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A Randomized controlled trial comparing the efficacy of a seven day regimen of co-amoxiclav versus a single dose second generation cephalosporin (cefoxitin) as prophylactic antibiotic therapy for third and fourth degree perineal lacerations among post-partum patients in a tertiary medical center / Samantha Quennie Wanasen-Razon; Lylah D. Reyes; Jennifer Co.

Contributor(s): Language: english Publication details: Fairview, Quezon City: Department of Obstetrics and Gynecology, FEU-NRMF, 2021.Description: 46 pages: illustrations, tables; (in folder) + with flash drive (soft copy)Content type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
Subject(s): LOC classification:
  • OB 2021 0005
Summary: Abstract: Episiotomy is a common obstetrical practice in the Philippines. However, particularly from midline episiotomy, a third- or fourth degree extension may not be prevented. This predisposes the episiotomy site to infection and wound breakdown due to bacterial contamination from the rectum. Compare the efficacy of single dose cefoxitin versus seven-day regimen of Co-amoxiclav in preventing wound infection of third- or fourth degree perineal tears among women who had episiotomy during vaginal delivery. Included were 64 women, 18 to 35 years old, who delivered vaginally and sustained a third or fourth degree laceration during episiotomy. Participants were randomly allocated to group A: single dose of Cefoxitin, 1 gram intravenous, given 30 minutes after delivery and group B: Co-amoxiclav, 750 mg twice a day for seven days postdelivery. Assessment for wound infection, pain/discomfort and adverse event rates as well as mean pain, REEDA scores and length of hospital stay between two groups were done right after episiorrphy, on the day of discharge and seven days after discharge. Wound infection, pain and discomfort were not noted for both treatment arms during the seven-day follow up period. The mean pain and REEDA scores tend to be higher among the participants in the co-amoxiclav group. There was also more adverse effects, such as nausea, dizziness and vomiting noted among those participants in the co-amoxiclav than in the cefoxitin group. Length of hospital stay ranged from 2 to 4 days with a mean of 2.98. Although, no statistically significant differences were noted between the two groups. Seven-day oral co-amoxiclav is comparable with single dose intravenous cefoxitin in preventing wound infection from third- or fourth degree perineal tears as well as safety. Thereby, compared to oral co-amoxiclav regimen, single dose cefoxitin is the cost-beneficial option among women with episiotomies having extension.
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Item type Current library Call number Status Notes Date due Barcode
Room Use Far Eastern University - Nicanor Reyes Medical Foundation Research OB 2021 0005 (Browse shelf(Opens below)) Available with flash drive (soft copy) R000876
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OB 2021 0002 A Comparative study on the effect of micronized progesterone and oral dydrogesterone in the treatment of threatened abortion in a tertiary medical center from 2015 to 2019 / OB 2021 0003 Association of fetal abdominal circumference with capillary blood glucose levels and perinatal outcome among women with gestational diabetes mellitus / OB 2021 0004 A Comparison of the efficacy of single dose cefazolin versus single dose cefazolin plus 7-day mupirocin ointment wound application in preventing surgical site infection among patients undergoing major obstetric and gynecologic procedures at a tertiary university hospital : a two-year single blinded randomized controlled trial / OB 2021 0005 A Randomized controlled trial comparing the efficacy of a seven day regimen of co-amoxiclav versus a single dose second generation cephalosporin (cefoxitin) as prophylactic antibiotic therapy for third and fourth degree perineal lacerations among post-partum patients in a tertiary medical center / OB 2021 0006 Lymphocyte immunotherapy in recurrent pregnancy loss : a case report / OB 2021 0007 "The Missing X" - profile of a 25-year old with turner syndrome : a case report / OB 2022 0001 Postabortal bleeding and endometrial cancer : a diagnostic dilemma /

Includes appendices and bibliographical references.

Abstract: Episiotomy is a common obstetrical practice in the Philippines. However, particularly from midline episiotomy, a third- or fourth degree extension may not be prevented. This predisposes the episiotomy site to infection and wound breakdown due to bacterial contamination from the rectum. Compare the efficacy of single dose cefoxitin versus seven-day regimen of Co-amoxiclav in preventing wound infection of third- or fourth degree perineal tears among women who had episiotomy during vaginal delivery. Included were 64 women, 18 to 35 years old, who delivered vaginally and sustained a third or fourth degree laceration during episiotomy. Participants were randomly allocated to group A: single dose of Cefoxitin, 1 gram intravenous, given 30 minutes after delivery and group B: Co-amoxiclav, 750 mg twice a day for seven days postdelivery. Assessment for wound infection, pain/discomfort and adverse event rates as well as mean pain, REEDA scores and length of hospital stay between two groups were done right after episiorrphy, on the day of discharge and seven days after discharge. Wound infection, pain and discomfort were not noted for both treatment arms during the seven-day follow up period. The mean pain and REEDA scores tend to be higher among the participants in the co-amoxiclav group. There was also more adverse effects, such as nausea, dizziness and vomiting noted among those participants in the co-amoxiclav than in the cefoxitin group. Length of hospital stay ranged from 2 to 4 days with a mean of 2.98. Although, no statistically significant differences were noted between the two groups. Seven-day oral co-amoxiclav is comparable with single dose intravenous cefoxitin in preventing wound infection from third- or fourth degree perineal tears as well as safety. Thereby, compared to oral co-amoxiclav regimen, single dose cefoxitin is the cost-beneficial option among women with episiotomies having extension.

Research - Department of Obstetrics & Gynecology

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