Abstract
Objectives
This study aims to examine associations, predictors and pharmacological treatment of chronic pain and mental health problems among Syrian refugees in a longitudinal perspective.
Design
Prospective cohort study.
Setting
We collected survey data among Syrian refugees in Lebanon granted resettlement to Norway (self-administered questionnaires) and at follow-up 1 year after arrival in Norway (structured telephone interviews).
Participants
Adult Syrian refugees attending mandatory pretravel courses in Lebanon in 2017–2018 were invited to participate. In total, 353 individuals participated at both time points.
Primary and secondary outcomes
We examined the cross-sectional associations between pain, mental health and migration-related exposures at baseline and follow-up and assessed whether associations changed significantly with time. Furthermore, we investigated the longitudinal association between mental health at baseline and pain at follow-up. We also evaluated temporal changes in use of analgesics and psychotropic drugs.
Results
While most refugees reported improved health from the transit phase in Lebanon to the early resettlement phase in Norway, a few had persisting and intertwined health problems. Most migration-related stressors were more closely associated with chronic pain and mental health problems after resettlement as compared with the transit phase. In parallel, poor mental health was associated with chronic pain in the follow-up (adjusted risk ratio (ARR) 1.5 (1.0, 2.2)), but not at baseline (ARR 1.1 (0.8, 1.5)). Poor mental health at baseline was a statistically significant predictor of chronic pain at follow-up among those not reporting chronic pain at baseline. At both timepoints, one in four of those with chronic pain used analgesics regularly. None with mental health problems used antidepressants daily.
Conclusions
Providers of healthcare services to refugees should be attentive to the adverse effect of postmigration stressors and acknowledge the interrelations between pain and mental health. Possible gaps in pharmacological treatment of pain and mental health problems need further clarification.
Keywords: mental health, public health, epidemiology
Strengths and limitations of this study.
This is a prospective longitudinal study investigating changes in health among refugees as they traverse international borders.
The study has a high response rate at follow-up, which is a rare feature in longitudinal studies among ‘hard-to-get’ populations such as refugees.
While most longitudinal studies among refugees solely consider mental health, this article incorporates somatic health encouraging a holistic approach in management and care.
The second wave of data collection was performed approximately 1 year postarrival, yet observation over a longer time span would yield a more throughout understanding of temporal changes in health among refugees.
The deliberate choice to change mode of data collection between baseline and follow-up to reduce attrition-related selection bias may have introduced acquiescence bias.
Introduction
Forced displacement of populations is not a temporary phenomenon but persists throughout our time as a global challenge. Public health endeavours towards refugees are increasingly urged to shift from short-term to long-term responses to accommodate protracted refugee situations.1 The healthcare needs of refugee populations will depend on the burden of disease in the country of origin, the demographic profile of the displaced group and migration experiences en route. Health reports commonly reported by refugees include pain conditions such as headache, musculoskeletal complaints and injuries as well as acute infections, dental, gastrointestinal and mental health problems.2–6 Importantly, health challenges may change along the migration stages.7
Somatic and mental health problems are interrelated and affected by social circumstances.8 Forcibly displaced individuals are often subjected to profound psychological distress, which may manifest as both mental health problems and bodily experiences such as pain.9 10 Most of the studies describing mental health symptoms and pain comorbidity among refugees evaluate clinic-based populations, particularly torture survivors.9 11 12 However, the relationship between prevalent mental health problems and pain in non-clinical refugee populations remains poorly examined, and, to our knowledge, has not been assessed in longitudinal studies.13
Somatic and mental health are also affected by life experiences. The effect of migration-related exposures on health has been explained by the theories of allostatic load14 and ‘the exhausted migrant’,15 which emphasise how stressors related to the migration experience add up over years and increase the risk of a wide range of diseases. Migration factors contributing to adverse health effects may include exposure to violence, loss of belongings and beloved ones, a precarious journey, economic hardship as well as communication barriers and uncertain prospects. It remains unsettled how pain and mental health are affected by migration experience at different stages of the migration trajectories of refugees.
