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Prevalence of chronic pain in a metropolitan area of a developing country: a population-based study

Prevalência de dor crônica em área metropolitana de um país em desenvolvimento: um estudo populacional

ABSTRACT

Objective

To estimate the prevalence of chronic pain (CP) in the adult population living in the city of São Paulo, Brazil, and to identify factors associated with CP in developing countries.

Methods

A cross-sectional study using a computer-assisted telephone interview in a two-stage stratified sample of adults living in households.

Results

2,446 subjects were interviewed. The mean age was 39.8 years old. The majority was female and 42.7% had less than 10 years of education. The prevalence of CP was 28.1%. The independent factors associated with CP were female gender (OR = 2.0; p < 0.001), age older than 65 years (OR = 1.4; p = 0.019) and less than 15 years of education (OR = 1.3-1.6; p < 0.04).

Conclusions

The prevalence of CP was high and similar to that which has been reported in developed countries. These results raise awareness about CP and may potentially help clinicians and policy makers to design better health care programs for CP treatment in these populations.

chronic pain; population; prevalence; developing countries

RESUMO

Objetivo

Estimar a prevalência de dor crônica (DC) na população adulta residente na cidade de São Paulo, Brasil, e assim identificar os fatores associados com DC em países em desenvolvimento.

Método

Estudo transversal utilizando entrevista por telefone auxiliada por computador em duas etapas numa amostra estratificada de adultos domiciliados em São Paulo.

Resultados

2446 indivíduos foram entrevistados. A média de idade foi 39,8 anos. A maioria foi do sexo feminino e 42,7% tinham menos de 10 anos de escolaridade. A prevalência de DC foi de 28,1%. Os fatores independentes associados à DC foram gênero feminino (OR = 2,0; p < 0,001), idade superior que 65 anos (OR = 1,4; p = 0,019) e menor que 15 anos de escolaridade (OR = 1,3-1,6; p < 0,04).

Conclusão

A prevalência de DC foi alta e próxima à reportada em países desenvolvidos. Estes resultados irão auxiliar profissionais de saúde e gestores a realizarem programas de avaliação e tratamento de dor crônica mais ajustados à realidade local.

