Sample Notes - The Osler Institute Board Review Courses

The Osler Institute
Excellence in Continuing Medical Education
“The Best of Series” Family Medicine Syllabus
DAY 1
Anemia RX and DX
Antibiotic Choices
Alternative Medicine
Evidence Based Medicine
Doctor Patient Interaction
Hypertension
Pain Management
Diabetes Mellitus
Maintenance of Certification
Test Taking Skills
Acid Base and Electrolytes
Renal Failure
Anticoagulation
Gyn Infections I and II
Abnormal Vaginal Bleeding
Menstrual Disorders and Menopause
DAY 4
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Reid Blackwelder
Evelyn Figueroa
Evelyn Figueroa
Evelyn Figueroa
DAY 2
Geriatric Nutrition
Vitamins and Minerals
Abuse and Neglect
Urinary Incontince
Delirium
Dementia
Mgt of Geriatric Behavioral Problems
Geriatric Pharmacology
Geriatric Screening and Prevention
Parathyroid
Thyroid
Growth and Growth Disorders
Adrenal and Gonadal Disorders
Common Eye Problems
Brian Krause
Brian Krause
Brian Krause
Brian Krause
Brian Krause
Brian Krause
Brian Krause
Eron Manusov
Eron Manusov
Eron Manusov
Eron Manusov
Eron Manusov
Eron Manusov
Eron Manusov
Eron Manusov
DAY 5
Larry Johnson
Larry Johnson
Larry Johnson
Larry Johnson
Larry Johnson
Larry Johnson
Larry Johnson
Larry Johnson
Larry Johnson
William Bryant
William Bryant
William Bryant
William Bryant
David Stager Jr
DAY 3
Fibromyalgia
Preventative Medicine
Congestive Heart Failure
Obstructive Sleep Apnea
Skin Disorders
Rheumatic Syndromes
Hyperlipidemia
Ped Exanthems
Adolescent Gynecology I and I
Infertility & ART
Contraception
Osteoporosis
Urinary Tract
Statistics and Epidemiology
HIV Testing and Counseling
Primary Care Management of HIV
Psychiatry I (Medical Psychiatry)
Psychiatry II (Psychopharmacology I)
Psychiatry III (Psychopharmacology II)
Psychiatry IV (Psychopharmacology III)
Psychiatry V (Psychiatric disorders)
Psychiatry VI (Substance Abuse)
Psychiatry VII (Ethics)
Pediatric Orthopedics
Hand and Wrist Injuries
Questions and Answers
Shoulder Pain
Foot and Ankle
Electrocardiograms
Cardiac Arrhythmias
White Cell Disorders
Signs, Symptoms and Evaluation,
and Cystic Fibrosis
Asthma and RSV Bronchiolitis
COPD
Restrictive Lung Disease
Sexual Assault
Breast Disease I and II
Pelvic Pain Evaluation I and II
Other OB Topics I and II
Neurology I
Neurology II
John Saito
John Saito
John Saito
John Saito
Robert Kauffman
Robert Kauffman
Robert Kauffman
Robert Kauffman
Ajay Gupta
Ajay Gupta
DAY 6
William Geiger
William Geiger
William Geiger
William Geiger
William Geiger
William Geiger
William Geiger
William Geiger
Melvin Thornton
Melvin Thornton
Melvin Thornton
Beth Fox
Beth Fox
Abass Hyderi
Abass Hyderi
Abass Hyderi
Peripheral Vascular Disease
Acute Coronary Syndrome
Trauma Assessment
Lower Back Problems
Sports Medicine
Mouth and Esophagus
GERD and Dyspepsia and Peptic Ulcers
GI Cancers
Small Bowel Disorders
Colitis and Colonic Diseases
Liver Disease and Cirrhosis
