In contrast to prior efforts to limit opioid use since the early 1900s,1 Portenoy and Foley2 reported a case series of 38 patients in 1986 and opined that long-acting opioids for chronic, noncancer pain (CNCP) were safe and effective and referenced other data supporting a less than 1% risk of addiction. Pharmaceutical companies then performed trials generally of not more than 3 months, claimed long-term safety and efficacy of opioids for chronic pain treatment, and marketed opioids to physicians and potential patients.3,4 Recognition of undertreatment of pain in many populations, legislative,5 litigation,6 regulatory,7–9 and health care accreditation-related activities10–13 further contributed to lowering barriers to, and rapid increases in opioid prescriptions, primarily for CNCP.14
In 2009, there were 201.9 million Schedule II through IV (including strong and weak) opioid prescriptions paid in the United States. It is estimated that 4.9% of US adults used opioids in the prior week and 2.0% used them regularly.15,16 Along with increased use of opioids, emergency department visits for nonmedical use of opioids increased 111% from 2004 to 2008.17
Opioid use and deaths associated with opioids have also risen closely together.18–27 Deaths related to opioids quadrupled from 1999 through 2010, increasing from 4000 to 16,000 deaths in 2010,28 occurring in both urban and rural areas.29,30 Opioids have surpassed motor vehicle crashes as the cause of death in several states.19,27,31–34
There have been an increasingly large number of policies and guidelines that have been developed to address opioids.35–63 Recent reviews of these opioid guidelines found widely varying quality.64,65 There was no guideline identified meeting current guidelines quality standards66 and addressing up-to-date and detailed opioid use guidance for nonmalignant pain management.
The American College of Occupational and Environmental Medicine (ACOEM) Opioids Guideline is designed to provide health care providers who are the primary target users of this guideline with evidence-based guidance on the use of opioids for treatment in the specific settings of acute (up to 1 month' duration), subacute (1 to 3 months' duration), chronic (>3 months' duration), and postoperative pain. This report summarizes findings from the 220-page ACOEM Opioids Guideline (960 references) and addresses the following questions developed by the Evidence-based Practice Opioids Panel:
- What evidence supports the need for a history and physical examination before prescribing opioids?
- Are opioids superior to other medications or other treatments for pain relief and functional improvement?
- Is screening for risk factors effective for reducing adverse effects of treatment from opioids?
- What is the dose–response relationship between morphine-equivalent dose and overdoses, fatalities, and other adverse effects?
- What evidence addresses the balance of risk and benefits of opioid use for acute, subacute, chronic, and postoperative pain?
- Are opioids efficacious for treatment of acute, subacute, chronic, and postoperative nonmalignant pain?
- Are opioid treatment agreements (opioid contract, doctor/patient agreement, or informed consent) effective?
- What is the prevalence of aberrant urine drug screening results among patients using opioids for treatment of chronic pain?
- What evidence supports the use of intrathecal drug delivery systems for treatment of chronic, nonmalignant pain?
- What tapering regimens are effective for weaning off opioids?
The primary target population is working-age adults, although the literature searches included articles addressing all adults. Thus, it is recognized that the principles may apply more broadly.
GUIDELINE DEVELOPMENT PROCESS
A detailed methodology document specifies evidence selection, scoring, incorporation of cost considerations,67 and formulation of recommendations.68–70 Briefly, the aim is to identify the highest-quality evidence on any given topic. The only noteworthy additions regarding this guideline are inclusion of large epidemiological studies for evidence of harms used for guidance and a change in the databases searched.
Guidance was drafted using tables of evidence that abstracted the epidemiological evidence. Draft text and tables were forwarded to the multidisciplinary Evidence-based Practice Opioids Panel (Michael S. Weiss, Kirk Bowden, Fernando Branco, Kimberly DuBrueler, Charl Els, Steven Mandel, David W. McKinney, Rafael Miguel, Kathryn L. Mueller, Robert J. Nadig, Michael I. Schaffer, Larry Studt, James B. Talmage, Russell L. Travis, and Thomas Winters). The Panel reviewed the evidence and finalized the text and recommendations. This guideline achieved 100% Panel agreement for all developed guidance.
