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Three-Year Outcomes of the Abre Venous Self-Expanding Stent System in Patients with Symptomatic Iliofemoral Venous Outflow Obstruction

Black, Stephen; Sapoval, Marc; Dexter, David J; Gibson, Kathleen; Kolluri, Raghu; Razavi, Mahmood; deFreitas, Dorian J; Wang, Hong; Brucato, Stephanie; Murphy, Erin; ,
PURPOSE/OBJECTIVE:To report 36-month outcomes and subgroup analysis of the ABRE study evaluating the safety and effectiveness of the Abre venous self-expanding stent system for the treatment of symptomatic iliofemoral venous outflow obstruction disease. METHODS:The ABRE study was a prospective, multicenter, nonrandomized study that enrolled and implanted Abre venous stents in 200 participants (mean age 51.5 years [SD ± 15.9], 66.5% women) with symptomatic iliofemoral venous outflow obstruction at 24 global sites. Outcomes assessed through 36 months included patency, major adverse events, stent migration, stent fracture, and quality-of-life changes. Adverse events and imaging studies were adjudicated by independent clinical events committee and core laboratories, respectively. RESULTS:Primary, primary-assisted, and secondary patency through 36 months by Kaplan-Meier estimates were 81.6%, 84.8%, and 86.3%, respectively. The cumulative incidence of major adverse events through 36 months was 10.2%, mainly driven by 12 thrombosis events. Subgroup analyses demonstrated a primary patency of 76.5% in the acute deep vein thrombosis group, 70.4% in the postthrombotic syndrome group, and 97.1% in the nonthrombotic iliac vein lesion group through 36 months. The overall mean lesion length was 112.4 mm (SD ± 66.1). There were no stent fractures or migrations in this study. Quality of life and venous functional assessments demonstrated significant improvements from baseline to 36 months across all patient subsets. CONCLUSIONS:Results from the ABRE study demonstrated sustained patency with a good safety profile after implantation of a dedicated venous stent in patients with symptomatic iliofemoral venous outflow obstruction disease.
PMID: 38336032
ISSN: 1535-7732
CID: 5691242

Sharing Perioperative Nursing Expertise Through Publication: A Guide for the Novice Author

Vortman, Rebecca; Darbyshire, Pamayla E; Talatala, Ray-An
Perioperative nurses can share their expertise by writing for publication in a peer-reviewed journal. Writing can help perioperative nurses grow their professional careers and advance the science of the perioperative nursing specialty. Despite the value and importance of publishing, perioperative nurses may lack confidence and fear rejection and negative feedback; increasing their knowledge and understanding of the authoring and publishing processes can assuage these fears. This education article describes concepts associated with scholarly publishing for authors and offers strategies to encourage perioperative nurses to share their practice experiences or research via peer-reviewed journals. Key steps associated with the writing and publication process are described. The article also explains the editorial and peer-review processes and provides supportive strategies for authors when a manuscript is not accepted initially.
PMID: 38407342
ISSN: 1878-0369
CID: 5691362

Outcomes of a 3-Year Quality Improvement Study to Improve Advance Care Planning in Patients With Decompensated Cirrhosis

Patel, Arpan; Bowman, Chip A; Prause, Nicole; Kilaru, Saikiran M; Nguyen, Andrew; Kogekar, Nina; Cohen, Cynthia; Channen, Lindsay; Harty, Alyson; Perumalswami, Ponni; Dietrich, Douglas; Schiano, Thomas; Woodrell, Christopher; Agarwal, Ritu
INTRODUCTION:To report outcomes of a 3-year quality improvement pilot study to improve advance directive (AD) completion. METHODS:The pilot consisted of champions, education, electronic health record templates, and workflow changes. We assessed changes, predictors, and effects of AD completion. RESULTS:The pilot led to greater (8.3%-36%) and earlier AD completion, particularly among those divorced, with alcohol-associated liver disease, and with higher Model of End-Stage Liver Disease-Sodium score. Decedents whose AD specified nonaggressive goals experienced lower hospital lengths of stay. DISCUSSION:Advance care planning initiatives are feasible and may reduce health care utilization among decedents requesting less aggressive care.
PMCID:10904002
PMID: 37934193
ISSN: 1572-0241
CID: 5691072

