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About 2,958 results

ALLMedicine™ Thrombotic Thrombocytopenic Purpura Center

Research & Reviews  1,001 results

Maternal and fetal outcomes of pregnancy occurring after a diagnosis of immune-mediated...
https://doi.org/10.1007/s00277-022-04936-2
Annals of Hematology; Brown J, Potugari B et. al.

Aug 7th, 2022 - Pregnancy is a well-established trigger for a first episode or relapse of immune thrombotic thrombocytopenic purpura (iTTP). Other outcomes of subsequent pregnancy after a diagnosis of iTTP are less well described. We conducted this retrospective ...

Real-world effectiveness of caplacizumab vs standard of care in immune thrombotic throm...
https://doi.org/10.1182/bloodadvances.2022008028
Blood Advances; Pascual Izquierdo MC, Mingot-Castellano ME et. al.

Aug 6th, 2022 - Immune thrombotic thrombocytopenic purpura (iTTP) is a thrombotic microangiopathy caused by anti-ADAMTS13 antibodies. Caplacizumab is approved for adults with an acute episode of iTTP in conjunction with PEX and immunosuppression. The objective of...

Incidence of thrombotic microangiopathies in Quebec: insight from a laboratory centrali...
https://doi.org/10.1186/s13023-022-02409-3
Orphanet Journal of Rare Diseases; Merlen C, Pépin E et. al.

Aug 5th, 2022 - Thrombotic microangiopathies (TMA) are serious medical conditions requiring a prompt diagnosis to adapt treatment. The determination of ADAMTS-13 activity enables discriminating thrombotic thrombocytopenic purpura (TTP) from other forms of TMA. Th...

Relapse of immune thrombotic thrombocytopenic purpura (iTTP) possibly triggered by COVI...
https://doi.org/10.1136/bcr-2021-247524
BMJ Case Reports; Fang F, Tse B et. al.

Jul 29th, 2022 - Thrombotic thrombocytopenic purpura (TTP) is a life-threatening disease that may be triggered by inflammation, including infection or vaccination. Since the start of the COVID-19 pandemic, several case reports were published on de novo or relapsed...

ADAMTS13 protease or lack of von Willebrand factor protects irradiation and melanoma-in...
https://doi.org/10.1111/jth.15820
Journal of Thrombosis and Haemostasis : JTH; Zheng L, Cao L et. al.

Jul 28th, 2022 - Severe deficiency of plasma ADAMTS13 activity may result in potentially fatal thrombotic thrombocytopenic purpura (TTP) and relative deficiency of plasma ADAMTS13 activity may be associated with adverse outcomes of certain malignancies. Here, we r...

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Guidelines  1 results

Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and o...
https://doi.org/10.1111/j.1365-2141.2012.09167.x
British Journal of Haematology; Scully M, Hunt BJ et. al.

May 26th, 2012 - Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies.|2012|Scully M,Hunt BJ,Benjamin S,Liesner R,Rose P,|diagnosis,pathology,therapy,diagnosis,pathology,therapy,

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Drugs  45 results see all →

Clinicaltrials.gov  41 results

Caplacizumab and Immunosuppressive Therapy Without Firstline Therapeutic Plasma Exchange in Adults With Immune-mediated Thrombotic Thrombocytopenic Purpura
https://clinicaltrials.gov/ct2/show/NCT05468320

Jul 21st, 2022 - The anticipated study duration per participant with the presenting episode therefore is a maximum of about 24 weeks (ie, 1 day of screening + maximum 12 weeks of treatment for the presenting episode + 12 weeks of follow-up).

A Prospective Study on the Long-Term Vascular Burden in Thrombotic Thrombocytopenic Purpura Patients
https://clinicaltrials.gov/ct2/show/NCT03187652

Jul 7th, 2022 - The investigators will conduct a prospective cohort study at the London Health Sciences Centre, Ontario, Canada. The investigators will identify 15-30 idiopathic thrombotic thrombocytopenic purpura and atypical hemolytic uremic syndrome patients w...

