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Dr GI Joe
Joseph Kumka
16 episodes
2 days ago
I'm Dr. Joseph Kumka, Gastroenterology Fellow, educator, and creator of this podcasts. Whether you're a resident gearing up for the boards, a fellow diving deep into subspecialty topics, or a practicing clinician hungry for high-yield updates—you’re in the right place. Subscribe, engage, and let's raise the bar together.
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Medicine
Education,
Health & Fitness
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All content for Dr GI Joe is the property of Joseph Kumka and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
I'm Dr. Joseph Kumka, Gastroenterology Fellow, educator, and creator of this podcasts. Whether you're a resident gearing up for the boards, a fellow diving deep into subspecialty topics, or a practicing clinician hungry for high-yield updates—you’re in the right place. Subscribe, engage, and let's raise the bar together.
Show more...
Medicine
Education,
Health & Fitness
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Inpatient IBD Flare
Dr GI Joe
15 minutes
1 month ago
Inpatient IBD Flare

Inpatient Management of Inflammatory Bowel Disease Flares with Bloody Stools

1.0 Purpose and Scope

This protocol provides a standardized, evidence-based framework for the systematic management of hospitalized patients presenting with inflammatory bowel disease (IBD) flares accompanied by bloody stools. Its strategic importance lies in ensuring timely, appropriate interventions and systematic risk stratification to improve patient outcomes while minimizing complications associated with both the disease and its treatments. This document outlines the critical first steps of patient evaluation upon hospital arrival, guiding clinicians through a structured pathway from initial stabilization to definitive therapy.


2.0 Immediate Assessment and Stabilization

The initial moments after a patient presents are critical for establishing a safe clinical course. Immediate stabilization and rapid initial diagnostics are paramount, as these actions form the foundation for all subsequent risk stratification and therapeutic decisions. The primary goals are to assess hemodynamic stability, correct fluid and electrolyte imbalances, and gather essential laboratory and stool studies before initiating disease-specific therapy.

Initial Orders and Interventions

  • Vital Signs: Assess and document BP, HR, temp, RR, and orthostatics to gauge hemodynamic stability.
  • Intravenous Access: Establish 2 large-bore IVs for fluid resuscitation and potential transfusion.
  • Fluid Resuscitation: Initiate IV fluids to correct dehydration and maintain hemodynamic stability.
  • Initial Laboratory Panels: Order a complete blood count (CBC), comprehensive metabolic panel (CMP), C-reactive protein (CRP) and/or erythrocyte sedimentation rate (ESR), a coagulation profile, and a Type & Cross.
  • Essential Stool Studies: Order stool studies to rule out infectious etiologies, including Clostridioides difficile toxin/PCR, stool culture for enteric pathogens, and ova and parasites if epidemiologically indicated.

Critical Directive: Hold all IBD-specific therapies, especially corticosteroids, until infection has been reasonably excluded, except in cases of fulminant colitis with an immediate life-threatening presentation.

These initial steps are designed to stabilize the patient while simultaneously initiating the workup to differentiate an infectious process from a true IBD flare.

3.0 Differentiating Infection from IBD Flare

Ruling out a superimposed infection is the single most critical decision point before initiating or escalating immunosuppressive therapy. Misdiagnosing an infection as a pure IBD flare and administering corticosteroids or biologics can lead to a fulminant course, increased morbidity, and worsened patient outcomes. Clinicians must be aware that highly sensitive multiplex PCR stool panels may detect pathogenic DNA that represents colonization rather than active infection. Therefore, a positive result must be interpreted in the full clinical context.

Prioritizing Infection Management

If a treatable pathogen—such as C. difficile, Cytomegalovirus (CMV), Salmonella, Shigella, or Campylobacter—is identified, the infection must be the primary target of therapy. Escalation of IBD-specific treatment should only be considered if symptoms of active colitis persist after 48-72 hours of appropriate antimicrobial or antiviral therapy.

