IBD III Flashcards

1
Q

Mild-Moderate Active UC

  • left sided disease within reach of ___
  • proctitis within reach of ___
  • extensive disease, pancolitis (i.e.,
    proximal disease, beyond splenic
    flexure) requires ___ tx
A
  • enemas
  • suppositories
  • systemic
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2
Q

Mild-Moderate Active UC

oral and/or topical ASAs
- if extensive disease: ___ 5-ASA
- left sided disease, topical mesalamine ___ (1 g/day)
- proctitis: mesalamine ___ (1 g/day)
- combo of ___ and ___ may be more effective for pts with left-sided/extensive disease

A
  • oral
  • enema
  • suppository
  • oral, topical
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3
Q

Mild-Moderate Active UC

if oral tx:
- ___ derivatives better tolerated than ___
- sulfasalazine: 2-6 g/day in divided doses
- mesalamine derivatives: 2-3 g/day

consider compliance, convenience, financial resources in product choice
* once daily dosing preferred

A
  • mesalamine, sulfasalazine
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4
Q

Mild-Moderate Active UC

if unresponsive to 5-ASA, can consider changing ___
* if unresponsive to standard-dose 5-ASA or moderate disease activity, AGA recommends high-dose ___ (> __ g/day) plus rectal ___

A

formulation
mesalamine, 3, mesalamine

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5
Q

Mild-Moderate Active UC

CR ___ is alternative (AGA also now
includes ___ as an option)
- especially when ___ to oral or topical 5-ASAs (can add to 5-ASA)
- limit budesonide use to < __ - __ weeks

PO corticosteroids ( ___ 40-60 mg/day) may be used for patients refractory to ASAs
* topical corticosteroids (foams, enemas, suppository) are effective for distal disease (ie, ___ , or ___ )

A
  • budesonide, prednisone
  • nonresponsive
  • 8-16
  • prednisone
  • left sided, proctitis
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6
Q

Mild-Mod. Active UC

T or F: oral and topical mesalamine should not be used together

A

FALSE: Remember: combo
oral and topical mesalamine can be more effective

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7
Q

Moderate-Severe Active UC

  • 4-6 stools per day, +/- blood in stool, some systemic symptoms
  • 5-ASA therapy possible for moderate, but not ___ disease
  • systemic corticosteroids (PO prednisone 40-60 mg/day)
  • for moderate can use oral ___

consider ___ inhibitors/biologics (potentially newer small molecules) in pts unresponsive to ASAs/other therapy, pts who are steroid dependent, pts who fail steroids

A
  • severe
  • budesonide
  • TNF-a
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8
Q

Moderate-Severe Active UC

TNF inhibitor (3)

anti-integrin (1)

IL12/IL-23 inhibitors (3)

JAK inhibitor (2)
- black box warning, only if failed TNF inhibitor

SP1 inhibitor (2)

A
  • infliximab, adalimumab, golimumab
  • vedolizumab
  • ustekinumab, mirikizumab, risankizuab
  • upadacitinib, tofacitinib
  • ozanimod, etrasimod
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9
Q

Moderate-Severe Active UC

AGA suggests against using ___ for induction or maintenance

___ monotherapy is option

thiopurine monotherapy should not be used for ___
- thiopurine monotherapy is option for ___
- AGA makes no recommendation regarding biologics monotherapy vs thiopurine monotherapy for maintenance

A
  • methotrexate
  • biologic
  • induction
  • maintenance
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10
Q

Moderate-Severe Active UC

AGA recommends combining TNF-antagonists, vedolizumab, or ustekinumab with ___ or ___ rather than monotherapy
- patients with less severe disease, or those who place relative value on minimizing ADRs vs maximizing efficacy may choose biologic monotherapy

AGA suggests ___ use of biologics (with/without immunomodulators) rather than gradual step-up (very low quality evidence)
- especially in moderate-severe disease at high risk of colectomy
- those with less severe disease who place a higher value on the safety of 5-ASA agents may prefer gradual step up

A
  • thiopurines, MTX
  • early
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11
Q

