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INFLAMMATORY BOWEL DISEASE ESTABLISHED AND EVOLVING THERAPIES Maruf Aberra(MD)

INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

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INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies. Maruf Aberra(MD). ULCERATIVE COLITIS. Making the diagnosis and assessing disease activity Clinical diagnosis, confirmed by objective findings from endoscopic and histological studies. - PowerPoint PPT Presentation

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Page 1: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

INFLAMMATORY BOWEL DISEASE

ESTABLISHED AND EVOLVING THERAPIES

Maruf Aberra(MD)

Page 2: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

ULCERATIVE COLITIS

Page 3: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

ULCERATIVE COLITIS, Disease activity• Mild -up to 4 bloody stools daily and no systemic

toxicity• Moderate - 4-6 bloody stools daily and minimal toxicity.• Severe- > 6 stools daily and signs of toxicity,

such as fever, tachycardia, anemia raised ESR.• Fulminant ulcerative colitis- > 10 bloody stools

daily, continuous bleeding, anemia requiring blood transfusion, abdominal tenderness, and colonic dilation on plain abdominal radiographs.

Disease activity index

Page 4: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Ulcerative Colitis, Natural history

The distribution of disease activity in a cohort of patients is constant each year

Half the patients are in clinical remission at any given time In the first 3–7 years after diagnosis 25% of patients were in remission 18% had activity every year 57% had intermittent relapses The only significant predictor of remission or relapse was

disease activity in the preceding year. After 10 years, the colectomy rate was 24%

Overall, patients with UC have a normal life expectancy

Page 5: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Medical Management UCInduction of response and remission

• First-line therapy for patients with mild to moderate ulcerative colitis is 5-aminosalicylic acid (mesalazine) cpds, which include oral and rectal mesalazine formulations.

• Oral pro-drugs – Sulfasalazine [5-ASA linked to sulfapyridine]

- Olsalazine [5-ASA dimer] - Balsalazide [5-ASA ,4-aminobenzoyl-β-

alanine]

Controversy exists about the optimum induction dose of 5-ASA

Generally Oral or topical doses of >1500 mg per day are sufficient to induce remission

Page 6: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Medical Management UC• Patients who do not respond to oral 5-ASA

compounds or rectal therapy or both should be treated with oral prednisone 40 mg per day up to 1 mg/kg per day or equivalent.

• Patients with severely active ulcerative colitis and those for whom oral corticosteroids have not worked, need to be admitted to hospital for intravenous corticosteroids.

• Cyclosporine, tacrolimus, and infliximab are all effective in patients with severe ulcerative colitis who do not respond to intravenous corticosteroids.

Page 7: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Ulcerative Colitis –Stepwise approach

Page 8: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Surgical management of UC• Emergency surgery - indicated in patients with

life threatening complications, such as perforation, refractory rectal bleeding, and toxic megacolon not responsive to medical management.

• Elective surgery-indicated in patients with dysplasia or cancer, ulcerative colitis refractory to medical management, or intolerance to long-term immunosuppression or other medical therapies.

• The most widely accepted surgical technique is total proctocolectomy with ileal J-pouch-anal

anastomosis.

Page 9: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies
Page 10: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Crohn’s Disease Disease activity Mild to moderate - ambulatory ,able to tolerate oral

alimentation , without manifestations of dehydration, toxicity, abdominal tenderness, painful mass, obstruction or >10% weight loss.

Moderate to severe disease - failure to respond to treatment for mild disease, more prominent symptoms of fever, weight loss, abdominal pain or tenderness, intermittent nausea and vomiting without obstruction, or significant anemia)

severe to fulminant disease- persisting symptoms on corticosteroids, high fevers, persistent vomiting, evidence of intestinal obstruction, rebound tenderness, cachexia, or evidence of an abscess.

Page 11: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Crohn’s Disease, natural history

Behavior of the disease varies substantially during its course

One year after diagnosis -10–30% of patients have an exacerbation -15–25% have low activity, and -55–65% are in remission. 13–20% of patients have a chronic active course of disease

activity 67–73% have a chronic intermittent course Only 10–13% remain in remission for several years. After 20 years, most patients will require surgery

The life expectancy of patients with Crohn’s disease is slightly reduced

Page 12: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Medical ManagementInduction of remission

First-line therapy for patients with mild to moderate disease is controversial.

