IMC 4.0 Flashcards

1
Q

? is the MC type of cardiomyopathy

What is the MC non-ischemic cause

What part of the heart if affected

A

Dilated

ETOH abuse
MCC- ischemic dz

All 4 chambers

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2
Q

Dilated Cardiomyopathy is characterized by ?

What heart sound is present

What Sxs can this present w/

A

Dec contraction strength- systolic dysfunction

S3- ventricular gallop

Fatigue
Edema
Exertion dyspnea
Displaced apical pulse (megaly)

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3
Q

? is the most definitive method to Dx Dilated Cardiomyopathy

What findings are Dx

What will be seen on EKG

A

Echo

Dilated ventricles
EF <50%, often <30%

Non-specific ST/T changes

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4
Q

What will be seen on CXR of Dilated Cardiomyopathy

How is this Tx

What med is added if increased contractility is needed

A

Balloon heart- megaly and pulmonary congestion

Loop+ACEI+BB
Transplant/LVAD

Digitalis

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5
Q

What medication is used in Dilated Cardiomyopathy to reduce remodeling

What medication is used to decrease the effects of excess catecholamines

Chronic use of ? street drug can lead to this

A

Angiotensin Converting Enzyme Inhibitors- ACEI

BBs

Cocaine

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6
Q

Define HOCM

What type of murmur does this have

What makes murmur louder/softer

A

Ventricular hypertrophy w/ diastolic dysfunction

Medium, mid-systolic cresc-decresc w/ S4

Dec- squat, grip, raise (increased preload)
Inc- valsalva, stand (dec preload)

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7
Q

How is HOCM genetically linked

This condition presents mimicking ?

What type of murmur is present

A

Autosomal dominant affect on sarcomeres

AS- angina, syncope, HF

S4 gallop w/ apical lift

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8
Q

What type of JVD wave is present in HOCM

How is this Dx

What is seen on EKG

A

Prominent A-wave

Echo- LVH, thick septum
MRI

LVH
Non-specific ST/T changes

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9
Q

How is HOCM Tx

What Rxs need to be avoided

What medication is c/i?

A

Diltiazem/Verapamil/Metoprolol
Exercise cessation
+syncope/arrest= ICD

Decrease preload: Diuretics ACEI Nitrates ARBs

Digoxin- increases contraction/obstruction

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10
Q

How does HOCM cause death

Define Restrictive Cardiomyopathy

What Hx is in the Pts report

A

Post-exertional ventricular arrhythmia

Noncompliant ventricles (MC- LV) that resist diastolic filling

Myocardial infiltration w/ abnormal tissue-
Amyloidosis- MC

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11
Q

What type of HF and sound is associated w/ Restrictive Cardiomyopathy

Half of these etiologies are ?

How is this Dx

A

Diastolic HF w/ S4

Idiopathic

Echo- normal EF, dilated atria, hypertrophy
Cath- high atrial pressure

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12
Q

What is seen on EKG of Restrictive Cardiomyopathy

If a Dx is in doubt after an Echo, what is the next step?

What would be seen on CXR

A

Non-specific ST/T changes
Low voltage complexes

MRI- abnormal textures

Pulmonary vascular congestion
Normal heart size

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13
Q

How is Restrictive Cardiomyopathy Tx

Why must Rxs be used cautiously

What populations are at higher risk for developing this condition

A

+edema/pulmonary congestion= diuretic
Definitive- transplant

Avoid lowering preload

Northern European men

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14
Q

Define ASD

What does this defect cause to occur

How common are these defects

A

Atrial wall defect causing L to R diastolic shunt

Volume overload of RA/RV

2nd MC behind VSD

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15
Q

Small ASDs can remain ASx as long as 30y/o but then ? occurs

This defect is often associated w/ ? d/t the stretching

This allows for ? event to occur

A

> 30: dyspnea, angina
50: Afib, RVF

Arrhythmia- RBBB

Paradoxical embolization- DVT causes stroke/brain abscess if septic

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16
Q

What happens to the S2 in an ASD

What kind of S1/S2 is present

How is this Dx

A

Shunting of blood equalizes blood volume entering ventricles- eliminates normally wide, split S2

Loud S1
Wide fixed split- lub dub-dub

Echo w/ bubble contrast

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17
Q

What is seen on EKG of ASDs

What is seen on CXR

How is this Tx

A

RAD
RVH
RBBB w/ rSR in V1

Megaly w/ dilated RA/RV

Small/central <3mm: observe
+Evidence of RV volume overload- surgical closure at 2-6y/o

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18
Q

Define PDA

How do Pts present

What type of murmur is produced

A

Systolic murmur d/t persistent ductus arteriosus (aorta to L-PA) causes L-R shunt

FTT
Poor feeding
Tachy/Tachy

Continuous machinery at 2nd LICS (patent your machine)

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19
Q

What are two common PE findings of PDA

What is seen on EKG

What is seen on CXR

A

Machinery murmur
Wide pulse pressure (arm>leg)

LVH, normal

LVH
Prominent LA, PA, aorta

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20
Q

How are PDAs Tx

Since these may be identified at birth, especially if premature, what is the next step

? congenital infection can cause a PDA

A

Indomethacin- decreases Prostaglandin E1/E2
Fluid restriction
Surgery/Catheter

Re-eval in 24hrs

Congenital Rubella

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21
Q

Define a VSD

? is this murmur the MC of

What type of murmur is created

A

Hole in septum causing L-R shunt between ventricles

MC congenital defect
MC pathological murmur of childhood

Harsh, loud holosystolic w/ systolic thrill

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22
Q

How is a VSD identified on PE

How is the Dx confirmed

How is this Tx

A

Pt supine
Diaphragm at tricuspid

Echo

Watchful expectation

Infant w/ CHF + growth retardation- digoxin + diuretic

Medical failure- surgery <6mon old

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23
Q

Peds w/ VSD need ? prophylaxis prior to procedures

What is being prevented

What is the MC outcome and the most UNCOMMON outcome

A

PCN/Amox
Allergy- Erythromycin

Bacterial endocarditis

MC: spontaneous closure
MUC- CHF secondary to VSD

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24
Q

Define Coarctation of Aorta

What is the usual PE finding

Half of these Pts will have ? defect putting them at risk for ? sequelae

A

Narrowing of aorta, MC below origin of left subclavian artery

Arm BP > Leg BP

Bicuspid aorta;
Berry aneurysm

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25
Q

What does Coarctation look like on EKG?

What does it look like on CXR

How is it definitively Dx

A

LVH

Rib scalloping/notching
Figure 3 sign

TTEcho or CT/MRA

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26
Q

How is Coarctation of Aorta Tx

How is Tx different if seen in neonates

Why would emergent surgical repair be needed

A

Balloon angioplasty w/ stent between 2-4y/o

Prostaglandin E1- keeps ductus arteriosus open

Shock
Megaly
Severe HTN/CHF

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27
Q

What happens if Coarcations are left untreated

Infantile Coarctation is associated w/ ? two defects

Unique fact of Tetrology of Fallot

A

Death by 50y/o d/t:
Rupture/dissection
CVA

PDA
Turner Syndrome- order karyotype analysis

Only cyanotic congenital heart dz on blueprint

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28
Q

What are the 4 features of Tetrology of Fallot

What makes this a Pentology

What is the resulting shunt created?

A

PS RVH Overriding VSD

ASD

PS- R to L through VSD

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29
Q

How is Tetrology of Fallot Dx

What is seen on CXR

What serial monitoring do Pts need

A

Echo

Boot shaped heart

EKG for QRS widening

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30
Q

How is Tetrology of Fallot Tx

What happens if these are left untreated

What are complications that arise after surgical correction

A

Surgery

Sudden cardiac death/HF <20y/o

HF
Outflow obstruction
PR
Arrhythmias

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31
Q

What hereditary T-cell disorder is associated w/ Tetrology of Fallot

What PE finding measures the severity of this condition

Infants/Peds will have ? common PE finding

A

DiGeorge Syndrome

PS

Cyanosis
Tet Spell= hypercyanotic

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32
Q

Define Primary HTN

What are the ranges for Normal, Elevated, Stage 1 and Stage 2

According to USPSTF, Pts need HTN screening starting at ? age and how often

A

SBP 130 or > or,
DBP 80 or >
On two readings, on two separate visits

N: <120 and <80
E: 120-29 and <80
1: 130-39 or 80-89
2: 140 or >, or 90 or >

Start at 3y/o, annual at 18y/o:
Normal- qYear
+RFs/SBP 120-29- q6mon

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33
Q

When measuring BP, Pts reasts x ?min

The cuff needs to cover ? much of arm

How big of width does bladder need

A

Rest >5min and >30min since tobacco/caffeine ingestion

80% of arm

40% of arm

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34
Q

BP discrepancy of ? in both arms needs further eval

When is anti-hypertensive therapy initiation indicated

What is the target BP for PTs w/ or w/out comorbidities

A

> 15mmHg

All Stage 2
Stage 1 w/ ASCVDz, DM2, CKDz or 10yr risk of 10% or more
140/90 w/out comorbidiites

<130/80
<60 w/ CAD/CKD/DM: <140/90
60/>: <150/90

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35
Q

When Tx HTN, how much salt intake is recommended

How much exercise is recommended

If medication is needed, ? is used per ethnicity

A

<2.3g/day (1tsp)

Mod intensity: 30min/day x 5d/wk
Vigorous intensity: 30min/day x 3d/wk

Non-black/DM:
ACEI/ARB
CCB
Thzd (chlorthalidone, indapamide)

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36
Q

What HTN Txs are recommended for Stage 2 HTN

When are ACEI/ARB, BB, or CCBs c/i for Tx

How long are therapies recommended

A

Two BP meds from different classes w/ lifestyle mod

ACEI/ARB- DM w/ proteinuria
BB- asthma
CCB- angina pectoris

F/u 1mon
Goal not met- increase dose or add 2nd med

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37
Q

What is done for HTN if BP is uncontrolled despite 2 anti-HTN meds

What is done if one med causes to much leg edema

What is done if the diuretic is not tolerated

A

ACEI/ARB and
Amlodipine and
Thzd-like

Substitude Amlodipine w/ Verapamil/Diltiazem

Use mineralcorticoid receptor agonist (Spironolactone)

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38
Q

S/e of ACEI

S/e of Spironolactone

S/e of BB

S/e of CCB

S/e of hydralazine

S/e of thiazides

A

Cough Angioedema HyperK (c/i- pregnant)

HyperK

Impotence (c/i asthma)

Leg edema

Lupus-syndrome (and Procainamide)
Pericarditis

HypoK

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39
Q

What are the 5 modifications used for Tx HTN and how much of a decrease is expected

? is the initial medical therapy for DM when starting HTN Tx

What EKG changes would be seen after long standing HTN

A
Weight loss: 5-20mm
DASH diet: 8-14mm
Na dec: 2-8mm
PT: 4-9mm
Dec ETOH: 2-4mm

ACEI- beneficial for neuropathy

LVH

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40
Q

What are two non-modifiable RFs for HTN

? anti-hypertensive agent has alpha and beta blocking activity

Pt w/ BP of 135/85, what is the next step and Tx

A

Age
FamHx CADz

Carvedilol

10yr HDz/stroke risk:
<10%- start lifestyle
>10%, CVDz, DM, CKD- start meds

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41
Q

Define Secondary HTN

When is this Dx suspected

What is the MC cause

A

130/80 or higher w/ identifiable cause

Severe BP
Refractory to HTN med

Primary aldosteronism- high Na, low K

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42
Q

What is the MC cause of curable HTN

? sweet diet finding can increase BP readings

When Tx HTN, lifestyle modification can be tried for how long before meds are used

A

Excessive ETOH and OCP combo usage

Licorice

6mon

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43
Q

When Tx HTN, a initial BP higher than ? indicates starting Tx w/ two med

Define Cardiogenic Shock

What is the MC cause

A

> 160mg

Pump fails, insufficient CO to maintain perfusion

Acute MI

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44
Q

What PE findings suggest cardiogenic shock

What vitals suggest this Dx

How is this Dx

A

Pulm congestion
AMS
Tachycardia
HOTN

JVD
UOP <20
SBP <90

Pulmonary capillary wedge pressure >15mm

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45
Q

How is Cardiogenic Shock Tx

How does this Dx present post-MI

What type of MI are at highest risk for this sequel

A

Fluids/Pressers: Dobutamine, NorEpi
Balloon pump

<72hrs post-MI as free wall rupture

Q-wave transmural
Lateral wall

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46
Q

Define O-HOTN

What criteria is used for Dx

What may be the cause in DM/older aged PTs

A

Excessive fall of BP when upright

Drop of >20 SBP
Drop of >10DBP
Both 2-5min after supine to standing

Autonomic dysfunction- HR inc <10bpm= tilt table

> 100bpm or inc by >30bpm= hypovolemia

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47
Q

How/why does post-postprandial O-HOTN occur

What is the DDx if during Bp checks Sxs present but no HOTN is present

How is O-HOTN Tx

A

Insulin response to high carb meal
Blood pools in GI tract
Alcohol worsens HOTN

POTS Dz

Inc Na/fluids
Fludrocortisone
Midodrine

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48
Q

? class of drug has the most common adverse effect of OHOTN

Define NSTEMI

What would be seen on EKG

A

MAOIs- inhibit enzymes that break down neurotransmitters

Myocardial necrosis w/out ST elevation/Q-waves d/t incomplete block (subendocardial infarct)

ST depression
T-wave inversion

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49
Q

What are the 3 cardiac biomarkers used during N/STEMI work ups

How are NSTEMIs Tx

A

Myoglobin:
1-4hrs; 12hrs; 24hrs

Troponin: most sensitive
2-4hrs; 12-24hrs; 7-10days

CK/CK0MG:
4-6hrs; 12-24hrs; 48-72hrs

MONA BNAH:
BB ASA Reperfusion-PCI Clopidogrel Heparin ACEI NTG Statin

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50
Q

Define STEMI

Since these are Tx similarly to NSTEMIs, what is done first

A

Myocardial necrosis w/ ST elevation/Q-waves d/t complete block (full wall thickness)

ASA and Clopidogrel
Reperfusion <12hrs of Sx onset
Gold Standard: PCI <90min
Thromolytic therapy <180min w/ TPA/Streptokinase

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51
Q

Where on EKG would abnormal be seen:

Anterior wall

Inferior wall

Lateral wall

Posterior wall

Anteroseptal

A

A: 1, aVL, V2-6; LAD

I: 2, 3, aVF RCA- SA/AV nodes

L: 1, aVL, V5-6 w/ reciprocal in 3, aVF; LCX

P: ST depression V1-3; RCA/LCX

AS: V1-V3; LAD/Septal

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52
Q

What are the 6 absolute c/is for fibrinolytic therapy for STEMI Tx

A

Suspected ADissection

Active bleeding/diathesis

Malignant intracranial neoplasm

Ischemic stroke <3mon

CV lesion

HTN, Intercranial

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53
Q

How long after Sxs do NSTEMI/Unstable Angina need angiography

Why is ASA used in N/STEMIs and TIAs

What is the MC type of MI and what is the ‘widow maker’

A

24-48hrs later

Decreases mortality

MC: Inferior (2, 3, aVF d/t RCA)
WM: LAD

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54
Q

What meds w/ Pts be d/c home w/ after NSTEMI

What med is held until d/c and why is it started then

When would BBs be with held from PTs

A

BB ACEI Ntg ASA Statin

ACEI- dec LVH/remodeling to increase EF

2nd/3rd* heart blocks

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55
Q

Why do Pts w/ inferior wall MIs have N/V/weakness and bradycardia

Define Stable Angina

Time frame for this Dx and possible presentation sign

A

Inc vagal tone
SA involvement

Pain/discomfort increased w/ exertion/emotion, predictable and relieved w/ rest/Nitro

<15min;
Levine sign

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56
Q

How is Stable Angina worked up

How is the Dx definitive and what wold be seen

How is this Tx

A

Stress test- reversible wall abnormalities/ST depression >1mm

Coronary angiography;
>70% stenosis

Nitro- sublingual/IV
BB
Angioplasty/Bypass

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57
Q

Stable Angina Pts have decreased prognosis if ?

What is the most sensitive clinical findings for Dx this condition

What is the most useful and cost-effective non-invasive test

A

LVEF <50%
Left main involved

Horizontal/down sloping ST depressions on EKG

Stress test: ST depression >1mm is pos

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58
Q

Pts w/ ? Hx have the highest risk for/are at the same risk for CADz compared to those w/ atherosclerosis

What is the most widely used test to Dx ischemic heart dz in Pts w/ classic angina Sxs

What is the TxOC for HF and what class increases these benefits

A

DM

Nuclear stress test

ACEI- dec morbidity and mortality
B1 selective BBs:
Bisprolol
Metoprolol succinate
Carvedilol
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59
Q

What causes BNP to be released and abnormally low

How is dyspnea early on in HF quantified

HF is a syndrome of ?

A

Released d/t inc ventricular pressures
Low- obesity

Amount of activity that precipitates Sxs

Ventricular dysfunction

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60
Q

Systolic LHF

A

S3 w/ dilated, thin LV from CADz/MI

LVEF <40%

Tx: Loop ACEI BB

Worse: O2 ACEI Nitro w/ IV diuretic at x2 PO dose, no BB until d/c

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61
Q

Diastolic LHF

A

S4 d/t hypertophied LV

Inc >55y/o w/ HTN

Normal EF

Tx: ACEI and BB/CCB; don’t use diuretics/digoxin

Exacerbation Tx- NOAL

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62
Q

RV HF

A

D/t P-HTN

No rales, JVD or edema

Dx w/ cardiac cath

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63
Q

High Output HF

A

Increased metabolic demand exceed CO

Hyperthyroid
Severe anemia
Beriberi/thiamine deficient

First- tachy, then systolic failure

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64
Q

How is HF Dx

What is the most important part of determining prognosis

BNP levels over ? amount means CHF is likely

A

Echo

EF:
Norm- 55-60; <35 increased mortality

> 100

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65
Q

What are the 4 NYHA HF classifications

A

1: no activity limitations
2: slight activity limitations; ordinary activity causes Sxs but comfortable at rest
3: marked limitation of activity; less than ordinary activity causes Sxs but comfortable at rest
4: unable to carry out activity, also have Sxs at rest

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66
Q

An S3 heart sound on inspiration most likely indicates ? type of HF

An S3 heart sound on expiration most likely indicates ? type of HF

? type of HF is associated w/ paroxysmal nocturnal dyspnea

A

Right sided

Left sided

Left sided

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67
Q

? antiarrhythmic is used to Tx Afib/flutter in Pts w/ HF

? drug affects RAAS, helps limit remodeling and adds to the effects of ACEIs

? is the most effective diuretic in Tx of HF

A

Digoxin

Spironolactone

Furosemide

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68
Q

? class medication is recommended in all stages of chronic HF

? 4 med classes are important in Tx HF because they all decrease mortality

How do they accomplish this benefit?

