In this study we developed a model for the prediction of prolonged work absence at 6 months follow-up in a cohort of workers on sick-leave due to LBP by the use of a broad spectrum of demographic, work, LBP and psychosocial related prognostic factors. We identified that moderate to poor job satisfaction, a higher score of fear avoidance beliefs, higher pain intensity at baseline, a longer duration of complaints and female gender were associated with a higher risk of not returning to work at 6 months.
Comparison with Findings in the Literature
In our study “moderate” and “poor” job satisfaction was found to be responsible for a longer time until RTW. Job satisfaction in relation to RTW is part of the evidence that work-related psychosocial characteristics might be relevant factors for workers to maintain work [8]. In a recent review it was concluded that there is strong evidence that job satisfaction is not associated with a longer time off work [6]. Adding our study to this review would result in conflicting evidence of job satisfaction as an important factor associated with sick-leave due to LBP. This indicates that job satisfaction might influence the course of disabling LBP and that evidence of this factor has to be confirmed.
There is a lack of prognostic studies in occupational health care that examine associations between psychological factors, like fear avoidance beliefs, and RTW [31]. Psychological beliefs have been identified as important factors in relation to the course of LBP and accompanying sick-leave [32]. The effect of fear avoidance beliefs on prolonged sick-leave in our study was small. A more pronounced relationship of fear-avoidance with future LBP work absence was shown by Fritz et al. [33]. Although the role of psychosocial beliefs in association with RTW is inconclusive [7], the presence of this association in the context of other potential prognostic factors in an occupational setting needs further attention.
A higher level of pain intensity at baseline and a longer duration of complaints at study inclusion have been identified as relevant prognostic factors in several studies before [32, 34]. The duration of complaints can be related to the severity of the LBP, which in turn may be responsible for a longer work absence. Von Korff et al. [34] stated that pain intensity is related to pain severity and limitations in functioning and work. Von Korff et al. showed that back pain does not have to be present all the time. The pain may be present in the background for a longer time at a lower level of pain intensity and may flare-up. Flare-ups are frequently seen in chronic LBP patients and are in combination with higher levels of functional limitations, like problems with work activities, responsible for higher pain severity and consequently work absence [34].
In the current study gender, i.e., female sex, was associated with a higher risk of sick-leave at 6 months follow-up. The review of Steenstra et al. [6] showed that female gender is associated with a longer time off work. An explanation of this gender difference on sick-leave duration can be found in the vulnerability hypothesis. This hypothesis states that due to differences in biological (e.g., hormone physiology) or psychological factors (e.g., coping strategies) similar exposures at work might have a larger negative effect on women than on men [35].
In our study, a more frequent exposure to daily stooping did not contribute to a higher risk of prolonged sick-leave. Daily exposure to stooping is an aspect of the high work load that workers experience if they are frequently exposed to it. This factor was associated with more sickness absence due to LBP in an etiological study [36]. However, the role of this factor on the prognosis of sick-leave in LBP patients is less obvious. Some prognostic studies did find an effect of high workload on longer sick-leave [37, 38], but others did not [39, 40]. We tested in the current study if the inclusion and exclusion of the variable stooping was responsible for a change in the estimates of the regression coefficients of other variables in the final model or if it caused a change in the model performance. In both test situations similar results were produced. Therefore, we choose to report the model without the inclusion of the variable daily exposure to stooping.
The explained variance of our prediction rule was 6%. In the study of Pransky et al. [41] an explained variance of 12% was reported. Dionne et al. [42] did not present a value for the explained variance. The explained variance of the prediction model in the study of Heymans et al. [43] was, 23.7%. Other studies that developed prognostic models for RTW in an occupational setting reported explained variances of 18–30% [39, 44]. Obvious is that the values of the explained variance strongly differ between studies but that they are not high in general. A low value for the explained variance means that prognostic factors can only explain a small fraction of the variance between individual patients. We still might have missed variables that may play a role in the complex environment of occupational health care and that may influence the prognosis of sick-leave, e.g., the maintenance of contact with the employer during the sick-leave period turned to be important in a recent study [45]. It also has to be noted that the explained variance of a Cox regression model is low in general even if there are strong and highly significant predictors in the model [46].
