Citations

Showing 10 of 108081 citations.

Management of Acute Surgical Pain in Plastic and Reconstructive Surgery
Saffari, Tiam M. , Saffari, Sara , Brower, Kristin I. , Janis, Jeffrey E.

Mayo Clinic

Plastic & Reconstructive Surgery | May 16, 2023 | Volume: 153 | Issue: 4 | Pages: 838e-849e

10.1097/prs.0000000000010694 | PMID 37189221 Get It

Summary: Fewer than half of all patients undergoing surgery report adequate postoperative pain relief. Poorly managed postoperative pain can lead to complications, increased hospital stays, prolonged rehabilitation, and a decreased quality of life. Pain rating scales are commonly used to identify, manage, and track the perceived intensity of pain. Changes in perceived pain severity and intensity are a key indicator for course of treatment. Postoperative pain is best treated with multimodal management with a variety of analgesic medications and techniques that target different receptors and mechanisms of action in the peripheral and central nervous systems. This includes systemic analgesia, regional analgesia, local analgesia (eg, topical and tumescent analgesia), and nonpharmacologic modalities. It is recommended that this approach is individually tailored and discussed through a shared decision-making approach. This review provides an overview of multimodal management for acute postoperative pain related to plastic surgery procedures. To increase patient satisfaction and provide effective pain control, it is recommended to educate patients on expectations of pain, multimodal options for pain control (including peripheral nerve blocks), complications of unrelieved pain, tracking and monitoring of pain by self-reporting, and how to reduce the use of opioid-based pain medication.
What Plastic Surgeons Should Know about Small-Joint Arthroplasty: Is This for Your Practice?
Rizzo, Marco , Chung, Kevin C.

Mayo Clinic

Plastic & Reconstructive Surgery | May 16, 2023 | Volume: 153 | Issue: 2 | Pages: 373e-382e

10.1097/prs.0000000000010693 | PMID 37189228 Get It

Summary: This article reviews the state of the art for arthroplasty of the metacarpophalangeal and proximal interphalangeal joints. Arthritis that affects these joints can result in significant pain and compromised function. The authors review indications for arthroplasty for each joint, types of implants to consider, technical considerations, patient expectations, and outcomes and complications.
Spatial transcriptomics herald a new era of transcriptome research
Saul, Dominik , Saul, Dominik , Kosinsky, Robyn Laura

Mayo Clinic

Clinical and Translational Medicine | May 16, 2023 | Volume: 13 | Issue: 5 | Pages: No page available

10.1002/ctm2.1264 | PMID 37190941 Get It

Phase-Amplitude Coupling Localizes Pathologic Brain with Aid of Behavioral Staging in Sleep
Křemen, Václav , Brinkmann, Benjamin H. , Duque, Juliano J., Carvalho, Diego Z. , Stead, Matt, Berry, Brent , Varatharajah, Yogatheesan , Kucewicz, Michal, Guragain, Hari, Brinkmann, Benjamin, Duque, Juliano, Brinkmann, Benjamin H , Kremen, Vaclav , Carvalho, Diego Z , Kucewicz, Michał T. , Guragain, Hari, Sieck, Gary C. , Worrell, Gregory A.

Mayo Clinic

Life | May 16, 2023 | Volume: 13 | Issue: 5 | Pages: 1186

10.3390/life13051186 | PMID 37240831 Get It

Low frequency brain rhythms facilitate communication across large spatial regions in the brain and high frequency rhythms are thought to signify local processing among nearby assemblies. A heavily investigated mode by which these low frequency and high frequency phenomenon interact is phase-amplitude coupling (PAC). This phenomenon has recently shown promise as a novel electrophysiologic biomarker, in a number of neurologic diseases including human epilepsy. In 17 medically refractory epilepsy patients undergoing phase-2 monitoring for the evaluation of surgical resection and in whom temporal depth electrodes were implanted, we investigated the electrophysiologic relationships of PAC in epileptogenic (seizure onset zone or SOZ) and non-epileptogenic tissue (non-SOZ). That this biomarker can differentiate seizure onset zone from non-seizure onset zone has been established with ictal and pre-ictal data, but less so with interictal data. Here we show that this biomarker can differentiate SOZ from non-SOZ interictally and is also a function of interictal epileptiform discharges. We also show a differential level of PAC in slow-wave-sleep relative to NREM1-2 and awake states. Lastly, we show AUROC evaluation of the localization of SOZ is optimal when utilizing beta or alpha phase onto high-gamma or ripple band. The results suggest an elevated PAC may reflect an electrophysiology-based biomarker for abnormal/epileptogenic brain regions.
Next-Generation Boron Drugs and Rational Translational Studies Driving the Revival of BNCT
Seneviratne, Danushka S. , Mackeyev, Yuri , Malouff, Timothy D. , Krishnan, Sunil , Mackeyev, Yuri , Krishnan, Sunil , Seneviratne, Danushka , Saifi, Omran

