Liver abscess
- Overview
- Theory
- Diagnosis
- Management
- Follow up
- Resources
Treatment algorithm
Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups: see disclaimer
suspected pyogenic abscess
empiric broad-spectrum antibiotic therapy including coverage for resistant organisms
Broad-spectrum antibiotic therapy should be started empirically when the diagnosis of liver abscess is suspected.[40]Hope WW, Vrochides DV, Newcomb WL, et al. Optimal treatment of hepatic abscess. Am Surg. 2008 Feb;74(2):178-82. http://www.ncbi.nlm.nih.gov/pubmed/18306874?tool=bestpractice.com [41]Ng FH, Wong WM, Wong BC, et al. Sequential intravenous/oral antibiotic vs. continuous intravenous antibiotic in the treatment of pyogenic liver abscess. Aliment Pharmacol Ther. 2002 Jun;16(6):1083-90. http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2036.2002.01266.x/full http://www.ncbi.nlm.nih.gov/pubmed/12030949?tool=bestpractice.com
Initial therapy should target gram-positive, gram-negative, and anaerobic organisms, including Bacteroides species.[8]Johannsen EC, Sifri CD, Madoff LC. Pyogenic liver abscesses. Infect Dis Clin North Am. 2000 Sep;14(3):547-63. http://www.ncbi.nlm.nih.gov/pubmed/10987109?tool=bestpractice.com [19]Feldman M, Friedman LS, Brandt LJ. Brandt. Sleisenger and fordtran's gastrointestinal and liver disease - 2: pathophysiology, diagnosis, management. 11th ed. Elsevier; 2022.
An antibiotic regimen that is particularly broad in its coverage is commenced when the patient is acutely ill with signs of shock or is receiving care in the intensive care unit (ICU).
Antibiotics that cover gram-negative organisms should be used, including piperacillin/tazobactam in monotherapy; imipenem/cilastatin in monotherapy; meropenem in monotherapy; ertapenem in monotherapy or one of cefepime, ceftriaxone, levofloxacin, or ciprofloxacin given with metronidazole.
A fluoroquinolone may be used when there is beta-lactam resistance or intolerance. A fluoroquinolone should not be used as initial empiric therapy if the rate of fluoroquinolone-resistant E coli exceeds 10% in the hospital or local community. Adverse effects may include tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[43]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. 19 March 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products
If a patient has risk factors for extended-spectrum beta-lactamase (ESBL)-producing organisms, treatment with a carbapenem antibiotic (e.g., imipenem/cilastatin, meropenem, or ertapenem) while awaiting culture results should be considered. ESBL-producing organisms have broad antibiotic resistance. Risk factors for infection with ESBL-producing organisms include increased length of stay in the hospital or ICU; presence of central venous catheter, arterial catheter, or urinary catheter; increased severity of illness; hemodialysis; ventilatory assistance; emergency abdominal surgery; prior administration of any antibiotic; gut colonization; and use of a gastrostomy or jejunostomy tube.[44]Giamarellou H. Multidrug resistance in Gram-negative bacteria that produce extended-spectrum beta-lactamases (ESBLs). Clin Microbiol Infect. 2005 Jul;11(suppl 4):1-16. http://www.ncbi.nlm.nih.gov/pubmed/15953019?tool=bestpractice.com [45]Jacoby GA, Munoz-Price LS. The new beta-lactamases. N Engl J Med. 2005 Jan 27;352(4):380-91. http://www.ncbi.nlm.nih.gov/pubmed/15673804?tool=bestpractice.com
Duration of antibiotic treatment depends on the patient's clinical course and the adequacy of drainage. Parenteral therapy is given initially. If the patient is improving and fever and leukocytosis have resolved, the patient can be switched to an oral anti-infective regimen.[41]Ng FH, Wong WM, Wong BC, et al. Sequential intravenous/oral antibiotic vs. continuous intravenous antibiotic in the treatment of pyogenic liver abscess. Aliment Pharmacol Ther. 2002 Jun;16(6):1083-90. http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2036.2002.01266.x/full http://www.ncbi.nlm.nih.gov/pubmed/12030949?tool=bestpractice.com Anti-infective agents can be stopped only if clinical symptoms and signs, including fever and leukocytosis, have resolved and the abscess has been adequately drained.