Background

The risks to firefighters’ respiratory health are well known. Reductions in lung function, increases in airway hyper-responsiveness, and the onset of other symptoms of respiratory illness have been reported in firefighters following exposures during firefighting duties [1,2,3,4,5,6].

Other reports indicate that firefighters have better lung function than the general population in both FEV1 and FVC: likely due to a strong healthy worker effect [7,8,9,10]. This makes the routine comparison of these values to a reference standard following a single pulmonary function test more challenging, and may serve to misclassify some firefighters’ lung function. For example, a firefighter with an FEV1 of 5.0 l (and 130% of predicted) could lose more than 1 litre before being below 100% of predicted normal, and more than two litres before being below the lower limit of normal (LLN) [11]. Serial measurements and subsequent analyses of the rate of change in lung function may represent the most useful way of monitoring firefighter respiratory health.

The long-term rate of change in FEV1 in healthy, non-smoking adults of working age was initially reported by Fletcher and Peto as − 36 mL/yr [12]. Further studies have reported rates of change ranging from around − 20 to − 38 mL per year [13,14,15,16,17,18,19,20,21], and as much as 56 mL per year [22]. Despite the known occupational hazards, it is not yet clear whether long-term routine firefighting leads to a greater rate of decline in lung function than would normally be expected. This review aims to answer the following questions: 1) What is the rate of change of lung function in professional urban firefighters? 2) How is this rate of change influenced by level of exposure to routine firefighting and non-routine firefighting (i.e. catastrophic events) and protective or deleterious factors? 3) How is the rate of change in lung function measured/calculated and reported in studies of professional firefighters?

Methods

This systematic review was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement guidelines [23], and the protocol was registered on the International Prospective Register of Systematic Reviews (PROSPERO) (registration number CRD42017058499).

Selection of studies

Studies selected for review had to satisfy three conditions: 1) FEV1 and/or FVC had to be measured in the same individuals on more than one occasion (if not using regression techniques), with a minimum observation period of 12 months; 2) The rate of change in either FEV1 or FVC had to be available directly or calculable from the presented data; and 3) Participants had to be adult (≥ 18 years of age) full-time professional urban firefighters; excluding part-time, volunteer and country/wildland firefighters. There was no restriction placed on publication date or language.

Search strategy

Relevant publications were initially sought with a systematic search conducted on March 8 2017, using the online electronic databases CINAHL, Embase, Medline, Medline (Epub ahead of print), Scopus and Web of Science. Under the advice of an academic librarian, the following keyword string was used to find candidate papers: ((“fire fighter*” or firefighter* or firem#n or “fire m#n”) or (fire [within three words] personnel)) AND ((“lung* function” or “pulmonary function” or respiratory) or (FEV* or “forced expiratory volume*” or FVC* or “vital capacit*” or spirometr*)). When available, the following subject headings were also combined with the keyword search (Firefighters/) AND (Lung/ or spirometry/ or vital capacity or forced vital capacity or forced expiratory volume or respiratory airflow). Two authors independently conducted all searches, collated all returned titles and abstracts and removed duplicate items.

Title and abstract screening

All titles and abstracts were independently screened to assess each item’s suitability for full-text review. When the title or abstract provided insufficient information to make a decision, the full-text paper was retrieved. The authors then independently reviewed all selected full-text papers and selected eligible papers for inclusion. Reference lists and citations (Google Scholar search March 29 2017) of eligible papers were then screened and the full-texts of relevant papers were examined: eligible papers were then included for review. Discrepancies were resolved at each stage of the selection process by discussion between the two authors, with a third author available for adjudication in case of disagreement.

Data extraction

Data from each included paper were independently entered into a database by two authors. Extracted information included, but was not limited to, the characteristics of the cohort(s) studied, study methodology and results. When the data were only reported graphically, they were extracted using an online tool [24]. When the rate of change in FEV1 and/or FVC was not reported and unavailable from the authors, it was calculated (and rounded to the nearest whole millilitre) as the difference between baseline and follow-up value divided by the time interval (or when more than two data points were available: calculated by using simple linear regression). When available, the respective rates of change were reported stratified by smoking status as well as for the entire cohort. When stratified data were not available, and the average rate of change for the entire cohort was reported alone, as well as the cohort’s smoking rate.

