LMCC II Flashcards
Pregnancy Hx
-Previous pregnancies: GPA Mode of delivery Sex weight length of labour complications -Hx present pregnancy GA, EDC Bleeding, N/V -Past medical history (DM, thyroid, htn, coagulopathy) -Past gene hx -Medications Prescription and no -Family hx genetic disease, birth defects, multiple gestations -Social Smoking, ETOH, drugs Domestic violence (50% begin in pregnancy) Social support, employment/finances, hx abuse, is mother prepared to raise a child
Gestational Age
weeks from the first day of last menstrual period
Estimated date conception (date when will give birth)
LMP + 7 days - 3 months
MSIGECAPS
- Mood (depressed)
- sleep (increased, decreased, early morning awakening)
- Interest
- Guilt/ worthlessness
- Energy
- concentration/ difficulty making decisions
- appetite/weight
- psychomotor activity
- suicidal ideation
MDD
- Requires 5 of MSIGECAPS over 2 week period
- 1/5 must be loss of interest or depressed mood
Health tips while pregnant
- abstinence from eton, smoking, drugs
- use of meds only after consulting MD
- healthy eating
Abortion age limits
- Latest in Canada is at 20 weeks
- preferably earlier at 16 weeks
Abortion medical options
<12 weeks: 12 weeks: prostaglandins (intra or extra amniotic) OR misoprostol
Surgical abortions
16 weeks: dilatation and evacuation, early induction of labour
Complications of abortion
- pain + discomfort commonly
- hemorrhage
- perforation of uterus
- laceration of cervix
- risk of infection/endometritis
- retained products of conceptions
Risk factors for breast cancer
Age over 50 Sex f over m Estrogen exposure Post menopausal In utero exposure to des Hrt Early menarche Nulliparity Pregnancy at older age Personal history of breast cancer Family history Genetics: brca Lifestyle; etoh, smoking, Exposure to chest radiation
preconception counselling supplementation
Folic acid within 8-12 weeks of conception (0.4-1 mg daily, 5 mg if previous NTD, anti-epileptic meds, DM or BMI > 35) and continue for T1
Iron supplementation
Prenatal vitamins
Ensure adequate calcium/ Vit D
preconception counselling: risk modification
- lifestyle: balanced nutrition and physical fitness
- infection screening: toxo, rubella, CMV, hepatitis B, VDRL, Pap smear, gon/chlam, HIV, TB, varicella
Investigation first pregnancy visit
CBC,blood group and type, Rh antibodies
Infectious screening
Urine C and S, screen proteinuria
Pelvic exam; Pap smear, chlam/gono, bacterial vaginosis
Air travel when pregnant
Allowed into second trimmest, discouraged after 36 weeks
Exercise during pregnancy absolute contraindications
- ruptured membranes
- pre-term labour
- hypertensive disorders of pregnancy
- incompetent cervix
- IUGR
- multiple gestation (>3)
- placenta previa >28 weeks
- persistent 2/3 trimester bleeding
- uncontrolled T1DM, thyroid disease
- other serious cardiovascular, respiratory or systemic disorder
Pre-natal visit: asess at every visit
- fetal movements
- uterine bleeding
- leaking
- cramping
P/E
-BP
-weight gain
-fundal height
Investigations
-urinanalysis for glucosuria, ketones, proteinuria
-fetal heart tones starting at 12 weeks using doppler
Symphysis pubic height
12 weeks: uteirne fundus at pubic symphysis
20 weeks: fundus at umbilicus, SFH should be within 2 cm of GA btw 20-36 weeks
37 weeks: fundus at sternum
Fetal movements
First noticed at 18-20 weeks
Prenatal screening: high risk population screening test
- Thalassemia (mediterranean, south east asian)
- Sickle cell (african, caribbean)
- Cystic fibrosis
- Tay Sachs
- Fragile X syndrome
T2DM in pregnancy fact sheet
- 2-4% pregnancies complicated by diabetes
- diagnosed 24-28 weeks
Treatment for pregnancy induced DM
- lifestyle modifications
- insulin (OHG controversial)