Sulfasalazine at doses of 3000–4500 mg per day is effective for induction of remission in active disease.

mesalazine has not consistently proved efficacious. Budesonide 9 mg per day is more effective than oral 5-ASA

4000 mg per day, and has similar efficacy to prednisolone. studies of antibiotics for active Crohn’s disease failed to

show efficacy for induction of remission. Patients who do not respond to the above, and outpatients

with moderate to severe disease are treated with oral prednisone 40 mg per day up to 1 mg/kg per day, or equivalent

Page 13: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

CD-ManagementManagement of fistulising Crohn’s disease

Close interaction b/n surgeon and gastroenterologist

Antibiotic therapy with ciprofloxacin 1000 mg per day or metronidazole is widely used for the first-line treatment of fistulas

Azathioprine or mercaptopurine are used as a second-line treatment.

Infliximab if above measures fail -Adalimumab fistulotomy or drainage with setons or both.

Page 14: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

CD Medical Management-stepwise

Page 15: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Crohn’s Disease, Surgical management

Will not cure Crohn’s disease Indications for emergency and elective surgery

are similar to those for ulcerative colitis. Specific indications - fibrotic strictures /symptomatic/ -fistulas / internal, enterovesical fistulas, and

enterocutaneous fistulas/

The optimum therapy for post-operative maintenance

Mesalazine, Azathioprine and mercaptopurine Metronidazole showed short-term efficacy, and Ordnidazole given for a year was effective

Page 16: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Emerging therapies for IBD emerging novel therapies—

Biological therapies—directed at cytokines (eg, infliximab, adalimumab, certolizumab pegol)

and receptors (eg, visilizumab, abatacept) T-cell activation, selective adhesion molecule blockers

(eg, natalizumab, MLN-02, alicaforsen) Anti-inflammatory cytokines (eg, interleukin 10) Modulation of the intestinal flora (eg, antibiotics,

prebiotics, probiotics) Leukocyte apheresis and many more monoclonal

antibodies, small molecules, recombinant growth factors MAP kinase inhibitors targeting various inflammatory

cells and pathways.

Page 17: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies
Page 18: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Safety and monitoring of medical treatments for IBD

Medical therapies of IBD , particularly immunosuppressant and modulators, are associated with Several side-effects.

Systemic corticosteroid toxicities Azathioprine and mercaptopurine toxicities pancreatitis, fever, rash, arthralgia, malaise, nausea, diarrhea,

thrombocytopenia, hepatitis, nodular regenerative hyperplasia, veno-occlusive disease, leucopenia, infection, and lymphoma.

Cyclosporine and tacrolimus toxicities hypertension, headaches, paraesthesias, seizure, gingival hyperplasia, hypertrichosis , anaphylaxis (ciclosporin only), infection renal insufficiency Anti-TNFα antibody (infliximab, adalimumab, certolizumab

pegol) Hypersensitivity reactions, autoantibody, demyelination (optic

neuritis,multiple sclerosis), drug-induced lupus, worsening of CHF, infections , NHL, and possibly solid tumour malignancies.

Page 19: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Neoplastic complications of IBD

increased risk of developing malignancies including colon cancer in patients with ulcerative colitis and Crohn’s colitis and small-bowel carcinoma in patients with Crohn’s enteritis.

A screening colonoscopy with a minimum of 30 mucosal biopsies should be done in patients with ulcerative colitis to rule out colonic neoplasia, dysplasia, or cancer, 8–10 years after onset of ulcerative colitis symptoms

Page 20: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

IBD-Nutrition-Related Concerns

• Review Nutrient Digestion & Absorption• DIET THERAPY for Specific Conditions• Nutrient-Drug Interactions• Potential Nutritional Interventions (omega-3 fatty acids, probiotics,

glutamine)

Page 21: INFLAMMATORY BOWEL DISEASE Established and Evolving Therapies

Thank You