GIT Flashcards

(48 cards)

1
Q

appendicitis

A

RF younger
Sx anorexia, fever, rif pain
OE rosvig pos, psoas and obturator, mcburny point tenderness.
Ix: USS,
Dx: clinica/imaging
Rx: OT.

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2
Q

ascending cholangitis - biliary tree bact infection secondary to statis of some form.

A

RF: >50, stones, primary/secondary cclorosing cholangitis, stricture of biliary tree. injury to bile duct (OT)
** Sx/OE: fever, ruq pain, jaundice.
Ix inflam markers, elevated bili/GGT/ALP; uSS/CT to identify cause of obstruction
Dx Sx and evidenc einflam (imaging/bloods)
Rx urgent OT, ERCP. amp/gent/met

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3
Q

cholecystitis

A

RF aging, FHx same, obesity, sudden weight changes, DM , pregnancy, ocp.
Sx severe RUQ pain, radiatse to back/shoudler, n/v/fever. often w colic sx
** OE (differentiates from colic), local peritonism. murphy pos. fever
Ix: USS, CBD > 6mm wall.. ECG/amylase.CXR for ddx, LFT but non specific.
Dx uss
Rx admit, lap chole, abx.

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4
Q

diveritculitis

A

RF age, smoking, obesity, low fibre diet
Sx LLQ pain, change in bowel habit, previous hx of same, n/v/fever/pr bleeding
OE usually LLQ tender, clinical sx cosntipation
Ix CT A/P w contrast
Dx CT/hx.
Rx :
- mild: tol PO intake and no comrobidity: bowel rest, simple anagliesa, low fibre diet 2-3 days.
- > 48 hours ongoing/worsenning/red sided Sx or immunosup: Aug DF BD 5 days, if severe then hospital iv gent/met/amp.

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5
Q

food intol: non immune mediated. ?sensitised nerve fibres.

A

RF: BS, hedaches…
Sx: any age, hours - days. variable reaction.
- bowel irritation, headaches, fatigue, mouth ulcers, sinus cnogestion, hives/swelling, sometimes eczema/rash
- often dose dependent…
- commonly: MSG, food additives, cereals, dairy.
Ix: elimination diet. no specific testing required.
Dx: clinical
Rx: dietary modification.

DDx oral allergy syndrome (raw fruit/veg w perioral sx/rhinitis), coeliac, tick bite (mammalian meat allergy), exercise induced food dept. allergy.

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6
Q

food alergy : igE mediated

A

RF IBS
Sx: childhood onset. allergenic reaction immediately (mins - hours), reproducible.
- rash aroudn mouth, urticaria, angioedema, vomitting, sob, anaphlyxais (varies on scale)
- commonly eggs milk peanut tree nut sesame crustaceans, wheat. soy.
Ix: skin prict tests, IgE specific allergenic test (RAST)
Dx: hx/ix.
Rx
- complete avoidance.
- non treanut/seafood allery improve w age.
- anaphylaxis managment plan.
- loratiadine vs. nocte doxylamine.
- consider referral for desensitisation.

DDx coleaic, tick bite (mammalian meat allergy), exercise induced food dept. allergy.

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7
Q

food allergy: non Ige mediated/mixed food allergy

A

coeliac
eosinophillic oesophagitis
FPIES. (food protein induced enterocollitis syndrome)
- cows milk, fish, chikcen, rice) - recurrent vomitting 1-4 hours after eating.

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8
Q

intersusseption

  • invagination of bowel onto itself
  • sequalae BO, congestion of mesenteric vessels, ischaemia of bowel wall.
A

RF: 2 months - 2 yeras. recent intussusception, meckels diveritumul, HSP, lymphoma, recent rotavirus vaccine, recent bowel surgeyr,.
Sx: intermittent abdo pain/distress (increases 12-24 hours), well between episodes. palpable abdo mass. red current jelly stools.
OE: sausage shaped mass in R abdomen. shock, peritonitis if per, distended if obstructed.
Ix: USS, can do AXR is BO/perf. but not diagnostic.
Dx: USS/clasically sx/age
Rx: analgesia, fluid bolus, NGT if BO, IV amox/gent/met, Surg review w NBM (can self reduce)

DDx

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9
Q

ischaemic colitis
- chronic ischaemic ischaemia = low flow to artery in mesentry, mild to gangrenous colitis/acute.