Quality assessment

Included studies were critically appraised to determine their risk of bias using the Research Triangle Institute Item Bank (RTI-IB) on Risk of Bias and Precision of Observational Studies [25], which provides a means to assess the quality of studies related to exposure outcomes. The RTI-IB is one of the only quality appraisal scoring tools available for observational studies, providing a comprehensive list of 29 questions covering a range of categories of bias [26]. The authors recommend the tool be modified based on its appropriateness to the literature. For this reason, questions 8, 12, 26 and 27 of the tool were omitted, due to their inapplicability to the topic, while a “cannot determine” response was added to question 13. The critical appraisal was carried out independently by two authors, with discrepancies being resolved by discussion. Each study was given a score based on the number of applicable RTI-IB items met and subsequently graded, based on previous publications [27,28,29] as low (0–.40), moderate (.41–.70), or high (.71–1) methodological quality/risk of bias.

Data analysis

A descriptive analysis was conducted due to the large heterogeneity of the included studies in terms of their population characteristics, type of assessment of exposure, and reporting of outcome measures.

Results

The searches yielded a total of 788 unique articles, including eight that were identified through reference checking (Fig. 1). Following the screening and review process, a total of 22 papers met the eligibility criteria and were included for review.

Fig. 1
figure 1

PRISMA flow diagram of included and excluded studies

Characteristics of included studies

Descriptive information about the included studies is summarised in Table 1 and includes study location and dates, the baseline characteristics of the study population and the methods of conducting spirometry and measuring exposure.

Table 1 Descriptive information. Studies are ordered by population type and year of publication

Within the 22 studies, all published between 1974 and 2016, there were 11 distinct firefighter populations: one from each of Australia [8] and South Korea [30], two from England [31, 32] and the remaining seven from the USA. These seven populations consisted of firefighters from Baltimore [33], Boston in both the 1960/1970s [34,35,36,37] and 1990s [38], Houston [39] and Phoenix [40,41,42,43], as well as New York firefighters exposed [44,45,46,47,48] or not-exposed to 9/11 [9]. The average age of active firefighters at study commencement ranged from 26.1 to 43.6 years, while recently-retired firefighters of one study [36] had an average age of 54.5 years. Seven studies involved both sexes (the highest proportion of female firefighters was 4%) and the remaining included males only. Eleven studies reported the proportions of different racial groups, with the majority of firefighters in each study (76.4 to 100%) being Caucasian/white and the rest being reported as African-American/black (0 to 6%), Hispanic (0 to 19.5%) or unspecified (0 to 14.4%). Two studies reported race without specifying proportions and nine did not report any racial information. Average follow-up time ranged from one to 12.2 years and each study measured lung function at least once, with the highest average number of measures reported being 10.3. Ten studies performed standardised spirometry based on published criteria, nine performed standardised spirometry (usually best or average of three trials) but not according to published standards and three did not report information on spirometry standardisation. The most common method of estimating firefighting exposure was self-report questionnaire (n = 15), and three of these studies combined this with an estimate of exposure based on fire department records (one of which did not use these data during analysis). One study obtained information by interview using a structured questionnaire and the remaining six either did not measure exposure, or did not report any measurement.

The rate of change in FEV1 and FVC

Routine firefighting

Sixteen studies reported on firefighter populations involved in routine firefighting (Table 2). Among nine studies reporting FEV1 change without stratifying by smoking status (smokers and non-smokers pooled together), six observed declines of between − 24.99 and − 39.6 mL/yr. [33, 35, 40,41,42,43] while the remaining three showed declines of − 68.2 to − 110 mL/yr. [30, 31, 37]. Within these nine studies, four included smoking status in their regression modelling: two studies observed significantly greater declines in both ever-smokers relative to never-smokers (additional 4.7 mL/yr. decline, p = 0.042) [42] and current smokers relative to non-smokers (Actual difference and p value not reported) [31], while the two others reported no significant effect [40, 41]. One study reported different rates of decline when stratified by occupational exposure, but observed no significant differences in smoking habits between the groups [37] while the remaining four studies did not report on the longitudinal effect of smoking on lung function [30, 33, 35, 43]. Five studies reported on the rate of change in FVC without stratifying by smoking status, observing declines of − 16.55 (66.75) [33], -40 [35], -76.7 [37], -103 [30] and − 107 [31] mL/yr. (SD (where available)). Among these studies, one reported significantly greater declines in current smokers relative to non-smokers (p value not reported) [31].

