Cargando…

Self-Report for Assessment of Pain and Quality of Life in Children with Sickle Cell Anemia in a Developing Country

PURPOSE: The specific assessment of pain and quality of life in children with sickle cell anemia (SCA) is still the subject of few studies and is traditionally evaluated through perception of their parents or guardians. Thus, this study aimed to evaluate pain, its characteristics, and impact on the...

Descripción completa

Detalles Bibliográficos
Autores principales:	Brito da Cunha, Valeska, Freitas de Andrade Rodrigues, Camila, Alves Rodrigues, Thiago, Silva Gomes de Oliveira, Eduardo José, Santos Garcia, João Batista
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove 2020
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727276/ https://www.ncbi.nlm.nih.gov/pubmed/33311996 http://dx.doi.org/10.2147/JPR.S261605

Ejemplares similares

Prejudice impairing quality of life in sickle cell disease patients in a developing country: faces of suffering
por: Rodrigues, Camila Freitas de Andrade, et al.
Publicado: (2023)

Food Consumption of People with Sickle Cell Anemia in a Middle-Income Country
por: Teixeira, Tamara Vilhena, et al.
Publicado: (2023)

Sexuality and sickle cell anemia
por: Côbo, Viviane de Almeida, et al.
Publicado: (2013)

Levels of inflammatory markers are differentially expressed in sickle cell anemia and sickle cell trait
por: Gomes, Ingrid Cristiane Pereira, et al.
Publicado: (2023)

Craniofacial geometric morphometrics in the identification of patients with sickle cell anemia and sickle cell trait
por: Ferreira, Warli de Brito, et al.
Publicado: (2020)

Is There a Difference in Fear-Avoidance, Beliefs, Anxiety and Depression Between Post-Surgery and Non-Surgical Persistent Spinal Pain Syndrome Patients?
por: Alves Rodrigues, Thiago, et al.
Publicado: (2022)

Left ventricular hypertrophy in children, adolescents and young adults with sickle cell anemia
por: Faro, Gustavo Baptista de Almeida, et al.
Publicado: (2015)

Clinical and laboratory profile of patients with sickle cell anemia
por: Sant’Ana, Phelipe Gabriel dos Santos, et al.
Publicado: (2017)

The role of academic leagues as a strategy for pain education in Brazil
por: Garcia, João Batista Santos, et al.
Publicado: (2019)

Induced Pluripotent Stem Cell for the Study and Treatment of Sickle Cell Anemia
por: Junqueira Reis, Luiza Cunha, et al.
Publicado: (2017)

Serum Hepcidin Concentration in Individuals with Sickle Cell Anemia: Basis for the Dietary Recommendation of Iron
por: Omena, Juliana, et al.
Publicado: (2018)

The influence of hydroxyurea on oxidative stress in sickle cell anemia
por: Torres, Lidiane de Souza, et al.
Publicado: (2012)

Genotypic Diversity among Angolan Children with Sickle Cell Anemia
por: Delgadinho, Mariana, et al.
Publicado: (2021)

Mortality in children, adolescents and adults with sickle cell anemia in Rio de Janeiro, Brazil
por: Lobo, Clarisse Lopes de Castro, et al.
Publicado: (2018)

Sociodemographic aspects and quality of life of patients with sickle cell anemia
por: dos Santos, Juliana Pereira, et al.
Publicado: (2013)

Immunological Hallmarks of Inflammatory Status in Vaso-Occlusive Crisis of Sickle Cell Anemia Patients
por: Silva-Junior, Alexander Leonardo, et al.
Publicado: (2021)

Genetic and biochemical markers of hydroxyurea therapeutic response in sickle cell anemia
por: Silva, Danilo Grunig Humberto, et al.
Publicado: (2013)

Physical exercise in sickle cell anemia: a systematic review
por: Pinto, Dayse Mota Rosa, et al.
Publicado: (2021)

Doppler velocimetry of the orbital arteries in patients with sickle cell anemia: relationship with biomarkers of hemolysis
por: Ferrão, Thiago de Oliveira, et al.
Publicado: (2017)

Transcranial doppler as screening method for sickling crises in children with sickle cell anemia: a latin America cohort study
por: Modolo, Gabriel Pinheiro, et al.
Publicado: (2022)

Transient red cell aplasia in two brothers with sickle cell anemia and erythrovirus B19 infection
por: Furtado, Marina dos Santos Brito Silva, et al.
Publicado: (2016)

Sickle cell anemia: hierarchical cluster analysis and clinical profile in a cohort in Brazil
por: Dutra, Valéria de Freitas, et al.
Publicado: (2023)

Association between inflammatory molecules, nitric oxide metabolites and leg ulcers in individuals with sickle cell anemia
por: Belisário, André Rolim, et al.
Publicado: (2022)

Pain measurement as part of primary healthcare of adult patients with sickle cell disease
por: Signorelli, Andreza Aparecida Felix, et al.
Publicado: (2013)

Comparative Analysis of Pain Behaviours in Humanized Mouse Models of Sickle Cell Anemia
por: Lei, Jianxun, et al.
Publicado: (2016)

How Hydroxyurea Alters the Gut Microbiome: A Longitudinal Study Involving Angolan Children with Sickle Cell Anemia
por: Delgadinho, Mariana, et al.
Publicado: (2022)

Use of an automated pyrosequencing technique for confirmation of sickle cell disease
por: de Martino, Camila Cruz, et al.
Publicado: (2019)

Oxidative status in sickle cell anemia
por: Magalhães, Silvia Maria Meira
Publicado: (2011)

Hepatobiliary Manifestations of Sickle Cell Anemia
por: Issa, Hussain, et al.
Publicado: (2010)

Sickle Cell Anemia and Babesia Infection
por: Beri, Divya, et al.
Publicado: (2021)

Precursors of Executive Function in Infants With Sickle Cell Anemia
por: Hogan, Alexandra M., et al.
Publicado: (2013)

Impact of iron overload on interleukin-10 levels, biochemical parameters and oxidative stress in patients with sickle cell anemia
por: Barbosa, Maritza Cavalcante, et al.
Publicado: (2013)

Risk factors in underweight older children with sickle cell anemia: a comparison of low- to high-income countries
por: Klein, Lauren Jane, et al.
Publicado: (2023)

Haptoglobin: an emerging candidate for phenotypic modulation of sickle cell anemia?()
por: Santos, Magnun Nueldo Nunes dos
Publicado: (2015)

Endothelial Activation by Platelets from Sickle Cell Anemia Patients
por: Proença-Ferreira, Renata, et al.
Publicado: (2014)

Sickle Cell anemia and hearing loss among children and youngsters: literature review
por: da Silva, Luzia Poliana Anjos, et al.
Publicado: (2015)

Sickle-cell Anemia and Latent Diastolic Dysfunction: Echocardiographic Alterations
por: Fattori, André, et al.
Publicado: (2015)

Aplastic anemia associated to systemic lupus erythematosus in an AIDS patient: a case report
por: de Oliveira, Leonardo Rodrigues, et al.
Publicado: (2013)

Frequency of Painful Crisis and Other Associated Complications of Sickle Cell Anemia Among Children
por: Sendy, Jana S, et al.
Publicado: (2023)

Mortality by sickle cell disease in Brazil
por: Arduini, Giovanna Abadia Oliveira, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_kbq8kogkafkrmot47sb4eg2t34