Background: In the 7 years after the WTC disaster, the annual number of FDNY retirements attributable to pulmonary disability increased nearly 4-fold. FDNY rescue workers evaluated for pulmonary disability at our subspecialty center were previously found to have an obstructed phenotype based on FEV1/FVC, Methacholine Challenge Test (MCT) reactivity, or bronchodilator (BD) reactivity (59% of N=1720). In this pilot study, we examined the long-term efficacy of treatment and its effect on disease progression in a subgroup (N=450) of individuals with subspecialty pulmonary testing who were referred for disability evaluation before and after a course of treatment. Methods: Our study cohort includes individuals that were symptomatic, had subspecialty pulmonary testing (pre-treatment), and were referred for disability evaluation after a full course of treatment (post-treatment). Disability evaluations were performed 30 days after weaning from inhaled medication. Individuals were excluded if their post-treatment PFT was less than three months after starting treatment. Change in lung function over time and post treatment were analyzed (N=415). Values are presented as medians with IQR. We defined statistical significance as P<0.05 using the paired t-test. Analyses were performed using GraphPad and SPSS software. Results: Individuals evaluated by MCT presented for disability evaluation earlier, with a shorter interval of treatment (7.5 months (5-10)) compared to those that received spirometry with BD, (14.5 months (8-25) p<0.0001). FEV1 %Pred and FEV1/FVC declined significantly; p<0.0001. FEV1 observed declined at a slower rate in the treatment group than in the entire WTC-exposed FDNY cohort, including those not referred for subspecialty evaluation: 15cc/year vs. 26cc/year. After treatment course, BD response was unchanged, but methacholine reactivity improved significantly. There was no difference between individuals receiving bronchodilator response and methacholine challenge in FEV1 or FEV1/FVC both pre- and post treatment, the decline FEV1 from pre- to post-treatment, time to entry into treatment cohort, or demographics (years of service, exposure, age at 9/11, or BMI). Conclusion: Treatment with removal from fire fighting, inhaled steroids and beta agonists did not improve spirometric measures, or BD response, but slowed the rate of decline and decreased hyper-reactivity to the MCT. Improvement in reactivity defined by MCT but not defined by BD response suggests that the pathways leading to BD response and MCT reactivity may be different and may respond differently to treatment.
Links with this icon indicate that you are leaving the CDC website.
The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website.
Linking to a non-federal website does not constitute an endorsement by CDC or any of its employees of the sponsors or the information and products presented on the website.
You will be subject to the destination website's privacy policy when you follow the link.
CDC is not responsible for Section 508 compliance (accessibility) on other federal or private website.
For more information on CDC's web notification policies, see Website Disclaimers.
CDC.gov Privacy Settings
We take your privacy seriously. You can review and change the way we collect information below.
These cookies allow us to count visits and traffic sources so we can measure and improve the performance of our site. They help us to know which pages are the most and least popular and see how visitors move around the site. All information these cookies collect is aggregated and therefore anonymous. If you do not allow these cookies we will not know when you have visited our site, and will not be able to monitor its performance.
Cookies used to make website functionality more relevant to you. These cookies perform functions like remembering presentation options or choices and, in some cases, delivery of web content that based on self-identified area of interests.
Cookies used to track the effectiveness of CDC public health campaigns through clickthrough data.
Cookies used to enable you to share pages and content that you find interesting on CDC.gov through third party social networking and other websites. These cookies may also be used for advertising purposes by these third parties.
Thank you for taking the time to confirm your preferences. If you need to go back and make any changes, you can always do so by going to our Privacy Policy page.