A

BBs

ACEI/ARB
BB
Spironolactone

Inc sympathetic stimulation and aldosterone production- regulates Na/water in body

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69
Q

Only valve w/ two leaflets

Classic AS presentation

Who gets fed during AS causing Sx

A

MV

Syncope
Angina
Dyspnea

1- coronary artery
2- carotids
3- L subclavian (arm pain)

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70
Q

Pt w/ angina is given Nitro and passes out, ? is underlying issue

What type of S2 will be heard

What additional heart sound may be heard

A

AS

Split S2

S4

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71
Q

? is the MC acquired heart valve stenosis

Where can this murmur radiate to

How is this best heard and what maneuvers will make this louder/softer

A

AS d/t calcification

Neck, apex

Leaning fwd w/ expiration;
Inc w/ squat
Dec w/ grip, straining

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72
Q

AS w/ ? suggests a congenital origin

What will be seen on PE if LVH is present

What type of abnormal microscopy result can be seen

A

Ejection sound

Apical impulse

Helmet cells (schistocytes)- fragmented RBCs from passing through calcified stenotic AV

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73
Q

What makes AS louder

What makes AS quiet

What is the MC cause of AS in younger PTs

A

Sit, lean fwd w/ exhale (valsalva)
Squat
Hand grip

Stand

Early onset calcification of congenital bicuspid valve

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74
Q

What is the MC cause of AR

What can Pts present w/ as c/c

What PE finding suggests AS has caused structural changes

A

Weak valve tissue from aging, floppy flaps

Aware of heart when laying down

Down, displaced apex

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75
Q

What term describes the pulses of the Pt w/ AR

What two findings suggest a large regurg flow is present

? congenital syndrome is associated w/ AR

A

Water hammer- increased pulse pressure

Mid-systolic
Austin flint

Marfans- MVP and AR

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76
Q

What is the best initial test for Pts w/ suspected AR

What does AR do to pulse pressures

What is the mainstay of Tx of AR

A

TTE

Widens

Dec after load until surgical correction

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77
Q

What is the difference in severity of mild/severe AR

What is the MC cause of MS

What is heard on exam

A

Severe AR- shorter murmur

Rheumatic heart dz

Apical opening snap (lateral decubitus)
+PHTN- palpable RV impulse
Loud S1
LAH- Tx w/ ACEI

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78
Q

MR is the MC ? murmur

What type of murmur is produced

What are 4 etiologies of MR

A
2nd MC (after AS)
MCC- MVP

Holosystolic at apex w/ dec S1, split S2 radiating to axilla, and apical S3

CADz
HTN
Infection
Rheumatic heart dz
MVP
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79
Q

What are two odd c/c Pts w/ MR may present w/

How is MR different from TR

Female w/ MVP have increased issues w/ ?

A

SOB worse w/ laying/activity
Inc nocturnal urination

Not louder w/ inspiration

Inc pulses- palpitations w/ exercise

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80
Q

What maneuvers change the features of MVP

What may be seen on EKG

How are these Pts Tx

A

Squat- delays
Standing- moves closer to S1

ST depression
PVCs
Early inferior repolarization
QTc prolongation

+palpitations: BB
Avoid smoke/caffeine
Surgical repair- especially w/ impaired LV systolic function

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81
Q

Where is TS heard

What makes murmur louder

What is the MC cause of this defect

A

Diastolic rumble at LLSB

Inspiration

Rheumatic valve heart dz

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82
Q

How is TS Tx

How does TR present

What is the MC cause

A

Percutaneous balloon valvotomy

Holosystolic at LLSB that radiates to sternum and inc w/ inspiration

RVF/dilation initiated from PHTN/LVF

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83
Q

How does TR change the JVD wave

How does PS present

What is the MC cause

A

Inc w/ large ‘V’ waves

Systolic murmur at pulmonic area that inc w/ inspiration

Congenital malformation in kids

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84
Q

What will be heard on PE of PS

What type of murmur is heard in PR

What causes PR

A

Widely split S2 w/ dec P2 w/ R sided S4

Diastolic decrescendo at pulmonic area that inc w/ inspiration

PV annular dilation/damage/congenital malformation

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85
Q

What is this murmur of PR AKA

Since PR can be indistinguishable from AR, how is it differentiated

How is this murmur Tx

A

Graham-Steel murmur

PR inc w/ inspiration, AR does not

Valve replacement

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86
Q

? is the MC cardiac arrhythmia and what is it’s biggest RF

The prevalence of this MC increases d/t ?

Why does this conduction irregularity develop

A

Afib d/t HTN- irregular, irregular w/out P-waves and narrow QRS

Age

SA node generation is overwhelmed/disorganized MC by pulmonary veins

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87
Q

What is the most important lab ordered for Afib work up

What two neurological issues can cause Afib

What is the best imaging for Dx

A

TSH to measure thyroxin (inc cellular metabolic rate); Graves present w/ Afib

Suabarachnoid hemorrhage
CVA

TTE- initial (valves, chamber/wall dimension)
TEE- most accurate (thrombus)

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88
Q

Where/what is the most common site of an embolus to develop during Afib

How is Afib Tx and w/ ? goal

How is rate control achieved w/ Rxs

A

LA appendage

1- Unstable: Cversion
2- >48hrs: anticoagulate x 21days
3- Afib + RVR= chemical conversion

<110bpm:
IV Diltiazem/SAME-olol
Low dose digoxin, slower/inadequate rate control

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89
Q

What is a s/e of using Sotalol for rate control of Afib

What is the drug of choice for Tx Afib in WPW

What med is best for rhythm control if there is/no CAD/CHF

A

Torsades

Procainamide- security detail to AV node

Flecainide: -CAD/CHF
Dronedarone: +CAD, -CHF
Amiodarone: +CHF

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90
Q

Why are CCBs used for rate control of Afib

DHP vs non-DHP CCBs

If using Amiodarone/Dronedarone for rhythm control, ? drug can’t also be used

A

Road block between SA/AV node (5 land to 2 lane)

Pine tree- outdoor
(CCBs w/ -pine, outpatient)
Non-pine (non-DHP)- no out-PT; Verapamil; Diltiazem

Dabigatran- DOAC for Afib d/t non-valvular d/o

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91
Q

When/why would Digoxin be used in the Tx of Afib

What alternatives to Warfarin are available and indication for use

How does AFlutter appear on EKG

A

HF and dec LV function;
Inc intracellular Ca

Dabigatran- DOAC for Afib d/t non-valvular d/o
Rivaro/Api-xaban: no antidote and no blood testing

Irr/Regular w/ sawtooth P-waves

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92
Q

How is AFlutter Tx

How is rate control in Aflutter different than Afib

If conversion is needed for Aflutter, how much energy is needed

A

Diltiazem
Flecainide
Dronedarone>Amiodarone

Rate control more difficult

50-100J

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93
Q

How is the need for anticoagulation for Afib/Flutter determined

What DOACs can be used

When/why would Warfarin be used and w/ ? goal

A

CHA2DS2-VASc:
0- none/ASA 81-325mg
1- ASA 81-325 or anticoag
2 or >- anticoagulate

Dabigatran
Edoxaban
Apixaban
Rivaroxaban

INR goal: 2.5:
Prosthetic valves
EGFR <30
Rx: Phenytoin, antiretrovirals
MS
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94
Q

What does the CHA2DS2-VASc stand for

? DOAC has a reversal agent if needed

Eliquis dosage needs to be lowered if used w/ ? ABX

A
CHF/LVEF 40% or less
HTN
Age 75 or >: 2pts
DM
Stroke/TIA/Emboli: 2pts
Vascular dz
Age 65-74
Female

Dabigatran

Clarithromycin

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95
Q

Define Paroxysmal AFib

When is this Dx changed to Persistent/Permanent Afib

Define Multifocal Atrial Tachycardia

A

Intermittent attacks that self resolve <7days

Persist:>7d
Permanent: >12mon

MC in COPD Pts w/ irregular, irregular rhythm and varying P-wave morphology

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96
Q

Nearly 90% of Afib PTs will present w/ ?

AFlutter may develop as a sequelae to ?

Aflutter Pts are more likely to present w/ ? c/c

A

ASx

Open heart surgery

Fatigue
Exercise intolerance

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97
Q

What is the main difference between Afib/Flutter Txs

? is the most rapid method to lower INR in PTs on Warfarin

Define PSVT

A

Aflutter cured w/ RFA

FPPlasma

SVT w/ abrupt start and stop in Pts w/out other structural heart Dz

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98
Q

What are the two types of PSVT

How are these Dx

How are these Tx

A

AVNRT: tachyarrhythmia developing above Bundle of His

WPW: abnormal pathway between atria and ventricles in Bundle of Kent

Holter monitor to capture episodes

Stable: Vagal, Carotid massage, Valsalva
Sxs: Adenosine
Regular: BB/CCBs
Definitive: RFA

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99
Q

What meds are avoided in Tx of WPW

What is the Tx oc choice for long term management

Why is Adenosine used for PSVT Tx w/ fear

A

Adenosine, CCBs

RFA

Transient asystole d/t T1/2 of 6sec

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100
Q

What are the 3 types of premature beats

What abnormal beat presentation can these have

A

PVC: wide/bizarre QRS w/out P-wave

PAC: abnormal P-wave, common in COPD Pts

PJC: narrow QRS w/ no/inverted P-wave

Trigeminy
Bigeminy

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101
Q

Pts w/ heart Dz and frequent PACs will soon develop ? issues

What are two etiologies of PVC

If Pt has palpitations, they describe them as ?

A

PSVT Afib/flutter

Hypoxemia
E+ imbalance

In throat

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102
Q

How are premature contractions Dx

How are these Tx

How is V-Tach Tx

A

EKG, Holter

PAC: reassure
PVC: BB, ablation
PJC: only Tx if >10/min or multifocal w/ lidocaine/antiarrhythmic

Stable: Amiodarone, Lidocaine, Procainamide
Unstable monomorphic: synchronized cardioversion starting at 100J
Unstable polymorphic: Dfib

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103
Q

How is VTach defined

This is a common complication d/t ?

? antiarrhythmic used for long term can cause hyper/hypo-thyoidism

A

3 or more consecutive premature ventricular beats

Acute MI
Dilated cardiomyopathy

Amiodarone- similar structure to thyroxine w/ iodine

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104
Q

What are the different classes of antiarrhythmic drugs?

S/e of using Procainamide

How is VFib Tx

A

1a: Na blocker
1b: fast Na blocker
1c: potent Na blocker
2: BB
3: K blocker
4: Ca blocker

Drug induced lupus eruption

CPR
Defib- non-synch conversion 120 150 180
Epi
Amiodarone 6mg, 12mg

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105
Q

Define VFib

This MC develops d/t ? myocardial abnormal

This rhythm can be caused by abusing ? two drug

A

Uncoordinated quivering of ventricle w/out useful contractions

MI- ischemia increases excitability of myocardium, predisposes heat to Vfib

Meth, Cocaine

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106
Q

? technique can providers use to Tx VFib if no defibrillator is present

Define 1* Heart Block and the Tx if needed

Define the two types of 2* Heart Blocks and their Txs

A

Precordial thump

PR >.20 (5 small squares): problem between SA/AV nodes; Tx w/ BBs

Mobitz Type 1: Wenckebach-
Long, long, drop; no Tx unless unstable- pacing

Mobitz Type 2:
Dropped QRS, Pwave w/out QRS; Tx w/ pacemaker

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107
Q

Define 3* Heart Block

What class of drug is c/i in all heart blocks

Only two blocks have constant R-Rs

A

Constant P-P, R-R interval
Erratic PR; Tx w/ pacer after r/o ischemic dz

CCBs

1st, 3rd degree

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108
Q

? is the MC cause of AV blocks

? is the only complete AV block

Why do Pts w/ Mobitz Type 2 need pacers

A

Idiopathic fibrosis/sclerosis
Ischemic heart dz

3rd degree

Always pathologic, almost always progress to 3rd degree blocks

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109
Q

? type of Dz infection can cause a 3* heart block

? is the MC cause of 3* blocks

Define Sick Sinus Syndrome

A

Lyme Dz

Myocardial ischemia

Dysfunction of sinus nodes automaticity and impulse generation

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110
Q

Define 4 abnormals seen in Sick Sinus Syndrome

What is the MC cause of the underlying sinus node dysfunction

Most PTs w/ SSS will need ? Tx

A

Sinus brady: <60bpm
Pause: <3 seconds
Arrest: >3 seconds
Tachy-Brady: alternates; Tx w/ pacemaker

Idiopathic SA fibrosis

Pacemaker
Use BB/CCB/Digoxin if prepared to transcutaneous pace

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111
Q

Define Acute and Subacute Endocarditis

MC cause in native valves infection is ? group

MC cause in IVDA

MC cause in prosthetic valves

A

Acute: Staph infects normal valves
Sub: Strep V infects abnormal valves

HACEK

Staph A w/ small vegetations

Staph epidermis

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112
Q

How does endocarditis of a fungal origin present

What is the time frame for presentation

What type of fungus will be cultured and how is it Tx

A

Contaminated line cause slowly grown, large vegetations

<2mon post-valve replacement

Candidia; Tx w/ Amphotericin B

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113
Q

? microbe is the MC cause of infective endocarditis

How does this microbe origin present

What are the peripheral findings of endocarditis

A

Strep viridians

Late complication of valve replacement w/ small vegetation/emboli

Splinter hemorrhages
Roth spots
Janeway- sign septic emboli
Osler node- painful
Spelnomegaly
Hematuria
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114
Q

How is endocarditis Dx

How is this condition Tx depending on valve type

A

TEE- gold standard
+Blood cultures, 3 sets, 1hr apart

Native w/out IVDA: Nafcillin Ampicillin Gentamicin

Prosthetic: Vanc Gentamicin Rifampin

IVDA: Nafcillin

PCN allergy- Vanc

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115
Q

What are Pts prophylactically Tx w/ post-endocarditis

Four RFs for developing infective endocarditis

Pts presenting w/ ? two Sxs signal suspected Dx

A

2g Amoxicillin
PCN allergy-Clinda

Prosthetic valve
Rheumatic heart dz
IVDA
Congenital defect

Fever- MC Sx
New murmur- TR/MR
Stroke

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116
Q

What are 3 possible adverse outcomes from infective endocarditis

Non-IVDA endocarditis MC affects ? valve

IVDA MC affects ?

A

Glomerulonephritis
Septic emboli
Splinter hemorrhages

Mitral

Tricuspid

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117
Q

5 criteria for Pts to need endocarditis prophylaxis

Pericarditis is MC from ? microbe and often leads to ? sequelae complication

? syndrome of pericarditis is seen 3-5d post-MI

A

Prosthetic valve
Prosthetic material repair
Hx endocarditis
Congential heart dz

Coxsackie;
Pericardial effusion

Dresslers

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118
Q

How is pericarditis Dx

What PE finding may be seen

How is it Tx

A

EKG w/ diffuse, ST elevation in 1/2, V5/6

Kussmaul sign- increased CVP w/ inspiration; common in constrictive pericarditis

NSAID/ASA x 7-14d
Sxs >48hrs- CCS

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119
Q

What are 3 autoimmune etiologies of pericarditis

What 2 inflammatory Dzs can cause this

What 2 medications can cause this

A

SLE RA Scleroderma

Sarcoidosis
Amyloidosis

Hydralazine
Procainamide

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120
Q

How do Pericardial Effusions present

What would be seen on EKGs

What would be seen on Echo

A

Same as pericarditis w/ fluid accumulation around heart

Low voltage QRS
Alternans
Tachy

Swinging heart
Water bottle sign

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121
Q

What are the “3-Ds” of a cardiac tamponade

What Triad is this AKA

What are two possible complications of an effusion

A

Muffled sounds
Elevated JVD w/ rapid x-descent, attenuated y-descent
HOTN

Beck’s Triad

Tamponade
Constrictive pericarditis

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122
Q

? is a classic finding on PE of cardiac tamponade

What would be seen in PTs VS

What is the gold standard of Dx

A

Pulsus paradoxus- SBP dec x 10mmHg w/ inspiration

Narrow pulse pressure

Echo

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123
Q

How is pericardial effusion different from tamponade

How is the tamponade Tx

? is the MC cause of non-traumatic tamponade

A

Effusion doesn’t cause RV collapse

Urgent- centesis
IV fluids to inc preload

Met malignancy

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124
Q

How do tamponades lead to death

? is one of the most consistent tamponade findings

What would make this consistent finding absent

A

IVC pressure decreases preload

Pulsus paradoxus

Hypovolume
Low press tamponade
LV

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125
Q

How do AAAs present

How do A-Dissections present

When is screening indicated

A

Back pain
Pulsatile mass
HOTN

Tearing pain radiating to back w/ different arm pulses

Male >65 w/ +smoking history

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126
Q

? is the difference between dissection and AAA in structural involvement

What is the initial and gold standard Dx test of choice for AAA

What is the CXR finding for aortic dissections and how are they Tx

A

AAA involves all 3 layers
Dissection- one layer, intima

US- initial
Angiography- gold standard

Widened mediastinum;
Ascending- surgery
Descending- BBs

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127
Q

What is the Dx test of choice for aortic dissections

How are AAAs managed depending on size

A

MRI angiography

<3cm- no more tests
3-4.4cm: annual
4.5-5cm: q6mom, refer
5-5.4cm: q3mon
>5.5 or >0.5cm expansion in 6mon- immediate repair even if ASx
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128
Q

Define Venous Insufficiency

What is a common PE finding

If ulcer present, they are commonly located ?

