Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment

scientific article

Survival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/PBC.25608
P698PubMed publication ID26173735

P50authorPhu-Quoc LêQ80465514
Laurence RozenQ82340353
P2093author name stringAlina Ferster
Catherine Heijmans
Christine Devalck
Laurence Dedeken
Sophie Huybrechts
Fleur Samantha Benghiat
Sophie Dupont
Béatrice Gulbis
Marie-Françoise Dresse
André Efira
Anna Vanderfaeillie
P2860cites workAcute clinical events in 299 homozygous sickle cell patients living in France. French Study Group on Sickle Cell DiseaseQ46846124
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonographyQ47906551
Matched-related donor transplantation for sickle cell disease: report from the Center for International Blood and Transplant Research.Q50697314
The effect of hydroxcarbamide therapy on survival of children with sickle cell disease.Q51065755
Trends in pediatric sickle cell disease-related mortality in the United States, 1983-2002.Q51946241
Bone marrow transplantation for sickle cell disease.Q54087053
Mortality in sickle cell disease. Life expectancy and risk factors for early death.Q55065788
Effectiveness of the 7-valent pneumococcal conjugate vaccine in children with sickle cell disease in the first decade of lifeQ57219845
Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East LondonQ58320124
Long-term results of related myeloablative stem-cell transplantation to cure sickle cell diseaseQ58416036
Management of sickle cell disease: summary of the 2014 evidence-based report by expert panel membersQ30459060
Pulmonary complications of sickle cell diseaseQ30515769
Hydroxyurea for sickle cell disease: a systematic review for efficacy and toxicity in childrenQ33382232
Risk factors for death in 632 patients with sickle cell disease in the United States and United KingdomQ33837174
Improved survival of children and adolescents with sickle cell diseaseQ33839801
How I use hydroxyurea to treat young patients with sickle cell anemiaQ33985120
Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatmentQ34187983
Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. Investigators of the Multicenter Study of Hydroxyurea in Sickle Cell AnemiaQ34308407
Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG).Q35097294
Survival of children with sickle cell diseaseQ35690101
Impact of hydroxyurea on clinical events in the BABY HUG trialQ36425423
Outcome of sickle cell anemia: a 4-decade observational study of 1056 patientsQ38471171
Sickle cell disease related mortality in the United States (1999-2009).Q42264563
The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS).Q43244775
An estimation of the incidence and demographic picture of the major hemoglobinopathies in Belgium (from a confidential inquiry).Q43916889
Impact of early transcranial Doppler screening and intensive therapy on cerebral vasculopathy outcome in a newborn sickle cell anemia cohortQ44448652
Hydroxyurea for sickle cell disease in children and for prevention of cerebrovascular events: the Belgian experience.Q45190220
P433issue11
P921main subjectBelgiumQ31
sickle-cell diseaseQ185034
hydroxycarbamideQ212272
P304page(s)1956-1961
P577publication date2015-07-14
P1433published inPediatric Blood & CancerQ15754342
P1476titleSurvival among children and adults with sickle cell disease in Belgium: Benefit from hydroxyurea treatment
P478volume62

Reverse relations

cites work (P2860)
Q280869792015 Clinical trials update in sickle cell anemia
Q39269713A reappraisal of the mechanisms underlying the cardiac complications of sickle cell anemia
Q28828635Cellular normoxic biophysical markers of hydroxyurea treatment in sickle cell disease
Q38898163Cellular therapy for sickle cell disease
Q38619234Clinical risks and healthcare utilization of haematopoietic cell transplantation for sickle cell disease in the U.S. using merged databases
Q89776833Cyclophosphamide improves engraftment in patients with SCD and severe organ damage who undergo haploidentical PBSCT
Q40460121Daily pain in adults with sickle cell disease-a different perspective.
Q90365516Decreased median survival of adults with sickle cell disease after adjusting for left truncation bias: a pooled analysis
Q33427950Effects of hydroxyurea treatment for patients with hemoglobin SC disease
Q50148088Evaluation of newborn sickle cell screening programme in England: 2010-2016.
Q38627797Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years
Q38851953Haematopoietic stem cell transplantation for sickle cell disease - current practice and new approaches
Q54735877Hydroxycarbamide adherence and cumulative dose associated with hospital readmission in sickle cell disease: a 6-year population-based cohort study.
Q39268375Hydroxyurea effectiveness in children and adolescents with sickle cell anemia: A large retrospective, population-based cohort
Q61908540Hydroxyurea for Children with Sickle Cell Anemia in Sub-Saharan Africa
Q46853675Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey.
Q38586282Hydroxyurea therapy for sickle cell anemia
Q39312525Implementation of multidisciplinary care reduces maternal mortality in women with sickle cell disease living in low-resource setting
Q40721306Improvement of medical care in a cohort of newborns with sickle-cell disease in North Paris: impact of national guidelines
Q26779359Indications and Results of HLA-Identical Sibling Hematopoietic Cell Transplantation for Sickle Cell Disease
Q48224577Lifespan care in SCD: Whom to transition, the patients or the health care system?
Q36913577Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognostication
Q37107206Minireview: Prognostic factors and the response to hydroxurea treatment in sickle cell disease
Q52666110Mortality in children, adolescents and adults with sickle cell anemia in Rio de Janeiro, Brazil.
Q38800491National registry of hemoglobinopathies in Spain (REPHem).
Q38689667Neonatal screening improves sickle cell disease clinical outcome in Belgium
Q38674500Patient Perspectives on Gene Transfer Therapy for Sickle Cell Disease.
Q56977890Point-of-Care Screening for Sickle-Cell Disease in Low-Resource Settings: a Multi-Center Evaluation of HemoTypeSC, a Novel Rapid Test
Q89777671Primum non nocere: the case against transplant for children with sickle cell anemia without progressive end-organ disease
Q48021426Realizing effectiveness across continents with hydroxyurea: Enrollment and baseline characteristics of the multicenter REACH study in Sub-Saharan Africa
Q90598059Sickle Cell Disease: Advances in Treatment
Q37585014Sickle cell anemia in sub-Saharan Africa: advancing the clinical paradigm through partnerships and research.
Q52795486Sickle cell disease.
Q48174073Sickle cell disease: a malady beyond a hemoglobin defect in cerebrovascular disease
Q37258852Study protocol for a randomized controlled trial to assess the feasibility of an open label intervention to improve hydroxyurea adherence in youth with sickle cell disease
Q91716403Targeted Hydroxyurea Education after an Emergency Department Visit Increases Hydroxyurea Use in Children with Sickle Cell Anemia
Q44223235Therapeutic advances in sickle cell disease in the last decade
Q30376725Time to Invest in Sickle Cell Anemia as a Global Health Priority.
Q37442387Translating sickle cell guidelines into practice for primary care providers with Project ECHO.
Q46235550Validity of simple clinical and biological parameters as screening tool for sickle cell anemia for referral to tertiary center in highly resource constraints.

Search more.