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JAMA Network logoLink to JAMA Network
. 2020 Jun 24;3(6):e207664. doi: 10.1001/jamanetworkopen.2020.7664

Assessment of Physician Prescribing of Muscle Relaxants in the United States, 2005-2016

Samantha E Soprano 1,2, Sean Hennessy 1,2,3,4, Warren B Bilker 1,2,5, Charles E Leonard 1,2,3,
PMCID: PMC7315288  PMID: 32579193

This cross-sectional study uses data from the National Ambulatory Medical Care Survey from 2005-2016 to assess continued and new physician prescribing of muscle relaxants in the United States.

Key Points

Question

What trends characterize the outpatient prescribing of skeletal muscle relaxants in the United States?

Findings

In this cross-sectional study of US physician visits, skeletal muscle relaxant prescribing doubled between 2005 and 2016. This increase was associated primarily with an increase in office visits with continuing use of skeletal muscle relaxants. New use of skeletal muscle relaxants was stable. Skeletal muscle relaxants were prescribed disproportionately to older adults, a high-risk population in whom these medications are potentially inappropriate, and were often prescribed concomitantly with opioids despite guidelines warning against this potentially dangerous combination.

Meaning

This evidence of increasing continuing use of skeletal muscle relaxants, their disproportionately high use in older adults, and their concomitant use with opioids all represent trends with potentially adverse clinical and public health consequences.

Abstract

Importance

Little is known to date about national trends in the prescribing of skeletal muscle relaxants (SMRs), the use of which is associated with important safety concerns, especially in older adults and in those who use concomitant opioids.

Objective

To measure national trends in SMR prescribing over a 12-year period.

Design, Setting, and Participants

This cross-sectional study used data from the National Ambulatory Medical Care Survey from January 2005 to December 2016. Data were analyzed from August 21, 2018, to July 18, 2019. The study included patients with ambulatory care visits who had encounters with non–federally funded, office-based physicians in the United States.

Exposures

SMR use, categorized as newly prescribed or continued therapy at the office visit.

Main Outcomes and Measures

Ambulatory care visits—overall and stratified by calendar year, geographic region, and patient age, sex, and race—in which an SMR was newly prescribed or continued were quantified. Among office visits in which an SMR was newly prescribed, diagnoses were assessed. Concomitant medications were quantified for all office visits, stratified by new or continued therapy. Survey visit weights were used to estimate nationally representative measures, and age-standardized rates were generated by geographic region using US Census data.

Results

This study included a total of 314 970 308 office visits (mean [SD] age, 53.5 [15.2] years; 194 621 102 [61.8%] men and 120 349 206 [38.2%] women). In 2016, there were 30 730 262 (95% CI, 30 626 464-30 834 060) US ambulatory care visits in which an SMR was either newly prescribed or continued as ongoing therapy. Patients in these visits were most frequently female (58.2% [95% CI, 57.9%-58.6%]), white (53.7% [95% CI, 53.4%-54.0%]), and aged 45 to 64 years (48.5% [95% CI, 48.2%-48.9%]). During the study period, office visits with a prescribed SMR nearly doubled from 15.5 million (95% CI, 15.4-15.6 million) in 2005 to 30.7 million (95% CI, 30.6-30.8 million) in 2016. Although visits for new SMR prescriptions remained stable, office visits with continued SMR drug therapy tripled from 8.5 million (95% CI, 8.4-8.5 million) visits in 2005 to 24.7 million (95% CI, 24.6-24.8 million) visits in 2016. Older adults accounted for 22.2% (95% CI, 21.8%-22.6%) of visits with an SMR prescription. Concomitant use of an opioid was recorded in 67.2% (95% CI, 62.0%-72.5%) of all visits with a continuing SMR prescription.

Conclusions and Relevance

This study found that SMR use increased rapidly between 2005 and 2016, which is a concern given the prominent adverse effects and limited long-term efficacy data associated with their use. These findings suggest that approaches are needed to limit the long-term use of SMRs, especially in older adults, similar to approaches to limit long-term use of opioids and benzodiazepines.

