pharm case study questions

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pharmantibotic.docx

Original work, answer the (3) questions below that go with the case study (this is NOT a paper just respond to the questions and cite if needed)

Case Study: Infectious Disease Drugs - Antibiotic

JT is a 29-year-old quadriplegic male with multiple chronic decubitus ulcers who presents to the emergency department with increasing malodorous, purulent drainage from his sacral wounds that started a few days ago. Additionally, he reports a 1-week history of increasing generalized pain and fatigue. JT resides in a long-term acute care facility and has limited mobility. 

Past Medical History:

Motor vehicle accident (5 years ago)

Quadriplegia 

Type II diabetes mellitus 

Peripheral vascular disease

Allergies:

Vancomycin – Red Man’s Syndrome

Vitals in the ED: 

Blood pressure: 110/72 mmHg; Pulse: 105 bpm; Respiratory rate: 22/min; Temperature: 101.2

Height: 5’9”; Weight: 72 kg

Imaging: Pending

Pertinent Labs (All others are within normal limits):

Values in the ED 

Normal range

Basic Metabolic Panel

CREATININE LEVEL (CREAT)

2.5 

0.5-1.0 mg/dL 

GLUCOSE LEVEL (GLUC)

152 

73-110 mg/dL 

A1c

6.9

4.2-6.3%

Inflammatory Markers

ESR

78

0-22 mm/hr

CRP

16

<10 mg/L

Complete Blood Count

WBC

18

4.5-11 cells/mcL

RBC

5

4.32-5.72 million cells/mcL

Platelet

422

150,000-450,000/mcL

JT is experiencing a sudden decrease in his urine output and his SCr has more than doubled since admission.

1. Which antibiotics (vancomycin, piperacillin/tazobactam, tobramycin) will be impacted by this new onset renal impairment?

The microbiology laboratory finally reports the identified organisms and antimicrobial susceptibilities. Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus are identified. Renal function has now improved back to baseline and JT is clinically stable. 

2. What are the intravenous antibiotic options for treatment of methicillin-resistant Staphylococcus aureus and Pseudomonas aeruginosa?

3. Since the patient is now clinically improving, you would like to continue piperacillin/tazobactam. However, you notice that the piperacillin/tazobactam MIC is high (at the clinical breakpoint) for Pseudomonas aeruginosa. 

a. What does the MIC mean? Minimum inhibitory concentration (MIC): The lowest concentration of antibiotic that results in no visible growth.

a. Describe the pharmacodynamic target for piperacillin/tazobactam that is associated with optimal activity. 

a. What dosing/administration strategies could you use to optimize the activity of piperacillin/tazobactam?