Skip to main content
Pain Medicine: The Official Journal of the American Academy of Pain Medicine logoLink to Pain Medicine: The Official Journal of the American Academy of Pain Medicine
. 2017 Sep 26;19(4):774–787. doi: 10.1093/pm/pnx208

Factors Associated with Opioid Initiation in OEF/OIF/OND Veterans with Traumatic Brain Injury

Teresa J Hudson 1,2,, Jacob T Painter 1,3, Laura E Gressler 1,3, Liya Lu 2, J Silas Williams 1, Brenda M Booth 2, Bradley C Martin 3, Mark D Sullivan 4, Mark J Edlund 5,6
PMCID: PMC6659014  PMID: 29036680

Abstract

Objective

These analyses examined opioid initiation and chronic use among Iraq (OIF) and Afghanistan (OEF/OND) veterans with a new diagnosis of traumatic brain injury (TBI) in the Veterans Health Administration (VHA).

Methods

Data were obtained from national VHA data repositories. Analyses included OEF/OIF/OND veterans with a new TBI diagnosis in 2010–2012 who used the VHA at least twice, had not received a VHA opioid prescription in the 365 days before diagnosis, and had at least 365 days of data available after TBI diagnosis.

Results

Analyses included 35,621 veterans. Twenty-one percent initiated opioids; among new initiators, 23% used chronically. The mean dose was 24.0 mg morphine equivalent dose (MED) daily (SD = 24.26); mean days supplied was 60.52 (SD = 74.69). Initiation was significantly associated with age 36–45 years (odds ratio [OR] = 1.09, 95% CI = 1.01–1.17, P = 0.04), female gender (OR = 1.22, P < 0.001), having back pain (OR = 1.38, P < 0.0001), arthritis/joint pain (OR = 1.24, P < 0.0001), or neuropathic pain (OR = 1.415, P < 0.02). In veterans age 36–45 years, those living in small rural areas had higher odds of chronic opioid use (OR = 1.31, P < 0.0001, and OR = 1.33, P = 0.006, respectively) and back pain (OR = 1.36, P = 0.003). Headache/migraine pain was associated with decreased odds of chronic opioid use (OR = 0.639, P = 0.003).

Conclusions

Prevalence of opioid use is relatively low among OEF/OIF/OND veterans with newly diagnosed TBI who are using VHA. Among those who initiated opioids, about 25% use them chronically. Prescribing was mostly limited to moderate doses, with most veterans using opioids for approximately two months of the 12-month study period.

Keywords: Opioid, Traumatic Brain Injury, Veteran, Pain

Introduction

Traumatic brain injury (TBI) has been called the “signature injury” of the conflicts in Iraq and Afghanistan [1,2]. An estimated 12–23% of veterans who served in Afghanistan (Operation Enduring Freedom [OEF]) and Iraq (Operation Iraqi Freedom [OIF] and Operation New Dawn [OND]) and who utilized Veterans Health Administration (VHA) care experienced a TBI while deployed [3]. Among the 613,391 returning veterans from Afghanistan and Iraq between 2009 and 2011, 40.2% have a primary pain diagnosis, 29.4% have a primary post-traumatic stress disorder (PTSD) diagnosis, and 9.6% have a primary TBI diagnosis. Among all veterans with TBI, a significant majority (62.5%) suffered from comorbidities related to pain and PTSD [4].

TBI is defined as a physical force to the brain sufficient to cause structural alteration or physiological disruption of brain functions that results in altered consciousness, amnesia, change in mental state, neurological deficits, or intracranial lesions [5]. TBI severity is generally categorized as mild, moderate, or severe, depending on the patient’s level of arousal/consciousness at the time of injury, the duration of any loss of consciousness, and the duration of post-traumatic amnesia [6]. An estimated 50% of injuries are mild, with fewer veterans presenting to VHA care having moderate to severe TBI. Symptoms associated with TBI are typically physical symptoms, cognitive impairment, and emotional/behavioral problems [5,7]. Symptoms can resolve in as little as a few minutes or over a few days to weeks, particularly in mild TBI. However, in some cases, symptoms continue for months to years, not just in patients with moderate to severe TBI, but also in those categorized as having a mild injury [8].

Among civilians, patients with TBI are five times more likely to report persistent pain compared with those without TBI [4,8,9]. An epidemiologic analysis of TBI among OEF/OIF/OND veterans from 2010–2012 found that 71% of those with TBI had head, back, or neck pain, compared with only 33% of those without TBI [10]. A review of 23 studies of chronic headaches after TBI reported a prevalence of 57.8% (95% CI = 55.5–50.2) when combining civilian and military cohorts [11,12]. Although there is evidence that pain may be more prevalent immediately following TBI, pain can persist and even worsen in the years after even a mild TBI. Indeed, pain related to TBI has been documented in veterans up to five years after the initial injury [13]. While a headache is the most commonly documented pain condition, back and neck pain and neuropathic pain are also common [8].

TBI is also associated with a range of mental health comorbidities, particularly PTSD and depression. Estimates of the prevalence of PTSD among veterans with mild TBI range from 14% to 77% [2,14–19]. Estimates of the prevalence of major depressive disorder comorbidity with TBI range from 3% to 53% [11,14,20–22]. This is particularly striking when considering that the 12-month prevalence of depression in the general adult population is approximately 6.7% [11,23].

The high rates of comorbid pain and mental health (MH) diagnoses are particularly concerning when considering risks of opioid use in veterans with TBI. Opioid medications have become a common treatment for noncancer pain [24–26]. Increased opioid use has been accompanied by increased opioid misuse, emergency department visits, overdoses, and automobile accidents [27–31]. Factors that increase the likelihood of chronic opioid use include chronic noncancer pain, having diagnoses of MH and substance use disorders (SUD; i.e., PTSD, depression, nonopioid SUD, opioid SUD, tobacco use), and demographic characteristics (male gender, younger age, Caucasian race) [32–37]. Among OEF/OIF/OND veterans with TBI and chronic noncancer pain, those with a PTSD diagnosis have a higher relative risk of receiving opioid medications for 20 or more consecutive days in the year following the pain diagnosis (TBI + PTSD adjusted relative risk [RR] = 2.95, 95% confidence interval [CI] = 2.79–3.12) than those without PTSD (TBI without PTSD adjusted RR = 1.77, 95% CI = 1.60–1.95, P < 0.01) [27]. However, there is little information about the factors, other than PTSD, associated with opioid initiation among veterans with TBI not previously using opioids, regardless of pain condition, nor is there information about the factors associated with chronic use after opioid initiation. The overarching goal of this work is to understand how opioids are used in patients with TBI. To that end, the current study identified a cohort of OEF/OIF/OND veterans who are regular users of VHA care and who had a recent diagnosis of TBI, but who had not used opioids in the 365 days prior to the TBI diagnosis. We hypothesized that diagnoses of chronic pain and comorbid diagnosis of PTSD, depression, or nonopioid SUD would be associated with opioid initiation and chronic opioid use among OEF/OIF/OND veterans with TBI.

