Skip to main content
Brazilian Journal of Physical Therapy logoLink to Brazilian Journal of Physical Therapy
. 2020 Dec 17;25(3):344–351. doi: 10.1016/j.bjpt.2020.12.005

Epidemiology of chronic back pain among adults and elderly from Southern Brazil: a cross-sectional study

Elizabet Saes-Silva a, Yohana Pereira Vieira a, Mirelle de Oliveira Saes a, Rodrigo Dalke Meucci a,b, Priscila Aikawa c, Ewerton Cousin d, Letícia Maria Almeida da Silva e, Samuel Carvalho Dumith a,b,
PMCID: PMC8134841  PMID: 33419714

Highlights

  • One in five individuals were affected by chronic back pain in the previous year.

  • The main factor associated with chronic back pain was higher level of stress.

  • The groups most affected were women, elderly, smokers, obese individuals, and those with fewer hours of sleep.

  • Chronic back pain worsen health perception, quality of life, and depressive symptoms.

  • Over a 12-month period, one third sought a physician and two third missed work because of back pain.

Keywords: Back pain, Prevalence, Quality of life, Spine, Physical therapy

Abstract

Background

Chronic back pain (CBP) can negatively affect one’s quality of life and health condition, posing significant social and economic burdens.

Objectives

(1) To determine the prevalence of CBP and analyze associated factors in adult and elderly individuals in a municipality in southern Brazil; (2) to verify who sought medical attention or missed work because of back pain; and (3) to estimate the impact of CBP on selected health outcomes.

Methods

This was a population-based cross-sectional study conducted with individuals aged 18 years and older. CBP was defined as “pain for three consecutive months in the cervical, thoracic, or lumbar regions in the last year.” Demographic, socioeconomic, behavioral, and physical and mental health information was collected. The impact of CBP was assessed by the etiological fraction method.

Results

The prevalence of CBP was 20.7% (95% CI: 18.3, 23.0) among the 1300 study participants. The factors associated with CBP were women, elderly, smokers, obesity, and sleeping fewer hours per night, as well as those with higher mental stress levels, history of fracture, arthritis/rheumatism, and work-related musculoskeletal disorder/repetitive strain injury. One-third of those with CBP missed work (31%) and 68% visited the physician over a 12-month period. All health outcomes analyzed (poor or very poor sleep quality, regular or poor health perception, worsened quality of life, depressive symptoms, perceived sadness) were significantly associated with CBP.

Conclusion

One in five adults or elderly reported having CBP over the previous 12 months. This condition was associated with poorer health perception, poorer quality of life, and depressive symptoms.

Introduction

Back pain is commonly termed non-specific as it is characterized by a range of biophysical, psychological, and social dimensions.1 When this condition persists beyond normal healing time, it can be regarded as chronic back pain (CBP). According to the International Association for the Study of Pain (IASP), acute and chronic pain are differentiated based on a three-month cutoff point in the occurrence of the symptoms.2

CBP can be highly disabling and cause significant social and economic burdens as it is one of the main reasons for work absenteeism3, 4 and disability.4, 5 The costs related to the occurrence of CBP can be direct (healthcare assistance) and indirect (work absenteeism and unproductivity).6, 7 In 2016, in the United States, indirect costs related to CBP reached 85% of expenses for the economy.6 In Brazil, in the same period, the economic burden of CBP to the healthcare system accounted for approximately 70% of hospitalizations and 65% of direct costs.7

CBP has been associated with poorer quality of life8 and poor sleep.9 Nevertheless, the impact of CBP on other health outcomes remains to be determined. There remains conflicting information in the literature regarding some factors associated to CBP, for instance, lower educational level,10, 11 age,11, 12 obesity,11, 12, 13 and smoking.11, 14 Furthermore, other variables, such as hours of sleep9 and history of fracture15 are still poorly studied or just described. In addition, CBP can negatively affect an individual's quality of life and health status,8 implicating a social and economic burden,3, 4 the identification of associated factors and prevalence of CBP is necessary to facilitate planning of specific preventive measures.16

We hypothesized that factors most associated with CBP are: older age, being a women, and having worse health conditions. Thus, this study aimed (1) to determine the prevalence of CBP and to analyze associated factors in adult and elderly individuals in a municipality in southern Brazil; (2) to determine the frequency of individuals with CBP who sought medical attention or missed work; and (3) to estimate the impact of CBP on some health outcomes.

Methods

This was a population-based cross-sectional study conducted in the municipality of Rio Grande, a coastal city in the far south of the state of Rio Grande do Sul, Brazil, with approximately 200 000 inhabitants (96% of them living in urban areas). Rio Grande has a Human Development Index (HDI) of 0.744 according to 2010 population census data.17 This study was part of a project entitled “Health of the Riograndina Population”, which addressed various health aspects in this population. Further methodological information about this project is published elsewhere.18

The study sample consisted of individuals aged 18 years or older, residing in the urban area of Rio Grande. Individuals admitted to nursing homes, hospitals, or prisons, and those with physical and/or cognitive disabilities — unable to answer the questionnaire, were considered ineligible. The sample size was calculated considering a CBP prevalence of 18% (lowest prevalence found in a national study),19 proportion of the exposed group from 10%, prevalence ratio of at least 1.8, and minimum 80% statistical power, indicating a sample size of 888 individuals. An additional 25% was included for the design effect and another 15% for confounding factors, totaling a sample size of 1243 individuals. Lastly, an additional 10% were included for possible sample losses and dropouts, for a final desired sample size of 1332 individuals.

