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      Manifestation of Borderline Personality Symptomatology in Chronic Pain Patients Under Stress: An Understated and Exacerbated Consequence of the COVID-19 Crisis

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      Journal of Pain Research
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          Abstract

          Introduction To the best of our knowledge, no one has ever suggested that it is “easy” to suffer from intractable chronic pain, with some subgroups impacted more than others. This burden has had a particularly strong impact in the United States, where the chronic pain treatment system has demonstrated failings with respect to access to care1–8 Because chronic pain is so poorly treated in the United States, patients have struggled not only with their pain and its sequelae but also with mounting frustration and downstream psychological consequences. Depression and suicidality have been linked to poorly controlled pain,9,10 and the authors of a recent study11 noted that these phenomena are a concern within the context of opioid tapering. Similarly, Lembke has recently acknowledged that even mention of tapering can trigger severe anxiety in chronic pain patients,12 with data supporting the relationship between undertreated chronic pain and anxiety.13,14 Although myriad investigations have supported the existence of a reciprocal relationship between chronic pain and depression15–17 as well as between chronic pain and anxiety,18–20 detailed discussion of causality is beyond the scope of this analysis. Personality Disorders and Chronic Pain Although depression and anxiety have been the most investigated psychological sequelae of chronic pain, they are hardly the only psychological conditions for which chronic pain sufferers are overrepresented. Several early reports and studies suggested that patients with personality disorders were significantly overrepresented in the chronic pain patient population.21–24 However, these studies were not particularly methodologically-robust, as clear issues of selection bias, small sample sizes, and reliance only upon semi-structured psychiatric interviews detracted from their validities. It was not until Gatchel et al25 published their prospective multi-site investigation of clinical predictors of psychopathology as strongly relating to low back pain patient outcomes in 1995 that more formidable scientific rigor was used to determine the incidence of personality disorders in the chronic pain population. The authors used a combination of a structured clinical interview and a 120-item patient questionnaire relating to the structured interview in addition to the Minnesota Multiphasic Personality Inventory (MMPI) to determine diagnoses for 324 chronic low back pain patients. Subjects were deemed either “disabled” or “nondisabled” based upon their current vocational statuses, with 36.1% of the disabled patients but only 22.3% of the nondisabled group identified as suffering from a personality disorder. Beyond the mere diagnosis of a personality disorder is the type of personality disorder from which a patient suffers. Based on the American Psychiatric Association’s Diagnostic and Statistical Manual of Mental Disorders (DSM),26 there are 3 “clusters” of personality disorders. Cluster A personalities include the paranoid, schizoid, and schizotypal, and these patients are often described as “odd or eccentric”. Cluster B personalities include the antisocial, borderline, histrionic, and narcissistic, and patients with such disorders are described as “dramatic, emotional, or erratic”. Finally, Cluster C personalities include the avoidant, dependent, and obsessive-compulsive, and are generally described as “anxious or fearful”. In pain management settings, it is the Cluster B patients who have received the most attention and raise the highest level of concern. In 1996, Elliot et al27 published the first study examining the prevalence of personality disorders in chronic pain patients in an outpatient program using a psychometric measure (the Millon Clinical Multiaxial Inventory (MCMI)) that had been validated for the identification of the specific personality disorders. The MCMI profiles yielded evidence of a personality disorder in 66% of the study’s sample, with 19% identified as suffering from Cluster B personality disorders. Not surprisingly, higher Narcissism Scale scores were associated with higher pain scale ratings at discharge, with higher Borderline Scale scores associated with earlier discharge from the program. Borderline Personality Disorder and Chronic Pain Of great concern to pain clinicians is the dramatic over-representation of patients with a comorbid Borderline Personality Disorder (BPD) (or even severe borderline personality features without meeting the full diagnostic criteria for a BPD diagnosis) in the chronic pain population. An excellent summary of the DSM-5 criteria for BPD can be found at: http://www.bpddemystified.com/what-is-bpd/symptoms/ . While data suggest a point prevalence of BPD in the general population of only 1.6%,28 figures as high as 62.5% among chronic pain patients have been identified in the empirical literature.29 Little work has been published on the prevalence of BPD in specific pain syndromes, although a 2012 study indicated that BPD patients are significantly over-represented in the fibromyalgia population.30 It has been noted that the percentage of patients with BPD in medical settings may be underestimated, as they are