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400 citation(s) found for "Aarhus, L L".

Posterior Lateral Meniscal Root and Oblique Radial Tears: The Biomechanical Evidence Supports Repair of These Tears, Although Long‐Term Clinical Studies Are Necessary
LaPrade, Robert F. , Geeslin, Andrew G. , Cohen, Moisés , Engebretsen, Lars , Faucett, Scott C. , Getgood, Alan , Inderhaug, Eivind , Johnson, Darren L., Kopf, Sebastian , Musahl, Volker , Negrín, Roberto , Riboh, Jonathan C. , Spalding, Tim , Engebretsen, Lars , LaPrade, Robert F , Chahla, Jorge , Krych, Aaron J. , Larson, Christopher Michael , Lind, Martin , Moatshe, Gilbert , Murray, Iain R. , Seil, Romain

Arthroscopy | November 30, 2022 | Volume: 38 | Issue: 12 | Pages: 3095-3101

10.1016/j.arthro.2022.09.015 | PMID 36462774 Get It

MGUS and SMM Plasma Cells Exhibit a Senescence-like Phenotype and Accumulation of Transposable Elements That May Contribute to Disease Progression
Guilatco, Angelo Jose, Hachfeld, Christine, Ruan, Ming, Royzenblat, Sonya , Xu, Ming, Kourelis, Taxiarchis , Kirkland, James L. , Weivoda, Megan , Borges, Gabriel Álvares , Edwards, Claire M. , Diaz‐delCastillo, Marta , Andersen, Thomas Levin , Tchkonia, Tamar , Drake, Matthew T.

Blood | November 28, 2022 | Volume: 140 | Issue: Supplement 1 | Pages: 9966-9967

10.1182/blood-2022-170571 Get It

Cardiac Resynchronization Therapy for Adult Patients With a Failing Systemic Right Ventricle: A Multicenter Study
Kharbanda, Rohit K. , Moore, Jeremy P. , Lloyd, Michael S. , Galotti, Robert, Bogers, Ad J.J.C. , Taverne, Yannick J.H.J. , Madhavan, Malini , McLeod, Christopher J. , Dubin, Anne M. , Mah, Douglas Y. , Chang, Philip M. , Kamp, Anna , Nielsen, Jens Cosedis , Aydın, Alper , Tanel, Ronn E. , Shah, Maully J. , Pilcher, Thomas , Evertz, Reinder , Tan, Reina Bianca , Czosek, Richard J. , Shivkumar, Kalyanam , Groot, Natasja M.S. de , Nielsen, Jens C , Khairy, Paul , Tan, Reina B , Czosek, Richard J , Shivkumar, Kalyanam , de Groot, Natasja M S , Dubin, Anne M , McLeod, Christopher J , Pilcher, Thomas A.

Journal of the American Heart Association | November 8, 2022 | Volume: 11 | Issue: 22 | Pages: No page available

10.1161/jaha.121.025121 | PMID 36346046 Get It

Background The objective of this international multicenter study was to investigate both early and late outcomes of cardiac resynchronization therapy (CRT) in patients with a systemic right ventricle (SRV) and to identify predictors for congestive heart failure readmissions and mortality. Methods and Results This retrospective international multicenter study included 13 centers. The study population comprised 80 adult patients with SRV (48.9% women) with a mean age of 45±14 (range, 18–77) years at initiation of CRT. Median follow‐up time was 4.1 (25th–75th percentile, 1.3–8.3) years. Underlying congenital heart disease consisted of congenitally corrected transposition of the great arteries and dextro‐transposition of the great arteries in 63 (78.8%) and 17 (21.3%) patients, respectively. CRT resulted in significant improvement in functional class (before CRT: III, 25th–75th percentile, II–III; after CRT: II, 25th–75th percentile, II–III; P =0.005) and QRS duration (before CRT: 176±27; after CRT: 150±24 milliseconds; P =0.003) in patients with pre‐CRT ventricular pacing who underwent an upgrade to a CRT device (n=49). These improvements persisted during long‐term follow‐up with a marginal but significant increase in SRV function (before CRT; 30%, 25th–75th percentile, 25–35; after CRT: 31%, 25th–75th percentile, 21–38; P =0.049). In contrast, no beneficial change in the above‐mentioned variables was observed in patients who underwent de novo CRT (n=31). A quarter of all patients were readmitted for heart failure during follow‐up, and mortality at latest follow‐up was 21.3%. Conclusions This international experience with CRT in patients with an SRV demonstrated that CRT in selected patients with SRV dysfunction and pacing‐induced dyssynchrony yielded consistent improvement in QRS duration and New York Heart Association functional status, with a marginal increase in SRV function.
Efficacy and Safety of Parathyroid Hormone Replacement With TransCon PTH in Hypoparathyroidism: 26-Week Results From the Phase 3 PaTHway Trial
Khan, Aliya , Rubin, Mishaela R. , Schwarz, Peter , Vokes, Tamara , Shoback, Dolores , Palermo, Andrea , Marcocci, Claudio , Clarke, B.L. , Abbott, Lisa G, Hofbauer, Lorenz C. , Kohlmeier, Lynn, Pihl, Susanne, An, Xuebei, Eng, Walter Frank, Ukena, Jenny, Sibley, Christopher T. , Shu, Aimee D , Khan, Aliya A , Gagnon, Claudia , Palermo, Andrea , Marcocci, Claudio , Clarke, Bart L , Shu, Aimee D , Hofbauer, Lorenz C , Schwarz, Peter , Smith, Alden Raymond , Rejnmark, Lars

