From: Cannabinoids and orthopedic surgery: a systematic review of therapeutic studies
Study | Population | Intervention | Control |
---|---|---|---|
Beaulieu [17] | Adults with post-operative PCA device | n = 20 (85% female) Nabilone 1 mg, n = 11 (n = 5 TKA or THA) Nabilone 2 mg, n = 9 (n = 6 TKA or THA) 4 total doses: 1-h post induction, then every eight hours with morphine PCA | n = 11 (90% female) (2 THA or TKA) Ketoprofen 50 mg n = 10 (60% female) (5 THA or TKA) Placebo |
Haroutounian et al [26] | Adults with chronic pain > 3 months | n = 206 (38% female) (14.6% attrition rate) (n = 76 musculoskeletal pain, n = 39 low back pain, n = 1 avascular necrosis of leg) n = 136 Smoked, n = 17 oral drops, n = 8 drops and smoked, n = 9 cookies, n = 6 cookies and drops Mean 43.2 g/month added to analgesic regiment THC 6–14% smoked and 11–19% oral CBD 0.2–3.8% smoked and 0.5–5.5% oral | None |
Hickernell et al. [9] | Adults post primary THA or TKA | n = 81 (65.4% female) (60.5% TKA) Dronabinol 5mg p.o. B.I.D with standard pain control during course of hospital stay | n = 162 (63.5% female) (57.4% TKA) matched, no placebo given |
Holdcroft et al. [25] | Adults with post-operative PCA | n = 65 (72% female) (n = 23 orthopaedic surgeries) Oral caplet of THC:CBD in 1:0.3 (in 5 mg group) and 1:0.5 ratio given at either 5, 10, and 15 mg of THC | Matched into 3 tiers of dosing, no placebo control |
Hunter et al.a [18] | Adults with knee osteoarthritis | n = 211 (100% knee osteoarthritis) Synthetic cannabidiol transdermal gel administered for 12 weeks dosed at: 125 mg B.I.D (N = 106) or 250mg B.I.D (N = 105) | n = 103 placebo gel |
Jain et al. [19] | Adults with acute fracture or postoperative pain | n = 40 (7.5% female) IM levonantradol given blinded as 1.5, 2, 2.5, or 3 mg doses in addition to meperidine IV, n = 10 each dose | n = 16 (1.25% female) IM placebo |
Levin et al. [20] | Perioperative patients with risk factors for post-operative nausea and vomiting | n = 172 (100% female) (n = 14 orthopaedic procedures, n = 9 spine procedures) 0.5 mg p.o. nabilone taken within 3 h prior to induction of anesthesia. | n = 168 (100% female) (n = 14 orthopaedic procedures, n = 9 spine procedures) Identical placebo |
Mondello et al. [27] | FBSS patients with moderate to severe pain after spinal cord stimulation therapy | n = 11 (45% female) CBD (< 1%)/THC(19%) oleic suspension p.o. mean dose 68.5 mg/day | None |
Notcutt et al. [22] | Patients with chronic pain recalcitrant to opioids | n = 34 (68% female) (0.9% attrition) (n = 8 post spine surgery, n = 3 post orthopaedic trauma, n = 1 arthralgia) Extracts > 95% purity administered sublingually randomized into four groups given for 2 weeks: 2.5 mg THC, 2.5 mg CBD, 2.5 mg CBD, and 2.5 mg CBD, placebo | None |
Poli et al. [28] | Adults with chronic pain recalcitrant to two analgesic treatments. | n = 725 (62% female) (n = 41 arthritis) (53.3% attrition rate over 12 months) 19%THC/< 1%CBD cannabis strain taken as a tea p.o.. Dosed at 28 mg/day, equating to 5 mg/day THC. Titrated up with “most” taking 10 mg THC/day | None |
Ware et al. [21] | Adults with chronic pain refractory to other treatments | N = 215 (49% female) (16.3% “nociceptive pain”) (31.2% attrition rate at 12 months) Herbal cannabis (n = 58 smoked, n = 130 combination, n = 17 oral) 12.5% THC +/-1.5%, median dose 2.5 g/day | n = 216 (64.8% female) (18.1% “nociceptive pain”) (15.7% attrition rate at 12 months) |
Yassin et al. [23] | Adults with low back pain or sciatica refractory to surgical treatment and/or opioid analgesics | n = 46 (52% female) (n = 9 post spinal fusion, n = 17 spinal stenosis, n = 20 disk herniation) (0% attrition) 150–175 mg Q.I.D. smoked in addition to tramadol and duloxetine | None |
Yassin et al. [24] | Adults with low back pain > 12 months, symptomatic fibromyalgia, and failure of opioid therapy | n = 31 (90% female) (n = 13 disk herniation, n = 21 degenerative changes of spine) (0% attrition) 2/3 g day of smoked cannabis without other analgesics. 1:4 THC:CBD, THC < 5% in addition to oxycodone | None |