A 51-year-old man presented to the emergency department with sudden onset of left-sided weakness, severe headache, slurred speech and left facial droop. His blood pressure was extremely elevated at 260/172. Imaging showed he had suffered a right basal ganglia hemorrhagic stroke. His history of poorly controlled hypertension due to non-adherence to medications was likely a major contributing factor to his stroke.
High prevalence of hypertension in older persons (nearly one of two subjects aged >60 years). It is a significant and often asymptomatic chronic disease. HTN is a major cause of morbidity and mortality among aged. Hypertension in older adults is generally defined by SBP ≥ 140 mmHg or DBP ≥ 90 mmHg over two clinic visits (systolodiastolic HTN)
Isolated systolic hypertension (ISH): SBP of ≥140 with a DBP of <90 mm Hg.
The recognition and treatment of HTN should be a priority among elderly. Controlled, RCTs have shown that treatment of hypertension decreases the incidence of complications in older adults.
It heterogeneous metabolic disorder characterized by common feature of chronic hyperglycemia with disturbance of carbohydrate fat and protein metabolism.
High prevalence of hypertension in older persons (nearly one of two subjects aged >60 years). It is a significant and often asymptomatic chronic disease. HTN is a major cause of morbidity and mortality among aged. Hypertension in older adults is generally defined by SBP ≥ 140 mmHg or DBP ≥ 90 mmHg over two clinic visits (systolodiastolic HTN)
Isolated systolic hypertension (ISH): SBP of ≥140 with a DBP of <90 mm Hg.
The recognition and treatment of HTN should be a priority among elderly. Controlled, RCTs have shown that treatment of hypertension decreases the incidence of complications in older adults.
It heterogeneous metabolic disorder characterized by common feature of chronic hyperglycemia with disturbance of carbohydrate fat and protein metabolism.
Recommendation 1
In the general population aged ≥60 years, initiate pharmacologic treatment to lower blood pressure (BP) at systolic blood pressure (SBP) ≥150 mm Hg or diastolic blood pressure (DBP) ≥90 mm Hg and treat to a goal SBP <150><90><140><60><90><60><140><140><90><140><90 mm Hg. (Expert Opinion – Grade E)
Recommendation 6
In the general nonblack population, including those with diabetes, initial antihypertensive treatment should include a thiazide-type diuretic, calcium channel blocker (CCB), angiotensin-converting enzyme inhibitor (ACEI), or angiotensin receptor blocker (ARB). (Moderate Recommendation – Grade B)
Recommendation 7
In the general black population, including those with diabetes, initial antihypertensive treatment should include a thiazide-type diuretic or CCB. (For general black population: Moderate Recommendation – Grade B; for black patients with diabetes: Weak Recommendation – Grade C)
Recommendation 8
In the population aged ≥18 years with CKD, initial (or add-on) antihypertensive treatment should include an ACEI or ARB to improve kidney outcomes. This applies to all CKD patients with hypertension regardless of race or diabetes status. (Moderate Recommendation – Grade B)
Recommendation 9
The main objective of hypertension treatment is to attain and maintain goal BP. If goal BP is not reached within a month of treatment, increase the dose of the initial drug or add a second drug from one of the classes in recommendation 6 (thiazide-type diuretic, CCB, ACEI, or ARB). The clinician should continue to assess BP and adjust the treatment regimen until goal BP is reached. If goal BP cannot be reached with 2 drugs, add and titrate a third drug from the list provided. Do not use an ACEI and an ARB together in the same patient. If goal BP cannot be reached using only the drugs in recommendation 6 because of a contraindication or the need to use more than 3 drugs to reach goal BP, antihypertensive drugs from other classes can be used. Referral to a hypertension specialist may be indicated for patients in whom goal BP cannot be attained using the above strategy or for the management of complicated patients for whom additional clinical consultation is needed. (Expert Opinion – Grade E)
1. Resistant Hypertension, complications, Target organ damage2. newly diagnosed stage-1 hypertension, rationale of use of ARB and comparison of Azilsartan with other ARBs3. Hypertension with bronchial asthma 4. Hypertension with Diabetes Mellitus with proteinuria5. Hypertension , Diabetes and IHD6. Gestational Hypertension , rationale of use of drugs7. Hypertension , Diabetes , ACS8. Hypertension, Diabetes and Syndrome X9. Hypertension and special situations
CME Sohag | internal medicine | Diabetes mellitusEmad Qasem
CME Sohag | internal medicine | Diabetes mellitus training session 22 may 2016 By Dr. Ahmed othman Abodooh, assistant lecturer of internal medicine, Sohag university
Hints about tuberculosis , Epididymis anatomy and functions, Epididymis infection with TB, Incidence, Clinical picture and complications of it, Hints about the diagnosis and treatment
Presented in the department of Urology, Sohag school of medicine
New trends in treatment of Infantile hemangiomaEmad Qasem
A short presentation about papers published in 2014 ( about 1050 research ) showing new modalities of treatment of infantile hemangioma.