dor crônica; população; prevalência; países em desenvolvimento

Chronic pain (CP) is defined as pain that persists after the normal period for lesion healing and continues for at least three months11. International Association for the Study of Pain. Classification of chronic pain. Seatle: IASP Press; 1986.. It can be continuous or intermittent. It is estimated that CP prevalence varies from 7%22. Breivik H, Collett B, Ventafridda V, Cohen R, Gallacher D. Survey of chronic pain in Europe: prevalence, impact on daily life, and treatment. Eur J Pain. 2006;10(4):287-333. doi:10.1016/j.ejpain.2005.06.009,33. Bowsher D, Rigge M, Sopp LP. Prevalence of chronic pain in the British population: a telephone survey of 1037 households. Pain Clin. 1991;4:223-30. to 48%44. Andersson HI, Ejlertsson G, Leden I, Rosenberg C, Centre BH, Bromölla. Chronic pain in a geographically defined general population: studies of differences in age, gender, social class, and pain localization. Clin J Pain. 1993;9(3):174-82. doi:10.1097/00002508-199309000-00004, depending on the population studied. Developing countries are defined as having a Human Development Index (HDI) bellow 0.9. While several studies have reported CP data in specific population samples from developing countries, such as the prevalence of CP in the elderly, and joint symptoms55. Silva VRL, Menezes AMB, Noal RB. [Chronic joint symptoms in adults from Pelotas, Rio Grande do Sul State, Brazil: prevalence and determinants]. Cad Saúde Pública. 2009;25(12):2571-582. Portuguese. doi:10.1590/S0102-311X2009001200005, data on CP prevalence in the general adult population in developing countries are still scarce. In fact, a systematic review in countries with a HDI bellow 0.9 published a few years ago included only a few studies reporting CP prevalence in these regions of the world66. Elzahaf RA, Tashani OA, Unsworth BA, Johnson MI. The prevalence of chronic pain with an analysis of countries with a Human Development Index less than 0.9: a systematic review without meta-analysis. Curr Med Res Opin. 2012;28(7):1221-9. doi:10.1185/03007995.2012.703132; most of them did not assess individuals from the general population. For instance, one of the studies included in the review was primarily aimed at mood disorders77. Tsang A, Von Korff M, Lee S, Alonso J, Karam E, Angermeyer MC et al. Common chronic pain conditions in developed and developing countries: gender and age differences and comorbidity with depression-anxiety disorders. J Pain. 2008;9(10):883-91. doi:10.1016/j.jpain.2008.05.005, and another included patients actively looking for primary care assistence88. Gureje O, Von Korff M, Simon GE, Gater R. Persistent pain and well-being: a World Health Organization study in primary care. JAMA. 1998;280(2):147-51. doi:10.1001/jama.280.2.147. Subsequently, the authors of this systematic review concluded that the low number of CP prevalence studies in low-HDI countries undermined their analyses and prevented further comparisons with the CP prevalence in high-HDI regions. Thus, while several studies have revealed the prevalence and risk factors for CP in developed countries22. Breivik H, Collett B, Ventafridda V, Cohen R, Gallacher D. Survey of chronic pain in Europe: prevalence, impact on daily life, and treatment. Eur J Pain. 2006;10(4):287-333. doi:10.1016/j.ejpain.2005.06.009,99. Català E, Reig E, Artés M, Aliaga L, López JS, Segú JL. Prevalence of pain in the Spanish population: telephone survey in 5000 homes. Eur J Pain. 2002;6(2):133-40. doi:10.1053/eujp.2001.0310,1010. Bouhassira D, Lantéri-Minet M, Attal N, Laurent B, Touboul C. Prevalence of chronic pain with neuropathic characteristics in the general population. Pain. 2008;136(3): 380-87. doi:10.1016/j.pain.2007.08.013, studies in developing countries are still scarce and heterogeneous1111. Sá KN, Baptista AF, Matos MA, Lessa I. Chronic pain and gender in Salvador population, Brazil. Pain. 2008;139(3): 498-506. doi:10.1016/j.pain.2008.06.008,1212. Cabral DM, Bracher ES, Depintor JD, Eluf-Neto J. Chronic pain prevalence and associated factors in a segment of the population of São Paulo City. J Pain. 2014;15(11):1081-91. doi:10.1016/j.jpain.2014.07.001 and the associated risk factors of CP are still a matter of debate. Population-based studies suggest that CP can be associated with age, gender, socio-economic level1111. Sá KN, Baptista AF, Matos MA, Lessa I. Chronic pain and gender in Salvador population, Brazil. Pain. 2008;139(3): 498-506. doi:10.1016/j.pain.2008.06.008, among other co-morbidities44. Andersson HI, Ejlertsson G, Leden I, Rosenberg C, Centre BH, Bromölla. Chronic pain in a geographically defined general population: studies of differences in age, gender, social class, and pain localization. Clin J Pain. 1993;9(3):174-82. doi:10.1097/00002508-199309000-00004,99. Català E, Reig E, Artés M, Aliaga L, López JS, Segú JL. Prevalence of pain in the Spanish population: telephone survey in 5000 homes. Eur J Pain. 2002;6(2):133-40. doi:10.1053/eujp.2001.0310,1313. Blyth FM, March LM, Brnabic AJ, Jorm LR, Williamson M, Cousins MJ. Chronic pain in Australia: a prevalence study. Pain. 2001;89(2-3):127-34. doi:10.1016/S0304-3959(00)00355-9,1414. Smith BH, Elliott AM, Chambers WA, Smith WC, Hannaford PC, Penny K. The impact of chronic pain in the community. Fam Pract. 2001;18(3):292-9. doi:10.1093/fampra/18.3.292,1515. Meana M, Cho R, DesMeules M. Chronic pain: the extra burden on Canadian women. BMC Womens Health. 2004;4, Suppl 1:S17. doi:10.1186/1472-6874-4-S1-S17.

Pain is a multidimensional experience that can vary according to cultural, emotional, physical and social characteristics. Cultural differences can be identified among countries or among different regions in the same country, interfering with the assessment of the prevalence of pain. Thus, the present study reports the results of the Brazilian Study of the Prevalence of Chronic Pain (EPI-DOR), which aimed to estimate the prevalence of CP, to describe pain characteristics and to identify possible factors associated with CP among the general population in the city of São Paulo, Brazil.

METHODS

Study design and setting

The present study was approved by our Institutions’ Ethics Review Board. The EPI-DOR, an observational, cross-sectional population-based survey assessed pain in adults living in households in São Paulo, Brazil. São Paulo has a population over of 10 million people; approximately 76% of its households have an active telephone line1616. Instituto Brasileiro de Geografia e Estatística – IBGE. Censo demográfico 2000. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2013 [cited 2003 jun]. Available from: http://www.ibge.gov.br/home/estatistica/populacao/censo2000/
http://www.ibge.gov.br/home/estatistica/...
,1717. Instituto Brasileiro de Geografia e Estatística – IBGE. Pesquisa mensal de emprego. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2015 [cited nov 2015]. Available: http://www.ibge.gov.br/home/estatistica/indicadores/trabalhoerendimento/pme_nova/pme_201507tm_01.shtm
http://www.ibge.gov.br/home/estatistica/...
,1818. Instituto de Pesquisa Econômica Aplicada – IPEA.IPEA data. [cited 2015 dec]. Available from: http://www.ipeadata.gov.br
http://www.ipeadata.gov.br...
.

