GI 8 lecture Flashcards

(35 cards)

1
Q

Describe the chronica abd pain with IBS

A

1) Cramping sensation with variable intensity & periodic exacerbations
2) Mild-to-severe
3) Relieved with defecation
4) Abdominal bloating with increased flatulence and/or belching

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2
Q

Describe the altered bowel habits with IBS

A

1) Diarrhea
2) Constipation
3) Alternating diarrhea and constipation
4) Normal BMs alternating with diarrhea and/or constipation

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3
Q

Describe the features of IBS

A

1) Many patients relate a life-long history of altered bowel habits
2) Associated conditions: fibromyalgia, PTSD, GAD, chronic fatigue syndrome
3) Fear of serious disease
4) Exacerbation of diarrhea may coincide with menstrual cycle
5) Bleeding, fever, weight loss, nocturnal awakening with diarrhea are NOT part of IBS (alarm features)

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4
Q

Define the following subtypes of IBS:
1) IBS with predominant constipation (IBS-C)
2) IBS with predominant diarrhea (IBS-D)

A

1) Patient reports that abnormal bowel movements are usually constipation (type 1 and 2 0n the BSFS)
2) Patient reports that abnormal bowel movements are usually diarrhea (type 6 and 7 in the BSFS)

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5
Q

Define the following subtypes of IBS:
1) IBS with mixed bowel habits (IBS-M)
2) IBS unclassified (IBS-U)

A

1) Patient reports that abnormal bowel movements are usually both constipation and diarrhea (more than one-fourth of all the abnormal bowel movements were constipation and more than one-fourth were diarrhea)
2) Patients who meet diagnostic criteria for IBS but cannot be accurately categorized into one of the other three subtypes

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6
Q

The _____________________________ should be used to record stool consistency with IBS

A

Bristol stool form scale (BSFS)

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7
Q

IBS:
1) What should Hx include?
2) What abt PE?

A

1) History: IBS features, BSFS, organic disease, med exposures, recent gastroenteritis, FHx (CRC, IBD, Celiac)
2) Usually normal, possible tender abdomen; include DRE for constipation

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8
Q

What labs should be done to exclude alternative Dx for IBS?

A

1) All IBS: CBC
2) IBS-D: fecal calprotectin or lactoferrin, stool test for giardia, Celiac serologies, CRP (if calprotectin or lactoferrin not available)
3) Colonoscopy: age-appropriate CRC screening in all pts

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9
Q

List the DDXs for IBS

A

IBS-D: Celiac disease, microscopic colitis, SIBO, IBD
IBS-C: dyssynergic defecation, slow colonic transit

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10
Q

Describe management for IBS

A

1) Clinician-patient relationship key to successful management
2) Direct therapy to the initial predominant symptom
3) Allow adequate time for visits
4) Schedule regular return visits
5) Provide patient with information, educational material
6) Be an empathic listener
7) Reassure patient this is a benign disorder
8) Refer for therapy when necessary

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11
Q

List 2 main causes of mesenteric ischemia and their etiologies

A

1) Occlusive: primary thrombosis or embolism
2) Low flow states: severe heart failure, sepsis, or hypotension

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12
Q

Describe mesenteric ischemia

A

1) Inadequate blood supply to the mesentery
2) Results from reduction in intestinal blood flow (arterial occlusion, venous occlusion, or arterial vasospasm)
3) Involves small intestine or colon (colonic ischemia)
4) Acute or chronic
5) Intestinal mucosa most sensitive to ischemia (under perfusion causes sloughing)

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13
Q

Mesenteric ischemia: Describe the parts of the intestinal vascular supply

A

1) Celiac artery (stomach & duodenum)
2) Superior mesenteric artery (SMA)(distal duodenum to mid-transverse colon)
3) Inferior mesenteric artery (IMA)(transverse colon to rectum)
4) Collateral pathways formed by natural anastomoses

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14
Q

Acute mesenteric ischemia: What are the main 2 types and how common are they? Where does each originate?

A

1) SMA embolism (50%): usually originates from the left atrium, left ventricle, cardiac valves, or proximal aorta. hypercoagulable states, inflammatory disorders, cirrhosis & portal hypertension
2) SMA thrombosis (15-20%): strangulating obstructions (adhesions, hernias, volvulus, metastatic malignancy, intussusceptions) and vasculitis (systemic lupus erythematosus, polyarteritis nodosa)

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15
Q

Acute mesenteric ischemia: List the 2 classifications and a variant

A

1) Low cardiac output & use of vasopressors (Non-Occlusive Mesenteric Ischemia (20-30%)
-Ischemic colitis (a variant; usually involves IMA)
2) Venous thrombosis (SMV, IMV, splenic vein, & portal vein)(5%)

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16
Q

Describe the prognosis of acute mesenteric ischemia

A

Survival: depends on early diagnosis & treatment
1) 70-90% mortality if delayed diagnosis & gangrene
2) Up to 90% survivability if no peritonitis
3) Mortality rate > 50%

17
Q

Colorectal obstruction:
1) How common is it?
2) What are 2 origins?
3) What is the most common benign cause?

