wound healing and GI Flashcards

1
Q

2 wound types and their description

A
  • Acute - generally heal in a couple days to weeks, but can become chronic E.g., surgery or trauma
  • Chronic- takes >12 weeks to heal E.g., Pressure ulcers, diabetic foot ulcers
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2
Q

Descriptions of ulcer stages

A
  • Stage 1 sores are not open wounds. The skin may be painful, but it has no breaks or tears.. In a dark-skinned person, the area may appear to be a different color than the surrounding skin Skin temperature is often warmer. And the stage 1 sore can feel either firmer or softer than the area around it.
  • At stage 2, the skin usually breaks open, wears away, or forms an ulcer. The sore expands into deeper layers of the skin. At this stage, some skin may be damaged beyond repair or may die.
  • During stage 3, the sore gets worse and extends into the tissue beneath the skin, forming a small crater. Fat may show in the sore, but not muscle, tendon, or bone.
    At stage 4, the pressure injury is very deep, reaching into muscle and bone and causing extensive damage. Damage to deeper tissues, tendons, and joints may occur.
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3
Q

Factors that impact wound healing

A
Nutrition-related
• Protein
• Energy
• Hydration
• Micronutrients 
• Hyperglycemia
Other factors: 
• Edema
• Circulation
• Smoking
• Stress
• Alcohol
• Medications: Corticosteroids and NSAIDs
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4
Q

Medical management/prevention of ulcers

A
• Minimize friction and pressure 
• Repositioning every 1-2 hours
• Incontinence (wet wounds won't heal)
- Scheduled toileting 
- Frequent changing
• Education
- Staff, resident, families
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5
Q

Phases of wound healing

A

3 main phases:
1. inflammatory:
- pro-inflammatory pathway involving cytokines. Redness, heat, swelling. Maybe pain
- coagulation pathway with platelets+fibrinogen to create a clot.
Inflammatory stage lasts 4-6 days; starts immediately
High need for energy, protein and micronutrients.
2. proliferative; Day 4-14
Also known as constructive phase
Epithelization begins- skin cells migrate to the wound to repair it- this also requires energy and nutrients
adequate blood supply is also required to deliver enough oxygen. this is gonna be a problem if there is not enough iron - impairment of oxygen delivery via hemoglobin
3. maturation: day 8-12 months
collagen is organized to increase tensile strength and form a scar- can take a long time

for the first 14 days- there are high energy, protein and micronutrient needs

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6
Q

Nutrients for healing

A

Adequate intakes for:
• Ca, Zn
• Vitamins A, D

Possibly elevated needs for:
• Energy
• Protein
• Vitamins C, E, K, 
• Fe, Se, Cu
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7
Q

Energy for healing reccs

A

high protein/ high energy diet
30-35kcal/kg for those at risk and for those with pressures ulcers
Use IBW for obese
Fortified foods and ON

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8
Q

Protein for healing reccs

A
  • 1.25-1.5g/kg for those at risk and for those with pressures ulcers
  • Use IBW for obese
  • Fortified foods and ONS
  • Arginine (stage 3-4 wound)- AA that helps transfer other AA into tissue, support protein production and insulin secretion
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9
Q

hydration reccs for wound healing

A
  • Use rule of thumb
  • Additional fluids if fever, vomiting, profuse sweating, diarrhea, heavily exuding wounds
  • If concerned about overhydration 1kcal/ml is a good place to start
  • Assess hydration status daily
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10
Q

vit/mineral reccs for wound healing

A

likely to need a vitamin and mineral supplement
• Multivitamin/mineral indicated
• Encourage food sources of zinc,
iron, copper, calcium, selenium, (ZICCS), vitamins A,D,E C, K-> not necessarily need to supplement them, especially in 1-2 stage
encourage food sources
• ONS for wounds might be indicated (stage 3-4)

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11
Q

what is celiac>

A

Celiac disease = autoimmune disease
• Immunological reaction to gluten
resulting in damage to intestinal mucosa

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12
Q

is there a genetic component with celiac?