A

RF: vasc RF. AF. age.
Sx: severe abdo pain, bloody diarrhoea, unwell. shock. RLQ usually.
OE: degree of illness out of proprtion to clinical signs.
Ix CT, colonoscopy /biopsy gold standard.
Dx colonoscopy urgent.

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10
Q

IBD extraarticualr

A

Ank Spond
uveitis
pyoderma gangrenosum
erythema nodosum
apthous ulcers
primary sclerosis cholangitis
vte

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11
Q

coelaic

A

Ix
- TTG, IgA level . +/- EMA
anti gliadin antibody is less specific.

Mx:

  • scope to confirm + repeat at 12 months post diagnosis
  • bloods repeat at 6-12 months post GF diet to see if resolved.
  • monitor b12/folate/TSH/vit D + BMD consideration.
  • screen family members
  • consider PTH/zinc.
  • DT

watch for lymphoma. adenocarcinoma. IBD, primary billiary cirrhosis, dermatitis herpetiformus.

join coeliac society.

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12
Q

IBS Dx/OE

A

cause not clear - visceral hypersensitivity/diet/gut micro/stress.
Ddx: functional; bact.overgrowth (if bloating/flat main issue)

Dx: abdo pain/discomfort > 3 / month, for 3 months, w > 2:

1) improvement w defecation
2) onset of Sx associated w change in bowel frequency
3) onset of Sx associated w change in stool appearance.

OE: not much to find - rule out ddx: coeliac (EMA/antiTTG)/ibd (calprotectin)/pancreatic insuf (fecal elastase)

  • often associated: migraines, dysmenorrhoea, FM, anxiety/dept/reflux/urinary frequ

no specific Ix for Dx.

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13
Q

IBS Mx

A

Mx:

  • non pharma:
  • reassure no long term sequalae, explain aeitology
  • often food intolerance related: exclusion diet, gradual reintroduce once found trigger. (DT)
  • stop smoking
  • weight reduction
  • optimise diet
  • reduce gums/fizzy drinks
  • reduce etOH
  • regular meals/sleephygiene

if diarrhoea PRN loperamide
if constipatino gentle fibre - metamucila good option, avoid bran.
if abdo pain; buscopan.
+/- SSRI.

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14
Q

Crohns (IBD)

A

PC: 20s usually.
mouth to anus, skip lesions. get fistulas/perianal disease.

Sx: abdo pain, diarrhoea, weight loss, mailaise, anorexia, obstructive/fistla/blood diarrhoea. nutritional def.
NOCTURNAL BO = IBD.

clue for Dx: pos faecal calprotectin. (elevated CRP, low labumin, iron def anaemia)

Dx : scopes

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15
Q

IBD Mx

A

RF for poor outcome:
- > 5kg weight loss, unable to manage ADLs, steroids at first presentation, not eating, longterm reliance on opioids for pain.

Mx:
- no cure, goal to treat active disease/improve wellbeing/maintain steroid free remission/prevent complications.
1) sulfasalazine, c/sterods for flare; with GE
metro for fistula flares.
2) regular review for sx severity/condition review
3) annual colonoscopic surveillance if high risk; otherwise 3-5 yearly.
4) DEXA
5) monitor bloods
6) PCV, HPV/HBV. avoid live if immunosuppressed.
7) 1-3 yearly CST if on immunomodulators.
8) quit smoking
9)psychological impact.

