| A | B |
|---|
| CHF - assessment findings | develop subtly - tires easily wt loss, diaphoresis |
| CHF - what we will see | fluid overload, periorbital and face edema, jugular, cool extremities |
| rheumatic fever - how get it | strep a |
| rheumatic fever affects | heart, joints, cns, tissue involvement |
| rheumatic fever when occurs | 1-3 weeks after strep |
| 1st indication of congenital heart defect | heart murmor |
| bradycardia is a significant warning sign of | cardiac arrest |
| jones criteria | 2 major or 1 major, 2 minor |
| jones - major | polyarthritis, carditis, chorea, erythema, subq nodules |
| jones - minor | fever spiking, hie erythrocyte sed rate |
| cystic fibrosis | leads to thick mucus in bronchioles, small I, pancreas, liver |
| cystic firosis - increased viscosity of secretions causes | obstruction of small passageway or organs |
| CF - lungs what happens | thick sticky secretions pool in bronchioles causing atelectasis and provide bacteria growth |
| CF - pancreas and small i - what happens | pancreas becomes damaged - diabetic - unable to absorb fats & protein |
| sickel cell replaces normal hemoglobin with | abnormal sickle shape |
| sickle cell causes | high blood viscosity - obstrusts blood flow - ischemia |
| factors that contribute to sickle cell | fever, altitude - extreme temp boose, pregnancy |
| sickel cell - most common reasons for hospitalization | acute painful episodes |
| sickle RBC causes 3 things | vaso occlusion, MI, ischemia |
| pain in sickle cell - areas | back, abd, chest, joint |
| sickle cell - nursing | hydration IV, ox, blood, PAIN meds, rest, resposition, joint pain |
| hemarthrosis - what to do | RICE |
| hemophilia - what is it | deficiency in clotting factors |
| hemophilia A VIII aka | classic hemophilia |
| hemarthrosis | bleeding in joints - |
| hemarthrosis - most common joints to bleed | knee, ankle, elbow |
| meds - hemophilia | DDAVP - med alert bracelet |
| teach hemophilia - | safety, s/s internal bleeding, soft toothbrush - NO ASA |
