First author, year, country | Design | Sample size | Age in years mean | Female% | Type of trauma or surgical procedure | Intervention (strategies) | Comparator | Outcomes | Results Mean or median, % (statistically significant results favoring intervention are in bold)a |
---|---|---|---|---|---|---|---|---|---|
Studies including trauma patients | |||||||||
 System-based | |||||||||
  Chambers 2021 USA [96] | Prospective cohort | 86 | 37 | 40% | Outpatient orthopaedic trauma surgery | Implementation of the Orthopaedic Trauma Association (OTA) pain management guidelines for acute musculoskeletal injuries | Before guidelines implementation | Cumulative MED | 6 weeks: I; 210.00; C: 225.00, 95% CI -85.00 - 20.00, p = 0.10 |
Proportion of patients who received opioid refill(s) | I: 2.00%; C: 2.00%, 95% CI -9.00 - 8.00, p = 1.00 | ||||||||
Proportion of patients using opioids (adherent vs non-adherent to guidelines for discharge prescription) | 6 weeks: Adherent: 17.00%; Non-adherent: 13.00% 95% CI − 22.00 - 13.00 p = 0.70 | ||||||||
  Chen 2020 USA [77] | Prospective cohort | 2,940 | 57 | 53% | Orthopaedic surgery including for traumatic fractures | A patient-specific protocol using an opioid taper calculator to standardize opioid prescribing at discharge after inpatient orthopaedic surgery | Before protocol implementation | MED | At discharge: I: 326.00; C: 427.00, p < 0.001 |
Refills mean | 1 month: I: 1.71; C: 1.58, p = 0.08 | ||||||||
  Reid 2020 USA [87] | Retrospective cohort | 753 | 57 | 56% | Orthopaedic trauma | State of Rhode Island legislation on strict opioid prescription limits. These limits prohibited providers from prescribing more than 30 MED per day, 150 total MED, or 20 total doses initially following a surgical procedure. | Idem as Reid 2019 | Cumulative MED | 1 month: I: 481.70; C: 677.40, p < 0.001 Opioid-tolerant: I: 880.00; C: 1,659.20, p = 0.04 Opioid-naïve: I: 478.10; C: 633.70, p < 0.001 30-90 days: I: 265.10; C: 256.70, p = 0.83 Opioid-tolerant: I: 923.80; C: 1,691.10, p = 0.10 Opioid-naïve: I: 241.10; C: 206.90, p = 0.90 |
  Wyles 2020 USA [97] | Retrospective | 4,523 | 63 | 51% | Orthopaedic and spine surgery including for traumatic fractures | Implementation of procedure-specific guidelines for discharge opioid prescriptions | Before guidelines implementation | MED | AT discharge: I: 375.00; C: 600.00 p < 0.001 |
Proportion of patients who received opioid refill(s) | 1 month: I: 24.00%; C: 25.00% p = 0.43 | ||||||||
  Choo 2019 USA [79] | Retrospective cohort | 830 | 63 | 48% | Orthopaedic surgery including for traumatic fractures | A quality improvement project using report sent to health professionals every two months, which showed median discharge MED per patient and reinforcement on multimodal pain management strategies | Before quality improvement project implementation | MED | At discharge: I: 450.00; C: 600.00, p < 0.001 |
Proportion of patients who received opioid refill(s) | Between discharge to 1 month: I: 24.00%; C: 25.70%, p = 0.58 Between 1 to 2 months: I: 14.90%; C: 14.20%, p = 0.77 Between 2 to 3 months: I: 7.80%; C: 6.50%, p = 0.58 | ||||||||
  Reid 2019 USA [86] | Retrospective cohort | 1,776 | 55 | 55% | Orthopaedic surgery including for traumatic fractures | Idem as Reid 2019 | Before legislation implementation | Cumulative MED | 1 month: I: 524.50; C: 790.00, p < 0.001 Opioid-Tolerant: I: 1,015.20; C: 1,304.10, p = 0.001 Opioid-Naïve: I: 446.57; C: 708.84, p < 0.001 Between 1 to 3 months: I: 208.50; C: 243.50, p = 0.007 Opioid-Tolerant: I: 804.60; C: 892.60, p = 0.08 Opioid-Naïve: I: 113.70; C: 141.00, p = 0.02 |
Proportion of patients using opioids | At 30 days: I: 24.00%; C: 28.00%, p = 0.03 | ||||||||
  Young 2019 USA [93] | Retrospective cohort | 218 | 75 | 72% | Minor non-surgical trauma | After Ohio's opioid prescription limit (opioids for 7 days and a total of 210 MEDs) | Before opioid prescription limit | Cumulative MED | 1 month: I: 105.00; C: 375.00, p = 0.02 |