Regression of role of corticosteroids, Progression of Propranolol role and Restriction of role of surgery are the most prominent points
A Case report of Hypothyroidism associated with cutaneous hemangioma is also explained inside
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
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
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
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.
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
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.
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
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.
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.
3. Case (1)
36 y/o white female
PMH
− Recently returned to work 10
weeks after the birth of first child
− Family history of diabetes
− No history of smoking
5. What is her BP stage?
normotensive
prehypertension
stage 1 hypertension
6. What is her BP stage?
normotensive
prehypertension
stage 1 hypertension
7.
8. What do you recommend
now?
A. Diet and lifestyle modification
B. Begin drug therapy
C. Ask her to come back for a BP
recheck in one week.
D. All of the above.
E. A & C
9. What do you recommend
now?
A. Diet and lifestyle modification
B. Begin drug therapy
C. Ask her to come back for a BP
recheck in one week.
D. All of the above.
E. A & C
10.
11. week Follow-up She returns in a
week. She’s begun a daily exercise
program and her BP on return is
138/88 mm Hg. What is the correct
diagnosis?
A. Normal BP
B. Prehypertension
C. Stage 1 hypertension
D. Not sure
12. 1-week Follow-up
she returns in a week. She’s begun a daily
exercise program and her BP on return is
138/88 mm Hg. What is the correct diagnosis?
A. Normal BP
B. Prehypertension
C. Stage 1 hypertension
D. Not sure
13. Treatment Alternatives, What is
the best treatment for her at this
point?
A. Diet and lifestyle modification,
and regular
follow-up of her BP
B. Drug therapy
C. Both of the above
D. Have her fill out her “bucket
list” and enjoy the
last year of her life.
14. Treatment Alternatives
What is the best treatment for Vicki
at this point?
A. Diet and lifestyle modification,
and regular follow-up of her BP
B. Drug therapy
C. Both of the above
D. Have her fill out her “bucket
list” and enjoy the
last year of her life.
18. RECOMMENDATIONS
1-5 –address questions 1 and 2 concerning
thresholds and goals for BP treatment.
6,7,8 – address question 3 concerning selection of
antihypertensive drugs.
9 – summary of strategies based on expert opinion
for starting and adding antihypertensive drugs.
19. Case 2
MR Ali is 70 year old ,complaining
from headache ,no evidence of
D.M,or CKD his blood pressure is
145/90 at the first reading then
140/85 at the second reading.
20. What will you do?
A- Start antihypertensive drug.
B-Diet modification and follow up
C-both A,B
21. What will you do?
A- Start antihypertensive drug.
B-Diet modification and follow up
C-both A,B
22. RECOMMENDATION 1
In the general population aged ≥60 years,
initiate pharmacological treatment to lower BP at
SBP of ≥150 mm Hg or
DBP of ≥ 90mm Hg and
treat to a goal
SBP < 150 mm Hg and
DBP <90 mmHg.
Strong recommendation – Grade A.
23. Corollary
Recommendation
In the General Population aged ≥60 yrs,
If pharmacological treatment for high BP results in
lower achieved SBP (for example <140 mm Hg) and
treatment is not assosciated with adverse effects on
health or quality of life, treatment does not need to be
adjusted.
Expert opinion – Grade E.