Sample size and participants

The sample size was determined by the primary aim of the study, which was to estimate the prevalence of CP. The estimated sample size was originally calculated to include 2,000 adults, based on a CP prevalence of 50%, maximum error of ± 2%, and a confidence interval of 95%. The sample size was then extended to 2,446 persons in order to cover the forecast losses of 20% of adults living in households.

A simple random, two-stage stratified sample design was used. The sampling process was as follows: (a) a systematic sample of 6,000 generated household telephone numbers was extracted, based on a telephone list obtained from the local telephone company; and (b) the telephone lines were re-sampled into 40 interpenetrating sub-samples, each including a sample of 200 telephone numbers. A random sample of the household member to be interviewed from each interpenetrating subsample was selected. Eligible subjects were required to (a) be 18 years of age or older and (b) live in a house with access to a landline telephone. Verbal informed consent was obtained from all respondents.

Data collection and measurements

Data were collected by telephone interview, using computer-assisted telephone interview software developed specifically for the present study. Some measures were adopted to prevent non-response and non-response bias. These included: (a) specific training of interviewers; (b) standardized content of the interviews, which included an introductory presentation as an initial part of the telephone contacts; and (c) standard operational procedures for contacts and callbacks in case of failed contact. Each selected telephone number was contacted up to 10 times on different days and at different time-periods of the day. In previous studies, up to six attempts were made1919. Neville A, Peleg R, Singer Y, Sherf M, Shvartzman P. Chronic pain: a population- based study. Isr Med Assoc J. 2008;10(10):676-80.. However, some individuals were unreachable after five to six attempts. Thus, in the present study ten attempts were arbitrarily defined as the standard operational procedure in case of failed contacts. The telephone contact occurred on weekdays and weekends from 8 a.m. to 9 p.m. A respondent was randomly selected from each household by the software, after identifying the number of household members who were 18 years of age or older. If an eligible subject agreed to participate, a verbal informed consent was obtained. The refusal rate and the time spent in each interview were recorded.

Structured telephone interview questionnaire

The survey instrument used in this study included 43 questions and was based on a Brazilian Pain Questionnaire for population-based surveys developed by Moreira Júnior and Souza2020. Moreira Junior ED, Souza MC. Epidemiologia da dor crônica: desenvolvimento de questionário para inquéritos populacionais. Rev Bras Med. 2003; 60(8):610-5.; the Brief Pain Inventory2121. Ferreira KA, Teixeira MJ, Mendonza TR, Cleeland CS. Validation of brief pain inventory to Brazilian patients with pain. Support Care Cancer. 2011;19(4):505-11. doi:10.1007/s00520-010-0844-7; and on the questionnaire proposed by Breivik and colleagues22. Breivik H, Collett B, Ventafridda V, Cohen R, Gallacher D. Survey of chronic pain in Europe: prevalence, impact on daily life, and treatment. Eur J Pain. 2006;10(4):287-333. doi:10.1016/j.ejpain.2005.06.009.

The questionnaire was composed of two parts. The first part assessed demographic and clinical characteristics (sex, age, level of education, religion, work/employment status, weight, height, co-morbidities, and nutritional status). The nutritional status of respondents was classified according to their body-mass index, considering the World Health Organization cut-off points. Self-reported weight and height were used to calculate body-mass index. The educational level of respondents was determined by years of education.

In the second part, regarding the presence of pain, subjects were asked, “throughout our lives, most of us have had pain from time to time (such as minor headache, sprains, and toothaches. Have you been suffering from pain in the last three months or longer?” The subjects who responded “NO” were classified as “no pain” and the interview was terminated. Responders who answered “YES” were then interviewed regarding pain characteristics using the second part of the questionnaire which assessed: (a) frequency, duration and intensity of pain; (b) location of pain; (c) use of pharmacological and non-pharmacological interventions to treat pain in the last 12 months; (d) who ordered or suggested the pain treatments; (e) other pain characteristics and pain interference, using the Brazilian version of the Brief Pain Inventory2121. Ferreira KA, Teixeira MJ, Mendonza TR, Cleeland CS. Validation of brief pain inventory to Brazilian patients with pain. Support Care Cancer. 2011;19(4):505-11. doi:10.1007/s00520-010-0844-7.

The Brief Pain Inventory asks patients to rate their intensity of pain (highest, lowest, and average), and the pain interference (with general activities, mood, walking ability, normal work, relationships with others, sleep, and enjoyment of life) on an 11-point scale ranging from 0 (no pain/no interference) to 10 (as bad as it can be), over the past 24 hours and over the last three months2121. Ferreira KA, Teixeira MJ, Mendonza TR, Cleeland CS. Validation of brief pain inventory to Brazilian patients with pain. Support Care Cancer. 2011;19(4):505-11. doi:10.1007/s00520-010-0844-7.

