Antibiotic Guideline for Adult Patients with Spontaneous Bacterial Peritonitis or Liver Cirrhosis with Upper Gastrointestinal Bleed Division & Speciality: Antibiotic Guideline for Adult Patients with Spontaneous Bacterial Peritonitis or Liver Cirrhosis with Upper Gastrointestinal Bleed. Drs Aithal, Ryder and Teli – Consultant Gastroenterologists Mr Tim Hills – Lead Pharmacist Antimicrobials and Infection Control Dr Steve Holden – Consultant Microbiologist. Riya Savjani – Senior Antimicrobial Pharmacist: (May 2017 update) Diagnostics and clinical support, microbiology Scope (Target audience, state if Trust Doctors, nurses, pharmacists Full Title of Guideline: Author (include email and role): wide): Review date (when this version goes out July 2017 of date): Explicit definition of patient group to which it applies (e.g. inclusion and Either patients diagnosed with Spontaneous Bacterial Peritonitis or has liver cirrhosis and an upper GI bleed exclusion criteria, diagnosis): Changes from previous version (not applicable if this is a new guideline, enter below if extensive): Summary of evidence base this guideline has been created from: st 1 line treatment for SBP amended from piperacillin/tazobactam due to shortage. st 1 line antibiotic prophylaxis for GI bleed in cirrhotic patient amended from piperacillin/tazobactam due to shortage SBP treatment in severe penicillin allergy: metronidazole amended from PO to IV Medline literature search 2012-2014 British Society of Gastroenterology Guidelines Recommended best practice based on clinical experience of guideline developers. The Sanford Guide To Antimicrobial Therapy 2012. John Hopkins Guides: Peritonitis, Spontaneous Bacterial & Secondary: Accessed 10/06/2014 This guideline has been registered with the trust. However, clinical guidelines are guidelines only. The interpretation and application of clinical guidelines will remain the responsibility of the individual clinician. If in doubt contact a senior colleague or expert. Caution is advised when using guidelines after the review date or outside of the Trust. Antibiotic Treatment and Prophylaxis of Spontaneous bacterial peritonitis Diagnosis Spontaneous Bacterial Peritonitis (SBP) is a frequent and serious complication of cirrhotic patients with ascites. Patients with SBP are frequently asymptomatic, it occurs in 15% of all those with ascites admitted to hospital irrespective of their symptoms. Diagnosis should also be suspected in cirrhotic patients with ascites presenting with: • Acute deterioration • Hepatic encephalopathy • Impairment of renal function • Peripheral leucocytosis without any obvious precipitating factor Investigations A diagnostic paracentesis is mandatory in all cirrhotic patients with ascites requiring hospital admission. • Inject ascitic fluid into FBC count bottle (lavender EDTA bottle) and send to haematology. Ask for WCC and neutrophils. This should be an urgent request and results should be followed up. SBP is confirmed if: Ascitic fluid WCC of >0.5 x 109/L (> 500 cells/mm3) or neutrophil count of >0.25 x 109/L ( >250 cells/mm3 ) • Ascitic fluid should be inoculated into a sterile universal container and into blood culture bottles at the bedside and sent to microbiology for culture. • DO NOT request glucose and lactate estimation in ascitic fluid routinely. Antibiotic Treatment Initial treatment in severe disease: Total duration for severe disease: 5-7 days 1st Line (including in mild penicillin allergy (e.g. rash only, no anaphylaxis, angioedema or immediate onset urticaria)) Cefuroxime IV 1.5g TDS +/- Metronidazole IV 500mg TDS Severe penicillin allergy/allergic to cephalosporins Ciprofloxacin PO 500mg BD (IV 400mg BD if oral route not available) plus Vancomycin IV Refer to antibiotic website for dosing, or use vancomycin dosing calculator available on the website. [monitor levels] +/- Metronidazole IV 500mg TDS Mild disease/Oral continuation treatment from severe above: (NB see IV to PO switch guideline on the antibiotic website) Total duration for mild disease: 5 days 1st Line Co-trimoxazole PO 960mg BD (Reduce dose to 480mg BD if CrCl <30ml/min - N.B. contains a sulphonamide and trimethoprim) Allergic to sulphonamides and/or trimethoprim Ciprofloxacin PO 500mg BD Nottingham Antibiotic Guidelines Committee Page 2 of 7 Written July 2014 Review July 2017 Antibiotic Prophylaxis Prophylaxis should be given to patients who have recovered from one previous episode of SBP Continuous Prophylaxis Regimen: 1st Line Co-trimoxazole PO 960mg OD (N.B. contains sulphonamide and trimethoprim) Allergic to sulphonamides and/or trimethoprim Ciprofloxacin PO 500mg OD Upper Gastrointestinal Haemorrhage in Patients with Liver Cirrhosis Introduction Bacterial infections occur in about 20% of patients with cirrhosis with upper gastrointestinal bleeding within 48 hours of admission, another 50% will have an infection during their hospital stay. A Cochrane review of randomised trials indicated that antibiotic prophylaxis reduces the risk of infection and mortality in this patient group. Antibiotic Prophylaxis Prophylaxis should be started on admission for all cirrhotic patients with upper gastrointestinal haemorrhage. 