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A comprehensive study guide for the nr507/ nr 507 midterm exam in advanced pathophysiology. It covers key concepts related to innate immunity, hypersensitivity reactions, and various types of anemia. The guide includes questions and answers, providing a valuable resource for students preparing for the exam.
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Innate immunity - ANSWER>> >>the immunity we are born with
Immune response: 3 levels/lines of protection - ANSWER>> >>1 st line: physical, mechanical, & biochemical barriers
2nd line: the inflammatory response
3rd line: lymphocyte production
most important immune defense - ANSWER>> >> intact skin and mucous membranes (impermeable barrier)
PAMP - ANSWER>> >>pathogen associated molecular pattern
surfaces of bacteria, viruses, and other microbes are covered with many foreign proteins
foreign
DAMP - ANSWER>> >>damage associated molecular pattern
many proteins are released from inside our cells when they are damaged
foreign
PRR - ANSWER>> >>pattern recognition receptors
surfaces of WBCs contain these receptor sites -continuously interact with any material they encounter to ID it as "self" or "non-self" (foreign; PAMP or DAMP)
Chemotaxis - ANSWER>> >> Cell movement that occurs in response to chemical stimulus
Phagocytosis - ANSWER>> >>"cell eating"
inside the lysosomes
Hypersensitivity Type 1:_____ - ANSWER>> >>Allergic reaction
Hypersensitivity: Type 1 Mediated by ______ - ANSWER>> >>IgE
Hypersensitivity: Type 1 Inflammation due to _____________ - ANSWER>> >>mast cell degranulation
Hypersensitivity: Type 1 local symptoms - ANSWER>> >>itching, rash
Hypersensitivity: Type 1 systemic symptoms - ANSWER>> >>wheezing
Hypersensitivity: Type 1 most dangerous form - ANSWER>> >>anaphylactic reaction-systemic response- hypotension, severe bronchoconstriction
Hypersensitivity: Type 1 main treatment ___________ - ANSWER>> >>epinephrine
Hypersensitivity Type 2: _________________ - ANSWER>> >> Cytotoxic reaction; tissue specific (example: thyroid tissue) hapten causes mediation of IgE or IgM
Hypersensitivity: Type 2 Primary effector cells involved - ANSWER>> >>macrophages
(MHC) alleles or non-MHC genes
Alloimmunity - ANSWER>> >>AKA isoimmunity immune system of one individual produces a reaction against tissues of another individual
Alloimmunity examples - ANSWER>> >>Neonatal disease where the maternal immune system becomes sensitized against antigens expressed by the fetus -Transplant rejection -Transfusion reaction
Hypersensitivity: Type 4 - ANSWER>> >>Tcell mediated delayed response
Does not involve antigen/antibody complexes
Hypersensitivity: Type 4 typical reaction - ANSWER>> >>localized contact dermatitis (symptoms usually occur a few days later)
Differentiating between type 1 and type 4 rash reactions - ANSWER>> >> Type I: IMMEDIATE hypersensitivity reactions, termed atopic dermatitis, are usually characterized by widely distributed lesions
Type 4: contact dermatitis (DELAYED hypersensitivity) consists of lesions only at the site of contact with the allergen -Example: poison ivy
How to treat Type 4 hypersensitivity rash - ANSWER>> >>nonsevere case of contact dermatitis: tx with topical corticosteroid
How to treat emergent Type 1 anaphylactic reactions - ANSWER>> >>epinephrine
Antihistamines act on _____________ - ANSWER>> >>H1 receptors
Primary immune deficiency - ANSWER>> >>congenital -caused generally by a genetic abnormality 60% of cases, symptoms within first 2 years of life
most primary immune deficiencies are the result of ______________ - ANSWER>> >>single gene defects
one of the most severe forms of primary immunodeficiency - ANSWER>> >>B- lymphocyte deficiency
secondary immune deficiency - ANSWER>> >>acquired -caused by illness, such as cancer or viral infection -caused by normal physiological changes, such as aging -more common than congenital
most common cause of secondary immunodeficiency worldwide - ANSWER>> >>malnutrition
most common symptom of immune deficiencies - ANSWER>> >> recurrent severe infections
hematopoiesis - ANSWER>> >>blood cell formation
most of our body's iron stores come from ____________________________ - ANSWER>> >>the recycling of iron from old RBCs
erythropoiesis - ANSWER>> >>formation of red blood cells (7 day process)