often simply identified as “difficult patients” rather than being diagnosed with BPD.31 Further, it has been determined that patients with BPD’s pain complaints are more difficult to medically substantiate than those without the characterological disturbance.32 Highlighting the issues that result in Cluster B Personalities’ presentations as challenging patients, Sansone and Sansone33 authored a review in 2007, focusing on specific strategies for treating chronic pain patients with comorbid BPD. The “paradox” of which they wrote are findings that while those with BPD seem impervious to self-inflicted pain (common among BPDs), their tolerance for non-self-inflicted pain has been found in numerous studies to be considerably lower than in patients without this Cluster B disorder. The authors also note challenges associated with findings of BPD patients’ higher prevalence of prescription opioid misuse, noting their tendency toward impulsivity and difficulties with self-regulation. This emotional dysregulation has been determined to contribute to pain sensitivity.34 Further, BPD patients are likely to report higher levels of pain than patients with other personality disorders.35 Regarding treatment of chronic pain patients with BPD, Sansone and Sansone33 emphasize the importance of helping patients understand that analgesics are unlikely to fully treat their pain, the benefits of non-opioid medications, the benefits of non-pharmacological approaches, conservative use of opioid analgesics, and careful monitoring of all opioid prescriptions. Frequent, brief appointments are suggested, along with the establishment of firm boundaries. Not surprisingly, a 2013 study by Tragesser et al determined that BPD in non-pain patients was associated with greater frequency and quantity of opioid abuse, higher risk for misuse as measured by the Revised Screener and Opioid Assessment for Patients with Pain (SOAPP-R), and more severe opioid-related consequences and dependence features.36 More severe borderline features were associated with an even greater risk of abuse. An earlier study indicated that 15% of patients suffering from BPD had histories of opioid abuse or dependence.37 Sansone et al came to similar conclusions among primary care outpatients with histories of opioid prescription, determining that those with BPD were at greater risk for abuse of prescription pain medications.38 The literature has also addressed similar issues regarding demands for excessive opioid analgesics in patients with BPD in palliative care settings.39 The authors of a recent investigation in which patients with chronic pain with comorbid BPD were more likely to misuse prescription opioids attributed this phenomenon to BPD sufferers’ unstable identities and self-harmful impulsivity.40 In a later analysis, Sansone and Sansone41 suggest that BPD symptomatology is often used to interpersonally engage others, with these symptoms, either consciously or unconsciously, used to elicit caretaking from those around them. However, given their tendencies toward unstable interpersonal relationships, extreme mood swings, and explosive anger, these relationships with health-care providers are unlikely to be maintained. This is consistent with Kalira et al's assessment,42 in which they note that patients with BPD are prone to provoking anger and frustration in others, potentially resulting in providers doubting the veracity of their symptoms. Suicidality has been documented as quite prevalent in borderline personalities, with an average of 3 suicide attempts during their lifetimes – primarily involving overdose.43 Further, other self-injurious behaviors (eg, superficial wrist cutting not intended to result in death but rather to relieve emotional tension) are also common among those with BPD,44 with these “parasuicides” too often resulting in unintended deaths. Importantly, longitudinal data have suggested that up to 10% of those suffering from BPD ultimately commit suicide.45 Unfortunately, a recent review concluded that there are no evidence-based guidelines for suicide prevention in BPD.46 For purposes of this analysis, it is important to consider a 2006 study that found that individuals with chronic pain are 2–3 times more likely to commit suicide than those without chronic pain47 – independent of personality disorder status. Similarly, Braden and Sullivan determined in a 2008 investigation that borderline personality traits were predictive of suicide among patients with self-reported chronic pain conditions.48 In 2015, the initial investigation of the specific relationship between chronic pain, BPD, and suicidality was published.49 BPD was associated with the utilization of higher dosages of opioids, the use of benzodiazepines and antidepressants, and medication nonadherence. Not surprisingly, those patients with BPD reported 6.6 times the likelihood of suicidal ideation over the past 12 months and 7.9 times the likelihood of a past-12-month suicide attempt compared to those without BPD. Yet another concern regarding comorbid chronic pain and BPD are findings that chronic pain sufferers with BPD are more likely to be receiving disability compensation than are those without BPD. For example, early work by Burton et al50 determined that workers compensation patients with BPD were less likely to return to work following functional restoration. A small 2003 study51 also found a positive relationship between disability and borderline personality symptoms, with the authors concluding from their finding that the perception