Peripheral Artery Disease Go-To Guide
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A Cross Sectional Study of Cutaneous Manifestations in 300 Patients of Diabetes Mellitus
International Journal of Advances in Medicine Khuraiya S et al. Int J Adv Med. 2019 Feb;6(1):150-154 http://www.ijmedicine.com pISSN 2349-3925 | eISSN 2349-3933 DOI: http://dx.doi.org/10.18203/2349-3933.ijam20190122 Original Research Article A cross sectional study of cutaneous manifestations in 300 patients of diabetes mellitus Sandeep Khuraiya1*, Nancy Lal2, Naseerudin3, Vinod Jain3, Dilip Kachhawa3 1Department of Dermatology, 2Department of Radiation Oncology , Gandhi Medical College, Bhopal, Madhya Pradesh, India 3Department of Dermatology, Dr. SNMC, Jodhpur, Rajasthan, India Received: 13 December 2018 Accepted: 05 January 2019 *Correspondence: Dr. Sandeep Khuraiya, E-mail: [email protected] Copyright: © the author(s), publisher and licensee Medip Academy. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. ABSTRACT Background: Diabetes Mellitus (DM) is a worldwide problem and one of the most common endocrine disorder. The skin is affected by both the acute metabolic derangements and the chronic degenerative complications of diabetes. Methods: The present study was a one-year cross sectional study from January 2014 to December 2014. All confirmed cases of DM with cutaneous manifestations irrespective of age, sex, duration of illness and associated diseases, willing to participate in the study were included in the study. Routine haematological and urine investigations, FBS, RBS and HbA1c levels were carried out in all patients. Results: A total of 300 patients of diabetes mellitus with cutaneous manifestations were studied. -
Note for Guidance on Clinical Investigation of Medicinal Products for the Treatment of Peripheral Arterial Occlusive Disease
The European Agency for the Evaluation of Medicinal Products Evaluation of Medicines for Human Use London, 25 April 2002 CPMP/EWP/714/98 rev 1 COMMITTEE FOR PROPRIETARY MEDICINAL PRODUCTS (CPMP) NOTE FOR GUIDANCE ON CLINICAL INVESTIGATION OF MEDICINAL PRODUCTS FOR THE TREATMENT OF PERIPHERAL ARTERIAL OCCLUSIVE DISEASE DISCUSSION IN THE EFFICACY WORKING PARTY September 1999 – September 2000 TRANSMISSION TO CPMP November 2000 RELEASE FOR CONSULTATION November 2000 DEADLINE FOR COMMENTS May 2001 DISCUSSION IN THE EFFICACY WORKING PARTY November 2001 – February 2002 TRANSMISSION TO CPMP April 2002 ADOPTION BY CPMP April 2002 DATE FOR COMING INTO OPERATION October 2002 Note: This revised Note for guidance will replace the previous Note for guidance (CPMP/EWP/233/95) , adopted in November 1995. 7 Westferry Circus, Canary Wharf, London, E14 4HB, UK Tel. (44-20) 74 18 84 00 Fax (44-20) 74 18 8613 E-mail: [email protected] http://www.emea.eu.int EMEA 2002 Reproduction and/or distribution of this document is authorised for non commercial purposes only provided the EMEA is acknowledged NOTE FOR GUIDANCE ON CLINICAL INVESTIGATIONS OF MEDICINAL PRODUCTS IN THE TREATMENT OF CHRONIC PERIPHERAL ARTERIAL OCCLUSIVE DISEASE TABLE OF CONTENTS 1. INTRODUCTION .................................................................................................... 4 2. GENERAL CONSIDERATIONS REGARDING PAOD TRIALS..................... 4 2.1 PAOD Classification and Epidemiological Background ...................................... 4 2.2 Clinical Trial Features ............................................................................................ -
IWGDF Guideline on Diagnosis, Prognosis and Management of Peripheral Artery Disease in Patients with a Foot Ulcer and Diabetes
IWGDF Guideline on diagnosis, prognosis and management of peripheral artery disease in patients with a foot ulcer and diabetes Part of the 2019 IWGDF Guidelines on the Prevention and Management of Diabetic Foot Disease IWGDF Guidelines AUTHORS Robert J. Hinchlife1, Rachael O. Forsythe2, Jan Apelqvist3, Ed J. Boyko4, Robert Fitridge5, Joon Pio Hong6, Konstantinos Katsanos7, Joseph L. Mills8, Sigrid Nikol9, Jim Reekers10, Maarit Venermo11, R. Eugene Zierler12, Nicolaas C. Schaper13 on behalf of the International Working Group on the Diabetic Foot (IWGDF) INSTITUTIONS 1 Bristol Centre for Surgical Research, University of Bristol, Bristol, UK 2 British Heart Foundation / University of Edinburgh Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, Scotland, UK 3 Department of Endocrinology, University Hospital of Malmö, Sweden 4 Seattle Epidemiologic Research and Information Centre-Department of Veterans Afairs Puget