Citations

Institution: Mayo Clinic Clear

Showing 10 of 108036 citations.

The Inclusive Sexual Function Index (ISFI): Adaptation and Validation in a Sample Diverse Across Racial/Ethnic, Sexual, and Gender Identities
Spencer, Katherine G., Vencill, Jennifer A. , Mark, Kristen P. , Girard, Abby , Arenella, Katherine , Rider, G. Nic , Rider, G. Nic

Journal of Sex & Marital Therapy | March 17, 2026 | Volume: 52 | Issue: 3 | Pages: 327-338

10.1080/0092623x.2026.2642874 | PMID 41841185 Get It

Advances in Stereotactic Navigation for Primary Spine and Pelvis Tumor Resection and Reconstruction: A Systematic Review
Subramanian, Tejas , Li, George, Vemu, Sree M. , Owusu-Sarpong, Stephane , Oles, Alexander R, Owusu-Sarpong, Stephane , Oles, Alexander R. , Song, Junho , Vaynrub, Max , Hirase, Takashi

HSS Journal®: The Musculoskeletal Journal of Hospital for Special Surgery | March 17, 2026 | Volume: 22 | Issue: 4 | Pages: 412-425

10.1177/15563316261418705 | PMID 41859436 Get It

Background: Primary spine/pelvic tumors are aggressive, and en bloc resection is often essential. While stereotactic navigation is increasingly used for instrumentation in spine surgery, its specific role in tumor resection remains incompletely defined. Purpose: We sought to describe (1) reported rates of achieving negative margins, (2) local recurrence, (3) complications attributed to navigation, and (4) comparative outcomes from studies involving nonnavigated controls. Methods: We conducted a systematic review according to preferred reporting items for systematic reviews and meta-analysis guidelines. Databases were queried for studies investigating the use of stereotactic navigation in primary spine/pelvic tumor surgery. Outcomes including surgical margin status, local recurrence, and complications were extracted and qualitatively synthesized using a best-evidence approach. Results: Twenty-one studies with 240 patients were included. The mean patient age was 46 years with follow-up of 33.4 months. Tumors were most often located in the sacrum/pelvis (81.3%), followed by the thoracic (8.3%), cervical (5.8%), and lumbar spine (4.6%). Chordoma (31.7%) and chondrosarcoma (27.1%) were the most frequently reported types. Negative surgical margins were achieved in 88.3% of cases. Local recurrence was reported in 16% of patients, with the highest observed in chondrosarcoma (32.4%). Complications occurred in 30.3% of patients; however, only 1% (2 cases) were attributed to navigation use. Two comparative studies examining navigated versus nonnavigated cohorts suggested improved bony margins and lower recurrence risk with navigation. Conclusion: Early studies suggest that stereotactic navigation may be a feasible and safe adjunct for the resection of primary spine/pelvic tumors, particularly in achieving adequate bony margins. However, the current evidence is limited to small retrospective studies with heterogeneity in methodology, tumor type, and follow-up. Level of Evidence: Level IV: Systematic review of level-III and level-IV studies.
Training for pediatric cannot intubate cannot oxygenate: surgical airway should replace needle cricothyrotomy
Lehman, Allison M.B., Amstutz, Paul, Moore, Jackson E. , Obersteadt, Christopher, Williams, Dominique, Waxman, Mary J., Blubaugh, Morgan , Parikh, Anaya, Walsh, Timothy R., Bruegger, Daniel E., Malik, Adrienne , Pirotte, Andrew, Johnson, Matthew D. , Obersteadt, Chris, Sood, Shawn , Pirotte, Andrew P.