[8]Johannsen EC, Sifri CD, Madoff LC. Pyogenic liver abscesses. Infect Dis Clin North Am. 2000 Sep;14(3):547-63. http://www.ncbi.nlm.nih.gov/pubmed/10987109?tool=bestpractice.com Follow-up imaging may help determine when anti-infective agents can be discontinued. The optimal duration of antibiotics for pyogenic liver abscess is not clear. Treatment duration typically ranges from 2 to 6 weeks with longer courses used in patients with hypervirulent Klebsiella pneumoniae, immunocompromise, inadequate source control.[1]Lam JC, Stokes W. Management of pyogenic liver abscesses: contemporary strategies and challenges. J Clin Gastroenterol. 2023 Sep 1;57(8):774-81. http://www.ncbi.nlm.nih.gov/pubmed/37249909?tool=bestpractice.com Normalization of C-reactive protein values may also help determine when antibiotics can be stopped.[27]Law ST, Li KK. Role of C-reactive protein in response-guided therapy of pyogenic liver abscess. Eur J Gastroenterol Hepatol. 2014 Feb;26(2):179-86. http://www.ncbi.nlm.nih.gov/pubmed/24025976?tool=bestpractice.com Future studies are needed to determine the optimal duration of antibiotics.
Primary options
piperacillin/tazobactam: 3.375 g intravenously every 6 hours
More piperacillin/tazobactamDose consists of 3 g piperacillin plus 0.375 g tazobactam.
OR
imipenem/cilastatin: 500 mg intravenously every 6 hours
More imipenem/cilastatinDose refers to imipenem component.
OR
meropenem: 1-2 g intravenously every 8 hours
OR
ertapenem: 1 g intravenously every 24 hours
OR
cefepime: 1-2 g intravenously every 8 hours
and
metronidazole: 500 mg intravenously every 8 hours
OR
ceftriaxone: 1-2 g intravenously every 12-24 hours
and
metronidazole: 500 mg intravenously every 8 hours
OR
levofloxacin: 500-750 mg intravenously every 24 hours
and
metronidazole: 500 mg intravenously every 8 hours
OR
ciprofloxacin: 400 mg intravenously every 12 hours
and
metronidazole: 500 mg intravenously every 8 hours
intravenous fluids + supportive care
Treatment recommended for ALL patients in selected patient group
In addition, general management of sepsis and septic shock, including resuscitative measures, intravenous fluid replacement, and supportive care, is commenced.[42]Evans L, Rhodes A, Alhazzani W, et al. Surviving sepsis campaign: international guidelines for management of sepsis and septic shock 2021. Crit Care Med. 2021 Nov 1;49(11):e1063-143. https://www.doi.org/10.1097/CCM.0000000000005337 http://www.ncbi.nlm.nih.gov/pubmed/34605781?tool=bestpractice.com
drainage
Treatment recommended for ALL patients in selected patient group
Urgent drainage is warranted if patients present with shock or multiorgan dysfunction.
Patients with severe illness and an Acute Physiology and Chronic Health Evaluation (APACHE) II Score (scoring that classifies severity of illness in intensive care unit patients) ≥15 may benefit from surgical resection rather than percutaneous drainage.[57]Hsieh HF, Chen TW, Yu CY, et al. Aggressive hepatic resection for patients with pyogenic liver abscess and APACHE II score > or =15. Am J Surg. 2008 Sep;196(3):346-50. http://www.ncbi.nlm.nih.gov/pubmed/18718219?tool=bestpractice.com
vancomycin
Treatment recommended for SOME patients in selected patient group
Consider adding vancomycin to any of the first-line (primary) antibiotic regimens above if the patient is severely ill, if MRSA or resistant enterococci are suspected, or if there are gram-positive cocci on the Gram stain of the abscess fluid.
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
antifungal therapy
Treatment recommended for SOME patients in selected patient group
When liver abscess is diagnosed in a patient who is immunocompromised or neutropenic, additional empiric therapy for Candida species should be considered. It is important to seek advice regarding the management of these patients from an infectious disease specialist.
Various possible antifungal agents may be used, including echinocandins (e.g., caspofungin, anidulafungin, and micafungin) or fluconazole. Fluconazole is indicated only for patients who do not have a prior history of azole antifungal therapy (e.g., patients receiving antifungal prophylaxis for bone marrow transplant).