The high prevalence of comorbidities related to pain and MH makes this veteran population more likely to use opioids and therefore more susceptible to possible adverse effects. Identifying the factors related to the initiation and chronic use of opioids could educate and inform clinicians as to the characteristics that may put patients at high risk for poor outcomes and could provide them with the ability to reevaluate treatment decisions to minimize these risks. The evidence gained from this investigation can also provide data to VHA policy makers and motivate changes in policies concerning this population.

Methods

Data Sources

Data for this study were obtained using three VHA data repositories: the Veterans Administration (VA) Corporate Data Warehouse (CDW), the OEF/OIF/OND Roster, and the VA Pharmacy Benefits Management Service (PBM). The project received approval from the institutional review boards of the Central Arkansas Veterans Healthcare System and the University of Arkansas for Medical Sciences. A data use agreement was executed with each repository.

Study Sample

We identified a study cohort of OEF/OIF/OND veterans who used VHA care at least twice in the 365 days prior to the index period but did not have an outpatient opioid prescription from a VHA provider in that time frame. This provided a cohort of patients who were known to be using VHA care and therefore had an opportunity to receive an opioid prescription from VHA but did not. As they were required to use the VHA at least twice, it implies some level of engagement in care and potentially increases the likelihood of getting prescription medications from the VHA rather than from an outside provider.

Included veterans had:

  1. at least one TBI diagnosis in FY10 or later (the date of the first TBI diagnosis identified was assigned as the veteran’s index date);

  2. at least 365 days of observation available prior to the date of TBI diagnosis (this requirement decreases the risk that the veteran had been receiving treatment for TBI outside VHA);

  3. at least two VHA outpatient visits in the 365 days after diagnosis.

Excluded veterans had:

  1. an opioid prescription or visit to a methadone clinic before the identified index date;

  2. residence in a VHA nursing home or domiciliary, or were enrolled in VHA hospice care in the 365 days prior to the index date;

  3. an opioid prescription in injectable or suppository form or had incomplete opioid prescription records 365 days after the index date;

  4. an average daily dose greater than 1,000 mg MED daily (these were treated as potentially invalid values and excluded from the analyses to protect against data entry errors);

  5. a date of opioid initiation 90 or fewer days from the end of the observation period (this was to ensure the possibility of measuring chronic opioid use).

The final cohort of veterans had a new TBI diagnosis within VHA in FY10 and were regular users of VHA care but were not living in an environment that would influence how prescription medications are managed (e.g., domiciliary or nursing home) or had conditions where opioid prescribing could systematically differ from prescribing for noncancer pain (e.g., cancer diagnosis or hospice care).

Opioid Use

Data from the VHA PBM were used to create variables for opioid use. This was based on the days covered by prescriptions issued by the VHA in the 12 months after the index date. Any opioid use was defined as a VHA outpatient opioid prescription for any length of time in the 12 months after the index date. Chronic opioid use was defined as 91 or more days of outpatient opioid use issued by a VHA pharmacy in the 12 months after the index date. To calculate the number of opioid days covered, the prescriptions for the 12 months after the index date were sorted into chronological order based on the date dispensed. If any two prescriptions overlapped by more than 20% or more than 10 days, the overlapping portions of the prescription were assumed to be taken concurrently and the overlapping days were only included once in the opioid days’ calculation. If the overlap was 20% or less and 10 or fewer days, the second prescription was shifted and the overlapping days from both the first and second prescription were included in the opioid days’ calculation. To further describe opioid use in this cohort, the mean daily opioid dose in morphine equivalents was calculated for each opioid user, referred to as the morphine equivalent dose. The MED was calculated by multiplying the quantity of each prescription by the strength of the prescription (milligrams of opioid per unit dispensed). The quantity–strength of the product was then multiplied by conversion factors derived from published sources to estimate the milligrams of morphine equivalent to the opioids dispensed in the prescription [38–40].

TBI Definition

The CDW was used to identify veterans with at least one outpatient visit coded with an ICD-9 code for TBI. These codes were selected based on a literature review [41,42] and VHA publications [5].

Other Variables

Demographic and diagnostic data included the following: date of birth, race, marital status, gender, zip code, and diagnosis codes (ICD-9). The zip code was used to classify veterans as living in an urban area, large rural city/town, small rural town, or isolated small rural town [43]. We identified common painful conditions experienced by veterans: neck, back, arthritis/joint, headache/migraine, neuropathic, and pain due to traumatic limb injuries, fractures, and amputations. These conditions were selected based on a literature search; they were found to be common among veterans, including those with TBI [9,44]. The definition of chronic pain requires at least two separate occasions of a pain diagnosis at least 30 but not more than 365 days apart. The ICD-9 codes used to identify veterans with these pain conditions are listed in Appendix Table A1. Veterans were categorized as having a painful condition if they had at least one outpatient visit coded with that condition within the 12-month period after the index date, and a second code for a painful condition at least 30 days but not more than 365 days later. While these are common chronic conditions, veterans in these analyses could have had chronic and nonchronic painful conditions we did not identify. However, given that these pain conditions are common among OEF/OIF/OND veterans and among those with TBI, they serve as appropriate tracer conditions in this cohort. Dummy variables were created to identify veterans with at least one recorded diagnosis of major depressive disorder, PTSD, alcohol use disorder, nonopioid SUD, opioid use disorder, or tobacco use. Definitions for these conditions are based on previous literature [34,45] and are consistent with definitions used by the VA Office of Mental Health Operations.

Military Characteristics

Military characteristics and education have been shown to be associated with persistent pain [9,46]. The OEF/OIF/OND Roster was used to identify both military characteristics including rank (enlisted, officer, warrant), component (reserve, guard, active duty), branch (Army, Navy, Air Force, Marines), and education level for subjects included in the analyses.

Analysis

Multivariable logistic regression was used to model the odds of initiating opioid use in the 12 months after the index date and to identify factors associated with chronic opioid use among opioid initiators. Veterans using VHA care are clustered within clinics that are clustered within medical centers. To avoid underestimating the standard error and erroneously identifying a variable as statistically significant, the VA Medical Center was specified as a random effect in each model.

Results

A total of 35,621 veterans met inclusion/exclusion criteria (see Table 1). The mean age of the cohort was 31.96 years (SD = 8.19). The cohort was generally Caucasian, male, had completed high school, and lived in urban areas. While serving in the military, the majority were enlisted and active duty military, rather than in the guard or reserve; the majority served in the Army. Less than 10% had an opioid or nonopioid SUD, 14% had an alcohol disorder, and 12% had documented tobacco use based on ICD-9 codes. Joint pain (7.08%) and back pain (6.14%) were the two most commonly diagnosed types of pain disorders. Opioids were initiated in 20.52% of the sample; 23.25% of those who initiated opioids used them chronically, defined as 90 or more days in the 365 days after the index date. Among opioid users, the mean dose was 24.0 mg MED daily (SD = 24.26). The mean days supplied was 60.52 (SD = 74.69), ranging from one to 365 days.

Table 1.

