Literature DB >> 16100161

Massive hemoptysis in cystic fibrosis.

Patrick A Flume1, James R Yankaskas, Myla Ebeling, Thomas Hulsey, Leslie L Clark.   

Abstract

BACKGROUND: Massive hemoptysis is a complication commonly reported in patients with cystic fibrosis (CF). An understanding of the pathophysiology of this complication and its consequences is important for the management of patients with CF.
OBJECTIVES: To identify risk factors associated with massive hemoptysis, and to determine the prognosis of patients following an episode of massive hemoptysis.
DESIGN: A retrospective, observational cohort study of the National CF Patient Registry between the years 1990 to 1999. PATIENTS: The Registry contained data on 28,858 patients with CF observed over 10 years at CF centers across the United States.
RESULTS: Massive hemoptysis occurred with an average annual incidence of 0.87% and in 4.1% of patients overall. There was no increased occurrence by sex, but it was more prevalent in older patients (mean age, 24.2 +/- 8.7 years [+/- SD]) with more severe pulmonary impairment (nearly 60% of patients who had an episode of massive hemoptysis had FEV1 < 40% predicted). The principal risks associated with an increased occurrence of massive hemoptysis included the presence of Staphylococcus aureus in sputum cultures (odds ratio [OR], 1.3) and diabetes (OR, 1.1). There was an increased morbidity (eg, increased hospitalizations and hospital days) and an increased 2-year mortality following massive hemoptysis.
CONCLUSION: Massive hemoptysis is a serious complication in CF patients, occurring more commonly in older patients with more advanced lung disease. Nearly 1 in 100 patients will have this complication each year. There is an attributable mortality to the complication and considerable morbidity, resulting in increased health-care utilization and a measurable decline in lung function.

Entities:  

Mesh:

Year:  2005        PMID: 16100161     DOI: 10.1378/chest.128.2.729

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  22 in total

1.  Patients with cystic fibrosis should be intubated and ventilated.

Authors:  Ian Ketchell
Journal:  J R Soc Med       Date:  2010-07       Impact factor: 5.344

2.  Risk of hemoptysis in cystic fibrosis clinical trials: A retrospective cohort study.

Authors:  V Thompson; N Mayer-Hamblett; M Kloster; D Bilton; P A Flume
Journal:  J Cyst Fibros       Date:  2015-02-25       Impact factor: 5.482

3.  Improvement in pulmonary function following closure of a patent foramen ovale in a man with cystic fibrosis.

Authors:  M Belton; K M Gyi
Journal:  J R Soc Med       Date:  2009-07       Impact factor: 5.344

4.  Treatment massive haemoptysis in cystic fibrosis with tranexamic acid.

Authors:  Matthew Hurley; Jayesh Bhatt; Alan Smyth
Journal:  J R Soc Med       Date:  2011-07       Impact factor: 5.344

Review 5.  Lung transplant referral for individuals with cystic fibrosis: Cystic Fibrosis Foundation consensus guidelines.

Authors:  Kathleen J Ramos; Patrick J Smith; Edward F McKone; Joseph M Pilewski; Amy Lucy; Sarah E Hempstead; Erin Tallarico; Albert Faro; Daniel B Rosenbluth; Alice L Gray; Jordan M Dunitz
Journal:  J Cyst Fibros       Date:  2019-03-27       Impact factor: 5.482

6.  Impact of Socioeconomic Position on Access to the U.S. Lung Transplant Waiting List in a Matched Cystic Fibrosis Cohort.

Authors:  Carli J Lehr; Aliza K Fink; Melissa Skeans; Albert Faro; Gabriela Fernandez; Elliott Dasenbrook; Maryam Valapour
Journal:  Ann Am Thorac Soc       Date:  2020-11

7.  Preprocedural planning with prospectively triggered multidetector row CT angiography prior to bronchial artery embolization in cystic fibrosis patients with massive hemoptysis.

Authors:  Don Hayes; Michael A Winkler; Stephen Kirkby; Patrizio Capasso; Heidi M Mansour; Anil K Attili
Journal:  Lung       Date:  2011-10-30       Impact factor: 2.584

Review 8.  A systematic approach to the management of massive hemoptysis.

Authors:  Christopher Radchenko; Abdul Hamid Alraiyes; Samira Shojaee
Journal:  J Thorac Dis       Date:  2017-09       Impact factor: 2.895

Review 9.  Is bronchoscopy an obsolete tool in cystic fibrosis? The role of bronchoscopy in cystic fibrosis and its clinical use.

Authors:  Lisa Paul
Journal:  J Thorac Dis       Date:  2017-09       Impact factor: 2.895

Review 10.  Contemporary approaches in the use of extracorporeal membrane oxygenation to support patients waiting for lung transplantation.

Authors:  Steven P Keller
Journal:  Ann Cardiothorac Surg       Date:  2020-01
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.