Please find the power point on Gestational Diabetes Mellitus (GDM) . I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
Please find the power point on Gestational Diabetes Mellitus (GDM) . I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
This talk was delivered for postgraduates and faculty of Dr. TMA Pai Hospital, Udupi on 07 March, 2017. This talk covered pathophysiology, screening, diagnosis, complications and management of diabetes mellitus in pregnancy.
Gestational diabetes mellitus (GDM) is a condition that develops during pregnancy when the body is not able to make enough insulin. GDM affects 2-10% of women during pregnancy.It is important to recognize and treat gestational diabetes as soon as possible to minimize the risk of complications to mother and baby.
Gestational diabetes Mellitus is defined as:
“Glucose intolerance of any severity with onset or first recognition during pregnancy”
This definition is applicable irrespective of whether the condition resolves after delivery or not.
It does not exclude the possibility that diabetes could have antedated pregnancy.
Diabetes during Pregnancy - Risk Factors, Detection, & TreatmentAshutosh Pandit
Diabetes during pregnancy can severely affect the health of both - mother & baby. Find out the symptoms and complications of Gestational Diabetes and learn how it can be detected & treated.
An intensive material on recent advances on contraception including the current contraceptive methods and a brief overview on immunocontraception and contraceptive vaccines
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 talk was delivered for postgraduates and faculty of Dr. TMA Pai Hospital, Udupi on 07 March, 2017. This talk covered pathophysiology, screening, diagnosis, complications and management of diabetes mellitus in pregnancy.
Gestational diabetes mellitus (GDM) is a condition that develops during pregnancy when the body is not able to make enough insulin. GDM affects 2-10% of women during pregnancy.It is important to recognize and treat gestational diabetes as soon as possible to minimize the risk of complications to mother and baby.
Gestational diabetes Mellitus is defined as:
“Glucose intolerance of any severity with onset or first recognition during pregnancy”
This definition is applicable irrespective of whether the condition resolves after delivery or not.
It does not exclude the possibility that diabetes could have antedated pregnancy.
Diabetes during Pregnancy - Risk Factors, Detection, & TreatmentAshutosh Pandit
Diabetes during pregnancy can severely affect the health of both - mother & baby. Find out the symptoms and complications of Gestational Diabetes and learn how it can be detected & treated.
An intensive material on recent advances on contraception including the current contraceptive methods and a brief overview on immunocontraception and contraceptive vaccines
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.
Systems approach,Principles of Adult learning & Learning process in Medical E...anitasreekanth
MEU WORKSHOP:Changing trends in the societal attitude calls for change in the medical education curriculum in India so that an INDIAN MEDICAL GRADUATE is of global significance
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.
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!
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stockrebeccabio
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stock
Telegram: bmksupplier
signal: +85264872720
threema: TUD4A6YC
You can contact me on Telegram or Threema
Communicate promptly and reply
Free of customs clearance, Double Clearance 100% pass delivery to USA, Canada, Spain, Germany, Netherland, Poland, Italy, Sweden, UK, Czech Republic, Australia, Mexico, Russia, Ukraine, Kazakhstan.Door to door service
Hot Selling Organic intermediates
- 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
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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
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
3. DEFINITION of GDM
• Any amount of carbohydrate intolerance diagnosed for the
first time during pregnancy
• It can be a PRE EXISTING DM or GESTATIONAL DM
• How to differentiate?
Do HbA1C….If > or equal to 6.5% it is pre existing
DM,FBS>126mg%,RBS>200mg%............OVERT
DIABETES
90% GDM & 10%PREXISTING DM
4. GESTATIONAL DIABETES MELLITUS
• Hyperglycemia during pregnancy that is not chronic
diabetes
• Hyperglycemia diagnosed for the first time during
pregnancy
• May occur anytime during pregnancy but most likely after
24 weeks
5. PREVALENCE
• 22 million women between 20 to 39 yrs have diabetes-
2010 data
• Expected to rise by 20 percent in next 10 years
• Women with IGT or pre diabetes have the potential to
develop GDM if they become pregnant
• In India prevalence is 1% to 14%percent
• GDM is more prevalent in urban areas compared to rural
areas
• Almost 50%will develop OVERT DM in next 10-15 years
• GDM leads to diabetes & obesity in the offspring
6. EFFECT OF PREGNANCY ON
GLUCOSE METABOLISM
• PREGNANCY IS A DIABETOGENIC STATE
• HPL,E,P,CORTISOL & ENZYME INSULINASE
• HPL,E,P & Cortisol cause insulin resistance
Increased insulinase activity destroys insulin
Pregnancy unmasks DM in latent diabetic subjects.
