Nichols + ??? 3 Flashcards

1
Q

Constipation

A

-Infrequent BM <3/week for 12 months with straining/feeling of incomplete evacuation/hard stool at least 25% of time

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2
Q

Normal Colonic Motility

A
  • motor function depends on contraction of circular layer of smooth muscle
  • has 3 patterns of contractions
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3
Q

Short Duration Colonic Contractions

A

Stationary Motor Contractions

  • Present over short areas of colon
  • Causes mixing of fecal material and extraction of water
  • Persists for <15 seconds
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4
Q

Long Duration Colonic Contraction

A
  • may be stationary or propagate for short distances
  • may travel in orad or aboral direction
  • assists in mixing and local propulsion of feces
  • migrates toward rectum in distal colon
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5
Q

Giant Migrating Complexes of Colon

A
  • propagates aborally aver extended distances
  • causes mass movement of feces
  • normally occurs 1-2 times/day
  • may be precipitated by colonic distention
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6
Q

Food Intake & Colonic Motility

A
  • food causes increased segmental activity
  • gastrocolic reflux-may be mediated by CCK
  • response is proportional to caloric content of meal
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7
Q

Hormones & Colonic Motility

A

CCk causes increased frequency & amplitude of segmental contractions
PgF
PgE
Serotonin

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8
Q

PgF

A

stimulates longitudinal muscle contraction

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9
Q

PgE

A

inhibits circular muscle contraction

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10
Q

Serotonin

A

mediates intestinal peristalsis and secretion in GI tract as well as modulation of pain perception

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11
Q

Role of Serotonin

A
  • serotonin (5-HT) is an important neurotransmitter in the brain-gut interaction (released by enterochromaffin cells)
  • 80% of total body 5-HT located in GI tract
  • 5-HT3 receptor antagonists have offered some help in alleviating pain in IBS and functional dyspepsia
  • 5-HT4 receptor agonists have a prokinetic effect in humans
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12
Q

Epidemiology of Constipation

A
  • 12-19% of people
  • more common in individuals with little daily physical activity, low income, and poor education
  • in patients 65 years of age, especially more in women
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13
Q

Constipation: Pediatric Etiology

A
95% functional 
5% organic 
-anatomic
-metabolic 
-neuropathic
-drugs
-endocrine connective tissue D/O
-lead intoxication or botulism
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14
Q

Functional Constipation

A
  • infants and pre-school

- 2 weeks duration Pebble-like, hard stools

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15
Q

Functional Fecal Retention

A
  • common cause of chronic constipation

- with fear and toilet refusal from infancy to 16 years old

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16
Q

Constipation: Elderly

A
  • endocrine and metabolic disease
  • neurologic disease
  • psychological conditions
  • structural abnormalities
  • lifestyle
  • iatrogenic (meds)
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17
Q

Constipation Diagnosis

A
  • H&P/other medical conditions
  • evaluate current meds
  • rule out thyroid disorders or electrolytes problem
  • colonoscopy or Barium Enema
  • colon transit of markers
  • anorectum manometry
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18
Q

Lab Data of Constipation

A

performed in patients with rectal bleeding, weight loss of >10lbs, a family history of colon cancer, IBD, anemia, positive fecal occult blood, short-term constipation

  • CBC
  • serum glucose, creatinine, calcium
  • TSH
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19
Q

Malabsorption

A
  • problem in GI lumen, Defects in epithelial absorptive surface, post-epithelum defect
  • steatorrhea, carbs, proteins
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20
Q

Steatorrhea

A

greater than 5% of dietary fat intake

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21
Q

Patients with steatorrhea?

A
  • weight loss
  • stool characteristics
  • osteomalacia
  • easy bruising
  • Fe deficiency anemia not due to blood loss
  • adult dev. of lactase insufficiency
  • gastric surgery, specially Billroth II
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22
Q

Steatorrhea Stool Characteristics?

A
  • floats
  • greasy
  • stinks
  • hard to flush
  • oil droplets with minimal stools
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23
Q

Mechanisms causing diarrhea in steatorrhea?

A
  • increase of osmotically active particles of mal-absorbed dietary constituents
  • hydroxylation of 10-hydroxy-oleate which acts as cathartic
  • fatty acids themselves impair fluid & electrolyte absorption
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24
Q

Diagnostic Studies with Steatorrhea?

