Literature DB >> 17955689

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

P Farrell1, S Joffe, L Foley, G J Canny, P Mayne, M Rosenberg.   

Abstract

There were four objectives in this study: (1) determine the incidence of cystic fibrosis (CF) in Ireland; (2) estimate the cost of diagnosing CF; (3) clarify the characteristics and outcomes of the nationwide diagnostic efforts and (4) identify disparities. Surveys were conducted to determine the number, methods, costs and outcomes for sweat tests in Ireland from 2001 through 2003. The results allowed us to determine that Ireland's CF incidence is the world's highest at 1:1353. The average cost for diagnosis was Euro 2663 per patient. Analyses of data in The Cystic Fibrosis Registry of Ireland revealed longer delays when diagnosis followed respiratory symptoms, rather than gastrointestinal signs, and also in girls compared to boys, particularly those presenting with respiratory symptoms. Although expenditures for diagnosing of CF in Ireland are relatively modest, the high incidence and age of diagnosis, as well as gender-related disparities, are sufficient to warrant investment in national newborn screening.

Entities:  

Mesh:

Year:  2007        PMID: 17955689

Source DB:  PubMed          Journal:  Ir Med J        ISSN: 0332-3102


  15 in total

1.  A decision-tree approach to cost comparison of newborn screening strategies for cystic fibrosis.

Authors:  Janelle Wells; Marjorie Rosenberg; Gary Hoffman; Michael Anstead; Philip M Farrell
Journal:  Pediatrics       Date:  2012-01-30       Impact factor: 7.124

Review 2.  A review of consanguinity in Ireland--estimation of frequency and approaches to mitigate risks.

Authors:  P Barrett
Journal:  Ir J Med Sci       Date:  2016-02       Impact factor: 1.568

3.  Effects of gender and age at diagnosis on disease progression in long-term survivors of cystic fibrosis.

Authors:  Jerry A Nick; Cathy S Chacon; Sara J Brayshaw; Marion C Jones; Christine M Barboa; Connie G St Clair; Robert L Young; David P Nichols; Jennifer S Janssen; Gwen A Huitt; Michael D Iseman; Charles L Daley; Jennifer L Taylor-Cousar; Frank J Accurso; Milene T Saavedra; Marci K Sontag
Journal:  Am J Respir Crit Care Med       Date:  2010-05-06       Impact factor: 21.405

4.  Cystic fibrosis in Sudanese children: First report of 35 cases.

Authors:  Salah A Ibrahim; Munadhil A Fadl Elmola; Zain A Karrar; Ali M E Arabi; Mohamed A Abdullah; Sulafa K Ali; Fathelrahman Elawad; Tag Elsir A Ali; Mashair B Abdulrahman; Salma O Ahmed; Abelrazzag S Gundi
Journal:  Sudan J Paediatr       Date:  2014

5.  Delayed cystic fibrosis presentation in children in the absence of newborn screening.

Authors:  A Jackson; L Foley; L Daly; P Fitzpatrick; M Harrington; S Zhou; C Kelleher
Journal:  Ir Med J       Date:  2010-04

6.  Estimating Direct Cost of Cystic Fibrosis Care Using Irish Registry Healthcare Resource Utilisation Data, 2008-2012.

Authors:  Abaigeal D Jackson; Andrew L Jackson; Godfrey Fletcher; Gerardine Doyle; Mary Harrington; Shijun Zhou; Fiona Cullinane; Charles Gallagher; Edward McKone
Journal:  Pharmacoeconomics       Date:  2017-10       Impact factor: 4.981

7.  Demographic and historical findings, including exposure to environmental tobacco smoke, in dogs with chronic cough.

Authors:  E C Hawkins; L D Clay; J M Bradley; M Davidian
Journal:  J Vet Intern Med       Date:  2010-05-11       Impact factor: 3.333

8.  National Newborn Screening for cystic fibrosis in the Republic of Ireland: genetic data from the first 6.5 years.

Authors:  Erina Sasaki; Marija Kostocenko; Niamh Lang; Tara Clark; Melissa Rogers; Rebecca Muldowney; Olivia Walsh; Loretta O'Grady; Gillian Edge; Alana Ward; Barry Linnane; Ingrid Borovickova; David E Barton; Sally Ann Lynch
Journal:  Eur J Hum Genet       Date:  2020-06-01       Impact factor: 4.246

9.  Is newborn screening for cystic fibrosis a basic human right?

Authors:  Philip M Farrell
Journal:  J Cyst Fibros       Date:  2008-02-11       Impact factor: 5.482

10.  A short-term evaluation of a prototype disposable Oscillating Positive Expiratory Pressure (OPEP) device in a cohort of children with cystic fibrosis.

Authors:  Kevin J O'Sullivan; Valerie Power; Barry Linnane; Deirdre McGrath; Magdalena Mulligan; Rebecca White; Leonard W O'Sullivan; Colum P Dunne
Journal:  BMC Pulm Med       Date:  2021-05-12       Impact factor: 3.317

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