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1.
Musculoskelet Surg ; 107(1): 55-68, 2023 Mar.
Article in English | MEDLINE | ID: mdl-34719773

ABSTRACT

PURPOSE: Metal ion release may cause local and systemic effects and induce hypersensitivity reactions. The aim of our study is first to determine if implant-related hypersensitivity correlates to patient symptoms or not; second, to assess the rate of hypersensitivity and allergies in shoulder arthroplasty. METHODS: Forty patients with shoulder replacements performed between 2015 and 2017 were studied with minimum 2-year follow-up; no patient had prior metal implants. Each patient underwent radiographic and clinical evaluation using the Constant-Murley Score (CMS), 22 metal and cement haptens patch testing, serum and urine tests to evaluate 12 metals concentration, and a personal occupational medicine interview. RESULTS: At follow-up (average 45 ± 10.7 months), the mean CMS was 76 ± 15.9; no clinical complications or radiographic signs of loosening were detected; two nickel sulfate (5%), 1 benzoyl peroxide (2.5%) and 1 potassium dichromate (2.5%) positive findings were found, but all these patients were asymptomatic. There was an increase in serum aluminum, urinary aluminum and urinary chromium levels of 1.74, 3.40 and 1.83 times the baseline, respectively. No significant difference in metal ion concentrations were found when patients were stratified according to gender, date of surgery, type of surgery, and type of implant. CONCLUSIONS: Shoulder arthroplasty is a source of metal ion release and might act as a sensitizing exposure. However, patch test positivity does not seem to correlate to hypersensitivity cutaneous manifestations or poor clinical results. Laboratory data showed small constant ion release over time, regardless of gender, type of shoulder replacement and implant used. LEVELS OF EVIDENCE: Level II.


Subject(s)
Arthroplasty, Replacement , Hypersensitivity , Shoulder Joint , Humans , Aluminum , Shoulder/surgery , Hypersensitivity/etiology , Hypersensitivity/diagnosis , Hypersensitivity/surgery , Metals/adverse effects , Arthroplasty, Replacement/adverse effects , Shoulder Joint/diagnostic imaging , Shoulder Joint/surgery
2.
Acta Biomed ; 85 Suppl 2: 102-6, 2014 Sep 24.
Article in English | MEDLINE | ID: mdl-25409728

ABSTRACT

In the follow up of Achille's tenorraphy, negativization of Thompson calf queezing test is not always omogeneous and absolute. Aim of the paper is to correlate Thompson test to different anatomical-ultrasound and functional parameters. We investigated clinically and by ultrasound 61 patients operated on of Achille's tenorraphy at Novara Hospital with follow-up of 10 to 46 months. Negative controls were contralateral tendons. We excluded patients with previous and/or contralateral Achille's tendon ruptures, those operated after 7 days, diabetics or with autoimmune diseases, if used topic steroids, < 18 years, those rejecting the study. Measured parameters were: age, gender, height, weight, side, open vs percutaneous approach, time from operation, neutral angle and range of motion of the ankle, maximal circumference of the leg, Single Heel Rise Test, Visual-Analogue-Scale Foot and Ankle (VAS FA) score; with ultrasound: length of tendons, mio-tendinous U.S.-structure, dynamic diastasis of tendon scar, tendon sliding. Thompson test is positive if no plantar-flexion of the foot occurs at calf squeezing, negative if plantar-flexion is normal (75% patients) and intermediate if reduced or slight reactive (25%).We found correlation of Thompson test with age (p<0,05) and with tendon length (p>0,05), being intermediate tests more represented in older patients and in those with longer healed tendons. In conclusion post-operative negativization of Thompson test can be incomplete as observed in older patients and in those healed with elongated tendon.


Subject(s)
Achilles Tendon/physiopathology , Achilles Tendon/surgery , Ankle , Muscle Contraction/physiology , Achilles Tendon/diagnostic imaging , Achilles Tendon/injuries , Adult , Female , Humans , Male , Middle Aged , Range of Motion, Articular , Recovery of Function , Retrospective Studies , Treatment Outcome
3.
Musculoskelet Surg ; 98 Suppl 1: 5-13, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24659198

ABSTRACT

PURPOSE: The aim of this study was to evaluate the short-term results after reverse shoulder arthroplasty (RSA) for proximal humeral fractures in elderly patients. METHODS: The same surgical technique was adopted in all patients: the procedure was performed through a deltopectoral approach, the subscapularis was always resected, and a positioning jig was used to implant the cemented humeral component in the desired height and in 20° of retroversion. Nineteen consecutive patients, affected by complex fractures of the proximal humerus, were operated in a 3-year period by the same surgeon at a single institution. All the patients were female, with a mean age of 75 years (range 70-83). RESULTS: Fifteen patients were evaluated at an average follow-up of 22 months (range 12-46 months). A postoperative infected hematoma was the only recorded complication. The absolute Constant score averaged 45.7 (range 19-69), while the relative and normalized scores averaged 65.1 (range 33-97) and 58.5 (range 24-91), respectively. The average Shoulder Pain and Disability Index (SPADI) score was 39 (range 6-89). X-rays showed healing of the greater tuberosity to the humeral diaphysis in nine shoulders. CONCLUSIONS: RSA is an established treatment option for elderly patients with proximal humeral fractures, particularly when general and local conditions are predictive of failure with hemiarthroplasty. Even though clinical results were quite variable in this series of patients, the adoption of a standardized surgical technique allowed to minimize postoperative complications. Subscapularis repair does not seem a critical factor for preventing implant dislocation, but its influence on functional results needs further investigation.


Subject(s)
Arthroplasty, Replacement , Arthroscopy , Frail Elderly , Rotator Cuff , Shoulder Fractures/surgery , Aged , Aged, 80 and over , Arthroplasty, Replacement/adverse effects , Arthroplasty, Replacement/instrumentation , Arthroplasty, Replacement/methods , Arthroscopy/methods , Female , Follow-Up Studies , Humans , Range of Motion, Articular , Retrospective Studies , Risk Factors , Rotator Cuff/surgery , Surgical Wound Infection/therapy , Treatment Outcome
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