A

big genetic component in developing celiac disease
Genetic and autoimmune linkages
• Major genes HLA-DQ2 and HLA-DQ8 in 95% of patients

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13
Q

WHat is the part of the gluten that is the root cause of problem

A

Gluten is made of prolamin and glutelin

Prolamin is the problematic part

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14
Q

What are the 3 main grains known for celiac triggers

A

wheat
rye
barley

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15
Q

Pathophysiology of Celiac Disease

A

• Gluten protein in lumen induces inflammatory response
- Cytokines released by WBC
- Cytotoxic T-cells
• Damage to villi; reduced height,
flattened
• Decreased enzyme function and surface area
• Maldigestion and malabsorption

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16
Q

celiac co-morbidities

A

• Osteoporosis: bone loss is multifactorial, but part of it is related to Vit D deficiency and calcium malabsorption
when celiac disease is treated, bone density will come back to normal in kids, but not in adults-> important to identify celiac disease early on to attenuate bone loss
• Thyroid dysfunction: as people with celiac are predisposed to other autoimmune disease like thyroid disease
• Anemia (B12, Iron, Folate): due to malabsorption
• Increased mortality due to increased risk of malignancy: as they are at risk of developing cancer
avoiding gluten decreases the risk
- Non-Hodgkin’s lymphoma (3-6x more likely)
- Oropharyngeal, esophageal, and small intestinal adenocarcinoma.

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17
Q

Clinical Manifestations of Celiac Disease

A

“Classic”
• Diarrhea, abdominal pain, cramping, bloating, gas

Extraintestinal symptoms can be present without any GI symptoms
• Bone and joint pain
• Muscle cramping, fatigue
• Peripheral neuropathy, seizures 
• Skin rash
• Mouth ulcerations
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18
Q

Common celiac symptoms

A
Diarrhea
• Fatigue
• Borborygmus- gurgling in intestines
• Abdominal pain
• Weight loss
• Abdominal distention 
• Flatulence
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19
Q

Uncommon celiac symptoms

A
  • Osteopenia/ osteoporosis
  • Abnormal liver function
  • Vomiting
  • Iron-deficiency anemia
  • Neurologic dysfunction
  • Constipation
  • Nausea
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20
Q

How many celiac cases present common vs uncommon symptoms

A

Up to 38 % Asymptomatic & ~85% non-classical symptoms- Screening is thus important in high risk groups
Not all symptoms follow the “classic” pattern. Can delay diagnosis.

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21
Q

what are the most common presenting symptoms?

A
  • abdominal pain (83%),
  • diarrhea (76%), and
  • weight loss (69%).
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22
Q

Diagnoses made prior to celiac disease included

A
  • anemia (40%),
  • stress (31%), and
  • irritable bowel syndrome (29%)

• Osteoporosis was common.

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23
Q

Those with __ symptoms are fewer than those __ or with__ symptoms

A

Those with outward symptoms are fewer than those asymptomatic or with less specific symptoms

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24
Q

Diagnosis & Treatment Overview steps

A
  • 1st: Physical exam and blood testing
  • 2nd: Duodenal biopsy
  • 3rd: Implement gluten-free diet
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25
Q

algorithm for evaluation of celiac disease

A

https://www.dynalife.ca/Portals/0/pdf/Symposium/2013/7%20-%20Celiac%20Disease%202013_Karina%20Capote.pdf

low suspicion
1. Blood work
wait for blood work results before biopsy
no antibodies-> look for other diagnosis
antibodies-> intestinal biopsy (as it confirms the diagnosis)

if high suspicion:
- blood testing right away: serology testing (looking for antibodies in the blood for gluten as antigen
- we screen for TTG and EMA antibodies )
step 2:
- intestinal biopsy
if there’s high suspicion, biopsy and blood tests will be done at the same time

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26
Q

What are the blood test that are done?

