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560 citation(s) found for "Yu, Mei".

Subcutaneous implantable cardioverter‐defibrillator noise following left ventricular assist device implantation
Khetarpal, Banveet Kaur , Javaid, Awad , Lee, Justin Z. , Mulpuru, Siva K. , Sorajja, Dan , Cha, Yong‐Mei , Mulpuru, Siva K , Kusumoto, Fred , Srivathsan, Komandoor

Journal of Arrhythmia | February 13, 2023 | Volume: 39 | Issue: 2 | Pages: 198-206

10.1002/joa3.12826 | PMID 37021015 Get It

AbstractBackgroundThe incidence and impact of noise in a subcutaneous implantable cardioverter defibrillator (S‐ICD) after left ventricular assist device (LVAD) implantation is not well established.MethodsWe performed a retrospective study of patients implanted with LVAD and with a pre‐existing S‐ICD between January 2005 and December 2020 at the three Mayo Clinic centers (Minnesota, Arizona, and Florida).ResultsOf the 908 LVAD patients, a pre‐existing S‐ICD was present in 9 patients (mean age 49.1 ± 13.7 years, 66.7% males), 100% with Boston Scientific third‐generation EMBLEM MRI S‐ICD, 11% with HeartMate II (HM II), 44% with HeartMate 3 (HM 3), and 44% with HeartWare (HW) LVAD. The incidence of noise from LVAD‐related electromagnetic interference (EMI) was 33% and was only seen with HM 3 LVAD. Multiple measures attempted to resolve noise, including using alternative S‐ICD sensing vector, adjusting S‐ICD time zone, and increasing LVAD pump speed, were unsuccessful, necessitating S‐ICD device therapies to be turned off permanently.ConclusionsThe incidence of LVAD‐related S‐ICD noise is high in patients with concomitant LVAD and S‐ICD with significant impact on device function. As conservative management failed to resolve the EMI, the S‐ICDs had to be programmed off to avoid inappropriate shocks. This study highlights the importance of awareness of LVAD‐SICD device interference and the need to improve S‐ICD detection algorithms to eliminate noise.
Outcome and safety of intraoperative defibrillation testing during device replacement: the Simpler trial
Nof, Eyal , Rav, Moshe , Beinart, Roy, Kutyifa, Valentina , Regev, Ehud , Biffi, Mauro , Cha, Yong‐Mei , Ovdat, Tal , Klempfner, Robert , Glikson, Michael , Goldenberg, Ilan , Milman, Anat , Rav Acha, Moshe , Beinart, Roy , Kutyifa, Valentina , Merkely, Béla , Regev, Ehud , Biffi, Mauro , Cha, Yong-Mei , Ovdat, Tal , Glikson, Michael

EP Europace | January 13, 2023 | Volume: 25 | Issue: 3 | Pages: 956-960

10.1093/europace/euac282 | PMID 36636968 Get It

AbstractAimsIntraoperative defibrillation testing (DT) during implant or replacement of implantable cardioverter-defibrillators (ICDs) has been a matter of debate for many years. This debate was put to rest by the Simple and Nordic ICD trials, and the practice of testing during new implantations has essentially been almost abandoned. Old registries demonstrated an increased incidence of significant findings in DT during replacements. The aim of the present study was to evaluate frequency of significant findings and safety of DT in subjects undergoing device replacement.Methods and resultsA prospective observational multi-centre study included consecutive patients undergoing ICD generator replacement. The primary outcome was a failure to terminate induced ventricular fibrillation (VF) with a single shock 10 J below the maximal capacity of the device. Secondary outcomes included complications of DT. Patients were followed-up at 1- and 6-months post-procedure. A total of 92 patients were eligible, and consented to the study, of which 84 underwent DT during battery replacement. The median age was 68 years and 79.8% were males. Induction of VF was successful in 84 patients as was a successful conversion on the first attempt in all. There were no procedure-related complications. During follow up one patient had two appropriate ICD shock events. In four patients, ICD programming was changed. None suffered inappropriate shock. There was no evidence of lead malfunction. Two deaths occurred, none of which was related to arrhythmia.ConclusionThe present study found DT was not associated with complications in patients undergoing ICD generator replacement but produced no clinically important information.
COVID-19 Deaths and the Impact of Health Disparities, Hospital Characteristics, Community, Social Distancing, and Health System Competition
Zhao, Mei , Hamadi, Hanadi , Haley, D. Rob , Xu, Jing , Tafili, Aurora , Spaulding, Aaron , Hamadi, Hanadi Y , Spaulding, Aaron , Haley, Donald Rob , Zhao, Mei

