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. 2026 Mar 3;11(2):e1417. doi: 10.1097/PR9.0000000000001417

Chronic pain is associated with disability: results from a large, population-based survey in South Africa

Murray McDonald a,*, Peter R Kamerman b, Romy Parker a
PMCID: PMC12959808  PMID: 41788787

Supplemental Digital Content is Available in the Text.

We show that chronic pain is associated with greater cognitive and physical disability, but not self-care, in a large population-based survey in South Africa.

Keywords: Chronic pain, High impact, Disability, South Africa

Abstract

Introduction:

Chronic pain significantly contributes to global disability, but data from South Africa and other low- and middle-income countries are limited.

Objectives:

We assessed the association between chronic pain (pain/discomfort ≥3 months) and disability using data from a large, population-based household survey. As an exploratory analysis, we also assessed for differences between individuals with high-impact chronic pain (HICP) (chronic pain with significant disability) to those with low-impact chronic pain (chronic pain with no disabilities) in demographics and health status variables.

Methods:

This cross-sectional, descriptive, secondary analysis used data collected in the 2016 South African Demographic and Health Survey, including 10336 adults. Disability was assessed using the Washington Group on Disability items. Statistical analyses were conducted using R v4.2.0 with the survey package.

Results:

Chronic pain prevalence was 18.3% (95% confidence interval [CI]: 16.9–19.7), with 27.8% (95% CI: 25.2–30.5) of individuals with chronic pain experiencing some form of disability. Chronic pain was associated with difficulties in cognition (adjusted odds ratio = 1.74 [95% CI: 1.41–2.14]) and mobility (AOR = 2.07 [95% CI: 1.70–2.52]), but not self-care (AOR = 1.07 [95% CI: 0.71–1.62]). The HICP group represented 1.7% (95% CI: 1.4–2.0) of the population and 9.2% (95%: 7.7–10.7) of those with chronic pain. Compared to the low-impact chronic pain group, the HICP group tended to be older and were more likely to be female, to receive a government grant, and to perceive their health as poor.

Conclusion:

Weak and moderately strong positive associations were found between chronic pain and greater cognitive and mobility disability, respectively.

1. Introduction

Chronic pain negatively affects physical function and participation in daily activities,7,53,54 including self-care.17,52 It also has a complex bidirectional negative relationship with psychological function, contributing to mood disturbances, anxiety, and cognitive decline.51,66 However, most reports on the disabling effects of chronic pain have been conducted in high-income settings. The findings from such settings may not fully apply to low- and middle-income settings where differences in disease burden (eg, communicable vs noncommunicable diseases), genetics, demographics, social norms, and healthcare systems may influence the impact of chronic pain.29,30

In this study, we investigated the association between chronic pain and disability across three domains: physical activity (impairment of walking or stair climbing), self-care (limited ability to wash and dress), and cognitive function (impaired ability to concentrate or remember) using data from a large, population-based survey in South Africa, an upper middle-income country that carries a significant burden of communicable (eg, HIV and tuberculosis infection) and noncommunicable disease (eg, diabetes mellitus and cardiovascular disease), has significant wealth and living standard disparities, including access to healthcare,1,12,43 but has a prevalence of chronic pain similar to that reported elsewhere.31

As an exploratory secondary aim, we investigated the concept of high-impact chronic pain (HICP), which refers to chronic pain that severely limits function, compared to low-impact chronic pain (LICP), which has less or no impact on function.52,63,65 Our aim was to determine whether individuals with HICP differed from those with LICP in demographics and health status variables.

2. Methods

2.1. Ethical approval

The study was approved by the South African Medical Research Council Ethics Committee (EC008-2/2015). Permission to use the data for a study titled, “Impact of pain in South Africa” was obtained from the Demographic and Health Surveys Program (https://dhsprogram.com).

2.2. Sampling

A total of 10336 adults aged 15 years or older were interviewed between April and November 2016 as part of the most recent South African Demographic and Health Survey funded by the South African government, the Global Fund to Fight AIDS, Tuberculosis and Malaria (Global Fund), the European Union, the United Nations Children's Fund, the United Nations Population Fund.25 This cross-sectional, descriptive national household survey aimed to provide estimates of demographic and health-related information for the country, achieving an 81% response rate for the adult health module (10336 out of 12717 eligible individuals). A brief outline of the sampling and interview processes is described below, with detailed descriptions in Supplement 1 (flowchart, http://links.lww.com/PR9/A386), Supplement 2 (sampling procedures, http://links.lww.com/PR9/A386), and Supplement 3 (fieldworker training procedures, http://links.lww.com/PR9/A386).

Eligible individuals were selected through a stratified 2-stage sampling procedure, detailed in Supplement 2 (http://links.lww.com/PR9/A386). The country was divided into primary sampling units (PSUs) using the Statistics South Africa Master Sample Frame based on the 2011 Census enumeration areas. In the first stage, 750 PSUs from 26 strata were selected with probability proportional to size. Within each PSU, a list of dwelling units was compiled to create the sampling frame for the second stage, which involved systematic selection of 20 dwelling units per PSU. In informal settlements, PSUs were segmented into groups of 20 dwelling units, with one segment randomly selected for sampling.

All households within selected dwelling units were eligible for interviews. In even-numbered dwelling units, all residents aged 15 years and older who were present the night before were eligible to complete the adult health module, excluding those unable to participate due to severe medical conditions or comprehension issues. The adult health module included key data for the analyses, such as demographic information, pain measures, disability assessments, and comorbidity evaluation. Modules were administered in-person (with no proxies) in one of South Africa's 11 official languages by 210 field workers organized into 30 teams. Each team consisted of a supervisor, three female interviewers, 1 male interviewer, 1 nurse, and 1 logistics officer/driver. All survey questions were rigorously forward and back translated and reviewed to ensure consensus before field deployment.

2.3. Outcome variables

Disability was assessed using questions sourced from the Washington Group on Disability Statistics developed under the United Nations Statistical Commission. These items are designed for large surveys and align with the International Classification of Functioning, Disability, and Health25 framework (https://www.washingtongroup-disability.com/question-sets/wg-short-set-on-functioning-wg-ss/). Six disability domains were assessed: problems with hearing, problems with seeing, problems with communicating, cognitive problems, problems with ambulation, and problems with self-care. We chose to use domains previously reported as being associated with pain, namely, cognitive problems,48,52 problems with ambulation,17,53 and problems with self-care.17,52 The questions used in the survey were worded as follows: (1) “do you have difficulty remembering or concentrating,” (2) “do you have difficulty walking a kilometre or climbing a flight of steps,” and (3) “do you have difficulty with self-care such as washing all over or dressing.” Each question was answered on a four-item Likert scale, ranging from no difficulty through to a complete loss of function. “Do not know” was a fifth option.