24. Case 3
MR Hemdan is 50 year old
,complaining from headache ,no
evidence of D.M,or CKD his blood
pressure is 145/90 at the first
reading then 140/90 at the second
reading.
25. What will you do?
A- Start antihypertensive drug.
B-Diet modification and follow up
C-both A,B
26. What will you do?
A- Start antihypertensive drug.
B-Diet modification and follow up
C-both A,B
27. RECOMMENDATION 2
In the general population < 60 yrs,
Initiate pharmacological treatment to lower BP
at DBP of ≥90 mmHg and
treat to a goal
DBP of lower than 90 mmHg.
For ages 30-59 years,Strong recommendation -Grade A.
For ages 18-29 years.Expert opinion –grade E.
28. DBP trials
HDFP(Hypertension Detection and Follow uP)
Hypertension – Stroke Cooperative
MRC
ANBP
VA Cooperative
Treatment to a lower DBP goal lower than 90 mm Hg reduces
cerebrovascular events,HF,overall mortality.
No benefit of treatment to a target DBP of 80,85 mm Hg compared to 90
mm Hg – HOT trial(not statistically significant in outcomes).
29. RECOMMENDATION 3
In the General Population younger than 60years,
initiate pharmacological treatment to lower BP
at SBP of ≥140 mm Hg and
treat to a goal SBP of < 140 mm Hg.
Expert opinion – Grade E.
30. Case 4
MR khaled admitted to hospital with
generalized body swelling and
decrease in urine output on
examination he has genealized
anasarca and his BP 135/85,he has
albumin+++ in urine and his 24 hr
urinary protein is 5000 mg with
serum creatinine is 3.2 mg/dl
31. What will you do?
A- Start antihypertensive drug.
B-no need to start
32. What will you do?
A- Start antihypertensive drug.
B- no need
33. RECOMMENDATION 4
In the Population aged 18 years or older with CKD,
Initiate pharmacological treatment to lower BP at
SBP of ≥ 140 mm Hg
or
DBP of ≥ 90 mmHg
and
treat to goal
SBP of < 140 mm Hg and
DBP < 90 mm Hg.
Expert opinion – grade E.
(Younger <70 yrs with eGFR or measured GFR <60 ml/min/1.73m2
People of any age with albuminuria >30mgalb/g of creatinine)
34. RECOMMENDATION 5
In the Population aged 18 years or older with diabetes,
initiate pharmacological treatment to lower BP at
SBP of ≥ 140 mm Hg or
DBP of ≥90 mm Hg
and treat to a
goal SBP < 140 mm Hg
goal DBP < 90 mm Hg
Expert opinion Grade E.
35. Back to MR ALI
MR Ali is 50 year old ,complaining
from headache ,no evidence of
D.M,or CKD his blood pressure is
145/90 at the first reading then
140/90 at the second reading.
36. With what you will start?
A-Thiazide diuretics
B-BB
C-loop diuretics(Lasix)
D-Aldomet
37. With what you will start?
A-Thiazide diuretics
B-BB
C-loop diuretics(Lasix)
D-Aldomet
38. RECOMMENDATION 6
In the General NonBlack population,including those with Diabetes,
initial AntiHypertensive treatment should include a
Thiazide -type Diuretic,
Calcium Channel Blocker(CCB),
Angiotensin Converting Enzyme inhibitor(ACEI),or
Angiotensin Receptor Blocker(ARB).
Moderate recommendation –GradeB.
39. Not recommended as first line drugs
Dual alpha1 +b blocking agents (Carvedilol)
Vasodilating b blocking agents (Nebivolol)
Central a2 adrenergic agonists (Clonidine)
Direct vasodilators (Hhydralazine)
Alodsterone receptor antagonists (Spironolactone)
Peripherally acting adrenergic antagonists (Reserpine)
Loop diuretics(Furosemide)
ONTARGET trial was not eligible because Hypertension was not
required for inclusion in the study.(Telmisartan,Ramipril).
40. RECOMMENDATION 7
In the General Black population,
including those with Diabetes,
initial antihypertensive treatment should include a
thiazide – type diuretic or CCB.
