4.5 Review

A systematic literature review of frequency of vaso-occlusive crises in sickle cell disease

Related references

Note: Only part of the references are listed.
Article Hematology

Evaluation of Longitudinal Pain Study in Sickle Cell Disease (ELIPSIS) by patient-reported outcomes, actigraphy, and biomarkers

Debra D. Pittman et al.

Summary: The study aims to develop tools to identify VOCs in SCD patients with or without health care utilization by accurately monitoring out-of-hospital pain using patient-reported VOC days as potential end points. The changes in biomarkers and activity measured by actigraphy may enable improved identification and assessment of VOCs.

BLOOD (2021)

Article Multidisciplinary Sciences

Epidemiology and disease burden of sickle cell disease in France: A descriptive study based on a French nationwide claim database

Henri Leleu et al.

Summary: This study estimated the prevalence of SCD in France between 19,800 and 32,400 patients in 2016, higher than previously published data. The study highlights the significant disease burden associated with vaso-occlusive events.

PLOS ONE (2021)

Review Hematology

The vaso-occlusive pain crisis in sickle cell disease: Definition, pathophysiology, and management

Deepika S. Darbari et al.

EUROPEAN JOURNAL OF HAEMATOLOGY (2020)

Article Oncology

Hydroxyurea use in young infants with sickle cell disease

Sarah B. Schuchard et al.

PEDIATRIC BLOOD & CANCER (2019)

Article Multidisciplinary Sciences

Sickle cell disease complications: Prevalence and resource utilization

Nirmish Shah et al.

PLOS ONE (2019)

Meeting Abstract Hematology

Sickle Cell Disease Burden in North Lebanon

Adlette Inati et al.

BLOOD (2019)

Article Psychology, Clinical

Integration of neuropsychology services in a sickle cell clinic and subsequent healthcare use for pain crises

Julie K. Janecek et al.

CLINICAL NEUROPSYCHOLOGIST (2019)

Article Infectious Diseases

Attrition from Care and Clinical Outcomes in a Cohort of Sickle Cell Disease Patients in a Tribal Area of Western India

Kapilkumar Dave et al.

TROPICAL MEDICINE AND INFECTIOUS DISEASE (2019)

Article Biochemistry & Molecular Biology

Gender-Related Differences in Sickle Cell Disease in a Pediatric Cohort: A Single-Center Retrospective Study

Giulia Ceglie et al.

FRONTIERS IN MOLECULAR BIOSCIENCES (2019)

Article Biochemistry & Molecular Biology

The Sub-Phenotypes of Sickle Cell Disease in Kuwait

Adekunle D. Adekile et al.

HEMOGLOBIN (2019)

Article Pediatrics

Clinical and hematological profile in a newborn cohort with hemoglobin SC

Paulo Rezende et al.

JORNAL DE PEDIATRIA (2018)

Article Hematology

Age is a predictor of a small decrease in lung function in children with sickle cell anemia

Shaina M. Willen et al.

AMERICAN JOURNAL OF HEMATOLOGY (2018)

Article Hematology

Aeroallergen sensitization predicts acute chest syndrome in children with sickle cell anaemia

Shaina M. Willen et al.

BRITISH JOURNAL OF HAEMATOLOGY (2018)

Review Medicine, General & Internal

Sickle cell disease

Russell E. Ware et al.

LANCET (2017)

Review Medicine, General & Internal

Sickle Cell Disease

Frederic B. Piel et al.

NEW ENGLAND JOURNAL OF MEDICINE (2017)

Article Multidisciplinary Sciences

Socio-environmental exposures and health outcomes among persons with sickle cell disease

Monika R. Asnani et al.

PLOS ONE (2017)

Article Hematology

Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven-year follow-up study

Charlotte F. J. van Tuijn et al.

AMERICAN JOURNAL OF HEMATOLOGY (2017)

Article Hematology

The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease Patients

Durjoy K. Shome et al.

INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION (2016)

Article Hematology

The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease Patients

Durjoy K. Shome et al.

INDIAN JOURNAL OF HEMATOLOGY AND BLOOD TRANSFUSION (2016)

Article Hematology

Factors predicting future ACS episodes in children with sickle cell anemia

Michael R. DeBaun et al.

AMERICAN JOURNAL OF HEMATOLOGY (2014)

Article Medicine, General & Internal

Priapism in Homozygous Sickle Cell Patients: Important Clinical and Laboratory Associations

Anazoeze Jude Madu et al.

MEDICAL PRINCIPLES AND PRACTICE (2014)

Review Hematology

Management of sickle cell disease from childhood through adulthood

Julie Kanter et al.

BLOOD REVIEWS (2013)

Review Hematology

Interplay between coagulation and vascular inflammation in sickle cell disease

Erica Sparkenbaugh et al.

BRITISH JOURNAL OF HAEMATOLOGY (2013)

Article Oncology

Hydroxyurea treatment of children with hemoglobin SC disease

Amber M. Yates et al.

PEDIATRIC BLOOD & CANCER (2013)

Article Oncology

Sickle Cell Disease Subphenotypes in Patients From Southwestern Province of Saudi Arabia

Abdulrahman Alsultan et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2012)

Article Medicine, General & Internal

Daily assessment of pain in adults with sickle cell disease

Wally R. Smith et al.

ANNALS OF INTERNAL MEDICINE (2008)

Article Multidisciplinary Sciences

DNA polymorphisms at the BCL11A, HBS1L-MYB, and β-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease

Guillaume Lettre et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)

Article Public, Environmental & Occupational Health

Gender differences in pain and healthcare utilization for adult sickle cell patients: The PiSCES project

DK McClish et al.

JOURNAL OF WOMENS HEALTH (2006)

Article Hematology

Foetal haemoglobin in homozygous sickle cell disease: a study of patients with low HBF levels

A Donaldson et al.

CLINICAL AND LABORATORY HAEMATOLOGY (2001)