Table 2 Rate of decline in FEV1. Studies are ordered by population type and year of publication. Values are means (SD), medians [IQR] or means [95% CI]

Six studies reported changes in lung function in firefighters involved in routine firefighting stratified by smoking status. Two studies observed significantly less negative rates of change in FEV1 in never smokers than other smoking groups [36, 38] and four studies found no significant differences [8,9,10, 32]. One study reported an FVC decline in never smokers of − 10 mL/yr. [36], significantly less negative than current smokers, while four others reported rates of change in FVC of − 19 [9], -27 (52) [34], -66, [32] -76.8 (10.7) [10], and + 11.2 (140.3) [8] mL/yr. (SD), with no significant differences compared to other smoking groups.

Six studies compared lung function changes in firefighters involved in routine firefighting to non-firefighter controls [8,9,10, 30, 32, 43]. One study showed a significantly greater rate of FEV1 decline in firefighters vs. industrial workers [30], one showed a significantly greater rate of decline in general population controls vs. firefighters [32], and four did not report any significant differences in changes in FEV1 compared to general population controls [8, 10], emergency medical workers [9] or paper-pulp mill and construction workers [43]. Five studies compared changes in the FVC of firefighters vs non-firefighters with two showing significantly greater FVC declines in firefighters [10, 30], one showing significantly greater FVC declines in non-firefighters [32], and two showing no significant differences [8, 9].

Non-routine firefighting

Six studies reported changes in lung function of firefighters exposed to non-routine firefighting [39, 44,45,46,47,48]. Firefighters involved in one study were exposed to smoke during a chemical warehouse fire [39], and experienced declines in FEV1 and FVC of − 81.3 and − 41.33 mL/yr., respectively, in the time between measurements after exposure and 18 months later. The remaining five studies reported on the changes in FEV1 observed in a cohort of New York firefighters following World Trade Centre site exposure after the terrorist attacks of September 11, 2001 (9/11). The pre-9/11 rate of change in FEV1 in firefighters and Emergency Medical Service (EMS) workers was reported as − 31 mL/yr. [44], while each group lost an average of 383 [95% CI, 374–393] mL and 319 [299–340] mL, respectively, in the first year following the disaster. In the 7 years after the initial reduction, the rate of change in FEV1 (adjusted for age, height, race and sex) of never-smoking firefighters was − 26 [95% CI, 20–31] mL/yr.: less than that of former or current smokers and significantly different from the − 40 [38,39,40,41,42] mL/yr. observed in never-smoking EMS workers [45]. A similar rate FEV1 decline of − 26.4 mL/yr. was observed in a follow-up study of the never-smoking firefighters after 13 years [46]. Compared to continuing smokers, the rate of change in FEV1 of former smokers who quit before or after 9/11 was significantly less negative. Two small subgroups of 9/11-responding firefighters were also studied, observing post-9/11 FEV1 declines of − 36.7 mL/yr. (adjusted for age, bronchial hyper-reactivity, height, race, steroid use and the initial loss of lung function related to 9/11 exposure) [47] and 37 mL/yr. (adjusted for age, height, interaction of smoking with AAT deficiency, length of FDNY tenure, race, sex, smoking, work assignment on 9/11 and WTC exposure intensity) [48].

In summary, most studies of non-smoking firefighters exposed to routine firefighting showed negative rates of change in FEV1 and FVC that were analogous to the rates observed in longitudinal studies of healthy non-smokers in the general population [12,13,14,15,16,17,18,19,20,21,22]. Those that showed greater rates of decline than would normally be expected were either less than [32] or not significantly different to [10] general population controls in direct comparisons, or were particularly limited by a lack of information on smoking status [30, 31, 37]. Firefighters exposed to non-routine events experienced significant reductions in lung function in the initial year after exposure, with long-term rates of change representing normal decline without recovery.

Influence of firefighting and protective or deleterious factors

Influence of firefighting exposure level

In their 1974 report of Boston firefighters, Peters and colleagues showed significant inverse relationships between self-reported fire exposure over a 12-month period and changes in FEV1 and FVC [37]. However, no significant relationship was observed in three [35] and six-year [34] follow-up studies on the same population, using self-reported exposure and estimates derived from fire department records. A significantly greater FEV1 decline was observed in active vs inactive firefighters in one study [33] but is contrasted by two others which showed trends of higher rates of decline in inactive vs active firefighters [34, 35], while a further study showed no difference [30]. No studies identified a relationship between service time and rate of change in FEV1 or FVC [10, 30, 31, 33, 35, 36]. One study reported significantly greater rates of FEV1 decline in firefighters who reported previous exposure to ammonia, however past chlorine exposure had no apparent effect [33].