90% of women show increased insulin secretion to counter
this insulin resistance.
Those 10% show insulin resistance.
Basically GDM unmasks chronic beta cell function of
pancreas.
11. RISK FACTORS FOR GDM
• Age >30yrs
• BMI >25kg/m2.Obese patients
• Family history of DM in first degree relatives
• Ethnicity:Prevalent in South Asians
• Previous OH:H/O GDM in prev pregnancies,Stillbirth,Repeated
miscarriages,Macrosomic baby,Unexplained perinatal loss
• Recurrent vaginal candiasis or polyhydramnios in present
pregnancy
12. MATERNAL COMPLICATIONS
• Early pregnancy:Spontaneous miscarriages
• Late pregnancy:PE 25%,UTI,Macrosomia,hydramnios
25%-50%
• Delivery:Preterm labour 26%, Instrumental delivery,
Traumatic delivery, CS, PPH, Maternal morbidity/mortality
• Puerperium:Infections,Lactation failure
• Long term complications:GDM in subsequent
pregnancy,DM,CVD
13. FETAL COMPLICATIONS
• DIABETIC EMBRYOPATHY:Congenital
malformations(increasing sugar levels r not favourable for
organogenesis).Risk is5% if HbA1C <8% & 25% if
HbA1C>10%
• FETAL MACROSOMIA:Shoulder dystocia,Traumatic
delivery,CS
• NEONATAL
COMPLICATIONS:Hypoglycemia,Hypocalcemia,Hypomagnese
mia,Hyperbilirubinemia,RDS,Cardiomyopathy
• Unexplained IUD:Risk is more in the last 4 to 6 weeks of
pregnancy
14.
15.
16. CAUSE OF IUD
• Uncontrolled diabetes…mat hyperglycemia….fetal
hyperinsulinemia….fetal hypoglycemia….hypoxia
• Fetal hyperinsulinemia….increased oxygen demand of
fetus
• HbA1C binds oxygen more but releases less
oxygen…fetal hypoxia
• Overt diabetes…vasculopathy…placental
insufficiency…FGR
17. HOW TO DIAGNOSE GDM.Screening
versus Diagnostic Test
• Purpose is to identify asymptomatic individuals with a high
probability of having or developing a specific disease
• UNIVERSAL SCREENING IS ADVISED FOR
DIAGNOSING GDM
18. WHOM TO SCREEN?
UNIVERSAL SCREENING IS THE OPTIMUM
APPROACH AS INDIAN WOMEN HAVE 11 FOLD RISK
OF DEVELOPING GLUCOSE INTOLERANCE DURING
PREGNANCY COMPARED TO CAUCASIAN WOMEN
19. HOW TO SCREEN?DIPSI CRITERIA
Diabetes in Pregnancy Study Group of
India
• ONE STEP APPROACH
• On 14th mar 2017,GOI asked for universal screening
• All women have to be screened at 24 to 28weeks of
gestation with 2 hrs 75 gms oral glucose
20. HOW DIPSI TEST IS PERFORMED?
• SINGLE STEP TEST
• No need to keep the patient fasting
• 75g glucose is orally administered by diluting in 300ml
water.
• Blood glucose levels are monitored after 2hrs
• If vomiting occurs within 30 minutes,the test has to be
repeated
• The threshold level of equal to or > than 140 is the cut off
for diagnosis of GDM
21. ADVANTAGES OF DIPSI
• SIMPLE,ECONOMICAL,ACCEPTABLE
• PATIENT DOES NOT NOT HAVE TO FAST
• DIPSI has got more sensitivity & negative predictive value
23. WHEN TO DO DIPSI?
• First booking visit
• 24-28 weeks[GOI/DIPSI}
• 32-34weeks{dipsi}
24. Why to do DIPSI?
• Identify & treat the patients
• Prevent diabetes in the 2 generations
25.