Two-stage sampling was used to obtain a representative sample of the urban population of Rio Grande. First, 72 (25%) census tracts were systematically selected based on the 2010 population census data, with probability proportional to the size of the sector. Second, a mean of 10 households per census tract was randomly selected, totaling 720 households. On average, there were two individuals aged 18 or older per household, which resulted in an estimated total of 1440 potentially eligible individuals.

Data were collected between April and July 2016 by previously trained interviewers who used a pre-coded questionnaire with closed questions. Field supervisors conducted telephone interviews with 10% of the sample to control the quality of the information and to address possible errors in the application of the questionnaire. A Kappa coefficient of 0.8 was obtained, which is considered substantial. Data were reviewed, coded, and double-entered by different examiners into EpiData version 3.1 software.

The outcome of interest was CBP, hereby defined as persistent pain (three months or more) in the cervical, thoracic, or lumbar regions in the previous year. The outcome was surveyed through the following questions:

  • 1)

    “Have you had back pain in the last 12 months, i.e., since <MONTH> last year?”;

  • 2)

    “Did such pain last more than 12 weeks, that is, three months in a row?”

Respondents had two answer options for both questions: “no” and “yes”. Respondents who answered positively to both questions were considered the numerator for calculating the prevalence of the outcome.

The independent variables investigated were sex (male; female), age group in years (18–39; 40–59; ≥60), skin color (white; other), marital status (single; married, divorced, or widowed), living alone (no; yes), schooling in full years (0–8; 9–11; ≥12), tertile asset index (lower; intermediate; higher),20 smoking (non-smoker; former smoker; smoker), leisure-time physical inactivity (no; yes), body mass index (BMI) (normal; overweight; obese), average sleep time per day (<6.0; 6.0–7.9; ≥8.0), tertile stress score (lower; intermediate; higher), history of fracture (no; yes), fall in the last year (no; yes), arthritis or rheumatism by medical diagnosis (no; yes), work-related musculoskeletal disorder/repetitive strain injury (WRMSD/RSI) (no; yes), chronic respiratory disease (no; yes), hypertension (no; yes). Information on work absenteeism in the last year because of back pain (no; yes) and seeking medical attention (no; yes) due to back pain were also collected. All variables were obtained by self-report.

The asset index variable considered household characteristics and ownership of some household goods through principal component analysis. After extraction, the first component explained 30.1% of the variability of all items (eigenvalue = 3.31). The leisure-time physical inactivity variable was created based on the leisure section of the International Physical Activity Questionnaire (IPAQ)21 and defined as “individuals who performed no physical activity during their leisure time (zero minutes per week)”. BMI was calculated using self-reported weight and height data and then categorized into normal (up to 24.9 kg/m2), overweight (25.0–29.9 kg/m2), or obese (≥30.0 kg/m2). The stress score was created based on the Perceived Stress Scale (PSS)22 and divided into tertiles. PSS score ranges from 0 to 56 points.

The variables considered as possible outcomes of CBP for calculating the Attributable Fraction or Etiological Fraction (EF) were: (1) poor or very poor sleep quality; (2) regular or poor health perception; (3) worsened quality of life; (4) depressive symptoms; (5) perceived sadness. Sleep quality was assessed by the question “How do you rate your sleep?” The following answers were possible: “very good”, “good”, “fair”, “poor”, and “very poor”. Health perception was surveyed through the following question: “Overall, how do you see your health”, with the possible answers: “excellent”, “very good”, “good”, “fair”, and “poor”.

Quality of life was measured by the WHOQOL-bref23 instrument of the World Health Organization (WHO). Subsequently, the standardized quality of life score was divided into quintiles, with the first quintile indicating the worst quality of life. Depressive symptoms were assessed by the Patient Health Questionnaire (PHQ-9)24 and dichotomized into “yes” or “no” based on the 9-point cutoff. Perceived sadness was defined by the face scale25 with those individuals who related themselves to the last three faces (sad, very sad, or extremely sad) being considered as sad.