A Blueprint for a Comprehensive, Multidisciplinary Pancreatic Cancer Screening Program

Fasullo, Matthew; Simeone, Diane; Everett, Jessica; Agarunov, Emil; Khanna, Lauren; Gonda, Tamas
PMID: 37782292
ISSN: 1572-0241
CID: 5691062

"A Light at the End of the Tunnel": Experiences With Peer Specialists in the Open Dialogue Model

Friesen, Phoebe; Wusinich, Christina; Lynch, Katherine; Russell, David
OBJECTIVE/UNASSIGNED:The authors examined participants' experiences with peer specialists in Parachute NYC, a community mental health program of support teams trained in Open Dialogue and intentional peer support. METHODS/UNASSIGNED:Qualitative interviews were conducted with eight enrollees and 10 network members (enrollees' family members). All excerpts coded as pertaining to peers were thematically analyzed. RESULTS/UNASSIGNED:Experiences with peer specialists were mostly positive. Participants especially valued peers' relatability and tendency to instill hope and engender empathy among enrollees and network members; peers' ability to foster community connections was also highly regarded. Generally, enrollees benefited from having peers and other health care professionals on a Parachute team because of their different forms of expertise. Concerns about peer specialists in dialogic care were reported by some network members, who questioned peers' degree of shared experiences, professionalism, and contributions to team unity. CONCLUSIONS/UNASSIGNED:Despite generally positive findings, the optimal role for peers within the Open Dialogue model needs further exploration.
PMID: 37752824
ISSN: 1557-9700
CID: 5691052

Leaving a Legacy: Allied Health Professionals' Perceptions of Fertility Preservation and Posthumous Reproduction for Adolescent and Young Adults with a Poor Cancer Prognosis

Barrett, Francesca; Sampson, Amani; Campo-Engelstein, Lisa; Caplan, Arthur; Vadaparampil, Susan T; Quinn, Gwendolyn P
PMCID:10877393
PMID: 37294937
ISSN: 2156-535x
CID: 5691012

Attention-deficit/hyperactivity disorder

Faraone, Stephen V; Bellgrove, Mark A; Brikell, Isabell; Cortese, Samuele; Hartman, Catharina A; Hollis, Chris; Newcorn, Jeffrey H; Philipsen, Alexandra; Polanczyk, Guilherme V; Rubia, Katya; Sibley, Margaret H; Buitelaar, Jan K
Attention-deficit/hyperactivity disorder (ADHD; also known as hyperkinetic disorder) is a common neurodevelopmental condition that affects children and adults worldwide. ADHD has a predominantly genetic aetiology that involves common and rare genetic variants. Some environmental correlates of the disorder have been discovered but causation has been difficult to establish. The heterogeneity of the condition is evident in the diverse presentation of symptoms and levels of impairment, the numerous co-occurring mental and physical conditions, the various domains of neurocognitive impairment, and extensive minor structural and functional brain differences. The diagnosis of ADHD is reliable and valid when evaluated with standard diagnostic criteria. Curative treatments for ADHD do not exist but evidence-based treatments substantially reduce symptoms and/or functional impairment. Medications are effective for core symptoms and are usually well tolerated. Some non-pharmacological treatments are valuable, especially for improving adaptive functioning. Clinical and neurobiological research is ongoing and could lead to the creation of personalized diagnostic and therapeutic approaches for this disorder.
PMID: 38388701
ISSN: 2056-676x
CID: 5691282

Surgical Considerations in the Management of Adolescent Endometriosis-An Expert Commentary