Sound Health Care System and the University of Washington, Seattle, Washington, USA 5 Vascular Surgery, The University of Adelaide, Adelaide, South Australia, Australia 6 Asan Medical Center University of Ulsan, Seoul, Korea 7 Patras University Hospital School of Medicine, Rion, Patras, Greece 8 SALSA (Southern Arizona Limb Salvage Alliance), University of Arizona Health Sciences Center, Tucson, Arizona, USA 9 Asklepios Klinik St. Georg, Hamburg, Germany 10 Department of Vascular Radiology, Amsterdam Medical Centre, The Netherlands 11 Helsinki University Hospital, University of Helsinki, Finland 12 Department of Surgery, University of Washington, Seattle, Washington, USA 13 Div. Endocrinology, MUMC+, CARIM and CAPHRI Institute, Maastricht, The Netherlands KEYWORDS diabetic foot; foot ulcer; guidelines; peripheral artery disease; surgery; diagnosis; prognosis; vascular disease www.iwgdfguidelines.org IWGDF PAD Guideline ABSTRACT The International Working Group on the Diabetic Foot (IWGDF) has published evidence-based guidelines on the prevention and management of diabetic foot disease since 1999. -
Hypertension and Coronary Heart Disease
Journal of Human Hypertension (2002) 16 (Suppl 1), S61–S63 2002 Nature Publishing Group All rights reserved 0950-9240/02 $25.00 www.nature.com/jhh Hypertension and coronary heart disease E Escobar University of Chile, Santiago, Chile The association of hypertension and coronary heart atherosclerosis, damage of arterial territories other than disease is a frequent one. There are several patho- the coronary one, and of the extension and severity of physiologic mechanisms which link both diseases. coronary artery involvement. It is important to empha- Hypertension induces endothelial dysfunction, exacer- sise that complications and mortality of patients suffer- bates the atherosclerotic process and it contributes to ing a myocardial infarction are greater in hypertensive make the atherosclerotic plaque more unstable. Left patients. Treatment should be aimed to achieve optimal ventricular hypertrophy, which is the usual complication values of blood pressure, and all the strategies to treat of hypertension, promotes a decrease of ‘coronary coronary heart disease should be considered on an indi- reserve’ and increases myocardial oxygen demand, vidual basis. both mechanisms contributing to myocardial ischaemia. Journal of Human Hypertension (2002) 16 (Suppl 1), S61– From a clinical point of view hypertensive patients S63. DOI: 10.1038/sj/jhh/1001345 should have a complete evaluation of risk factors for Keywords: hypertension; hypertrophy; coronary heart disease There is a strong and frequent association between arterial hypertension.8 Hypertension is frequently arterial hypertension and coronary heart disease associated to metabolic disorders, such as insulin (CHD). In the PROCAM study, in men between 40 resistance with hyperinsulinaemia and dyslipidae- and 66 years of age, the prevalence of hypertension mia, which are additional risk factors of atheroscler- in patients who had a myocardial infarction was osis.9 14/1000 men in a follow-up of 4 years. -
Coronary Microvascular Dysfunction
Journal of Clinical Medicine Review Coronary Microvascular Dysfunction Federico Vancheri 1,*, Giovanni Longo 2, Sergio Vancheri 3 and Michael Henein 4,5,6 1 Department of Internal Medicine, S.Elia Hospital, 93100 Caltanissetta, Italy 2 Cardiovascular and Interventional Department, S.Elia Hospital, 93100 Caltanissetta, Italy; [email protected] 3 Radiology Department, I.R.C.C.S. Policlinico San Matteo, 27100 Pavia, Italy; [email protected] 4 Institute of Public Health and Clinical Medicine, Umea University, SE-90187 Umea, Sweden; [email protected] 5 Department of Fluid Mechanics, Brunel University, Middlesex, London UB8 3PH, UK 6 Molecular and Nuclear Research Institute, St George’s University, London SW17 0RE, UK * Correspondence: [email protected] Received: 10 August 2020; Accepted: 2 September 2020; Published: 6 September 2020 Abstract: Many patients with chest pain undergoing coronary angiography do not show significant obstructive coronary lesions. A substantial proportion of these patients have abnormalities in the function and structure of coronary microcirculation due to endothelial and smooth muscle cell dysfunction. The coronary microcirculation has a fundamental role in the regulation of coronary blood flow in response to cardiac oxygen requirements. Impairment of this mechanism, defined as coronary microvascular dysfunction (CMD), carries an increased risk of adverse cardiovascular clinical outcomes. Coronary endothelial dysfunction accounts for approximately two-thirds of clinical conditions presenting with symptoms and signs of myocardial ischemia without obstructive coronary disease, termed “ischemia with non-obstructive coronary artery disease” (INOCA) and for a small proportion of “myocardial infarction with non-obstructive coronary artery disease” (MINOCA). More frequently, the clinical presentation of INOCA is microvascular angina due to CMD, while some patients present vasospastic angina due to epicardial spasm, and mixed epicardial and microvascular forms. -