Statistical analysis

Data were analyzed in STATA software version 11.2 (StataCorp LP, College Station, Texas, USA). Univariate analysis was performed using absolute and relative frequency to describe the sample according to each variable of interest. Bivariate analysis was used to calculate the prevalence of the outcome according to independent variables. Multivariate analysis was performed following a hierarchical model to determine the order of entry of the variables in the analysis.26 The hierarchical model was built on three levels: the first level included demographic and socioeconomic variables (sex, age, skin color, marital status, living alone, schooling, and asset index); the second level consisted of behavioral variables (smoking, leisure-time physical inactivity, sleeping hours, and stress score) and BMI; and the third level included health-related variables (history of fracture, fall in the previous year, arthritis/rheumatism, WRMSD/RSI, chronic respiratory disease, and hypertension). In each hierarchical level, variables associated with CBP with P-value ≤0.20 were maintained as possible confounding factors in the adjusted model.27 Poisson regression with robust variance adjustment was used to calculate the crude and adjusted prevalence ratios (PR) and their corresponding 95% confidence intervals (95% CI) and P values. The Wald test was used to check for heterogeneity (dichotomous or nominal exposures) and for linear trend (ordinal exposures). A significance level of 5% was considered for two-tailed tests.

Interactions related to sex, age range, and variables with P < 0.10 were tested and described in the results. An analysis of individuals who sought medical attention and/or missed work because of back pain was also performed. Significant results (P < 0.05) are reported in the text. All statistically significant variables associated with CBP were controlled in the CBP-related outcome analysis.

To assess the impact of CBP on each of five health outcomes, the Attributable Fraction or Etiological Fraction (EF) was calculated. This measure represents the maximum reduction of the associated disease if exposure to the population of interest was to be completely eliminated.28 The EF was calculated through the following formula:

EF = [PO * (PR − 1.0)]
1 + [(PO * (PR − 1))]

Where, PO = prevalence of the outcome; PR = crude prevalence ratio.

Ethical aspects

This protocol for the study was approved by the Health Research Ethics Committee at the Universidade Federal do Rio Grande (FURG), Rio Grande, RS, Brazil under protocol no. 20/2016 (CAAE: 52939016.0.0000.5324). The ethical principles established by the National Health Council were followed according to Resolution 466/12. Study participants were informed of their right to refuse participation and on confidentiality procedures. Those who agreed to participate in the study signed an Informed Consent Form.

Results

A total of 1300 out of 1429 eligible individuals participated in the study, which corresponded to a response rate of 91.0%. The effect of the sample design (ESD) for CBP was 1.08, that is, 8%. More than half of the respondents were females (57%), 83% had white skin color and 54% were married, divorced, or widowed. The average ± standard deviation age was 46 ± 17, ranging from 18 to 96 years. The median per capita household income was US$ 250 (interquartile range: 150, 440). Most respondents (90%) did not live alone and nearly half (42%) had 8 years or less of schooling. As for behavioral factors, 18% of the sample were smokers, 67% physically inactive, and 12% slept less than 6 h a day. Nearly a quarter of the sample (24%) was obese, one third (33%) had a history of fracture, and 18% had fallen in the previous year. Hypertension was the most frequent morbidity (28%), followed by respiratory diseases (16%), WRMSD/RSI (14%), and arthritis/rheumatism (12.2%) (Table 1).

Table 1.

Characteristics of participants from Rio Grande, Brazil, 2016 (N = 1300).

Variable N %
Sex
 Male 564 43.4
 Female 736 56.6
Age group (years)
 18–39 508 39.1
 40−59 477 36.7
 60 or + 315 24.2
Skin color
 White 1077 83.0
 Others 221 17.0
Marital status
 Single 602 46.3
 Married. Divorced, or widowed 698 53.7
Living alone
 No 1174 90.4
 Yes 125 9.6
Schooling (year)
 0–8 543 41.8
 9–11 400 30.8
 ≥12 355 27.4
Asset index (tertiles)
 Lower 447 34.4
 Intermediate 419 32.3
 Higher 433 33.3
Smoking
 Non-smoker 733 56.4
 Former smoker 333 25.6
 Smoker 234 18.0
Physically inactive
 No 433 33.3
 Yes 862 66.7
Body mass index
 Euthrophic 477 38.4
 Overweight 471 37.9
 Obese 294 23.7
Sleep time (hours per day)
 <6.0 163 12.5
 6.0–7.9 525 40.4
 ≥8.0 612 47.1
Stress level (tertiles)
 Lower 438 33.8
 Intermediate 475 36.7
 Higher 382 26.5
History of fracture
 No 863 66.5
 Yes 435 33.5
Fall in the last year
 No 1060 81.7
 Yes 237 18.3
Arthritis or rheumatism
 No 1141 87.8
 Yes 159 12.2
WRMSD/RSI
 No 1125 86.5
 Yes 175 13.5
Chronic respiratory disease
 No 1078 84.3
 Yes 201 15.7
Hypertension
 No 933 71.8
 Yes 366 28.2

WRMSD/RSI: work-related musculoskeletal disorder/repetitive strain injury.

