This document defines diabetes and provides classifications of the different types of diabetes. It discusses the key characteristics of type 1 diabetes, type 2 diabetes, and other specific types. Criteria are provided for diagnosing diabetes and prediabetes based on HbA1c levels, fasting plasma glucose levels, and oral glucose tolerance tests. Guidelines are also given for screening and diagnosing gestational diabetes.
Objetivos en diabetes: de la "evidencia" al sentido común Rafael Bravo Toledo
Objetivos en diabetes: de la "evidencia" al sentido común
José Manuel Millaruelo Trillo. Centro de Salud Torrero La Paz. Zaragoza. Miembro de la red GEDAPS Aragón
Our aim is to reduce morbidity and mortality related to Non communicable diseases such as hypertension, diabetes, cardiovascular disease, stroke, Obesity, Cancer and lifestyle diseases among those least able to withstand the burden of the disease.
Objetivos en diabetes: de la "evidencia" al sentido común Rafael Bravo Toledo
Objetivos en diabetes: de la "evidencia" al sentido común
José Manuel Millaruelo Trillo. Centro de Salud Torrero La Paz. Zaragoza. Miembro de la red GEDAPS Aragón
Our aim is to reduce morbidity and mortality related to Non communicable diseases such as hypertension, diabetes, cardiovascular disease, stroke, Obesity, Cancer and lifestyle diseases among those least able to withstand the burden of the disease.
This is part 1 for the "All Things Taboola" series in which we'll cover everything you need to know about our discovery platform. Why this is the best thing for your agency and how to pitch it to your clients.
Join us and become an expert in a few steps. Speakers: Lena Chudasam, Sr. success manager at Taboola, Christophe Butlin CEO of Stringo media and Jonathan Riftin, Taboola Partners lead
Memorias Conferencia Científica Anual sobre Síndrome Metabólico 2017 - Programa Científico
Futuro en el tratamiento de la DM2
Dr. Guillermo E. Umpierrez
Professor of Medicine in the Division of Endocrinology at Emory University School of Medicine, Section Head, Diabetes and Endocrinology. USA. Editor en Jefe del BJM Open Diabetes Research and Care
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
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Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
These lecture slides, by Dr Sidra Arshad, offer a quick overview of physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
1. Diabetes
Universidad de Sucre
Visible para todos
Jesús Turizo Hernández
Universidad de Sucre | Facultad de Ciencias de la Salud | Programa de Medicina
2. Atlas de la Diabetes de la Federación Internacional de Diabetes, 2013
3. Definición
La diabetes es un grupo de enfermedades metabólicas caracterizada por
hiperglucemia resultante de defectos en la secreción de insulina, la acción
de la insulina, o ambos.
Diagnosis and Classification of Diabetes Mellitus. (2009). Diabetes Care, 33 (Supplement 1), pp. S62-S69.
Etimología
El término diabetes: aspectos históricos y lexicográficos. Panacea. Vol. V, n° 15. Marzo, 2004.
Del griego diabétes.
Del verbo diabaíno, ‘caminar’.
Del prefijo dia-, ‘a través de’ y báino, ‘andar, pasar’.
Ojos
Riñones
Nervios
Corazón
Vasos sanguíneos
Hiperglicemia crónica
Diagnosis and Classification of Diabetes Mellitus. (2009). Diabetes Care, 33 (Supplement 1), pp. S62-S69.
Definición
4.
5. Número estimado de personas con diabetes en el mundo
y por región en 2015 y 2040 (20-79 años)
20. Epidemiología
La prevalencia de la diabetes mellitus tipo 2 en Colombia es
aproximadamente del 7,4% en hombres y del 8,7% en mujeres mayores de
30 años.
La incidencia de diabetes mellitus tipo 1 en Colombia es relativamente baja
(de 3-4 por 100.000 niños <15 años) y la prevalencia se estima en un
0,07%.
Los puntos de corte de cintura que mejor discriminan el exceso de grasa
visceral en Latinoamérica corresponden a 94 cm para hombres y 88 cm para
mujeres.
Aschner, P. (2015). Epidemiología de la diabetes en Colombia. Avances en Diabetología 31(3): 95-100.
21. Clasificación
Diabetes tipo 1 (DM1).
Diabetes tipo 2 (DM2).
Otros tipos específicos de diabetes.
Diabetes gestacional (DMG).
Diagnosis and Classification of Diabetes Mellitus. (2009). Diabetes Care, 33 (Supplement 1), pp. S62-S69.