Frontiers in Disaster and Emergency Medicine | March 17, 2026 | Volume: 4 | Issue: No issue available | Pages: No page available

10.3389/femer.2026.1772381 | PMID 41928873 Get It

Failed pediatric endotracheal intubation, prompting surgical airway management via emergency front of neck access (eFONA), is an intrinsically challenging topic. While rare, all emergency airway providers must be equipped to handle these complex clinical scenarios, both through initial training and maintenance of competency. Needle cricothyrotomy is a commonly taught method in cannot intubate cannot oxygenate (CICO) scenarios for children under age eight. However, needle cricothyrotomy is technically difficult, profoundly rare, and maintaining competency is a challenge. From a multidisciplinary perspective, we examine the utility of continuing to teach needle cricothyrotomy and explore alternatives. This project group suggests that pediatric eFONA training across disciplines should focus on surgical tracheotomy rather than needle cricothyrotomy, with consideration given to specialty-specific human performance factors.
Synergistic Anticancer Activity of Cannabinoids and Terpenes Against Triple-Negative Breast Cancer Resistance
Aare, Mounika , Lazarte, Jassy Mary, Nathani, Aakash , Boirie, Breana, Turley, Tamiel N. , Copland, John A. , Sachdeva, Mandip , Singh, Mandip , Lazarte, Jassy Mary S.

International Journal of Molecular Sciences | March 17, 2026 | Volume: 27 | Issue: 6 | Pages: 2730

10.3390/ijms27062730 | PMID 41898593 Get It

Triple-negative breast cancer (TNBC) remains highly aggressive and refractory to conventional treatments, underscoring the need for novel combination strategies. Here, we employed 2D and 3D in vitro models, transcriptomic profiling, and in vivo xenograft studies to evaluate the anticancer efficacy of cannabinoids combined with the terpene β-caryophyllene (BC) in resistant TNBC models. Among the tested cannabinoids, cannabichromene (CBC) exhibited the greatest potency, and its combination with BC at sub-toxic concentrations significantly reduced IC50 values, enhanced cytotoxicity in spheroids, and suppressed colony formation and migration. The combination treatment induced pronounced G1 cell cycle arrest and increased apoptotic cell death. Western blot analyses revealed downregulation of PARP, Survivin, mTOR, Vimentin, Glypican-5, and PD-L1, while RNA sequencing demonstrated suppression of proliferative and migratory signaling pathways alongside activation of apoptosis, autophagy, and ferroptosis-related pathways. In vivo, CBC + BC significantly inhibited tumor growth in MDA-MB-231 xenografts, outperforming single-agent treatments. Collectively, these findings demonstrate that BC synergistically enhances cannabinoid activity, yielding superior antiproliferative and anti-migratory effects, and highlight this combination as a promising therapeutic strategy for resistant TNBC.
Monoclonal gammopathy of thrombotic significance in a nutshell
Kanack, Adam J. , Mauch, Emily, Murray, David , Padmanabhan, Anand , Mauch, Emily E

British Journal of Haematology | March 17, 2026 | Volume: 208 | Issue: 5 | Pages: 1551-1554

10.1111/bjh.70438 | PMID 41841750 Get It

Summary This nutshell review discusses the pathophysiology, diagnostic features, treatment strategies and avenues for future research in a recently identified thrombotic entity, monoclonal gammopathy of thrombotic significance (MGTS). MGTS is an anti‐platelet factor 4 (PF4) antibody‐mediated disorder distinct from heparin‐induced thrombocytopenia (HIT) and vaccine‐induced thrombotic thrombocytopenia (VITT), as it involves the production of persistent, monoclonal anti‐PF4 antibodies. Several subtypes of MGTS, including ‘HIT‐like’, ‘VITT‐like’ and ‘non‐HIT/VITT‐like’, exhibit unique serological profiles that can complicate diagnosis. Recognition of ‘HIT‐like’ MGTS is critical to avoid heparin exposure in these patients, which can result in adverse effects like those seen in heparin‐exposed HIT patients. ‘Non‐HIT/VITT‐like’ MGTS antibodies have only been detected in PF4‐enhanced functional testing; therefore, we recommend using these platelet‐based tests as the front‐line assay for detecting MGTS antibodies. Mass profiling using mass spectrometry is critical for the ‘fingerprinting’ of monoclonal antibodies to establish a diagnosis of MGTS. Treatments used in HIT and VITT, such as non‐heparin anticoagulants and intravenous immunoglobulin G, are typically insufficient for managing MGTS. Emerging MGTS therapies, such as plasma cell‐directed drugs and Bruton tyrosine kinase inhibitors, are discussed. The review concludes with an emphasis on areas of future research in MGTS.
Preferred standard‐of‐care carfilzomib dosing in multiple myeloma: An international survey of haematologists/oncologists
Banerjee, Rahul, Dong, Sharlene , McCaughan, Georgia , Mehra, Nikita , Wang, Bo, Sperling, Adam S. , Cowan, Andrew J., Anderson, Lee, Rajkumar, S. Vincent, Rajkumar, S. Vincent , Banerjee, Rahul , Banerjee, Rahul , Rajkumar, S Vincent , Sperling, Adam S , Cowan, Andrew J. , Anderson, Larry D. , Kaur, Gurbakhash