2.4. Variables of interest

Chronic pain was defined as having pain or discomfort either all the time, or on and off, for more than 3 months. High-impact chronic pain was defined as chronic pain (as defined above) accompanied by significant difficulty or complete inability in at least one of the following domains: remembering and/or concentrating, walking a kilometer and/or climbing stairs, washing and/or dressing. Low-impact chronic pain was defined as chronic pain (as defined) without any difficulty in any of the 3 domains. We extracted data on age, sex, literacy, government grant receipt (a needs-based monthly payment to qualifying South African residents),25 health insurance coverage, healthcare use, location and number of unique pain sites, self-perceived health status, and comorbid conditions (see below) from the dataset.

2.5. Covariates

Participant age (in years), sex (female or male), literacy (cannot read, partly able, able to read), government grant receipt (yes or no), residence location (urban or nonurban), and the presence or absence of other sources of disability were included as covariates in the statistical models (see statistical analysis for model details). Other sources of disability included: (1) having had a stroke; (2) having had a heart attack or angina/chest pains; (3) having chronic obstructive pulmonary disease; (4) having had, or currently having, cancer; and (5) having had tuberculosis (TB).

2.6. Statistical analyses

All statistical analyses were conducted using the R v4.2.059 and the survey package,40 a package that factors in the complex sampling design and sampling weights in the calculation of summary and inferential statistics.

“Do not know” answers for the three disability questions were infrequent, accounting for less than 0.12% of answers. Instead of using listwise deletion of participant data when “Do not know” was provided as an answer, we took the conservative step of reclassifying all “Do not know” responses as having no disability.

For the primary question, we investigated the association between chronic pain and function in each of the three disability domains. Statistical models were generated for each disability domain using multiple ordinal regression with the Likert score as the dependent variable, chronic pain as the independent variable of interest, and age, sex, literacy, residence (urban vs non-urban), government grant receipt, and other potential sources of disability (TB, stroke, heart attack, chronic obstructive pulmonary disease, cancer) as covariates. All covariates were decided on a priori as factors that may affect the outcome and not following univariate screening of variables or using forward/backward selection on multivariable models. The 95% confidence intervals (CIs) of the odds ratios were used to interpret the direction, magnitude, and precision of the relationship between chronic pain and a disability.

To check for multicollinearity between model covariates, variance inflation factors were calculated for all models, and values of 5 or greater were taken to indicate collinearity. In the case of multiple ordinal regression models, the proportional odds assumption could not be directly tested for models constructed from a survey with a complex design. To overcome this problem, Likert scale cut-points were redefined into all possible binary combinations and binary logistic regression models, using a quasibinomial distribution family, were generated for each new binary cut-point. The estimates from each model, with their 95% CIs, were plotted and significant deviations in estimates were assessed by looking at the overlap between estimates and their CIs.

For the exploratory secondary question in those individuals with chronic pain, we compared people living with chronic pain and high disability (HICP; defined as the presence of chronic pain and a complete inability or a lot of difficulty in at least one of the domains of cognition, mobility, and self-care) to people living with chronic pain and no disability (LICP; defined as the presence of chronic pain without any difficulty in cognition, mobility, and self-care). We investigated whether age, sex, and number of unique pain sites (assessed using a “yes” or “no” question for a list of body regions: head/face, neck/shoulders, chest, abdomen, back, limbs, other) differed between the HICP and LICP groups. We also assessed whether having HICP (compared to LICP) was associated with worse health outcomes (self-perceived health status: poor vs average/good/excellent, receipt of government grants: “yes” or “no”, presence of healthcare seeking behaviour in the past 12 months: “yes” or “no”). As an exploratory analysis, we only performed univariate analyses. The relationship between HICP status and age and number of pain sites was assessed using linear regression, whereas the relationship between HICP status and binary variables was assessed by binary logistic regression models, using a quasibinomial distribution family. As an exploratory analysis, we do not report P-values, relying instead on interpretation of regression estimates (95% CIs) to assess the direction, magnitude, and precision of the relationships being assessed. No model checks were made or R2 values calculated for the linear regression models because data weighting and the use of stratification and clustered sampling can result in complex residual behaviours that cannot be interpreted using standard model check and fit metrics. All analysis scripts are available on Zenodo (DOI: 10.5281/zenodo.17182169), the data are available through the Demographic and Health Surveys Program (https://dhsprogram.com), and our reporting was aided by the STROBE guideline.61

3. Results

3.1. General description of the sample

Table 1 summarises the demographic and disease-related data for the entire cohort (NObserved = 10336; pain prevalence = 18.3% [95% CI: 16.9–19.7]). In disability, about 7% of the cohort had difficulty concentrating, about 9% had difficulty walking or climbing stairs, and about 1.5% had difficulty caring for themselves. The average age was ∼39 years, and there were fewer males than females (∼40% male). Two-thirds of the cohort lived in urban areas, and literacy was poor (∼22% were unable or only partly able to read). Overall, ∼90% of all participants rated their health as average, good, or excellent. Consistent with these ratings, ∼88% had not sought healthcare in the past 12 months. Access to health insurance was low (16% had access). About 1% of the cohort had been diagnosed with cancer, having had a stroke, or having chronic obstructive pulmonary disease. Approximately 3% of the cohort had had a heart attack/angina, and ∼5% had being infected by TB.

Table 1.

Demographic and disease characteristics for the full sample.

Characteristic Full sample (NObserved = 10336)
Mean (95% CI)
Age (y)* 38.9 (38.3–39.6)
Characteristic Full sample (NObserved = 10336)
Percent (95% CI)*
Had chronic pain 18.3 (16.9–19.7)
Had any difficulty remembering or concentrating 7.1 (6.5–7.8)
Had any difficulty walking 1 km or climbing stairs 8.8 (8.1–9.5)
Had any difficulty washing or dressing self 1.4 (1.1–1.6)
Female 59.3 (58.1–60.4)
Lived in an urban area§ 66.5 (64.3–68.7)
Literacy
 Cannot read 9.5 (8.6–10.4)
 Partly able 13.1 (12.0–14.1)
 Able to read 77.5 (75.9–79.0)
Perceived health status
 Poor 10.2 (9.4–11.0)
 Average 30.8 (29.4–32.2)
 Good 43.7 (42.2–45.2)
 Excellent 15.3 (14.0–16.6)
Accessed healthcare in the past 12 mo 11.8 (10.8–12.7)
Had health insurance 16.0 (13.9–18.0)
Received government grant 20.1 (18.8–21.4)
Diagnosed with tuberculosis (TB) 5.5 (4.9–6.1)
Diagnosed with stroke 1.4 (1.1–1.7)
Diagnosed with heart disease 3.2 (2.7–3.6)
Diagnosed with cancer 1.1 (0.8–1.4)
Diagnosed with chronic obstructive pulmonary disease 1.5 (1.1–1.8)
*

Age (y) percentiles: 0 (minimum) = 15, 25th = 24, 50th (median) = 35, 75th = 51, 100th (maximum) = 95.