  Earp 2018 USA [80] | Retrospective cohort | 518 | 54 | 61% | Hand and upper-extremity surgeries including for traumatic fractures | Postoperative opioid-limit prescribing protocol | Before protocol implementation | MED | At discharge Tierb 1: I: 39.20; C: 113.60, p < 0.001 Tier 2: I: 61.40; C: 171.10, p < 0.001 Tier 3: I: 131.20; C: 229.60, p < 0.001 Tier 4: I: 208.10; C: 264.80, p < 0.02 Tier 5: I: 246.90; C: 369.90, p < 0.003 MED decreased by a minimum of 97.80% and a maximum of 176.00% (p < 0.05 for all tiers) |
Proportion of patients who received opioid refill | 1 refill: I: 1.70%; C: 6.50%, p < 0.001 2 refills: I: 0.00%; C: 1.70%, p < 0.001 | ||||||||
 Pharmacological | |||||||||
  Cunningham 2021 USA [98] | Retrospective cohort | 230 | 64 | 65% | Distal femur fracture surgery | Regional anesthesia | Without regional anesthesia | Cumulative MED | 6 weeks: I: 95.10; C:74.90 Incident rate ratio : 1.27, 95% CI 1.01-1.59, p = 0.03 3 months: I: 112.10; C:85.00 Incident rate ratio : 1.33, 95% CI (1.07, 1.66), p = 0.01 Between 6 weeks to 3 months: I : OR 1.85 95% IC (1.14, 3.04) p = 0.014 |
  Cunningham 2021 USA [99] | Retrospective | 230 | 41 | 35% | Pelvis and acetabulum fracture surgery | Regional anesthesia | Without regional anesthesia | Cumulative MED | 6 weeks: I: 177.20; C:145.20 Incident rate ratio : 1.22, 95% CI 0.99-1.51, p = 0.06 3-months: I: 207.90; C:156.80 Incident rate ratio 1.33, 95% CI 1.06-1.65, p = 0.01 |
Opioid fill | Between 6 weeks to 3 months: IÂ : OR 2.05, 95% CI 1.24- 3.46, p = 0.006 | ||||||||
  Bhashyam 2018 USA [63] | Prospective cohort | 500 | 50 | 50% | Orthopaedic trauma | Recreational use or self-medication with marijuana I1: Prior user I2: Use during recovery | Never use marijuana | Total prescribed MED | 6 months: Marijuana used during recovery compared to never users (mean difference = 343.00, p = 0.03) |
Duration of opioid use (days) | Marijuana used during recovery compared to never users (mean difference = 12.50, p = 0.03) | ||||||||
Proportion of patients using opioids (%) | Persistent Use for > 3 months : I1: 25.90%; I2: 21.70%; C: 17.60%, no significance test | ||||||||
  Radi 2017 USA [94] | Retrospective cohort | 216 | NS | 37% | Orthopaedic trauma | Peri-operative regional nerve block (single shot) | No block | Proportion of patients using opioids | 3 months: I: 44.20%; C: 34.80%, p = 0.22 6 months: I: 7.70%; C: 14.60%, p = 0.19 |
  Yazdani 2016 Iran [75] | Randomized controlled trial | 60 | 32 | 17% | Trauma: ORIF of a recent mandibular unilateral body fracture | A 100 mg dose of Amantadine one hour before surgery | Placebo capsule | Cumulative MED | 6 months: I: 121.70; C: 106.00, p = 0.61 |
  Gray 2011 Australia [66] | Randomized controlled trial | 90 | 36 | 17% | Burn injury | Pregabalin (75 mg to 300 mg titration according to pain level) twice daily for 28 days and weaned and ceased over the next 6 days. | Placebo capsules | Morphine Parenteral Equivalent/ day | 1 month: I: 14.92; C: 14.92, p = 0.09 |
 Educational | |||||||||
  Bérubé 2021 Canada [100] | Randomized controlled trial | 49 | 41 | 25% | Traumatic injury requiring hospital- ization. Patients receiving > 2 doses/ day of opioid at discharge and with at least one risk factor for chronic opioid use | TOPP-Trauma programme + UC. This educational program (2 x 10 min session prior discharge and max 6 x 15 min opioid tapering counselling session every 2 weeks after discharge) focused on multimodal pain management strategies and guidance about opioid tapering | UC + an educational pamphlet received before discharge | Reported MED/day | 6 weeks: I: 1.20; C: 12.20, 95% CI –22.00-0.10 3 months : I: 0.40; C: 4.10, 95% CI – 8.30-0.70 |
Total MED delivered | 6 weeks: I: 618.19; C: 1,009.00, 95% CI –1,324.00-542.10 3 months : I: 679.00; C: 1,443.40, 95% CI – 1,781.60-248.60 | ||||||||
Proportion of patients using opioids (%) | 6 weeks: I: 17.00%; C: 29.00%, p > 0.05 3 months: I: 12.00%; C: 16.00%, p > 0.05 | ||||||||
  Syed 2018 USA [53] | Randomized controlled trial | 134 | 59 | 32% | Arthroscopic rotator cuff repair | Formal education detailing recommended postoperative opioid usage, side effects, dependence, and addiction | Preoperative education regarding surgery | Cumulative MED | 6 weeks: I: 40.40; C: 60.60, p = 0.02 3 months: I: 51.20; C: 87.20, p = 0.01 |
Opioids discontinua-tion | Between 6 weeks to 3 months: OR: 2.19, 95% CI 1.10-4.39, p = 0.03 | ||||||||