lab values for: Iron Deficiency Anemia - ANSWER>> >>Serum ferritin level: Decreased RBC distribution width: Increased Serum iron level: Decreased Total iron-binding capacity: Increased Transferrin saturation: Decreased
lab values for: Thalassemia - ANSWER>> >>Serum ferritin level: Increased RBC distribution width: Normal to incrased Serum iron level: Normal to increased Total iron-binding capacity: Normal Transferrin saturation: Normal to increased
lab values for: Anemia of Chronic Disease - ANSWER>> >> Serum ferritin level: Normal to increased RBC distribution width: Normal Serum iron level: Normal to decreased Total iron-binding capacity: Slightly decreased
Major lab marker for anemia - ANSWER>> >> Increased RBC distribution width (RDW) is one of the earliest lab markers in developing microcytic or macrocytic anemia
Folate deficiency can cause a _______________ - ANSWER>> >> megaloblastic anemia
megaloblastic anemia - ANSWER>> >>a blood disorde r characterized by anemia in which the red blood cells are larger than normal
who is at risk for folate deficiency - ANSWER>> >>alcoholics
Symptoms of Vit B12 deficiency - ANSWER>> >>Fatigue Dyspnea Peripheral neuropathy in BLE
Vit B12 deficiency risk factors - ANSWER>> >>older adults H-pylori infection vegan (its in meat, fish, poultry, dairy)
Hemolytic anemia - ANSWER>> >>anemia caused by the destruction of red blood cells -mismatched blood types-destroys RBCs (cytotoxic type 2) -autoimmune hemolytic anemia due to autoantibodies against erythrocytes the immune system perceives as an antigen and attacks -Allergic reaction to a drug
Trauma victims who are losing blood are at risk for what type of anemia? - ANSWER>> >>Acute blood loss anemia
a normocytic-normochromic type of anemia
Aplastic anemia is characterized by: __________ Dx: ___ - ANSWER>> >>failure of bone marrow to produce red blood cells Dx made by blood tests and bone marrow biopsy -granulocyte count < -platelet count <20,
Aplastic anemia is a __________-__________ type of anemia - ANSWER>> >>
Sickle Cell Anemia - ANSWER>> >>Hemoglobinopathy Inherited autosomal recessive genetic disorder Inherit 2 abnormal genes, one from each parent, if only one abnormal Hb gene inherited then person has sickle cell trait
Sickle cell anemia pathophysiology: _______________________ - ANSWER>> >>single amino acid change on beta-chain (valine replaces glutamic acid)
Sickle cell anemia increases the risk for: - ANSWER>> >>stroke and splenic damage
Thalassemia - ANSWER>> >>Hemoglobinopathy Inherited autosomal recessive genetic disorder that causes decreased circulating hemoglobin -abnormal gene from both parents
Thalassemia has __________genetic mutations - ANSWER>> >>many possible
Thalassemia relation to malaria - ANSWER>> >> abnormal RBCs are more resistant to infection by parasite that causes malaria, shortened life span doesn't allow malaria parasite to complete life cycle *more prevalent in Africa
Anatomy of Heart: Flow through heart (Valves in order) - ANSWER>> >>. Tricuspid valve
Blood flow through the heart: - ANSWER>> >>1-Superior & Inferior Vena Cava 2-Rt Atrium 3-Tricuspid Valve 4- Rt Ventricle 5-Pulmonary Valve 6-Pulmonary Artery 7- Lungs-pick up oxygen 8-Pulmonary Veins
Hemorrhage can ___________ afterload due to decreased volume - ANSWER>> >>decrease
Increased preload __________ stroke volume (in the healthy heart)-the heart is able to __________ to the extra volume. - ANSWER>> >>increases, compensate
__________ preload caused by hemorrhage, dehydration-anything that reduces blood volume - ANSWER>> >>Decreased
Types of heart failure - ANSWER>> >>Left heart failure (CHF) Right heart failure (Cor Pulmonale) High-output failure
Left heart failure - ANSWER>> >>Inability of left ventricl e to provide adequate blood flow into systemic circulation
Causes of left heart failure - ANSWER>> >>systemic hypertension (most common) LV MI LV hypertrophy (often secondary to cardiac damage) Aortic semilunar or bicuspid valve damage Secondary to right heart failure
Left heart failure process - ANSWER>> >>1. high systemic vasular pressure
-right heart failure=biventricular heart failure
underlying pathophysiology of heart failure - ANSWER>> >> less cardiac output to meet bodys oxygen demands
