Intra-Abdominal Candidiasis,

Intra-Abdominal Candidiasis,
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Intra-abdominal candidiasis is an important clinical entity with diverse manifestations and risk factors. Learn about its classification, common forms, microbiology, clinical features, and management strategies. Explore the spectrum of disease and understand the different types of peritonitis associated with Candida infections.

  • Candidiasis
  • Peritonitis
  • Microbiology
  • Clinical Manifestations
  • Risk Factors

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  1. Intra-Abdominal Candidiasis, Candida peritonitis Paschalis Vergidis, MD, MSc Infectious Diseases Consultant Manchester University NHS Foundation Trust

  2. Learning Objectives To understand the different forms of intra-abdominal candidiasis To discuss the risk factors for intra-abdominal candidiasis To review the management and outcomes of intra-abdominal candidiasis

  3. Spectrum of Disease Kullberg BJ, Arendrup M. NEJM 2015; 373: 1445-1456

  4. Intra-Abdominal Candidiasis Common form of deep-seated candidiasis Poorly studied compared to candidaemia Accounts for ~10% of all cases of peritonitis Bacterial co-infection is common

  5. Classification Primary peritonitis No apparent breach of the GI tract Secondary Peritonitis Follows perforations, surgical leaks, trauma or other pathological process Tertiary Peritonitis Persistence or recurrence of intra-abdominal infection following treatment Intra-Abdominal Abscess Localized infection resulting from pathological process or breach of the GI tract Infected Pancreatic Necrosis Infection of the non-vitalized pancreatic tissue Cholecystitis, cholangitis Vergidis et al. PLoS ONE. 2016; 11(4). e0153247

  6. Risk factors Recurrent GI surgery GI tract perforations GI anastomosis leakage Acquisition can be: Community-acquired Hospital-acquired Healthcare-associated Prolonged broad-spectrum antibiotics Acute renal failure Total parenteral nutrition ICU stay Diabetes mellitus Immunosuppression Bassetti et al. Intensive Care Med. 2013; 39(12): 2092-106

  7. Microbiology Candidaalbicans (65-82%) C. glabrata <20% C. tropicalis <10% C. parapsilosis <5% Other non-albicans Candida spp. ~2% Mixed Candida spp. ~5%

  8. Clinical manifestations Fever Abdominal pain (+/- guarding/rebound tenderness) Nausea, vomiting Purulent discharge from abdominal drains Leucocytosis Electrolyte abnormalities Hypokalaemia, hypernatremia Acidosis Raised inflammatory markers Clinical presentation is similar to bacterial peritonitis Bacterial co-infection is common

  9. Diagnosis Direct microscopy Intra-operative peritoneal or abscess fluid Culture Peritoneal or abscess fluid Blood culture In situ drains Dialysis effluent Non-culture based diagnostics Serum -D-Glucan Candida PCR

  10. Treatment Source control Drainage of abscesses/collections Repair of anatomical defects Antifungals Antifungal treatment has been shown to improve outcomes Echinocandin Fluconazole (if not critically ill) Prophylaxis Fluconazole in high-risk surgical patients Dupont et al. Arch Surg. 2002. 137 (12):134-6 Montravers et al . Crit Care Med. 2006; 34 (3): 646-52 Vergidis et al. PLoS ONE. 2016; 11(4). e0153247

  11. Source control Drainage Percutaneous (CT-, ultrasound-guided) Transgastric Surgical procedures Laparotomy to repair anatomical defects

  12. Prognosis Survival analysis by type of intra-abdominal candidiasis Early source control and antifungal treatment are associated with improved outcomes Mortality ~30% in recent studies Mortality higher in patients admitted to the ICU Vergidis et al. PLoS ONE. 2016;11(4): e0153247

  13. Predictors of mortality Increased likelihood for survival: Presence of abscess Antifungal therapy Septic shock High APACHE II* Score Upper GI tract source Nosocomial peritonitis Inadequate source control *Acute Physiology and Chronic Health Evaluation II Dupont et al. Arch Surg. 2002; 137 (12):134-6 Montravers et al . Crit Care Med. 2006; 34 (3): 646-52 Vergidis et al. PLoS ONE. 2016; 11(4). e0153247

  14. Summary Intra-abdominal candidiasis is as common as Candida bloodstream infections Mortality rates are comparable to that of candidaemia Early source control and antifungal treatment are associated with improved outcomes

  15. END

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