Antimicrobials are the most widely prescribed therapeutic agents, yet as much as 50 percent of hospital antibiotic use may be unnecessary. Numerous reports suggest that inappropriate and unnecessary antibiotic use leads to increased selection of resistant pathogens resulting in increased morbidity, mortality and cost of health care. Prior antibiotic drug exposure is a strong risk factor for colonization and infection due to drug-resistant bacteria. Control of antibiotic use may be one of the few modifiable risk factors for acquisition of resistant bacteria.
What are our program goals?
The goals of antimicrobial stewardship are to improve patient care, outcomes and safety by optimizing antibiotic selection, dosing, route and duration. We also strive to decrease the unintended consequences of toxicity, adverse drug events, the selection of pathogenic organisms, the emergence of resistance and cost related to antibiotic use.
Meet our team
- Sandra Arnold, MD -Sandra Arnold, MD, is a medical co-director of the Antimicrobial Stewardship Service and the division chief of Pediatric Infectious Diseases. She is also an associate professor at the University of Tennessee Health Science Center and an associate program director of the pediatric residency program .
- Bindiya Bagga, MD -Bindiya Bagga, MD, is the medical co-director of the Antimicrobial Stewardship Service and an assistant Professor at the University of Tennessee Health Science Center. She is also an associate program director of the pediatric residency program.
- Kelley Lee, Pharm.D., BCPS -Kelley Lee, Pharm.D., BCPS, is co-director of the Antimicrobial Stewardship Service and a clinical pharmacy specialist in antimicrobial stewardship. She is also a professor in the Department of Clinical Pharmacy at the University of Tennessee Health Science Center
- Chasity Shelton, Pharm.D., BCPS, BCNSP -Chasity Shelton, PharmD, BCPS, BCNSP, is a clinical pharmacy specialist in antimicrobial stewardship and an assistant professor in the Department of Clinical Pharmacy at the University of Tennessee Health Science Center.
- Rebecca Chhim, Pharm.D., BCPS - Rebecca Chhim, PharmD, BCPS, is a clinical pharmacy specialist in antimicrobial stewardship and an assistant professor in the Department of Clinical Pharmacy at the University of Tennessee Health Science Center.
For any questions regarding antimicrobial stewardship or our program please contact Kelley Lee, PharmD, at 901-287-5969 or kelley.lee@lebonheur.org.
Our guidelines
Our guidelines were developed in collaboration with our specialists and are based on current literature reviews, including national guidelines and the current Le Bonheur antibiogram. Print versions of the Le Bonheur guidelines are available to hospital staff. Any departures from the guidelines are based on the clinical judgment of care providers. Below is a list of all of our current guidelines and terminology.
Empiric therapy
Antibiotic therapy administered to a patient for suspected bacterial infection prior to the identification of etiology of infection. This is based on the most common organisms causing the suspected infection and the institution’s antibiogram.
Prophylactic Therapy
Antibiotics used to prevent an infection before it occurs as deemed necessary by national guidelines.
Definitive Therapy
Antibiotic therapy selected for bacterial infection based on antimicrobial susceptibility results.
De-escalation
Changing antibiotic therapy (narrower spectrum, reducing number of antibiotics, transitioning IV to oral, determining duration of therapy) based on cultures, susceptibilities, and clinical course. Typically occurs 24 to 48 hours after initiation of antibiotics.
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Obtain wound cultures for all admitted patients when feasible
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Empiric therapy for MRSA is recommended due to the high percentage of methicillin-resistant isolates at our institution.
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Many MRSA isolates are susceptible to clindamycin and trimethoprim/sulfamethoxazole (note: trimethoprim/sulfamethoxazole does not reliably treat Streptococcal infection).
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Once positive cultures return, transition to most narrow-spectrum agent (e.g., penicillin for Group A Streptococcus)
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Transition patients requiring initial IV therapy to PO therapy once improving
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Unstable patients or suspected necrotizing infections, consult ID service
Abscesses
- central induration or fluctuance- Incision and Drainage (obtain culture)
- Empiric antibiotics based on severity of presentation
- Mild with small lesion 1-2 cm (no systemic signs and symptoms1): I&D only
- Moderate with larger lesion and/or fever: oral trimethoprim/sulfamethoxazole x 5 – 7 days
- Severe (failed oral antibiotics, systemic signs of infection1, immunocompromised): vancomycin until appropriate response then consider oral therapy for total of 10 days
Cellulitis (default if unclear if cellulitis vs abscess)
-indistinct edges, peau d’orange, no pus- Empiric antibiotics
- Clindamycin for mild infection
- Vancomycin if penetrating trauma, purulent drainage, or systemic signs of infection1
- Consider additional coverage depending on exposure risks (e.g., traumatic wound associated with soil or water, call ID)
- Duration of therapy: 5-7 days, transition to PO when able (clindamycin alone, or TMP/SMX AND amoxicillin)
Bite Wounds
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Empiric antibiotics directed towards both aerobic and anaerobic bacteria
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Ampicillin-sulbactam, consider MRSA coverage (vancomycin or trimethoprim-sulfamethoxazole) for severe or worsening infections
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Tetanus toxoid administration to patients without appropriate vaccination; consider rabies prophylaxis if animal bite
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Duration of therapy: 7-10 days, transition to PO when able (amoxicillin/clavulanate alone, or with TMP/SMX if MRSA is suspected)
- High Risk – concern for joint involvement, face, eye, dental, labial, peri-rectal, concern for NEC, immunocompromised patient, major trauma, critically ill- consider ID Consult
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Empiric therapy for MRSA is recommended, due to the high percentage of methicillin-resistant isolates at our community.
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Many MRSA isolates are susceptible to clindamycin and trimethoprim/sulfamethoxazole.
Abscesses
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Incision and Drainage (obtain culture)
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Empiric antibiotics based on severity of presentation
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Mild with small lesion 1-2 cm (no systemic signs and symptoms1): I&D only
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Moderate with larger lesion and/or fever: oral trimethoprim/sulfamethoxazole x 5 – 7 days
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Cellulitis
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Antibiotics – clindamycin for mild infection
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Duration of therapy: 5-7 days
Bite Wounds
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Antibiotics directed towards both aerobic and anaerobic bacteria
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amoxicillin-clavulanate
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Tetanus toxoid administration to patients without appropriate vaccination
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Duration of therapy: 7-10 days
National guidelines
- Acute Bacterial Rhinosinusitis
- Methicillin-Resistant Staphylococcus Aureus
- Antimicrobial Prophylaxis in Surgery
- Community-Acquired Pneumonia in Infants and Children Older Than 3 Months of Age
- Intra-abdominal Infection
- Skin and Soft Tissue Infections
- Streptococcal Pharyngitis
- Intravascular Catheter-Related Infection
- The Diagnosis and Management of Acute Otitis Media
- Urinary Tract Infection: Clinical Practice Guideline for the Diagnosis and Management of the Initial UTI in Febrile Infants and Children 2 to 24 Months
- Therapeutic Monitoring of Vancomycin in Adult Patients