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16
Q

UC

A

PC: large intestine/retrograde from rectum. continuous.
commonly bloody diarrhoea.
- watch for toxic megacolon complication

Mx: as above, also consider surgical removal of large intestine if severe/refractory.
localised enemas w mesalazine/PR steroid etc. THEn PO

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17
Q

IBD e/articular Sx

A
  • large joint arthorpathy
  • ank spond
    uveitis
    iritis
    episcelritis
    conjunctivitis
    pyoderma gangrenosum (ulcer)
    erthema nodosum (painful)
    apthous ulcers
    primary sclerosing cholangitis
    VTE
    gallstones
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18
Q

lactase def

A

frothy, watery, explosive diarrhoea - soon after ingestion of lactose.

most commonly associated w acute GI post infection / loss of enzyme, can go on for 1-2 weeks.
- ddx: zollinger eliison syndrome/sensory loss w Dm arthroapthy, progressive diasabiltiy w CF, whipples, tropical sprue, HIV enetropathy, coealiac spru.

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19
Q

barrets

A

relative risk increased for adenocarinoma oesphagus
absolute risk < 2% life time risk.
RF: central obesity, smoking, fhx cancer, sex,a ge, hx GORD.
Dx: endsocopy - metaplasia from squamous to columnar

Mx:
endoscopy screening program. modify RF w lifestyle changes.
consider PPI - wont regress but helps symptomatically.

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20
Q

PPI SFX

A

long term:
micronutrient def - b12/folate
OP
infections such as GE
hypomagnesemia
alopecia
photosesitivity
impaired LFTs

21
Q

EoE

A

same as GORD; but intermittent bolus obstructions.
specific food trigger often.

RF male > female, atopic hx
Dx: endoscopic appearans/histo findings. peristent gastric eosinophillia after PPI trial (GORD will improve)

if severe: risk boerhaave syndrome.

Mx:
NON PHARMA
-dietary exclusion - consider allergy patch testing
-6 food elimination: milkd, wheat, egg, soy, nuts then reintroduce.
PHARMA
-topical fluticasone (swallow MDI rather than inhale, 2 puffs BD)
-SFX: candidiasis.
final: dilatataion

22
Q

GORD red flags

A

red flags

  • dyaphagia, odonyphagia
  • haematemeis
  • weight loss
  • > 55
  • iron def +/- anaemia
  • nocturnal abdo pain
  • persistent
  • FHx?Phx barrets/GI maliganncy
  • new or changing Sx, particularly in older person
  • inadequate reponse to PPI.
23
Q

GORD Ix + HPylori

A

only Ix if red flags/Sx refractory to Rx/diagnosis unclear.

1) endoscopy, 2/4 patients will have negative endoscopye.
2) consider HPylori - post Rx confirm if negative at 6 weeks.
- do for all < 55 yo. or if any RF: (lower SES, migrant/refugee, fhx PUD/gastric cancer)

Dx otherwise based on therapeutic trial of PPI 2weeks.
- if no red flags, and improved w PPI, then reduce to prn

24
Q

GORD Mx

A

Non pharma
- raise bed head, weight loss, smoking cessation, small/regular meals,. avoid acidic foods/hot drinks, avoid lying down after eating, fluid in between meals not prior, eat > 3 hours until bed.

Pharma
- cease nsaids/bisphosphonates, avoid drugs relaxing LOS: ccb/nitrates/cholinergics
- Rx Hpylori (calrithro/amoxyl/ppi), if pos (2 weeks better)
- PRN gastrogel 10-20mL/ H2 receptor antag ranitidine 150mg,
+ PPI 20 –> if insuff 20 BD –> 40 BD if ongoing but refer at this point.
- trial PPI for 4-8 weeks; then down titrate slowly then PRN only.

