Pain Experience, Physical Function, Pain Coping, and Catastrophizing in Children With Sickle Cell Disease Who Had Normal and Abnormal Sensory Patterns

Author:

Hyacinth Octavia,Machado Silva-Rodrigues Fernanda,Darezzo Rodrigues Nunes Michelle,Carlos Lopes Luís,Fernandes Ananda,Castanheira Nascimento Lucila,Jacob Eufemia

Funder

UCLA Council of Research

UCLA Ralph Research Bunche Center

UCLA School of Nursing

National Institutes of Health

National Heart, Lung, and Blood Institute

Publisher

Elsevier BV

Subject

Anesthesiology and Pain Medicine,Clinical Neurology,General Nursing

Reference94 articles.

1. Sickle cell disease;Ware;Lancet,2017

2. Sickle cell disease;Kato;Nat Rev Dis Primers,2018

3. Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions;Piel;PLoS Med,2013

4. Estimated life expectancy and income of patients with sickle cell disease compared with those without sickle cell disease;Lubeck;JAMA,2019

5. Depression, anxiety, and quality of life in children and adolescents with sickle cell disease;Graves;Pediatr Nurs,2016

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