Cohort characteristics (N = 35,621)

Entire Cohort
No Opioid
Any Opioid Use
P—Comparing No Opioid Use and Any Opioid Use
Variable Level No.* % No.* % No.* % P
Demographic characteristics
 Age, y 18–25 7,482 21 5,933 20.96 1,549 21.19 0.366
26–35 18,961 53.23 15,130 53.44 3,831 52.4
36–45 6,150 17.27 4,835 17.08 1,315 17.99
46–55 2,596 7.29 2,065 7.29 531 7.26
>55 432 1.21 347 1.23 85 1.16
 Race White 24,889 69.87 19,632 69.35 5,257 71.91 <0.0001
Nonwhite 5,906 16.58 4,707 16.63 1,199 16.4
Unknown 4,826 13.55 3,971 14.03 855 11.69
 Marital status Married 14,160 39.75 11,235 39.69 2,925 40.01 <0.0001
Not married 16,675 46.81 13,421 47.41 3,254 44.51
Unknown 4,786 13.44 3,654 12.91 1,132 15.48
 Gender Female 2,053 5.76 1,567 5.54 486 6.65 0.0003
Male 33,568 94.24 26,743 94.46 6,825 93.35
 Education BS or higher 1,991 5.59 1,695 5.99 296 4.05 <0.0001
High school 31,222 87.65 24,702 87.26 6,520 89.18
Some college 2,408 6.76 1,913 6.76 495 6.77
 Rural/urban status Urban 28,267 79.35 22,464 79.35 5,803 79.37 0.9886
Large rural 4,099 11.51 3,253 11.49 846 11.57
Small rural 1,860 5.22 1,480 5.23 380 5.2
Isolated small rural 1,395 3.92 1,113 3.93 282 3.86
Military characteristics
 Rank while in military Enlisted 34,386 96.53 27,260 96.29 7,126 97.47 <0.0001
Officer 1,095 3.07 937 3.31 158 2.16
Warrant Officer 140 0.39 113 0.4 27 0.37
 Military component Guard 7,122 19.99 5,770 20.38 1,352 18.49 0.0005
Active 24,570 68.98 19,396 68.51 5,174 70.77
Reserve 3,929 11.03 3,144 11.11 785 10.74
 Branch of military Army 24,975 70.11 19,604 69.25 5,371 73.46 <0.0001
Air Force 1,383 3.88 1,099 3.88 284 3.88
Marines 7,006 19.67 5,809 20.52 1,197 16.37
Navy 2,257 6.34 1,798 6.35 459 6.28
Clinical characteristics
 PTSD diagnosis No 17,401 48.85 13,875 38.95 3,526 9.9 0.2329
Yes 18,220 51.15 11,435 40.52 3,785 10.63
 Depression No 25,028 70.26 19,998 56.14 5,030 14.12 0.0022
 Diagnosis Yes 2,281 10,593 8,312 23.33 2,281 6.4
 Alcohol disorder No 30,752 86.33 24,436 68.6 6,316 17,073 0.8600
Yes 4,869 13.67 3,874 10.88 995 2.79
 Nonopioid SUD No 33,549 94.18 26,724 75.02 6,825 19.16 0.0007
Yes 2,072 5.82 1,586 4.45 486 1.36
 Opioid SUD No 35,204 98.83 27,995 78.59 7,209 20.24 0.0453
Yes 417 1.17 315 0.88 102 0.29
 Tobacco use No 30,271 84.98 24,060 67.54 6,211 17.44 0.9431
Yes 4,250 11.93 1,100 3.09 5,350 15.02
Painful conditions
 At least 1 chronic No 30,481 85.57 24,370 68.41 6,111 17.16 <0.0001
 Condition Yes 5,140 14.43 3,940 11.06 1,200 3.37
 Neck pain No 35,210 98.85 28,005 78.62 7,205 20.23 0.0078
Yes 411 1.15 305 0.86 106 0.3
 Back pain No 33,434 93.86 26,699 74.95 6,735 18.91 <0.0001
Yes 2,187 6.14 1,611 4.52 576 1.62
 Arthritis/joint pain No 33,099 92.92 26,410 74.14 6,689 18.78 <0.0001
Yes 2,522 7.08 1,900 5.33 622 1.75
 Headache/migraine pain No 34,024 95.52 27,039 75.91 6,985 19.61 0.9104
Yes 1,271 3.57 326 0.92 1,597 4.48
 Neuropathic pain No 35,386 99.34 28,143 79.01 7,243 20.33 0.0014
Yes 235 0.66 167 0.47 68 0.19
 Amputation pain No 35,542 99.78 28,245 79.29 7,297 20.49 0.5369
Yes 79 0.22 65 0.18 14 0.04
Opioid use
 Opioid No 28,310 79.48 28,310 100 0 0 <0.0001
Yes 7,311 20.52 0 0 7,311 100
 Chronic opioids No 33,921 95.23 28,310 100 5,611 76.75 <0.0001
Yes 1,700 4.77 0 0 1,700 23.25
Mean SD Mean SD Mean SD P
CCI score 0.0789 0.34 0.08 0.33 0.08 0.37 0.6100
Age at index 31.88 8.13 31.86 8.13 31.96 8.16 0.3500

CCI = Charlson Comorbidity Index; PTSD = post-traumatic stress disorder; SUD = substance use disorder.

*

Some numbers do not add up to total number of patients because of missing data.

Some percentages do not add up to 100 because of rounding.

P value is the difference between no opioid use and any opioid use.

Results of a logistic regression model examining factors associated with opioid initiation are in Table 2. Cohort members age 36–45 had an 8.3% greater odds of receiving opioids compared with the age 26–35 reference group (OR = 1.08, 95% CI = 1.00–1.17, P = 0.04). Nonwhite persons and those with unknown race had lower odds of opioid initiation compared with white veterans. Women had higher odds of opioid initiation compared with men (OR = 1.22, 95% CI = 1.10–1.36, P ≤ 0.001). Veterans who had a bachelor’s degree or higher had significantly lower odds of initiating opioids compared with those who completed high school only (OR = 0.65, 95% CI = 0.55–0.77, P < 0.0001). There were no statistically significant findings related to opioid initiation based on rank while in the military. Those veterans who served in the National Guard had lower odds of initiating opioids compared with active duty personnel (OR = 0.86, 95% CI = 0.78–0.95, P < 0.001). Compared with those in the Navy, Marines had significantly lower odds of opioid initiation (OR = 0.84, 95% CI = 0.74–0.95, P = 0.005). Among clinical characteristics, the only statistically significant finding was that veterans with back pain (OR = 1.38, 95% CI = 1.24–1.53, P < 0.001), arthritis/joint pain (OR = 1.23, 95% CI = 1.11–1.36, P < 0.001), and neuropathic pain (OR = 1.42, 95% CI = 1.06–1.89, P < 0.019) had higher odds of initiating opioid medications.

Table 2.