Clasificación
Diabetes tipo 1 (DM1):
Destrucción de las células β, lo que conduce a la deficiencia
absoluta de insulina.
A. Inmunomediada.
B. Idiopática.
Diagnosis and Classification of Diabetes Mellitus. (2009). Diabetes Care, 33 (Supplement 1), pp. S62-S69.
Clasificación
Diabetes tipo 2 (DM2):
A. Predominantemente insulinorresistente con deficiencia
relativa de insulina.
B. Predominantemente con un defecto secretor de la insulina
con o sin resistencia a la insulina.
Diagnosis and Classification of Diabetes Mellitus. (2009). Diabetes Care, 33 (Supplement 1), pp. S62-S69.
Clasificación
Diagnosis and Classification of Diabetes Mellitus. (2009). Diabetes Care, 33 (Supplement 1), pp. S62-S69.
Otros tipos específicos de diabetes:
A. Defectos genéticos de la función de las células β:
1. Cromosoma 12, HNF-1α (MODY3).
2. Cromosoma 7, glucocinasa (MODY2).
3. Cromosoma 20, HNF-4α (MODY1).
4. Cromosoma 13, factor promotor de insulina-1 (IPF-1;
MODY4).
5. Cromosoma 17, HNF-1α (MODY5).
6. Cromosoma 2, NeuroD1 (MODY6).
7. ADN mitocondrial.
8. Otros.
B. Defectos genéticos en la acción de la insulina:
1. Resistencia a la insulina tipo A.
2. Leprechaunismo.
3. Síndrome de Rabson-Mendenhall.
4. Diabetes lipoatrófica.
5. Otros.
C. Enfermedades del páncreas exocrino:
1. Pancreatitis.
2. Trauma del páncreas.
3. Pancreatectomía.
4. Neoplasia del páncreas.
5. Fibrosis quística.
6. Hemocromatosis.
7. Pancreatopatía fibrocalculosa.
8. Otros.
D. Endocrinopatías:
1. Acromegalia.
2. Síndrome de Cushing.
3. Glucagonoma.
4. Feocromocitoma.
5. Hipertiroidismo.
6. Somatostinoma.
7. Aldosteronoma.
8. Otros.
E. Inducida por drogas o químicos:
1. Vacor.
2. Pentamidina.
3. Ácido nicotínico.
4. Glucocorticoides.
5. Hormonas tiroideas.
6. Diazóxido.
7. Agonistas β-adrenérgicos.
8. Tiazidas.
9. Fenitoína.
10. γ-interferón.
11. Otros.
F. Infecciones:
1. Rubéola congénita
2. Citomegalovirus
3. Otros.
G. Formas poco comunes de diabetes mediada Inmunológicamente:
1. Síndrome del hombre rígido.
2. Anticuerpos contra el receptor de la insulina.
3. Otros.
H. Otros síndromes genéticos algunas veces asociados con
diabetes:
1. Síndrome de Down.
2. Síndrome de Klinefelter.
3. Síndrome de Turner.
4. Síndrome de Wolfram.
5. Ataxia de Friedreich.
6. Corea de Huntington.
7. Síndrome de Lawrence-Moon-Biedl.
8. Distrofia miotónica.
9. Porfiria.
10. Síndrome de Prader-Willi.
11. Otros.
23. Atlas de la Diabetes de la Federación Internacional de Diabetes, 2013
24. Criteria for the diagnosis of diabetes
FPG ≥126 mg/dL (7.0 mmol/L). Fasting is defined as no caloric intake for at least 8
h.
OR
2-h PG ≥200 mg/dL (11.1 mmol/L) during an OGTT. The test should be performed
as described by the WHO, using a glucose load containing the equivalent of 75 g
anhydrous glucose dissolved in water.
OR
A1C ≥6.5% (48 mmol/mol). The test should be performed in a laboratory using a
method that is NGSP certified and standardized to the DCCT assay.
OR
In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a
random plasma glucose ≥200 mg/dL (11.1 mmol/L).
