Exam 2 Blueprint Flashcards

1
Q

How long does it take for acute HIV symptoms to appear?

A

2-4 weeks from exposure

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2
Q

What are the symptoms of acute HIV?

A

Flu like symptoms:
Fatigue
Headache
low-grade fever
Night sweats
persistent generalized lymphadenopathy (swollen lymoh nodes)

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3
Q

What happens for your CD4 and viral count during acute HIV infection?

A

High viral load (very contagious)
Low CD4+ T count ( 200 to 500 cells/μl)

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4
Q

(T/F) In acute HIV infection, bone marrow is still able to produce enough CD4+ T cells

A

True

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5
Q

(T/F) Once HIV develops to AIDS, your immune system is severely compromised

A

True

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6
Q

What is the five criterias of AIDS?

Not all have to be met to be diagnosed with AIDS

A
  1. CD4+ T-cell count drops less than 200 cells/μL,
  2. specific opportunistic infections,
  3. specific opportunistic cancers,
  4. wasting syndrome, or
  5. AIDS dementia complex.

  1. Wasting syndrome, also called cachexia, is a complicated metabolic syndrome related to underlying illness and characterized by muscle mass loss with or without fat mass loss
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7
Q

What are the ways HIV is transmitted?

There are three ways

A

Sexual (semen, vaginal secretions, bloof)
Blood and blood products (Needle sharing, needle stick, transfusions (usually not from the U.S due to protocol)
Perinatal (pregnancy or delivery, breastfeeding)

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8
Q

What are the two diagnostic tests for HIV/AIDS?

A

ELISA
Western Blot

Blood or saliva tests, early false negatives are possible

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9
Q

What is the normal range for CD4?

A

500-1500

Anything below indicates poor immune system status (200)

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10
Q

What are the goals of ART?

There are five

Think what are does for the viral load, CD4 count, and HIV symptoms/transmission

A

(1) decrease the viral load
(2) maintain or increase CD4 cell counts
(3) prevent HIV-related symptoms and opportunistic diseases
(4) delay disease progression
5) prevent HIV transmission

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11
Q

What education should be given to patients about ART?

A

Early intervention, drug adherence, family planning, psychological factors/support (social stigma)

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12
Q
A
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13
Q

What viral load count makes it so HIV cannot be transmitted

A

200 and less

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14
Q

What is an example of an ART drug?

There is only one

A

Biktarvy (Bictegravir/entricitabine/tenofovir)

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15
Q

(T/F) ART kills the virus

A

False

It helps stop viral replication in the body by blocking different stages in virus life cycle

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16
Q

What are adverse reaction/side effects of ART?

There are seven, two important

A

Hepatitis B exacerbation
Autoimmune disorders
Nephrotoxicity. hepototxicity
Neutropenia
Pancreatitis
Nausea/vomiting/diarrhea

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17
Q

What are contraindications of ART?

There are three

A

Hepatitis B
Poor kidney or liver function
Breast feeding

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18
Q

(T/F) There are no concerns with drug interactions between OTC drugs and ART

A

False

Many drug interactions, beware OTC and supplements used with ART

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19
Q

(T/F) SLE (Systemic Lupus Erythematosus) is an autoimmune disease

A

True

Chromic multisystem inflammatory autoimmune disease with alternating remission and exacerbation

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20
Q

What are clinic manifestations to SLE?

Two important ones

A

Butterfly rash
Alopecia
Fever,
Weight loss,
Joint pain,
Excessive fatigue precede worsening disease
activity

Alopecia is hair loss

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21
Q

What systems of the body does SLE affect?

There are six

A

Skin
Muscles
Lining of lungs
Heart
Nervous tissue
Kidneys

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22
Q

What are the symptoms of SLE in the skin

A

Alopecia
CCLE (discoid (round) lesions on scalp and face)
SCLE (red, ring-shaped lesions where disease active; butterfly rash) (these lesions do not scar or itch, and are not thick or scaly)
Oral or nasopharyngeal ulcers

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23
Q

What are muscoskeletal symptoms in SLE?

