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Mayo Clinic

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Postoperative pain management after ureteroscopy: focused approaches to reducing opiate dependence
Ballantyne, Christopher, Stern, Karen , Ballantyne, Christopher C, Stern, Karen L

Pain Management | June 5, 2025 | Volume: 15 | Issue: 7 | Pages: 401-411

10.1080/17581869.2025.2515001 | PMID 40468954 Get It

Incidental aneurysm rupture during endovascular thrombectomy for acute ischaemic stroke
Dong, Selina X. , Hendriks, Eef J. , Dong, Selina , Huynh, Thien , Volders, David

BMJ Case Reports | June 5, 2025 | Volume: 18 | Issue: 6 | Pages: e265481

10.1136/bcr-2025-265481 | PMID 40473323 Get It

Acute ischaemic stroke remains a leading cause of disability and mortality worldwide. Treatments include systemic fibrinolysis and more recently, endovascular thrombectomy (EVT). The presence of incidental intracranial aneurysms may increase procedural risk during EVT, particularly given their potential higher prevalence in patients with stroke due to shared risk factors such as smoking and hypertension. We present the case of an elderly woman who experienced rupture of an unrecognised intracranial aneurysm during EVT. This case underscores the importance of meticulous preprocedural imaging review, awareness of high-risk anatomical locations and cautious selection of EVT techniques. We also provide a brief review of the literature regarding the incidence, mechanisms and management of intraprocedural aneurysm rupture.
Risk factors, impact, and healthcare use related to initial suicide attempts: comprehensive analysis of Swedish population
Hu, Kejia , Dung, Nguyen Thi Thuy , Borges, Karen, Kuja‐Halkola, Ralf , Butwicka, Agnieszka , Brikell, Isabell , Crowley, James J, D’Onofrio, Brian M. , Larsson, Henrik , Lu, Yi , Crowley, James J. , Nguyen, Thuy-Dung , Rück, Christian , Hu, Kejia , Kuja-Halkola, Ralf , Lu, Yi , Brikell, Isabell , Crowley, James J, Chang, Zheng, Lichtenstein, Paul , Bulik, Cynthia Marie , Sullivan, Patrick F. , Fang, Fang

BMJ Medicine | June 5, 2025 | Volume: 4 | Issue: 1 | Pages: e001129

10.1136/bmjmed-2024-001129 | PMID 40510927 Get It

Objective To provide a comprehensive analysis of initial suicide attempts, covering incidence, risk factors, outcomes, and healthcare use in the month before and the month after the attempts. Design Comprehensive analysis of the Swedish population that included three designs: a retrospective cohort study to investigate incidence and healthcare use, a nested case-control study to investigate risk factors, and a matched cohort study to examine subsequent suicide attempts and mortality. Setting Comprehensive Swedish national registers that include patient diagnoses from hospitals and specialist outpatient care, and cause of death information updated to the end of 2019. Participants 3.7 million people born in Sweden in 1963-98 and followed from age 10 to 57 years. Main outcome measure First lifetime suicide attempt identified in patient and death registers using ICD (international classification of diseases) codes for intentional self-harm, any self-harm with lethal methods or requiring hospital admission, or any self-harm resulting in death. Results The lifetime risk of an initial suicide attempt in the study population was 4.6%, with greater risk in females and highest risk between ages 18 and 24. One in 10 families in Sweden had at least one family member who attempted suicide. Overdose and poisoning were the most common methods. Previous psychiatric disorders, general medical diseases, and adverse life events were associated with increased risk of initial suicide attempt, while higher socioeconomic status was associated with decreased risk. People with an initial suicide attempt were at substantially increased risk of subsequent attempts (hazard ratio 23.4), death by suicide (16.4), and all cause mortality (7.3). At least 60% of those who made an initial suicide attempt had a healthcare contact in the month before the attempt. Conclusions This study provides comprehensive data on the incidence, risk factors, outcomes, and healthcare use of initial suicide attempts in the Swedish population, highlighting the need for systematic prevention efforts for people who have attempted suicide for the first time.
Bronchoscopic lung volume reduction: model for assisted target lobe selection
Hostetter, Logan , Brown, Leah M, Rajagopalan, Srinivasan , Dulohery-Scrodin, Megan, Edell, Eric S. , Lester, Michael , Maldonado, Fabien , Lentz, Robert J. , Bartholmai, Brian J. , Peikert, Tobias, Dulohery-Scrodin, Megan M, Bartholmai, Brian J , Brown, Leah M

BMJ Open Respiratory Research | June 5, 2025 | Volume: 12 | Issue: 1 | Pages: e002903