Pancreatitis and Pancreatic Cancer
Acute Abdomen
Palliative and End of Life Care
Cancer Detection
Eric Coris
Eric Coris
Eric Coris
Eric Coris
Eric Coris
Leslie Smith
Leslie Smith
Leslie Smith
Leslie Smith
Leslie Smith
Leslie Smith
Leslie Smith
Leslie Smith
Lenny Salzberg
Lenny Salzberg
Questions or comments on this or any other Osler products please contact us at (800)356-7537 or [email protected]
The Osler Institute
Excellence in Continuing Medical Education
“The Best of Series” Family Medicine Syllabus
Reid B. Blackwelder , MD
Professor & Director of Med Student Education
ETSU Quillen College of Medicine
Robert P. Kauffman , MD
Professor of Obstetrics and Gynecology
Texas Tech University HSC School of Medicine
William P. Bryant , MD
Assistant Professor
Children's Hospital at Scott and White
Brian D. Krause , MD
Psychiatrist
Private Practice
Eric E. Coris , MD
Professor
USF College of Medicine
Eron G. Manusov , MD
Director,
Family Medicine Residency
Southern Regional AHEC
Evelyn Figueroa , MD
Associate Program Director
University of IL
Hosp & Health Sciences System
Beth A. Fox , MD
Associate Professor
ETSU Quillen College of Medicine
William J. Geiger , MD, FAAFP
Professor
Medical College Of Wisconsin
Ajay Gupta , MD
Associate Professor of Neurology
Cleveland Clinic Foundation
Abbas Hyderi , MD, MPH
Associate Professor
University of IL Hospital & Health Sciences
System
Larry E. Johnson , MD, PhD
Assoc. Professor of Geriatrics & Family Med.
University of Arkansas
John Saito , MD
President & CEO
Pulmonary & Sleep Disorder Consultants
Lenard Salzberg , MD
Associate Director
Family Medicine Residency
Southern Regional AHEC
Leslie C. Smith , MD, MS, MA
Professor
University of IL
David Stager, Jr , MD
Assistant Clinical Professor of Ophthalmology
Children's Medical Center
Melvin H. Thornton II , MD
Associate Professor of OB/GYN REI
Columbia University
Review of Anemias
Reid B. Blackwelder, M.D.
([email protected])
Professor Family Medicine
East Tennessee State University
Goals
Review the terminology used to discuss
anemias
Address clues in the history and exam that can
direct the evaluation
Describe one approach to using lab tests
to suggest a diagnosis
Review some aspects of treatment of
common anemias
Definitions
Normal values vary according to age and
gender (and lab)
On the boards, you will always be given the
normals in parentheses
Definitions
Anemia refers to a reduction in the number
or volume of RBCs to less than a normal
level.
May occur due to:
Acute/chronic blood loss
Decreased production
Breakdown of blood (hemolysis)
Definitions & Interpretation
Specific lab values must be interpreted in
context of patient and illness
Are Hgb levels of 14.0 in a male smoker, or
of 12.5 in a severely volume contracted
woman, "normal”?
Clinical context and condition of patient
determine urgency of Dx and Rx
But the boards will not try to trick you!