Any difficulty = complete inability, a lot of difficulty, or some difficulty with remembering or concentrating, walking a kilometer or climbing stairs, and/or washing or dressing themselves.

Sex was recorded as a binary variable (male or female).

§

Original categories consisted of urban, rural, and traditional places of residence, but we combined the rural and traditional categories into a single “non-urban” category.

3.2. Primary outcomes

The results of the primary analyses comparing chronic pain and disability are presented in Table 2.

Table 2.

Chronic pain associations with disability.

Characteristic Chronic pain Adjusted odds ratio (95% CI)* McFadden Pseudo-R* (%)
No (NObserved = 8389) Yes (NObserved = 1947)
Percent (95% CI)*
Difficulty remembering or concentrating 1.74 (1.41–2.14) 16.0
 No difficulty 94.6 (94.0–95.2) 85.1 (83.1–87.2)
 Some difficulty 4.2 (3.7–4.8) 11.8 (10.0–13.5)
 A lot of difficulty 1.0 (0.8–1.3) 2.8 (2.1–3.5)
 Cannot at all 0.1 (0.1–0.2) 0.3 (0.1–0.5)
Difficulty walking 1 km or climbing stairs 2.07 (1.7–2.52) 24.0
 No difficulty 93.7 (93.1–94.4) 80.0 (77.6–82.3)
 Some difficulty 4.3 (3.8–4.8) 13.2 (11.2–15.1)
 A lot of difficulty 1.7 (1.4–2.0) 6.2 (5.0–7.3)
 Cannot at all 0.3 (0.2–0.4) 0.8 (0.4–1.1)
Difficulty washing or dressing self 1.07 (0.71–1.62) 21.3
 No difficulty 98.9 (98.7–99.2) 97.4 (96.7–98.1)
 Some difficulty 0.7 (0.5–0.9) 1.7 (1.1–2.2)
 A lot of difficulty 0.3 (0.1–0.4) 0.5 (0.2–0.9)
 Cannot at all 0.1 (0.1–0.2) 0.4 (0.1–0.6)
*

Reference level: no chronic pain.

Percentage of model deviance explained compared to the null model.

Adjusted for age; sex; literacy; government grant receipt; urban/nonurban residence; diagnosed with chronic obstructive pulmonary disease; diagnosed as having had heart disease (heart attack and/or angina pectoris); diagnosed with having, or having had, cancer; diagnosed with having had a stroke; diagnosed with having had tuberculosis.

3.3. Model checks

All models had variance inflation factors less than 5 (ie, no indication of multicollinearity between variables in the models). Visual checks of the proportional odds assumption of ordinal regression models indicated no serious deviations from the assumption (Supplement 4, http://links.lww.com/PR9/A386).

3.4. Cognition

Chronic pain was associated with higher odds of having a cognitive disability compared to those without chronic pain (adjusted odds ratio = 1.74 [95% CI: 1.41–2.14]). However, with the likelihood of residual confounding and inherent measurement error, we interpreted this effect as being weak. Most participants, regardless of chronic pain status, reporting “no difficulty remembering or concentrating,” with few participants in either group reporting “a lot of difficulty” or “could not remember or concentrate at all.”

3.5. Mobility

The findings for the ability to walk or climb stairs were similar to those for cognitive function, such that chronic pain was associated with greater disability (adjusted odds ratio = 2.07 [95% CI: 1.70–2.52]); the relationship was moderately strong. Again, the vast majority, regardless of pain presence, reported “no difficulty walking or climbing stairs.”

3.6. Self-care

Almost all participants (∼98%), regardless of chronic pain status, reporting no difficulty with self-care. Consistent with these data, the point estimate indicated a very weak, positive association (adjusted odds ratio = 1.07), but the 95% CI for the adjusted odds ratio was ambiguous, ranging from 0.71 to 1.62, and based on the likelihood of residual confounding and inherent measurement error, we interpreted this effect as being very unlikely to be positive.

3.7. Secondary outcomes

The results of the secondary analyses, which assessed differences between the HICP group and the low-impact chronic pain group (chronic pain with no disabilities) in demographics and health status, are shown in Table 3.

Table 3.

Exploratory analysis of variables associated with having high-impact chronic pain.

Variable LICP* (NObserved = 1350) HICP (NObserved = 234) Estimate (95% CI)
Mean (95% CI) Beta coefficient
Age (y) 41.7 (40.2–43.1)§ 63.8 (61.3–66.3) 22.2 (19.3–25.0)
No. of unique pain sites 1.3 (1.2–1.3) 1.6 (1.5–1.8) 0.4 (0.2–0.5)
Variable LICP* (NObserved = 1350) HICP (NObserved = 234) Estimate (95% CI)
Percent (95% CI) Odds ratio
Female 61.0 (56.8–65.0) 77.1 (71.3–82.8) 2.16 (1.49–3.13)
Received a government grant 19.9 (17.1–22.9) 70.6 (63.2–78.0) 9.62 (6.49–14.25)
Accessed healthcare in the past 12 mo 16.1 (13.5–18.7) 21.7 (16.0–27.4) 1.44 (0.98–2.13)
Perceived health status was poor 17.1 (14.5–19.7) 54.0 (46.2–61.7) 5.69 (3.93–8.23)
*

Low-impact chronic pain (LICP) = chronic pain without any difficulty remembering and/or concentrating, walking a kilometre and/or climbing stairs, and/or washing or dressing themselves.

High-impact chronic pain (HICP) = chronic pain with complete inability or a lot of difficulty with remembering and/or concentrating, walking a kilometer and/or climbing stairs, and/or washing or dressing themselves.

Reference level: LICP.

§

LICP age (y) percentiles: 0 (minimum) = 15, 25th = 27, 50th (median) = 39, 75th = 56, 100th (maximum) = 95.

HICP age (y) percentiles: 0 (minimum) = 20, 25th = 54, 50th (median) = 66, 75th = 76, 100th (maximum) = 95.

Those with HICP represented 1.7% (95% CI: 1.4–2.0) of the total cohort and 9.2% (95%: 7.7–10.7) of those with chronic pain. Compared to individuals with LICP, those with HICP were more likely to be female (HICP ∼75% female; LICP ∼60% female). Those with HICP were also older by about 20 years on average (large effect size—beta coefficient—and narrow CI), and about half rated their health as being poor (∼3 fold higher than the LICP group; the effect size—odds ratio—was large, and although the CI was wide, the lower limit was still consistent with a large effect size). Most (70%) of the HICP group received some form of government grant (almost 4-fold higher than the LICP group; the effect size—odds ratio—was very large, but precision of the estimate was low). On average, people with HICP had greater number of unique pain sites than people in the LICP group, but the magnitude of the effect size—beta coefficient—was marginal. Moreover, despite substantially more people in the HICP group rating their health as being poor compared to people in the LICP group, healthcare seeking behaviour was about the same in the 2 groups (small effect size—odds ratio—with ambiguous CI).