Introduction

In response to the opioid epidemic, clinicians and patients are increasingly seeking alternatives to opioids for the management of musculoskeletal conditions. Centrally acting skeletal muscle relaxants (SMRs), such as baclofen, carisoprodol, chlorzoxazone, cyclobenzaprine, metaxalone, methocarbamol, orphenadrine, and tizanidine, are labeled for acute musculoskeletal conditions including spasms and lower back pain; they are used off-label for neuropathic pain, chronic noncancer pain, temporomandibular disorder pain, and numerous nonpain conditions.1 A 2003 systematic review concluded that SMRs are effective for acute low back pain (although their comparative effectiveness vs analgesics or nonsteroidal anti-inflammatory drugs for acute low back pain is unknown), the evidence for chronic low back pain is less convincing, and SMRs must be used with caution because of central nervous system adverse effects, such as drowsiness and dizziness.2 Because of the lack of evidence regarding the long-term efficacy and safety of SMRs and the unquantified risk of abuse, dependence, and overdose,1,3 recommendations generally limit the use of SMRs to a maximum duration of 2 to 3 weeks.4 Despite such recommendations, a 1988-1994 study found that 44.5% of people taking SMRs were continuously treated for longer than 1 year.5 Carisoprodol, chlorzoxazone, cyclobenzaprine, methocarbamol, metaxalone, and orphenadrine are all considered potentially inappropriate medications in older adults,6,7 in whom these agents are associated with sedation, cognitive impairment, and fracture.8 An additional concern regarding the inappropriate use of SMRs is the potential for drug-drug interactions, particularly with opioids.9

We sought to characterize national trends in SMR prescribing, both overall and in older adults, and to examine the concomitant prescribing of SMRs with opioids. Therefore, we examined nationally representative data from the National Ambulatory Medical Care Survey (NAMCS) for the 12-year period spanning from 2005 to 2016.

Methods

We conducted a retrospective cross-sectional analysis of SMR prescribing using publicly available NAMCS data from January 2005 to December 2016. NAMCS is a US-based, annual survey of non–federally funded office-based physicians engaged in direct patient care.10 Survey data are collected from sampled health care professionals by trained proctors. Office visit records are weighted based on the most recently available census data to provide a nationally representative view of all ambulatory care visits in the United States. The survey captures information about the office visit, such as the reason for the encounter and diagnoses, medications, and demographic information about the patient, as well as information about the provider and their practice.

We identified all office visits in which an SMR was recorded as either newly prescribed or continued ongoing drug therapy, referred to herein as an SMR visit. To limit the data set to records of interest, we generated a list of Lexicon Plus (Cerner Multum Inc) drug identification codes for baclofen, carisoprodol, chlorzoxazone, cyclobenzaprine, metaxalone, methocarbamol, orphenadrine, and tizanidine. From these records, we extracted visit information, patient demographic characteristics, and record weights to generate national estimates. We examined the total number of visits per year; the race, ethnicity, and sex of the patient; and the region of the visit. Furthermore, we stratified counts by SMR agent and whether the SMR was newly prescribed or continued drug therapy.

We identified patients who were newly prescribed an SMR during the recorded visit by linking the new or continued status of reported medications (NCMed) variable to the SMR drug identification code. The NCMed variable indicates whether the medication was newly prescribed during the office visit or the patient was instructed to continue the medication as a part of their ongoing drug therapy. We examined the number of visits per year, the patient’s primary reason for the office visit, and all recorded diagnoses. All concomitant medications were examined for new SMR visits, and concomitant opioids were examined for continued SMR visits. A list of variables used, corresponding NAMCS variable names, and the population in which they were examined are presented in eTable 1 in the Supplement. For variables permitting multiple entries per visit, we included all entries without regard to ordering, eg, using all 5 diagnosis fields recorded in the 2016 survey.

We conducted analyses using the Statistical Package for Social Scientists, version 25 (IBM Corp) from August 21, 2018, to July 18, 2019. The University of Pennsylvania’s Office of Regulatory Affairs determined that this research did not require institutional review board oversight because the NAMCS is a publicly available data set. This article complies with the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline for cross-sectional studies.11