10.1136/bmjresp-2024-002903 | PMID 40473270 Get It

Introduction Bronchoscopic lung volume reduction with endobronchial valves (EBV) is an effective procedure for patient with severe emphysema to improve lung function, exercise tolerance, dyspnoea and quality of life. Optimisation of patient and treatment lobe selection is essential for successful EBV outcomes. While clinical selection criteria are rigorous, many centres use a multidisciplinary team and rely on previous clinical experience for the selection process. To aid objective clinical decision making, we present a mathematical model to facilitate patient and target lobe selection. Methods A multidisciplinary team reviewed quantitative high-resolution computed tomography (HRCT) analysis from 119 patients to select candidates for EBV and to select a treatment lobe. Two logistic regression models, (1) candidacy for EBV placement and (2) target-lobe selection, were developed based on the normalised distributions of the four quantitative HRCT variables (fissure completeness score, per cent of voxel density with HU < −910 and HU < −950, and lobar volumes) across all five lung lobes. An external cohort of 50 patients (25 candidates and 25 non-candidates) was used to validate the prediction model. Results Performance measures of the training cohort demonstrated an area under the curve (AUC) of 0.91, accuracy of 81%, sensitivity of 93% and specificity of 78% compared with the multidisciplinary teams’ target lobe selection. The validation cohort demonstrated an AUC of 0.89, accuracy of 84%, sensitivity of 88% and specificity of 83% compared with the multidisciplinary team decision making. Conclusions Endobronchial valve lung volume reduction remains a potent palliative measure to improve quality of life in patients with hyperinflated emphysema. Our model for target lobe selection harnesses the multidisciplinary experience at a tertiary care centre to objectively select candidates and target lobes to assist clinicians’ decision making. Future studies investigating prediction of lobar collapse and functional improvement after target lobe selection using our model are needed.
Author Reply to “Regarding ‘The Primary Risk Factors for Season‐Ending Injuries in Professional Basketball Are Minutes Played Per Game and Later Season Games’”
Menon, Sanjit , Morikawa, Landon , Buckner‐Petty, Skye , Chhabra, Anikar , Tummala, Sailesh, Buckner-Petty, Skye, Chhabra, Anikar , Tummala, Sailesh V , Tummala, Sailesh V.

Arthroscopy | June 5, 2025 | Volume: 41 | Issue: 9 | Pages: 3283-3285

10.1016/j.arthro.2025.05.032 | PMID 40480480 Get It

Impact of Pretransplant Antimicrobial Sulfonamide Allergy Label in Kidney Transplant Recipients
Cuellar, Cesar Campos, Venugopal, A. , Pleqi, Vasili, Hochwald, Alex, Ma, Yaohua , Gonzales, Alexei, Powers, Harry Ross, Wadei, Hani M , Venugopal, Amogharvasha, Powers, Harry Ross, Wadei, Hani M. , Cuellar, Cesar Campos, Venugopal, Amogharvasha, Gonzales, Alexei

Transplant Infectious Disease | June 5, 2025 | Volume: 27 | Issue: 4 | Pages: No page available

10.1111/tid.70063 | PMID 40468705 Get It

ABSTRACT Background Sulfa antibiotic allergy labels (SALs) are encountered frequently in kidney transplant recipients (KTs). This often results in patients receiving second‐line prophylaxis for both Pneumocystis jiroveci and urinary tract infections (UTIs). The effect of SAL on outcomes including UTIs after KT is unclear. Methods In our single‐center retrospective cohort study, we investigated the effect of SALs on bacteriuria after KT. We identified patients with pre‐KT SALs from 2011 to 2022. A matched cohort was then created using KT with no pretransplant SALs. The groups were compared using proportional analysis and univariable and multivariable Cox proportional regression models. The primary outcome of interest was the proportion of individuals experiencing one or more episodes of bacteriuria within 1 year posttransplant. Secondary outcomes included bacteremic UTIs, acute kidney injury, and opportunistic infections. Results We found that the proportion of individuals experiencing bacteriuria within the first‐year posttransplant was significantly greater in the SAL group versus the control group ( n = 21, 28% vs. n = 22, 14.7%, p = 0.012). This result was also seen in univariable and multivariable survival analysis. In addition, episodes of UTI with associated bacteremia ( n = 11, 14.7% vs. n = 5, 3.3%, p = 0.002) were statistically significantly higher in the SAL group. Conclusion There was a significantly greater number of episodes of bacteriuria in the first‐year posttransplant in subjects with pretransplant SAL. Based on our findings, we suggest that all KTs with pretransplant SALs undergo evaluation and intervention prior to transplantation. image
Real-world survival outcomes and MDM2 prevalence in US patients with metastatic dedifferentiated liposarcoma
Robinson, Steven I. , Klein, Alyssa , Stanhope, Stephen A., Evans, Kathryn , Agulnik, Mark , Robinson, Steven I