Criterios diagnósticos
Standards of Medical Care in Diabetes—2017. Diabetes Care. Volume 40, Supplement 1, January 2017
25. Criteria for testing for diabetes or prediabetes in asymptomatic adults
1. Testing should be considered in overweight or obese (BMI ≥25 kg/m² or ≥23
kg/m² in Asian Americans) adults who have one or more of the following risk
factors:
A1C ≥5.7% (39 mmol/mol), IGT, or IFG on previous testing
first-degree relative with diabetes
high-risk race/ethnicity (e.g., African American, Latino, Native American, Asian
American, Pacific Islander)
women who were diagnosed with GDM
history of CVD
hypertension (≥140/90 mmHg or on therapy for hypertension)
HDL cholesterol level <35 mg/dL (0.90 mmol/L) and/or a triglyceride level >250
mg/dL (2.82 mmol/L)
women with polycystic ovary syndrome
physical inactivity
Criterios diagnósticos
Standards of Medical Care in Diabetes—2017. Diabetes Care. Volume 40, Supplement 1, January 2017
26. Criterios diagnósticos
Standards of Medical Care in Diabetes—2017. Diabetes Care. Volume 40, Supplement 1, January 2017
Categories of increased risk for diabetes (prediabetes)
FPG 100 mg/dL (5.6 mmol/L) to 125 mg/dL (6.9 mmol/L) (IFG)
OR
2-h PG in the 75-g OGTT 140 mg/dL (7.8 mmol/L) to 199 mg/dL (11.0 mmol/L) (IGT)
OR
A1C 5.7 – 6.4% (39 – 47 mmol/mol)
27. Criteria for Clinical Diagnosis of the Metabolic Syndrome
Measure Categorical Cut Points
Elevated waist circumference
Population and country specific
definitions
Elevated triglycerides (drug treatment for
elevated triglycerides is an alternate
indicator)
≥150 mg/dL (1.7 mmol/L)
Reduced HDL-C (drug treatment for
reduced HDL-C is an alternate indicator)
<40 mg/dL (1.0 mmol/L) in males;
<50 mg/dL (1.3 mmol/L) in females
Elevated blood pressure
(antihypertensive drug treatment in a
patient with a history of hypertension is
an alternate indicator)
Systolic ≥130 and/or diastolic ≥85 mmHg
Elevated fasting glucose (drug treatment
Alberti, K., et al. (2009). Harmonizing the Metabolic Syndrome. Circulation, 120(16), pp.1640-1645.
Criterios diagnósticos
28. Screening for and diagnosis of GDM
One-step strategy
Perform a 75-g OGTT, with plasma glucose measurement when patient is fasting
and at 1 and 2 h, at 24 – 28 weeks of gestation in women not previously diagnosed
with overt diabetes.
The OGTT should be performed in the morning after an overnight fast of at least 8 h.
The diagnosis of GDM is made when any of the following plasma glucose values are
met or exceeded:
Fasting: 92 mg/dL (5.1 mmol/L)
1 h: 180 mg/dL (10.0 mmol/L)
2 h: 153 mg/dL (8.5 mmol/L)
Standards of Medical Care in Diabetes—2017. Diabetes Care. Volume 40, Supplement 1, January 2017
Criterios diagnósticos
29. Screening for and diagnosis of GDM
Two-step strategy
Step 1: Perform a 50-g GLT (nonfasting), with plasma glucose measurement at 1 h,
at 24–28 weeks of gestation in women not previously diagnosed with overt diabetes.
If the plasma glucose level measured 1 h after the load is ≥130 mg/dL, 135 mg/dL,
or
140 mg/dL (7.2 mmol/L, 7.5 mmol/L, or 7.8 mmol/L), proceed to a 100-g OGTT.
Step 2: The 100-g OGTT should be performed when the patient is fasting.
The diagnosis of GDM is made if at least two of the following four plasma glucose
levels (measured fasting and 1 h, 2 h, 3 h after the OGTT) are met or exceeded:
Standards of Medical Care in Diabetes—2017. Diabetes Care. Volume 40, Supplement 1, January 2017
Criterios diagnósticos
30. Standards of Medical Care in Diabetes—2017. Diabetes Care. Volume 40, Supplement 1, January 2017
Criterios diagnósticos
Screening for and diagnosis of GDM
Two-step strategy
Carpenter/Coustan NDDG
Fasting 95 mg/dL (5.3 mmol/L) 105 mg/dL (5.8 mmol/L)
1 h 180 mg/dL (10.0 mmol/L) 190 mg/dL (10.6 mmol/L)
2 h 155 mg/dL (8.6 mmol/L) 165 mg/dL (9.2 mmol/L)
3 h 140 mg/dL (7.8 mmol/L) 145 mg/dL (8.0 mmol/L)
or
31. Metas de control
Summary of glycemic recommendations for many
nonpregnant adults with diabetes
A1C <7.0% (53 mmol/mol).