A

Impaired venous return causing skin change, edema, pain

Stasis Dermatitis

Medial malleolus

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129
Q

How is Chronic Venous Insufficiency Dx

How are they Tx

Define Varicose Veins

A

US, D-dimer

Elevation, compression
Ulcers- wound care, compression

Dilatd superficial veins in lower extremities w/out obvious cause

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130
Q

If symptomatic, what do varicose veins present w/

How are these Tx

Define Acute Bronchitis

A

Pain w/ exertion
Full/pressure
Hyperesthesia

Compression
Elevation
Wound care
Sclerotherapy
Surgery

Cough lasting >5days

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131
Q

? Sx is unusual for bronchitis and it’s presence should shift Dx to ?

95% of bronchitis is d/t ? etiology

If caused by bacteria, ? microbes can cause this

A

Fever;
Pneumonia

Viral

M Catarrhalis- MC bacterial cause of acute bronchitits
H influenzae
Strep pneumoniae

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132
Q

How is acute bronchitis Dx

How are these cases Tx

Acute exacerbations of chronic bronchitis d/t bacteria are Tx w/ ?

A

CXR

Tx Sxs, >95% are viral:
Cough: Dextromethorphan, Guaifenesin
Wheeze/Pulm Dz: albuterol

1st: 2-Gen Cephalosporin
2nd: 2-Gen Macrolide or TMP/SMX

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133
Q

When are ABX indicated for the Tx of Acute Bronchitis

How does Acute Sinusitis present

What is the MC cause

A

Elderly
+CardioPulm Dz and cough x 7-10days
ImmComp

Sinus pain w/ drainage
Sxs worsen 5-7d or do not improve >10days

Strep pneumo

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134
Q

What is First, Second, and Third Line Tx for Acute Sinusitis

What is the gold standard and other form of imaging method if needed

? microbe is the MC cause of chronic sinusitis

A

1st: Augmentin
2nd: Doxy
3rd: Levaquin

CT- gold standard
X-ray w/ waters view

Staph A

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135
Q

Time frame for acute sinusitis

When is this converted to chronic sinusitis

Time frame for sub-acute sinusitis

A

<4wks w/ sudden onset

> 12 consecutive wks

4-12wks

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136
Q

What are the indications to use ABX for Tx of Sinusitis

What ABX are options for first line Tx

Why would second line ABX be needed and what can be used

A

Sxs >10d w/out improving
Fever >102
+purulent d/c
Improvement w/ rapid worsening of Sxs

Augmentin*
Amoxicillin
PCN allergy- Doxy, Cefixime or Cefpodoxime w/ or w/out Clindamycin

No improvement in 7d;
Augmentin 2g BID
Levofloxacin
Moxifloxacin
PCN allergy- Doxy, Levoflox, Moxiflox
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137
Q

How is Chronic Sinusitis Tx

How is sinusitis in Peds Tx

Why do Sinusitis Pts lose sense of smell

A

3wk Tx course of:
Augmentin
PCN allergy- Clinda

Augmentin
PCN allergy: Cefpodoxime, Cefdinir

Olfactory epithelium destroyed by viral infection/chronic sinusitis

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138
Q

? is the MC microbe to cause acute bacterial sinusitis in adults?

? is the MC type of bacterial pneumonia that is MC seen in Pts >40y/o

This MC type if common in Pts w/ ? MedHx

A

Staph A

Strep pneumonia- rust colored sputum

Splenectomy

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139
Q

How does Staph A pneumonia present

How is it Tx if MRSA is suspected

Pseudomonas causes pneumonia in ? populations

A

Salmon colored sputum after influenza

Vanc

ICU ventilator
CF w/ Vit A deficiency
Bronchiectasis
Malignancy
COPD
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140
Q

When/where is mycoplasma pneumonia more commonly seen

What two findings indicate this Dx

MC microbe to cause pneumonia in drinkers w/ aspiration

A

Pts <40y/o in dorms

Cold agglutinins
Bullous myringitis
Erythema Multiforme

Klebsiella

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141
Q

Strep Pneumo, H influenza induced pneumonia usually present w/ ? S/Sxs

Atypicals like Mycoplasma, Chlamydia and viruses present w/ ? S/Sxs

What two Pt populations are most frequently admitted for CAP

A

Productive cough
Fever, high
Tachy/Tachy

Non-productive cough w/ fever

Elderly
COPD

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142
Q

How do the 3 typical microbes (Hflu, Morax, Strep Pneumo) that cause pneumonia appear on CXR

How do the 3 atypicals (Legion Mycoplasma C-pneumonia) appear on CXR

A

Lobar pneumonia and sicker Pt

Interstitial infiltrates, Pt not as sick

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143
Q

? is the MC nosocomial infection

? is the 2nd MC

? is the MC type of pneumonia in older adults and is more common in winter month

A

UTI d/t foley

Pneumonia w/ Strep Pneumo

Pneumococcal pneumonia d/t Strep Pneumo

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144
Q

What vaccine is used to help reduce CAP

What Pts should get this vaccine

? is the biggest lymph node of the body

A

PCV-13, 1 year later;
PPV-23
Annual influenza

Age >65y/o
Smokers
Sickle cell dz
DM
Indian/Inuit
Chronic liver Dz

Spleen- largest Ab maker in body

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145
Q

How is CAP Tx outpatient w/ no ABX use x 90days

How is CAP Tx outpatient if +ABX use x 90days or +comorbidities

How is CAP tx in areas w/ macrolide resistance

A

Macrolide (Azith/Clarith) or,
Doxy

M/L/G-floxacin or,
Macrolide (A/C-mycin) and Augmentin (Beta-lactam)

M/L/G-floxacin or,
Macrolide (A/C-mycin) and Augmentin (Beta-lactam)

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146
Q

How is CAP Tx in ICU

How is this Tx regiment changed it Pt has COPD

? is the MC atypical pneumonia and MC pneumonia in younger adults w/ ? outbreak trend

A

M/L/G-floxacin or Azith and
Cefotax/Ceftriax or Ampicillin (antipseudomona w/ beta lactam coverage)

Levofloxacin (Levaquin) becomes 1st

Mycoplasma in adults <40y/o w/ summer/fall outbreaks

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147
Q

How does Mycoplasma Walking Pneumonia present on CXR

How is it Tx

How does Legionella induced pneumonia present

A

Patchy infiltrates more extensive than exam

1- Azith/Clarith-romycin
2- Doxy/Augmentin
3- Levofloxacin (Levaquin)

HypoNa Diarrhea Fever

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148
Q

What is the CURB-65 scale used for

How is anaerobic pneumonia Tx

A
Pneumonia ICU admission:
Confused
Urea >20
RR 30/>
BP: <90/60
65 or older
Each one= 1pt
0-1: low risk
2pts: mod risk, consider admit
3-5: high risk, ICU admit

Augmentin
Amox/PCN and Metronidazole

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149
Q

? PE finding is a constant finding in Legionnaires pneumonia

What are the two distinct clinical presentations of this Dz

What does it look like on CXR

A

Bradycardia

1st- Pontiac fever; viral-like syndrome
2nd- pneumonia

Mid/lower lobe w/ patchy infiltrate
Inc LDH= pleural effusion

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150
Q

How is Legionairres Pneumonia Dx

How is this form of pneumonia Tx

Define Pneumocystic Carinii Pneumonia

A

IFA and ELISA
Sputum DFA
Legionella urine Ag

1- Azithromycin
2- Levofloxacin (Levaquin)
3- Doxy

Pneumocystis jiroveci- unicellular fungi in ImmComp Pts (AIDS CD4 <200)

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151
Q

How does Pneumocystis jiroveci present

How does it appear on CXR

How is this type Dx

A

F/C
Dyspnea, low PO2
Dry cough x wks

Bilateral, perihilar infiltrates w/ inflamed alveolar cells

Bronchial lavage/biopsy

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152
Q

How is the degree of lung injury in Pneumocystis Jiroveci measured

How is this Tx

What s/e may be seen d/t this medication

A

LDH level

TMP/SMX (+ Dapsone)
Allergy- Pentamidine

Pancreatitis
Renal failure
Prolong QT

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153
Q

Chlamydia pneumonia is associated w/ ? Hx but lacks ? presenting Sx

What 3 forms are pathogenic to humans

How is it passed along

A

Birds;
Afebrile

Pneumoniae
Psittaci
Trachomatis

Inhalation of dried feces

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154
Q

How is Chlamydia Psittaci Tx

? are the 3 MC causes of viral pneumonia

A

1- Doxy
2- Azithromycin

Influenza
Adenovirus
Parainfluenza

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155
Q

How is Viral Pneumonia in Peds Dx

How is an RSV etiology tested for

How will they present

A

PCR testing for Adenovirus

Nasal wash

Tachypneic w/ wheeze

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156
Q

How is RSV pneumonia Tx

What will these Pts be at risk for later in life

Pts w/ pneumonia and Tx w/ Macrolides but bounce back now need to be Tx w/?

A

1- Ribavirin
2- Palivizumab

Reactive airway dzs

Levofloxacin (Levaquin)

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157
Q

Peds w/ CAP are Tx w/ ?

How is CAP Tx outpatient w/ no comorbidities, recent ABX use and low resistance rate

What is the s/e of using Macrolide or Fluoroquinolone class ABXs

A

1st- Amoxicillin, <5y/o
2nd- Azithromycin, >5y/o

1- Azith/Erythromycin
2- Clarithromycin/Doxy

Prolonged QT interval

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158
Q

MC cause of viral pneumonia in adults

MC cause of viral pneumonia in kids

MC cause of fungal pneumonia in western states

A

Influenza

RSV

Valley Fever d/t Coccidioides

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159
Q

MC cause of fungal pneumonia from caves/zoos in Ohio/MS river valley

? fungal spore is found in soil and can lead to meningitis

MC fungal pneumonia etiology in COPD/TB

A

Histoplasma capsulatum

Cryptococcus

Pulmonary aspergillosis

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160
Q

? is a major RF for CAP

? microbe is a tag along but exacerbator of H Influenza pneumonia

Histoplasma Capsulatum looks like ? on CXR

A

Recent hospitalization

M Catarrhalis

Sarcoidosis

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161
Q

What are 3 positive PE findings seen in pneumonia

Poor dental hygiene can cause pneumonia from ? type of microbes

? beta-lactam ABX is used in the Tx of CAP

A

Tactile fremitus
Egophony: spoken ‘ee’ heard as ‘ay’
Dull percussion

Anaerobes

Ceftriaxone

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162
Q

How is Klebsiella Pneumonia Tx

Pneumovax can be given to Pts w/ increased risk of pneumococcal dz starting at ? age

? is the TxOC for Peds w/ Chlamydial Pneumonia

A

3rd Gen: Cefotaxime

23mon

Erythromycin/Sulfisoxazole

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163
Q

What is seen on CXR of hypersensitivity pneumonitis

How is Coccidioides Pneumonia Dx

How Coccidioides and Aspergillosis Tx ?

A

Diffuse nodular densities

EIA for IgG/IgM

C/A: Flu/Itra-conazole

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164
Q

How is Crypto/Histoplasma capsulatum pneumonia Tx

When/what is used in AIDS Pts for daily prophylaxis against Jiroveci

A

Amphotericin B and Flucytosine

TMP/SMX;
Hx of PJP infection
CD4 <200

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165
Q

How is Viral Pneumonia differentiated from Mycoplasma Pneumonia

How is Viral Pneumonia Dx

If Sxs <48hrs, what is used for Tx depending on strain of influenza

A

Adeno- fast onset w/ GI Sxs x7days
Myco- slow, insidious

Rapid Influenza Ag
RSV nasal swab
Neg agglutinin titer

A/B: Zan/Oselt-amivir
A only: Ama/Riman-tadine

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166
Q

? is the MC cause of lower respiratory tract infections in kids worldwide

This is the leading cause of ? two Dxs in infants

? is the MC pathogen of Bronchiolitis

A

RSV, almost all will have it by 3y/o

Bronchiolitis
Pneumonia

RSV

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167
Q

How is RSV Dx

What is seen on PE

What does this look like on CXR

How is it Tx

A

Nasal RSV Ag test

Fever
Wheezing cough
Rhinorrhea
Flaring nares

Diffuse infiltrates

Steroids

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168
Q

When does Pt w/ RSV need to be admitted

When is prophylaxis indicated

What is used for prophylaxis

A

Feeding difficulty
O2 desat
Retractions
Tachypnea

28wk, 6 day or < and <12mon at start of RSV season
<12mon w/ CH/LDz, 
Congenital airway abnormality
ImmComp
<24mon w/ CF

Palivizumab

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169
Q

What organism causes TB

How is it transmitted

What are the classic findings on PE

A

Mycobacterium tuberculosis

Respiratory droplet

Fever
Anorexia
Weight Loss
Night sweat

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170
Q

When are TB PPDs read as positive

A

Induration= raised area

>5mm:
\+CXR
ImmComp/HIV
Pred equivalent of 15mg/day >1mon
Close contacts
>10mm:
IVDA
High prevelance immigrant
High risk living
Bypass surgery
Medical employees

> 15mm:
No RFs

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171
Q

How is TB Dx

What would be seen on CXR

What would be seen on biopsy results

A

Sputum smear/culture for Acid Fast Bacilli and staining

Upper cavitary lesion
Apical Ghon complex

Caseating granuloma

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172
Q

What is the name of TB spread out of the lungs

What are two types

A

Miliary

Potts- TB to spine
Scrofula- TB to cervical nodes

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173
Q

How is TB Tx

How long is Tx done per med type

A

+PPD= CXR
Neg CXR= Isoniazid x 9mon w/ B6 (Pyridoxine) to prevent neuropathy or sideblastic anemia

Active TB= RIPE w/ baselines prior to Tx:
Rifampin
Isonizid
Pyrazinamide
Ethambutol

RIPE x 2mon
IR x 4mon

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174
Q

What are the s/e of RIPE Tx drugs

When is a Pt w/ active TB considered for therapy cessation

What is used for prophylaxis for PTs living w/ +TB

A

Rif: orange fluids
INH: neuropathy
Pyra: gout
Emb: optic neuritis, red/green blindness

Neg AFB x 2 in a row

Isoniazid x 12mon

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175
Q

What part of RIPE Tx needs to be adjusted if CrCl is <30mL/min

What PT education is given w/ RIPE Tx

Which meds can cause hepatotoxicity

A

E/P to 3x/wk

Take meds on empty stomach

RIP

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176
Q

RIPE Tx can interact w/ ? other Tx method

CXR finding of a Ghon complex indicated ? Dx

What part of the lung is MC involved w/ these complexes

A

Raltegravir for HIV, double dose for HIV Tx

Primary TB

Lower lobes

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177
Q

How is L-TB Tx

Administration of ? drug can reactivate a latent infection

Mycobacterium MC affects ? part of lung

A

INH x 9mon or,
Rifampin x 4mon or,
RIF and PZA x 2mon w/ infected contact

Exogenous CCS

Upper lobes

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178
Q

TB is the MC cause of ? endocrine d/o in the world

PPDs need to be read w/in ? time frame

Why do Pts w/ Rheumatoid Arthritis need TB tests prior to Tx

A

Addisons Dz

48-72hrs

Etanercept: anti-cytokine agent, can reactivate dormant TB

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179
Q

+HIV Pt w/ positive PPD is Tx how

Define Asthma

What PE finding indicates emergency

A

INH and RFN

Chronic, reversible, inflammatory airway dz

Lack of wheezing

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180
Q

How is Asthma Dx

Define FEV

Define FVC

A

Peak expiratory flow rate (Dec FEV1:FVC ratio)

Forced Expiratory Volume- measures how much air exhaled w/ forced breath

Total amount exhaled during FEV test

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181
Q

What are the 4 asthma classifications and Ts

A

Intermittent:
Sx <2x/wk
or 2/< wake up/wk
Tx: SABA PRN

Mild: 
Sx >2/wk or 3-4 wake up/mon
SABA >2d/wk
Minor  limitations
Tx: Low ICS daily
Moderate:
Daily Sxs
 >1 waking >wk
Daily SABA use
Some activity limits
Tx 3: Low ICS+LABA daily
Tx 4: Med ICS+ LABA daily
Severe:
Daily Sxs
Wake 7x/wk
Multiple SABA daily
Extremely limited activity
Tx 5: High ICS+LABA daily
Tx 6: High ICS+LABA+PO CCS
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182
Q

How is an asthma exacerbation Tx

When Tx Asthma, considered SQ allergen immunotherapy for ? Steps

Consider consult at ? step

A

PO CCS
Iprtropium bromide
Nebulized SABA
O2

2-4

Step 3

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183
Q

How is exercise induced asthma prophylactically Tx

What is the ICS used for Asthma Txs

? PE finding suggests improvement of an asthma attack after Tx

A

Albuterol- B2 agonist

Nedocromil
Beclomethasone
Cromolyn

Inc FEV1

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184
Q

What is the MOA of Salmeterol for Asthma Tx

COPD is umbrella term for what two Dxs

What causes the risk for infection and loss of lung recoil to occur

A

Relaxation of bronchial smooth muscles

Chronic bronchitis
Emphysema

Dec ciliary/WBC function
Frayed elastin fibers

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185
Q

How is COPD Dx

What is the criteria for chronic bronchitis Dx

What are common findings seen in these Pts

A

PFT: FEV1/FVC 50%

Productive cough >3mon x 2yrs

Inc Hgb/Hct (polycythemia)
P-HTN

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186
Q

How is COPD Tx

What is the single most important medication fro Tx

What vaccines are highly recommended

A

Mild: SABA (FEV1>80)
Mod: LABA (Tiotropium) + ICS (Fluticasone, Salmeterol)

Low O2- too much removed respiratory drive
PaO2 <55mmHg/ PaCO2>55mmHg
SpO2 <88% or 89% w/ CorPulmonale

Flu
Pneumoccocal

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187
Q

? is the inhaler of choice for COPD Pts

Define Emphysema

Why are Blue Bloaters blue and why are Pink Puffers pink

A

Ipratropium bromide- anticholinergic blocks constrictive effect of Ach on airway muscles

Enlarged air spaces d/t destruction of alveolar septae

Blue: Chronic hypoxia
Pink: CO2 retention

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188
Q

? CXR finding is pathognemonic for Emphysema

Pts <40y/o w/ COPD need ? test

Hallmark of blue bloater

A

Parenchymal Bullae (subpleural blebs)

Alpha-1 antitrypsin

Productive cough

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189
Q

3 parts of PFT that are decreased in COPD

2 parts that are increased

? drugs is used in COPD Tx for preventing nocturnal bronchospasms

A

Max vent volume
Tidal volume
Vital capacity

Total lung capacity
Residual volume

Theophylline- xanthing drug prevents spasms and prolongs dilation

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190
Q

What microbes cause infections in COPD PTs

What ABX are used during COPD exacerbation

? are the indications to use these ABX

A

H influenza
Strep Pneumo
Moraxella
Strep Viridians

1- macrolide
2- Cefuroxime Cefpodoxime, Fefdinir
3- Doxy

Inc quantity and purulence

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191
Q

COPD Pts >65y/o are predisposed to infections by ?

