Sandbox/intraabdominal
Overview
Definitions
From a clinical view, intra-abdominal infections can be classified in:[1][2][3]
- Uncomplicated, in which the infectious process involves only a single organ and there is no anatomical disruption
- Complicated, in which the infectious process extends beyond the hollow viscus into the peritoneal space and is associated with abscess formation or peritonitits.
Patients with uncomplicated intra-abdominal infections usually do not need antimicrobial therapy besides perioperative prophylaxis and can be managed with surgery alone (i.e. appendicitis).
A health care-associated infection is a new term that describe patients that have a close contact with health systems, they include community-onset infection and hospital-onset infection. The following table describes the two types of health care-associated infection that would guide the therapeutic regimen. [1]
Community-onset infection | Hospital-onset infection |
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Includes patients with 1 or more of the following conditions: | Includes patients with positive culture results obtained >48 h after admission. Patients might also have 1 of the conditions described in community-onset infection. |
Principles of Therapy for Complicated Intra-abdominal Infection
The following table describes the factors that define a high risk infection, due to an increase chance of treatment failure and a more severe infection.[4]
Clinical factors for high risk patients |
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Delay in the initial intervention (>24 h) |
APACHE II score ≥ 15 |
Advanced age (>70 years) |
Comorbidity and degree of organ dysfunction |
Low albumin level |
Poor nutrition status |
Degree of peritoneal involvement or diffuse peritonitis |
Inability to achieve adequate debridement or control of drainage |
Presence of malignancy |
- All patients should undergo a source control procedure to clear infected foci.[5]
- Patients should undergo fluid resuscitation to restore cardiovascular homeostasis. For patients with septic shock, follow The Surviving Sepsis Campaign guidelines for managing septic shock.[6]
- If the diagnosis of intra-abdominal infection is confirmed or is considered highly likely, antibiotics should be initiated immediately.
- Patients without septic shock should receive the proper [antibiotics]] in the emergency department.[6]
- Only cultures from the site of infection should be obtained from higher-risk patients, for patients with lower-risk community-acquired infection, cultures are optional.[1]
- Sensibility testing for Pseudomonas, Proteus, Acinetobacter, Staphylococcus aureus, and Enterobacteriaceae should be done, as this organisms have shown higher resistance rates in recent years.[7]
- Lower-risk patients with community-acquired intra-abdominal infection which show favorable clinical progress do not require modification of therapy.
- If microorganisms with high pathogenic potential are found, susceptibility results should be used to determine antibiotic therapy in high-severity community-acquired or health care-associated infection.
- The recommended duration of therapy is 4-7 days.[8]
- Completion of the antibiotic course with oral presentations can be considered if the patient evolves favorably, is able to tolerate an oral diet and if his susceptibility studies do not show resistant microorganisms.[9]
Extra-biliary Complicated Intra-abdominal Infection
Community-Acquired
▸ Click on the following categories to expand treatment regimens.
Children ▸ Single agent ▸ Combination Adults - Mild to Moderate ▸ Single agent ▸ Combination Adults - Severe ▸ Single agent ▸ Combination |
|
Health Care-Associated
▸ Click on the following categories to expand treatment regimens.
▸ Gram-Negative Bacilli (<20% multidrug resistance) ▸ ESBL-Enterobacteriaceae ▸ P. aeruginosa (>20% resistant to ceftazidime) ▸ Methicillin-resistant S. aureus ▸ Candida spp |
|
Biliary Infection
Community-acquired Acute Cholecystitis
▸ Click on the following categories to expand treatment regimens.
Acute Cholecystitis ▸ Mild-to-moderate ▸ Severe Special Considerations ▸ Acute Cholangitis after Bilio-enteric Anastomosis ▸ Acute Cholecystitis in Advanced age ▸ Acute Cholecystitis in Immunocompromised
|
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Health Care-Associated Biliary Infection
Biliary Infection of any severity |
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▸ Meropenem 1 g IV q8h OR ▸ Imipenem/Cilastatin 500 mg IV q6h or 1 g q8h OR ▸ Doripenem 500 mg IV q8h OR ▸ Piperacillin-Tazobactam 3.375 g IV q6h OR ▸ Ciprofloxacin 400 mg IV q12h OR ▸ Levofloxacin 750 mg IV q24h OR ▸ Cefepime 2 g IV q8-12h |
PLUS |
▸ Metronidazole 500 mg IV q8-12h OR ▸ Metronidazole 1.5 g IV q24h |
PLUS |
▸ Vancomycin 15–20 mg/kg IV q8-12h |
References
- ↑ 1.0 1.1 1.2 Solomkin JS, Mazuski JE, Bradley JS, Rodvold KA, Goldstein EJ, Baron EJ; et al. (2010). "Diagnosis and management of complicated intra-abdominal infection in adults and children: guidelines by the Surgical Infection Society and the Infectious Diseases Society of America". Clin Infect Dis. 50 (2): 133–64. doi:10.1086/649554. PMID 20034345.
- ↑ Mazuski JE, Solomkin JS (2009). "Intra-abdominal infections". Surg Clin North Am. 89 (2): 421–37, ix. doi:10.1016/j.suc.2008.12.001. PMID 19281892.
- ↑ Blot S, De Waele JJ (2005). "Critical issues in the clinical management of complicated intra-abdominal infections". Drugs. 65 (12): 1611–20. PMID 16060697.
- ↑ Koperna T, Schulz F (1996). "Prognosis and treatment of peritonitis. Do we need new scoring systems?". Arch Surg. 131 (2): 180–6. PMID 8611076.
- ↑ Marshall JC, Maier RV, Jimenez M, Dellinger EP (2004). "Source control in the management of severe sepsis and septic shock: an evidence-based review". Crit Care Med. 32 (11 Suppl): S513–26. PMID 15542959.
- ↑ 6.0 6.1 Dellinger RP, Levy MM, Rhodes A, Annane D, Gerlach H, Opal SM; et al. (2013). "Surviving Sepsis Campaign: international guidelines for management of severe sepsis and septic shock, 2012". Intensive Care Med. 39 (2): 165–228. doi:10.1007/s00134-012-2769-8. PMID 23361625.
- ↑ Hawser SP, Bouchillon SK, Hoban DJ, Badal RE (2009). "In vitro susceptibilities of aerobic and facultative anaerobic Gram-negative bacilli from patients with intra-abdominal infections worldwide from 2005-2007: results from the SMART study". Int J Antimicrob Agents. 34 (6): 585–8. doi:10.1016/j.ijantimicag.2009.07.013. PMID 19748234.
- ↑ Solomkin JS, Mazuski JE, Baron EJ, Sawyer RG, Nathens AB, DiPiro JT; et al. (2003). "Guidelines for the selection of anti-infective agents for complicated intra-abdominal infections". Clin Infect Dis. 37 (8): 997–1005. doi:10.1086/378702. PMID 14523762.
- ↑ Solomkin JS, Dellinger EP, Bohnen JM, Rostein OD (1998). "The role of oral antimicrobials for the management of intra-abdominal infections". New Horiz. 6 (2 Suppl): S46–52. PMID 9654311.