1
Indices
MCV (mean corpuscular volume)
Useful index for distinguishing anemias
If homogenous RBC population
Normal MCV 82-97 fL
Macrocytosis > 97 fL
Microcytosis < 82 fL
Peripheral Smear
Spherocytes/Ovalocytes
Sickle cells
Schistocytes
Traumatic hemolysis
Prosthetic valve
DIC
TTP
Hemolytic-uremic
syndrome
Indices
RDW (red blood cell distribution width)
If elevated, indicates variability of RBC
(anisocytosis)
Unreliable value in diagnosis
Peripheral Smear
"Teardrop" cells
Bone marrow disease
(fibrosis, tumor)
Oval macrocytes and
hypersegmented polys:
Megaloblastic anemia
Immature (blast) cells
Leukemia
History Associated with Anemia
“Evaluation of Anemia”
Evaluation of a Patient with Anemia
Patient, not Disease-centered
Presence of Inherited Anemia
Spherocytosis, ovalocytosis
Hemoglobinopathy
Presence of Chronic Illness
Chronic infection
Diabetes
Hypothyroid, renal, hypoadrenal
Collagen vascular diseases
Malignancy
2
Social Hx Associated with Anemia
Nutritional
Strict vegan (B12)
Few fruits/veggies (folate)
Alcohol use (folate, marrow suppression, liver
disease)
Symptoms attributable to anemia alone
History Associated with Anemia
Surgery
Partial or total gastrectomy
Medications can cause
Bone marrow depression
Hemolysis (G-6-PD deficiency)
Review of Systems
Pregnancy & Menses
Symptoms suggesting undiagnosed medical
problem
Physical findings
Pallor of oral mucosa/conjunctiva
Usually not present until Hgb level less than 7-8
g/dl
No correlation between level and signs/symptoms
Often not present if anemia develops slowly
Physical findings – Volume Status
Orthostasis
Baseline tachycardia
Widened pulse pressure
Flow murmurs
Flat neck veins
Decreased urine output
Decreased turgor
Palmar crease pallor suggests hgb <7 g/dl
Fun fact to amaze students with your wisdom
Physical findings - Skin
Jaundice (hemolysis)
Petechiae/ecchymoses (bleeding disorders)
Lymphadenopathy (malignancy/infection)
Glossitis, macroglossia (pernicious anemia)
Angular cheilitis (Fe deficiency)
3
Physical findings - Neurologic
Paresthesias
Dementia
Ataxia
Decreased proprioception/vibration sense
(pernicious anemia)
Laboratory Tests
Approach varies greatly depending upon
reference, anecdotal experience,
circumstances, etc
Regardless of approach, have a rationale
Recognize the difference between patient in
office vs in hospital (usually acutely ill)
Try not to "shotgun" (though we all do it!)
Absolute Reticulocyte Count
Abs Retic Count = Retic Count x RBC
Abs retic count < 100,000 suggests defect in
RBC production
Abs retic count > 100,000 suggests acute
bleeding or hemolysis
Physical findings
Heme positive stool (GI loss)
Splenomegaly
Hemolysis
Sequestration
Malignancy
One Approach
CBC
Peripheral smear
Check retic count
Various Pearls
Serum Fe
Negative acute phase reactant
Decreases with any stress (fever, etc)
TIBC
Only elevated in Fe deficiency
Also a negative acute phase reactant
% Saturation
Decreases in both Fe def and ACD
4
Various Pearls - Ferritin
Proportional to body's iron stores
Generally both increase with age
Less than 16-35 ng/dl suggests depleted stores
If older than 65, less than 45 ng/dl
Even though it is a positive acute phase reactant,
must have Fe to elevate.
Can have ferritin of 50-60 ng/mL and still have
Fe-deficiency
Bone marrow iron stores: "gold standard"
Potential Evaluation
Pathway
Microcytic Anemia (MCV < 82fL)
Suspect Anemia
Check CBC, peripheral smear, Retic count
Evaluation of Microcytic Anemia
MCV, Abs Retic Count
Microcytic Anemia
MCV < 82fL
Ferritin Level
Low
Normal or High
Check serum Fe
Low
Normal or High
Fe Deficiency Anemia
AOCD
Check serum lead
High
Normal
Hgb Electrophoresis
Lead Toxicity
Check Ferritin level
Low value (generally<30 ng/mL) suggests/confirms
iron def
Normal or high value - check serum iron
Serum Fe
Low Fe - anemia of chronic disease (ACD)
Normal or increased - check serum lead level
Lead Level
High - lead toxicity
• Anemia is late sequellae, by the way
Normal - do Hgb electrophoresis
Thalassemia
Thalassemia, Other
Fe-Deficiency vs.
