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1.
J Cardiol Cases ; 23(3): 108-111, 2021 Mar.
Article En | MEDLINE | ID: mdl-33717373

Flush occlusions of coronary arteries present with multiple challenges during primary percutaneous coronary intervention (PPCI). We describe a case of anterior ST-elevation myocardial infarction in cardiogenic shock, where it was not possible to identify the origin of left anterior descending artery (LAD) as it was flush occluded and initial attempts to place a coronary guidewire in the LAD during PPCI were unsuccessful. After failed attempts with multiple guidewires, a combined pharmacological-mechanical approach resulted in successful timely revascularization and subsequent recovery of the patient. .

4.
Cardiovasc Drugs Ther ; 35(3): 427-440, 2021 06.
Article En | MEDLINE | ID: mdl-32918656

Lopinavir-ritonavir combination is being used for the treatment of SARS-CoV-2 infection. A low dose of ritonavir is added to other protease inhibitors to take advantage of potent inhibition of cytochrome (CYP) P450 3A4, thereby significantly increasing the plasma concentration of coadministered lopinavir. Ritonavir also inhibits CYP2D6 and induces CYP2B6, CYP2C19, CYP2C9, and CYP1A2. This potent, time-dependent interference of major hepatic drug-metabolizing enzymes by ritonavir leads to several clinically important drug-drug interactions. A number of patients presenting with acute coronary syndrome and acute heart failure may have SARS-CoV-2 infection simultaneously. Lopinavir-ritonavir is added to their prescription of multiple cardiac medications leading to potential drug-drug interactions. Many cardiology, pulmonology, and intensivist physicians have never been exposed to clinical scenarios requiring co-prescription of cardiac and antiviral therapies. Therefore, it is essential to enumerate these drug-drug interactions, to avoid any serious drug toxicity, to consider alternate and safer drugs, and to ensure better patient care.


COVID-19 Drug Treatment , Heart Diseases/drug therapy , Lopinavir/administration & dosage , Ritonavir/administration & dosage , SARS-CoV-2 , Anticoagulants/therapeutic use , Drug Interactions , Drug Therapy, Combination , Humans , Hypolipidemic Agents/therapeutic use , Platelet Aggregation Inhibitors/therapeutic use
6.
Postgrad Med J ; 96(1137): 412-416, 2020 Jul.
Article En | MEDLINE | ID: mdl-32527756

Coronavirus infection outbreaks have occurred frequently in the last two decades and have led to significant mortality. Despite the focus on reducing mortality by preventing the spread of the virus, patients have died due to several other complications of the illness. The understanding of pathological mechanisms and their implications is continuously evolving. A number of symptoms occur in these patients due to the involvement of various endocrine glands. These clinical presentations went largely unnoticed during the first outbreak of severe acute respiratory syndrome (SARS) in 2002-2003. A few of these derangements continued during the convalescence phase and sometimes occurred after recovery. Similar pathological and biochemical changes are being reported with the novel coronavirus disease outbreak in 2020. In this review, we focus on these endocrine changes that have been reported in both SARS coronavirus and SARS coronavirus-2. As we battle the pandemic, it becomes imperative to address these underlying endocrine disturbances that are contributing towards or predicting mortality of these patients.


Adrenal Gland Diseases/physiopathology , Betacoronavirus/physiology , Coronavirus Infections/physiopathology , Diabetes Mellitus/physiopathology , Pandemics , Pneumonia, Viral/physiopathology , Severe Acute Respiratory Syndrome/physiopathology , Severe acute respiratory syndrome-related coronavirus/physiology , Adrenal Gland Diseases/metabolism , Adrenal Gland Diseases/virology , COVID-19 , Coronavirus Infections/metabolism , Coronavirus Infections/virology , Diabetes Mellitus/virology , Humans , Hyperglycemia , Pneumonia, Viral/metabolism , Pneumonia, Viral/virology , Practice Guidelines as Topic , SARS-CoV-2 , Severe Acute Respiratory Syndrome/metabolism , Severe Acute Respiratory Syndrome/virology
7.
Cardiovasc Revasc Med ; 20(12): 1165-1171, 2019 12.
Article En | MEDLINE | ID: mdl-30685340

Plaque rupture or plaque erosion leads to intracoronary thrombus formation resulting in coronary artery occlusion and ST-segment elevation myocardial infarction. Early restoration of blood flow in occluded coronary artery is the mainstay of therapy and it can be achieved by either thrombolytic therapy or primary percutaneous coronary intervention (P-PCI) or a combination of these two in many different ways. It has been proved that primary PCI is better than thrombolytic therapy in establishing early and effective recanalization of infarct related artery, reducing major adverse cardiovascular events (MACE) and increasing survival. There have been tremendous advances in PCI techniques over the years with newer stents, thrombectomy devices, and adjunctive pharmacotherapy. However, intracoronary thrombus continues to be the bane of interventional cardiologists. Failure of recanalization, suboptimal results, distal embolization, no reflow and impaired myocardial perfusion are some of the unresolved difficulties, regularly seen during PCI of patients with large intracoronary thrombus burden indicating an unmet need. This review focuses on emerging evidence about the usefulness of intracoronary thrombolytic therapy as an adjunct to PCI in patients with large intracoronary thrombus burden.