A
  • Polyarthralgia (pain in multiple joints)
  • Deformities like:
    Swan neck deformity in fingers
    Ulnar deviation
    Subluxation with hyperlaxity of joints
  • Increased risk of bone loss and fracture
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24
Q

What are cardiopulmonary symptoms involved in SLE?

A

Tachypnea and cough
Pleurisy (inflammation of the pleura)
Dysrhythmias (leading cause of death in SLE patients)

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25
Q

What are renal symptoms of SLE?

A

Nephropathy
Mild proteinuria to rapidly progressive glomerulonephritis
Scarring, permanent damage can lead to ESRD (End-Stage Renal Disease)

Proteinuria is a condition where an excessive amount of protein is present in the urine
Glomerulonephritis is inflammation and damage to the filtering part of the kidneys (glomeruli).

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26
Q

What is the goal of treatment for renal problems in SLE?

A

Slow progression of nephropathy and preserve renal function

27
Q

What are treatments for renal problems in SLE?

There are four

A

Corticosteroids and immunosuppresive agents
Belimumab (human monoclonal antibody)
Voclosporin

28
Q

What are nervous system problems associated with SLE?

A

Neuropsychiatric (Ranging from headaches to cerebrovascular disease)
NPSLE
* Focal: Caused by clots; Stroke or aseptic meningitis may occur;
Headaches are common;
Can be severe during a flare-up;
Vasculopathy in chronic disease
* Diffuse
Inflammatory process;
Psychosis, anxiety, depression, confusion, cognitive problems

NPSLE stands for Neuropsychiatric Systemic Lupus Erythematosus

29
Q

What are hematological problems associated with SLE?

A

Anemia
Leukopenia
Thrombocytopenia
Coagulation disorders

30
Q

What medication can help decrease risk of clots?

A

Hydroxychloroquine

31
Q

(T/F) Vaccinations are safe for patients with SLE

32
Q

(T/F) Patients receiving corticosteroids or cytotoxic drugs must avoid live virus vaccines

33
Q

What medications will you use for SLE?

There are six

Think about symptoms of SLE and what you would use to treat/manage. Honestly not THAT important to remember

A

NSAIDs
Antimalarial drugs
Corticosteriods
Immunosuppresive drugs
Anticoagulants
Topical immunodilators

34
Q

What will you monitor for when taking immunosuppresive drugs?

A

Toxicity and side effects

Suppresses immune system, reduce end-organ damage

35
Q

What do topical immunodilators do and what symptoms of SLE do they manage

A

Lesions and butterfly rash
Suppresses immunity activity of the skin

36
Q

What should SLE patients avoid to avoid flare ups?

A

Fatigue,
Sun exposure
Emotional stress
Infection
Drugs,
Surgery

37
Q

What are the early/first symptoms of Guillain-Barre Syndrome (GBS)?

A

Weakness, paresthesia, and hypotonia of limbs
Reflexes in affected limbs may be weak or absent
Maximum weakness occurs at 4 weeks

38
Q

(T/F) There is symmetric weakness of limbs with GBS

39
Q

What clinical signs do you look for for diagnosis of GBS?

A

Progressive weakness of more than 1 limb
Decreased or absent reflexes

40
Q

What tests will you order to help diagnose GBS?

Not that important to know, be more aware of clinical signs for diagnosis

A

Electrolytes, liver function tests, CPK, ESR
CSF analysis
EMG and NCS

Electromyography (EMG) and Nerve Conduction Study (NCS)

Cerebrospinal Fluid (CSF) Analysis

41
Q

What interventions wil you use for the acute phase of GBS?

A

Ventilatory support
ICU–hemodynamic monitoring
Immunomodulating treatments (PE and High dose IVIG)

PE: Plasma Exchange (plasmapheresis)
IVIG: IV immunoglobulin

42
Q

When is IVIG and PE most effective?

A

In the first 2 weeks on symptom onset

43
Q

(T/F) PE and IVIG therapies have little value after 4 weeks past disease onset

44
Q

What assessment will you conduct for patients with GBS?