The prevalence of CBP was 20.7% (95% CI: 18.3, 23.0), ranging from 13% in individuals with lower stress level and 14% in males to 42% in individuals with WRMSD/RSI and 47% in those with arthritis or rheumatism (Table 2). The factors significantly associated with CBP in the crude analysis were: female sex, age of 60 or older, smoking, physical inactivity, obesity, less than 6 h of sleep per day, higher stress level, history of fracture, fall in the previous year, arthritis/rheumatism, WRMSD/RSI, chronic respiratory disease, and hypertension (Table 2). Following adjustment for potential confounding factors, the variables physical inactivity, fall in the previous year, chronic respiratory disease, and hypertension, were no longer associated with CBP.

Table 2.

Crude and adjusted analysis of chronic back pain among adults and elderly from urban population of Rio Grande, Brazil, 2016 (N = 1300).

Level Variable Chronic back pain (%) Crude analysis Adjusted analysis
PR (95% CI) PR (95% CI)
1 Sex
 Male 13.7 1.00 1.00
 Female 26.0 1.90 (1.48, 2.43) 1.88 (1.47, 2.41)
1 Age group (years)
 18−39 17.9 1.00 1.00
 40−59 20.8 1.16 (0.88,1.53) 1.16 (0.88, 1.52)
 60 or + 24.8 1.38 (1.05, 1.82) 1.34 (1.01, 1.76)
1 Skin color
 White 20.5 1.00 1.00
 Others 21.3 1.04 (0.83, 1.29) 1.08 (0.90, 1.36)
1 Marital status
 Single 19.4 1.00 1.00
 Married, divorced or widowed 21.6 1.11 (0.89, 1.39) 1.01 (0.76, 1.35)
1 Living alone
 No 20.4 1.00 1.00
 Yes 23.2 1.14 (0.82, 1.59) 0.99 (0.69, 1.42)
1 Schooling (year)
 0–8 22.7 1.24 (0.96, 1.60) 1.10 (0.82, 1.50)
 9–11 19.8 1.08 (0.79, 1.48) 1.05 (0.76, 1.45)
 ≥12 18.3 1.00 1.00
1 Asset index (tertiles)
 Lower 23.0 1.22 (0.91, 1.62) 1.21 (0.91, 1.61)
 Intermediate 19.8 1.05 (0.80, 1.38) 1.07 (0.81, 1.41)
 Higher 18.9 1.00 1.00
2 Smoking
 Non-smoker 18.1 1.00 1.00
 Former smoker 21.6 1.19 (0.93, 1.52) 1.18 (0.91, 1.52)
 Smoker 26.9 1.48 (1.15, 1.91) 1.67 (1.31, 2.12)
2 Physically inactive
 No 17.1 1.00 1.00
 Yes 22.4 1.31 (1.00, 1.72) 1.06 (0.84, 1.33)
2 Body mass index
 Euthrophic 18.2 1.00 1.00
 Overweight 17.8 0.98 (0.73, 1.32) 1.06 (0.80, 1.39)
 Obese 28.9 1.59 (1.20, 2.09) 1.64 (1.26, 2.13)
2 Sleep time (hours per day)
 <6.0 32.5 1.78 (1.32, 2.40) 1.58 (1.16, 2.15)
 6.0–7.9 19.6 1.07 (0.82, 1.40) 1.18 (0.91, 1.54)
 ≥8.0 18.3 1.00 1.00
2 Stress level (tertiles)
 Lower 13.0 1.00 1.00
 Intermediate 17.7 1.36 (0.98, 1.89) 1.28 (0.91, 1.79)
 Higher 33.3 2.56 (1.92, 3.40) 2.16 (1.62, 2.86)
3 History of fracture
 No 18.4 1.00 1.00
 Yes 24.8 1.35 (1.10, 1.65) 1.26 (1.03, 1.54)
3 Fall in the last year
 No 18.8 1.00 1.00
 Yes 28.7 1.53 (1.23, 1.90) 1.11 (0.87, 1.42)
3 Arthritis or rheumatism
 No 17.0 1.00 1.00
 Yes 46.5 2.74 (2.16, 3.47) 1.85 (1.42, 2.41)
3 WRMSD/RSI
 No 17.2 1.00 1.00
 Yes 42.3 2.45 (1.97, 3.05) 1.91 (1.50, 2.91)
3 Chronic respiratory disease
 No 19.0 1.00 1.00
 Yes 27.4 1.44 (1.10, 1.88) 1.14 (.087, 1.48)
3 Hypertension
 No 18.9 1.00 1.00
 Yes 24.9 1.32 (1.05, 1.66) 1.06 (0.82, 1.38)

WRMSD/RSI: work-related musculoskeletal disorder/repetitive strain injury.

PR: Prevalence ratio; 95% CI: 95% confidence interval.

The variable sex interacted significantly only with age and physical inactivity. In other words, the association between older age group (60 years or older) and CBP was found only in females, whereas the association between physical inactivity and CBP was significant only in males — and no longer observed after adjustment. The variable age interacted only with marital status, with a lower prevalence of CBP among not-single individuals aged 40–59 years.