- tight glycemic control: post-prandial blood glucose
- 1 hr post prandial <5.3,
- monitor 24 hour urine protein and creat clearance, retinal exam, hga1c
T2DM and labour
- monitor glucose q1hr
- pt should be on insulin and dextrose drip
- 3.5-6.5
Risk factors for gestational diabetes
- age >25
- obesity
- ethnicity (aboriginal, hispanic, asian, african)
- Fhx of DM
- previous hx GDM
- previous child with birthweight > 4 kg
GDM and long term prognosis
-50% risk of developing DM in next 20 yrs
Complications of DM
- Obstetric: htn/PET, polyhydramnios, pre-term, stillbirth
- Fetal: macrosomia OR IUGR, RDS (hyperglycemia interferes with surfactant synthesis), congenital abnormalities
- Mom: hypoglycemia, DKA
Defn pre-eclampsia, criteria for diagnosis
- Systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg, and
- Proteinuria ≥0.3 grams in a 24-hour urine specimen or protein:creatinine ratio ≥0.3, or
- Signs of end-organ dysfunction (platelet count 1.1 mg/dL or doubling of the serum creatinine, elevated serum transaminases to twice normal concentration)
PET investigations
MAHA picture (CBC, D-dimer, fibrinogen, blood smear, hap to, bill)
LFT
Creat
Thrombocytopenia < 100
Labour management PET
-hourly ins and outs
-urine dip q12
-hourly Neuro vitals
-continuous FHR monitoring
-anticonvulsant therapy: mag sulfate
-anti-hypertensive therapy:
hydralazine 5-10 mg IV bolus over 5 mins q 15-30 mins
labetolol 20-50 mg IV q 10 mins
2nd line: nifedipine 10-20 mg PO q 20-60 mins
ACEi contraindicated
Post partum management PET
- early admission (36 weeks)
- mag sulfate (continue mg sulfate in first 12-24 hours post partum: seizure risk increased)
- IV hydralazine
- 2nd line: labetolol
- 3rd line: nifedipine
- vitals q 1h
- most return normotensive in 2 weeks
PET symptoms P/E
- persistent headache
- sudden weight gain over 1-2 days/edema
- RUQ pain
- Persistent and/or severe headache
- Visual abnormalities (scotomata, photophobia, blurred vision, or temporary blindness)
- Nausea, vomiting
- Dyspnea
- decreased urination
Eclampsia defn
PET + CNS involvement (decreased LOC and seizures)
HELLP syndrome
variant of PET
- hemolysis
- elevated LFT
- low platelets
4 types of pregnancy-related hypertensive disorders
- preeclampsia/eclampsia/hellp
- Chronic/pre-existing htn
- pre-eclampsia superimposed upon chronic/pre-existing htn
- gestational hypertension
chronic pre-existing htn
- > 140/90
- pre-dates pregnancy OR present before 20 weeks and persists longer than 12 weeks post partum
pre-eclampsia superimposed upon chronic preexisting htn
- new onset proteinuria or other end organ dysfunction after 20 weeks
- if had proteinuria + htn before pregnancy then defined by worsening or resistant htn in last half pregnancy or development os S and S of severe spectrum of disease
Gestational htn
-htn without proteinuria or signs of PET that develops > 20 weeks and should resolve within 12 weeks post partum
Prevalence PET
7.5% pregnancies worlwide
more prevalent in first pregnancies
Late onset (>34 weeks) more common than early onset <34 weeks
10-15% of direct maternal deaths are associated with PET/clampsia
PET increased maternal risk for
- progession to eclampsia=> seizures
- stroke (hemorrhagic)
- pulmonary edema
- AKI
- hepatic failure or rupture
- DIC (bleeding problems)
- placental abruption
- maternal and fetal death (rarely)
- fetal risks: prematurity, IUGR, hypoxia
Risk factors for PET
- hx PET
- first pregnancy
- fam hx PET
- pre-existing medical conditions including DM, htn, antiphospholipid antibodies, high BMI, CKD
- twin pregnancies
- advanced maternal age
PET increases fetal risk of
- malnutrition
- hypoxia
- IUGR
- prematurity
- death
treatment PET
- delivery is curative!
