Assi Milwidsky

Dr. Assi Milwidsky

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Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 January 2017 in Biomarkers
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Journal Article
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AMAssi Milwidsky
Assi Milwidsky
TZTomer Ziv-Baran
Tomer Ziv-Baran
SLSevan Letourneau-Shesaf
Sevan Letourneau-Shesaf
GKGad Keren
Gad Keren
PTPhilippe Taieb
Philippe Taieb
YSYacov Shacham
Yacov Shacham
Context: There is a known association between C-reactive protein (CRP) levels and adverse outcomes in patients presenting with ST-elevation myocardial infarction (STEMI). The optimal time frame to measure CRP for risk stratification is not known. Objective: The aim of the current study was to evaluate the relation between the change in CRP velocity (CRPv) and 30-d mortality among STEMI patients. Material and methods: We included consecutive patients with a diagnosis of STEMI who presented to Tel-Aviv Medical Center between 2008 and 2014 and had their CRP measured with a wide range assay (wr-CRP) at least twice during the 24 h after admission. CRPv was defined as the change in wr-CRP concentration (mg/l) divided by the change in time (in hours) between the two measurements. Results: The study population comprised of 492 patients, mean age was 62 ± 14, 80% were male. CRPv was significantly higher among patients who died within 30 d of admission (1.42 mg/l versus 0.18 mg/l, p < 0.001). In a multivariate regression model adjusted to multiple confounders, CRPv was independently associated with 30-d mortality (OR 1.39, 95% CI: 1.20–1.62, p < 0.001). Conclusion: CRPv might be an independent and rapidly measurable biomarker for short-term mortality in patients presenting with STEMI.

28 May 2021 in Catheterization and Cardiovascular Interventions
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Journal Article
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AMAssi Milwidsky
Assi Milwidsky
MVMiguel Alvarez Villela
Miguel Alvarez Villela
JWJose Wiley
Jose Wiley
CSCristina Sanina
Cristina Sanina
SPSnehal R. Patel
Snehal R. Patel
UJUlrich Jorde
Ulrich Jorde

15 September 2015 in Cardiovascular Diabetology
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Journal Article
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AMAssi Milwidsky
Assi Milwidsky
EMElad Maor
Elad Maor
SKShaye Kivity
Shaye Kivity
ABAnat Berkovitch
Anat Berkovitch
SZSagit Ben Zekry
Sagit Ben Zekry
RKRafael Kuperstein
Rafael Kuperstein
Left ventricular (LV) diastolic dysfunction (LVDD) is a well-established and early echocardiographic characteristic of diabetic cardiomyopathy. However, there are limited data on the association between impaired fasting glucose (IFG) and LVDD. To determine whether IFG is associated with LVDD among middle age adults. Amongst 3781 subjects screened in an annual health survey program and referred for an echocardiogram, 2971 individuals without LV systolic dysfunction or valvular heart disease were selected. Mean age of study population was 59 ± 12 years and 75 % were men. The subjects were categorized into three groups: euglycemia (N = 2025), IFG (N = 534) and diabetes mellitus (DM; N = 412). Doppler echocardiography readers were blinded to glycemic state. Subjects with impaired LV relaxation, pseudo-normal or restrictive filling patterns were defined as having LVDD. LVDD was diagnosed in 574 (19 %) of subjects and it was more prevalent among patients with IFG and DM than in euglycemic individuals (27, 30 and 15 %, respectively; p < 0.001). Patients with IFG and DM had lower ratios of early (E) to late (A) trans-mitral flow (0.9 ± 0.3 and 0.9 ± 0.3 vs. 1.1 ± 0.4, respectively, p < 0.001). LV hypertrophy (LVH) was also more prevalent among patients with IFG and DM (11 and 18 %, respectively, vs. 9 %; p < 0.001). Multivariate binary logistic regression model adjusted to age, gender, obesity, LVH, renal function, total, high and low density lipoprotein cholesterol, triglycerides, ischemic heart disease, hypertension and LV ejection fraction showed that patients with IFG were 43 % more likely to have LVDD compared with euglycemic subjects (95 % confidence interval 1.12–1.83, p = 0.004). IFG is independently associated with a significant increase in the likelihood for the presence of LVDD in middle aged adults.