Population Health Management | December 28, 2022 | Volume: 25 | Issue: 6 | Pages: 807-813

10.1089/pop.2022.0144 | PMID 36576382 Get It

The United States has one of the highest cumulative mortalities of coronavirus disease 2019 (COVID-19) and has reached 1 million deaths as of May 19th, 2022. Understanding which community and hospital factors contributed to disparities in COVID-19 mortality is important to inform public health strategies. This study aimed to explore the potential relationship between hospital service area (1) community (ie, health professional shortage areas, market competition, and uninsured percentage) and (2) hospital (ie, teaching, system, and ownership status) characteristics (2013–2018) on publicly available COVD-19 (February to October 2020) mortality data. The study included 2514 health service areas and used multilevel mixed-effects linear model to account for the multilevel data structure. The outcome measure was the number of COVID-19 deaths. This study found that public health, as opposed to acute care provision, was associated with community health and, ultimately, COVID-19 mortality. The study found that population characteristics including more uninsured greater proportion of those over 65 years, more diverse populations, and larger populations were all associated with a higher rate of death. In addition, communities with fewer hospitals were associated with a lower rate of death. When considering region in the United States, the west region showed a higher rate of death than all other regions. The association between some community characteristics and higher COVID-19 deaths demonstrated that access to health care, either for COVID-19 infection or worse health from higher disease burden, is strongly associated with COVID-19 deaths. Thus, to be better prepared for potential future pandemics, a greater emphasis on public health infrastructure is needed.
Cloned antibodies from patients with HIT provide new clues to HIT pathogenesis
Zhu, Wen , Zheng, Yongwei , Yu, Mei , Wu, Ya‐Ling , Wei, Jianhui, Fu, Guoping, Schneider, Nicholas O. , Jones, Curtis G., Irani, Mehraboon S. , Padmanabhan, Anand , Aster, Richard H. , Wang, Demin , Wen, Renren , Zhou, Lu , Schneider, Nicholas , Padmanabhan, Anand , Wang, Demin , Wen, Renren , Yu, Mei, Wu, Yaling, Lü, Zhou

Blood | December 9, 2022 | Volume: 141 | Issue: 9 | Pages: 1060-1069

10.1182/blood.2022017612 | PMID 36493339 Get It

AbstractHeparin-induced thrombocytopenia (HIT) is a serious adverse drug reaction characterized by antibodies that recognize platelet factor 4/heparin complexes (PF4/H) and activate platelets to create a prothrombotic state. Although a high percentage of heparin-treated patients produce antibodies to PF4/H, only a subset also makes antibodies that are platelet activating (PA). A close correlation between PA antibodies and the likelihood of experiencing HIT has been demonstrated in clinical studies, but how PA (presumptively pathogenic) and nonactivating (NA) (presumptively benign) antibodies differ from each other at the molecular level is unknown. To address this issue, we cloned 7 PA and 47 NA PF4/H-binding antibodies from 6 patients with HIT and characterized their structural and functional properties. Findings showed that PA clones differed significantly from NA clones in possessing 1 of 2 heavy chain complementarity-determining region 3 (HCDR3) motifs, RX1-2R/KX1-2R/H (RKH) and YYYYY (Y5), in an unusually long complementarity-determining region 3 (≥20 residues). Mutagenic studies showed that modification of either motif in PA clones reduced or abolished their PA activity and that appropriate amino acid substitutions in HCDR3 of NA clones can cause them to become PA. Repertoire sequencing showed that the frequency of peripheral blood IgG+ B cells possessing RKH or Y5 was significantly higher in patients with HIT than in patients without HIT given heparin, indicating expansion of B cells possessing RKH or Y5 in HIT. These findings imply that antibodies possessing RKH or Y5 are relevant to HIT pathogenesis and suggest new approaches to diagnosis and treatment of this condition.
Comparison of Allogeneic Hematopoietic Cell Transplantation Outcomes from Younger Matched Unrelated Donor Versus Older Sibling Donor for Acute Myeloid Leukemia
Estrada‐Merly, Noel, Zhang, Mei‐Jie , Bredeson, Christopher , Litzow, Mark R. , Saber, Wael , Abid, Muhammad Bilal , Chen, Karen , Allan, David , Sabloff, Mitchell , Kebriaei, Partow