Logistic regression model of opioid initiation (N = 35,621)*

Variable Level Odds ratio 95% CI P
Demographic characteristics
 Age, y 18–25 1.060 0.991 1.135 0.0915
26–35 Ref
36–45 1.083 1.004 1.168 0.0395
46–55 1.084 0.969 1.212 0.1580
56–65 1.142 0.881 1.470 0.3038
 Race Nonwhite 0.889 0.826 0.957 0.0019
Unknown 0.786 0.723 0.854 <0.0001
White Ref
 Marital status Married 1.060 0.999 1.124 0.0552
Unknown 1.246 1.149 1.352 <0.0001
Not married Ref
 Gender Female 1.221 1.095 1.362 0.0003
Male Ref
 Education BS or above 0.651 0.548 0.774 <0.0001
Some college 0.942 0.845 1.049 0.2746
High school Ref
 Rural/urban status Isolated rural 1.003 0.873 1.153 0.9642
Large rural 0.984 0.903 1.072 0.7122
Small rural 0.992 0.879 1.120 0.8961
Urban Ref
Military characteristics
 Rank while in military Officer 0.926 0.578 1.485 0.7497
Warrant Officer Ref
Enlisted 1.051 0.683 1.619 0.8199
 Military component Guard 0.859 0.775 0.952 0.0037
Reserve Ref
Active 1.023 0.935 1.118 0.6234
 Branch of military Air Force 1.064 0.897 1.263 0.4731
Marines 0.835 0.737 0.946 0.0047
Navy Ref
Army 1.117 0.998 1.251 0.0548
Clinical characteristics
 Depression diagnosis Yes vs no 1.036 0.974 1.100 0.2704
 PTSD diagnosis Yes vs no 1.010 0.954 1.069 0.7422
 Alcohol disorder Yes vs no 0.968 0.890 1.053 0.4461
 Nonopioid SUD Yes vs no 1.187 1.054 1.336
 Opioid SUD Yes vs no 1.134 0.892 1.443 0.3047
 Tobacco use Yes vs no 0.976 0.905 1.053 0.5361
Painful condition
 Neck pain Yes vs no 1.140 0.901 1.441 0.2741
 Back pain Yes vs no 1.376 1.236 1.531 <0.0001
 Arthritis/joint pain Yes vs no 1.231 1.112 1.363 <0.0001
 Headache/migraine Pain Yes vs no 0.887 0.778 1.011 0.0733
 Neuropathic pain Yes vs no 1.415 1.056 1.896 0.0199
 Amputation pain Yes vs no 0.709 0.393 1.276 0.2513

CI = confidence interval; PTSD = post-traumatic stress disorder; SUD = substance use disorder.

*

All models controlled for physical health comorbidities with Charlson Comorbidity Score.

Table 3 provides the results of the logistic regression model of chronic opioid use. Only 89% (N = 6,518) of opioid initiators were included in this model as 11% started opioids within 90 days of the end of the observation period and did not have sufficient time to meet the definition of chronic opioid use. Veterans who were married or had unknown marital status had much higher odds than unmarried veterans of using opioids chronically (OR = 1.27, 95% CI = 1.13–1.43, P < 0.001, and OR = 1.88, 95% CI = 1.63–2.16, P < 0.001, respectively). Veterans with a bachelor’s degree or higher were significantly less likely to use opioids chronically compared with those who completed high school only (OR = 0.49, 95% CI = 0.34–0.72, P = 0.0002). Veterans living in rural areas had greater odds than those in urban areas of receiving opioids chronically, although this was only statistically significant for those living in small rural areas (OR = 1.33, 95% CI = 1.08–1.64, P = 0.006). Although women were more likely to initiate opioid medications, they were less likely to use them chronically. Members of the National Guard compared with the Reserve were more likely to use opioids chronically (OR = 1.04, 95% CI = 0.87–1.24, P < 0.0001). Veterans in the Army were less likely to use opioids chronically compared with those who served in the Navy (OR = 0.915, 95% CI = 0.697–1.20, P < 0.001). Veterans with a history of tobacco use were less likely to use opioids chronically (OR = 0.84, 95% CI = 0.72–0.97, P = 0.02). Veterans with back pain were more likely to use opioids chronically (OR = 1.37, 95% CI = 1.11–1.67, P = 0.003), while veterans with headache/migraine pain were less likely to use them chronically (OR = 0.634, 95% CI = 0.48–0.86, P = 0.003). There were no other statistically significant clinical characteristics associated with chronic opioid use. Interestingly, those with a diagnosis of chronic pain were not statistically more likely to use opioids chronically, nor were those with a diagnosis of depression, PTSD, alcohol disorders, or other substance use disorders.

Table 3.

Model of chronic opioid use among opioid initiators (N = 6,518)*

Variable Level Odds ratio 95% CI P
Demographic characteristics
 Age, y 18–25 0.990 0.867 1.131 0.885
26–35 Ref
36–45 1.310 1.145 1.499 <0.0001
46–55 1.026 0.826 1.274 0.8187
56–65 1.095 0.665 1.803 0.7213
 Race Nonwhite 0.593 0.507 0.695 <0.0001
Unknown 1.895 1.626 2.163 <0.0001
White Ref
 Married Married 1.273 1.134 1.429 <0.0001
Unknown 1.875 1.626 2.163 <0.0001
Not married Ref
 Gender Female 0.840 0.662 1.066 0.151
Male Ref
 Education BS or above 0.495 0.342 0.716 0.0002
Some college 0.996 0.817 1.214 0.9689
High school Ref
 Rural/urban status Isolated rural 1.113 0.860 1.440 0.4165
Large rural 1.156 0.990 1.350 0.0675
Small rural 1.334 1.084 1.641 0.0065
Urban Ref
Military characteristics
 Rank while in military Officer 1.064 0.413 2.743 0.8974
Warrant Officer Ref
Enlisted 0.996 0.817 1.214 0.6804
 Military component Guard 1.040 0.873 1.238 0.0097
Reserve Ref
Active 0.768 0.629 0.938 0.6624
 Branch of military Air Force 1.344 0.950 1.900 0.0948
Marines 1.560 1.199 1.952 0.5204
Navy Ref
Army 0.915 0.697 1.200 0.0006
Clinical characteristics
 Depression diagnosis Yes vs no 0.975 0.867 1.097 0.6776
 PTSD diagnosis Yes vs no 1.008 0.905 1.122 0.8853
 Alcohol disorder Yes vs no 0.843 0.708 1.003 0.0546
 Nonopioid SUD Yes vs no 0.845 0.649 1.099 0.2088
 Opioid SUD Yes vs no 1.462 0.909 2.353 0.1171
 Tobacco use Yes vs no 0.835 0.716 0.973 0.0213
Painful conditions
 Neck pain Yes vs no 1.277 0.822 1.982 0.2766
 Back pain Yes vs no 1.366 1.110 1.670 0.0027
 Arthritis/joint pain Yes vs no 1.082 0.884 1.324 0.4470
 Headache/migraine pain Yes vs no 0.639 0.477 0.855 0.0026
 Neuropathic pain Yes vs no 1.353 0.783 2.337 0.2784
 Amputation pain Yes vs no 1.076 0.424 2.734 0.8770

CI = confidence interval; PTSD = post-traumatic stress disorder; SUD = substance use disorder.

*

All models controlled for physical health comorbidities with the Charlson Comorbidity Score.

