The document provides a history of diabetes from ancient times to the present. It describes how diabetes was first described in writing in 1500 BC India and how the word "diabetes" was coined in 250 BC by Apollonius of Memphis to mean "to siphon" referring to the disease draining fluids. Early treatments for diabetes were ineffective and dangerous. A key breakthrough was the discovery of insulin by Banting, Best, Collip and Macleod at the University of Toronto in 1921-1922, allowing those with diabetes to live longer lives. The mass production of insulin began in the 1920s, and refinements to insulin continued, including the development of recombinant DNA human insulin in 1978 and modern designer insulins in the
14. a case study on diabetes mellitus type 1 with diabetic ketoacidosis cp in...Dr. Ajita Sadhukhan
A 26 year old male patient was admitted to the male medicine ward with complaints of nausea, vomiting, generalised weakness, anxiety, decreased appetite, headache since noon.
14. a case study on diabetes mellitus type 1 with diabetic ketoacidosis cp in...Dr. Ajita Sadhukhan
A 26 year old male patient was admitted to the male medicine ward with complaints of nausea, vomiting, generalised weakness, anxiety, decreased appetite, headache since noon.
Hypertension or high blood pressure has become a common health problem.
•High blood pressure may cause coronary artery disease, stroke, heart failure, atrial fibrillation, peripheral vascular disease, vision loss, chronic kidney disease and dementia.
•The narrower your arteries are, the higher your blood pressure will be.
•Your blood pressure measurement takes into account how much blood is passing through your blood vessels and the amount of resistance the blood meets while the heart is pumping.
•High blood pressure generally develops over many years, and it affects nearly everyone eventually.
•Fortunately, high blood pressure can be easily detected. And once you know you have high blood pressure, you can work with your doctor to control it.
Get more details @
Diabetes mellitus (DM) is a group of diseases characterized by high levels of blood glucose resulting from defects in insulin production, insulin action, or both.
The term diabetes mellitus describes a metabolic disorder of multiple aetiology characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both.
The effects of diabetes mellitus include long–term damage, dysfunction and failure of various organs.
Hypertension or high blood pressure has become a common health problem.
•High blood pressure may cause coronary artery disease, stroke, heart failure, atrial fibrillation, peripheral vascular disease, vision loss, chronic kidney disease and dementia.
•The narrower your arteries are, the higher your blood pressure will be.
•Your blood pressure measurement takes into account how much blood is passing through your blood vessels and the amount of resistance the blood meets while the heart is pumping.
•High blood pressure generally develops over many years, and it affects nearly everyone eventually.
•Fortunately, high blood pressure can be easily detected. And once you know you have high blood pressure, you can work with your doctor to control it.
Get more details @
Diabetes mellitus (DM) is a group of diseases characterized by high levels of blood glucose resulting from defects in insulin production, insulin action, or both.
The term diabetes mellitus describes a metabolic disorder of multiple aetiology characterized by chronic hyperglycaemia with disturbances of carbohydrate, fat and protein metabolism resulting from defects in insulin secretion, insulin action, or both.
The effects of diabetes mellitus include long–term damage, dysfunction and failure of various organs.
Rethinking Diabetes: What Science Reveals About Diet, Insulin, and Successful...Lucky Gods
Break Free from the Blood Sugar Rollercoaster: Rethinking Diabetes insulin, diet, effective treatments
Forget everything you thought you knew about diabetes! This isn't a one-size-fits-all story, it's a transformative journey through the cutting-edge science of managing your blood sugar and thriving. ✨
Imagine this:
Waking up energized, your body a temple of strength and vitality.
Fueling your days with delicious, nutritious meals that don't feel like restrictions.
Taming stress and conquering cravings with science-backed tools.
**Unlocking the secrets of insulin and metabolic flexibility for lasting results.
Discovering a thriving community of support and understanding.
This ebook is your cheat code to unlocking a healthier, happier you. We'll equip you with the knowledge and tools to:
Ditch the myths and embrace the evidence-based truth about diabetes.
