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Purpose: To intra-individually compare discomfort levels and patient satisfaction after arterial access closure using the ExoSeal(®) vascular closure device (VCD) and manual compression (MC) in a prospective study design.
Methods: Patients undergoing two planned interventions from 07/2013 to 09/2014 could participate in the study. Access closure was performed with an ExoSeal(®)-VCD in one and MC in the other intervention. Patients were clinically and sonographically examined and were given questionnaires 1 day after intervention [groin- and back-pain during bedrest (100-point visual analog scale; 0: no pain); comfortability of bedrest (10-point Likert scale, 1: comfortable), satisfaction with closure (10-point Likert scale, 1: very satisfied)]. Results were analyzed in a cross-over design.
Results: 48 patients (29 male, median age 62.5 (32-88) years) were included. An ExoSeal(®)-VCD was used first in 25 cases. As four of these subsequently refused MC as second intervention, data from 44 patients could be analyzed. All closures were technically successful (successful device deployment) without major complications. Groin- and back-pain after VCD-use/MC was 0 (0-15) vs. 10 (0-80) and 0 (0-75) vs. 25 (0-90), respectively (p < 0.0001). Bedrest after VCD-use was more comfortable than after MC [1 (range 1-7) vs. 6 (2-10); p < 0.0001]. Satisfaction with the closure procedure and with the intervention in general was higher after VCD-use compared to MC [1 (1-3) vs. 5 (2-10) and 1 (1-2) vs. 2 (1-4), respectively; p < 0.0001].
Conclusion: Intra-individual comparison showed pain levels and discomfort to be significantly lower after ExoSeal(®) use compared to MC. VCD closure was associated with higher satisfaction both with the closure itself and with the intervention in general.
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http://dx.doi.org/10.1007/s00270-015-1204-2 | DOI Listing |
J Robot Surg
September 2025
Orlando Health Advanced Robotic Surgery Center, Orlando, FL, USA.
Teleproctoring offers a remote alternative to traditional surgical mentoring, addressing logistical barriers in robotic surgery education. We conducted a prospective trial to assess the feasibility and trainee perception of teleproctoring using the Proximie platform. Eighteen surgeons with limited robotic experience performed a standardized enterotomy closure on synthetic bowel models using the da Vinci Si system, while receiving real-time remote guidance from an expert located 2570 km away.
View Article and Find Full Text PDFClin Spine Surg
August 2025
Department of Orthopaedic Surgery, Rothman Orthopaedic Institute at Thomas Jefferson University Hospital, Philadelphia, PA.
Study Design: Pilot Evaluation Study.
Objective: To assess the ease-of-use and performance of TissueStat, a novel minimally invasive spine surgery (MIS) fascial closure device, compared with conventional suturing techniques.
Summary Of Background Data: Wound issues in spine surgery can be a major source of morbidity and decreased patient satisfaction.
Spine (Phila Pa 1976)
August 2025
Department of Anesthesiology and Intensive Care, Aarhus University Hospital, Aarhus, Denmark.
Study Design: A randomized blinded trial with three groups.
Objective: To evaluate whether a single intraoperative methadone dose reduces postoperative opioid requirements and pain intensity in patients undergoing lumbar fusion surgery.
Summary Of Background Data: Spine fusion is associated with significant acute postoperative pain.
Cureus
August 2025
Plastic Reconstructive and Aesthetic Surgery, Adichunchanagiri Institute of Medical Sciences, Bala Gangadharanatha Nagara, IND.
Background: Pressure ulcers (PUs) present a therapeutic challenge in bedridden or neurologically impaired patients and represent a significant healthcare burden, affecting millions of patients worldwide. Current standard treatment approaches often fall short in achieving optimal healing outcomes, necessitating the development of advanced therapeutic interventions. Biological skin substitutes - high-purity type I collagen (HPTC) and dehydrated human amnion/chorion membrane (dHACM) - have emerged as promising therapeutic alternatives to traditional wound care approaches.
View Article and Find Full Text PDFSurg Case Rep
August 2025
Department of Gastroenterology and Transplant Surgery, Hiroshima University Hospital, Hiroshima, Hiroshima, Japan.
Introduction: Surgical site infection (SSI)-associated wound dehiscence offers management challenges, often requiring frequent and prolonged wound care to achieve healing. Dehiscence may result in evisceration, requiring careful attention to infection management and organ protection, leading to extended hospitalization, poor cosmesis, increased costs, and higher risks of incisional hernias, all of which reduce patient satisfaction. Herein, we outline 3 cases in which the combination of negative pressure wound therapy with instillation and dwell time (NPWTi-d) and deep cavity wound dressing and protective agent (Sorbact) enabled safe and early wound healing.
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