EVIDENCE REVIEW AND GRADING
All evidence related to opioids in prior ACOEM Practice Guidelines39,71–78 after searching seven databases was included in this guideline (MEDLINE, EBM Online, Cochrane, TRIP, CINAHL, EMBASE, and PEDro). Comprehensive searches for epidemiological evidence were performed with both PubMed and Google Scholar through October 2013 to help ensure complete study capture. There was no limit on the year of publication. Search terms for this report are available at: http://www.acoem.org/PubMedSearchDetails.aspx. Reference lists of included articles were reviewed for inclusion. All included studies were scored for quality.68–70 Articles scoring moderate or high quality were included.68–70
The search strategies identified a total of 264,617 article titles, which were screened, with all potentially appropriate study abstracts reviewed and evaluated against specified inclusion and exclusion criteria. A total of 263 studies were included in these analyses. Articles reporting the studies were critically appraised and scored, and a total of 157 were of high and moderate quality addressing pain treatment.
COMMENTS AND MODIFICATION
Guidance was developed with sufficient detail to facilitate assessment of compliance (Institute of Medicine [IOM]) and auditing/monitoring (Appraisal of Guidelines for Research and Evaluation [AGREE]).66,67 Alternative options to manage conditions are provided in other ACOEM guidelines when comparative trials are available.39,71–78
The only AGREE67 and IOM criterion not adhered to is incorporation of the views of the target population. Patients taking opioids, those with current or past opioid dependence or addiction, or other affected patient groups were not involved on the Panel or external review process, nor were advocates for or against the use of opioids. In accordance with the IOM's Trustworthy Guidelines, this guideline underwent external peer review by 27 external reviewers, and subsequent revisions to the guidance, and detailed records of the peer review processes are kept, including responses to external peer reviewers.66
The Evidence-based Practice Opioids Panel and the Research Team have complete editorial independence from ACOEM and Reed Group, which have not influenced the guideline. The literature is routinely monitored and formally searched at least annually for evidence that would materially affect this guidance. This guideline is planned to be updated at least every 3 years or more frequently should evidence require it.
A separate report on this guideline's findings concerning the use of opioids for safety sensitive work is available elsewhere.79 All treatment recommendations are guidance based on synthesis of the evidence plus expert consensus. These are recommendations for practitioners, and decisions to adopt a particular course of action must be made by trained practitioners on the basis of available resources and the particular circumstances presented by the individual patient.
Comprehensive History and Physical Examination
No quality studies assess the utility of a history and physical examination. Nevertheless, the Panel's consensus recommendation is that a careful history and physical examination are highly important for appropriate pain management and consideration of opioid prescriptions regardless of pain acuity (Table 1). The Panel recommended to evaluate current and prior pharmacological and nonpharmacological methods for safe and effective control of pain, associated symptoms, and function.63,80–82 A comprehensive evaluation and documentation include a history, prior treatment, vocation, avocational activities, current functional level, medical history, family history, social history including substance(s) use (tobacco, alcohol, and illicit substances), review of systems, laboratory testing, and imaging studies as appropriate.62,63,80,81,83,84 This systematic approach should result in a clear diagnosis to treat as evidence indicates.63,80,83 In many cases of chronic pain, the most accurate “diagnosis” may be a symptom rather than a pathophysiological diagnosis, for example, chronic low back pain (LBP). An evidence-based treatment plan should focus on addressing the diagnosis or symptoms. Obstacles for treatment and rehabilitation should be identified and addressed.