Among the individuals with CBP (n = 268), 31% (n = 83) missed work and 68% (n = 183) sought medical attention due to painful symptoms. The frequency of work absenteeism was higher in the following groups: individuals living alone, with lower socioeconomic status, with higher stress level, and diagnosed with WRMSD/RSI. Meanwhile, the frequency of individuals who sought medical attention was higher among elderly, single individuals, and among those with arthritis or rheumatism.

The association between CBP and health-related outcomes is shown in Table 3. The prevalence of poor or very poor sleep quality was 11%; 34% of the sample perceived their health as fair or poor; one fifth (20%) were within the group with the poorest quality of life; 28% had depressive symptoms; and 9% felt sad or very sad. All outcomes were significantly associated with CBP in both the crude and adjusted analyses (Table 3). The EF ranged from 12% for perceived sadness and 15% for lesser sleep quality to 23% for depressive symptoms, 25% for poor health perception, and 26% for lower quality of life score.

Table 3.

Association of chronic back pain with possible outcomes and the respective etiological fraction among adults and elderly from Rio Grande, Brazil, 2016 (N = 1300).

Outcome Prevalence Crude analysis Adjusted analysisa Etiological fraction
% PR (95% CI) PR (95%CI) % (95% CI)
Poor or very poor sleep quality 10.7 2.60 (1.81, 3.74) 1.59 (1.07, 2.35) 14.6 (12.7, 16.5)
Regular or poor health perception 33.9 1.97 (1.71, 2.27) 1.38 (1.17, 1.62) 24.7 (22.4, 27.1)
Worsened quality of life 20.0 2.71 (2.15, 3.41) 1.50 (1.16, 1.94) 25.5 (23,1, 27.9)
Depressive symptoms 28.4 2.07 (1.75, 2.45) 1.29 (1.08, 1.53) 23.3 (21.0, 25.6)
Perceived sadness 9.0 2.49 (1.81, 3.41) 1.59 (1.14, 2.20) 11.8 (10.1, 13.5)

PR: Prevalence ratio; 95% CI: 95% confidence interval.

a

Adjusted for: sex, age group, socioeconomic status, smoking, body mass index, hours of sleep, stress, history of fracture, arthritis/rheumatism, work-related musculoskeletal disorder/repetitive strain injury.

Discussion

This study recruited a representative sample of the adult and elderly population and had a low percentage of sample losses and refusals (9.0%), which allowed us to obtain statistically valid data for the subgroups. The prevalence of CBP found in this population was 20.7% (95% CI: 18.3, 23.0) and was associated with females, elderly, smokers, obesity, poor sleep, a history of fracture, and WRMSD/RSI.

The results of this study were consistent with data from studies conducted in Germany (21%)29 and São Paulo, Brazil (22%).14 Another relevant study,19 used data from the 2013 National Health Survey (PNS in Portuguese), which assessed CBP across all states of Brazil. The authors reported a CBP prevalence of 18.5%, which is very similar to that observed in our study. Importantly, different classifications for CBP have been proposed in the literature, as follows: over 7 days,10 7 weeks or more,11 3 months or more,12, 14, 30 previous 12 months,13, 29, 31 or solely an indication of CBP.8, 9, 19 Hence, different prevalence ratios of CBP have been reported worldwide (from 15.4% to 75.5%)8, 10, 13, 29,30 and in Brazil (from 18.5% to 82.9%).9, 11, 12, 14,19 Such variability may be due to different methods for defining the outcome(s), age groups, research instrument, and methods used for data acquisition.9

Previous studies have shown that women are more likely to develop CBP than are males,8, 9, 10, 11, 12, 13, 14, 19, 29, 30 which is consistent with our findings. Females were almost twice as likely to have CBP as compared to males.

Despite being frequent at all ages, CBP was associated with the age group 60 years and older, with a statistically significant P values observed only for females. However, the literature mentions that the same changes also occur in men32 and our findings do not show a causal relationship between aging and CBP in men. In addition, the middle-aged population is more affected by CBP, although in the elderly CBP is more severe.32

Consistent with other studies,10, 30 a greater percentage of smokers (26.9%) reported having CBP when compared to non-smokers (18.0%). These results can be explained by the deleterious effects of smoking on the musculoskeletal system through mechanisms such as increased of osteoporosis and fractures, decreased bone density, and more frequent degenerative changes in the spine.3 Some authors suggest a reduction in extracellular matrix in the intervertebral disc nucleus, which could progress to intervertebral disc degeneration.33

Another important associated factor for CBP was obesity. Obese individuals had a 64.0% higher probability of having CBP in comparison with those classified as non-obese. In addition to exerting mechanical effects that cause intervertebral disc degeneration, obesity seems to influence intervertebral disc homeostasis through adipokine-mediated inflammatory effects, especially leptin and adiponectin.34 A study35 showed that leptin increases the production and expression of degrading and pain-generating molecules by intervertebral disc cells, which may potentiate the degenerative process. Collectively, these findings provide evidence on a possible biochemical link between intervertebral disc degeneration, back pain, and obesity.

