Ischemic Disease - Bradleys Flashcards

1
Q

Epidemiology of stroke: What % of strokes are Ischemic? What are the long term morbidities of strokes?

A

88% of strokes are Ischemic. Morbidity of stroke: 30 % require assitance with ADLs, 20 require assistance with ambulation, and 16% require insitutional care.

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2
Q

What are non-modifiable stroke risk factors? (Five)

A

age, male gender, ethnicity, family history, and prior history of stroke

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3
Q

What are modifiable stroke risk factors? lifestyle + Non-lifestyle + Non-lifestyle without much proof.

A

smoking + drug use NON-LIFESTYLE hypertension, dyslipidemia SES - low arterial hypertension Heart disease Asymptomatic carotid artery disease Sickle Cell NON-LIFESTYLE risk factos which have yet to be shown to decrease risk when modified - Hypertension - Homocysteinuria - Left Ventricular hypertrophy

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4
Q

What inherited diseases are associated with nonatherosclerotic vasculopathies? Think 1. collagen-vascular 2. cardiac 3. hemtological 4. inherited mitochondrial disorders. Mnemonic: CHIC (collagen-vascular, hematological, inherited mitochondrial, cardiac)

A

Ehlers Danlos Type IV Marfans Rendu-Osler-weber disease (Hereditary hemorrhagic telengectiasias) Sturge Weber Syndrome CARDIAC - familial atrial myxomas -hereditary cardiomyopathies - hereditary cardiac conduction disorders HEMATOLOGICAL - protein C and S or antithrombindeficiencies Inherited Mitochondrial disorders - Fabry - MELAS - Homocystinuria

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5
Q

What is the pathophysiology of cerebral ischemia?

A

* loss of aerobic glycolysis * intracellular accumulation of sodium and calcium ions * release of excitotoxic neurotransmitters, * elevation of lactate levels with local acidosis, free radical production, cell swelling, overactivation of lipases and proteases, and cell death. * Apoptosis of many neurons.

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6
Q

What are the three most predictive examination findigns for the diagnosis of acute stroke (UPTODATE)?

A
  1. Facial Paresis 2. Arm drift/weakness 3. Abnormal Speech
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7
Q

What are immediate lab tests you need for Strokes?

A

CT Head Serum Glucose O2 saturation Ischemic and Hemorrhagic Stroke - EKG, - cardiac enzymes - CBC + Plts - lytes, urea, creatinine - INR - PTT - APTT

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8
Q

What does CT perfusion in normal brain show? MTT, CBF, CBV

A

Normal perfusion parameters are: gray matter MTT: 4 s CBF: 60 ml/100 g/min CBV: 4 ml/100 g white matter MTT: 4.8 s CBF: 25 ml/100 g/min CBV: 2 ml/100 g

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9
Q

What does CT perfusion in ischemic penumbra show?

A

Prolonged MTT

>> MODERATELY reduced CBF

Near normal or INCREASED CBV

CBVVVVV VERRRRY GOOD. — if CBV is increased - that’s good. penumbra is larger!

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10
Q

What does CT perfusion in infarct core show?

A
  • Prolonged MTT,
  • markedly DECREASED CBF,
  • markedly DECREASED CBV
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11
Q

What options for antiHTN medications are available for ICH?

A

Labetalol, Nicardipine are first line agents. Nitroprusside should be considered second-line therapy. It has added risks of increasing ICP and affecting PLT function

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12
Q

What is the recurrence rate for extracranial dissections? Name risks for recurrence (3) What is the recurrence rate for ischemic events?

A

1% per year Young patients, FMD, Fam history of dissections 0-13%, highest in the first few weeks after presentation

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13
Q

Name the causes of extracranial dissections (lots)

A

Blunt or penetrating trauma FMD Marfan Ehlers Danlos type IV Pseudoxanthoma elasticum Coarctation of the aorta Menke’s disease Alpha-1 antitrypsin deficiency Mucopolysaccharidosis Osteogenesis imperfecta Adult polycystic kidney disease Elevated arterial elastase content Lentiginosis Atherosclerosis Vessel tortuosity Moya Moya Homocysteinuria Pharyngeal Infections Sympathomimetic drug abuse Luetic (syphilitic) arteritis

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14
Q

What are the diagnostic criteria for Moya Moya?

A

Review Suzuki’s 6 angiographic stages

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15
Q

What are conditions associated with the formation of aneurysms

A

AD inherited polycystic kidney disease (13% risk increases with age >60 to 23%) Ehlers Danlos syndrome type IV Fibromuscular dysplasia Coarctation of the aorta (10% risk) Moya Moya Pseudoxanthoma elasticum Alpha-1 antitrypsin deficiency SLE Sickle cell anemia Bacterial endocarditis Fungal infections NF1 Tuberous sclerosis Pheochromocytoma AV Malformations Anomalous carotid-vertebrobasilar anastomoses Cocaine use Cigarettes Family History

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16
Q

What is Terson Syndrome?

A

SAH + vitreous hemorrhage. Associated with worse outcomes and more severe SAH

17
Q

What is the timeline for Xanthochromia in CSF

A

appears about 12 hours after symptom onset, lasts several weeks.

18
Q

How do you choose between clipping and coiling?

A

COILING: Advanced age, poor clinical grade, systemic illness, top of the basilar , high surgical risk, patient preferance. CLIPPING: medically well, wide neck-Body ratio aneursms, normal arterial branches arising from dome or body. MCA arter aneurysms, aneurysms associated with large parechnymal hematoma CLIPPINGS have worse prognosis and mortality ISAT study: - risk reduction for coiling (better than clipping). Coiling has risk of aneurysm recurrence or rebleeding but still preferred compared to clipping.

19
Q

What are some DDX in CNS vasculitis?

A

Primary angiitis of the CNS GCA Systemic vasculitides (Behcet’s, ANCA, PAN) Cryoglobulinemic vasculitis Systemic inflammatory conditions (SLE, RA APLAS (more likely a thrombotic syndrome than a vasculitic one)) Infectious (syphilis, lyme, bartonella, TB, HIV) Lymphoma

20
Q

What are Risk factors for RCVS?

A

Women Post-partum Migraine history Drugs: Ergots, other anti-migraine therapies, SSRI’s Sympathomimetics OTC Cocaine Marijuana

21
Q

WHat are EGPA (pANCA) diagnostic Criteria?

A
  • Asthma (with or without pulmonary opatcities on imaging) - Blood eosinophils > 1.5g/L (or > 10% of leukocytes) - Vasculitis (systemic)
22
Q

What are GPA (CANCA) diagnostic criteria?

A

At least two of: -Nasal or oral inflammation -Abnormal CXR -Urinary sediment, microhematuria -Granulomatous inflammation on biopsy When it is meningeal, GPA usually involves the lower CNS structures.

23
Q

What are diagnostic criteria for Behcet’s?

A

Recurrent oral ulceration (recurring at least 3x/year) plus two of: -Recurrent genital ulcers -Skin lesions (erythema nodosum, acneiform lesions, papulopustular eruption, psueodfolliculitis -Eye lesions (anterior uveitis, posterior uveitis, retinal vasculitis) -Positive pathergy test

24
Q

WHAT is the CHADS2 score? And what is the conferred stroke risk?

A
25
Q

WHAT is the CHADS2-VASC score?

A
26
Q

How do you treat ivTPA angioedema?

A

STOP THE OFFENDING DRUG!!!!

Hydrocortisone 100 mg IV

Benadryl 50 mg IV

Ranitidine 50 mg