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blood substitute (Volplex / Volplex)

✓ Approved

Sinclair · 细胞治疗 · 细胞治疗

什么是 blood substitute?

blood substitute 是一种细胞治疗,由Sinclair研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Intravenous (IV)。

药物档案

商品名Volplex, Volplex
公司Sinclair
药物类别细胞治疗
给药途径Injectable (Others), Intravenous (IV)
状态Approved

治疗适应症

blood substitute 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Surgical and medical proceduresAdjuvant therapy✓ Approved

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[Blood Loss in Open Spine Surgeries - Preoperative Estimate vs Reality].

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Intraoperative blood loss represents a critical challenge in spinal surgery, with the potential to increase morbidity, mortality, and healthcare costs. Significant blood loss is associated with postoperative complications such as respiratory failure, infections, and hematomas. This paper evaluates current methods of estimating blood loss and highlights the discrepancy between intraoperative clinical estimates and the actual total blood loss, with a specific focus on the phenomenon of hidden blood loss (HBL). The concept of Total Blood Loss (TBL) is analyzed as the sum of Visible Blood Loss (VBL), consisting of blood in suction canisters, sponges, and drains, and HBL, which results from hemolysis and sequestration of blood into tissues. Mathematical formulas, specifically the Gross equation and Nadler's formula for patient blood volume, are discussed as tools for calculating TBL based on hematocrit changes. Visual estimation is consistently shown to be inaccurate, often leading to significant underestimation, especially in losses exceeding 1,000 ml. Research indicates that in major spinal procedures, approximately 21% of the total intraoperative blood loss is captured in surgical sponges. For practical intraoperative monitoring, a "28% coefficient" should be added to the volume in the suction canister to provide a realistic estimate of the blood trapped in textiles. Furthermore, HBL accounts for at least 30% of the total perioperative loss. In extensive posterior thoracolumbar fusions, the visible blood in the suction canister may represent about half of the actual TBL only. Younger patients are paradoxically more susceptible to higher HBL due to more dynamic transcapillary refill and greater vascular compliance.

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Arthroscopy for the Painful Shoulder Arthroplasty: Indications, Outcomes, and Technical Considerations.

Jackson Garrett R GR, Koetting Sean S, Childers Justin T JT, Kenter Keith K et al.

Persistent pain, stiffness, or suspected infection following shoulder arthroplasty remains a challenging clinical problem. Arthroscopy has emerged as a minimally invasive diagnostic and therapeutic tool in selected patients with painful anatomic total shoulder arthroplasty, reverse shoulder arthroplasty, or hemiarthroplasty. This review summarizes the current evidence regarding indications, outcomes, complications, and technical considerations for arthroscopy in the setting of pain following prior shoulder arthroplasty. Shoulder arthroscopy after arthroplasty has been described for glenoid component loosening, polyethylene wear, rotator cuff pathology, biceps tendon disease, postoperative stiffness, impingement, and suspected periprosthetic joint infection. Reported outcomes suggest that arthroscopy may improve pain and function in selected patients, particularly after glenoid component removal, biceps procedures, capsular release, and lysis of adhesions. Arthroscopic tissue biopsy also demonstrates greater diagnostic utility than aspiration or serum inflammatory markers for suspected periprosthetic shoulder infection. Technical strategies, including initial subacromial evaluation and controlled glenohumeral entry through the rotator interval, may reduce iatrogenic implant damage during arthroscopic evaluation. Arthroscopy can be both diagnostic and therapeutic in well-selected patients with painful or stiff shoulder arthroplasty. Although it is not a substitute for revision surgery in cases of clear implant failure, instability, or massive cuff insufficiency, it may help clarify the diagnosis, treat focal pathology, and delay or avoid open revision in selected patients.

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Arthroscopy-Assisted Core Decompression Combined with Octacalcium Phosphate/Gelatin Composite Implantation for Osteonecrosis of the Femoral Head: A Study Protocol for a Single-Center Externally Controlled Trial.

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Background/Objectives: Osteonecrosis of the femoral head is a progressive disease that frequently leads to femoral head collapse and secondary osteoarthritis. Although total hip arthroplasty provides reliable outcomes, its use in younger patients is limited due to concerns regarding implant longevity. Joint-preserving procedures such as core decompression have been widely used; however, their efficacy remains controversial. This study aims to evaluate a combined approach using arthroscopy-assisted core decompression and an osteoconductive bone substitute. Methods: This study is designed as a single-center, externally controlled trial conducted at Tohoku University Hospital. Patients with osteonecrosis of the femoral head (Japanese Investigation Committee Stage 1-3B, Type B-C2) will undergo arthroscopy-assisted core decompression combined with octacalcium phosphate/gelatin composite implantation. A total of 25 patients will be prospectively enrolled. Outcomes will be compared with a propensity score-matched historical control cohort. The primary outcome is disease progression within 1 year, defined as radiographic progression or conversion to total hip arthroplasty. Secondary outcomes include radiographic changes, clinical outcomes, and bone remodeling assessed by computed tomography. Expected Results: This study is expected to provide preliminary clinical evidence regarding the feasibility and potential effectiveness of arthroscopy-assisted core decompression combined with octacalcium phosphate/gelatin composite implantation for osteonecrosis of the femoral head. The intervention may promote bone remodeling and contribute to the prevention of femoral head collapse. Conclusions: The findings of this study may contribute to the development of improved minimally invasive joint-preserving treatment strategies for osteonecrosis of the femoral head and provide a basis for future large-scale clinical trials.

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