British Journal of Haematology | March 17, 2026 | Volume: 208 | Issue: 5 | Pages: 1831-1835

10.1111/bjh.70435 | PMID 41841734 Get It

Top 10 Tips Palliative Care Clinicians Should Know About Navigating Physician Job Transitions
Lawton, Andrew J. , Zehm, April , Dow, Lindsay , Webb, Jason A., Malhotra, Sonia, Strand, Jacob J. , Berns, Stephen , Newport, Kristina , Jones, C. P. , Lindenberger, Elizabeth, Webb, Jason A., Buss, Mary K. , Santivasi, Wil L.

Journal of Palliative Medicine | March 17, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1177/10966218261433847 | PMID 41841451 Get It

Most palliative care (PC) physicians will change jobs over the course of their career, yet few supports exist to guide them through this often unfamiliar process. Job transitions frequently elicit stress and uncertainty, as individuals balance personal and professional priorities, navigate complex negotiations, and assume the inherent risks of pursuing new opportunities. Yet, when approached intentionally, a job transition can also be a transformative process that allows for self-discovery, cultivation of new skills and connections, and reshaping of one’s professional identity. This article, written by a team of PC physicians who have made job transitions themselves, offers 10 tips for navigating this professional step successfully. With emphases on authentic communication, skilled mentorship, relationship building, and exploration of local culture—the article offers practical advice to help PC physicians navigate a job transition confidently, while staying grounded in their personal values and the work they find most meaningful.
FADIS: Fast-food attributed diabetes index study: An ecological State-level exploration of nutritional transitions and diabetes burden in India
Nammi, Jeevan Yadav, Pasala, Roshini, Nammi, Jeevan

The Indian Journal of Medical Research | March 17, 2026 | Volume: 163 | Issue: No issue available | Pages: 237-242

10.25259/ijmr_1802_2025 | PMID 41949142 Get It

Background and objectives India’s rapid urbanisation, economic liberalisation, and rising fast food consumption are driving a nutritional transition that parallels the growing epidemic of non communicable diseases, particularly type 2 diabetes mellitus. This study examines the association between fast food expenditure and diabetes prevalence across 18 Indian States, stratified by gender and urban-rural residence. Methods The fast-food attributed diabetes index study (FADIS) utilised publicly available State-level data to evaluate correlations between fast food spending and diabetes prevalence. A novel framework, DIAGRAM (diabetes and intake gradient analysis model), was applied to parse these associations across urban and rural men and women. The WEIGHT (women’s elevated intake and glucose-health evaluation tracker) model assessed the prevalence of overweight as a predictor of diabetes in women. Results We found a strong positive correlation between fast food expenditure and diabetes prevalence among urban populations, specifically urban men (r=0.653, P =0.003) and urban women (r=0.619, P =0.0062). Rural patterns were less consistent and weaker. The WEIGHT model identified the prevalence of overweight as a significant contributor to diabetes risk among women. Interpretation and conclusions In this ecological analysis, we found that fast-food expenditure had a strong correlation with diabetes prevalence, particularly among urban men and women. In women, overweight prevalence rather than fast-food expenditure emerged as the significant predictor in multivariable analyses. These findings highlight the need for gender-sensitive and region-specific public health strategies to address India’s evolving nutritional transitions and diabetes burden.
Foundation Models for Volumetric Medical Imaging: Opportunities, Challenges, and Future Directions
Guo, Junlin , Singh, Yashbir, Younis, Khaled, Kuanar, Shiba , Faghani, Shahriar, Farina, Eduardo Moreno Judice De Mattos, Huo, Yuankai, Maleki, Farhad, Singh, Yashbir , Faghani, Shahriar , Huo, Yuankai , Maleki, Farhad , Faghani, Shahriar , Singh, Yashbir , Maleki, Farhad , Ghosh, Tapotosh , Sheikhi, Farnaz , Farina, Eduardo Moreno Júdice de Mattos

