| | Relationship Between Quality of Life and Self-Efficacy in Persons With Spinal Cord InjuriesAbstract Middleton J, Tran Y, Craig A. Relationship between quality of life and self-efficacy in persons with spinal cord injuries. ObjectiveTo study the interaction between quality of life in people with spinal cord injury (SCI) and expectations of daily living (self-efficacy) and pain. DesignCross-sectional study with multiple independent measures. ParticipantsIncluded 106 persons with SCI of 12 months or more in duration who were living in the community and had enrolled from past admission lists in a rehabilitation unit. InterventionParticipants received no treatments as part of the study but were asked to complete 2 questionnaires by postal survey in their postrehabilitation stage. Main Outcome MeasuresThe Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) and the Moorong Self-Efficacy Scale. ResultsPersons with SCI were found to have lowered quality of life (QOL) compared with the Australian general population. Low self-efficacy and pain intensity were found to reduce QOL across all SF-36 domains even further. Factors such as completeness of lesion, sex, age at time of injury, and time since injury were not associated with reduced QOL. Tetraplegia was associated with lower QOL in physical functioning and greater limitation due to bodily pain. A combination of low self-efficacy and pain intensity was associated with an increased reduction in QOL compared with reductions seen for these factors by themselves. ConclusionsRehabilitation strategies may need to concentrate on improving QOL by targeting factors like low self-efficacy. THERE IS NO QUESTION that acquiring a spinal cord injury (SCI) negatively influences physical and psychologic aspects of health and quality of life (QOL).1, 2, 3, 4, 5, 6, 7, 8 It is generally a debilitating disorder that can have a profound impact on independence and lifestyle, related to loss of motor and sensory function as well as associated problems such as bladder, bowel, and sexual dysfunction, chronic pain, increased risk of mental health problems and drug dependence, increased risk of rehospitalization, relationship and marital difficulties, and poor vocation prospects.1, 6, 9, 10, 11, 12, 13, 14, 15 Medical treatments are initially designed to preserve the life of the person who has suffered an SCI and then to minimize the trauma and loss.8 However, although improvements in health and living can be made with medical, physical, psychologic, and technologic interventions,1, 8, 9, 16 gains are generally limited due to the challenges of the above problems, such as social disadvantage and pain.1, 4, 17, 18 Objective measures of rehabilitation outcome commonly assess level or extent of impairment and activity limitation (disability). However, these types of measures alone are recognized as inadequate for explaining most of the variation in community integration outcomes (participation) postdischarge after rehabilitation.19 It is considered that more than objective measures of functional capacity are needed to assess aspects of well-being in a person with SCI,2, 20 and thus the construct of QOL was developed and has become widely used.21 QOL measures are largely subjective in that they assess the judgment of people about their own health and life status.2 Nevertheless, QOL measures have become established tools in SCI-related research, assessing health from a multidimensional perspective including physical, psychologic, social, and vocational aspects.2, 17, 21, 22 Although there have been many QOL measures used to assess persons with SCI,2, 21 some are becoming recognized as being valid and scientifically robust measures of health.2, 4, 21 The Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36) is considered a reliable measure of QOL and has been frequently used in measuring the impact of disease,8, 23, 24 with a number of studies having now shown that SCI negatively impacts QOL, using the SF-36.4, 7, 8, 13, 18, 25 Additionally, factors such as neuropathic pain have been shown to decrease QOL even further in people with SCI,26 although factors such as negative mood, spasticity, socioeconomic disadvantage, and medical complications have also been found to be associated with lower QOL.4, 8, 18 Furthermore, even the caregivers of people with SCI have been shown to have lowered QOL in comparison with age-matched healthy controls, using the SF-36.27 Factors such as level of lesion, age, time since injury, and completeness have not been consistently found to be associated with lower QOL.8 Self-efficacy and perceived control constructs have been investigated comprehensively and been shown to be important factors influencing health in diverse areas28 including the addictions,29 coronary heart disease,30 weight loss,31 improvement after stroke,32 