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Table 1 Articles included in the review analyzing the use of dexmedetomidine in periarticular infiltrations

From: Periarticular infiltration used in total joint replacements: an update and review article

Name

Type of study

Number of patients

Groups and findings

Dosage of DM

Duration of DM

Main findings

Complications (postop delirium, Nausea, Hypotension, Bradycardia

Exclusion criteria

Zhao et al. [2]

RCT

116 total knee arthroplasty patients

Control (Ropivicaine) (1)

Epinephrine + Ropivicaine (2)

Dexmedetomidine + Ropivicaine(3)

DM had lower pain scores at 6 h

DM + Epinephrine had lower pain scores for first 24 h

2.0 ug/kg

Good pain relief 6–12 h after surgery

Lower levels of proinflammatory cytokines. Prolong sensory block and minimize motor block effect

No complications

Allergies to the medications; severe knee deformities;history of a knee infection;Long-term opioid usage; history of neuromuscular disorders;diagnosis of severe cardiovascular disease

Nickar et al. [3]

RCT

75 total knee arthroplasty patients

DM + Ropivicaine(1)

Ketorolac + Ropivicaine (2)

Control (Ropivicaine) (3)

1.0 ug/kg

150 min  ±  54.22 pain relief

Ketorolac demonstrated better pain relief compared to DM

No complications

Patients with a history of infection or malignant disease; cardiac disease(receiving Beta-Blockers, calcium channel blockers or alpha-methyldopa, coagulopathy, hepatic or kidney disease, allergic reaction to medications

Salem et al. [4]

RCT

45 knee arthroscopy patients

Control (1)

DM (2)

Fentanyl (3)

100 ug

505 min pain relief

Fentanyl had the longest pain relief (693 min)

First 6 h had same pain relief between Fentanyl + DM

No complications

Advanced renal or hepatic disease;psychiatric disorders;prolonged intake of NSAIDS, patients taking beta-blockers-tricyclic antidepressants; allergic reactions to medications

Pangrahi et al. [5]

RCT

60 arthroscopy patients

(1) Control

(2) DM (1 ug/kg)

(3) DM (2 ug/kg)

1–2 ug/kg

757.3  ± 207.68 min in group 3

Group 3 demonstrated significant lower pain scores in first 12 h, lower analgesic requirement and lower intensity of pain

No complications

Allergy to medications;pregnancy or lactation;hepatic-renal-cardiopulmonary abnormality; alcoholism,diabetes,bleeding diathesis,patients of Beta-blockers,clonidine,alpha-methyldopa; patients using opioid or non-opioid analgesia

Mohamed et al. [6]

RCT

90 abdominal hysterectomy patients

(1) Bupivicaine 0.25% + 2 mg/kg Ketamine

(2) Bupivicaine 0.25% + DM 2 ug/kg

2 ug/kg

(1) Ketamine – 7.6 ±  4.16 h

(2) DM – 6.00  ± 3.73 h

Rescue analgesia, first dose of analgesia, VAS score was less in Ketamine + DM group with Ketamine doing slightly better than DM

6.7% of patients had sedation + hypotension in DM group

Significant cardiac,respiratory,renal or hepatic diseases, coagulation disorders, patients with infection, patients with psychiatric illnesses

Hao et al. [7]

RCT

120 patients undergoing tonsillectomies or adenoinectomies

(1) GA + Ropivicaine + DM

(2) GA + Ropivicaine

1 ug/kg

10 h (9.4–11.4)

Pain scores were significantly lower at the 8th,16th,20th and 24th hour after surgery

None documented

Patients with cardiovascular,respiratory and endocrine disorders; Patients with known allergies to local anesthetics

Azemati et al. [8]

RCT

60 pediatric patients undergoing unilateral herniorraphy

(1) Bupivicaine 0.5% + DM

(2) Bupivicaine 0.5%

1 ug/kg

2 h

Pain scores were better in the first 2 h for the DM group

Heart rate was statistical lower in the DM group in the first 20 min after injection. Sedation was also significantly more in the DM for the first 3 h

Patients with history of seizures, coagulopathies,sensitivity to DM, congenital heart disease, history of bleeding disorders, liver or kidney failure, neurological diseases

Abo Elfadl et al. [9]

RCT

90 children undergoing tonsillectomies

(1) Levobupivicaine 0.25% + DM

(2) Levobupivicaine 0.25%

1 ug/kg

644.31 ± 112.89 min

The DM group consumed less analgesia in the first 24 h and had a higher total oral intake

No side effects

Obstructive sleep apnea syndrome;cardiovascular,liver,renal disease,coagulation disorders,relevant drug allergies,neurological or psychiatric illness

Mitra et al. [10]

RCT

45 undergoing elective lumbar discectomies

(1) Ropivicaine 0.5%

(2) Ropivicaine 0.5% + Tramadol

(3) Ropivicaine 0.5% + DM

0.5 ug/kg

930 min (854.3–1005.7)

DM group demonstrated statistical longer time to rescue analgesia. Pain scores and Diclofenac consumption in the first 24 h was statistically lower in the DM

No side effects

ASA grade ¾;History of allergy to relevant drugs;patients with severe systemic disease,pregnancy,psychiatric illness,seizure disorder

Li et al.[11]

RCT

57 patients with elective posterior lumbar fusion

(1) Ropivicaine 0.5%

(2) Ropivicaine 0.5% + DM

1 ug/kg

10.5  ± 3.7 h

Significantly less Morphine + PCA requirements in the DM. Analgesic request was delayed and Vas core reduced up to 16 h after surgery

No side effects

Allergies to relevant medications; long-term treatment with opioids;renal or hepatic insufficiency;neoplastic disorders;BMI >  = 30, local sepsis;unbalanced cardiopathy or pneumopathy, severe diabetes;preoperative psychiatric or cognitive disorders,coagulation abnormalities

Yu et al. [12]

RCT

140 patients undergoing laparoscopic cholecystectomy

(1) Placebo group (saline)

(2) Ropivacaine 0.5%(skin); + Saline(deltoid muscle)

(3) ropivacaine 0.5% + DM (Skin); and Saline at the deltoid muscle

(4) Ropivicaine 0.5% (skin); and DM at the deltoid muscle

1 ug/kg

12 h

DM did demonstrate lower Vas score scores compared to Ropivicaine + saline up to 12 h. The Ropivicaine + DM combined at the sking performed the best

No adverse events. Slight decrease in diastolic + systolic blood Pressure in DM groups (no statistical significant)

BMI >  = 30; renal or hepatic disorders, opioid usage;history of alcohol or drug abuse;ASA status or 3 or greater;contraindications of use(hypotension or bradycardia);pregnancy, patients with history of chronic pain; allergic to relevant medications

Luan et al. [13]

RCT

50 patients undergoing an open gastrectomy

(1) Ropivicaine 0.3%

(2) Ropivicaine 0.3% + DM

1 ug/kg

Didn’t record first time to analgesia

No difference in VAS scores between groups. Higher Sufentanil consumption in the first 24 h

No adverse events

Allergy to relevant medications; BMI >  = 30; opioids addiction; chronic pain, psychiatric diseases