Among people living with HIV on chronic opioid therapy, few report receiving guideline concordant monitoring practices. Among those receiving monitoring, high satisfaction was reported. Risk of opioid misuse was not associated with receiving monitoring practice nor satisfaction with that monitoring.
Keywords: HIV, opioid, COT, monitoring, patient perspective
Abstract
Background
Chronic opioid therapy (COT) is common in people living with human immunodeficiency virus (PLHIV), but is not well studied. We assessed opioid risk behaviors, perceptions of risk, opioid monitoring, and associated Current Opioid Misuse Measure (COMM) scores of PLHIV on COT.
Methods
COT was defined as ≥3 opioid prescriptions ≥21 days apart in the past 6 months. Demographics, substance use, COMM score, and perceptions of and satisfaction with COT monitoring were assessed among PLHIV on COT from 2 HIV clinics.
Results
Among participants (N = 165) on COT, 66% were male and 72% were black, with a median age of 55 (standard deviation, 8) years. Alcohol and drug use disorders were present in 17% and 19%, respectively. In 43%, the COMM score, a measure of potential opioid misuse, was high. Thirty percent had an opioid treatment agreement, 66% a urine drug test (UDT), and 12% a pill count. Ninety percent acknowledged opioids’ addictive potential. Median (interquartile range) satisfaction levels (1–10 [10 = highest]) were 10 (7–10) for opioid treatment agreements, 9.5 (6–10) for pill counts, and 10 (8–10) for UDT. No association was found between higher COMM score and receipt of or satisfaction with COT monitoring.
Conclusions
Among PLHIV on COT, opioid misuse and awareness of the addictive potential of COT are common, yet COT monitoring practices were not guideline concordant. Patients who received monitoring practices reported high satisfaction. Patient attitudes suggest high acceptance of guideline concordant care for PLHIV on COT when it occurs.
In the past 2 decades, there has been a dramatic increase in the use of prescription opioids in the United States. Since 1999, the consumption of hydrocodone has more than doubled and oxycodone use has increased by nearly 500% [1]. During the same period, the number of drug overdose deaths has more than tripled, totaling 64070 in 2016, with 63% of the overdose deaths related to opioids in 2015 [2, 3]. Half of opioid-related deaths involve a prescription opioid. Forty-five percent of people who use heroin are addicted to prescription opioids, and a history of prescription opioid use remains the strongest predictor of heroin use [4, 5].
Pain accounts for 20.7% of ambulatory healthcare visits, and chronic pain has been reported in 30%–90% of human immunodeficiency virus (HIV)–infected adults, compared to 30% of the general US population [6–9]. Furthermore, 31% of people living with HIV (PLHIV) in the Veterans Aging Cohort Study were prescribed opioids for pain in a 12-month period [10]. The importance of appropriate monitoring for patients on chronic opioid therapy (COT) has been highlighted with the publication of the first Centers for Disease Control and Prevention opioid prescribing guidelines [11, 12], as well as guidelines tailored specifically to PLHIV by the Infectious Diseases Society of America [13]. Despite guidelines that recommend incorporation of opioid treatment agreements, urine drug tests (UDTs), pill counts, use of prescription drug monitoring programs, and use of risk assessment tools into pain management care delivery, few clinicians currently follow these best practices [14–17]. To date, little is known about opioid monitoring practices among PLHIV on COT, nor the patients’ perceptions of those monitoring practices, when applied. To address the current epidemic of prescription opioid drug use disorder, it is important to better understand current monitoring practices and barriers to implementing practice-improvement programs, from the vantage point of patients [18].
In this study, we describe patients’ opioid risk behaviors, perceptions of opioid risk, and the receipt of and satisfaction with opioid monitoring (ie, opioid treatment agreements, UDTs, pill counts) using baseline data from an observational study of PLHIV on COT (ClinicalTrials.gov identifier NCT02525731). We explored differences in the study population, stratified by Current Opioid Misuse Measure (COMM) score (<9 or ≥9), a measure of misuse of opioid pain medications [19]. Finally, we explored the association between the COMM, and (1) the extent of appropriate monitoring and (2) patient satisfaction with monitoring.