25
alcoholic liver disease
stages: 1) alcoholic fatty liver- worry when AST/ALT \> 1.5 2) alcoholic hepatitis - AST usually 3 x the ALT. /rapidly progressive sx inc. RUQ pain/jaundice/fever/neutrophillia 3) alcoholic liver cirrhosis. OE: plethroic face thickenend greasy skin macroglosia telangiectasia suffused conjunctivae rosacea parotid swelling chleitis Ix: bloods inc. caeroplasmins/viral heaptitis, cmv for alt cause. USS +/- fibroscan Mx: stop etOH, prevent progression. MDT: DT, GE, psychiatrists/psychologist manage withdrawl: thiamine repacement/bzd. stop smoking/manage obesity which is often associated vaccinate Hep B + A, and PCV/influenza.
26
CLD causes
etOH fatty liver autoimmune chronic viral primary biliary cirrhosis haemachromatosis drugs cryptogenic (no cause) OE: alcoholic faceies spider naevia, caput medusae gynaecomastia splenomegaly (portal HTN) ascites hepatomegaly (vs. small and nodular) bruising, peripheral oedema/neuorpathy atrophied testes/spare pubic hair.
27
NASH
cause: insulin resistance, etOH, obesity. +/- AN, rapid weight loss, lipodystrophy, drugs inc. oestrogens. c/steroid/mtx. increases risk DM/metabolic syndrome/cvasc disease + some cancers, can cause cirrhosis --\> HCC. spectrum 1) simple steatosis. 2) steatohepatitis (NASH) 3) cirrhosis more likely to have cirrhosis if: AST/ALT \> 1, ALT raised, old, serum albumin + platelets low, obesity, hyperglycaemia, DM, metabolic syndrome. uss consider fibroscan. and use NAFL fibrosis score. Mx: if LFTs OK and no evidence cirrhosis/portal HTN on uss --\> 6 month aggresively lifestyl changes and if LFTs still off --\> GE.
28
metabolic syndrome
fasting TIG \> 1.7 or on statin fasting HDL \<1 BP \> 130/85 or on Rx FBG: \> 5.6mmol/L + T2DM aim remember: male wcc \< 94, female \< 80.
29
haematchromatosis
HFE gene testing. - only C282Y homozygotes + sometimes heterozygotes, get clinically significantly overloaded worry re: fibrosis, cirrhosis, hcc, cardiac arrithmia, cardiomyopathy, DM , arthropathy, skin hyperpigmentation w overload. if venesection dependent: 500mL 1-2 weekly, red cross lifeblood = free. aim for ferritin 50-100. screen family if homozycgote C282Y.
30
Hep B
- HBsAg pos = acute + anti HBc IgM - HBsAg pos = chronic + anti HBc IgG - HbSAg neg, antiHBc IgG pos + anti HBs pos = resolved infection - only anti HBs pos = vaccinated Rx - most people clear + becomes HBsAg negative within 6 months - if still positive then chronic hep B (95% of people) - if fulminant hepatitis/liver failure + ongoing at 6 months = Rx. - Rx w specialist/prescriber for entecavir. : check HbV DNA 4-6 monthly, then 6 monthly. if not being treated but chronic hep B: LFT 6 monthly + HBV DNA annually
31
Hep C
RF: prison, IVDU, sexual partner w HCV, HIV, MSM, child w mum w HCV, liver disease, birth in high prevalent area. blood transusion prior 1990. tatoo/piercings HCV antibody positive; then go and do PCR , dont need genotype now (as non pbs criteria) but if treatment resitent then do it. Rx - need to be a registered prescriber. - exclude cirrhosis with biopsy/fibroscan + AST/platelet ratio. - consider coinfection w HIV/HBV - review meds for interactions (LFT related) - exclude pregnancy --\> first line: direct acting antiviral drugs. 8-12 weeks. failure : treatment non adherence, reinfection, virological failure (rare) --\> specialist.
32
hepatitis Rx - GP role
GP role if not prescriber - monitoring adherence - social support - drug SFx monitoring - level of RNA monitoring
33
hep c sequalae/long term monitoring
sequalae: 2-5% annual risk of HCC. - if cirrhosis: need 6 monthly uss + AFP - if abnormal LFT: exclude alt causes / specialist re-refer. - if no CLD, no cirrhosis: no long term f/u required. - if RF for reinfection: repeat HCV RNA yearly after new exposures. abstain from etOH if possible - 4 s.d/day = increased risk of rapidly progressive liver diasese. - ensure vaccines for HBV + HAV + PCV up to date
34
HCV transmission info
