FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2598532529> ?p ?o ?g. }

• W2598532529 endingPage "3731" @default.
• W2598532529 startingPage "3731" @default.
• W2598532529 abstract "Abstract Introduction: thrombotic thrombocytopenic purpura (TTP) is a rare, life-threatening thrombotic microangiopathy, with a reported incidence of 2-6 cases/million/year and a 10-20% mortality. TTP is associated with the severe deficiency of the von Willebrand factor cleaving protease, ADAMTS13, due to congenital defects in the ADAMTS13 gene (congenital TTP) or to the development of autoantibodies against ADAMTS13. The Milan TTP Registry is a digital database developed and curated at the Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico (Milan, Italy), including demographic, clinical and laboratory data of patients with a confirmed diagnosis of congenital or acquired thrombotic thrombocytopenic purpura (TTP). Aims: to report the natural history of patients affected with acquired TTP enrolled in the Milan TTP Registry, including demographic, clinical and laboratory data. Methods: acquired TTP patients enrolled in the Milan TTP Registry for an acute episode of TTP occurred between January 2002 and November 2015, and followed until May 2016, were included in this study. Acquired TTP was defined as the occurrence of thrombocytopenia and microangiopathic hemolytic anemia, in the absence of alternative causes. Patients with acquired TTP secondary to cancer and bone-marrow transplant were excluded from this analysis. Demographic and disease-related information were collected by a standardized clinical questionnaire. ADAMTS13-related measurements were performed in a centralized laboratory in Milan. Remission of an acute TTP episode was defined as two days after normalization of the platelet count (≥150 x 109/l). Results: 416 patients with a confirmed diagnosis of acquired TTP were included in the Milan TTP Registry, for a total of 837 acute events. Demographic, clinical and laboratory data are reported in Tables 1 and 2. The majority of patients were female (77%), of white ethnicity (98%) and Italian origin (82%). The median age at the first TTP episode was 40 years (interquartile range [IQR] 30-52). A history of other autoimmune diseases, cancer (non-active at the time of the TTP event), HIV infection and other diseases such as stroke, acute myocardial infarction and hypertension was reported in 34% of the patients. Among potential triggers of acute episodes (defined as occurring within three months before onset), infections were the most prevalent (22% of all patients), followed by the assumption of estroprogestinic drugs (5%). At TTP episode onset, systemic, bleeding and neurological signs and symptoms were present in 70%, 68% and 44% of acute events, respectively, whereas a lower prevalence of renal (19%) and cardiovascular (10%) signs and symptoms was observed. Clinical characteristics and hematologic laboratory parameters were less severe in relapsing episodes compared with first episodes (Table 2). Almost all acute events were treated by plasma exchange procedures and steroids. Rituximab therapy was administered in 12% of acute TTP episodes. In 197 acute TTP episodes with available ADAMTS13-related measurements at baseline, ADAMTS13 activity was severely reduced (<10%) in 85%, moderately reduced (10% to lower limit of normal range) in 12% and normal in 3% of events, respectively. Anti-ADAMTS13 antibodies were positive in 93% of acute TTP. The TTP-related mortality in our population of acquired TTP patients was 5%. In survivors, the median time to remission was 13 days (IQR 7-24, n=313), shorter for relapses than first events (median difference 8 days, 95% confidence interval 5-11). In 348 patients who survived the first TTP episode and had a follow-up period of at least 6 months, 178 (51%) experienced only one episode of acquired TTP, whereas 170 (49%) developed a recurrent form of the disease. This results might be overestimated due to the tertiary nature of our center. Conclusions: acquired TTP is a rare, potentially fatal disease, which may require a long hospitalization and presents in a recurrent form in nearly half of the patients. Digital registries, such as the Milan TTP Registry, represent a powerful and necessary tool to systematically collect epidemiologic, clinical and laboratory data which may ultimately improve our understanding and management of acquired TTP. Our registry, in collaboration with those of other international centers, might answer the most relevant questions in this field. Disclosures Peyvandi: Novo Nordisk: Other: research funding paid to Luigi Villa Foundation, Research Funding, Speakers Bureau; CSL Behring: Speakers Bureau; SOBI: Speakers Bureau; Biotest: Other: research funding paid to Luigi Villa Foundation, Research Funding, Speakers Bureau; Ablynx: Membership on an entity's Board of Directors or advisory committees, Other: research funding paid to Luigi Villa Foundation, Research Funding; Octapharma: Consultancy; Alexion: Other: research funding paid to Luigi Villa Foundation, Research Funding; Bayer: Speakers Bureau; Grifols: Speakers Bureau; LFB: Consultancy; Kedrion Biopharma: Consultancy, Other: research funding paid to Luigi Villa Foundation, Research Funding." @default.
