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1.
Eur Heart J Cardiovasc Imaging ; 25(4): 491-497, 2024 Mar 27.
Article in English | MEDLINE | ID: mdl-37936296

ABSTRACT

AIMS: The aim of the study is to assess the impact of the baseline plaque composition on the DREAMS 3G luminal late loss and to compare the serial plaque changes between baseline and 6 and 12 months (M) follow-up. METHODS AND RESULTS: A total of 116 patients were enrolled in the BIOMAG-I trial. Patients were imaged with optical coherence tomography (OCT) pre- and post-DREAMS 3G implantation and at 6 and 12 M. OCTPlus software uses artificial intelligence to assess composition (i.e. lipid, calcium, and fibrous tissue) of the plaque. The differences between the OCT-derived minimum lumen area (MLA) post-percutaneous coronary intervention and 12 M were grouped into three terciles. Patients with larger MLA differences at 12 M (P = 0.0003) had significantly larger content of fibrous tissue at baseline. There was a reduction of 24.8% and 20.9% in lipid area, both P < 0.001, between the pre-DREAMS 3G OCT and the 6 and 12 M follow-up. Conversely, the fibrous tissue increased by 48.4% and 36.0% at 6 and 12 M follow-up, both P < 0.001. CONCLUSION: The larger the fibrous tissue in the lesion at baseline, the larger the luminal loss seen at 6 and 12 M. Following the implantation of DREAMS 3G, favourable healing of the vessel coronary wall occurs as shown by a decrease in the lipid area and an increase in fibrous tissue.


Subject(s)
Coronary Artery Disease , Drug-Eluting Stents , Percutaneous Coronary Intervention , Plaque, Atherosclerotic , Humans , Absorbable Implants , Artificial Intelligence , Coronary Angiography , Coronary Vessels , Lipids , Tomography, Optical Coherence/methods , Treatment Outcome
2.
J Prim Care Community Health ; 14: 21501319231199014, 2023.
Article in English | MEDLINE | ID: mdl-37740500

ABSTRACT

BACKGROUND AND OBJECTIVE: Meta-analysis of randomized controlled trials have demonstrated the efficacy of telemedicine in blood pressure (BP) management when compared to conventional care. We initiated a hypertension telehealth clinic in our urban primary care clinic and through this study aim to evaluate the strengths and limitations of telemedicine in hypertension (HTN) control. The primary outcome of the study is to identify the proportion of patients with improved HTN. Secondary outcomes included identifying: predictors for lower BP, predictors of missing telehealth appointments, and comorbid conditions that are more likely to necessitate use of more than 1 antihypertensive medication. METHODS AND ANALYSIS: Patients seen in the HTN telehealth clinic from May 1st, 2022 to October 31st, 2022 were identified. A retrospective chart review was done to compare the BP during in-person visit prior to first telehealth visit, telehealth visit home BP readings and last recorded in-office BP on chart at end of study period. Descriptive statistical analysis, Chi Square test, and multivariable logistic regression was used to analyze data. RESULTS: Of the 234 appointments, 83% were conducted and 154 patients were seen. A remarkable decrease in percentage of patients with BP >140/90 was seen when comparing in-office visit BP to first telehealth visit home BP, 72% versus 45% respectively. No remarkable difference was noted in percentage of patients with BP >140/90 when comparing first telehealth visit home BP to last in-office BP recorded on chart, 45% and 41% respectively. Patients with diabetes had lower odds of missing appointments, adjusted odds ratio (aOR): 0.34 ([0.12-0.91], P = .03). Patients with partners were more likely to have lower BP at the telehealth visit, aOR:3.2 ([1.15-9.86], P = .03) while patients with obstructive sleep apnea (OSA) (aOR 0.27 ([0.08-0.77], P = .02) and CAD, aOR 0.24 ([0.06-0.8], P = .03) were less likely to have lower BP. CONCLUSION: The study demonstrated telemedicine as a great tool to prevent overtreatment of hypertension as significant difference between in-office BP and home BP during telehealth visits was noted. We did not see a significant change in blood pressure when comparing home BP at first telehealth visit to the last in-person clinic BP at end of study period.


Subject(s)
Hypertension , Telemedicine , Humans , Blood Pressure , Hypertension/drug therapy , Primary Health Care , Retrospective Studies
3.
JACC Case Rep ; 4(1): 59-62, 2022 Jan 05.
Article in English | MEDLINE | ID: mdl-35036946

ABSTRACT

We present the case of a 25-year-old woman with desmoplakin cardiomyopathy-related myocarditis. Her high-sensitivity troponin and symptoms improved with pulse steroid therapy and mycophenolate mofetil. The literature lacks data to effectively guide the management of recurrent myocarditis in desmoplakin cardiomyopathy. (Level of Difficulty: Advanced.).

4.
Neuron ; 73(4): 729-42, 2012 Feb 23.
Article in English | MEDLINE | ID: mdl-22365547

ABSTRACT

Following damage to peripheral nerves, a remarkable process of clearance and regeneration takes place. Axons downstream of the injury degenerate, while the nerve is remodeled to direct axonal regrowth. Schwann cells are important for this regenerative process. "Sensing" damaged axons, they dedifferentiate to a progenitor-like state, in which they aid nerve regeneration. Here, we demonstrate that activation of an inducible Raf-kinase transgene in myelinated Schwann cells is sufficient to control this plasticity by inducing severe demyelination in the absence of axonal damage, with the period of demyelination/ataxia determined by the duration of Raf activation. Remarkably, activation of Raf-kinase also induces much of the inflammatory response important for nerve repair, including breakdown of the blood-nerve barrier and the influx of inflammatory cells. This reversible in vivo model identifies a central role for ERK signaling in Schwann cells in orchestrating nerve repair and is a powerful system for studying peripheral neuropathies and cancer.


Subject(s)
MAP Kinase Signaling System/physiology , Nerve Regeneration/genetics , Peripheral Nerve Injuries/physiopathology , Proto-Oncogene Proteins c-raf/metabolism , Schwann Cells/physiology , Animals , Animals, Newborn , Benzamides/pharmacology , Cell Movement/drug effects , Cyclin D1/metabolism , Cytokines/metabolism , Diphenylamine/analogs & derivatives , Diphenylamine/pharmacology , Estrogen Antagonists/pharmacology , Gene Expression Regulation/drug effects , Gene Expression Regulation/genetics , Leukocytes/pathology , MAP Kinase Signaling System/drug effects , MAP Kinase Signaling System/genetics , Male , Mast Cells/pathology , Mice , Mice, Inbred C57BL , Mice, Transgenic , Microscopy, Confocal , Microscopy, Electron, Transmission , Microscopy, Immunoelectron , Motor Activity/drug effects , Motor Activity/genetics , Myelin Sheath/genetics , Myelin Sheath/metabolism , Nerve Regeneration/drug effects , Neutrophils/metabolism , Neutrophils/pathology , Peripheral Nerve Injuries/pathology , Proto-Oncogene Proteins c-raf/genetics , Reaction Time/drug effects , Reaction Time/genetics , Receptor, Nerve Growth Factor/genetics , Receptor, Nerve Growth Factor/metabolism , Receptors, Estrogen/genetics , Recovery of Function/drug effects , Recovery of Function/genetics , Schwann Cells/ultrastructure , T-Lymphocytes/metabolism , T-Lymphocytes/pathology , Tamoxifen/pharmacology , Time Factors
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