Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach

Background/objective: Recurrent hemoptysis is a debilitating complication of cystic fibrosis (CF) and likely results from mucosal erosions into abnormal bronchial blood vessels due to chronic respiratory infection. We hypothesize that the use of beta-blockade will decrease mean arterial pressure res...

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Main Authors: John Moua, Eliezer Nussbaum, Eileen Liao, Inderpal S. Randhawa
Format: Article
Language:English
Published: SAGE Publishing 2013-08-01
Series:Therapeutic Advances in Respiratory Disease
Online Access:https://doi.org/10.1177/1753465813482744
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spelling doaj-eec6de0c79e44b668fc8377adff19dfe2020-11-25T02:59:18ZengSAGE PublishingTherapeutic Advances in Respiratory Disease1753-46581753-46662013-08-01710.1177/1753465813482744Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approachJohn MouaEliezer NussbaumEileen LiaoInderpal S. RandhawaBackground/objective: Recurrent hemoptysis is a debilitating complication of cystic fibrosis (CF) and likely results from mucosal erosions into abnormal bronchial blood vessels due to chronic respiratory infection. We hypothesize that the use of beta-blockade will decrease mean arterial pressure resulting in lower bronchial artery blood flow and, subsequently, decrease the frequency and severity of hemoptysis, rate of hospitalizations, and usage of intravenous antibiotics. Methods: Retrospective chart review was performed on 12 CF patients with recurrent hemoptysis, aged 13–40 years old, along with a follow-up telephone survey to assess the effectiveness of beta-blockade for hemoptysis, tolerance of inhaled respiratory medications, activity tolerance, and potential adverse effects. A beta-blocker, specifically atenolol, was initiated in all subjects within 24 hours after experiencing recurrent hemoptysis episodes. Results: A majority of patients (72.7%) had complete cessation of hemoptysis. There were significant decreases in the frequency of hemoptysis ( p = 0.02) and the amount of hemoptysis ( p = 0.004). The rate of hospitalizations significantly decreased from 1.33 to 0.67 ( p = 0.05) after initiation of atenolol. There was a trend toward statistical significance in the reduction of intravenous antibiotics use ( p = 0.08). No statistical difference was found when comparing the pre- and post-treatment means of forced expiratory volume in 1-second ( p = 0.59). Very minimal adverse effects were observed with only one patient reporting intermittent facial flushing. Conclusion: Beta-blockade, particularly with atenolol, appears to successfully treat, if not resolve, recurrent hemoptysis refractory to conservative therapy in CF. Beta-blocker therapy appears to maintain an effective safety profile in CF.https://doi.org/10.1177/1753465813482744
collection DOAJ
language English
format Article
sources DOAJ
author John Moua
Eliezer Nussbaum
Eileen Liao
Inderpal S. Randhawa
spellingShingle John Moua
Eliezer Nussbaum
Eileen Liao
Inderpal S. Randhawa
Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach
Therapeutic Advances in Respiratory Disease
author_facet John Moua
Eliezer Nussbaum
Eileen Liao
Inderpal S. Randhawa
author_sort John Moua
title Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach
title_short Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach
title_full Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach
title_fullStr Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach
title_full_unstemmed Beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach
title_sort beta-blocker management of refractory hemoptysis in cystic fibrosis: a novel treatment approach
publisher SAGE Publishing
series Therapeutic Advances in Respiratory Disease
issn 1753-4658
1753-4666
publishDate 2013-08-01
description Background/objective: Recurrent hemoptysis is a debilitating complication of cystic fibrosis (CF) and likely results from mucosal erosions into abnormal bronchial blood vessels due to chronic respiratory infection. We hypothesize that the use of beta-blockade will decrease mean arterial pressure resulting in lower bronchial artery blood flow and, subsequently, decrease the frequency and severity of hemoptysis, rate of hospitalizations, and usage of intravenous antibiotics. Methods: Retrospective chart review was performed on 12 CF patients with recurrent hemoptysis, aged 13–40 years old, along with a follow-up telephone survey to assess the effectiveness of beta-blockade for hemoptysis, tolerance of inhaled respiratory medications, activity tolerance, and potential adverse effects. A beta-blocker, specifically atenolol, was initiated in all subjects within 24 hours after experiencing recurrent hemoptysis episodes. Results: A majority of patients (72.7%) had complete cessation of hemoptysis. There were significant decreases in the frequency of hemoptysis ( p = 0.02) and the amount of hemoptysis ( p = 0.004). The rate of hospitalizations significantly decreased from 1.33 to 0.67 ( p = 0.05) after initiation of atenolol. There was a trend toward statistical significance in the reduction of intravenous antibiotics use ( p = 0.08). No statistical difference was found when comparing the pre- and post-treatment means of forced expiratory volume in 1-second ( p = 0.59). Very minimal adverse effects were observed with only one patient reporting intermittent facial flushing. Conclusion: Beta-blockade, particularly with atenolol, appears to successfully treat, if not resolve, recurrent hemoptysis refractory to conservative therapy in CF. Beta-blocker therapy appears to maintain an effective safety profile in CF.
url https://doi.org/10.1177/1753465813482744
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