Anemia of Chronic Disease
s
Fe-Def
Serum Fe (40-150 mcg/dl) Low
TIBC(Transferrin)(200-400µg/dl)
High
% Sat (Fe/TIBC) (16-60%) Low
Ferritin: m: 16-200 ng/ml
f: 4-160 ng/ml
Low
ACD
Low
Nl or Low
Low
Causes of Iron-Deficiency Anemia
Increased need
Pregnancy
Normal growth
Nl or High
5
Causes of Iron-Deficiency Anemia
Causes of Iron-Deficiency Anemia
Decreased Intake or Absorption
Increased blood loss
Childhood
Gastric surgery
Achlorhydria
Celiac sprue
Fe-Deficiency Anemia
10-25% young women
1% men
Up to 10% elderly
10-20% pts w/Fe def anemia have CA
Up to 50% pts have GERD/PUD
GERD, PUD, gastritis
Inflammatory Bowel Disease
Malignancy
Menstruation
Treatment
Retic count up by 2 weeks
Anemia corrected by 6 weeks
4-6 months to correct depleted Fe stores
Fe-Def vs AOCD?
To distinguish Fe-def vs. AOCD in an
elderly ill patient
Consider empiric trial of Fe replacement.
Be sure to follow retic and Hgb
If no change in 2-3 weeks, stop Fe
Potential Evaluation
Pathway
Normocytic Anemia (MCV 82-97 fL)
6
MCV 82-97 fL
Evaluation of Normocytic Anemia
Corrected Abs Retic Count
Changes of Marrow failure
Yes
No
Bone Marrow
Bx
ACD
Check Corrected Absolute Reticulocyte
Count
High
Low or Normal
LDH, Haptoglobin
Normal
Response to
Blood loss
Abnormal
If Low or Normal…
Any changes suggesting marrow failure?
Coombs
Positive
Negative
Hemolytic Dz
Splenomegaly
No
Yes
Hypersplenism, Drug,
Infection, Hemoglobinopathy
Evaluation of Normocytic Anemia
Any changes suggesting marrow failure?
Yes
Do bone marrow biopsy
• Myelodysplasia
• Infiltrative disease
• Aplastic anemia
Evaluation of Normocytic Anemia
Corrected Absolute Reticulocyte Count…
High:
Check LDH, haptoglobin
Normal - can be expected response to blood
loss
Abnormal - check Coombs
No
Dx is AOCD
Evaluation of Normocytic Anemia
Corrected Absolute Reticulocyte Count…High:
Any splenomegaly?
Yes - Check RBC morphology and Coombs
Negative Coombs - hypersplenism, drug effect,
infection, hemoglobinopathy
Positive Coombs - hemolytic disease
No
Hemolytic disease
Causes of Normocytic Anemia
Decreased RBC production
Bone marrow failure
Aplastic anemia
RBC destruction/loss
Acute blood loss (may be occult)
Hypersplenism
Hemolytic anemia
7
Hemolytic anemia
Anemia of Chronic Disease - Rx
Intrinsic RBC anomalies
If AOCD, iron replacement doesn't help and
may be detrimental
Consider erythropoietin therapy
Spherocytosis
G6PD defects
Hemoglobinopathies
Check epo levels, iron studies
Provide Fe as well
May or may not be appropriate Rx now
Extrinsic factors
Mechanical
Infectious (DIC)
Autoimmune antibodies
Goal Hgb level 10-12
Higher increases morbidity and mortality
MCV >97fL
Evaluate smear for megalocytes
Present
Examples of Evaluation
Pathways
Macrocytic Anemia (>97 fL)
Absent
Megaloblastic Anemia
Non-Megaloblastic Anemia
Check B12, Folate
Abs Corr Retic Count
Low
Normal
High
Low or Normal
Deficiency
Drug, Idiopathic
Liver/Thyroid Dz
Schilling’s
Bone Marrow Bx
Hemolytic Dz
Acute Blood Loss
Hypersplenism
No
Yes
Aplastic Anemia
Evaluation of Macrocytic Anemia
Look for macrocytes, hypersegmented polys
If Present - Megaloblastic anemia
Check B12, Folate levels
One or both low - deficiency (replace)
If levels normal - consider due to drug or
idiopathic
• Referral for eval, bone marrow
Evaluation of Macrocytic Anemia
Look for macrocytes, hypersegmented polys
If Absent - Non-megaloblastic anemia
Review Abs Corrected Retic Count
8
Evaluation of Macrocytic Anemia
If Absolute corrected Retic Count is:
Low or Normal
Eval for liver disease, hypothyroidism
If absent, aplastic anemia
High
Hemolytic disease
Acute blood loss
Hypersplenism
Evaluation of Macrocytic Anemia
The most common cause of macrocytosis?