25 October 2018 in Biomarkers
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Journal Article
Closed access
AMAssi Milwidsky
Assi Milwidsky
EFEyal Fisher
Eyal Fisher
RBRafael Y. Brzezinski
Rafael Y. Brzezinski
MEMichal Ehrenwald
Michal Ehrenwald
GSGabi Shefer
Gabi Shefer
OROri Rogowski
Ori Rogowski
Introduction: Metabolic syndrome (MetS) and high-sensitivity cardiac troponin T (hs-TnT) are associated with higher risk for cardiovascular diseases (CVD). Our aim was to assess the relation between hs-TnT elevation and MetS in a general population sample. Materials and methods: Individuals participating in an annual health survey program between 2010 and 2016 were included in the study. Blood samples including hs-TnT levels were collected. The study population was divided into three groups based on hs-TnT levels – undetectable (<5 ng/L), intermediate (5–14 ng/L) and elevated (>14 ng/L). Results: A total of 5994 subjects were included in the study, the mean age was 48.5 and 4336 (72%) were males. Compared with subjects with undetectable hs-TnT the prevalence of MetS was higher in those with detectable and elevated levels – 392 (10%) vs. 270 (15%) and 51 (33%), respectively (p < 0.001). In a multivariate model adjusted for age, gender and multiple co-morbidities, the number of MetS components and presence of MetS were significantly associated with an increased risk for detectable hs-TnT levels (OR = 1.02 {for each component}; 95% CI [1.00–1.05], p = 0.04) and (OR = 1.13; 95% CI [1.07–1.2], p < 0.001) respectively. Only the waist, glucose and hypertension components of the MetS were significantly associated with elevated troponin. Conclusions: The MetS and its distinct components have a cumulative impact on hs-TnT levels in apparently healthy subjects.

27 January 2022 in ESC Heart Failure
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Journal Article
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AMAssi Milwidsky
Assi Milwidsky
SFShir Frydman
Shir Frydman
MLMichal Laufer-Perl
Michal Laufer-Perl
BSBen Sadeh
Ben Sadeh
OSOrly Sapir
Orly Sapir
OHOfer Havakuk
Ofer Havakuk
Aims Routine, intermittent inotropic therapy (IIT) is still applied in advanced heart failure (HF) patients either as a bridge to definitive treatment or as a mean to improve quality of life (QOL), despite limited evidence to support its' use. Given recent reports of improved QOL and reduced HF hospitalization, with levosimendan compared with placebo in advanced HF patients, we aimed to assess the effects of switching a small group of milrinone-treated patients to levosimendan. This was performed as part of a protocol for changing our ambulatory HF clinic milrinone-based IIT to levosimendan. Methods and results Single-centre study of consecutive ambulatory advanced HF patients that received ≥4 cycles of once-weekly milrinone IIT at our HF outpatient clinic, who were switched to levosimendan IIT. All patients had left ventricular ejection fraction ≤35%, elevated B-natriuretic peptide (BNP), and were in New York Heart Association Classes III–IV despite maximally tolerated guideline directed medical therapy. Patients were evaluated using BNP levels, echocardiography, cardio-pulmonary exercise test, and HF QOL questionnaire before and after 4 weeks of levosimendan IIT. The cohort included 11 patients, 10 (91%) were male and the mean age was 76 ± 12 years. After 4 weeks of levosimendan therapy, maximal O2 consumption improved in 8/9 (89%) by a mean of 2.28 mL/kg [95% CI −0.22–3.38, P = 0.05]. BNP levels decreased in 9/11 (82%) levosimendan treated patients, from a median of 1015 ng/L [261–1035] to 719 ng/L [294–739], (P < 0.01). QOL as measure by the EQ-5D-5L questionnaire improved in 8/11 (82%) patients after levosimendan IIT, by a median of two points [95% CO −4.14–0.37, P = 0.09]. On echocardiography, peak systolic annular velocity (S') increased after levosimendan IIT by an average of 3 cm/s [95% CI 0.16–2.10, P = 0.03]. Conclusions In this small-scale study of ambulatory advanced HF patients, we observed improvements in right ventricular systolic function, maximal O2 consumption, and BNP after switching from milrinone to levosimendan based IIT.

1 May 2016 in Heart & Lung
Verified
Journal Article
Closed access
GAGalit Aviram
Galit Aviram
ESEugene Soikher
Eugene Soikher
ABAchiude Bendet
Achiude Bendet
TZTomer Ziv-Baran
Tomer Ziv-Baran
SBShlomo Berliner
Shlomo Berliner
YTYan Topilsky
Yan Topilsky