Data

A Double-Blinded, Randomised, Placebo-Controlled Trial of Antibiotic Prophylaxis in Elective Non-Hysterectomy Laparoscopic Surgery for Benign Gynaecological Conditions

University of New South Wales
Lim, Claire ; Abbott, Jason ; Roydhouse, Stephanie ; McCormack, Lalla ; Deans, Rebecca ; Nesbitt-Hawes, Erin
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.26190/unsworks/1632&rft.title=A Double-Blinded, Randomised, Placebo-Controlled Trial of Antibiotic Prophylaxis in Elective Non-Hysterectomy Laparoscopic Surgery for Benign Gynaecological Conditions&rft.identifier=https://doi.org/10.26190/unsworks/1632&rft.publisher=UNSW, Sydney&rft.description=This dataset is for a study that aims to determine the feasibility of a double-blinded randomised, placebo-controlled study in determining the effectiveness of antibiotic prophylaxis in preventing postoperative infections in elective non-hysterectomy laparoscopic procedures for benign gynaecological conditions. Participants were randomly allocated into one of two groups - receiving 2g cephazolin and placebo (10mL normal saline) preoperatively. Data was collected pre-, intra- and post-operatively, including follow-up data collected at 2- and 6-weeks postoperatively. Primary outcomes analaysed include feasibility of a large-scales study and postoperative infection rates in both group. Secondary outcomes analysed include length of hospital stay, re-admission to hospital, unscheduled presentations to healthcare facilities and antibiotic-related reactions. It contains de-identified patient data including demographics, pre-, intra- and post-operative data, as well as follow-up data at 2-weeks and 6-weeks. Patients who have been withdrawn after randomisation are highlighted in yellow.&rft.creator=Lim, Claire &rft.creator=Abbott, Jason &rft.creator=Roydhouse, Stephanie &rft.creator=McCormack, Lalla &rft.creator=Deans, Rebecca &rft.creator=Nesbitt-Hawes, Erin &rft.date=2022&rft.coverage=Australia&rft_rights= https://creativecommons.org/licenses/by-nc/4.0/&rft_subject=minimally invasive surgery&rft_subject=pelvic surgery&rft_subject=gynaecology&rft_subject=postoperative infections&rft_subject=surgical prophylaxis&rft_subject=Obstetrics and gynaecology&rft_subject=Reproductive medicine&rft_subject=BIOMEDICAL AND CLINICAL SCIENCES&rft_subject=Medical microbiology&rft_subject=HEALTH&rft.type=dataset&rft.language=English Access the data
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This dataset is for a study that aims to determine the feasibility of a double-blinded randomised, placebo-controlled study in determining the effectiveness of antibiotic prophylaxis in preventing postoperative infections in elective non-hysterectomy laparoscopic procedures for benign gynaecological conditions. Participants were randomly allocated into one of two groups - receiving 2g cephazolin and placebo (10mL normal saline) preoperatively. Data was collected pre-, intra- and post-operatively, including follow-up data collected at 2- and 6-weeks postoperatively. Primary outcomes analaysed include feasibility of a large-scales study and postoperative infection rates in both group. Secondary outcomes analysed include length of hospital stay, re-admission to hospital, unscheduled presentations to healthcare facilities and antibiotic-related reactions. It contains de-identified patient data including demographics, pre-, intra- and post-operative data, as well as follow-up data at 2-weeks and 6-weeks. Patients who have been withdrawn after randomisation are highlighted in yellow.

Issued: 2022

Data time period: 2019-02-21 to 2021-04-22

Data time period: Study period based on number of participants recruited

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Spatial Coverage And Location

text: Australia

Subjects
Biomedical and Clinical Sciences | Health | Medical Microbiology | Obstetrics and Gynaecology | Reproductive Medicine | gynaecology | minimally invasive surgery | pelvic surgery | postoperative infections | surgical prophylaxis |

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