A

Testing for gliadin antibodies
• is no longer recommended
• low sensitivity and specificity for celiac disease

Antiendomysial IgA antibodies (EMA) and tissue transglutaminase (tTG) antibodies.
• tTG, has 95-98% sensitivity
• EMA has 85-98% sensitivity
• Returns to normal if treatment adhered to 4-6 months.
• If detected after that may suggest incompliance or hidden gluten

Confirmatory testing, including small bowel biopsy, advised

these tests can also be used for monitoring treatment
If a person has been following gluten-free diet, after 4-6 months these antibodies will go back to normal
If after 6 months, there still are these antibodies present in blood test, this is a sign that patient still has gluten in his diet coming from hidden sources of gluten

27
Q

Antibodies Associated with Celiac Disease: sensitivity and specificity

A

Anti-gliadin: least specific and sensitive
Anti-endomysial: 2nd most sensitive, most specific
Anti-tissue transglutaminase: most sensitive, 2nd most specific

28
Q

When can antibody testing be false positive, false negative?

A

Any test will be False Negative with IgA deficiency e.g. during an infection
Anti-tissue transglutaminase: False Positive tTG in IBD

29
Q

Reference Values (Mayo Clinic) tTG IgA

A

<4.0 U/mL (negative)
4.0-10.0 U/mL (weak positive)
>10.0 U/mL (positive)

30
Q

sensitivity vs specificity

A

sensitivity- ability to diagnose patients with disease

specificity- ability to diagnose patients w/o disease

31
Q

If patient tested negative with IgA deficiency or positive with tTG deficiency-> next step?

A

If patient tested negative with IgA deficiency or positive with tTG deficiency-> move to biopsy to confirm the diagnosis

32
Q

Small Intestine Biopsy: when is it required?

A

Required to confirm the diagnosis for most

Should also be considered in patients:
• with negative serologic test results who are at high risk or
• in whom the physician strongly suspects celiac disease.

33
Q

Small Intestine Biopsy: how can it look with celiac

A
  • Mucosal changes may vary from:
  • partial to total villous atrophy,
  • may be characterized by subtle crypt lengthening • increased epithelial lymphocytes.
34
Q

To avoid false negative results on endoscopic biopsy:

A

• at least 4 tissue samples used, which increases the sensitivity of the test.

35
Q

benefits of gluten-free diet in celiac patients

A
  • Villous height generally returns to normal
  • Maldigestion and malabsorption resolve
  • Physical signs and symptoms resolve
36
Q

how long does it take to see improvement when following GFD?

A
  • Symptomatic improvement after 2 weeks in 70-95%
  • Micronutrient biochemistry should be re-checked in 2-3 months
  • Serology negative after 4-6 months
37
Q

What is refractory celiac disease?

A

Refractory coeliac disease (1% of patients)
some patients still experience symptoms even after being placed on gluten-free diet
-> continued villous damage
- Can be due to unknown gluten contamination or due to presence of co-existing disease like colitis

38
Q

Challenges of gluten free diet (GFD)

A
  • Compliance
  • Palatability
  • Affordability
39
Q

What has to be done if the patient was following GD diet before testing?

A
  • If on a gluten free diet prior to dx, “the standard of care in such cases is to perform a ‘gluten challenge’ whereby the patient consumes the equivalent of two servings of gluten containing foods per day for up to 8 weeks, and then returns for serological testing and duodenal biopsy.”
  • Short-course 14-28 d on a 3 or 7.5 g gluten/d diet

As little as 3 g of gluten per day induces damage to the GI tract based on histological assessments

40
Q

A panel convened by the National Institutes of Health identified six elements essential to treating celiac disease once it is diagnosed

A

C: Consultation with a skilled registered dietitian
E: Education about the disease
L: Lifelong adherence to a gluten-free diet
I: Identification and tx of nutritional deficiencies
A: Access to an advocacy group
C: Continuous long-term follow-up.

41
Q

why may patients still experience symptoms despite GF diet?