Statistical analyses

Computerized weighting was used in the analyses. Data from each subject were weighted by the number of adult household members to compensate for any differences in the probabilities of selection among eligible respondents in each house. To reduce the bias due to the non-respondents and make estimations for São Paulo’s general population, the distributions of the study sample according to age, sex, and level of education (12 population strata) were compared and adjusted to the distribution in the city of São Paulo, using data from the 2000 Brazilian census (the version available when the study was designed) carried out by the Brazilian Institute of Geography and Statistics.

Statistical analyses were performed using the Statistical Package for the Social Sciences, Version 15.0® (Chicago, IL). Descriptive statistics were generated on the sample characteristics. Univariate and multivariate analyses were used to identify factors associated with CP. The Chi-square test and multiple logistic regression models (adjusted odds ratio) were applied to examine the association between CP (dependent variable) and demographic characteristics (independent variables). Multiple logistic regression models were performed to measure the association between CP and presence of comorbidities, controlling for sex, age, and level of education. These demographic characteristics were included in the models because they were independently and significantly associated with the presence of CP. For all tests, a p value < 0.05 was considered statistically significant. We used a stepwise forward procedure and the Wald test.

The values left blank were treated as system-missing values. Missing data were not treated in any special manner or for any statistical method, such as imputation.

Supplementary Statistical analyses

Weighting

Prevalence estimates and statistical analyses utilized weighted data. Two steps of weights were used. One step adjusted for different probabilities of selection among respondents; and a second one was post-stratification weights adjusting for imbalances, due to non-response and non-coverage bias, between the study sample and the population of São Paulo in relation to distribution by age, sex, and educational level. The educational level of respondents was determined by years of school completed.

Data from each respondent were weighted by the number of adults living in each household. After this step, the distributions of the study sample and the São Paulo population were compared according to age, sex, and educational level. We analyzed data from the 2,000 Brazilian National Census carried out by the Brazilian Institute of Geography and Statistics (Table 1). The observed frequencies of individuals aged 40 years of age or more were higher in the sample than in the population of São Paulo, as well as the frequency of females, and individuals with 11 or more years of school completed. Thus, in order to correct for these sample imbalances, post-stratification weights were adjusted. These weights were obtained from the distribution of the sample within 12 strata, considering the population distribution according to age, sex, and educational level (Tables 2 and 3).

Table 1
Distribution of the study sample and the population of São Paulo according to age, sex, and level of education.
Table 2
Distribution of the study sample and the population of São Paulo according to age, sex, and level of education.
Table 3
Sample weights applied in the post-stratification adjustment.

RESULTS

A total of 2,446 persons were interviewed to cover the forecast losses of 20% of adults living in household. There was a refusal rate of 12.4% (n = 418; 10.2% refused to schedule an interview and 2.2% refused to participate in the study after being informed of the aims and procedures of the research). The average interview lasted 7.7 minutes. The Figure summarizes the recruitment of subjects. The mean age was 39.8 years (range = 18–91). The majority was female (53.5%), had completed up to 10 years of education (57.3%), and was currently employed (59.8%). About one-third (33.4%) of the respondents were considered overweight and 12.7% were obese (Table 4).

Figure
Study inclusion flow diagram.

Table 4
Sociodemographic characteristics of respondents adjusted to the structure of the Brazilian general population.

Prevalence of chronic pain

The presence of current CP with a duration ≥ 3 months was reported by 713 respondents, which represented a prevalence of 28.1% (95%CI: 25.0–31.4%). The prevalence of CP according to sociodemographic characteristics of the population is presented in Table 5.

Table 5
Prevalence of chronic pain according to sociodemographic characteristics.

The prevalence of CP was higher in women than in men (34.7% vs. 20.6%; p = 0.001) and in the 45–64 year age group (33.9%), followed by the 30–44 year age group (p < 0.001). Pain had a tendency to be more prevalent with increasing age (p < 0.001) and with fewer years of schooling (p < 0.001). Separated/divorced (39.0%) and widowed individuals (37.9%) reported CP more frequently than single and married responders (p = 0.021).

We observed a higher prevalence of CP among obese and overweight individuals, but this association was not statistically significant. There was no significant association between CP and work status (p = 0.78) or between CP and religion (p = 0.20).