4. Discussion

4.1. Chronic pain and disability in South Africa

Using data from a large, population-based survey in South Africa, we investigated the association between chronic pain and disability across three domains: physical activity, cognitive function, and self-care. Our secondary aim was to determine whether individuals with HICP differed from those with LICP in selected demographic and health status variables. For our primary objective, we found weak and moderately strong positive associations between chronic pain and greater cognitive and mobility disability domains, respectively, but not with self-care. For our exploratory secondary objectives, we found that compared to the LICP group, the HICP group were more likely to be older, female, rate their health as “poor,” and receive a government grant, yet they were no more likely to use healthcare.

Previous South African studies have shown that chronic pain impairs function and limits activity in people attending primary care,53 HIV clinics,20 palliative care clinics,9,16 and in people suffering from conditions such as inflammatory arthritis.5 The data from this study show that this relationship is present at a population level for disability in cognition and mobility. However, caution should be taken when interpreting the cognition and mobility results. First, for both these domains, very few people, irrespective of whether they had chronic pain, had severe disability. That is, when disability was present, it tended to be mild to moderate in severity. Second, the relationship between chronic pain and disability may be bi-directional, as disabling conditions can also lead to chronic pain, so cause and effect cannot be confirmed through these associations.11,19,51

Cognitive function encompasses several domains, including executive function, language processing, motor skills, attention, and memory.32 Previous studies have associated cognitive impairment with chronic pain,32,48 suggesting it may be a risk factor for cognitive decline with age.66 Chronic pain may impact cognitive function through mechanisms such as competing resources, neuroplasticity, and/or dysregulated neurochemistry.48 In this study, cognitive impairment was assessed only in attention and memory, which does not provide a comprehensive measure of cognition. In addition, sleep and depression, which are notable mediating or moderating factors in this relationship,34 were unavailable in this dataset.

The association between chronic pain and reduced physical function is well established in international populations7,54 and has been observed in local primary care, rural, and urban populations.15,26,53 In this study, physical function was measured by assessing walking and stair-climbing abilities. Although these activities may reflect the higher occurrence of limb and back pain in our sample, walking and stair-climbing might not necessarily be as affected by pain in other areas e.g. neck pain. A more comprehensive measure of physical function may have yielded a higher level of dysfunction, and thus affected the association with chronic pain. In addition, this relationship may be moderated by factors such as physical fitness, depression, anxiety, and analgesic use.6,3739

Previous studies have identified self-care difficulties as common consequences of chronic pain.17,52 A U.S. study found self-care limitations only in those with HICP, who had nearly three times the self-care disability rate as our sample (∼3.7% vs ∼1.4%).52 Similarly, a Spanish study found chronic pain affected washing/dressing least among 13 activities.17 The lack of association between chronic pain and self-care limitations in South Africa may be due to underreporting or a true lack of effect. Underreporting could stem from perceived stigma associated with being sick and potential causes of that illness (eg, HIV infection). Alternatively, a true lack of association might be due to the low prevalence of self-care limitations, the perceived importance or prioritisation of other activities, or having sufficient help with self-care tasks from family or carer support.24,28,41,45,55,56,65

South Africans with chronic pain were more likely to seek healthcare, particularly from public facilities, compared to those without chronic pain. Painful conditions are among the most common reasons for seeking medical care both globally22 and in South Africa.33 If chronic pain is driving increased demand for healthcare services, it could substantially burden the public healthcare system. This may have significant economic consequences in an increasingly ageing population,14,36 necessitating health system strengthening to meet and manage the demand.8,57

4.2. High-impact chronic pain in South Africa

We defined HICP as chronic pain with significant cognitive, mobility or self-care difficulties, and found that ∼1.7% of South Africans experience HICP. Other countries have also attempted to define HICP,3,17,62 but a consensus definition remains elusive,18 making comparisons challenging due to different methodologies. For example, in the United States, HICP prevalence was estimated at 8% using a definition of pain on most days for the last 6 months with significant limitations in life or work activities.13 In Saudi Arabia, the prevalence was 4% using a definition of chronic pain affecting activities of daily living for 3 months or more, with pain severity of at least 7 on a 0 to 10 scale. In Spain, a prevalence of 2.4% was found using a definition of chronic pain on at least 4 to 5 days per week for 3 months and cluster analysis of 13 impairments, limitations, and restrictions.17

Due to survey limitations, we were unable to analyse the relationship between HICP and life role restrictions such as employment, interpersonal relationships, or community engagement. However, compared to people with chronic pain but without disability (LICP), our HICP group shows a strong association with poor self-perceived health, and a strong association with receiving financial support from the government via a social grant. Therefore, we consider our definition and analysis a valid representation of HICP.18

South Africans with HICP are more likely to be older and female than those with chronic pain who are not disabled. The association between age and HICP aligns with studies from the United States,52 Saudia Arabia,3 and Spain,17 possibly due to the relationship between age and disability.58,64 However, although the relationship between female sex and HICP was found in Saudi Arabia,3 it was not observed in the United States,52 or Spain.17 This discrepancy could be due to methodological differences or societal and gender role factors in disability.10,46,47

Interestingly, we found no meaningful association between number of unique pain sites and HICP, aligning with some studies17 but in disagreement with others.17,63 This discrepancy may be due to methodological differences or indicate that a single pain location can cause significant disability.

In our sample, those with HICP were more likely to rate their health as “poor” compared to others with chronic pain but were no more likely to seek healthcare in the previous 12 months, which contrasts with international data.3,17,52 Our study and others suggest that South Africans with chronic pain show higher levels of care seeking.33,44 However, South Africans with disability (especially in cognition and mobility domains) exhibit higher levels of depression and barriers to healthcare,23,50 which might explain the lower than expected healthcare usage in our HICP group. This could also be due to a lack of access to care, availability of care, and/or transport2,21,60 especially considering that they were older and more than 50% were from nonurban areas.60 Further investigation into the care needs and barriers of this group should be a research priority.

5. Limitations

We used a metric for disability and HICP that was relatively narrow in domain and cut-offs that were relatively strict to represent the people living with disabilities. Using this restricted definition may underrepresent the extent of disability/HICP in this population,23,27,35,42 which would affect the generalisability of our findings to other populations.

These data were collected in 2016 and published in 2019 thus may not reflect the current state of pain-related disability. However, the burden of noncommunicable disease1 and socioeconomic circumstances are unlikely to have changed remarkably4,49 and may reasonably reflect the current state of pain-related disability.