A
  • chemical fat balance, D-xylose absorption, secretin test, X-ray (flat plate of abdomen, CT scan, barium)
  • hydrogen breath test, aspiration of duodenal content for giardia & quant
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25
Stages of Malabsorption
1. Intraluminal Stage 2. Intestinal Stage 3. Lymphatic Transport Stage
26
What Causes the most Steatorrhea?
pancreatic insufficiency
27
Intraluminal Stage
-chronic pancreatitis -Zollinger-Ellison Syndrome -Post-gastrectomy -cystic fibrosis Solubilization: bile acid insufficiency -cholestatic liver disease, terminal lleum resection, bacterial overgrowth in small intestine, reduced CCK released
28
Effects of Impaired Circulation of Bile Salts
- diarrhea and if severe steatorrhea - increased proportion of the bile acids pols conjugated with glycine vs. taurine - increased proportion of deoxycholate in bile - a reduced bile salt pool size
29
Intestinal Stage
Epithelial cell surface digestion - Disaccharidase Insufficiency - Stasis Syndrome
30
Intestinal Stage: Intestinal Cell Dysfunction
- gluten sensitivity enteropathy - stasis syndrome - whipple's disease - intestinal ischemia - radiation enteritis - tropical sprue - genetic disorders such as cystinuria - anderson's disease - abetalipoproteinemia
31
Causes of Malabsorption of GSE
- Cells at surface of intestine are immature: - intestine is in a secretory state (Na-Cl-water) - conc. of bile salts above their CMC is reduced - absorptive functions of mature enterocytes (disaccharidases, Fe, Ca) are reduced - complex lipid synthesis is reduced - Endocrine Cells that produce CCK are reduced - absorptive area of intestine is greatly reduced
32
GSE Pathogenesis & Treatment
- inciting agent is gluten in a person with the right genetic background - treatment: remove exposure to gluten foods - clinical response to the gluten exclusion diet is mandatory to sustain a diagnosis of GSE - If NO response: patient is exposed to hidden sources, patient has GSE plus pancreatic insufficiency or the stasis syndrome, patient has a cause of villous atrophy other than GSE
33
Diagnosis of GSE
IgA antibody ELSIA in detection of GSE sen. 95-98% spec. 94-95%
34
Unexplained Causes of Steatorrhea
- giardiasis - adrenal insufficiency - amyloid - diabetes - hyperthyroidism - combined variable immunodeficiency
35
Lymphatic Transport Stage
-lymphatic duct obstruction: lymphoma, Whipple, Intestinal lymphangectasia, TB, carcinoid
36
Pathology: Celiac Sprue/Gluten Sensitive Enteropathy
villous blunting CD8 -noninfectious cause
37
Viral Gastroenteritis
temporary dissacharidase deficiency
38
Whipple Disease
- rare intestinal, lymph node, cerebral, cardiac and joint infection with Tropheryma whippelii - PAS stain-positive actinomycete - late middle age white males
39
Radiography with Constipation
- plain films of abdomen: megacolon, impaction - barium enema - colon transit study (sitz marker) - defecography
40
Sitzmarks
- different techniques - Pt takes 1 capsule on day 0, check X-ray day5 - if over 80% of the marker are passed by day 5 than colon transit normal
41
Severe idiopathic chronic constipation
- mostly women | - complaints include infrequent defecation, excessive straining when defecating, or both
42
Sitz marker study
- Normal Colonic Transit - Colonic inertia: with delayed passage of marker through proximal colon and no increase in motor activity after meals or with the administration of laxatives - outlet delay: in which markers move normally through colon but stagnate in rectum (more common in pelvic floor dyssenergia)
43
Pelvic Floor Dyssynergia
Defecation Normally: involves relaxation of puborectalis and external anal sphincter muscles, together with increased intraabdominal pressure and inhibition of colonic segmenting activity In Dyssynergic Defecation: ineffective defecation is associated with a failure to relax, or inappropriate contraction of, the puborectals and external anal sphincter muscles
44
Severe Idiopathic Constipation
- in one study frequency of the different abnormalities that can produce severe idiopathic chronic constipation - slow transit constipation 11% - dyssynergic defecation 13% - combo 5% - IBS 71%
45
Treatment of Constipation
``` Education: increase fluid & fiber intake Laxatives Lubiprostone: Cl channel activator 5HT4 agonists: Prucalopride Bio-feedback Surgery: sub-total colectomy with ileorectal anastomosis Suppositories: glycerin or bisacodyl Disimpaction: patients with fecal impaction ```
46
Fiber & Laxatives
Fiber: improve symptoms, bulk forming laxatives, Metamucil, methylcellulose, Ca poycarbopphil Stool softners: docusate sodium Osmotic Agents: polethylene glycol, lactulose Stimulant Laxatives: bisacodyl, senna