Treatment course: ≥2 weeks of intravenous therapy depending on clinical course.
Primary options
caspofungin: 70 mg intravenously once daily on day 1, followed by 50 mg once daily
OR
anidulafungin: 200 mg intravenously once daily on day 1, followed by 100 mg once daily
OR
micafungin: 100 mg intravenously once daily
OR
fluconazole: 800 mg intravenously/orally once daily on day 1, followed by 400 mg once daily
standard empiric broad-spectrum antibiotic therapy
Broad-spectrum antibiotic therapy should be started empirically when the diagnosis of liver abscess is suspected.[40]Hope WW, Vrochides DV, Newcomb WL, et al. Optimal treatment of hepatic abscess. Am Surg. 2008 Feb;74(2):178-82. http://www.ncbi.nlm.nih.gov/pubmed/18306874?tool=bestpractice.com [41]Ng FH, Wong WM, Wong BC, et al. Sequential intravenous/oral antibiotic vs. continuous intravenous antibiotic in the treatment of pyogenic liver abscess. Aliment Pharmacol Ther. 2002 Jun;16(6):1083-90. http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2036.2002.01266.x/full http://www.ncbi.nlm.nih.gov/pubmed/12030949?tool=bestpractice.com In stable patients, antibiotic therapy may be deferred until after drainage or aspiration if the procedure can be performed soon after the diagnosis is suspected.
Initial therapy should target gram-positive, gram-negative, and anaerobic organisms, including Bacteroides species.[8]Johannsen EC, Sifri CD, Madoff LC. Pyogenic liver abscesses. Infect Dis Clin North Am. 2000 Sep;14(3):547-63. http://www.ncbi.nlm.nih.gov/pubmed/10987109?tool=bestpractice.com [19]Feldman M, Friedman LS, Brandt LJ. Brandt. Sleisenger and fordtran's gastrointestinal and liver disease - 2: pathophysiology, diagnosis, management. 11th ed. Elsevier; 2022.
A fluoroquinolone should not be used as initial empiric therapy if the rates of fluoroquinolone-resistant E coli exceed 10% in the hospital or local community. Adverse effects may include tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[43]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. 19 March 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products
Once the infective organism is confirmed on culture, the regimen can be adjusted appropriately. Any of the fluoroquinolones may be used when there is beta-lactam resistance or intolerance.
Duration of antibiotic treatment depends on the patient's clinical course and the adequacy of drainage. Parenteral therapy is given initially. If the patient is improving and fever and leukocytosis have resolved, the patient can be switched to an oral anti-infective regimen.[41]Ng FH, Wong WM, Wong BC, et al. Sequential intravenous/oral antibiotic vs. continuous intravenous antibiotic in the treatment of pyogenic liver abscess. Aliment Pharmacol Ther. 2002 Jun;16(6):1083-90. http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2036.2002.01266.x/full http://www.ncbi.nlm.nih.gov/pubmed/12030949?tool=bestpractice.com Anti-infective agents can be stopped only if clinical symptoms and signs, including fever and leukocytosis, have resolved and the abscess has been adequately drained.[8]Johannsen EC, Sifri CD, Madoff LC. Pyogenic liver abscesses. Infect Dis Clin North Am. 2000 Sep;14(3):547-63. http://www.ncbi.nlm.nih.gov/pubmed/10987109?tool=bestpractice.com Follow-up imaging may help determine when anti-infective agents can be discontinued. The optimal duration of antibiotics for pyogenic liver abscess is not clear. Treatment duration typically ranges from 2 to 6 weeks with longer courses used in patients with hypervirulent Klebsiella pneumoniae, immunocompromise, inadequate source control.[1]Lam JC, Stokes W. Management of pyogenic liver abscesses: contemporary strategies and challenges. J Clin Gastroenterol. 2023 Sep 1;57(8):774-81. http://www.ncbi.nlm.nih.gov/pubmed/37249909?tool=bestpractice.com Normalization of C-reactive protein values may also help determine when antibiotics can be stopped.[27]Law ST, Li KK. Role of C-reactive protein in response-guided therapy of pyogenic liver abscess. Eur J Gastroenterol Hepatol. 2014 Feb;26(2):179-86. http://www.ncbi.nlm.nih.gov/pubmed/24025976?tool=bestpractice.com Future studies are needed to determine the optimal duration of antibiotics.