Preprandial capillary plasma glucose 80–130 mg/dL (4.4–7.2 mmol/L).
Peak postprandial capillary plasma glucose <180 mg/dL (10.0 mmol/L).
Standards of Medical Care in Diabetes—2017. Diabetes Care. Volume 40, Supplement 1, January 2017
32.
33.
34.
35.
36.
37.
38. Section changes
The section was updated to include a new consensus on the staging of
type 1 diabetes and a discussion of a proposed unifying diabetes
classification scheme that focuses on b-cell dysfunction and disease
stage as indicated by glucose status.
Section 2. Classification and Diagnosis of Diabetes
39. Staging of type 1 diabetes
Stage 1 Stage 2
Stage
Autoimmunity
Normoglycemia
Presymptomatic
Autoimmunity
Dysglycemia
Presymptomatic
Diagnostic
criteria
Multiple
autoantibodies
No IGT or IFG
Multiple autoantibodies
Dysglycemia: IFG and/or IGT
FPG 100–125 mg/dL (5.6–6.9 mmol/L
2-h PG 140–199 mg/dL (7.8–11.0 mm
A1C 5.7–6.4% (39–47 mmol/mol) or ≥
Section changes
Section 2. Classification and Diagnosis of Diabetes
40. Section changes
The recommendation to test women with gestational diabetes mellitus
for persistent diabetes was changed from 6–12 weeks’ postpartum to
4–12 weeks’ postpartum to allow the test to be scheduled just before
the standard 6-week postpartum obstetrical checkup so that the results
can be discussed with the patient at that time of the visit or to allow the
test to be rescheduled at the visit if the patient did not get the test.
Section 2. Classification and Diagnosis of Diabetes
41. Section changes
To reflect new evidence showing an association between B12
deficiency and long-term metformin use, a recommendation was added
to consider periodic measurement of B12 levels and supplementation
as needed.
Section 5. Prevention or Delay of Type 2 Diabetes
42. Section changes
Based on recommendations from the International Hypoglycemia
Study Group, serious, clinically significant hypoglycemia is now
defined as glucose <54 mg/dL (3.0 mmol/L), while the glucose alert
value is defined as ≥70 mg/dL (3.9 mmol/L). Clinical implications are
discussed.
Section 6. Glycemic Targets
43. Classification of hypoglycemia
Level Glycemic criteria Description
Glucose alert value
(level 1)
≤70 mg/dL (3.9
mmol/L)
Sufficiently low for treatment with
fast-acting carbohydrate and dose
adjustment of glucose-lowering
therapy
Clinically significant
hypoglycemia (level 2)
<54 mg/dL (3.0
mmol/L)
Sufficiently low to indicate serious,
clinically important hypoglycemia
Severe hypoglycemia
(level 3)
No specific
glucose threshold
Hypoglycemia associated with severe
cognitive impairment requiring
external assistance for recovery
Section changes
Section 6. Glycemic Targets
44. Section changes
To optimize maternal health without risking fetal harm, the
recommendation for the treatment of pregnant patients with diabetes
and chronic hypertension was changed to suggest a blood pressure
target of 120–160/80–105 mmHg.
Section 9. Cardiovascular Disease and Risk Management
45.
46. Blood Glucose Meters Accuracy Requirements
The minimum accuracy performance criteria are:
At glucose levels <100 mg/dL (5.55 mmol/L), 95% of results should be
within ±15 mg/dL (0.83 mmol/L) of laboratory results.
At glucose levels ≥100 mg/dL (5.55 mmol/L), 95% of results should be
within ±15% of laboratory results.
System Accuracy Requirement A: Accuracy Plot
47. Blood Glucose Meters Accuracy Requirements
The minimum accuracy performance criteria are:
99% of results must be within zones A & B of the Consensus Error Grid
(CEG) for type 1 diabetes.
System Accuracy Requirement B: Consensus Error Grid
48. Blood Glucose Meters Accuracy Requirements
System Accuracy Requirement B: Consensus Error Grid
Zone A No effect on clinical action
Zone B Altered clinical action – little or no effect on clinical outcome
Zone C Altered clinical action – likely to affect clinical outcome
Zone D Altered clinical action – could have signifcant medical risk
Zone E Altered clinical action – could have dangerous consequences