Discussion

In these analyses, opioids were initiated in slightly more than 20% of the OEF/OIF/OND TBI cohort, but among opioid initiators, almost 25% used opioids chronically. This chronic use, however, is lower than in all veterans. In other analyses, we found that among all opioid users with chronic noncancer pain in the VHA nationwide, almost 57% of opioid users received them chronically [24]. This may suggest that opioid prescribing from VA providers is lower among OEF/OIF/OND veterans with TBI compared with other veteran cohorts. This finding may also be a function of the sample. We observed this cohort for 365 days after the index period. It is possible that opioid initiation may occur later than the first year after a diagnosis, suggesting that other pain management strategies may be used during that time. It is also possible that patients with new TBI diagnoses within the VA are less likely to initiate opioids within the VA compared with veterans who are treated in other health care systems before coming to the VA. The doses and number of days using opioids in the 365-day observation period were modest, with most people taking only 25 mg MED/day and using opioids for 60 or fewer days. Generally, low-dose morphine is approximately 10–40 mg MED/day, moderate is 40–120 mg MED/day, and high-dose is more than 120 mg MED/day [47]. Opioid initiators were more likely to have at least one pain diagnosis compared with those who did not initiate opioid medications. It is also important to note that diagnoses such as alcohol disorder and SUDs were not associated with opioid initiation.

Several of our findings are notably different than other studies examining opioid use in veterans. Other authors have found that male gender was associated with opioid use, including chronic opioid use [24,34,36]. However, in the current analyses, women were more likely to initiate opioids but not to use them chronically. This is a particularly interesting finding given that other studies have found that painful conditions such as musculoskeletal, headache, and back pain may be more common among women veterans, particularly those who served in Iraq and Afghanistan, than among their male counterparts [48]. Female veterans are more likely than male veterans to report severe pain and pain that interferes in their daily lives, to have an emergency department or primary care visit for a pain-related problem, to have a service-connected disability rating, and to have a rating of at least 50% [9,48–50]. In our cohort, 20% of women had a chronic pain diagnosis, compared with only 14% of men (X2 = 46.82, P < 0.0001).

In these analyses, education appeared to have a protective effect. Veterans in this cohort who had a bachelor’s degree or higher were less likely to initiate opioids or use them chronically. Improving education among veterans may offer a target for a policy initiative that could benefit veterans and decrease risk of opioid initiation and chronic use.

In our analyses, neither PTSD nor depression was associated with opioid initiation or chronic opioid use. Previous work found that PTSD and depression were associated with increased odds of receiving opioids and of receiving them chronically, but most of those studies were in cohorts of veterans known to have chronic, painful conditions and used data from as far back as 2005. It is important to note that these analyses depended on diagnoses of mental health conditions that were documented in the VA medical record. It is possible that veterans in this cohort had comorbid mental health conditions that were undiagnosed or not documented in the VA electronic health record. Data for the current analyses are from 2010 and later. In 2009 and 2010, the VHA implemented new policies designed to decrease chronic opioid use and increase monitoring to identify opioid misuse [51–53]. The lack of association between opioid use and depression and PTSD may be a result of these policies. We reported earlier that depression, PTSD, and substance use disorders were not associated with opioid continuation beyond 90 days of use in the veteran population, as we have found in the civilian population [54].

The proportion of veterans with documented smoking in this study was approximately 12%. In other studies, smoking prevalence was approximately 23–30% [34,45]. This difference is likely related to the way we identified smoking in the cohort. We used one ICD-9 CM code for smoking (305.1, tobacco use disorder) and no V codes or supplementary codes for a history of smoking. Other authors used a wide range of codes that included the history of tobacco use; we limited the code used to identify current tobacco use only. Given the difference in identification of tobacco use and that it was not associated with opioid initiation but was associated with statistically lower odds of chronic use, it will be important to further examine this issue in future research.

Approximately 15% of the cohort had a pain diagnosis, which is lower than the epidemiologic estimates of pain conditions among veterans with TBI [10–12]. This low prevalence is likely due to the definition of a painful condition. The first date of TBI diagnosis in FY10 or later was considered the index date; veterans were followed for the 365-day period following the index date. The definition of chronic pain required at least two separate occasions of a pain diagnosis at least 30 but not more than 365 days apart. However, the goal was not to determine whether opioids were prescribed only in response to a pain diagnosis or to identify all diagnoses for which opioids are prescribed. The goal was to identify factors associated with opioid initiation among veterans with TBI as a cohort who had not used opioids in the previous 365-day period and had a relatively new TBI diagnosis, thereby making it possible to understand opioid initiation. The numerous pain conditions in this study served as tracer conditions to help understand the clinical conditions of these veterans, a strategy used in other studies [25]. Therefore, the findings likely cannot be generalized to all veterans or others with TBI or pain. However, it does help to understand how opioids are used in OEF/OIF/OND veterans with TBI who have a relatively new diagnosis.

Limitations

One of the challenges of studying TBI using data repositories is that there is no way to account for the severity of TBI or how recently it occurred. While the proposed inclusion/exclusion criteria used in these analyses will not necessarily completely identify veterans with a “new” TBI diagnosis, TBI not being coded by a VA provider in the previous 12 months may suggest that treatment related to TBI was not a key clinical focus in the 365 days prior to the index date. Other studies have noted that mild TBI is the most common type of TBI presenting to the VHA for care, so it is likely that most of the cases identified in these analyses are also mild TBI. It is also possible that some veterans who experienced TBI may not be diagnosed. Therefore, it is likely that the current findings are most generalizable to veterans who are newly diagnosed with TBI in the VHA.

Another key limitation of this study is the lack of information about opioid use and receipt of medical care outside the VHA. Identifying opioid prescriptions obtained from non-VHA providers is very difficult. To decrease the risk of underestimating opioid use because of non-VHA prescribing, we identified veterans who used VHA care at least twice in the 365 days prior to the index period but who did not have an outpatient opioid prescription from a VHA provider in that time frame. This implies some level of engagement in care and potentially increases the likelihood of veterans mainly getting their prescription medications from the VHA rather than from an outside provider. Therefore, the findings from these analyses are likely generalizable to veterans within VHA who are using VHA care regularly. These veterans are also the ones most likely to be affected by system-wide policies and interventions related to opioid use.

Conclusion

These data suggest that the prevalence of opioid use is relatively low among OEF/OIF/OND veterans with newly diagnosed TBI who are using the VHA, but among those who initiated opioids, about 25% use them chronically. Prescribing was mostly limited to moderate doses, with most veterans using opioids for approximately two months of the 12-month study period. Future analyses should seek to better understand factors that influence outcomes of TBI and opioid use in this cohort, including longer observation periods to examine the trajectory of opioid use and gender-related differences in chronic use among opioid initiators.

Acknowledgments

The authors thank Ms. Cynthia Brace for editing and formatting the manuscript.

Appendix

Table A1.