Results

Patient demographic characteristics for SMR visits are shown in Table 1. The cross-sectional analysis included a total of 314 970 308 office visits (mean [SD] age, 53.5 [15.2] years; 194 621 102 [61.8%] men and 120 349 206 [38.2%] women). In 2016, there were 30 730 262 (95% CI, 30 626 464-30 834 060) US ambulatory care visits in which an SMR was either newly prescribed or continued as ongoing therapy. Patients prescribed an SMR in 2016 tended to be female (58.2% [95% CI, 57.9%-58.6%] women vs 41.8% [95% CI, 41.4%-42.1%] men). Racial demographic characteristics for SMR users in 2016 were as follows: 53.7% white (95% CI, 53.4%-54.0%), 10.2% African American (95% CI, 9.7%-10.6%), 1.2% Asian (95% CI, 1.0%-1.5%), and 2.2% Native American or Alaska Native (95% CI, 2.0%-2.5%). There were no data available for Native Hawaiians, and 1.5% (95% CI, 1.3%-1.8%) of patients had more than 1 race reported. As shown in eTable 2 in the Supplement and Figure 1, the number of US office visits in which an SMR was either newly prescribed or continued doubled from 15.5 million (95% CI, 15.4-15.6 million) visits in 2005 to 30.7 million (95% CI, 30.6-30.8 million) visits in 2016. During this 12-year period, the number of office visits resulting in new SMR prescriptions remained relatively stable at approximately 6 million (95% CI, 6.0-6.3 million) per year, whereas office visits for continued SMR drug therapy tripled from 8.5 million (95% CI, 8.4-8.5 million) to 24.7 million (95% CI, 24.6-24.8 million).

Table 1. Demographic Distributiona of Patients in All SMR Office Visits, 2005-2016.

Variable Year
2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016
Sex
Female 61.9 (61.5-62.3) 58.1 (57.7-58.3) 61.2 (60.9-61.4) 65.4 (65.0-65.6) 67.3 (67.0-68.5) 62.9 (62.7-63.1) 65.7 (65.5-65.9) 61.0 (60.9-61.1) 59.0 (58.9-59.1) 65.2 (65.0-65.2) 57.5 (54.2-60.7) 58.2 (57.9-58.6)
Male 38.1 (37.7-38.6) 41.9 (41.6-42.3) 38.9 (38.6-39.1) 34.6 (34.3-34.9) 32.7 (32.4-32.9) 37.1 (36.8-37.3) 34.3 (34.0-35.5) 38.9 (38.9-39.1) 41.0 (40.9-41.1) 34.8 (34.7-35.0) 42.5 (42.0-43.0) 41.8 (41.4-42.1)
Age, y
<15 0.7 (0.4-1.1) 1.0 (0.6-1.4) 0.2 (0.00-0.4) 0.9 (0.7-1.1) 0.5 (0.3-0.8) 0.2 (0.1-0.2) 1.2 (09-1.3) 0.7 (0.1-1.5) 0.4 (0.3-0.5) 0.6 (0.6-0.7) 0.3 (0.2-0.4) 0.3 (0.1-0.5)
15-24 7.4 (7.0-7.8) 8.7 (8.4-9.1) 5.3 (5.0-5.6) 3.4 (3.1-3.7) 2.5 (2.3-2.7) 4.2 (3.9-4.5) 2.6 (2.3-2.8) 3.7 (3.6-3.8) 3.6 (3.5-3.7) 2.9 (2.2-3.1) 1.8 (1.4-2.2) 4.1 (3.7-4.4)
25-44 31.2 (30.8-31.7) 33.8 (33.4-34.0) 37.2 (36.8-37.4) 32.4 (32.1-32.7) 26.8 (26.6-27.0) 28.2 (27.9-29.3) 29.1 (28.9-29.3) 26.8 (26.7-26.9) 23.3 (23.1-23.3) 24.7 (24.6-24.8) 21.0 (20.6-21.3) 24.9 (24.6-25.2)
45-64 41.8 (40.9-42.0) 42.7 (42.2-43.0) 41.6 (41.3-41.8) 42.6 (42.3-42.9) 52.4 (52.2-52.7) 50.4 (50.2-50.7) 49.4 (49.1-49.6) 49.1 (49.0-49.2) 51.9 (51.8-52.0) 49.3 (48.6-49.5) 48.7 (48.3-49.0) 48.5 (48.2-48.9)
≥65 16.4 (15.9-16.8) 17.6 (16.2-17.9) 15.8 (15.4-16.0) 20.7 (20.4-21.0) 17.8 (17.5-18.3) 17.0 (16.8-17.3) 17.8 (17.6-17.9) 19.7 (19.6-19.7) 20.9 (20.7-21.0) 22.5 (22.4-22.6) 28.3 (27.8-28.7) 22.2 (21.8-22.6)
Race/ethnicity
White 87.8 (87.4-88.2) 84.3 (83.9-84.6) 57.7 (57.5-57.9) 56.2 (55.9-56.5) 69.4 (69.1-69.7) 66.3 (66.0-66.8) 65.3 (65.0-65.4) 56.7 (56.6-56.8) 58.6 (58.5-58.7) 64.7 (64.5-64.8) 60.4 (60.1-60.8) 53.7 (53.3-54.0)
African American 10.3 (9.9-10.7) 12.7 (12.3-13.0) 10.3 (9.9-10.6) 10.1 (9.8-10.4) 11.2 (10.9-11.5) 13.7 (13.4-13.9) 8.8 (8.4-9.0) 7.9 (7.8-8.0) 10.8 (10.6-10.9) 7.7 (7.6-7.8) 11.5 (11.2-11.7) 10.2 (9.7-10.6)
Asian 1.4 (1.1-1.7) 1.3 (0.9-1.5) 1.0 (0.7-1.3) 1.1 (0.9-1.2) 0.7 (0.5-0.8) 0.3 (0.2-0.4) 1.7 (1.0-2.0) 1.1 (1.1-1.3) 1.8 (1.2-2.0) 2.2 (2.2-2.7) 0.4 (2.8-6.1) 1.2 (1.0-1.5)
Native Hawaiian NR 0.9 (0.7-1.1) NR NR NR NR NR 0.2 (0.0-0.3) 0.8 (0.0-0.1) 1.3 (1.0-1.4) NR NR
Native American or Alaska Native NR 2.2 (0.5-1.3) 0.4 (0.1-0.5) NR 0.1 (0.0-0.2) 0.2 (0.1-0.2) 0.4 (0.2-0.5) 0.3 (0.2-0.4) 0.2 (0.1-0.2) 0.7 (0.6-0.8) 0.2 (0.1-0.3) 2.2 (2.0-2.5)
>1 Race/ethnicity reported NR 0.1 (0.0-0.1) NR 0.7 (0.0-0.1) 0.3 (0.0-0.4) NR NR 0.3 (0.2-0.4) 0.2 (0.1-0.3) 0.3 (0.2-0.3) NR 1.5 (1.3-1.8)