As state parties or signatories of international treaties recognising health-related human rights, hosting countries are obliged to provide adequate medical care for refugees.16 Furthermore, in cases where somatic and mental health problems are interrelated, the conditions should be managed in a holistic approach. Nevertheless, many studies report barriers preventing forcibly displaced individuals from accessing healthcare services.17 Less is known about the access to pharmacological treatment, hence a knowledge gap remains concerning the use of relevant medication for pain and mental health problems among refugees.2
In this study, we aim to examine associations, predictors and use of pharmacological treatment for chronic pain and mental health problems among Syrian refugees over time. We explore the main aim from three angles. First, we assess the cross-sectional associations between chronic pain, mental health and migration-related exposures among refugees in the transit and the early postmigration phase and investigate if associations change significantly between these two migration phases. Second, we examine whether poor mental health in the transit period predicts chronic pain in the early postmigration phase. Third, we describe the temporal changes in use of pharmacological treatment for chronic pain and mental health symptoms in the transit and early postmigration phase.
Methods
Study design, setting and data collection
This is a prospective cohort study surveying Syrian refugees in a conflict-near setting in the Middle East with follow-up approximately 1 year after arrival in Northern Europe. The study is part of the Changing Health and health care needs Along the Syrian Refugees’ Trajectories to Norway project recruiting Syrian refugees registered with the United Nations High Commissioner for Refugees in Lebanon and granted resettlement in Norway.18
We invited all Syrian refugees aged 16 and above participating in the mandatory pre-travel courses organised by the International Organization for Migration in Lebanon in the period August 2017 to April 2018. At baseline, respondents self-completed a questionnaire in Arabic. Project staff assisted those with low literacy level and healthcare workers were available to respond to potential signs of retraumatisation. Based on consent from the participants, contact details after resettlement in Norway were obtained from The Directorate of Integration and Diversity and local public immigration offices. The follow-up data collection was carried out during 2018–2019, approximately 1 year after the arrival of respondents in Norway and was completed as a structured telephone interview facilitated by Arabic-speaking study staff. The current study includes refugees who participated both at baseline in Lebanon and at follow-up in Norway.
Measures
Dependent variables
The outcomes in this study are chronic pain, anxiety/depression symptoms and use of analgesics and psychotropics.
We examined chronic pain using a single, validated item asking: ‘Do you have physical pain now that has lasted more than 6 months?’19
Symptoms of anxiety and/or depression were assessed by the Hopkins Symptom Checklist (HSCL-10).20 21 The HSCL-10 item asks respondents to rate the extent to which they have suffered from various symptoms of anxiety and depression during the last week on a 4-point Likert scale. We employ a mean HSCL-10 score of 1.85 (range 1–4) as a cut-off indicating clinically relevant anxiety or depression in line with suggestions from the literature.21
Furthermore, we assessed the use of painkillers and psychotropics, including antidepressants, tranquillisers and sedatives, using questions from the Oslo Health Study.22
Independent variables
Sociodemographic variables recorded included: age, gender, mother tongue, marital status, number of children, level of education and work participation. The Single General Trauma Item was used to identify exposure to traumatic events connected to being forcibly displaced.23 Further, we sought to map various exposures relating to the respondent’s migration journey and developed questions on length of stay, migration without family members and residence permit in transit country.
To answer the first research question, anxiety/depression symptoms were treated as an explanatory variable, and chronic pain as the outcome variable. Additionally, a single question on sleep quality, considered a clinically interesting topic, was extracted from the HSCL-10 item and investigated separately as an explanatory variable. Post-traumatic stress symptoms were assessed by the Harvard Trauma Questionnaire (HTQ).24 25 The HTQ uses the same time frame and response scale as HSCL-10. We adhere to the manual suggesting a mean HTQ score of 2.5 (range 1–4) as a threshold for clinical post-traumatic stress disorder (PTSD). Both HSCL-10 and HTQ are validated instruments widely used among refugees and have exhibited satisfactory psychometric properties among Arabic speakers.
