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A Randomised Clinical Trial of Buffered Tumescent Local Anaesthesia During Endothermal Ablation for Superficial Venous Incompetence.
Nandhra, Sandip; Wallace, Tom; El-Sheikha, Joe; Leung, Clement; Carradice, Dan; Chetter, Ian.
Afiliación
  • Nandhra S; Academic Vascular Surgery, Hull-York Medical School, Hull Royal Infirmary, Hull, UK. Electronic address: sjnandhra@gmail.com.
  • Wallace T; Academic Vascular Surgery, Hull-York Medical School, Hull Royal Infirmary, Hull, UK.
  • El-Sheikha J; Academic Vascular Surgery, Hull-York Medical School, Hull Royal Infirmary, Hull, UK.
  • Leung C; Academic Vascular Surgery, Hull-York Medical School, Hull Royal Infirmary, Hull, UK.
  • Carradice D; Academic Vascular Surgery, Hull-York Medical School, Hull Royal Infirmary, Hull, UK.
  • Chetter I; Academic Vascular Surgery, Hull-York Medical School, Hull Royal Infirmary, Hull, UK.
Eur J Vasc Endovasc Surg ; 56(5): 699-708, 2018 11.
Article en En | MEDLINE | ID: mdl-30392525
OBJECTIVE/BACKGROUND: Endovenous thermal ablation (EVTA) is the recommended first line intervention for superficial venous incompetence (SVI). While the infiltration of perivenous tumescent local anaesthesia (TLA) is key to procedural success, it is paradoxically the predominant source of patient reported discomfort. This randomised controlled trial investigates the potential to reduce peri-procedural pain and improve patient reported outcome measures (PROMs), including quality of life (QoL) using TLA buffered to physiological pH. METHODS: Patients undergoing great saphenous vein EVTA with concomitant phlebectomies were randomised to either standard (ST) or buffered (BT) TLA. Follow up assessments were performed at weeks 1, 6, and 12. The primary outcome was patient reported peri-procedural pain on a 100 mm visual analogue scale (VAS). Secondary outcomes were one week post-procedural pain VAS and analgesia use, QoL (disease specific: Aberdeen Varicose Vein Questionnaire [AVVQ]; generic: Short Form-36 [SF-36] and EuroQol 5 Dimensions Questionnaire [EQ-5D]), patient satisfaction VAS, technical success on duplex ultrasound (DUS) examination, and complications. RESULTS: Ninety-seven patients were randomised: 50 to ST and 47 to BT. The groups had comparable baseline demographics, Clinical Etiologic Anatomic Pathological, Venous Clinical Severity Score, QoL, and DUS parameters. Equally, intra-procedural parameters (volume of TLA, length of ablation, and linear energy delivered) were also comparable. Peri-procedural pain scores were significantly lower in the BT group with a mean ± SD score of 2.86 ± 3.57 versus 4.44 ± 2.94 (p = .001). Pain scores and analgesia use over the subsequent week were equivalent. SF-36 Bodily Pain domain scores were significantly better in the BT group at week 1 (77 vs. 62; p = .008). AVVQ, SF-36, and EQ-5D scores were otherwise similar between the groups throughout follow up, significantly improving over baseline. Technical success was high in both groups, with no major complications and few minor complications. CONCLUSION: Buffered TLA offers a significantly lower peri-procedural pain experience for patients undergoing EVTA and should replace current tumescent formulae.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vena Safena / Insuficiencia Venosa / Ablación por Catéter Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Vasc Endovasc Surg Asunto de la revista: ANGIOLOGIA Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Vena Safena / Insuficiencia Venosa / Ablación por Catéter Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Vasc Endovasc Surg Asunto de la revista: ANGIOLOGIA Año: 2018 Tipo del documento: Article