of greater disability in the borderline personality group as representing an “unconscious tendency to reestablish their life roles as victims” (p. 442). Two European studies52,53 similarly identified a strong positive association between the use of disability benefits/pensions and BPD. Most recently, BPD features were associated with a greater likelihood of receiving disability for chronic pain, even when the authors controlled for anxiety, depression, and other aspects of patients’ pain.54 The authors offered 3 explanations for their findings. First, negative interpersonal relationships can cause problems with maintaining employment. Second, that those with BPDs have diminished social support networks that could provide a buffer to stress may result in an inability to function at a sufficiently high level to maintain employment. Most relevant to this analysis, the third explanation offered is that those with BPD are more likely to find themselves in conflictual relationships with health-care providers, thus interfering with the quality of care they receive and, consequently, less favorable pain care outcomes. “Diathesis-Stress”, Borderline Personality, and Chronic Pain Many individuals who present at any given time with symptoms of BPD do not do so throughout their lives. In fact, many may carry what are essentially “latent” features of BPD until stress levels become so overwhelming that borderline personality features become manifest. Despite the DSM-V’s26 characterization of the traits that define BPD as “enduring”, there exists considerable disagreement regarding this concept. Crowell et al,55 among numerous others, have suggested a purely psychosocial model of BPD, while others, such as Perez-Rodriguez et al,56 have more recently focused on the neurobiological underpinnings of the disorder. A biopsychosocial conceptualization of BPD could combine these two positions, and numerous experts57–60 on the disorder have considered a biological predisposition toward BPD to put certain individuals at greater risk for the onset of the disorder and more severe manifestations of its symptoms when under considerable psychosocial stress. A diathesis-stress model has also been proposed to help understand why certain individuals will develop chronic pain while others will not do so. Among the early proponents of such a model were Flor and Turk,61,62 who conceptualized chronic pain as an interaction between biological and psychological predispositions (diathesis) and the stress of injury and resulting disability. The copious body of empirical investigation supporting the model has been reviewed in a textbook chapter by Weisberg and Keefe.63 Most relevant to this analysis is the work by Weisberg and Keefe,64 Weisberg,65 and Weisberg et al66 on the possibility that stress of chronic pain and the losses associated with it serving to “trigger” personality disorders to which a patient had been predisposed, yet had not yet manifested themselves. These authors have posited the existence of a bidirectional relationship between chronic pain and personality disorders, as well as claiming that their model provides a rational explanation for the over-representation of personality disorders in the chronic pain population that was discussed earlier in this analysis. Supporting this explanation is their observation that descriptions of many chronic pain patients’ premorbid personality functioning differ dramatically from those observed following the development of their chronic pain. As discussed earlier, whether the predisposing diathesis or diatheses are psychosocial, physiological, or a combination of the two has yet to be firmly established empirically. More relevant is the conceptualization of chronic pain as a “disease of the person” that affects the sufferer beyond the physical sensation of pain itself. Rather, chronic pain affects individuals’ qualities of life by causing potential deficits in function and can have a dramatic impact on a patient vocationally, financially, legally, recreationally, socially, sexually, emotionally, and even spiritually. The COVID-19 Crisis, Chronic Pain, and Borderline Personality Expression: A Potentially Bad Storm To this point, we have elucidated the challenges associated with being a patient with the comorbidities of chronic pain and BPD, as well as treating such patients under normal circumstances. The worldwide COVID-19 crisis has greatly exacerbated these challenges, which will be discussed in the remainder of this analysis. Accepting the diathesis-stress model of chronic pain and BPD, the role of stress in exacerbating pain symptoms cannot be understated. Whether infected with the virus, living with loved ones who are infected or in a high-risk category, or fearing for our lives and/or livelihoods, everyone is under a heightened sense of stress. Much has been written about the levels of individual and societal stress associated with the crisis, and detailed description of all of the related stressors is beyond the scope of this analysis. What is important is the formidable body of literature unequivocally supporting the notion that stress exacerbates chronic pain.67–69 Although the impact of stress on chronic pain experience has been studied extensively, investigation of the impact of societal stress on chronic pain has been limited. Scientists have already begun to address issues of chronic pain treatment as affected by the COVID-19 crisis. Eccleston et al70 have noted that the crisis and response of social distancing have resulted in many having