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Clostridium difficile Infection (CDI
from Antimicrobial Guide
by uri703
RECURRENT EPISODES
No. of Recurrences Recommended Regimens
1st Recurrence
Vancomycin 125 mg PO Q6H for 10-14 days Vancomycin Pulsed-Taper Regimen: 125 mg PO Q6H for 10-14 days 125 mg PO Q12H for 7 days 125 mg PO once daily for 7 days 125 mg PO every 2-3 days for 2-8 weeks
OR
Fidaxomicin200 mgPO Q12H for 10 days If fidaxomicin was used for the initial episode: Vancomycin 125 mg PO Q6H for 1014 days
2nd Recurrence
Consult ID for tailoring antibiotic therapy. Vancomycin Pulsed-Taper Regimen (outlined above)
OR
Fidaxomicin200 mgPO Q12H for 10 days
OR
Consult ID team for possible: • Vancomycin 125 mg PO Q6H for 10-14 days then rifaximin 400mgPO TID for 20 days1, • Referral for fecal microbiota replacement therapy1,
≥ 3 recurrences Consult ID team • Possible referral for fecal microbiota replacement therapy1 • Consider restarting vancomycin taper OR fidaxomicin200 mg PO Q12H OR vancomycin followed by rifaximin1
RISK FACTORS FOR CDI
• ≥ 64 years of age • Exposure to antibiotics in last 90 days • Hospitalization in last 30 days • Recent GI surgery • Exposure to CDI (household family member with CDI) • Long-term care facility or nursing home resident • Gastric acid reducing agent (PPIs) • Tube feedings
INFECTION CONTROL
• Screening for C. difficile in hospitalized patients without diarrhea is not recommended • Asymptomatic carriers should not be treated • Patients should be placed in a private room or with other patients who have CDI • Continue contact precautions for CDI patients until 48 hours from resolution of symptoms • Place contact precautions plus sign on patient’s door • Hand hygiene and barrier precautions (gloves and gowns) • Place dedicated stethoscope in patient’s room • When patient discharged or symptoms resolve, room should be terminally cleaned
MISCELLANEOUS
• Repeat CDI PCR testing not recommended due to the likelihood of false positives. Toxin A, B, and
TC may remain positive for as long as 30 days in patient with symptom resolution.
CDI= Clostridium difficile infection; GI= gastrointestinal; H= hour(s); ID= Infectious Diseases; PCR= Polymerase Chain Reaction; PO= by mouth; Q= every; TC= Toxigenic Culture
Extended Spectrum Beta-Lactamase (ESBL) Infection Extended Spectrum Beta-Lactamase (ESBL) Infection Extended Spectrum Beta-Lactamase(ESBL) Infection
CLINICAL SYNDROME PREFERRED REGIMEN ALTERNATIVE REGIMEN CLINICAL CONSIDERATIONS
CLINICAL SYNDROME PREFERRED REGIMEN ALTERNATIVE REGIMEN CLINICAL CONSIDERATIONS Extended Spectrum Extended Spectrum Beta-Lactamase (ESBL) Beta-LactamaseInfection (ESBL) Infection Carbapenem-resistant Carbapenem-resistantEnterobacteriaceae Enterobacteriaceae (CRE) (CRE)
Meropenem 2 gm IV Consult ID Please DO NOT treat Meropenem Q8H 2 gm IV colonization, or a “dirty Q8H (Use maximum doses) (Use maximum doses) Consult ID urine” sample Consult ID The optimal treatment for infection due to CRE is uncertain and antibiotic options are limited. Management of infections due to CRE should be done in
consultation with ID
Consult ID Consult ID
Consult ID Please DO NOT treat colonization, ora “dirty urine” sample
The optimal treatment for infectiondue to CRE isuncertain and antibiotic optionsare limited. Management of infections due to CRE should be done in
consultation withID
Febrile Neutropenia Febrile Neutropenia Febrile Neutropenia
CLINICAL SYNDROME PREFERRED REGIMEN ALTERNATIVE REGIMEN CLINICAL CONSIDERATIONS
CLINICAL SYNDROME PREFERRED REGIMEN ALTERNATIVE REGIMEN CLINICAL CONSIDERATIONS
Febrile Neutropenia Cefepime 2gmIV Q8H Meropenem 1 gmIV Ifpatient has indwelling Febrile Neutropenia High risk: anticipated prolonged (>7 days duration) AND profound neutropenia (ANC ≤100 cells/mm3 High risk: anticipated prolonged (>7days duration) AND profound neutropenia (ANC≤100 cells/mm3 following cytotoxic Cefepime 2gm IV Q8H OR Piperacillin/tazobactam 3.375gm IV Q4H (18gm/day) OR Piperacillin/tazobactam 3.375gm IV Q4H (18gm/day) Meropenem Q8H Q8H 1 gm IV If patient has indwelling catheter, is persistently febrile OR previously colonized with MRSA: ADD vancomycin catheter,is persistently febrile OR previously colonized with MRSA: ADD vancomycin Consult ID for following cytotoxic chemotherapy)+/- Consult ID for Anti-fungaltherapy; chemotherapy) +/-significant co-morbid Anti-fungaltherapy; Considerwhen fever significant co conditions: -morbid Consider when fever failsto respond after conditions: hypotension, fails to respond after 3-7days oftherapy hypotension, pneumonia, new-onset 3-7 days of therapy pneumonia, new-onset abdominal pain, or abdominal pain, or neurologic changes neurologic changes ANC= Absolute neutrophil count; CRE= Extended SpectrumBeta-Lactamase;ESBL= ExtendedSpectrum Beta-Lactamase; ANC= Absolute neutrophil count; CRE= Extended Spectrum Beta-Lactamase; ESBL= Extended Spectrum Beta-H= hour(s); ID=InfectiousDiseases;IV=intravenous;MRSA= Methicillin-Resistant S. aureus;Q= every Lactamase; H= hour(s); ID= Infectious Diseases; IV= intravenous; MRSA= Methicillin-Resistant S. aureus; Q= every
NOTE: Dosingbased on normalrenal function.Referto Table of Contents forsection on AntimicrobialDosingfor Adult NOTE: Dosing based on normal renal function. Refer to Table of Contents for section on Antimicrobial Dosing for Adult Patients Basedon Renal Function,Aminoglycoside High DoseOnceDaily (HDOD)andMonitoringin AdultPatients, and
Patients Based on Renal Function, Aminoglycoside High Dose Once Daily (HDOD) and Monitoring in Adult Patients, and Vancomycin Dosing and Monitoringin Adult Patients. Vancomycin Dosing and Monitoring in Adult Patients.