A
  • Might experience lactose intolerance for ~ 1 month
  • Consider contamination sources
  • Refractory celiac disease
42
Q

Food labelling – Canada vs USA and Europe

A

Canada
• Gluten-free: < 20 ppm gluten: 20 mg/kg of food
• 10 mg gluten in 1/8th of teaspoon of wheat flour • 1/350th of a slice of bread
• USA & Europe: <20 ppm

43
Q

Typical Foods to Avoid

A

• Barley (flakes, flour, pearl)
• Beer, ale, lager
• Breading and bread stuffing
• Bulgur; Couscous; Croutons; Farina
• Hydrolyzed wheat protein
• Rye bread and flour
• Wheat bran, Wheat flour, Wheat germ, Wheat starch
• Dinkel (also known as spelt)
• Durum ; Einkorn
• Emmer ; Farro or Faro (also known as spelt)
• Kamut ; Spelt (also known as farro or faro, dinkel)
• Atta (chapatti flour); Brewers yeast; Communion wafers
• Fu **
• Graham flour; Malt, malt extract, malt syrup and malt flavouring, Malt vinegar, Malted milk
** Fu is a dried gluten product derived from wheat that is sold as thin sheets or thick round cakes. Used as a protein supplement in Asian dishes such as soups.
• Matzoh, matzoh meal; Modified wheat starch
• Oatmeal, oat bran, oat flour and whole oats **; Pastas; Seitan ****
• Semolina; Triticale
**
Oats are contaminated unless “gluten free”. ** Seitan is meat-like from wheat gluten used in many vegetarian dishes; sometimes called “wheat meat”

44
Q

Safe grains

A

corn, rice, buckwheat, wild rice, amaranth, quinoa, teff, millet, sorghum

45
Q

Other ‘safe’ foods:

A

• All vegetables, legumes, fruits, natural meats (not deli meats), fish, shellfish,
eggs, natural dairy products and nuts as well as potatoes, tapioca and
arrowroot.
• Question these foods if processed, in sauces, etc. (read labels!)

46
Q

What is the allowed quantity of the “pure oats”

A

❑Moderate amounts of pure oats can be safely ingested by most patients
❑No conclusive evidence of a certain amount tolerated each day
the amount of pure oats considered within safe limits is 50 to 70 g/ day for adults and 20 to 25 g/day for children

47
Q

what is the definition of uncontaminated oats

A

< 20 ppm defines uncontaminated oats (free of wheat, rye and barley)

48
Q

fibre and oats. consequences

A

The fibre content of an oat containing diet is often higher than the typical gluten-free diet. When adding oats to the diet, individuals may experience a change in stool pattern or mild gastrointestinal symptoms, including abdominal bloating and gas. These symptoms should resolve within a few days. Therefore, it is advised to start with a small amount of oats per day [adults 25-70 grams (1/4-3/4 cup dry rolled oats) and children 10-25 grams (1/8-1/4 cup)] and gradually increase as tolerated.

49
Q

sources of away-from-home contamination

A

Away from home, be aware of sources of cross contamination:
• Products in bulk bins can become contaminated by using the scoops in more than
one bin. There is no assurance that the other customers will be as cautious as
you. Also, flour dust in the air around these bins can cause a problem.
• At the deli counter, where gluten free meats are being cut using the same utensils
without cleaning in between or where cut meats often overlap on the counter.
• Buffet lunches, where the chef tests the temperatures in all the dishes using one
thermometer, or spoons are used for more than one dish.
• French fries cooked in oil where battered foods have been fried.
• Meat cooked on a grill which hasn’t been cleaned after cooking regular food with gluten

50
Q

GFD and weight gain/loss

A

Weight Loss might be a sign that gluten is still being present in the diet as the patient is experiencing symptoms and losing weight
Gluten free diet often causes weight gain as gluten free diet’s tend to be a nutrient dense as companies add fat to make up for loss of taste
Also monitor blood lipid levels

51
Q

Parts of nutrition assessment with celiac?

A
• Body weight (loss or gain) 
• Diarrhea and other NIS
-  Steatorrhea
- Fat soluble vitamin deficiencies 
• Micronutrient deficiencies
- Iron
- Folate
- Vitamin B12 
- Zinc
- Magnesium
• Low fibre
52
Q

What should be managed with celiac?

