Intravenous antibiotics are overused in hospitals. Many infections can be managed with oral antibiotics.Oral antibiotics avoid the adverse effects of intravenous administration. They are also usually less expensive.When intravenous antibiotics are indicated, it may be possible to switch to oral therapy after a short course. There are guidelines to aid the clinician with the timing of the switch so that there is no loss of efficacy.Infections that may be suitable for a short course of intravenous antibiotic include pneumonia, complicated urinary tract infections, certain intra-abdominal infections, Gram-negative bacteraemia, acute exacerbations of chronic lung disease, and skin and soft tissue infections.Bone and joint infections and infective endocarditis are managed with prolonged courses of intravenous antibiotics. However, there is research looking at the feasibility of an earlier switch to oral antibiotics in these conditions. third of almost 2000 days of antibiotic therapy was unnecessary. 3
Using oral rather than parenteral antibioticsMajor advantages of oral over the intravenous route are the absence of cannula-related infections or thrombophlebitis, a lower drug cost, and a reduction in hidden costs such as the need for a health professional and equipment to administer intravenous antibiotics. Oral therapy may potentially enable an early discharge from the hospital 4,5 or directly from the emergency department. 6 For example, a single dose of intravenous antibiotic for paediatric uncomplicated urinary tract infections did not reduce the rate of representation or readmission. This suggests most children with a urinary tract infection can be managed with oral antibiotics alone. 7 A key consideration is the bioavailability of oral antibiotics. This varies in comparison to intravenous formulations (Tables 1 and 2). Some oral antibiotics have equivalent bioavailability to the intravenous drug. They could be substituted, depending on the condition being treated and the required site of drug penetration.In a small prospective trial, patients with moderately severe cellulitis were randomised to receive either oral cefalexin monohydrate or parenteral cefazolin. Parenteral administration was changed to oral once the cellulitis had stopped progressing and the patient was afebrile. There was no statistically significant REFERENCES