heart failure: over time there is decreased _________, decreases __________, increased ____________________________. - ANSWER>> >> contractility, stroke volume, left ventricular end-diastolic volume (LVEDV)
When contractility is decreased, stroke volume falls, and left ventricular end-diastolic volume (LVEDV) increases. This causes dilation of the heart and an increase in __________ - ANSWER>> >>preload
Heart failure: major risk factor in its development - ANSWER>> >>longstanding hypertension Sometime right-sided heart failure can occur without there being left-sided heart failure; This usually occurs because the person has _________________________________. - ANSWER>> >>long-standing pulmonary issues (COPD)
Right heart failure - ANSWER>> >> Inability of RV to provide adequate blood flow into pulmonary circulation
Right heart failure causes - ANSWER>> >>pulmonary disease RV MI RV hypertrophy pulmonary semilunar valve or tricuspid valve damage Secondary to left heart failure
Characteristic of right heart failure - ANSWER>> >>JVD
Right heart failure process - ANSWER>> >>1. high pulmonary vascular pressure
-jugular distension, hepatosplenomegaly, peripheral edema -Left heart failure = biventricular heart failure
High-Output Failure (HOF) - ANSWER>> >> Inability of heart to pump sufficient amounts of blood to meet the circulatory needs of the body, despite the normal blood volume and cardiac contractility
High-output failure causes - ANSWER>> >>severe anemia nutritional deficiencies hyperthyroidism
NYHA Functional Classification - ANSWER>> >>Stage I: mild - no limitation of physical activity
Stage II: mild - slight limitation of physical activity Stage III: moderate - marked decrease in physical activity
Stage IV: severe - inability to carry on any physical activity without discomfort
Mitral stenosis murmur characteristics - ANSWER>> >>-rumbling, decrescendo diastolic murmur heard at apex of heart -low-pitched murmur auscultated at apex of heart -opening snap
mitral stenosis s/s - ANSWER>> >>As it progresses, symptoms of decreased CO occur: SOB exercise intolerance JVD crackles in bases pulmonary congestion/edema cough fatigue pounding/racing heart
mitral regurgitation murmur characteristic - ANSWER>> >>-blowing, holosystolic murmur -blowing pansystolic murmur heard best at the hearts apex and radiates to the back and axilla
Mitral regurgitation s/s - ANSWER>> >>SOB JVD crackles in bases
aortic stenosis murmur characteristic - ANSWER>> >>mid-systolic crescendo- decrescendo murmur heard loudest at the base and radiating to the neck
aortic regurgitation presents with - ANSWER>> >>-early, high pitched diastolic decrescendo murmur heard loudest at the left lower sternal border
aortic regurgitation s/s - ANSWER>> >>fatigue syncope SOB palpitations
wide pulse pressure (SBP-DBP) LV dilation -can have extra heart sound (S3) or displaced PMI
chest xray may show signs of pulmonary edema and cardiomegaly with what type of heart valve disorder? - ANSWER>> >>aortic regurgitation
mitral valve prolapse (MVP) s/s - ANSWER>> >>-many asymptomatic -atypical chest pain -palpitations -SOB -mid-systolic click certain arrhythmias mitral valve prolapse increases the risk for: - ANSWER>> >>infective endocarditis progression to mitral regurgitation
Fainting and chest pressure upon exercising are symptoms of ___________. - ANSWER>> >>aortic stenosis
Aortic stenosis has __________, laterally displaced ___________. - ANSWER>> >>sustained, apical pulse
what kind of heart valve disorder will have a S4 gallop present - ANSWER>> >> aortic stenosis
Spirometry that indicates obstructive pulmonary disease - ANSWER>> >> decreased FEV low FEV1/FEV ratio <70%
Spirometry that indicates restrictive pulmonary disease - ANSWER>> >> FEV1/FVC ratio above 70%
Asthma - ANSWER>> >>obstructive pulmonary disease airways are constricted two forms: intrinsic or extrinsic
asthma characterized by: - ANSWER>> >>airway inflammation bronchial hyperreactivity and smooth muscle spasm
Diagnostic PFT for COPD - ANSWER>> >> reveals airway obstruction (decreased FEV1) that is progressive and unresponsive to bronchodilators
COPD consists of _______ and _______ - ANSWER>> >> chronic bronchitis and emphysema
risk factors for COPD - ANSWER>> >>smoking airborne irritants -air pollutants, chemical fumes, dust anything that affects lung growth during gestation - smoking, antibiotic use, preterm, air pollution inherited mutation of alpha-antitrypsin gene -genetic cause of COPD
