From: Periarticular infiltration used in total joint replacements: an update and review article
Name | Type of study | Patients | Groups | Main findings | Complications | Exclusion criteria |
---|---|---|---|---|---|---|
Reddy et al. [27] | Prospective randomized controlled trial | 140 patients MP group 70 patients Non steroid group—70 patients | Periarticular cocktail (PAI) 60 ml of 0.2% Ropivacaine; 8 mg Morphine; 0.3 mg Epinephrine; 60 mg Ketorolac MP group received an additional 100 mg of MP while the second group received only Saline | Lower VAS score in PAI group with Methylprednisolone 8 h after surgery, POD 1 and POD 2; No difference in ROM between the groups | Not listed | Bilateral of revision total knee arthroplasty procedures; General or Epidural anesthesia; severe renal insufficiency; uncontrolled DM, Bleeding disorders; history of vascular surgery involving the femoral vessels on operative side; History of arrhythmias and seizures; History of chronic pain, or alcohol or drug abuse, Allergies to medication, local infection, sepsis |
Kulkarni et al. [28] | Randomized controlled trial | 50 patients undergoing bilateral TKA | Both knees received a PAI, but the second knee also received methylprednisolone (40 mg) as part of the PAI | Lower VAS at 24 h and 72 h in the PAI with Methylprednisolone group. Greater ROM at 24 h and 72 h after surgery in the PAI with methylprednisolone group | No infections or further operations in the subsequent 6 months | Renal insufficiency; poorly controlled DM (HBA1C > 7.0); history of inflammatory arthritis;Allergy to medication; history of knee infection or prolonged QT interval |
Chia et al. [25] | Randomized Controlled trial | 127 patients | 3 groups. One control group, 1 low dose steroid group (40Â mg Triamcinolone acetonide) and 1 high dose steroid (80Â mg) group | No significant differences between pain scores and ROM between the groups | One PJI in the high dose steroid group | Unstable Diabetes, Immunosuppression,Chronic renal failure, Allergic reaction |
El-Boghdadly et al. [29] | Randomized controlled trial | 140 patients 72 patients—saline group 68 patients—Dexamethasone group | PAI consisted of 300 mg Ropivicaine, 30 mg Ketorolac; 0.6 mg of Epinephrine Patients randomized to receive 8 mg of Dexamethasone or Saline | Dexamethasone group had lower rates of Nausea + Vomiting POD 0 and 1, They had a shorter hospital stay of 7.7 h; Dexamethasone group demonstrated greater ROM on POD 1 and mobilized a longer distance that the control group; Decrease in total inpatient opioid consumption and need for patient controlled rescue analgesia in the Dexamethasone group. Total morphine consumption in the first 24 h were comparable.No long-term benefits seen with usage of Dexamethasone | No adverse events | Allergic reactions; Bilateral TKA procedures; Chronic opioid usage |
Tsukada et al. [35] | Double blinded Randomized Controlled trial | 75 patients 38—Methylprednisolone group 37—Saline group | PAI—300 mg Ropivacaine; 8 mg Morphine; 0.3 mg Epinephrine; 50 mg Ketoprofen In the one group they added 40 mg Methylprednisolone (MP) and the second group they only added Normal Saline | MP group had lower cumulative pain scores in the 24 h postoperative. No difference in VAS score at rest between groups but VAS score lower with activity in the first 24 h in the MP group; Some trend of better flexion and extension angle in the MP in the first 10 days | No adverse events. 5 patients develop a peroneal palsy due to the injection at the area—all resolved within 24 h | Poorly controlled DM(HBA1C > 7); Contraindications to spinal anesthetic;Regular opioid usage, Renal insufficiency; Prolonged Q-interval |
Christensen et al. [36] | Double blinded prospective Randomized Controlled trial | 76 patients MP group 39 patients; No steroid group—37 patients | PAI—80 mg Bupivacaine Hydrochloride; 4 mg Morphine, 0.3 mg Epinephrine; 100ug Clonidine; 750 mg Cefuroxime MP group received an additional 40 mg MP and the no steroid group received Saline | LOS was statistical better in the MP group; No difference between the groups regarding total narcotic consumption on first day or pain score on the first 24 h or upon discharge between the groups No difference in ROM between the two groups | Three patient in the MP had complications compared o none in the no steroid group. The complications included joint sepsis with subsequent death; 2 MUA | Renal disease, Allergic reactions to drugs used, chronic opioid usage, Rheumatoid arthritis; history of a knee infection |