  Stanek 2015 USA [52] | Retrospective cohort | NS | NS | NS | Hand surgery including for traumatic fractures | Implementation of an educational assist device to serve as a memory prompt of narcotic guidelines | Before implementation of the educational assist device | Reduction in opioid prescription (%) | 3 months: Repair of a metacarpal fracture: 20.00% reduction, p = 0.04 |
  Holman 2014 USA [5] | Retrospective cohort | 613 | 43 | 38% | Orthopaedic trauma | A standardized discussion with patients aiming to inform them that they would receive opioids for a maximum of 6 weeks postoperatively | No standardized discussion but limited postoperative opioids prescriptions to 12 weeks | Proportion of patients using opioids | 6 weeks: I: 27.00%; C: 36.00%, p = 0.01 3 months: I: 20.00%; C: 20.00%, p = 0.90 |
 Multimodal | |||||||||
  Singer 2021 USA [101] | Retrospective cohort | 620 | 49 | 32% | Hospitalized trauma patients | Multimodal analgesia protocol and corresponding electronic medical record order set (including opioids, NSAID and gabapentin who were adjusted for age and medical condition) | Before implementation of multimodal protocol. | Cumulative outpatient MED | 6 months: I: 210.00; C: 263.00, p = 0.03 |
Proportion of patients using opioids chronically (opioid prescription at 6 mo) | I: 3.20%; C:3.10%, p = 0.62 | ||||||||
 Alternatives | |||||||||
  Crawford 2019 USA [55] | Randomized controlled trial | 233 | 45 | 39% | Lower extremity surgery including for traumatic injuries (military population) | Standard care and modified battlefield acupuncture with semi-permanent needles | C1: standard care + small adhesive bandages on the ear C2: standard care + placebo auricular acupuncture with semi-permanent needles | Cumulative MED | 1 month: I: 257.00; C1: 358.00; C2: 266.00, p = 0.22 |
 Psychological | |||||||||
Studies including non-trauma surgical patients: orthopeadic and spine | |||||||||
 System-based | |||||||||
  Chalmers 2021 USA [102] | Retrospective cohort | 19428 | 63 | 53% | THA or TKA | Modification of routine discharge MED (C = 750 MED, I1 = 520 MED, I2 = 320 MED) | Before routine discharge reduction (C) | Cumulative MED (mean) | 3 months Total population: I1: 798.00; I2: 556.00; C: 1,009.00, p < 0.001 |
Postoperative refill in MED (mean) | Total population: I1: 859.00; I2: 682.00; C: 1,017.00, p < 0.001 | ||||||||
Proportion of patients who received opioid refill(s) | Total population: I1: 33.00%; I2: 33.00%; C: 28.00%, p < 0.001 | ||||||||
  Cunningham 2021 USA [103] | Retrospective cohort | 4,592 | 61 | 57% | ACDF, ACLR, CTR, RCR, TAA, THA, TKA, trapeziec-tomy with suspension-plasty | North Carolina legislation. The STOP Act requires to review a patient’s 12-month history before issuing an initial prescription for an opioid and instituting a 5-day limit on initial prescriptions for acute pain and a 7-day limit on postoperative prescriptions + institutional educational materials for practitioners and patients about responsible opioid prescribing, opioid use, and North Carolina law (I1: immediately after implementation; I2: 1 year after implementation) | Before implementation of the STOP Act legislation and departmental policies (C) | Total MED prescribed | 6 weeks: I1:126.15; I2: 120.30; C: 184.95, p < 0.001 |
Proportion of patients who received more than one prescription | I1: 30.50%; I2: 31.70%; C: 37.20%, p < 0.001 | ||||||||
  Raji 2021 USA [104] | Retrospective case-control | 334 | 69 | 65% | Different types of shoulder arthroplasty | After Ohio legislation which limit opioid prescriptions to no more than 7 days at a time for adults, with a maximum allotted dose per day of 30 morphine milligram equivalents | Before implementation of Ohio legislation | Total MED | 1 month: Total: I: 300.00; C: 570.00, p < 0.001 Opioid tolerant: I: 740.00; C: 825.00, p = 0.551 Oioid naïve: I: 210.00; C: 450.00, p < 0.001 Between 1 to 2 months: Total: I: 0.00; C: 0.00, p = 0.88 Opioid tolerant: I: 360.00; C: 300.00, p = 0.449 Oioid naïve: I: 0.00; C: 0.00, p = 0.779 Between 2 to 3 months: Total: I: 0.00; C: 0.00, p = 0.47 Opioid tolerant: I: 405.00; C: 300.00, p = 0.506 Oioid naïve: I: 0.00; C: 0.00, p = 0.853 Between discharge to 3 months: Total: I: 450.00; C: 600.00, p < 0.001 Opioid tolerant: I: 1,680.00; C: 1,455.00, p = 0.802 Oioid naïve: I: 210.00; C: 487.50, p < 0.001 |