Alcohol
Transfusion
Avoid transfusion "triggers"
Plan for autologous blood if possible
Administer
unit-by-unit
based
on
reassessment
Transfuse to relieve symptoms related to
blood loss when other replacement has
failed
Evaluation of Macrocytic Anemia
Many drugs can cause macrocytosis without
megaloblasts
Phenytoin
OCs
Methotrexate
Barbiturates
TMP-SMX
Zidovudine
Treatment of Macrocytic Anemia
Must be tailored to cause
Discontinue offending drugs/agents
Replacement
Folic acid: 1 mg/d
Vit B12
• 1000 microgram/d IM for 5 days, then
weekly until Hct normal, then monthly for
life (medical myth)
• Studies suggest po replacement as effective
Closing Clinical Pearls
Remember to put the numbers into the
clinical context
Labs done on ill patients in the hospital are
different than in an outpatient evaluation
Try not to shotgun
Or at least admit we are doing it!
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A Clinical Approach to
Antibiotic Use
Reid Blackwelder, MD
Professor, Family Medicine
James H. Quillen College of
Medicine
Goals
Review how to choose an antibiotic
Discuss the factors involved in this
dance
Review antibiotic classes (not all)
Consider specific indications
Review adverse reactions
Suggest some selections based on
particular infections
Choosing an Antibiotic
Identify the organism!
Or at least consider the most likely ones
This can seem unimportant
Clinical “Pathways” or “Protocols” make
decisions for you
Gram stains seem less commonly used
It requires a good history, exam and
clinical thinking
Clinical Decision Making
If you are uncertain about exactly
what antibiotic to prescribe…
Challenge yourself to think or write
down the most likely organism…
And the clinical context
This is a dying art!
The History and Exam
Still the most likely ways to help
prioritize likely causes, and what the
boards use most!
1
The History –
Likely Cause of Pneumonia for…
Shaking chill and rust-colored sputum
Pneumococcal
A farmer who delivered a sick calf,
with myalgias, fever
Q fever
2 weeks of illness with onset of sore
throat, cough
The Physical Exam –
Likely cause of Pneumonia if…
A vesicular lesion on the tympanic
membrane in a patient with an
atypical presentation
Mycoplasma
The black necrotic lesion of ecthyma
gangrenosum
Pseudomonas
Mycoplasma
The Lab (Gram stain) –
Likely cause of Pneumonia if…
Gram positive lancet-shaped
diplococci
Strep Pneumoniae
Large gram positive bacilli
Klebsiella
Small pleomorphic gram negative
coccobacilli
Haemophilus influenzae
Boards and Practice
Obviously, these skills are critical in
your daily practice
Patients usually present with less
than the “classic” history or physical
findings
Board questions are much more likely
to present a “typical” picture
Pharmacokinetics
The antibiotic must be able to reach the
site of infection at adequate
concentration
Not all antibiotics can reach the prostate
Skin infections
Meningitis
And do so not to fool you
2
As a class, Penicillins are:
Bactericidal
Inhibits cell wall mucopeptide
synthesis
Penicillin G
Drug of choice for
Syphillis
Neisseria meningitidis
Pasteurella multocida
Actinomyces
Active against most anaerobes
Not useful against
Penicillin G
Drug of choice for streptococcus
Resistance becoming an issue
Broad penetration into tissues
Main ADR is allergy
Aminopenicillins
Ampicillin, Amoxicillin
Activity
Less active against streptococci
Improved gram-neg activity
Active against H. flu
Gram negative organisms
H. Influenzae
Penicillinase resistant Penicillins
Oxacillin, nafcillin, methicillin
Drug of choice for S. aureus
As a class, Cephalosporins are:
Bactericidal
Inhibit cell wall mucopeptide synthesis
Not MRSA
Less active against strep, anaerobes
3