Future Oncology | June 5, 2025 | Volume: 21 | Issue: 14 | Pages: 1797-1807

10.1080/14796694.2025.2502319 | PMID 40468683 Get It

Progress in Pharmacogenomics Implementation in the United States: Barrier Erosion and Remaining Challenges
Smith, D. Max , Aquilante, Christina L. , Deverka, Patricia A. , Devine, Emily Beth , Dunnenberger, Henry M. , Empey, Philip E. , Hertz, Daniel L. , Monte, Andrew A. , Moyer, Ann M. , Pratt, Victoria M. , Saulsberry, Loren , Oni‐Orisan, Akinyemi , Douglas, Michael P , Devine, Beth , Dunnenberger, Henry M , Empey, Philip E , Hertz, Daniel L , Moyer, AM , Patel, Jai N , Pratt, Victoria M , Saulsberry, Loren , Scott, Stuart A , Voora, Deepak , Woodahl, Erica L , Whirl-Carrillo, Michelle , Oni-Orisan, Akinyemi , Smith, D Max , Scott, Stuart A. , Whirl‐Carrillo, Michelle

Clinical Pharmacology & Therapeutics | June 5, 2025 | Volume: 118 | Issue: 4 | Pages: 778-789

10.1002/cpt.3736 | PMID 40468601 Get It

Barriers to incorporating pharmacogenetics into routine clinical practice in the United States are well documented. Initial surveys by the Clinical Pharmacogenetics Implementation Consortium (CPIC) in 2009 and 2010 identified barriers across four key domains that have hindered the widespread adoption of clinical pharmacogenetic testing. These are presented verbatim as: (i) absence of a definition of the processes required to interpret genotype information and to translate genetic information into clinical actions; (ii) need for recommended drug/gene pairs to implement clinically now; (iii) clinician resistance to consider pharmacogenetic information at the bedside; and (iv) concerns about test costs and reimbursement. Over time, many of these challenges have been overcome, and clinical pharmacogenetic testing has subsequently reached broader implementation. Despite this progress, several barriers remain that block further adoption. This narrative review used authors' expertise and experience to identify and describe current barriers to pharmacogenetic implementation across seven domains in the United States: equity and inclusion; guidelines and supporting evidence; regulatory agency oversight; payer coverage and insurance; availability of quality pharmacogenetic tests; electronic health records; and provider and patient education. Within each domain, it revisits past successes and challenges and explores remaining barriers. We also propose solutions to address ongoing challenges across these domains, including further expansion of recommendations beyond pharmacogenetic‐specific guidelines, standards for designing clinical decision support tools, and broader pharmacogenetics education. Addressing these remaining obstacles directs work to enable broader adoption of clinical pharmacogenetic implementation to ultimately improve patient outcomes.
Biologic Therapies for Managing Cutaneous Immune‐Related Adverse Events in Cancer Patients Receiving Immune Checkpoint Inhibitors
Tran, Tung S, Piche, Shannon L., Wetter, David A. , Nguyen, Giang Huong , Tran, Tung S. , Tran, Tung S , Nguyen, Giang H

International Journal of Dermatology | June 5, 2025 | Volume: 64 | Issue: 11 | Pages: 2140-2142

10.1111/ijd.17894 | PMID 40468559 Get It

Real World Performance of an Individualized Antitachycardia Pacing Algorithm
Jackson, Troy , Yee, Raymond, Taepke, Robert T., Cheng, Alan , Birgersdotter‐Green, Ulrika , Cha, Yong‐Mei , Taepke, Robert, Singh, Jagmeet P , Yee, Raymond

Journal of Cardiovascular Electrophysiology | June 5, 2025 | Volume: 36 | Issue: 8 | Pages: 1875-1885

10.1111/jce.16747 | PMID 40468565 Get It

ABSTRACT Background A novel individualized antitachycardia pacing (IATP) algorithm using the post‐pacing interval for real‐time control has been introduced. Performance information is limited to a small safety and feasibility study with additional single‐center and case studies. A larger‐scale analysis is needed to better understand algorithm performance. Methods Deidentified remote monitoring transmissions from devices with the IATP therapy applied were randomly selected. Rhythms were classified and effects of the novel algorithm were assessed. For monomorphic ventricular tachycardias (MVTs) proportions of successful therapy, shock‐free episodes, and acceleration were calculated using generalized estimating equations to correct for multiple episodes and compute statistics of the algorithm's performance. Results There were 2259 MVT episodes in 336 patients. IATP succeeded in 87.1% of MVT episodes with 89.9% of MVT episodes ultimately free of shock therapy. Based on multivariate analysis, significant factors in therapy success were programming of at least the recommended number of sequences (90% at least recommended vs 73%, p = 0.00088) and female sex (95% for females vs 86%, p = 0.002). A trend to higher success was found for MVT with a cycle length of 320 ms or greater (90% vs. 83%, p = 0.10). The IATP accelerated 3.6% of MVT episodes. None of the available factors was significantly associated with acceleration in the multivariate analysis. Conclusions The IATP algorithm succeeded in a large proportion of MVT episodes and with low acceleration in patients randomly selected from remote monitoring transmissions. Using at least the recommended number of sequences had the strongest association with successful therapy.