Sickle Cell Disease in Childhood From Newborn Screening Through Transition to Adult Medical Care

被引：66
|
作者：
Quinn, Charles T. [1 ,2 ]
机构：
[1] Cincinnati Childrens Hosp Med Ctr, Div Hematol, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Dept Pediat, Coll Med, Cincinnati, OH 45229 USA
来源：
PEDIATRIC CLINICS OF NORTH AMERICA | 2013年 / 60卷 / 06期
关键词：
Sickle cell disease; Genetics; Diagnosis; Pathophysiology; Treatment; Survival; ACUTE CHEST SYNDROME; PULMONARY-HYPERTENSION; ADVERSE OUTCOMES; CHILDREN; ANEMIA; STROKE; TRANSFUSIONS; HOSPITALIZATION; DEXAMETHASONE; HYDROXYUREA;
D O I：
10.1016/j.pcl.2013.09.006
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Sickle cell disease (SOD) is the name for a group of related blood disorders caused by an abnormal hemoglobin molecule that polymerizes on deoxygenation. SOD affects the entire body, and the multisystem pathophysiology begins in infancy. Thanks to prognostic and therapeutic advancements, some forms of SOD-related morbidity are decreasing, such as overt stroke. Almost all children born with SOD in developed nations now live to adulthood, and lifelong multidisciplinary care is necessary. This article provides a broad overview of SOD in childhood, from newborn screening through transition to adult medical care.
引用
收藏
页码：1363 / +
页数：20
相关论文
共 50 条
  • [41] Newborn screening for sickle cell disease in a Nigerian hospital
    Odunvbun, M. E.
    Okolo, A. A.
    Rahimy, C. M.
    PUBLIC HEALTH, 2008, 122 (10) : 1111 - 1116
  • [42] Pediatric to Adult Transition in Sickle Cell Disease: Survey Results from Young Adult Patients
    Travis, Kate
    Wood, Anthony
    Yeh, Peter
    Allahabadi, Sachin
    Chien, Ling-Chen
    Curtis, Sara
    Hammond, Allexa
    Kohn, Jaden
    Ogugbuaja, Christine
    Rees, Matthew
    Shumway, John
    Sheehan, Vivien
    ACTA HAEMATOLOGICA, 2020, 143 (02) : 163 - 175
  • [43] Newborn Screening for Sickle Cell Disease: Indian Experience
    Colah, Roshan B.
    Mehta, Pallavi
    Mukherjee, Malay B.
    INTERNATIONAL JOURNAL OF NEONATAL SCREENING, 2018, 4 (04)
  • [44] Identification of Risk Factors for an Unsuccessful Transition from Pediatric to Adult Sickle Cell Disease Care
    Andemariam, Biree
    Owarish-Gross, Jasmine
    Grady, James
    Boruchov, Donna
    Thrall, Roger S.
    Hagstrom, J. Nathan
    PEDIATRIC BLOOD & CANCER, 2014, 61 (04) : 697 - 701
  • [45] Newborn screening for sickle cell disease: 4 years of experience from California's newborn screening program
    Shafer, FE
    Lorey, F
    Cunningham, GC
    Klumpp, C
    Vichinsky, E
    Lubin, B
    JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1996, 18 (01) : 36 - 41
  • [46] Newborn Screening for Sickle Cell Disease in India: The Need for Defining Optimal Clinical Care
    Jyotish Patel
    Graham R. Serjeant
    The Indian Journal of Pediatrics, 2014, 81 : 229 - 230
  • [47] Beyond the transition of adolescents and young adults with sickle cell disease to adult care: Role of geography
    Anderson, Nina
    Eckman, James R.
    Ballas, Samir K.
    AMERICAN JOURNAL OF HEMATOLOGY, 2017, 92 (06) : E110 - E112
  • [48] Perspectives on Building Sustainable Newborn Screening Programs for Sickle Cell Disease: Experience from Tanzania
    Bukini, Daima
    Nkya, Siana
    McCurdy, Sheryl
    Mbekenga, Columba
    Manji, Karim
    Parker, Michael
    Makani, Julie
    INTERNATIONAL JOURNAL OF NEONATAL SCREENING, 2021, 7 (01)
  • [49] Characterization of mortality in children with sickle cell disease diagnosed through the Newborn Screening Program
    Sabarense, Alessandra P.
    Lima, Gabriella O.
    Silva, Livia M. L.
    Viana, Marcos Borato
    JORNAL DE PEDIATRIA, 2015, 91 (03) : 242 - 247
  • [50] Cardiac Manifestations in Adult Sickle Cell Disease Patients at a Tertiary Care Hospital in Chhattisgarh, India
    Shrivastava, Smit
    Chaudhary, Animesh
    Pandey, Prabhat
    JOURNAL OF EVOLUTION OF MEDICAL AND DENTAL SCIENCES-JEMDS, 2021, 10 (21): : 1567 - 1574
12345