Risk Factors in Abdominal Aortic Aneurysm and Aortoiliac Occlusive
OPEN Risk factors in abdominal aortic SUBJECT AREAS: aneurysm and aortoiliac occlusive PHYSICAL EXAMINATION RISK FACTORS disease and differences between them in AORTIC DISEASES LIFESTYLE MODIFICATION the Polish population Joanna Miko ajczyk-Stecyna1, Aleksandra Korcz1, Marcin Gabriel2, Katarzyna Pawlaczyk3, Received Grzegorz Oszkinis2 & Ryszard S omski1,4 1 November 2013 Accepted 1Institute of Human Genetics, Polish Academy of Sciences, Poznan, 60-479, Poland, 2Department of Vascular Surgery, Poznan 18 November 2013 University of Medical Sciences, Poznan, 61-848, Poland, 3Department of Hypertension, Internal Medicine, and Vascular Diseases, Poznan University of Medical Sciences, Poznan, 61-848, Poland, 4Department of Biochemistry and Biotechnology of the Poznan Published University of Life Sciences, Poznan, 60-632, Poland. 18 December 2013 Abdominal aortic aneurysm (AAA) and aortoiliac occlusive disease (AIOD) are multifactorial vascular Correspondence and disorders caused by complex genetic and environmental factors. The purpose of this study was to define risk factors of AAA and AIOD in the Polish population and indicate differences between diseases. requests for materials should be addressed to J.M.-S. he total of 324 patients affected by AAA and 328 patients affected by AIOD was included. Previously (joannastecyna@wp. published population groups were treated as references. AAA and AIOD risk factors among the Polish pl) T population comprised: male gender, advanced age, myocardial infarction, diabetes type II and tobacco smoking. This study allowed defining risk factors of AAA and AIOD in the Polish population and could help to develop diagnosis and prevention. Characteristics of AAA and AIOD subjects carried out according to clinical data described studied disorders as separate diseases in spite of shearing common localization and some risk factors. -
Origin of the Microangiopathic Changes in Diabetes
ORIGIN OF THE MICROANGIOPATHIC CHANGES IN DIABETES A. H. BARNETT Birmingham SUMMARY its glycosidally linked disaccharide units. Such alterations The mechanism of development of microangiopathy is lead to abnormal packing of the peptide chains producing incompletely understood, but relates to a number of excessive leakiness of the membrane. The exact mech ultrastructural, biochemical and haemostatic processes. anisms of thickening and leakiness of basement mem These include capillary basement membrane thickening, brane and their relevance to diabetic complications are not non-enzymatic glycosylation, possibly increased free rad entirely clear, but appear to involve several biochemical ical activity, increased flux through the polyol pathway mechanisms. and haemostatic abnormalities. The central feature Non-enzymatic Glycosylation appears to be hyperglycaemia, which is causally related to the above processes and culminates in tissue ischaemia. In the presence of persistent hyperglycaemia glucose This article will briefly describe these processes and will chemically attaches to proteins non-enzymatically to form discuss possible pathogenic interactions which may lead a stable product (keto amine or Amadori product) of which to the development of the pathological lesion. glycosylated haemoglobin is the best-known example. In long-lived tissue proteins such as collagen the ketoamine Microangiopathy is a specific disorder of the small blood then undergoes a series of reactions resulting in the vessels which causes much morbidity and mortality in dia development of advanced glycosylation end products betic patients. Diabetic retinopathy is the commonest (AGE) (Fig. 1).5 AGE are resistant to degradation and con cause of blindness in the working population of the United tinue to accumulate indefinitely on long-lived proteins. -
Pvd-Vs-Pad.Pdf
