Spontaneous bacterial peritonitis medical therapy: Difference between revisions
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# Patients with ascites admitted to the hospital should undergo abdominal paracentesis. Paracentesis should be repeated in patients (whether in the hospital or not) who develop signs or symptoms or laboratory abnormalities suggestive of infection (e.g., abdominal pain or tenderness, fever, encephalopathy, renal failure, acidosis, or peripheral leukocytosis). | # Patients with [[ascites]] admitted to the hospital should undergo abdominal [[paracentesis]]. [[Paracentesis]] should be repeated in patients (whether in the hospital or not) who develop signs or symptoms or laboratory abnormalities suggestive of [[infection]] (e.g., [[abdominal pain]] or [[tenderness]], [[fever]], [[encephalopathy]], [[renal failure]], [[acidosis]], or peripheral [[leukocytosis]]). | ||
# Patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm<sup>3</sup> in a community-acquired setting in the absence of recent beta-lactam antibiotic exposure should receive empiric antibiotic therapy, e.g., an intravenous third-generation cephalosporin, preferably cefotaxime 2 g every 8 hours. | # Patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm<sup>3</sup> in a community-acquired setting in the absence of recent beta-lactam antibiotic exposure should receive empiric antibiotic therapy, e.g., an intravenous third-generation cephalosporin, preferably cefotaxime 2 g every 8 hours. | ||
# Patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm<sup>3</sup> in a nosocomial setting and/or in the presence of recent beta-lactam antibiotic exposure should receive empiric antibiotic therapy based on local susceptibility testing of bacteria in patients with cirrhosis. | # Patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm<sup>3</sup> in a nosocomial setting and/or in the presence of recent beta-lactam antibiotic exposure should receive empiric antibiotic therapy based on local susceptibility testing of bacteria in patients with cirrhosis. |
Revision as of 21:22, 16 June 2014
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aditya Govindavarjhulla, M.B.B.S. [2], Chetan Lokhande, M.B.B.S [3], Guillermo Rodriguez Nava, M.D. [4], Alejandro Lemor, M.D. [5]
Overview
Empiric broad-spectrum intravenous antibiotic, preferably with a third generation cephalosporin such as cefotaxime, is warranted for suspected or established spontaneous bacterial peritonitis (SBP) to cover the most common isolates including Escherichia coli, Klebsiella pneumoniae, and Streptococcus pneumoniae. Oral ofloxacin may be considered in selected cases. Albumin should be reserved for patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm3 and clinical suspicion of SBP, who also have a serum creatinine >1 mg/dL, blood urea nitrogen >30 mg/dL, or total bilirubin >4 mg/dL.
Empiric Therapy Adapted from AASLD Practice Guidelines: Management of Adult Patients with Ascites Due to Cirrhosis.[1]
Spontaneous Bacterial Peritonitis |
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Preferred Regimen |
▸ Cefotaxime 2 g IV q8h (or 2 g IV q4h if life-threatening) OR ▸ Ticarcillin–Clavulanate 3.1 g IV q4–6h OR ▸ Piperacillin–Tazobactam 3.375 g IV q6h (or 4.5 g IV q8h) OR ▸ Ceftriaxone 1–2 g IV q12–24h OR ▸ Ertapenem 1 g IV q24h |
For ESBL–producing Enterobacteriaceae, check susceptibility testing. |
▸ Doripenem 500 mg IV q8h (1–hr infusion) OR ▸ Ertapenem 1 g IV q24h OR ▸ Imipenem–Cilastatin 0.5–1 g IV q6–8h OR ▸ Meropenem 1 g IV q8h OR ▸ Ciprofloxacin 400 mg IV q12h OR ▸ Levofloxacin 750 mg IV q24h OR ▸ Moxifloxacin 400 mg IV q24h |
- Empiric antibiotic therapy should be administered to patients with ascitic fluid PMN counts greater than or equal to 250 cells/mm3 in a clinical setting compatible with ascitic fluid infection or those who have convincing signs or symptoms of infection (fever, abdominal pain, or unexplained encephalopathy) regardless of the PMN count in the ascitic fluid.[2][3]
- The 3 most common isolates from the ascitic fluid are Escherichia coli, Klebsiella pneumoniae, and Streptococcus pneumoniae.
