Fluid overload due to intravenous fluid therapy for vaso‐occlusive crisis in sickle cell disease: incidence and risk factors
Author:
Affiliation:
1. Department of Hematology Amsterdam UMCAmsterdamThe Netherlands
2. Department of Pediatric Hematology Emma Children’s Hospital Amsterdam UMC AmsterdamThe Netherlands
3. Department of Internal Medicine Flevo Hospital Almere The Netherlands
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.17696
Reference41 articles.
1. Pathophysiologically based drug treatment of sickle cell disease
2. Mortality In Sickle Cell Disease -- Life Expectancy and Risk Factors for Early Death
3. The painful crisis of homozygous sickle cell disease: clinical features
4. Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease
5. Impact of sickle cell disease on patientsʼ daily lives, symptoms reported, and disease management strategies: Results from the international Sickle Cell World Assessment Survey ( SWAY )
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4. Intravenous fluid therapy and hospital outcomes for vaso‐occlusive episodes in children, adolescents, and young adults with sickle cell disease;Pediatric Blood & Cancer;2023-11-27
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