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Acute Idiopathic Thrombocytopenic Purpura of Childhood ... - sepeap

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Panepinto and Brousseau Pediatric Emergency Care Volume 21, Number 10, October 2005<br />

Instructions for the Pediatric Emergency Care CME Program Examination<br />

To earn CME credit, you must read the designated article and complete the examination below, answering at least 80%<br />

<strong>of</strong> the questions correctly. Mail a photocopy <strong>of</strong> the completed answer sheet to the Office <strong>of</strong> Continuing Education, Wolters<br />

Kluwer Health, 530 Walnut Street, 8th Floor East, Philadelphia, PA 19106. Only the first answer form will be considered for<br />

credit and must be received by Wolters Kluwer Health by December 15, 2005. Answer sheets will be graded and certificates<br />

will be mailed to each participant within six to eight weeks after WKH receipt. The answers for this examination will appear in<br />

the January 2006 issue <strong>of</strong> Pediatric Emergency Care.<br />

Credits<br />

Wolters Kluwer Health designates this educational activity for a maximum <strong>of</strong> 1 category 1 credit toward the AMA<br />

Physician’s Recognition Award. Each physician should claim only those credits that he/she actually spent in the activity.<br />

Accreditation<br />

Wolters Kluwer Health is accredited by the Accreditation Council for Continuing Medical Education to provide<br />

continuing medical education for physicians.<br />

CME EXAMINATION<br />

October 2005<br />

Please mark your answers on the ANSWER SHEET.<br />

<strong>Acute</strong> <strong>Idiopathic</strong> <strong>Thrombocytopenic</strong> <strong>Purpura</strong> <strong>of</strong> <strong>Childhood</strong>—Diagnosis and Therapy, Panepinto and Brousseau<br />

1. The clinical manifestations <strong>of</strong> ITP are due to:<br />

a) altered platelet function<br />

b) decreased production <strong>of</strong> platelets in the bone marrow<br />

c) autoimmune destruction <strong>of</strong> platelets<br />

d) increased consumption <strong>of</strong> platelets from mucosal<br />

bleeding<br />

2. All <strong>of</strong> the following are common signs/symptoms in ITP<br />

except:<br />

a) splenomegaly<br />

b) petechiae<br />

c) ecchymoses<br />

d) hemorrhagic blisters in the mouth<br />

e) epistaxis<br />

3. Which <strong>of</strong> the following treatments would be least appropriate<br />

for a child with ITP and mild to moderate<br />

symptoms?<br />

a) oral corticosteroids<br />

b) IVIg<br />

c) platelet transfusion<br />

d) IV anti-D Ig<br />

4. A child with known ITP presents with the acute onset <strong>of</strong> a<br />

severe headache and focal neurological findings. Which<br />

treatment(s) should be given or strongly considered at this<br />

time?<br />

a) high-dose IV steroids<br />

b) platelet transfusion<br />

c) IVIg<br />

d) splenectomy<br />

e) all <strong>of</strong> the above<br />

5. Which <strong>of</strong> the following is correct about the treatment <strong>of</strong><br />

childhood ITP?<br />

a) Observation is never indicated due to the risk <strong>of</strong><br />

intracranial hemorrhage.<br />

b) Treatment should be based on the platelet count alone.<br />

c) The natural course <strong>of</strong> ITP is a return to normal platelet<br />

count without sequelae.<br />

d) A bone marrow aspiration is required for all children<br />

treated for ITP.<br />

e) Children between 3 and 5 years <strong>of</strong> age have the<br />

highest risk <strong>of</strong> progression to chronic ITP.<br />

696 n 2005 Lippincott Williams & Wilkins<br />

Copyright © Lippincott Williams & Wilkins. Unauthorized reproduction <strong>of</strong> this article is prohibited.

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