For general black population:Moderate Recommendation –GradeB.
For black patients with diabetes:Weak recommendation –GradeC.
41. RECOMMENDATION 8
In the population aged 18 years or older
with CKD and hypertension,
initial (or add-on) antihypertensive treatment should include
ACEI or ARB to improve kidney outcomes.
This applies to all CKD patients with hypertension regardless
of race or diabetes status.
Moderate Recommendation – GradeB.
42. What if patient is a black and having CKD?
In black patients with CKD and proteinuria,an ACEI or ARB is
recommended as initial therapy because of the higher likelihood
of progression to ESRD. AASK trial.
JAMA.2002;288(19):2421-2431
In black patients with CKD but without proteinuria,the choice
for initial therapy is less clear and includes a thiazide- type
diuretic,CCB,ACEI or ARB.
ACEI /ARB can be used as an initial drug or second line drug.
43. Case 5
Fahmy Amer
55 y/o male presents for follow-up.
Past Medical History
− Blood pressure on initial presentation was 160/95,
now 15o/90
− Non-smoker, no known CAD
− Fasting glucose 140 mg/dL (repeated from previous
visit, when it was 142 mg/dL); A1C: 8.2%
− Initial therapy: Diet modification, increased exercise,
and started 25 mg of HCTZ
44. Next action?
A. Continue dietary modification and
exercise recommendations
B. Begin therapy with an ACEi, ARB, or
CCB
C. Refer to dietitian for diet counseling
D. Begin metformin
E. All of the above
F. A & B only
45. Next action?
A. Continue dietary modification
and exercise recommendations
B. Begin therapy with an ACEi, ARB,
or CCB
C. Refer to dietitian for diet
counseling
D. Begin metformin
E. All of the above
F. A & B only
46. 2-Week Follow-Up
Mr. Amer returns, having visited with the dietitian
and is trying to implement his recommendations.
He has started walking daily. His BP at this visit is
140/90; 2hr postprandial glucose is 126 mg/dL.
What should we consider next?
A. Increase the dose of the ACEi/ARB or CCB
B. Consider additional up-titration or new
medications for diabetes, High BP or cholesterol as
needed.
C. Initiate a dose of aspirin, if not already started
D. All of the above
47. 2-Week Follow-Up
Mr. Amer returns, having visited with the dietitian
and is trying to implement his recommendations.
He has started walking daily. His BP at this visit
is 136/84; 2hr postprandial glucose is 126 mg/dL.
What should we consider next?
A. Increase the dose of the ACEi/ARB or CCB
B. Consider additional up-titration or new
medications for diabetes, High BP or cholesterol
as needed.
C. Initiate a dose of aspirin, if not already started
D. All of the above
48. 1-Month Follow-Up
Mr. Amer returns for follow-up.
His BMI is 29;
2hr postprandial glucose is 92
mg/dL;
HgA1c is 6.8% and his BP is 120/75.
55. RECOMMENDATION 9
If goal BP is not reached within a month of treatment,
Increase the dose of the initial drug or
add a second drug from one of the classes in recommendation6 (thiazide-
type diuretic,CCB,ACEI,ARB).
If goal BP cannot be reached with 2 drugs,
add and titrate a third drug from the list provided.
Donot use an ACEI and ARB together in the same patient.
If goal BP cannot be reached using the drugs in recommendations, because
of a contraindication or the need of > 3 drugs to reach goal
BP,antihypertensive drugs from other classes can be used.
Referral to a hypertension specialist.
Expert opinion –GradeE.
56.
57.
58.
59.
60. Case 6
51 year old man admitted to an
outside hospital
CC: Sudden onset of left-sided
weakness, severe headache, slurred
speech and left facial droop
BP 260/172
Head CT Scan showed Right basal ganglia
hemorrhage with shift
HPI: Transported by ambulance to
SUH.
Intubated en route due to declining
mental status
61. Case 6
PMH - Hypertension - according to
wife, patient was non-adherent
with prescribed medications
Out patient medications and allergies -
not available
Family History +for HTN/CVA
Exam SUH - BP 196/130
Positive for Left dense hemiparesis
62. Case 6
Hospital day 2
Dilated right pupil
Emergent right frontotemporal
craniotomy and evacuation of clot
Subsequent Hospital Course
Difficult to control BP
Pneumonia
65. Question 1
What is the primary reason for
hypertensive emergencies today?
