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Randomized Controlled Trial
. 2018 Jun;97(24):e11181.
doi: 10.1097/MD.0000000000011181.

The effects of preoperative single-dose thoracic paravertebral block on acute and chronic pain after thoracotomy: A randomized, controlled, double-blind trial

Affiliations
Randomized Controlled Trial

The effects of preoperative single-dose thoracic paravertebral block on acute and chronic pain after thoracotomy: A randomized, controlled, double-blind trial

Xiu-Liang Li et al. Medicine (Baltimore). 2018 Jun.

Abstract

Background: Patients undergoing thoracotomy frequently experience acute pain and chronic post-thoracotomy pain (CPTP). There are few articles relating to the investigations on the effects of preoperative single-dose thoracic paravertebral block (PSTPVB) on acute pain and CPTP. We tested the hypothesis that adding PSTPVB to intravenous (IV) patient-controlled analgesia (PCA) would reduce acute pain scores and decrease the incidence and intensity of CPTP.

Methods: Fifty-six patients undergoing elective thoracotomy were randomized to receive PSTPVB in addition to IV PCA (group T) or IV PCA alone (group C). A single 20-mL injection of 0.50% ropivacaine plus 10 mg dexamethasone in saline was administered preoperatively under ultrasound guidance; sufentanil was used for IV PCA. The acute pain intensity at rest and at coughing based on verbal rating scale, postoperative sufentanil consumption, and complications were evaluated at 6, 24, 48, and 72 hours after surgery. The incidence and intensity of CPTP were evaluated at 3 months after surgery.

Results: Group T had significantly less acute pain compared with group C at all measurement times both at rest and at coughing (P < .05). The PCA cumulative sufentanil consumption, complications, and the incidence of CPTP between the 2 groups was not statistically significant (P > .05). The intensity of CPTP was significantly higher in group C than in group T (P < .05).

Conclusion: This study indicated that adding PSTPVB to IV PCA improved acute postoperative pain and chronic pain in patients undergoing thoracotomy, but did not reduce the incidence of CPTP.

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Conflict of interest statement

The authors have no conflicts of interest to disclose.

Figures

Figure 1
Figure 1
Consolidated standards of reporting trials (CONSORT) flow diagram.
Figure 2
Figure 2
Acute pain scores (VRS) during 72 hours after surgery at rest. Data are presented as mean ± SD. The pain scores were significantly lower in group T than in group C at all time points at rest (P < .05). VRS = verbal rating scale.
Figure 3
Figure 3
Acute pain scores (VRS) during 72 hours after surgery at coughing. Data are presented as mean ± SD. The pain scores were significantly lower in group T than in group C at all time points at coughing (P < .05). VRS = verbal rating scale.
Figure 4
Figure 4
Number of patients with VRS scores ≤3 cm (ie, sufficient postoperative analgesia) during 72 hours after surgery at rest and at coughing. VRS = verbal rating scale.
Figure 5
Figure 5
The cumulative sufentanil consumption by intravenous patient-controlled analgesia (μg). The difference between the groups was not statistically significant at all time points. PCA = patient-controlled analgesia.

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