and improvement in stuttering.33 Self-efficacy has been defined as a person’s belief or sense of confidence in his/her own ability to perform a particular task or behavior successfully in the future.34 However, few studies have examined the relationship between self-efficacy and SCI,28 and there are very few known to the authors that have examined the relationship between QOL and self-efficacy in persons with SCI. A further limitation of studies in this area has been that researchers have measured self-efficacy narrowly based on physical function only35 or used a generic self-efficacy scale.36, 37 Horn et al35 found significant associations between low self-efficacy and level of neurologic impairment. Hampton36, 37 studied the contribution of self-efficacy beliefs to QOL in Chinese people with SCI. Self-efficacy was found to be a very significant contributor to QOL when compared with a range of disability variables.36 Hampton37 also found that self-efficacy, social support, and health status contributed a substantial amount to life satisfaction compared with education level, age, sex, and disability factors. Hampton’s37 findings also suggested that, irrespective of social support, people with higher levels of self-efficacy appeared to be more satisfied with their lives than did people with low self-efficacy. Craig et al38 found that low self-confidence in the SCI person’s perceived ability to control their behavior (similar construct to low self-efficacy) was related to long-term risks of depressive mood. Self-efficacy (perceived control) in persons with SCI has been found to increase during cognitive behavior therapy.39 The above self-efficacy research raises the likelihood that QOL in people with SCI is substantially influenced by attitudinal factors like self-efficacy rather than just disability-related factors, such as completeness of the lesion, level of the lesion, and so on.40, 41 There are no specific self-efficacy measures designed to assess a range of relevant life domains, not only functional, but also social, leisure, and vocational activities in people with SCI, and this lack led to the development and validation of the Moorong Self-Efficacy Scale (MSES).28 The MSES specifically targets the beliefs of SCI people and was found to be a reliable and valid construct with 2 major factors, these being perceptions about daily activities and social functioning.28 Given that self-efficacy is a potentially important factor in health and QOL outcomes, the aim of this study was to investigate the relationship between QOL as measured by the SF-36 and the MSES. A second aim was to examine additional relationships between QOL and factors such as pain, sex, age, level and completeness of neurologic lesion, and time since injury. Methods  Participants Participants included persons with SCI of at least 12 months in duration who had received treatment in a specialized rehabilitation unit after an acute injury or community readmission over the previous 5 years and were now living in the community. Altogether, we sent out 233 invitations asking the persons with SCI to complete the SF-36 and the MSES. Seventeen were sent to incorrect postal addresses, 19 were returned unopened, and 87 were not returned. A total of 110 persons completed and returned the questionnaires, resulting in a reasonable return rate of 51.6%. However, 4 of the 110 had not completed the questionnaires correctly, leaving 106. Of the 106, there were 80 men and 26 women who participated with a mean age ± standard deviation (SD) of 46.7±15.8 years. The majority of the persons with SCI had paraplegia (63% with paraplegia, 37% with tetraplegia), but 39% were assessed as having complete lesions based on the American Spinal Injury Association guidelines for impairment classification.42 This meant that for an incomplete injury, some sensory and or motor function was determined to have been preserved below the level of lesion, including at the S4-5 level. The mean time since the injury was 8.6±10.9 years. Measures Measures were the SF-36 and the MSES. The SF-36 has been shown to have acceptable reliability and validity with a variety of populations including Australia,23, 24, 43, 44 and normative Australian data are available.45 The SF-36 questionnaire was scored by summing and transforming raw data for each of the 8 domains, using the formula in the SF-36 manual.24 Higher scores on the 8 domains suggest higher QOL. The MSES measures a person’s self-efficacy (that is, their belief or sense of confidence in his/her own ability) and is a 16-item questionnaire that has been found to have acceptable reliability and validity. It is scored by summing all 16 items on a 7-point Likert scale ranging from 1 (very uncertain) to 7 (very certain).28 Example items include: “I can avoid having bowel accidents”; I can accomplish