APPENDIX 6
IV TO ORAL SWITCH
1. INTRODUCTION
Unnecessary prolonged courses of Intravenous (IV) antimicrobials are associated with longer length of hospital stay, increased risk of morbidity and mortality related to IVline infections, as well as higher treatment cost1-3. Therefore, one of the core elements in antimicrobial stewardship (AMS) programme is to promote timely oral (PO) antimicrobials conversion (IVOC) once the patient is clinically stable, able to tolerate oral feeding and has no contraindications4-6.
Multiple studies have highlighted the benefits of IVOC, including decreased risk of healthcare-associated and cannula-related infections, reduced medical and hospitalisation costs, shorter hospital length-of-stay, with increased patient mobility and comfort2,3,5,7-10. Early IVOC also has been demonstrated to be safe and equally effective to prolonged IV antimicrobial courses with no negative impact on patient outcomes in terms of mortality, readmission or adverse drug reactions3, 9, 11.
2. TIMING OF INTRAVENOUS ANTIMICROBIAL REVIEW
IVOC should be considered within 48 to 72 hours of IV antimicrobial therapy5, 10, 12, 13. This period of time allows the clinician to evaluate patients’ microbiology results and assess their response to treatment.
3. CRITERIA FOR INTRAVENOUS TO ORAL ANTIMICROBIAL CONVERSION (IVOC)
3.1 Considerations for Early IVOC2, 6, 10
3.1.1 Criteria of Patients for Early IVOC9-13
Stable vital signs
- Temperature >36°C and <38°C for 24 to 48 hours
- Stable blood pressure (no unexplained hypotension)
- No tachycardia (heart rate below 90 beats/min)
- No tachypnoea (respiratory rate below 20 breaths/min)
Stable immune response
- White cell count between 4 and 12 x 109/L or normalising
- C-reactive protein reducing trend
Gastrointestinal tract intact and functional
- Oral fluids/food are tolerated (at least 1L/day of oral fluids or 40mL/hour of enteral nutrition)
- No concerns about malabsorption
Oral absorption is not compromised
- No diarrhoea, vomiting, malabsorptive disorder, short bowel syndrome or swallowing disorder
An appropriate oral antimicrobial is available, considering oral bioavailability, any clinically significant drug interactions or patient allergies
No significant concerns over patient adherence to oral antimicrobial treatment
3.1.2 Types of infections where IVOC may be considered
Pneumonia
Skin and soft tissue infections
Urinary tract infections
Intra-abdominal infections without deep-seated collection
Uncomplicated Gram-negative bacteraemia
3.2 Conditions where early IVOC is NOT appropriate
Early IVOC is not appropriate in infections which warrant prolonged course of IV antimicrobial or require very high tissue concentration which cannot be delivered via equivalent oral antimicrobial preparations such as5, 6, 10, 11:
Bone and joint infections
Central nervous system infections: meningitis, encephalitis, intracranial abscess
Deep-seated abscess, abscess without incision or inadequately drained
Endocarditis
Exacerbation of cystic fibrosis or bronchiectasis
Empyema
High-risk neutropenia or severe infections during chemotherapy-related neutropenia
Infections of implants/prostheses/IV catheters
Melioidosis (at least 14 days of IV therapy)
Septicaemia or critical infection with high risk of mortality
Severe soft tissue infections such as: necrotising fasciitis, Group A Streptococcal infections etc.
Severely immunocompromised: solid organ transplant, bone marrow transplant
Staphylococcus aureus bacteraemia
Treatment for liver abscesses, adequately drained abscesses and empyema, osteomyelitis and septic arthritis can be changed to oral therapy after ≥ 2 weeks of IV therapy
4. IV TO ORAL ANTIMICROBIAL CONVERSION PROTOCOL
5. ANTIMICROBIALS FOR CONVERSION/STEP-DOWN THERAPY
References:
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