Chapter 32: Idiopathic Thrombocytopenia Purpura (ITP) (Children) Flashcards
Immune Thrombocytopenia (ITP)
cause is unknown
- disorder of increased platelet destruction caused by antiplatelet antibodies
- these antiplatelet antibodies attach to the child’s own platelets, and the body’s immune system eliminates the platelets, erroneously identifying them as bacteria
Characteristic Features
- thrombocytopenia (abnormal decrease in the number of blood platelets)
- purpura (discoloration caused by hemorrhage beneath the skin)
How is ITP Classified?
by duration; lasting a few months to a year or chronic, lasting longer than a year
Chronic Immune Thrombocytopenia
lasts longer than 12 months
Signs and Symptoms
clinical presentation of ITP is generally a previously healthy child who may have had a recent viral infection
- petechiae
- bruising
- mucocutaneus bleeding
- epistaxis
- menorrhagia
- internal bleeding such as a intracranial hemorrhage (rare)
Diagnosis
- hx and physical exam
- mostly appear healthy, with the exception of bruising and bleeding
- no tests confirm diagnosis
- newly diagnosed ITP is often benign, self-limiting, and often occurs in children younger than 10 after an upper respiratory infection; after childhood diseases such as measles, rubella, mumps, and chickenpox; and even after infection with parvovirus B19
Diagnosing Idiopathic (immune) Thrombocytopenia Purpura
-no definitive tests to establish the diagnosis
-other disorders such as lupus, leukemia, and lymphoma must be ruled out
>numerous tests to confirm diagnosis:
-CBC and peripheral smear examination, coagulation analysis, and possible bone marrow aspirate to rule out underlying malignancy
>CBC often shows isolated and usually severe thrombocytopenia (platelet count of less than 20,000)
>Peripheral smear is often normal with the exception of thrombocytopenia with normal-size to large platelets
Normal Platelet Count vs Thrombocytopenia
- CBC will often show severe thrombocytopenia: platelet count less than 20,000
- Normal: 150,000 to 400,000
Nursing Care
-most patients with acute ITP may have spontaneous resolution with no tx
-tx for ITP among pediatric hematologists is not consistent
>General Guidelines:
-children who have a platelet count greater than 20,000 and are asymptomatic do not require treatment and platelet counts are monitored
-small toddlers and active children with bruising and petechiae with platelet counts less than 20,000 are treated aggressively to avoid the most serious complication of a life-threatening intracranial bleed
-unless severe life-threatening bleeding is present, transfusion of platelets is not recommended to treat acute ITP because the antibodies attach to the infused platelets and destroy the new platelets in a similar fashion as the destruction of the patient’s own platelets
General Guidelines to Follow for Treatment
- children who have a platelet count greater than 20,000 and are asymptomatic do not require treatment and platelet counts are monitored
- small toddlers and active children with bruising and petechiae with platelet counts less than 20,000 are treated aggressively to avoid the most serious complication of a life-threatening intracranial bleed
- unless severe life-threatening bleeding is present, transfusion of platelets is not recommended to treat acute ITP because the antibodies attach to the infused platelets and destroy the new platelets in a similar fashion as the destruction of the patient’s own platelets
Medical Care
-steroid administration
-intravenous immune gamma globulin (IVIG)
-anti-D antibody (WinRho SDF)
>children with low platelet counts and acute bleeding require inpatient hospitalization and close observation b/c of potential of a cerebrovascular bleed
>my also receive a 2 to 3 day course of IVIG intravenously; IVIG is to prevent antibody attachment to the platelets, thereby preventing platelet destruction in the spleen; see a rise in platelet cunts within 48 hours
>inpatient care includes bedrest, monitoring of vital signs and adverse reactions during IVIG therapy and daily blood counts
Administration of IV anti-D antibody
newest treatment for acute ITP with an Rh(D)-positive blood type
-action: to bind to the RBCs, which are selectively destroyed in the spleen of instead platelets
-the anti-D antibody coats the Rh(D)-positive RBCs with antibody, only for Rh(D)-positive patients
-the anti-D coated cells saturate the capacity of the spleen receptors, and the platelets are spared
>side effect: hemolytic anemia that often resolves as the IgG disperses; other side effects: fever, chills, or headache after infusion)
Immune Gamma Globulin (IVIG)
used to prevent antibody attachment to the platelets, thereby preventing platelet destruction in the spleen
- rise in platelet count within 48 hours
- care includes bedrest, monitoring of vital signs and adverse reactions to IVIG, and daily blood counts
Surgical Care: Splenectomy
for whom medical tx has failed and there have been acute life-threatening bleeding episodes
- must be older than 5 years old
- have low platelet counts that impact their activities of daily living
Post-operative Nursing Care
- monitoring vital signs as per policy until condition stabilized
- administering IV fluids, pain medications, and antibiotics if ordered
- assessing surgical site for the signs and symptoms of bleeding or infection
- monitoring intake and output