- no use of antihypertensives unless BP >150/100 or symptomatic
- admit hospital 36 weeks for monitoring; may need to admit earlier with steroids and earlier delivery
Management of pregnancy induced hypertension (severe)
- control BP with IV labetolol or hydrazine (target BP <160/110)
- prevent seizures with mg so4
- delivery by induction or C section when stable with prophylaxis 24 hours post partum
Eclampsia
ABC + supplemental O2 Mg SO4 g over 20 mins then drip -If seizures occur use IV diazepam -control BP with labetolol/hydralazine -initiate delivery when mother stable
PE on EKG
S1Q3T3
Deep S in lead I
Q wave lead III
T wave lead III
Hampton hump
Peripheral wedge shaped opacity
Westermark sign
Focus of oligemia; secondary to proximal pulmonary artery dilatation and peripheral vasoconstriction (hypoxic)
Life threatening causes of CP
MI Tamponade Tension pneumothorax Aortic dissection PE Esophageal rupture
Nasal prong L translated into FiO2
2L=> 26% 3L=> 30% 4L=> 35% 6L=> 40% 40% considered maximum inspired oxygen obtainable without high flow mask such as ventimask
DTaP-IPV Diptheria Tetanus acellular Pertussis Inactivated Polio vaccine
2, 4, 6 months
18 months
DTap at 14-16 yrs
Tetanus and diptheria q 10 yrs
MMR
12, 18 months
Pneumo-C
pneumococcal 7 valent conjugated vaccine
2, 4, 6, 15
Men-C
Meningococcal C conjugate vaccine
2, 4, 6, OR 12
Var
15 months
Hep B
0, 1, 6 months
Vaccines at 2, 4, 6
DTaP-IPV + 18 + teens + adult
Men-C (6 or 12)
Pneu-C + 15 months
HiB + 18
Hib
2, 4, 6, 18
Live vaccines
MMR
Varicella
**can give to pts with CD4 > 200
Contraindications to all vaccines
moderate to severe illness +/- fever (common URTI fine)
allergy to vaccine component (yeast or gelatin?)
MMR contraindications
- allergy egg or neomycin
- pregnancy
- immunocompromised (except healthy HIV positive children)
Varicella contraindications
- Pregnancy or planning to get pregnant within 3 months
- anaphylaxis
HPV
between age 9-26 at 0, 2, 6 months
Contraindications to pertussis component
Hx of progression neuro disorder or epilepsy
Somatoform disorder (diseases)
Conversion Somatization Pain disorder Hypochondriasis Body dysmorphic disorder
Malingering
Intentional production of false or grossly exaggerated physical or psych symptoms motivated by external reward (missing work)
Factitious disorder
intention production or feigning of physical or psych signs or symptoms to assume the sick role where external incentives are absent
Conversion disorder
symptoms affecting voluntary motor or sensory function that mimic neuro disorder
-symptoms preceded by stress or conflict
(blindness, inability to speak, numbness)
Somatization disorder
recurrent multiple clinically significant complaints which result in pt seeking txt or having impaired functioning
- 4 pain sx to four different sites
- 2 GI sx (not including pain)
- 1 sexual
- 1 pseudo-neural
Pain disorder
pain as primary symptom
Hypochondriasis
- preoccupation with fear of having serious disease based on misinterpretation of bodily signs or symptoms
- belief is not delusional
Body dysmorphic disorder
preoccupation with imagined defect in appearance or excess concern around slight anomaly; usually related to face
Treatment of somatoform disorders
- brief frequent visits
- focus psychological not physical symptoms
- minimize medical investigations
- minimize psychotropic drugs; anxiolytics in short term only, antidepressants for depressive symptoms
- attend to transference and countertransference
Joints of ankle
Tibio-talar: dorsi and plantar flex
Subtalar: talar-calcenal joint
Transverse tarsal: forefoot
Talar drawer sign
laxity indicates anterior talo-fibular ligament rupture
talar tilt
transverse tarsal joint; laxity indicates tear in medial or lateral tendons (calcaneo-fibular or deltoid)
Treatment of sprains
RICE: Rest Ice Compression Elevation
Grading ankle sprain
1: stretched ligament fiber
2: partial tear with pain and swelling
3: complete ligament separation
CAGE questionnaire
Cut back
people Annoyed
Guilty
Eye-opener
HEEADSS