Abbreviations: NR, not reported; SMR, skeletal muscle relaxant.

a

Values are expressed as percentage (95% CI).

Figure 1. National SMR Utilization Stratified by New vs Continued Use, 2005-2016.

Figure 1.

SMR indicates skeletal muscle relaxant.

Adults older than 65 years accounted for 22.2% (95% CI, 21.9%-22.6%) of SMR visits in 2016, although this group accounted for just 14.5% of the US population.12 In 2016, the demographic characteristics of the other age groups were as follows: 0.3% (95% CI, 0.1%-0.5%) younger than 15 years, 4.1% (95% CI, 3.7%-4.4%) aged 15 to 24 years, 24.9% (95% CI, 24.6%-25.2%) aged 25 to 44 years, and 48.5% (95% CI, 48.2%-48.9%) aged 45 to 65 years. As shown in Figure 2, the proportion of visits that were SMR visits among patients 65 years and older increased 3-fold (from 1.3 SMR visits [95% CI, 1.0-1.7] per 100 office visits in 2005 to 4.3 SMR visits [95% CI, 4.1-4.6] per 100 office visits in 2016). The prescription of SMRs to older adults considered potentially inappropriate medications in this population (ie, carisoprodol, chlorzoxazone, cyclobenzaprine, metaxalone, methocarbamol, and orphenadrine) approximately doubled from 2.2 million (95% CI, 2.1-2.4 million) office visits in 2005 to 4.3 million (95% CI, 4.2-4.5 million) office visits in 2016.

Figure 2. National SMR Utilization Rates Among Adults Aged 65 Years or Older, Stratified by New vs Continued Use, 2005-2016.

Figure 2.

SMR indicates skeletal muscle relaxant.

The most common diagnoses between 2005 and 2015 reported for new SMR visits are shown in Table 2; the diagnosis coding system used for the NAMCS data shifted from the International Classification of Diseases, Ninth Revision, Clinical Modification to the International Classification of Diseases, Tenth Revision, Clinical Modification in 2016. The most common diagnoses during these visits were related to back pain and other musculoskeletal conditions; this pattern was maintained in 2016. As shown in Table 2, among new SMR visits, hydrocodone-acetaminophen was the most common concomitant therapy. Other analgesics, such as ibuprofen, naproxen, and tramadol, were also commonly used. As shown in eTable 3 in the Supplement, in 2016, 67.2% (95% CI, 62.0%-72.5%) of continuing SMR visits recorded concomitant therapy with an opioid, in contrast to 10.3% (95% CI, 9.8%-13.2%) of all ambulatory care visits nationally.