Moderate-Severe Active UC

in patients who have achieved remission with biologic agents and/or immunosuppressives or tofacitinib, AGA recommends ___ continuing
5-ASA for induction or maintenance

A

AGAINST

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12
Q

Mod. -Severe Active UC

T or F: certolizumab is approved for UC

A

FALSE
IMPORTANT: certolizumab is NOT approved for UC; golimumab IS approved for UC

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13
Q

Severe-Fulminant UC

require inpatient tx
- consider ___ (bowel rest)

parenteral corticosteroids
- methylprednisolone (16-20 mg q 6 h, AGA recommends 40-60 mg/day)
- hydrocortisone (100 mg q 8 h)
- generally treat __ - __ days (then transition to PO)

consider TNF-α inhibitors ( ___ ) or ___ in pts unresponsive to IV steroids
- cyclosporine: start IV, transition to PO, with transition to ___ or ___
- effective, but may delay rather than prevent colectomy

___ has similar efficacy to ___

A
  • NPO
  • 3-7
  • infliximab, cyclosporine
  • 6-P, AZA
  • infliximab, cyclosporine
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14
Q

UC: Maintenance of Remission

generally use an ___ , a TNF-α antagonist
( ___ and ___ ), ___ , or ___
- choice depends on part in the tx required to induce remission
- no role for ___ ; ___ not studied

ASAs
- newer ___ derivatives better tolerated than ___ (2-3 g/day mesalamine equiv)
- use mesalamine ____ (if left-sided disease) or ___ (if proctitis)
- may use ___ of topical/systemic (more effective than either alone)

in pts who are steroid dependent or unresponsive to ASAs
- ___ or 6- ___ (slow to work: 3-6 months)

TNF-α antagonist for pts who required a TNF-α antagonist for induction (or who fail ___ )
* possibly with AZA
* ___ , ___ , or ___

A
  • ASA, infliximab, adalimumab, AZA, 6-MP
  • corticosteroids, budesonide
  • mesalamin, sulfasalazine
  • enemas, suppositories
  • combo
  • AZA, 6-MP
  • AZA
  • infliximab, adalimumab, golimumab
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15
Q

UC: Maintenance of Remission

anti-integrin (1)

IL12/IL-23 inhibitors (3)

JAK inhibitor (2)
* black box warning, only if failed TNF inhibitor

SP1 inhibitor (2)

A
  • vedolizumab
  • ustekinumab, mirikizumab, risankizumab
  • upadacitinib, tofacitinib
  • ozanimod, etrasimod
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16
Q

Mild-Moderate Active CD

___ marginally effective for treating symptoms of mild/mod colonic CD
- not isolated small bowel CD
- does not result in mucosal ___

mesalamine derivatives have ___ efficacy, no longer recommended, should not be used
- despite this, mesalamine derivatives frequently tried since well tolerated/familiar
- consider formulation and site of action

A
  • sulfasalazine
  • healing
  • minimal
17
Q

Mild-Moderate Active CD

controlled release ___
- option for pts with ilealeocecal ( ___ ) or ___ sided disease

antibiotics
- e.g. metronidazole +/- ciprofloxacin
- variable efficacy, possible option if perianal disease, fistulizing disease, unresponsive to sulfasalazine
- not recommended as primary therapy

A
  • budesonide
  • distal, right
18
Q

Mild-Moderate Active CD

T or F: mesalamine has no efficacy in CD

A

True
- sulfasalazine has marginal efficacy

19
Q

Moderate-Severe Active CD

failed treatment for mild/mod disease, systemic symptoms (fever, wt. loss, abd. pain/tenderness, anemia, vomiting, diarrhea, etc)
- systemic corticosteroids ( __ prednisone 40-60 mg/day)
- tx until resolution of sx and resumption of ___
- may be more effective than ___

hospitalized patients may receive ___ corticosteroids
- methylprednisolone (16-20 mg q 6 h) or hydrocortisone (100 mg q 8 h)