  Sabesan 2021 USA [105] | Retrospective cohort | 143 | 73 | 56% | Primary reverse shoulder arthroplasty | After Florida House bill 21 law (restriction of 3 to 7-days supply of opiates for acute pain) | Before House Bill 21 law. | Cumulative MED | 3 months: I: 461.90; 1750.7, p = 0.035 |
Proportion of patients who received opioid refill(s) | I: 17.80%; C: 70.1%, p < 0.001 | ||||||||
Proportion of patients using opioids chronically (for 3 or more months of continuous usage) | I: 12.50%; C: 23.00%, p < 0.043 | ||||||||
  Eley 2020 USA [81] | Retrospective cohort | 246 | 59 | 38% | Spine surgery | Implementation of an opioid prescription-limit protocol | Before protocol implementation | MED | At discharge: I: 120.60; C: 286.90, p < 0.001 |
Proportion of patients who received opioid refill | 3 months: I: 17.10%; C: 16.50%, p = 0.98 | ||||||||
Proportion of patients transitioning to chronic opioid use | I: 2.40%; C: 4.60%, p = 0.70 | ||||||||
  Joo 2020 USA [83] | Retrospective cohort | 83 | 67 | 1% | Spine surgery | An individualized discharge opioid prescribing and tapering protocol | Before protocol implementation | Cumulative MED (median) Proportion of patients who received opioid refill(s) | 6 months: I:300.00; C:900.00, p < 0.01 I: 36.80%; C: 40.00%, p = 0.77 |
  Tamboli 2020 USA [89] | Retrospective cohort | 49 | 68 | 8% | THA | Multidisciplinary patient-specific opioid prescribing and tapering protocol | Before protocol implementation | Cumulative MED (median) | 6 weeks: I: 295.00; C: 900.00 MD: 721, 95% CI 127.00-1,316.00, p = 0.007 |
Proportion of patients who received opioid refill | I: 54.00%; C: 48.00%, p = 0.67 > 1 refill: I: 54.00%; C: 67.00%, p = 0.69 | ||||||||
  Whale 2020 USA [91] | Retrospective cohort | 1,994 | 68 | 62% | THA or TKA | After Ohio Opioid Prescribing Guidelines | Before implementation of prescribing guidelines | Cumulative MED | Total (acute and chronic follow-ups): TKA cohort: All: I: 1,145.80; C: 1,602.60, p < 0.01 THA cohort: All: I: 878.30; C: 1,302.30, p < 0.01 Between discharge to < 3 months (acute) TKA cohort: I: 390.70; C: 519.70, p = 0.02 THA cohort: I: 178.60; C: 232.10, p = 0.27 ≥ 3 month (chronic) TKA cohort: All: I: 148.80; C: 178.10, p = 0.48 THA cohort: All: I: 69.00; C: 121.80, p = 0 .12 |
Proportion of patients who received opioid refill(s) | Acute: TKA: I: 47.20%; C: 41.50%, p = 0.50 THA: I: 25.70%; C: 18.30%, p = 0.01 Chronic: TKA: I: 12.00%; C: 12.70%, p = 0.72 THA: I: 9.50%; C: 10.00%, p = 0.83 | ||||||||
  Chen 2019 USA [78] | Retrospective cohort | 60,056 | 65 | 7% | TKA (veteran population) | Opioid safety initiative that combined education, guideline dissemination with audit and feedback using dashboards | Before opioid safety initiative implementation | Proportion of patients using opioids chronically (for greater than 3 months in a 6-month period) | 6 months: Post-operative chronic user: I: 14.10%; C: 26.90%, p < 0.001 |
  Holte 2019 USA [82] | Retrospective cohort | 399 | 61 | 52% | TKA and THA | Implementation of strict postoperative opioid prescription guidelines and mandatory preoperative patient education session led by nursing staff regarding postoperative pain management with an emphasis on opioid use | Before implementation of guidelines | MED | At discharge: I: 387.30; C: 751.50 p < 0.0001 |
Total postoperative refill in MED | 3 months: I: 84.00; C: 253.00, p = 0.004 | ||||||||
Number of refills (mean) | I: 0.30; C: 0.50, p = 0.02 | ||||||||
Number of call-ins pertaining to pain management (mean) | I: 0.40; C: 0.70, p = 0.03 | ||||||||
  Reid 2019 USA [88] | Retrospective cohort | 1,125 | 67 | 62% | THA or TKA | State of Rhode Island legislation on strict opioid prescription limits. These limits prohibited providers from prescribing more than 30 MED per day, 150 total MED, or 20 total doses initially following a surgical procedure. | Before legislation implementation | Cumulative MED | 1 month: I: 632.00; C: 907.00, p < 0.001 Opioid-Tolerant: I: 1,288.00; C: 1,398.00, p = 0.06 Opioid-Naïve: I: 501.00; C: 796.00, p < 0.001 1to 3 months: I: 270.00; C: 279.00, p = 0.19 Opioid-Tolerant: I: 1,119.00; C: 898.00, p = 0.96 Opioid-Naïve: I: 100.00; C: 139.00, p = 0.17 |