26. MANAGEMENT OF GDM
• Educate the patient
• Tight glycemic control.Target FBS 90mg%,1 hr PPBS
140mg% & 2nd hour PPBS 140mg%
• Monitoring the patient and the fetus
• Labour management
• Multidisciplanary
approach:obstretician,diabetologist,dietician,neonatologist
27. EDUCATING A GDM PATIENT
• DIETARY CHANGES:replace with low glycemic foods
• Discuss appropriate weight gain during pregnancy
• EXERCISE :Daily 30mins to I hour of moderate exercise
• Start with MNT
• IF UNCONTROLLED:INSULIN THERAPHY Or
METFORMIN THERAPHY(OHAs)
• Self monitoring of glucose
• Self administration of insulin
28. MNT(MEDICAL NUTRITION
THERAPHY)
• Adequate nutrition.Well balanced diet
• Adequate weight gain
• Prevention of ketosis(overt diabetes)
• Prevention of postprandial hyperglycemia
• If within 2 weeks glucose levels r not under control ..switch to
drugs
• GDM DIET-30kcal/kg/d in normal weight women,24kcal/kg/d for
overweight women & 12kcal/kg/d for morbidly obese patients
Diet should have 40%carb,30%protein & 30% fat
Usually 3 meal & 3 snacks with breakfast 10%,lunch30% &
dinner 30%,30% snacks
29.
30. TARGET WEIGHT GAIN IN GDM
• BMI<18.5kg/m29(underweight)----12.5kg-18kgs
• BMI18.5-24.9kg/m2(ideal)---11.5-16kgs
• BMI25-29.9kg/m2(overweight)--------7-11.5kgs
• BMI>30kg/m2(obese)--------5-9kgs
31. Insulin Initiation During Pregnancy
• About 50% women treated with diet alone will require additional
theraphy with insulin
• GDM patients require low doses of insulin compared to pre
existing DM patients
• Insulin is given subcutaneously
• Recombinant human insulin is most preferred
• Start with 4 units of premixed(30/70)insulin BB.Give 30mins
BB.If not controlled increase every 4th day by 2 U till 10
units.Usually they don’t need >20units
• Insulin dose has to be individualised………0.7units/kg daily
• Two thirds of insulin is administered in the morning & 1/3rd in
the evening with 1:2 ratio of short to intermediate or long acting
insulin
32.
33. Insulin options safe in pregnancy
name type onset peak duration dosage
Aspart Rapid
acting
15min 60min 2hrs Start of
each meal
Lispro Rapid
acting
15min 60min 2hrs Start of
each meal
Reg insulin Intermediat
e acting
60mins 2-4hrs 6hrs 60-90mins
before
meal
NPH Intermed
acting
2hrs 4-6hrs 8hrs Every 8 hrs
Detemir Long acting 2hrs 12hrs Every
12hrs
34.
35. OHA /INSULIN IN GDM
• Metformin or insulin can be started if MNT fails.Insulin is
the first choice & metformin can be given after 20 WOG
• Insulin can be started anytime during pregnancy
• Metformin max dose is 2g/day
36. MONITORING BLOOD
GLUCOSE(SMBG)
• Atleast 4 times self monitoring
• Fasting & three 2hrs postprandial
• If target levels r achieved,lab monitoring to be done once a
month till 28 weeks
• 28-32 weeks,lab monitoring of plasma glucose done every 2
weeks
• >32 weeks…once a week
• Do FUNDOSCOPY,MONITORING MICROALBUMINURIA
37. GLYCAEMIC TARGETS
• Mean plasma glucose of 105mg/dl
• Fasting plasma glucose at 90mg/dl & PP at 120mg/dl
• Mean plasma glucose not to go below 86
38. MONITORING DURING PREGNANCY
• FIRST TRIMESTER
• Clinical exam,Dating scan,NT scan,Double marker
test,Color doppler for prediction of PIH
• SECOND TRIMESTER
• Clinical exam,Anomaly scan,fetal 2D echo at 24 weeks
• THIRD TRIMESTER
• Clinical exam,DFKC,Growth scans at 28,32,36
weeks,Color doppler if indicated,AFI,NST(32 weeks
onward)