In order to identify exposures related to the respondent’s lived migration experience, we used items from the WHO Quality of Life Scale (WHOQOL-BREF).26 Variables included satisfaction with personal relationships, support from friends, safety, physical environment, economy, information, leisure activities, living place, access to healthcare and transportation rated on a 5-point Likert scale. The items were dichotomised into binary measures where either not at all and a little or very dissatisfied and dissatisfied were merged as indicative of poor outcome. The WHOQOL-BREF has demonstrated good psychometric properties, reliability and validity in Arab populations.26
We used standardised procedure to translate, double back-translate and pilot the study instrument among the target population.27
Statistical analysis
Sociodemographic and migration-related characteristics of the study cohort were described as crude prevalence proportions and medians and IQR. We assessed for selection bias in background variables between the cohort and the loss-to-follow-up group using Fisher’s exact-test and Student’s t-test. Additionally, we used logistic regression to evaluate bias related to associations between sociodemographic characteristics and missing values for key outcomes.
Because of the high prevalence for most of the outcomes, risk ratios were judged as a more appropriate measure of association than odds ratios. Poisson regression was chosen above log-binomial regression to estimate risk ratios due to failing convergence.28 The association between migration-related stressors and chronic pain and poor mental health, respectively (online supplemental DAG figure 1A) was first investigated in baseline data and follow-up data separately using Poisson regression with robust error variance (sandwich estimation) and reported as risk ratios with 95% CIs. We ran unadjusted regression models and models adjusted for age and gender. We used the same statistical procedure to study associations between poor mental health and chronic pain (online supplemental DAG figure 1B) and included models additionally adjusted for trauma as such exposure may be associated both with poor mental health and pain. We assessed whether the cross-sectional associations changed significantly between the two time points using generalised estimation equation (GEE) with log as link-function, Poisson distribution and exchangeable working correlation structure and included an interaction term between exposure and timepoint. The p value for the interaction term is reported as a test for change in association over time.
bmjopen-2020-046454supp001.pdf (341.3KB, pdf)
Furthermore, Poisson regression was used to investigate whether poor mental health stratified by chronic pain in transit (baseline) predicted chronic pain in the early resettlement phase (follow-up) both in crude models and models adjusted for age and gender. We evaluated whether association varied significantly depending on pain status at baseline by including interaction terms between poor mental health and pain at baseline and report the p value for the interaction term of the adjusted models.
Last, we used GEE regression to assess the temporal change in use of painkillers stratified by reporting chronic pain. There were too few users of psychotropics to allow equivalent statistical analysis.
Missing values were handled with listwise deletion in all regression models. All tests were two sided with the level of statistical significance set to 0·05. Analyses were conducted in Stata IC V.16·0.
Patient and public involvement
Syrian refugees were represented in the reference groups of the study, which were consulted during the development, including formulation of research question and design. During recruitment, participants provided helpful information to identify reasons for non-response. Result will be disseminated to the Syrian community in Norway primarily through schools offering a mandatory 2-year educational programme for newly arrived refugees as well as through public channels.
Results
Altogether, 506 Syrian refugees participated in the study at baseline in Lebanon. Of these, 464 were confirmed resettled in Norway and 353 participated at follow-up, resulting in an attrition rate of 24%. Reasons for lost-to-follow-up included: no contact information (13), did not answer phone/wrong phone number (60), did not wish to participate (38).
The final study population of 353 respondents who participated both at baseline and follow-up is described in table 1.
Table 1.
Sociodemographic and migration-related factors (n=353)
| Sociodemographic factors at baseline | ||
| Gender (n, %) | ||
| Women | 181 | 51 |
| Men | 171 | 49 |
| Age in years (median, IQR) | 34 | 27–41 |
| Mother tongue (n, %) | ||
| Arabic | 335 | 95 |
| Kurmanji | 15 | 4 |
| Marital status (n, %) | ||
| Married | 265 | 75 |
| Living with partner if married | 260 | 98 |
| Number of children (median, IQR) | 3 | 2–4 |
| Education in years (median, IQR) | 8 | 6–10 |
| Work participation prior to flight (n, %) | 187 | 38 |
| Migration-related factors at baseline | ||
| Time since flight from Syria in years (median, IQR) | 5 | 4–6 |
| No residence permit in Lebanon (n, %) | 242 | 69 |
| Migrating without family from Syria to Lebanon (n, %) | 55 | 16 |
| Exposure to traumatic event(s) (n, %)* | 135 | 40 |
| Migration-related factors at follow-up | ||
| Time since arrival in Norway at follow-up in months (median, IQR) | 14 | 12–15 |
| Migrating without family from Lebanon to Norway (n, %) | 8 | 2 |
*Measured by the Single General Trauma Item.