Primary options
levofloxacin: 500-750 mg intravenously/orally every 24 hours
and
metronidazole: 500 mg intravenously/orally every 8 hours
OR
ciprofloxacin: 400 mg intravenously every 12 hours, or 750 mg orally twice daily
and
metronidazole: 500 mg intravenously/orally every 8 hours
OR
moxifloxacin: 400 mg intravenously/orally every 24 hours
and
metronidazole: 500 mg intravenously/orally every 8 hours
OR
ceftriaxone: 1-2 g intravenously every 12-24 hours
and
metronidazole: 500 mg intravenously every 8 hours
OR
cefotaxime: 1-2 g intravenously every 6-8 hours
and
metronidazole: 500 mg intravenously every 8 hours
drainage
Treatment recommended for SOME patients in selected patient group
For most abscesses, drainage is an important step in treatment, along with antibiotic therapy. For liver abscesses <3 cm in diameter, antibiotics alone may be sufficient to treat the abscess.[40]Hope WW, Vrochides DV, Newcomb WL, et al. Optimal treatment of hepatic abscess. Am Surg. 2008 Feb;74(2):178-82. http://www.ncbi.nlm.nih.gov/pubmed/18306874?tool=bestpractice.com
The abscess can be drained by needle aspiration (most commonly under radiographic guidance), placement of an indwelling catheter (most commonly under radiographic guidance), open or laparoscopic surgical drainage, surgical resection of the abscess, or endoscopic drainage (in cases of a biliary origin of infection).
The choice as to which type of drainage procedure is performed depends on several factors, including the size, location, and complexity of the abscess.
antifungal therapy
Treatment recommended for SOME patients in selected patient group
When liver abscess is diagnosed in a patient who is immunocompromised or neutropenic, additional empiric therapy for Candida species should be considered. It is important to seek advice regarding the management of these patients from an infectious disease specialist.
Various possible antifungal agents may be used, including echinocandins (e.g., caspofungin, anidulafungin, and micafungin) or fluconazole. Fluconazole is indicated only for patients who do not have a prior history of azole antifungal therapy (e.g., patients receiving antifungal prophylaxis for bone marrow transplant).
Treatment course: ≥2 weeks of intravenous therapy depending on clinical course.
Primary options
caspofungin: 70 mg intravenously once daily on day 1, followed by 50 mg once daily
OR
anidulafungin: 200 mg intravenously once daily on day 1, followed by 100 mg once daily
OR
micafungin: 100 mg intravenously once daily
OR
fluconazole: 800 mg intravenously/orally once daily on day 1, followed by 400 mg once daily
alternative empiric broad-spectrum antibiotic therapy
Alternative antibiotics may be used when drug-resistant or gram-negative pathogens are suspected. Antibiotics that cover gram-negative organisms include piperacillin/tazobactam, imipenem/cilastatin, meropenem, ertapenem, and cefepime administered with metronidazole.
A carbapenem antibiotic (e.g., imipenem/cilastatin, meropenem, or ertapenem) should be considered with risk factors for extended-spectrum beta-lactamase-producing organisms. Risk factors include increased length of stay in the hospital or intensive care unit; presence of central venous catheter, arterial catheter, or urinary catheter; increased severity of illness; hemodialysis; ventilatory assistance; emergency abdominal surgery; prior administration of any antibiotic; gut colonization; and use of a gastrostomy or jejunostomy tube.[44]Giamarellou H. Multidrug resistance in Gram-negative bacteria that produce extended-spectrum beta-lactamases (ESBLs). Clin Microbiol Infect. 2005 Jul;11(suppl 4):1-16. http://www.ncbi.nlm.nih.gov/pubmed/15953019?tool=bestpractice.com [45]Jacoby GA, Munoz-Price LS. The new beta-lactamases. N Engl J Med. 2005 Jan 27;352(4):380-91. http://www.ncbi.nlm.nih.gov/pubmed/15673804?tool=bestpractice.com
If amebic abscess is considered (not as the most likely diagnosis but as a consideration along with other infective causes of liver abscess), then metronidazole should be included as part of the antibiotic regimen. This is preferable to using tinidazole because metronidazole also covers anaerobic pathogens.
