Literature DB >> 27469176

Background and Epidemiology.

Don B Sanders1, Aliza K Fink2.   

Abstract

Cystic fibrosis (CF) is the most common autosomal-recessive disease in white persons. Significant advances in therapies and outcomes have occurred for people with CF over the past 30 years. Many of these improvements have come about through the concerted efforts of the CF Foundation and international CF societies; networks of CF care centers; and the worldwide community of care providers, researchers, and patients and families. There are still hurdles to overcome to continue to improve the quality of life, reduce CF complications, prolong survival, and ultimately cure CF. This article reviews the epidemiology of CF, including trends in incidence and prevalence, clinical characteristics, common complications, and survival.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BMI; Cystic fibrosis; FEV(1); MRSA; Mortality; Newborn screening; Pseudomonas aeruginosa

Mesh:

Year:  2016        PMID: 27469176      PMCID: PMC4967225          DOI: 10.1016/j.pcl.2016.04.001

Source DB:  PubMed          Journal:  Pediatr Clin North Am        ISSN: 0031-3955            Impact factor:   3.278


  90 in total

1.  Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis.

Authors:  Michael W Konstan; Wayne J Morgan; Steven M Butler; David J Pasta; Marcia L Craib; Stefanie J Silva; Dennis C Stokes; Mary Ellen B Wohl; Jeffrey S Wagener; Warren E Regelmann; Charles A Johnson
Journal:  J Pediatr       Date:  2007-06-22       Impact factor: 4.406

Review 2.  Improving chronic care delivery and outcomes: the impact of the cystic fibrosis Care Center Network.

Authors:  Peter J Mogayzel; Jordan Dunitz; Laura C Marrow; Leslie A Hazle
Journal:  BMJ Qual Saf       Date:  2014-04       Impact factor: 7.035

3.  Cystic fibrosis mutations and genotype-pulmonary phenotype analysis.

Authors:  Andrew T Braun; Philip M Farrell; Claude Ferec; Marie Pierre Audrezet; Anita Laxova; Zhanhai Li; Michael R Kosorok; Marjorie A Rosenberg; William M Gershan
Journal:  J Cyst Fibros       Date:  2005-11-04       Impact factor: 5.482

4.  Recommendations for the classification of diseases as CFTR-related disorders.

Authors:  C Bombieri; M Claustres; K De Boeck; N Derichs; J Dodge; E Girodon; I Sermet; M Schwarz; M Tzetis; M Wilschanski; C Bareil; D Bilton; C Castellani; H Cuppens; G R Cutting; P Drevínek; P Farrell; J S Elborn; K Jarvi; B Kerem; E Kerem; M Knowles; M Macek; A Munck; D Radojkovic; M Seia; D N Sheppard; K W Southern; M Stuhrmann; E Tullis; J Zielenski; P F Pignatti; C Ferec
Journal:  J Cyst Fibros       Date:  2011-06       Impact factor: 5.482

5.  Longevity of patients with cystic fibrosis in 2000 to 2010 and beyond: survival analysis of the Cystic Fibrosis Foundation patient registry.

Authors:  Todd MacKenzie; Alex H Gifford; Kathryn A Sabadosa; Hebe B Quinton; Emily A Knapp; Christopher H Goss; Bruce C Marshall
Journal:  Ann Intern Med       Date:  2014-08-19       Impact factor: 25.391

Review 6.  Exacerbations in cystic fibrosis. 1: Epidemiology and pathogenesis.

Authors:  Christopher H Goss; Jane L Burns
Journal:  Thorax       Date:  2007-04       Impact factor: 9.139

7.  Association between respiratory tract methicillin-resistant Staphylococcus aureus and survival in cystic fibrosis.

Authors:  Elliott C Dasenbrook; William Checkley; Christian A Merlo; Michael W Konstan; Noah Lechtzin; Michael P Boyle
Journal:  JAMA       Date:  2010-06-16       Impact factor: 56.272

8.  Novel CFTR variants identified during the first 3 years of cystic fibrosis newborn screening in California.

Authors:  Lisa Prach; Ruth Koepke; Martin Kharrazi; Steven Keiles; Danieli B Salinas; Maria Carmen Reyes; Mark Pian; Harry Opsimos; Kimberly N Otsuka; Karen Ann Hardy; Carlos E Milla; Jacquelyn M Zirbes; Bradley Chipps; Susan O'Bra; Muhammad M Saeed; Reddivalam Sudhakar; Susan Lehto; Dennis Nielson; Gregory F Shay; Mary Seastrand; Sanjay Jhawar; Bruce Nickerson; Christopher Landon; Ann Thompson; Eliezer Nussbaum; Terry Chin; Henry Wojtczak
Journal:  J Mol Diagn       Date:  2013-06-28       Impact factor: 5.568