Home -where, with who, relations with family, recent moves, ever run away? Education -attending school? grades? failures? suspensions? future plans, goals Eating -habits, hx AN, obesity Activities -extracuricular, sports, work -best friends -social clubs -car -gangs Drugs -types/amount -with friends or alone Sexuality -dating, types experiences -contraception, pregnancies, STD -sexual abuse Suicide -self harm thoughts -prior attempts -depression
Special test for appendicitis
Psoas sign
Obturator sign
Rosving’s
Obturator sign (appendicitis)
hips and knees flexed
hold ankle and knee
internal rotation
-to identify a pelvic appendix
Psoas sign
raise leg against resistance
Rosving’s sign
palpate LLQ which produces RLQ pain
Approach to neonatal jaundice
Conjugated vs Unconjugated
Hemolysis vs no hemolysis
If hemolysis; Coombs + or negative
Conjugated Hyperbilli is ALWAYS PATHOLOGICAL
Causes of conjugated hyperbilli
Hepatic;
- infectious (TORCH)
- metabolic (lipid storage, galactosemia, hypothyroid)
- drugs
- TPN
Post hepatic
- biliary atresia
- choledochal cysts
- sepsis
- UTI
Work-up
U/S +/- HIDA scan
ALWAYS PATHOLOGIC
Causes unconjugated hyperbilli
Hemolysis
Coombs +
- ABO incompatibility
- SLE
- drug induced
- idiopathic
Coombs-
RBC defects: G6PD, hemoglobinopathy, hereditary spherocytosis, HUS
No hemolysis
- physiologic jaundice of newborn
- breast milk jaundice
- breast feeding jaundice
- Gilbert/crigler-najjar
- hypothyroid
- pyloric stenosis
- sepsis
Physiologic jaundice of newborn
- occurs at day 2-3 NEVER ON DAY 1
- resolves by 1 week (but could last a bit longer if premature)
- diagnosis of exclusion
Breast milk jaundice
- 5-7 days into breast feeding, peaks at 3 weeks
- mild unconj hyperbilli
- considered normal
- substances in breast milk increase enterohepatic circulation
Breast feeding jaundice
- failure to breast feed
- caused by decreased intake with excessive weight and fluid loss
- nutritional inadequacy causes increases EHC of bill
- change to formula, frequent feeding
- *take good breast feeding history
Txt of hyperbillirubinemia
If unconjugated
- phototherapy
- exchange RBC
W/U of hyperbilli
- LFT
- neonatal and maternal blood type
- Coombs
- Blood smear
- CBC+ retics
- septic w/u +/- CSF
Acute billirubin encephalopathy
acute rise in bill in CNS
lethargy, decreased feeding, hypotonic, high pitched cry
Kernicterus is the chronic sequelae of acute bill encephalopathy
Differential for microscopic hematuria in adults
CA Stones Infection GN BPH
Psych history
Past psychiatric hx -suicide attempts -hospitalizations -pharmacology/ECT Past medical/surgical hx (head trauma, seizures) Family psychiatric hx
Mental status exam: ASEPTIC
A: Appearance
-dress, posture, stated age, psychomotor agitation/depressionm attentive, eye contact
S: Speech
-rate (pressured or slow), rhythm, volume, tone, articulation
E: Emotions
-Mood (how do you feel?)
-Affect (how do they seem; range of expression, flattened affect)
P: Perception
-illusions (misperception of real stimulus)
-hallucination: perception in absence of stimulus
-derealization, depersonalization
T: thought process and content
-coherent, tangential, loose association
-content: suicidality/homicidality, obsessions, delusions
I: insight and judgement
-Judgement: dr’s own of patient
C: Cognition
-MMSE, intellect
Bacterial vaginosis
- grayish/white fishy discharge
- clue cells
- +whiff test (also sometimes positive in trichomonas)
- NOT sexually transmitted
- can cause PID
- Treat with metronidazole or clinda (Amox in pregnancy)
- High pH (>5)
Trichomonas
-motile trichomonads on microscopy
-STI
yellow/green frothy discharge
-Motile flagellated organisms on microscopy
-treat partner
-can cause PID
-treat with flagyl
->pH (>5)
Yeast infection
- cottage cheese d/c
- erythematous/pruritic
- high pH R/O yeast infection
Chlamydia
- Asymptomatic in 80% of women
- Muco-purulent endocervical discharge/urinary sx/pelvic pain/post coital bleeding
- Test with cervical culture/PCR/urine test
- Reportable disease
- Treat with doxy X 7 days OR azithro X 1 (safe in pregnancy)
- In pregnancy=> re-test for cleared infection 3-4 weeks after txt
Gonorrhea