Duration of antibiotic treatment depends on the patient's clinical course and the adequacy of drainage. Parenteral therapy is given initially. If the patient is improving and fever and leukocytosis have resolved, the patient can be switched to an oral anti-infective regimen.[41]Ng FH, Wong WM, Wong BC, et al. Sequential intravenous/oral antibiotic vs. continuous intravenous antibiotic in the treatment of pyogenic liver abscess. Aliment Pharmacol Ther. 2002 Jun;16(6):1083-90. http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2036.2002.01266.x/full http://www.ncbi.nlm.nih.gov/pubmed/12030949?tool=bestpractice.com Anti-infective agents can be stopped only if clinical symptoms and signs, including fever and leukocytosis, have resolved and the abscess has been adequately drained.[8]Johannsen EC, Sifri CD, Madoff LC. Pyogenic liver abscesses. Infect Dis Clin North Am. 2000 Sep;14(3):547-63. http://www.ncbi.nlm.nih.gov/pubmed/10987109?tool=bestpractice.com Follow-up imaging may help determine when anti-infective agents can be discontinued. The optimal duration of antibiotics for pyogenic liver abscess is not clear. Treatment duration typically ranges from 2 to 6 weeks with longer courses used in patients with hypervirulent Klebsiella pneumoniae, immunocompromise, inadequate source control.[1]Lam JC, Stokes W. Management of pyogenic liver abscesses: contemporary strategies and challenges. J Clin Gastroenterol. 2023 Sep 1;57(8):774-81. http://www.ncbi.nlm.nih.gov/pubmed/37249909?tool=bestpractice.com Normalization of C-reactive protein values may also help determine when antibiotics can be stopped.[27]Law ST, Li KK. Role of C-reactive protein in response-guided therapy of pyogenic liver abscess. Eur J Gastroenterol Hepatol. 2014 Feb;26(2):179-86. http://www.ncbi.nlm.nih.gov/pubmed/24025976?tool=bestpractice.com Future studies are needed to determine the optimal duration of antibiotics.
Primary options
piperacillin/tazobactam: 3.375 g intravenously every 6 hours
More piperacillin/tazobactamDose consists of 3 g piperacillin plus 0.375 g tazobactam.
OR
imipenem/cilastatin: 500 mg intravenously every 6 hours
More imipenem/cilastatinDose refers to imipenem component.
OR
meropenem: 1-2 g intravenously every 8 hours
OR
ertapenem: 1 g intravenously every 24 hours
More ertapenemOnce-daily dosing, does not cover Pseudomonas.
OR
cefepime: 1-2 g intravenously every 8 hours
and
metronidazole: 500 mg intravenously every 8 hours
vancomycin
Treatment recommended for SOME patients in selected patient group
Vancomycin may be included when the patient is not improving with first-line antibiotics, when Gram stain reveals gram-positive cocci, or when a resistant enterococcal or staphylococcal infection is suspected.
Primary options
vancomycin: 15-20 mg/kg intravenously every 8-12 hours
drainage
Treatment recommended for SOME patients in selected patient group
For most abscesses, drainage is an important step in treatment, along with antibiotic therapy. For liver abscesses <3 cm in diameter, antibiotics alone may be sufficient to treat the abscess.[40]Hope WW, Vrochides DV, Newcomb WL, et al. Optimal treatment of hepatic abscess. Am Surg. 2008 Feb;74(2):178-82. http://www.ncbi.nlm.nih.gov/pubmed/18306874?tool=bestpractice.com
The abscess can be drained by needle aspiration (most commonly under radiographic guidance), placement of an indwelling catheter (most commonly under radiographic guidance), open or laparoscopic surgical drainage, surgical resection of the abscess, or endoscopic drainage (in cases of a biliary origin of infection).
The choice as to which type of drainage procedure is performed depends on several factors, including the size, location, and complexity of the abscess.
antifungal therapy
Treatment recommended for SOME patients in selected patient group
When liver abscess is diagnosed in a patient who is immunocompromised or neutropenic, additional empiric therapy for Candida species should be considered. It is important to seek advice regarding the management of these patients from an infectious disease specialist.