Number of refills | 1 month: I: 2.20; C:1.90, p < 0.001 Opioid-Tolerant: I: 3.0; C: 2.50, p = 0.03 Opioid-Naïve: I: 2.10; C: 1.80, p < 0.001 | ||||||||
  Reid 2019 USA [85] | Retrospective cohort | 211 | 52 | 54% | Spine Surgery | Idem | Idem | Number of prescriptions (n) | 1 month: I: 1.70; C:1.60, p = 0.42 |
Cumulative MED | 1 month: I: 444.10; C: 877.90, p < 0.001 Opioid-Tolerant: I: 632.20; C: 1,122.90, p < 0.001 Opioid-Naïve: I: 363.40; C: 730.10, p < 0.001 Between 1 to 2 months: I: 129.50; C: 181.00, p = 0.25 Opioid-Tolerant: I: 407.90; C: 546.20, p = 0.23 Opioid-Naïve: I: 150.30; C: 207.00, p = 0.13 61 to 90 days: I: 91.90; C: 153.60, p = 0.19 Opioid-Tolerant: I: 226.70; C: 272.20, p = 0.82 Opioid-Naïve: I: 87.90; C: 126.10, p = 0.30 91 to 120 days: I: 131.20; C: 136.80, p = 0.08 Opioid-Tolerant: I: 181.20; C: 274.00, p = 0.21 Opioid-Naïve: I: 53.70; C: 81.00, p = 0.07 | ||||||||
  Vaz 2019 USA [90] | Prospective cohort | 196 | 68 | 58% | THA or TKA | Standardized opioid prescription protocol: maximum of 30 pills (370 MED) for THA and 40 pills (490 MED) for TKA | Postoperative analgesic prescription at provider’s discretion | Cumulative MED | 1 month: TKA cohort: I: 200.00; C: 504.00, p < 0.001 THA cohort: I: 432.00; C: 902.00, p < 0.001 |
Proportion of patients who received opioid refill(s) | TKA cohort: I: 50.00%; C: 29.00%, p = 0.04 THA Cohort: I: 16.00%; C: 8.00%, p = 0.2 | ||||||||
  Wyles 2019 USA [92] | Retrospective cohort | 2573 | 67 | 53% | TKA or THA | Clinicians were recommended to prescribe a maximum MED for an opioid prescription based on the procedure level: Level 1 = 100 MED, Level 2 = 200 MED, Level 3 = 300 MED, and Level 4= 400 MED | Prescriptions without guidelines | Cumulative MED (median) | 1 month (median): TKA cohort: I: 388.00; C: 750.00, p < 0.001 THA cohort: I: 388.00; C: 750.00, p < 0.001 |
Proportion of patients who received opioid refill(s) | TKA cohort: I: 35.00%; C: 35.00%, p = 0.77 THA cohort: I: 17.00%; C: 16.00%, p = 0.55 | ||||||||
 Pharmacological | |||||||||
  Burns 2021 USA [106] | Randomized controlled trial | 157 | 61 | 52% | Scheduled shoulder arthroplasty (group 1) or ARCR (group 2) | Celecoxib 200 mg twice daily for 3 weeks | Placebo medication | Difference in MED between I and C group (ß) | 6 weeks: Total population: –198.80 p = 0.01 Group 1 –270.00 p = 0.04 Group 2: –94.50 p = 0.31 |
  Zhuang 2020 China [76] | Randomized controlled trial | 246 | 68 | 80% | TKA | Supplied sequential treatment with intravenous parecoxib 40 mg (every 12 hours) for the first 3 days after surgery, followed by oral celecoxib 200 mg (every 12 hours) for up to 6 weeks | Placebo medication | Cumulative MED (median) | 1 month: I: 53.33; C: 166.50 Median difference: 112.02, 95% CI 43.12-150.92, p < 0.001 6 months: I: 58.00; C: 180.35 Median difference: 120.92, 95% CI 57.34-181.81, p < 0.001 |
  Starr 2019 USA [72] | Randomized controlled trial | 11,614 | 66 | 6% | TKA (veteran population) | β-blocker within 90 days prior to surgery, β-blocker as an inpatient on postoperative day 0 or 1, and refill prescription for a β-blocker within 90 days after surgery | No β-blocker | Cumulative MED | 1 month: I: 86.10; C: 90.40, p = 0.004 |
Proportion of patients using opioids | 1 month: OR 0.89, 95% CI 0.80-0.99, p = 0.02 3 months: OR 1.00, 95% CI 0.87-1.15, p = 0.965 12 months: OR 1.04, 95% CI 0.90-1.20, p = 0.54 | ||||||||
  Fenten 2018 Netherlands [65] | Randomized controlled trial | 153 | 65 | 54% | TKA | LIA of the posterior capsule and a FNB catheter | Periarticular LIA with ropivacaine 0.2% for postoperative analgesia | Proportion of patients using opioids | 3 months: I: 7.90%; C: 13.00% No significance test 12 months: I: 5.40%; C: 2.60% No significance test |
  Hah 2018 USA [67] | Randomized controlled trial | 410 | 57 | 58% | Surgeries: orthopeadic (80% of patients), thoracotomy, and breast | Four capsules of gabapentin, 300mg preoperatively and two capsules of gabapentin, 300 mg, 3 times a day postoperatively (10 total doses) | Placebo capsules | Proportion of patients using opioids | 6 months: I: 2.40%; C: 2.00% OR 1.22, 95% CI 0.32-4.66, p = 0.80 12 months: I: 1.90%; C: 1.50% OR 1.28, 95% CI 0.28-5.87, p = 0.70 |