The multiple logistic regression analyses confirmed the association between CP and sex, age, and level of education (Table 6). Female gender (OR = 2.0; p < 0.001), age higher than 65 years compared with the 18–29 year age group (OR = 1.4; p = 0.019), and fewer years of education (< 15 years) were associated with higher odds of having CP (OR = 1.3–1.6; p < 0.04) (Table 7). The greatest chance of having CP was observed among respondents reporting concomitant muscular complaints (adjusted OR = 6.4; p = 0.016), fibromyalgia (adjusted OR = 4.7; p = 0.031), spinal disorders (adjusted OR = 3.8; p < 0.001), heart diseases lasting one year or less (adjusted OR = 3.7; p = 0.007), arthritis (adjusted OR = 3.5; p < 0.001), rheumatism (adjusted OR = 3.4; p = 0.007), depression (adjusted OR = 3.3; p = 0.003), and anxiety/psychiatric disorders (adjusted OR = 3.3; p = 0.0001).

Table 6
Factors associated with the presence of chronic pain among the São Paulo general population: multivariate model.
Table 7
Association between reported presence of medically diagnosed co-morbidities or medical conditions and the prevalence of chronic pain among the São Paulo general population.

Pain characteristics and treatment

The mean intensity of the average pain in the past 24 hours was 6.8 (SD = 2.4) (Table 8). The most frequent body location of pain was legs and feet (22.5%), followed by the back and the neck (21.1%), and chest (17.2%). The duration of pain was often prolonged (55.8 ± 84.1 months). Only 25% of the respondents had suffered from CP for less than one year.

Table 8
Clinical characteristics of chronic pain and its treatment.

The interviewers asked respondents whether their pain was being treated in any way in the past 12 months. Most respondents (58.5%) had taken medications for their pain in the last 12 months, but only 16% of respondents had used non-pharmacological methods, remedies or therapies for pain.

DISCUSSION

It is still unknown whether pain is more prevalent in countries with a low HDI, and this is mainly due to the lack of studies assessing CP exclusively in this populations1111. Sá KN, Baptista AF, Matos MA, Lessa I. Chronic pain and gender in Salvador population, Brazil. Pain. 2008;139(3): 498-506. doi:10.1016/j.pain.2008.06.008,1212. Cabral DM, Bracher ES, Depintor JD, Eluf-Neto J. Chronic pain prevalence and associated factors in a segment of the population of São Paulo City. J Pain. 2014;15(11):1081-91. doi:10.1016/j.jpain.2014.07.001. One could expect a higher prevalence of CP in low-HDI populations since HDI is defined by three dimensions (i.e., longevity, mean years of schooling and income) and two of these dimensions are known to be associated with CP (years of schooling and income)2222. Eriksen J, Jensen MK, Sjøgren P, Ekholm O, Rasmussen NK. Epidemiology of chronic non-malignant pain in Denmark. Pain. 2003;106(3):221-8. doi:10.1016/S0304-3959(03)00225-2,2323. Vieira EBM, Garcia JB, Silva AA, Araújo RLM, Jansen RC. Prevalence, characteristics, and factors associated with chronic pain with and without neuropathic characteristics in São Luız, Brazil. J Pain Symptom Manage. 2012;44(2):239-51. doi:10.1016/j.jpainsymman.2011.08.014. Also, the prevalence of some diseases associated with CP — such as HIV/AIDS2424. Asamoah-Odei E, Garcia Calleja JM, Boerma JT. HIV prevalence and trends in sub-Saharan: no decline and large subregional differences. Lancet. 2004;364(9428):35-40. doi:10.1016/S0140-6736(04)16587-2 and leprosy — is higher in developing countries, which have a significant proportion of cases located in the sub-Saharan Africa2424. Asamoah-Odei E, Garcia Calleja JM, Boerma JT. HIV prevalence and trends in sub-Saharan: no decline and large subregional differences. Lancet. 2004;364(9428):35-40. doi:10.1016/S0140-6736(04)16587-2. In the present study, the observed prevalence of CP, defined as daily pain lasting for three months or longer, was 28.1%. This was similar to previous studies that used the same CP definition and were conducted in other countries such as Spain (23.4%)99. Català E, Reig E, Artés M, Aliaga L, López JS, Segú JL. Prevalence of pain in the Spanish population: telephone survey in 5000 homes. Eur J Pain. 2002;6(2):133-40. doi:10.1053/eujp.2001.0310, Finland (35.1%)2525. Mäntyselkä PT, Turunen JH, Ahonen RS, Kumpusalo EA. Chronic pain and poor self-rated health. JAMA. 2003;290(18):2435-42. doi:10.1001/jama.290.18.2435, France (31.7%)1010. Bouhassira D, Lantéri-Minet M, Attal N, Laurent B, Touboul C. Prevalence of chronic pain with neuropathic characteristics in the general population. Pain. 2008;136(3): 380-87. doi:10.1016/j.pain.2007.08.013, and the USA (26.0%)2626. Toblin RL, Mack KA, Perveen G, Paulozzi LJ. A population-based survey of chronic pain and its treatment with prescription drugs. Pain. 2011;152(6):1249-55. doi:10.1016/j.pain.2010.12.036. Some studies used the World Health Organization’s six-month definition of CP, while most studies employed the International Association for the Study of Pain’s three-month cut-off11. International Association for the Study of Pain. Classification of chronic pain. Seatle: IASP Press; 1986.,66. Elzahaf RA, Tashani OA, Unsworth BA, Johnson MI. The prevalence of chronic pain with an analysis of countries with a Human Development Index less than 0.9: a systematic review without meta-analysis. Curr Med Res Opin. 2012;28(7):1221-9. doi:10.1185/03007995.2012.703132. However, in some instances, CP was defined as the presence of “painful symptoms lasting longer than 45 days”55. Silva VRL, Menezes AMB, Noal RB. [Chronic joint symptoms in adults from Pelotas, Rio Grande do Sul State, Brazil: prevalence and determinants]. Cad Saúde Pública. 2009;25(12):2571-582. Portuguese. doi:10.1590/S0102-311X2009001200005 and in others, CP was defined as any pain lasting more than three months in the individual’s life, given that it was also present in at least one episode in the preceding 30 days1212. Cabral DM, Bracher ES, Depintor JD, Eluf-Neto J. Chronic pain prevalence and associated factors in a segment of the population of São Paulo City. J Pain. 2014;15(11):1081-91. doi:10.1016/j.jpain.2014.07.001. For instance, Cabral et al.1212. Cabral DM, Bracher ES, Depintor JD, Eluf-Neto J. Chronic pain prevalence and associated factors in a segment of the population of São Paulo City. J Pain. 2014;15(11):1081-91. doi:10.1016/j.jpain.2014.07.001 found a 42% prevalence of CP using this latter definition in a sample of individuals living in a neighborhood of São Paulo, while persistent pain, defined as pain present in 50% of the days in the preceding three months, was reported to occur in only 28.5% of this sample.