Craft a personalized plan for success, based on your unique needs and preferences.
Master the art of mindful eating and discover the power of food as medicine.
Unleash the potential of your own body with effective exercise and lifestyle strategies. ♀️
Navigate the world of medications and treatments with confidence.
Build resilience, overcome challenges, and celebrate every victory along the way.
This isn't just about managing diabetes; it's about reclaiming your health and embracing a vibrant, fulfilling life.
So, ditch the doubt, grab your curiosity, and let's rewrite the story of diabetes together!
Nina Teicholz in her book The Big Fat Surprise. According to her, we have been approaching the very real problem of heart attack risk from the wrong angle for many years.
Infertility is defined as the inability of a couple to conceive after at least one year of regular unprotected intercourse.
Male infertility refers to a male's inability to cause pregnancy in a fertile female.
IDD situation in our country has improved
A good number of thyroid disorder patients are either undiagnosed and or untreated
Thyroid disorder in pregnancy- Rate high
As a sound thyroid functioning status is crucial for growth, development in children; reproduction, psychological and general wellbeing in adults, we must be proactive in screening, diagnosing and treating our patients.
Over the past several years it has been proved that maternal thyroid disorder influence the outcome of mother and fetus, during and also after pregnancy. The most frequent thyroid disorder in pregnancy is maternal hypothyroidism. It is associated with fetal loss, placental abruptions, pre-eclampsia, preterm delivery and reduced intellectual function in the offspring.1 In pregnancy, overt hypothyroidism is seen in 0.2% cases2 and sub clinical hypothyroidism in 2.3% cases3. Fetal loss, fetal growth restriction, pre-eclampsia and preterm delivery are the usual complications of overt hyperthyroidism (low TSH and high T3, T4) seen in 2 of 1000 pregnancies whereas mild or sub clinical hyperthyroidism (suppressed TSH alone) is seen in
1.7% of pregnancies and not associated with adverse outcomes4. Autoimmune positive euthyroid pregnancy shows doubling of incidence of miscarriage and preterm delivery. Worldwide more than 20 million people develop neurological sequel due to intra uterine, iodine deprivation5. Other problems of thyroid disorders in pregnancy are post partum thyroiditis, thyroid nodules and cancer, hyper emesis gravidarum etc. Debates and disputes persist regarding several protocol and management plan in this specific spectrum of diseases.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
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.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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
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
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Title: Sense of Smell
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 primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
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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
1. Diabetes:
Past, Present and Future
Dr Shahjada Selim
Assistant Professor
Department of Endocrinology
Bangabandhu Sheikh Mujib Medical University, Dhaka
Email: selimshahjada@gmail.com
April 1, 2016 Shahjada Selim, MD, MACE.
2. Shahjada Selim, MD, MACE.
In 1500 BC
Diabetes First Described In Writing
Hindu healers wrote that flies and ants were
attracted to urine of people with a
mysterious disease that caused intense
thirst, enormous urine output, and wasting
away of the body.
April 1, 2016
3. Shahjada Selim, MD, MACE.
250 BC
The Word Diabetes First Used
• Apollonius of Memphis coined the name
"diabetes” (διαβήτηςδιαβήτης) meaning "to go through"
‘‘to stand apart’’ or siphon. He understood that
the disease drained more fluid than a person
could consume.
April 1, 2016
4. Shahjada Selim, MD, MACE.
250 BC
The Word Diabetes First Used
• Gradually the Latin word for honey, "mellitus,"
was added to diabetes because it made the urine
sweet.
• FirstFirst recordedrecorded inin EnglishEnglish inin aboutabout 14251425 asas
‘diabetes’‘diabetes’.
April 1, 2016
5. Shahjada Selim, MD, MACE.
Diabetes is a wonderful affection, not very
frequent among men, being a melting down of
the flesh and limbs into urine…The flow is
incessant, as if from the opening of
aqueducts…it takes a long period to form, but
the patient is short-lived…for the melting is
rapid, the death speedy.