There were four quality trials of acute pain patients treated with opioids compared with placebo, with a small overall magnitude of benefit, whereas the adverse effects profile was high. Among trials for treatment of acute pain, ibuprofen was reportedly superior to codeine or acetaminophen for acute injuries including fractures.85 Diflunisal was equivalent to codeine for sprains, strains, and mild to moderate LBP.86 Valdecoxib* was better tolerated and trended toward greater pain relief than tramadol for ankle sprains.87 Valdecoxib was equivalent to oxycodone as assessed by pain ratings, but trended toward less rescue medication use and had fewer adverse effects among patients with spine and extremity pain.88 Global ratings for LBP showed that carisoprodol was superior to propoxyphene and has fewer adverse effects.89 Ketorolac was equivalent for pain relief, but superior to meperidine regarding adverse effects for treating severe LBP.90 Ketorolac was also superior to codeine/acetaminophen for acute LBP treated in emergency departments.91 Diflunisal was superior to codeine/APAP for LBP.92 One trial suggests that transcutaneous electrical stimulation was equivalent to codeine/acetaminophen for acute trauma.†93 There are many emergency department trials of up to a few hours of treatment and no follow-up, with minimal if any differences, and thus of somewhat unclear utility for guidance.94–105 No quality trials suggest superiority of opioids to other active treatments. Prolonged use of opioids after an acute event has been associated with worse functional outcomes.106–108 Quality evidence indicates that safety profiles are considerably worse for opioids.
Routine use of opioids for treatment of acute pain is strongly not recommended and the recommendation for select use of opioids based purely on the evidence is downgraded from “A” to “C” (Table 1). Although there are a few trials of patients with acute pain treated with opioids compared with placebo, the overall magnitude of benefit is small while the adverse effects profile is sufficiently high that this resulted in the recommendation being downgraded. When needed, the lowest effective dose of a short-acting opioid is recommended for those with acute, severe pain uncontrolled by other agents such as nonsteroidal anti-inflammatory drugs (NSAIDs).109 Based on expert opinion, NSAIDs or acetaminophen should generally accompany an opioid prescription. Lower potency opioids are recommended when sufficient for pain relief. As-needed dosing rather than scheduled is generally indicated. Dispensing quantities should be only what is needed to treat the pain. Short-acting opioids are recommended for treatment of acute pain. Long-acting opioids are not recommended. If parenteral administration is required, ketorolac has demonstrated superior efficacy compared with opioids for acute severe pain.90,91 The maximum daily oral dose recommended based on risk of overdose/death is 50-mg morphine equivalent dose (MED)110 (Fig. 1). Exceeding that dose should be based on documented need, and incremental functional gain increased surveillance for adverse effects and frequent reconsideration of benefit versus risk. Lower doses are also indicated in the elderly, women,111 and those of low body weight. Prescription drug monitoring program databases are recommended to be checked. Considerable caution is recommended among those receiving other CNS-depressing medications such as benzodiazepines or depressant medications, and patients with concomitant psychiatric disorders or other risk factors for adverse effects, overdose, and death (Table 2).17,29,30,32,112–133 Because of risk of impairment and lost time from work due to medication effects,134,135 opioids should be prescribed at night or while not working when possible.136 The Panel recommends tapering the opioid in 1 to 2 weeks. Potential benefits of prescribing opioids are improved short-term pain control and accelerated functional recovery, whereas potential harms are numerous (Table 2).
Findings and recommendations for postoperative pain management with opioids are mostly comparable with those treating acute pain (Table 1). Nevertheless, studies also include at least one trial showing modestly improved long-term knee range of motion and less opioid use with pregabalin for 14 days plus epidural and opioid management after total knee arthroplasty.240 Another trial found superior range of motion and fewer venous thromboses after continuous femoral nerve catheter analgesia instead of solely using oral narcotics.241 Ketorolac appeared superior as a primary pain treatment supplemented with opioids compared with opioids alone for spine and joint procedures.242 Data also suggest that patient-controlled analgesia may not be superior to intramuscular opioids.243,244 Thus, opioids may have deleterious postoperative effects if not used solely as adjunctive medications. Preoperative consultation with anesthesiology and/or pain management specialists may be needed for those taking chronic opioids preoperatively. Additional differences from the acute pain recommendations above include administration of NSAIDs at the time of surgery without undue complications,245–250 although these studies would likely be underpowered for rare complications. For major surgeries, scheduled opioid medication is frequently required. Opioids sufficient to participate in therapeutic exercise (eg, progressive ambulation) and allow sleep may be needed. It is recommended to dispense only what is needed to avoid either overmedication and/or diversion. Weaning should begin as soon as function is recovering and pain is subsiding. Also, closely monitored inpatient settings may somewhat moderate the cautions about the recommended MED limit of 50 mg and overdoses (Fig. 1). Nevertheless, the evidence that early ambulation is critical to functional recovery is strong. Therefore, oversedation that interferes with function is a concern. For patients on chronic opioids preoperatively, especially moderate to high doses, consultation with a physician experienced in managing these complex cases may be necessary. Thus, thoughtful use of short-acting opioids for postoperative pain management is recommended for limited use as adjunctive therapy to more effective treatments with recommendations summarized in Table 1. Prescription drug monitoring programs should be checked. Psychiatric and/or mental health consultation should be considered for those who do not improve as expected and require high doses or ongoing opioid use. For those requiring opioid use beyond 1 month, the subacute/chronic opioid use recommendations given later apply.