METHODS
Setting and Study Sample
The Atlanta-based clinic is an urban Ryan White HIV/AIDS Program–funded clinic, affiliated with the largest area safety-net hospital in Georgia. The clinic serves >6000 uninsured or underinsured patients who are predominantly African American and economically disadvantaged. The vast majority of these patients carry an AIDS diagnosis and those who do not have an AIDS diagnosis are either ≤24 years of age, pregnant, severely mentally ill, have a substance use disorder, or have complicating medical comorbidities [20]. The Boston-based clinic is also affiliated with Boston’s largest safety-net hospital and serves a population where approximately 70% of patients come from underserved populations, including low-income families, minorities, and immigrants. It has been in operation since 1988 and serves 1400 patients. Neither clinic had an official policy to guide COT initiation or monitoring at the time the study was conducted. The Boston clinic had a co-located addiction specialist in the clinic who could provide consults or co-management of complex cases. Atlanta lacked an addiction specialist.
Inclusion criteria for the observational cohort were the following: age ≥18 years; HIV-infected; English-speaking; and receiving COT (defined as having ≥3 opioid prescriptions written at least 21 days apart during the prior 6 months). This working definition of COT has been used as a pragmatic means of identifying individuals who receive opioids daily for chronic pain [21]. A list of potential participants was generated from the medical record using an algorithm to identify patients meeting entry criteria. Clinicians on the research team then reviewed the medical records of those identified to confirm eligibility. Research assistants contacted potential participants within the HIV clinics or by telephone to describe the study and offer participation. Eligible and interested participants were invited for a final screening and baseline assessment. After informed consent, participants completed a 60- to 90-minute research assistant–administered survey. Study participants were compensated with $35 (cash or gift card equivalent) for participation in the survey.
Demographic, Clinical, and Behavioral Measures
The following domains were assessed in the survey: demographics; HIV transmission risk and date of diagnosis; antiretroviral therapy use; hepatitis C virus testing; education level [22]; housing instability and financial insecurities (adapted from Kim et al [23]); food insecurity [24]; depressive symptoms (Center for Epidemiologic Studies Depression Scale [CES-D]) [25]; medications with medical record reconciliation (HIV, opioids, nonopioid pain relievers, psychiatric medications); anxiety (State-Trait Anxiety Inventory) [26]; posttraumatic stress disorder (PTSD) scores (PTSD Checklist for the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition) [27]; substance use (Addiction Severity Index and Texas Christian University Drug Screen II) [28, 29]; opioid misuse (COMM) [19]; and perceptions of COT, satisfaction with COT monitoring, and receipt of naloxone [30, 31]. Research assistants entered data from the survey-based interviews directly into REDCap (Research Electronic Data Capture). Project managers completed quality assurance data reviews. The complete survey is included in the Supplementary Appendix.
Current Opioid Misuse Measure
Guidelines recommend the use of the COMM as part of the assessment for patients on COT [17]. The COMM is a 17-question patient self-report assessment of aberrant behavior related to opioids in the past 30 days. Aberrant behaviors in this context are behaviors concerning for addiction or taking the medication other than how it was prescribed, including taking pain medication for symptoms other than pain, seeking early or outside prescriptions for pain medications, or using someone else’s prescription opioids. A COMM score of ≥9 was determined to be a good measure of prior 30-day prescription opioid misuse when validated in patients receiving care in specialty pain management clinics. In a subsequent study, Meltzer et al [32] demonstrated that a COMM score of ≥13 had high sensitivity and specificity of predicting those patients with a prescription drug use disorder. We used the high COMM score as an indicator of potential opioid misuse.
Statistical Analysis
Descriptive statistics were evaluated for subject characteristics overall and stratified by COMM score (<9 vs ≥9). Differences by COMM score were compared using χ2 test, Fisher exact test, 2-sample t test, and Wilcoxon rank-sum test, as appropriate. Post hoc logistic regression analyses explored the relationship between the main independent variable, COMM scores, and the outcomes extent of monitoring and patient satisfaction with monitoring. Six outcomes were explored in regression analyses: 3 COT monitoring practices (ie, opioid treatment agreements, UDTs, pill counts) and, among those who received each monitoring practice, satisfaction with those practices. The satisfaction outcome variables were dichotomized at 10 (ie, 10 = satisfied, <10 = not satisfied), due to the distributions of scores. The following covariates were controlled for due to potential confounding based on the literature and clinical knowledge: age, gender, race, substance use disorder within the previous 12 months, and ever having an opioid overdose. Due to a limited number of events, only gender and substance use disorder were controlled for in analyses of pill count, satisfaction with pill count, and satisfaction with opioid treatment agreements. Post hoc exploratory evaluations of the association between CES-D on reported monitoring practices as well as an evaluation of the Brief Pain Inventory score and medication misuse were also conducted. Given the exploratory, hypothesis-generating nature of these analyses, no adjustment was made for multiple comparisons.