150 BC
Aretaeus the Cappadocian
April 1, 2016
6. Shahjada Selim, MD, MACE.
Moreover, life is disgusting and painful; thirst
unquenchable; excessive drinking…and one
cannot stop them either from drinking or
making water... they are affected with
nausea, restlessness, and a burning thirst;
and at no distant term they expire.
150 BC
Aretaeus the Cappadocian
April 1, 2016
9. Shahjada Selim, MD, MACE.
Early Diabetes Treatments
• In 1000, Greek physicians recommended
horseback riding to reduce excess urination
• In the 1800s, bleeding, blistering, and doping
were common
• In 1915, Sir William Osler recommended
opium
• Overfeeding was commonly used to
compensate for loss of fluids and weight
• In the early 1900s a leading American
diabetologist, Dr. Frederick Allen,
recommended a starvation diet.
April 1, 2016
10. Shahjada Selim, MD, MACE.
Early Research
• In 1798, John Rollo documented excess
sugar in the blood and urine
• In 1813, Claude Bernard linked diabetes to
glycogen metabolism
• In 1869, Paul Langerhans, a German
medical student, discovered islet cells in the
pancreas.
April 1, 2016
11. Shahjada Selim, MD, MACE.
Early Research
• In 1889, Joseph von Mehring and Oskar
Minkowski created diabetes in dogs by
removing the pancreas
• In 1910, Sharpey-Shafer of Edinburgh
suggested a single chemical was missing
from the pancreas. He proposed calling this
chemical "insulin."
April 1, 2016
12. Shahjada Selim, MD, MACE.
Near Miss
• In 1908, a young internist in Berlin, Georg
Ludwig Zuelzer created a pancreas extract
named acomatrol.
• After injecting acomatrol into a dying diabetic
patient, the patient improved at first, but died
when the acomatrol was gone.
April 1, 2016
13. Shahjada Selim, MD, MACE.
Near Miss
• Zuelzer filed an American patent in 1911 for a
"Pancreas Preparation Suitable for the
Treatment of Diabetes”
• Disappointing results, however, caused his
lab to be taken over by the German military
during WWI
April 1, 2016
14. Shahjada Selim, MD, MACE.
Other “Pancreas Extractors”
• American scientist E. L. Scott was partially
successful in extracting insulin with alcohol.
• A Romanian, R. C. Paulesco, made an extract from
the pancreas that lowered the blood glucose of
dogs.
• Some claim Paulesco may have been the first to
discover insulin about 10 years before Banting and
Best.
April 1, 2016
15. Shahjada Selim, MD, MACE.
Before Insulin
Before insulin was discovered in 1921, everyone
with type 1 diabetes died within weeks to years of
its onset.
JL on 12/15/22 and 2 mos later
April 1, 2016
16. Sir William Osler, in the year 1915, is said to
have even recommended opium! Early research
linked diabetes to glycogen metabolism, and the
islet cells of pancreas were discovered by Paul
Langerhans, a young German medical student.
April 1, 2016 Shahjada Selim, MD, MACE.
17. In 1916, Sharpey-Shafer of Edinburgh
suggested that a single chemical was missing
from the pancreas and proposed its name as
“insulin.” The term insulin originates from the
word Insel, which is German for an islet or
island.
April 1, 2016 Shahjada Selim, MD, MACE.
19. Researchers like E.L. Scott and Nikolae
Paulesco were successful in extracting insulin
from the pancreas of experimental dogs. The key
breakthrough, though, came from the Toronto
University with the discovery of insulin in 1921.
April 1, 2016 Shahjada Selim, MD, MACE.
21. BantingBanting andand BestBest managedmanaged toto getget throughthrough
dozensdozens ofof dogsdogs tryingtrying differentdifferent methodsmethods toto
getget thethe pancreaspancreas toto failfail andand thenthen toto replacereplace it.it.
DespiteDespite theirtheir poorpoor science,science, andand poorpoor records,records,
theythey eventuallyeventually ‘stumbled’‘stumbled’ onon somethingsomething
Promising.Promising.
