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1.
Cardiovasc Intervent Radiol ; 40(8): 1164-1168, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28289842

ABSTRACT

BACKGROUND: Bronchial artery embolisation (BAE) is recommended for the treatment of massive haemoptysis in cystic fibrosis (CF), but there are no randomised controlled trials of this therapy and its role in sub-massive haemoptysis is unclear. This study aimed to determine the outcomes and safety of BAE in adults with CF. MATERIALS AND METHODS: All patients with CF undergoing BAE at our centre between March 2011 and January 2015 were identified at the time of the procedure. Patient records were reviewed at hospital discharge, death or one month post-procedure (whichever was soonest). Follow-up continued to January 2016. Severity of haemoptysis was classified as: massive (>240 ml/24 h or >100 ml/day for ≥2 days), moderate-severe (>20 ml/24 h) or mild (<20 ml/24 h). RESULTS: Twenty-seven patients underwent 51 BAE procedures over a median follow-up period of 26 months (range 1-54). Ten patients (37%) required more than one BAE during the study. BAE was performed for massive haemoptysis in 18 cases (35%). Haemoptysis recurred after 31 (61%) of BAE procedures with no difference in recurrence rates between massive and sub-massive haemoptysis. Side effects were reported after 61% of procedures with chest pain the most common adverse event . Mortality after first BAE in the study was 3.9% at 30 days and 14.8% at 12 months. No significant predictors of mortality were identified. CONCLUSIONS: BAE is often effective in controlling haemoptysis but is associated with considerable morbidity and high recurrence rates.


Subject(s)
Bronchial Arteries , Cystic Fibrosis/complications , Embolization, Therapeutic/methods , Hemoptysis/therapy , Adolescent , Adult , Aged , Female , Follow-Up Studies , Hemoptysis/etiology , Humans , Male , Middle Aged , Prospective Studies , Recurrence , Severity of Illness Index , Treatment Outcome , Young Adult
2.
Int J Biometeorol ; 58(9): 1845-51, 2014 Nov.
Article in English | MEDLINE | ID: mdl-24452385

ABSTRACT

The effect of changes in the weather on the respiratory health of patients with cystic fibrosis (CF) is unclear. We conducted a prospective study to determine the impact of climate and season on the incidence of viral respiratory infections (VRI) and pulmonary exacerbations (PEx) among adults with CF. Between December 2010 and April 2012, 98 adults with CF were followed for 12 months. Polymerase chain reaction assays for nine viruses were performed on sputum, nose and throat swabs every 2 months and additionally at onset of PEx. Hourly temperature and relative humidity measurements were recorded throughout the study. Statistical analysis utilized generalized estimating equation (GEE) models. Pre-specified criteria for VRI and PEx were met at 29% and 37% of visits, respectively. Rhinovirus accounted for 72% of identified viruses. Incidence of rhinovirus peaked in autumn while non-rhinovirus VRI peaked in winter. Rhinovirus was associated with increased mean temperatures (OR 1.07; p = 0.001), while non-rhinovirus VRI was associated with lower mean temperatures (OR 0.87; p < 0.001). PEx occurred frequently throughout the study with no clear seasonal pattern observed. There was no significant association between climate variables and the incidence of either PEx or antibiotic prescription. There is a seasonal pattern to VRI in adults with CF. The incidence of VRI but not PEx is associated with changes in ambient temperature.


Subject(s)
Climate , Cystic Fibrosis/epidemiology , Respiratory Tract Infections/epidemiology , Virus Diseases/epidemiology , Weather , Adult , Comorbidity , Cystic Fibrosis/diagnosis , Female , Humans , Male , Population Surveillance , Prevalence , Risk Factors , Temperature , United Kingdom/epidemiology , Virus Diseases/diagnosis , Young Adult
3.
Thorax ; 67(7): 645-9, 2012 Jul.
Article in English | MEDLINE | ID: mdl-21680564

ABSTRACT

A review is presented of key clinical papers published in Thorax and elsewhere between 2008 and April 2011 which have advanced our understanding of cystic fibrosis (CF), primary ciliary dyskinesia and non-CF bronchiectasis. Studies were identified through searches of the Thorax archive and the Medline database. Within the field of CF, the following key themes were studied: diagnosis in equivocal CF, assessment of CF lung disease, novel therapies addressing the basic defect in CF, maintenance pulmonary therapies, management of early Pseudomonas infection, the microbiology of CF lung disease, renal impairment in CF and controversies in lung transplantation in CF.


Subject(s)
Bronchiectasis/diagnosis , Cystic Fibrosis/diagnosis , Kartagener Syndrome/diagnosis , Diagnosis, Differential , Humans
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