This study was reviewed and approved by the institutional review boards at the Boston University Medical Campus and Emory University School of Medicine, and the Grady (Health System) Research Oversight Committee.
RESULTS
Out of 280 individuals identified as eligible by medical record review, 48 could not be reached for screening, 61 declined screening, and 171 completed screening, 100% of whom were eligible to be enrolled. One individual was unable to provide informed consent due to illness severity, 2 individuals did not have complete data, and 4 individuals did not complete the baseline survey, leaving 165 who comprised the study sample. Study participant demographics are stratified by COMM score (<9 or ≥9) and shown in Table 1. The median age was 55 years (interquartile range [IQR], 49–59 years) with 66.1% men, 72.1% African American/black, and 9.1% Hispanic. Substance use data, not presented in table form, are described here. Eighty-one (48.8%) participants reported using a substance, other than alcohol, in the previous 12 months. Among patients with drug use in the previous 12 months, 64.2% (52/81) reported marijuana as the substance they most frequently used and 21% (17/81) reported crack/cocaine as the substance they most frequently used. One-quarter (44/165 [26.7%]) of participants met criteria for a substance use disorder during the previous year. Drug use disorders were present in 19.3% and alcohol use disorders in 16.9%. Overall, baseline characteristics appeared similar by COMM score.
Table 1.
Demographic and Social Characteristics of People Living with Human Immunodeficiency Virus on Chronic Opioid Therapy for Chronic Pain
Characteristic | Overall | COMM Score ≥9 | COMM Score <9 | P Value |
---|---|---|---|---|
(n = 165) | (n = 71) | (n = 94) | ||
Age, y, median (IQR) | 55 (49–59) | 53 (49–57) | 56 (50–60) | .15 |
Age group, y | ||||
25–34 | 4 (2.4) | 1 (1.4) | 3 (3.2) | |
35–44 | 13 (7.9) | 9 (12.7) | 4 (4.3) | |
45–54 | 69 (41.8) | 33 (46.5) | 36 (38.3) | |
55–64 | 72 (43.6) | 26 (36.6) | 46 (48.9) | |
≥65 | 7 (4.2) | 2 (2.8) | 5 (5.3) | |
Male | 109 (66.1) | 41 (57.7) | 68 (72.3) | .05 |
African American | 119 (72.1) | 54 (76.1) | 65 (69.1) | .33 |
Hispanic | 15 (9.1) | 7 (9.9) | 8 (8.5) | .57 |
Sexuality | .34 | |||
Straight/heterosexual | 112 (67.9) | 51 (71.8) | 61 (64.9) | |
Gay/lesbian/queer/homosexual | 37 (22.4) | 12 (16.9) | 25 (26.6) | |
Bisexual | 15 (9.1) | 7 (9.9) | 8 (8.5) | |
Other | 1 (0.6) | 1 (1.4) | 0 (0.0) | |
Housing | .06 | |||
Own/rent | 140 (84.8) | 56 (78.9) | 84 (89.4) | |
Education | .27 | |||
Graduated high school | 110 (66.7) | 44 (62.0) | 66 (70.2) | |
Health insurance | 152 (92.1) | 66 (93.0) | 86 (91.5) | .73 |
Ran out of money for basic necessities (prior 12 mo) | .73 | |||
Never | 62 (37.6) | 25 (35.2) | 37 (39.4) | |
Occasionally | 55 (33.3) | 26 (36.6) | 29 (30.9) | |
Monthly/weekly/daily | 48 (29.1) | 20 (28.2) | 28 (29.8) | |
Food insecurity (prior 30 d) | 21 (12.7) | 11 (15.5) | 10 (10.6) | .35 |
Jail or prison (prior 12 mo) | 14 (8.5) | 6 (8.5) | 8 (8.5) | .99 |
Data are presented as No. (%) unless otherwise indicated.
Abbreviations: COMM, Current Opioid Misuse Measure; IQR, interquartile range.
Table 2 shows opioid misuse, risk of misuse, and patient beliefs about pain medications. Only 8 (4.8%) reported illicit opioid use in the prior 12 months, while 26.1% reported any history of illicit opioid use. Many patients met criteria for being high risk for opioid misuse, based on the COMM score, with close to half (43.0%) scoring ≥9 and almost one-quarter (22.9%) ≥13. Participants reported a perceived danger of pain medications with 89.8% responding affirmatively to a question about the addiction potential of opioids. With response choices of 0–5 (0 = do not agree at all, 5 = agree very much) the median scores were as follows, when asked about agreement with the statements: “Pain medicine is very addictive” was 5 (IQR, 3–5) and “There is a danger of becoming addicted to pain medicine” was 5 (IQR, 4–5). There appeared to be stronger agreement to “Pain medicine is very addictive” in the COMM ≥9 group.
