Page last updated: 2024-10-28

hydroxyurea and Cerebrovascular Disorders

hydroxyurea has been researched along with Cerebrovascular Disorders in 9 studies

Cerebrovascular Disorders: A spectrum of pathological conditions of impaired blood flow in the brain. They can involve vessels (ARTERIES or VEINS) in the CEREBRUM, the CEREBELLUM, and the BRAIN STEM. Major categories include INTRACRANIAL ARTERIOVENOUS MALFORMATIONS; BRAIN ISCHEMIA; CEREBRAL HEMORRHAGE; and others.

Research Excerpts

ExcerptRelevanceReference
"Sickle cell disease is a common and life-threatening haematological disorder that affects millions of people worldwide."2.55Sickle cell disease. ( Abboud, MR; de Montalembert, M; Tshilolo, L; Ware, RE, 2017)
"Hydroxyurea has proven efficacy in numerous clinical trials as a disease-modifying treatment for patients with sickle cell anemia (SCA) but is currently under-used in clinical practice."1.42Optimizing hydroxyurea therapy for sickle cell anemia. ( Ware, RE, 2015)
"Stroke is a common cause of morbidity and mortality in sickle cell disease (SCD) and silent cerebral infarction is the most common form of neurologic injury."1.39Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: a single center prospective survey in adult Italians. ( Calvaruso, G; Iannello, S; Maggio, A; Pecoraro, A; Rigano, P; Steinberg, MH, 2013)
"Hydroxyurea can increase fetal hemoglobin (HbF) and improve the clinical course of sickle cell disease (SCD) patients."1.29A cautionary note regarding hydroxyurea in sickle cell disease. ( Lubin, BH; Vichinsky, EP, 1994)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (22.22)18.2507
2000's0 (0.00)29.6817
2010's5 (55.56)24.3611
2020's2 (22.22)2.80

Authors

AuthorsStudies
Bernaudin, F1
Rankine-Mullings, A1
Reid, M1
Soares, D1
Taylor-Bryan, C1
Wisdom-Phipps, M1
Aldred, K1
Latham, T1
Schultz, WH1
Knight-Madden, J1
Badaloo, A1
Lane, A1
Adams, RJ1
Ware, RE4
Ansari, J1
Moufarrej, YE1
Pawlinski, R1
Gavins, FNE1
Rigano, P1
Pecoraro, A1
Calvaruso, G1
Steinberg, MH2
Iannello, S1
Maggio, A1
de Montalembert, M2
Tshilolo, L1
Abboud, MR1
Brousse, V1
Gandhi, S1
Height, S1
Dick, MC1
O'Driscoll, S1
Abihsera, G1
Rees, DC1
Vichinsky, EP1
Lubin, BH1
Kinney, TR1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Pilot Study of the Use of Oral Ketamine for Treatment of Vaso-Occlusive Pain in Adolescents and Young Adults[NCT05378555]Phase 310 participants (Anticipated)Interventional2023-05-01Recruiting
Prospective Clinical Study on Early Inflammatory, Cell Adhesion and Hemostatic Plasmatic Markers of Endothelial Dysfunction in Children With Sickle Cell Disease (SCD)[NCT04839159]41 participants (Anticipated)Interventional2012-05-10Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

3 reviews available for hydroxyurea and Cerebrovascular Disorders

ArticleYear
What is the place of hematopoietic stem cell transplantation in the management of cerebral vasculopathy in children with sickle cell anemia?
    Hematology/oncology and stem cell therapy, 2020, Volume: 13, Issue:3

    Topics: Allografts; Anemia, Sickle Cell; Cerebrovascular Disorders; Child; Hematopoietic Stem Cell Transplan

2020
Sickle cell disease: a malady beyond a hemoglobin defect in cerebrovascular disease.
    Expert review of hematology, 2018, Volume: 11, Issue:1

    Topics: Anemia, Sickle Cell; Antisickling Agents; Cell Communication; Cerebrovascular Disorders; Disease Pro

2018
Sickle cell disease.
    Lancet (London, England), 2017, 07-15, Volume: 390, Issue:10091

    Topics: Anemia, Sickle Cell; Antisickling Agents; Blood Transfusion; Cerebrovascular Disorders; Chronic Dise

2017
Sickle cell disease.
    Lancet (London, England), 2017, 07-15, Volume: 390, Issue:10091

    Topics: Anemia, Sickle Cell; Antisickling Agents; Blood Transfusion; Cerebrovascular Disorders; Chronic Dise

2017
Sickle cell disease.
    Lancet (London, England), 2017, 07-15, Volume: 390, Issue:10091

    Topics: Anemia, Sickle Cell; Antisickling Agents; Blood Transfusion; Cerebrovascular Disorders; Chronic Dise

2017
Sickle cell disease.
    Lancet (London, England), 2017, 07-15, Volume: 390, Issue:10091

    Topics: Anemia, Sickle Cell; Antisickling Agents; Blood Transfusion; Cerebrovascular Disorders; Chronic Dise

2017

Trials

1 trial available for hydroxyurea and Cerebrovascular Disorders

ArticleYear
Hydroxycarbamide treatment reduces transcranial Doppler velocity in the absence of transfusion support in children with sickle cell anaemia, elevated transcranial Doppler velocity, and cerebral vasculopathy: the EXTEND trial.
    British journal of haematology, 2021, Volume: 195, Issue:4

    Topics: Adolescent; Anemia, Sickle Cell; Antisickling Agents; Blood Flow Velocity; Cerebrovascular Circulati

2021

Other Studies

5 other studies available for hydroxyurea and Cerebrovascular Disorders

ArticleYear
Cerebrovascular events in sickle cell-beta thalassemia treated with hydroxyurea: a single center prospective survey in adult Italians.
    American journal of hematology, 2013, Volume: 88, Issue:11

    Topics: Adult; Aged; Anemia, Sickle Cell; Antisickling Agents; beta-Thalassemia; Cerebral Infarction; Cerebr

2013
Optimizing hydroxyurea therapy for sickle cell anemia.
    Hematology. American Society of Hematology. Education Program, 2015, Volume: 2015

    Topics: Anemia, Sickle Cell; Antisickling Agents; Blood Transfusion; Cerebrovascular Disorders; Drug Adminis

2015
Combined blood transfusion and hydroxycarbamide in children with sickle cell anaemia.
    British journal of haematology, 2013, Volume: 160, Issue:2

    Topics: Adolescent; Anemia, Sickle Cell; Blood Transfusion; Brain Ischemia; Cerebral Infarction; Cerebral Re

2013
A cautionary note regarding hydroxyurea in sickle cell disease.
    Blood, 1994, Feb-15, Volume: 83, Issue:4

    Topics: Adult; Anemia, Sickle Cell; Blood Transfusion; Cerebral Hemorrhage; Cerebrovascular Disorders; Femal

1994
Hydroxyurea: an alternative to transfusion therapy for stroke in sickle cell anemia.
    American journal of hematology, 1995, Volume: 50, Issue:2

    Topics: Adult; Anemia, Sickle Cell; Blood Group Incompatibility; Blood Transfusion; Cerebrovascular Disorder

1995