1. Renovascular Disease
2. Pheochromocytoma
3. Non-adherence to anti-hypertensive
medication
4. Hyperaldosteronism
5. Erythropoeitin
66. What is the primary reason
for hypertensive emergencies
in the USA today?
1. Renovascular Disease
2. Pheochromocytoma
3. Non-adherence to
anti-hypertensive
medication
4. Hyperaldosteronism
5. Erythropoeitin
10
67. Hypertensive Emergency
According to the Joint National
Committee on Hypertension Report
Severely elevated blood pressure with
signs and symptoms of acute end organ
damage
Requires hospitalization
Requires parenteral medication
68. Hypertensive Urgency
Severely elevated blood pressure
without signs and symptoms of
acute end organ damage
Can be managed as an outpatient
Can be managed with oral
medications
71. Etiology
Essential hypertension : Inadequate blood pressure control and noncompliance are
common precipitants (MOST COMMON)
Renovascular
Eclampsia/pre-eclampsia
Acute glomerulonephritis
Pheochromocytoma
Anti-hypertensive withdrawal syndromes
Head injuries and CNS trauma
Renin-secreting tumors
Drug-induced hypertension
Burns
Vasculitis
Post-op hypertension
Coarctation of aorta (very rare)
2nd common
72. Question 2
What is the most common complaint in
hypertensive emergency?
1. Neurologic defect
2. Gross Hematuria
3. Chest pain
4. Headache
5. Epistaxis
73. What is the most common complaint
in hypertensive emergency?
1. Neurologic defect
2. Gross Hematuria
3. Chest pain
4. Headache
5. Epistaxis
74. Clinical Presentation
Variable
Zampaglione et al (Hypertension
27:144, 1996)
14, 209 ER visits in one year period
108 met definition of hypertensive
emergency (0.8%)
Mean Systolic BP 210 + 32
Mean Diastolic BP 130 + 15
75. Clinical Presentation
Frequency of signs and symptoms
Chest Pain 27%
Dyspnea 22%
Neuro defect 21%
Interestingly….
Headache was only 3% and epistaxis was 0%
in this study
76. Question 3
Hypertensive emergency is associated with
a threshold BP of
1. Systolic > 225 mm Hg
2. Diastolic > 110 mm Hg
3. Systolic > 250 mm Hg
4. Diastolic > 120 mm Hg
5. All of the above
77. Hypertensive emergency is
associated with a threshold
BP of
1. Systolic > 225 mm Hg
2. Diastolic > 110 mm Hg
3. Systolic > 250 mm Hg
4. Diastolic > 120 mm Hg
5. Non of the above
78. Threshold BP
There is no specific BP where hypertensive
emergencies occur
But, organ dysfunction is rare with diastolic
BPs < 130 mm Hg
Rate of increase may be more important
Hence, encephalopathy will occur at lower BPs
in pregnancy and in children
79. Initial Evaluation
Focused history
History of hypertension?
How well is hypertension controlled?
What antihypertensives?
Adherence to antihypertensive regimen?
Last dose of antihypertensive?
81. Initial Evaluation
Confirm BP in both arms
Use appropriate sized BP cuff
Cuff that is too small
BP cuffs that are too small falsely
elevate BP measurements in
obese patients
82.
83. Initial Evaluation
Assess for end-organ damage
Vascular Disease
Assess pulses in all extremities
Auscultate over renal arteries for bruits
Cardiopulmonary
Listen for rales (CHF)
Murmurs or gallops
86. Lab Testing
Aortic Dissection?