Tyson, Nichole; Shim, Jessica; Lee, Ted; King, Cara R; Einarsson, Jon; Hornstein, Mark D; Laufer, Marc R
Given the complexities and controversies that exist in diagnosing adult endometriosis, as well as optimizing medical and surgical management, it is not surprising that there is even more ambiguity and inconsistency in the optimal surgical care of endometriosis in the adolescent. This collaborative commentary aimed to provide evidence-based recommendations optimizing the role of surgical interventions for endometriosis in the adolescent patient with input from experts in minimally invasive gynecologic surgery, pediatric and adolescent gynecology, and infertility/reproductive medicine.
PMID: 38325581
ISSN: 1553-4669
CID: 5691232

Intralesional Injections of a TNF-α Inhibitor to Treat Orofacial Granulomatosis

Lee, Jasmine; Kurien, Lisa; Marciano, Tuvia
PMID: 38243814
ISSN: 1536-4844
CID: 5691182

TROPHY-U-01, a phase II open-label study of sacituzumab govitecan in patients with metastatic urothelial carcinoma progressing after platinum-based chemotherapy and checkpoint inhibitors: updated safety and efficacy outcomes

Loriot, Y; Petrylak, D P; Rezazadeh Kalebasty, A; Fléchon, A; Jain, R K; Gupta, S; Bupathi, M; Beuzeboc, P; Palmbos, P; Balar, A V; Kyriakopoulos, C E; Pouessel, D; Sternberg, C N; Tonelli, J; Sierecki, M; Zhou, H; Grivas, P; Barthélémy, P; Tagawa, S T
BACKGROUND:Sacituzumab govitecan (SG) is a Trop-2-directed antibody-drug conjugate containing cytotoxic SN-38, the active metabolite of irinotecan. SG received accelerated US Food and Drug Administration approval for locally advanced (LA) or metastatic urothelial carcinoma (mUC) previously treated with platinum-based chemotherapy and a checkpoint inhibitor, based on cohort 1 of the TROPHY-U-01 study. Mutations in the uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene are associated with increased adverse events (AEs) with irinotecan-based therapies. Whether UGT1A1 status could impact SG toxicity and efficacy remains unclear. PATIENTS AND METHODS/METHODS:TROPHY-U-01 (NCT03547973) is a multicohort, open-label, phase II registrational study. Cohort 1 includes patients with LA or mUC who progressed after platinum- and checkpoint inhibitor-based therapies. SG was administered at 10 mg/kg intravenously on days 1 and 8 of 21-day cycles. The primary endpoint was objective response rate (ORR) per central review; secondary endpoints included progression-free survival, overall survival, and safety. Post hoc safety analyses were exploratory with descriptive statistics. Updated analyses include longer follow-up. RESULTS:Cohort 1 included 113 patients. At a median follow-up of 10.5 months, ORR was 28% (95% CI 20.2% to 37.6%). Median progression-free survival and overall survival were 5.4 months (95% CI 3.5-6.9 months) and 10.9 months (95% CI 8.9-13.8 months), respectively. Occurrence of grade ≥3 treatment-related AEs and treatment-related discontinuation were consistent with prior reports. UGT1A1 status was wildtype (∗1|∗1) in 40%, heterozygous (∗1|∗28) in 42%, homozygous (∗28|∗28) in 12%, and missing in 6% of patients. In patients with ∗1|∗1, ∗1|∗28, and ∗28|∗28 genotypes, any grade treatment-related AEs occurred in 93%, 94%, and 100% of patients, respectively, and were managed similarly regardless of UGT1A1 status. CONCLUSIONS:With longer follow-up, the ORR remains high in patients with heavily pretreated LA or mUC. Safety data were consistent with the known SG toxicity profile. AE incidence varied across UGT1A1 subgroups; however, discontinuation rates remained relatively low for all groups.
PMID: 38244927
ISSN: 1569-8041
CID: 5691202