April 1, 2016 Shahjada Selim, MD, MACE.
22. 19211921 andand AllAll That……That……
Banting,Banting,
Best,Best,
Collip,Collip,
andand
McLeodMcLeod
At theAt the
UniversityUniversity
ofof
Toronto.Toronto.
April 1, 2016
Shahjada Selim, MD, MACE.
23. FG Banting and JJR Macleod were awarded the
Nobel Prize for Physiology or Medicine in 1923.
They shared their prize money with CH Best and
JB Collip who were “left out” by the prize
committee.
April 1, 2016 Shahjada Selim, MD, MACE.
25. Banting and Best injected the crude pancreatic
extract “thick brown muck” into a 14-year-old
boy named “Leonard” in January 1922. His
blood sugar levels dropped significantly, but an
abscess developed at the injection site making
him acutely ill.
April 1, 2016 Shahjada Selim, MD, MACE.
26. A refined extract was again administered after 6
weeks, causing drop in blood sugar levels from 520
mg/dl to 120 mg/dl within 24 h. Leonard lived for
13 years before dying of pneumonia (another
disease for which no cure was available in those
days)
April 1, 2016 Shahjada Selim, MD, MACE.
28. McLeod brought in a
leading biochemist to
help with purification –
James Bertram Collip.
Collip was working on
calcium but agreed to
work with McLeod
during a 1 year
sabbatical.
April 1, 2016 Shahjada Selim, MD, MACE.
The Solution
29. RegardedRegarded asas thethe firstfirst
personperson toto everever receivereceive
insulininsulin onon 11th11th
JanuaryJanuary 19221922 agedaged 1414
HeHe livedlived forfor 1313 yearsyears
beforebefore dyingdying inin aa carcar
accidentaccident
April 1, 2016 Shahjada Selim, MD, MACE.
Leonard
31. Recognition
InIn 1923,1923, BantingBanting andand McLeodMcLeod werewere
awardedawarded the Nobelthe Nobel PrizePrize forfor MedicineMedicine
BantingBanting gavegave halfhalf hishis prizeprize immediatelyimmediately toto
Best,Best, andand McLeodMcLeod gavegave halfhalf ofof hishis toto
Collip.Collip.
April 1, 2016 Shahjada Selim, MD, MACE.
32. TheThe DiabeticDiabetic Association,Association, waswas setset upup inin 19341934 byby
novelistnovelist HGHG WellsWells andand DrDr RDRD Lawrence “ToLawrence “To promotepromote
thethe study,study, thethe diffusiondiffusion ofof knowledge,knowledge, andand thethe properproper
treatmenttreatment ofof diabetesdiabetes inin thisthis country.”country.”
1923 - “I’ve got some insulin. It works. Come back quick.”
April 1, 2016 Shahjada Selim, MD, MACE.
33. On May 1922, Eli Lilly signed an agreement to
pay royalties to the Toronto University to
increase the production of insulin. In 1923,
August Krogh and Hans Christian Hagedorn
began the mass production of insulin extracted
from porcine pancreas in Denmark.
April 1, 2016 Shahjada Selim, MD, MACE.
34. The Nordisk Insulin Laboratorium (now Novo
Nordisk) was thus established. In 1955, Sir
Frederick Sanger characterized the amino acid
sequence of human insulin, making it the first
protein to whose sequence was determined. He
was awarded the 1958 Nobel Prize in Chemistry
for this work.
April 1, 2016 Shahjada Selim, MD, MACE.
35. Subsequently, Hans Christian Hagedorn
discovered the prolonged effect of insulin by
adding protamine to the insulin molecule. Various
intermediate acting preparations were formulated
to provide 24-h control of blood glucose.
April 1, 2016 Shahjada Selim, MD, MACE.
36. Purified versions of animal insulin were developed
in 1974 by chromatographic techniques (less than 1
pmol/l of protein impurities) known as
“monocomponent MC” “single peak” insulin in
order to reduce the allergic reactions and
lipodystrophy.