Suspect with severe tearing chest pain, unequal
pulses, widened mediastinum
Contrast Chest CT Scan or MRI
Pulmonary Edema/CHF
Transthoracic Echocardiogram
Differentiate between systolic dysfunction,
diastolic dysfunction, mitral regurgitation
87. Management
Elevated BP without target organ
damage
Hypertensive urgency
Oral meds
Goal - gradual reduction of BP over
24 - 48 hours
88. ORAL DRUGS FOR HTN
URGENCIES
Drug Initial dose Onset duration Adverse effects
89. Management
Elevated BP with target organ
damage
Hypertensive emergency
Parenteral meds
Goal - Reduce diastolic BP by 10-
15% or to 110 mm Hg over a period
of 30 - 60 minutes
90. GOAL reduce MAP by no more than 20-25%,
DBP to 100-110mm Hg within few minutes to 2 hours.
More aggressive and rapid BP reduction (Acute
Pulmonary edema ,Aortic dissection)
More slowly for acute cerebrovascular damages with
monitoring of neurological status.
Constant infusion of intravenous agents required (no
intermittent IV boluses/oral/sublingual drugs- drastic
BP fall).
91. Normalisation of BP is usually not
recommended*
How fast and how much BP to be lowered to be given importance.
92. Why ??
Sudden fall in BP may cause acute hypoperfusion of vital organs
and results in myocardial ischemia or infarction, hemiplegia,or
acute renal failure.
Older patients with long lasting hypertension and preclinical organ
involvement (LVH, atherosclerosis and arteriolar remodelling) are
at risk of these complications as the lower limit of autoregulation
shifted to right.
93. Management
Where?
ICU with close monitoring
Severe requires intra-arterial BP
monitoring
Which Parenteral meds?
Depends on the situation
94. Question 4
Which of the following drugs should not be
used to treat hypertensive emergency?
1. Sublingual Nifedipine
2. Labetolol
3. ACE Inhibitors
4. Nicardipine
5. 1 and 3
95. Which of the following drugs should not
be used to treat hypertensive
emergency?
1. Sublingual
Nifedipine
2. Labetolol
3. ACE Inhibitors
4. Nicardipine
5. 1 and 3
97. Sodium nitroprusside
Potent short acting arterial and venous dilator
(reduces pre- and after- load)
Rapid onset of action.(seconds)
Continuous intra-arterial BP monitoring required.
Infusion chamber and tubing to be covered.
intracranial pressure (caution in intracerebral hemorrhage)
Induces coronary steal (non selective coronary vasodilation)
Increases mortality in pts with acute MI. (NEJM,1982)
Thiocyanate toxicity (nausea,vomiting,lactic acidosis and altered mental status)
Usually rare, seen in pts with renal ,hepatic dysfunction.
98. Fenoldopam
A peripheral dopamine-1 receptor antagonist (DA1). {highly
specific}
10 –fold more potent than dopamine as a renal vasodilator.
Antihypertensive effect by combined natriuretic and vasodilatory effect
(esp. intrarenal arteries)
Not to be used as prophylactic agent for preventing CIN
(CAFCIN Trial)
Agent of choice in hypertensive emergencies assosciated with renal
dysfunction.
Adv effects – hypotension ,hypokalemia
99. Nicardipine
Second generation DHP CCB.
Strong cerebral and coronary vasodilation.
Onset of action 5-15 min, Duration being 2-6 hrs.
Increases both stroke volume and coronary blood flow with a favourable effect on
myocardial oxygen balance.
CAD with Systolic HF. C/I in Aortic stenosis.
Dosage independent of weight.
Infusion rate of 5mg/h – 2.5 mg/h increments every 5 min –max being 15 mg/h.
IV Nicardipine maintained BP in Treatment range > IV Labetalol (CLUE trial)
J Emerg Med 1987:5:463-473
100. Clevidipine
Third generation, intravenous, dihydropyridine caclium channel
antagonist.
FDA approval (2008)
Ultra short half life of about 1 min.
Potent arterial vasodilation (no effect on venous capacitance,
myocardial contractility)*
No significant adverse effect on heart rate’.
Injectable emulsion.
99.9% bound to protein.
Safe in pts with renal,hepatic dysfunction.
C/I –allergies to soy products,eggs and egg products,defective lipid
metabolism.
*Rivera et al .,2010,Polly et al 2011.
50mg/100ml
101. Dosage
•An IV infusion at 1–2 mg/hour is recommended for initiation and
should be titrated by doubling the dose every 90 seconds.