How are these Pts Tx w/ ABX

Blue Bloater is common in ? smoking Hx

A

Pseudomonas

1- Cipro/Levofloxacin
2- Augmentin
3- Doxy

> 40pk/year

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192
Q

Difference in CXR between Blue Bloater and Pink Puffer

? is the most effective Tx for COPD

What will ABGs of chronic bronchitis show

A

Blue: diaphragm not flat

Cessation

Resp acidosis

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193
Q

COPD Gold Categories

A

A: breathless if hurrying on level ground; less Sxs, 0-1 exacerbation past 12mon w/ no admission
Tx: SABA/SAMA

B: walks slower than others; more Sxs, 0-1 exacerbation past 12mon w/ no admission
Tx: LABA/LAMA w/ SABA

C: breathless if hurrying on level ground; less Sxs
2/> exacerbation/year w/ 1 or more admission
Tx: LAMA, SABA

D: walks slower than others; more Sxs; 2/> exacerbation/year w/ 1 or more admission
Tx: LAMA+LABA+SABA

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194
Q

Define Centriacinar Emphysema

This form of emphysema is associated w/ ?

What part of the lung is affected

A

Morphological pattern of destruction to bronchioles and central acini

Smoking

Upper lobe

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195
Q

COPD Pts w/ ? other Dx have increased risk for mortality

Why do emphysema PTs breathe through pursed lips

COPD exacerbation are managed w/ ? 3 meds

A

Bronchiectasis

Inc pressure in airway prevents collapse

Systemic steroids
ABX
Antivirals

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196
Q

SABAs for COPD Tx

SAMAs for COPD Tx

LABAs for COPD Tx

LAMAs for COPD Tx

A

Levabuterol
Albuterol
Pirbuterol

Ipratropium Bromide

Salmeterol
Olodaterol
Formoterol
Arformoterol

Aclidinum bromide
Tiotropiium Bromide
Umeclidinium
Glycopyronium bromide

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197
Q

Interstitial lung Dzs

Which one is MC of the interstitial dzs

This is MC caused by four etiologies

A

-Pulmonary alveolar proteinosis
-Eosinophilic Pulm -Syndrome
Interstitial pneumonia
-Diffuse interstitial pneumonia
Sarcoidosis

Interstitial pneumonia

Medication
Environment
Occupation
Infection

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198
Q

What is the MC type of interstitial pneumonia

What histological pattern is seen

What is no pattern is seen by the lab

A

Pulmonary fibrosis

Usual Interstitial Pneumonia

IPF

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199
Q

3 criteria used to Dx Pts >65y/o w/ IPF/UIP

What are the three methods to Dx this condition

How are these Pts Tx as long as they don’t have IPF

A

Inspiratory crackles
Restrictive PFT
CXR findgins
Pleural honey combing

BAL- esp P Jirovecii
Lung biopsy- standard
Transbronchial biopsy

Pred: 1-2mg/kg/day x 2mon

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200
Q

How are PTs w/ IPF Tx

What is the only definitive Tx fo IPF

How is sarcoidosis Dx and Tx

A

Nintedanib and
Pirfenidone

Transplant

Biopsy w/ non-caseating granulomas
Tx: Pred 1mg/kg/day

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201
Q

How is Sarcoidosis Tx if refractory to steroid Tx

What is a good/poor prognosis for these PTs

A

Methotrexate
Azathioprine
Infliximab

Good: only hilar adenopathy

Bad: lung parenchyma involvement

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202
Q

Define Pulmonary Alveolar Proteinosis

MC presenting c/c

CXR findings

How is this Tx

A

Phospholipid accumulation in alveolar spaces

Dyspnea

Bilateral alveolar infiltrates

Whole lung lavage
GM-CSF: granulocyte macrophage colony stimulating factor

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203
Q

What can cause Eosinophilic Pulm Syndromes

What syndrome can be seen here

One third of cases are idiopathic d/t ?

How is this Tx

A

Helminth infection
Filariae infecition

Loffler: helminthe larva infiltrate into pulmonary passage

Chronic: female w/ asthma
Acute: febrile illness w/ cough/dyspnea

Pred

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204
Q

What are the 7 types of Occupational Pulmonary Dzs

A

Pneumoconioses

Hypersenstivity Pneumonitis

Obstructive airway d/o

Toxic lung injury

Cancer

Pleural Dz

Other

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205
Q

Define Pneumoconioses

What are the 3 types of Penumoconiose Dzs

How are all Tx

A

Fibrotic lung dz from inhaled inorganic dusts

Coal Worker:
Silicosis
Asbestosis

Supportive

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206
Q

How does Coal Worker Pneumoconiosis appear on CXR

? RF does not play into this conditions severity

Complicated Coal Workers is AKA ?

Coal Workers + Rheumatoid Arthritis causes ?

A

Diffuse opacities in upper lobes

Smoking

Progressive Massive Fibrosis- contraction of upper lobes, similar to Complicated Silicosis

Caplan Syndrome

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207
Q

How does Silicosis appear on CXR

These PTs are at increased risk for ? future Dx

Asbestosis Pts usually don’t seek Tx until ? long after exposure

A

Egg shell calcification throughout lungs

Pulmonary TB

> 15yrs

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208
Q

How is Asbestosis best Dx

? tissue finding suggests significant exposure

What finding characterizes Hypersensitivity Pneumonitis

A

CT- detects parenchymal fibrosis

Ferruginous body

Interstitial infiltrates of lymphocytes and plasma cells w/ noncaseating granulomas

209
Q

What causes Farmers Lung

What causes Humidifier Lung

What causes Bird Fancier Lung

A

Moldy Hay

Contaminated humidifier/heating systems

Bird serum/excretions

210
Q

What causes Bagassosis

What causes Sequoisis

What causes Maple Bark Stripper Dz

A

Moldy sugar cane

Modly redwood dust

Rotting maple tree bark

211
Q

What causes Mushroom Picker Dx

What causes Suberosis

What causes Detergent Workers Dz

A

Moldy compost

Moldy cork dust

Enzyme additives

212
Q

What are the 3 Occupational Obstructive Airway Dzs

A

Occupational Asthma- Dx w/ bronchial provocation

Industrial Bronchitis- exposured coal dust, hemp, cotton, flax

Byssinosis- textile worker; Sxs worse on first day back to work; leads to Chronic Bronchitis

213
Q

Example of Toxic Lung Injury

What is a later complication experienced and how can this be prevented

? flavoring can cause a Toxic Lung Injury

A

Silo Filler- inhaled Nitrogen Dioxide

Bronchiolitis obliterans;
Early CCS Tx

Diacetyl- butter flavored popcorn

214
Q

What three toxic inhalations lead to the development of bronchogenic carcinomas

? inhalation causes small-cell carcinomas

Pleural Dzs can develop d/t exposure to ? two inhalants

A

Cigarette, Asbestos, Radon gas

Chloromethyl methyl ether

Asbestos
Talc

215
Q

Define Berylliosis

Systemic Sxs manifest mimicking ?

Size requirements for pulmonary nodule or mass

A

Pulmonary d/o from mining materal for fluorescent lamps

Sarcoidosis

<3cm- nodule
>3cm- mass

216
Q

Pulmonary nodules are AKA ?

What are the steps for work up

A

Coin lesions

1- Incidental CXR

2- CT

3- Suspicious (ill-defined border, lobular, spiculated)- biopsy

4- non-suspicious (calcified, smooth edges) <1cm: f/u 3mon, 6mon and yearly x 2yrs

217
Q

Coin lesion that has not grown in ? time is considered benign

What CXR finding is suspicious

What diameter is suggestive of benign/malignant

A

2yrs or more

Volume doubling from 21-40 days

<1.5cm: benign
>5.3cm: Ca
Exception: Abscess, Wegener, Hydatid cyst

218
Q

PTs <35y/o, nonsmoking w/ incidental lung nodule finding needs ? next step if no prior CXRs are avail

Non-small cell lung Ca has ? four sub-types

? is the MC type seen in non-smoking females

A

CT scan of chest

Adeno- MC lung Ca
Squamous- MC in smoker
Large- Dx of exclusion, rapid grower
Carcinoid

Bronchogenic Adenocarcinoma-

219
Q

MC presentation of adenocarcinoma

What CXR finding indicates Squamous Cell Ca

What CXR finding suggest adenocarcinoma

A

Pleural effusion w/ inc LDH

Central mass w/ hemoptysis

Peripheral mass

220
Q

What CXR finding suggests large/carcinoid

What is Small Cell Lung Ca so deadly

What lab findings signal Small Cell Lung Ca

A

Throughout lung

Almost always in smoker
Mets early/at Dx
Rarely surgical

ADH= SIADH: HypoNa, HyperCa
ACTH= Cushing Synd.
221
Q

What syndrome can Small Cell Lung Ca cause

How are lung Cas Dx

Pancoast tumor of lung are most likely ? type

A

Lambert Eaton Myasthenic Syndrome- muscle weakness d/t ACTH/ADH

Bronchoscopy w/ biopsy (central) or,
Fine needle transthoracic

Squamous
Adenocarcinoma

222
Q

Pt presents w/ facial/arm swelling means a Pancoast Tumor is causing ?

Pancoast Syndrome is ? trifecta

How is Non-Small Cell Ca Tx

A

Superior Vena Cava Syndrome

Shoulder pain
Horners
Bone destruction (PTH from squamous Ca)

Stage 1-2: surgery
Stage 3: chemo then surgery
Stage 4: palliative

223
Q

How is Small Cell Ca Tx

Small Cell Ca is AKA ?

How is Carcinoid Syndromes Dx

A

Non-surgical= Chemo

Oat Cell Carcinoma

CT scan w/ Octreoscan
UA- inc 5-HIAA
CXR- pedunculated sessile growth in central bronchi

224
Q

Squamous Cell and Small Cell both start ?

? type of lung Ca starts in the pleura

A

Centrally (SCs start central; all others start peripheral)

Mesothelioma (asbestosis), not a bronchogenic carcinoma

225
Q

Define Carcinoid Syndrome

Why is there a hormonal excess

Where are the tumors located

A

Specific to carcinoids- serotonin increases bronchoconstriction (asthma), peristalsis (diarrhea) and facial flushing*

Tryptophan converted into serotonin instead of niacin/proteins

Colon
Appendix- Peds pts
Bronchials
Small intestine

226
Q

What lab result indicates Pt has Carcinoid Syndrome

What other lab result is elevated and decreased

? nutritional dz may be c/c presentation

A

5-HIAA- serotonin elevated in urine

Inc: chromogranin A, protein of carcinoid Ca
Dec: tryptophan

Pellagra- niacin deficiency

227
Q

What heart valve lesions may be present during Carcinoid Syndromes

How are these Tx

What is the MC site for these tumors to mets to

A

TIPS:
Tricuspid insufficiency
Pulmonic Stenosis

Surgical excision (resistant to Chemo/Rad)
Octerotide- somatostatin analogue to decrease serotonin secretion
Niacin (Vit B3)

Liver to lungs

228
Q

What is the mnemonic for Carcinoid Syndrome and why is this

Normal pulmonary BP is ? so P-HTN is then defined as ?

What is the MC of P-HTN

A

FDR:
Flushing: inc histamine/bradykinin
Diarrhea: pellagra
R-sided valves: collagen thickens d/t inc serotonin

15/5;
>25mmHg at rest

MS

229
Q

How is P-HTN Dx

What would be seen on EKG

How is this Tx depending on the etiology

A

Right heart cath- gold standard

T-wave inversion V1-V4,
2, 3, aVF

2* LVF: Diuretic Anticoagulant Digoxin

Cardiogenic- (pulm artery HTN) Prostanoids, Phosphodiesterase inhibitor, Endothelin antagonist

230
Q

What structural changes does P-HTN cause

? respiratory drug is used for P-HTN Tx

O2 saturation of 90% correlates to ? PO2 value

A

Smooth muscle hypertrophy
Initmal fibrosis in Pulm Arteries

Bosentan- endothelin antagonist to decrease vascular resistance

60mmHg

231
Q

DVT presents w/ ? PE finding

Females older than 35y/o should have ? birth control d/t inc risk

How are these Dx

A

Homan- extend leg, push foot to head, +pain

Progestin only

D-Dimer
Venography w/ Duplex US- gold standard

232
Q

How are DVTs Tx

If Pt has recurrent DVTs, how is Tx changed

Where are DVTs more commonly developed

A

LMWH
Fondaparinux

Lifetime anticoagulation

Left iliac- compressed by aortic bifurcation

233
Q

How do PEs present

How are these Dx

How are they Tx

A

SOB w/ tachycardia*- MC Sx of PE

Spiral CT
VQ scan (pregnant)

Heparin w/ Xa inhib (Riva/Apixa/Edoxaban) then Dabigatran (DOAC)
Renal insuff- Warfarin (INR 2-3)
Heme-unstable: thrombolytic

234
Q

? part of the lung is more commonly affected by PEs

If PE is a fat emboli from long bone Fx, how does the Pt present

How is the probability of a PE calculated

A

Lower lobes

Hypoxemia
Neuro abnormals
Petechial rash

Wells Score:
>4- PE likely, image
=4- unlikely, D-dimer

235
Q

What do ABGs during PEs show

What would be seen on EKG

What CXR terms may be seen

A

Respiratory alkalosis

S1Q3T3

Westermark
Hampton hump

236
Q

Where does the obstruction in OSA tend to occur

What are the RFs for OSA

How can this present

A

Ooropharynx

Alcohol
Hypothyroidism
Sedatives
Obesity
FamHx
Anatomical obstruction
Personality change
Dec intellect
Dec libido
Monring HAs
Polycythemia
237
Q

How is OSA Dx and differentiated from CSA

What is an alternative test for Pts w/ high suspicion but no medical comorbidity

How is this Tx by severity

A

Polysomnography w/:
>5 apneas w/ comorbidity
15/> regardless of comorbidity

Home sleep apnea test

Mild-Mod:
PO appliance
Pos pressure therapy

Sev: CPAP
Uvulopalatopharyngoplasty
Tracheostomy- life threatening OSA

238
Q

During OSA work ups, Cheyne Stokes respiration are commonly seen in PTs w/ ? Dx

How is the severity of sleep-disordered breathing measured

What are the 3 categories of severity

A

CHF

Apneic + hypopneic episodes/hr

Normal AHI <5
Mild: 5-15
Mod: 15-30
Sev: >30

239
Q

When is OSA Tx indicated

? class medication is c/i in these Pts

What are the different types of pneumothorax

A

Sx w/ AHI >5
All AHI >15

Benzos

Spot- ruptured bleb
Secondary Spot- cough/lung dz
Traumatic
Tension- leads to shock

240
Q

What will be seen on PE of Pneumothorax

How are these Tx

How do Pts w/ Sarcoidosis present

A

Dec sounds
Dec tactile fremitus

<20% diameter self resolve
Needle aspiration
Chest tube
CXR q24hrs

Spiking fever
Erythema Nodosum

241
Q

How is Sarcoidosis Dx

What lab result will be elevated

What would be seen on a PFT

How is it Tx

A

Tissue biopsy- noncaseating granulomas

HyperCa
ACE higher 4x normal

Restrictive pattern

PO Pred and ACEI

242
Q

Define Sarcoidosis

What is the hallmark CXR finding

What are 3 DDxs for this hallmark finding

A

Systemic granulomatous dz w/ noncaseating granulomas

Mediastinal adenopathy

Young female: sarcoidosis
Ohio kid/zookeeper w/ fever- Histo
Old ceramic worker- beryllosis

243
Q

What is used for assessing Sarcoidosis progression and Tx guides

How is this Tx

What is the leading cause of death for this population

A

Serial PFTs

CCS
ACEI for HTN
Methotrexate

Pulmonary fibrosis

244
Q

What are the 4 organs MC involved in sarcoidosis in sequence

What are the 4 stages of this Dz

A

Lung
Nodes
Skin
Eye

1- bilat adenopathy
2- bilat adenopathy and reticular opacities
3- reticular opacities
4- opacities w/ volume loss and fibrosis

245
Q

Define Transudate

What is the MC cause

What are other possible causes

A

“Transient” thin water fluid from pulmonary circulation back pressure/dec osmotic pressure

CHF

Cirrhosis w/ ascites
Hypoalbumin- nephrotic syndrome

246
Q

Define Exudate

What is the MC cause

What are other possible causes

A

Thicker fluid from tissue infection, damage, inflammation allowing blood protein/water to escape

Pneumonia

Ca PE TB Pancreatitis

247
Q

What criteria is used for pleural effusions as an exudate

A
Lights Criteria: one of three=
(Inc Protein, Inc LDH)
1- pleural protein:serum protein >0.5
2- pleural LDH:serum LDH >0.6
3- pleural LDH >2/3 upper limit of lab's normal serum LDH
248
Q

Isolated L-sided pleural effusion is most likely a ?

Isolated R-sided pleural effusion is most likely as ?