- Can infect cervix, oropharynx (sore throat), anorectal area
- Txt: ceftriaxone IM or cefixime OR cipro
- if pregnant: use cephalosporins (avoid quinolones)
- treat co-infection with chlam
- Re-test in pregnancy
HSV of vulva
classically HSV-1 above belt
HSV-2 below belt
-presents 2-21 days following contact
-prodromal sx: burning, tingling, pruritus
-multiple painful shallow ulcerations with vesicles appear 7-10 days after initial infection
-lesions are infectious
-treat first episode of acyclovir 7-10 days, second episode for 3-5 days
-can use suppressive therapy if 6-8 recurrences/year
-C-section if active genital lesion
-suppression therapy for pregnant women with first episode or hx HSV from 36 weeks on
Grading muscle strength
0-no contraction
1-visible muscle twitch but no movement of joint
2-weak contraction insufficient to overcome gravity
3-weak contraction able to overcome gravity with no additional resistance
4-weak contraction able to overcome some resistance but not full resistance
5-normal able to overcome full resistance
Reflex grading
0-no reflex 1-trace reflex 2-normal reflex 3-very brisk 4-clonus
Hoffman reflex
Upper motor Babinski
Flick index finger downwards and watch for reflex flexion of thumb
C4 dermatome
below mandible to clavicle (neck anterior and posterior)
C5 dermatome
Strip on medial arm not including hand
C6 dermatome
Strip on external arm (lateral to C5) including thumb
C7 dermatome
Strip on outer arm including index and middle finger
C8 dermatome
trip on lateral arm including elbow and ring and pinky fingers
muscles innervated T1
Hand intrinsics
Adduction of fingers
Adduction/abduction of thumb (involves T1 and C8)
Muscles innervated by C5
Deltoids
Biceps
Weakness
- shoulder abduction
- elbow flexion
Muscles innervated C6
Biceps
Wrist extensors
Weakness
- flexion
- wrist extension
Muscles innervated C7
Triceps
Wrist flexors
Finger extension
Weakness
- triceps
- wrist flexion
Muscles innervated C8
Finger intrinsics
Thumb ad/abduction (C8/T1)
Weakness hand grip
Thumb abd/adduction
Median nerve sensory innervation
Palmar aspect: thumb, indexm, middle and medial half of ring
Dorsal aspect: distal half of index, middle fingers and medial half of distal ring
Radial nerve sensory innervation
Dorsal aspect of hand including thumb and proximal 1/2 index and middle
Ulnar nerve sensory innervation
Palmar aspect: hypothenar eminence, pinky and distal half of ring finger
Dorsal aspect: proximal half/lateral half middle finger, wring finger and pinky
Motor innervation median nerve
thenar muscle
flex at metacarpophalangeal joints of index and middle finger
motor innervation of ulnar nerve
flexion/adduction wrist
flexion fingers
intrinsic muscles of fingers
Damaging ulnar nerve
commonly occurs with medial epicondyle fracture
Classic sign: can flex wrist but is accompanied by abduction, cannot abduct fingers, cannot grip pager
Tinel’s sign
tap on palmar surface of wrist + if elicits shooting parasthesias in median nerve distn
Phalen’s sign
maximally flex both wrists but pushing the dorsi of hands together for 30-60 sec+ if elicits median nerve distribution numbness/paresthesias
Exam for pt with new petecchiae
Skin, nails for nutritional status Stigmata liver disease Liver/spleen size/tenderness Lymphadenopathy Lungs for effusions Thyroid exam (high association with ITP)
NO RECTAL EXAM GIVEN RISK OF BLEEDING
Blood tests Thrombocytopenia
R/O plt clumping CBC, coags, LFT Blood smear Hemolytic w/u R/O infection (HIV, Hep)
TXT of BPH
Proscar (finasteride) (5 alpha reductase blocker)
Flomax (alpha blocker)
Referral to urology for TURP
When should an LP be performed in the setting of a febrile seizure
- if meningeal signs on exam
- if vaccination status of strep pneumo of Hib uncertain
- if on antibiotics since can mask signs and symptoms of meningitis
Defn Febrile seizure
- age 6 months -18 months (typically btw 12-18)
- convulsions associated with T >38
- no CNS infection/inflammation, no metabolic cause
- no hx of afebrile seizures
Simple febrile seizures
- last less than 15 minutes
- have no focal features
- occur once in a 24-hour period.