• As the blood pressure approaches goal, the infusion rate should be
increased in smaller increments and titrated less frequently.
•The maximum infusion rate for Cleviprex is 32 mg/hour.
•Most patients in clinical trials were treated with doses of 16 mg/hour
or less.
No more than 1000 mL (or an average of 21 mg/hour) of Cleviprex
infusion is recommended per 24 hours..
Am J Cardiovascular Drugs 2009;9;117-134
102. Labetalol
Combined selective 1 adrenergic and non selective β
adrenergic receptor blocker (1:7).
Hypotensive effect – in 2-5 min after IV admin.
Maintains cardiac output (unlike other BB).
Reduces SVR, but does not decrease PBF.
Cerebral,renal,coronary blood flow maintained.
Less placental transfer can be used in pregnancy induced HTN
emergency.
Metabolised by liver.
Oral/IV.
103. Esmolol
Ultrashort acting cardioselective β adrenergic blocking agent.
Ideal β blocker in critical cases.
Useful in severe postoperative HTN.
Onset of action is within 60 sec
Duration of action being 10-20min.
Rapid hydrolysis of ester linkages by RBC esterases(metabolism), not
dependent on renal or hepatic function.
0.5 to 1mg/kg loading dose over 1min,followed by an infusion -
50ug/kg/min.(max 300ug/kg/min)
104. Not to use
Sublingual NifedipineDrug is poorly soluble, not absorbed through buccal mucosa
Sudden uncontrolled and severe reductions in BP,may precipitate
cerebral,renal and myocardial ischemic events.
Lack of clinical documentation attesting to a benefit from its use.
The Cardiorenal Advisory Committee of the FDA has concluded “that
the practice of administering SL/oral nifedipine should be abandoned
because this agent is not safe nor efficacious”.
.
106. CVA or Ischemic Stroke
BP elevation after CVA or ischemic
stroke can be protective to preserve
cerebral perfusion
Hold on aggressive lowering unless
Thrombolytic therapy anticipated or
BP excessively high ( SBP > 220 mm Hg or
DBP >120)
BP Goal for thrombolytic therapy is to
lower SBP if > 185 or DBP >110
110. Sympathetic Crisis
Generally in association with
recreational drugs such as cocaine,
amphetamine or phencyclidine
Sudden cessation of clonidine or
Beta-adrenergic antagonist
Pheochromocytoma - rare
111. Question 5
Which of the following drugs should be
avoided in sympathetic crises with
hypertensive emergency?
1. Phentolamine
2. Benzodiazepine
3. Labetolol
4. Nicardipine
5. Fenoldopam
112. Which of the following drugs should be
avoided in sympathetic crises with
hypertensive emergency?
1. Phentolamine
2. Benzodiazepine
3. Labetolol
4. Nicardipine
5. Fenoldopam
113. Sympathetic Crisis
Beta-adrenergic antagonists will result in
unopposed alpha-adrenergic stimulation
In cocaine use, Beta blockers can
Increase blood pressure
Worsen coronary artery vasoconstriction
Decrease survival
Avoid beta blockade (including non selective
agents such as labetolol)
115. Aortic Dissection
Treatment is paramount
75% of patients with ascending aortic
dissection die in 2 weeks of the acute
episode without successful therapy
5 year survival is 75% with successful
intervention
Khan et al. Chest 2002, 122:311
Kouchoukos New Engl J Med 1997; 336:1876
117. Aortic Dissection
Standard therapy
Beta-adrenergic blocker plus
vasodilator
Esmolol + Nicardipine or
fenoldopam
Nitroprusside can be used as
well
118. Acute Post Operative Hypertension
Frequent in post-operative state (20-75%)
Hyper-responsiveness to surgical trauma
Increased stress hormones?
Activation of RAA?
Also hypothermia, hypoxia, carbon dioxide
retention, bladder distention
119. Acute Post Operative Hypertension
Prevention
Safe to give antihypertensives pre-op
Hold diuretics
Treatment - BP thresholds vary
Control pain and anxiety
While NPO use nicardipine, esmolol or
labetolol
Resume oral medications when possible