How are these Tx

A

Exudate

Transudate

Thoracentesis
Chronic/recurrent: pleurodesis or indwelling cath

249
Q

Define Empyema

Usually these are Tx how

Define Decortication

A

infected pleural effusion

Chest tube

Thoracotomy and removal of infected fibrous rings from around lung

250
Q

Define ARDS

What is the MC cause

Usually ? other organs will fail too

How is this Tx

A

Respiratory failure d/t Inflammation of lungs and fluid accumulation in alveoli decrease O2 sats

1-Sepsis (2- trauma, 3- aspiration/near-drown)

Kidney Liver

Intubate for mechanical PEEP, PaO2 >60/SaO2 >90

251
Q

What physiological process causes ARDS

This process allows for ? to develop

How is this Dx

A

Inc alveolar-capillary membrane permeability

Non-cardiogenic pulmonary edema (protein rich)

CXR w/ air bronchograms and bilateral fluffy infiltrates

252
Q

Define Delirium

This is common in hospitalized PTs d/t ?

What is the 4 criteria needed for Dx

A

Acute onset of temporary AMS

Drugs
Infection
Dehydration

Dec consciousness
Cognitive change
Rapid onset
Evidence physical condition

253
Q

Testing to Dx Delirium includes ?

How is this Tx

? are the MC type of hallucinations experienced by these Pts

A

CT/MRI

Tx cause
Supportive care
Sedation

Visual

254
Q

? antipsychotic is used for delirium Tx

What is the MC cause of delirium

What is the saying for anticholinergic ODs

A

Haloperidol

ETOH abuse

Hot as Hades
Mad as a hatter
Dry as a bone
Red as a beet
Blind as a bat
255
Q

How do Cluster HAs present

What will Pt look like

How are these Tx

A

Unilateral eye pain w/ lacrimation and nasal congestion x 15-180min

Same time, every day attack causing pacing/rubbing head

O2 12-15L via non-rebreather
Sumatriptan

256
Q

What is used of Cluster HA prophylaxis

How do Migraine HAs present

How is this Tx in order

A

Lithium
Divalproex
Verapamil
Topiramate

Unilateral throb/pulsating HA w/ photo/phono-phobia and N/V

NSAID
5-HT1 agonist (Triptan- constrict dilated vessels)
Atenolol
Ergotamine
Reglan + Benadryl
257
Q

When are migraine Tx c/i

How are these Dx

When is neuroimaging indicated

A

Cardiac dz
Cerebrovasc dz
PVDz

PIN:
Photophobia
Impairment, job/life
Nausea

New onset >50y/o
Changed pattern
Atypical/unremitting
Prolonged/bizarre aura

258
Q

When is migraine prophylaxis indicated

What is used for prophylaxis

A

4/> HA/mon
8/> HA days/mon

1st line:
Divalproex
Topiramate
PMT-olol

2nd:
Amytriptyline
Venlafaxine
A/N-olol

3rd:
Botox
CHRP monoclonal Abs

259
Q

? is the MC form of aura w/ migraines

Define Migraine Equivalent

When are these Dx as Chronic Migraines

A

Ophthalmic

Migraine aura w/out HA

> 15d/mon x 3mon

260
Q

How do Tension HAs present

How are they Tx

What are two categories of these HAs

A

Bilateral front/occipital HA in ‘band-like’ pattern

1st: NSAID
2nd: ASA/caffeine
Ergotamine

Episodic: <15d/mon
Chronic: 15/>d/mon

261
Q

What is used for Tension HA prophylaxis

Medication overuse HAs must be avoided by limiting abortive agent use to ?

How does an esophageal stricture tend to present

A

TCA: amytriptyline
CBTherapy

No more than 2d/wk

Dysphagia to solids w/ gradual progression

262
Q

MCC of esophogeal strictures is d/t ?

Define Esophageal Web

Define Schatzki Ring

A

Benign peptic strictures from GERD

Thin mucosal membrane growing across lumen

Eosphageal ring at B-junction, MC from hiatal hernia

263
Q

Define Plummer-Vinson Syndrome

Define Steakhouse Syndrome

How are esophageal strictures Dx

A

Dysphagia
Iron deficient anemia
Cheilosis
Esophageal webs

Progressive dysphagia to solids, worse after heavy meal that was wolfed down

Initial- barium swallow
Dx- Upper Endoscopy

264
Q

How are esophageal strictures Tx

? esophageal stricture is PROXIMAL/MID and not distal

What are the 3 types of hernias

A

Endoscopy w/ dilation
H2 antagonist
PPI

Infectious esophagitis

Diaphragmatic
Ventral
Umbilical- refer >2y/o

265
Q

How are hernias Dx

Define Direct Hernia

Define Indirect Hernia

A

US/Clinical

Intestine goes through external ring at Hesselbach Triangle, rarely into scrotum; felt on side of finger

MC; intestine goes through inguinal ring into canal; felt on tip of finger; congenital/<1y/o Pt
(“i” indirect through “i” of inguinal)

266
Q

? type of hernia have high incidence of strangulation

What are the 5 types of non-infectious esophagitis

What is the hallmark Sx of infectious esophigitis

A

Femoral d/t femoral ring rigidity

Medication
Eosinophilic
Radiation
Corrosive
Reflux

Odynophagia- pain w/ swallowing liquid or solid

267
Q

How does Fungal Esophagitis present

How does HSV Esophagitis present

How does CMV esophagitis present

How does Eosinophilic Esophagitis present

A

Linear white/yellow plaques; Tx Fluconazole

Mulitiple punched out lesions on EGD; Tx Acyclovir

Solitary ulcer/erosion on EGD; Tx Ganciclovir

MedHx of asthma and multiple corrugated rings on swallow; Tx inhaled steroid

268
Q

How is Esophagitis Dx

How is Corrosive Esophagitis Tx

How is Bisphosphonate induced esophagitis Tx

A

Endoscopy w/ biopsy and culture

CCS

Take w/ 4oz of water, avoid laying down x60min

269
Q

? is the MCC of esophagitis

Esophagitis induced from chemo/rad is expected after ? much radiation

What are these PTs at risk for developing

A

GERD

5000cGy

Strictures

270
Q

What are the two main types of esophageal Ca

How are these Cas Tx

How do these usually present

A

SCC, MC world- d/t smoking and ETOH
Adeno, MC in US- d/t Barrett’s esophagus

Resection-no mets
Rad/Chemo w/ 5-FU

Dysphagia to solids progressing to liquids w/ adenopathy

271
Q

Adenocardinoma of the esophagus is usually found in ? area and d/t ? progression

How are esophageal Ca Dx and staged

Barretts Esophagitis need endoscopic screenings ? often

A

Distal esophagus: GERD to Barretts

Dx: upper endoscopy
Stage: CT

q3-5yrs

272
Q

How is GERD Dx

What is an upper GI study used for

? presenting GERD c/c is often overlooked

A

pH probe: Gold Standard
Endoscoyp w/ cytologic washing

Anatomy, not reflux

Chronic cough

273
Q

How is GERD Tx

What are 5 meds that can cause LES relaxation

What is an uncommon Sx seen in GERD

A

H2 antagonist BID
Persistent Sxs- switch to PPI (most effective)
Once Sxs stop, continue x 8wks

CCBx
Diazepam
Theophylline
Meperidine
Morphine

Odynophagia

274
Q

Two common presenting Sxs of gastritis

What are the two types of gastritis

A

Dyspepsia
Abdominal pain

Acute: rapid developed lesion in gastric antrum

Chronic:
Type A- slow lesions in fundus d/t Ab w/ risk for adenocarcinoma
Type B- ASx slow lesions in antrum from NSAID/Pylori w/ PUD risk

275
Q

How is gastritis Dx

How is this Tx

What are four s/e of medical therapy

A

Endoscopy w/ four biopsies

H2RA: Famotidine, Cimetidine, Omeprazole- D/c when ASx x 8wks

PPI causes:
Hypochloride
Dec Ca (hip Fxs)
Dec serum B12
Dec Mg
276
Q

Gastritits Tx can make Pts at increased risk for ?

What two infections can cause gastritis

? is the MCC

A

Pneumonia
C Diff

HSV
CMV

H Pylori

277
Q

Microscopic shape of H Pylori

What are the two types of ulcers seen in PUDz

How can the location be hinted at on PE

A

Gram-neg spiral bacillus

Duodenal
Gastric

Food decreases pain of duodenal ulcer

278
Q

What type of PUD ulcer is more common

Both types of ulcers are MC caused by ?

What anatomic plane are these usually found on

A

Duodenal > Gastric

H Pylori

Anterior duodenum

279
Q

Rarely, duodenal ulcers can be caused by ? syndrome

PUD is the MC cause of ?

How does this MC usually present

A

Zollinger-Ellison: gastrinoma tumor of pancreas causing excess gastrin to be produced; Dx w/ serum gastrin >200pg

Non-hemorrhagic GI bleeds

Melena

280
Q

How is PUDz Dx

How is PUD Tx w/ Triple Therapy

What is the next step if H Pylori was suspected

A

Upper endoscopy w/ biopsy

PPI
\+H Pylori= 
Omeprazole
Amoxicillin
Metronidazole/Clarithromycin
Quad therapy: add Bismuth

Eradication confirmation in 4wks

281
Q

How are NSAID induced PUD Tx

How is Zollinger Ellison Tx

When is PPI Tx used w/ caution

A

D/c NSAID
PPI x 8wks minimum

PPI
Tumor resection

Hepatic impairment

282
Q

4 RFs for gastric Ca

How are these Dx

How are they Tx

A

FamHx
Ulcers
H Pylori
Pernicous anemia

Guiac
CBC- micro/hypo
EGD w/ biopsy

Gastrectomy

283
Q

What are the MC Sxs of gastric Ca

? is the most important RF

What are two metastatic signs

A

Early: pain, indigestion
MC: Weight loss

H Pylori

Virchow node- L-supraclavicular
Mary Joseph- umbilical

284
Q

What EGD finding indicates a gastric Ca Dx

What does the mnemonic WEAPON stand for

A

Linitis Plastic- thickening of stomach wall

Weight loss
Emesis
Anorexia
Pain
Obstruction
Nausea
285
Q

Virchows node is associated w/ L-supraclavicular, what is associated w/ the R side

What causes Celiac Dz

What does this Dz cause to occur

A

Hodgkin’s lymphoma: right nodule drains mediastinum, a common origin site

Autosomal recessive inheritance of an immunologic response to gluten

Injury to proximal intestine mucosa

286
Q

? is a dermatological manifestation of Celiac Dz

How is this Dx

How is a Dx confirmed after a positive Dx test

A

Derm. herpetiformis- European male w/ painful, pruritic bilateral extensor lesions
Dx: punch biopsy
Tx: Dapsone, diet

IgA endomysial Ab- inc spec, lower sense

IgA transglutaminase AB- + in most Pts on gluten free diet

Endoscopic intestinal biopsy

287
Q

Why are Pts sensitive to gluten in Celiac Dz

What causes lactose intolerance

How is this Dx

A

Sensitivity to gliadins- alcohol-water soluble fraction of gluten

No lactase enzyme: digests lactose into glucose/galactose

Hydrogen breath test >20ppm <90min
Stool acidity- E Coli/Rotavirus

288
Q

What is the difference in appearance of Crohns and UC

What is the difference in areas involved

A

Crohns- transmural cobblestone, skip lesions
UC- limited to sub/mucosa crypt abscess

Crohns- spares rectum, +abdominal pain

289
Q

? radiographic findings are pathognemonic fo Crohns and UC

? one is protected by smoking

? Ab test is used for UC

A

Crohns: Terminal ileum string sign
UC: lead pipe d/t loss of haustra

UC

p-ANCA

290
Q

What upper GI Sx can indicate Crohns

What is the MC site

What Ab test is used

A

Aphthous ulcer

Terminal ileum

ASCA

291
Q

How is UC and Crohns Tx w/ 5-ASAs

What Rx is used if there is no response

What is the next step if there is still no response

A

Sulfasalazine w/ supplemental folate
Mesalamine

Metronidazole

Azathioprine
6-Mercaptopurine

292
Q

Which IBDz can be cured w/ surgery

What medical therapy needs to be avoided in these PTs

What are 3 extraintestinal manifestations of IBDz

A

UC

Anti-diarrheals- induces ileus

Uveitis
Erythema nodosum
Arthritis

293
Q

How is IBS standardized by Sx-based criteria

What are labs not needed for Dx

What med is used for Tx as an anti-spasmodic

A
Rome criteria:
Pain 3d/mon x 3mon w/ two of:
Improved w/ BM
Changed frequency
Changed consistency

Routine studies are normal in IBS

Hyoscycamine- anticholinergic

294
Q

IBS is a ? d/o

? infection leads to increased prevalence of IBS

? is the MC vessel blocked leading to intestinal ischemia

A

Functional, not organic

Giardia lamblia

Superior mesenteric artery

295
Q

Mesenteric ischemia presents as pain after ? and relieved by ?

What will be seen on x-ray

How is this Dx

How is it Tx

A

<30min after eating;
Relief w/ laying/squat

Thumb-printing of small bowel

Mesenteric angiography- gold standard
Colonoscopy

Revascularization

296
Q

What meds can help prevent future poly growth after polypectomy

Colonic polys are the MC cause of ? in Peds

Where are adenomatous polyps commonly found

A

ASA
Cox-2 inhibitors

Painless rectal bleeding

Distal colon/rectum

297
Q

Polyps located ? are more likely to be malignant

What type of polyp has a 30-70% chance of malignant transformation

How are these Dx

A

Proximal colon

Villous adenoma

Colonoscopy for Dx and therapeutic q/ f/u q3-5yrs

298
Q

Define Familial Adenomatous Polyposis

What screening is needed for first degree relatives

When is a sigmoidoscope recommended

A

> 100 polyps by 15y/o and Ca by 40y/o

Genetic screen at 10y/o

12y/o

299
Q

What two RFs trigger the start to colon Ca screenings

What types of screening are recommended for Pts that have no Sxs/RFs

Under routine circumstances, when should Pts start and stop getting screening colonoscopies

A

Adenomatous polyp or 1st* relative w/ Dx- start at 40y/o or 10yrs younger than age of Dx

> 50:
Colon- q10yrs
Flex sig, contrast enema, tumor cells- q5yrs

45y/o - 75y/o

300
Q

Colon Ca is the ? leading cause of death

How is colon Ca Dx

How are these Tx

A

3rd
Lung, skin, colon

Colonoscopy w/ biopsy
Enema= apple core lesion

Resection
Chemo w/ 5-FU

301
Q

What lab result is monitored in colon Ca Pts during Tx

Where is Diverticulitis MC found

How is this Dx

A

CEA- carcinoembryonic antigen

Descending colon
Western society- sigmoid

CT w/out contrast- fat stranding w/ wall thickening
NO colonoscopy

302
Q

Diverticulitis is the MC cause of ?

How is diverticulitis Tx

What 3 PE findings is suggestive of positive Diverticuosis Dx

A

Painless, massive lower GI bleeds

Cipro or,
Augmentin + Metronidazole

No vomit
Inc CRP >5mg
LLQ pain

303
Q

? is NOT a complication of Diverticulosis

? two microbes cause the inflammatory process of diverticulitis

? criteria is used to define constipation

A

Colon Ca

E Coli
Bacteroides fragilis

Rome 3

304
Q

Pts >50y/o w/ constipation need ? r/o

How much fiber is recommended during Tx

A

Ca

20-25g/day

305
Q

What are the bulking laxatives

What are the osmotic laxatives

What are the softener suppositories

A

Psyllium seed
Methycellulose
Ca polycarbophil
Wheat dextrin

Polyethylene glycol

Glycerin
Bisacodyl

306
Q

Constipation lasting longer than ? long needs further work up

? anti-HTN med class doesn’t cause constipation

? is the MC organic cause of constipation in Peds

A

> 14days

BBs

Hirschprung dz

307
Q

Define Hep A

Where does this cause outbreaks

How is it Dx

A

RNA virus transmitted via fecal-oral

Military
Enclosed environment
Daycare

Early: anti-HAV IgM
Late: anti-HAV IgG, remains elevated for life

308
Q

How is Hep A Tx

When are vaccines given

Define Hep B

A

IgG globulin no more than 14d after exposure

<24mon, just as effective as immune globulin injections

DNA virus ‘Dane” particle via blood, IVDA, intercourse

309
Q

When can pregnant females get Hep B vaccine

? is the first sign of infection

What is the 2nd sign

What is the 3rd sign

A

27-36wks

HBsAg- subway, serological hallmark of HBV infection

HBeAg- egg= replication and infectious

HBcAg- intracellular Ag in liver cell

310
Q

? lab result means Dx of acute Hep B

? lab result means decreased viral replication

? lab result appears after clearance of the HBsAg or indicates vaccination

A

anti-HBc (Ab IgM)

anti-HBe (Ab IgM)

anti-HBs (Ab IgM)

anti-HBs

311
Q

How does Chronic Hep B develop

? test is used to differentiate from passive and active Hep B immunity

What lab result will indicate health care worker is Hep B immunized

A

HBsAg is always positive, ‘e’ can occasionally develop >6mon after infection

Core Abs
IVDA: +cAbs
Healthcare: -cAbs

anti-HBs (we never exposed to the core)

312
Q

How is Hep B Tx

Define Hep C

Incubation period and these Pts are at risk for ?

A

Hep B DNA vaccine

Single strand RNA in post-transfusion/transplant/IVDA Pts

2wks-6mon;
Hepatocellular Ca

313
Q

How is Hep C Dx

How is Hep C Tx

Define Hep D

How is D transmitted

A

anti-HCV Abs in serum

Interferon, controls chronic Hep C

RNA virus requiring HBsAg for infection

Clotting factors
Drug users

314
Q

? infection causes 50% of fulminate hepatitis infections

This infection puts Pts at increased risk for ?