most things I set out to do”; and “I can deal with unexpected problems that come up in life.” The full 16 items can be found in another article.28 High scores on the MSES suggest high self-efficacy or stronger beliefs in the person’s ability to control their behavior and outcomes, such as personal hygiene, household participation, maintaining relationships, and accessing community and leisure pursuits.28 Data Analysis We calculated mean values for the 8 SF-36 domains and MSES score for the entire group and SF-36 QOL comparisons made to Australian population norms standardized for age and sex. The influence of the MSES on QOL was determined by dichotomizing subjects on the basis of the MSES median sample (N=106) score of 89. Therefore, scores equal to or less than 89 became group 1 and scores above 89 became group 2. Although dichotomizing on the basis of the median leaves middle-ranking scores in the analysis, a significant advantage of using the median is that the power of the analysis is not decreased as it would be if, for instance, one analyzed only subjects scoring on the low and high end of the scale. A multivariate analysis of variance (MANOVA) was then conducted to determine differences in QOL among the 8 SF-36 domains as a function of high versus low self-efficacy. Scheffé contrasts were then calculated to determine where significant differences occurred. This same MANOVA procedure was performed to determine whether factors such as neurologic level (tetraplegia vs paraplegia), completeness of lesion (complete vs incomplete), sex (male vs female), age at injury (group of 106 split into young and older groups when the injury occurred, the split occurring at the median age of 34 years), and pain intensity (Q.7 in the SF-36 where a score of 0 represents extreme pain levels, 22 represents severe pain, 42 moderate pain, 64 mild pain, and 88 represents very mild pain and 100 no pain; a median score of 42 was used with ≤42 forming group 1 and >42 forming group 2). A chi-square test was performed to determine the overlap between the number of subjects who reported low levels of self-efficacy and high levels of pain intensity. Results  Table 1 shows the descriptive statistics for the entire group of 106 as well as for able-bodied Australians. The SCI group was found to have significantly lower QOL scores on all 8 SF-36 domains when compared with Australian norms standardized for age and sex. Table 1 also shows the mean MSES level for the 106 persons with SCI. Pearson correlation analyses failed to find any significant associations between self-efficacy (MSES scores) and sex, age, level or completeness of lesion, and time since injury. Only level of lesion was found to be significantly associated with the QOL physical functioning domain (r=.34, P<.05; tetraplegia associated with lower QOL scores). No other significant relationships were found between QOL and age, sex, time since injury, and completeness of the lesion. | | |  | Variable | Mean ± SD | 95% CI | SE | Mean Australian Norms ± SE | t | Effect Size |  |
|---|
 | Physical functioning | 37.5±25 | 32.7–42.3 | 2.43 | 82.5±0.2 | 18.5⁎ | 1.80 |  |  | Role–physical | 42.2±39 | 34.7–49.7 | 3.79 | 79.8±0.4 | 9.9⁎ | 0.96 |  |  | Bodily pain | 51.9±29 | 46.2–57.6 | 2.87 | 76.8±0.3 | 8.6⁎ | 0.85 |  |  | General health | 55.6±26 | 50.6–60.6 | 2.53 | 71.6±0.2 | 6.4⁎ | 0.61 |  |  | Vitality | 52.7±22 | 48.4–57.1 | 2.17 | 64.5±0.2 | 5.4⁎ | 0.54 |  |  | Social functioning | 65.7±29 | 59.9–71.4 | 2.88 | 84.9±0.2 | 6.6⁎ | 0.66 |  |  | Role–emotional | 70.4±32 | 62.9–78.0 | 3.80 | 82.8±0.3 | 3.2⁎ | 0.39 |  |  | Mental health | 69.3±20 | 65.5–73.2 | 1.94 | 75.9±0.2 | 3.4⁎ | 0.33 |  |  | MSES score | 84.5±21 | 80.4–88.6 | 2.06 | NA | NA | NA |  | | | |
The MSES correlated significantly with all the SF-36 domains (r=.38 for bodily pain; r=.41 for mental health and role−physical; r=.43 for role−emotional; r=.54 for physical functioning; r=.60 for vitality; r=.64 for general health and social functioning, variances ranging from 14% to 41%). This consistent mild to moderate positive relationship between QOL and MSES (high self-efficacy related to higher QOL) was supported by the finding of substantial differences in QOL as a function of self-efficacy. Figure 1 shows the influence on the 8 SF-36 QOL domains as a function of self-efficacy level, that is, low self-efficacy versus high self-efficacy. MANOVA confirmed that significant differences existed between the 2 groups over the 8 measures (Wilks λ=.53, F8,97=10.7, P<.001). Scheffé post hoc tests showed that significant differences existed (df=104, P<.001) in all SF-36 domains between the 2 groups. Table 2 shows that effect sizes for QOL differences between population norms and persons with SCI possessing low self-efficacy ranged from moderate to very large, but effect sizes for the difference between the high self-efficacy group and the general population on QOL were moderate to large for only 3 domains (physical functioning, role−physical, bodily pain). No substantial differences existed between the general population and those persons with SCI having high self-efficacy for the remaining 5 domains (general health, vitality, social functioning, role−emotional, mental health). | | |  | Variable | Mean Low Self-Efficacy ± SD | Difference to Norms (effect size) | Mean High Self-Efficacy ± SD | Difference to Norms (effect size) | Mean Australian Norms ± SE |  |