47
Lubiprostone
-locally acting chloride channel activator that enhances chloride-rich intestinal fluid secretion (anticonstipation)
48
Misoprostol
prostaglandin analog
49
Prucalopride
5HT4 prokinetic agent | not in US
50
Hirschsprung Disease
-congenital disorder: obstipation from birth and colonic dilatation proximal to a spastic, non-relaxing and nonpropulsive segment of distal bowel MEGA COLON
51
Hirschsprung Disease: Pathogenesis
absence of ganglion cells in large bowel, functional obstruction and proximal dilatation
52
Hirschsprung Disease: Epidemiology
1:5000-8000 males>females 4:1 10% of cases in Down's Syndrome most sporadic, few familial
53
Hirschsprung Disease: Heterogeneous defects in genes regulating
1. migration and survival of neuroblasts 2. neurogenesis 3. receptor tyrosine kinase activity
54
Hirschsprung Disease: Presentation
- failure to pass meconium - obstructive constipation, occasional passage of stool - bouts of diarrhea, abdominal distention
55
Physiological Definition of Diarrhea?
>200gm stool per day
56
Normal stool frequency?
3 bm a week to 3 bm per day
57
Fluid Input Into Gut?
``` Ingestion 2L Saliva 1.5L Gastric Secretions 2L Bile 0.5L Pancreatic Secretions 1.5L Small Intestinal Secretions 1L ```
58
Function of Na+ in Fluid Absorption: Small Intestinal Villi
- Na+/glucose co-transporter | - Na+/H+ exhanger
59
Function of Na+ in Fluid Absorption: Large Intestinal Crypts
-epithelial Na+ channel (ENaC)
60
Increased Intraluminal Fluid: Pathophysiological Mechanisms
1. Decreased Absorption (osmotic) - ingestion of unabsorbable solute - osmotic draw of fluid into the gut lumen 2. Increased Secretion - active secretion of electrolytes + fluid into lumen - electrolytes comprise most stool osmolality 3. Inflammation - mediators stimulate secretion - epithelial barrier compromised by cell death
61
Causes of Osmotic Diarrhea
1. Non-absorbable carbohydrates - lactose (milk, yougert, cheese) - sorbitol, mannitol - lactulose 2. Non-absorbable electrolytes (laxatives) - Mg2+ compounds - Golytely (PEG) prep for colonoscopy - fleet phoshphosoda prep 3. Miscellaneous
62
Key to Secretory Diarrhea?
-excessive Cl- secretion into the gut
63
Osmotic VS Secretory
volume: moderate vs voluminous, watery resolves w/fasting vs persists during fasting much flatulence vs no flatulence stool ph < 5.3 vs ph 6-7 osmolar gap > 125 vs <50
64
Causes of Secretory Diarrhea
1. Bacterial toxins (cholera, heat stable e.coli, yersinia) 2. Laxatives: senna, phenolphthalein, bisacodyl, ricinoleic acid (caster oil) 3. meds: cholinergics, prostaglandins 4. Chemical irritants: bile, arsenic, caffeine, ETOH 5. Neuroendocrine tumors: VIPoma, carcinoid, medullary carcinoma of thyroid
65
Acute Diarrhea
``` < 3 weeks infectious secretory or inflammatory self-limited supportive care (mostly) ```
66
Most common cause of Diarrhea in US?
- viral - E. coli - campylobacter (bloody) - salmonella, shigella (bloody) - giardia (bad water) - cryptosporidium (aids) - c. difficile (hospital)
67
Diarrhea cause in third world?
- viral - campylobacter - E. coli - vibrio cholerae - entameba histolytical - salmonella, shigella - cryptosporidium (infants)
68
Traveler's Diarrhea
20-60% of travelers to third world Prophylaxis recommendations: cooked food only, bottled beverages, no ice, wash hands before meals, peptobismol -if diarrhea: fluids, anti-diarrheals, ciprofloxacin if severe
69
Traveler's Diarrhea: most common cause
E. Coli (40%)
70
C. Difficile Colitis
Risk factors: abx use, extremes of age, hospitalization, institutionalization Cause: Cytotoxins A & B Diagnosis: pseudomembranous colitis on endoscopy, stool assay Treatment: stop abx, metronidazole or vancomycin po, cholestyramine to bind toxins
71
Chronic Diarrhea
``` > 3 week duration -infectious, immune-mediated, malabsorption -osmotic, secretory (no mucosal injury) -inflammatory (mucosal injury) variable prognosis -special interventions required ```
72
Clinical Features of Lactase Deficiency
1. osmotic diarrhea 2. flatulence 3. acidic stool pH
73
Irritable Bowel Syndrome
-common cause of chronic diarrhea in US -disorder of motility & pain perception -Diagnosis-abdominal pain, bloating, symptoms associated with bowel functions, no weight loss, bleeding, malnutrition, or anemia Treatment: anti-cholinergic meds (diarrhea), 5-HT receptor antagonists (constipation), reassurance
74
Microscopic Colitis
2 Types -Lymphocytic colitis -Collagenous colitis Chronic watery, non-bloody diarrhea in adults Treat: bismuth, aminosalisylates, steroids
75
Behcet's Disease
``` generalized vasculitis -oral & genital aphthous ulcers -uveitis -GI tract ulcers -non-erosive arthritis Treatment: immunosuppressives ```