Mastering SBP Guidelines for SCE Hepatology Success

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Hepatology SCE
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Published by TalkingCases

Nov 21, 2025

Mastering Spontaneous Bacterial Peritonitis (SBP) Guidelines for SCE Hepatology Success

Spontaneous Bacterial Peritonitis (SBP) is a common, life-threatening complication of cirrhotic ascites. For candidates tackling the Specialty Certificate Examination (SCE) in Gastroenterology or Acute Medicine, mastery of current SBP management guidelines is non-negotiable. SBP frequently appears in vignettes testing your immediate diagnostic, therapeutic, and prophylactic decision-making skills.

As an examiner and specialist, I can confirm that the SCE often tests the subtle details of patient selection, antibiotic choice, and albumin usage. Here is your definitive guide to acing SBP management for the exam.


1. The Diagnostic Imperative: Paracentesis

The cornerstone of SBP diagnosis is prompt diagnostic paracentesis. The SCE assumes you know the indications and interpretation of ascitic fluid analysis.

Indications for Diagnostic Paracentesis:

  1. Any patient admitted to the hospital with cirrhosis and ascites. Crucial point: Do not wait for classical signs of infection.

  2. Fever (even low grade).

  3. Abdominal pain or tenderness.

  4. Unexplained encephalopathy or deterioration in renal function.

  5. Gastrointestinal bleeding (high risk of SBP).

Diagnostic Criteria:

SBP is confirmed if the Ascitic Fluid Neutrophil Count (Polymorphonuclear Leukocytes - PMNs) is ≥ 250 cells/mm³, irrespective of culture results.

  • Culture Negative Neutrocytic Ascites (CNNA): PMNs ≥ 250 cells/mm³ but negative culture. Treated identically to culture-positive SBP.

  • Monomicrobial Non-neutrocytic Bacterascites (MNB): PMNs < 250 cells/mm³ but positive culture. Re-paracentesis is mandatory. If PMNs remain low, treat if symptomatic; if PMNs rise, treat as SBP.

  • Secondary Peritonitis: PMNs ≥ 250 cells/mm³ and often very high protein (> 10 g/L), LDH, and multiple organisms on culture. This requires surgical review and broad-spectrum antibiotics (often Metronidazole added to cover anaerobes).


2. Acute Management: Antibiotics and Albumin

Once SBP is diagnosed, immediate empirical treatment is essential to reduce mortality.

A. Empirical Antibiotic Therapy

The standard first-line treatment targets Gram-negative enteric organisms, which are responsible for the majority of cases.

Regimen Agent & Dose Duration Key Rationale for SCE
First-Line Third-generation cephalosporin (e.g., Cefotaxime 2g IV TDS or Ceftriaxone 1-2g IV OD) 5–7 days High coverage for E. coli and Klebsiella (the most common culprits). Ceftriaxone is often favoured for simplicity.
In Quinolone Prophylaxis Consider Piperacillin/Tazobactam or Carbapenems (if septic shock/severe illness or high local resistance) 5–7 days If the patient is already on quinolone prophylaxis, resistance is highly likely.
Hospital-Acquired/Resistant Meropenem or other Carbapenems (local guidelines apply) 7 days Reserved for patients with a recent hospital stay, MDR risk, or failure to respond to first-line agents.

Response to Treatment: A repeat paracentesis 48 hours after starting treatment is only necessary if the patient shows no clinical improvement (e.g., PMN count should drop by > 50% or be < 250 cells/mm³).

B. Albumin Infusion: The Renal Shield

Albumin administration is a vital component, reducing the risk of developing Circulatory Dysfunction and Hepatorenal Syndrome (HRS), thereby improving survival.

Indications for IV Albumin (Crucial for SCE):

Albumin is indicated if the patient meets any of the following high-risk criteria:

  1. Ascitic fluid PMN count ≥ 250 cells/mm³ (i.e., definitive SBP).

  2. Creatinine > 1 mg/dL (88 µmol/L).

  3. Urea > 40 mg/dL (14.3 mmol/L).

  4. Bilirubin > 4 mg/dL (68 µmol/L).

Dosing Schedule:

  • Day 1: 1.5g/kg body weight within 6 hours of diagnosis.

  • Day 3: 1.0g/kg body weight.

Focus for SCE: If the vignette describes a patient with SBP and signs of renal impairment (high Cr/Urea) or severe liver disease (high Bilirubin), including albumin in the management plan is mandatory.


3. Preventing Recurrence: SBP Prophylaxis

SBP has a high recurrence rate, making prophylaxis essential in survivors and high-risk patients.

A. Secondary Prophylaxis (Post-SBP)

  • Indication: All patients who survive an episode of SBP require long-term prophylaxis until transplantation or resolution of ascites.

  • Agent: Oral Norfloxacin 400 mg daily or Ciprofloxacin 500 mg daily.

  • Duration: Long-term/lifelong.

B. Primary Prophylaxis (High-Risk Patients)

This is offered to patients who have never had SBP but are at extremely high risk.

  • High-Risk Criteria (Need to memorize for SCE):

    1. Low Ascitic Protein: Ascitic fluid protein concentration < 1.5 g/dL AND impaired renal function (Cr ≥ 1.2 mg/dL or Urea ≥ 25 mg/dL or Na ≤ 130 mEq/L) OR severe liver failure (Child-Pugh score ≥ 9 with Bilirubin ≥ 3 mg/dL).

    2. Patients with Acute Gastrointestinal Hemorrhage (GIH): Prophylaxis is given for 7 days during the hospital stay (e.g., Ciprofloxacin 500 mg BD or IV Ceftriaxone).

  • Agent: Oral Norfloxacin 400 mg daily or Ciprofloxacin 500 mg daily.


SCE Hot Spots and Clinical Pearls

  1. When to suspect Secondary Peritonitis? Look for refractory SBP, or ascitic fluid analysis showing protein > 10 g/L, LDH above serum level, or mixed flora. This requires a CT abdomen to exclude bowel perforation/abscess.

  2. SBP in the Outpatient Clinic? If a patient with known ascites presents with non-specific symptoms, remember to test for SBP. The threshold for paracentesis must be low.

  3. Drug Interactions: Be mindful of quinolones (Ciprofloxacin) and their interactions, especially regarding QT prolongation, which can be tested in the pharmacy/prescribing section of the SCE.

By mastering these guidelines—from prompt diagnosis and appropriate antibiotic/albumin use to lifelong prophylaxis—you will demonstrate the specialized clinical knowledge required to excel in your SCE.

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