|---|
 | Physical functioning | 27.7±21 | 2.61 | 48.0±25 | 1.38 | 82.5±0.2 |  |  | Role–physical | 29.7±37 | 1.35 | 55.7±37 | 0.65 | 79.8±0.4 |  |  | Bodily pain | 42.2±29 | 1.19 | 62.4±27 | 0.53 | 76.8±0.3 |  |  | General health | 42.3±24 | 1.22 | 70.1±20 | 0.07 | 71.6±0.2 |  |  | Vitality | 41.6±20 | 1.14 | 64.8±18 | −0.02 | 64.5±0.2 |  |  | Social functioning | 49.8±29 | 1.21 | 82.8±19 | 0.11 | 84.9±0.2 |  |  | Role–emotional | 58.2±41 | 0.60 | 83.6±32 | −0.02 | 82.8±0.3 |  |  | Mental health | 63.1±21 | 0.61 | 76.0±17 | −0.00 | 75.9±0.2 |  | | | |
No significant differences were found in the QOL domains as a function of sex, completeness of lesion (complete vs incomplete), time since injury, or age at injury. However, neurologic level (tetraplegia vs paraplegia) was found to influence QOL significantly in some domains (fig 2). MANOVA detected significant differences between the 2 groups (Wilks λ=.79, F8,95=3.2, P<.01) and Scheffé post hoc tests found significant differences between the tetraplegic and paraplegic groups (df=104, P<.05) only in the physical functioning and pain SF-36 domains. Figure 3 shows the QOL domains that differed as a function of pain intensity (low pain vs high pain group, median split of 42 on the SF-36 pain intensity Q.7). MANOVA analysis detected significant differences between the high and low pain intensity groups in QOL (Wilks λ=.69, F7,98=6.4, P<.001). Scheffé post hoc tests (df=104, P<.01) confirmed that differences existed between the 2 groups in all SF-36 domain functions except physical functioning (see fig 3). Table 3 displays a 2×2 contingency table showing the number of participants with SCI who reported they had high versus low levels of pain intensity as a function of low versus high levels of self-efficacy. There was a significant tendency (χ12 test=6.25, P<.05) for people with high levels of pain to have low levels of self-efficacy, and vice versa (low levels of pain and high levels of self-efficacy). The positive predictive value or likelihood of pain being associated with low self-efficacy was found to be high (P=.67), with an odds ratio of 2.7 for someone with high pain intensity having low self-efficacy. A question may arise concerning the independence of the self-efficacy construct, that is, that self-efficacy is just another measure of pain. This is unlikely given that the strength of the relationship between self-efficacy and pain intensity was not strong (ϕ=.24, P<.05; ϕ2=.06 [or variance explained 6%]). Furthermore, reference to table 3 shows that 40 of the sample (38%) had self-efficacy and pain scores inconsistent with the notion that self-efficacy is another measure for pain intensity. The combination effect of a person with SCI having 2 QOL risk factors, that is, low self-efficacy and high pain intensity, was determined. The QOL differences (effect sizes [ES]) with the general population were increased even more in comparison with decreases associated with low self-efficacy and high pain intensity individually except for physical functioning (mean ± SD, 29.9±21; ES=2.5; mean role−physical, 21.9±36; ES=1.6; mean general health, 36.9±15; ES=2.3; mean vitality, 35.4±23; ES=1.3; mean social functioning, 37.9±18; ES=2.6; mean role−emotional, 48.7±41; ES=.83; mean mental health, 59.1±22; ES=.76). | | |  | Self-Efficacy | High Pain (≤42) | Low Pain (>42) | Percentage |  |
|---|
 | Low self-efficacy (≤89) | 37 (35) | 18 (17) | 52 |  |  | High self-efficacy (>89) | 22 (21) | 29 (27) | 48 |  |  | Percentage | 56 | 44 | 100 |  | | | |