  Thompson 2018 USA [74] | Retrospective cohort | 44 | 70 | 68% | TEA | Liposomal bupivacaine mixture through indwelling interscalene catheter | Indwelling interscalene catheter | Cumulative MED | 3 months: I: 1,198.60; C: 1,762.50, p = 0.19 |
  Sun 2017 USA [73] | Retrospective cohort | 120,080 | 57 | 61% | TKA | Nerve Block | No nerve block | Proportion of patients using opioids chronically (having filled 10 or more prescriptions or >120 days’ supply within the first year of surgery, excluding the first 90 postoperative days) | 12 months: Opioid naïve: I: 1.78%; C: 1.81%, p = 0.744 Adjusted for patient demographics, comorbidities, and preoperative medication use (ARR): 0.98, 98.3% CI 0.847-1.14, p = 0.79 Chronic user: I: 67.60%; C: 67.80%, p = 0.761 Intermittent user: I: 6.08%; C: 6.15%, p = 0.787 |
  Hyer 2015 USA [69] | Randomized controlled trial | 70 | 53 | 48% | Spinal surgery | Duloxetine once a day 2 weeks before and more then 3 months after surgery | Placebo capsule | Opioid use | 1 month: p > 0.05 |
  Aguirre 2012 Switzerland [62] | Randomized controlled trial | 72 | 58 | 51% | Minimally invasive hip surgery | 20 mL ropivacaine 0.3% applied into the wound as a bolus before wound closure followed with a continuous infusion of ropivacaine 0.3% at 8 mL/h for 48 hours after surgery | NaCl 0.9% placebo | Opioid use | 3 months: p > 0.05 |
  Nader 2012 USA [70] | Randomized controlled trial | 62 | 65 | 70% | TKA | Continuous femoral analgesia for 24 hours | Oral opioid analgesia | Median daily MED | 1 month: I: 10.00 mg; C: 18.00 mg, p = 0.12 6 months: I: 0.00; C: 0.00, p = 0.63 |
  Chevet 2011 France [64] | Prospective cohort | 107 | 72 | 72% | TKA | An intravenous dose of 15 mg/kg of ATX between induction and incision, renewed at the end of surgery | No ATX | Proportion of patients using mild opioids | 6 months: I: 20.00%; C: 33.00%, p = 0.18 |
  Schroer 2011 USA [71] | Randomized controlled trial | 107 | 67 | 58% | TKA | Celecoxib 200 mg to twice daily for 6 weeks after discharge | Placebo capsules | Number of opioid pills used (dosage NS) | 12 months: I: 76.30; C: 138.00, p = 0.003 |
 Educational | |||||||||
  Cheesman 2020 USA [107] | Randomized controlled trial | 140 | 58 | 32% | ARCR | Formal opioid education (recommended postoperative opioid use, side effects, dependence, and addiction) + a 2-minute computer-based presentation concerning opioid abuse and its consequences + a paper outline on the most important points of the presentation | Standard preoperative education followed by a discussion of risks and benefits. No formal education on opioid use, dependence, and addiction. | Total MED | 24 months : Total population: I: 375.00; C:725.00 p = 0.27 Opioid-naïve patients: I: 375.00; C: 535.00 p = 0.42 Prior opioid use: I: 1,612.00; C:2,475.00 p = 0.57 |
Proportion of opioid dependence (6 opioid prescriptions from the date of surgery) | Total population: I: 11.40%; C: 25.70% p = 0.5 Opioid-naïve patients: I: 3.70%; C: 16.70% p = 0.04 Prior opioid use: I: 37.50%; C: 47.60% p = 0.78 | ||||||||
No of prescriptions filled | Total population: I: 2.90; C: 6.30 p = 0.03 Opioid-naïve patients: I: 1.20; C: 3.40 p = 0.6 Prior opioid use: I: 8.90; C: 13.20 p = 0.56 | ||||||||
  Campbell 2019 USA [50] | Randomized controlled trial | 159 | 60 | 45% | THA or TKA | Traditional perioperative education + automated text messages included recovery instructions paired with encouraging and empathetic statements, personalized video messages from their surgeon, and short instructional videos | Traditional perioperative education, which included a preoperative clinic appointment and perioperative instructions | Time to opioids cessation (days) | 6 weeks: I: 22.50; C: 32.40 Mean difference: -10.0, 95% CI -14.2-(-5.7), p < 0.001 |
  Smith 2018 USA [51] | Randomized controlled trial | 561 | 66 | 60% | TKA or THA | Usual care + pharmacist intervention Usual care: an educational session that advised patients on the risks and benefits of surgery, pain control measures and exercise recommendations. Pharmacist intervention: mailed brochures describing what patients should expect regarding opioid use and pain control after and follow-up telephone call from a pharmacist. | Usual Care (handouts and a class in preparation for surgery that advised patients on the risks and benefits of surgery, pain control measures, exercise recommenda-tions, and the need for postsurgical assistance) | Total dispensing of opioid medications | 3 months: Adjusted mean difference for patients sociodemographics and probability of long-term opioid use: 0.92 95% CI 0.69-1.21 No readmission for pain control during the study period. |