A

Hep D

Inc severity of Hep B attacks
Chronic hepatitis
Cirrhosis

315
Q

Define Hep E

How is this transmitted

Pt wants to be tested to see if they have Hep A, ? lab is ordered

A

Similar to Hep A d/t trasmission and prevalence in young adults

Fecal-oral

Anti-HAV IgM

316
Q

What Hep B lab result would a PA-C and IVDA have in common

What lab test says Pt is actively infectious

What lab result would be positive in chronic Hep B Pt

A

Anti-HBs

HBeAg

HBsAg

317
Q

Hep D needs / part of Hep B to exist

What is the first evidence of infection w/ Hep B

What is the lab result needed for Dx of Hep B

What lab result indicated Hep B virus replication and infection

A

HBsAg

Anti-HBs

Anti-HBc

HBeAg

318
Q

What Hx does Hep A present w/

What are two PE findings

How long are they contagious

A

Travel to Asia

Hepatomegaly and jaundice

1wk of jaundice

319
Q

How are Hep A Pts Dx

What Pt education goes w/ Dx

What do family members get for Tx

A

IgM anti-HAV

Immune for life

IV-IGg

320
Q

How does Hep B present to clinic

What lab result means Pt is immune

? lab result means Pt is positive for infection

A

Flu-like w/ jaundice

anti-HBs

HBsAg

321
Q

? lab result mean acute Hep B

? lab result means chronic Hep B

Hep E outbreaks is associated w/ ?

How is it Dx

A

Anti-HBc IgM

Anti-HBc IgG

Waterborne outbreaks

IgM anti-HEV

322
Q

When are Hep C screenings recommended

What anti-virals are used for tx

How is Chronic Hep E Tx

A

18-79y/o

Sofosbu-vir
Velpatas
Daclatas
Glecapre

Ribavirin

323
Q

Define Cirrhosis

What PE findings may present late in the Dz process

What skin changes can be seen

A

Hepatic fibrosis d/t regenerative nodules surrounded by fibrotic tissue preventing regeneration

Terrys nail- white bed
Ascites
Gynecomastia

Palmar erythema
Caput medusae
Spider angioma

324
Q

How is Cirrhosis Dx

Once Dx, all PTs need ? f/u imaging

What abnormal lab results will be seen

A

Gold Standard: biopsy

EGD

AST > ALT
Anemia
Dec platelets
Inc unconjugated bili
Inc PTT
325
Q

What scoring system is used for Cirrhosis Mortality

What meds are sued for prophylaxis against variceal hemorrhage

What is used if encephalopathy is present and what is avoided

A

Child-Pugh:
Class A: 5-6pts
Class B: 7-9pts
Class C: 10-15pts

Non-selective BBs:
Nadolol
Propranolol

Lactulose+Neomycin; Sedatives

326
Q

What is used in cirrhosis if pruritis is present

Cirrhosis Pts w/ sudden onset fever and abdominal pain need ? Dx r/o

Why can cirrhosis Pts present w/ foul breath

A

Cholestyramine

Bacterial peritonitis

Fetor Hepaticus- musty breath d/t sulfur in blood passing into lungs

327
Q

What are 3 features of decompensated liver cirrhosis

Define Palm Tree Sign

? tumor marker is used for liver Ca

A

Jaundice
Encephalopathy
Ascites

Caput Medusae: enlarged superficial epigastric veins in umbilicus

alpha-Fetoprotein

328
Q

Hepatocellular carcinoma occurs in the setting of ? two Dxs

How are these worked up if <1cm

Inc alpha-fetoprotein in ? two populations should raise concern

A

Chronic liver dz
Cirrhosis

MRI
Neg= US q3mon

Cirrhosis
Hep B

329
Q

How are liver Cas Tx

What Tx option is not attempted d/t ineffectiveness

What are the 5 F’s of Cholelithiasis

A

Transplant if tumor is <5cm or,

3/< tumors, all 3/

330
Q

Define Cholelithiasis

What is the best test to Dx Cholelithiasis

What is the cardinal Sxs

A

Stones in gallbladder w/out inflammation

RUQ US, best after NPO x 8hrs to fill/distend gallbladder

Biliary colic d/t temporary obstruction

331
Q

Define Boas Sign

What are the 3 potential complications that can arise from this condition

A

Right subscapular pain d/t biliary colic

Cholecystitis- cystic duct obstruction

Choledocholithiasis- gallstones in biliary tree

Cholangitis- biliary tract infection d/t obstructed stones

332
Q

How is Choledocholithiasis Tx

How is Cholangitis Dx

What lab result will be elevated if bile flow is obstructed, specific to the biliary tree, and what Dx is then likely

What lab result is used to confirm this lab elevation

A

ERCP stone extraction

ERCP

Alkaline phosphatase (ALK-P)- cholestasis

GGT

333
Q

The liver’s ability to synthesize clotting factors is reflected by ? lab result

What clotting factors does it make

How is Cholelithiasis Tx

A

Prothrombin time

1 2 5 8 9 10 12 13

Cholecystectomy

334
Q

? ABX is a major cause of biliary sludge

This ABX can cause ? type of stones to be formed

Define Cholecystitis

A

Ceftriaxone- binds Ca in bile w/in gallbladder

Frank stones

Inflamed gallbladder d/t obstruction of biliary duct

335
Q

What is the most specific test to Dx cholecystitis

What PE finding helps w/ Dx

How is this Dx

A

HIDA Scan

Murphy’s Sign

RUQ US then,
HIDA

336
Q

How is cholecystitis Tx

Define Cholangitis

What is the MC microbe involved

A

Lap Cholecystectomy

Infected obstruction in bile duct

E Coli

337
Q

Define Charcots Triad

Define Reynold’s Pentad

How is Cholangitis Dx

A

RUQ pain
Jaundice
Fever

HOTN
Confusion

RUQ US then,
ERCP for Dx and Tx

338
Q

? is the top 3 MCC of acute cholangitis

What are the 3 products secreted by the pancreas

What is the MCC of acute and chronic pancreatitis

A

Choledocholithiasis
ERCP
Tumor

Amylase
Insulin
Glucagon

Acute: gallstone
Chronic- ETOH

339
Q

How is pancreatitis Dx

How is this Tx

? RF increases the risk for pancreatic Ca

A

Abdominal CT

Analgesia
Bowel rest
IV fluids

Smoking

340
Q

What tumor marker is used to track pancreatic Ca

How does pancreatitis present

What is the mnemonic for causes of pancreatitis

A

CA 19-9

Steatorrhea
Pain radiating to back, better w/ leaning fwd

GET SMASHED:
Gallstone
Ethanol
Trauma
Steroid
Mumps
Autoimmune
Scorpion
HyperCa
HyperLipid
ERCP
Drugs
341
Q

What criteria is used to predict the severity of pancreatitis

What are the indications at admission

What are the indications at 48hrs

A

Ranson’s criteria

Glucose >200
Age >55y/o
Leukocyte >16K
LDH >350
AST >250
Arterial PAO2 <60
BiCarb <20
Ca <8
BUN inc x 1.8
Hct dec x 10%
Sequestered >6L
342
Q

What is the triad of chronic pancreatitis

What extra finding may be seen on imaging

? lab result is sens and spec for Dx

A

Pancreatic calcification
Steatorrhea
DM

Pseudocyst- Pt will have palpable mass and jaundice

Lipase > 3x normal

343
Q

How is Pancreatitis Dx

What would be seen on x-ray

How is Chronic Pancreatitis Dx

A

Abdominal CT w/ contrast

Sentinal loops

CT
MRI w/ MRCP

344
Q

How is pancreatitis Tx

What is the best part of Tx

When are hemorrhoids more prevalent

A

NPO
IV analgesia, fluid bowel rest

Fluids

Pregnancy
Post-child birth

345
Q

How are hemorrhoids Tx

What are the 3 types

A

Stool softener
CCS sitz bath
Internal- rubber band ligation

External: distal to dentate
Internal: prox to dentate
Mixed; prox and distal

346
Q

What are the 4 degrees of hemorrhoids

Pts w/ anal fistulas need ? other Dx considered

What is an uncommon PE finding in anorectal abscesses

A

1: no prolapse
2: prolapse, spot reduction
3: prolapse, need manual reduction
4: irreducible, risk for strangulation

Crohns

Fevers- more likely in deep abscesses

347
Q

Define Anorectal Fistula

When/why is imaging needed for abscesses

How is anal fistula Dx

A

Tract between two areas d/t deep anorectal abscess

CT if recurrent

Anoscopy

348
Q

How are anorectal abscess/fistulas Tx

Vit B3 deficiency is AKA ?

What would be seen on PE

A

InD
Softener w/ inc fiber
Fistula- surgery

Niacin- Pellagra; 4 D’s: dermatitis diarrhea dementia death

Bright red tongue

349
Q

What populations are at risk for Vit B3/niacin deficiency

What Rx can cause Niacin/Vit B3 deficiency

What is VitB1 deficiency

A

ETOH
Mal-absorption syndrome

INH therapy

BerBeri- burning feet syndrome

350
Q

What is the MCC of VitB1 deficiency

What issue can present in these populations

What is VitB2 deficiency and what does it present w/

A

Alcoholics

Wernickes encephalopathy- abnormal eye movement, abnormal stance/gait, AMS

Riboflavin- cheilosis, angular stomatitis, magenta tongue

351
Q

What is VitB6 deficiency

What does this deficiency present w/

How is this Tx

A

Pyidoxine-

Seb Derm-like eruption
Atrophic glossitis w/ ulcers
Conjunctivitis
Neuorpathy

INH OD Tx

352
Q

What is the first sign of Vit A deficiency

Who does this present in

How does Vit C deficiency present

A

Night blindness

CF
Mal-absorption
Spruce/pancreatic d/o

Scuvy- easily bleeds/bruises, hair/tooth loss, joint pain/swelling

353
Q

Prolonged Vit D deficiency leads to

What other chronic Dz can lead to this deficiency

Where is Vit K synthesized and what does it control

A

Rickets

End stage renal dz- can’t activate Vit D to absorb Ca in intestine

Liver; any Dz impacting liver- dec K
PT and PTT

354
Q

What population is at inc risk for Vit K deficiency

Define Phenylketonuria

This is the MC ? and w/out Tx ? develops

A

Exclusively breast fed infants

Genetic d/o preventing normal use of protein

Inborn error or protein metabolism;
Brain development

355
Q

First vaccine given to infant

Second shot given is ?

What is the 3rd test

A

Hep B

Vit K

PKU

356
Q

Define Kwashiorkor Deficiency

Define Marasmus

Folate deficiency can cause ?

A

Inadequate intake of protein leading to edema

Inadequate intake of ALL energy forms

Neural tube defect

357
Q

Vit B12 deficiency can lead to ?

? is the MC type of kidney stone and what prevention can dec incidence

If the stone is infected, most likely a ? stone infected by ?

A

Cobalamin- degeneration of spinal cord

Calcium oxylate- grapefruit juice

Struvite- Proteus Klebsiella Pseudomonas Staph

358
Q

Kidney stones larger than ? will probably need surgical help

What is the MC location for these to get lodged

Best method to Dx is ?

A

> 5mm- need lithotripsy

UVJ

Abdominal/pelvic CT w/out contrast

359
Q

How are kidney stones Tx

What are the 4 types of kidney stone and what are they associated w/

All of these are radiopaque except for ? type

A

1st: toradol
2nd morphine
3rd: opiate
4: Tamsulosin/CCB

Ca Oxalate- MC
Struvite- chronic UTI w/ Klebsiella/Proteus
Uric Acid- acidic urine d/t meat/alcohol/gout
Cystine- genetic

Cystine- lucent

360
Q

When do kidney stones need to be admitted

What Tx method is best for stones >5mm but <2cm

What Tx method is best if the above method fails and is best for stones >2cm

A

Uncontrolled pain
Anuria
Renal colic and UTI/fever

Lithotripsy

Percutaneous nephrolithotomy

361
Q

? is the primary intervention of choice for struvite kidney stones

? is the MC and 2nd MC microbe to cause cystitis

How is this Tx w/ 1st, 2nd line meds and during pregnancy

A

Percutaneous nephrolithotomy

1st- E Coli
2nd- Enterococcus/Saprophytics (sexually active female)

1st: TMP/SMX
2nd: Cipro
Pregnant- Nitrofurantoin/Cephalexin
Pain- Phenazopyridine
Complicated- Cipro

362
Q

Define Cystitis

How can this present in Peds

? is the MC cause of recurrent cystitis in men

A

Infection of bladder causing dysuria w/out d/c

New onset incontinence in previously toilet trained Pt

Chronic bacterial prostatits

363
Q

How is cystitis Dx

What lab results indicated Dx

When/why would imaging be needed

A

Urine culture- gold standard
Urine dipstick w/ + nitrites, luekocyte esterase

> 100K CFU women
1K CFU men/cath Pts

Pyelo
Recurrent
Anatomic abnormals

364
Q

When would ASx cystitis in geriatric need Tx

How are postcoidal UTIs Tx

How is Pediatric Cystitis Tx depending on renal involvement

A

DM
+ structure abnormals

TMPSMX
Cephalexin

Low risk- Keflex
High risk- 3rd gen (Cefix, Cefdinir, Ceftibuten)

365
Q

When working up female cystitis, squamous cells are seen on UA. What is the next step

Define Pyelonephritis

How does this present

A

Repeat UA w/ clean catch, squamous epithelial cells indicate vaginal flora

Ascending UTI that reaches renal pelvis

CVA tenderness w/ F/C/N/V

366
Q

What is the MC microbe that causes Pyelonephritis

What lab result is pathognomonic for dx

How is this Tx outpatient, admitted and pregnant

A

E Coli

WBC casts

Cipro/Levo/Cephalexin
IV Ceftriax
Preg: IV Ceftriax

367
Q

Define Nephrotic Syndrome

Pts w/ this syndrome are at increased risk for ?

What is the MCC in adults and Peds

A

Protieinuria >3.5g/24hrs
Hypoalbuminemia
Hypercholesterol
Normal renal function

DVT- hypercoagulable

Adult: DM
Peds: post-viral infection

368
Q

How is nephritic syndrome different from nephrotic syndrome

What are the two classifications of nephrotic syndrome

Why is there proteinuria in nephrotic syndrome

What two lab results suggest a Dx of Nephrotic Syndrome

A

Neph: Hematuria
1-3g/day proteinuria
HTN
Oliguria

Primary: kidney biopsy
Secondary: systemic dz

Podocytes damaged by IgG Abs

Fatty cast w/ maltese cross
Oval fat bodies

369
Q

What are the MC primary cause of Nephrotic Syndrome

A

Membranous Nephropathy- MC in non-DM w/ malignancy/infection w/ Hep B

Minimal Change- MCC in kids; assume Dx w/ idiopathic nephrotic syndrome improved w/ CCS

Focal Segmental Glomerulosclerosis: occurs in obese, heroine, AfAm w/ HIV

370
Q

What are the MC secondary causes of Nephrotic Syndrome

How is Nephrotic Syndrome Dx

How is this Tx

A

Lupus
DM
Pre-eclampsia
Amyloidosis

24hr urine w/ >3.5g of protein

Statin
Angiotensiin inhibition
Na restriction
Diuretic
Steroids/Cyclosporine
371
Q

MC first Sx of nephrotic syndrome in Peds is seen as ?

What does HyperK look like on EKG

How is it Tx

A

Facial swelling

Peak T
Prolonged QRS
Muscle fatigue

Bicarb Insulin Gluconate

372
Q

What does HypoK look like on EKG

How is this Tx

What needs to be avoided

A

Flat/inverted T wave
U-wave

Replete K and Mg

Avoid Dextrose fluids

373
Q

What can cause HyperVolemic, HypoNa

What can cause Euvolemic HypoNa

What can cause HypoVolemic NypoNa

A

CHF
Nephrotic syndrome
RF
Cirrhosis

SIADS
Steroids
Hypothyroid

Na loss

374
Q

How is ASx HypoNa Tx

How is Moderate HypoNa Tx

How is severe HypoNa Tx

Correcting serum Na should be done how fast in order to prevent ?

A

Water restriction

IV NS, Loop diuretic

50mL bolus w/ 3% NS

= 10mEq.L over 24hrs;
Osmotic demyelination syndrome

375
Q

What lab result indicates underlying

How is this Tx

What adverse outcomes can occur from Tx

What lab results indicates HyperNa d/t Diabetes Insipidus

A

BUN/Cr >20:1 d/t decreased flow to kidneys, more urea remains in blood

D5W

Cerebral edema
Pontine herniation

Urine osmolality <250 w/ HyperNa

376
Q

MCC of HypoCa

What EKG/PE findings can be seen

How is HypoCa Tx

A

Hypoparathyroidism

QT prolongation
Traousseaus
Chvosteks

Calcium gluconate
Calcium chloride

377
Q

MCCC of HyperCa

What ‘saying’ goes with this condition

What does EKG look like

How is this Tx

A

Hyperparathyroid

Stone Bones Groans Moans

Shortened QT interval

NS w/ Furosemide

378
Q

What is the 3 step approach to Acid-Base d/os

DDx for metabolic acidosis

How is anion gap calculated

A

pH: 7.35-7.45
PCO2: 35-45
HCO3: 20-26

MUDPILES:
Methanol
Uremia
DKA
Paraldehyde
Infection
Lactive acidosis
Ethylene glycol
Salicylates

Na - (Cl+HCO3)= 10-16

379
Q

DDx for low anion gap <16

Define Orchitis

Since this is usually d/t a virus, bacterial orchitis is MC d/t?

A

Loss of BiCarb d/t:
Pancreatic/biliary drainage
Renal tubular acidosis
Diarrhea

Unilateral testicular inflammation d/t mumps

Concurrent epididymitis

380
Q

How is Orchitis Dx

How is this Tx

When/why would ABX be used

A

UA w/ culture
Pyuria
Bacteruria

NSAIDs
Scrotal support
ABX
Ice/Rest

<35/sexually active post-puberty male:
Ceftriax and Doxy or,
Azith and Doxy (PCN allergy)

> 35w/out STI suspected:
Levofloxacin or TMP/SMX

381
Q

Where is the epididymis located and what does it do

In Pts <35y/o this is usually d/t ? and Tx w/

In Pts >35y/o this is usually d/t ? and Tx w/?