Discussion  The findings of this research confirmed the results of a number of prior studies that have investigated the QOL of people with SCI.4, 7, 8, 25 The SCI sample that participated in the present study had consistently lower QOL scores than those in the Australian general population across all the 8 SF-36 domains. Not surprisingly, SCI had a large impact on physical functioning, physical role limitations, and pain. These 3 areas were found to have large effect sizes ranging from 1.8, .96, to .85, respectively, but general health difference between the SCI and general population was moderate (ES=.61). This comes as no surprise because prior studies have established that persons with SCI judge areas such as physical loss and limitations and ongoing debilitating pain to have severe long-term implications for their health and QOL.4, 8 Negative impacts for social functioning and vitality (ES=.66, ES=.54) were also found, but smaller though still impressive differences were found for the psychologic domains such as emotional role limitations (ES=.39) and mental health (ES=.33). This is also not surprising given that the social disadvantages arising from impairment and social participation restrictions are perceived as a major problem after SCI.8, 18 Additionally, given that poor mental health is a risk for a substantial minority with SCI,1, 10, 14 it was expected that psychologic aspects of QOL would also be reduced compared with the general population. Interestingly, some studies have not found significant differences between persons with SCI and the general population in the SF-36 mental health domain.4 Factors such as completeness of lesion, sex, age at injury, and time since injury have been inconsistently found to be related to lower QOL,2, 8, 18 and were not found to be associated with QOL in the present research. Women have been found to have a lower QOL after SCI,8 though this could be due to the unbalanced sex samples often used in research. Persons who are older at the time of the injury have been found to have lower QOL. Westgren and Levi8 found a poorer QOL in those over 20 years than those under 20 years of age at injury, and Stensman46 found this effect in those over 34 years at the time of the injury. It is thought older age reduces QOL after SCI due to lowered capacity (eg, reduced physiologic reserve, decreased vitality, aging body) to cope with the impairment.46 Obviously, more work needs to occur to clarify the influence of factors like age and time since injury. Level of neurologic impairment was found to be a significant factor interacting with QOL. People with higher lesions (tetraplegia) were found to have lower QOL, though differences occurred only in 2 SF-36 domains, these being physical functioning and bodily pain domains. It has not been clear from the literature that a higher lesion level will lower QOL relative to a lower lesion, though people with tetraplegia have been shown in recent research to have lower global QOL scores as well as the physical functioning domain.4, 8, 18 Unlike the findings of the present research, Haran et al4 found lower QOL related to bodily pain in people with paraplegia than in those with tetraplegia. Obviously, more work needs to be conducted on differences in QOL between paraplegia and tetraplegia.17 One of the major findings of this research was the substantial association found between QOL and a measure of self-efficacy specifically targeted to SCI. Prior research has produced data to suggest that expectations of control are associated with health quality in people with SCI35, 36, 37, 38, 39 and this was further supported by the findings of the present study. Persons with SCI with low levels of self-efficacy reported significantly lower levels of QOL than SCI persons with higher levels of self-efficacy and moreover, differences occurred in all 8 SF-36 domains. Table 2 shows the effect sizes for the SF-36 domain differences between persons with SCI having low versus high self-efficacy, as well as the SF-36 domains for the Australian general population. Scrutinizing these effect sizes, it becomes clear that self-efficacy beliefs are strongly associated with life quality. For those who believe they have low control over their behavior and life outcomes (ie, low self-efficacy), effect sizes ranged from moderate (mental health, role−emotional) to quite large effect sizes (the remaining 6 domains). In contrast, those SCI persons who believed they had some degree of control (high self-efficacy) had lower QOL for only 3 domains (physical functioning, role−physical, bodily pain), but the remaining 5 domains were no different from the QOL for the general population. This replicates research that has found that persons with SCI can have levels of QOL similar to able-bodied members of society,2 suggesting that certain factors may act to lower QOL in persons with SCI. Clearly, low self-efficacy can negatively impact QOL. Therefore, if this is the case, and research is suggesting it is, rehabilitation strategies should be designed to counter the influence of low self-efficacy. This would involve using cognitive behavior therapy, for instance, to challenge negative attitudes such as “I cannot deal with problems in my life” and “My life is ruined by not being able to avoid having bowel accidents.” If not challenged and changed, these types of self-statements or beliefs may result in increased risks of depressive mood and anxiety.1 Although physical and medical dimensions of SCI often attract most attention in the early stages