The prevalence of CP and its associated characteristics in the general population of developing countries has been rarely assessed, with varying definitions and sample sizes1111. Sá KN, Baptista AF, Matos MA, Lessa I. Chronic pain and gender in Salvador population, Brazil. Pain. 2008;139(3): 498-506. doi:10.1016/j.pain.2008.06.008,1212. Cabral DM, Bracher ES, Depintor JD, Eluf-Neto J. Chronic pain prevalence and associated factors in a segment of the population of São Paulo City. J Pain. 2014;15(11):1081-91. doi:10.1016/j.jpain.2014.07.001. The present study provided information regarding sex, age, level of education, and a high response rate to the telephone interviews was obtained, reaching a total of 2,446 participants. The minimum sample size recommended for population-based surveys has been reported to be 2,000 individuals per city22. Breivik H, Collett B, Ventafridda V, Cohen R, Gallacher D. Survey of chronic pain in Europe: prevalence, impact on daily life, and treatment. Eur J Pain. 2006;10(4):287-333. doi:10.1016/j.ejpain.2005.06.009,2727. Monteiro CA, Moura EC, Jaime PC, Lucca A, Florindo AA, Figueiredo IC et al. Surveillance of risk factors for chronic diseases through telephone interviews. Rev Saude Publica. 2005;39(1):47-57. doi:10.1590/S0034-89102005000100007, and this is the largest study available so far in low HDI individuals1111. Sá KN, Baptista AF, Matos MA, Lessa I. Chronic pain and gender in Salvador population, Brazil. Pain. 2008;139(3): 498-506. doi:10.1016/j.pain.2008.06.008,1212. Cabral DM, Bracher ES, Depintor JD, Eluf-Neto J. Chronic pain prevalence and associated factors in a segment of the population of São Paulo City. J Pain. 2014;15(11):1081-91. doi:10.1016/j.jpain.2014.07.001.

In the city of São Paulo, the landline telephone coverage is approximately 76% and can be considered adequate for studies such as this. Nevertheless, to reduce the bias due to sample and population distribution differences, the data underwent post-stratification weighting. The study design weights were adjusted to the distribution of age, sex, and level of education of the São Paulo’s population. This procedure ensures the sample representativeness and internal validity and has rarely been employed previously.