to postpone evaluation and the initiation of treatment due to the misguided view that pain management is “elective.” As the authors express concern that patients with pain will turn to the streets and seek potentially deadly illicit opioids, they recommend that technologies such as telemedicine and digital therapeutics emphasizing effective self-management should be used more widely. Cohen et al71 have recently developed a best practices guideline for chronic pain management during the COVID-19 pandemic and other public health crises. The authors note that “Traditionally, pain management has not been considered a high priority in austere environments or times of crisis” (p. 5). Like Eccleston et al,70 they support telehealth, and opine that utilization of mobile approaches for psychological treatment of chronic pain is perhaps even more compelling than such approaches for physical treatment. Certainly to their credit, in discussing appropriate triage, Cohen et al note the importance of assessing psychiatric considerations. Further, they cite the empirical literature indicating that psychological stress increases the risk for opioid abuse, noting that many patients consciously or unconsciously use opioids to reduce psychological symptoms that may emerge or be exacerbated by the stress of a pandemic. Unique stressors, including those associated with being quarantined, are outlined. Overall, the body of literature on BPD and chronic pain strongly supports our concerns regarding treating previously diagnosed BPD patients. Moreover, it is important to be aware of the likelihood that those who are predisposed to the characterological disturbance will manifest BPD in response to the severe stress of the COVID-19 crisis. Social media has suggested that myriad patients were unable to find adequate pain treatment prior to the onset of the pandemic, reporting that they were discharged from multiple practices “without cause”. It is our sense that many of these patients suffer from BPD, and as clinicians, we understand why physicians may not desire to work with these individuals. However, we also believe that pain management should be provided to all in need of such, and discrimination against these individuals presents an ethical imbroglio. All patients suffering from chronic pain deserve a chance to lead quality lives, even if they are at risk for impulsivity, suicidality, opioid misuse, and disruptive or even violent behavior. While medical systems tend to place the blame on patients for behaviors associated with their personality disorders,72 doing so is a violation of epistemic justice,73,74 and serves to further marginalize an already stigmatized, vulnerable group of patients. We conclude by recommending that at this particularly stressful time, the key to solving the BPD and chronic pain dilemma is more routine screening for personality disorders among all patients receiving pain management services. With progressive frequency, physicians who treat patients with pain are administering screening measures for depression and anxiety, with recent recommendations made for such screening among patients in chronic pain management involving opioid therapy,75 prior to spine surgery,76 in cancer care,77 and in primary care practice, generally.78–80 Further, some suggest that more frequent urine drug testing (UDT) is actually an answer to the opioid misuse problem in the pain management setting,81 with recommendations that all patients receiving chronic opioid therapy undergo monthly UDT – not to exclude patients from treatment – but rather to determine which patients require a higher degree of monitoring in order to optimize treatment safety and efficacy. This approach is similar to one proposed in a recent study of total hip and total knee arthroplasty patients, in which the authors stress screening not as a deterrent to arthroplasty, but rather as a tool to identify patients who would potentially benefit from a higher level of support and to minimize unnecessary utilization of resources.82 Would routine of screening for BPD for chronic pain patients seeking treatment not potentially result in similar outcomes, with benefits to both the patient and physician practices? Effective screening for depression and anxiety is not necessarily less time-consuming than screening for BPD, although more numerous brief screening measures for depression and anxiety have been validated. Undoubtedly, the choice of a BPD screening measure is an important one. Although structured and semi-structured interviews are considered the “gold standards” for the diagnosis of personality disorders, these approaches require a considerable amount of training, expertise and physician time to administer. Accordingly, they cannot be considered practical for use in the pain setting for screening patients for BPD. While a number of screening measures for personality disorders exist, we believe that the most effective and practical for routine screening of BPD in the pain management setting is the McLean Screening Instrument for Borderline Personality Disorder (MSI-BPD).83 Numerous screening measures for all of the DSM personality disorders have been published,84 yet as they screen for multiple personality disorders, they tend to be lengthy and screen for disturbances that may not be particularly relevant to chronic pain management. The MSI-BPD is a 10-item measure specific to BPD. Its balance of sensitivity (0.81) and specificity (0.85) have been determined to be good.83 While not widely used in investigations of