Wang et al. [30] | Prospective double blind randomized controlled trial | 102 patients: 50 control group and 52 in corticosteroid group | PAI—0.2% Ropivacaine; 2ug/ml Epinephrine Steroid group—0.1 mg/ml Dexamethasone (DM) | VAS scores were statistical lower at 6 + 12 h at rest in the DM group and in the first 24 h with activity. DM had statistical lower overall morphine consumption; IL-6 + CRP was statistical lower in the DM in the first 2 days postoperatively; Longer ambulation and better ROM in the DM only on POD 1.No difference in LOS, nausea + vomiting or glucose levels | No difference in complication rates between the two groups | Other diagnosis than OA (i.e. RA, traumatic arthritis); Allergic reaction; Flexion or varus–valgus deformity >  = 30 degrees; history of knee surgery or infection; history of excessive opioid or alcohol consumption; history of narcotic dependency; Psychiatric illness or cognitive impairment; Thrombotic events |
Sean et al. [33] | Prospective double blind randomized controlled trial | 100 patients; 50 steroid group and 50 patients in the control group | PAI—0.5 ml/kg of 0.5% Bupivacaine with 1:200 000 Epinephrine; Steroid group received 40 mg Triamcinolone acetonide | Significant less pain POD 2—5 in the steroid group; Less morphine consumption in the steroid group; in the steroid group they observed decrease LOS,quicker ability to achieve straight leg raise and better ROM which was significant POD 2 onward. The ROM persisted to be better even at 6 months postop. At 2 years no difference in clinical outcome between the groups | Both groups had 1 infection with a no culture in the steroid group while the control group grew MRSA infection | Diabetes, immunodeficiency, previous surgery to the knee; hypothyroidism, renal failure or allergies to medications |
Yue et al. [31] | Prospective randomized controlled study | 72 patients; 36 in the steroid group and 36 in the control group | PAI—30 ml of 0.75% Ropivicaine; 0.5 ml of 1:1000 Epinephrine Steroid group—1 ml Betamethasone; The steroid group injected the mixture in thee periarticular tissues but did not inject the steroid in the subcutaneous tissues | No difference in VAs at rest or activity; No difference in ROM or overall morphine consumption; KSS was statistically better at the 1 and 3 month mark in the steroid group but similar after 6 months. Celecoxib usage was shorter in the steroid group | No complications in either group | Know allergies to the medications; Major systemic illnesses (heart failure, renal impairment); psychological problems, narcotic dependence; chronic opioid users |
Kwon et al. [26] | Randomized controlled trial | 76 staged knee replacements. the first knee was randomized to either receive steroids or no steroids. The second staged knee then received the opposite treatment | PAI—300 mg Ropivicaine; 10 mg Morphine Sulfate; 30 mg Ketorolac, 300ug of 1:1000 Epinephrine Steroid group—40 mg Triamcinolone Acetonide | Statistical lower pain on the night of the operation in the steroid group; Steroid group demonstrated earlier straight leg raise ability, but no difference in maximal flexion; No difference in rescue medication; No difference in flexion,patient satisfaction or PROMS at 6 months | No difference in complication rates | GI bleeding, congestive heart failure, Delirium or failed spinal anesthesia |
Kim et al. [32] | Prospective randomized double blind study | 270 patients—divided in 6 groups of 45 patients each | All the groups received 400 mg Ropivicaine + 0.6 mg Epinephrine; Group 1—as above; Group 2—Morphine (5 mg) in addition; Group 3 Ketorolac (30 mg) in addition; Group 4 Morphine and Ketorolac in addition; Group5 Morphine, Ketorolac and Methylprednisolone (40 mg) in addition | Lower pain scores first 12 h in Group 4 + 5 compared to the other groups; No difference between Group 4 and 5 however. Lower opioid consumption in the first 24 h in group 4 + 5 but total opioid consumption the same; Group 5 demonstrated lower CRP values until POD 4 and better ROM until POD 2 | No difference in complication rates | Inflammatory arthritis, previous surgical procedure to the knee; allergy to the medications |