Blood | November 28, 2022 | Volume: 140 | Issue: Supplement 1 | Pages: 909-910

10.1182/blood-2022-162742 Get It

Genomic and Transcriptional Profiling Stratifies Vq Myeloma Lines into Two Clusters with Distinct Risk Signatures and Drug Responses
Flietner, Evan, Yu, Mei , Zhou, Yun , Feng, Yubin, Wen, Zhi , Sun, Yuqian, Burns, Robert, Patnaik, Mrinal M. , Asimakopoulos, Fotis , Zhang, Jing , Rajagopalan, Adhithi , Veltri, Anthony J. , Lasho, Terra L. , Callander, Natalie S. , Wang, Demin

Blood | November 28, 2022 | Volume: 140 | Issue: Supplement 1 | Pages: 9935-9936

10.1182/blood-2022-162827 Get It

Younger Matched Unrelated Donors Confer a Decreased Relapse Risk As Compared to Older Sibling Donors for Adult B-Cell ALL Patients Undergoing Allogeneic Hematopoietic Cell Transplantation
Estrada‐Merly, Noel, Zhang, Mei‐Jie , Chen, Karen , Bredeson, Christopher , Litzow, Mark R. , Saber, Wael , Abid, Muhammad Bilal , Allan, David , Sabloff, Mitchell , Kebriaei, Partow

Blood | November 28, 2022 | Volume: 140 | Issue: Supplement 1 | Pages: 10540-10541

10.1182/blood-2022-163517 Get It

Comparative Effectiveness of Lenalidomide/Dexamethasone-Based Triplet Regimens for Treatment of Relapsed and/or Refractory Multiple Myeloma in Subgroups Defined By Cytogenetic Risk
Sanchez, Larysa , Cheng, Mu, Cherepanov, Dasha , DerSarkissian, Maral , Stull, Dawn Marie, Hilts, Annalise, Duh, Mei Sheng , Huang, Fei, Chun, Justin, Ailawadhi, Sikander

Blood | November 28, 2022 | Volume: 140 | Issue: Supplement 1 | Pages: 4308-4309

10.1182/blood-2022-156320 Get It

CTNI-16. NRG-RTOG 9802 OBSERVATION ARM - LONG TERM RESULT
Polley, Mei‐Yin C. , Shaw, Edward , Buckner, Jan C. , Barger, Geoffrey, Coons, Stephen Joel , Ricci, Peter E. , Gilbert, Mark, Brown, Paul D. , Stelzer, K. , Rogers, Leland , Schultz, Christopher J. , Howard, Steven , Fisher, Barbara, Haddock, Michael G. , Won, Minhee , IWAMOTO, FABIO MASSAITI , Coons, Stephen, Suh, John H. , Kim, Michelle H. , Huang, Jiayi , Mehta, Minesh P.

Neuro-Oncology | November 14, 2022 | Volume: 24 | Issue: Supplement_7 | Pages: vii73-vii73

10.1093/neuonc/noac209.282 Get It

Abstract BACKGROUND Radiation Therapy Oncology Group 9802 was a phase III trial for patients with centrally confirmed LGG (WHO grade II). Participants ³ 40 years or those with neurosurgeon defined less than gross total resection (GTR) were randomized to radiotherapy (RT) +/- PCV. In a separate cohort, adults age < 40 years with neurosurgeon defined GTR were observed by MRI every 6 months without adjuvant therapy. At last report, outcome for the observation cohort was immature with median follow-up of only 4.4 years. Here, we present mature outcomes for the observation arm. METHODS Eligible adults (as above) were observed by MRI every 6 months. OS and PFS were estimated by Kaplan-Meier method and estimated hazard ratios to characterize the prognostic variables. RESULTS There were 111 eligible patients (median age 30; median KPS = 100). Median follow-up was 16.1 years with 71 (64%) alive at the last follow-up. 79 patients (71%) had progressed with median PFS of 6.9 years. 5, 10, and 15 year-PFS and OS rates were 54%, 39%, 28% and 94%, 77%, and 65%. 1p19q status was codeleted in 32%, IDH1/2 mutant in 78% and MGMT promoter methylated in 39% of tested cases. Multivariate Cox analyses showed that preoperative tumor size ³ 4 cm (HR = 2.43 for PFS, p = 0.001; HR = 2.58 for death, p = 0.016) and residual disease on imaging ³ 1 cm (HR = 2.97 for PFS, P < 0.001; HR = 2.02 for death, p = 0.05) were associated with worse outcomes. Analyses based on molecular results will be presented. CONCLUSION A subset of low-grade gliomas can be observed after the initial resection based on younger age, smaller tumor size, and no residual disease on neuroimaging. This can likely be further refined by prognostic molecular markers. Patients with the most favorable prognostic factors can avoid or delay the acute and long-term side effects of RT and chemotherapy for several years.