1st Line whilst NBM (including in mild penicillin allergy (e.g. rash only, no anaphylaxis, angioedema or immediate onset urticaria)) Cefuroxime IV 1.5g TDS converting once able to Co-trimoxazole PO 960mg BD (Reduce dose to 480mg BD if CrCl <30ml/min - N.B. contains a sulphonamide and trimethoprim) Total duration of antibiotic prophylaxis (IV+PO) is usually 5 days Severe penicillin allergy/allergic to cephalosporins Discuss with medical microbiologist/gastroenterologist Allergic to sulphonamides and/or trimethoprim Discuss with medical microbiologist/gastroenterologist Nottingham Antibiotic Guidelines Committee Page 3 of 7 Written July 2014 Review July 2017 Appendix - Audit tools Spontaneous Bacterial Peritonitis Hospital No. Date of audit: Ascitic tap results WCC >0.5 Y/N Ascitic culture sent Y/N Ascitic Culture results: sensitivity results if positive Blood culture results: sensitivity results if positive Initial SBP antibiotic treatment prescribed: Prophylaxis in line with guidelines Y/N In no, clear justification for deviation in the medical notes: Y/N Changed to PO within 24 hours of patient meeting the IV-PO switch guideline criteria? Y/N In no, clear justification for deviation in the medical notes: Y/N Secondary Antibiotic Prophylaxis prescribed: Prophylaxis in line with guidelines Y/N In no, where was the deviation? Was there a clear justification for deviation in the medical notes: Y/N Subsequent SBP infections whilst on prophylaxis.- Y/N if yes details – organism – resistant to prophylaxis Y/N no. of days after starting prophylaxis: Nottingham Antibiotic Guidelines Committee Page 4 of 7 Written July 2014 Review July 2017 Upper GI bleed. Hospital No. Date of audit: Evidence of cirrhosis Y/N Antibiotic Prophylaxis prescribed: Prophylaxis in-line with guidelines: Y/N In no, clear justification for deviation in the medical notes: Y/N Switched to oral within 24 hours of oral route becoming available: Y/N In no, clear justification for deviation in the medical notes: Y/N Nottingham Antibiotic Guidelines Committee Page 5 of 7 Written July 2014 Review July 2017 Equality Impact Assessment Report 1. Name of Policy or Service Response to external best practice policy 2. Responsible Manager Tim Hills Lead pharmacist antimicrobials and Infection control 3. Name of person Completing EIA Tim Hills Lead pharmacist antimicrobials and Infection control 4. Date EIA Completed 17/6/2014 5. Description and Aims of Policy/Service This guideline describes the management, treatment and prophylaxis of adult patients with spontaneous bacterial peritonitis and adult patients with liver cirrhosis and an upper gastrointestinal haemorrhage. 6. Brief Summary of Research and Relevant Data See information within evidence base on front page 7. Methods and Outcome of Consultation Consultations have been carried out with the following: Antibiotic guidelines committee Comments from the above consultations have been received and incorporated where appropriate. Nottingham Antibiotic Guidelines Committee Page 6 of 7 Written July 2014 Review July 2017 8. Results of Initial Screening or Full Equality Impact Assessment: Equality Group Assessment of Impact Age No Impact Identified Gender No Impact Identified Race No Impact Identified Sexual Orientation No Impact Identified Religion or belief No Impact Identified Disability No Impact Identified Dignity and Human Rights No Impact Identified 9. Working Patterns No Impact Identified Social Deprivation No Impact Identified Decisions and/or Recommendations (including supporting rationale) From the information contained in the procedure, and following the initial screening, it is my decision that a full assessment is not required at the present time. 10. Equality Action Plan (if required) N/A 11. Monitoring and Review Arrangements Review July 2017 Nottingham Antibiotic Guidelines Committee Page 7 of 7 Written July 2014 Review July 2017
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