of rehabilitation, it is becoming clearer that attitudinal issues are at least equally important in contributing to life satisfaction and well-being in the long-term. It would be a critical mistake to believe that a traumatic injury like SCI will necessarily result in low QOL just because of the onset of severe physical impairment. Pain intensity seems also to be an influential factor in reducing life quality as shown in figure 3. Those with high pain intensity were found to have significantly lower QOL than those with lower levels of pain intensity for all the SF-36 domains other than physical functioning. Given that the pain intensity data was based on 1 item (Q.7) from the SF-36 scale itself, this finding will need replication using an independent pain measure. However, others have also found that pain amplifies the decrease in QOL associated with SCI.8, 26 The question may arise whether self-efficacy is independent of the pain measure, that is, is it just a surrogate measure of pain? This is unlikely given the low strength of the association found between the 2 variables shown in table 3. One can assume then that both self-efficacy and pain are independent factors, and this raises some pertinent issues. Inspecting the data in table 3 suggests that it is likely that if someone has low self-efficacy then they have a higher risk of experiencing debilitating pain (P=.67). It is of course not possible to argue causally; however, the odds are high (2.7 times) that a person with SCI possessing low self-efficacy will have a problem with pain (or perhaps vice versa). This may have important therapeutic implications as evidence emerges to suggest that cognitive-behavioral interventions are feasible to run and likely to be effective for individuals with SCI,47, 48 in similar fashion to other chronic pain conditions, where higher pain self-efficacy beliefs have been shown to predict reduced pain and avoidance behaviors.49 People who believe that they have no ability to bring about their desired outcomes in life (be it vocational, social, behavioral, physical, and so on) due to negative thinking, may place themselves at a higher risk of negative medical outcomes such as pain, or negative mood (depression) and chronic anxiety. In turn, this may lead to a decrease in social participation, which is known to reduce life satisfaction.40, 41 Certainly, the connections between all these factors need to be further explored with greater consideration given to them during the rehabilitation process. A further point needs to be made. The negative impact on QOL and life satisfaction may well be cumulative. The combination of the 2 negative factors “low self-efficacy” and “pain intensity” was associated with an even greater reduction in QOL than the reduction in QOL associated with each of the 2 factors independently. This reduction was seen in all SF-36 domains except for physical functioning. This is a concerning finding and needs to be addressed in rehabilitation and in community-based interventions for people with SCI. Study Limitations A limitation of this research involved surveying SCI persons and obtaining around a 50% return. Therefore, future research should prospectively explore the factors that negatively impact on QOL for persons with SCI, as well as investigate the nature of any synergistic effects, to assist development of enhanced therapeutic approaches. A further limitation involved the lack of control for the numerous symptoms that are associated with SCI when examining the relationship between pain intensity, self-efficacy, and QOL. Conclusions  Future studies will need to control for major variables such as age, completeness, time since injury, and so on, so that the influence of pain and self-efficacy is delineated. References  1. 1Craig A, Hancock K, Dickson H, Chang E. Immunizing against depression and anxiety following spinal cord injury. Arch Phys Med Rehabil. 1998;79:375–377. Abstract |
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a Rehabilitation Studies Unit, Faculty of Medicine, University of Sydney & Royal Rehabilitation Centre, Sydney, NSW, Australia b Department of Medical and Molecular Biosciences, University of Technology, Sydney, NSW, Australia. Reprint requests to Ashley Craig, PhD, Dept of Medical and Molecular Biosciences, University of Technology, Sydney, NSW, Australia
Supported by the NSW Premier SCI Grant (grant no. R1PG4). No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the author(s) or upon any organization with which the author(s) is/are associated. PII: S0003-9993(07)01551-1 doi:10.1016/j.apmr.2007.09.001 © 2007 American Congress of Rehabilitation Medicine and the American Academy of Physical Medicine and Rehabilitation. Published by Elsevier Inc. All rights reserved. | |
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