Journal of Bone and Mineral Research | October 21, 2022 | Volume: 38 | Issue: 1 | Pages: 14-25

10.1002/jbmr.4726 | PMID 36271471 Get It

ABSTRACT Conventional therapy for hypoparathyroidism consisting of active vitamin D and calcium aims to alleviate hypocalcemia but fails to restore normal parathyroid hormone (PTH) physiology. PTH replacement therapy is the ideal physiologic treatment for hypoparathyroidism. The double-blind, placebo-controlled, 26-week, phase 3 PaTHway trial assessed the efficacy and safety of PTH replacement therapy for hypoparathyroidism individuals with the investigational drug TransCon PTH (palopegteriparatide). Participants (n = 84) were randomized 3:1 to once-daily TransCon PTH (initially 18 μg/d) or placebo, both co-administered with conventional therapy. The study drug and conventional therapy were titrated according to a dosing algorithm guided by serum calcium. The composite primary efficacy endpoint was the proportion of participants at week 26 who achieved normal albumin-adjusted serum calcium levels (8.3–10.6 mg/dL), independence from conventional therapy (requiring no active vitamin D and ≤600 mg/d of calcium), and no increase in study drug over 4 weeks before week 26. Other outcomes of interest included health-related quality of life measured by the 36-Item Short Form Survey (SF-36), hypoparathyroidism-related symptoms, functioning, and well-being measured by the Hypoparathyroidism Patient Experience Scale (HPES), and urinary calcium excretion. At week 26, 79% (48/61) of participants treated with TransCon PTH versus 5% (1/21) wiplacebo met the composite primary efficacy endpoint (p < 0.0001). TransCon PTH treatment demonstrated a significant improvement in all key secondary endpoint HPES domain scores (all p < 0.01) and the SF-36 Physical Functioning subscale score (p = 0.0347) compared with placebo. Additionally, 93% (57/61) of participants treated with TransCon PTH achieved independence from conventional therapy. TransCon PTH treatment normalized mean 24-hour urine calcium. Overall, 82% (50/61) treated with TransCon PTH and 100% (21/21) wiplacebo experienced adverse events; most were mild (46%) or moderate (46%). No study drug-related withdrawals occurred. In conclusion, TransCon PTH maintained normocalcemia while permitting independence from conventional therapy and was well-tolerated in individuals with hypoparathyroidism. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR). Abstract TransCon PTH is an investigational once-daily prodrug providing sustained release of active PTH designed to maintain stable PTH levels in the physiological range for 24 hours/day. The PaTHway trial met all primary and key secondary endpoints with statistically significant differences from placebo. Most adverse events (AEs) were mild/moderate. Injection-site reactions and headaches were the most common treatment-related AEs.
Cardiac computed tomography following Watchman FLX implantation: device-related thrombus or device healing?
Kramer, Anders , Korsholm, Kasper , Jensen, Jesper Møller , Nørgaard, Bjarne Linde , Peelukhana, Srikara, Herbst, Thomáš, Horton, Rodney , Kar, Saibal , Saw, Jacqueline , Alkhouli, Mohamad , Nielsen‐Kudsk, Jens Erik , Kramer, Anders Dahl , Alkhouli, Mohamad , Korsholm, Kasper , Møller Jensen, Jesper , Nørgaard, Bjarne Linde , Peelukhana, Srikara Viswanath

European Heart Journal - Cardiovascular Imaging | October 20, 2022 | Volume: 24 | Issue: 2 | Pages: 250-259

10.1093/ehjci/jeac222 | PMID 36336848 Get It

Abstract Aims Cardiac computed tomography (CT) is increasingly utilized during follow-up after left atrial appendage closure (LAAC). Hypoattenuated thickening (HAT) is a common finding and might represent either benign device healing or device-related thrombosis (DRT). The appearance and characteristics of HAT associated with the Watchman FLX have not been previously described. Therefore, we sought to investigate cardiac CT findings during follow-up after Watchman FLX implantation with a focus on HAT and DRT. Methods and results Retrospective single-centre, observational study including all patients with successful Watchman FLX implantation and follow-up cardiac CT between March 2019 and September 2021 (n = 244). Blinded analysis of CT images was performed describing the localization, extent, and morphology of HAT and correlated to imaging and histology findings in a canine model. Relevant clinical and preclinical ethical approvals were obtained. Overall, HAT was present in 156 cases (64%) and could be classified as either subfabric hypoattenuation (n = 59), flat sessile HAT (n = 78), protruding sessile HAT (n = 16), or pedunculated HAT (n = 3). All cases of pedunculated HAT and five cases of protruding sessile HAT were considered as high-grade HAT (n = 7). Subfabric hypoattenuation and flat sessile HAT correlated with device healing and endothelialization in histological analysis of explanted devices. Conclusion Subfabric hypoattenuation and flat sessile HAT are frequent CT findings for Watchman FLX, likely representing benign device healing and endothelialization. Pedunculated HAT and protruding HAT are infrequent CT findings that might represent DRT.