Evolution of sickle cell disease from a life‐threatening disease of children to a chronic disease of adults: The last 40 years

S Chaturvedi, MR DeBaun - American journal of hematology, 2016 - Wiley Online Library
Over the past 40 years, public health measures such as universal newborn screening,
penicillin prophylaxis, vaccinations, and hydroxyurea therapy have led to an impressive …

Management of sickle cell disease: a review for physician education in Nigeria (sub‐saharan Africa)

AS Adewoyin - Anemia, 2015 - Wiley Online Library
Sickle cell disease (SCD) predominates in sub‐Saharan Africa, East Mediterranean areas,
Middle East, and India. Nigeria, being the most populous black nation in the world, bears its …

Estimating the risk of child mortality attributable to sickle cell anaemia in sub-Saharan Africa: a retrospective, multicentre, case-control study

B Ranque, R Kitenge, DD Ndiaye, MD Ba… - The Lancet …, 2022 - thelancet.com
Background Many children with sickle cell disease living in sub-Saharan Africa die before
reaching age 5 years. We estimate the child mortality associated with sickle cell anaemia …

Mortality by sickle cell disease in Brazil

GAO Arduini, LP Rodrigues… - Revista brasileira de …, 2017 - SciELO Brasil
This work aimed to characterize mortality by sickle cell disease in Brazil. The MEDLINE
electronic database was searched using the terms 'mortality'and 'sickle cell disease'and …

The intersection between asthma and acute chest syndrome in children with sickle-cell anaemia

MR DeBaun, RC Strunk - The Lancet, 2016 - thelancet.com
Acute chest syndrome is a frequent cause of acute lung disease in children with sickle-cell
disease. Asthma is common in children with sickle-cell disease and is associated with …

Clustering of end‐organ disease and earlier mortality in adults with sickle cell disease: A retrospective‐prospective cohort study

S Chaturvedi, DL Ghafuri, N Jordan… - American journal of …, 2018 - Wiley Online Library
Chronic end‐organ complications result in morbidity and mortality in adults with sickle cell
disease (SCD). In a retrospective‐prospective cohort of 150 adults with SCD who received …

Debating the future of sickle cell disease curative therapy: haploidentical hematopoietic stem cell transplantation vs. gene therapy

AA Kassim, A Leonard - Journal of Clinical Medicine, 2022 - mdpi.com
Hematopoietic stem cell transplantation (HSCT) is a well-established curative therapy for
patients with sickle cell disease (SCD) when using a human leukocyte antigen (HLA) …

Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia–lessons learned for prophylaxis

S Alkindi, AR Al-Ghadani… - Journal of …, 2021 - journals.sagepub.com
Objective To assess the clinical and laboratory predictors of venous thromboembolism (VTE)
in patients with sickle cell anaemia (SCA) and its relationship to morbidity and mortality …

Current perspectives of sickle cell disease in Nigeria: changing the narratives

OO Ojewunmi, TA Adeyemo, OC Ayinde… - Expert Review of …, 2019 - Taylor & Francis
Introduction: Sickle cell disease (SCD) is an inherited blood disorder characterized by
clinical heterogeneity that may be influenced by environmental factors, ethnicity, race, social …

[HTML][HTML] Cervical precancer screening with HPV DNA testing and mobile colposcopy in women with sickle cell disease in Accra, Ghana

Y Dei-Adomakoh, K Effah, E Tekpor… - …, 2023 - ncbi.nlm.nih.gov
Background Worldwide, about 20–25 million people are affected by sickle cell disease
(SCD), with 60% of patients living in sub-Saharan Africa. Despite recent therapeutic …