6. Recommendations

This research shows that chronic pain is significantly associated with disability in a large, nationally representative population of an upper middle-income country. We recommend that chronic pain should be increasingly included in the national healthcare agenda and encourage further research into the relationship between chronic pain and disability, particularly in LMIC. The concept of HICP appears to be relevant to the South African context and warrants further conceptual refinement and investigation into its utility. We also recommend that any future SADHS or similar survey monitor pain treatments and barriers to healthcare to better understand how chronic pain is managed in South Africa.

Disclosures

The authors have no conflict of interest to declare.

Supplemental digital content

Supplemental digital content associated with this article can be found online at http://links.lww.com/PR9/A386.

Footnotes

Sponsorships or competing interests that may be relevant to content are disclosed at the end of this article.

Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal's Web site (www.painrpts.com).

Contributor Information

Peter R. Kamerman, Email: peter.kamerman@wits.ac.za.

Romy Parker, Email: romy.parker@uct.ac.za.

References

  • [1].Achoki T, Sartorius B, Watkins D, Glenn SD, Kengne AP, Oni T, Wiysonge CS, Walker A, Adetokunboh OO, Babalola TK, Bolarinwa OA, Claassens MM, Cowden RG, Day CT, Ezekannagha O, Ginindza TG, Iwu CCD, Iwu CJ, Karangwa I, Katoto PD, Kugbey N, Kuupiel D, Mahasha PW, Mashamba-Thompson TP, Mensah GA, Ndwandwe DE, Nnaji CA, Ntsekhe M, Nyirenda TE, Odhiambo JN, Oppong Asante K, Parry CDH, Pillay JD, Schutte AE, Seedat S, Sliwa K, Stein DJ, Tanser FC, Useh U, Zar HJ, Zühlke LJ, Mayosi BM, Hay SI, Murray CJL, Naghavi M. Health trends, inequalities and opportunities in south Africa's provinces, 1990–2019: findings from the global burden of disease 2019 study. J Epidemiol Community Health 2022;76:471–81. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [2].Allen EM, Call KT, Beebe TJ, McAlpine DD, Johnson PJ. Barriers to care and health care utilization among the publicly insured. Med Care 2017;55:207–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [3].Almalki MT, BinBaz SS, Alamri SS, Alghamdi HH, El-Kabbani AO, Al Mulhem AA, Alzubaidi SA, Altowairqi AT, Alrbeeai HA, Alharthi WM, Alswat KA. Prevalence of chronic pain and high-impact chronic pain in Saudi Arabia. Saudi Med J 2019;40:1256–66. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [4].World Bank. The world bank in South Africa. Vol. 2025. Washington, DC: World Bank, 2024. [Google Scholar]
  • [5].Benitha R, Tikly M. Functional disability and health-related quality of life in South Africans with rheumatoid arthritis and systemic lupus erythematosus. Clin Rheumatol 2007;26:24–9. [DOI] [PubMed] [Google Scholar]
  • [6].Blyth FM, Noguchi N. Chronic musculoskeletal pain and its impact on older people. Best Pract Res Clin Rheumatol 2017;31:160–8. [DOI] [PubMed] [Google Scholar]
  • [7].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;10:287–333. [DOI] [PubMed] [Google Scholar]
  • [8].Briggs AM, Jordan JE, Sharma S, Young JJ, Chua J, Foster HE, Haq SA, Huckel Schneider C, Jain A, Joshipura M, Kalla AA, Kopansky-Giles D, March L, Reis FJJ, Reyes KAV, Soriano ER, Slater H. Context and priorities for health systems strengthening for pain and disability in low- and middle-income countries: a secondary qualitative study and content analysis of health policies. Health Policy Plan 2022;38:129–49. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [9].Brownstein AJ, Ziganshin BA, Kuivaniemi H, Body SC, Bale AE, Elefteriades JA. Genes associated with thoracic aortic aneurysm and dissection: an update and clinical implications. Aorta (Stamford) 2017;5:11–20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [10].Burstein R, Henry NJ, Collison ML, Marczak LB, Sligar A, Watson S, Marquez N, Abbasalizad-Farhangi M, Abbasi M, Abd-Allah F, Abdoli A, Abdollahi M, Abdollahpour I, Abdulkader RS, Abrigo MRM, Acharya D, Adebayo OM, Adekanmbi V, Adham D, Afshari M, Aghaali M, Ahmadi K, Ahmadi M, Ahmadpour E, Ahmed R, Akal CG, Akinyemi JO, Alahdab F, Alam N, Alamene GM, Alene KA, Alijanzadeh M, Alinia C, Alipour V, Aljunid SM, Almalki MJ, Al-Mekhlafi HM, Altirkawi K, Alvis-Guzman N, Amegah AK, Amini S, Amit AML, Anbari Z, Androudi S, Anjomshoa M, Ansari F, Antonio CAT, Arabloo J, Arefi Z, Aremu O, Armoon B, Arora A, Artaman A, Asadi A, Asadi-Aliabadi M, Ashraf-Ganjouei A, Assadi R, Ataeinia B, Atre SR, Quintanilla BPA, Ayanore MA, Azari S, Babaee E, Babazadeh A, Badawi A, Bagheri S, Bagherzadeh M, Baheiraei N, Balouchi A, Barac A, Bassat Q, Baune BT, Bayati M, Bedi N, Beghi E, Behzadifar M, Behzadifar M, Belay YB, Bell B, Bell ML, Berbada DA, Bernstein RS, Bhattacharjee NV, Bhattarai S, Bhutta ZA, Bijani A, Bohlouli S, Breitborde NJK, Britton G, Browne AJ, Nagaraja SB, Busse R, Butt ZA, Car J, Cárdenas R, Castañeda-Orjuela CA, Cerin E, Chanie WF, Chatterjee P, Chu DT, Cooper C, Costa VM, Dalal K, Dandona L, Dandona R, Daoud F, Daryani A, Das Gupta R, Davis I, Davis Weaver N, Davitoiu DV, De Neve JW, Demeke FM, Demoz GT, Deribe K, Desai R, Deshpande A, Desyibelew HD, Dey S, Dharmaratne SD, Dhimal M, Diaz D, Doshmangir L, Duraes AR, Dwyer-Lindgren L, Earl L, Ebrahimi R, Ebrahimpour S, Effiong A, Eftekhari A, Ehsani-Chimeh E, El Sayed I, El Sayed Zaki M, El Tantawi M, El-Khatib Z, Emamian MH, Enany S, Eskandarieh S, Eyawo O, Ezalarab M, Faramarzi M, Fareed M, Faridnia R, Faro A, Fazaeli AA, Fazlzadeh M, Fentahun N, Fereshtehnejad SM, Fernandes JC, Filip I, Fischer F, Foigt NA, Foroutan M, Francis JM, Fukumoto