Sensitivity analyses comparing the cohort and the loss-to-follow-up group did not support selection bias related to attrition (online supplemental table 1), nor did we find indications of bias associated with missing values for key outcomes (online supplemental tables 2,3).
Various key migration-related stressors were found to be associated with reporting chronic pain both in crude models and adjusted models (figure 1, online supplemental table 4). Trauma exposure and poor economy were associated with chronic pain both at baseline and follow-up. Poor safety, poor information, poor living place, poor access to healthcare and poor transportation were all associated with chronic pain at follow-up only. The association between poor information and chronic pain showed statistically significant interaction with migration stage (p=0.034).
Figure 1.
Associations between migration-related factors (exposure) and chronic pain (outcome) in baseline and follow-up. Separate Poisson regression models for each exposure with robust standard errors adjusted for age and gender. Chronic pain measured by asking: ‘Do you have physical pain now that has lasted more than 6 months?’ RR, relative risk.
Several migration-related stressors were also associated with poor mental health outcome (figure 2, online supplemental table 5). Trauma exposure, poor support from friends, poor safety and poor living place were associated with poor mental health both at baseline and follow-up. We found statistically significant interaction with migration stage in the association between poor mental health and poor personal relationships, poor support from friends, poor safety, poor economy and poor information, respectively.
Figure 2.
Associations between migration-related factors (exposure) and anxiety/depression (outcome) in baseline and follow-up. Separate Poisson regression models for each exposure with robust standard errors adjusted for age and gender. Anxiety/depression measured by the Hopkins Symptoms Checklist 10 with cut-off for suspected anxiety/depression 1.85. RR, relative risk.
Table 2 shows the cross-sectional association between mental health and chronic pain at baseline and follow-up separately. While the number reporting symptoms indicating anxiety/depression decreased from baseline to follow-up (118 to 39), the proportion reporting chronic pain among those with anxiety/depression symptoms increased (33% to 50%) between the two timepoints (table 2).
Table 2.
Associations between mental health (exposure) and chronic pain (outcome) at baseline and follow-up (n=353)
| Baseline | Follow-up | Interaction test§ | |||||||||
| N | Chronic pain, n (%) | RR (95% CI) | N | Chronic pain, n (%) | RR (95% CI) | P | |||||
| Model 1* | Model 2† | Model 3‡ | Model 1* | Model 2† | Model 3‡ | ||||||
| Anxiety/depression symptoms¶ | |||||||||||
| No | 235 | 66 (28.6) | 1 | 1 | 1 | 314 | 79 (25.2) | 1 | 1 | 1 | |
| Yes | 118 | 38 (32.5) | 1.1 (0.8 to 1.6) | 1.1 (0.8 to 1.6) | 1.1 (0.8 to 1.5) | 39 | 19 (50.0) | 2.0 (1.4 to 2.9) | 1.7 (1.2 to 2.4) | 1.5 (1.0 to 2.2) | 0.197 |
| PTSD symptoms** | |||||||||||
| No | 296 | 80 (27.4) | 1 | 1 | 1 | 339 | 89 (26.4) | 1 | 1 | 1 | |
| Yes | 14 | 6 (42.9) | 1.6 (0.8 to 2.9) | 1.3 (0.6 to 2.7) | 1.1 (0.5 to 2.4) | 7 | 6 (85.7) | 3.2 (2.3 to 4.6) | 2.8 (1.7 to 4.6) | 2.3 (1.4 to 3.8) | 0.095 |
| Poor sleep | |||||||||||
| No | 295 | 84 (29.0) | 1 | 1 | 1 | 323 | 76 (23.7) | 1 | 1 | 1 | |
| Yes | 52 | 19 (36.5) | 1.3 (0.8 to 1.9) | 1.2 (0.8 to 1.8) | 1.1 (0.7 to 1.7) | 30 | 22 (73.3) | 3.1 (2.3 to 4.1) | 2.4 (1.7 to 3.5) | 2.2 (1.5 to 3.2) | 0.011 |
*Unadjusted estimates from Poisson regression with robust standard errors, separate models for baseline and follow-up.