- Relatively broad-spectrum therapy, preferably with cefotaxime, is warranted until the results of susceptibility testing are available.
- Infection with multiresistant organism including Extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae, Pseudomonas aeruginosa, methicillin-resistant Staphylococcus aureus (MRSA), and Enterococcus faecium is associated with an increased mortality. Risk factors for multiresistant infections include:[4]
- Nosocomial origin of infection
- Long-term norfloxacin prophylaxis
- Recent infection with multiresistant bacteria
- Recent use of beta-lactams
- Oral ofloxacin may be used alternatively in selected cases such as patients without vomiting, shock, grade II (or higher) hepatic encephalopathy, or serum creatinine greater than 3 mg/dL.[5]
Adjunctive Therapy
- Albumin infusion should be administered to cirrhotic patients with spontaneous bacterial peritonitis in the following conditions:[6]
- Serum creatinine> 1 mg/dL
- Blood urea nitrogen >30 mg/dL
- Total bilirubin >4 mg/dL
- Adjunctive intravenous albumin at a dose of 1.5 g/kg at the time of diagnosis, followed by 1 g/kg on day 3 is associated with a reduced incidence of renal impairment and death in comparison with treatment with an antibiotic alone.[7]
- The use of non-selective beta blockers in cirrhotic patients with SBP should be discouraged since it is associated with an increased risk for hemodynamic compromise, prolonged hospitalization, hepatorenal syndrome, acute kidney injury.[8]
AASLD Recommendations for the Management of Spontaneous Bacterial Peritonitis
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References
- ↑ "Management of Adult Patients with Ascites Due to Cirrhosis: Update 2012" (PDF).
- ↑ Runyon, Bruce A (2013-04). "Introduction to the revised American Association for the Study of Liver Diseases Practice Guideline management of adult patients with ascites due to cirrhosis 2012". Hepatology (Baltimore, Md.). 57 (4): 1651–1653. doi:10.1002/hep.26359. ISSN 1527-3350. PMID 23463403. Unknown parameter
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ignored (help); Check date values in:|date=
(help) - ↑ Hoefs, J C (1982-08). "Spontaneous bacterial peritonitis". Hepatology (Baltimore, Md.). 2 (4): 399–407. ISSN 0270-9139. PMID 7095741. Unknown parameter
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(help) - ↑ Fernández, Javier (2012-05). "Prevalence and risk factors of infections by multiresistant bacteria in cirrhosis: a prospective study". Hepatology (Baltimore, Md.). 55 (5): 1551–1561. doi:10.1002/hep.25532. ISSN 1527-3350. PMID 22183941. Unknown parameter
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(help) - ↑ Navasa, M (1996-10). "Randomized, comparative study of oral ofloxacin versus intravenous cefotaxime in spontaneous bacterial peritonitis". Gastroenterology. 111 (4): 1011–1017. ISSN 0016-5085. PMID 8831596. Unknown parameter
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(help) - ↑ Sigal, Samuel H (2007-04). "Restricted use of albumin for spontaneous bacterial peritonitis". Gut. 56 (4): 597–599. doi:10.1136/gut.2006.113050. ISSN 0017-5749. PMC 1856861. PMID 17369392. Unknown parameter
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(help) - ↑ Sort, P (1999-08-05). "Effect of intravenous albumin on renal impairment and mortality in patients with cirrhosis and spontaneous bacterial peritonitis". The New England journal of medicine. 341 (6): 403–409. doi:10.1056/NEJM199908053410603. ISSN 0028-4793. PMID 10432325. Unknown parameter
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ignored (help) - ↑ Mandorfer, Mattias (2014-06). "Nonselective β Blockers Increase Risk for Hepatorenal Syndrome and Death in Patients With Cirrhosis and Spontaneous Bacterial Peritonitis". Gastroenterology. 146 (7): 1680–1690.e1. doi:10.1053/j.gastro.2014.03.005. ISSN 1528-0012. PMID 24631577. Unknown parameter
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(help)