the impact of BPD on chronic pain outcomes, the general psychometric properties of the measure are sufficiently strong to justify it as a quick screener for BPD. Positive scores on the MSI-BPD should never be used to exclude a patient with pain from treatment. As it is merely a screener, the tool should be used to identify patients who may likely benefit from psychological or psychiatric evaluation prior to continuing with treatment. Screening should be provided to all patients in a pain practice in order to 1) avoid stigmatizing those suspected of having a BPD, and 2) identify those who potentially do suffer from a BPD yet have not manifested it in their interactions with a practice, yet have the potential to manifest the symptoms in response to high levels of stress. This is particularly important during the ongoing COVID-19 crisis, as patients with chronic pain are dealing not only with their “normal” pain-related stressors but also with remote treatment or a complete lack of treatment, as well as concerns regarding medication shortages and lack of access to alternative and multimodal care.70 Chronic pain patient advocates have expressed concern that identification of patients with BPD will result in many not being able to receive treatment. This is hardly the recommendation that we are making. Should a patient receive a diagnosis of a BPD, he/she should be more closely monitored than non-characterologically-disturbed patients, just as those with greater potential for prescription opioid misuse should be monitored for such more closely than those at lower risk.85,86 Perhaps the analogy of patients at higher risk for substance abuse can be taken further in considering those with BPD. It has been recommended that patients at higher risk for substance abuse can be effectively treated in outpatient pain clinic settings, provided that they work concomitantly with a substance abuse counselor and/or an addiction medicine specialist.87 Accordingly, we recommend not that those with BPD are excluded from necessary treatment that is often necessitated for patients to lead lives of reasonable quality, but that they also receive concomitant mental health services (including Dialectical Behavioral Therapy) in order to help them minimize the behaviors that have too often resulted in their discharge from pain care and often futile efforts to find new pain management specialists to treat them. A perusal of social media over the past 3 months is suggestive of widespread psychological deterioration of many chronic pain patients, with evidence of high levels of vitriol, frank paranoia, and threats regarding self-destructive behaviors (eg, seeking illicit opioids on the streets, suicidality) and outward violence more frequent than had been the case prior to the onset of the COVID-19 crisis. We appreciate that several months of social media posts hardly represent empirical “data”, and that changes in the social media environment may occur as the pandemic progresses, stagnates, or diminishes. Irrespective, we find the trends in borderline types of posts disturbing, and are concerned that many patients will experience difficulties in finding and/or maintaining the relationships necessary to access reasonable-quality pain management. Having made recommendations for screening, referral, and enhanced monitoring, we understand that they will not be universally accepted. Further, we recognize that there will undoubtedly be a degree of variance regarding how patients with comorbid chronic pain and BPD are most effectively managed within individual pain management practices. Irrespective, it would perhaps behoove pain management physicians and their patients to ask themselves 1) are outcomes under the current paradigm of treating all patients presenting for treatment satisfactory?, and 2) can risks to both patients and their physicians be further mitigated by screening for BPD? BPDs are not “going away”, and it appears likely that the COVID-19 crisis is not going to “go away” anytime soon. The stress of poorly managed chronic pain, according to the diathesis-stress theory, is likely to result in increasing levels of stress and, accordingly, increased emotional dysregulation and related behaviors among those suffering from BPD as the COVID-19 crisis persists. Although not a panacea, the simple act of screening all chronic pain patients for BPD may represent an important initial step in identifying patients in pain practices that can benefit from further mental health evaluation and increased monitoring. Perhaps we should have looked at such a paradigm as prudent since the inception of the management of chronic pain. Irrespective, the ongoing COVID-19 crisis gives us even more reason to institute a minor paradigmatic revision in our assessment and treatment of patients with chronic pain.

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          Mental illness-related stigma in healthcare

          Mental illness-related stigma, including that which exists in the healthcare system and among healthcare providers, creates serious barriers to access and quality care. It is also a major concern for healthcare practitioners themselves, both as a workplace culture issue and as a barrier for help seeking. This article provides an overview of the main barriers to access and quality care created by stigmatization in healthcare, a consideration of contributing factors, and a summary of Canadian-based research into promising practices and approaches to combatting stigma in healthcare environments.