†Estimates from Poisson regression with robust standard errors, adjusted for age and gender. Separate models for baseline and follow-up.
‡Estimates from Poisson regression with robust standard errors, adjusted for age, gender and trauma exposure. Separate models for baseline and follow-up.
§P value for interaction term between exposure variable and time (baseline/follow-up) for GEE model including both baseline and follow-up data with adjustment for age, gender and trauma exposure. Test for effect modification by migration phase.
¶Measured by the Hopkins Symptoms Checklist 10, cut-offf or suspected anxiety/depression 1.85.
**Measured by the Harvard Trauma Questionnaire, cut-offf or suspected PTSD 2.5.
GEE, generalised estimation equation; PTSD, post-traumatic stress disorder; RR, relative risk.
Similarly, the number experiencing symptoms compatible with PTSD was reduced from baseline to follow-up (14 to 7), but the proportion reporting chronic pain among those with likely PTSD rose (43% to 86%). Anxiety/depression symptoms were associated with chronic pain in the follow-up in all models (table 2). However, at baseline, we did not find any statistically significant association between anxiety/depression symptoms and chronic pain. The same pattern was seen for PTSD and poor sleep. Associations with chronic pain were in general stronger at follow-up than at baseline, but the test for interaction was only significant for poor sleep.
In table 3, we assess whether mental health problems at baseline predict chronic pain at follow-up. In stratified analyses, anxiety/depression symptoms at baseline were a statistically significant predictor of chronic pain at follow-up among those not reporting chronic pain at baseline (table 3).
Table 3.
Mental health at baseline (exposure) as a predictor of chronic pain at follow-up (outcome) stratified by pain at baseline (n=353)
| RR (95% CI) | Interaction‡ | ||||
| Model 1* | Model 2† | P | |||
| Pain at baseline | No pain at baseline | Pain at baseline | No pain at baseline | ||
| Anxiety/depression symptoms at baseline | 0.8 (0.5 to 1.3) | 1.8 (1.2 to 2.8) | 0.9 (0.5 to 1.4) | 1.7 (1.1 to 2.7) | 0.039 |
| PTSD symptoms at baseline | 0.8 (0.2 to 2.5) | 1.1 (0.3 to 3.9) | 1.0 (0.3 to 3.0) | 1.0 (0.3 to 3.0) | 0.916 |
| Poor sleep at baseline | 0.6 (0.3 to 1.3) | 1.5 (0.8 to 2.6) | 0.6 (0.3 to 1.3) | 1.4 (0.8 to 2.4) | 0.075 |
*Unadjusted estimates from Poisson regression with robust standard errors.
†Estimates from Poisson regression with robust standard errors, adjusted for age and gender.
‡P value for interaction term between exposure variable and pain status at baseline from GEE model with log-link, Poisson distribution and adjustment for age and gender.
GEE, generalised estimation equation; PTSD, post-traumatic stress disorder; RR, relative risk.
We found an increase in daily use of painkillers among those reporting chronic pain (21% to 29%) (table 4). At the same time, there was a reduction in daily use of painkillers over time among those not reporting chronic pain (7% to 2%). Among those reporting symptoms indicating anxiety/depression, there were no daily users of antidepressants neither in the transit phase nor in the early resettlement phase.
Table 4.
Changes in use of pharmacological treatment of for chronic pain and mental health symptoms from baseline to follow-up (n=353)
| Baseline | Follow-up | Change* | ||||
| n (%) | n (%) | RR (95% CI) | ||||
| Chronic pain | No chronic pain | Chronic pain | No chronic pain | Chronic pain | No chronic pain | |
| Painkillers daily | 22 (21) | 16 (7) | 28 (29) | 4 (2) | 1.3 (0.9, 2.2) | 0.2 (0.1, 0.7) |
| Painkillers last 4 weeks | 66 (64) | 86 (36) | 67 (68) | 78 (31) | 1.1 (0.9, 1.3) | 0.9 (0.7, 1.1) |
|
Anxiety/
depression |
No anxiety/
depression |
Anxiety/
depression |
No anxiety/
depression |
Anxiety/
depression |
No anxiety/
depression |
|
| Antidepressants daily | 0 (0) | 1 (0) | 0 (0) | 0 (0) | – | – |
| Antidepressants last 4 weeks | 3 (3) | 4 (2) | 2 (5) | 0 (0) | – | – |
*Change in use of medicines from the transit phase to the early resettlement phase stratified by experiencing health problems or not.