Table 2.
Patient Report of Opioid Use, Misuse, and Perception of Risk in a Cohort of People Living with Human Immunodeficiency Virus on Chronic Opioid Therapy for Chronic Pain
Characteristic | Overall | COMM Score ≥9 | COMM Score <9 | P Value |
---|---|---|---|---|
(n = 165) | (n = 71) | (n = 94) | ||
History of illicit opioid use | 43 (26.1) | 17 (23.9) | 26 (27.7) | .59 |
Use of illicit opioid in past 12 mo | 8 (4.8) | 4 (5.6) | 4 (4.3) | .73 |
Ever overdosed on opioids | 12 (7.3) | 5 (7.0) | 7 (7.4) | .92 |
Patient beliefs about pain medicationa | ||||
Pain medicine is very addictive, median (25th, 75th percentile) | 5 (3, 5) | 5 (4, 5) | 5 (3, 5) | .04 |
There is a danger of becoming addicted to opioid pain medicine, median (25th, 75th percentile) | 5 (4, 5) | 5 (4, 5) | 5 (4, 5) | .87 |
Answered ≥3 on either of the above 2 questions | 153 (92.7) | 68 (95.8) | 85 (90.4) | .19 |
Data are presented as No. (%) unless otherwise indicated.
Abbreviation: COMM, Current Opioid Misuse Measure.
aScale from 0 to 5 (0 = do not agree at all, 5 = agree very much).
Patient report of COT monitoring and satisfaction with the monitoring are shown in Table 3. Self-report of having received COT monitoring was low overall. Referring to their current clinic, 30.3% reported ever signing an opioid treatment agreement, two-thirds reported ever having a UDT, and 12% reported ever having a pill count. Less than 5% received all 3 types of monitoring; those in the COMM ≥9 group had a higher proportion receiving all 3 types; however, the results were not statistically significant. Twenty-four percent did not receive any type of monitoring and only 10.3% had ever been prescribed naloxone. On a scale from 1 to 10 (1 = not satisfied at all, 10 = extremely satisfied) among those with monitoring, median satisfaction (25th, 75th percentile) with opioid treatment agreements was 10 (7, 10), with UDTs was 10 (8, 10), and with pill counts was 10 (6, 10). COMM scores (using cutoffs at ≥9 or ≥13) were not significantly associated with opioid treatment agreements, UDTs, or pill counts. COMM scores were also not significantly associated with satisfaction with any of the monitoring modalities. Odds ratios for adjusted and unadjusted analyses are reported in Table 4 for COMM ≥9. Models for COMM ≥13 did not appreciably differ from the ≥9 model (data not shown). In a post hoc, exploratory analysis (Supplementary Table 1), no significant association was observed between CES-D and any of the opioid monitoring/satisfaction outcomes. A possible association was found between higher brief pain inventory score (both severity and interference scales) (Supplementary Table 2) and higher odds of responding affirmatively to medication misuse questions on the COMM tool.
Table 3.
Chronic Opioid Therapy (COT) Monitoring and Patient Satisfaction With COT Monitoring in a Cohort of People Living with Human Immunodeficiency Virus on COT for Chronic Pain
Characteristic | Overall | COMM Score ≥9 | COMM Score <9 | P Value |
---|---|---|---|---|
(n = 165) | (n = 71) | (n = 94) | ||
COT monitoring | ||||
Ever signed opioid treatment agreement at current clinic | 50 (30.3) | 28 (39.4) | 22 (23.4) | .05 |
Ever had pain medication stopped due to not following rules of agreement | 11 (18.6) | 7 (23.3) | 4 (13.8) | .34 |
Ever had urine drug test at current clinic | 110 (66.7) | 49 (69.0) | 61 (64.9) | .38 |
Ever had pill count at current clinic | 20 (12.1) | 11 (15.5) | 9 (9.6) | .25 |
Received all 3: treatment agreement, urine drug test, and pill count | 8 (4.8) | 6 (8.5) | 2 (2.1) | .08 |
Patient satisfaction with COT monitoringa | ||||
Opioid treatment agreement, median (25th, 75th percentile) | 10 (7, 10) | 10 (7, 10) | 10 (7, 10) | .25 |
Urine drug test, median (25th, 75th percentile) | 10 (8, 10) | 10 (8, 10) | 10 (8, 10) | .93 |
Pill count, median (25th, 75th percentile) | 10 (6, 10) | 9 (7, 10) | 10 (5, 10) | .81 |
Ever received naloxone | 17 (10.3) | 7 (9.9) | 10 (10.6) | .87 |
Data are presented as No. (%) unless otherwise indicated.