A CLINICIAN'S GUIDE Helping Your Patients with Peripheral Artery Disease (PAD) Peripheral Artery Disease Definition Peripheral artery disease is a disease of the blood vessels outside the heart. This condition is caused by a narrowing of vessels that carry blood away from the heart to other parts of the body. Peripheral artery disease (PAD) is often used interchangeably with the term “peripheral vascular disease (PVD).” The term “PAD” is recommended to describe this condition because it includes venous in addition to arterial disorders. PAD stems from structural changes in the blood vessels resulting from fatty buildup (atherosclerosis) in the inner walls of the arteries. These deposits hinder and block normal blood flow. Why is peripheral artery disease dangerous? In the most common type of PAD, lower extremity PAD, blood flow is reduced to the legs and feet. Left untreated, PAD can lead to gangrene and limb amputation. Patients with PAD are at heightened risk for death from both heart attack and stroke. PAD can result in poor kidney circulation, leading to high blood pressure, or blood pressure that is difficult to control with lifestyle changes and medications. In some cases, blockage of the kidney arteries may progress to loss of kidney function or kidney failure. What are the symptoms of PAD? The most common symptom of PAD is “claudication,” which is cramping, fatigue, aching, pain or discomfort in the legs and buttocks caused by poor blood circulation. The symptoms occur during activity and usually go away with rest. Claudication can often decrease the distance you can walk, and can negatively affect your ability to function at home and at work. -
Atherosclerosisatherosclerosis
AtherosclerosisAtherosclerosis Atherosclerotic Cardiovascular Disease (ASCVD) Smooth m. proliferation Endothelial injury Lipids (cholesterol) Pathogenesis of atherosclerosis 1 Normal Artery Structure Lipoprotein particle 2 XX 60,00060,000 xx 180,000180,000 Robert Hamilton, Ph.D. EM: Negative staining Cardiovascular Research Inst., UCSF 3 The cholesterol in LDL accounts for ©Medscape approx. 70% of the plasma cholesterol Arteriosclerosis (Hardening of the arteries) Arterial wall thickening + loss of elasticity Monckeberg medial Arteriolosclerosis Atherosclerosis calcific sclerosis hyaline hyper- plastic ¾Age 50 -small arteries/arterioles -aorta & branches + ¾Radiologic calcif. -hyaline type / hyperplastic coronary arteries ¾Lumen intact -hypertension / diabetes -ASCVD causes 38% of ¾Clinically insignif. all deaths in N. America 4 ATHEROSCLEROSIS: response-to-injury model Atherosclerosis is a chronic inflammatory response of the arterial wall to endothelial injury. 1. Chronic endothelial injury 2. Accumulation of lipoproteins (LDL mainly) basic tenets 3. Monocyte adhesion to endothelium 4. Platelet adhesion 5. Factors releasedÆSMC recruitment 6. SMC proliferation and ECM production 7. Lipid accumulation: extracellular/mac-SMC Risk Factors for Atherosclerosis •Hyperlipidemia •Smoking •Hypertension •Turbulence •Genetics 5 Endothelial injury Early Chronic—repetitive injury non- denuding endothelial dysfunction -cig. smoke toxins -homocysteine -?? Infectious agents -cytokinesÆgenes for Endothelial injury Early Chronic—repetitive injury non- -
A Case of Malignant Hypertension-Induced Thrombotic Microangiopathy with Gradually Improved Renal Function Using Appropriate Antihypertensives
10.5152/turkjnephrol.2021.4404 Case Report A Case of Malignant Hypertension-Induced Thrombotic Microangiopathy with Gradually Improved Renal Function Using Appropriate Antihypertensives Feyza Bora1 , Fatih Yılmaz2 , Hasan Sözel3 , Bahar Akkaya4 1Department of Nephrology, Akdeniz University School of Medicine, Antalya, Turkey 2Department of Nephrology, Antalya Atatürk State Hospital, Antalya, Turkey 3Department of Internal Medicine, Akdeniz University Hospital, Antalya, Turkey 84 4Department of Pathology, Akdeniz University Hospital, Antalya, Turkey Abstract Malignant hypertension sometimes causes microangiopathic hemolytic anemia (MAHA) and thrombotic microangiopathy (TMA). TMA results in the obstruction of arterioles and capillaries due to microvascular thrombosis. The pathological di- agnosis of TMA is done by tissue biopsy. In this process, malignant hypertension-induced TMA must be distinguished from thrombotic thrombocytopenic purpura (TTP) and hemolitic uremic syndrome (HUS). We describe the case of a 45-year-old man with malignant hypertension, MAHA, and severe renal failure. Plasmapheresis was performed until the ADAMTS -13 activity was reported as normal. The patient’s blood pressure was reduced in a controlled