When and when not to administer intravenous antibiotics
When and when not to administer intravenous antibiotics
When and when not to administer intravenous antibiotics
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<strong>When</strong> <strong>and</strong> <strong>when</strong> <strong>not</strong> <strong>to</strong> <strong>administer</strong><strong>intravenous</strong> <strong>antibiotics</strong>• Reliable diagnosis of an infection requiring IV rather than oraltherapy as the IV route should only be used if the antibioticcan<strong>not</strong> be <strong>administer</strong>ed by any other route.• IV antibiotic treatment via a peripheral cannula should <strong>not</strong>normally exceed two weeks duration, if treatment is expected<strong>to</strong> last longer than two weeks a central line or PICC line(Peripherally inserted central catheter) should be considered
Why Antibiotics• Antibiotics are used <strong>to</strong> treat infectious diseases by killing or inhibitingthe growth of microorganisms.• Antibiotics may be <strong>administer</strong>ed orally, <strong>intravenous</strong>ly or intramuscularly.• In some patients the absorption of <strong>antibiotics</strong> taken orally from thegastrointestinal system can be unpredictable <strong>and</strong> <strong>antibiotics</strong> may begiven <strong>intravenous</strong>ly.• Intravenous administration can cause complications <strong>and</strong> will also putgreater dem<strong>and</strong>s on staff resources.
Benefits of IV Antibiotic Therapy.• Direct administration of antibiotic in<strong>to</strong> the bloodstream allowing tissue penetration quickly.• Levels easily controlled.• Fast acting
Indications for IV Antibiotics
Oral route compromised• Vomiting• Nil by mouth• Severe diarrhoea• Swallowing disorder• Unconscious
Continuing Sepsis2 or more of the following:Temp >38°C or 90bpmRespira<strong>to</strong>ry rate >20 bpmWCC >12 or
Special Indications requiringprolonged high dose IV <strong>antibiotics</strong>• Endocarditis• Meningitis• Staph. aureus bacteraemia• Immunosuppression• Bone/joint infection• Deep abscess• Cystic fibrosis• Prosthetic infection
Other clinical signs•Febrile with neutropenia•Hypotension/shock:a low blood pressure is associatedwith reduced blood flow <strong>to</strong> the gut<strong>and</strong> reduced/unpredictable drugabsorption.•For skin <strong>and</strong> soft tissue infections:IV therapy indicated if there isheat, erythema <strong>and</strong> indurationor sepsis syndrome.
Risks of IV Antibiotic Therapy.• Anaphylaxis• Phlebitis – MechanicalChemicalBacterial• Speed Shock• CRBI – Bacteraemia• AKI <strong>and</strong> liver function
The indications for IV <strong>to</strong> oral switch• Medication should be changed <strong>to</strong> oral treatment at theearliest opportunity (usually 3 days). There must be acompletion date or date of review of treatment if needed.• Ideal for pathway treatments such as cellulitis which canachieve an IV <strong>to</strong> Oral switch much quicker.Usual guidelines include: clinical signs of improvement –• Inflamma<strong>to</strong>ry markers, clinical signs, etc.• Haemodynamic stability• Oral route available & working
Guidelines for switchingSelection of oral switch agent also critical <strong>and</strong> must haveappropriate characteristics• Undertaken under the advice of the Microbiologist• MDT decision• Must have reliable absorption• Must achieve suitable blood levels• No underlying resistance issues
The benefits of oral <strong>antibiotics</strong>• Reduction in the likelihood of hospital acquired bacteraemia, phlebitis <strong>and</strong>infected/IV lines• Patient is more likely <strong>to</strong> receive <strong>antibiotics</strong> at the correct time <strong>and</strong> missfewer doses• Potential reduction in the risk of adverse effects; errors in preparation aresignificantly higher with IV drugs, compared <strong>to</strong> oral• Reduces patient discomfort <strong>and</strong> enables improved mobility<strong>and</strong> the possibility of earlier discharge from the hospital• Saves both medical <strong>and</strong> nursing time• Potential reduction in treatment costs allowing
The role of risk assessmentsin IV therapy• Choosing the correct vascular access device– central or peripheral• Know the pH <strong>and</strong> osmolality of the IV therapy.• Ensuring the patient is <strong>not</strong> allergic <strong>to</strong> anycomponent of the treatment• Pathway based treatment <strong>to</strong> ensure correctactions are undertaken at the correct time.• Awareness of antibiotic resistance• S<strong>to</strong>p or review dates.
Tips <strong>and</strong> advice for safe <strong>and</strong> effective IVtherapy in practice
OPAT Service.• Patients being discharged with IV <strong>antibiotics</strong> canbe managed in the community by the OPAT team• Save bed days• Better patient experience• Cost saving• Nurse led
Ambula<strong>to</strong>ry Care Pathways• Cellulitis pathway• Admission avoidance• Initially 3 days IV antibiotic bolus• Early oral switch
Multidisciplinary team working• Vascular Access, IV Therapy <strong>and</strong> OPAT CNS• Infection Prevention <strong>and</strong> Control CNS• Consultant Microbiologist• Cystic Fibrosis CNS• Clinical team• Medical Day Unit• ED <strong>and</strong> Minor injury unit• Medical Assessment• Community In-reach
Safe IV Therapy in Practice• Regular IV administration updates for staff• St<strong>and</strong>ardisation of training <strong>and</strong> practice throughoutthe Trust• Learning form incidents through safer meds group• Proactive approach <strong>to</strong> poor practice, embracingclinical supervision.• Competency assess high risk IV therapyadministration –TPN• Care bundles for CVC <strong>and</strong> peripheral cannulas
The Benefits of SuccessfulPeripheral cannulation• Ideal for most IV Antibiotic therapy.• Improve pain initiative outcomes.• Reduce PICC usage based upon more peripheral catheterisations.• Reduce CRBSIs by achieving cannulisation in fewer attempts..• Fewer delays in antibiotic treatments.
Reduce the risk of cannula associatedIV therapy complications• Site cannula with ultrasound or infrared• Site a smaller lumen cannula in the largest veinas far down the arm as possible• Avoid joints <strong>and</strong> bony prominents.This will avoid chemical, mechanical <strong>and</strong> bacterial phlebitis <strong>and</strong>CRBIs.
Vascular Access• Peripheral cannula - Up <strong>to</strong> a week of IVtherapy, can be discharged on OPAT(indwell time 96hours with VIP 0)• Midline Catheter – up <strong>to</strong> 6 weeks, IV bolus withpH range 5-9• PICC up <strong>to</strong> 6 months + - suitable for all IVtherapy• Ports that are in-situ for other therapies can beused (Excluding Parenteral Nutrition)
Other Routes<strong>When</strong> a patient has an enteral tube (e.g. N/G or PEG) in place, oralantibiotic medication may be considered provided that gastricmotility has been established. Consult microbiology team foradvice.Care must be taken <strong>when</strong> <strong>administer</strong>ing <strong>antibiotics</strong> via theenteral tube due <strong>to</strong> the potential for interactions with feeds e.g.ciprofloxacin, flucloxacillin.
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