Registration for a live webinar on 'Precision medicine treatment for anticancer drug resistance' is now open.
See webinar detailsWe noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- What is aplastic anemia (AA)
- Estimated annual incidence
- History and definition of AA
- Diagnostic criteria of AA
- Bone marrow biopsy
- Etiology of aplastic anemia (AA)
- Pathogenesis of aplastic anemia (AA)
- Discovery of immune pathogenesis in AA
- Karyotypic abnormalities in patients with AA
- Somatic gene mutations in leukocytes
- GPI depleted cells in patients with acquired AA
- HLA-allelic loss due to 6pUPD in patients with AA
- Escape hematopoiesis by HSCs that lack HLA-class I alleles in patients with AA
- Classification of aplastic anemia severity
- Symptoms of aplastic anemia
- Diagnosis of acquired aplastic anemia
- Bone marrow smear
- Differential diagnosis
- Inter-relationship between AA and related BM failure
- Overlapping histology of AA and MDS cases
- Why does thrombocytopenia precede pancytopenia in AA?
- Clinical consequences of aplastic anemia
- Treatment options for aplastic anemia
- Targets of treatment for aplastic anemia
- First line treatment of severe aplastic anemia (1)
- First line treatment of severe aplastic anemia (2)
- First line treatment of SAA and non-severe AA requiring transfusions in Japan
- Comparison between HSCT and IST
- Comparing event-free survival in patients with SAA after HSCT
- Second line treatment of severe aplastic anemia
- Efficacy of thrombopoietin-receptor agonists in the treatment of refractory aplastic anemia
- Second line treatment of severe aplastic anemia
- First line treatment of non-severe AA without a need of transfusions in Japan
- Failure-free survival rates in SAA patients after IST
- Age-adjusted cost-effective analysis in patients treated with HSCT or IST
Topics Covered
- Aplastic anemia (AA)
- Diagnostic criteria of AA
- Classification of aplastic anemia severity
- Inter-relationship between AA and related bone marrow failure
- Treatment options for aplastic anemia
- First line treatment of severe aplastic anemia
- Comparison between hematopoietic stem cell transplantation (HSCT) and immunosuppressive therapy (IST)
- Second line treatment of severe aplastic anemia
Talk Citation
Nakao, S. (2023, August 31). Aplastic anemia: epidemiology, diagnosis, treatment, and health economics [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 21, 2024, from https://doi.org/10.69645/RVMR4188.Export Citation (RIS)
Publication History
Financial Disclosures
- The financial disclosure includes honoraria received from Kyowa Kirin, Novartis Pharma, Sanofi, and Alexion.
A selection of talks on Clinical Practice
Transcript
Please wait while the transcript is being prepared...
0:00
Hello. My name is Shinji Nakao.
I'm now working at the Japanese
Red Cross Ishikawa Blood Center
as the Director General.
I'm going to talk about the
epidemiology, diagnosis, treatment
and health economics
of aplastic anemia.
0:19
Aplastic anemia, AA,
is a syndrome characterized
by pancytopenia
and bone marrow hypoplasia
caused by a persistent decrease
in the number of hematopoietic
stem cells, HSCs.
There are two forms.
One is congenital, and
the other is acquired.
The decrease of HSCs
is mostly induced by
an immune attack against
HSCs in acquired AA.
In patients with congenital AA,
germline mutations cause
functional abnormalities in HSCs,
leading to the failure to
produce mature blood cells.
1:04
The estimated annual
incidence of AA
is 1.5 - 2.3 per million
in Western countries,
while in Asian countries the
incidence is 3.0 - 7.5 per million,
two to three times higher
than in Western countries.
There are two age peaks.
One is around 20 years of age,
and the other is
around 70 years.
1:32
The first patient was described
by Paul Ehrlich in 1888.
Louis Henri Vaquez named the disease
"anemia aplastique" in 1904.
AA is not really only an anemia,
but instead is a pancytopenia
in which leukopenia,
anemia and thrombocytopenia
are almost always found,
and is defined as a syndrome
caused by a persistent decrease
in the number of HSCs without
any extrinsic factors,
such as chemotherapies
and chemicals.
The top photo of this slide
shows blood collection tubes
Hide