A

Posterior testis;
Connect efferent duct w/ vas deferens

Chlamydia/Gonorrhea;
Ceftriax and Doxy

E-Coli/Pseudomonas; Cipro

382
Q

What PE sign is seen in epididymitis

MCC for ED

How is this Tx and when is this drug class c/i

A

Prehns: elevation brings relief

Psychogenic

Sildenafil- empty stomach 1hr prior, lasts 8hrs
Tadalafil- 2hrs prios, lasts 36hrs
Verdenafil- take w/ non-fatty food, lasts 8hrs
CAD/CVA

383
Q

What is the biggest RF for ED

What are 3 common causes of priapisms

How are these Tx

A

Atherosclerosis

Trazadone
Cocaine
Sickle Cell Dz

Stair climbing
Sudafed

384
Q

If Pt experiences erection during sleep, cause of ED is most likely d/t?

What causes the Sxs of BPH

This is Tx w/ any drug w/ ? class

A

Psychogenic

Residual volume d/t increased cell numbers increasing urinary resistance

-sin: a- blockers
Prazosin Terazosin Tamulosin
-ride:
Finasteride- 5a reductase, inhibits T converted to DHT; dec size of prostate

385
Q

What 3 classes of drugs need to be avoided when Tx BPH

How is BPH Dx

What lab marker for Ca is usually elevated and needs to be checked

A

Anticholinergics
Sympathomimetics
Opioids

DRE- uniform, large, firm and rubbery prostate

PSA:
<4 normal
>4 w/ BPH- prostatitis/Ca

386
Q

How is BPH Tx if refractory to meds

? is the MC non-cutaneous Ca among males

When does screening begin for this MC

A

TURP- transurethral resection of prostate

Prostate

PSA test at 50
+1st* relative/AfAM at 40

387
Q

What type of Ca is prostate Ca

What is the MC site this Ca will mets to

What RF leads to an increased risk while ? may be protective

A

Adenocarcinoma

Bone

High fat diet increases risk;
Soy decreases risk

388
Q

When is a transrectal biopsy for prostate Ca indicated

What presenting c/c indicates prostate Ca has metastesized

What will be felt on PE

A

PSA >10
Abnormal transrectal US

Back pain

Hard, nodular and asymmetric

389
Q

PSA >4 next step

PSA >10 next step

How is prostate Ca Tx but w/ ? adverse outcome

A

US w/ needle biopsy

Bone scan r/o mets

Protatectomy- ED

390
Q

How is prostate Ca w/ mets Tx

What monitoring is needed

? is the MC type of bladder Ca in the USA

A

Androgen deprivation therapy- Leuprolide

PSA <0.1

Urothelial carcinoma- AKA transitional cell carcinoma

391
Q

SCC bladder Ca is associated w/ ? infection

How does bladder Ca present

How is it Dx

How is it Tx

A

Schistosoma haematobium

Painless hematuria w/ +smoking Hx

Cystoscopy w/ biopsy- gold standard

Chemo, surgery, cystoscopy q3mon

392
Q

What are the 5 types of incontinence

A

Urge: detrusor overactivity; MC elderly, nursing home
Dx: urodynamic study

Stress: weak floor after delivery; r/o infection w/ UA

Overflow: impaired detrusor contractility; high postvoid volume/nocturnal wetting, common in DM/neuro d/os

Functional: can’t reach toilet in time d/t physical/mental blockades

Mixed: stress and urge- MC

393
Q

How is urinary incontinence Dx

A

UA- r/o UTI (only mandatory study for Peds w/ enuresis)

Postvoid residual:
overflow= high PVR
stress/urge- low/norm PVR

Urodynamic-
stress- normal contraction
urge- inc contraction during filling

US w/ cystoscope- anatomic abnormals

394
Q

How is Urge incontinence Tx

How is stress Tx

How is Overflow Tx

A

Bladder training
Anticholinergics (oxybutynin)
TCA (Imipramine)

Kegels
Estrogen
Pessary
Sling, mid-urethral

Intermittent self-cath
Cholinergic- Bethanechol, inc contractions
A-blocker- Tera/Doxazosin- dec sphincter resistance

395
Q

How is functional incontinence tx

How is Mixed incontinence Tx

? is the most definitive Tx for primary enuresis

A

Scheduled voidings

Lifestyle mod w/ pelvic floor exercises

Desmopressin

396
Q

How does prostatitis present

How is this Tx

A

Hesitency w/ dec flow
Saddle tenderness

<35: C/G
>35: Ecoli, pseudomonas;
Doxy/Ofloxacin/Ceftriax
>35: EColi/Pseudo; Cipro/TMPSMX

397
Q

How does acute bacterial prostatits present on DRE

? is the MC form of prostatitis

How are acute and chronic cases Tx

A

Boggy, warm and tender- do not massage (sepsis)

Chronic bacterial w/ enlarged, nontender prostate

Acute:
<35: Ceftriax and Doxy
>35: Flqln/TMP-SMX

Chronic- Flqnln or TMP-SMX

398
Q

? is the MC type of renal malignancy

? does this originate

This is more common in ? population

A

Renal Cell Ca

Proximal renal tubular epithelium

AfAm

399
Q

How does Renal Cell Ca present

What labs would be abnormal

What are the 1st and 2nd MC types

A

Weight loss
Hematuria
Palpable mass

Normo/Normo anemia (EPO flare)
HTN w/ hyperCa

Clear cell carcinoma
Transitional cell

400
Q

What is the biggest RF for Renal Cell Ca

How is this Dx

How is it Tx

A

Smoking

Abdominal CT or US

Surgery w/ nephrectomy

401
Q

? is the MC type of testicular Ca and the two types

When does this tend to appear

What is seen on PE

A

Germ cell:
Seminoma
Non-seminomatous

20-34y/o w/ cryptorchidism/orchitis

Painless, swollen and hard testi

402
Q

What are the 3 most important tumor markers for Dx testicular Ca

? lab result isolates Dx to NSGCT testicular tumor

What lab result is sen in both Seminomas and NSGCT

A

bHCG
AFP
LDH

AFP

HCG

403
Q

What does LDH indicate for testicular Ca

How is testicular Ca Tx

? tumor marker is used to monitor for relapse

A

High burden- seminoma, recurrence of NSGCT

Orchiectomy
Seminomatous- radiation
NSGCT- radioresistant

AFP

404
Q

How does Acute RF look on lab results

What can cause this

What is the first and second MC cause of Chronic RF

A

Inc Cr/BUN
Dec GFR

ACEI w/ bilat stenosis
Hypovolemia
Infection
Nephritic syndrome
Tubular necrosis

1st: DM
2nd: HTN

405
Q

What type of UA results is seen in Chronic RF

What are the 3 mechanisms of Acute RF

A

Broad Waxy Casts

Prerenal: perfusion
Renal: glomerular, tubular, interstistial
Postrenal: obstruction

406
Q

Prerenal SpecGrav, BUN, Osmolality and FENA

Renal SpecGrav, BUN, Osmolality and FENA

A

> 1.030
20
500
<1

<10.10
<10
<300
>1

407
Q

What types of casts are seen on UA during acute tubular necrosis

What other lab result is seen d/t this damage

What 3 lab results make this Dx likely

A

Muddy borwn

Unable to concentrate urine- high FENa

FENa >2%
Muddy casts
High osmolality

408
Q

What lab results suggest Interstitial Nephritis

What results are seen in Glomerulonephritis

Why does CKDz develop Vit D deficiency and Hyperphosphate

A

WBC casts Eosinophils

Oliguria
Hematuria
RBC casts

Vit D cant be made into Calcitriol
Dec excretion

409
Q

How is CKDz defined

? is the MC cause

What are the 5 stages

A
eGFR <60ml x 3mon or any 3:
Albuminuria >30mg
Proteinuria >0.2
Hematuria
Structural abnormals

HTN

1: GFR 90mL or > w/ albuminuria or hreditary dz
2: 60-89
3: 30-59
4: 15-29
5: <15

410
Q

How is CKDz Dx

? is the marker for kidney damage

What meds are used to slow Dx progression

A

Cockcroft Gault formula for GFR

Proteinuria

ACEI/ARB w/ pneumococcal vaccine

411
Q

How does RA present

What joints does it primarily affect

What syndromes can these Pts develop

A

Warm, swollen and symmetrically stiff joints x 1hr every morning

MCP
PIP
Wrist

Felty- RA, Splenomegaly, and Neutropenia
Caplan- pneumoconiosis and RA

412
Q

What type of effusion is seen in RA PTs

? rheum lab results will be positive in most PTs and which one is more specific

What type of anemia could be seen

A

Exudative

RF, C1M;
Anti-CCP more spec for RA

Normo/Normo

413
Q

? monotherapy is the best initial Tx medication for early RA w/ poor prognosis

? is used 2nd line for Tx

What is the s/e of using this 2nd line Tx

A

Methotrexate

Hydroxychloroquine

Eye toxicity

414
Q

What drugs are used 1st through 4th line for Tx of RA

What is the pathophysiologic reason for RA Dz

What two PE findings suggest OA Dx

A

Methotrexate
Hydroxychloroquine
Sulfasalzine (HMS- triple therapy)
Infliximab

Synovial inflammation

PIP Bouchard
DIP Heberden

415
Q

What is the first medication elderly PTs w/ OA are Tx w/

What three x-ray findings aid w/ Dx

OA in the knee commonly causs ?

A

Tylenol

Narrowing
Oseophyte
Sclerosis

Baker’s cyst

416
Q

How does SLE present

? syndrome do these Pts have that put them at risk for DVTs

How is this Tx

? monoclonal Ab can be used to inhibit B-cell factors

A

Fatigue
Hand/wrist joint pain
Malar rash

417
Q

What are 4 medications that can cause lupus

Define Discoid Lupus

What two tests are 100% specific for SLE Dx

A

Procainamide
Isoniazid
Quinidine
Hydralazine

Annular, erythematous patches on face/scalp that heal w/ scars

Antidouble strand DNA (dsDNA) and,
Anti-Smit Ab (anti-SM)

418
Q

Why do women w/ SLE have increased risk for miscarriages

What lab results will be decreased during flares

What two lab positives put neonates at higher risk for neonate lupus

A

B2 glycoprotein 1 Ab

Complement- C3, C4, CH50

Anti-Ro, Anti-La

419
Q

? lab result positive is highly sensitive for drug induced lupus

How is SLE Dx confirmed

A

Antihistone Ab

4 or more RASHNIA4
Renal d/o
Arthralgia
Serositis
Heme d/o
Neuro d/o
Imm derangement
ANA
4 rashes: malar, discoid, photosensitive
mucosal
420
Q

How is SLE Tx

? is the MC constitutional Sx associated w/ SLE

? is the most specific Ab for SLE and ? has the most sensitivity for screening

A

Sun protection
Hydroxychloroquine*
NSAIDs/Tyelenol

Fatigue

Anti-Smith;
ANA

421
Q

How is Systemic Sclerosis characterized on PE

What syndrome do these PTs develop

? is the MC GI Sx

A

Thickened skin from accumulation of collagen

CREST- 
Calcinosis
Raynauds
Esophageal dysfunt
Sclerdactyly
Telangiectasis

GERD

422
Q

How is Scleroderma Dx

How is it Tx during renal crisis or Raynauds crisis

A

Anti-centromere A- limited crest but better prognosis

Antiscl70- diffuse/multiple organs involved

Anti-tropoisomerase Ab

ACEI- Captopril
CCB/Prostacyclin

423
Q

How is Scleroderma induced P-HTN Tx

? three GI infection can stimulate Retiers

How is Ankylosing Tx

A

Ambrisentan and Tadalafil

Shigella
Salmonella
Campylobacter

PT w/:
Indomethacin
Methotrexate/Sulfasalazine
Pred- flares
Etanercept/Infliximab
424
Q

Define Ankylosing

How does this present

What 4 systemic issues can this present w/

A

Seronegative spondyloarthropathy affecting SI joint and spine

Morning back pain that dec w/ activity

Psoriasis
IBDz
Anterior uveitis
Aortic regurg

425
Q

? is the gold standard to Dx Ankylosing

How is Reiters Tx

What would be seen on a synovial aspiration result

A

X-ray

Indometh/Diclofenac
Doxy for Chlamydia
Sulfasal/Methotrex
Etanercept/Infliximab

Aseptic w/ negative bacterial culture

426
Q

? is the MC form of inflammatory arthritis

This MC is a d/o of ?

? is the underlying physiologic issue

A

Gout

Purine metabolism

Hyperuricemia

427
Q

? medication can induce gout

How is this Dx

How is this Tx

How does Tx change if cause is pseudogout

A

Thiazides

Needle shaped monosodium urate crystals w/ negative biregringence (pos fringence/rhomboid- pseudo)

1st: Indomethicin/Naproxen/Ibuprofen
2nd: Colchicine

Steroids

428
Q

? is usually the first sign of gout attack

What x-ray findings signal pseudogout

When is gout prophylaxis indicated

A

Podagra- MTP of great toe

Chondrocalcinosis- linear radiodensities

2 or more flares/year:
Allopurinol- dec uric acid production
Probenecid- inc urine excretion

429
Q

How is Firbomyalgia Tx

? is the preferred method of exercise PT

? is the Sjogrens Dx test and ? lab result is Dx

A

TCA
Pregabalin- only FDA approved Tx

Swimming

Schirmers tear test: <5mm of lacrimation in 5min
Anti-RO and antiLA (Anti-SSA, Anti-SSB)

430
Q

? part of the body does Sjogrens affect

How is this Tx

Define Giant Cell Arteritis

A

Exocrine glands- salivary/lacrimal w/ parotid enlargement

Tears
Pilocarpine- cholinergic
Cevimeline- muscarinic stimulation

Autoimmune viral infection causes monocyte activation/cytokine production leading to tissue destruction

431
Q

The vasculitis of GCA affects ? structures

This is MC in ? population w/ ? Dx

How is this Dx

A
Extracranial branch of carotid:
Posterior ciliary 
Occipital 
Ophthalmic 
Temporal

Female >50 w/ Polyalgia Rheumatica

ESR >100
Biopsy

432
Q

Define Polymyalgic Rheumatica

? other Dx is closely related w/ this population

How is this Tx

A

Idiopathic inflammation of synovitis, bursitis, tenosynovitis causing proximal joint stiffness

GCA

Methotrexate, CCS

433
Q

Define Polyarteritis Nodosa

One quarter of Pts will have ? underlying Dx

How is this Dx

A

Systemic vasculitis of arteries in men 40-50y/o

Hep B/C

Biopsy- necrotizing arteritis

434
Q

? lab result is seen in Polyarteritis Nodosa

How is this Tx and ? is done if refractory

How is this Tx if underlying Hep B is present

A

ANCA negative

Steroids; Cyclophosphamide

Plasmapheresis

435
Q

Cephalosporin Generation endings

A

1st: Fa/Pha
2nd: everything else
3rd: one/ten/me
4th: Pi
5th: Rol

436
Q

Define Hyperthyroidism

What is the preferred method for Tx hyperthyroidism during pregnancy

How can Pts present

A

PTU

Excess production of thyroxine hormone

Weight loss
Anxiety
Tachycardia/PVCs

437
Q

? is the MCCC of hyperthyroidism

What lab result will be seen and what will be seen if condition is causes by the MCC

How is it Tx

A

Graves dz- antithyrotropin Ab (TSHR-Ab) against TSH receptor

Low TSH, inc F-T4/T3
Graves Dz: low TSH, inc T3

Methimazole
Propylthiouracil

438
Q

Thyroid storm occur in ? two populations

How does this lead to death

How is Graves Abs tested for

A

Graves Dz
Toxic Multinodular goiter

Cardiogenic shock
CV collapse

TSI, TBII

439
Q

How are the cardiac Sxs of Graves Dz Tx

Define Hypothyroidism

What is the MCC and what would be seen on lab results

A

Atenolol

Thyroid gland doesn’t produce enough thyroid hormone

Hashimotos-
Inc TSH, low FT4

440
Q

What does Primary Hypothyroidism look like on lab results

What does Secondary Hypothyroidism look like

? lab result is not sensitive for the Dx of hypothyroidism

A

Inc TSH, low FT4

Low TSH, low FT4

T3

441
Q

How is a Dx of Hashimoto’s confirmed

Anemia is often present, ? type

? other CMP lab result will be high in primary hypothyroidism

A

Anti-TPO Abs

Normo/Normo

Cholesterol

442
Q

How is Hypothyroidism Tx

? is a severe form of hypothyroidism seen nondiagnosed/under Tx cases

? presentation should suggest a Dx of Hashimotos Thyroiditis

A

L-Thyroxine/Synthroid

Myxedema Coma

Goiter w/ tenderness
+MedHx recent viral illness

443
Q

What lab result would be elevated during Hashimotos Thyroiditis

? type of thyroid activity is seen in postpartum thyroiditis

Define Quevains Thyroiditis

A

Anti-TPO Abs

Hyper x 5-7mon

MCC of thyroid pain after infection; starts hyper, progresses to hypo

444
Q

What are two drugs that can cause drug induced thyroiditis

? causes Bacterial Thyroiditis

? lab result should indicate Pt w/ heat, pain, swelling has a bacterial form

A

Lithium
Amiodarone

Staph, Strep

Inc WBC

445
Q

4 etiologies of a painful thyroiditis

3 etiologies of a nonpainful thyroiditis

A

DeQuervains/Granulomatous
Infectious
Radiation
Trauma

Postpartum
Drug induced
Hashimotos

446
Q

How is Hashimotos’ Thyroiditis Tx

How is Subacute/Postpartum Thyroiditis Tx

How is Drug induced Thyroiditis Tx

How is Bacterial Thyroiditis Tx

A

Chronic hypo- T4 substitution

BBs and ASA

D/c offender

Surgical drainage of abscess and specific ABX

447
Q

? is the MC RF for thyroid carcinoma

? is the MC form

? is the MC beign nodule

A

Radiation exposure

Papillary

Adenoma

448
Q

? PE findings suggest thyroid Ca

What Lab/US results also suggest a Dx

How is thyroid Ca Dx

A

Firm/hard
Fixed w/ swallowing
Swollen lymph nodes

Microcalcification
Irregular margin
Size >1cm
Solid

US w/ biopsy if >1cm

449
Q

How is a thyroid nodule determined to be benign or malignant

What is the next step if uptake shows Ca

How is this Tx

A

Cold- no iodine uptake, Ca
Hot, takes up iodine, non-Ca

Fine needle aspiration

Removal of thyroid
Anaplastic Ca- Tx w/ chemo/rad

450
Q

Define Hyperparathyroidism

When do PTs become symptomatic

What causes primary and secondary hyperparathyroidism

A

Aver active, secretes PTH, leads to hypercalcemia

Ca >12

Primary: parathyroid adenoma
Secondary: CKDz

451
Q

What is the saying for hyperparathyroidism

How is this condition Tx

Define Hypoparathyroidism

A

Bones Stones Groans Psychic moans

Ectomy
Furosemide/Calcitonin
Bisphosphonates

Dec PTH causing low Ca levels

452
Q

What do Pts w/ hypoparathyroidism present w/

What triad is used for Dx

What is seen on EKG

A

Chvosteks’s sign
Trousseaus sign

Dec Ca
Inc DTRs
Dec PTH
Inc Phosphate

Prolonged QTc

453
Q

How is hypoparathyroidism Tx short term

How is this Tx if tetany is present

How is this Tx long term

A

Vit D, Ca

IV Ca gluconate

Recombinant human PTH

454
Q

Define Paget’s Dz

What form of bone Ca is most associated w/ this condition

? parts of the body are most affected

A

Bone remodeling d/o causing weaker bone

Osterosearcoma

Femur
Lumber
Pelvis*
Skull*

455
Q

How can Pts w/ Paget’s Dz present

How is this Dx

How is it Tx

A

Arthritis
Bone pain
Excessive warmth
Deafness

Inc Alk Phos
Lytic lesions/thickened cortices on x-ray

Bisphosphonates
Calcitonin

456
Q

Total cholesterol is desired to be below ?