April 1, 2016 Shahjada Selim, MD, MACE.
37. In 1978, recombinant DNA technology was used
to produce synthetic human insulin in E. coli. In
early 1980s, mass production of rDNA human
insulin was commenced.
April 1, 2016 Shahjada Selim, MD, MACE.
38. By the mid of nineties, the structure of human
insulin was modified by altering the amino acid
sequence (addition, deletion, or exchange of
amino acids) to produce insulins with better
pharmacokinetic properties, which came to be
known as a “modern insulin” or “designer
April 1, 2016 Shahjada Selim, MD, MACE.
45. InIn 2005 Incretin based therapy wasIncretin based therapy was
introduced.introduced.
April 1, 2016 Shahjada Selim, MD, MACE.
46. Shahjada Selim, MD, MACE.
Demands On Intelligent Devices
• Intuitive interface and language
• Must be impartial and fair
• Outcome driven – user feels better and
is more confident about control
• Compatible with clinic workflow
• Well funded
• Able to rapidly evolve as errors appear
• Must close the data loop between user
and MD
April 1, 2016
47. Shahjada Selim, MD, MACE.
Smart Phones And PDAs
• Fast internet & email communication
• Convenient remote insulin delivery
• Larger food and carb database
• Better graphics for BG analysis,
display of patterns, etc
• Larger event database for long-term
analysis
April 1, 2016
48. Shahjada Selim, MD, MACE.
Intelligent Devices
• 300 personal carb selections
with accurate carb counts
• Carb factor (1:1 TO 1:100)
• Correction factor (1:4 to 1:
400)
5 sec microdraw BG meter
0.1 unit precision motor
Non-volatile memory
3,000 events
Bluetooth data transfer
April 1, 2016
49. Shahjada Selim, MD, MACE.
Thoughts And Developments
For The Future
April 1, 2016
50. Shahjada Selim, MD, MACE.
New: Rapid Basal Reduction
A rapid basal reduction offsets excess BOB and
eliminates the need to eat at bedtime.April 1, 2016
51. Shahjada Selim, MD, MACE.
New: The Super Bolus
A Super Bolus helps cover high GI foods and prevent
postmeal hyperglycemia. A 3 or 4 hour block of basal
insulin is turned into a bolus to speed its effect.
A Super Bolus
can be
activated at a
user-selected
quantity, such
as 40 or 50
grams
April 1, 2016
52. Shahjada Selim, MD, MACE.
New: The Super Bolus
• To ensure safety and success, the Super Bolus will
require some clinical testing:
– How long can basal delivery be stopped or reduced
without increasing the risk for clogging of the infusion line
– How long (3, 4, 5 hours?) can the basal be lowered before
a rebound high will occur once the Super Bolus is gone?
– Is a reduction of the basal delivery rather than complete
stoppage a better policy?
– If a person sets their basal delivery too low or too high, will
this affect a Super Bolus?
April 1, 2016
53. Shahjada Selim, MD, MACE.
New: High BG Super Bolus
If a pumper misjudges the carb content of a meal, a
super bolus enables a faster, safe correction.
April 1, 2016
54. Shahjada Selim, MD, MACE.
New: A Reminder Timer
• A simple timer alerts the user 25 minutes after a
bolus that it is safe to begin eating a high GI meal.
April 1, 2016
55. Shahjada Selim, MD, MACE.
New: An Intelligent Reminder
An intelligent
pump alerts the
user when their
BG is likely to
cross a selected
threshold value,
such as 120
mg/dl. They can
then eat without
exposure to
extremely high
readings.
April 1, 2016
56. Shahjada Selim, MD, MACE.
New: Less Glucose Exposure
The lower the blood
glucose is at the
start of a meal, the
less exposure to
glucose there will
be.
