A placebo-controlled, double-blind trial of the long-term effects of albuterol administration in patients with cystic fibrosis.

Author: BarberoG J, KönigP, PoehlerJ

Paper Details 
Original Abstract of the Article :
This placebo-controlled study was designed to confirm a previously performed open label study that showed significant improvement in spirometry on maintenance therapy with albuterol for 1 year. In a double-blind, cross-over trial, albuterol (by metered dose inhaler) 180 microg b.i.d. or placebo were...See full text at original site
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引用元:
https://doi.org/10.1002/(sici)1099-0496(199801)25:1<32::aid-ppul3>3.0.co;2-q

データ提供:米国国立医学図書館(NLM)

Albuterol for Cystic Fibrosis: A Long-Term Perspective

My dear researchers, cystic fibrosis (CF) is a complex disease, a challenging desert landscape for those who live with it. This study investigates the long-term effects of albuterol administration in patients with CF, a journey of seeking relief and improving quality of life in the face of adversity.

A Journey of Relief and Hope

The study found that maintenance therapy with albuterol led to significant improvements in spirometry, a measure of lung function, in patients with CF. It's like finding a source of water in the desert, providing a temporary respite from the harsh conditions. The researchers also noted a reduction in hospitalizations among patients on albuterol, offering a glimmer of hope for a more stable and comfortable existence.

Navigating the Desert of CF

This study underscores the potential benefits of long-term albuterol therapy in managing CF. While further research is needed to fully understand the mechanisms at play, this research provides a promising avenue for improving lung function and quality of life for patients with CF. It's a reminder that even in the most challenging of journeys, there is always the possibility of finding relief and hope along the way.

Dr. Camel's Conclusion

This study offers valuable insights into the long-term benefits of albuterol therapy in managing cystic fibrosis. While further research is needed to fully understand the mechanisms at play, this research provides a promising avenue for improving lung function and quality of life for patients with CF. Just as a wise traveler in the desert learns to adapt to the changing environment, we must continue to explore and refine treatment strategies to ensure the well-being of those living with this complex disease.

Date :
  1. Date Completed 1998-04-02
  2. Date Revised 2019-09-14
Further Info :
SNS
PICO Info
in preparation
Languages

English

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