There are five

A

Neurological assessment (motor and sensory evaluation)
Respiratory assessment
Cardiac assessment
Fever
Nutrition

Motor: ascending paralysis, reflexes, CN function (gag, cornea, swallow), and LOC
Respiratory: Monitor ABGs and vital capacity
Cardiac: Monitor BP and heart rate and rhythm
Fever: Sputum and blood cultures; antibiotics
Nutrition: Delayed gastric emptying, paralytic ileus, risk for aspiration; Enteral or parenteral nutrition

45
Q

How is the recovery process for GBS patients?

A

Recovery starts at approc 28 days
80% walk independently at 6 months
60% have full recovery in 1 year

46
Q

What asculation findings will you find in pneumonia patients?

A

Fine or coarse crackles over affected region

47
Q

What asculation findings will you find in pneumonia patients with consolidation?

A

Bronchial breath sounds
Egophony
Increased fremitus

48
Q

What asculation findings will you find in pneumonia patients with pleural effusion?

A

Dullness to percussion over affected area

49
Q

What are the goals for patients with pneumonia?

There are six

A

1. No signs of hypoxemia
2. Normal breathing patterns
3. Clear breath sounds
4. Normal chest x-ray
5. Normal WBC count
6. No complications

50
Q

What are risk factors for pneumonia?

There are five

A

Advanced age
Immunosuppression
History of antibiotic use
Prolonged mechanical ventilation
Contact with high population numbers

51
Q

What are diagnostic tests for TB?

A

TST skin test (aka Mantoux test) (PPD)
Blood test
Chest x-ray (cannot make definitive diagnosis and only suggestive)
TB sputum culture x3

PPD: Immunocompromised: >/= 5mm is positive
Risk factor for TB: >/= 10 mm positive
No risk factor for TB: >/= 15 mm positive

IGRAs for blood testing

Sputum culture x3 is golden standard

52
Q

How long is a TB patient infectious?

A

First two weeks after starting treatment if sputum is positive (Restrict visitors and public exposure; have strict hand and oral hygeine)

53
Q

What infection control measures will you take with TB patients?

A

Teach patient to prevent spread
◦ Cover nose and mouth with tissue when coughing, sneezing, or producing sputum; dispose in trash or flush
◦ Hand washing after handling sputum-soiled tissues
Patient wears face mask if outside of negative-pressure room
Identify and screen close contacts
Airborne precautions

54
Q

What is the Bacille-Calmette-Guerin (BCG) Vaccine for regarding TB?

A

Live, attenuated strain of Mycobacterium bovis
Given to infants in parts of world with high prevalence of TB

The important part is it’s a live strain and given to infants in parts of world with high prevalence of TB

55
Q

What is the medication adherence used for patients with active TB?

Acryonym RIPE

A

The first phase is intensive medication treatment with 4 drugs: Rifampin, Isoniazid, Pyrazinamide, and Ethambutol)
Second phase is continuation of two drugs (Isoniazid and rifapin)

First phase is RIPE, second is RI

56
Q

Isonizaid increases risk for what?

A

Hepatoxicity

57
Q

When do you exclude Pyrazinamide from treatment?

A

When pregnant and/or with hepatitis

58
Q

When would you stop Ethambutol?

A

If susecptible for all 4 drugs

59
Q

How can you ensure adherence to treatment for TB patients?

A

DOT (directly observed treatment)
Teach adverse effects and when to seek medical care (Baseline LFTs and every 2-4 weeks)

Liver function tests

60
Q

What is medication treatment for latent TB?

What is the standard, those not infected with MDR bacill, those resistant to isoniazid, and those with HIV and fibrotic lesions

A

Standard - Isoniazid for 9 months (or 6 months if medical adherence is an issue)
Alternative 3-month regimen of Isoniazid and rifapentine for those not infected with MDR bacill
4 months of rifampin for those resistant to isoniazid
HIV patients and those with fibrotic lesions on chest x-ray should take Isoniazid for 9 months

61
Q

What is COPD?

A

Chronic obstructive pulmonary disease

62
Q

(T/F) COPD is a progressive lung disease characterized by persistent airflow limitation

63
Q

What are the main causes of COPD?

A

Smoking
Noxious particles and gases

64
Q

What is the difference between chronic bronchitis and emphysema?