Coronary Artery Disease/therapy , Coronary Thrombosis/therapy , Fibrinolytic Agents/administration & dosage , Myocardial Infarction/therapy , Percutaneous Coronary Intervention , Thrombolytic Therapy , Coronary Artery Disease/diagnostic imaging , Coronary Artery Disease/mortality , Coronary Artery Disease/physiopathology , Coronary Thrombosis/diagnostic imaging , Coronary Thrombosis/mortality , Coronary Thrombosis/physiopathology , Fibrinolytic Agents/adverse effects , Humans , Myocardial Infarction/diagnostic imaging , Myocardial Infarction/mortality , Myocardial Infarction/physiopathology , Percutaneous Coronary Intervention/adverse effects , Percutaneous Coronary Intervention/mortality , Risk Factors , Thrombolytic Therapy/adverse effects , Thrombolytic Therapy/mortality , Treatment Outcome
8.
Cardiovasc Revasc Med ; 15(5): 308-10, 2014.
Article En | MEDLINE | ID: mdl-24880912

Dual antiplatelet therapy including aspirin and a P2Y12 ADP receptor antagonist is given after percutaneous coronary intervention to avoid catastrophic complication of stent thrombosis. Dual antiplatelet therapy is associated with increased bleeding risk and may not be tolerated by many patients. This article presents the patients, which had to be given single antiplatelet therapy after percutaneous coronary intervention and discusses the possible factors responsible for the success of single antiplatelet therapy strategy in these patients, in the current era of newer antiplatelet agents and coronary stents.


Drug Hypersensitivity , Drug-Eluting Stents , Percutaneous Coronary Intervention , Platelet Aggregation Inhibitors/therapeutic use , Thrombosis/drug therapy , Aspirin/adverse effects , Female , Humans , Male , Middle Aged , Percutaneous Coronary Intervention/methods , Treatment Outcome
9.
BMJ Case Rep ; 20132013 Apr 22.
Article En | MEDLINE | ID: mdl-23608860

A young man presented with a 2-month history of fever and malaise. Cardiac auscultation revealed the presence of a diastolic murmur. Subsequently, a cardiac echocardiogram was done, which showed a large vegetation adherent to an anterior mitral leaflet. The blood culture was positive for Brucella species. The patient was given antibiotic therapy for brucellosis and referred for surgery. Brucella endocarditis is one of the rarest, yet most notorious complications of this infection. This condition requires a high degree of clinical suspicion in order to facilitate prompt diagnosis and treatment.


Agricultural Workers' Diseases/diagnosis , Agricultural Workers' Diseases/drug therapy , Agricultural Workers' Diseases/microbiology , Brucellosis/diagnosis , Brucellosis/drug therapy , Endocarditis/diagnosis , Endocarditis/drug therapy , Endocarditis/microbiology , Adult , Animals , Anti-Bacterial Agents/therapeutic use , Diagnosis, Differential , Drug Therapy, Combination , Echocardiography , Humans , Male , Radiography, Thoracic
10.
Catheter Cardiovasc Interv ; 78(1): 72-5, 2011 Jul 01.
Article En | MEDLINE | ID: mdl-21061245

Thrombus remains the bane of interventional cardiology. The use of thrombus extraction devices and distal protection devices has been controversial. Pharmacological modulation using intracoronary (IC) thrombolytic therapy during percutaneous coronary intervention (PCI) is also not an established choice although intravenous thrombolytic therapy is widely accepted and applied treatment of choice for acute ST-elevation myocardial infarction (STEMI). This case report shows successful management of a patient of STEMI using a combination of IC thrombolytic therapy, thrombectomy device, and PCI.


Angioplasty, Balloon, Coronary , Coronary Thrombosis/therapy , Myocardial Infarction/therapy , Thrombectomy , Thrombolytic Therapy , Adult , Angioplasty, Balloon, Coronary/instrumentation , Combined Modality Therapy , Coronary Angiography , Coronary Thrombosis/complications , Coronary Thrombosis/diagnosis , Humans , Male , Metals , Myocardial Infarction/diagnosis , Myocardial Infarction/etiology , Prosthesis Design , Stents , Thrombectomy/instrumentation , Treatment Outcome
11.
J Invasive Cardiol ; 20(12): 655-8, 2008 Dec.
Article En | MEDLINE | ID: mdl-19057030

Thrombosis late after implantation is an infrequent but increasingly recognized complication following revascularization with drug-eluting stents (DES). The window of vulnerability for this complication with DES remains undefined. Intermediate-term follow up from pivotal trials and registries suggests continuous separation of event curves out to at least 3 years. We briefly review the evolving body of literature on DES thrombosis and report a case of very late thrombosis 53 months after implantation of a sirolimus-eluting stent. The event occurred despite chronic aspirin monotherapy and represents the longest latency from implantation to thrombosis described in the literature for a DES.


Angioplasty, Balloon, Coronary , Coronary Artery Disease/therapy , Coronary Restenosis/etiology , Coronary Thrombosis/etiology , Drug-Eluting Stents/adverse effects , Humans , Male , Middle Aged , Time Factors
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