Various possible antifungal agents may be used, including echinocandins (e.g., caspofungin, anidulafungin, and micafungin) or fluconazole. Fluconazole is indicated only for patients who do not have a prior history of azole antifungal therapy (e.g., patients receiving antifungal prophylaxis for bone marrow transplant).
Treatment course: ≥2 weeks of intravenous therapy depending on clinical course.
Primary options
caspofungin: 70 mg intravenously once daily on day 1, followed by 50 mg once daily
OR
anidulafungin: 200 mg intravenously once daily on day 1, followed by 100 mg once daily
OR
micafungin: 100 mg intravenously once daily
OR
fluconazole: 800 mg intravenously/orally once daily on day 1, followed by 400 mg once daily
suspected amebic abscess
nitroimidazole
Patients with amebic liver abscess (either confirmed or presumed highly likely as the cause of the abscess) are treated with a nitroimidazole.[60]Haque R, Huston CD, Hughes M, et al. Amebiasis. New Engl J Med. 2003 Apr 17;348(16):1565-73. http://www.ncbi.nlm.nih.gov/pubmed/12700377?tool=bestpractice.com [61]Stanley SL Jr. Amoebiasis. Lancet. 2003 Mar 22;361(9362):1025-34. http://www.ncbi.nlm.nih.gov/pubmed/12660071?tool=bestpractice.com [68]Fung HB, Doan TL. Tinidazole: a nitroimidazole antiprotozoal agent. Clin Ther. 2005 Dec;27(12):1859-84. http://www.ncbi.nlm.nih.gov/pubmed/16507373?tool=bestpractice.com If a patient is unable to take oral medications or is severely ill, intravenous metronidazole can be used.
Treatment course: 7-10 days (metronidazole) or 3 days (tinidazole).
Primary options
metronidazole: 500-750 mg orally three times daily; or 500 mg intravenously every 8 hours
OR
tinidazole: 2000 mg orally once daily
drainage
Treatment recommended for SOME patients in selected patient group
Drainage of the abscess is not usually required but is necessary if the patient does not respond to antibiotic therapy, the abscess is >5 cm in diameter, there are left-lobe lesions, there is high risk of rupture, or the exact diagnosis is still in doubt.[11]Petri WA Jr, Singh U. Diagnosis and management of amebiasis. Clin Infect Dis. 1999 Nov;29(5):1117-25. https://academic.oup.com/cid/article/29/5/1117/337264/Diagnosis-and-Management-of-Amebiasis http://www.ncbi.nlm.nih.gov/pubmed/10524950?tool=bestpractice.com [60]Haque R, Huston CD, Hughes M, et al. Amebiasis. New Engl J Med. 2003 Apr 17;348(16):1565-73. http://www.ncbi.nlm.nih.gov/pubmed/12700377?tool=bestpractice.com [61]Stanley SL Jr. Amoebiasis. Lancet. 2003 Mar 22;361(9362):1025-34. http://www.ncbi.nlm.nih.gov/pubmed/12660071?tool=bestpractice.com [62]Chavez-Tapia NC, Hernandez-Calleros J, et al. Image-guided percutaneous procedure plus metronidazole versus metronidazole alone for uncomplicated amoebic liver abscess. Cochrane Database Syst Rev. 2009 Jan 21;(1):CD004886. http://onlinelibrary.wiley.com/doi/10.1002/14651858.CD004886.pub2/full http://www.ncbi.nlm.nih.gov/pubmed/19160244?tool=bestpractice.com
Percutaneous drainage is the most common method, but other drainage techniques (e.g., surgical drainage) may be used.
pyogenic abscess: following response to intravenous antibiotic therapy
switch to oral therapy
The duration of antibiotic therapy (with or without antifungal therapy) depends on the patient's clinical course and the adequacy of drainage.
Parenteral therapy is given initially. If the patient is improving and fever and leukocytosis have resolved, the patient can be switched to an oral antibiotic (with or without oral antifungal) regimen.[41]Ng FH, Wong WM, Wong BC, et al. Sequential intravenous/oral antibiotic vs. continuous intravenous antibiotic in the treatment of pyogenic liver abscess. Aliment Pharmacol Ther. 2002 Jun;16(6):1083-90. http://onlinelibrary.wiley.com/doi/10.1046/j.1365-2036.2002.01266.x/full http://www.ncbi.nlm.nih.gov/pubmed/12030949?tool=bestpractice.com The choice of oral regimen depends on the specific pathogen isolated and the reported sensitivities.
