Difference between revisions of "Immune Thrombocytopenia"
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m (Protected "Immune Thrombocytopenia" ([edit=sysop] (indefinite) [move=sysop] (indefinite))) |
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| Line 14: | Line 14: | ||
Discuss with medical officer | Discuss with medical officer | ||
| − | Acceptable if more than 6 months from | + | ===Childhood disease=== |
| + | |||
| + | Acceptable If single episode of ITP as a child with complete resolution | ||
| + | |||
| + | ===Adult disease=== | ||
| + | |||
| + | Acceptable for BM only if more than 6 months from complete rceovery (platelet count <150). | ||
| + | |||
| + | Unacceptable if chronic or has required multiple lines of therapy | ||
Unacceptable if recurrent ITP. | Unacceptable if recurrent ITP. | ||
Revision as of 12:05, 1 June 2016
Contents
Acceptability at Recruitment
QUALIFIED
Acceptability at CT / Work-Up
QUALIFIED
Individual at Risk
Donor / Recipient
Explanation of Condition
Autoimmune condition leading to destruction of platelets. Severe types may lead to life-threatening bleeding as a consequence.
Guidance
Discuss with medical officer
Childhood disease
Acceptable If single episode of ITP as a child with complete resolution
Adult disease
Acceptable for BM only if more than 6 months from complete rceovery (platelet count <150).
Unacceptable if chronic or has required multiple lines of therapy
Unacceptable if recurrent ITP.
If received IVIG then see Transfusion.
Inform transplant centre in every case.
Pseudonyms or Related Conditions
ITP
Immune Thrombocytopenic Purpura
Version
Version 1, Edition 1
Date of Last Update
15th June 2012