Clinical Characteristics and Outcomes of SLE Patients Admitted to Critical Care Unit
https://clinicaltrials.gov/ct2/show/NCT05418855

Jun 14th, 2022 - Systemic lupus erythematosus (SLE) is a systemic heterogeneous autoimmune disease with a highly variable course and prognosis that many different organs may be affected . It has wide spectrum of clinical presentation that affects all ages and ethn...

Improvement of Immunologic and Molecular Techniques for the Diagnosis and Follow-up of Patients With Thrombotic Thrombocytopenic Purpura
https://clinicaltrials.gov/ct2/show/NCT05046717

May 27th, 2022 - The lack of ADAMTS13 is the only biological marker that is specific for aTTP diagnosis8 and the assessment of ADAMTS13 is of clinical importance because it is essential for the rapid differential diagnosis between aTTP and other TMA. Furthermore, ...

.German TTP-Registry (Thrombotic Thrombocytopenic Purpura)
https://clinicaltrials.gov/ct2/show/NCT05389007

May 24th, 2022 - 1.) Identification of predictive markers for morbidity and mortality in acute TTP and in TTP relapses using a prospective long-term registry and 2.) Investigation of the pathophysiological processes in acute bouts and in remission by recording the...

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News  94 results

Spreading Newfound Treatment Strategies in Hematologic Malignancies in Seattle
https://www.onclive.com/view/spreading-newfound-treatment-strategies-in-hematologic-malignancies-in-seattle

Oct 6th, 2021 - We recently traveled to Seattle, California for an OncLive® State of the Science Summit™ on Hematologic Malignancies. At the meeting, faculty from Seattle Cancer Care Alliance provided insight on current and evolving standards of care in leukemia,...

Double Hit: Epstein-Barr Virus Causing Infectious Mononucleosis Followed by Hemolytic Uremic Syndrome
https://www.mdedge.com/fedprac/avaho/article/245913/infectious-diseases/double-hit-epstein-barr-virus-causing-infectious
Oday Elmanaseer, MD (elmanao@amc.edu), Alzira Avelino, MD et. al.

Sep 9th, 2021 - Introduction Epstein-Barr virus (EBV) is a herpes virus that commonly causes infectious mononucleosis (IM) and linked to different hematological conditions. Here we present a case of EBV-triggered Hemolytic Uremic Syndrome (HUS) with pulmonary inv.

Transplant-Associated Thrombotic Microangiopathy: New Insights, Emerging Treatments
https://www.onclive.com/view/transplant-associated-thrombotic-microangiopathy-new-insights-emerging-treatments

Jul 22nd, 2021 - Transplant-associated thrombotic microangiopathy (TA-TMA) is a complication of stem cell transplants that can occur with peripherally mobilized stem cells or bone marrow-derived stem cells. TA-TMA remains a difficult complication to address, with ...

Challenges of Accurate Diagnosis of TA-TMA After Hematopoietic Stem Cell Transplant
https://www.onclive.com/view/challenges-of-accurate-diagnosis-of-ta-tma-after-hematopoietic-stem-cell-transplant

Apr 8th, 2021 - Samer Khaled, MD: That is a good segue to our next segment about the challenges of a prompt and accurate diagnosis of TA-TMA [transplant-associated thrombotic microangiopathy]. One of the challenges is to identify TA-TMA early in the course of the...

Real-world outcomes of caplacizumab for iTTP comparable to clinical trial results
https://www.mdedge.com/hematology-oncology/article/238288/bleeding-disorders/real-world-outcomes-caplacizumab-ittp
Mark S. Lesney, PhD

Apr 7th, 2021 - Real-world data for caplacizumab outcomes matched those seen in randomized controlled trials (RCTs) for the treatment of immune-mediated thrombotic thrombocytopenic purpura (iTTP), according to the results of a retrospective study. Data collected.

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Patient Education  1 results see all →