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            Managing patients with chronic pain during the COVID-19 outbreak: considerations for the rapid introduction of remotely supported (eHealth) pain management services

            1. Introduction Across the world, pain treatment centres have closed their doors. Because of the COVID-19 pandemic, healthcare providers are abruptly changing their care delivery to protect patients and staff from infection and to reallocate resource towards the greatest acute needs. Elective, routine, and nonemergency casework has stopped in secondary and tertiary centres, while in primary care, patients are requested to stay away or “socially distance,” and in residential care facilities and hospices, strict isolation and separation protocols have been introduced. Before the COVID-19 pandemic, telemedicine and eHealth approaches were being developed and tested in a gradual fashion with many studies focusing on lessons learned and barriers to using digital solutions. 3,37,39,51 Overnight, however, treating or supporting people with non-urgent and long-term conditions at a distance from healthcare providers has become imperative. These immediate changes are happening across healthcare systems. Telemedicine is being used to demand-manage the flow of patients with respiratory distress accessing emergency departments 25 ; video consultation is being introduced in multiple settings 23 ; and using social media is being discussed positively for its potential to direct people to trusted resources, to counteract misinformation, and to provide psychological first aid. 36 Pain management providers face the challenge of delivering face-to-face service through different modes. Fortunately, there is a rich stream of research and clinical experience in the use of different technological solutions. Table 1 provides a summary of the definitions and terminology in use. Table 1 Definitions and terminology used in remotely supported pain management. We consider 4 related factors to help guide healthcare professionals caring for patients with chronic pain: (1) the public health consequences of COVID-19 for patients with pain; (2) the consequences of not treating these patients for the unknown duration of this pandemic; (3) options for remote assessment and management; and (4) clinical evidence supporting remote therapies. Finally, we provide guidance for those attempting to rapidly transition to remote care with technology and discuss the lessons for the future of the pain treatment centre. 2. Public health considerations Pain prevention and control—particularly for chronic pain—will inevitably be disrupted by the COVID-19 pandemic. Diversion of resources will be planned (eg, cancelling elective surgery and outpatient procedures for chronic disease management) and unplanned (eg, medication shortages due to panic buying and inaccessibility of remaining healthcare options during movement restrictions). Longer-term, healthcare workers are likely to be at higher risk of lasting psychological morbidity based on evidence from the 2002 to 2003 SARS epidemic. 33 The effect of the pandemic on pain burden will be differentially distributed across and within populations, depending on population characteristics emerging as determinants of the pandemic, including older age, population density, socioeconomic gradient, smoking prevalence, levels of chronic disease morbidity, availability of diagnostic testing, and access to health care. Some of these characteristics are also associated with higher levels of chronic pain prevalence and burden (eg, older age, socioeconomic status, smoking prevalence, chronic disease comorbidity, and access to health care). 5 Therefore, populations with higher existing pain burden are more likely to experience higher incidence of COVID-19 infections, greater disruption to their usual healthcare access, and worse downstream consequences of abruptly altered health care. In addition, some at-risk population subgroups also have poor access to technologies used in remote care.48 Prevention of chronic pain within populations currently depends on best practice management of acute pain and early recognition of the risk of progression to chronic pain. 6 Drivers of acute pain burden include injury-related pain and treatment-related pain (eg, after surgery). Social isolation measures will directly influence the number and type of injuries experienced within populations (eg, fewer road traffic and workplace accidents, increases in conflict/interpersonal violence, and domestic injuries). Changes in the overall volume and type of surgery (more emergency and high acuity elective surgery) are occurring as health systems pivot to respond to the pandemic. Preventing chronic pain is complex at the best of times, but in a global health pandemic, risk factors for pain morbidity and mortality will be magnified. 3. Not treating chronic pain The high prevalence of chronic pain risks inuring us to suffering, one can easily mistake common for trivial. When people with chronic pain are denied assessment and treatment, their condition can worsen significantly; spontaneous recovery is rare. People living with chronic pain have the largest global morbidity, measured by years lived in disability. 44 People waiting for assessment often report severe levels of pain that interfere with their ability to function, and reports of severe pain are associated with more severe levels of depression in 50% and suicidal thinking in 34.6%. 10 Children and adolescents also report high symptom burden when awaiting evaluation. 43 Furthermore, people waiting over 6 months for assessment experience deteriorating health-related quality of life, increased pain, and increased depression. 