Pharmaceutical Care of Gastrointestinal patients 2 UC and Crohn's Flashcards

1
Q

Inflammatory bowel disease (IBD) is a term mainly used to describe two conditions. list these two conditions

A

ulcerative colitis and Crohn’s disease

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2
Q

what is Ulcerative Colitis?

  • causes?
  • which part of the GI tract becomes inflamed?
  • does it go away?
A

1) Ulcerative Colitis is a condition that causes inflammation and ulceration of the inner lining of the rectum and colon
2) Small ulcers develop on the surface of the intestinal lining and these may bleed and produce pus
3) Only the surface of the intestine becomes inflamed
4) UC is sometimes described as a chronic condition
5) Long periods of good health (remission) as well as relapses or flare-ups
6) Cause: unknown, but environmental, genetic and bacterial may play a role

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3
Q

what is Crohn’s Disease?

  • can it spread?
  • can it be cured?
  • which part of the body does it affect?
A

1) Crohn’s disease is a chronic inflammatory disease of the gastrointestinal tract
2) Inflammation extends all the way through the intestinal wall from mucosa to serosa
3) Crohn’s disease is a relapsing and remitting disease
4) Initially only a small segment of the gastrointestinal tract may be involved, but Crohn’s disease can progress
5) Smoking and genetic predisposition are two important factors that are likely to play a role
6) Although surgical resection of inflamed segments may temporarily arrest symptoms, subsequent inflammation is likely to recur. Resection is not curative in Crohn’s disease, which is in contrast to ulcerative colitis

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4
Q

what are the symptoms of Crohn’s Disease?

  • when is pain exacerbated?
  • list some non GI symptoms
A

1) Patients present with diarrhoea and insidious abdominal pain
2) Pain is often exacerbated after feeding
3) Diarrhoea is usually non-bloody (helps differentiate from ulcerative colitis)
4) Patients can frequently have fever and weight loss
5) Non-intestinal manifestations can include: mouth ulcers (immune response), arthritis, erythema nodosum (inflammation of fat cells under skin)

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5
Q

compare the anatomy of crohn’s disease vs ulcerative colitis. is there a difference in where each disease is typically present?

A

1) Crohn’s Disease: mainly on the ascending colon and parts of the ilium
2) Ulcerative Colitis: mainly on the descending colon

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6
Q

the main difference between Crohn’s and Ulcerative Colitis is the type of inflammation. compare the difference in the type of inflammation

A

1) in Crohn’s the inflammation goes all the way through the wall
- All Layers of Bowel Inflamed
2) in ulcerative colitis: inflammation is on the surface
- Only Lining of Bowel Inflamed

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7
Q

describe the differences in the appearance of the intestines in crohn’s disease vs ulcerative colitis

A

1) ulcerative colitis: ulceration, crypt distortion, pseudopolyps (surviving mucosa)
2) crohn’s disease: cobble stoning, thickened wall , fissure all may be present

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8
Q

compare the majour differences in the symptoms of Crohn’s Disease & Ulcerative colitis

A

1) rectal bleeding: usual in Ulcerative Colitis only sometimes in Crohn’s Disease
2) cigarette smoking: not usually involved in ulcerative colitis but common in crohn’s disease.
3) discrete ulcers are rare in ulcerative colitis but common in crohns
4) aphthoid ulcers are rare but common in crohns
5) cobble stone lesions never occur in ulcerative colitis but are common in crohns

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9
Q

what is Proctosigmoiditis?

A

Proctosigmoiditis is a form of ulcerative colitis and affects the rectum and sigmoid colon (the S-shaped last part of the large intestine, leading into the rectum).

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10
Q

what is Proctitis?

A

inflammation of the anus (the opening) and lining of the rectum (lower part of the intestine leading to the anus)

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11
Q

list the tests conducted to diagnose Inflammatory Bowel Disease

A

1) full blood count (FBC)
2) CT bowel
3) Sigmoidoscopy or colonoscopy
4) CRP
5) Stool sample (rule out c.diff)
6) Liver function tests (LFTs)
7) Temperature
8) Faecal calprotectin

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12
Q

what is Faecal calprotectin and what two conditions does it help differentiate between?

A

1) released into the intestines in excess when there is any inflammation there. Its presence can mean a person has an inflammatory bowel disease such as Crohn’s disease or ulcerative colitis.
2) Help with differential diagnosis of IBD and IBS as symptoms are can be similar

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13
Q

outline some complications that can occur as a result of Crohn’s Disease.

