Postoperative Antibiotic Requirements Following Immediate Breast Reconstruction
Bacterial Infection, Anti-infective Agents, Breast Implantation
About this trial
This is an interventional treatment trial for Bacterial Infection focused on measuring Surgical Site Infection, Breast Reconstruction, Antibiotics
Eligibility Criteria
Inclusion Criteria:
- All patients presenting to Stony Brook University Medical Center Plastic Surgery clinic for immediate breast reconstruction using a tissue expander.
- Age 18 years or older
Exclusion Criteria
- Delayed or revision implant reconstruction
- Refusal or inability to consent
- Contraindications to surgery as determined by attending physician
- Contraindications to both penicillin/cephalosporin and clindamycin antibiotics (significant allergies)
- Patients with serious existing systemic infection, defined as 2 or more of the following:
Peripheral body temperature >38 degrees Celsius CRP >5g/L Leukocytes > 12,000/microliter
Sites / Locations
- Stony Brook University Medical Center
Arms of the Study
Arm 1
Arm 2
Other
Experimental
Antibiotics until Drain Removal
Early discontinuation of antibiotics
All patients will receive 24 hours of IV Cefazolin, as is universal practice for clean breast surgery. The control group will receive oral outpatient Cefadroxil until the final drain is removed. In case of significant penicillin allergy (defined as a history of urticaria or anaphylaxis associated with penicillin) patients will receive Clindamycin.
All patients will receive 24 hours of IV Cefazolin, as is universal practice for clean breast surgery. The interventional group will then discontinue antibiotics.