RR, relative risk.
Discussion
Main findings
Overall, most of the refugees in this study exhibit a resilient pattern with decreasing mental health problems, while a few seem to have complex, interrelated and long-lasting health problems. Migration-related stressors appear to be more closely related to both chronic pain and poor mental health in Norway compared with the earlier transit phase. Correspondingly, poor mental health and chronic pain were significantly associated in the early postmigration phase in Norway but we were not able to detect the same association in the transit phase in Lebanon. Furthermore, poor mental health at baseline was a predictor of chronic pain at follow-up, highlighting the intertwined nature of these two conditions. In both migration phases, around one in four of those with chronic pain use painkillers daily, while none of those with symptoms of mental ill health use antidepressants.
Most of the assessed migration-related exposures in this study were more closely associated with poor health outcomes in the early resettlement phase compared with the previous transit phase. The proximity to the horrors of the war in time and space in the transit phase might be an important driver for mental health symptoms. After arrival in Northern Europe, most of our respondents are more content with their socioeconomic situation. However, with larger geographical and temporal distance to the conflict, worries related to socioeconomic factors might receive higher attention among those experiencing poor health. Postmigration stressors, such as socioeconomic, social and interpersonal factors, as well as factors relating to the asylum process and immigration policy, have previously been demonstrated to be related with poor mental health.29 Associations have also been shown between pain and postmigratory stressors as assessed by the 17-item Postmigration Living Difficulties Checklist.9 Our results are in line with an emerging string of the literature, suggesting postsettlement factors to be of greater importance than premigratory conditions for the mental health of resettled refugees.30 31 As a clinical tool, information about adverse lived migration experiences in the post-migration phase may serve as yellow flags when evaluating pain and mental health disorders among refugees.
Several studies have evaluated longitudinal changes in mental health among refugees.32 33 However, research examining patterns of pain among refugees over time is scanty.13 Pain in refugees has predominantly been assessed in cross-sectional studies and in clinical settings among torture survivors or patients with PTSD.9 11 34 Furthermore, we are not aware of prior population-based studies investigating the associations between mental health and pain among forcibly displaces individuals.
The frequently observed concurrence of PTSD and pain has been explained by ‘the mutual maintenance theory’ describing how these conditions perpetuate each other.35 Interrelatedness of poor mental health and chronic pain may have several potential explanations.36 The phenomena may have a common source representing a shared vulnerability towards developing both health problems. Shared vulnerability is also the reason why we adjusted for trauma exposure in our analyses. Furthermore, poor mental health may exacerbate chronic pain and vice versa, constituting a mutually maintaining relationship.35 This is highlighted by studies indicating a dose-response relation between pain and score on the HSCL for anxiety/depression.11 37 Importantly, both mechanisms may apply simultaneously. In this study, the number reporting mental health problems decline, but among these, the proportion reporting chronic pain increases. Thus, we find an aggregation of individuals with concomitant complaints in the resettlement phase. We hypothesise that individuals with milder and more context-sensitive mental health problems may recover after transfer to a less stressful context in the resettlement phase in a ‘salutogenic’ manner.38 Individuals with persisting symptoms may have more resistant mental health challenges and more frequently exhibit concurrent reports of pain. This concentration of fewer, but more complex cases of anxiety/depression, may explain why we observe a stronger association between mental health and pain in the resettlement phase. Our findings support our hypothesis that poor mental health in the transit setting predicts chronic pain at follow-up, confirming our postulated direction of causality between mental health problems and pain.
