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Rheumatic Fever & Kawasaki Syndrome

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Rheumatic Fever   serious inflammatory connective tissue disorder  
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rheumatic fever follows   an infection of some strains of group A beta hemolytic streptococci  
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rheumatic fever affects the   heart, joints, brain and skin  
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the exact cause of rheumatic fever is   unknown  
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rheumatic fever can occur at any age but is more common in children between ages   6-15  
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common s/s of a strep infection   sore throat, red and swollen tonsils, fever, h/a, muscle aches, many times, however, the initial strep infection may not cause any sumptoms  
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major manifestations of rheumatic fever   1-3 wks after an untreated streptococcal infection, hallmark signs or rheumatic fever may occur, caridits, arthritis, subQ nodules, skin rash, sydenham chorea(st. Vitus dance)  
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erythema marginatum   skin rash  
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minor manifestations of rheumatic fever   joint pain, fever, previous rheumatic fever, abnormal heart beat, blood testing indicating inflammation, new heart murmurs  
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diagnosing rheumatic fever   presence of 2 of the major criteria OR presence of 1 major plus 2 minor criteria  
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In all cases of rheumatic fever evidence of a preceding _____________ infection is key to making a dx.   strep throat  
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lab test for rheumatic fever diagnosis   antistrptolysin-O titer  
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complications of rheumatic fever   during a 1st attack about 1/2 of people develop heart inflammation, in some cases there may be scarring of 1 or more of the heart's valves, permanent heart damage is known as rheumatic heart disease  
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most people recover fully after 6 weeks, T or F?   True  
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In rare cases, heart damage is so extensive it leads to congestive heart failure(CHF), T or F?   True  
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A rheumatic valve has fibrous rolled edges, T or F?   True  
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clinical tx for rheumatic fever   antibiotics(pcn,sulfadiazine or erythromycin), ASA, NSAID's, steroids(used for severe cariditis w/CHF)  
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Long term antibiotic prophylaxis   american heart assoc recommends daily or monthly antibiotic prophylaxis continuing long term, perhaps for life. Low dose antibiotics, esp in 1st 3-5 yrs after initial attack  
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monthly injections of long acting ____________ for a period of up to 5 yrs, if carditis is present maybe up to __________yrs   penicillin, 40 yrs  
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long term antibiotics are used in rheumatic fever to...   reduce the chance of another attack  
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nursing management for rheumatic fever   prevention, during acute phase VS q 4hrs, auscultate heart sounds, observe for changes in skin & joints, administer antibiotics and ASA as ordered, plan quiet activities, educate parents regarding future sore throats and long term antibiotics  
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Kawasaki Syndrome   an acute febrile, systemic inflammatory illness  
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cause of kawasaki syndrome is   unknown, but maybe an infectious agent such as a virus  
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2 leading causes of acquired heart disease in US   Kawasaki syndrome and rheumatic fever  
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kawasaki syndrome is most common in   children under age 5  
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kawasaki syndrome can occur in any race but is more common in those with ___________ancestry   asian  
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greatest incidence of kawasaki's syndrome occurs in....   winter and spring  
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lowest incidence of kawasaki's syndrome occurs in...   summer  
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kawasaki's syndrome is usually preceded by an...   upper respiratory infection  
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kawaski's syndrome affects...   small arteries including the coronary arteries  
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3 stages kawasaki's syndrome occurs in...   acute, subacute, and convalescent  
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acute phase of kawasaki's syndrome   can last 2wks:irritability,persistent fever(>102 x 5days),severe redness in the eyes,red throat,swollen hands and feet(poss red/purplish color), rash on trunk&perineal area,unilateral enlargement of the cervical lymph node, diarrhea,hepatic dysfunction  
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subacute phase   2 wks after fever, cracking lips and strawberry tongue, peeling of the skin on the tips of fingers and toes, joint pain, cardiac dx(do echo), thrombocytosis(increased platelets)  
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coronary artery damage can lead to   aneurysms, MI's or ischemic heart disease  
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convalescent phase of kawasaki's syndrome   occurs at about 6-8 wks after dx onset, child appears normal, lingering signs of inflammation may be present  
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diagnosing kawasaki's syndrome   there is no specific diagnostic test, occurs when a high spiking fever over 102 is present x5 days or more along w/4 of the 5 criteria not explained by another disease process  
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fiver criteria of kawasaki's syndrome   B/L conjunctivitis w/out exudate, dry,swollen cracked lips and a strawberry tongue, dermatitis of the extremities, intense palmar & plantar erythema w/peeling, dermatitis of trunk w/rash, acute cervical lymphadenopathy  
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complications of kawasaki's syndrome   if tx'ed w/in 10 days of the 1st symptom, usually no heart problem develops, if untreated can lead to vasculitis of the coronary arteries  
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myocardium, valves and pericardium can become inflamed in kawaskai's syndrome, T or F?   True  
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What can develop in kawasaki's syndrome?   arrhythmias  
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clinical treatment for kawasaki's syndrome   IV immunoglobulins(purified antibodies), ASA, high doses of ASA given while the fever is high, corticosteroids may be give(if fever persists and a second dose of immunoglobulins are ineffective)  
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Nursing Management for Kawasaki's syndrome   monitor temp Q 4hrs and prior to each dose of ASA, carefully assess extremities for edema, redness & peeling Q 8hrs, examine eyes for conjuctivitis & mucous membranes for inflammation, assess heart sounds carefully,  
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Flu vaccine can prevent Reyes syndrome from ASA, T or F?   True  
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