• W2598532529 created "2017-04-07" @default.
• W2598532529 creator A5024573108 @default.
• W2598532529 creator A5034493215 @default.
• W2598532529 creator A5042034318 @default.
• W2598532529 creator A5047898833 @default.
• W2598532529 creator A5051527815 @default.
• W2598532529 creator A5057745623 @default.
• W2598532529 creator A5061651325 @default.
• W2598532529 creator A5065562432 @default.
• W2598532529 creator A5086300600 @default.
• W2598532529 date "2016-12-02" @default.
• W2598532529 modified "2023-10-17" @default.
• W2598532529 title "Natural History of Patients Affected with Thrombotic Thrombocytopenic Purpura: Milan TTP Registry" @default.
• W2598532529 doi "https://doi.org/10.1182/blood.v128.22.3731.3731" @default.
• W2598532529 hasPublicationYear "2016" @default.
• W2598532529 type Work @default.
• W2598532529 sameAs 2598532529 @default.
• W2598532529 citedByCount "0" @default.
• W2598532529 crossrefType "journal-article" @default.
• W2598532529 hasAuthorship W2598532529A5024573108 @default.
• W2598532529 hasAuthorship W2598532529A5034493215 @default.
• W2598532529 hasAuthorship W2598532529A5042034318 @default.
• W2598532529 hasAuthorship W2598532529A5047898833 @default.
• W2598532529 hasAuthorship W2598532529A5051527815 @default.
• W2598532529 hasAuthorship W2598532529A5057745623 @default.
• W2598532529 hasAuthorship W2598532529A5061651325 @default.
• W2598532529 hasAuthorship W2598532529A5065562432 @default.
• W2598532529 hasAuthorship W2598532529A5086300600 @default.
• W2598532529 hasConcept C126322002 @default.
• W2598532529 hasConcept C187212893 @default.
• W2598532529 hasConcept C2777878052 @default.
• W2598532529 hasConcept C2778585876 @default.
• W2598532529 hasConcept C2779134260 @default.
• W2598532529 hasConcept C2779338263 @default.
• W2598532529 hasConcept C2780653079 @default.
• W2598532529 hasConcept C2780921031 @default.
• W2598532529 hasConcept C2781127562 @default.
• W2598532529 hasConcept C71924100 @default.
• W2598532529 hasConcept C89560881 @default.
• W2598532529 hasConceptScore W2598532529C126322002 @default.
• W2598532529 hasConceptScore W2598532529C187212893 @default.
• W2598532529 hasConceptScore W2598532529C2777878052 @default.
• W2598532529 hasConceptScore W2598532529C2778585876 @default.
• W2598532529 hasConceptScore W2598532529C2779134260 @default.
• W2598532529 hasConceptScore W2598532529C2779338263 @default.
• W2598532529 hasConceptScore W2598532529C2780653079 @default.
• W2598532529 hasConceptScore W2598532529C2780921031 @default.
• W2598532529 hasConceptScore W2598532529C2781127562 @default.
• W2598532529 hasConceptScore W2598532529C71924100 @default.
• W2598532529 hasConceptScore W2598532529C89560881 @default.
• W2598532529 hasIssue "22" @default.
• W2598532529 hasLocation W25985325291 @default.
• W2598532529 hasOpenAccess W2598532529 @default.
• W2598532529 hasPrimaryLocation W25985325291 @default.
• W2598532529 hasRelatedWork W17016037 @default.
• W2598532529 hasRelatedWork W2022810605 @default.
• W2598532529 hasRelatedWork W2124400226 @default.
• W2598532529 hasRelatedWork W2292506600 @default.
• W2598532529 hasRelatedWork W2619798956 @default.
• W2598532529 hasRelatedWork W2808596725 @default.
• W2598532529 hasRelatedWork W2946198964 @default.
• W2598532529 hasRelatedWork W3045579636 @default.
• W2598532529 hasRelatedWork W3104949179 @default.
• W2598532529 hasRelatedWork W4285801222 @default.
• W2598532529 hasVolume "128" @default.
• W2598532529 isParatext "false" @default.
• W2598532529 isRetracted "false" @default.
• W2598532529 magId "2598532529" @default.
• W2598532529 workType "article" @default.