Chronic Noncancer Pain
There are 67 high- or moderate-quality placebo-controlled clinical trials addressing opioid use for patients with chronic pain. Of these, 52% lasted up to 1 month, 12% were 1 to 2 months, and 34% were 3 months in duration. Only one trial was longer than 3 months at 16 weeks.251 There is only one quality trial that targeted subacute pain, finding flupirtine equivalent to tramadol for subacute LBP.252 As tolerance develops quickly, guidance for subacute and chronic pain are combined.
For treatment of subacute and chronic pain, there is quality evidence that other medications and treatments are at least equivalent if not superior for subacute or chronic pain (eg, NSAIDs,253–256 nortriptyline,257 clonidine,258 and flupirtine.252) No quality trials suggest superiority of opioids to other medications or treatments. One trial suggests that morphine is superior to benztropine for pain, but not function.259 Among trials for treatment of subacute or chronic pain, one trial failed to find superiority of morphine to nortriptyline for treatment of chronic lumbar radiculopathy.257 Another found neither morphine nor mexiletine superior to placebo.260 Another found celecoxib superior to tramadol for chronic LBP.253 Diclofenac was superior to dextropropoxyphene/APAP for treatment of hip or knee osteoarthritis.254 Diclofenac was approximately equivalent to tramadol in another trial.256 Naproxen was equivalent to oxycodone for treatment of chronic LBP.255 There are no trials documenting improved objective functional outcomes, with more than 100 studies documenting many adverse effects.261 There is quality evidence that opioids are associated with reduced pain thresholds.262 Thus, there is considerable evidence that other medications and treatments should be used prior to consideration of an opioid prescription for chronic/subacute pain patients.263
Tramadol is a synthetic opioid and is a controlled substance in some US states. Tramadol is associated with potential abuse264 and has a similar adverse effect profile as other opioids. Nevertheless, death risks, while elevated, seem to be somewhat lower than other opioids. Tramadol seems to be a better initial option than more potent opioids. Nevertheless, with the long-term use, especially higher dose, it may be considered equivalent to other opioids for purposes of this guideline. It has also been associated with motor vehicle crashes.79
For subacute and chronic pain, an opioid trial, preceded by full informed consent and a trial agreement, is recommended if other evidence-based approaches for functional restorative pain therapy have been implemented, with documented adherence, and with inadequate improvement in function63,81 (Tables 1 and 3). Pain or pain scales alone are recommended as insufficient reasons.82,113,265–276 Examples of functional gains to track include walking distance, numbers of repetitions of specific exercises, return to work, and return to modified work. Maintenance opioids are recommended for those achieving functional gains (Table 3).
Treatment Agreements and Informed Consent
Although there are no quality studies to document efficacy of opioid consent forms and/or opioid treatment agreement contracts, they are commonly used to monitor patients on opioids.39,41,62,63,277,278 These agreements usually include provision for urine drug testing for assessing compliance for use of that particular opioid, as well as ascertaining other illicit substances use.62,63,279–282 This guideline developed a combined Opioid Consent Form and Opioid Treatment Agreement into one form that is recommended for subacute and chronic pain patients (available at: www.mdguidelines.com/documents/stateguidelines/apg3_opioid_06_treatment_agreement.pdf).