 Multimodal | |||||||||
  Urban 2021 USA [108] | Retrospective cohort | 267 | 67 | 63% | TKA | Preoperative cryoneurolysis (1 min 45 sec cycle in the infrapatellar branches of the saphenous nerve near the knee and branches of the femoral cutaneous nerves in the mid-to-distal anterior thigh + standard multimodal regiment. | Standard multimodal regiment (preoperative protocol + postoperative : oral acetaminophen 500 mg every 6 hours, oral meloxicam 7.5mg twice daily, oral tramadol 50 mg every 6 hours as needed for pain, oral oxycodone 5 mg every 3 hours as needed) | Cumulative MED | 6 weeks: Mean: I: 894; C: 1,406.00 Ratio estimate : 0.64 95% CI 0.57-0.71, p < 0.001 |
Proportion of patients who received ≥1 prescription at 6 weeks | I: 12.00%; C: 20.00% Ratio estimate : 0.61 95% CI 0.29-1.28, p < 0.19 | ||||||||
  Buys 2020 USA [109] | Retrospective cohorte | 336 | 65 | 10 % | RCR, THA, TKA, TSA (veteran population) | Implementation of a Transitional Pain Service. Multidisciplinary providers work together to deliver comprehensive pain management for any surgical patient at risk for CPSP and COU in preoperative, surgical hospitalization and postoperative period up to 6 months. | Before Transitional Pain Service implementation | Proportion of patients still using opioids | 3 months: Patients with history of COU I: 33.40%; C: 23.30% p = 0.002 Opioid-naïve patients I: 0.70%; C: 8.40% p = 0.004 |
  Li 2020 USA [110] | Prospective cohort | 143 | 66 | 45% | TKA | Multimodal pain management + opioid PRN | Opioid-only analgesia | Cumulative MED | 1 month: Mean: I: 386.40; C: 582.50 p = 0.0006 |
Proportion of patients who required a refill | I: 51.40%; C; 74.60% p = 0.004 | ||||||||
  Fleischman 2019 USA [57] | Randomized controlled trial | 235 | 63 | 46% | THA | I1: Multimodal analgesic regiment (acetaminophen 1000 mg tid x 4w + Gabapentin 200 mg bid x 4 w + Meloxicam 15 mg die x 2w + Omeprazole 20 mg die x 2 w) + narcotic for emergency pain relief only I2: Multimodal analgesic regiment + narcotic as needed | No standing dose regimen (acetaminophen 500 mg QID PRN x 4w + Oxycodone q. 4h PRN + tramadol 50 mg q 6 hours PRN) | Cumulative MED | 1 month: I1: mean difference: -0.77, p < 0.001); I2: -0.30, p = 0.04 compared to C I1: mean difference: -0.46, p = 0.002 compared to I2. |
Proportion of patients who received opioid refill (%) | 3 months: I1: 10.50%; I2: 6.50%; C: 15.60%, No significance test | ||||||||
Proportion of patients using opioids | I1: 0.00%; I2: 1.30%; C: 2.60%, No significance test | ||||||||
  Hannon 2019 USA [68] | Randomized controlled trial | 304 | 65 | 54% | THA or TKA | Prescriptions of acetaminophen, meloxicam, gabapentin, tramadol, and 30 pills of 5 mg OxyIR (oxycodone) as a second breakthrough pain medication | Idem as experimental group and 90 pills of 5 mg OxyIR (oxycodone) | Cumulative MED | 1 month : I: 456.70; C: 455.60, p = 0.980 3 months: I: 777.10; C: 1089.70, p < 0.001 |
Proportion of patients who received opioid OxyIR refill(s) (%) | 3 months: I: 26.70%; C: 10.50%, p < 0.001 | ||||||||
  Padilla 2019 USA [84] | Retrospective cohort | 669 | 65 | 58% | THA | Opioid sparing pain management protocol (intravenous acetaminophen, periarticular injection of liposomal bupivacaine, pre-emptive analgesia in postoperative period) | Before implementation of the opioid sparing protocol | Cumulative MED | 3 months: I: 13.90; C: 80.10, p < 0.001 |
  Tan 2018 Australia [58] | Prospective cohort | 230 | 64 | 66% | THA | ERAS program (multimodal analgesia, early mobilization with physiotherapy) | Before ERAS implementation | MED/day | 6 weeks: I: 0.00; C: 0.00, p > 0.99 |
Proportion of patients using opioids (%) | The proportion of patients with zero MED consumption at week 6 increased from 56.60% to 80.00% (RR 1.34, 95% CI 1.13-1.58). | ||||||||