A

1) Strictures
2) Perforations
3) Fistulae- Uncommon in UC

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14
Q

what is the Harvey-Bradshaw Index for Crohn’s?

A

1) The tool is used to quantify the stage of disease
2) This helps determine treatments options, as the disease has a variety of symptoms that effect QoL
3) Treatment options vary depending on the stage of disease or ‘flare’

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15
Q

describe the mild, moderate and severe scores for ucerative Colitis

A

1) Mild: fewer than four stools daily, no more than small amounts of blood in stools, no anaemia, pulse rate not above 90, no fever and normal ESR and CRP.
2) Moderate: four to six stools a day with more blood in stools than for mild disease. No anaemia, pulse rate not above 90, no fever and normal ESR and CRP.
3) Severe: six or more stools per day, visible blood in stools and at least one feature of systemic upset (temperature above 37.8°C, pulse rate greater than 90, anaemia, ESR above 30).

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16
Q

for each of the following parts of the GI system state what is absorbed:

1) colon
2) duodenum
3) jejunum
4) ileum

A

1) Colon – site of water absorption
2) Duodenum – iron and calcium ions
3) Jejunum – folic acid
4) Ileum – fat and vitamin B12 absorption

17
Q

describe the WHO analgesic pain ladder

A

1) step 1 mild : Non-opioid + Optional adjuvant If pain persists or increases, go to step 2
2) step 2 moderate: Weak opioid + Non-opioid + Optional adjuvant If pain persists or increases, go to step 3.
3) step 3 severe: Strong opioid + Non-opioid + Optional adjuvant Freedom from pain.

18
Q

Discuss the use of Steroids in UC and crohns.

  • when are they used?
  • risk of long term use?
  • what is the dose?
A

1) Indication: both Crohn’s and UC in mod-severe relapse
2) No role in maintenance
- 40mg OD prednisolone reduced slowly 2/52
-

19
Q

for each of the following Rectal preparations state the site of action:

1) Suppository
2) Foam
3) enema

A

1) Suppository: Rectum, Proctitis
2) Foam: Sigmoid Colon, Procto-sigmoiditis
3) enema: Descending colon to splenic flexure, Left sided colitis

20
Q

what dose of 5-aminosalicylic acid (Mesalazine) should be used in crohns and UC

A

1) Crohn’s – no evidence for doses >4g
2) UC –Induction of remissions ≥ 4g/day
- Maintenance of remission ≥ 2g/day
3) Rectal preparations (PINCE) : 15% past splenic flexure: 2g bd oral + 1g OD rectal (64% remission at week 8 vs 43% oral) - this is a combined oral and rectal

21
Q

using the Harvey–Bradshaw Index for Crohn’s disease give scores indicative of the following:
1) remission 16

A

1) remission 16

22
Q

how do you optimise the use of steroids

A

1) Correct dose: Start at 40mg and slow reduction
2) Correct formulation- Know where the disease is located
3) Prevent osteoporosis
4) Consider infection risk
5) rectal steroids Only for patient not responding to rectal mesalazine

23
Q

where is mesalazine normally absorbed, what is its method of action and why are MR preparations used?

A

1) Mesalazine - orally would be extensively absorbed from the upper GIT, with little of the drug reaching the colon.
2) MR preparations used - release the drug in the terminal ileum and colon (local action)
3) Mesalazine is an anti-inflammatory drug structurally related to the salicylates
4) Mesalazine is the active moiety of sulfasalazine, which is metabolized to sulfapyridine and mesalazine.
5) Inhibits prostaglandin and leukotriene synthesis, release of reactive oxygen species and other actions

24
Q

outline the active moiety of Sulfasalazine

A

1) prodrug- not active in its ingested form. It is broken down by bacteria in the colon into its two components, 5-aminosalicylic acid (5-ASA), and sulfapyridine.
2) 5-ASA (mesalazine) →poorly absorbed →induced remission in UC by :
- inbibiting COX, PAF, cytokines
- inhibiting IL-1 and TNF α
3) sulfapyridine is rapidly absorbed in the colon → acetylated in the liver → excreted in urine → no therapeutic action in UC

25
Q

list the different formulations of mesalazine available and state their site of action

A

1) Asacol MR- EC therefore delayed release pH>7
- Site: terminal ileum + large bowel
2) Octasa MR– EC therefore delayed release pH>7
- Site: Terminal ileum and colon
3) pentasa- Ethylcellulose coated microgranules to allow slow continuous release – diffusion through semi-permeable membrane
- Site: Duodenum to rectum
4) Sulfasalazine and other azo-bonded:- cleaved by intestinal bacteria – azoreductase pH >7.
- Site: colon

26
Q

what other things do you need to consider for UC and crohns patients with regards to their treatment ?
- what needs to be monitored what is recommended?