The majority of the factors associated with CP observed in the present study were similar to results reported in other studies in developed countries. Women reported CP more frequently than men (34.7% vs. 20.6%). In European countries and Canada the difference between men and women varied from 16.9% to 56% for women, and from 11% to 28% for men99. Català E, Reig E, Artés M, Aliaga L, López JS, Segú JL. Prevalence of pain in the Spanish population: telephone survey in 5000 homes. Eur J Pain. 2002;6(2):133-40. doi:10.1053/eujp.2001.0310,1313. Blyth FM, March LM, Brnabic AJ, Jorm LR, Williamson M, Cousins MJ. Chronic pain in Australia: a prevalence study. Pain. 2001;89(2-3):127-34. doi:10.1016/S0304-3959(00)00355-9,1414. Smith BH, Elliott AM, Chambers WA, Smith WC, Hannaford PC, Penny K. The impact of chronic pain in the community. Fam Pract. 2001;18(3):292-9. doi:10.1093/fampra/18.3.292,1515. Meana M, Cho R, DesMeules M. Chronic pain: the extra burden on Canadian women. BMC Womens Health. 2004;4, Suppl 1:S17. doi:10.1186/1472-6874-4-S1-S17,2222. Eriksen J, Jensen MK, Sjøgren P, Ekholm O, Rasmussen NK. Epidemiology of chronic non-malignant pain in Denmark. Pain. 2003;106(3):221-8. doi:10.1016/S0304-3959(03)00225-2. Although epidemiologic studies clearly demonstrated that women have a higher pain prevalence than men, animal and human experimental pain studies are not strongly consistent. According to some recent reviews, women have greater pain sensitivity (lower levels of threshold and tolerance), activate specific brain regions in response to pain stimuli, and inhibit pain less than men (difference in endogenous pain modulation). In addition, psychosocial factors and gonadal hormones, mainly estradiol, have been shown to increase the risk of pain occurrence. The prevalence of CP increases progressively with age. This association was observed previously99. Català E, Reig E, Artés M, Aliaga L, López JS, Segú JL. Prevalence of pain in the Spanish population: telephone survey in 5000 homes. Eur J Pain. 2002;6(2):133-40. doi:10.1053/eujp.2001.0310,1313. Blyth FM, March LM, Brnabic AJ, Jorm LR, Williamson M, Cousins MJ. Chronic pain in Australia: a prevalence study. Pain. 2001;89(2-3):127-34. doi:10.1016/S0304-3959(00)00355-9,1414. Smith BH, Elliott AM, Chambers WA, Smith WC, Hannaford PC, Penny K. The impact of chronic pain in the community. Fam Pract. 2001;18(3):292-9. doi:10.1093/fampra/18.3.292,2222. Eriksen J, Jensen MK, Sjøgren P, Ekholm O, Rasmussen NK. Epidemiology of chronic non-malignant pain in Denmark. Pain. 2003;106(3):221-8. doi:10.1016/S0304-3959(03)00225-2,2828. Schmidt CO, Raspe H, Pfingsten M, Hasenbring M, Basler HD, Eich W et al. Back pain in the German adult population: prevalence, severity, and sociodemographic correlates in a multiregional survey. Spine. 2007;32(18):2005-11. doi:10.1097/BRS.0b013e318133fad8. In one study, the prevalence was higher among people aged 67 years or more than among the 16–24 year age group2222. Eriksen J, Jensen MK, Sjøgren P, Ekholm O, Rasmussen NK. Epidemiology of chronic non-malignant pain in Denmark. Pain. 2003;106(3):221-8. doi:10.1016/S0304-3959(03)00225-2. In the present study, the CP prevalence was higher in the 45–64 year age group than in other groups reporting CP. This higher prevalence of CP among middle-age adults was also observed in Israel and France1010. Bouhassira D, Lantéri-Minet M, Attal N, Laurent B, Touboul C. Prevalence of chronic pain with neuropathic characteristics in the general population. Pain. 2008;136(3): 380-87. doi:10.1016/j.pain.2007.08.013,1919. Neville A, Peleg R, Singer Y, Sherf M, Shvartzman P. Chronic pain: a population- based study. Isr Med Assoc J. 2008;10(10):676-80..