T, Fullman N, Gallus S, Gebre DG, Gebrehiwot TT, Gebremeskel GG, Gessner BD, Geta B, Gething PW, Ghadimi R, Ghadiri K, Ghajarzadeh M, Ghashghaee A, Gill PS, Gill TK, Golding N, Gomes NGM, Gona PN, Gopalani SV, Gorini G, Goulart BNG, Graetz N, Greaves F, Green MS, Guo Y, Haj-Mirzaian A, Haj-Mirzaian A, Hall BJ, Hamidi S, Haririan H, Haro JM, Hasankhani M, Hasanpoor E, Hasanzadeh A, Hassankhani H, Hassen HY, Hegazy MI, Hendrie D, Heydarpour F, Hird TR, Hoang CL, Hollerich G, Rad EH, Hoseini-Ghahfarokhi M, Hossain N, Hosseini M, Hosseinzadeh M, Hostiuc M, Hostiuc S, Househ M, Hsairi M, Ilesanmi OS, Imani-Nasab MH, Iqbal U, Irvani SSN, Islam N, Islam SMS, Jürisson M, Balalami NJ, Jalali A, Javidnia J, Jayatilleke AU, Jenabi E, Ji JS, Jobanputra YB, Johnson K, Jonas JB, Shushtari ZJ, Jozwiak JJ, Kabir A, Kahsay A, Kalani H, Kalhor R, Karami M, Karki S, Kasaeian A, Kassebaum NJ, Keiyoro PN, Kemp GR, Khabiri R, Khader YS, Khafaie MA, Khan EA, Khan J, Khan MS, Khang YH, Khatab K, Khater A, Khater MM, Khatony A, Khazaei M, Khazaei S, Khazaei-Pool M, Khubchandani J, Kianipour N, Kim YJ, Kimokoti RW, Kinyoki DK, Kisa A, Kisa S, Kolola T, Kosen S, Koul PA, Koyanagi A, Kraemer MUG, Krishan K, Krohn KJ, Kugbey N, Kumar GA, Kumar M, Kumar P, Kuupiel D, Lacey B, Lad SD, Lami FH, Larsson AO, Lee PH, Leili M, Levine AJ, Li S, Lim LL, Listl S, Longbottom J, Lopez JCF, Lorkowski S, Magdeldin S, Abd El Razek HM, Abd El Razek MM, Majeed A, Maleki A, Malekzadeh R, Malta DC, Mamun AA, Manafi N, Manda AL, Mansourian M, Martins-Melo FR, Masaka A, Massenburg BB, Maulik PK, Mayala BK, Mazidi M, McKee M, Mehrotra R, Mehta KM, Meles GG, Mendoza W, Menezes RG, Meretoja A, Meretoja TJ, Mestrovic T, Miller TR, Miller-Petrie MK, Mills EJ, Milne GJ, Mini GK, Mir SM, Mirjalali H, Mirrakhimov EM, Mohamadi E, Mohammad DK, Darwesh AM, Mezerji NMG, Mohammed AS, Mohammed S, Mokdad AH, Molokhia M, Monasta L, Moodley Y, Moosazadeh M, Moradi G, Moradi M, Moradi Y, Moradi-Lakeh M, Moradinazar M, Moraga P, Morawska L, Mosapour A, Mousavi SM, Mueller UO, Muluneh AG, Mustafa G, Nabavizadeh B, Naderi M, Nagarajan AJ, Nahvijou A, Najafi F, Nangia V, Ndwandwe DE, Neamati N, Negoi I, Negoi RI, Ngunjiri JW, Thi Nguyen HL, Nguyen LH, Nguyen SH, Nielsen KR, Ningrum DNA, Nirayo YL, Nixon MR, Nnaji CA, Nojomi M, Noroozi M, Nosratnejad S, Noubiap JJ, Motlagh SN, Ofori-Asenso R, Ogbo FA, Oladimeji KE, Olagunju AT, Olfatifar M, Olum S, Olusanya BO, Oluwasanu MM, Onwujekwe OE, Oren E, Ortega-Altamirano DDV, Ortiz A, Osarenotor O, Osei FB, Osgood-Zimmerman AE, Otstavnov SS, Owolabi MO, P AM, Pagheh AS, Pakhale S, Panda-Jonas S, Pandey A, Park EK, Parsian H, Pashaei T, Patel SK, Pepito VCF, Pereira A, Perkins S, Pickering BV, Pilgrim T, Pirestani M, Piroozi B, Pirsaheb M, Plana-Ripoll O, Pourjafar H, Puri P, Qorbani M, Quintana H, Rabiee M, Rabiee N, Radfar A, Rafiei A, Rahim F, Rahimi Z, Rahimi-Movaghar V, Rahimzadeh S, Rajati F, Raju SB, Ramezankhani A, Ranabhat CL, Rasella D, Rashedi V, Rawal L, Reiner RC, Jr, Renzaho AMN, Rezaei S, Rezapour A, Riahi SM, Ribeiro AI, Roever L, Roro EM, Roser M, Roshandel G, Roshani D, Rostami A, Rubagotti E, Rubino S, Sabour S, Sadat N, Sadeghi E, Saeedi R, Safari Y, Safari-Faramani R, Safdarian M, Sahebkar A, Salahshoor MR, Salam N, Salamati P, Salehi F, Zahabi SS, Salimi Y, Salimzadeh H, Salomon JA, Sambala EZ, Samy AM, Santric Milicevic MM, Jose BPS, Saraswathy SYI, Sarmiento-Suárez R, Sartorius B, Sathian B, Saxena S, Sbarra AN, Schaeffer LE, Schwebel DC, Sepanlou SG, Seyedmousavi S, Shaahmadi F, Shaikh MA, Shams-Beyranvand M, Shamshirian A, Shamsizadeh M, Sharafi K, Sharif M, Sharif-Alhoseini M, Sharifi H, Sharma J, Sharma R, Sheikh A, Shields C, Shigematsu M, Shiri R, Shiue I, Shuval K, Siddiqi TJ, Silva JP, Singh JA, Sinha DN, Sisay MM, Sisay S, Sliwa K, Smith DL, Somayaji R, Soofi M, Soriano JB, Sreeramareddy CT, Sudaryanto A, Sufiyan MB, Sykes BL, Sylaja PN, Tabarés-Seisdedos R, Tabb KM, Tabuchi T, Taveira N, Temsah MH, Terkawi AS, Tessema ZT, Thankappan KR, Thirunavukkarasu S, To QG, Tovani-Palone MR, Tran BX, Tran KB, Ullah I, Usman MS, Uthman OA, Vahedian-Azimi A, Valdez PR, van Boven JFM, Vasankari TJ, Vasseghian Y, Veisani Y, Venketasubramanian N, Violante FS, Vladimirov SK, Vlassov V, Vos T, Vu GT, Vujcic IS, Waheed Y, Wakefield J, Wang H, Wang Y, Wang YP, Ward JL, Weintraub RG, Weldegwergs KG, Weldesamuel GT, Westerman R, Wiysonge CS, Wondafrash DZ, Woyczynski L, Wu AM, Xu G, Yadegar A, Yamada T, Yazdi-Feyzabadi V, Yilgwan CS, Yip P, Yonemoto N, Lebni JY, Younis MZ, Yousefifard M, Yousof HSA, Yu C, Yusefzadeh H, Zabeh E, Moghadam TZ, Bin Zaman S, Zamani M, Zandian H, Zangeneh A, Zerfu TA, Zhang Y, Ziapour A, Zodpey S, Murray CJL, Hay SI. Mapping 123 million neonatal, infant and child deaths between 2000 and 2017. Nature 2019;574:353–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [11].Casey CY, Greenberg MA, Nicassio PM, Harpin ER, Hubbard D. Transition from acute to chronic pain and disability: a model including cognitive, affective, and trauma factors. PAIN 2008;134:69–79. [DOI] [PubMed] [Google Scholar]
  • [12].Chatterjee A, Czajka L, Gethin A. Wealth inequality in South Africa, 1993–2017. World Bank Econ Rev 2022;36:19–36. [Google Scholar]
  • [13].Dahlhamer J, Lucas J, Zelaya C, Nahin R, Mackey S, DeBar L, Kerns R, Von Korff M, Porter L, Helmick C. Prevalence of chronic pain and high-impact chronic pain among adults—United States, 2016. MMWR Morb Mortal Wkly Rep 2018;67:1001–6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [14].Solanki G, Kelly G, Cornell J, Daviaud E, Geffen L. Population ageing in South Africa: trends, impact, and challenges for the health sector. South Afr Health Rev 2019;2019:175–82. [PMC free article] [PubMed] [Google Scholar]
