Tuyển tập các báo cáo nghiên cứu về hóa học được đăng trên tạp chí sinh học quốc tế đề tài : Multi-modal-analgesia for pain management after Hallux Valgus surgery: a prospective randomised study on the effect of ankle block | Journal of Orthopaedic Surgery and Research BioMed Central Research article Multi-modal-analgesia for pain management after Hallux Valgus surgery a prospective randomised study on the effect of ankle block Ibrahim Turan 1 Hamid Assareh 1 Christer Rolft2 and Jan Jakobsson 1 Address 1Karolinska Institutet Foot Ankle Surgical Centre Stockholm Sweden and 2Sheffield Centre of Sports Medicine University of Sheffield UK Email Ibrahim Turan Hamid Assareh Christer Rolf christerrolf@ Jan Jakobsson Corresponding author tEqual contributors Open Access Published 18 December 2007 Received 5 July 2007 Journal of Orthopaedic Surgery and Research 2007 2 26 doi 1749-799X-2-26 Accepted 18 December 2007 This article is available from http content 2 1 26 2007 Turan et al licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License http licenses by which permits unrestricted use distribution and reproduction in any medium provided the original work is properly cited. Abstract Background Pain and emesis are the two major complaints after day case surgery. Local anaesthesia has become an important part of optimizing intra and post-operative pain treatment but is sometimes not entirely sufficient. The aim of the present study was to study the effect of adding an ankle block to a multi-modal analgesic approach on the first 24-hour-need for rescue analgesia in patients undergoing elective Hallux Valgus surgery. Type of study Prospective randomized patient-blind study comparing ankle block with levo-bupivacaine lidocaine and Saline placebo control. Methods Ninety patients were studied comparing ankle block 15 cc using levo-bupivacaine mg ml lidocaine 10 mg ml or placebo saline on day-case elective Hallux Valgus surgery supported by general anaesthesia in all cases. Primary study endpoint was .
