The Use of Ceftaroline as Surgical Prophylaxis in Surgery With Risk of MRSA Infection

The study is a randomized double-blinded study comparing ceftaroline to standard of care
therapy with cefazolin and vancomycin as surgical prophylaxis for high risk orthopedic and
cardiac surgeries. Study participants will be enrolled from those undergoing cardiothoracic
surgery involving sternotomy and those undergoing prosthetic joint replacement of either hip
or knee. Consenting patients will be randomized 2:1 to receive either ceftaroline or
cefazolin/vancomycin. This study will be blinded by the use of placebo vancomycin infusions
and placebo cephalosporin infusions. Study participants will be enrolled from 2 populations
of patients; those undergoing cardiothoracic surgery with sternotomy and those undergoing
prosthetic joint replacement of either hip or knee.

Subjects will be identified by the primary surgical service. Adult subjects 18 years and
older will be notified of the study and if agreeable will be interviewed by a study
coordinator who will explain the study and study procedures and determine eligibility.
Informed consent will be obtained from potential participants. Enrollment and consent may be
obtained up to seven days prior to surgery.

Consented participants will have a detailed history performed with particular reference to
prior surgical infections, risk factors such as diabetes, smoking, prior skin infections and
obesity. Participants will undergo a physical examination. Patients will be assessed for
nares colonization with methicillin-resistant Staphylococcus aureus (MRSA) as per the
primary surgeon's standard procedure. Patients identified as positive for MRSA colonization
will be decolonized with mupirocin. Female participants will have a serum beta-human
chorionic gonadotrophin (HCG) assay performed to exclude pregnancy.

Consented participants will be randomized 2:1 to receive either ceftaroline or
cefazolin/vancomycin, the current regimen for high risk individuals. Randomization will be
performed by a blinded individual using a randomization program. Within each group,
participants will be allocated in the 2:1 ratio.

On the day of surgery, all patients will be evaluated for changes in medical history, vital
signs recorded and bilateral nares swabs obtained for Staphylococcal screening for both MRSA
and methicillin-sensitive Staphylococcus aureus (MSSA) carriage. All patients will receive
pre-operative toweling of the operative site with chlorhexidine, and a surgical skin
preparation of chlorhexidine/alcohol (Duraprep).

Consented participants will receive two blinded infusions. Study infusions will be prepared
by an unblinded pharmacist to match the active medications. Placebo and study medication
will be matched in volume and appearance. Dosing of vancomycin and cefazolin will be weight
based up to 120 kg at 15 mg/kg and 25 mg/kg respectively. ceftaroline will be administered
at a dose of 600 mg in individuals with estimated creatinine clearance of greater than 50
ml/min and 400 mg for those with creatinine clearance rates of 30-50 ml/min. Vancomycin or
placebo1 will be started 120 minutes prior to incision and completed within 60 minutes prior
to surgery. The cefazolin or ceftaroline will be started 60 minutes before surgery and
completed 30 minutes prior to incision. Each participant will thus receive 2 infusions at
T-120 and T-60 minutes from time of skin incision.

Patients will be redosed with antibiotics between 1.5 to 2 half-lives (cefazolin or
ceftaroline at 4hrs hours post skin incision and vancomycin/placebo 1 at 12 hrs) in
prolonged procedures. One post-operative dose of of cefazolin/ceftraroline will be given in
the recovery room 4 hours after skin incision for those patients who were not redosed during
the procedure for orthopedic procedures and 2 doses will be administered for cardiothoracic
procedures.

Pharmacokinetic substudy:

Because of the variation in the pharmacokinetics previously identified for patients
undergoing extracorporeal circulation, we will perform a pharmacokinetic analysis on a
subset of 50 patients in the cardiac surgery arm of the study to allow data on at least 30
patient receiving ceftaroline. Plasma samples will be collected at the start of infusion
(time = 0, Sample #1), end of infusion (time = 30 minutes, Sample #2), 15 minutes post
infusion (Sample #3), at the time of skin incision (Sample #4) at commencement of
cardiopulmonary bypass (CPB) (Sample # 5), at completion of CPB (Sample # 6) and at the time
of skin closure (Sample #7). Samples will be analyzed by high pressure liquid chromatography
(HPLC) to determine ceftaroline levels using known plasma standards with appropriate quality
controls.

Patients will undergo a wound inspection by study personnel prior to discharge from
hospital. Microbiological cultures will be obtained from all surgical site infections. All
isolates will be reported out. Patients will be interviewed and examined at day 30 for the
presence of evidence of surgical site infection at any operative site. Subjects will be
questioned with regard to the presence of fever, redness or drainage or other manifestations
of infection. Physical examination findings by the surgical team at prior post-operative
visits will be reviewed and correlated with the data obtained from the subject. The primary
end point will be the development of a surgical site infection within 30 days of surgery.

30 day surgical site infection rates at either the primary surgical site or any remote
surgical site (e.g. vein donor site for CABG procedures) will be used as the principal
outcome measure. Surgical site infections will be characterized as superficial (above the
fascia) or complex (deep (extending below the fascia) and organ involving), Secondary
endpoints recorded will include (i) other infections, viz. pulmonary, UTI, line related);
(ii) Drug related, viz., rash, itching; and (iii) nausea, vomiting and (iiii) return to OR.

Inclusion Criteria:

- Informed Consent

- Age - 18 years and older

- Patients undergoing either hip or knee arthroplasty or cardiac surgery with
sternotomy

- Body mass index (BMI) between 18 and 30 kg/m2 inclusive.

- Female subjects must have a negative serum pregnancy test and be using appropriate
contraception.

Exclusion Criteria:

- Pregnancy

- Hypersensitivity or allergic reaction to any β-lactam antibiotic or vancomycin.

- Presence of cardiovascular shock,

- Receipt of chronic concomitant systemic corticosteroids, 40 mg of prednisone
equivalent;

- Severe renal impairment (i.e. Creatinine clearance ≤ 30 mL/min);

- Significant hepatic impairment (i.e. known acute viral hepatitis, aspartate
aminotransferase or alanine aminotransferase concentration 10-fold the upper limit of
normal (ULN) or total bilirubin 3-fold the ULN or manifestations of end-stage liver
disease, such as ascites or hepatic encephalopathy),

- Hematological impairment with current or anticipated neutropenia with less than 500
neutrophils/mm3 or thrombocytopenia with platelet count of 60 000 cells/mm3

- HIV infection which at the time of screening meets 2008 CDC criteria for AIDS.

- Patients undergoing revision surgery for infected prosthetic joint replacement.

- Body mass index (BMI) less than 18 or greater than 30 kg/m2.

- Concurrent antibiotics