Week 6- Pharmaceutical care considerations in IBD + Pharmaceutical care - Drugs used in IBD Flashcards

1
Q

why do patients with IBD have a risk of getting infections?

A
  • due to IBD treatment that can suppress the immune system and increase the risk
  • to prevent infection they should get immunisation history and infection history
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2
Q

when using steroids for patients with IBD what is the aim and why?

A

-to use and slowly reduce till they can stop
-Prolonged steroid use is associated with: increased infection risk, osteoporosis,
adrenal suppression, diabetes, weight gain, cardiovascular disease

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3
Q

when a patient is taking steroids what else should they be given to help monitor their bone health?

A
  • calcium and vitamin D as it help with uptake of calcium

- should have calcium and vitamin D levels checked and risk of deficiency checked

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4
Q

why is malnutrition common in IBD?

A

increased nutritional demand due to chronic inflammation and poor absorption due to inflammation or surgery

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5
Q

what vitamin deficiencies are important to consider for the patient?

A
  • magnesium
  • calcium
  • potassium
  • vitamin D
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6
Q

why do patients with IBD have iron defiency?

A

-due to excess excretion of iron and bleeding to to inflammation, decrease of intake of iron due to changes in diet

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7
Q

what type of patients with IBD tend to smoke more?

A

crohns disease

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8
Q

what are the risks of smoking as a patient with IBD?

A

Continuation of smoking is linked to worse disease course, higher risk of
surgery and worst outcomes after surgery

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9
Q

what are some of the risk of using NSAIDs with IBD?

A
  • May to lead to increase disease activity – esp. in Crohn’s colitis
  • May precipitate a relapse
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10
Q

what cancer is IBD a risk factor for?

A

bowel cancer

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11
Q

what are some ways to reduce the risk of colorectal cancer in IBD patients?

A

• Receive and take appropriate treatment to manage inflammation
• Regular specialist reviews – at least annually
• Regular colonoscopy – frequency dependent on presence of additional risk factors
(FHx) and specific disease characteristics (disease activity/presence of stricture)
• Usually 1-5 yearly
• Additional ways to reduce risk – physical activity, high fibre, reducing
red/processed meat, limiting alcohol, ?supplementing vitamin D if deficient

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12
Q

what are some issues with adherence for IBD patients?

A
  • Chronic disease with long term medical treatment
  • Remission
  • Topical treatments
  • Need for monitoring
  • Adverse effects
  • Patients beliefs
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13
Q

what are the consequences of poor adherence to medication for IBD patients?

A

Worse patient outcomes – increased disease activity, relapse, loss of response,
higher morbidity and mortality, poor QOL, higher disability

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14
Q

what are some other pharmaceutical considerations to make about IBD treatment and patients?

A
  • stoma patient information
  • ‘short gut syndrome’= lack of functioning small bowel maybe affect nutritional absorption
  • drug consideration= magnesium giving diarrhoea, pain relief should only be paracetamol
  • anxiety and depression
  • pain and fatigue
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15
Q

what type of drug is the main treatment for UC?

A

aminosalicylates

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16
Q

where is mezalazine in its unaltered form absorbed ?

A

small intestine

17
Q

what is the structure of sulfasalazine?

A

mesalazine bound t sulfapyridine via an azo bond, the presence of the Colonic bacterial azoreductase breaks the bond.
-The azo bond prevents absorption in the upper testinal tract

18
Q

where is sulfapyridine absorbed, metabolised and excreted?

A

in the colon, metabolised by the liver and excreted in the urine and is responsible for adverse effects

19
Q

what are some contraindications for the use of sulfasalazine?

A

-hypersensitivity to sulfasalazine/sulfonamides or 5-aminosalicylate/ salicylates

20
Q

what are some of the cautions for the use of sulfasalazine?

A
-History of asthma can cause 
cough
Risk of haematological toxicity
Renal and hepatic impairment
Glucose-6-dehydrogenase (G6PD) deficiency
Slow acetylator status
21
Q

what are some of the side effects of sulfasalazine?

A

-Headache, nausea, fever, rash, raised temperature,
reversible infertility in men, reduced WBC
-Pancreatitis
-Hepatitis, pneumonitis, skin reaction (i.e. Stevens-Johnson
syndrome), haemolysis, inflammation of the kidney

22
Q

what are some of the monitoring that occurs for the treatment of sulfasalazine?

A

-full blood count
-liver function test
-renal function
more intensely at the beginning of therapy

23
Q

what are some preparations that can be done to aminosalicylates to help release the drug to a certain area

A

-prepartions can be coated with an enteric coat with a specific agent to release at specific pH to prevent early disintergration in the stomach and upper GI
-wanting time dependant microspheres of mesalazine encapsulated in ethylcellulose semi-permeable
membrane = time and moisture dependent release (pH independent)
-multi-matrix, Mesalazine incorporated into lipophilic matrix and enterically coated (dissolution pH >7)
• Matrix swells to form a gel (potentiating slow diffusion) – terminal ileum and entire colon release

24
Q

how long is the delayed effect of thiopurines?

A

3-6 months

25
Q

what are some contradictions for thiopurines?

A

Hypersensitivity, serious infection, pancreatitis, impaired bone
marrow

26
Q

what are some cautions for thiopurines?

A

Reduce TPMT

Renal and hepatic impairment

27
Q

when should patients inform their doctors when using thiopurine?

A

ulceration of the throat, fever, infections, bruising, bleeding
= signs of myelosuppression

28
Q

what should be the dose if a patient is using allopurinol?

A

Interaction with allopurinol – reduce azathioprine dose to ¼ of the usual dose