Pharmacological treatment is not always indicated nor advisable in treating chronic pain and poor mental health. However, pharmacological treatment may also be a cornerstone in the treatment of conditions thresholding a certain severity level. Three in five of those with chronic pain in our study had used analgesics over the last 4 weeks, and this might represent both barriers to obtain medication, sufficient use or even overmedicalisation at the expense of other coping strategies. The corresponding rate of analgesics use over the last 4 weeks in the general Norwegian population is 60% in women and 37% in men, regardless of pain reporting.39 Further research should explore coping strategies for chronic pain among refugees in depth. None of our respondents used antidepressants daily, and this finding might indicate barriers to pharmacological treatment yet the subject needs further scrutiny. The majority of intervention studies targeting mental ill health in refugees involve non-pharmacological treatment options, and studies evaluating the effect of antidepressants among refugees with trauma-related disorders have provided ambiguous evidence.40 Importantly, regular treatments, such as antidepressants, are vulnerable to conflict-driven disruption in continuity of care.
In expanding our understanding of the dynamics between two health reports frequently reported among refugees, namely pain disorders and mental health challenges, our findings have important implications for stewards of healthcare systems as well as clinicians providing healthcare for refugees. While most of our respondents recover from the transit to the early postmigration phase, previous research reveals that declining health outcomes among refugees become evident only after several years postresettlement.41 42 This study highlights the need to identify the minority of vulnerable individuals with entwined somatic and mental health problems and be attentive to adverse postmigration experiences that may make way for deteriorating health among all refugees.
Strengths and weaknesses
Some methodological concerns regarding our study should be noted. First, health effects of migration-related stressors, as explained by the ‘exhausted migrant’ theory, develop over years. While beyond the scope of this study, an observation time over at least a decade would yield a more rigorous understanding of temporal changes in associations, predictors and treatment for chronic pain and poor mental health in refugees.
Second, we deliberately chose to change the mode of data collection between baseline and follow-up from self-completion of questionnaires to structured telephone interviews to prevent selection bias related to attrition with the risk of introducing acquiescence bias. Additionally, this study does not include clinical data, and the reporting of pain and mental health problems relies on self-assessment. Finally, the items assessing chronic pain and use of medicines have not been validated among refugees or Arab-speaking populations.
Conclusion
Most refugees recover from mental health problems from the transit to the early resettlement phase, while a few have persisting problems. Among these, mental health and chronic pain are interrelated and associated with a range of postmigration stressors. Thus, our results illustrate a resilient majority and a concentration of the most vulnerable. Healthcare planners and clinicians providing healthcare services to newly arrived refugees should acknowledge interrelations between pain and mental health disorders, seek information about lived migration experiences and prevent discontinuity of care.
Supplementary Material
Acknowledgments
The authors would especially like to thank all participating refugees for taking part in the study. The authors would also like to thank the International Organisation for Migration, the Norwegian Directorate of Integration and Diversity and Bergen and Kristiansand municipality for aid in the data collection process of this study. The views expressed in this publication are those of the authors and not necessarily those of our collaborators.
Footnotes
Twitter: @EMStromme
Contributors: ED, BNK, LTF, JH-Y and EMS contributed to the conception of the study. ED, JH-Y, WH and EMS took part in acquisition of data. EMS and JI performed the analyses. All authors took part in interpretations, contributed substantially to writing and approved the final manuscript.
Funding: The CHART study was funded by the Research Council of Norway (grant 269835). The funder of the study had no role in study design, data collection, data analysis, data interpretation or writing of the manuscript.
Competing interests: None declared.
Provenance and peer review: Not commissioned; externally peer reviewed.
Supplemental material: This content has been supplied by the author(s). It has not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been peer-reviewed. Any opinions or recommendations discussed are solely those of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and responsibility arising from any reliance placed on the content. Where the content includes any translated material, BMJ does not warrant the accuracy and reliability of the translations (including but not limited to local regulations, clinical guidelines, terminology, drug names and drug dosages), and is not responsible for any error and/or omissions arising from translation and adaptation or otherwise.
Data availability statement
No data are available. The data generated in this study is not publicly available due to data protection regulations in Norway.
Ethics statements
Patient consent for publication
Not required.
Ethics approval
The study was approved by the Regional Committee for Medical and Health Research Ethics of South East Norway (ref. no. 2017/377) and the International Organisation for Migration. We obtained informed consent from all respondents both before study enrolment and at follow-up.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
bmjopen-2020-046454supp001.pdf (341.3KB, pdf)
Data Availability Statement
No data are available. The data generated in this study is not publicly available due to data protection regulations in Norway.


