Literature DB >> 11875155

Health supervision for children with sickle cell disease.

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Abstract

Sickle cell disease (SCD) is a group of complex genetic disorders with multisystem manifestations. This statement provides pediatricians in primary care and subspecialty practice with an overview of the genetics, diagnosis, clinical manifestations, and treatment of SCD. Specialized comprehensive medical care decreases morbidity and mortality during childhood. The provision of comprehensive care is a time-intensive endeavor that includes ongoing patient and family education, periodic comprehensive evaluations and other disease-specific health maintenance services, psychosocial care, and genetic counseling. Timely and appropriate treatment of acute illness is critical, because life-threatening complications develop rapidly. It is essential that every child with SCD receive comprehensive care that is coordinated through a medical home with appropriate expertise.

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Year:  2002        PMID: 11875155     DOI: 10.1542/peds.109.3.526

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  46 in total

Review 1.  Managing sickle cell disease.

Authors:  Susan Claster; Elliott P Vichinsky
Journal:  BMJ       Date:  2003-11-15

2.  Meningeal signs and facial edema in a child with sickle cell disease.

Authors:  Marie Gauthier; Rochelle Winikoff
Journal:  CMAJ       Date:  2010-05-10       Impact factor: 8.262

3.  Prognostic significance of early vaso-occlusive complications in children with sickle cell anemia.

Authors:  Charles T Quinn; Elizabeth P Shull; Naveed Ahmad; Nancy J Lee; Zora R Rogers; George R Buchanan
Journal:  Blood       Date:  2006-08-29       Impact factor: 22.113

Review 4.  Sickle cell diseases: current therapeutic options and potential pitfalls in preventive therapy for transcranial Doppler abnormalities.

Authors:  Sharada A Sarnaik
Journal:  Pediatr Radiol       Date:  2005-02-10

Review 5.  New Ways to Detect Pediatric Sickle Cell Retinopathy: A Comprehensive Review.

Authors:  Daniel A Pahl; Nancy S Green; Monica Bhatia; Royce W S Chen
Journal:  J Pediatr Hematol Oncol       Date:  2017-11       Impact factor: 1.289

6.  Association between Hospital Volume and Within-Hospital Intensive Care Unit Transfer for Sickle Cell Disease in Children's Hospitals.

Authors:  Jean L Raphael; Troy Richardson; Matt Hall; Suzette O Oyeku; David G Bundy; Ram V Kalpatthi; Samir S Shah; Angela M Ellison
Journal:  J Pediatr       Date:  2015-10-23       Impact factor: 4.406

7.  Health-related quality of life in children and adolescents with sickle cell disease.

Authors:  Juanita Conkin Dale; Cindy J Cochran; Lonnie Roy; Ethel Jernigan; George R Buchanan
Journal:  J Pediatr Health Care       Date:  2010-04-02       Impact factor: 1.812

8.  Methodological quality of national guidelines for pediatric inpatient conditions.

Authors:  Gabrielle Hester; Katherine Nelson; Sanjay Mahant; Emily Eresuma; Ron Keren; Rajendu Srivastava
Journal:  J Hosp Med       Date:  2014-03-28       Impact factor: 2.960

9.  Optical Coherence Tomography Angiography and Ultra-widefield Fluorescein Angiography for Early Detection of Adolescent Sickle Retinopathy.

Authors:  Daniel A Pahl; Nancy S Green; Monica Bhatia; Margaret T Lee; Jonathan S Chang; Maureen Licursi; Courtney Briamonte; Elana Smilow; Royce W S Chen
Journal:  Am J Ophthalmol       Date:  2017-08-30       Impact factor: 5.258

10.  Preventive Care Delivery to Young Children With Sickle Cell Disease.

Authors:  David G Bundy; John Muschelli; Gwendolyn D Clemens; John J Strouse; Richard E Thompson; James F Casella; Marlene R Miller
Journal:  J Pediatr Hematol Oncol       Date:  2016-05       Impact factor: 1.289

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