Study Design:
This is a follow-up to the original pilot study (HS# 2009-7015 at UCI/587-08 at LBMMC). This study is also designed to be a prospective, non-randomized, non-blinded trial of the effects of obesity on adequacy of antimicrobial (cefazolin) concentrations with increased doses (from 2 grams to 3 grams) of preoperative prophylactic antibiotics within adipose tissues at the time of cesarean delivery.
Inclusion Criteria:
• Patients at term (\>37 weeks) undergoing a cesarean delivery at LBMMC and UCI.
Exclusion criteria:
* pre-gestational diabetes
* chronic hypertension
* collagen vascular disease
* renal impairment
* multiple gestation
* contraindications to cefazolin administration (known anaphylactic reaction to penicillin's or known cephalosporin allergy)
* any exposure to cephalosporins in one week prior to cesarean section
* need for emergent cesarean delivery or diagnosis of chorioamnionitis
Study Procedure:
All patients requiring cesarean delivery under non-emergent circumstances, as determined by their physician, will be approached for participation in study by co-investigators. They will be approached on Labor and Delivery during their intake evaluation on the day of their scheduled procedure. Based on published literature and preliminary power analysis we expect that each of the 2 study groups will need 1414 subjects to demonstrate statistically significant difference in antibiotic concentrations within adipose tissue. The two groups will consist of:
1. OBESE GROUP (BMI 30-40)
2. MORBIDLY OBESE GROUP (BMI \>40)
1. All subjects will receive cefazolin at least 30, but no more than 60 minutes prior to skin incision.
2. At the time of cesarean delivery, the following tissue samples will be collected:
* adipose tissue immediately following skin incision (prior to incision of the fascia) and
* adipose tissue prior to skin closure
* serum sample after skin incision but prior to completion of the operative procedure
Approximately 2 grams of tissue sampled from each site and 5 cc of blood will be required for analysis.
All samples will be collected by Dr. Swank, Dr. Wing or a physician who had previously been proctored in the proper tissue collecting techniques by either of the above mentioned investigators. Upon collection, tissue specimens will be blotted to remove residual blood and debris, weighed, and placed in a freezer (-80'C) until analysis. Serum samples will be drawn into red top tubes and immediately placed on wet ice. Immediately following completion of the surgery, they will then be centrifuged for 10 minutes at 3G (3200 rpm) and placed in a locked -80'C freezer until analysis.
Tissue and serum samples will then be sent to David P. Nicolau, PhD, FCCP, FIDSA, at the Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut. Samples will be batched and sent all together at the completion of study enrollment. Dr. Swank and the study nurse will be responsible for securely packing samples on dry ice and overnight shipping them to Dr. Nicolau. Once with Dr. Nicolau, the tissue samples will be homogenized and analyzed to determine zones of inhibition. The Cefazolin concentrations will be determined in the serum samples using a previously validated high-performance liquid chromatography method. 16 Tissues and serum will be sent without direct identifiers. Dr. Nicolau will not have access to the identity of the research subjects providing the samples.