COPD has decreased _______ due to expiratory airway obstruction from ______________________ - ANSWER>> >> decreased FVC, mucus, edema, loss of elastic recoil
COPD causes air trapping in the lungs which leads to: - ANSWER>> >> chest to hyper expand causing increased work of breathing -hypoventilation -hypercapnia
COPD chest xray reveal - ANSWER>> >>flattened diaphragm distended lung fields increased thoracic diameter
COPD GOLD staging - ANSWER>> >> GOLD guidelines are based on the degree of airway limitation: Gold 1: Mild - FEV1 ≥ 80% predicted Gold 2: Moderate - 50% ≤ FEV1 < 80% predicted Gold 3: Severe - 30% ≤ FEV1 < 50% predicted Gold 4: Very Severe - < 30% predicted
perfusion - ANSWER>> >> the actual exchange of O2 and CO2 in the bloodstream -occurs via the alveoli and pulmonary capillaries
ventilation - ANSWER>> >>air movement in/out of the lung -critical to ensure sufficient perfusion
damage from Emphysema occurs in the ___________ - ANSWER>> >>alveoli
emphysema impairs _________ - ANSWER>> >>gas exchange
emphysema s/s - ANSWER>> >>air trapping pursed-lip breathing increased A&P diameter barrel chest prolonged expiration dyspnea
damage from chronic bronchitis occurs in the __________ - ANSWER>> >>airway dyspnea wheezing rhonchi chronic bronchitis s/s - ANSWER>> >>Productive cough with copious amount of sputum cyanosis of the skin and mucus membranes prolonged expiration
chronic bronchitis characterized by: - ANSWER>> >>chronic productive cough: -persisting for at least 3 consecutive months for at least 2 successive years bronchial inflammation hypersecretion of mucus
Chronic Granulomatous Disease (CGD) is what type of immunodificiency? - ANSWER>> >>Primary immunodeficiency
what is a predominant cause of secondary immune deficiency worldwide? - ANSWER>> >>malnutrition
Pneumocystis Carinii is what type of immunodeficiency? - ANSWER>> >> secondary immunodeficiency -caused by something external to immune system (yeast-like fungus)
contact dermatitis is an example of type ______ hypersensitivity reaction - ANSWER>> >>type 4
"first responders" of the innate immune system - ANSWER>> >>neutrophils -appear 1st in any immune response anaphylaxis is an example of a type ____ hypersensitivity reaction - ANSWER>> >> type 1
antigens
anemia types are classified by: - ANSWER>> >>size -normocytic, microcytic, macrocytic color -normochromic, hypochromic, hyperchromic variability -anisocytosis (size), poikilocytosis (shape) sideroblastic thalassemia microcytic-hypochromic anemias - ANSWER>> >>iron deficiency
microcytic-normochromic - ANSWER>> >>anemia of inflammation and chronic disease
microcytic-hyperchromic - ANSWER>> >>hereditary spherocytosis infection transfusion reaction causes of hemolytic anemia - ANSWER>> >>RBC's are destroyed: hemolytic disease of newborn (Rh incompatability) Autoimmune reaction drug-induced
aplastic anemia - ANSWER>> >>failure of blood cell production in the bone marrow
what valve disorder is associated with a hx of rheumatic heart disease - ANSWER>> >>mitral stenosis
an ECG may demonstrate atrial fibrillation and left ventricular hypertrophy in _______ - ANSWER>> >>mitral stenosis
4 main categories of interstitial lung diseases (ILD) - ANSWER>> >>ExposureRelated ILD Connective Tissue Disease Idiopathic Interstitial Pneumonias Other ILDs ILDs observed almost solely in current or past smokers - ANSWER>> >> Respiratory bronchiolitis-interstitial lung disease (RB-ILD) Desquamative interstitial pneumonia (DIP) Pulmonary Langerhans cell histiocytosis
Meds that can cause Medication-Induced ILD - ANSWER>> >>Amiodarone Nitrofurantoin Methotrexate
ILD s/s - ANSWER>> >>dyspnea non-productive cough hypoxemia fine (velcro-like) crackles fever clubbing extrapulmonary symptoms hemoptysis, chest pain, wheezing -relatively uncommon but can occur
interstitial lung disease (ILD) excludes: - ANSWER>> >> infectious and neoplastic diseases alterations of alveolar and airway architecture ILD characterized by: - ANSWER>> >>interstitial inflammation and fibrosis -scarring around alveolar sacs
ILD 4 diagnostic tests - ANSWER>> >>1. High resolution chest CT
What are the most diagnosed ILD's - ANSWER>> >>Radiation pneumonitis Pneumoconioses Hypersensitivity Pneumonitis