International Classification of Disease, Ninth Revision, Clinical Modification (ICD9-CM) codes used to identify pain diagnoses

Pain Diagnoses ICD9-CM Codes
Neck pain
  • 721.0, .1

  • 722.0, .31, .4, .71, .81, .91

  • 723.0, .1, .2, .3, .5, .6, .7, .8, .9

  • 739.1

  • 784.1

  • 847.0

Back pain
  • 720.1, .2, .81, .89, 7.9

  • 721.2, .3, .41, .42, .5, .6, .7, .8, .9, .91

  • 722.10, .11, .2, .30, .32, .39, .51, .52, .6, .70, .72, .73, .80, .82, .83, .90, .92, .93

  • 724.00, .01, .02, .03, .09, .1, .2, .3, .4, .5, .6, .70, .71, .79, .8, .9

  • 737.10, .11, .12, .19, .20, .21, .22, .29, .30, .31, .32, .33, .34, .39, .40, .41, .42, .43, .8, .9

  • 738.4, .5

  • 739.2, .3, .4

  • 756.10, .11, .12, .13, .19

  • 839.20

  • 846.0

  • 847.1, .2, .3, .4, .9

Arthritis/joint pain
  • 359.4, .5, .6, .71, .79, .81, .89, .9

  • 524.69, .61, .62, .63, .69

  • 696.0

  • 710.0, .1, .2, .3, .4, .5, .8, .9

  • 711.00, .02, .03, .04, .05, .06, .07, .08, .09, .10, .11, .12, .13, .14, .15, .16, .17, .18, .19, .20, .21, .24, .25, .26, .27, .29, .30, .31, .33, .34, .37, .39, .40, .41, .42, .43, .44, .45, .46, .47, .49, .50, .51, .53, .54, .56, .57, .58, .59, .60, .66, .67, .68, .69, .70, .71, .77, .80, .81, .82, .83, .84, .85, .86, .87, .88, .89, .90, .91, .92, .93, .94, .95, .96, .97, .98, .99

  • 712.10, .11, .12, .13, .14, .15, .16, .17, .18, .19, .20, .21, .22, .23, .24, .25, .26, .27, .28, .29, .30, .31, .32, .33, .34, .35, .36, .37, .38, .39, .80, .81, .82, .83, .84, .86, .87, .88, .89, .90, .91, .92, .93, .94, .95, .96, .97, .98, .99

  • 713.0, .1, .2, .3, .4, .5, .6, .7, .8

  • 714.0, .1, .2, .30, .31, .32, .33, .4, .81, .89, .9

  • 715.00, .04, .09, .10, 11, .12, .13, .14, .15, .16, .17, .18, .20, .21, .22, .23, .24, .25, .26, .27, .28, .30, .31, .32, 33, .34, .35, .36, .37, .38, .80, .89, .90, .91, .92, .93, .94, .95, .96, .97, .98

  • 716.00, .01, .02, .03, .04, .05, .06, .07, .09, .10, .11, .12, .13, .14, .15, .16, .17, .18, .19, .20, .21, .22, .23, .24, .25, .26, .27, .28, .29, .30, .31, .32, .33, .34, .35, .36, .37, .38, .39, .40, .41, .42, .43, .44, .45, .46, .47, .48, .49, .50, .51, .52, .53, .54, .55, .56, .57, .58, .59, .60, .61, .62, .63, .64, .65, .66, .67, .68, .80, .81, .82, .83, .84, .85, .86, .87, .88, .89, .90, .91, .92, .93, .94, .95, .96, .97, .98, .99

  • 717.0, .1, .41, .42, .43, .49, .5, .7, .81, .82, .83, .84, .85, .89, .9

  • 718.00, .01, .02, .03, .04, .05, .07, .08, .09, .20, .21, .22, .23, .24, .25, .26, .27, .28, .29, .30, .31, .32, .33, .34, .35, .36, .37, .38, .39, .40, .41, .42, 43, .44, .45, .46, .47, .48, .49, .50, .51, .52, .53, .54, .55, .56, .57, .58, .59, .60, .65, .71, .73, .74, .75, .76, .77, .78, .79, .80, .81, .82, .83, .84, .85, .86, .87, .88., 89, .90, .91, .92, .93, .94, .95, .96, .97, .98, .99

  • 719.20, .21, .22, .23, .24, .25, .26, .27, .28, .29, .30, .31, .32, .33, .34, .35, .36, .37, .38, .39, .40, .41, .42, .43, .44, .45, .46, .47, .48, .49

  • 720.0

  • 725.0

  • 726.0, .10, .11, .12, .19, .30, .31, .32, .33, .39, .4, .5, .60, .61, .62, .63, .64, .65, .69, .71, .72, .73, .79, .8, .9, .91

  • 727.00, .01, .02, .09, .2, .3, .50, .59, .60, .61, .62, .63, .64, .65, .66, .67, .68, .69, .81, .82, .83, .89, .9

  • 728.0, .10, .11, .12, .13, .19, .3, .79, .81, .86, .89, .9

  • 729.0, .1, .4

  • 730.30, .31, .32, .34, .35, .36, .37, .38, .39

  • 731.0, .1, .2, .3, .8

  • 732.0, .1, .2, .3, .4, .5, .6, .7, .8, .9

  • 733.6, .7, .92

  • 736.00, .01, .02, .03, .04, .05, .06, .07, .09, .1, .20, .21, .22, .29, .30, .31, .32, .39, .41, .42, .5, .6, .70, .71, .72, .73, .74, .75, .76, .79, .89, .9

  • 737.0

  • 738.2, .3, .6

  • 739.5, .6, .7

  • 840.4, .7

  • 845.09

Headache/migraine pain
  • 307.81

  • 339.00, .01, .02, .03, .04, .05, .10, .11, .12, .20, .21, .22, .3, .41, .42, .43, .44, .81, .82, .83, .84, .85, .89

  • 346.00, .01, .02, .03, .10, .11, .12, .13, .20, .21, .22, .23, .30, 31, .32, .33, .40, .41, .42, .43, .50, .51, .52, .53, .60, .61, .62, .63, .70, .71, .72, .73, .80, .81, .82, .83, .90, .91, .92, .93

  • 784.0

Neuropathic pain
  • 336.8

  • 337.0

  • 338.0

  • 339.09

  • 340.0

  • 350.1

  • 352.1

  • 353.0, .1, .2, .3, .4, .6, .8, .9

  • 354.0, .1, .2, .3, .4, .5, .8, .9

  • 355.0, .1, .2, .3, .4, .5, .6, .71, .79, .8, .9

  • 356.0, .2, .4, .8, .9

  • 357.0, .1, .2, .3, .4, .5, .6, .7, .81, .82, .89, .9

  • 723.4

  • 729.2

  • 806.00, .01, .02, .03, .04, .05, .06, .08, .09, .10, .13, .14, .15, .18, .19, .20, .21, .23, .24, .25, .26, .27, .28, .29, .30, .34, .35, .36, .37, .39, .4, .5, .6, .61, .62, .69, .70, .72, .79, .8, .9

  • 907.2, .3, .4, .5, .9

  • 952.00, .01, .02, .03, .04, .05, .06, .07, .08, .09, .10, .11, .12, .13, .14, .15, .16, .17, .18, .19, .2, .3, .4, .8, .9