Antibiotics and antifungals can be stopped only if clinical symptoms and signs, including fever and leukocytosis, have resolved and the abscess has been adequately drained.[8]Johannsen EC, Sifri CD, Madoff LC. Pyogenic liver abscesses. Infect Dis Clin North Am. 2000 Sep;14(3):547-63. http://www.ncbi.nlm.nih.gov/pubmed/10987109?tool=bestpractice.com Normalization of C-reactive protein values may help determine when antibiotics can be stopped.[27]Law ST, Li KK. Role of C-reactive protein in response-guided therapy of pyogenic liver abscess. Eur J Gastroenterol Hepatol. 2014 Feb;26(2):179-86. http://www.ncbi.nlm.nih.gov/pubmed/24025976?tool=bestpractice.com Follow-up imaging may also help determine when antibiotics and antifungals can be discontinued. The optimal duration of antibiotics for pyogenic liver abscess is not clear. Treatment duration typically ranges from 2 to 6 weeks with longer courses used in patients with hypervirulent Klebsiella pneumoniae, immunocompromise, inadequate source control.[1]Lam JC, Stokes W. Management of pyogenic liver abscesses: contemporary strategies and challenges. J Clin Gastroenterol. 2023 Sep 1;57(8):774-81. http://www.ncbi.nlm.nih.gov/pubmed/37249909?tool=bestpractice.com Future studies are needed to determine the optimal duration of antibiotics.
Oral regimens should be based on antimicrobial susceptibilities.
Adverse effects of fluoroquinolones may include tendonitis, tendon rupture, arthralgia, neuropathies, and other musculoskeletal or nervous system effects.[43]European Medicines Agency. Quinolone- and fluoroquinolone-containing medicinal products. 19 March 2019 [internet publication]. https://www.ema.europa.eu/en/medicines/human/referrals/quinolone-fluoroquinolone-containing-medicinal-products
Primary options
levofloxacin: 500-750 mg orally every 24 hours
and
metronidazole: 500 mg orally every 8 hours
OR
ciprofloxacin: 500-750 mg orally twice daily
and
metronidazole: 500 mg orally every 8 hours
OR
moxifloxacin: 400 mg orally every 24 hours
and
metronidazole: 500 mg orally every 8 hours
OR
amoxicillin/clavulanate: 500 mg orally every 8 hours, or 875 mg orally every 12 hours, or 2000 mg orally (extended-release) every 12 hours
amebic abscess: following response to nitroimidazole therapy
luminal agent
Patients who have responded to treatment for amebic abscess with nitroimidazoles, with or without aspiration, should also be commenced on a luminal agent (e.g., paromomycin) to eradicate gut colonization and prevent relapse of amebiasis.[65]Drugs for parasitic infections. Med Lett. 2004 Aug;46:e1-12. This is commenced following completion of the acute antibiotic course.
Treatment course: 7 days.
Primary options
paromomycin: 25-35 mg/kg/day orally given in 3 divided doses
abscess recurrence
retreatment + investigation for biliary abnormalities
There are no set guidelines or recommendations for treatment of a recurrent abscess that differ from the first occurrence. Patients with underlying biliary disease have the highest rate of recurrence (25%).[66]Cheng HC, Chang WL, Chen WY, et al. Long-term outcome of pyogenic liver abscess: factors related with abscess recurrence. J Clin Gastroenterol. 2008 Nov-Dec;42(10):1110-5. http://www.ncbi.nlm.nih.gov/pubmed/18458641?tool=bestpractice.com Potential etiologies include biliary obstruction and a fistula between the biliary tree and the intestine. If a liver abscess recurs, the authors would recommend that expert consultation by a gastroenterologist and investigation for biliary abnormalities by endoscopic retrograde cholangiopancreatography or magnetic resonance cholangiopancreatography should be considered.
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Please note that formulations/routes and doses may differ between drug names and brands, drug formularies, or locations. Treatment recommendations are specific to patient groups. See disclaimer
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