Clinical Characteristics and Predictors of Reduced Survival for Adult-diagnosed Cystic Fibrosis Analysis of the Canadian CF Registry

被引:18
作者
Desai, Sameer [1 ]
Wong, Hubert [1 ]
Sykes, Jenna [3 ,4 ]
Stephenson, Anne L. [3 ,4 ]
Singer, Joel [1 ,5 ]
Quon, Bradley S. [2 ,6 ,7 ]
机构
[1] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC, Canada
[2] Univ British Columbia, Dept Med, Div Resp Med, Vancouver, BC, Canada
[3] Univ Toronto, Div Respirol, Toronto, ON, Canada
[4] St Michaels Hosp, Adult Cyst Fibrosis Program, Toronto, ON, Canada
[5] St Pauls Hosp, Canadian HIV Trials Network, Vancouver, BC, Canada
[6] St Pauls Hosp, Ctr Heart Lung Innovat, Vancouver, BC, Canada
[7] Univ British Columbia, Vancouver, BC, Canada
关键词
cystic fibrosis; adult-diagnosed; survival; prognosis; epidemiology; MANIFESTATIONS; POPULATION; FOUNDATION; GUIDELINES; MORTALITY; DISEASE; AGE;
D O I
10.1513/AnnalsATS.201801-037OC
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Rationale: Individuals diagnosed with cystic fibrosis (CF) as adults represent a growing subpopulation of CF cases, but there are limited studies describing their characteristics and prognosis. Objectives: The objectives of this study were to describe the clinical characteristics of individuals with adult-diagnosed CF, estimate survival rates in this population, and identify clinical predictors of reduced survival at baseline. Methods: The Canadian CF Patient Registry was used to identify patients with CF who were >= 18 years of age at diagnosis and received a diagnosis between 1990 and 2014. Clinical characteristics were described and the Kaplan-Meier method was used to estimate lung-transplant-free survival. Multivariable Cox regression analysis and adjusted survival curves were employed to identify important predictors of reduced survival at the time of diagnosis (i.e., baseline) and to produce adjusted effects. Results: A total of 362 adults were diagnosed with CF during the study period. The median follow-up time was 7.7 years and 48 individuals experienced an event (15 transplants, 33 deaths without transplant). The median age at diagnosis was 34.3 years, with the majority of individuals presenting with pulmonary and/or gastrointestinal symptoms (71%). Lung-transplant-free survival was 88% at 10 years and 86% at 15 years. Age at diagnosis (hazard ratio [HR], 1.24 per 5-year increase, 95% confidence interval [CI], 1.09-1.43), diabetes (HR, 4.19; 95% CI, 1.35-13.01), and lung function (HR, 1.35 per 5% decrease in forced expiratory volume in 1 second % predicted; 95% CI, 1.24-1.48) at baseline were important predictors of reduced survival. Conclusions: CF care providers can use this information to inform individuals who received a diagnosis of CF as adults about their prognosis and to guide the necessity of treatments, specifically with regard to those who are at high risk for a worse prognosis.
引用
收藏
页码:1177 / 1185
页数:9
相关论文
共 31 条
  • [21] Diagnosis of Adult Patients with Cystic Fibrosis
    Nick, Jerry A.
    Nichols, David P.
    [J]. CLINICS IN CHEST MEDICINE, 2016, 37 (01) : 47 - +
  • [22] Effects of Gender and Age at Diagnosis on Disease Progression in Long-term Survivors of Cystic Fibrosis
    Nick, Jerry A.
    Chacon, Cathy S.
    Brayshaw, Sara J.
    Jones, Marion C.
    Barboa, Christine M.
    Clair, Connie G. St.
    Young, Robert L.
    Nichols, David P.
    Janssen, Jennifer S.
    Huitt, Gwen A.
    Iseman, Michael D.
    Daley, Charles L.
    Taylor-Cousar, Jennifer L.
    Accurso, Frank J.
    Saavedra, Milene T.
    Sontag, Marci K.
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2010, 182 (05) : 614 - 626
  • [23] Update of Literature From Cystic Fibrosis Registries 2012-2015. Part 6: Epidemiology, Nutrition, and Complications
    Salvatore, Donatello
    Buzzetti, Roberto
    Mastella, Gianni
    [J]. PEDIATRIC PULMONOLOGY, 2017, 52 (03) : 390 - 398
  • [24] Survival Comparison of Patients With Cystic Fibrosis in Canada and the United States A Population-Based Cohort Study
    Stephenson, Anne L.
    Sykes, Jenna
    Stanojevic, Sanja
    Quon, Bradley S.
    Marshall, Bruce C.
    Petren, Kristofer
    Ostrenga, Josh
    Fink, Aliza K.
    Elbert, Alexander
    Goss, Christopher H.
    [J]. ANNALS OF INTERNAL MEDICINE, 2017, 166 (08) : 537 - +
  • [25] A contemporary survival analysis of individuals with cystic fibrosis: a cohort study
    Stephenson, Anne L.
    Tom, Melissa
    Berthiaume, Yves
    Singer, Lianne G.
    Aaron, Shawn D.
    Whitmore, G. A.
    Stanojevic, Sanja
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2015, 45 (03) : 670 - 679
  • [26] A standardized approach to estimating survival statistics for population-based cystic fibrosis registry cohorts
    Sykes, Jenna
    Stanojevic, Sanja
    Goss, Christopher H.
    Quon, Bradley S.
    Marshall, Bruce C.
    Petren, Kristofer
    Ostrenga, Josh
    Fink, Aliza
    Elbert, Alexander
    Stephenson, Anne L.
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 2016, 70 : 206 - 213
  • [27] DAGitty A Graphical Tool for Analyzing Causal Diagrams
    Textor, Johannes
    Hardt, Juliane
    Knueppel, Sven
    [J]. EPIDEMIOLOGY, 2011, 22 (05) : 745 - 745
  • [28] Therneau T.M., 2015, ADJUSTED SURVIVAL CU
  • [29] Multiple imputation of discrete and continuous data by fully conditional specification
    van Buuren, Stef
    [J]. STATISTICAL METHODS IN MEDICAL RESEARCH, 2007, 16 (03) : 219 - 242
  • [30] Communicating a diagnosis of cystic fibrosis to an adult: What physicians need to know
    Widerman, E
    [J]. BEHAVIORAL MEDICINE, 2002, 28 (02) : 45 - 52