Abbreviations: COMM, Current Opioid Misuse Measure; COT, chronic opioid therapy.
aSatisfaction (scale of 1–10: 1 = not satisfied at all, 10 = extremely satisfied) was assessed only among the subgroup who had ever received each respective type of monitoring (ie, for the overall group, opioid treatment agreement, n = 51; urine drug test, n = 110; pill count, n = 20).
Table 4.
Association Between Current Opioid Misuse Measure Score With Receipt of Monitoring and With Satisfaction Toward the Monitoring in a Cohort of Human Immunodeficiency Virus–Infected Patients on Chronic Opioid Therapy for Chronic Pain
Independent Variable | Outcome | No.a | Unadjusted OR (95% CI) | Adjusted OR (95% CI) |
---|---|---|---|---|
COMM score ≥9 | Pain treatment agreementb | 156 | 2.02 (1.02–3.99) | 1.82 (.89–3.74) |
Urine drug testb | 162 | 1.10 (.56–2.13) | 1.01 (.50–2.04) | |
Pill countc | 165 | 1.73 (.68–4.44) | 1.59 (.60–4.26) | |
Satisfaction with pain treatment agreemente | 50 | 0.38 (.11–1.24) | 0.36 (.10–1.25) | |
Satisfaction with urine drug screend | 110 | 0.55 (.25–1.20) | 0.54 (.22–1.29) | |
Satisfaction with pill counte | 20 | 0.67 (.11–3.92) | 0.52 (.05–5.05) |
Abbreviations: CI, confidence interval; COMM, Current Opioid Misuse Measure; OR, odds ratio.
aSample size varies because individuals who responded “I don’t know” were excluded. Sample size for satisfaction only includes those who responded affirmatively to receiving the respective monitoring practice.
bAdjusted for: age, gender, race, past year substance use disorder, ever had opioid overdose.
cAdjusted for: gender, substance use disorder in the past 12 months.
dAdjusted for: age, gender, race, substance use disorder in the past 12 months, ever had opioid overdose.
eAdjusted for: gender, substance use disorder in the past 12 months.
DISCUSSION
Among PLHIV on COT, 3 findings were most notable: patients clearly understood the significant risk of addiction to their pain medications; patients had high risk of opioid misuse; and yet, patients reported receiving minimal monitoring regarding COT. Patient knowledge of risk of addiction is consistent with a qualitative study of patients on COT in San Francisco [33]. The combination of high risk of misuse and minimal monitoring yields potential for bad outcomes, for both patients’ and the public’s health. Despite the limited monitoring that occurred, patients who did receive it were accepting of the monitoring and reported very high levels of satisfaction with it.
Consistent with other reports, the UDT was the one monitoring practice that a majority (two-thirds) had received at least once in the past [34]. We hypothesize that UDTs are used most because it is an easy task to accomplish for the provider, completed by simply writing an order for the test. However, we do not have information on the extent to which the UDT results were followed up, which is what likely makes UDTs an effective monitoring practice. Few patients in the current cohort reported signing an opioid treatment agreement or having a pill count. However, the current study does report higher levels than earlier studies [34–36]. This follows the logic that systems-level changes may be necessary to effect the uptake of more time and human resource–intensive procedures, such as reviewing and signing an opioid treatment agreement, performing pill counts, and following up the UDT results [37–39]. Guideline concordant care would require patients to receive opioid treatment agreements, UDTs, and pill counts, the 3 of which were received by a negligible percentage of patients [14].
A large proportion of patients had high COMM scores, a predictor of opioid misuse. Though no associations between COMM scores and COT monitoring practices were statistically significant, potentially due to lack of power, the effect sizes we observed between higher COMM score and treatment agreement and having received all 3 practices were notable. These findings should be further explored with a larger sample. We found that other aspects of safe prescribing, such as prescribing naloxone alongside opioids, was only reported by 10% of the patients and did not appear to correlate with COMM-based risk. This represents an opportunity to increase naloxone distribution as a way to improve safe prescribing, as was done by the Department of Veterans Affairs in 2014 [40].
