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. 2014 Nov 17;2014(11):CD008726. doi: 10.1002/14651858.CD008726.pub2

Jyothi 2010.

Methods RCT. Individual women. 2‐arm study.
Participants Inclusion criteria
  • “Women who were scheduled to undergo hysterectomy for benign disease and elective cesarean delivery were enrolled in this trial”. However, only women underwent CS will be included in the review.

  • N = 122 women having elective CS (60 having hysterectomy)


Exclusion criteria
  • “We excluded patients who gave history of hypersensitivity to penicillin or cephalosporin; or signs of pre‐existing infections and those who had received antibiotic therapy within the last seven days prior to surgery.”

Interventions Intervention: cephalosporin (B1).
  • Cefazolin 2 g, administered IV.

  • Medication was administered as a single dose.

  • Immediately after clamping the umbilical cord.

  • Total number randomised: N = 67.


Comparison: penicillin (A4) combination.
  • Amoxycillin‐clavulanic acid 2.4 g (co‐amoxyclav) ‐ administered IV.

  • Medication was administered as a single dose.

  • Immediately after clamping the umbilical cord.

  • Total number randomised: N = 55

Outcomes Outcomes: fever and infection, endometritis.
Reported outcomes: postoperative hospital stay, wound infection, asymptomatic bacteriuria, total infection, postoperative urinary infection.
Notes Setting: Kasturba Hospital, Manipal, Karnataka, India, April 2004 to September 2005.
Subgroups
  1. Elective CS.

  2. After cord clamping.

  3. Systemic ‐ IV administration.

  4. Single dose.

  • Comparisons 1 (subgroup 2); 2; 3; 4; 6.

  • No information about funding source for study.

Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Unclear risk No information provided.
Allocation concealment (selection bias) Unclear risk No information provided.
Blinding of participants and personnel (performance bias) 
 All outcomes Unclear risk No information provided.
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk No information provided.
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No loss of follow‐up was reported.
Selective reporting (reporting bias) Unclear risk The study protocol is unavailable.
Other bias Unclear risk Baseline characteristics were similar for: age; BMI; associated disease; type of surgery (primary CS or not). Other possible biases were unclear. No information about funding source for study.