Firefighters responding to the 9/11 disaster experienced dramatic declines in FEV1 in the first year following exposure [44,45,46,47,48]. Measured by self-reported arrival time, a significant dose-response relationship was observed between exposure intensity and loss of FEV1 [44]. Firefighters that reported the greatest dust exposure (those arriving earliest) also experienced the greatest rate of FEV1 decline in the subsequent 7 and 13-year follow-ups [45, 46].

The included studies show a dose-response relationship between changes in lung function and exposure level in non-routine severe firefighting events, but results were inconsistent regarding the presence of such an effect of exposure level in routine firefighting.

Influence of respiratory protection

Four studies investigated the effect of respiratory protection on changes in FEV1. In one study, firefighters who reported ‘never or rarely’ using their respiratory protection during fire knockdown had higher odds of ‘accelerated’ FEV1 decline (greater than 50 mL/yr) compared with those who used it ‘often or frequently’ (Odds Ratio = 2.20, 95% Confidence Interval = 1.02–4.74, p = .044) [8]. Another study observed a greater FEV1 decline in firefighters who reported ‘never’ vs ‘ever’ using a mask while extinguishing fires (− 68.44 vs − 30.90 mL/yr), but the association was only significant in those with non-repeatable spirometry [33]. There was no significant difference in changes of FEV1 based on mask-use during fire overhaul (clean-up). A further study showed no relationship between the rate of change in FEV1 and the stated tendency of firefighters to wear protective respiratory apparatus [34] while there was also no identifiable protective effect of using any type of protective mask during the response to the 9/11 disaster [44].

Influence of other factors

In the five studies that included covariates in their models to estimate changes in lung function, four included race, sex and smoking status as well as baseline age and height [44,45,46, 48], while one included only race as well as baseline age and height: due to the absence of females and separate analyses with smokers [9]. Three of these studies included weight at baseline [9, 45, 46] with one also including weight change in a separate model [9]. These five variables as well as a further 20 were included in subsequent modelling to investigate factors that affect the rate of change in lung function (all variables listed in Table 2). Overall, noteworthy predictors included weight gain, which was associated with a significantly greater decline in FEV1 in two studies [9, 46] and close to being significant in another [41], while four studies observed significantly increased or decreased rates of FEV1 decline based on different variations in gene expressions [40,41,42, 48]. One study associated the development of bronchial hyper-reactivity with a significant increase in FEV1 decline in 9/11-exposed firefighters, while the use of steroids was associated with a less negative rate of change in FEV1 [47].

Calculation/measurement and reporting of the rate of change in FEV1 and FVC

Eight studies calculated the rate of change in FEV1 and/or FVC as the change in volume divided by the change in time using data from two time-points [8, 10, 33,34,35,36,37, 47]: four of which had measured lung function on more than two occasions [34,35,36]. Five studies used simple linear regression [32, 40,41,42,43], five used linear mixed models [9, 44,45,46, 48], while a further four did not report on the rate of change, or did not report their method of calculation [30, 31, 38, 39]. There was no apparent indication that any technique was more biased toward positive, negative or null results.

Six studies reported on the proportion of firefighters with a decline in FEV1 or FVC that was greater than a particular cut-off: often referred to as an ‘accelerated’ or ‘greater than expected’ decline. The cut-offs (proportion of firefighters above cut-off) were set at declines of > 50 mL/yr. (Fire: 26%, Controls: 39%) [8], > 60 mL/yr. (18.4% [42], 23% [40]), > 64 mL/yr. (19.5%) [46], ,> 75 mL/yr. (50.8%) [38] and > 90 mL/yr. (4.8%) [43], with the latter study also using a relative cut-off of > 2.1% per year (5.6%) [43]. One study also reported on FVC declines of greater than 75 mL/yr. (35.1%) [38].

Quality assessment/risk of bias

Two articles were rated as high quality/low risk of bias, 12 as moderate quality/moderate risk of bias, and eight as low quality/high risk of bias (Table 3).

Table 3 Summary of individual study quality/risk of bias assessment using the RTI-IB. Studies are ordered by population type and year of publication

The most evident biases were performance bias, information bias and attrition bias. Studies generally failed to use valid and reliable means of measuring exposures and did not report them with great detail in respect to the measurement and reporting of confounding variables. Seven studies reported loss to follow-up of greater than 30%, yet none investigated any potential effect of this through sensitivity analyses or other adjustment methods.

Biases that were the most unclear were selection bias/confounding, detection bias, performance bias and precision. The most common issues were around the clarity of inclusion/exclusion criteria, the lack of clarity in reporting blinding of assessors to exposure status as well as the appropriateness of statistical techniques: although this was mainly a reflection of the age of the studies.

