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Outcomes of non-cystic fibrosis-related bronchiectasis post-lung transplantation.
Kennedy, Jessica L; Walker, Anne; Ellender, Claire M; Steinfort, Kate; Martin, Catherine; Smith, Catherine; Snell, Gregory; Whitford, Helen.
Afiliação
  • Kennedy JL; Department of Allergy, Immunology and Respiratory Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
  • Walker A; School of Medicine, Dentistry and Health Science, Melbourne University, Melbourne, Victoria, Australia.
  • Ellender CM; Department of Respiratory and Sleep Medicine, Austin Hospital, Melbourne, Victoria, Australia.
  • Steinfort K; Department of Allergy, Immunology and Respiratory Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
  • Martin C; Department of Thoracic Medicine, Royal Adelaide Hospital, Adelaide, South Australia, Australia.
  • Smith C; Department of Allergy, Immunology and Respiratory Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
  • Snell G; Department of Respiratory and Sleep Medicine, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
  • Whitford H; Department of Allergy, Immunology and Respiratory Medicine, Alfred Hospital, Melbourne, Victoria, Australia.
Intern Med J ; 52(6): 995-1001, 2022 06.
Article em En | MEDLINE | ID: mdl-33656222
ABSTRACT

BACKGROUND:

Lung transplantation is a recognised treatment for end-stage lung disease due to bronchiectasis. Non-cystic fibrosis (CF) bronchiectasis and CF are often combined into one cohort; however, outcomes for non-CF bronchiectasis patients vary between centres, and in comparison with those for CF.

AIMS:

To compare lung transplantation mortality and morbidity of bronchiectasis (non-CF) patients with those with CF and other indications.

METHODS:

Retrospective analysis of patients undergoing lung transplantation between 1 January 2008 and 31 December 2013. Time to and cause of lung allograft loss was censored on 1 April 2018. A case-note review was conducted on a subgroup of 78 patients, to analyse hospital admissions as a marker of morbidity.

RESULTS:

A total of 341 patients underwent lung transplantation; 22 (6%) had bronchiectasis compared with 69 (20%) with CF. The 5-year survival for the bronchiectasis group was 32%, compared with CF (69%), obstructive lung disease (OLD) (64%), pulmonary hypertension (62%) and ILD (55%) (P = 0.008). Lung allograft loss due to chronic lung allograft dysfunction with predominant infection was significantly higher in the bronchiectasis group at 2 years. The rate of acute admissions was 2.24 higher in the bronchiectasis group when compared with OLD (P = 0.01). Patients with bronchiectasis spent 45.81 days in hospital per person year after transplantation compared with 18.21 days for CF.

CONCLUSIONS:

Bronchiectasis patients in the present study had a lower 5-year survival and poorer outcomes in comparison with other indications including CF. Bronchiectasis should be considered a separate entity to CF in survival analysis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bronquiectasia / Transplante de Pulmão / Fibrose Cística Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bronquiectasia / Transplante de Pulmão / Fibrose Cística Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article