liping Chen ◽  
Chenyu Xu ◽  
Lanhua Liu ◽  
...  

Abstract Background: To investigate at what extent breastfeeding and vaginal delivery can increase mother-to-child transmission of cytomegalovirus (CMV) and to observe the clinical outcomes of postnatal CMV infection in infants. Methods: In this secondary study of prospectively collected clinical data and serum samples, April 2012 through March 2015, 380 pregnant women with CMV IgG positive/CMV IgM negative and their 384 infants (4 twin pairs) with gestational age ≥32 weeks were included. CMV IgG and IgM were measured with enzyme-linked immunosorbent assay. Results: Of 384 infants followed up at 10.2 ± 2.3 months age, 177 (46.1%) were defined with CMV infection based on the presence of higher CMV IgG levels than in their mothers. The infection rate in 190 breastfed infants was higher than in 194 formula-fed infants (62.6% vs 29.9%, P < 0.001). Vaginally delivered infants (172) had higher CMV infection rate than 212 infants delivered by caesarean section (55.2% vs. 38.7%, P = 0.001). Compared with formula feeding and caesarean section, breastfeeding and vaginal delivery increased postnatal CMV infection respectively (OR = 3.801, 95% CI 2.474‒5.840, P < 0.001; OR = 1.818, 95% CI 1.182‒2.796, P = 0.007). Nevertheless, CMV-infected infants normally developed and did not show adverse clinical outcomes compared to uninfected infants. Conclusions: Breastfeeding and vaginal delivery can increase postnatal CMV infection; however, the infection does not cause adverse events in term or late preterm infants. Detection of CMV DNA in breastmilk should not be routinely performed, and breastfeeding should be encouraged in these infants.


1987 ◽  
Vol 10 (2) ◽  
pp. 138-144 ◽  
Author(s):  
J.R. Thompson ◽  
R.M. Hutton ◽  
B.R. Moir-Bussy

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