Patients reported higher levels of satisfaction with opioid monitoring practices than we expected. At a time when patient satisfaction has become such an important metric in many healthcare settings, these results are encouraging as they suggest patients are receptive to opioid monitoring practices. This result is particularly susceptible to the selection bias of a cohort study, as it is possible that patients dissatisfied with opioid prescribing practices may have left the current clinics. However, the result suggests that interventions to improve guideline-concordant prescribing and monitoring may be well received by patients. Despite not finding a statistically significant association between COMM scores and satisfaction with monitoring, the effect sizes observed in this exploratory study were notable from a clinical perspective and should be further investigated in a larger-scale study. If confirmed, this may represent a subgroup of patients who need particular attention to engage in the monitoring process.
The study has several limitations. Recall bias and social desirability bias associated with the survey-based interview may have affected results, as patient self-report was not corroborated in the medical record. The baseline assessments were conducted at a time when opioids and the opioid epidemic were prominent in the media, which could have affected patient perception. The patient reports about receiving COT monitoring practices (ie, opioid treatment agreement, UDTs, pill counts) were reported as ever having received that practice at the current clinic. This may overestimate the true amount of monitoring taking place as optimal monitoring requires things such as UDT and pill counts to occur with some regularity. Additionally, given lack of quantifiable data around UDT and pill counts, we are unable to discern if patients are satisfied with the practice itself or if there is a role that frequency, or lack thereof, plays to drive satisfaction. Post hoc analyses exploring the relationship between COMM scores and extent of monitoring or patient satisfaction with monitoring were likely underpowered due to relatively small samples, particularly for outcomes related to pill count. Despite these limitations, the current study had strengths including the following: systematically administered interviews, quality assurance mechanisms including verification of medications with those in the medical record, a thorough review of the study assessment by an additional staff member, and logic checks by the data management team; in addition, the multisite design assessed >1 distinct patient population, providing some heterogeneity in the baseline data.
CONCLUSIONS
Among PLHIV on COT, opioid misuse and awareness of the addictive potential of COT are common. COT monitoring practices among PLHIV are not the norm, with two-thirds ever receiving a UDT, one-third signing an opioid treatment agreement, and only 12% having a pill count. Surprisingly, patients who received these COT monitoring practices reported high satisfaction. Effective implementation of guidelines for care of PLHIV on COT merits attention from HIV clinical teams. Optimal approaches to accomplish this goal are needed, but it is reassuring that patient attitudes suggest high acceptance of such practices.
Supplementary Data
Supplementary materials are available at Clinical Infectious Diseases online. Consisting of data provided by the authors to benefit the reader, the posted materials are not copyedited and are the sole responsibility of the authors, so questions or comments should be addressed to the corresponding author.
Supplementary Material
Notes
Acknowledgments. We thank the patients who participated in the cohort and contributed their time to this study. We appreciate the assistance of the entire TEACH (Targeting Effective Analgesia in Clinics for HIV) team, including Christopher Shanahan and Kristen O’Connor. We thank Vincent C. Marconi, Minh Nguyen, Cameron England, and Jeselyn Rhodes of the Emory Center for AIDS Research Infectious Disease Program Registry team and Linda Rosen at the Boston Medical Center’s Clinical Data Warehouse for assistance in identifying eligible patients for the cohort.
Disclaimer. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute on Drug Abuse (NIDA), the National Institute of Allergy and Infectious Diseases (NIAID), or the National Institutes of Health (NIH).
Financial support. This work was supported by NIDA/NIH (grant number R01DA037768 to J. H. S. and C. d. R.) and by NIAID/NIH Emory Center for AIDS Research (grant number P30AI050409 to C. d. R. and J. C.).