Table 2. Visit Diagnoses (2005-2015a) and Concomitant Medications (2005-2016) Among New SMR Visits.

Variable Office visits, No. (95% CI)
Diagnosis (ICD-9-CM code) (n = 78 671 742)b
Other and unspecified disorders of back (724.9) 26 496 352 (25 635 583-27 357 121)
Sprains and strains of other and unspecified parts of back (847.9) 10 148 115 (9 559 679-10 736 551)
Spinal stenosis in cervical region (723.0) 8 205 661 (7 448 293-8 963 029)
Other disorders of soft tissues (729.99) 6 512 583 (5 996 830.56-7 028 335)
Essential hypertension (401.1) 6 049 615 (5 708 365-6 390 866)
Intervertebral disc disorders (722.90) 6 030 779 (5 425 636-6 635 922)
Disorders of muscle, ligament, and fascia (728.79) 4 585 666 (4 254 719-4 916 613)
Anxiety state (300.0) 3 167 519 (2 303 704-4 031 334)
Other and unspecified disorders of joint (719.98) 2 989 405 (2 688 389-3 290 421)
Disorders of lipoid metabolism (272.9) 2 694 600 (2 362 481-3 026 719)
Concomitant medication (n = 84 850 041)c
Hydrocodone-acetaminophen 14 096 447 (13 380 518-14 812 376)
Ibuprofen 12 531 204 (12 004 039-13 058 369)
Naproxen 9 820 338 (9 321 411-10 319 265)
Tramadol 5 011 229 (4 680 556-5 341 902)
Lisinopril 4 208 202 (1 105 116-7 311 288)
Meloxicam 4 069 328 (3 556 643-4 582 013)
Aspirin 3 969 403 (3 649 823-4 288 983)
Omeprazole 3 927 795 (3 455 672-4 399 919)
Albuterol 3 781 380 (3 376 754-4 186 006)
Diclofenac 3 752 475 (3 545 994 -3 958 956)

Abbreviations: ICD-9-CM, International Classification of Diseases, Ninth Revision, Clinical Modification; SMR, skeletal muscle relaxant.

a

2016 excluded because of transition to International Classification of Diseases, Tenth Revision, Clinical Modification.

b

Among all new SMR office visits from 2005 to 2015.

c

Among all new SMR office visits from 2005 to 2016.

Table 3 shows the number of office visits and age-standardized rates of SMR visits for 2005 and 2016 stratified by geographic region and by new vs continued SMR. In the Northeast, age-standardized new SMR visit rates changed by −33.4% (95% CI, −31.7% to −36.4%), whereas continued SMR visit rates increased by 325.1% (95% CI, 320.2% to 342.4%). We observed a similar pattern in the South, with a −15.8% (95% CI, −15.2% to −17.0%) change in new SMR visits accompanied by a 79.1% (95% CI, 68.8% to 82.2%) increase in continued SMR visits. In the Midwest, new and continued SMR visit rates increased by 26.9% (95% CI, 22.1% to 28.9%) and 297.6% (95% CI, 273.8% to 307.5%), respectively. We observed similar but less marked increases in new and continued SMR visit rates in the West, with increases of 5.4% (95% CI, 3.8% to 5.6%) and 91.6% (95% CI, 87.4% to 93.2%), respectively.

Table 3. 12-Year Change in SMR Utilization by Geographic Region, 2005-2016.