The literature presents little evidence related to sleep and CBP.9 Our findings showed that more than a third of the population who slept less than six hours a night had CBP. A study36 showed that people with CBP have poorer sleep quality and higher levels of insomnia as compared with healthy controls, i.e., those with CBP may potentially suffer from sleep disorders. This is consistent with what was observed in our study, where a strong association between few hours of sleep and CBP was observed. However, answering whether poor sleep is a cause or consequence of CBP remains elusive.

The factor most strongly associated with CBP was higher stress level, in that individuals who were more stressed were more than twice as likely to develop CBP than those reporting a lower stress level. Consistent with this, a study37 conducted in 43 low- and middle-income countries reported that higher levels of stress sensitivity were significantly associated with back pain or CBP.

Consistent with other reports,9, 38 arthritis/rheumatism and WRMSD/RSI were the most prevalent CBP-related conditions, which remained associated even after adjustment. These conditions can aggravate the symptomatology of CBP and cause functional limitations and disabilities, thereby affecting the individual’s quality of life and leading to work absenteeism. Individuals experiencing CBP seek health care more frequently and, therefore, they account for increased economic burden to the public healthcare system.3, 7, 38

Currently, CBP is considered one of the leading causes of work absenteeism.3, 4 In our study, one in three participants with CBP missed work due to pain. Direct (health care) and indirect (work absenteeism and unproductivity) costs6, 7 related to CBP could be dramatically reduced if preventive measures were implemented. Education and physical exercises have been reported as the most effective measures both in the prevention of CBP and in reducing its worsening.39 Beliefs and attitudes are not learned intentionally, so the indirect message of an educational program can influence someone’s attitudes and beliefs.40

The impact of CBP on some health outcomes is one of the strengths of this study. If complete elimination of CBP from this population was possible, parameters such as worsened health perception, poor quality of life, and the prevalence of depressive symptoms could be reduced by 25%. These results provide an idea of how much the burden to healthcare services, cost of medicines, and withdrawal from social activities, work, and leisure, could be reduced if individuals with CBP could be effectively treated. But, no solution will be effective without the collaborative efforts of people with CBP, policy makers, doctors, physical therapists and researchers to develop and implement effective interventions.39

This study also has important limitations to consider. First, its cross-sectional design does not allow establishing any temporality relationship between the events and, thereby, may be subjected to reverse causality bias. For instance, it is possible for more stressed individuals to develop back pain, but the opposite may also be true. Second, the pain assessment performed in our study did not consider information on pain intensity or duration and no clinical examination to validate whether individuals had CBP was conducted. Lastly, the extrapolation of the results to the general population should be interpreted with caution. The majority of the population had, for example, white skin color and were from urban zone, which may differ from other municipalities in Brazil and in the world.

Longitudinal studies are recommended to better understand the causes and consequences of CBP and to identify the factors contributing to greater susceptibility and severity of this condition in the population.

Conclusion

The prevalence of CBP in this study was 20%. Our exploratory analyses showed that CBP was associated with stress, poor sleep, female sex, elderly, smokers, and obesity. One in three individuals with CBP missed work and two in three individuals sought medical attention within a 12-month period. CBP can contribute significantly to poorer health perception, poorer quality of life, and depressive symptoms.

Conflicts of interest

The author declares no conflicts of interest.

Acknowledgements

E Saes-Silva, YP Vieira, E Cousin received scholarships from CAPES (Coordination for the Improvement of Higher Education Personnel, Brazil). SC Dumith is a research productivity fellow at the CNPq (National Council for Scientific and Technological Development, Brazil). This study was funded by FAPERGS (Foundation for Research Support of the State of Rio Grande do Sul – FIRST PROJECTS PROGRAM – ARD/PPP 2014), under grant number 16/2551-0000359-9.

