Seminar SP 25 Final Review Flashcards
(215 cards)
the presence of air in the pleural space, which can lead to partial or complete collapse of the lung
Pneumothorax
a serious complication of blood transfusion characterized by acute pulmonary edema due to circulatory overload
Diagnostic criteria include new or worsening respiratory distress, evidence of fluid overload, and radiographic findings of pulmonary edema
TACO
a complication of blood transfusion characterized by acute pulmonary edema due to circulatory overload, rather than an immune-mediated process
TACO
a serious complication of blood transfusion characterized by acute onset of non-cardiogenic pulmonary edema, typically occurring within 6 hours of transfusion
TRALI
chest radiograph characterized by bilateral patchy infiltrates without signs of heart failure
TRALI
a genetic bleeding disorder caused by a deficiency in clotting factors, specifically factor VIII and IX
Hemophilia
Factor 8 Deficiency
Hemophilia A
Factor 9 Deficiency
Hemophilia B
Ventricular Septal Defect (VSD)
Pulmonary Stenosis
Overriding Aorta
Right Ventricular Hypertrophy
Tetralogy of Fallot
Tetralogy of Fallot
Ventricular Septal Defect (VSD)
Pulmonary Stenosis
Overriding Aorta
Right Ventricular Hypertrophy
a palliative surgical technique used for patients with single-ventricle physiology, meaning only one ventricle is functional enough to support circulation
Fontan Procedure
Pulmonary Autograph
Ross Procedure
DOE, orthopnea, paroxysmal nocturnal dyspnea, cough, crackles/rales. fatigue
Left-Heart Failure
Peripheral edema, JVD, hepatomegaly, ascites, fatigue
Right-Heart Failure
Behavioral abnormalities, aphasia (if dominant cortex is involved), and contralateral lower limb weakness and sensory deficits
Anterior Cerebral Artery Sroke
Hypochloremic, hypokalemic metabolic alkalosis
Pyloric Stenosis
ETT Size= (Age/4) +4
Uncuffed ETT Sizing
ETT Size= (Age/4) + 3.5
Cuffed ETT Sizing
A rare autosomal dominant genetic mutation on chromosome 11 that affects the C1-inhibitor protein
Can also occur due to spontaneous genetic mutation in up to 25% of cases
This results in cutaneous and mucosal swelling
Hereditary Angioedema
Treatment for HAE
C1 Esterase Inhibitor
Bradykinin B2 receptor antagonist
Kallikrein Inhibitor
Anxiety,Stress
Viral infections
Minor local trauma
Surgery**
Triggers for Hereditary Angioedema
Medications contraindicated in HAE
ACE Inhibitors
Estrogens
NSAIDs
Multi-system: urticaria (hives), hypotension, wheezing, GI distress
Skin involvement often present (hives, flushing)
Bronchospasm, hypotension, shock
Tryptase test to confirm
Anaphylaxis
Localized swelling (face, lips, airway, GI) without hives
Airway swelling, especially tongue/larynx
CV sx - Rare (except in airway obstruction)
HAE- Hereditary Angioedema