A

1) Osteoporosis risk
2) Nutrition
3) anaemia
4) Opportunistic infections - vaccines
5) Side effects
6) DVT risk

27
Q

discuss how tablet size and frequency can lead to adherence problems in patients . how can pharmacists help?

A

1) Tablet size can be a particular problem especially when the patient is acutely unwell
2) Swallowing a large tablet or a number of large tablets can feel overwhelming
3) Talk to your patient to aid adherence and compliance to their treatment regimens
4) Does the frequency of tablets affect
- their daily life?
- what is their work/life pattern?

28
Q

what are Thiopurines?

A

Thiopurines are a class of drugs that are used to suppress the normal activity of the body’s immune system. Examples of thiopurine drugs include azathioprine

29
Q

discuss the use of Thiopurines in IBD.

  • what test should be conducted first?
  • which enzyme is tested for?
A

1) A TPMT test is used to check whether a person is at risk of developing severe side effects after taking a type of medication called thiopurine
2) Assess thiopurine methyltransferase (TPMT) activity before offering azathioprine or mercaptopurine.
3) Do not offer azathioprine or mercaptopurine if TPMT activity is deficient (very low or absent).
4) Consider azathioprine or mercaptopurine at a lower dose if TPMT activity is below normal but not deficient

30
Q

outline the Mechanism of Action of thiopurines in particular Azathioprine.

  • what is its most severe side effect
  • can it be given in conjunction with purine analogues?
A

1) Azathioprine is an immunosuppressive drug
2) Class of agents is purine analogues
3) Prodrug for mercaptopurine (active metabolite)
4) Azathioprine acts to inhibit purine synthesis
5) Its most severe side effect is bone marrow suppression, and it should not be given in conjunction with purine analogues such as allopurinol

31
Q

outline the use of Methotrexate in IBD

  • what is the dose?
  • what should be monitored
  • how often should it be administered
  • what other drug should it be taken with
A

1) Used in active and relapsing Crohn’s
2) 25mg/week PO or IV/SC
3) Monitor FBC and LFTs
4) Maintenance dose to prevent remission
5) ONCE weekly dosing
6) Concomitant folic acid
- give patient methotrexate dosage record booklet

32
Q

what is Ciclosporin used to treat ?

  • how should it be administered?
  • what dose?
  • what should be monitored?
A

1) Therapy for acute severe ulcerative colitis
2) Consider adding intravenous ciclosporin to intravenous corticosteroids or consider surgery for people:
- who have little or no improvement within 72 hours of starting intravenous corticosteroids or
- whose symptoms worsen at any time despite corticosteroid treatment.
3) Take into account the person’s preferences when choosing treatment
4) 2mg/kg PO/IV
5) Baseline BP, FBC, cholesterol, LFTS, GFR, Mg2+

33
Q

if there is an inadequate response to oral prednisolone after 2–4 weeks in Mild-moderate UC, what other drug can be added to the regime to induce remission?

A

1) Consider adding oral tacrolimus to oral prednisolone to induce remission
2) Mild to moderate ulcerative colitis if there is an inadequate response to oral prednisolone after 2–4 weeks.

34
Q

discuss the use of Monoclonal antibodies (MABs) for the treatment of IBD.

  • name a brand of MAB
  • when should MAB’s be considered?
  • how long is the planned treatment course?
  • when are they not recommended?
A

1) Infliximab is licensed for the management of severe active Crohn’s disease and severe UC
2) Not responded adequately to treatment with corticosteroid and a conventional drug that affects the immune response/intolerant
3) Planned course of treatment for 12 months or until treatment failure
4) Not recommended for treatment of subacute manifestations of moderate-severe active UC that would be managed in OP setting
5) Acute exacerbations of UC when ciclosporin is C/I

35
Q

Describe the mechanism of action of Infliximab

A

1) TNF-α has been implicated in numerous autoimmune diseases
2) Regulates inflammation
3) Infliximab is a chimeric monoclonal antibody that targets and binds to TNF-α.
4) By inactivating TNF-α, the inflammatory process is significantly diminished