April 1, 2016
57. Shahjada Selim, MD, MACE.
New: An Intelligent Reminder
An intelligent pump
alerts the user
when their blood
glucose is low
enough to begin
eating
April 1, 2016
59. Shahjada Selim, MD, MACE.
Future Pattern Management
• Finding problem patterns enables solutions
• Set BG targets
• Gather and record data
• Analyze patterns in data
• Assess factors that influence
patterns
• Recommend action
April 1, 2016
60. Shahjada Selim, MD, MACE.
Only A Few Patterns
The relatively low number of BG patterns in
diabetes makes them easy to identify:
• High most of the time
• Frequent lows
• High mornings (lunches, dinners, bedtime)
• Low mornings (lunches, dinners, bedtime)
• Postmeal spiking
• High to low
• Low to high
• Poor control with little or no pattern
April 1, 2016
61. Shahjada Selim, MD, MACE.
Low High Pattern Alert
• Insulin dose suggestions and an alert about
past overtreatment of lows.
April 1, 2016
62. Shahjada Selim, MD, MACE.
Low High Pattern Alert
• An intelligent device can provide a
person’s precise carb requirement when
the blood glucose is tested.
April 1, 2016
63. Shahjada Selim, MD, MACE.
Overnight Basal Patterns
bedtime 2 am breakfast
100
200
300
basal too low
Dawn
Phenomeno
n
just right
too high
Goal for overnight BG change = +/- 30 mg/dl
just right
April 1, 2016
64. Shahjada Selim, MD, MACE.
User Interface – Critical Component
Despite 30 years of pump and meter development,
device communication to the user is still in it’s infancy.
April 1, 2016
65. Shahjada Selim, MD, MACE.
Future Intelligent Devices
• Carb database for accurate carb counts.
April 1, 2016
66. Shahjada Selim, MD, MACE.
Future Intelligent Devices
• Suggestion for carb intake or to limit intake based
on weight/calorie/carb goals
April 1, 2016
67. Shahjada Selim, MD, MACE.
Future Intelligent Devices
• A high glucose can be analyzed to
determine the magnitude of the error
April 1, 2016
69. Shahjada Selim, MD, MACE.
Future Intelligent Devices
• New dose recommendations based on A1c,
% of TDD given as correction boluses, and
frequency of hypoglycemia
April 1, 2016
70. Shahjada Selim, MD, MACE.
Future Intelligent Devices
• Pattern alerts and advice
April 1, 2016
71. Shahjada Selim, MD, MACE.
Future Intelligent Devices
• Fast lab results without calling. Messaging allows
physician to make recommendations.
April 1, 2016
72. Shahjada Selim, MD, MACE.
Pump Plus Continuous Monitor
• Automatic basal and bolus testing
• Trends allow exact short-term BG
predictions for rapid recognition of
pending highs or lows
• Both user and device can relate problems
to their source
Unfortunately, insulin delivery from an
external pump is too slow to create an
effective artificial pancreas with this
combination
April 1, 2016
External controllers like these will be preferred by some users. For instance a cell phone could deliver a bolus discretely to a pump worn under clothing, or a PDA could hold a massive carb and nutrition database for someone who eats a wide variety of food, or who is on a sodium or phosphorous restricted diet.
Devices can come in all forms. Not yet in production, this is my design for an intelligent insulin pen which accurately delivers increments as small as 0.1 unit, calculates carb and correction doses, tracks bolus-on-board (BOB), predicts where the blood glucose will go when sufficient BG test data is available, communicates easily via a Bluetooth connection, and suggests the best time to begin eating after a meal bolus has been given, such as alerting the user when an elevated premeal blood glucose has reached a preselected value, such as 150 mg/dl (8.3 mmol).
The dial to the right of the LCD scrolls through the choices on the LCD, and the button to its right will select that choice or the button to the left of the LCD will move the previous screen.
This is a simple example of how some of today’s pumpers deal with excess Bolus on Board at bedtime. This person has a 2 unit excess of bolus insulin even though their bedtime reading is slightly high at 150 mg/dl (8.3 mmol). To compensate, they use a temporary insulin reduction to remove 2 units from their basal delivery. This eliminates the need for a bedtime snack if the basal has been correctly set. This could be done automatically by today’s pumps.