  • [15].de Villiers M, Maree JE, van Belkum C. The influence of chronic pain on the daily lives of underprivileged South Africans. Pain Manage Nurs 2015;16:96–104. [DOI] [PubMed] [Google Scholar]
  • [16].Dekker AM, Amon JJ, le Roux KW, Gaunt CB. “What is killing me most”: chronic pain and the need for palliative care in the Eastern Cape, South Africa. J Pain Palliat Care Pharmacother 2012;26:334–40. [DOI] [PubMed] [Google Scholar]
  • [17].Dueñas M, Salazar A, de Sola H, Failde I. Limitations in activities of daily living in people with chronic pain: identification of groups using clusters analysis. Pain Pract 2020;20:179–87. [DOI] [PubMed] [Google Scholar]
  • [18].Eccleston C, Begley E, Birkinshaw H, Choy E, Crombez G, Fisher E, Gibby A, Gooberman-Hill R, Grieve S, Guest A, Jordan A, Lilywhite A, Macfarlane GJ, McCabe C, McBeth J, Pickering AE, Pincus T, Sallis HM, Stone S, Van der Windt D, Vitali D, Wainwright E, Wilkinson C, de C Williams AC, Zeyen A, Keogh E. The establishment, maintenance, and adaptation of high- and low-impact chronic pain: a framework for biopsychosocial pain research. PAIN 2023;164:2143–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [19].Ehde DM, Jensen MP, Engel JM, Turner JA, Hoffman AJ, Cardenas DD. Chronic pain secondary to disability: a review. Clin J Pain 2003;19:3–17. [DOI] [PubMed] [Google Scholar]
  • [20].Farrant L, Gwyther L, Dinat N, Mmoledi K, Hatta N, Harding R. The prevalence and burden of pain and other symptoms among South Africans attending HAART clinics. South Afr Med J 2012;102:499–500. [DOI] [PubMed] [Google Scholar]
  • [21].Gil-González D, Carrasco-Portiño M, Vives-Cases C, Agudelo-Suárez AA, Castejón Bolea R, Ronda-Pérez E. Is health a right for all? An umbrella review of the barriers to health care access faced by migrants. Ethn Health 2015;20:523–41. [DOI] [PubMed] [Google Scholar]
  • [22].Gureje O, Von Korff M, Simon GE, Gater RJJ. Persistent pain and well-being: a World Health Organization study in primary care. JAMA 1998;280:147–51. [DOI] [PubMed] [Google Scholar]
  • [23].Hanass-Hancock J, Myezwa H, Carpenter B. Disability and living with HIV: baseline from a cohort of people on long term ART in South Africa. PLoS One 2015;10:e0143936. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [24].Hansen C, Sait W. “We too are disabled”: disability grants and poverty politics in rural South Africa. Bristol: Disability and Poverty: Policy Press, 2011. pp. 93–118. [Google Scholar]
  • [25].Health NDo, International I, Council SAMR, Africa SS. South Africa demographic and health survey 2016. Fairfax: ICF International, 2019. [Google Scholar]
  • [26].Igumbor EU, Puoane TR, Gansky SA, Plesh O. Chronic pain in the community: a survey in a township in Mthatha, Eastern Cape, South Africa. South Afr J Anaesth Analgesia 2011;17:329–37. [Google Scholar]
  • [27].Inge D, Pedro Celestino ÁV, Ximena Del Carmen PB, Celia Katherine RA, Peter P, Jo L. Lessons from disability counting in Ecuador, with a contribution from primary health care. Int J Environ Res Public Health 2021;18:5103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [28].Jelsma J, Mkoka S, Amosun SL. Health-related quality of life (HRQoL) domains most valued by urban IsiXhosa-speaking people. Qual Life Res 2008;17:347–55. [DOI] [PubMed] [Google Scholar]
  • [29].Johnson MI, Elzahaf RA, Tashani OA. The prevalence of chronic pain in developing countries. Pain Manag 2013;3:83–6. [DOI] [PubMed] [Google Scholar]
  • [30].Kamerman P, Madden V, Arendse G, Bedwell G, Cajee D, Chinaka T, Mason B, McDonald M, Mqadi L, van der Walt J, Parker R. A nation in pain: high-quality local research as a crucial step to improve pain prevention and care. South Afr J Anaesth Analgesia 2024;30:76–8. [Google Scholar]
  • [31].Kamerman PR, Bradshaw D, Laubscher R, Pillay-van Wyk V, Gray GE, Mitchell D, Chetty S. Almost 1 in 5 South African adults have chronic pain: a prevalence study conducted in a large nationally representative sample. PAIN 2020;161:1629–35. [DOI] [PubMed] [Google Scholar]
  • [32].Khera T, Rangasamy V. Cognition and pain: a review. Front Psychol 2021;12:673962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [33].Labadarios D. South African national health and nutrition examination survey. In: Academy of Science of South Africa Changing patterns of non-communicable diseases: proceedings report. Pretoria: Academy of Science of South Africa, 2014. pp. 102–7. [Google Scholar]
  • [34].Landrø NI, Fors EA, Våpenstad LL, Holthe Ø, Stiles TC, Borchgrevink PC. The extent of neurocognitive dysfunction in a multidisciplinary pain centre population. Is there a relation between reported and tested neuropsychological functioning? PAIN 2013;154:972–7. [DOI] [PubMed] [Google Scholar]
  • [35].Lauer EA, Henly M, Coleman R. Comparing estimates of disability prevalence using federal and international disability measures in national surveillance. Disabil Health J 2019;12:195–202. [DOI] [PubMed] [Google Scholar]
  • [36].Lehohla P. Census 2011: profile of older persons in South Africa. Pretoria: Statistics South Africa Pretoria, 2014. [Google Scholar]
  • [37].Leveille SG, Bean J, Ngo L, McMullen W, Guralnik JM. The pathway from musculoskeletal pain to mobility difficulty in older disabled women. PAIN 2007;128:69–77. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [38].Lipat A, Peterson J, Johnson A, Clark DJ, Cruz-Almeida Y. Higher pressure pain sensitivity may contribute to reduced mobility in older adults with chronic pain. J Pain 2023;24:82. [Google Scholar]
