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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술대회자료
- 저자정보
- 발행연도
- 2021.3
- 수록면
- 145 - 145 (1page)
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Introduction and Background
We aimed to compare the clinical efficacy and safety of arthroscopy-guided continuous suprascapular nerve block(AS-SSNB) with ultrasound-guided continuous interscalene block (US-ISB) for patients with arthroscopic rotator cuff repair.
Material and Method
A prospective study was performed between March and June 2020. Totally, 75 patients were included and divided into two groups: In 38 patients of group 1 (AS-SSNB), indwelling catheter was introduced via Neviaser portal under arthroscopic view just before closing the portal at the end of the surgery. In 37 patients of group 2 (US-ISB), indwelling catheter was inserted towards the interscalene brachial plexus just prior to the surgery under US control. The primary outcome was the pain score measured by a visual analog scale (VAS) at postoperative 8 hours during admission, which was most painful in pilot study. Comparison was conducted at different times (postoperative 4, 8, 24, and 48 hours). The secondary outcome was th ... 전체 초록 보기
We aimed to compare the clinical efficacy and safety of arthroscopy-guided continuous suprascapular nerve block(AS-SSNB) with ultrasound-guided continuous interscalene block (US-ISB) for patients with arthroscopic rotator cuff repair.
Material and Method
A prospective study was performed between March and June 2020. Totally, 75 patients were included and divided into two groups: In 38 patients of group 1 (AS-SSNB), indwelling catheter was introduced via Neviaser portal under arthroscopic view just before closing the portal at the end of the surgery. In 37 patients of group 2 (US-ISB), indwelling catheter was inserted towards the interscalene brachial plexus just prior to the surgery under US control. The primary outcome was the pain score measured by a visual analog scale (VAS) at postoperative 8 hours during admission, which was most painful in pilot study. Comparison was conducted at different times (postoperative 4, 8, 24, and 48 hours). The secondary outcome was th ... 전체 초록 보기
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UCI(KEPA) : I410-ECN-0101-2021-514-001737469