References

  • 1.Walker J. Back pain: pathogenesis, diagnosis and management. Nurs Stand. 2012;27(14):49–56. doi: 10.7748/ns2012.12.27.14.49.c9478. [DOI] [PubMed] [Google Scholar]
  • 2.Merskey H., Bogduk N. Introduction. In: Merskey H., Bogduk N., editors. Classification of Chronic Pain: Descriptions of Chronic Pain Syndromes and Definition of Pain Terms. 2nd ed. IASP Press; 1994. pp. ix–xv. [Google Scholar]
  • 3.Rubin D.I. Epidemiology and risk factors for spine pain. Neurol Clin. 2007;25(2):353–371. doi: 10.1016/j.ncl.2007.01.004. [DOI] [PubMed] [Google Scholar]
  • 4.Lambeek L.C., van Tulder M.W., Swinkels I.C., Koppes L.L., Anema J.R., van Mechelen W. The trend in total cost of back pain in the Netherlands in the period 2002 to 2007. Spine (Phila Pa 1976) 2011;36(13):1050–1058. doi: 10.1097/BRS.0b013e3181e70488. [DOI] [PubMed] [Google Scholar]
  • 5.Meziat Filho N., Silva G.A. Disability pension from back pain among social security beneficiaries, Brazil. Rev Saúde Pública. 2011;45(3):494–502. doi: 10.1590/s0034-89102011000300007. [DOI] [PubMed] [Google Scholar]
  • 6.Waters H., Graf M. 2020. The Costs of Chronic Disease in the US.https://assets1b.milkeninstitute.org/assets/Publication/ResearchReport/PDF/ChronicDiseases-HighRes-FINAL.pdf . [Accessed 13 June 2020] [Google Scholar]
  • 7.Carregaro R.L., da Silva E.N., van Tulder M. Direct healthcare costs of spinal disorders in Brazil. Int J Public Health. 2019;64(6):965–974. doi: 10.1007/s00038-019-01211-6. [DOI] [PubMed] [Google Scholar]
  • 8.Husky M.M., Farin F.F., Compagnone P., Fermanian C., Kovess-Masfety V. Chronic back pain and its association with quality of life in a large French population survey. Health Qual Life Outcomes. 2018;16(1):195. doi: 10.1186/s12955-018-1018-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Igutti A.M., Bastos T.F., Barros M.B.d.A. Back pain in adults: a population-based study in Campinas, São Paulo State, Brazil. Cad Saude Publica. 2015;31(12):2546–2558. doi: 10.1590/0102-311X00178114. [DOI] [PubMed] [Google Scholar]
  • 10.Schneider S., Randoll D., Buchner M. Why do women have back pain more than men?: a representative prevalence study in the Federal Republic of Germany. Clin J Pain. 2006;22(8):738–747. doi: 10.1097/01.ajp.0000210920.03289.93. [DOI] [PubMed] [Google Scholar]
  • 11.Ferreira G.D., Silva M.C., Rombaldi A.J., Wrege E.D., Siqueira F.V., Hallal P.C. Prevalence and associated factors of back pain in adults from southern Brazil: a population-based study. Braz J Phys Ther. 2011;15(1):31–36. [PubMed] [Google Scholar]
  • 12.Candotti C.T., Noll M., Marchetti B.V. Prevalence of back pain, functional disability, and spinal postural changes. Fisioter Mov. 2015;28(4):711–722. [Google Scholar]
  • 13.Großschädl F., Freidl W., Rásky É., Burkert N., Muckenhuber J., Stronegger W.J. A 35-year trend analysis for back pain in Austria: the role of obesity. PLoS One. 2014;9(9) doi: 10.1371/journal.pone.0107436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Depintor J.D.P., Bracher E.S.B., Cabral D.M.C., Eluf-Neto J. Prevalence of chronic spinal pain and identification of associated factors in a sample of the population of São Paulo, Brazil: cross-sectional study. São Paulo Med J. 2016;134(5):375–384. doi: 10.1590/1516-3180.2016.0091310516. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Gerhardt A., Hartmann M., Blumenstiel K., Tesarz J., Eich W. The prevalence rate and the role of the spatial extent of pain in nonspecific chronic back pain—a population-based study in the south-west of Germany. Pain Med. 2014;15(7):1200–1210. doi: 10.1111/pme.12286. [DOI] [PubMed] [Google Scholar]
  • 16.Großschädl F., Stolz E., Mayerl H., Rásky É., Freidl W., Stronegger W. Educational inequality as a predictor of rising back pain prevalence in Austria sex differences. Eur J Public Health. 2015;26(2):248–253. doi: 10.1093/eurpub/ckv163. [DOI] [PubMed] [Google Scholar]
  • 17.Brazil Instituto Brasileiro de Geografia e Estatística . IBGE; Rio de Janeiro: 2011. Demographic Census 2010. [Google Scholar]
  • 18.Dumith S.C., Paulitsch R.G., Carpena M.X. Planning and execution of a population health survey by means of a multidisciplinary research consortium. Sci Med. 2018;28(3):30407. [Google Scholar]
  • 19.Malta D.C., Oliveira M.M.d., Andrade S.S.C.d.A., Caiaffa W.T., Souza M.d.F.M.d., Bernal R.T.I. Factors associated with chronic back pain in adults in Brazil. Rev Saúde Pública. 2017;51:9s. doi: 10.1590/S1518-8787.2017051000052. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Jollife I.T. Springer; 2002. Principal Component Analysis. [Google Scholar]
  • 21.Matsudo S., Araujo T., Matsudo V. Internacional physical activity questionnaire (IPAQ): study of validity and reliability in Brazil. Rev Bras Ativ Fís Saúde. 2001;6(2):5–18. [Google Scholar]
