Thoracic epidural versus paravertebral blockade for reducing chronic post thoracotomy pain (TOPIC 2): an open label, allocation concealed, multicentre, randomised controlled trial

Structured Abstract

Importance Many patients undergoing thoracotomy suffer from debilitating chronic post-thoracotomy pain (CPTP) lasting months or years postoperatively. The effectiveness of the commonly used two analgesic techniques, paravertebral blockade (PVB) and thoracic epidural blockade (TEB), on the incidence of CPTP is unknown.

Objective To test the hypothesis that PVB reduces the incidence of CPTP compared with TEB.

Design Pragmatic, open-label, allocation-concealed randomized controlled trial. Participants were recruited between January 8th, 2019 and September 29th, 2023.

Setting 15 UK thoracic centers.

Participants 770 eligible adult patients undergoing thoracotomy were randomly assigned (1:1) to TEB or PVB using a web-based randomization service.

Intervention(s) Participants in the PVB group received three single-shot paravertebral injections of local anesthetic before knife-to-skin, followed by placement of a paravertebral catheter. Participants in the TEB group had a thoracic epidural catheter placed and loaded with local anaesthetic before knife-to-skin.

Main Outcome(s) and Measure(s) The primary outcome was the incidence of CPTP at 6 months post-randomization, defined as a 100mm Visual Analogue Score (VAS) greater than or equal to 40mm (indicating moderate pain) when considering ‘worst chest pain over the last week’. Secondary outcomes included additional measures of chronic/acute pain, complications and quality of life.

Results The trial enrolled 770 patients (342 female patients (44.4%); mean (SD) age, 66.6 (11.0) years). After 33 post-randomisation exclusions of patients who did not proceed to thoracotomy, 737 were included in the modified intention-to-treat population (364 PVB, 373 TEB). At 6-months, 59 (22%) of 272 participants in the PVB group and 47 (16%) of 292 participants in the TEB group developed CPTP (adjusted risk ratio=1·32 [95%CI 0·93 to 1·86]; adjusted risk difference=0·05 [95%CI –0·01 to 0·11]; p=0·12). During the acute phase, pain was greater on day 1 with PVB, but not different on days 2-3. Hypotension was less common in the PVB group; complications were similar otherwise.

Conclusions and Relevance PVB did not reduce the incidence of CPTP at 6 months compared to TEB. TEB appeared to provide marginally better acute pain relief on postoperative day 1, but there was no difference thereafter. Postoperative complications were comparable between groups. The findings support the ongoing utility of both techniques.

Trial Registration This trial is registered with ClinicalTrials.gov, NCT03677856.

Funding Organisation NIHR HTA reference-16.111.111

Question Does paravertebral blockade (PVB) reduce the incidence of chronic post-thoracotomy pain (CPTP) compared to thoracic epidural blockade (TEB)?

Findings In this open-label, allocation-concealed, multicenter randomised clinical trial that included 770 adults, paravertebral blockade did not significantly reduce the incidence of CPTP six months postoperatively compared to thoracic epidural blockade (22% with PVB vs 16% with TEB).

Meaning In adult patients undergoing thoracotomy, providing acute perioperative analgesia with PVB does not reduce the incidence of CPTP compared to TEB.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

NCT03677856

Clinical Protocols

https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-023-07463-1

Funding Statement

This project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment (HTA) programme (NIHR 16/111/111)

Author Declarations

I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.

Yes

The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Ethics committee of South-East Scotland Research Ethics Committee (REC 18/SS/0131) gave ethical approval for this work.

I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.

Yes

I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).

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I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.

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Data Availability

The datasets generated during the current study will be made available by the Chief Investigator upon reasonable request and in accordance with the Birmingham Clinical Trials Unit's research collaboration and data transfer guidelines.

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