Discussion

To our knowledge, this is the first study to systematically review the literature measuring longitudinal changes in lung function of professional urban firefighters and its associations with occupational exposure. Among firefighters exposed to routine firefighting, the reported rates of change in lung function were variable and ranged from normal rates of decline to what could be considered accelerated: particularly among current smokers. There is a general lack of evidence of a relationship between measures of routine firefighting exposure and long-term changes in lung function: though this may be primarily due to limitations in exposure measurement itself. In contrast, exposure to non-routine disastrous events is more clearly related to reductions in lung function.

The large variability in the reported rates of change in lung function of firefighters exposed to routine firefighting make definitive conclusions difficult. Most observations among never-smokers were consistent with other longitudinal studies of the general population, or were at least no more negative than non-firefighter general population controls. However, the range of findings and low rating in quality assessments among included studies, and the fact that there is no clear upper limit of normal lung function decline, precludes any definitive conclusions about the risks of accelerated longitudinal declines in lung function of professional urban firefighters in relation to routine firefighting.

Among studies of routine firefighters, the study with the highest score (0.63) in the quality rating/lowest risk of bias assessment consisted of 5 years of annual measurements and provides the best evidence of the effect of contemporary firefighting on lung function [9]. Firefighters in this study experienced a longitudinal rate of change in FEV1 of − 45 mL/yr. which was equal to that of unexposed controls. While this is greater than the rate of decline reported in most longitudinal studies of healthy adult non-smokers, it is still less than is reported by others such as Tashkin et al. [22] This highlights the difficulties associated with comparing rates of change in lung function between studies of different periods, which utilised different recruitment strategies as well as different equipment and standards of lung function testing. For these reasons, studies that make direct comparisons to a well-matched (yet unexposed) reference group who are sampled in the same way, are particularly valuable, but equally scarce.

One of the few studies employing a control population made a surprising observation of an increase in FEV1 and FVC in non-smoking firefighters concurrent to a decline in age-matched, non-smoking general population controls [8]. Although this may be somewhat influenced by the inclusion of younger firefighters whose lungs may still be maturing, the mean changes in FEV1 and FVC for firefighters aged 36–45 years were positive. This is contradictory to the notion that lung function declines after peaking during in the third decade of life [15, 21, 49,50,51]. Caution, though, is needed in interpreting these results, as this study would have benefited from further follow-up in order to reduce any possible effect of statistical regression to the mean.

In attempting to quantify the effect of routine firefighting exposures on changes in lung function, multiple different strategies have been employed, each with limited success. The number of responses to fires has not been meaningfully associated with negative changes in FEV1 or FVC, either through estimates based on fire department records (FDR) or recalled by firefighters themselves [33,34,35,36]. Musk et al. [35] also reported a poor correlation between the two methods, which may suggest that firefighters cannot accurately recall their exposures over a twelve-month period, that the FDR method of estimation was unreliable, or both. Service/employment time has also been a poor index of exposure [10, 31, 33, 35, 36], and has questionable validity given the way in which firefighters can move between active and inactive roles throughout their careers. This movement of workers also undermines any assumptions that active firefighters have had greater exposures than inactive firefighters, given that firefighters may self-select out of active roles as a direct result of poor health following work-related exposure. Further crude indices of exposure have included self-reported heavy smoke exposure, informally described as “shellackings” [35, 37], “lungers” or “pastings” [34], as well as absence from work following exposure to smoke [31], showing no significant associations with changes in lung function.

Examined separately from studies of firefighters exposed to routine firefighting, studies investigating changes in lung function following severe exposure reveal consistent outcomes of accelerated declines in lung function. Observing firefighters immediately following exposure to a chemical warehouse fire, Unger et al. [39] reported a high average rate of decline in FEV1 over the subsequent 18 months. While a lack of pre-exposure data is a limitation of the study, the rate of decline may have even been underestimated, if there were cases of lung function recovery, over the course of follow-up. This may provide an example of how studies involving ‘non-routine events’ could bias the estimate of the rate of change in lung function following the event and supports the separate interpretation of the results in this review. This issue also applies to the studies which followed firefighters after 9/11 [44,45,46,47,48]. In addition, some of these studies included firefighters who retired during follow-up and thereby removing them from firefighting exposures which may further affect estimates of the rate of change in lung function. Notwithstanding these issues, these studies were among the highest quality rated studies with the lowest risk of bias and have benefitted from the presence of several years of pre-exposure data. They provide unequivocal evidence of the dramatic long-term negative effect of this exposure on lung function and highlight the importance of routine lung function surveillance in firefighters.

