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Literature DB >> 18262856

Is newborn screening for cystic fibrosis a basic human right?

Abstract

Because it is clearly in the best interests of children with cystic fibrosis to be diagnosed early at <2 months, which can only be achieved routinely by newborn screening, it can be argued that this should be a human right. However, if more harm than good is likely, or if regional "readiness" does not exist, newborn screening should be deferred.

Entities: Disease Species

Mesh：

Year: 2008 PMID： 18262856 PMCID： PMC2504861 DOI： 10.1016/j.jcf.2008.01.001

Source DB: PubMed Journal: J Cyst Fibros ISSN： 1569-1993 Impact factor: 5.482

22 in total

1. Analysis of the costs of diagnosing cystic fibrosis with a newborn screening program.

Authors: Don S Lee; Marjorie A Rosenberg; Andrew Peterson; Linda Makholm; Gary Hoffman; Ronald H Laessig; Philip M Farrell
Journal: J Pediatr Date: 2003-06 Impact factor: 4.406

2. The meaning of "early" diagnosis in a new era of cystic fibrosis care.

Authors: Philip M Farrell
Journal: Pediatrics Date: 2007-01 Impact factor: 7.124

3. Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy.

Authors: Erika J Sims; Allan Clark; Jonathan McCormick; Gita Mehta; Gary Connett; Anil Mehta
Journal: Pediatrics Date: 2007-01 Impact factor: 7.124

4. Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report.

Authors: Anne Marie Comeau; Frank J Accurso; Terry B White; Preston W Campbell; Gary Hoffman; Richard B Parad; Benjamin S Wilfond; Margaret Rosenfeld; Marci K Sontag; John Massie; Philip M Farrell; Brian P O'Sullivan
Journal: Pediatrics Date: 2007-02 Impact factor: 7.124

Review 5. Overview of published evidence on outcomes with early diagnosis from large US observational studies.

Authors: Margaret Rosenfeld
Journal: J Pediatr Date: 2005-09 Impact factor: 4.406

6. Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany).

Authors: D Siret; G Bretaudeau; B Branger; A Dabadie; M Dagorne; V David; M de Braekeleer; V Moisan-Petit; G Picherot; G Rault; V Storni; M Roussey
Journal: Pediatr Pulmonol Date: 2003-05

Is newborn screening for cystic fibrosis a basic human right?

1. Analysis of the costs of diagnosing cystic fibrosis with a newborn screening program.

2. The meaning of "early" diagnosis in a new era of cystic fibrosis care.

3. Cystic fibrosis diagnosed after 2 months of age leads to worse outcomes and requires more therapy.

4. Guidelines for implementation of cystic fibrosis newborn screening programs: Cystic Fibrosis Foundation workshop report.

Review 5. Overview of published evidence on outcomes with early diagnosis from large US observational studies.

6. Comparing the clinical evolution of cystic fibrosis screened neonatally to that of cystic fibrosis diagnosed from clinical symptoms: a 10-year retrospective study in a French region (Brittany).

Review 7. Potential impact of newborn screening for cystic fibrosis on child survival: a systematic review and analysis.

8. Diagnosis of cystic fibrosis in the Republic of Ireland: epidemiology and costs.

9. Longitudinal evaluation of bronchopulmonary disease in children with cystic fibrosis.

10. Cognitive function of children with cystic fibrosis: deleterious effect of early malnutrition.

1. Newborn Screening for Cystic Fibrosis: Over the Hump, Still Need to Fine-Tune It.