Electronics | March 17, 2026 | Volume: 15 | Issue: 6 | Pages: 1245

10.3390/electronics15061245 Get It

Foundation models, known as the large-scale, pretrained models capable of generalizing across diverse tasks, have significantly advanced the field of medical image analysis. While most early applications focused on 2D modalities, the unique challenges and opportunities associated with volumetric medical imaging have recently attracted growing interest. This study provides a comprehensive overview of the current landscape of foundation models tailored for volumetric medical image analysis, with a focus on CT, MRI, and PET imaging. We examine key components of these models, including 3D architectures, training strategies, and supported modalities. In addition, we highlight their contribution to major clinical tasks such as classification and prediction, segmentation, image registration, quality enhancement, and visual question answering. Critical challenges of these models, including high computational cost, limited and less diverse 3D datasets, and domain adaptation, are discussed alongside the promising solutions and future research directions. By synthesizing recent advances in volumetric foundation models and outlining key technical and clinical challenges, this review provides a thorough roadmap toward the development of scalable, generalizable, and clinically applicable AI systems for volumetric medical images.
Comparative Proteomic Profiling of Responses to Standard Systemic Treatment Regimens in Pancreatic Cancer
Mansouri, Amirsalar , Hart, Olivia , Aslanabadi, Sina , Hartupee, Conner, Yalcin, Dicle , Sinha, Devbarna, Cios, Aleksandra , Cheng, Zetao , Ammanamanchi, Sudhakar , Zabaleta, Jovanny , Stewart, John H. , West, John T. , Borad, Mitesh J., Nagalo, Bolni Marius , Adamec, Jiří , Moaven, Omeed , Sinha, Garima , Cios, Aleksandra , Ammanamanchi, Sudhakar , Zabaleta, Jovanny , Nagalo, Bolni , Adamec, Jiri , Moaven, Omeed , Hartupee, Conner Daniel, Chabu, Chiswili Yves , Borad, Mitesh J.

Cells | March 17, 2026 | Volume: 15 | Issue: 6 | Pages: 531

10.3390/cells15060531 | PMID 41892321 Get It

Pancreatic ductal adenocarcinoma (PDAC) is an aggressive malignancy with a 5-year survival rate of 13.3%. First-line treatment relies on two chemotherapy regimens, FOLFIRINOX (FOLFNX) or gemcitabine plus nab-paclitaxel (GEMPAC). However, direct clinical comparisons between these regimens have yielded inconsistent results across survival and toxicity endpoints, and the molecular basis of heterogeneous treatment responses remains poorly defined. To investigate regimen-specific tumor-cell-intrinsic mechanisms, we performed quantitative proteomic profiling of a primary PDAC-derived MIA PaCa-2 cell line following treatment with FOLFNX or GEMPAC. Differentially expressed proteins were analyzed using Gene Ontology, KEGG, and Ingenuity Pathway Analysis to define pathway-level alterations, and findings were contextualized using TCGA transcriptomic data. Proteomic analyses revealed that FOLFNX and GEMPAC engage in distinct cytotoxic programs. FOLFNX predominantly suppressed ribosome biogenesis and mitochondrial translation, consistent with sustained metabolic and biosynthetic stress, whereas GEMPAC preferentially disrupted mitotic cytokinesis and phosphatidylinositol phosphate biosynthesis, consistent with mitotic failure. Integration with TCGA data showed that FOLFNX-altered proteins aligned with favorable prognostic expression signatures, whereas GEMPAC-associated proteins were enriched among adverse profiles, reflecting engagement of distinct tumor-intrinsic programs. Together, these findings provide mechanistic insight into differential chemotherapy responses and establish a foundation for proteomics-based biomarkers to guide personalized chemotherapy selection in PDAC.