Urine Drug Screening
Most evidence documents aberrant drug screen prevalence rates of 32% to 45%.277,280,281,283–286 Drug screening may identify both aberrant use and other substance use outside a treatment agreement.280,281 Urine drug screening, qualitative and quantitative, is recommended at baseline, randomly at least two to four times a year and at termination for patients prescribed opioids for the treatment of subacute or chronic pain; these tests are to evaluate presence or absence of the drug, its metabolites, and other substance(s) use.63 Higher frequencies of drug screening are recommended among those consuming more than 50 mg of MED (Fig. 1). It is recommended to be performed in a federally certified laboratory with a two-step process including confirmatory gas chromatography–mass spectroscopy. In certain situations, other screenings (eg, hair particularly for information regarding remote use287–292) or blood (for acute toxicity) may be appropriate. Standard urine drug/toxicology screening processes are recommended (consult a qualified medical review officer).279,293,294 To be useful, one must choose a test that the laboratory states will detect the presence of the opioid (and metabolites) being prescribed, assuming that the patient is actually taking and not diverting the medication. It is also important that the test chosen is able to detect the drugs that might be used/abused surreptitiously, and that increases the risk of accidental overdose mortality (eg, benzodiazepines, barbiturates). If there is an aberrant drug screen result (either positive for unexpected drugs or unexpected metabolites or unexpectedly negative results), there should be a careful evaluation of whether there is a plausible explanation (eg, drug not tested, drug metabolite not tested, laboratory cutpoint, and dosing interval would not capture the drug/metabolite, laboratory error). In the absence of a plausible explanation, those patients with aberrant test results should have the opioid discontinued or weaned.40,81
Conversion of opioids to an MED is helpful to transfer from one opioid to another. This is most commonly performed to attempt to achieve a better functional outcome and/or to reduce adverse effects. Quality evidence to support this practice has not been published. Several resources are available295,296 that include a spreadsheet-based calculator297 and on-line converting tool.298 To avoid drug overdoses, when transferring from one opioid to another, the MED prescribed should be approximately 50% of the prior dose.299–302
Many studies have described widely varying rates of tapering opioids, mostly ranging from 10% per week to 50% per day.40,56,303,304 Nevertheless, there are no high- or moderate-quality studies among the desired target population to define the best methods. The clinical approach is, therefore, largely empirical.
Non–cancer-related breakthrough pain (BTP) has been treated with opioids.305–308 There are cases in which BTP may indicate hyperalgesia, or potentially, insufficient treatment of pain. Nevertheless, in treating BTP, functional gain is recommended to be documented; otherwise, the total dose should revert to the prior dose level. The treatment of BTP with opioids is likely a common means of dose escalation.309 Thus, treatment of nonmalignant BTP in the absence of overt trauma is not recommended.
No quality studies document efficacy of intrathecal opioid delivery systems for treatment of chronic nonmalignant pain. Intrathecal opioid delivery systems are invasive and costly, with possible significant adverse effects, including potential long-term sequelae from both implantation/retention of the devices, including granuloma formation, and those associated with the concurrent use of intrathecal opioids.137,138,310–313 Thus, with a lack of documented efficacy, invasiveness, serious adverse effects, and marked costs, these devices are not recommended. For new patients, there are few barriers for implementing this guideline, whereas for existing patients, this guideline should not be interpreted as requiring device removal.
Opioids have been associated with numerous adverse effects, which differ somewhat on the basis of the specific drug and route of administration. In aggregate, these effects include (see also Table 2) opioid-induced hyperalgesia,139,140 lower pain thresholds (hyperalgesia), nausea, vomiting, delayed gastric emptying, constipation, pruritus, drowsiness, sedation, respiratory depression,54,141–178 clouding of consciousness or “mental fog,” dysphoria, decreased concentration, lack of coordination, myoclonus, muscle rigidity, dizziness, euphoria, sexual dysfunction, bladder dysfunction, immune system effects, hair loss, anaphylaxis, sleep disturbance,62,138,179–192 motor vehicle crashes,136,193–196 lower return to work status,197 injuries and other accidents,132 disability,197,198 and drug tolerance.199 Deaths from unintentional and intentional overdoses, misuse, and therapeutic misadventures occur, although they are infrequent relative to the adverse events listed previously.