30 The risks of harm from undertreatment can be exacerbated further by the risk of harm from inappropriate treatment. In many countries, most notably the United States and Canada, chronic pain management is practiced in the shadow of a crisis of the oversupply and overuse of opioids.47 Given that best practice for prevention of opioid harms is unclear, referral to pain professionals for pain medicine management is common. 4 In the United States, few pain clinics can care for high volumes of patients, and referring everyone for opioid stewardship is unrealistic. 11 In North America, we already see an increase in serious mental health problems as some turn to illicit sources of opioids, while others suffer in silence. 24 Not treating chronic pain will have consequences for individuals, healthcare systems, and providers in the short- and long-term, increasing quantity, severity, and complexity of need. 4. Distance assessment and treatment with technology To address the needs of people with chronic pain, one should look first to pervasive and inexpensive technology such as the telephone. 40 Telemedicine, including telephone consultation, short message services, and video conferencing are used worldwide and are broadly analogous to traditional care, although the benefits and costs of telemedicine are still largely unknown. 28,34 They are minimally disruptive and require a broadly similar healthcare resource. Clinical assessment relying on patient-reported outcome measures can be undertaken remotely. Mobile telephones with camera technology allow for shareable images of paper assessments. In addition, many local electronic health record systems already allow for electronic administration of measures. Several web-based systems have been optimised for people with pain, such as the CHOIR system in the United States 9 or the PAIN OUT system in Europe. 41 Such systems allow clinicians to review measures before appointments. Interdisciplinary evaluations can be modified for distance use before the visit, supporting history and interview. Even aspects of the physical examination can be undertaken virtually, for example, in judging appearance, movement, or in self-examination under guidance. Although there are limitations to the lack of hands-on physical examination possible with telehealth, a modified virtual examination may allow an initial treatment plan to be started. Pain self-management options are available using different technologies (eg, the internet, email, computers, and “smart” phones), which play a central role in health care provided to patients. Most studies have been concerned with remotely delivered self-management interventions for chronic pain, undertaken at one's convenience and without having to leave the home. 12,14,15,42,45 These interventions aim to provide the same information and training in self-management skills as provided in face-to-face pain management programs but use technology in different ways. Interventions have been examined in controlled trials. 20,46 The focus on technology promises increased access and scalability, although evaluations of their impact in reaching scale are scarce. Several of these interventions are already freely available in some parts of the world, and many others are commercially in development or are being offered. 16 A caveat on commercially developed interventions, however, is the current lack of quality control over the content, security, and marketing claims. The burgeoning app market is a good example, and caution should be exercised. 28 Table 2 summarises guidance for those unfamiliar with telemedicine and digital treatments who are tasked with their rapid deployment. Table 2 Practical recommendations for the rapid introduction of remotely supported pain management. 5. Evidence for efficacy and harm of telemedicine and DTx interventions Although telephones are in common clinical use, full-scale telemedicine for people with chronic pain is rare. In general, the evidence is similar to that from primary care studies and is cautiously optimistic but recognizes barriers to implementation, unforeseen harm, and potential for inequity in access and use. 17,21,31,39 Most innovation has been in the development of internet-delivered therapies for people with chronic pain. Many remotely delivered programs can be accessed directly and have minimal requirements. In children and adolescents with mixed chronic pain (eg, sickle cell disease, musculoskeletal pain, juvenile idiopathic arthritis, and headache), remote psychological therapies delivered through the internet or mobile applications show small beneficial effects for reducing pain intensity, including headache severity, after treatment, but not maintained at follow-up. 20 The first Cochrane systematic review of technological interventions for chronic pain in adults found 15 studies with 2000 participants. 18 Several systematic reviews have been published since. 7,13,32,46 Reviews identify small to moderate reductions in pain, disability, and distress in intervention groups compared with any control (including active, standard care, or waitlist control). 7,32 Unsurprisingly, when compared with only active control (eg, face-to-face therapies), no difference in treatment effect was found between remote and in-person therapies. 32 Remotely delivered physical exercise interventions are also available, with benefits comparable with usual care for reducing pain and beneficial compared with no treatment. 1 Although promising, there are concerns related to the evidence underlying remote therapies; relatively few studies assessed for harm, and dropout can be substantial. Access and engagement are important to track and report, particularly as disadvantaged groups use technology less (eg, older adults and disabled people). 2 “Therapeutic alliance” is important but may be more challenging to establish, foster, and maintain remotely. That said, a large trial delivering psychological therapy through an online pain course showed improvement in pain, disability, and emotional functioning compared with waiting list but few differences between groups with varying amounts of therapist contact. 