9.  Early Life Growth Trajectories in Cystic Fibrosis are Associated with Pulmonary Function at Age 6 Years.

Authors:  Don B Sanders; Aliza Fink; Nicole Mayer-Hamblett; Michael S Schechter; Gregory S Sawicki; Margaret Rosenfeld; Patrick A Flume; Wayne J Morgan
Journal:  J Pediatr       Date:  2015-09-02       Impact factor: 4.406

10.  Is chest CT useful in newborn screened infants with cystic fibrosis at 1 year of age?

Authors:  Lena P Thia; Alistair Calder; Janet Stocks; Andrew Bush; Catherine M Owens; Colin Wallis; Carolyn Young; Yvonne Sullivan; Angie Wade; Angus McEwan; Alan S Brody
Journal:  Thorax       Date:  2013-10-16       Impact factor: 9.139

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  27 in total

1.  Elexacaftor-Tezacaftor-Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele.

Authors:  Peter G Middleton; Marcus A Mall; Pavel Dřevínek; Larry C Lands; Edward F McKone; Deepika Polineni; Bonnie W Ramsey; Jennifer L Taylor-Cousar; Elizabeth Tullis; François Vermeulen; Gautham Marigowda; Charlotte M McKee; Samuel M Moskowitz; Nitin Nair; Jessica Savage; Christopher Simard; Simon Tian; David Waltz; Fengjuan Xuan; Steven M Rowe; Raksha Jain
Journal:  N Engl J Med       Date:  2019-10-31       Impact factor: 91.245

2.  Succinate links mitochondria to deadly bacteria in cystic fibrosis.

Authors:  Speranza Esposito; Valeria Rachela Villella; Federica Rossin; Antonella Tosco; Valeria Raia; Alessandro Luciani
Journal:  Ann Transl Med       Date:  2019-12

3.  Mucoid Pseudomonas aeruginosa and regional inflammation in the cystic fibrosis lung.

Authors:  Sankalp Malhotra; Don Hayes; Daniel J Wozniak
Journal:  J Cyst Fibros       Date:  2019-04-26       Impact factor: 5.482

Review 4.  Cystic Fibrosis and Pseudomonas aeruginosa: the Host-Microbe Interface.

Authors:  Sankalp Malhotra; Don Hayes; Daniel J Wozniak
Journal:  Clin Microbiol Rev       Date:  2019-05-29       Impact factor: 26.132

5.  Evaluation of Frequency and Characteristics of Drug Allergy in Pediatric Patients with Cystic Fibrosis.

Authors:  Zeynep Şengül Emeksiz; Pınar Metbulut; Şule Selin Akyan Soydaş; Gökçen Tuğcu; Güzin Cinel; Emine Dibek Mısırlıoğlu
Journal:  Pediatr Allergy Immunol Pulmonol       Date:  2022-05-18       Impact factor: 0.885

6.  Epidemiology of Eosinophilic Esophagitis in Patients with Cystic Fibrosis: A Population-Based 5-Year Study.

Authors:  Omar Alaber; Ramy Sabe; Virginia Baez-Socorro; Senthilkumar Sankararaman; Erica Roesch; Thomas J Sferra
Journal:  Pediatr Gastroenterol Hepatol Nutr       Date:  2022-07-06

Review 7.  Stem cells and lung regeneration.

Authors:  Kalpaj R Parekh; Janna Nawroth; Albert Pai; Shana M Busch; Christiana N Senger; Amy L Ryan
Journal:  Am J Physiol Cell Physiol       Date:  2020-08-12       Impact factor: 4.249

8.  Telerehabilitation Using Fitness Application in Patients with Severe Cystic Fibrosis Awaiting Lung Transplant: A Pilot Study.

Authors:  Aimee M Layton; Andrew M Irwin; Erin C Mihalik; Emily Fleisch; Claire L Keating; Emily A DiMango; Lori Shah; Selim M Arcasoy
Journal:  Int J Telemed Appl       Date:  2021-02-26

9.  Combined Liver-Lung-Kidney Transplant in a Patient with Cystic Fibrosis.

Authors:  Lori Shah; Geoffrey Dube; Lorna Dove; Amy C McLaughlin; Jean Emond; Lloyd Rattner; Frank D'Ovidio; Emily DiMango
Journal:  Am J Case Rep       Date:  2021-06-24

10.  A retrospective 'real-world' cohort study of azole therapeutic drug monitoring and evolution of antifungal resistance in cystic fibrosis.

Authors:  M Di Paolo; L Hewitt; E Nwanko; M Ni; A Vidal-Diaz; M C Fisher; D Armstrong-James; A Shah
Journal:  JAC Antimicrob Resist       Date:  2021-03-16
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