manner first using antihyperten- sives, and TMA was confirmed by a kidney biopsy. Based on the normal ADAMTS-13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13) activity, other possible conditions that might cause TMA were eliminated, and malign hypertension-induced TMA was diagnosed. After two years, the glomerular filtration rate was found to have increased from 22 to 59.5 ml/min. In cases of severe hypertension associated with TMA, it may sometimes not be easy to establish whether TMA is caused by malignant hypertension or other associated diseases. The treatment of hyperten- sion-induced TMA aims to control hypertension, which leads to the resolution of TMA over time. -
Cutaneous Collagenous Vasculopathy: Papular Form
Volume 25 Number 8| August 2019| Dermatology Online Journal || Photo Vignette 25(8):8 Cutaneous collagenous vasculopathy: papular form Alberto Conde-Ferreirós1, Mónica Roncero-Riesco1, Javier Cañueto1, Concepción Román-Curto1, Ángel Santos-Briz2 Affiliations: 1Department of Dermatology, University Hospital of Salamanca, Paseo de San Vicente, 58-182, 37007, Salamanca, Spain, 2Department of Pathology, University Hospital of Salamanca, Paseo de San Vicente, 58-182, 37007, Salamanca, Spain Corresponding Author: Dr. Alberto Conde Ferreirós, University Hospital of Salamanca, Department of Dermatology, Paseo San Vicente, 58-182, 37007, Salamanca (Spain), Email: [email protected] [email protected], Tel: 34-923-29100/34-691-010273 Introduction Abstract Cutaneous collagenous vasculopathy is a rare Cutaneous collagenous vasculopathy is a rare clinicopathological entity; it was first described in clinicopathological entity, first described in 2000. 2000 by Salama and Rosenthal [1]. Cutaneous Cutaneous collagenous vasculopathy has been considered a form of microangiopathy of superficial collagenous vasculopathy has been considered a dermal vessels and produce lesions that appear as form of microangiopathy, which affects superficial telangiectasia. We present a patient with cutaneous vessels. It is characterized by the deposit histopathologic features of cutaneous collagenous of a homogeneous eosinophilic hyaline material in vasculopathy and scattered erythematous papules vascular walls. To date, all cases clinically consist in on the trunk with a striking dermatoscopic finding. progressive asymptomatic cutaneous We propose the term of “cutaneous papular telangiectasias. collagenous vasculopathy” as a new clinical manifestation of this disease. Case Synopsis Keywords: cutaneous collagenous vasculopathy, collagen We report a 68-year-old man with a history of IV, microangiopathy, cutaneous telangiectasias hyperuricemia, hypertension, atrial fibrillation, gout, A B A B Figure 1. -
Atherosclerosis
Atherosclerosis Circulating the Facts About Peripheral Vascular Disease Brought to you by the Education Committee of the Society for Vascular Nursing 1 www.svnnet.org Society for Circulating the Facts About Peripheral Artery Disease: Vascular Atherosclerosis Nursing ATHEROSCLEROSIS ● What is ATHEROSCLEROSIS? ● Signs and symptoms ● Risk factors ● Prevent further disease ● Diagnostic tests What Is Atherosclerosis? Blood flows through tubes called arteries which carry oxygen and food to your body and internal organs. Atherosclerosis is a buildup of cholesterol and fat in the artery and is also known as plaque. Arteries become blocked and narrowed due to atherosclerosis and this affects blood flow to your body. Atherosclerosis can affect any artery in the body, including arteries in the heart, brain, arms, legs, pelvis, and kidneys. Signs and Symptoms Signs and symptoms of atherosclerosis are related to the location and amount of narrowing (plaque) that causes decreased blood flow through arteries. The following arteries can be affected by atherosclerosis: Carotid Arteries Blood flows to your brain through the carotid arteries located on either side of the neck. Plaque that narrows or blocks blood flow in the carotid arteries may cause: ● Sudden body weakness ● Weakness/ unable to move one side of the body ● Sudden imbalance or falling ● Droop on one side of the mouth or face ● Temporary or permanent blindness or loss of the vision in one eye ● Difficulty speaking and understanding words ● Memory loss or sudden confusion ● Loss of consciousness ● Sudden and severe headache ● Difficulty with breathing Updated 09052014 1 Society for Circulating the Facts About Peripheral Artery Disease: Vascular Atherosclerosis Nursing Coronary Arteries Blood flows to your heart through the coronary arteries.