Clinique Chénieux
Limoges, France
NCT Number: NCT04189731
Shoulder surgery is performed usually under interscalene block considered as a gold standard. This anesthesia is well suited for hospitalized patients but not for outpatients. The Orthopedic Surgery Department of Clinique Chénieux has been operating patients requiring arthroscopic shoulder surgery with a short interscalene block relayed by a long suprascapular block. The main objective is to evaluate the effectiveness of this method by measuring the average pain over 3 days after the operation.
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Notify Me18 year–70 year
All sexes
Observational
Limoges, France
The surgery of the shoulder is usually performed under interscalene block (ISB), considered as a gold standard. This anesthesia is well suited for hospitalized patients but not for outpatients. Indeed, the ISB entails, in addition to a sensory block, a motor block often useless and important since it extends beyond the shoulder to the entire upper limb. It can also be a source of anxiety and cause the risk of compression in the limb operated because of the extended sensorimotor block. It is also responsible for a painful bounce almost constant with sometimes the very rapid installation of intense pain when the effect of the sensory block disappears. This pain can be difficult to relieve despite frequent use of opioids.
The Orthopedic and Traumatologic Surgery Department of the Clinique Chénieux has been operating patients requiring arthroscopic surgery of the shoulder according to the following technique. It involves the establishment of a short ISB (between 2h and 4h) relayed by a supra-scapular block (SSB) long (72h) through the placement of a perineural catheter thus allowing a continuous diffusion of Naropein® by an elastomeric pump. The same day or the day after the operation, the patients return to their home and are followed by nurses.
The objective of this technique is to better manage postoperative pain, thus allowing the management of patients in outpatient surgery. A prospective non-interventional study will make it possible, in a context of common practice, to obtain data on the management of pain in operated patients and then to consider a generalization of this practice to other centers.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Day1
Score of average pain at D1, D2 and D3 by a numeric pain scale (NPS) <4/10
Time frame: Day2
core of average pain at D2 by a numeric pain scale (NPS) <4/10
Time frame: Day 3
core of average pain at D3 by a numeric pain scale (NPS) <4/10
Time frame: Day 7
Number of readmissions the first week after the operation
Time frame: Day 0
Number of painful peaks on awakening and leaving the block on the day of the operation
Time frame: Day 1, Day 2, Day 3, Day 4 and Day 7
Amount and types of analgesics consumed / consumed non-opioid during the operation and the first week after the operation
Time frame: Day 4, Day 7, Day 15 and Day 30
Score of minimum, maximum, average pain the month before the operation and by a numeric pain scale (NPS). Scale from 0 to 10.
Time frame: Day 30
Satisfied patient rate determined by using a satisfaction questionnaire with 4 responses: very satisfied, somewhat satisfied, somewhat dissatisfied and very dissatisfied
Time frame: Month 3
Number of postoperative complications at 3 month
Time frame: Month 6 and Month 12
Cartilaginous Toxicology at 6 months and 12 months determined by radiograph of the shoulder of face in 3 rotations
University Hospital, Limoges
Other
Acronym: BSS-CHIR
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