- blood/blood contact. - not to donate blood - not to share toothpaste/razor - mother to baby transmission is low - but possible. - avoid BF with cracked/bleeding nipples. - sexual transmission is low amongst monogamous heterosexual partners (0.5%/year) = but possible - needle exchange program
35
autoimmune hepatitis
10-40 yo female fatigue/anorexia/jaundice. ddx alcoholic hepatitis, viral heptatitis. NAFLD pos ANA sm Abdy antiLKM1 igG high Dx: biopsy Rx: pred, azathioprine. 3-5 yearly mortality if not Rx
36
cirrhosis clinical signs/monitring
Sx: anorexia, nausea, vomitting, peripheral oedema, bloating/distension, bleeding tendency, drowsiness, ecephalopathy OE: look for alcoholic facies spider naevi palmar erythema peripheral oedema/ascietes jaundice hepatosplenomegaly. if not small/fibrotic liver ascites gynaecomastia monitorign: 6/12 uss + AFP/LFTs + regular scopes for varices assessment. hcc risk 2-5%/year.
37
complications cirrhosis
sbp encephalopathy heptaorenal syndrome hypernatremia portal HTN w varices portal vein thrombosis renal failure often associated w OP, vit D def, malnutrition.
38
primary billiary cirrhosis
uncommon cause of CLD women, 30-60. ``` Dx: obstructive pattern of liver biochem AMA pos (antimit abdy). ``` Rx: specialist complications: fat solubile vit def, hypercholesterolaemia, BMD.
39
wilsons disease
genetic copper excess 5-35yo usually --\> cirrhosis w copper accumulation + presents w kayser fleischer rings. Dx: usually via corneal findings + caeruplasmin low. + high 24 hour urinary copper excretion Rx: specialist.
40
haemorrhoids
mx: * adequate fibre intake * hydration * avoid straining * respond to urge to defect + try not to initiatie defecation without urge * sitz baths for comfort * procetosedyl: hydrocort/ciclocaine for short term use - SFX; candidaisis, localsied SFX w dermatitis. if bleeding: surg. / unable to reduce, or if large thrombosed external: no Rx required - should spontneously rupture + pain settled at 102 weeks. if severe --\> surg.
41
proctalgia fugax
short attacks of sharp stabbling pain near anal area. wakes pt from sleep. painless when not having episode no clear cause Rx: reassurance, explanation - ?muscular spasm: local warmth, ingestion of food, firm pressure to perineum. if severe: specialist - anecdotal evidence salb/gtn/ccb
42
bowel cancer prevention
- identify risk per Red book/cancer network guidliens - # 1' and 2' realtives - prevention * adopt healthy lifestyle * regular exercise * diet low in fat, high in veggies * high in fibre * avoid smoking * avoid excessive alcohol * individual specific CRC screening * consider low dose aspirin if high risk bewteen 50-50 for 2.5 years. * early recognition of sx
43
Iron def sx
* reduced aeorbic work performance * dev delay * adverse pregnancy outcome * ipaired immune function * glossitis * pica * angular chelitis
44
b12 def
Sx * peripheral neuropathy * spinal cord dmage * otic atrophy * dementia * angular chelitis * glossitis * Rx: IMI alternative days for 2 weeks; then 3 monthly (or if less severe just 3 monthly) , usually life long requierd * ensure IF negative (pernicious anaemia). /cause identified.
45
pyloric stenosis (child)
2-6 week chronological age. progressive non billious vomitting. often projectiled + soon after feeds. can also be blood stained see visible gastric peristalsis + pyloric mass in RUQ (olive) Rx: ED. concern re hypocholareamic hypokalaemic me alkalosis. Surg review
46
carcinoid syndrome
wheezing, flushing, diarrhoea. cause mostly liver mets from pancreatic/gut tumours excessiev serotonin/histmine Mx: oncology/pal acre
47
hirschprungs
first yaer of life vomitting, abdo distension, enterocolitis. RF: trismy 21. = colonic functional obstruction w assocated absence of ganglion cells. Sx: vomitting, explosive passage of liquid/foul stools + abdo distension usually clue: delaeyd mec. Dx: AXR. --\> ED.
48
albendazole
- use for tapeworm (dog/fox) + heliminth infection/strongyloides. (instead of ivermectin). + cutaneous larva migrans.