Complex febrile seizures
- last >30 mins
- focal neuro symptoms
- occur >1 in 24 hours
Prognosis febrile seizure
- 2/3 never have another febrile seizures
- 1/3 will have further febrile seizures
- 3% will go on to have seizures without fever
- 2% develop lifelong epilepsy
W/U febrile seizures
- Chem 7/CBGM
- CBC
- Cultures
- imaging with CT/EEG indicated only in specific situations
Txt febrile seizures
- treat seizure lasting > 5 mins with lorazepam (0.05-0.1 mg/kg)
- Tylenol
- use of anti epileptics for complex seizures should be individualized
Dysphagia solids vs liquids
Solids indicate mechanical obstruction
Liquids indicate neuromuscular dysfunction (often occurs swallowing either liquids or solids)
Approach to esophageal dysphagia
Solids
- mechanical obstruction
- intermittent: esophageal ring
- Progressive: if chronic heartburn indicates peptic sricture, if B sx malignant
Liquids/Solids
- suggests motor dysfunction
- Intermittent: DES
- Progressive: scleroderma, achalasia
W/U esophageal dysphagia
Barium swallow (diagnose stricture or achalasia) Manometry if concern re achalasia Endoscopy
Secondary causes of Htn
Primary renal disease Vascular -Renovascular disease (RAS) -Coarctation aorta Endo -Renin/Aldo -Hypercortisolism -Pheochromocytoma -Hyperthyroidism
Test coarctation aorta
BP UE>LE
brachial-femoral delay
Diagnosis of HTN
1) First visit:
- take three readings, discard first and average 2/3
- If BP >140/90: schedule visit two within 1 month
2) 2nd Visit
- If BP >180/110 diagnose HTN
- If BP > 140/90 AND evidence of macro vascular target organ damage, DM, CKD diagnose HTN
Diagnose HTN if
-BP >160/100 averaged across first three visits
OR
-BP>140/90 averaged across five visits
ABPM
- if mean awake SBP >135, DBP >85
- mean 24 hours SBP >130/80
Home BP measurement
- >135/85 average
Htn urgency
BP >180/110 often with mild headache
No signs of acute end organ damage
-reduction of BP gradually over hours to days
-can use Acei, Lasix, clonidine acc uptodate
-rapid BP lowering not recommended in pts with known aortic or intracranial aneurysm (BP lowering over course of hours); arguably pts high risk for stroke or MI also
Diagnosis HTN on ABPM
awake BP >135/85
OR
mean 24 hour BP >130/80
Examples of target organ damage in HTN
- CVA
- Vascular dementia
- htn retinopathy
- LV dysfunction/hypertrophy
- CAD/angina/CHF
- renal disease/albuminuria
- PAD/claudication
Hx of extra-intestinal manifestations of IBD
- iritis/uveitis
- arthritis
- mouth ulcers
- anal ulcers
- skin lesions
- kidney stones
HTN emergency
BP >180/110 with evidence of end organ damage; Cerebrovascular -Htn encephalopathy, ICH/SAH Cardiac -acute aortic dissection/LV failure/MI/after CABG Renal -Acute GN, post kidney transplant, MAHA Eclampsia
Arcus senilis
evidence of familial hypercholesterolemia in the eyes
Guidelines to ECHO pts with a symptomatic heart murmurs
- diastolic murmur
- continuous
- late systolic murmur
- murmurs associated with ejection clicks
- murmurs that radiate to the neck or back
- grade 3 or louder mid peaking systolic murmurs
- Other indications (class IIa): associated with abnormal physical findings, associated with abnormal ECG or CXR
Qualifying heart murmurs
Intensity (grade I-VI)
Pitch (high or low, rumbling, blowing, musical)
Configuration (shape; cresc/decresc)
Location
Timing (midsystolic, holosystolic, early or late systolic, continuous)
Grading murmur
I: faint, heard with difficulty
II: faint
III: moderate
IV: associated with palpable thrill
V: loud but cannot be heard without stethoscope
VI: loud and can be heard without stethescope
Timing of systolic murmurs
Midsystolic: begins after S1 and ends before S2 (both S1S2 audible)
Holosystolic: obscures both S1S2
Early systolic: obscures S1, audible S2
Late systolic: starts after S1, obscures S2
Timing of diastolic murmurs
