BMJ· 2026Q1
Kronik post-torakotomi ağrısını azaltmak için torasik epidural ve paravertebral blokajın karşılaştırılması (TOPIC-2): açık etiketli, paralel gruplu, üstünlük, çok merkezli, randomize kontrollü çalışma
Thoracic epidural versus paravertebral blockade for reducing chronic post-thoracotomy pain (TOPIC-2): open label, parallel group, superiority, multicentre, randomised controlled trial
- 2atıf
- Q1SCImago
- 2026yıl
Kısa özet
Paravertebral blokaj, altı ayda torasik epidurale kıyasla kronik post-torakotomi ağrısını azaltmadı; ağrı insidansında anlamlı bir fark bulunmadı (%22'ye karşı %16).
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Ana noktalar
- Paravertebral blokaj, torasik epidurale kıyasla altı ayda kronik post-torakotomi ağrısını azaltmadı (%22'ye karşı %16 insidans).
- Torasik epidural ameliyat sonrası 1. günde daha iyi akut ağrı kesici etki sağladı, sonrasında fark kalmadı.
- Paravertebral blokaj ile hipotansiyon ve kaşıntı daha az görülürken, idrar retansiyonu daha sık görüldü.
- İki grup arasında genel ameliyat sonrası komplikasyon oranları benzerdi.
Yapay zekâ ile başlık ve abstract'tan üretildi; tam metin okunmaz.
Özet (abstract)
Abstract Objectives To evaluate the effectiveness of paravertebral blockade versus thoracic epidural during the perioperative period in reducing chronic post-thoracotomy pain. Design Open label, parallel group, superiority, multicentre, randomised controlled trial. Setting 15 thoracic centres in the UK. Participants Adult patients undergoing thoracotomy randomised (1:1) to either paravertebral blockade or thoracic epidural using a web based service between January 2019 and September 2023. Interventions Participants in the paravertebral group received three single-shot paravertebral injections of local anaesthetic before incision f ollowed by placement of a paravertebral catheter. Participants in the epidural group had a thoracic epidural catheter placed and loaded with local anaesthetic before incision. Main outcome measure The primary outcome was incidence of chronic post-thoracotomy pain at six months after randomisation, defined as a 100 mm visual analogue score greater than or equal to 40 mm (indicating moderate pain) when considering worst chest pain over the past week. Secondary outcomes included acute pain (visual analogue score of 100 mm) and complications. Results 770 patients were enrolled, of which 428 (56%) were male (mean (standard deviation, SD) age 66.6 (11.0) years). After 33 exclusions of patients after randomisation who did not proceed to thoracotomy, 737 remained in the modified intention-to-treat population (364 in the paravertebral group, 373 in the epidural group). Six months after randomisation, 59 (22%) of 272 participants in the paravertebral group and 47 (16%) of 292 participants in the epidural group developed chronic post-thoracotomy pain (adjusted risk ratio 1.32 (95% confidence interval (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, worst and average pain was greater on day 1 with paravertebral blockade (adjusted mean difference 7.7 mm (95% CI 2.8 to 12.5 mm) and 7.0 mm (95% CI 2.7 to 11.2 mm), respectively), but no different on days 2-3. Hypotension was less common in the paravertebral group than the epidural group (12% v 18%, respectively, adjusted risk ratio 0.66 (95% CI 0.46 to 0.94), adjusted risk difference -0.06 (95% CI -0.11 to -0.01)), as was pruritis (4% v 12%, adjusted risk ratio 0.37 (95% CI 0.21 to 0.64), adjusted risk difference -0.07 (95% CI -0.11 to -0.03)), although more participants in this group experienced urinary retention (12% v 6%, adjusted risk ratio 2.21 (95% CI 1.35 to 3.61), adjusted risk difference 0.05 (95% CI 0.01 to 0.09)), complications were similar otherwise. Conclusions Paravertebral blockade did not reduce chronic post-thoracotomy pain at six month follow-up compared to thoracic epidural. Thoracic epidural provided marginally better acute pain relief one day after the operation, but showed no difference thereafter. Postoperative complications were comparable between groups. The findings support the ongoing use of both techniques. Trial registration ClinicalTrials.gov NCT03677856 .
Yazarların özeti; kaynağından alınmıştır. BMJ, 2026 · DOI ↗
Ücretsiz hesapla devam et
Makaleye Sor ile bu makaleye günde 3 soru ücretsiz; makaleyi kaydet, kaynakçasını al, ilgi alanına göre her gün yeni özetler. Çıkarımlar Premium.
Web'de ücretsiz devam etGoogle ya da Apple hesabınla giriş; kart istemez. Bu makaleye geri dönersin.
Telefonda:
Alan: Anesteziyoloji ve Ağrı Tıbbı
Anesthesiology and Pain MedicineMedicine