Potential conflicts of interest. D. M. C. has received payments from Janssen and grants from the NIH. W. S. A. has received payments from the HIV Medicine Association. All other authors report no potential conflicts of interest. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
References
- 1. Kolodny A, Courtwright DT, Hwang CS, et al. The prescription opioid and heroin crisis: a public health approach to an epidemic of addiction. Annu Rev Public Health 2015; 36:559–74. [DOI] [PubMed] [Google Scholar]
- 2. Centers for Disease Control and Prevention. Annual surveillance report of drug-related risks and outcomes—United States, 2017. Surveillance special report 1. Available at: https://www.cdc.gov/drugoverdose/pdf/pubs/2017cdc-drug-surveillance-report.pdf. Accessed 22 December 2017. [Google Scholar]
- 3. Centers for Disease Control and Prevention. Provisional counts of drug overdose deaths as of August 6, 2017. Available at: https://www-cdc-gov.proxy.library.emory.edu/nchs/data/health_policy/monthly-drug-overdose-death-estimates.pdf. Accessed 22 December 2017. [Google Scholar]
- 4. Centers for Disease Control and Prevention. Prescription opioid overdose data. Available at: https://www.cdc.gov/drugoverdose/data/overdose.html. Accessed 7 March 2017. [Google Scholar]
- 5. Compton WM, Jones CM, Baldwin GT. Relationship between nonmedical prescription-opioid use and heroin use. N Engl J Med 2016; 374:154–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6. Daubresse M, Chang HY, Yu Y, et al. Ambulatory diagnosis and treatment of nonmalignant pain in the United States, 2000-2010. Med Care 2013; 51:870–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Merlin JS, Cen L, Praestgaard A, et al. Pain and physical and psychological symptoms in ambulatory HIV patients in the current treatment era. J Pain Symptom Manage 2012; 43:638–45. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8. Miaskowski C, Penko JM, Guzman D, Mattson JE, Bangsberg DR, Kushel MB. Occurrence and characteristics of chronic pain in a community-based cohort of indigent adults living with HIV infection. J Pain 2011; 12:1004–16. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9. Parker R, Stein DJ, Jelsma J. Pain in people living with HIV/AIDS: a systematic review. J Int AIDS Soc 2014; 17:18719. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10. Edelman EJ, Gordon K, Becker WC, et al. Receipt of opioid analgesics by HIV-infected and uninfected patients. J Gen Intern Med 2013; 28:82–90. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. US Department of Health and Human Services, Office of the Surgeon General. Facing addiction in America: the surgeon general’s report on alcohol, drugs, and health. Washington, DC: DHHS, 2016. [PubMed] [Google Scholar]
- 12. Dowell D, Haegerich TM, Chou R. CDC guideline for prescribing opioids for chronic pain—United States, 2016. MMWR Recomm Rep 2016; 65:1–49. [DOI] [PubMed] [Google Scholar]
- 13. Bruce RD, Merlin J, Lum PJ, et al. 2017 HIVMA of IDSA clinical practice guideline for the management of chronic pain in patients living with HIV. Clin Infect Dis 2017; 65:e1–37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Nuckols TK, Anderson L, Popescu I, et al. Opioid prescribing: a systematic review and critical appraisal of guidelines for chronic pain. Ann Intern Med 2014; 160:38–47. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Morasco BJ, Duckart JP, Dobscha SK. Adherence to clinical guidelines for opioid therapy for chronic pain in patients with substance use disorder. J Gen Intern Med 2011; 26:965–71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16. Sullivan MD, Bauer AM, Fulton-Kehoe D, et al. Trends in opioid dosing among Washington State Medicaid patients before and after opioid dosing guideline implementation. J Pain 2016; 17:561–8. [DOI] [PubMed] [Google Scholar]
- 17. Chou R, Fanciullo GJ, Fine PG, et al. American Pain Society-American Academy of Pain Medicine Opioids Guidelines Panel Clinical guidelines for the use of chronic opioid therapy in chronic noncancer pain. J Pain 2009; 10:113–30. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Hansen L, Penko J, Guzman D, Bangsberg DR, Miaskowski C, Kushel MB. Aberrant behaviors with prescription opioids and problem drug use history in a community-based cohort of HIV-infected individuals. J Pain Symptom Manage 2011; 42:893–902. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Butler SF, Budman SH, Fernandez KC, et al. Development and validation of the current opioid misuse measure. Pain 2007; 130:144–56. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Colasanti J, Kelly J, Pennisi E, et al. Continuous retention and viral suppression provide further insights into the HIV care continuum compared to the cross-sectional HIV care cascade. Clin Infect Dis 2016; 62:648–54. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21. Starrels JL, Becker WC, Alford DP, Kapoor A, Williams AR, Turner BJ. Systematic review: treatment agreements and urine drug testing to reduce opioid misuse in patients with chronic pain. Ann Intern Med 2010; 152:712–20. [DOI] [PubMed] [Google Scholar]