early ___ therapy (with/without immunomodulators) may be beneficial

A
  • PO
  • weight gain
  • budesonide
  • IV
  • biologic
20
Q

Moderate-Severe Active CD

TNF-α antagonists effective
v can use in patients failing immunosuppressive tx, steroid
dependent pts
v infliximab + AZA (or possibly MTX) may be more effective
than either alone
v adalimumab may be used
* SC administration
* possible option in pts who lose response to infliximab
v AGA suggests infliximab or adalimumab plus thiopurine
for induction and maintenance over monotherapy in those
naïve to biologics and immunomodulators
v certolizumab may be used (AGA recommends other
agents over certolizumab based on results of meta
analysis)

A
21
Q

Moderate-Severe Active CD

Agents targeting leukocyte trafficking
v vedolizumab
* with or without immunomodulator
v natalizumab
* not preferred
* only use for maintenance if JC negative
* IL-12/IL-12 and IL-23 antagonists
v ustekinumab
v risankizumab
* JAK inhibitor
v upadacitinib à if failed TNF inhibitor

A
22
Q

Moderate-Severe Active CD

immunomodulator (AZA and 6-MP) monotherapy not
recommended to induce remission (may help
maintain remission after induced w steroids, may be
steroid sparing)
v may use monotherapy in maintenance of remission
* MTX (up to 25 mcg weekly IM or SC) may be used
to induction (esp in steroid-dependent CD) and for
maintaining remission
* cyclosporine should NOT be used for CD
* 5-ASA or sulfasalazine should not be used

A
23
Q

Severe-Fulminant CD

persistent sx/systemic toxicity despite corticosteroid
or biologic txt, cachexia, rebound tenderness,
obstruction, or abscess; CDAI > 450
* require inpatient tx
* consider NPO (bowel rest)
* supportive care
* parenteral corticosteroids (if no abscess)
v methylprednisolone (16-20 mg q 6 h) or hydrocortisone
(100 mg q 8 h)
v generally treat 3-7 days (then transition to PO)
* may consider infliximab (or other biologic) if not
attempted prior
v infliximab may be preferred if fulminant

A
24
Q

CD: Maintenance of Remission

minimal evidence sulfasalazine and PO mesalamine
derivatives are effective
v may try due to favorable adverse effect profile
v not recommended in moderate-severe CD
* no role for systemic corticosteroids
* budesonide has minimal long-term efficacy à not
recommended for >4 months
150

A
25
Q

CD: Maintenance of Remission

AZA and 6-MP are effective
v esp. in steroid-induced or infliximab-induced remission
* MTX
v alternative to AZA and 6-MP, esp. in pts w initial response
to MTX
v SQ only (PO not recommended)

A
26
Q

CD: Maintenance of Remission

TNF-α antagonists are options for CD maintenance
v ADA suggests use of infliximab or adalimumab in
combination with AZA or 6-MP in patients who are naïve
to biologics and immunomodulators
v certolizumab
v ant-integrin: vedolizumab
v Il-12/IL-23 antagonists: , ustekinumab, risankizumab
v natalizumab not recommended
v clinical controversy: bottom-up or top-down approach
* in moderate-severe disease, AGA suggest early introduction with a
biologic +/- and immunomodulator vs delaying their use while
trying 5-ASAs and/or corticosteroids
152

A
27
Q

Social Determinants of Health (SDH) and IBD

SDH: economic stability, education access/quality,
health care access/quality, neighborhood,
social/community
* IBD à chronic diseases with complex courses,
requiring regular follow-up, access to specialists,
invasive diagnostics, complex and potentially
expensive treatments, often diagnosed during most
economically productive years of adulthood
* lower socioeconomic status may be associated with
worse outcomes in IBD (health care utilization, ICU
admission, corticosteroids, death)

A
28
Q

Social Determinants of Health

(SDH) and IBD

consider:
v access to specialists, infusion resources, laboratories
v navigating insurance and patient assistance programs
v delivery and storage of expensive drugs
v importance of achieving and maintaining remission on
employment, educational success, caregiver
responsibilities, social activities

A
29
Q
A