Literature DB >> 28232958

Dynamics of Disease Progression and Gastrostomy Tube Placement in Children and Adolescents with Cystic Fibrosis: Application of Joint Models for Longitudinal and Time-to-Event Data.

Rhonda Szczesniak1, Weiji Su2, J P Clancy3.   

Abstract

BACKGROUND: Previous small-sample studies have examined the effect of gastrostomy (g-) tube placement on weight, height, and lung function in adolescent patients with cystic fibrosis (CF), but there are no RCTs to date reporting efficacy. The goal of this study was to implement a dynamic prediction model to 1) understand the role of rapid lung function decline in g-tube placement in real-world clinical settings; 2) provide a prognostic tool with the potential to aid clinicians in optimizing the timing of g-tube placement, in relation to rate of lung function decline and current nutrition status.
METHODS: A dynamic prediction model was developed, utilizing data on patients 6-21 years of age from the Cystic Fibrosis Foundation Patient Registry (1997-2013). A joint model was implemented, which coupled a semiparametric mixed model to characterize rapid lung function decline with a time-to-event model to identify risk factors for g-tube initiation.
RESULTS: The 4,034 individuals (21.3%) who underwent g-tube placement during adolescence or young adulthood had poorer nutrition and lung function at baseline and initially had increased rates of pancreatic enzyme use, infection and gastroesophageal reflux disease, compared to those who did not receive g-tubes; these associations changed over follow up. Rapid lung function decline was associated with increased risk of g-tube supplementation.
CONCLUSIONS: By jointly modeling longitudinal patterns of lung function decline with g-tube delivery, it is possible to construct prognostic aids to evaluate treatment delivery in relation to the onset of rapid lung function decline and other important clinical markers. These algorithms have the potential to enable more effective monitoring of disease progression and promote more timely treatment delivery.

Entities:  

Keywords:  cystic fibrosis patient registry; functional data analysis; individualized prediction; longitudinal analysis; nutrition; pulmonary function

Year:  2016        PMID: 28232958      PMCID: PMC5319388          DOI: 10.18103/imr.v2i9.163

Source DB:  PubMed          Journal:  Intern Med Rev (Wash D C)


  20 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

2.  Spirometric reference values from a sample of the general U.S. population.

Authors:  J L Hankinson; J R Odencrantz; K B Fedan
Journal:  Am J Respir Crit Care Med       Date:  1999-01       Impact factor: 21.405

Review 3.  Basic concepts and methods for joint models of longitudinal and survival data.

Authors:  Joseph G Ibrahim; Haitao Chu; Liddy M Chen
Journal:  J Clin Oncol       Date:  2010-05-03       Impact factor: 44.544

Review 4.  Enteral tube feeding for cystic fibrosis.

Authors:  Alison Morton; Susan Wolfe
Journal:  Cochrane Database Syst Rev       Date:  2015-04-09

5.  Comparison of the use of body mass index percentiles and percentage of ideal body weight to screen for malnutrition in children with cystic fibrosis.

Authors:  Zhumin Zhang; HuiChuan J Lai
Journal:  Am J Clin Nutr       Date:  2004-10       Impact factor: 7.045

Review 6.  Tackling the increasing complexity of CF care.

Authors:  Gregory S Sawicki; Christopher H Goss
Journal:  Pediatr Pulmonol       Date:  2015-10

7.  A semiparametric approach to estimate rapid lung function decline in cystic fibrosis.

Authors:  Rhonda D Szczesniak; Gary L McPhail; Leo L Duan; Maurizio Macaluso; Raouf S Amin; John P Clancy
Journal:  Ann Epidemiol       Date:  2013-10-05       Impact factor: 3.797

8.  A comparison of change point models with application to longitudinal lung function measurements in children with cystic fibrosis.

Authors:  Angela Moss; E Juarez-Colunga; Farouk Nathoo; Brandie Wagner; Scott Sagel
Journal:  Stat Med       Date:  2016-01-05       Impact factor: 2.373

9.  Joint modelling of longitudinal and survival data: incorporating delayed entry and an assessment of model misspecification.

Authors:  Michael J Crowther; Therese M-L Andersson; Paul C Lambert; Keith R Abrams; Keith Humphreys
Journal:  Stat Med       Date:  2015-10-29       Impact factor: 2.373

Review 10.  Evidence-based practice recommendations for nutrition-related management of children and adults with cystic fibrosis and pancreatic insufficiency: results of a systematic review.

Authors:  Virginia A Stallings; Lori J Stark; Karen A Robinson; Andrew P Feranchak; Hebe Quinton
Journal:  J Am Diet Assoc       Date:  2008-05
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  1 in total

Review 1.  Harnessing repeated measurements of predictor variables for clinical risk prediction: a review of existing methods.

Authors:  Lucy M Bull; Mark Lunt; Glen P Martin; Kimme Hyrich; Jamie C Sergeant
Journal:  Diagn Progn Res       Date:  2020-07-09
  1 in total

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