  • 953.0, .1, .2, .3, .4, .5, .8, .9

  • 954.0, .1, .8, .9

  • 955.0, .1, .2, .3, .4, .5, .6, .7, .8, .9

  • 956.0, .1, .2, .3, .4, .5, .8, .9

  • 957.0, .1, .8, .9

Amputation pain
  • 878.0, .1, .2, .3, .4, .5, .6, .7, .8, .9

  • 885.0, .1

  • 886.0, .1

  • 887.0, .1, .2, .3, .4, .5, .6, .7

  • 894.2

  • 895.0, .1

  • 896.0, .1, .2, .3

  • 897.0, .1, .2, .3, .4, .5, .6, .7, .9

  • 997.60, .61

  • 998.30

  • E87.85

  • V49.60, .61, .62, .63, .64, .65, .66, .67, .70, .71, .72, .73, .74, .75, .76, .77

  • V54.10, .11, .12, .13, .14, .15, .16, .17, .19

References

  • 1. Taylor B, Hagel EM, Cutting A et al. , Fiscal year 2011 VA utilization report for Iraq and Afghanistan war veterans diagnosed with TBI. Prepared for the VA Polytrauma and Blast-Related Injuries QUERI #PLY 05-2010-2. 2012. Available at: http://www.queri.research.va.gov/ptbri/docs/FY10-TBI-Diagnosis-HCU-Report.pdf (accessed September 2014).
  • 2. Tanielian T, Jaycox LH, Adamson DM et al. , Invisible Wounds of War: Psychological and Cognitive Injuries, Their Consequences, and Services to Assist Recovery. Santa Monica, CA: RAND Corporation; 2008. [Google Scholar]
  • 3. O'Neil ME, Carlson KF, Storzbach D et al. , Complications of mild traumatic brain injury in veterans and military personnel: A systematic review. VA-ESP Project #05-225. 2013. Available at: http://www.hsrd.research.va.gov/publications/esp/mild_tbi-REPORT.pdf (accessed September 2014). [PubMed]
  • 4. Cifu DX, Taylor BC, Carne WF et al. , Traumatic brain injury, posttraumatic stress disorder, and pain diagnoses in OIF/OEF/OND veterans. J Rehabil Res Dev 2013;50:1169–76. [DOI] [PubMed] [Google Scholar]
  • 5.Minneapolis Veterans Affairs Medical Center, Minnesota Evidence Synthesis Program, Center for Chronic Disease Outcomes Research. The assessment and treatment of individuals with history of traumatic brain injury and post-traumatic stress disorder: A systematic review of the evidence. Available at: http://www.hsrd.research.va.gov/publications/esp/TBI-PTSD-2009-REPORT.pdf (accessed September 2014). [PubMed]
  • 6. Fabrizio KS, Keltner NL.. Traumatic brain injury in Operation Enduring Freedom/Operation Iraqi Freedom: A primer. Nurs Clin North Am 2010;45: 569–80, vi. [DOI] [PubMed] [Google Scholar]
  • 7. Silver JM, McAllister TW, Arciniegas DB.. Depression and cognitive complaints following mild traumatic brain injury. Am J Psychiatry 2009;166:653–61. [DOI] [PubMed] [Google Scholar]
  • 8. Sherman KB, Goldberg M, Bell KR.. Traumatic brain injury and pain. Phys Med Rehabil Clin N Am 2006;17:473–90, viii. [DOI] [PubMed] [Google Scholar]
  • 9. Higgins DM, Kerns RD, Brandt CA et al. , Persistent pain and comorbidity among Operation Enduring Freedom/Operation Iraqi Freedom/Operation New Dawn veterans. Pain Med 2014;15:782–90. [DOI] [PubMed] [Google Scholar]
  • 10. Taylor BC, Campbell E, Nugent S et al. , Fiscal year 2012 VA utilization report for Iraq and Afghanistan war veterans diagnosed with TBI. Prepared for the VA Polytrauma and Blast-Related Injuries. QUERI #PLY 05-2010-2. 2014. Available at: http://www.queri.research.va.gov/ptbri/docs/FY12-TBI-Diagnosis-HCU-Report.pdf (accessed September 2014).
  • 11. Sullivan-Singh SJ, Sawyer K, Ehde DM et al. , Comorbidity of pain and depression among persons with traumatic brain injury. Arch Phys Med Rehabil 2014;95:1100–5. [DOI] [PubMed] [Google Scholar]
  • 12. Nampiaparampil DE. Prevalence of chronic pain after traumatic brain injury: A systematic review. JAMA 2008;300:711–9. [DOI] [PubMed] [Google Scholar]
  • 13. Brickell TA, Lange RT, French LM.. Health-related quality of life within the first 5 years following military-related concurrent mild traumatic brain injury and polytrauma. Mil Med 2014;179:827–38. [DOI] [PubMed] [Google Scholar]
  • 14. Hoge CW, McGurk D, Thomas JL et al. , Mild traumatic brain injury in U.S. soldiers returning from Iraq. N Engl J Med 2008;358:453–63. [DOI] [PubMed] [Google Scholar]
  • 15. Carlson KF, Nelson D, Orazem RJ et al. , Psychiatric diagnoses among Iraq and Afghanistan war veterans screened for deployment-related traumatic brain injury. J Trauma Stress 2010;23:17–24. [DOI] [PubMed] [Google Scholar]
  • 16. Congress of the United States, Congressional Budget Office. The Veterans Health Administration's treatment of PTSD and traumatic brain injury among recent combat veterans. 2012. Available at: http://www.cbo.gov/sites/default/files/cbofiles/attachments/02-09-PTSD.pdf (accessed September 2014).
  • 17. Taber KH, Hurley RA.. OEF/OIF deployment-related traumatic brain injury. PTSD Res Quart 2010;21: 1–8. Available at: http://www.ptsd.va.gov/professional/newsletters/research-quarterly/v21n1.pdf (accessed September 2014). [Google Scholar]
  • 18. Lippa SM, Fonda JR, Fortier CB et al. , Deployment-related psychiatric and behavioral conditions and their association with functional disability in OEF/OIF/OND veterans. J Trauma Stress 2015;28:25–33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Carlson KF, Kehle SM, Meis LA et al. , Prevalence, assessment, and treatment of mild traumatic brain injury and posttraumatic stress disorder: A systematic review of the evidence. J Head Trauma Rehabil 2011;26:103–15. [DOI] [PubMed] [Google Scholar]
  • 20. Hart T, Brenner L, Clark AN et al. , Major and minor depression after traumatic brain injury. Arch Phys Med Rehabil 2011;92:1211–9. [DOI] [PubMed] [Google Scholar]
  • 21. Gould KR, Ponsford JL, Johnston L, Schonberger M.. The nature, frequency and course of psychiatric disorders in the first year after traumatic brain injury: A prospective study. Psychol Med 2011;41: 2099–109. [DOI] [PubMed] [Google Scholar]
  • 22. Bombardier CH, Fann JR, Temkin NR et al. , Rates of major depressive disorder and clinical outcomes following traumatic brain injury. JAMA 2010;303: 1938–45. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Kessler RC, Chiu WT, Demler O, Merikangas KR, Walters EE.. Prevalence, severity, and comorbidity of 12-month DSM-IV disorders in the National Comorbidity Survey Replication. Arch Gen Psychiatry 2005;62:617–27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Edlund MJ, Austen MA, Sullivan MD et al. , Patterns of opioid use for chronic noncancer pain in the Veterans Health Administration from 2009 to 2011. Pain 2014;155:2337–43. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Sullivan MD, Edlund MJ, Fan MY et al. , Trends in use of opioids for non-cancer pain conditions 2000-2005 in commercial and Medicaid insurance plans: The TROUP study. Pain 2008;138:440–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Braden JB, Fan MY, Edlund MJ et al. , Trends in use of opioids by noncancer pain type 2000-2005 among Arkansas Medicaid and HealthCore enrollees: Results from the TROUP study. J Pain 2008;9: 1026–35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Seal KH, Shi Y, Cohen G et al. , Association of mental health disorders with prescription opioids and high-risk opioid use in US veterans of Iraq and Afghanistan. J Am Med Assoc 2012;307:940–7. [DOI] [PubMed] [Google Scholar]