There is no quality literature to identify which patients can be safely prescribed opioids without escalation of dose or other adverse risks. This caused a downgrading of the level of evidence from “C” to “I” especially when combined with evidence of adverse effects (see Table 2) in addition to concerns regarding the inability to control escalating doses.309 Prescribing opioids may initiate the path to opioid dependency, addiction, and other adverse effects. Tolerance is a common occurrence, although generally not significantly problematic. Addiction and drug-seeking behaviors are less common.259,314–318 Yet, approximately 80% of patients experience some adverse effects from opioids and approximately 33% to 80% do not finish a clinical trial with opioids due primarily to these adverse effects (the large range in estimates is in part due to trial design such as whether a washout phase was included, length of treatment, and severity of pain).319–321
Although the clinical interview remains an important method to identify risk for aberrant drug-related behaviors,322,323 it is neither systematic nor efficient. Thus, there are many screening/monitoring methods that have been developed.41,322–342 The three tools with the largest volume of research seem to be the Screener and Opioid Assessment for Patients with Pain (SOAPP) and its revised version (SOAPP-R), the Pain Medication Questionnaire, and the Current Opioid Misuse Measure. All three of these tools have undergone partial validations, although none of them has been fully validated to document prevention of opioid misuse/abuse.200,262,271,273,322,323,325–328,331,340,341,343–354 The Pain Disability Index is also widely used; it is also wholly subjective and has somewhat fewer supportive data.355,356
Opioid deaths have been associated with CYP2D6 and OPRMI gene variations,357–361 with the CYP cytochromes (CYP 3A4/3A5, CYP2D6, CYP2C9, CYP2D9) responsible for metabolism through the cytochrome P450 system,362 and genetic variations impairing opioid metabolism. As one example of potential clinical impacts, there is a strong tendency for those of Chinese ancestry, as well as some whites, not to metabolize codeine to morphine. Currently, screening for genetic risks prior to opioid treatment is not in widespread use.363–366 Cytochrome-blocking drugs367 and cytochrome-inducing pharmaceuticals also influence efficacy and toxicity.364–366,368,369–387
Opioids are moderate to high cost, depending on the duration of treatment. Provider and organizational barriers to implement recommendations to prescribe nonopioid medications and therapies are low, consisting primarily of altering practice habits. Barriers regarding dose limit recommendations are similarly low, consisting primarily of altering practice habits. Barriers to dose reduction are greater for established patients, especially on higher doses. Tools are identified to assess functional progress, assessing opioid risk, and guidance to assist with tapering. Urine drug testing guidance has been developed.
None of 28 comparative effectiveness trials reviewed reported that opioids are superior to other medications or treatments for acute, subacute, chronic, or postoperative pain. Several trials suggested that opioids are inferior to other medications, generally NSAIDs. Reported magnitudes of benefit of opioids compared with placebo are modest. As there currently is none, high-quality evidence regarding objective gains in function from treatment with opioids for chronic pain is a particularly important need.
For chronic pain, there are no placebo-controlled trials lasting more than 4 months. Thus, long-term efficacy of opioids for chronic pain is unknown. There also is no quality literature to identify which patients can safely be prescribed opioids without escalation of dose or other adverse risks. This caused a downgrading of the level of evidence from “C” to “I” especially when combined with evidence of major adverse effects reviewed elsewhere in addition to concerns regarding the inability to control escalating doses.309 The ability to prospectively identify patients who are able to realize both long-term safety and efficacy of opioids is another area of much-needed research.