Mayo Clinic

Cells | May 16, 2023 | Volume: 12 | Issue: 10 | Pages: 1398

10.3390/cells12101398 | PMID 37408232 Get It

BNCT is a high-linear-energy transfer therapy that facilitates tumor-directed radiation delivery while largely sparing adjacent normal tissues through the biological targeting of boron compounds to tumor cells. Tumor-specific accumulation of boron with limited accretion in normal cells is the crux of successful BNCT delivery. Given this, developing novel boronated compounds with high selectivity, ease of delivery, and large boron payloads remains an area of active investigation. Furthermore, there is growing interest in exploring the immunogenic potential of BNCT. In this review, we discuss the basic radiobiological and physical aspects of BNCT, traditional and next-generation boron compounds, as well as translational studies exploring the clinical applicability of BNCT. Additionally, we delve into the immunomodulatory potential of BNCT in the era of novel boron agents and examine innovative avenues for exploiting the immunogenicity of BNCT to improve outcomes in difficult-to-treat malignancies.
Immune checkpoint inhibitors and their interaction with proton pump inhibitors–related interstitial nephritis
Miao, Jing , Miao, Jing , Herrmann, Sandra M.

Mayo Clinic

Clinical Kidney Journal | May 16, 2023 | Volume: 16 | Issue: 11 | Pages: 1834-1844

10.1093/ckj/sfad109 | PMID 37915905 Get It

ABSTRACT Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy and outcomes, leading to an expanding use in millions of patients worldwide. However, they can cause a spectrum of immune-related adverse events (irAEs). Essentially, any organs can be affected by irAEs, which have emerged as therapy-limiting side effects. In the kidneys, ICI-associated acute interstitial nephritis (ICI-AIN) leads to acute kidney injury (AKI) in 2%–5% of patients on ICI therapy. AKI associated with ICI therapy pathologically presents with AIN in nearly 90% of the cases, but the pathophysiology of ICI-AIN remains to be defined. The generation of autoreactive T cells in patients receiving AIN-inducible drugs, such as proton pump inhibitors (PPIs), is one of the leading theories, supported by a higher incidence of ICI-AIN in patients on these AIN-inducible drugs. In this review, we will discuss our understanding of the incidence, potential pathophysiological mechanisms, clinical presentations, risk factors, diagnosis, and management of PPI-related AIN and its interaction with ICI therapy.
Weight loss with subcutaneous semaglutide versus other glucagon‐like peptide 1 receptor agonists in type 2 diabetes: a systematic review
Stretton, Brandon , Kovoor, Joshua G. , Bacchi, Stephen , Chang, Shantel , Ngoi, Benjamin , Murray, Tess, Heng, Jonathan, Ovenden, Christopher D. , Heilbronn, Leonie K. , Rayner, Christopher K. , Horowtiz, Michael, Kovoor, Joshua , Thompson, Campbell H , Rayner, C K , Bristow, Thomas C., Gupta, Aashray K. , Maddern, Guy John , Boyd, Mark Alastair , Talley, Nicholas J.

Mayo Clinic

Internal Medicine Journal | May 16, 2023 | Volume: 53 | Issue: 8 | Pages: 1311-1320

10.1111/imj.16126 | PMID 37189293 Get It

AbstractGlucagon‐like peptide 1 receptor agonists (GLP‐1 RAs) reduce elevated blood glucose levels and induce weight loss. Multiple GLP‐1 RAs and one combined GLP‐1/glucose‐dependent insulinotropic polypeptide agonist are currently available. This review was conducted with the aim of summarising direct comparisons between subcutaneous semaglutide and other GLP‐1 RAs in individuals with type 2 diabetes (T2D), particularly with respect to efficacy for inducing weight loss and improving other markers of metabolic health. This systematic review of PubMed and Embase from inception to early 2022 was registered on PROSPERO and was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta‐Analyses and Meta‐Analysis of Observational Studies in Epidemiology guidelines. Of the 740 records identified in the search, five studies fulfilled the inclusion criteria. Comparators included liraglutide, exenatide, dulaglutide and tirzepatide. In the identified studies, multiple dosing regimens were utilised for semaglutide. Randomised trials support the superior efficacy of semaglutide over other GLP‐1 RAs with respect to weight loss in T2D, but tirzepatide is more effective than semaglutide.
The Spectrum of Duodenal Histologic Findings in Patients With Trisomy 21
Alexander, Erin , Stahl, Marisa G. , Weaver, Amy L. , Devara, Janaki , Fahey, Lisa M. , Singh, Arunjot , Leonard, Maureen M. , Weisbrod, Vanessa , Shull, Mary , Silvester, Jocelyn A. , Kramer, Zachary , Kerzner, Benny, Liu, Edwin , Absah, Imad , Silvester, Jocelyn A , Weisbrod, Vanessa