Early diastolic: begins with A2/P2 and extends into diastole for variable duration Mid diastolic: starts after S2 terminates before S1 Late diastolic (presystolic) starts well after S2 and extends to S1
Continuous murmur
begins in systole and continues through diastole without interruption, encompassing S2
Mid systolic murmurs, causes
Most often benign
-Flow murmurs: increased flow rate across normal semilunar valve (thyrotoxicosis, pregnancy, anemia) or aortic valve sclerosis
-ASD with left to right shunting
Benign if NOT associated with other cardiac signs
Diff’ll holosystolic murmur
MR
TR
VSD
MR
Holosystolic best heard in left lateral decubitus with bell stethoscope Blowing/high pitch Apex Radiate to axilla/scapula Increases with manoeuvres that increase LV volume ex leg raising or when after load increases (squatting, handgrip) Decreases with valsalva or with standing little respiratory variation
TR
Holosystolic
Diaphragm
Left lower sternal border
Murmur increases with increased venous return; inspiration, leg raising
Decreases with standing (decreasing venous return)
c-v wave JVP, pulsatile, increase with inspiration due to increased in venous return (Kussmaul)
VSD
holosystolic
loud, can be associated with thrill
LL sternal border
Late systolic murmur
MVP
TVP
Ischemic MR
MVP
- late systolic
- diaphragm
- apex
- -usually preceded by single or multiple clicks
- murmur increases with increasing preload (squatting, elevation legs, hand grip)
early diastolic murmur
AR
Pulmonic regurgitation
Mid diastolic murmur
MS
TS
Inspiration as it portends to right and left sided venous return
Increases right sided and decrease left sided venous return
Increases right sided murmurs (TR, PR)
Decreases murmur of MVP
Abrupt standing as it portends to heart murmurs
Decreases venous return to heart
Decrease intensity AS
Decrease MR/TR
Increases HCM
Squatting as it portends to heart murmurs
Increase venous return (preload) with increased after load
- Increases MR (after load)
- Increases VSD
- decreases HCM (after load increases effective orifice size of outflow tract)
HCM
crescendo-decrescendo murmur
apex and LLSB
radiate axilla and base, usually not to neck
Increases by increasing obstruction; squatting to standing, valsalva
Decreases by attenuation of obstruction; handgrip, passive elevation of legs
Valsalva
Decreases venous return to both right and left ventricle
- Decreases AS, MR and TR
- increases HCM (decrease LVOT with decrease venous return)
hand grip
increase SVR, increase LV volume
Most useful to differentiate AS v MR
AS: decrease
MR: increase
AS
- systolic
- RUSB
- harsh
- crescendo/decrescendo
- radiates carotids/clavicle
- musical radiation to apex (gallaverdin)
OPQRST hx
Onset Progression/provoking Quality Radiation Severity Timing Relieving/exacerbating
Hx of spinal stenosis
Pain worse with activity, resolves with rest
Pain worse lying down
Lower extremity dermatomes
L2-L1 Upper thigh Inner lower leg L3: Inner thighs over medial knee L4: Medial to calf L5: dorsal foot (plantar foot) S1: outer foot
Low back pain history
- OPQRST
- Neuro sx: weakness, parasthesias
- bladder/bowel incontinence
- B symptoms
- Infectious sx
- trauma
- arthralgias, skin lesions
LBP exam
Observation:
- Gait, toe walk (S1), heel walk (L4L5 weakness)
- observe back for scoliosis, kyphosis
Palpate: spinuous processes, paraspinals, deeper into facet joint areas
- PSIS: transition lumbar to S1 joint
- sacroiliac joint
Passive ROM:
- forward bending/extension
- lateral flexion
- straight leg raise
Motor
- Hip flexors (flex/ex/int/ext rotation)
- Knees
- Ankle
Neuro
- reflexes
- sensory (test dermatomes)
- Babinski
- Ankle clonus
- saddle anasthesia
- rectal tone
Vascular
Peripheral pulses
Quads
L234
Hamstrings
L4L5S1S2
plantar flexion: Anterior tibili
L4L5
Toe extension
extensor hallucis longus
L5
Ankle eversion
S1