These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
124 related articles for article (PubMed ID: 32770822)
1. Quality improvement initiative to improve pulmonary function in pediatric cystic fibrosis patients. Filbrun AG; Enochs C; Caverly L; Rajala K; Powell C; Merrick E; Nasr SZ Pediatr Pulmonol; 2020 Nov; 55(11):3039-3045. PubMed ID: 32770822 [TBL] [Abstract][Full Text] [Related]
2. The impact of re-education of airway clearance techniques (REACT) on adherence and pulmonary function in patients with cystic fibrosis. Zanni RL; Sembrano EU; Du DT; Marra B; Bantang R BMJ Qual Saf; 2014 Apr; 23 Suppl 1():i50-5. PubMed ID: 24608551 [TBL] [Abstract][Full Text] [Related]
3. Pulmonary function disparities exist and persist in Hispanic patients with cystic fibrosis: A longitudinal analysis. McGarry ME; Neuhaus JM; Nielson DW; Burchard E; Ly NP Pediatr Pulmonol; 2017 Dec; 52(12):1550-1557. PubMed ID: 29082671 [TBL] [Abstract][Full Text] [Related]
4. Implementation of standardized cystic fibrosis care algorithm to improve the center data-quality improvement project international collaboration. Gokdemir Y; Eralp EE; Ergenekon AP; Yilmaz Yegit C; Yanaz M; Mursaloğlu H; Uzunoglu B; Kocamaz D; Tastan G; Kenis Coskun O; Filbrun A; Enochs C; Bouma S; Iwanicki C; Karakoc F; Nasr SZ; Karadag B J Cyst Fibros; 2023 Jul; 22(4):710-714. PubMed ID: 37037703 [TBL] [Abstract][Full Text] [Related]
5. Lung function determinants and mortality of children and adolescents with cystic fibrosis in South Africa 2007-2016. Vandenbroucke NJ; Zampoli M; Morrow B Pediatr Pulmonol; 2020 Jun; 55(6):1381-1387. PubMed ID: 32176840 [TBL] [Abstract][Full Text] [Related]
6. Increased adherence to CFF practice guidelines for pulmonary medications correlates with improved FEV1. Moore BM; Laguna TA; Liu M; McNamara JJ Pediatr Pulmonol; 2013 Aug; 48(8):747-53. PubMed ID: 22997186 [TBL] [Abstract][Full Text] [Related]
7. Analysis of a large cohort of cystic fibrosis patients with severe liver disease indicates lung function decline does not significantly differ from that of the general cystic fibrosis population. Polineni D; Piccorelli AV; Hannah WB; Dalrymple SN; Pace RG; Durie PR; Ling SC; Knowles MR; Stonebraker JR PLoS One; 2018; 13(10):e0205257. PubMed ID: 30307979 [TBL] [Abstract][Full Text] [Related]
8. Improved recognition of lung function decline as signal of cystic fibrosis pulmonary exacerbation: a Cystic Fibrosis Learning Network Innovation Laboratory quality improvement initiative. List R; Solomon G; Bichl S; Horton BJ; Shen S; Corcoran B; Sadeghi H; Britto MT; Ren C; Albon D; BMJ Open Qual; 2023 Dec; 12(4):. PubMed ID: 38154821 [TBL] [Abstract][Full Text] [Related]
9. Heterogeneity in Survival in Adult Patients With Cystic Fibrosis With FEV Ramos KJ; Quon BS; Heltshe SL; Mayer-Hamblett N; Lease ED; Aitken ML; Weiss NS; Goss CH Chest; 2017 Jun; 151(6):1320-1328. PubMed ID: 28115168 [TBL] [Abstract][Full Text] [Related]
10. Advance care planning in adolescents with cystic fibrosis: A quality improvement project. Kazmerski TM; Weiner DJ; Matisko J; Schachner D; Lerch W; May C; Maurer SH Pediatr Pulmonol; 2016 Dec; 51(12):1304-1310. PubMed ID: 27749020 [TBL] [Abstract][Full Text] [Related]
11. The impact of transforming healthcare delivery on cystic fibrosis outcomes: a decade of quality improvement at Cincinnati Children's Hospital. Siracusa CM; Weiland JL; Acton JD; Chima AK; Chini BA; Hoberman AJ; Wetzel JD; Amin RS; McPhail GL BMJ Qual Saf; 2014 Apr; 23 Suppl 1():i56-i63. PubMed ID: 24608552 [TBL] [Abstract][Full Text] [Related]
12. Rhinovirus-associated pulmonary exacerbations show a lack of FEV1 improvement in children with cystic fibrosis. Cousin M; Molinari N; Foulongne V; Caimmi D; Vachier I; Abely M; Chiron R Influenza Other Respir Viruses; 2016 Mar; 10(2):109-12. PubMed ID: 26493783 [TBL] [Abstract][Full Text] [Related]
13. Relationship between lung function and Modified Shuttle Test performance in adult patients with cystic fibrosis: a cross-sectional, retrospective study. Doeleman WR; Takken T; Bronsveld I; Hulzebos EH Physiotherapy; 2016 Jun; 102(2):184-8. PubMed ID: 27101722 [TBL] [Abstract][Full Text] [Related]
14. Variation in lung function is associated with worse clinical outcomes in cystic fibrosis. Heinzmann-Filho JP; Pinto LA; Marostica PJ; Donadio MV J Bras Pneumol; 2015; 41(6):509-15. PubMed ID: 26785959 [TBL] [Abstract][Full Text] [Related]
16. Effect of supervised training on FEV1 in cystic fibrosis: a randomised controlled trial. Kriemler S; Kieser S; Junge S; Ballmann M; Hebestreit A; Schindler C; Stüssi C; Hebestreit H J Cyst Fibros; 2013 Dec; 12(6):714-20. PubMed ID: 23588193 [TBL] [Abstract][Full Text] [Related]
17. Association of nutritional status, plasma, albumin levels and pulmonary function in cystic fibrosis. Souza dos Santos Simon MI; Drehmer M; de Abreu E Silva FA; Hoffmann A; Druck Ricachinewsky C; de Fonseca Andrade Procianoy E; Scattolin I; Saldanha Menna Barreto S Nutr Hosp; 2011; 26(6):1322-7. PubMed ID: 22411378 [TBL] [Abstract][Full Text] [Related]
19. The Short-Term Effect of Breathing Tasks Via an Incentive Spirometer on Lung Function Compared With Autogenic Drainage in Subjects With Cystic Fibrosis. Sokol G; Vilozni D; Hakimi R; Lavie M; Sarouk I; Bat-El Bar ; Dagan A; Ofek M; Efrati O Respir Care; 2015 Dec; 60(12):1819-25. PubMed ID: 26374905 [TBL] [Abstract][Full Text] [Related]
20. Growth failure in cystic fibrosis. McNaughton SA; Stormont DA; Shepherd RW; Francis PW; Dean B J Paediatr Child Health; 1999 Feb; 35(1):86-92. PubMed ID: 10234643 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]