A

• Gluten-free diet is often nutrient dense
- Weight gain is a common outcome of this diet
- Elevated lipid profile
• GF foods are not fortified or enriched
• Common to recommend a multivitamin/mineral supplement

53
Q

what should be reassessed at a follow up?

A
  • food records
  • labs: iron, vit B12, Hb
  • vit D: risk of osteopenia
  • weight- of losing weight, make sure there is no gluten in the diet
  • cholesterol levels
  • compliance
  • affordability
  • barriers to compliance
54
Q

CSI: Celiac Symptom Index

A

• 16-item questionnaire
• scores of 30 or less
- associated with both high quality of life (mean visual analog scale score of 86.5) and excellent GFD adherence (mean diet score of 1.8),
- suggestive of clinical remission

• scores of 45 or greater

  • were associated with relatively poor quality of life (mean visual analog scale score of 69.3) and worse GFD adherence (mean diet score of 2.4),
  • suggesting ongoing active celiac disease
55
Q

what are the possible etiologies of gastroparesis?

A

The most common of these are diabetes mellitus, postvagotomy syndrome, postviral gastroparesis, and narcotics or other agents that slow motility.

56
Q

When obtaining a diet history of a pt with SB motility disorder, the clinician should evaluate the following:

A
  • Changes in appetite and nausea, vomiting, or diarrhea
  • Problems chewing or swallowing, which can affect one’s ability to ingest certain foods
  • The patient’s typical daily dietary intake
  • The use of supplemental nutrition (oral, enteral, or parenteral)
  • Food intolerances or allergies
  • Use of supplements, such as vitamins, minerals, herbs, or protein powders
  • Use of stool-bulking agents or laxatives
  • History of severe constipation
  • Medications known to slow gastric emptying
57
Q

Medications Known to Delay Gastric Emptying

A
Aluminum-containing antacids
Anticholinergics
Atropine
Beta-agonists
Calcitonin
Calcium channel blockers
Dexfenfluramine
Diphenhydramine
Ethanol
Glucagon
Interleukin-1
L-Dopa
Lithium
Octreotide
Ondansetron
Narcotics
Nicotine
Potassium salts
Progesterone
Selective serotonin reuptake inhibitors
Sucralfate
Tricyclic antidepressants
58
Q

dietary modifications in gastroparesis

A

Dietary modification focuses on eating multiple small meals throughout the day; these meals should be limited in fat and fiber content, both of which can slow gastric emptying. In more severe cases, patients tolerate liquids better than solids, and these patients may require a liquid diet, at least initially.

59
Q

advise for glucose control in gastroparesis

A
  • If gastroparesis is a result of diabetes mellitus, maximize glucose control.
  • Monitor the need to change the timing or the overall requirements for insulin in order to have consistent delivery of nutrients with optimal total calories ingested.
  • Expect an increase in insulin requirements because improved symptom control will likely result in an increase in total calories ingested.
  • In general, dietary restrictions (eg, diabetic or heart healthy diets) should be lifted during the trial
60
Q

Formula selection/ Delivery in gastric motility problems

A
  • most patients with motility disorders—including those with diabetes mellitus—tolerate standard, polymeric formulas.
  • Because the stomach is bypassed, a formula that contains fiber may be tolerated; however, indigestible fiber may aggravate symptoms if small intestinal bacterial overgrowth (SIBO) is a chronic problem
  • Bolus is not tolerated well; pump or gravity feed over a long time is preferred
61
Q

Is PN recommended in gastroparesis?

A

should only be considered as a last resort

62
Q

is energy expenditure elevated in Crohn’s disease patients?

A

no

perhaps because physical activity decreases during periods of disease exacerbation.

63
Q

should fiber be restricted in crohn’s

A

no as that will inturn lower veggie and vitamin intake-> lower vitamin and mineral intake
fiber may also improve the outcome of inflammatory bowel disease