  • 28. Beaudoin FL, Straube S, Lopez J, Mello MJ, Baird J.. Prescription opioid misuse among ED patients discharged with opioids. Am J Emerg Med 2014;32:580–5. [DOI] [PubMed] [Google Scholar]
  • 29. Atluri S, Sudarshan G, Manchikanti L.. Assessment of the trends in medical use and misuse of opioid analgesics from 2004 to 2011. Pain Physician 2014;17:E119–28. [PubMed] [Google Scholar]
  • 30. Cicero TJ, Lynskey M, Todorov A, Inciardi JA, Surratt HL.. Co-morbid pain and psychopathology in males and females admitted to treatment for opioid analgesic abuse. Pain 2008;139:127–35. [DOI] [PubMed] [Google Scholar]
  • 31. Gwira Baumblatt JA, Wiedeman C, Dunn JR et al. , High-risk use by patients prescribed opioids for pain and its role in overdose deaths. JAMA Intern Med 2014;174:796–801. [DOI] [PubMed] [Google Scholar]
  • 32. Burgess DJ, Nelson DB, Gravely AA et al. , Racial differences in prescription of opioid analgesics for chronic non-cancer pain in a national sample of veterans. J Pain 2014;15(4):447–55. [DOI] [PubMed] [Google Scholar]
  • 33. 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]
  • 34. Dobscha SK, Morasco BJ, Duckart JP, Macey T, Deyo RA.. Correlates of prescription opioid initiation and long-term opioid use in veterans with persistent pain. Clin J Pain 2013;29:102–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Weimer MB, Macey TA, Nicolaidis C et al. , Sex differences in the medical care of VA patients with chronic non-cancer pain. Pain Med 2013;14: 1839–47. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Macey TA, Morasco BJ, Duckart JP, Dobscha SK.. Patterns and correlates of prescription opioid use in OEF/OIF veterans with chronic noncancer pain. Pain Med 2011;12:1502–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Wu PC, Lang C, Hasson NK, Linder SH, Clark DJ.. Opioid use in young veterans. J Opioid Manag 2010;6:133–9. [DOI] [PubMed] [Google Scholar]
  • 38. Ashburn MA, Lipman AG, Carr D, Rubingh C.. Principles of Analgesic Use in the Treatment of Acute Pain and Cancer Pain, 5th edition Glenview, IL: American Pain Society; 2003. [Google Scholar]
  • 39. Vieweg WVR, Carlyle Lipps WF, Fernandez A.. Opioids and methadone equivalents for clinicians. Prim Care Companion J Clin Psychiatry 2005;7: 86–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. US Department of Justice, Drug Enforcement Administration, Office of Diversion Control. Controlled substance schedules. Available at: http://www.deadiversion.usdoj.gov/schedules/index.html (accessed Sepetember 2014).
  • 41. Taylor BC, Hagel EM, Carlson KF et al. , Prevalence and costs of co-occurring traumatic brain injury with and without psychiatric disturbance and pain among Afghanistan and Iraq war veteran V.A. users. Med Care 2012;50:342–6. [DOI] [PubMed] [Google Scholar]
  • 42. Gironda RJ, Clark ME, Ruff RL et al. , Traumatic brain injury, polytrauma, and pain: Challenges and treatment strategies for the polytrauma rehabilitation. Rehabil Psychol 2009;54:247–58. [DOI] [PubMed] [Google Scholar]
  • 43. Rural Health Research Center. RUCA data: Using RUCA data. 2012. Available at: http://depts.washington.edu/uwruca/ruca-uses.php (accessed September 2014).
  • 44.Epidemiology Program, Post-Deployment Health Group, Office of Public Health, Veterans Health Administration, Department of Veterans Affairs. Analysis of VA health care utilization among Operation Enduring Freedom (OEF), Operation Iraqi Freedom (OIF), and Operation New Dawn (OND) veterans: Cumulative from 1st Qtr FY 2002 through 4th Qtr FY 2013 (October 1, 2001–September 30, 2013). 2014. Available at: http://www.publichealth.va.gov/docs/epidemiology/healthcare-utilization-report- fy2013-qtr4.pdf (accessed September 2014).
  • 45. Morasco BJ, Duckart JP, Carr TP, Deyo RA, Dobscha SK.. Clinical characteristics of veterans prescribed high doses of opioid medications for chronic non-cancer pain. Pain 2010;151:625–32. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Hudson TJ, Edlund MJ, Steffick DE, Tripathi SP, Sullivan MD.. Epidemiology of regular prescribed opioid use: Results from a national, population-based survey. J Pain Symptom Manage 2008;36:280–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47. Agency Medical Directors Group. Interagency guideline on opioid dosing for chronic non-cancer pain: An educational aid to improve care and safety with opioid therapy. 2010. Available at: http://www.agencymeddirectors.wa.gov/Files/OpioidGdline.pdf (accessed September 2014).
  • 48. Frayne SM, Phibbs CS, Friedman SA et al. , Sourcebook: Women Veterans in the Veterans Health Administration, Volume 2. Sociodemographics and Use of VHA and Non-VA Care (Fee). Washington, DC: Women's Health Evaluation Initiative, Women's Health Services, Veterans Health Administration, Department of Veterans Affairs; 2012. [Google Scholar]
  • 49. Kaur S, Stechuchak KM, Coffman CJ, Allen KD, Bastian LA.. Gender differences in health care utilization among veterans with chronic pain. J Gen Intern Med 2007;22:228–33. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Haskell SG, Brandt CA, Krebs EE et al. , Pain among veterans of Operations Enduring Freedom and Iraqi Freedom: Do women and men differ? Pain Med 2009;10:1167–73. [DOI] [PubMed] [Google Scholar]
  • 51. US Department of Veterans Affairs, Office of Acquisition and Logistics (OAL). VA directives and handbooks. 2013. Available at: http://www.va.gov/oal/library/dms.asp (accessed September 2014).
  • 52. Veterans Health Administration, Department of Defense. VA/DoD clinical practice guideline for the management of opioid therapy for chronic pain, version 2.0. 2010. Available at: http://www.healthquality.va.gov/guidelines/Pain/cot/COT_312_Full-er.pdf (accessed September 2014).
  • 53.US Department of Veterans Affairs, Veterans Health Administration. VHA directive 2009-053: Pain management. 2009. Available at: http://www.va.gov/vhapublications/ViewPublication.asp?pub_ID=2781 (accessed September 2014).
  • 54. Vanderlip E, Sullivan M, Edlund M et al. , National study of discontinuation of long-term opioid therapy among veterans. Pain 2014;155:2673–9. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Pain Medicine: The Official Journal of the American Academy of Pain Medicine are provided here courtesy of Oxford University Press

RESOURCES