15 Understanding who struggles to engage and use eHealth provision is crucial to maximise effectiveness, as are concerns about privacy, transparency (eg, therapist-generated vs automated messages), and training needs of staff accustomed to face-to-face working. Virtual and augmented reality are rarely used with chronic pain but have potential for remote use, going beyond distraction, with a focus on improving function and reducing distress. 18 Early studies are promising but small. 22,26 6. Discussion COVID-19 will have consequences for people with chronic pain, a large population with the greatest global burden of disease. The downstream consequences of disrupting treatments for chronic pain have yet to be modelled but are likely to be substantial. Many healthcare professionals specialising in pain have skills directly relevant to the acute response to the pandemic and so will be redeployed; others may be able to maintain some service delivery to affected individuals. Telemedicine and eHealth interventions for service delivery will be attempted and will be novel for many. Ubiquitous communication technology is relatively inexpensive to access. It is practically possible to communicate with patients if the personnel and infrastructure are available. In some treatments, such as psychologically orientated self-management, investment in developing web-based or application-based platforms delivering pain self-management has produced some evidence of efficacy, and some products are freely available to download. Healthcare providers need to be aware that many of the behavioural components of eHealth self-management are not only potentially helpful for managing pain but also for emotional distress related to the COVID-19 pandemic. In Table 3, we suggest research priorities to improve the evidence for distance interventions and learn from this abrupt change in our practice. Table 3 Research priorities for remotely supported (eHealth) pain management services. Changing practice in such an unplanned way will have positive and negative consequences, many unforeseen. Systems can establish protocols that can enable them to oversee, monitor, and capture important patient and provider outcomes and perspectives. When we come to redesign services after the pandemic, we will need to share that experience and use it to learn what works, to modify what does not work, and to build new models of care for people living with chronic pain. Conflict of interest statement The authors have no conflicts of interest to declare.
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              Chronic pain-associated depression: antecedent or consequence of chronic pain? A review.

              To determine the current status for the association of chronic pain and depression and to review the evidence for whether depression is an antecedent or consequence of chronic pain (CP). A computer and manual literature review yielded 191 studies that related to the pain-depression association. These reports were reviewed and sorted into seven categories relating to the topic of this paper. Eighty-three studies were then selected according to inclusion criteria and subjected to a structured review. Any medical treatment setting including pain treatment as inclusion criteria for selection of studies. Any patients with any type of chronic pain. The reviewed studies were consistent in indicating that there is a statistical relationship between chronic pain and depression. For the relationship between pain and depression, there was greater support for the consequence and scar hypotheses than the antecedent hypothesis. Depression is more common in chronic pain patients (CPPs) than in healthy controls as a consequence of the presence of CP. At pain onset, predisposition to depression (the scar hypothesis) may increase the likelihood for the development of depression in some CPPS. Because of difficulties in measuring depression in the presence of CP, the reviewed studies should be interpreted with caution.
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                Author and article information

                Journal
                J Pain Res
                J Pain Res
                JPR
                jpainres
                Journal of Pain Research
                Dove
                1178-7090
                15 June 2020
                2020
                : 13
                : 1431-1439
                Affiliations
                [1 ]Department of Biopsychology, Tufts University , Medford, MA, USA
                [2 ]Department of Anesthesia, Critical Care and Pain Medicine, Harvard Medical School/Massachusetts General Hospital , Boston, MA, USA
                [3 ]Department of Diagnostic Sciences, Tufts University School of Dental Medicine , Boston, MA, USA
                [4 ]Department of Public Health and Community Medicine, Tufts University School of Medicine , Boston, MA, USA
                Author notes
                Correspondence: Michael E Schatman Tel +1 425 647-4880 Email Michael.Schatman@tufts.edu
                Author information
                http://orcid.org/0000-0002-4722-9158
                http://orcid.org/0000-0003-3282-3952
                http://orcid.org/0000-0002-1019-0413
                Article
                264761
                10.2147/JPR.S264761
                7304780
                32606909
                3982cab2-fb03-4492-b244-0a8455139d73
                © 2020 Shapiro et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 28 May 2020
                : 02 June 2020
                Page count
                References: 87, Pages: 9
                Categories
                Editorial

                Anesthesiology & Pain management
                Anesthesiology & Pain management

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