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Abedi, Armita Armina

https://orcid.org/0000-0002-1803-3981

Mayo Clinic

Copenhagen University Hospital

Citations 3

Harnessing the Biologic Power of Bacteriophages to Improve the Treatment of Periprosthetic Joint Infection
Abdelbary, Hesham , Malko, Sasha , Powell, James Nelson, Abedi, Armita Armina , Suh, Gina A. , Çıtak, Mustafa , Taha, Mariam , Crawley, Angela M , Abedi, Armita Armina , Suh, Gina A , Citak, Mustafa , Abdelbary, Hesham

Journal of Bone and Joint Surgery | July 28, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.2106/jbjs.26.00339 Get It

➢ Periprosthetic joint infection (PJI) remains the most common cause of failure after total joint arthroplasty, with current standard therapies associated with failure rates between 10% and 30%. ➢ The 2025 International Consensus Meeting in Istanbul, Türkiye, highlighted the potential benefits of bacteriophage (phage) therapy in managing PJI. ➢ One of the barriers to integrating phage therapy into standard clinical PJI care is the knowledge gap between preclinical research and clinical practice. ➢ This Expert Review summarizes the key therapeutic advantages of using phages as an adjuvant therapeutic platform for PJI. It also highlights the current challenges that are continuing to limit the integration of phages into standard PJI care.
Imaging modalities demonstrate moderate and heterogeneous diagnostic accuracy for periprosthetic joint infection: A systematic review and meta‐analysis
Abedi, Armita Armina , Glaudemans, Andor Waltherus Johannes Maria, Parvizi, Javad, Force, the Imaging Working Group for the Unified PJI Definition Task, Glaudemans, Andor W.J.M. , Tarabichi, Saad , Abedi, Armita Armina , Parvizi, Javad

Knee Surgery, Sports Traumatology, Arthroscopy | June 3, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1002/ksa.70423 Get It

Abstract Purpose The diagnostic accuracy of imaging modalities in periprosthetic joint infections (PJIs) remains uncertain. This study assessed and compared the performance of different imaging techniques for diagnosing PJI. Methods A systematic review and meta‐analysis of studies published in PubMed and Embase (1 January 2000 to 1 March 2024) was conducted. Eligible studies included adults (≥18 years), applied a valid reference standard for PJI diagnosis, and provided sufficient data to construct 2 × 2 contingency tables. Imaging modalities included white blood cell scintigraphy (WBCS), FDG‐PET/CT, antigranulocyte scintigraphy (AGS), bone scintigraphy (BS), magnetic resonance imaging (MRI), computed tomography (CT) and related combinations. Risk of bias was assessed using the QUADAS‐2 tool. A bivariate random‐effects model estimated pooled diagnostic odds ratios, sensitivities, and specificities with 95% confidence intervals (CIs). Results Forty studies (1263 PJI cases, 4700 controls) were included. Pooled sensitivity and specificity were as follows: WBCS‐SPECT/CT: 87.1% (95% CI, 31.7–99.0) and 94.1% (95% CI, 87.5–97.3); WBCS‐BMS: 79.7% (95% CI, 58.3–91.7) and 94.2% (95% CI, 91.0–96.3); WBCS: 88.1% (95% CI, 73.8–95.1) and 80.0% (95% CI, 62.2–90.7); FDG‐PET (±PET/CT): 88.1% (95% CI, 79.9–93.2) and 87.2% (95% CI, 76.3–93.5); BS‐WBCS: 59.5% (95% CI, 43.2–73.9) and 96.6% (95% CI, 92.2–98.6); BS: 89.3% (95% CI, 80.9–94.2) and 74.1% (95% CI, 59.0–85.0); AGS: 89.1% (95% CI, 76.8–95.3) and 73.0% (95% CI, 63.1–81.0). No eligible studies were identified for MRI or CT. Substantial heterogeneity was observed. Conclusion Diagnostic performance varied substantially, and no modality consistently demonstrated superior accuracy. WBCS showed the most stable results, particularly when combined with BS or BMS. Given the heterogeneity and variability in specificity, imaging should complement comprehensive diagnostic evaluation rather than be used in isolation. Level of Evidence 2a–3a, systematic review and meta‐analysis of retrospective cohort and case‐control studies.
2025 International Consensus Meeting on Musculoskeletal Infection: Summary From the Biofilm Workgroup on Biofilm Formation, Persistence, and Host‐Environment Interactions
Muthukrishnan, Gowrishankar , Coraça‐Huber, Débora C., Abbaszadeh, Ahmad , Abedi, Armita A., Abuhussein, Ezzuddin , Bingham, Joshua S. , Cichos, Kyle H. , Drago, L., Hamilton, John , Hickok, Noreen J., Iannotti, Ferdinando , Jensen, Louise Kruse, Li, Bingyun , Manzary, Mojieb, Moriarty, T. Fintan, McDonald, Katya , Nishitani, K., Norton, Nicholas, Oral, Ebru, Parvizi, Javad M., Raafat, Dina, Saeed, Kordo B. A., Sallai, Imre , Em, Schwarz, Siverino, Claudia , Tate, J.C. , Trobos, Margarita , Tubbs, Andie R., Hamilton, John L. , Saeed, Kordo , Abedi, Armita Armina , Bingham, Joshua S , Drago, Lorenzo , Hickok, Noreen J , Iannotti, Ferdinando , Moriarty, T Fintan , McDonald, Katya , Schwarz, Edward M , Abedi, Armita Armina , Coraça-Huber, Débora Cristina , Atkins, Gerald J. , Coenye, Tom , Jennings, Jessica Amber , Jensen, Louise Kruse , Nishitani, Kohei, Norton, Nicholas , Oral, Ebru , Parvizi, Javad , Raafat, Dina , Sekar, Amita

Journal of Orthopaedic Research | January 9, 2026 | Volume: 44 | Issue: 1 | Pages: No page available

10.1002/jor.70130 Get It

ABSTRACT Musculoskeletal infection (MSKI) remains a major problem after trauma and elective orthopedic surgery. Chronic MSKI is related to the formation of biofilm, which impairs diagnosis and effective treatments. Therefore, to understand and communicate global standards and best practices, the 2025 International Consensus Meeting (ICM) on MSKI created a Biofilm Section to address crucial aspects of biofilm biology pertaining to its mechanisms of drug resistance and immune evasion, and potential approaches to overcome them. This featured a 2‐year process, with final voting and discussion on May 8–10, 2025, in Istanbul, Turkey. This Consensus Article is the effort of the Biofilm Basic Mechanisms Workgroup, which interpreted the results on ICM questions related to (1) the infectious microenvironment; (2) appropriate inocula in preclinical research; (3) biofilm behavior in infected tissues; and (4) synergy within biofilms and with other comorbidities. Collectively, we find that this field has the necessary research tools to discover the pathophysiology of orthopedic implant‐associated biofilm development and maturation, perform clinically relevant studies in animal models, and elucidate mechanisms that allow opportunistic infections in compromised tissues and patients with other health issues.