A

1) 25% of all intestinal obstructions
2) Functional or mechanical (partial or complete)
3) Volvulus (5-15%)
-Sigmoid volvulus most common cause of large bowel obstruction

18
Q

List some other causes of colorectal obstruction

A

Post-op adhesions, strictures due to diverticular disease, hernia with colonic incarceration

19
Q

Colorectal obstruction:
1) 70% occurs where?
2) What labs are needed?

A

1) At or distal to transverse colon
2) Assess for hypovolemia, metabolic abnormalities
Cancer markers

20
Q

Describe the Sx of acute (complete or near-complete) colorectal obstruction

A

1) Bloating, abdominal pain, obstipation
2) +/- nausea, +/- vomiting
3) Infra-umbilical, cramping pain
4) Paroxysms of pain q20-30 minutes

21
Q

List the risk factors for colorectal obstruction

A

1) Malignancy (colorectal, pancreatic & ovarian cancer; lymphoma)
2) Postoperative adhesive bowel disease
3) Stricture due to prior colorectal resection
4) Stricture due to repeated inflammation (diverticulitis)
5) Hernia with colonic incarceration
6) Volvulus (due to anatomic or physiologic abnormalities)

22
Q

Describe the initial management of colorectal obstruction

A

1) Supportive care, decompression of sigmoid volvulus
2) Surgical management: Urgent for acute complete or near complete (benign or malignant etiology)

23
Q

________________ & ___________ are the most useful & practical studies for colorectal obstruction

A

Plain films & CT

24
Q

Describe the workup of colorectal obstruction

A

1) CBC with diff, CMP, lipase, UA
2) Acute abdominal series
3) If no clear cause, consider CT
4) NPO
5) Pain Control
6) Medical or Surgical Management

25
Describe colorectal polyps
1) Discrete mass lesions that protrude into the intestinal lumen 2) Most commonly sporadic 3) May be due to familial polyposis syndrome 4) 70% removed during colonoscopy are adenomatous (precancerous) 5) Usually asymptomatic 6) May ulcerate & bleed 7) May cause intestinal obstruction (large polyps)
26
Toxic megacolon: 1) Define it and its main etiologies 2) What are some other etiologies?
1) Total or segmental non-obstructive colonic dilatation occurring in context of systemic toxicity -Potentially lethal complication of IBD (most common UC) or infectious colitis 2) C. diff infection, infectious colitis (Salmonella, Shigella, Campylobacter), amoebic colitis, CMV colitis (in HIV/AIDS)
27
What are some precipitating risk factors for toxic megacolon?
Hypokalemia, antimotility agents (loperamide), opiates, anticholinergics, antidepressants
28
What are the symptoms of toxic megacolon?
1) Signs & symptoms of acute colitis (resistant to therapy) usually present for 1 week prior to dilatation 2) Severe bloody diarrhea most common presenting symptom 3) Diarrhea may improve prior to onset of megacolon 4) Malaise, abdominal pain, distention
29
What may you find in the Hx of a patient with toxic megacolon?
1) Prior IBD attacks (especially UC) 2) Extraintestinal manifestations of IBD 3) Recent travel 4) Antibiotic or chemotherapy use 5) Use of antimotility agents 6) HIV/AIDS status
30
List the diagnostic criteria for toxic megacolon
Radiographic evidence of colonic distention 1) **PLUS at least 3:** fever (>38C, >100.4F), HR >120 BPM, neutrophilic leukocytosis (>10,500/microL), anemia 2) **PLUS at least 1:** dehydration, AMS, electrolyte disturbances, hypotension
31
Describe the diagnostic eval of toxic megacolon
1) CT abd/pelvis with PO & IV contrast (rectal contrast CT), then serial plain films 2) Baseline plain abdominal films upon admission 3) Labs: CBC/diff, BMP or CMP, CRP or ESR, stool studies (culture, micro, C. diff) 4) Limited endoscopy for selected patients
32
What is the pathogenesis of toxic megacolon?
Severe inflammation of smooth muscle layer --> paralysis of colonic smooth muscle --> dilatation
33
What are the signs of toxic megacolon on PE?
-Toxic-appearing patient with altered sensorium -Tachycardia -Fever -Postural hypotension -Lower abdominal distention & tenderness + peritoneal signs *Large doses of steroids, analgesics, & AMS may mask S/Sx
34
Toxic megacolon: How do you Dx?
Based on clinical signs of systemic toxicity with radiographic evidence of colonic dilatation (> 6 cm) (use diagnostic criteria)
35
List some DDxs for toxic megacolon
Congenital megacolon (Hirschsprung’s disease), acquired megacolon (due to chronic constipation), colonic pseudo-obstruction (Ogilvie syndrome), diffuse gastrointestinal dysmotility, acute colonic obstruction, volvulus, pelvic tumors, & intraluminal obstructive tumors.