Incidence, diagnosis, and outcome of immune‐mediated thrombotic thrombocytopenic purpura: A nationwide survey by the Spanish registry of thrombotic thrombocytopenic purpura. Issue 4 (29th March 2021)
- Record Type:
- Journal Article
- Title:
- Incidence, diagnosis, and outcome of immune‐mediated thrombotic thrombocytopenic purpura: A nationwide survey by the Spanish registry of thrombotic thrombocytopenic purpura. Issue 4 (29th March 2021)
- Main Title:
- Incidence, diagnosis, and outcome of immune‐mediated thrombotic thrombocytopenic purpura: A nationwide survey by the Spanish registry of thrombotic thrombocytopenic purpura
- Authors:
- Pascual‐Izquierdo, Cristina
del Rio‐Garma, Julio
de la Rubia, Javier
Viejo, Aurora
Mingot, Eva
Cid, Joan
Solanich, Xavier
Fernández‐Sojo, Jesús
Martín‐Sánchez, Jesús
Hernández, Luis
García‐Gala, José María
Alonso, Nieves
González, Victoria
Oliva, Ana
Gómez‐Seguí, Inés
Goterris, Rosa
Guerra, Luisa
García‐Candel, Faustino
Fernández‐Docampo, Marta
Antelo, María Luisa
Salgado‐Barreira, Ángel
Salinas, Ramón - Abstract:
- Abstract: Background: Immune‐mediated thrombotic thrombocytopenic purpura (iTTP) is a rare disease characterized by the presence of anti‐ADAMTS13 autoantibodies. Achieving accurate information on incidence and customary disease management is important to provide appropriate diagnostic and therapeutic resources. The aim of this study was to determine the incidence and outcomes of iTTP in Spain. Study design and methods: A cross‐sectional survey was carried out among Spanish hospitals, focused on iTTP patients ≥16 years old attended between 2015 and 2017, and those at follow‐up before that interval. Incidence, prevalence, mortality, refractoriness, exacerbations, treatment complications, relapses, and sequelae were estimated. Results: Forty‐two hospitals covering roughly 20 million inhabitants answered the survey and reported 203 episodes (138 newly‐diagnosed and 65 relapses), of which 193 (95.1%) were treated. Incidence was 2.67 (95% CI 1.90‐3.45) patients per million inhabitants per year and prevalence 21.44 (95% CI% 19.10‐23.73) patients per million inhabitants. At diagnosis, ADAMTS13 activity and anti‐ADAMTS13 autoantibody were measured in 97% and 84.3% of reported episodes, respectively. Fifteen patients (7.4%) died as a direct consequence of iTTP, 6 of them before receiving any iTTP‐specific treatment. Thirty‐one (16.1%) of the 193 treated episodes were refractory to plasma exchange and corticosteroids, and 51 (26.4%) suffered at least one exacerbation. Conclusion: iTTPAbstract: Background: Immune‐mediated thrombotic thrombocytopenic purpura (iTTP) is a rare disease characterized by the presence of anti‐ADAMTS13 autoantibodies. Achieving accurate information on incidence and customary disease management is important to provide appropriate diagnostic and therapeutic resources. The aim of this study was to determine the incidence and outcomes of iTTP in Spain. Study design and methods: A cross‐sectional survey was carried out among Spanish hospitals, focused on iTTP patients ≥16 years old attended between 2015 and 2017, and those at follow‐up before that interval. Incidence, prevalence, mortality, refractoriness, exacerbations, treatment complications, relapses, and sequelae were estimated. Results: Forty‐two hospitals covering roughly 20 million inhabitants answered the survey and reported 203 episodes (138 newly‐diagnosed and 65 relapses), of which 193 (95.1%) were treated. Incidence was 2.67 (95% CI 1.90‐3.45) patients per million inhabitants per year and prevalence 21.44 (95% CI% 19.10‐23.73) patients per million inhabitants. At diagnosis, ADAMTS13 activity and anti‐ADAMTS13 autoantibody were measured in 97% and 84.3% of reported episodes, respectively. Fifteen patients (7.4%) died as a direct consequence of iTTP, 6 of them before receiving any iTTP‐specific treatment. Thirty‐one (16.1%) of the 193 treated episodes were refractory to plasma exchange and corticosteroids, and 51 (26.4%) suffered at least one exacerbation. Conclusion: iTTP incidence and prevalence were somewhat higher than those documented in neighboring countries. Together with data on treatments and outcomes, this information will allow us to better estimate what is needed to improve diagnosis and prognosis of iTTP patients in Spain. … (more)
- Is Part Of:
- Journal of clinical apheresis. Volume 36:Issue 4(2021)
- Journal:
- Journal of clinical apheresis
- Issue:
- Volume 36:Issue 4(2021)
- Issue Display:
- Volume 36, Issue 4 (2021)
- Year:
- 2021
- Volume:
- 36
- Issue:
- 4
- Issue Sort Value:
- 2021-0036-0004-0000
- Page Start:
- 563
- Page End:
- 573
- Publication Date:
- 2021-03-29
- Subjects:
- ADAMTS13 -- immune‐mediated thrombotic thrombocytopenic purpura -- incidence -- Spain -- treatment
Hemapheresis -- Periodicals
Blood -- Transfusion -- Periodicals
Blood -- Transfusion, Autologous -- Periodicals
Cell separation -- Periodicals
Leukapheresis -- Periodicals
Plasmapheresis -- Periodicals
615.39 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1098-1101 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jca.21894 ↗
- Languages:
- English
- ISSNs:
- 0733-2459
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4958.381500
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- 18438.xml