  Dasa 2016 USA [56] | Retrospective cohort | 100 | 38 | 70% | TKA | Administering perioperative cryoneurolysis and multimodal analgesics regimen | Multimodal analgesics regimen alone. | Cumulative MED | 3 months: I: 2,069.12; C: 3,764.42, p < 0.0001 |
 Surgical | |||||||||
  Bovonratwet 2021 USA [111] | Retrospective cohort | 611 | 63 | 81% | THA | Direct anterior approach | Posterior approach | MED | No data available on the amount of prescribed or consumed opioids |
Proportion of patients who required a refill | 3 months: I: 14.77%; C: 20.73: p = 0.077 I relative to C: relative risk = 0.95, 95% CI 0.55-1.64, p = 0.864 | ||||||||
  Varady 2021 USA [112] | Retrospective cohort | 92, 506 | 57 | 52% | TJA | Outpatient (no overnight stay) | Inpatient | Proportion of new opioid persistent use (patient still filling opioid prescriptions >90 days postop) | 3 months: I: 8.20; C: 10.60 p < 0.001 OR, 1.21; 95% CI 1.11-1.32; p < 0.001 |
  Walega 2019 USA [61] | Randomized controlled trial | 68 | 66 | 60% | TKA | Genicular nerve radiofrequency aoublation | Sham procedure: simulated GN-RFA using identical supplies and devices | MED/day | 6 months: I: 0.00; C: 0.00, p = 0.58 |
  Verla 2018 USA [60] | Retrospective cohort | 46 | 58 | 54% | Spine surgery | Transforaminal lumbar interbody fusions | Direct lateral lumbar interbody fusions | Postoperative opioids duration in months | All level: I: 5.20; C: 4.80, p = 0.82 L4-L5 only: I: 4.30; C: 3.14, p = 0.5 |
  Della Valle 2010 USA [59] | Randomized controlled trial | 72 | 63 | 68% | THA | Mini-incision approach | 2 incisions approach | MED/day | 6 weeks: I: 1.30; C: 1.40, p = 0.79 |
 Alternative | |||||||||
  Collinsworth 2019 USA [54] | Randomized controlled trial | 40 | 20 | 22% | Shoulder surgery (military population) | Usual care and BFA (semipermanent acupuncture needles emplaced on the subjects’ ears for 3–5 days within 24 hours after shoulder surgery. BFA was reapplied, as needed, up to 6 weeks post-surgically) | Usual postsurgical care (include surgery specific protocols, therapeutic modalities and prescribed/ over-the-counter pain medications | Daily opioid use | 6 weeks: mean difference: 3.75, 95% CI -3.335-10.825, p = 0.29 |
 Psychological | |||||||||
  Hanley 2021 USA [113] | Randomized controlled trial | 118 | 65 | 62% | THA, TKA | One 20 minutes session of mindfulness of breath (I1) or mindfulness of pain (I2) 3 weeks preop | One 20 minutes session of cognitive-behavioral pain psychoeducation (C) | Opioid use | Until 28 days postoperatively Both MoB and MoP decreased postoperative opioid use relative to C, F(8, 83) = 16.66, p < 0.001 |
  Hah 2020 USA [114] | Randomized controlled trial | 104 | 66 | 52% | THA, TKA | Motivational interviewing and guided opioid tapering support added to usual care (phone call weekly for postoperative weeks 2-7 and monthly up to 1 year or to opioid cessation) | Usual care + standardized verbal and written instructions on the proper analgesic use of opioids before surgery | Time to base line opioid use return (days) | I: 34.60; C: 67.80, HR 1.62; 95% CI 1.06- 2.46; p = 0.03 |
Proportion of patients using opioids at 3 months | Overall: I: 2.70%; C:2.00, p > 0.05 Opioid naïve: I: 2.70%; C: 9.50%, p > 0.05 Preoperative user: I: 8.30%; C: 23.10%, p > 0.05 | ||||||||
Proportion of patients using opioids at 6 months | Overall: I:0.00%; C:5.50%, p > 0.05 Opioid naïve: I: 0,00%; C: 2,40%, p > 0.05 Preoperative user: I: 0.00%; C: 15.40%, p > 0.05 | ||||||||
Time to postoperative opioid cessation (days) | I: 41.1; C: 76.4 HR 1.57; 95% CI 1.01- 2.44; p = 0.05 | ||||||||
Proportion of opioid cessation | I: 91.80%; C: 87.3%, p = 0.5 | ||||||||
  Dindo 2018 USA [95] | Randomized controlled trial | 75 | 63 | 6% | Orthopedic surgeries (no trauma) | Acceptance and Commitment Therapy (ACT) and treatment as usual | Treatment as usual (a nurse-led patient education class + analgesia with opioids +/- nonopioids, anticonvulsants or anxiolytics regular or as need. Discharge combination of an opioid and acetaminophen | Time to opioid cessation (days) | I: 42.50; C: 51.00; HR 1.44, 95% CI 0.74-2.78 |
Proportion of patients using opioids | At 7 weeks: I: 29.00%; C: 52.00%, OR= 0.39; 95% CI 0.14-1.08 |