Among all studies included in the review that made the comparison, most studies observed greater rates of decline in never-smoking firefighters compared to current-smoking firefighters. Although the significance of this difference was not always tested statistically, the excess declines in current smokers were comparable to those observed in general smoking population [52, 53]. Cigarette smoking has the potential to be particularly dangerous to firefighters, given that it has been linked with reductions in immune responses [54], which may leave them more vulnerable to the dangers of fire smoke. Based on the information available in this review, however, it was not possible to speculate any further than this.

Along with smoke exposure, both from fires and cigarettes, one of the most important variables affecting firefighter lung function trajectories is the use of respiratory protection, which has undergone many changes across the time periods of the included studies. The US-based National Fire Protection Association (NFPA) produced its first Standard for Respiratory Protective Equipment for Firefighters (NFPA 19B) in 1971, with the aim of prohibiting filter-type canister masks for firefighters and permitting only self-contained breathing apparatus (SCBA) [55]. The regularly updated standard has overseen improvements in technology that are likely to have influenced the frequency with which SCBA is utilised by firefighters, which may have implications on respiratory health. In their pioneering studies of the early 1970s Boston, Musk et al... found no relationship between firefighters’ “self-stated tendency” to use respiratory protection and changes in FEV1, but provided no further information on the frequency of use [34]. Tepper and colleagues later compared changes in the FEV1 of firefighters who reported ‘never’ vs ‘ever’ using a mask while extinguishing fires, showing little association [33]. This method, though, may lack sensitivity due to the use of the broad term ‘ever’, which may have grouped together those who have used it once only, or at every response. Two decades later, Schermer et al [8] showed that firefighters who reported ‘never or rarely’ using respiratory protection during fire suppression were significantly more likely than others to experience greater declines in FEV1. They were also less likely to not use respiratory protection during fire overhaul: the period following extinguishment of visible flame, when exposures are still dangerous [56, 57]. These firefighters were also more likely to be older, suggesting a possible cohort effect whereby use of respiratory protection increases with each new generation of firefighters. Among responders to the 9/11 disaster in New York in 2001, there was no identifiable protective effect of using any type of protective mask [44]. However, this is likely due to the fact that most firefighters were entirely unprotected, or wore only a disposable mask in the first 2 days of the event [58].

Studies that received the highest quality assessment/lowest risk of bias scores tended to be among the most recently published studies, and employed more contemporary statistical methods of analysis [9, 44,45,46,47,48]. Among the remaining studies, there was no discernible relationship between publication date and quality. Mixed models approaches offer several advantages over other ‘pre-post’ analyses, with the latter being more susceptible to influence by measurement error. Further, given the natural variability in lung function measurements, studies with more than two measures of lung function over five or more years of follow-up can more precisely and reliably evaluate the rate of change in lung function [18]. Those studies that met this criterion tended to report normal rates of decline in FEV1 or FVC. None of the included studies assessed for non-linear changes in lung function.

A limitation of this review was the absence of meta-analytical techniques, which were precluded by the lack of homogeneity across studies published over several decades. The review may also be limited by publication bias, as it did not include evidence that was unpublished or pending publication. Additionally, the minimum follow-up time for studies to be included was 1 year. Given the value of repeated measurements over long periods [18], approximately half of the studies included may be too short to provide truly meaningful insights into the way lung function changes over time. Further, due to the manner in which published data were reported, some data were estimated from graphical figures using computer software, or calculated from the data that were available and this may have reduced the precision of estimates of rate of change. Moreover, the focus of this review was on professional urban firefighters, whose exposures may differ in type, intensity and duration to those of wildland firefighters. Although exposure to wildland firefighting has produced cross-shift [59] and cross-seasonal [60] reductions in lung function, further studies are needed to investigate the long-term effects of such firefighting.

Conclusions

The data provided by longitudinal studies, which were mostly concerned with FEV1, are highly variable and provide an unclear picture of how the rate of change in lung function of firefighters relates to routine exposures and how it compares to the rate of change expected in a non-exposed working-age population. Firefighters who abstain from cigarette smoking and who routinely wear respiratory protection are more likely than otherwise to have a normal rate of decline in lung function. Exposure to catastrophic events, such as 9/11, significantly increases the rate of decline in lung function but there is limited evidence detailing the effect of routine firefighting and future studies will benefit from more robust methods of measuring exposure.