dc.contributor.author |
Carrera, C.
|
|
dc.contributor.author |
Cullell, N.
|
|
dc.contributor.author |
Torres-Águila, N.
|
|
dc.contributor.author |
Muiño, E.
|
|
dc.contributor.author |
Bustamante, A.
|
|
dc.contributor.author |
Dávalos, A.
|
|
dc.contributor.author |
López-Cancio, E.
|
|
dc.contributor.author |
Ribó, M.
|
|
dc.contributor.author |
Molina, C.A.
|
|
dc.contributor.author |
Giralt-Steinhauer, E.
|
|
dc.contributor.author |
Soriano-Tárraga, C.
|
|
dc.contributor.author |
Mola-Caminal, M.
|
|
dc.contributor.author |
Jiménez-Conde, J.
|
|
dc.contributor.author |
Roquer, J.
|
|
dc.contributor.author |
Vives-Bauza, C.
|
|
dc.contributor.author |
Navarro, R.D.
|
|
dc.contributor.author |
Obach, V.
|
|
dc.contributor.author |
Arenillas, J.F.
|
|
dc.contributor.author |
Segura, T.
|
|
dc.contributor.author |
Serrano-Heras, G.
|
|
dc.contributor.author |
Martí-Fàbregas, J.
|
|
dc.contributor.author |
Freijo, M.
|
|
dc.contributor.author |
Cabezas, J.A.
|
|
dc.contributor.author |
Tatlisumak, T.
|
|
dc.contributor.author |
Heitsch, L.
|
|
dc.contributor.author |
Ibañez, L.
|
|
dc.contributor.author |
Cruchaga, C.
|
|
dc.contributor.author |
Lee, J.M.
|
|
dc.contributor.author |
Strbian, D.
|
|
dc.contributor.author |
Montaner, J.
|
|
dc.contributor.author |
Fernández-Cadenas, I.
|
|
dc.date.accessioned |
2020-05-13T05:51:26Z |
|
dc.identifier.uri |
http://hdl.handle.net/11201/152327 |
|
dc.description.abstract |
[eng] OBJECTIVE: To validate the Genot-PA score, a clinical-genetic logistic regression score that stratifies the thrombolytic therapy safety, in a new cohort of patients with stroke. METHODS: We enrolled 1,482 recombinant tissue plasminogen activator (rtPA)-treated patients with stroke in Spain and Finland from 2003 to 2016. Cohorts were analyzed on the basis of ethnicity and therapy: Spanish patients treated with IV rtPA within 4.5 hours of onset (cohort A and B) or rtPA in combination with mechanical thrombectomy within 6 hours of onset (cohort C) and Finnish participants treated with IV rtPA within 4.5 hours of onset (cohort D). The Genot-PA score was calculated, and hemorrhagic transformation (HT) and parenchymal hematoma (PH) risks were determined for each score stratum. RESULTS: Genot-PA score was tested in 1,324 (cohort A, n = 726; B, n = 334; C, n = 54; and D, n = 210) patients who had enough information to complete the score. Of these, 213 (16.1%) participants developed HT and 85 (6.4%) developed PH. In cohorts A, B, and D, HT occurrence was predicted by the score (p = 2.02 × 10-6, p = 0.023, p = 0.033); PH prediction was associated in cohorts A through C (p = 0.012, p = 0.034, p = 5.32 × 10-4). Increased frequency of PH events from the lowest to the highest risk group was found (cohort A 4%-15.7%, cohort B 1.5%-18.2%, cohort C 0%-100%). The best odds ratio for PH prediction in the highest-risk group was obtained in cohort A (odds ratio 5.16, 95% confidence interval 1.46-18.08, p = 0.009). CONCLUSION: The Genot-PA score predicts HT in patients with stroke treated with IV rtPA. Moreover, in an exploratory study, the score was associated with PH risk in mechanical thrombectomy-treated patients. |
|
dc.format |
application/pdf |
|
dc.relation.isformatof |
https://doi.org/10.1212/WNL.0000000000007997 |
|
dc.relation.ispartof |
Neurology, 2019, vol. 93, num. 9, p. e851-e863 |
|
dc.rights |
, 2019 |
|
dc.subject.classification |
57 - Biologia |
|
dc.subject.other |
57 - Biological sciences in general |
|
dc.title |
Validation of a clinical-genetics score to predict hemorrhagic transformations after rtPA |
|
dc.type |
info:eu-repo/semantics/article |
|
dc.date.updated |
2020-05-13T05:51:27Z |
|
dc.embargo |
10000-01-01 |
|
dc.subject.keywords |
stroke |
|
dc.subject.keywords |
clinical practice |
|
dc.subject.keywords |
genetic score |
|
dc.subject.keywords |
tissue plasminogen activator (rTPA) |
|
dc.subject.keywords |
hemorrhagic transformation (HT) |
|
dc.rights.accessRights |
info:eu-repo/semantics/closedAccess |
|
dc.identifier.doi |
https://doi.org/10.1212/WNL.0000000000007997 |
|