Cargando…

Frequency of Painful Crisis and Other Associated Complications of Sickle Cell Anemia Among Children

Background Sickle cell disease (SCD) represents a group of inherited health conditions that affect red blood cells. SCD is a relatively common genetic disorder in Saudi Arabia, with the highest prevalence found in the Eastern Province region. The most common complications of SCD include acute chest...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sendy, Jana S, Alsadun, Mohammed S, Alamer, Sarah S, Alazzam, Shujon M, Alqurashi, Mansour M, Almudaibigh, Adel H
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2023
Materias:	Pediatrics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10691739/ https://www.ncbi.nlm.nih.gov/pubmed/38046719 http://dx.doi.org/10.7759/cureus.48115

Ejemplares similares

Ophthalmic Self-Medication Practices and Associated Factors of Using Steroid Eye Drops Among Adult Ophthalmic Patients
por: Alamer, Sarah S, et al.
Publicado: (2023)

Effect of Weather on Frequency of Vaso-Occlusive Crisis in Children With Sickle Cell Disease
por: Almuqamam, Mohamed, et al.
Publicado: (2021)

Infantile-onset Pompe disease complicated by sickle cell anemia: Case report and management considerations
por: Starosta, Rodrigo Tzovenos, et al.
Publicado: (2022)

Mineral bone disorders and kidney disease in hospitalized children with sickle cell anemia
por: Batte, Anthony, et al.
Publicado: (2023)

Association of laboratory markers and cerebral blood flow among sickle cell anemia children
por: Adanho, Corynne Stéphanie Ahouéfa, et al.
Publicado: (2022)

Blood Transfusion Vs. Hydroxyurea for Stroke Prevention in Children With Sickle Cell Anemia: A Systematic Review and Meta-Analysis
por: Hafiz, Tamara A, et al.
Publicado: (2022)

Septic Arthritis Associated With Hip Joint Subluxation and Epiphyseal Plate Deformation as a Sequala of Sickle Cell Anemia
por: Nathani, Harsh R, et al.
Publicado: (2023)

Impact of Mode of Delivery on the Survival Rate of Very Low Birth Weight Infants: A Single-Center Experience
por: AlQurashi, Mansour A
Publicado: (2020)

Sex and frequency of pain episodes are associated with acute pain trajectories in adolescents with sickle cell disease
por: Astles, Rachel, et al.
Publicado: (2023)

Life-Threatening Infectious Complications in Sickle Cell Disease: A Concise Narrative Review
por: Ochocinski, Dominik, et al.
Publicado: (2020)

Frequency and Risk Factors of Endocrine Complications in Turkish Children and Adolescents with Sickle Cell Anemia
por: Özen, Samim, et al.
Publicado: (2013)

The perception of pediatric sickle cell anemia patient's caregivers toward hematopoietic stem cell transplantation (single-center experience, Saudi Arabia)
por: Monagel, Dania A., et al.
Publicado: (2023)

Early Hyporegenerative Anemia Complicating Hemolytic Disease of the Newborn Secondary to Rhesus Alloimmunization
por: Acosta, Catalina, et al.
Publicado: (2021)

Frequency distribution of sickle cell anemia, sickle cell trait and sickle/beta-thalassemia among anemic patients in Saudi Arabia
por: Elsayid, Mohieldin, et al.
Publicado: (2015)

Splenic Complications of Sickle Cell Anemia and the Role of Splenectomy
por: Al-Salem, Ahmed H.
Publicado: (2011)

Duodenal perforation: an unusual complication of sickle cell anemia
por: Acıpayam, Can, et al.
Publicado: (2014)

A Presumed Sickle Cell Anemia Crisis Revealed To Be Medium Vessel Vasculitis
por: Badeeb, Arwa
Publicado: (2023)

Microcytic Anemia Hiding Vitamin B12 Deficiency Anemia
por: Busaleh, Fadi, et al.
Publicado: (2021)

P105: BLOOD MICROVESICLES AS BIOMARKERS TO PREDICT VASO-OCCLUSIVE CRISIS IN SICKLE CELL ANEMIA
por: Chebbi, M, et al.
Publicado: (2022)

Screening for Neurodevelopmental Delay for Preterm Very Low Birth Weight Infants at Tertiary Care Center in Saudi Arabia
por: Al-Hindi, Mohammed Y, et al.
Publicado: (2021)

Hematopoietic Cell Transplantation for Sickle Cell Disease
por: Krishnamurti, Lakshmanan
Publicado: (2021)

Neurological Complications following Blood Transfusions in Sickle Cell Anemia
por: Alharbi, Hana, et al.
Publicado: (2017)

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

Moyamoya Syndrome in Children With Sickle Cell Disease in Saudi Arabia: A Single-Center Experience
por: Zayed, Abdalla M, et al.
Publicado: (2023)

Frequency of Immediate Neonatal Complications (Hypoglycemia and Neonatal Jaundice) in Late Preterm and Term Neonates
por: Salman, Muhammad, et al.
Publicado: (2021)

Clinical Characteristics of Newborn Infants Delivered to Pregnant Women With Laboratory-Confirmed COVID-19: A Single-Center Experience From Saudi Arabia
por: AlQurashi, Mansour A, et al.
Publicado: (2021)

Rapidly Progressing Autoimmune Hemolytic Anemia in a Pediatric Patient With COVID-19
por: Kononowicz, Julia E, et al.
Publicado: (2023)

Haplotype Map of Sickle Cell Anemia in Tunisia
por: Moumni, Imen, et al.
Publicado: (2014)

Haematological Profile of Children With Sickle Cell Anaemia in Steady State
por: Aliu, Rasaki, et al.
Publicado: (2020)

Role of Steroids in Sickle Cell Patients With Acute Chest Syndrome
por: Jeyamurugan, Kokila, et al.
Publicado: (2022)

Genome editing for sickle cell disease: still time to correct?
por: Ceglie, Giulia, et al.
Publicado: (2023)

Salmonella pyomyositis complicating sickle cell anemia: a case report
por: Wong, Vanessa K, et al.
Publicado: (2010)

Changes in Urine Microalbumin-to-Creatinine Ratio in Children with Sickle Cell Disease over Time
por: Shatat, Ibrahim F., et al.
Publicado: (2016)

Hypertensive Crisis in Pediatric Patients: An Overview
por: Raina, Rupesh, et al.
Publicado: (2020)

Chronic Thromboembolic Pulmonary Hypertension in a Child With Sickle Cell Disease
por: Spencer, Robert, et al.
Publicado: (2020)

An unusual ultrasound appearance of renal hemosiderosis in acute sickle cell nephropathy
por: Kocher, Madison, et al.
Publicado: (2019)

Management of fever and acute painful crises in children with sickle cell disease in emergency departments: a tertiary hospital experience
por: Almahmoud, Tameem, et al.
Publicado: (2023)

Higher hydroxyurea adherence among young adults with sickle cell disease compared to children and adolescents
por: Reddy, Paavani S., et al.
Publicado: (2022)

Pain frequency, severity and QT dispersion in adult patients with sickle cell anemia: correlation with inflammatory markers
por: Garadah, Taysir S, et al.
Publicado: (2016)

Hydroxyurea Use Among Children With Sickle Cell Disease at King Abdulaziz University Hospital in Jeddah City
por: Alzahrani, Fatma, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_j7of4rcqai1linf8058k82em4h