Mayo Clinic

Journal of Pediatric Gastroenterology and Nutrition | May 15, 2023 | Volume: 77 | Issue: 2 | Pages: 184-190

10.1097/mpg.0000000000003825 | PMID 37184455 Get It

Objectives:Patients with Trisomy 21 (T21) commonly have gastrointestinal symptoms and diseases that prompt evaluation with esophagogastroduodenoscopy (EGD). Our objective is to characterize duodenal histological abnormalities in these patients when undergoing EGD. A secondary aim is to explore associations of histologic findings with different therapies.Methods:Patients 30 years old or younger with T21 who underwent EGD from 2000 to 2020 at 6 hospitals were included in this retrospective cohort study. Duodenal biopsies were categorized based on reported histopathology findings as normal or abnormal. Abnormal pathology reports were reviewed and categorized into villous atrophy (VA) and duodenitis without VA. The VA group was further categorized based on the presence or absence of celiac disease (CD).Results:We identified 836 patients with T21 who underwent EGD, 419 (50.1%) of whom had duodenal histologic abnormalities. At the time of the first (index) abnormal duodenal biopsy, 290 of 419 had VA and of those, 172 of 290 met CD diagnostic criteria, while 118 of 290 did not meet CD criteria (nonspecific VA). Among the patients with an abnormal biopsy, acid suppression at the time of the index biopsy was less common in patients with VA‐CD compared to patients without VA or patients with nonspecific VA (12.2% vs 45.7% vs 44.9%).Conclusions:Half of the T21 patients in this cohort had abnormal duodenal biopsies including a subgroup with nonspecific VA. In this cohort, acid suppression use was more prevalent in patients with abnormalities other than CD.
Outcomes of limited versus extensive surgery for chronic rhinosinusitis: A systematic review and meta‐analysis
Ramkumar, Shreya P. , Marks, Lisa , Lal, Devyani , Marino, Michael J. , Lal, Devyani , Marks, Lisa A

Mayo Clinic

International Forum of Allergy & Rhinology | May 15, 2023 | Volume: 13 | Issue: 11 | Pages: 2096-2100

10.1002/alr.23178 | PMID 37184241 Get It

Key points There is no consensus on the extent of appropriate surgery for chronic rhinosinusitis (CRS), particularly CRS without polyps (CRSsNP). There is wide heterogeneity in the definition of “limited” and “extensive” endoscopic sinus surgery (ESS). Studies on the appropriate extent of surgery for CRS are needed.
Dying To Find Out: The Cost of Time at the Dawn of the Multicancer Early Detection Era
Klein, Eric A. , Madhavan, Sarina , Beer, Tomasz M. , Bettegowda, Chetan , Liu, Minetta C. , Hartman, Anne‐Renee , Hackshaw, Allan , Klein, Eric A , Beer, Tomasz M , Bettegowda, Chetan

Mayo Clinic

Cancer Epidemiology, Biomarkers & Prevention | May 15, 2023 | Volume: 32 | Issue: 8 | Pages: 1003-1010

10.1158/1055-9965.epi-22-1275 | PMID 37255363 Get It

Abstract Cancer is a significant burden worldwide that adversely impacts life expectancy, quality of life, health care costs, and workforce productivity. Although currently recommended screening tests for individual cancers reduce mortality, they detect only a minority of all cancers and sacrifice specificity for high sensitivity, resulting in a high cumulative rate of false positives. Blood-based multicancer early detection tests (MCED) based on next-generation sequencing (NGS) and other technologies hold promise for broadening the number of cancer types detected in screened populations and hope for reducing cancer mortality. The promise of this new technology to improve cancer detection rates and make screening more efficient at the population level demands the development of novel trial designs that accelerate clinical adoption. Carefully designed clinical trials are needed to address these issues.