Age group, ya No. of office visits Age-standardized rate per million populationb % Difference (95% CI)
2005 2016 2005 2016
New SMR visits
Northeast 806 072 604 326 14 884 9917
<18 59 485 NR 1142 NR −33.4 (−31.7 to −36.4)
18-24 142 000 NR 2866 NR
25-44 171 266 112 423 3156 2288
45-64 410 995 356 956 7326 5690
≥65 22 326 134 952 393 1938
Midwest 1 308 190 1 755 480 20 073 25 466
<18 56 558 NR 863 NR 26.9 (22.1 to 28.9)
18-24 122 191 111 327 1928 1667
25-44 310 611 625 067 4845 10 681
45-64 729 940 413 552 11 048 5642
≥65 88 890 605 534 1390 7476
South 3 100 314 2 433 079 22 997 19 362
<18 248 784 68 892 2314 610 –15.8 (−15.2 to −17.0)
18-24 448 217 315 016 4391 2688
25-44 984 557 201 379 9255 1872
45-64 949 278 1 159 135 9181 9270
≥65 469 478 688 656 4562 4922
West 1 160 469 1 385 413 17 773 18 728
<18 22 919 197 263.0 321 2752 5.4 (3.8 to 5.6)
18-24 71 311 153 745 1078 2042
25-44 373 064 396 164 5300 5603
45-64 537 379 612 761 8487 8020
≥65 155 796 25 480 2587 311
Overall US 6 375 045 6 178 298 22 017 18 855 –14.4 (−12.3 to −15.1)
Continued SMR visits
Northeast 1 324 873 5 763 559 23 768 101 030
<18 NR NR NR NR 325.1 (320.2 to 342.4)
18-24 4466 242 937 90 44 441
25-44 339 226 2 312 550 6252 168 064
45-64 682 694 2 191 924 12 169 141 183
≥65 298 487 1 016 148 5258 117 659
Midwest 1 662 278 7 086 853 25 627 101 891
<18 13 411 92 265 205 1461 297.6 (273.8 to 307.5)
18-24 5777 50 600 91 758
25-44 787 613 2 106 184 12 286 35 989
45-64 659 845 3 051 307 9987 41 626
≥65 195 632 1 786 498 3058 22 057
South 3 641 577 7 804 048 34 745 62 232
<18 NR NR NR NR 79.1 (68.8 to 82.2)
18-24 432 NR 4 NR
25-44 1 133 092 11 341 547 10 651 10 544
45-64 1 770 148 4 724 147 17 120 37 782
≥65 717 800 1 945 345 6974 13 905
West 1 822 159 4 086 159 28 189 54 004
<18 46 457 40 390 650 563 91.6 (87.4 to 93.2)
18-24 NR 64 101 NR 852
25-44 513 580 951 051 7296 13 451
45-64 879 499 2 424 176 13 891 31 756
≥65 382 623 606 442 6352 7411
Overall US 8 450 887 24 740 620 29 144 75 430 158.8 (143.2 to 164.0)

Abbreviations: NR, not reported; SMR, skeletal muscle relaxant.

a

Regions defined by the US Census Bureau.

b

2005 US population used as the reference group for age standardization.

Discussion

This analysis of nationally representative office visit data found that SMR use doubled from 2005 to 2016 and that there was a disproportionately high use of these drugs in older adults, a population in which SMR use is potentially inappropriate. These increasing rates did not appear to have an association with the decline in opioid prescribing that began in 2012 in both the general ambulatory care population and in the older adult population.13 Furthermore, among visits with a continuing SMR, 67.2% of patients were concomitantly treated with an opioid—a combination that has the potential to cause serious drug-drug interactions, such as potentiated central nervous system depression and an increased risk of opioid overdose.9 As expected, among new users of SMRs, we found that the most common diagnoses were related to back pain and other musculoskeletal conditions. Interestingly, although the frequency of new initiation of SMR therapy remained stable, the number of office visits in which SMR therapy was continued tripled, indicating a potential shift in duration of use of these drugs. This trend is a concern given the limited evidence of long-term efficacy and the risk of serious central nervous system adverse effects and drug-drug interactions.

Although prior papers have examined the use of SMRs in veterans4 and older adults,14,15 the present study is, to our knowledge, the first study since 20045,16 to examine SMR use in the general population. The strengths of this study stem from the design of the NAMCS that permits us to make projections to US physician office visits.

Limitations

This study has some limitations. The NAMCS does not capture patients leaving the hospital with an SMR prescription or allow researchers to follow patients over time or assess clinical outcomes. In addition, these data are limited to the United States, and we are unaware of recent analogous data from other countries.

Conclusions

Given their prominent adverse effects and the limited evidence for their long-term efficacy, growth in the continued use of SMRs, particularly in older adults and concomitantly with opioids, is concerning. Given the findings of this cross-sectional study, efforts to limit the long-term use of SMRs may be needed, especially for older adults, similar to efforts used to limit the long-term use of opioids17 and benzodiazepines.18

Supplement.

eTable 1. NAMCS Variable and Population of Analysis

eTable 2. Number of US Office Visits with a Skeletal Muscle Relaxant Prescription, 2005-2016

eTable 3. Office Visits With Newly Prescribed or Continued Opioid Therapy, 2016

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplement.

eTable 1. NAMCS Variable and Population of Analysis

eTable 2. Number of US Office Visits with a Skeletal Muscle Relaxant Prescription, 2005-2016

eTable 3. Office Visits With Newly Prescribed or Continued Opioid Therapy, 2016


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