Once infection is deemed unlikely or is being appropriately treated, the next step is to formally stratify the severity of the IBD flare.

4.0 Severity Stratification

Accurate severity stratification is essential for guiding the intensity and timing of medical therapy. This assessment allows clinicians to match the treatment approach to the patient's risk profile, ensuring that severe disease receives aggressive inpatient management while milder cases are not over-treated. This distinction is critical: UC severity is driven by mucosal inflammation and its systemic effects (stool frequency, bleeding, toxicity), whereas CD severity is primarily defined by its transmural nature and propensity for structural complications (obstruction, abscess, perforation).

4.1 Ulcerative Colitis (UC) Severity

Severity in UC is primarily determined by stool frequency, the presence of blood, and signs of systemic toxicity, as defined by the Truelove & Witts criteria.

Severe UC: Defined as having ≥6 bloody stools per day PLUS at least one sign of systemic toxicity:

  • Fever >37.8°C (100.0°F)
  • Heart Rate >90 beats per minute
  • Hemoglobin <10.5 g/dL
  • Erythrocyte Sedimentation Rate (ESR) ≥30 mm/hr

Practical Laboratory Cutoff: In modern practice, a CRP >30 mg/L is also consistent with a severe flare.

Fulminant UC: >10 stools per day, continuous bleeding, abdominal tenderness/distention, transfusion requirement.

Moderate UC: 4-6 stools per day, intermediate between mild and severe.

Mild UC: <4 stools per day, small amounts of blood, no systemic toxicity.

4.2 Crohn's Disease (CD) Severity

In contrast to UC, the severity of a Crohn's disease flare is primarily driven by the presence of systemic illness and structural complications, not stool frequency.

Severe/Fulminant CD: Defined by the presence of one or more of the following:

  • High fever and cachexia
  • Persistent vomiting
  • Evidence of intestinal obstruction
  • Signs of peritonitis (rebound tenderness)
  • Intra-abdominal abscess
  • Massive hemorrhage

Practical Laboratory Cutoff: A CRP >45 mg/L is associated with severe disease activity and a higher risk of steroid failure.

This severity assessment directly informs the initial set of inpatient management orders.

5.0 Core Inpatient Management Orders

Beyond disease-specific medical therapy, a standardized set of core supportive care orders is crucial for all hospitalized IBD patients. These orders are designed to manage symptoms, prevent complications, and improve patient tolerance to treatment.

  • Diet: The patient should be placed on Nil Per Os (NPO) or clear liquids initially. The diet can be advanced as tolerated based on clinical improvement.
  • Intravenous Fluids: Provide maintenance and replacement IV fluids, with close monitoring and correction of electrolyte abnormalities.
  • VTE Prophylaxis: Pharmacologic prophylaxis (e.g., low-molecular-weight heparin) is mandatory for all hospitalized patients with an IBD flare, even in the presence of bloody stools. The risk of venous thromboembolism (VTE) is elevated 2- to 3-fold in this population and significantly outweighs the bleeding risk in most cases. Prophylaxis should only be held in cases of massive hemorrhage causing hemodynamic instability.
  • Medications to Avoid: Explicitly discontinue and avoid Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) and opioids, as both are associated with worse clinical outcomes in acute IBD flares.

These core orders are complemented by diagnostic procedures to confirm disease severity and guide the therapeutic strategy.

6.0 Endoscopic and Imaging Strategy

The strategic use of endoscopy and imaging is essential to confirm the severity of a flare, rule out complications, and obtain tissue for histology. The approach must balance the diagnostic yield of a procedure against the potential risks in an acutely inflamed bowel.

6.1 Ulcera...

Dr GI Joe
I'm Dr. Joseph Kumka, Gastroenterology Fellow, educator, and creator of this podcasts. Whether you're a resident gearing up for the boards, a fellow diving deep into subspecialty topics, or a practicing clinician hungry for high-yield updates—you’re in the right place. Subscribe, engage, and let's raise the bar together.