Regarding education, individuals with fewer years of schooling had a higher chance of having CP than those with higher levels of schooling, as reported previously1313. Blyth FM, March LM, Brnabic AJ, Jorm LR, Williamson M, Cousins MJ. Chronic pain in Australia: a prevalence study. Pain. 2001;89(2-3):127-34. doi:10.1016/S0304-3959(00)00355-9,1919. Neville A, Peleg R, Singer Y, Sherf M, Shvartzman P. Chronic pain: a population- based study. Isr Med Assoc J. 2008;10(10):676-80.,2222. Eriksen J, Jensen MK, Sjøgren P, Ekholm O, Rasmussen NK. Epidemiology of chronic non-malignant pain in Denmark. Pain. 2003;106(3):221-8. doi:10.1016/S0304-3959(03)00225-2,2828. Schmidt CO, Raspe H, Pfingsten M, Hasenbring M, Basler HD, Eich W et al. Back pain in the German adult population: prevalence, severity, and sociodemographic correlates in a multiregional survey. Spine. 2007;32(18):2005-11. doi:10.1097/BRS.0b013e318133fad8. These data suggested that independent of the country’s development level, people with lower educational levels present a higher risk for CP. The reasons for this are manyfold, and may reflect different degrees of cognitive reserve2929. Farfel JM, Nitrini R, Suemoto CK, Grinberg LT, Ferretti RE, Leite RE et al. Very low levels of education and cognitive reserve: a clinicopathologic study. Neurology. 2013;81(7):650-7. doi:10.1212/WNL.0b013e3182a08f1b and coping in more and less educated individuals. In fact, it has been suggested that patients with a better cognitive reserve may present with less CP after surgery3030. Attal N, Masselin-Dubois A, Martinez V, Jayr C, Albi A, Fermanian J et al. Does cognitive functioning predict chronic pain? Results from a prospective surgical cohort. Brain. 2014;137(3):904-17. doi:10.1093/brain/awt354. However, cross-sectional studies do not allow one to infer causal relationships between these associated factors. For example, since the duration of pain was relatively high in our sample, it cannot be ruled out that long-lasting CP negatively interfered with patients’ quality of life and daily activities to a point where the number of years of education was also reduced because of the burden of CP. Regardless of sex, age, and educational level, CP was associated with co-morbidities. Respondents who reported muscular disorders, fibromyalgia, back and spine diseases, heart diseases in the last year, arthritis, rheumatism, depression, and anxiety or any other psychiatric disorder were more than twice as likely to report CP.

There are some limitations to this study that should be considered. The first limitation is the use of cross-sectional data, which limits our ability to draw conclusions about the direction of effects. Data collection was conducted through structured telephone interviews, which may have overlooked other potential contributors to CP risk in adults. Differences in outcomes of interest according to methods for collecting data may introduce bias to the study, so it is important to highlight that the prevalence of CP in the general population should be followed up throughout the year because pain profiles may change over time. Differences in health measurements between telephone and face-to-face interviews may cause some researchers to question the suitability of telephone surveys. Concerning the external validity of the study, São Paulo has the largest population in Brazil, and about 10% of the general Brazilian population lives in its metropolitan area. In fact, compared to Brazilian data, São Paulo has a similar life expectancy (77 years, compared to 73 in Brazil), lower than 0.9 HDI (0.80, compared to 0.744 in Brazil), men:women ratio (0.89, compared to 0.95 in Brazil), percentage of the population in poverty (28.1%, compared to 31.7% in Brazil), and illiteracy (10.8% compared to 9.6% in Brazil)1616. Instituto Brasileiro de Geografia e Estatística – IBGE. Censo demográfico 2000. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2013 [cited 2003 jun]. Available from: http://www.ibge.gov.br/home/estatistica/populacao/censo2000/
http://www.ibge.gov.br/home/estatistica/...
,1717. Instituto Brasileiro de Geografia e Estatística – IBGE. Pesquisa mensal de emprego. Rio de Janeiro: Instituto Brasileiro de Geografia e Estatística; 2015 [cited nov 2015]. Available: http://www.ibge.gov.br/home/estatistica/indicadores/trabalhoerendimento/pme_nova/pme_201507tm_01.shtm
http://www.ibge.gov.br/home/estatistica/...
,1818. Instituto de Pesquisa Econômica Aplicada – IPEA.IPEA data. [cited 2015 dec]. Available from: http://www.ipeadata.gov.br
http://www.ipeadata.gov.br...
,3131. United Nations Development Programme. Work for human development: briefing note for countries on the 2015 Human Development Report: Brazil. 2015 [cited nov 2015]. (Human Development Report 2015). Available from: http://hdr.undp.org/sites/all/themes/hdr_theme/country-notes/BRA.pdf
http://hdr.undp.org/sites/all/themes/hdr...
.

In conclusion, the prevalence of CP was high in the city of São Paulo and similar to the prevalence observed in developed countries. The highest prevalence was found in women, in the 34–64 year age group, in respondents reporting low educational level (< 15 years) and several co-morbidities. The present study provides evidence on the high prevalence and burden of CP in a developing country population and should be used to support treatment and prevention policies in this population.

ACKNOWLEDGEMENTS

Data collection was supported by Janssen-Cilag Brazil. The authors had full access to the data, and performed all the analyses and wrote the manuscript. No third party company was employed.

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  • Support: Janssen-Cilag Farmacêutica, Brazil, and Centro de Dor, Departamento de Neurologia, Universidade de São Paulo, Brasil.

Publication Dates

  • Publication in this collection
    Dec 2016

History

  • Received
    03 May 2016
  • Accepted
    01 Sept 2016
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