39. WHEN TO DELIVER?
• Deliver in a tertiary care hospital
• Timing & mode of delivery
GDM controlled on diet alone & no complications:deliver
at 40 weeks
GDM on insulin theraphy:induction at 38 weeks
Vaginal delivery is allowed if macrosomia is ruled out
Morning dose of insulin is omitted
Glucose levels r checked hourly with glucometer
IV infusion of NS started
If glucose levels <70mg%,D5 is started
If glucose levels>140mg% regular insulin is
administered in IV infusion
40. INSULIN DOSAGE IN LABOUR ACC TO
BG LEVELS
Blood glucose mg/dl Insulin dosage Iv fluids at 125ml/hr
<100 0 D5
100-140 1 D5
141-180 1.5 NS
181-220 2 NS
>220 2.5 NS
41. • If baby weight >4kgs deliver by CS
• If uncontrolled sugar levels or any other complicating
factor,deliver the fetus
• If preterm…steroids r to be given with strict monitoring of
BG levels
42. INTRAPARTUM CARE
• FIRST STAGE
• If hyperglycemia controlled on diet & spont labour…admission
CTG,PARTOGRAM,GLUCOMETER MONITORING 2
HRLY[Sugars 80 to 120}
• If hyperglycemia controlled by insulin/metformin,spont
labour…….same as above & IV fluid as per blood sugar levels
• INSTITUTIONAL DELIVERY
• EXPERT OBST
• CONTINUOUS CTG
43. • SECOND STAGE
1. Controlled ARM
2. Anticipate shoulder dystocia
3. Neonatologist
• THIRD STAGE
1. AMTSL
2. Prevent traumatic or atonic PPH
44. POSTPATUM CARE
• Careful glucose monitoring for 2 hrs postdelivery & for 48
hrs
• Regular postnatal care
• OGTT at 6 weeks postpartum
• Note:maternal insulin requirements fall significantly
immediately after delivery and continue to decline(insulin
drip can be reduced or stopped after delivery)
45. IMMEDIATE POSTPARTUM CARE
• STOP insulin AS GLUCOSE CONTROL WILL BE
ACHIEVED IN MOST WOMEN IMMEDIATELY AFTER
DELIVERY
• CONTINUE PREPRANDIAL BGL FOR 24 HRS
• IF preprandial BG 72-126…discontinue monitoring
• If BG <72 OR >126…MED OPINION
• 1-8% may be glucose intolerant & need OHAs
• Metformin,glibenclamide,glyburide r safe during lactation
46. RISK FACTORS FOR PERSISTENT
DIABETES
• Pregnant FBS >126
• Diagnosis of GDM during first trimester
• A prior history of GDM
47. MONITOR FOR PERSISTENT
DIABETES(longterm consequences)
• OGTT to be done at 6 weeks postpartum to screen for
persistent diabetes
• 50%o f GDM will develop type 2 DM within 15 yrs of
delivery
• If GDM on insulin,50% will develop type 2 DM in 5 years
• Recommended lifelong screening for diabetes every 3 yrs
• Early glucose monitoring in future pregnancy(risk of
recurrence is 30% -50%)
49. FETAL LONGTERM CONSEQUENCES
• Increased risk of developing OBESITY,DIABETES
• FETAL ONSET OF ADULT DISEASE
• GESTATIONAL PROGRAMMING:process whereby
stresses or stimuli that occur at sensitive periods of fetal
dev permanently change structure,physiology and
metabolism that predisposes individuals to diseases in
adult life.intrauterine exposure to diabetogenic
environment is risk factor fpr dev of DM in adult life.
50. CONCLUSION(KEY POINTS)
Universal testing of all pregnant women
Testing to be done twice in pregnancy..once at 1st visit &
second at 24-28 weeks
Single step test recommended
Start on MNT for patients with positive OGTT test>140mg/dl
If not controlled start on OHA or insulin
In uncontrolled diabetes or those with obstetric indication
early delivery recommended after steroid theraphy
Vaginal delivery preferred but LSCS for
macrosomia/obstetric indication
Neonatal monitoring for hypoglycemia & other
complications
Postpartum evaluation of glycemic status at 6 weeks to be
done postdelivery