  • 22.Reis R.S., Hino A.A.F., Rodriguez-A-ez C.R. Perceived stress scale reliability and validity study in Brazil. J Health Psychol. 2010;15(1):107–114. doi: 10.1177/1359105309346343. [DOI] [PubMed] [Google Scholar]
  • 23.Fleck M.P., Louzada S., Xavier M. Application of the Portuguese version of the abbreviated instrument of quality life “WHOQOL-bref”. Rev Saude Publica. 2000;34(2):178–183. doi: 10.1590/s0034-89102000000200012. [DOI] [PubMed] [Google Scholar]
  • 24.Santos I.S., Tavares B.F., Munhoz T.N. Sensitivity and specificity of the Patient Health Questionnaire-9 (PHQ-9) among adults from the general population. Cad Saude Publica. 2013;29(8):1533–1543. doi: 10.1590/0102-311x00144612. [DOI] [PubMed] [Google Scholar]
  • 25.Andrews F.M., Withey S.B. Plenum Press; New York: 1976. Social Indicators of Well-being. [Google Scholar]
  • 26.Victora C.G., Huttly S.R., Fuchs S.C., Olinto M.T. The role of conceptual frameworks in epidemiological analysis: a hierarchical approach. Int J Epidemiol. 1997;26:224–227. doi: 10.1093/ije/26.1.224. [DOI] [PubMed] [Google Scholar]
  • 27.Maldonado G., Greenland S. Simulation study of confounder-selection strategies. Am J Epidemiol. 1993;138(11):923–936. doi: 10.1093/oxfordjournals.aje.a116813. [DOI] [PubMed] [Google Scholar]
  • 28.Gordis L. 4a.ed. Revinter; Rio de Janeiro: 2010. Epidemiology. [Google Scholar]
  • 29.Kuntz B., Hoebel J., Fuchs J., Neuhauser H., Lampert T. Social inequalities in the prevalence of chronic back pain among adults in Germany. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2017;60(7):783–791. doi: 10.1007/s00103-017-2568-z. [DOI] [PubMed] [Google Scholar]
  • 30.Jhun H.-J., Park J.-Y. Estimated number of Korean adults with back pain and population-based associated factors of back pain: data from the fourth Korea National Health and Nutrition Examination Survey. J Korean Neurosurg Soc. 2009;46(5):443. doi: 10.3340/jkns.2009.46.5.443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Schmidt C.O., Raspe H., Pfingsten M. Back pain in the German adult population: prevalence, severity, and sociodemographic correlates in a multiregional survey. Spine (Phila Pa 1976) 2007;32(18):2005–2011. doi: 10.1097/BRS.0b013e318133fad8. [DOI] [PubMed] [Google Scholar]
  • 32.Hartvigsen J., Hancock M.J., Kongsted A. What low back pain is and why we need to pay attention. Lancet. 2018;391(10137):2356–2367. doi: 10.1016/S0140-6736(18)30480-X. [DOI] [PubMed] [Google Scholar]
  • 33.Nakahashi M., Esumi M., Tokuhashi Y. Detection of apoptosis and matrical degeneration within the intervertebral discs of rats due to passive cigarette smoking. PLoS One. 2019;14(8) doi: 10.1371/journal.pone.0218298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Sharma A. The role of adipokines in intervertebral disc degeneration. Med Sci. 2018;6(2):34. doi: 10.3390/medsci6020034. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Segar A.H., Fairbank J.C., Urban J. Leptin and the intervertebral disc: a biochemical link exists between obesity, intervertebral disc degeneration and low back pain—an in vitro study in a bovine model. Eur Spine J. 2019;28(2):214–223. doi: 10.1007/s00586-018-5778-7. [DOI] [PubMed] [Google Scholar]
  • 36.Van de Water A.T., Eadie J., Hurley D.A. Investigation of sleep disturbance in chronic low back pain: an age-and gender-matched case-control study over a 7-night period. Man Ther. 2011;16(6):550–556. doi: 10.1016/j.math.2011.05.004. [DOI] [PubMed] [Google Scholar]
  • 37.Stubbs B., Koyanagi A., Thompson T. The epidemiology of back pain and its relationship with depression, psychosis, anxiety, sleep disturbances, and stress sensitivity: data from 43 low-and middle-income countries. Gen Hosp Psychiatry. 2016;43:63–70. doi: 10.1016/j.genhosppsych.2016.09.008. [DOI] [PubMed] [Google Scholar]
  • 38.Oliveira M.M.d., Andrade S.S.C.d.A., Souza C.A.V.d., Ponte J.N., Szwarcwald C.L., Malta D.C. Chronic back complaints and diagnosis of self-reported work-related musculoskeletal disorders (WMSDs) in Brazil: National Health Survey, 2013. Epidemiol Serv Saude. 2015;24(2):287–296. [Google Scholar]
  • 39.Foster N.E., Anema J.R., Cherkin D. Prevention and treatment of low back pain: evidence, challenges, and promising directions. Lancet. 2018;391(10137):2368–2383. doi: 10.1016/S0140-6736(18)30489-6. [DOI] [PubMed] [Google Scholar]
  • 40.Leysen M., Nijs J., Van Wilgen P. Attitudes and beliefs on low back pain in physical therapy education: a cross-sectional study. Braz J Phys Ther. 2020;(August) doi: 10.1016/j.bjpt.2020.08.002. S1413-3555(19)30994-3, In press. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Brazilian Journal of Physical Therapy are provided here courtesy of Associação Brasileira de Pesquisa e Pós-Graduação em Fisioterapia

RESOURCES