Many of the studies have low sample sizes and the designs of the trials vary, especially for treatment of chronic pain. In those studies that include all patients in a randomized controlled trial, overall dropout rates (including washout phases, run-in phases, conversion phases, titration phases, trial “enrichment” phases, as well as those who drop out during the trial) and adverse effect profiles each frequently exceed 50% and several are more than 75%.261,308,314,319,388–393 Studies that include or require prior chronic opioid use and/or have early washout and/or run-in phase(s) likely remove patients who (i) cannot tolerate the adverse effects, (ii) are unwilling to endure the adverse effects for a duration of time, (iii) recognize prior adverse impacts on function, and/or (iv) have lower psychological and substances use profiles. Consequently, the bulk of reported chronic pain trials likely have artificially lower adverse-effect profiles than treatment of the general population.394 Ergo, fewer than 50% of patients with chronic pain appear likely to tolerate opioids, even if they are potentially indicated.308,314,319,388,390–393
The vast majority of the trials of opioids either are industry-sponsored or have significant conflicts of interest. By contrast, epidemiological studies of motor vehicle crash risk associated with opioids show no significant conflicts of interest.79 Sponsored studies have been frequently reported to have better apparent results and lower complication rates than studies conducted by independent investigators.395–398 A prior review of 546 pharmaceutical trials found that 63% were primarily funded by industry, 14% by government, and 23% by nonprofit or nonfederal organizations.395 Industry sponsorship revealed in the present systematic review and guideline on opioid use was greater still especially for chronic pain. For acute pain, 42.1% of 19 trials for patients with acute pain, 60.0% of 20 perioperative and postoperative trials, and 87.1% of 93 chronic pain patient trials with sponsorship identified had partial or full industry sponsorship. When analyzing only the studies that had a minimum level of follow-up time (1, 7, and 30 days for acute, postoperative, and chronic pain, respectively), 80.0%, 80.0%, and 93.9% had partial or full industry sponsorship, respectively.
The number of comparative trials with nonopioid treatment arms compared to an opioid is fairly limited and focused on a few medications. Altogether, there are 9 acute pain, 7 peri/postoperative, and 12 chronic pain comparative trials that scored high or moderate quality. Industry sponsorship of these is similarly 73.9%. Thus, the large majority of evidence regarding efficacy of opioids is at least partially industry-sponsored or with conflicts of interest. These analyses provide additional direction for needed nonconflicted research.
APPLICABILITY AND IMPLEMENTATION ISSUES
Strengths of this guideline include its systematic synthesis of many quality studies. The evidence is largely consistent for many of the guideline questions, including both strong and weak opioids. Findings include a lack of studies showing superiority of opioids for pain treatment. The dose–response relationship between morphine equivalent dose and risk of fatality has been reproduced, and duplicated between acute and chronic pain patients. Therefore, the overall evidence base is strongly supportive of most of this guideline's recommendations. This guideline has also identified additional interventions that, if implemented, would likely reduce the adverse effects and mortality.
Weaknesses of this guideline include the relatively few comparative trials and heavy industry sponsorship of trials and conflicts of interest in the vast majority of studies. Implementation of this guideline could potentially result in pain, which could be undertreated when it may be successfully treated with opioids, although the guideline includes provisions to avoid that.
The ACOEM Evidence-based Practice Opioids Panel concludes that quality evidence currently fails to demonstrate superiority of opioids to other medications and treatments for treatment of pain. It recommends comprehensive history and physical examinations. Selective use of the lowest effective, short-acting opioid dose is recommended as adjunctive treatment for patients with acute and postoperative pain that is inadequately treated with NSAIDs or other treatments. The strongest risk factors for overdose and deaths include concomitant use of benzodiazepines, illicit substances, unemployment status, psychiatric disorders, and a substance(s) abuse history. Opioid consent and treatment agreements are recommended for treatment of subacute and chronic pain with opioids. Carefully conducted trials on highly select patients with subacute and chronic pain are recommended, as well as opioid maintenance only with documented functional gain(s). A strong and reproducible dose–response relationship identifies a recommended MED limit of 50 mg/day for acute or chronic pain. Higher doses are recommended to require documented commensurately greater functional benefit(s).
The Evidence-based Practice Opioids Panel recognizes the considerable work of the managing editors: Marianne Dreger, MA (Production), and Julie A. Ording, MPH (Research). The Opioids Panel also much appreciates the research for this guideline that was conducted by the research team: Ulrike Ott, MSPH; Atim C. Effiong, MPH; Deborah G. Passey, MS; William G. Caughey, MS; Holly Uphold, PhD; Alzina Koric, MPP; Zac Carter, BS; Zachary C. Arnold, BS; Katherine Schwei, BS; Kylee Tokita, BS; Leslie M. Cepeda-Echeverria; Ninoska De Jesus; and Jeremiah L. Dortch, BS. Drs Hegmann and Thiese also conducted research for this guideline. Dr Harris served as the Opioids Panel methodologist.
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* Valdecoxib is currently withdrawn from the market.
† Flupirtine also has evidence of efficacy, although not currently approved in the United States.