- 22. National Institute on Drug Abuse. Seek, test, treat and retain initiative. HIV/HCV/STI testing status and organizational testing practices questionnaire. Available at: http://www.drugabuse.gov/researchers/research-resources/data-harmonization-projects/seek-test-treat-retain/addressing-hiv-among-vulnerable-populations. Accessed 22 December 2017. [Google Scholar]
- 23. Kim TW, Walley AY, Heeren TC, et al. Polypharmacy and risk of non-fatal overdose for patients with HIV infection and substance dependence. J Subst Abuse Treat 2017; 81:1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Vogenthaler NS, Hadley C, Lewis SJ, Rodriguez AE, Metsch LR, del Rio C. Food insufficiency among HIV-infected crack-cocaine users in Atlanta and Miami. Public Health Nutr 2010; 13:1478–84. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25. Lewinsohn PM, Seeley JR, Roberts RE, Allen NB. Center for Epidemiologic Studies Depression Scale (CES-D) as a screening instrument for depression among community-residing older adults. Psychol Aging 1997; 12:277–87. [DOI] [PubMed] [Google Scholar]
- 26. Tilton SR. Review of the State-Trait Anxiety Inventory (STAI). News Notes 2008; 48:1–3. [Google Scholar]
- 27. Blake DD, Weathers FW, Nagy LM, et al. The development of a clinician-administered PTSD scale. J Trauma Stress 1995; 8:75–90. [DOI] [PubMed] [Google Scholar]
- 28. McLellan AT, Luborsky L, Woody GE, O’Brien CP. An improved diagnostic evaluation instrument for substance abuse patients. The Addiction Severity Index. J Nerv Ment Dis 1980; 168:26–33. [DOI] [PubMed] [Google Scholar]
- 29. Institute of Behavioral Research. Texas Christian University drug screen II. Fort Worth: Texas Christian University, Institute of Behavioral Research, 2007. [Google Scholar]
- 30. Hansen L, Penko J, Guzman D, Bangsberg DR, Miaskowski C, Kushel MB. Aberrant behaviors with prescription opioids and problem drug use history in a community-based cohort of HIV-infected individuals. J Pain Symptom Manage 2011; 42:893–902. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31. Vijayaraghavan M, Penko J, Bangsberg DR, Miaskowski C, Kushel MB. Opioid analgesic misuse in a community-based cohort of HIV-infected indigent adults. JAMA Intern Med 2013; 173:235–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32. Meltzer EC, Rybin D, Saitz R, et al. Identifying prescription opioid use disorder in primary care: diagnostic characteristics of the Current Opioid Misuse Measure (COMM). Pain 2011; 152:397–402. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33. Hurstak EE, Kushel M, Chang J, et al. The risks of opioid treatment: perspectives of primary care practitioners and patients from safety-net clinics. Subst Abus 2017; 38:213–21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34. Khalid L, Liebschutz JM, Xuan Z, et al. Adherence to prescription opioid monitoring guidelines among residents and attending physicians in the primary care setting. Pain Med 2015; 16:480–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35. Önen NF, Barrette EP, Shacham E, Taniguchi T, Donovan M, Overton ET. A review of opioid prescribing practices and associations with repeat opioid prescriptions in a contemporary outpatient HIV clinic. Pain Pract 2012; 12:440–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Lum PJ, Little S, Botsko M, et al. BHIVES Collaborative Opioid-prescribing practices and provider confidence recognizing opioid analgesic abuse in HIV primary care settings. J Acquir Immune Defic Syndr 2011; 56:S91–7. [DOI] [PubMed] [Google Scholar]
- 37. Liebschutz JM, Xuan Z, Shanahan CW, et al. Improving adherence to long-term opioid therapy guidelines to reduce opioid misuse in primary care: a cluster-randomized clinical trial. JAMA Intern Med 2017; 177:1265–72. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38. Westanmo A, Marshall P, Jones E, Burns K, Krebs EE. Opioid dose reduction in a VA health care system—implementation of a primary care population-level initiative. Pain Med 2015; 16:1019–26. [DOI] [PubMed] [Google Scholar]
- 39. Wiedemer NL, Harden PS, Arndt IO, Gallagher RM. The opioid renewal clinic: a primary care, managed approach to opioid therapy in chronic pain patients at risk for substance abuse. Pain Med 2007; 8:573–84. [DOI] [PubMed] [Google Scholar]
- 40. US Department of Veterans Affairs. Pharmacy benefit management services: opioid overdose education and naloxone distribution. Available at: https://www.pbm.va.gov/PBM/academicdetailingservice/Opioid_Overdose_Education_and_Naloxone_Distribution.asp. Accessed 27 November 2017. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.