  • [39].Lipat AL, Peterson JA, Clark DJ, Cruz-Almeida Y. Decreased cognitive function is associated with impaired spatiotemporal gait performance in community dwelling older adults with chronic musculoskeletal pain. Brain Cogn 2022;159:105862. [DOI] [PubMed] [Google Scholar]
  • [40].Lumley T. Analysis of complex survey samples. J Stat Softw 2004;9:1–19. [Google Scholar]
  • [41].Maart S, Eide AH, Jelsma J, Loeb ME, Ka Toni M. Environmental barriers experienced by urban and rural disabled people in South Africa. Disabil Soc 2007;22:357–69. [Google Scholar]
  • [42].Madans JH, Loeb ME, Altman BM. Measuring disability and monitoring the UN convention on the rights of persons with disabilities: the work of the Washington Group on Disability Statistics. BMC Public Health 2011;11(suppl 4):S4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [43].Maphumulo WT, Bhengu BR. Challenges of quality improvement in the healthcare of South Africa post-apartheid: a critical review. Curationis 2019;42:1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [44].Mash B, Fairall L, Adejayan O, Ikpefan O, Kumari J, Mathee S, Okun R, Yogolelo WJP. A morbidity survey of South African primary care. PLoS ONE, 2012;7:e32358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [45].Mitra S. The capability approach and disability. J Disabil Pol Stud 2006;16:236–47. [Google Scholar]
  • [46].Mitra S, Posarac A, Vick B. Disability and poverty in developing countries: a multidimensional study. World Develop 2013;41:1–18. [Google Scholar]
  • [47].Moodley J, Graham L. The importance of intersectionality in disability and gender studies. Agenda 2015;29:24–33. [Google Scholar]
  • [48].Moriarty O, McGuire BE, Finn DP. The effect of pain on cognitive function: a review of clinical and preclinical research. Prog Neurobiol 2011;93:385–404. [DOI] [PubMed] [Google Scholar]
  • [49].OECD. OECD economic surveys: South Africa 2022. Vol. 2025. Paris: OECD, 2022. [Google Scholar]
  • [50].Parker R, Madden VJ, Devan D, Cameron S, Jackson K, Kamerman P, Reardon C, Wadley A. Barriers to implementing clinical trials on nonpharmacological treatments in developing countries: lessons learnt from addressing pain in HIV. Pain Rep 2019;4.e783. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [51].Pincus T, Burton AK, Vogel S, Field AP. A systematic review of psychological factors as predictors of chronicity/disability in prospective cohorts of low back pain. Spine 2002;27:E109–E120. [DOI] [PubMed] [Google Scholar]
  • [52].Pitcher MH, Von Korff M, Bushnell MC, Porter L. Prevalence and profile of high-impact chronic pain in the United States. J Pain 2018;20:146–60. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [53].Rauf W, Meyer H, Marcus T, Becker P. The impact of chronic pain on the quality of life of patients attending primary healthcare clinics. South Afr J Anaesth Analgesia 2014;20:122–6. [Google Scholar]
  • [54].Reid KJ, Harker J, Bala MM, Truyers C, Kellen E, Bekkering GE, Kleijnen JJC, Opinion. Epidemiology of chronic non-cancer pain in Europe: narrative review of prevalence, Curr Med Res Opin 2011;27:449–62. [DOI] [PubMed] [Google Scholar]
  • [55].Rohwerder B. Disability stigma in developing countries. K4D helpdesk report. Brighton: Institute of Development Studies, 2018. [Google Scholar]
  • [56].Sadiki MC, Radzilani-Makatu M, Zikhali MP. Acquired physical disability: personal meanings in a rural South African setting. J Psychol Africa 2018;28:514–7. [Google Scholar]
  • [57].Sharma S, Blyth FM, Mishra SR, Briggs AM. Health system strengthening is needed to respond to the burden of pain in low- and middle-income countries and to support healthy ageing. J Glob Health 2019;9:020317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [58].Tas Ü, Verhagen AP, Bierma-Zeinstra SM, Odding E, Koes BW. Prognostic factors of disability in older people: a systematic review. Br J Gen Pract 2007;57:319–23. [PMC free article] [PubMed] [Google Scholar]
  • [59].Team RC. R: A language and environment for statistical computing. Vienna, Austria: R Foundation for Statistical Computing, 2022. [Google Scholar]
  • [60].Vergunst R, Swartz L, Mji G, MacLachlan M, Mannan H. “You must carry your wheelchair”—barriers to accessing healthcare in a South African rural area. Global Health Action 2015;8:29003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [61].Von Elm E, Altman DG, Egger M, Pocock SJ, Gøtzsche PC, Vandenbroucke JP. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. Lancet 2007;370:1453–7. [DOI] [PubMed] [Google Scholar]
  • [62].Von Korff M, DeBar L, Krebs E, Kerns R, Deyo R, Keefe FJ. Graded chronic pain scale revised: mild, bothersome, and high-impact chronic pain. PAIN 2020;161:651–61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [63].Von Korff M, Scher AI, Helmick C, Carter-Pokras O, Dodick DW, Goulet J, Hamill-Ruth R, LeResche L, Porter L, Tait R, Terman G, Veasley C, Mackey S. United States national pain strategy for population research: concepts, definitions, and pilot data. J Pain 2016;17:1068–80. [DOI] [PubMed] [Google Scholar]
  • [64].Wahrendorf M, Reinhardt JD, Siegrist J. Relationships of disability with age among adults aged 50 to 85: evidence from the United States, England and Continental Europe. PLoS One 2013;8:e71893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [65].WHO. International classification of functioning, disability and health. Vol. 2017. Switzerland: World Health Organization, 2017. [Google Scholar]
  • [66].Zhang X, Gao R, Zhang C, Chen H, Wang R, Zhao Q, Zhu T, Chen C. Evidence for cognitive decline in chronic pain: a systematic review and meta-analysis. Front Neurosci 2021;15:737874. [DOI] [PMC free article] [PubMed] [Google Scholar]

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