An intelligent device could provide precise estimates about when a basal reduction would work. For instance, in a situation where the BG is 90 mg/dl (5 mmol), but the amount of BOB suggests that the BG will drop too far before a reduction in basal delivery could begin to offset this drop, an intelligent device would not offer a basal reduction as an option for treatment and instead suggest how many carbs will be required to counter the BOB.
The Super Bolus borrows basal to pay bolus. By stacking insulin at the time of a bolus, more insulin becomes available sooner. The corresponding reduction in basal delivery prevents hypoglycemia.
Although this is a fairly straightforward idea, some testing will be required. Pump companies have already done testing to determine how long a basal delivery can be reduced or suspended before occlusions become more common, and research has already been done on the decay in insulin action after basal delivery is suspended.
Use of a Super Bolus to lower high blood sugars increases the velocity to goal and reduces glucose exposure greatly.
This simple concept is brilliant and was brought to my attention by a Roche employee (call me with your name please!) after a presentation I gave for them. Ideally, all meals would be started 20 to 30 minutes later to allow insulin, which has almost no effect on the blood glucose for the first 20 minutes, to begin to work before the quick impact of a meal begins.
An intelligent device takes this further. A pump or device has all the data it needs to predict where the blood glucose will be up to 4 or 5 hours later and can alert the user to test their BG at the time they are likely to cross a certain desired threshold.
This is why a smart timer is important. The A1c level rises higher the more we are exposed to glucose. Here, a pumper finds they have a BG of 300 mg/dl (16.7 mmol) before a meal. Should they eat right away? The “area under the curve” above reveals glucose exposure when a timer alerts the user to begin eating when their blood glucose has reached 100 mg/dl (5.6 mmol) as shown in blue, compared to if they begin to eat right away shown in red (plus green plus blue).
Here, a Suger Bolus is added for a faster drop in the glucose level, while a Smart Timer sounds when they have likely reached 120 mg/dl. They can then retest their glucose to ensure it is OK to eat. An intelligent device would also use this second BG test to check its own accuracy and check over time to ensure the basals and boluses are correctly set.
Screen shots from an intelligent device showing a simple reminder on top that today’s pumps could do, and on the bottom more detailed information provided by an intelligent device that predicts what the blood glucose level will be at a particular time or when a particular threshold will be reached.
Checking the overnight basal lets you sleep soundly. A middle of the night test clarifies how to adjust these basals.
Contains a 500 food or larger personally selected database or carbs, glycemic index, calories, fat, etc, to allow for exact determination of carb and calorie intakes. A carb bolus recommendation is made immediately after the entire meal is selected.
Carb intake can be tracked and recommendations given, such as in the top screen where a certain carb intake would be higher than the user’s preselected daily limit. The built-in food database can track total calories as well as carbs to reach a weight goal. The bottom screen shows a specific carb intake needed at that time to cover a low blood glucose, taking into account the BOB.
The user enters the intensity (based on a 1 to 10 personal scale) and duration (in 5 minute increments) of exercise or activity. The device can then make specific recommendations for carb intake or insulin dose reductions. The device can “learn” over time how to evaluate one individual’s interpretation of the intensity of their exercise from their resulting blood sugars. A timer could be automatically started to alert the user when to test during or after exercise based on the intensity and duration.
Here, the device alerts the user about an elevated current A1c value obtained via the Bluetooth connection, an excessive use of correction bolus insulin from data stored in the pen, and that low blood sugars are rare at this time from the BG record also stored in the pen. An increase in insulin doses is recommended based on the information. Entry of the Lantus or other long-acting insulin dose is done on another screen.
Here specific patterns are addressed. In the bottom screen, due to a pattern of night lows following a certain intensity and duration of exercise that day, a basal reduction of a certain percentage and duration can be recommended to prevent a night low. The device keeps track of how well this basal reduction works to make more precise adjustments in the future.
Bluetooth allows fast transfer of lab results and other information, such as this A1c result from the doctor’s office.