With respect to calibration, the slope index of our prediction model was 0.90. This means that the observed and predicted probabilities are well in agreement. The bootstrap-corrected c-index of our model of 0.63 was moderate. We found three similar prediction rules for LBP patients in an occupational setting that used the outcome measure RTW. Dionne et al. [42] developed a prediction tool to identify workers at high risk of adverse occupational outcomes. Pransky et al. [41] developed a practical screening model to predict length of disability after acute occupational LBP. Heymans et al. [43] developed a nomogram to predict work status in chronic LBP patients. Their nomogram had presented a slope index of 0.91 and a c-index of 0.76. Both slightly higher than in our current study. The studies of Pransky et al. [41] and Dionne et al. [42] did not report on calibration or discrimination of their prediction tools. Pransky et al. also did not report on PPV or NPV. Dionne et al. reported PPVs of 33–57% and NPVs for their model of 74–91%. The study of Heymans et al. [43] reported PPVs in the range of 70–95% and NPVs in the range of 33–100%. With respect to the practical implication of our prediction rule we are aware that prudence has to be taken when using the prediction rule in practice. Considering an adequate cut point, at the score level of 2 the NPV is 98%, which means that the majority of patients with a score lower than 2 will not receive an intervention, which is correct. At the score levels of 6 and 10 the NPV of 89 and 84%, respectively are still high. The PPV of 41% at the score level of 10 is moderate, which means that 41% of the patients with a score of 10 and higher (i.e., patients with a poor prognosis) correctly receive an intervention. However, 59% (100%-PPV) of the patients with a score of 10 and higher receive an intervention despite their good prognosis. This may lead to misusing health care resources, high treatment costs, potential for iatrogenesis or that sick-leave duration takes longer than expected because patients think that treatments should be completed before full RTW is reached. However, from an employers’ perspective it seems more attractive to refer each patient with a score of 10 or higher to a specific treatment to stimulate work ability and work resumption.
Remarks on Our Study: Choices in the Data Analysis
In our prediction model we adjusted for the treatment effects that were examined in each RCT that delivered the patient data. Therefore, treatment effects may have influenced prediction of RTW. However, the treatment effect of usual care [11–13], and low and high intensity back schools were small [13]. The graded activity intervention showed a beneficial effect on RTW in one RCT [11] and an opposite effect on RTW in another study [12]. These interventions will therefore have a small impact on prediction of RTW. A workplace intervention proved to stimulate RTW [12]. The prognostic score of a patient may slightly improve when he will be referred to this intervention. Whether the risk scores obtained by our prediction rule can be improved in new patients by specific interventions has to be confirmed in a future RCT. We therefore present our prediction rule without involvement of the treatment variable.
Study Strengths and Limitations
The strength of our study is that we were able to include almost all variables that are mentioned in the literature as prognostic factors. Moreover, the selection of relevant predictors was not only based on evidence in the literature but also on clinical expertise of OPs. This may enhance clinical applicability of the prediction rule. According to the Dutch occupational health care guidelines, workers have to visit their OP when they are on sick-leave for not more than 8 weeks due to LBP, which was also the case in our study. Therefore, our study results are generalizable to Dutch occupational health care practice.
The success of using clinical prediction rules in practice depends among other things on how much time it will take for the patient and/or clinician to determine the final risk score and probability of outcome. Our prediction rule consists of five variables that can easily be answered by the patient. Most variables consist of one question only, i.e., job satisfaction, pain intensity, duration of complaints and gender. For the variable fear avoidance beliefs 16 questions have to be answered, which makes a total of 20 questions. The prediction rule can easily be offered via a desktop computer, in an Excel format or as a web application. In this form it will take 5–10 min to fill in the prediction rule and might it be feasible to administer the rule on a routine basis just before or during the appointment with the clinician.
A limitation of our study is that we did not test the generalizability of the prediction rule in new similar patients (external validation) [29]. Even after correction for optimism the performance of the model may decrease due to other population characteristics. The need for external validation after adjusting for optimism was for example reported in the study of Bleeker et al. [47]. However, there are good indications that internal validation by using bootstrap-corrected indices of discrimination produce estimates that can also be expected in future patients [48].
A limitation of our study is the low explained variation and moderate clinical performance of the prediction rule. This means that not each individual risk profile might be accurate enough so that it can be used in practice to guide treatment decisions. As a consequence prudence has to be taken when using the prediction rule in practice.