92 results match your criteria: "Sisli Florence Nightingale Hospital[Affiliation]"

Objective: The aim of the study was to evaluate prostate awareness in the general male population and discover the common misinformation about prostate diseases (PDs).

Material And Methods: A cross-sectional population sampling was performed in the general population for men between the ages of 18-70 with a survey conducted by medical students. The survey consisted of 15 questions addressing different aspects of PDs and common misinformation in the general population.

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Primary hyperoxaluria is a rare hereditary metabolic disorder resulting in accumulation of calcium oxalate in visceral organs, including the heart. We report a 19-year-old male with non- compaction cardiomyopathy combined with patent ductus arteriosus awaiting combined liver-kidney transplantation for primary hyperoxaluria. After surgical closure of the patent ductus arteriosus, the patient underwent a successful renal and subsequent liver transplantation.

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Article Synopsis
  • The study aimed to investigate QT dispersion (QTd) and P-wave dispersion in patients with conversion disorder (CD), focusing on their potential link to arrhythmias and sudden cardiac death.
  • Involved 60 CD patients without known organic diseases and 60 healthy controls, with assessments for anxiety and depression, as well as 12-lead ECG measurements to calculate QTd and P-wave dispersion.
  • Results showed significantly higher anxiety and depression scores in CD patients, along with increased QTc and QTd intervals compared to controls, indicating a possible heightened risk of ventricular arrhythmia in this group.
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Sinusoidal obstruction syndrome/veno-occlusive disease: current situation and perspectives-a position statement from the European Society for Blood and Marrow Transplantation (EBMT).

Bone Marrow Transplant

June 2015

1] Josep Carreras Leukaemia Research Institute, Barcelona, Spain [2] Haematology Department, Hospital Clinic, Barcelona, Spain [3] Spanish Bone Marrow Donor Program, Josep Carreras Foundation, Barcelona, Spain.

Sinusoidal obstruction syndrome or veno-occlusive disease (SOS/VOD) is a potentially life-threatening complication of hematopoietic SCT (HSCT). This review aims to highlight, on behalf of the European Society for Blood and Marrow Transplantation, the current knowledge on SOS/VOD pathophysiology, risk factors, diagnosis and treatments. Our perspectives on SOS/VOD are (i) to accurately identify its risk factors; (ii) to define new criteria for its diagnosis; (iii) to search for SOS/VOD biomarkers and (iv) to propose prospective studies evaluating SOS/VOD prevention and treatment in adults and children.

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Acute multicoronary occlusion is an extremely rare clinical and angiographic finding. Prompt diagnosis and treatment are extremely important. Herein, we present a 38-year-old man suffering from concomitant anterior and inferior myocardial infarctions due to simultaneous total occlusion of both the left anterior descending and right coronary arteries.

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The aim of this study was to investigate whether anticoagulant and antiaggregant agents have protective effects against oxidative damage induced by peripheral ischemia-reperfusion (I/R). Groups were created as follows: control group, I/R group (sham group), I/R plus acetylsalicylic acid (Group I), I/R+clopidogrel (Group II), I/R+rivaroxaban (Group III), I/R+bemiparin sodium (Group IV), and I/R+enoxaparin sodium (Group V). In Groups I, II, III, IV, and V, drugs were administered daily for 1 week before I/R creation.

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Introduction: Epileptic, migrainous, and vascular pathologies may cause transient global amnesia (TGA); however, the mechanism of causation remains unclear. We investigated possible vascular causes of TGA.

Methods: We retrospectively evaluated the clinical and radiologic studies of 13 patients with TGA.

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Symptoms after hospital discharge following hematopoietic stem cell transplantation.

Indian J Palliat Care

January 2014

Department of Nursing, Bahcesehir University Faculty of Health Sciences, Ciragan Caddesi Osmanpasa Mektebi Sokak, Besiktas, Istanbul, Turkey.

Aims: The purposes of this study were to assess the symptoms of hematopoietic stem cell transplant patients after hospital discharge, and to determine the needs of transplant patients for symptom management.

Materials And Methods: The study adopted a descriptive design. The study sample comprised of 66 hematopoietic stem cell transplant patients.

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Glasgow coma scale and APACHE-II scores affect the liver transplantation outcomes in patients with acute liver failure.

Hepatobiliary Pancreat Dis Int

December 2013

Organ Transplantation Center, Sisli Florence Nightingale Hospital, Istanbul, Turkey; Department of Gastroenterology, Istanbul Bilim University, Medical School, Istanbul, Turkey.

Background: The timing and selection of patients for liver transplantation in acute liver failure are great challenges. This study aimed to investigate the effect of Glasgow coma scale (GCS) and APACHE-II scores on liver transplantation outcomes in patients with acute liver failure.

Method: A total of 25 patients with acute liver failure were retrospectively analyzed according to age, etiology, time to transplantation, coma scores, complications and mortality.

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Congress summary: the 20th congress of the international society for rotary blood pumps.

Artif Organs

September 2013

Prof of Cardiovascular Surgery Director of Cardiac Transplantation and Mechanical Circulatory Support Dept., Istanbul Sisli Florence Nightingale Hospital, Abide-i Hurriyet Cad. 164, Sisli, Istanbul, 34381, Turkey.

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Although several left ventricular assist devices (LVADs) have been used widely, remote monitoring of LVAD parameters has been available only recently. We present our remote monitoring experience with an axial-flow LVAD (HeartAssist-5, MicroMed Cardiovascular, Inc., Houston, TX, USA).

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Hepatorenal syndrome is defined as renal failure caused by acute or chronic liver failure without any laboratory or histological reasons. The exact etiology of this syndrome is unknown. However, vasodilatation in the splanchnic area as a result of cirrhosis and portal hypertension, reflex systemic and splanchnic vasoconstriction are the basic pathophysiological reasons of this syndrome.

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Background: In liver transplantation or resection for hepatocellular carcinoma (HCC), patient selection depends on morphological features. In patients with HCC, we performed a clinicopathological analysis of risk factors that affected survival after liver transplantation.

Methods: In 389 liver transplantations performed from 2004 to 2010, 102 were for HCC patients.

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Right-lobe liver transplant from donors with Gilbert syndrome.

Exp Clin Transplant

February 2012

Sisli Florence Nightingale Hospital, Department of General Surgery and Organ Transplantation, Sisli, Istanbul, Turkey.

Objectives: Donor safety is one of the most important aspects of living-donor liver transplant. The preoperative evaluation of candidates for such transplants essentially starts with serologic and biochemical analyses. However, some potential liver donors with normal liver function test results may have isolated mild hyperbilirubinemia (serum indirect bilirubin level > 20.

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Foreign body perforation of the gastrointestinal (GI) tract has diverse clinical manifestations, and the correct preoperative diagnosis is seldom made. We report the case of a 69-year-old woman who experienced severe pain in the right iliac fossa. The presumptive diagnosis was acute purulent appendicitis or diverticulitis.

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The prevalence of carotid artery diseases increases with age and exposure to cardiovascular risk factors. Significant carotid artery stenosis is closely associated with the development of stroke and cerebrovascular events. Doppler ultrasound imaging is a noninvasive and useful modality for the examination of carotid and vertebral arteries.

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Gaucher disease (GD) is the most common lysosomal storage disorder. Deficiency of the lysosomal enzyme glucocerebrosidase results in the intracellular accumulation of undegraded substrates in the spleen, liver and bone marrow. Enzyme replacement therapy (ERT) is a standard approach for type 1 GD.

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