LDL is desired to be below ?

HLD is desired to be below? ?

A

<200

<100

<40: low
>60: high

457
Q

What are the LDL goals if <1RF, 2RFs, DM/CADz, 10yr risk of >20%

A

<160- normal population, 1RF

<130 for 2RFs

<100- DM, CADz

<70- 10yrs risk of 20%, recent MI, CAD w/ DM/current smoking

458
Q

How is hypercholesterol Tx

What is a s/e of Tx, especially over ? dose

When are lipid screening began depending on organization recommending

A

1st: lifestyle
2nd: statin

Rhabdo, >80mg- check serum creatine kinase

USAPSTF: 35y/o
NCEP: 20y/o

459
Q

How is hypertriglycerides Tx

What bile sequestrant is used for DM w/ hypertriglyceride

A

1st: Fibrates (gemfibrozil)
2nd: Niacin, Omega-3, Bile sequestrant (Resin)

Colesevelam hydrochloride

460
Q

Pts w/ LDL of 190/> are Tx w/ ?

How is DM between 40-75y/o Tx

A

High intensity statin:
Atorva: 40-80
Rosuva: 20mg

ASCVD 7.5/>: high intensity
ASCVD <7.5: moderate intensity
Atorva- 10mg
Rosuva- 10mg
Simva- 20-40mg
Prava- 40-80mg
Lova- 40mg
Flu XL- 80mg
Flu- 40mg BID
Pita- 2-4mg
461
Q

How are non-DM w/ LDL >190 Tx

What are the two types of hypertriglycerides

A

ASCVD 7.5/>: moderate intensity
ASCVD <7.5: lifestyle

Combines- 2b; total, LDL and Tgd all elevated
Familial hyper- 4; normal LDL, elevated Tgd

462
Q

Hypertriglycerides >500 put PTs at risk for ?

Levels over 2000 put Pts at risk for ?

? type of hypertriglyceride causes palmar xanthomas

A

Pancreatitis
Xanthomas
Lipemia retinalis

Chlomicronemia- N/V/pain/pancreatitis

Type 3

463
Q

How often are fasting lipid panels needed

What is the next step if triglycerides are found to be >150mg

What is the next step if levels are found to be >1000

A

Start at 20y/o,
No comorbiditeis- repeat q5yrs

+ comorbidities- repeat q12mon

Fast x 12-16hr and recheck

Beta-quantification and electrophoresis

464
Q

? 3 meds are used to lower triglyceride levels

What causes Type 1 DM to emerge

A

Statins
Fibrates
Niacin
Fish oil

B-cells fail to respond and are destroyed

465
Q

Define Dawn Phenomenon

Define Somogyi effect

A

Dec insulin sensitivity and surge of regulator hormones during fasting; Tx inc night time insulin

Nocturnal hypoglycemia w/ rebound hyperglycemia d/t GH surge; Tx w/ dec nighttime insulin

466
Q

How is DM Dx

How is this Tx

? vaccines do these Pts need

A

Random >200 w/ Sxs
Fasting 126 or >
A1c 6.5% or >

A1c goal <7
Basal (Glargine)
Rapid (Humalog)

Flu
Tdap
PCV12
Pneumococcal

467
Q

Bolus-rapid insulin

Bolus short acting insulin

Basal-immediate

Basal-long acting

A

Post-prandial control:
Lispro Aspart Glulisine

Fasting control:
Regular: Humulin-R, Novolin-R

NPH: Humulin-N, Novolin-N

Glargine Detemir

468
Q

MOA and S/e of Metformin

A

Dec liver glucose production, peripheral glucose utilization, and intestinal absorption

Lactic acidosis

469
Q

MOA and s/e of Sulfonylureas

A

Stimulate pancreatic B-cells to release insulin

Hypoglycemia
Weight gain

470
Q

MOA and s/e of thiazolidinediones

A

Inc insulin sensitivity at peripheral receptor sites

Fluid retention/edema

471
Q

MOA and s/e of a-glucosidase inhibitor

A

Delays glucose absorption in intestine

Inc LFT/hepatitis

472
Q

MOA and s/e of Meglitinides

A

Stimulate b-cell insulin release

Hypglycemia

473
Q

MOA and s/e of GLP-1 agonists

A

Mimicks incretin to cause insulin secretion, decreases glucagon and delays gastric emptying

Hypoglycemia
Gastroparesis

474
Q

MOA and s/e of DDP-4 inhibitors

A

Inhibits degradation of GLP-1

Pancreatitis
RF

475
Q

MOA and s/e of SGLT2 inhibitors

A

Dec renal glucose threshold to increase urinary eexcretion

UTIs

476
Q

Normal fasting glucose is ?

Criteria for DM Dx

Criteria for Pre-DM Dx

A

70-100

A1c 6.5/>
Fasting 126/>
2hr 200/>
Random 200/> w/ Sxs

A1c 5.7-6.4
Fasting 100-125
2hr w/ 75g- 140-199

477
Q

How often is A1c checked for controlled and uncontrolled DM

MCC of gynecomastia in infant/boys

MCC of gynecomastia in men

A

Control: q6mon
Uncontrol: q2mon

Physiologic gynecomastia

Drugs (spironolactone)
Idiopathic
Persistent pubertal
gynecomastia

478
Q

How is Osteoporosis Dx

What scores mean porotic/penic

How are these Tx and w/ ? Pt education

A

DEXA on all females 65/>

Porotic:
T-score -2.5 or <
Penia:
T-score -1 - 2.4

PO Bisphosphonates (Alendronate, Risedronate)
Take w/ water, remain upright x 30min to avoid jaw necrosis
479
Q

How often are f/u DEXA scans needed depending on T-scores

How is this Tx if PT can’t tolerate PO Bisphosphonates

What medication is sued for Tx in PTx w/ very high risk of Fx (-3.5/>)

A

-1 - -1.5: q5yrs
-1.5 - -2: q3-5yrs
>-2; q1-2yrs

IV Zoledronic Acid

Teriparatide- recombinant PTH

480
Q

How to remember Addisons Dz

What E+ findings are seen on lab results

A

ADrenal Down
ADD hormone for Tx

HyperK
HypoNa

481
Q

Primary adrenocortical insufficiency is AKA and d/t?

What lab results will be seen

Define secondary adrenocortical insufficiency and lab results seen

A

Addisons Dz- adrenal destruction causing dec cortisol/aldosterone

Inc ACTH
Dec cortisol
Dec aldosterone

Pituitary failure;
Dec ACTH
Dec cortisol
Normal aldosterone

482
Q

? are the two etiologies of secondary adrenocortical insufficiency

How is this Dx

A

Exogenous steroids- MCC
Hypopituitarism

8AM ACTH w/ ACTH stimulation test

Inc ATCH and low cortisol= primary Dx

Low ACTH, low cortisol= secondary Dx

483
Q

? two stimulation tests are used toDx adrenal insufficiency

A

ACTH Cosyntropin:
IM ACTH given
Normal: cortisol levels rise
Insufficiency: little/no increase

CRH stimulation- differs the cuase of the insufficiency
Primary- high ACTH, low cortisol
Secondary- low ACTH, low cortisol

484
Q

How is Addison’s Tx

How is Secondary Insufficiency Tx

What lab results suggest Cushings Syndrome

A

Cortisol replacement

Hydrocortisone
Fludrocortison

Inc cortisol
Inc BP
Dec K+

485
Q

Cushings Dz is MCC by ?

? body types is seen here

How is Cushings Syndrome Dx

A

Pituitary adenoma

Buffalo hump
Moon facies
Pigmented striae

Low dose Dexamethasone suppression and,
24hr urine cortisol (gold standard)

486
Q

How is the cause of Cushing Syndrome differentiated

A

High dose dexamethasonze suppression test-
Suppressed cortisol- pituitary ACTH secreting tumor

ACTH level:
dec ACTH= adrenal tumor
Norm/Inc ACTH: ectopic ACTH tumor

487
Q

How is Cushings Dz Tx

What med is used for Pts ineligible for the primary Tx

Adrenal neoplastic Dz is AKA ?

A

Transsphenoidal surgery

Ketoconazole

Pheochromocytoma

488
Q

Define Pheochromocytoma

This Dx is associated in ? other d/os

What are the 5Ps of episodic Sxs

A

Catecholamine (Epi, NorEpi) secreting adrenal tumor

NF-1
MEN2A/2B
Von Hippel Lindau Dz

Pressure, Inc BP
Pain, HA
Persipiration
Palpation, tachy
Pallor
489
Q

How is a Pheo Dx

How is this Tx

What must be doe prior to Tx

A

24hr catecholamine w/ metabolites (metanephrine and vanilymandelic acid)

Complete adrenalectomy

Non-sel A-block: phenoxybenzamine/phentolamine
Then, BBs

490
Q

Gigantism and Acromegaly are both caused by ?

What are these rarely caused by

What is the difference between Gigantism and Acromegaly

A

Pituitary adenomas secreting excess GH

Non-pituitary tumor secreting GHRH

G: GH hypersecretion begins in childhood, before epiphyses closure
A: hypersecretion in adulthood

491
Q

How is Acromegaly/Gigantism Dx

What lab result is used to track therapy response

How are both cases Tx

A

IGF-, 2-10x normal

IGF-1

Surgery/radiation
Non-surgical= Octreotide/Lanreotide to suppress HG

492
Q

Define Diabetes Insipidus

What are the two types

A

Deficient/resistant ADH resulting in massive polyuria

Central- no ADH production

Nephrogenic- partial, complete insensitivity to ADH

493
Q

How is Diabetes Insipidus Dx

How is the etiology of the Dx determined

A

Water Deprivation test- pos- diluted urine production despite water restriction

Desmopressin stimulation test:
Central= dec urine output
Nephrogenic= continued production of diluted urine

494
Q

How is Diabetes Insipidus Tx depending on the etiology

Define Glomerulonephritis

What is the MCC

A

Central: Desmopressin
Nephro: Na/Protein restriction w/ Hydrochlorothiazide or indomethacine

Sudden onset of hematuria, proteinuria and RBC casts d/ glomeruli inflammation

Post-infection GABHS/Strep species
World: Beurgers Dz

495
Q

How is Post-Infectious Glomerulonephritis Dx

? is the MCC of this worldwide

How does the worldwide MC present

A

ASO titer and,
Low C3/C4

IgA Nephropathy- Bergers Dz

Hematuria
URI
Flank pain

496
Q

How is IgA Nephropathy/Berer’s Dx

Define Alports Syndrome

How is this Dx

A

IgA deposits in mesangium on staining

Isolated, persistent hematuria in kids w/ RF, HL and anterior lenticonus on Opto exam

C3/C4 levels

497
Q

What causes Membranoproliferative Glomerulonephritis

How is this Dx

What lab result suggests a Dx of Rapidly Progressive Glomerulonephritis

A

SLE/Viral hepatitis induced damage to glomerulus

Low C3,C4 levels

Crescent formation on biopsy d/t fibrin/plasma protein deposition

498
Q

How is Goodpastures Syndrome Dx

How is it Tx

What is seen on vasculitis induced glomerulonephritis

A

+anti-GM Abs
Linear IgG deposits

Steroids
Plasmapheresis w/ cyclophosphamide

ANCA Abs

499
Q

How is glomerulonephritis Dx

What lab is needed if Pt has recent strep infection

What is the gold standard for Dx

A

Hematuria (>3RBCs/field)
RBC casts
Proteinuria

Antistreptolysin-o titer

Renal biopsy

500
Q

What lab result is often decreased in glomerulonephritis

How is this Tx

What are the cysts in Polycystic KDz made of

A

C3

ACE/ARB is protective
Post-strep- use Nifedipine
Steroids/Na/Fluid restriction

Epithelial cells from renal tubules

501
Q

? is one of the MC human genetic d/os

What ER c/c can these Pts have

What Cardiac issues can they have

A

Autosomal dominant PCKDz

Brain aneurysm induced worst HA ever

MVP, LVH

502
Q

How is PCKDz Dx

Genetic studies for ? can be done prior to Sx onset

How is this condition Tx

A

US

PDK1/PKD2

ACEI/ARB
Transplant

503
Q

? is the MC form of anemia

What type of anemia is seen

What are the two MCCs

A

Fe deficient

Micro/Hypo

Dyfunctional uterine bleeding
GI bleed (men)
504
Q

How is Fe Deficient Anemia Tx

What is the first, second and last sing of this condition developing

What lab result suggest lead poisoning and how is it Tx

A

Ferrous sulfate

1st: low ferritin
2nd: rising TIBC
3rd: micro/hypo

Pt w/ neuro Sxs-
Basophilic stippling, Sideroblastic anemia
Thalassemia;
Tx EDTA

505
Q

What is seen on a peripheral smear of Fe Defficient anemia

How long does Tx take

How often do these Pts need f/u

A

Poikilocytes- pencil/cigar shaped

6wks corrects anemia
6mon replaces Fe stores

q3mon x 12mon

506
Q

When Tx Fe Deficient anemia, taking meds w/ ? can increase absorption

? lab result suggests Tx is working

? are the MCC of Anemia of Chornic Dz

A

Vit C

Inc reticulocyte counts

Chronic RF
CT d/o

507
Q

How is Anemia d/t Renal Failure Dx

How is this Tx

What does B12 Deficiency anemia look like

A

+RF and dec EPO levels

Recombinant EPO- Procrit, Epogen when Hgb <10
Fe supplements

Hypersegmented neutrophils
Neuropathy- loss of vibratory/proprioception
Inc Methylmalonic acid

508
Q

B12 Anemia leading to pernicious anemia is d/t ?

How is B12 Anemia Dx

What other lab results are elevated

A

Dec intrinsic factor

Macrocytosis and,
Hypersegmented neutrophils

MMA
Homocysteine

509
Q

What is seen in Folate Deficient Anemia

Of the two macro anemias (B12/Folate) hos does Folate appear differently

What is the risk if mother has tthis during pregnancy

A

Dec folate
Inc MCV- macro

Folate- no Neuro Sxs

Inc risk neural tube defects

510
Q

How is Folate Deficient Anemia Dx

How is this Tx

What causes hemolytic anemia

A

Magaloblastic
Folate <3
Normal MMA

400-1000ug/day of Folate

Premature RBC breakdown

511
Q

What are the two etiologies of the premature RBC breakdown of Hemolytic Anemia

A

Intracorpuscular:
RBC membrane defects (spherocytosis)

Extracorpuscular:
Autoimmune (+Coombs, Tx Pred)
G6PD
Chemo s/e

512
Q

How does Hemolytic Anemia present

What test will be positive if cause is autoimmune

What four results indicated the other causes

A

Splenomegaly
Inc indirect bili
Inc LDH

Direct Coombs (Abs to RBCs, Indirect- Abs in serum)

Spherocytosis- fragility test
G6PD- Heinz body
Sickle- inc retic count w/ pain
Thalassemia: very low MCV w/ normal TIBC/Ferritin

513
Q

? lab result pentad is the hallmark of hemolytic anemia

How are these Tx

Define Aplastic Anemia

A

Corrected Retic >2
Falling Hgb
Inc indirect bili
Inc LDH

Autoimmune: steroids
Spherocytosis: splenectomy

Normo/Normo from loss of blood cell precursors causing anemia w/out reticulocytes

514
Q

Unique fact about Aplastic Anemia

When is this Dx suspected

What is the most accurate test

A

Only one where all 3 lines are dec: WBC RBC Platelet

WBC <1500
Platelet <50K

Marrow biopsy- hypocellular marrow w/ fatty infiltrates

515
Q

How is Aplastic Anemia Tx

How is Tx changed in PTs ?50y/o

What med is used to decrease risk of infections

A

RBC transfusion w/ leuko-reduced, platelet transfusion

Anti-thymocyte globulin + cyclosporine/Pred

Figrastim- G-CSF

516
Q

How is Sickle Cell inherited

? lab result is used to track crisis progress

What does the punnet square look like

A

Homozygous of HgbS

Retic count

HbSS- Dz
HbSA- trait
Two parents w/ trait= 1/4 chance of kid w/ HbSS

517
Q

How is Sickle Cell Dx

? bodies are seen in lab results

? med is used to decrease frequency of crisis

A

HgbSS on electrophoresis

Howell Jolly- nuclear remains not phagocytosed

Hydroxyurea

518
Q

Define Thalassemia

Thalassemia and Fe Deficient are both micro/hypo, how is Thalassemia different

What other lab finding helps w/ Dx

A

Autosomal recessive blood d/o w/ abnormal Hgb formation

Higher RBC count
More micro/hypo than Fe deficient

Nucleated erythroblasts

519
Q

Stopped on B-Thalassemia

A

b